jpcrd628 PDF
jpcrd628 PDF
jpcrd628 PDF
1880–2002
James S. Chickosa…
Department of Chemistry, University of Missouri-St. Louis, St. Louis, Missouri 63121
0047-2689Õ2003Õ32„2…Õ519Õ360Õ$37.50 519 J. Phys. Chem. Ref. Data, Vol. 32, No. 2, 2003
520 J. S. CHICKOS AND W. E. ACREE, JR.
Substance T/K range Vapor pressure range/Pa ⌬ vapH m 共298.15 K兲 kJ mol⫺1 Classification
a,d
C3 H8 O 1-propanol 333–378 20 E⫹3–135 E⫹3 47.45⫾0.1 Primary
C5 H12 pentaneb,d 269–315 2.0 E⫹4 –1.2 E⫹5 26.42⫾0.1 Primary
C6 F6 hexafluorobenzenea,d 290–377 7.5 E⫹3–2.1 E⫹5 35.71⫾0.07 Primary
C6 H6 benzenea,c,d 286 –383 7.0 E⫹3–2.3 E⫹5 33.83⫾0.07 Primary
C6 H14 hexaneb,d 286 –343 1.2 E⫹4 –1.0 E⫹5 31.52⫾0.13 Primary
C7 H16 heptaneb,d 299–372 6.4 E⫹3–1.0 E⫹5 36.57⫾0.15 Primary
C8 H18 octaneb,d 326 – 400 7.7 E⫹3–1.0 E⫹5 41.56⫾0.17 Primary
C9 H20 nonaneb,d 344 – 425 6.4 E⫹3–1.0 E⫹5 46.55⫾0.19 Primary
C10H8 naphthalened 353– 434 1.0 E⫹3–2.3 E⫹4 55.65⫾2.8 Secondary
C10H22 decaneb,d 268 –348 1.7 E⫹1–3.2 E⫹3 51.42⫾0.21 Primary
C11H24 undecaneb,d 294 –382 4.1 E⫹1– 6.4 E⫹3 56.58⫾0.57 Primary
C12H26 dodecaneb,d 313– 403 5.8 E⫹1–7.3 E⫹3 61.52⫾0.62 Primary
C13H28 tridecaneb,d 323– 402 4.7 E⫹1–3.7 E⫹3 66.68⫾0.67 Primary
C14H30 tetradecaneb,d 344 – 422 7.6 E⫹1– 4.4 E⫹3 71.73⫾0.72 Primary
C16H32 hexadecaneb,d 364 – 452 5.5 E⫹1– 4.7 E⫹3 81.35⫾0.81 Primary
C18H38 octadecaneb,d 312–590 1.0 E⫺1–1.0 E⫹5 91.44⫾1.83 Primary
C20H42 eicosaneb,d 344 –380 4.1 E⫺1–9.1 E⫹0 101.81⫾2.0 Primary
H2 O waterd 273–373 6.1 E⫹1–1.0 E⫹5 43.99⫾0.07 Primary
a
Reference 12.
b
Reference 13.
c
Cancer suspect agent.
d
Reference 5.
reasonably exhaustive version of these databases covering in Table 1. The temperature range, the corresponding vapor
the literature to the present has recently been published and pressures, and the recommended molar vaporization enthal-
is also available on line at http://webbook.nist.gov/ pies at T⫽298.15 K are also included in the table. Some of
chemistry/. Combined with fusion and sublimation enthalp- these reference materials are solids at T⫽298.15 K and
ies appropriately adjusted to T⫽298.15 K, vaporization en- therefore the vaporization enthalpies are hypothetical values.
thalpies ⌬ vapH m (298.15 K), complete a thermochemical The reader should consult the literature cited at the bottom of
cycle that can be used to assess the quality of the available the table to obtain the vaporization enthalpy at the tempera-
data. Application of this thermochemical cycle is illustrated ture of interest.
below. A goal of the present contribution has been to provide
an exhaustive coverage of the literature from about 1880 to
2002; regrettably however, this compilation is probably still 3. Heat Capacity Adjustments
incomplete.
Vaporization enthalpies, like their sublimation counter-
2. Reference Materials for Vaporization parts, are measurements based on mass transport and as such
Enthalpy Measurements are directly or indirectly dependent upon vapor pressure. The
vapor pressure of different liquids at a given temperature can
Calibration is a fundamental requirement in every thermo- vary many orders of magnitude. In order to obtain a reason-
chemical measurement of vaporization enthalpy. Regardless able amount of mass transport, it is frequently necessary to
of which technique is used, the measurement ultimately de- conduct these measurements at temperatures that differ sub-
pends either directly or indirectly on vapor pressure. Vapor stantially from the standard reference temperature, 298.15 K.
pressures of liquids vary over many orders of magnitude. An The actual temperature of measurement depends on the sen-
experimental technique calibrated with a standard in one sitivity of the instrument or apparatus and the properties of
pressure or temperature regime does not in itself guarantee the substance of interest. Vaporization enthalpy measure-
the same accuracy in another. Substantial variations in vapor- ments are often conducted as a function of temperature.
ization enthalpy are revealed in the tables that follow. This The magnitude of the vaporization enthalpy is dependent
variance clearly establishes the importance of documenting on temperature. Figure 1 and Eqs. 共1兲 and 共2兲 illustrate the
the accuracy of the measurements through the use of appro- origin of this temperature dependence in terms of a thermo-
priate reference materials that approximate the temperature dynamic cycle. If the heat capacities of the liquid and gas
and pressure regimes of the measurements of interest. phase are known, C p l and C p g , respectively, then the vapor-
A series of compounds have been recently proposed as ization enthalpy at T⫽298.15 K can be related to the experi-
reference materials for vaporization enthalpy.5 These have mental measurements by using Eq. 共1兲. This equation, gen-
been classified as primary, secondary, or tertiary reference erally referred to as Kirchhoff’s equation, can be used to
materials, on the basis of various criteria. The materials clas- adjust sublimation enthalpy measurements to any reference
sified as primary and secondary reference materials are listed temperature. The term T m represents either the temperature
⫹ 冕 Tm
298.15
共 C p l ⫺C p g 兲 dT 共1兲
planatory. The R terms in this table represent variable groups
and are not included in the value. Values in brackets should
be considered as tentative assignments. The use of these
⌬ vapH m 共 298.15 K兲 ⬇⌬ vapH m 共 T m 兲 group values is illustrated with the examples in Table 3. Es-
timations of C p c (298.15 K) for these compounds follow the
⫹ 共 C p l ⫺C p g 兲共 T m ⫺298.15兲 共2兲
same protocol.
over narrow ranges of temperature. Treating the heat capaci- Groups are defined on the basis of their substitution and
ties of the two phases as independent of temperature and hybridization patterns. These groups are further subdivided
integrating Eq. 共1兲 results in Eq. 共2兲. Since the magnitude of into cyclic, acyclic and aromatic categories. The estimation
the heat capacity of the gas phase is usually smaller than that of C p l (298.15 K) for propionic acid illustrates how directly
of the liquid phase 共l兲, vaporization enthalpies increase with C p values can be estimated. Identification of the appropriate
decreasing temperature. group is important. Although not shown in Table 3, the same
Experimental heat capacities for many liquids at T protocol is used for estimating C p c (298.15 K). Estimation of
⫽298.15 K are available.8 Experimental gas phase heat ca- the heat capacity of piperadine is similar. In this case it is
pacities for compounds that are liquids at T⫽298.15 K are important to use the appropriate cyclic group. Once the
unavailable and generally need to be estimated. Gas phase proper groups are identified, the estimation is direct. Di-t-
heat capacities can be calculated from statistical mechanics butyl ether is estimated in a similar fashion. Benzothiazole
or estimated by group additivity methods. A number of group illustrates the estimation of an aromatic molecule containing
additivity methods have been developed to estimate gas a heterocyclic ring. The aromatic ring carbons are selected
phase heat capacities.9,10 However, group values for some based on their substitution pattern; the sulfur and nitrogen
functional groups are not available. Equation 共3兲 is an ex- atoms of the thiazole ring are identified as cyclic atoms; the
ample of an attempt to circumvent the lack of sufficient nitrogen atom is identified on the basis of its hybridization
group values.11 The term C p l (298.15 K) refers to the heat and substitution pattern. 2-Methylcyclohexanone is another
capacity of the liquid at T⫽298.15 K. This term may either example of an estimation of a cyclic molecule. This estima-
be estimated or experimental values may be used if avail- tion includes the contributions of a cyclic carbonyl, four cy-
able. The uncertainty associated with the term in brackets in clic methylene groups, a methyl, and a cyclic tertiary me-
Eq. 共3兲 is ⫾30 J mol⫺1 共⫾2兲 thine group. The estimation of limonene illustrate an
example of a molecule that contains both cyclic and acyclic
共 C p l ⫺C p g 兲 兵 T m ⫺298.15其
double bonds. Additional examples can be found in the
⫽ 关 10.58⫹0.26C p l 共 298.15 K兲兴共 T m ⫺298.15兲 . 共3兲 literature.4,11
Heat capacities calculated according to the protocol just
The vaporization enthalpies reported in this compendium described have been used when necessary in conjunction
have not been adjusted to T⫽298.15 K unless done so by the with Eqs. 共4兲–共6兲 to adjust vaporization, sublimation, and
authors reporting the measurements. The vaporization en- fusion enthalpies to 298.15 K. These temperature adjust-
thalpies are reported at the mean temperature of measure- ments are necessary in illustrating the thermochemical cycle
ment wherever possible. This allows the reader to verify the described below. Equations 共4兲–共6兲 have been used in those
reported data and to adjust for temperature in a consistent cases where the measurements were referenced to some other
manner. Authors have applied different methods to adjust for temperature
共A兲 Group values for estimating the C p l (298.15 K) and C p c (298.15 K) of hydrocarbons.a
Hydrocarbon groups
secondary sp C 2
⫽CH2 25.8 46 2
tertiary aromatic sp C ⫽Ca H– 21.8 17.5
tertiary sp 2 C ⫽CH– 27.8 21.4 quaternary aromatic sp 2 C ⫽Ca R– 15.3 8.5
quaternary sp 2 C ⫽C– 21.7 6.9 internal quaternary aromatic C ⫽Ca R– 关16兴 关9.1兴
tertiary sp C ⬅C–H 34.3 37.1
quaternary sp C ⬅C– 28.9 15.5
J mol⫺1 K⫺1
TABLE 2. Group values ⌫ 1 and ⌫ c for estimating C p l (298.15 K) and C p c (298.15 K)—Continued
J mol⫺1 K⫺1
⫻ 共 T m ⫺298.15兲 ⫺ 关 10.58⫹0.26C p l 共 298.15 K兲兴 the two enthalpies on the right hand side of the equation.
Since fusion enthalpies of solids usually decrease when ad-
⫻ 共 T m ⫺298.15兲 . 共6兲 justed to 298.15 K, the latter contributes a smaller amount to
the sublimation enthalpy, particularly if the melting point of
the material is high. Thus an accurate vaporization enthalpy
An uncertainty 共⫾2 兲 of one third the temperature adjust-
can tolerate a less accurately determined fusion enthalpy.
ment has been associated with the use of Eqs. 共5兲 and 共6兲 in
This is fortunate since as discussed below, there is a physical
Table 4. The uncertainty has been assigned arbitrarily.
basis for variance in fusion enthalpy.
Many solids exhibit polymorphism or undergo solid-solid
phase transitions. These may occur unnoticed. Solid-solid
phase transitions occurring below T⫽298.15 K generally do
not pose a problem if the vaporization and sublimation en-
thalpy measurements are conducted at temperatures above
the phase change. Enthalpic differences between polymor-
phic forms generally tend to be small in relation to solid-gas,
liquid-gas transitions. Since the smaller ⌬ fusH m (298.15 K)
term in Eq. 共7兲 is the one affected by polymorphism, this
phenomena should not have a large effect on the quality of
the thermochemical cycle, even if the sublimation and fusion
enthalpy measurements are conducted on different polymor-
phic forms. In many cases the sublimation enthalpy mea-
sured directly should compare favorably with the sum of the
fusion and vaporization enthalpy. Yet often this is not the
case.
FIG. 2. A hypothetical molecule illustrating the different hydrocarbon groups The results given in Table 4 illustrate some of the situa-
in estimating C p . tions that can arise when constructing a thermochemical
a
See Ref. 8.
b
See Ref. 14.
cycle based on phase changes. The sublimation enthalpy of served between three of the four sublimation values.
p-nitroaniline has been measured frequently and reproduc- Acetanilide provides a different but similar example. The
ibly. The value of 共100.9⫾1.0兲 kJ mol⫺1 is the mean value of sublimation enthalpies calculated using Eq. 共6兲 are slightly
nine measurements. Two measurements of the fusion and larger than the two direct measurements. The data suggest a
vaporization enthalpy are also available. Both fusion enthal- vaporization enthalpy of 73.9 and a sublimation enthalpy of
pies are in good agreement with each other; the mean value 90 kJ mol⫺1 at T⫽298.15 K.
is reported in Table 4. Comparison of the vaporization en- The vaporization and sublimation enthalpies of
thalpies at T⫽298.15 K results in values with a 12 kJ mol⫺1 4-chlorobiphenyl have been reported a number of times. One
discrepancy. In this instance the experimental sublimation set of sublimation enthalpies cluster around 83 kJ mol⫺1 and
enthalpy falls halfway between the two values calculated by the other around 75 kJ mol⫺1. A distinction between these
Eq. 共7兲. The experimental data suggest a vaporization en- two possibilities is possible by examining the vaporization
thalpy of 85.5 kJ mol⫺1. This is an instance where the vapor- enthalpies of the isomeric 2- and 3-chlorobiphenyls 共see
ization enthalpies are in disagreement; disagreement between Table 6兲. The vaporization enthalpies of these isomeric ma-
sublimation enthalpies is the more common occurrence. terials would be expected to be similar. On this basis, a va-
Data for 1,6-hexanedioic acid represents results that are porization of around 72 kJ mol⫺1 and a sublimation enthalpy
more typical. The fusion and vaporization enthalpies have of approximately 83 kJ mol⫺1 for 4-chlorobiphenyl at T
been measured once while the sublimation enthalpy has been ⫽298.15 K is selected for 4-chlorobiphenyl.
reported three times. In this instance good agreement is ob- Benzil is a case where all the available data appear to be
TABLE 4. A comparison of experimental sublimation enthalpies and those calculated using Eq. 共6兲; enthalpies in kJ mol⫺1; C p in J mol⫺1 K⫺1 a
⌬ subH m
⌬ fusH m ⌬ vapH m ⌬ subH m ⌬ fusH m ⌬ vapH m 共298 K兲 ⌬ subH m
(T fus) T fus /K (T m /K) T m /K (T m ) T m /K C pl C pc 共298 K兲 共298 K兲 关Eq. 共6兲兴 共298 K兲a
C6 H6 N2 O2 4-nitroaniline 21.1 420.7 77.9 488 100.7 298 235.8 164.7 15.4⫾1.9 91.5⫾4.5 106.9⫾4.9 100.9
70 430 79.5⫾3.2 94.9⫾3.7
C6 H10O4 1,6-hexanedioic acid 34.85 426.4 92 447 133.6 298 302.4 213.8 27.6⫾2.4 105.3⫾3.5 132.9⫾4.3 133.6
129.3 383 132.1⫾0.9
140 306.5 140.3⫾0.1
C8 H9 NO acetanilide 21.65 387.5 64.8 488 80.6 313.5 239.1 177.0 17.6⫾1.3 78.6⫾4.6 96.2⫾4.7 81.0⫾0.1
66.3 402 87.2 326.5 73.9⫾2.4 91.4⫾2.8 88.0⫾0.3
C12H9 Cl 4-chlorobiphenyl 13.32 348.6 71.6 298 86 278 272.9 211.7 10.8⫾0.8 71.6 82.4⫾0.8 85.3⫾0.2
66.8 368 73.7 326 72.5⫾1.7 83.3⫾1.9 74.6⫾0.3
59 384 66.0⫾2.1 76.8⫾2.2
65.9 466 79.6⫾4.0 90.4⫾4.1
C14H10O2 benzil 23.1 368 69.2 416 98.4 329 351.6 248.0 18.6⫾1.5 81.2⫾2.8 99.8⫾2.2 99.62.0
C14H22O 2,6-di-t-butylphenol 16.57 310.7 60.4 401 84.6 298 401.8 311.1 15.7⫾0.3 72.2⫾2.4 88.0⫾2.5 84.6
81.5 298 81.5
110.9 298 110.9
C16H10 fluoranthene 18.8 383.3 62.3 518 98.3 298 310.5 226.6 14.0⫾1.6 82.4⫾5.3 96.4⫾5.5 98.3
86.2 495 84.6 303 104.2⫾4.7 118.2⫾5.0 84.8⫾0.1
77.4 398 99.2 298 86.5⫾2.4 100.5⫾2.9 99.2
102.1 340 103.6⫾0.5
102.6 328 103.6⫾0.3
C17H34O2 methylhexadecanoate 68.16 307.2 69.6 302 152.3 296 579.6 490.1 67.4⫾0.3 70.2⫾0.1 137.6⫾0.3 152.⫾0.1
82.4 426 54.7⫾0.2 103.0⫾3.1 170.6⫾3.1
82.6 393 97.9⫾2.3 165.3⫾2.3
71.4 437 93.8⫾3.3 161.2⫾3.3
55.35 305.2 125.0⫾0.2
157.8⫾3.1
152.6⫾2.3
148.5⫾3.3
a
See Ref. 7. ⌬ fusH m (T fus) and ⌬ vapH m (T m ) refer to the fusion and vaporization enthalpy at the melting point and mean temperaure of measurement; fusion
enthalpies are from Chickos et al.6 and Domalski and Hearing14; sublimation enthalpies from Chickos and Acree;7 vaporization enthalpies from Table 6;
uncertainties in fusion and vaporization enthalpies 共⫾2 兲 are those associated with the temperature adjustment only.
internally consistent. The fusion enthalpy reported is the av- the boiling point and are accurate to a few %. Some require
erage of two literature values.14 Similarly with 2,6-di-t- critical constants and other parameters that may have to be
butylphenol and fluoranthene. The sublimation enthalpies estimated themselves. A summary of some of the existing
measured directly and those calculated by Eq. 共7兲 agree methods and their applications can be found in the book
within ⫾4.0 kJ mol⫺1, which is the accuracy typical of many edited by Lyman et al.10 共see also Ref. 15兲. The estimation of
experimental sublimation and vaporization enthalpy mea- vaporization enthalpy at or near the boiling point continues
surements. to be a topic of recurring interest.16 –23
The scatter of data obtained for methyl hexadecanoate il- A number of methods and equations for the estimation of
lustrate another common situation that can arise when data vaporization enthalpies at T⫽298.15 K have also been de-
from the literature are examined. Two fusion enthalpies and veloped. Some model vaporization enthalpies on concepts of
several vaporization enthalpies have been reported which are group additivity while some are based on other thermody-
not in particularly good agreement. Using the value of the namic principles.24 –35 Details on the application of some of
sublimation enthalpy as a guide, consistent results are ob- these methods in estimating vaporization enthalpies are
tained if the fusion enthalpy of 54.7 kJ mol⫺1 共298.15 K兲 is available.4,10,25
combined with the mean of the last three vaporization enthal-
pies, 98.3⫾5.3 kJ mol⫺1, resulting in a sublimation enthalpy
of 152.9⫾5.4 kJ mol⫺1.
7. Vaporization Enthalpy Compendium
TABLE 5. A list of acronyms and abbreviations used in Tables 6 and 7 of Organic Compounds by Stephenson and Malanowski pub-
lished in 1987 by Elsevier Science Publishing Co. Some of
A calculated from the vapor pressure data reported by the
method of least squares the data included in this compendium, notably for the higher
B calculated from the difference of the enthalpies of n-alkanes and haloalkanes, appears to be data that have been
sublimation at temperature T, and fusion at the melting estimated.36,37 Estimated vaporization enthalpies are gener-
point ally not included in Table 5 unless the data are reported in
BG Bourdon gauge
C calorimetric determination
the Stephenson and Malanowski compendium or the source
GC gas chromatography is identified. The reader should exercise some caution when
GCC gas chromatography-calorimetry using data that are not referenced to the primary literature.
CGC correlation gas chromatography Additionally, some of the information has originated from
DM diaphram manometer non-English language journals with translations occasionally
DSC differential scanning calorimeter
EB ebullometry
provided by the author’s students. These tables, having been
EST estimated value complied over a period of twenty years, have gone through
GS gas saturation, transpiration numerous revisions. Some errors have been corrected; how-
HG Heise gauge ever it is unlikely that all of them have been detected. The
HSA head space analysis reader is encouraged to consult the original literature when
I isoteniscope
IPM inclined piston manometry
using this data.
ME mass effusion–Knudsen effusion Several sources of data contains vapor pressure data rep-
MG McLeod gauge resented in the form of the Antoine equation 关Eq. 共8兲兴, where
MM mercury manometer P represents the vapor pressure, T is the temperature in K,
NA not available at the time of publication and A, B, and C are the Antoine constants obtained from
OM oil manometer
RG Rodebush gauge
treatment of the vapor pressure-temperature data
SG spoon gauge log10 P⫽A⫺B/ 共 C⫹T 兲 . 共8兲
STG strain gauge
T tensimeter Vaporization enthalpies were calculated from the Antoine
TE torsion effusion constants in one of two ways. A Lotus macro was written to
UV ultraviolet absorption calculate vapor pressures using the Antoine constants over a
30 K temperature range; the resulting vapor pressure–
temperature data were reformulated in terms of the integrated
form of the Clausius–Clapeyron equation. A ln P versus 1/T
Compounds are arranged according to molecular formula. linear regression analysis provided ⌬ vapH m (T m )/R at the
The compound’s name, occasionally a synonym, and the mean temperature, T m , of the 30 K range. The 30 K tem-
CAS registry number are included on the first line. The range perature range was chosen closest to T⫽298.15 K but within
of temperatures studied is the next entry in the table. For the temperature range specified. Alternatively, vaporization
measurements performed at a constant temperature or when enthalpy was calculated using the Antoine constants from the
not specified, this entry is left blank. The vaporization en- following equation:
thalpy at the mean temperature of measurement,
⌬ vapH m (T m ), is the next entry followed by the mean tem- ⌬ vapH m 共 T m 兲 ⫽2.303RB 关 T m / 共 T m ⫹C兲兴 2 . 共9兲
perature (T m /K), an acronym or abbreviation briefly de- Temperatures were chosen to lie with the range of measure-
scribing the type of measurement and the reference to the ment, often at the mean temperature. In a number of in-
original work. In some cases the type of measurement was stances, the authors only provide vapor pressure–
not available, or recorded. In these instances this entry was temperature data. In these instances, a vaporization enthalpy
left blank. If the authors of the work have adjusted their was calculated from the data as described above.
results to 298.15 K, then this information along with the An examination of data in Tables 6 and 7 reveals that
reference is entered on the third line. This information is many compounds have been measured repeatedly. All the
repeated for multiple measurements. The measurements are data here are treated equally; there has been no attempt to
arranged in reverse chronological order. Entries for com- recommend or identify recommended values. A critical
pounds with deuterium substitution are listed after the unla- evaluation of the data is beyond the scope of this compen-
beled parent. dium. However, the reader should be aware of a number of
The authors have made an effort to present the data accu- critical reviews that are available. The IUPAC monograph,
rately and without error. Much of the earlier data have been ‘‘Enthalpies of Vaporization of Organic Compounds by Ma-
retrieved with the aid of existing compendia that have been jer and Svoboda12 is among the most extensive evaluations
published over the years. Most of these compendia include available. Others are included in the references associated
references to the original literature. A notable exception is with Tables 6 and 7. The reader is encouraged to consult
the very useful reference Handbook of the Thermodynamics these references before deciding on the best value to use.
CF4 O4 S trifluoromethylperoxyfluorosulfonate
共233–286兲 27.7 共259兲 关60/15兴
CF4 O5 S2 fluorosulfonic acid trifluoromethane sulfonic acid anhydride 关21595-44-8兴
共308 –338兲 32.9 共323兲 A 关87/5兴关99/16兴
CF4 O6 S2 trifluoromethyl fluorodisulfate
共292–351兲 34.4 共321兲 关60/15兴
CF5 NO pentafluoromethoxyamine 关4217-93-0兴
共167–210兲 18.5 共195兲 A 关87/5兴关65/19兴
CF5 OPS phosphorothionic difluoride, S-trifluoromethyl ester 关52752-66-6兴
共293–353兲 23.1 共323兲 关99/16兴
CF5 OPS trifluoromethylthiosphoryl difluoride
23.0 关74/38兴
CF5 O3 P trifluoromethoxyphosphoryl difluoride
共225–264兲 27.4 共245兲 关73/37兴
CF5 O3 P difluoroperoxyphosphoric acid trifluoromethyl ester 关39125-42-3兴
共241–280兲 32.0 共265兲 A 关87/5兴关73/37兴
CF5 PS trifluoromethyl thiodifluorophosphine
24.3 关74/38兴
CF6 N2 O2 S2 N,N⬘-共difluoromethylene兲bisimidosulfuryl fluoride 关20094-83-1兴
共283–308兲 36.0 共295兲 关68/21兴
CF6 N2 S2 difluoromethane bis共S,S-difluorosulfilimine兲 关17686-45-2兴
共230–313兲 36.0 共245兲 A 关87/5兴关99/16兴
CF6 PS difluoro共trifluoromethylthio兲phosphine 关52752-65-5兴
共293–353兲 22.3 共323兲 关99/16兴
CF8 OS pentafluoro共trifluoromethoxy兲 sulfur 关1873-23-0兴
共217–262兲 24.4 共247兲 A 关87/5兴关64/18兴
CF8 S trifluoro共pentafluorothio兲methane 关373-80-8兴
共223–252兲 20.2 共253兲 I 关01/22兴
共205–262兲 23.8 共247兲 A 关87/5兴关99/16兴
CF9 NOS tetrafluoro共difluoroamino兲共trifluoromethoxy兲 sulfur
共257–298兲 28.7 共272兲 A 关87/5兴关64/19兴
CF10O5 S2 关-共carbonodiperoxato兲兴decafluoro disulfur 关60672-59-5兴
38.1 关76/31兴
CIN cyanogen iodide 关506-78-5兴
共419– 426兲 40.0 共423兲 A 关87/5兴
共298 – 414兲 58.3 共313兲 关47/5兴
CN4 O8 tetranitromethane 关509-14-8兴
共286 –373兲 43.1 共301兲 A 关87/5兴
共313–373兲 42.9 共328兲 A 关87/5兴关84/9兴
关52/15兴
共273–313兲 46.6 共288兲 关87/5兴关84/9兴
关49/19兴
CO carbon monoxide 关630-08-0兴
共68 –108兲 6.0 共93兲 A 关87/5兴
共69– 83兲 6.0 共81兲 关32/3兴
6.0 共81兲 C 关32/3兴
COS carbonyl sulfide 关463-58-1兴
共161–284兲 20.4 共176兲 关99/16兴
共284 –379兲 18.3 共299兲 关99/16兴
共140–224兲 19.5 共209兲 A 关87/5兴
19.0⫾0.1 共214兲 关39/5兴
共162–224兲 19.5 共209兲 关37/2兴
CO2 carbon dioxide 关124-38-9兴
共273–304兲 16.7 共288兲 A 关87/5兴
共216 –273兲 16.4 共258兲 A 关87/5兴
共267–303兲 16.5 共282兲 关72/6兴
共179–198兲 25.9 共188兲 关56/1兴
CS2 carbon disulfide 关75-15-0兴
共255–354兲 28.7 共270兲 关99/16兴
共354 –552兲 27.1 共369兲 关99/16兴
共260–353兲 28.5 共275兲 A 关87/5兴
共338 – 408兲 27.4 共353兲 A 关87/5兴
共388 – 497兲 27.0 共403兲 A 关87/5兴
共490–533兲 28.7 共505兲 A 关87/5兴
C2 H7 NO 2-aminoethanol 关141-43-5兴
共310– 444兲 61.7 共325兲 A 关87/5兴
共379– 443兲 54.7 共394兲 关59/1兴
共273–301兲 U50.8 共287兲 A, GS 关57/25兴
共338 – 443兲 58.9 共353兲 关50/1兴关84/9兴
C2 H7 O3 P dimethyl phosphite 关868-85-9兴
39.5 关93/20兴
共346 – 456兲 38.7 共361兲 A 关87/5兴关70/16兴
C2 H8 ClN dimethylammonium chloride 关506-59-2兴
共429–533兲 95.6 共444兲 A 关87/5兴
共533–569兲 143.9 共548兲 A 关87/5兴
C2 H8 ClN ethylammonium chloride 关557-66-4兴
共382– 480兲 34.3 共397兲 A 关87/5兴
C2 H8 N2 1,1-dimethylhydrazine 关57-14-7兴
共267–303兲 34.1 共284兲 关00/18兴
共238 –292兲 36.5 共277兲 A 关87/5兴关53/3兴
关84/9兴
C2 H8 N2 1,2-dimethylhydrazine 关540-73-8兴
共274 –297兲 41.0 共286兲 A 关87/5兴关51/15兴
关84/9兴
C2 H8 N2 ethylenediamine 关107-15-3兴
共303–391兲 43.9 共318兲 A 关87/5兴
共284 – 419兲 45.9 共299兲 A, IPM 关87/5兴关75/4兴
45.0⫾0.1 共298兲 C 关69/2兴
46.0⫾0.2 共298兲 IPM 关65/8兴关70/11兴
共299–390兲 45.6 共314兲 关34/2兴关84/9兴
C3 BrClF6 O4 perchloric acid, 1,1,2,3,3,3-hexafluoro-2-bromopropyl ester 关38126-26-0兴
共273–293兲 38.1 共283兲 A 关87/5兴关73/19兴
C3 BrF5 O 2-bromo-2,3,3,3-tetrafluoropropionyl fluoride 关6129-62-0兴
共224 –282兲 30.2 共267兲 A 关87/5兴
C3 BrF6 NO N,N-bis共trifluoromethyl兲 carbamoyl bromide
共233–293兲 30.7 共278兲 A 关87/5兴
C3 BrF9 N2 N-bromo-tris共trifluoromethyl兲hydrazine
共283–333兲 36.8 共308兲 关66/31兴
C3 BrF10NS bromotrifluoro关1,1,1,2,3,3,3-heptafluoro-2-propanaminoato共2-兲兴 sulfur 关62977-73-5兴
35.1 共394兲 I 关77/15兴
C3 Br2 F6 O 共trifluoromethyl兲共1,2-dibromo-1,2,2-trifluoroethyl兲 ether 关2356-57-2兴
共299–335兲 34.6 共314兲 A 关87/5兴
C3 Br3 F6 NO 1,1,1,1⬘,1⬘,1⬘-hexafluoro-N-共tribromomethoxy兲dimethylamine 关29528-78-7兴
共297–338兲 28.9 共312兲 A 关87/5兴
C3 ClF4 NO2 chloro共trifluoroacetyl兲carbamic fluoride 关42016-32-0兴
39.3 共371兲 关73/21兴
C3 ClF5 O chloropentafluoroacetone 关79-53-8兴
共232–303兲 27.3 共247兲 A 关87/5兴关64/6兴
关84/9兴
C3 ClF5 O 2-chloro-2,3,3,3-tetrafluoropropionyl fluoride 关28627-00-1兴
共195–273兲 23.9 共258兲 A 关87/5兴
C3 ClF6 NO2 O-共chloroformyl兲-N,N-bis共trifluoromethyl兲hydroxylamine 关15496-01-2兴
共227–286兲 34.5 共271兲 A 关87/5兴
C3 ClF6 NS chloro共hexafluoroisopylidenimino兲 sulfur
37.7 共368兲 I 关72/22兴
C3 ClF7 O heptafluoroisopropyl hypochorite 关22675-68-9兴
共196 –287兲 26.7 共272兲 A 关87/5兴
共194 –273兲 22.7 共258兲 A 关87/5兴
C3 ClF8 N N-chloro-N-1,2,2,2-pentafluoro-1-共trifluoromethyl兲ethylamine 关33757-13-0兴
共240–311兲 28.8 共255兲 A 关87/5兴关71/17兴
C3 ClF8 NOS 共heptafluoropropyl兲imidosulfuryl chloride fluoride 关74366-14-6兴
26.7 共346兲 I 关80/10兴
C3 ClF10NS chlorotrifluoro关1,1,1,2,3,3,3-heptafluoro-2-propanaminoato共2-兲兴 sulfur 关62977-71-3兴
33.5 共391兲 I 关77/15兴
C3 Cl2 F5 N 2,2-difluoro-1,2-dichloro-N-共trifluoromethyl兲ethylidenimine
共283–318兲 31.2 共298兲 A 关87/5兴
C3 Cl2 F6 1,2-dichlorohexafluoropropane 关661-97-2兴
共296 –307兲 28.1 共301兲 关80/9兴
C3 H6 I2 1,3-diiodopropane 关627-31-6兴
54.1 共298兲 GC 关94/19兴
C3 H6 N2 O4 1,1-dinitropropane 关601-76-3兴
共323–383兲 57.9 共338兲 A 关87/5兴
C3 H6 N2 O4 2,2-dinitropropane 关595-49-3兴
共363–553兲 46.3 共378兲 A 关87/5兴
C3 H6 N2 O6 1,2-propanediol dinitrate 关6423-43-4兴
共288 –328兲 63.8 共303兲 A 关87/5兴关70/16兴
C3 H6 N2 O6 1,3-propanediol dinitrate 关3457-90-7兴
共293–313兲 74.3⫾4.6 共303兲 A, GS 关87/5兴关57/5兴
C3 H6 N6 O6 hexahydro-1,3,5-trinitro-1,3,5-triazine 关121-82-4兴
共503–523兲 84.4 共513兲 A 关87/5兴
C3 H6 O 2-propen-1-ol 关107-18-6兴
共323–373兲 47.3 共298兲 CGC 关95/21兴
C3 H6 O oxetane 关503-30-0兴
29.8 共298兲 C 关81/8兴
C3 H6 O acetone 关67-64-1兴
共329– 488兲 29.9 共344兲 A 关87/5兴
共178 –243兲 32.9 共228兲 A 关87/5兴
共203–269兲 33.8 共254兲 A 关87/5兴
共323–379兲 30.6 共338兲 A 关87/5兴
共374 – 464兲 29.5 共389兲 A 关87/5兴
共457–508兲 29.7 共472兲 A 关87/5兴
26.1 共373兲 C 关86/18兴
21.7 共423兲 C 关86/18兴
15.3 共473兲 C 关86/18兴
9.2 共498兲 C 关86/18兴
共285–329兲 31.9 共300兲 EB 关86/10兴
共305–333兲 31.8 共319兲 关84/23兴
共259–351兲 32.8 共274兲 A 关87/5兴关74/6兴
关75/8兴
31.3 共298兲 关75/8兴
共261–328兲 32.7 共276兲 A, EB 关87/5兴关72/6兴
共278 –293兲 32.6 共285兲 关63/25兴
共310–329兲 31.1 共319兲 关57/3兴
共204 –339兲 35.0 共253兲 MG 关26/7兴
共204 –339兲 32.1 共293兲 MG 关26/7兴
共204 –339兲 30.7 共313兲 MG 关26/7兴
C3 H6 O allyl alcohol 关107-18-6兴
共310–340兲 44.6 共325兲 关02/45兴
共253–370兲 46.7 共268兲 A 关87/5兴
NA 关36/2兴
共283–313兲 44.8 共298兲 关35/3兴
C3 H6 O methyl vinyl ether 关107-25-5兴
共278 – 412兲 23.4 共293兲 A 关87/5兴
C3 H6 O propanal 关123-38-6兴
共263–373兲 31.5 共278兲 关77/24兴
共286 –321兲 NA 共301兲 关74/8兴
28.3 共321兲 关72/4兴
29.4 共303兲 关72/4兴
30.3 共286兲 关72/4兴
29.6 共298兲 关72/4兴
共290–322兲 30.3 共305兲 A 关87/5兴关70/16兴
共250–330兲 31.9 共265兲 EB 关87/5兴关51/8兴
C3 H6 O propylene oxide 关75-56-9兴
共225–308兲 31.6 共240兲 A 关87/5兴关70/16兴
共292–345兲 28.5 共307兲 关66/3兴
27.9 共298兲 C 关62/28兴
共249–308兲 30.1 共264兲 关59/1兴
共285–322兲 28.2 共303兲 关37/7兴
共243–306兲 32.9 共273兲 关35/5兴
C3 H6 O2 1,3-dioxolane 关646-06-0兴
共305–347兲 34.6 共326兲 关89/3兴
共280–323兲 35.8 共295兲 A 关87/5兴
关78/14兴
C4 F12O3 S oxobis共trifluoromethyl兲bis共trifluoromethoxy兲 sulfur 关66632-46-0兴
共273–335兲 33.4 共288兲 A, I 关87/5兴关78/14兴
C4 F12P2 S di关bis共trifluoromethyl兲phosphino兴 sulfide
共273–335兲 42.2 共304兲 T 关64/31兴
C4 F12P4 1,2,3,4-tetrakis共trifluoromethyl兲tetraphosphetane 关393-02-2兴
共313–375兲 43.2 共328兲 A, SG 关87/5兴关58/10兴
C4 F12S difluorobis共pentafluoroethyl兲 sulfur 关33622-15-0兴
共284 –341兲 34.0 共299兲 A 关87/5兴
32.2 关71/34兴
C4 F12S difluoro共heptafluoropropyl兲 共trifluoromethyl兲 sulfur 关31206-31-2兴
32.8 关71/34兴
C4 F13NOS trifluoro关1,1,1,2,3,3,3-heptafluoro-2-propanaminoato共2-兲兴-共trifluoromethanolato兲 sulfur 关65844-09-9兴
33.9 共389兲 I 关78/14兴
C4 F15N2 O2 P phosphorous bis关bis共trifluoromethyl兲nitroxide兴 difluoride
共303–370兲 37.6 共336兲 关73/24兴
C4 F16S2 hexadecafluoro-octahydro-1,4-dithiane 关4556-31-4兴
共323– 408兲 40.5 共365兲 关99/16兴关73/38兴
C4 N4 dicyanoacetylene 关1071-98-3兴
共295–350兲 27.3 共310兲 A 关87/5兴
C4 HBrF7 N 1-bromo-2-fluoro-N,N-bis共trifluoromethyl兲vinylamine 关25273-49-8兴
共321–342兲 29.8 共331兲 A 关87/5兴
C4 HBrF9 N 2-bromo-1,1,2-trifluoro-N,N-bis共trifluoromethyl兲ethylamine
共308 –342兲 31.9 共323兲 A 关87/5兴
C4 HBrF9 N 2-bromo-1,2,2-trifluoro-N,N-bis共trifluoromethyl兲ethylamine 关4905-96-8兴
共301–332兲 33.8 共316兲 A 关87/5兴
C4 HBr2 F6 N trans 1,2-dibromo-N,N-bis共trifluoromethyl兲vinylamine
共355–382兲 33.4 共369兲 A 关87/5兴
C4 HCl2 F5 O2 3,4-dichloro-2,2,3,4,4-pentafluorobutyric acid 关375-07-5兴
共373– 456兲 54.8 共388兲 A 关87/5兴关57/17兴
C4 HF5 3,3,4,4,4-pentafluoro-1-butyne 关7096-51-7兴
共203–261兲 23.6 共246兲 A 关87/5兴
C4 HF6 N N,N-bis共trifluoromethyl兲ethynylamine 关13747-21-2兴
共229–271兲 26.0 共256兲 A 关87/5兴
C4 HF7 O2 perfluorobutyric acid 关375-22-4兴
共310– 426兲 50.1⫾0.2 共320兲 EB 关02/21兴
共310– 426兲 45.9⫾0.2 共360兲 EB 关02/21兴
共310– 426兲 41.0⫾0.5 共400兲 EB 关02/21兴
共329– 493兲 47.8 共344兲 A 关87/5兴
共353–393兲 47.3 共368兲 A 关87/5兴
C4 HF8 N N,N-bis共trifluoromethyl兲-1,2-difluorovinylamine 关13747-24-5兴
共276 –296兲 28.8 共286兲 A 关87/5兴
C4 HF8 N N,N-bis共trifluoromethyl兲-2,2-difluorovinylamine 关13747-23-4兴
共274 –291兲 27.7 共282兲 A 关87/5兴
C4 HF8 NO 2,2,3,3,5,5,6,6-octafluoromorpholine 关375-17-7兴
共273–323兲 32.7 共288兲 A 关87/5兴
C4 HF8 NOS 2,2,3,3,4,4,5,5-octafluoro-1,1,2,3,4,5-hexahydro-1-iminothiophene-1-oxide 关77589-47-0兴
28.0 共397兲 关81/15兴
C4 HF9 N2 OS 1,1,1-trifluoro-N-关2,2,2-trifluoro-1-共trifluoromethyl兲ethylidene兴-methanesulfonimidamide 关62609-65-8兴
37.2 共388兲 I 关77/19兴
C4 HF9 O2 S trifluoromethanesulfinic acid, 2,2,2-trifluoro-1-共trifluoromethyl兲ethyl ester 关52225-50-0兴
39.3 共362兲 HG 关74/25兴
C4 HF10N 1,1,1,2,3,3,3-heptafluoro-N-共pentafluoroethyl兲ethanamine 关54566-81-3兴
26.4 共306兲 关75/19兴
C4 HF10N 1,1,1,2,3,3,3-heptafluoro-N-共trifluoromethyl兲-2-propanamine 关53684-05-2兴
28.1 共309兲 关75/21兴
C4 HF10NOS S,S-bis共pentafluoroethyl兲sulfoximine 关34556-24-6兴
35.6 共366兲 I 关72/25兴
C4 H2 1,3-butadiyne 关460-12-8兴
共237–283兲 26.1 共268兲 A 关87/5兴关71/21兴
共191–282兲 26.4 共267兲 关47/5兴
共188 –234兲 33.4 共219兲 关33/10兴关84/9兴
共195–273兲 25.4 共258兲 关26/3兴关84/9兴
C4 H2 BrF6 N 1-bromo-N,N-bis共trifluoromethyl兲vinylamine 关19451-87-7兴
C4 H4 N2 pyrimidine 关289-95-2兴
49.8⫾0.3 共298兲 C 关62/37兴
C4 H4 N2 pyridazine 关289-80-5兴
53.5⫾0.4 共298兲 C 关62/37兴
C4 H4 N4 O7 furazandimethanol 关57449-43-1兴
dinitrate
共399– 433兲 58.7 共414兲 A 关87/5兴关75/18兴
C4 H4 N4 O8 furazandimethanol dinitrate, 2-oxide 关57449-44-2兴
共413– 453兲 64.3 共428兲 A 关87/5兴关75/18兴
C4 H4 O furan 关110-00-9兴
共238 –356兲 30.2 共253兲 A 关87/5兴
共227–323兲 28.2 共298兲 关70/36兴
共275–334兲 28.6 共290兲 关52/17兴关84/9兴
C4 H4 O2 diketene 关674-82-8兴
共297–388兲 42.9 共312兲 A 关87/5兴
42.9⫾0.1 共298兲 C 关68/19兴
C4 H4 O3 succinic anhydride 关108-30-5兴
共401–534兲 57.3 共416兲 A 关87/5兴
C4 H4 O4 1,4-dioxane-2,5-dione 关502-97-6兴
共376 –513兲 50.4 共391兲 A 关87/5兴关47/5兴
C4 H4 S thiophene 关110-02-1兴
共267–381兲 35.8 共282兲 关99/16兴
共333–373兲 34.8 共348兲 I 关71/3兴
34.6 共298兲 关71/28兴
共300–366兲 34.1 共315兲 EB 关52/9兴
共311–393兲 33.7 共326兲 关49/7兴
33.6⫾0.1 共319兲 C 关49/7兴
32.7⫾0.1 共336兲 C 关49/7兴
31.5⫾0.1 共357兲 C 关49/7兴
共344 –363兲 32.6 共353兲 关45/8兴
C4 H5 Cl 2-chloro-1,3-butadiene 关126-99-8兴
共243–263兲 29.6 共253兲 A 关87/5兴
共279–333兲 29.6 共294兲 A 关87/5兴关71/21兴
共293–333兲 30.9 共308兲 关64/7兴关84/9兴
C4 H5 ClO methacryloyl chloride 关920-46-7兴
共313–372兲 36.1 共328兲 A 关87/5兴
C4 H5 ClO3 ethyl chloroglyoxylate 关4755-77-5兴
共268 – 408兲 44.9 共283兲 关47/5兴
C4 H5 Cl3 O2 ethyl trichloroacetate 关515-84-4兴
共293– 440兲 49.0 共308兲 A 关87/5兴
51.0⫾0.1 共298兲 C 关72/41兴
共317–368兲 47.5 共332兲 关59/9兴关84/9兴
C4 H5 Cl5 1,2,2,3,4-pentachlorobutane 关2431-52-9兴
共368 – 498兲 62.6 共383兲 A 关87/5兴关68/29兴
C4 H5 F2 I 1,1-difluoro-4-iodo-1-butene
共318 –342兲 40.6 共330兲 A 关87/5兴
C4 H5 F3 O vinyl 2,2,2-trifluoroethyl ether 关406-90-6兴
共293–317兲 32.0 共305兲 A 关87/5兴
C4 H5 F3 OS trifluorothioacetic acid, S-ethyl ester 关383-64-2兴
共273–313兲 42.0 共288兲 A 关87/5兴
C4 H5 F3 O2 trifluoroacetic acid, ethyl ester 关383-63-1兴
34.7 共335兲 HG 关73/20兴
C4 H5 F5 1,1,1,3,3-pentafluorobutane 关406-58-6兴
共303–358兲 29.2 共318兲 关02/12兴
C4 H5 F5 O 1,1,1,2,2-pentafluoro-3-methoxypropane 关378-16-5兴
共283–321兲 31.6 共298兲 I 关02/19兴
C4 H5 F5 O 1-共difluoromethoxy兲-1,1,2-trifluoroethane 关69948-24-9兴
共283–316兲 31.7 共298兲 I 关02/19兴
C4 H5 F6 OP ethyl bis共trifluoromethyl兲phosphinite
共248 –328兲 33.2 共288兲 关59/21兴
C4 H5 N 3-butenenitrile 关109-75-1兴
共293– 417兲 40.3 共308兲 A 关87/5兴
40.0 共298兲 关69/14兴
共254 –392兲 41.6 共268兲 关47/5兴
C4 H6 1-butyne 关107-00-6兴
共205–289兲 26.0 共274兲 A 关87/5兴
23.7 共298兲 关71/28兴
25.8⫾0.1 共263兲 C 关50/10兴
24.5⫾0.1 共281兲 C 关50/10兴
C4 H6 2-butyne 关503-17-3兴
共240–308兲 29.0 共255兲 A 关87/5兴
26.7 共298兲 关71/28兴
26.9⫾0.1 共291兲 C 关41/2兴
C4 H6 cyclobutene 关822-35-2兴
共206 –275兲 24.7 共260兲 A 关87/5兴
共196 –275兲 24.6 共260兲 关41/8兴关84/9兴
C4 H6 ClFO2 2-chloroethyl fluoroacetate
共273–333兲 56.4 共288兲 A, GS 关87/5兴关48/14兴
关71/21兴
C4 H6 ClF3 O 2-chloro-1,1,2-trifluoroethyl ethyl ether 关310-71-4兴
37.5⫾0.1 共298兲 C 关84/7兴
36.5⫾0.1 共313兲 C 关84/7兴
35.3⫾0.1 共328兲 C 关84/7兴
34.2⫾0.1 共343兲 C 关84/7兴
32.9⫾0.1 共358兲 C 关84/7兴
C4 H6 Cl2 3,4-dichloro-1-butene 关760-23-6兴
共320–396兲 38.0 共335兲 A 关87/5兴
C4 H6 Cl2 trans 1,3-dichloro-2-butene 关7415-31-8兴
共306 – 401兲 39.3 共321兲 A 关87/5兴
C4 H6 Cl2 trans 1,4-dichloro-2-butene 关110-57-6兴
共340–379兲 45.6 共355兲 A 关87/5兴
C4 H6 Cl2 O2 2-chloroethyl chloroacetate 关3848-12-2兴
共319– 478兲 53.3 共334兲 A 关87/5兴关47/5兴
C4 H6 Cl2 O2 ethyl dichloroacetate 关535-15-9兴
50.6⫾0.1 共298兲 C 关72/41兴
共283– 430兲 46.2 共298兲 A 关87/5兴关47/5兴
C4 H6 Cl4 1,2,3,3-tetrachlorobutane 关13138-51-7兴
共349– 464兲 54.2 共364兲 A 关87/5兴关68/29兴
C4 H6 FN 4-fluorobutyronitrile 关407-83-0兴
共273–333兲 45.2 共288兲 A, GS 关87/5兴关48/14兴
关71/21兴
C4 H6 F2 O2 2-fluoroethyl fluoroacetate
共273–333兲 55.1 共288兲 A, GS 关87/5兴关48/14兴
关71/21兴
C4 H6 F3 I 1,1,1-trifluoro-3-iodobutane 关540-87-4兴
共304 –321兲 32.4 共312兲 A 关87/5兴
C4 H6 F3 I 1,1,1-trifluoro-3-iodo-2-methylpropane 关26653-47-4兴
共298 –368兲 30.4 共313兲 A 关87/5兴
C4 H6 F3 NO3 methyl N-trifluoromethyl-N-methoxyurethane
39.0 关79/28兴
C4 H6 F4 O 1-ethoxy-1,1,2,2-tetrafluoroethane 关512-51-6兴
共283–330兲 33.0 共298兲 I 关02/19兴
C4 H6 F4 O 1,1,2,2-tetrafluoro-3-methoxypropane 关60598-17-6兴
共293–347兲 35.2 共308兲 I 关02/19兴
C4 H6 F6 N2 O 1,1-dimethyl-2,2-bis共trifluoromethyl兲hydrazine-2-oxide 关30295-33-1兴
共287–356兲 36.4 共302兲 A 关87/5兴
C4 H6 F6 P2 S methyl共trifluoromethyl兲phosphinothious acid, anhydrosulfide 关26348-88-9兴
共316 –342兲 46.7 共329兲 关70/26兴
C4 H6 N2 O dimethylfurazan 关4975-21-7兴
共353– 427兲 51.1 共368兲 A 关87/5兴关71/6兴
C4 H6 N2 O2 dimethylfurazan-2-oxide 关2518-42-5兴
共353– 493兲 57.0 共368兲 A 关87/5兴关71/6兴
C4 H6 N4 O8 1,1,1,3-tetranitro-2-methylpropane 关42216-58-0兴
共304 –327兲 75.7 共316兲 A 关87/5兴
C4 H6 N4 O11 2-nitro-2-hydroxmethyl-1,3-propanedioltrinitrate 关20820-44-4兴
共313–353兲 72.9 共328兲 A 关87/5兴
C4 H6 O trans crotonaldehyde 关123-73-9兴
共314 – 411兲 36.6⫾0.1 共320兲 EB 关02/15兴
C4 H8 O2 2-methyl-1,3-dioxolane 关497-26-7兴
共270–308兲 43.0⫾0.6 GS 关98/21兴关02/32兴
C4 H8 O2 cis 2-butene-1,4-diol 关6117-80-2兴
共373–508兲 74.7 共388兲 A 关87/5兴
C4 H8 O2 1,1-dimethoxyethene
共303–362兲 39.6 共333兲 关95/29兴
C4 H8 O2 butanoic acid 关107-92-6兴
共391– 429兲 50.3 共406兲 EB 关01/15兴
共278 –308兲 58.5⫾0.3 共293兲 GS 关00/6兴
共278 –308兲 58.2⫾0.3 共298兲 GS 关00/6兴
共353–393兲 60.7 共298兲 CGC 关95/21兴
共437–592兲 47.7 共452兲 A 关87/5兴
共301–358兲 51.1 共316兲 A 关87/5兴
共355– 453兲 53.2 共370兲 A 关87/5兴关71/21兴
monomer 40.5⫾0.1 共298兲 C 关70/8兴
58⫾4 共298兲 C 关70/8兴
共363– 436兲 52.0 共378兲 关49/1兴关84/9兴
C4 H8 O2 1,3-dioxane 关505-22-6兴
39.1⫾0.1 共298兲 C 关82/9兴
35.6⫾0.4 关59/23兴
C4 H8 O2 1,4-dioxane 关123-91-1兴
共285–375兲 38.0 共300兲 A 关87/5兴
共329–372兲 36.5 共350兲 关84/20兴
38.6⫾0.1 共298兲 C 关82/9兴
共293–398兲 37.3 共308兲 关63/22兴关84/9兴
共283–353兲 37.0 共318兲 关36/6兴
C4 H8 O2 ethyl acetate 关141-78-6兴
共300–390兲 34.1 共315兲 关97/11兴
共313–353兲 35.0 共298兲 CGC 关95/21兴
共271–373兲 36.7 共286兲 关81/11兴关84/9兴
35.6⫾0.1 共298兲 C 关80/13兴
34.6⫾0.1 共313兲 C 关80/13兴
31.4⫾0.1 共343兲 C 关80/13兴
33.8⫾0.1 共326兲 C 关77/12兴
33.4⫾0.1 共331兲 C 关77/12兴
32.4⫾0.1 共344兲 C 关77/12兴
31.9⫾0.1 共351兲 C 关77/12兴
31.0⫾0.1 共363兲 C 关77/12兴
34.0 共320兲 关76/8兴
31.9 共350兲 关76/8兴
35.1⫾0.2 共298兲 C 关66/2兴
共288 –351兲 35.7 共303兲 A 关87/5兴关65/3兴
关71/21兴
C4 H8 O2 3-hydroxy-2-butanone 关513-86-0兴
共273– 418兲 38.4 共288兲 A 关87/5兴
C4 H8 O2 2-methylpropanoic acid 关79-31-2兴
共278 –308兲 55.8⫾0.3 共293兲 GS 关00/6兴
共278 –308兲 55.5⫾0.3 共298兲 GS 关00/6兴
共344 – 445兲 51.6 共359兲 EB 关87/9兴
共288 – 428兲 50.9 共303兲 A 关87/5兴
共428 –562兲 45.4 共443兲 A 关87/5兴
共228 –243兲 53.4⫾3 共398兲 TE 关79/4兴
monomer 35.5⫾0.1 共298兲 C 关70/8兴
53⫾4 共298兲 C 关70/8兴
C4 H8 O2 isopropyl formate 关625-55-8兴
共221–342兲 34.5 共236兲 A 关87/5兴关47/5兴
C4 H8 O2 methyl propionate 关922-67-8兴
共313–363兲 28.9 共298兲 CGC 关95/21兴
35.6⫾0.4 共298兲 GC 关87/17兴
共231–353兲 39.1 共246兲 A 关87/5兴
共353– 486兲 32.8 共368兲 A 关87/5兴
35.9⫾0.1 共298兲 C 关80/13兴
34.9⫾0.1 共313兲 C 关80/13兴
36.3⫾0.3 共298兲 GCC 关80/5兴
C5 H6 F6 N2 S 2,2,2-trifluoro-N,N-dimethyl-N⬘-关共trifluoromethyl兲thio兴-ethanimidamide 关62067-11-2兴
40.4 共400兲 I 关77/18兴
C5 H6 F6 O 1,1,1,2,3,3-hexafluoro-4-methoxybutane 关58705-93-4兴
共293–360兲 37.0 共308兲 I 关02/19兴
C5 H6 F6 N2 S dimethylamino共hexafluoroisoproplidenimino兲 sulfur
39.7 共383兲 I 关72/22兴
C5 H6 F6 O2 S trifluoromethanesulfinic acid, 2,2,2-trifluoro-1,1-dimethylethyl ester 关52225-49-7兴
35.6 共388兲 HG 关74/25兴
C5 H6 F6 O5 S2 3,3-bis关共trifluoromethyl兲sulfonyl兴-1-propanol 关61915-97-7兴
共333– 418兲 32.8 共348兲 A, I 关87/5兴关77/17兴
关99/16兴
C5 H6 N2 dimethylmalononitrile 关7321-55-3兴
共322– 413兲 47.5 共337兲 A 关87/5兴关67/20兴
C5 H6 N2 2-methylpyrazine 关109-08-0兴
共288 –392兲 42.4 共340兲 关95/4兴
C5 H6 N2 glutaronitrile 关544-13-8兴
共364 –560兲 60.1 共379兲 A 关87/5兴
共277–303兲 66.8 共290兲 A 关87/5兴关72/20兴
C5 H6 O 2-methylfuran 关534-22-5兴
共289–337兲 32.4 共304兲 关02/30兴
共251–338兲 34.4 共266兲 A 关87/5兴
共288 –303兲 32.5 共295兲 关72/20兴
共333–373兲 30.9 共348兲 关71/3兴关84/9兴
共215–360兲 32.2 共298兲 关70/36兴
C5 H6 O2 5-methyl-2(3H)-furanone 关591-12-8兴
共324 – 442兲 40.3 共339兲 A 关87/5兴
C5 H6 O2 共dl兲 5-methyl-2共5H兲-furanone 关591-11-7兴
共356 – 481兲 48.2 共371兲 A 关87/5兴
C5 H6 O2 furfuryl alcohol 关98-00-0兴
共304 – 443兲 53.6 共319兲 A 关87/5兴关47/4兴
C5 H6 O2 5-hydroxy-3-pentyn-2-one 关15441-65-3兴
共273–333兲 64.4 共288兲 A 关87/5兴关72/20兴
C5 H6 O3 glutaric anhydride 关108-55-4兴
共373–560兲 60.9 共388兲 A 关87/5兴关47/5兴
C5 H6 O3 (dl) monomethylsuccinic anhydride 关4100-80-5兴
共342–521兲 59.3 共357兲 A 关87/5兴关47/5兴
C5 H6 S 2-methylthiophene 关554-14-3兴
共333–373兲 36.8 共348兲 I 关71/3兴关84/9兴
38.7 共298兲 关71/28兴
共324 –391兲 37.2 共339兲 A, EB 关87/5兴关52/9兴
关99/16兴
C5 H6 S 3-methylthiophene 关616-44-4兴
共326 –398兲 36.8 共357兲 关99/16兴
共333–373兲 37.4 共348兲 I 关71/3兴关84/9兴
39.5 共298兲 关71/28兴
共327–399兲 37.5 共342兲 A, EB 关87/5兴关52/9兴
C5 H7 ClO3 acetic acid, chlorooxo, propyl ester 关54166-91-5兴
共282–396兲 52.7 共297兲 A 关87/5兴关47/5兴
C5 H7 FO2 allyl fluoroacetate
共273–333兲 48.9 共288兲 A, GS 关87/5兴关48/14兴
关72/20兴
C5 H7 N cyclobutanecarbonitrile 关4426-11-3兴
44.3 共298兲 C 关83/6兴
共328 – 402兲 39.6 共347兲 BG 关71/2兴
40.0⫾0.4 共298兲 BG 关71/2兴
C5 H7 N 2-ethylacrylonitrile
共244 –387兲 37.1 共259兲 关87/5兴关47/5兴
C5 H7 N angelic acid, nitrile 关20068-02-4兴
共265– 413兲 42.8 共280兲 A 关87/5兴关47/5兴
C5 H7 N 1-methylpyrrole 关96-54-8兴
共333–373兲 38.0 共343兲 I 关71/3兴
共321– 423兲 39.0 共336兲 A, EB, IPM 关87/5兴关68/4兴
关72/20兴
C5 H7 N 共Z兲 2-pentenenitrile 关25899-50-7兴
关65/7兴关72/20兴
共283–323兲 36.9 共303兲 关37/9兴
C5 H10O pentanal 关110-62-3兴
共313–353兲 38.3 共298兲 CGC 关95/21兴
共290–385兲 U50.0 共305兲 A 关87/5兴
38.1⫾0.1 共298兲 关81/18兴
共305–377兲 37.3 共320兲 关79/15兴
C5 H10O pivaldehyde 关630-19-3兴
共308 –336兲 34.2 共322兲 关89/2兴
C5 H10O 3,3-dimethyloxetane 关6921-35-3兴
33.9⫾0.3 共298兲 C 关71/25兴
C5 H10OS S-propyl thiolacetate 关2307-10-0兴
44.1⫾0.2 共298兲 C 关66/2兴
C5 H10OS S-isopropyl thiolacetate 关926-73-8兴
42.3⫾0.2 共298兲 C 关66/2兴
C5 H10OS 1-共methylthio兲-2-共vinyloxy兲ethane 关6607-53-0兴
共316 –347兲 47.5 共331兲 A 关87/5兴关99/16兴
C5 H10O2 tetrahydrofurfuryl alcohol 关97-99-4兴
共393– 453兲 46.2 共408兲 A 关87/5兴
共333– 443兲 46.5 共388兲 关79/21兴
C5 H10O2 2,2-dimethyl-1,3-dioxolane 关2916-31-6兴
共278 –318兲 41.1⫾0.2 GS 关98/21兴关02/32兴
C5 H10O2 4-methyl-1,3-dioxane 关1120-97-4兴
共273–313兲 43.7⫾0.3 GS 关98/21兴关02/32兴
C5 H10O2 1-methoxy-2-butanone 关50741-70-3兴
共297– 408兲 44.9 共312兲 A 关87/5兴关34/3兴
关72/20兴
C5 H10O2 3-hydroxy-3-methyl-2-butanone 关115-22-0兴
共317– 419兲 41.1 共332兲 A 关87/5兴关72/20兴
关50/11兴
C5 H10O2 4-hydroxy-3-methyl-2-butanone 关3393-64-4兴
共375–528兲 58.3 共390兲 A 关87/5兴关72/20兴
共317– 458兲 59.0 共332兲 关47/5兴
C5 H10O2 butyl formate 关592-84-7兴
共295–380兲 37.9 共310兲 A 关87/5兴
41.3⫾0.1 共298兲 C 关80/13兴
40.1⫾0.1 共313兲 C 关80/13兴
39.0⫾0.1 共328兲 C 关80/13兴
38.7⫾0.1 共346兲 C 关76/14兴
38.1⫾0.1 共355兲 C 关76/14兴
37.3⫾0.1 共363兲 C 关76/14兴
C5 H10O2 sec butyl formate 关589-40-2兴
共238 –367兲 37.7 共253兲 A 关87/5兴
C5 H10O2 ethyl propionate 关105-37-3兴
共315– 420兲 36.7 共330兲 关97/11兴
共372–538兲 34.4 共387兲 A 关87/5兴
39.3⫾0.1 共298兲 C 关80/13兴
38.2⫾0.1 共313兲 C 关80/13兴
36.6⫾0.1 共336兲 C 关77/12兴
36.0⫾0.1 共344兲 C 关77/12兴
35.5⫾0.1 共351兲 C 关77/12兴
34.5⫾0.1 共363兲 C 关77/12兴
39.1⫾0.1 共298兲 C 关72/3兴
共306 –372兲 38.2 共321兲 A 关87/5兴关65/3兴
关72/20兴
C5 H10O2 isobutyl formate 关542-55-2兴
共371–507兲 36.6 共386兲 A 关87/5兴
共240–372兲 38.6 共255兲 A 关87/5兴关47/5兴
C5 H10O2 isopropyl acetate 关108-21-4兴
共313–353兲 37.0 共298兲 CGC 关95/21兴
37.2⫾0.2 共298兲 C 关66/2兴
共235–362兲 38.8 共250兲 A 关87/5兴关47/5兴
共273–363兲 36.3 共288兲 A 关29/5兴
C5 H10O2 methyl butyrate 关623-42-7兴
54.4 关86/10兴
C7 H7 BrS 4-bromothioanisole 关104-95-0兴
55.7 关86/10兴
C7 H7 Cl benzyl chloride 关100-44-7兴
共276 –309兲 50.1⫾0.3 共298兲 GS 关02/29兴
49.9 共298兲 CGC 关02/29兴
共320–390兲 48.6 共335兲 A, I 关87/5兴关76/11兴
50.1⫾0.5 共298兲 关76/11兴关99/16兴
共295– 453兲 48.6 共310兲 关87/5兴关47/5兴
C7 H7 Cl 2-chlorotoluene 关95-49-8兴
共370– 432兲 41.6 共385兲 关99/16兴
共345– 430兲 45.3 共298兲 关84/9兴关91/2兴
共345– 430兲 42.5 共361兲 关84/9兴
共338 – 493兲 42.8 共353兲 A 关87/5兴关73/18兴
关70/14兴
共278 – 432兲 44.8 共293兲 关47/5兴
共273–348兲 45.8 共288兲 关40/5兴
C7 H7 Cl 3-chlorotoluene 关108-41-8兴
共373– 435兲 41.9 共388兲 关99/16兴
共277– 436兲 43.7 共292兲 A 关87/5兴关47/5兴
共273–348兲 46.2 共288兲 关40/5兴
C7 H7 Cl 4-chlorotoluene 关106-43-4兴
共362– 435兲 41.8 共375兲 关99/16兴
共304 – 436兲 41.7 共319兲 A 关87/5兴
共340– 430兲 46.0 共298兲 关84/9兴关91/2兴
共338 – 433兲 43.5 共353兲 关84/9兴
共279– 435兲 44.1 共293兲 关47/5兴
C7 H7 ClO 2-chloroanisole 关766-51-8兴
49.4 关86/10兴
共388 – 460兲 48.3 共403兲 A 关87/5兴关73/18兴
关99/16兴
C7 H7 ClO 3-chloroanisole 关2845-89-8兴
48.1 关86/10兴
C7 H7 ClO 4-chloroanisole 关623-12-1兴
47.7 关86/10兴
C7 H7 ClS 2-chlorothioanisole 关17733-22-1兴
53.6 关86/10兴
C7 H7 ClS 3-chlorothioanisole 关4867-37-2兴
51.9 关86/10兴
C7 H7 ClS 4-chlorothioanisole 关123-09-1兴
53.1 关86/10兴
C7 H7 F benzyl fluoride 关350-50-5兴
共278 –318兲 46.2⫾0.3 共298兲 GS 关02/29兴
46.5 共298兲 CGC 关02/29兴
共278 –318兲 46.3⫾0.3 共298兲 GS 关97/14兴
共297– 410兲 43.7 共312兲 A 关87/5兴
共298 –356兲 44.3 共312兲 I 关76/11兴
44.5⫾0.4 共298兲 关76/11兴
C7 H7 F 2-fluorotoluene 关95-52-3兴
共248 –388兲 42.0 共263兲 关99/16兴
共452–531兲 31.5 共465兲 关99/16兴
共453–530兲 32.3 共468兲 关84/16兴
共308 –348兲 38.0 共323兲 关74/26兴关84/9兴
共295–388兲 38.7 共310兲 A 关87/5兴关51/9兴
共248 –387兲 40.5 共264兲 关47/5兴
C7 H7 F 3-fluorotoluene 关352-70-5兴
共250–390兲 41.6 共265兲 关99/16兴
共293–390兲 39.2 共308兲 A 关87/5兴关51/9兴
共250–389兲 40.7 共266兲 关47/5兴
C7 H7 F 4-fluorotoluene 关352-32-9兴
共340– 430兲 39.5 共298兲 关84/9兴关91/2兴
共340– 429兲 37.0 共355兲 A 关87/5兴关51/9兴
关99/16兴
C7 H7 F2 N N,N-difluorobenzylamine 关23162-99-4兴
C7 H9 N 3-ethylpyridine 关536-78-7兴
共334 –373兲 44.6 共349兲 A 关87/5兴关73/18兴
C7 H9 N 2-ethylpyridine 关100-71-0兴
共323–373兲 43.7 共338兲 A 关87/5兴关73/18兴
C7 H9 N 4-ethylpyridine 关536-75-4兴
共333–372兲 45.3 共348兲 A 关87/5兴关73/18兴
C7 H9 N N-methylaniline 关100-61-8兴
共309– 469兲 53.6 共324兲 A 关87/5兴
C7 H9 N o-toluidine 关95-53-4兴
共290–517兲 57.8 共300兲 EB, IPM 关94/17兴
共290–517兲 54.5 共340兲 EB, IPM 关94/17兴
共290–517兲 51.5 共380兲 EB, IPM 关94/17兴
共290–517兲 48.6 共420兲 EB, IPM 关94/17兴
共290–517兲 45.7 共460兲 EB, IPM 关94/17兴
共290–517兲 42.7 共500兲 EB, IPM 关94/17兴
共391– 474兲 50.0 共406兲 A 关87/5兴关49/1兴
关84/9兴
C7 H9 N m-toluidine 关108-44-1兴
共394 – 477兲 51.1 共409兲 A 关87/5兴关49/1兴
关84/9兴
C7 H9 N p-toluidine 关106-49-0兴
共393– 474兲 51.1 共408兲 A 关87/5兴
共315– 473兲 54.9 共330兲 关47/5兴
C7 H9 N 1-cyclohexene-1-carbonitrile 关1855-63-6兴
53.6⫾0.1 共298兲 C 关70/21兴
C7 H9 N bicyclo关3.1.0兴hexane-1-carbonitrile 关31357-72-9兴
共366 – 444兲 U43.2 共382兲 BG 关71/2兴
C7 H9 NO 2-methoxyaniline 关90-04-0兴
共334 – 492兲 57.5 共349兲 A 关87/5兴关47/5兴
C7 H10 bicyclo关2.2.1兴hept-2-ene 共norbornene兲 关498-66-8兴
共338 – 406兲 35.1⫾0.2 共298兲 EB 关96/5兴
共301–350兲 34.3 共316兲 A 关87/5兴
C7 H10 bicyclo关4.1.0兴hept-3-ene 关16554-83-9兴
共333–384兲 36.7 共348兲 A 关87/5兴
38.4⫾0.6 共298兲 EB 关74/20兴
C7 H10 tricyclo关 2.2.1.02,6兴 heptane 关279-19-6兴
共302–337兲 38.3 共317兲 A 关87/5兴
C7 H10 tricyclo关 4.1.0.02,4兴 heptane
36.5⫾0.5 共298兲 EB 关74/20兴
C7 H10 tricyclo关 4.1.0.02,6兴 heptane 关187-26-8兴
共322–373兲 35.3 共337兲 A 关87/5兴
C7 H10N2 2,3,5-trimethylpyrazine 关14667-55-1兴
53.9⫾1.6 共298兲 C 关96/2兴
C7 H10N2 diallylcyanamide 关538-08-9兴
共369– 495兲 52.3 共384兲 A 关87/5兴
C7 H10N2 1,5-dicyanopentane 关646-20-8兴
共306 –331兲 74.5 共318兲 A 关87/5兴
C7 H10N2 2,4-diaminotoluene 关95-80-7兴
共379–553兲 67.7 共394兲 A 关87/5兴关47/5兴
C7 H10N2 4-tolyhydrazine 关539-44-6兴
共355–515兲 65.4 共370兲 A 关87/5兴关47/5兴
C7 H10O 1-ethynyl-1-cyclopentanol 关17356-19-3兴
共323–373兲 62.1 共298兲 CGC 关95/21兴
C7 H10O 7-norbornanone 关10218-02-7兴
共322–348兲 47.9 共335兲 EB 关94/16兴
C7 H10O 2-norbornanone 关497-38-1兴
50.0 共298兲 GC 02/37兴
共343–383兲 51.5 共298兲 CGC 关95/21兴
共343–383兲 49.6 共298兲 CGC 关95/21兴
C7 H10O2 5-methyl-5-hexene-2,4-dione 关20583-46-4兴
共323–363兲 26.4 共338兲 A 关87/5兴关73/18兴
C7 H10O3 3-acetyl-2,4-pentanedione 关815-68-9兴
共369– 477兲 54.9 共384兲 A 关87/5兴
C7 H10O3 glycidyl methacrylate 关106-91-2兴
50.2⫾0.4 关87/14兴
C7 H14O2 2,2,4-trimethyl-1,3-dioxane
41.9⫾1.2 共298兲 关67/37兴
C7 H14O2 2-methyl-2-propyl-1,3-dioxolane 关4352-98-1兴
共278 –313兲 46.3⫾0.3 共298兲 GS 关98/21兴关02/32兴
C7 H14O2 2-methyl-2-isopropyl-1,3-dioxolane 关4405-16-7兴
共274 –303兲 43.9⫾0.2 共298兲 GS 关02/32兴
共273–303兲 44.6⫾0.2 GS 关98/21兴
C7 H14O2 关共1-methylpropoxy兲methyl兴oxirane 关3814-55-9兴
45.2⫾1.8 关87/14兴
C7 H14O2 heptanoic acid 关111-14-8兴
共283–328兲 72.5⫾0.8 共306兲 GS 关00/6兴
共283–328兲 72.9⫾0.8 共298兲 GS 关00/6兴
共353–393兲 75.7 共298兲 CGC 关95/21兴
76.0 共266兲 关82/4兴
共271–291兲 72.0⫾1.5 共298兲 TE 关79/4兴
共351– 495兲 68.3 共366兲 A 关87/5兴关47/5兴
C7 H14O3 tert-butylperoxymethyloxirane 关33415-52-0兴
53.9⫾0.4 关87/14兴
C7 H14O3 2-propoxyethylacetate 关20706-25-6兴
55.6⫾0.1 共298兲 C 关70/17兴
C7 H14O3 (dl) butyl lactate 关138-22-7兴
共339– 456兲 58.7 共354兲 A 关87/5兴
C7 H14O3 3-ethoxypropionic acid, ethyl ester 关763-69-9兴
共312– 446兲 45.5 共327兲 A 关87/5兴
C7 H14O3 1-heptene ozonide 关768-63-8兴
共353–373兲 44.4 共363兲 A 关87/5兴关77/9兴
C7 H14O3 4-共2-hydroxyethyl兲-4-methyl-1,3-dioxane
共329– 455兲 51.7 共344兲 A 关87/5兴
C7 H14O3 3-hydroxypropionic acid, butyl ester
共361–382兲 60.3 共371兲 A 关87/5兴关73/18兴
C7 H14O3 3-methoxypropionic acid, propyl ester 关5349-56-4兴
共323– 433兲 47.0 共338兲 A 关87/5兴
C7 H14O3 3-propoxypropionic acid, methyl ester 关14144-39-9兴
共323– 453兲 46.6 共338兲 A 关87/5兴
C7 H14O3 (dl) butyric acid, 2,3-dihydroxypropyl ester 关557-25-5兴
共392– 449兲 80.4 共407兲 A 关87/5兴
C7 H14O3 2-butoxypropionic acid 关14620-87-2兴
共373– 473兲 52.8 共388兲 A 关87/5兴关73/18兴
C7 H14S allyl tert-butyl sulfide 关37850-75-2兴
共319–339兲 41.9 共332兲 关99/16兴
共319–339兲 43.1 共329兲 A, EB 关87/5兴关62/16兴
共319–339兲 44.8 共298兲 EB 关62/16兴
C7 H15Br 1-bromoheptane 关629-04-9兴
共341– 481兲 47.0 共356兲 关99/16兴
共323–363兲 50.2 共298兲 CGC 关95/21兴
50.8⫾0.1 共298兲 C 关68/1兴
50.4⫾0.2 共298兲 C 关66/2兴
共333– 483兲 47.5 共348兲 A, EST 关87/5兴关61/13兴
C7 H15Br (dl) 2-bromoheptane 关1974-04-5兴
共333– 440兲 45.0 共348兲 A 关87/5兴关99/16兴
C7 H15Cl 1-chloroheptane 关629-06-1兴
共326 – 462兲 45.1 共341兲 关99/16兴
共313–353兲 47.9 共298兲 CGC 关95/21兴
共300– 430兲 47.0 共298兲 关84/9兴关91/2兴
共307– 434兲 46.9 共322兲 A, DTA 关87/5兴关69/5兴
47.7⫾0.1 共298兲 C 关68/1兴
C7 H15Cl (dl) 2-chloroheptane 关1001-89-4兴
共313– 424兲 44.8 共328兲 A 关87/5兴关99/16兴
C7 H15Cl2 N N-methyl-bis共2-chloropropyl兲amine 关52802-03-6兴
共273–333兲 54.6 共288兲 A, GS 关87/5兴关48/13兴
关73/18兴
C7 H15Cl2 N N-propyl-bis共2-chloroethyl兲amine 关621-68-1兴
共273–369兲 56.8 共288兲 A, GS 关87/5兴关48/13兴
关73/18兴
C7 H15F 1-fluoroheptane 关661-11-0兴
共294 – 416兲 40.3 共309兲 关99/18兴
共287– 417兲 40.8 共302兲 A, EST 关87/5兴关61/13兴
C7 H15I 1-iodoheptane 关4282-40-0兴
共373–513兲 47.8 共388兲 A, EST 关87/5兴关61/13兴
关70/14兴
C7 H15N N-ethylpiperidine 关766-09-6兴
共274 –313兲 41.1⫾0.6 共294兲 GS 关98/12兴
共274 –313兲 40.8⫾0.6 共298兲 GS 关98/12兴
C7 H15N octahydroazocine 关1121-92-2兴
共273–313兲 46.5 共288兲 A 关87/5兴
C7 H15NO N,N-dimethyl-tert-butylcarboxamide
55.1⫾0.4 共298兲 ME 关95/3兴关93/19兴
C7 H15NO 1-共diethylamino兲-2-propanone 关1620-14-0兴
共278 –318兲 47.7⫾0.3 共298兲 GS 关94/3兴
C7 H15NO2 methyl 2-共N,N-dimethylamino兲-2-methylpropanoate
共278 –308兲 49.2⫾1.0 共293兲 GS 关92/13兴
C7 H15NO2 lactic acid, N-butylamide 关30220-58-7兴
共365– 433兲 77.4 共380兲 A 关87/5兴
C7 H15NO2 lactic acid, N-sec-butylamide
共368 – 418兲 74.6 共383兲 A 关87/5兴
C7 H15NO2 lactic acid, N-isobutylamide
共388 – 418兲 73.5 共403兲 A 关87/5兴
C7 H15NO2 共l兲 leucine methyl ester 关2666-93-5兴
共320–353兲 39.4 共366兲 A 关87/5兴
C7 H16 heptane 关142-85-5兴
共330–371兲 34.7 共345兲 关02/8兴
36.6 共298兲 关94/12兴
共298 –363兲 36.1 共313兲 关84/27兴
共298 –338兲 36.1 共313兲 关84/15兴
36.6⫾0.1 共298兲 C 关79/13兴
35.6⫾0.1 共313兲 C 关79/13兴
34.4⫾0.1 共333兲 C 关79/13兴
33.1⫾0.1 共353兲 C 关79/13兴
36.55 共298兲 关71/28兴
共288 –348兲 36.4 共303兲 关67/10兴
共297–375兲 36.1 共312兲 A 关87/5兴关49/6兴
34.5⫾0.1 共331兲 C 关47/10兴
33.2⫾0.1 共350兲 C 关47/10兴
共313–398兲 35.4 共328兲 关46/4兴
共299–372兲 36.0 共314兲 MM 关45/2兴
32.0 共371兲 C 关40/6兴
共310–397兲 35.5 共325兲 EB 关40/14兴
C7 H16 2-methylhexane 关591-76-4兴
共296 –365兲 34.6 共311兲 A 关87/5兴
34.9⫾0.1 共298兲 C 关79/13兴
33.9⫾0.1 共313兲 C 关79/13兴
32.7⫾0.1 共333兲 C 关79/13兴
31.3⫾0.1 共353兲 C 关79/13兴
34.8 共298兲 关71/28兴
共273–318兲 34.8 共298兲 关61/16兴
共291–364兲 34.8 共306兲 关49/6兴
C7 H16 (dl) 3-methylhexane 关589-34-4兴
共289–366兲 35.1 共304兲 A 关87/5兴
35.1⫾0.1 共298兲 C 关79/13兴
34.2⫾0.1 共313兲 C 关79/13兴
32.9⫾0.1 共333兲 C 关79/13兴
31.7⫾0.1 共353兲 C 关79/13兴
35.1 共298兲 关71/28兴
共293–366兲 34.9 共308兲 关49/6兴
C7 H16 2,2-dimethylpentane 关590-35-2兴
32.4⫾0.1 共298兲 C 关98/16兴
31.8⫾0.1 共308兲 C 关98/16兴
关70/14兴
C8 H6 Cl2 2,6-dichlorostyrene 关28469-92-3兴
53.8⫾1.5 共298兲 GS 关01/1兴
共321– 490兲 50.4 共336兲 A 关87/5兴关47/5兴
关70/14兴
C8 H6 Cl2 3,4-dichlorostyrene 关2039-83-0兴
共330–503兲 53.3 共345兲 A 关87/5兴关47/5兴
关70/14兴
C8 H6 Cl2 3,5-dichlorostyrene 关2155-42-2兴
共326 – 498兲 55.1 共341兲 A 关87/5兴关70/14兴
C8 H6 Cl2 O 3-共chloromethyl兲benzoyl chloride 关63024-77-1兴
共424 – 464兲 54.7 共439兲 A 关87/5兴关99/16兴
C8 H6 Cl2 O 4-共chloromethyl兲benzoyl chloride 关876-08-4兴
共440– 466兲 68.3 共453兲 A 关87/5兴关99/16兴
C8 H6 Cl4 2,3,4,6-tetrachloro-1-ethylbenzene 关877-08-7兴
共350–543兲 53.6 共365兲 A 关87/5兴关47/5兴
C8 H6 Cl4 3,4,5,6-tetrachloro-1,2-dimethylbenzene 关877-08-7兴
共367–547兲 63.6 共382兲 A 关87/5兴关70/14兴
C8 H6 F12O3 S bis共1,1,1,3,3,3-hexafluoro-2-methyl-2-propanol兲 sulfite 关53602-64-5兴
46.5 关75/43兴
C8 H6 O 2,3-benzofuran 关271-89-6兴
共323– 403兲 46.2 共338兲 A 关87/5兴
C8 H6 O 2-ethynylphenol 关5101-44-0兴
共300–373兲 33.5 共315兲 A 关87/5兴
C8 H6 O2 phenyl glyoxal 关1074-12-0兴
共348 – 467兲 59.7 共363兲 A 关87/5兴关47/5兴
C8 H6 O2 phthalide 关87-41-2兴
共368 –563兲 59.3 共383兲 A 关87/5兴关47/5兴
C8 H6 O3 piperonal 关120-57-0兴
共310–353兲 65.7 共331兲 关53/5兴
共360–536兲 60.6 共375兲 A 关87/5兴关47/5兴
C8 H6 S benzo关b兴thiophene 关95-15-8兴
共349– 424兲 52.1 共364兲 关99/16兴
共424 – 498兲 47.9 共439兲 关99/16兴
共498 – 631兲 45.0 共513兲 关99/16兴
共310–542兲 54.3 共320兲 关91/13兴
共310–542兲 52.0 共360兲 关91/13兴
共310–542兲 49.7 共400兲 关91/13兴
共310–542兲 46.2 共460兲 关91/13兴
共310–542兲 43.8 共500兲 关91/13兴
共310–542兲 41.2 共540兲 关91/13兴
47.2 共425兲 关81/1兴
42.8 共505兲 关81/1兴
36.1 共605兲 关81/1兴
共306 –346兲 53.8 共326兲 关81/2兴关99/16兴
C8 H7 Br 2-bromostyrene 关2039-88-5兴
共378 –543兲 48.7 共393兲 A 关87/5兴关70/14兴
C8 H7 Br 4-bromostyrene 关2039-82-9兴
共393– 420兲 48.5 共406兲 关99/16兴
共383–543兲 49.9 共398兲 A 关87/5兴关70/14兴
C8 H7 Cl 2-chlorostyrene 关2039-87-4兴
共363–523兲 46.0 共378兲 A 关87/5兴关70/14兴
C8 H7 Cl 3-chlorostyrene 关2039-85-2兴
共298 – 463兲 46.1 共313兲 A 关87/5兴关47/5兴
关70/14兴
C8 H7 Cl 4-chlorostyrene 关1073-67-2兴
共363–523兲 48.1 共378兲 A 关87/5兴关47/5兴
关70/14兴
C8 H7 ClO 4⬘-chloroacetophenone 关99-91-2兴
共404 – 623兲 54.0 共419兲 A 关87/5兴关99/16兴
共395– 485兲 50.7 共410兲 关49/1兴关84/9兴
C8 H7 ClO phenylacetyl chloride 关103-80-0兴
共321– 483兲 56.5 共336兲 A 关87/5兴关47/5兴
关99/16兴
关70/14兴
C8 H8 Cl2 1,4-bis共chloromethyl兲benzene 关93-52-7兴
共412–504兲 50.8 共427兲 关99/16兴
C8 H8 Cl2 O2 2-共2,4-dichlorophenoxy兲ethanol 关120-67-2兴
共484 –560兲 65.1 共499兲 关59/1兴关84/9兴
A 关99/16兴关87/5兴
C8 H8 Cl2 O3 3,5-dichloro-2,6-dimethoxyphenol
共293–323兲 70.4 共308兲 CGC 关99/13兴
C8 H8 Cl3 O3 PS O,O-dimethyl-O-共2,4,5-trichlorophenyl兲thiophosphate 关299-84-3兴
共298 –373兲 56.8 共313兲 A 关87/5兴
C8 H8 N2 O2 1,4-bis共2-hydroxyethyl兲piperazine 关122-96-3兴
共413–507兲 67.8⫾5.3 关98/7兴
C8 H8 N2 O3 2⬘-nitroacetanilide 关552-32-9兴
共473–593兲 44.0 共488兲 A 关87/5兴
C8 H8 O acetophenone 关98-86-2兴
共360–520兲 55.4⫾0.4 共298兲 EB 关96/3兴
共343–383兲 53.4 共298兲 CGC 关95/21兴
共343–383兲 52.7 共298兲 CGC 关95/21兴
共343–383兲 57.9 共298兲 CGC 关95/21兴
共375– 603兲 49.7 共390兲 A 关87/5兴
共383– 437兲 41.9 共398兲 GS, EB 关65/7兴
共310– 476兲 51.2 共325兲 关47/5兴
C8 H8 O 2,5-dihydrobenzo-3,4-furan 关496-14-0兴
共285–510兲 53.7⫾0.4 共298兲 EB 关96/4兴
C8 H8 O phenylacetaldehyde 关122-78-1兴
共283–333兲 54.5 共298兲 A 关87/5兴
C8 H8 O2 1,4-benzodioxan 关493-09-4兴
共400– 486兲 50.4 共415兲 A 关87/5兴
50.4 关58/25兴
C8 H8 O2 benzyl formate 关104-57-4兴
共298 –357兲 51.6 共313兲 A 关87/5兴
C8 H8 O2 2⬘-hydroxyacetophenone 关118-93-4兴
共369– 491兲 58.3 共384兲 A 关87/5兴
50.2 关86/10兴
C8 H8O2 2-methoxybenzaldehyde 关135-02-4兴
55.2 关86/10兴
C8 H8 O2 4-methoxybenzaldehyde 关123-11-5兴
共348 –521兲 58.4 共363兲 A, EB 关85/9兴
共283–323兲 60.4 共298兲 A 关87/5兴关55/8兴
共346 –521兲 57.1 共361兲 A 关87/5兴关47/5兴
C8 H8 O2 methyl benzoate 关93-58-3兴
共358 –517兲 51.1⫾0.2 共360兲 EB 关02/15兴
共358 –517兲 48.5⫾0.2 共400兲 EB 关02/15兴
共358 –517兲 45.8⫾0.2 共440兲 EB 关02/15兴
共358 –517兲 43.0⫾0.4 共480兲 EB 关02/15兴
57.2⫾0.1 共303兲 C 关98/6兴
共313–353兲 53.4 共298兲 CGC 关95/21兴
共313–363兲 53.8 共298兲 CGC 关95/21兴
共433– 473兲 54.7 共298兲 CGC 关95/21兴
共334 – 428兲 50.7 共379兲 BG 关88/2兴
共334 – 428兲 48.3 共410兲 BG 关88/2兴
共283–323兲 53.9 共298兲 A 关87/5兴
共373–533兲 49.7 共388兲 A 关87/5兴
55.6⫾0.1 共298兲 C 关72/1兴
共341– 433兲 52.8 共363兲 BG 关71/2兴
C8 H8 O2 m-toluic acid 关99-04-7兴
共473–533兲 62.8 共503兲 A 关87/5兴关70/34兴
C8 H8 O2 phenyl acetate 关122-79-2兴
共313–363兲 53.3 共298兲 CGC 关95/21兴
共433– 473兲 53.6 共298兲 CGC 关95/21兴
共313–353兲 53.1 共298兲 CGC 关95/21兴
共311– 469兲 51.7 共326兲 A 关87/5兴关47/5兴
C8 H8 O2 phenylacetic acid 关103-82-2兴
共370–539兲 65.0 共385兲 A 关87/5兴
C8 H9 N 2-methyl-5-vinylpyridine 关140-76-1兴
共342– 457兲 55.2 共357兲 A 关87/5兴
共342– 457兲 54.5 共357兲 关61/19兴关84/9兴
C8 H9 N N-methylbenzaldehyde-imine
共283–318兲 51.1⫾0.2 共301兲 GS 关97/9兴
共283–318兲 51.2⫾0.2 共298兲 GS 关97/9兴
C8 H9 NO acetanilide 关103-84-4兴
共473–577兲 64.8 共488兲 A 关87/5兴
共387–577兲 66.3 共402兲 关47/5兴
C8 H9 NO2 anthranilic acid, methyl ester 关134-20-3兴
共299–333兲 62.3 共314兲 A, ME 关87/5兴关54/7兴
C8 H9 NO2 2-nitro-1,3-dimethylbenzene 关81-20-9兴
共284 –323兲 57.2⫾0.8 共303兲 GS 关00/15兴
57.5⫾0.8 共298兲 关00/15兴
共373– 498兲 49.7 共388兲 A 关87/5兴
C8 H9 NO2 4-nitro-1,3-dimethylbenzene 关89-87-2兴
共368 –518兲 56.7 共383兲 A 关87/5兴
共338 –517兲 57.3 共353兲 关47/5兴
C8 H9 NO2 1,2-dimethyl-3-nitrobenzene 关83-41-0兴
共383–518兲 59.4 共398兲 关84/9兴
C8 H9 NO2 1,2-dimethyl-4-nitrobenzene 关99-51-4兴
共399–536兲 63.6 共414兲 关84/9兴
C8 H9 NO2 2-nitro-1-ethylbenzene 关612-22-6兴
共284 –323兲 62.7⫾0.4 共303兲 GS 关00/15兴
63.0⫾0.4 共298兲 关00/15兴
共353– 422兲 56.3 共368兲 A 关87/5兴
C8 H9 NO2 4-nitro-1-ethylbenzene 关100-12-9兴
共353– 433兲 59.4 共368兲 A 关87/5兴
C8 H9 N3 2,2-dicyanohexanenitrile
共288 –323兲 61.0⫾0.2 GS 关94/5兴
C8 H10 1,2-dimethylbenzene 关95-47-6兴
共373– 423兲 42.9 共298兲 CGC 关95/21兴
共333– 419兲 41.1 共348兲 A 关87/5兴
共416 – 473兲 38.0 共431兲 A 关87/5兴
共471–571兲 36.7 共486兲 A 关87/5兴
共567– 630兲 36.7 共582兲 A 关87/5兴
共386 – 416兲 39.8 共401兲 关82/3兴
43.4 共298兲 关71/28兴
43.4⫾0.1 共298兲 C 关47/7兴
共337– 419兲 40.8 共352兲 MM 关45/2兴关49/6兴
共273–323兲 45.0 共288兲 关43/1兴关84/9兴
C8 H10 1,3-dimethylbenzene 关108-38-3兴
共360– 410兲 39.2 共375兲 关02/9兴
共327– 412兲 40.7 共342兲 关89/7兴
共267–301兲 44.7 共282兲 A 关87/5兴
共412– 462兲 37.5 共427兲 A 关87/5兴
共461–554兲 36.4 共476兲 A 关87/5兴
共550– 617兲 36.2 共565兲 A 关87/5兴
共380– 411兲 38.7 共395兲 关83/2兴
42.7 共298兲 关71/28兴
42.7⫾0.1 共298兲 C 关47/7兴
共331– 415兲 40.4 共346兲 MM 关87/5兴关45/2兴
关49/6兴
共273–333兲 43.2 共288兲 关43/1兴关84/9兴
C8 H10 1,4-dimethylbenzene 关106-42-3兴
共373– 423兲 42.3 共298兲 CGC 关95/21兴
共293–323兲 43.0⫾0.1 共298兲 关90/3兴
42.3⫾0.01 共298兲 关88/16兴
40.3 共353兲 关88/7兴
共411– 463兲 37.3 共426兲 A 关87/5兴
共460–553兲 36.1 共475兲 A 关87/5兴
共551– 616兲 36.2 共566兲 A 关87/5兴
36.0⫾0.1 共411兲 C 关85/10兴
34.5⫾0.1 共436兲 C 关85/10兴
关99/16兴
C8 H17Cl2 N N-isobutyl bis共2-chloromethyl兲amine 关87289-70-1兴
共273–345兲 60.3 共288兲 A, GS 关87/5兴关48/13兴
关99/16兴
C8 H17F 1-fluorooctane 关463-11-6兴
49.7 共298兲 关U/1兴关85/6兴
共307– 446兲 44.1 共322兲 A, EST 关87/5兴关61/13兴
关70/14兴
C8 H17I 1-iodooctane 关629-27-6兴
共391–554兲 50.7 共406兲 A, EST 关87/5兴关61/13兴
关70/14兴
C8 H17NO N-propylpiperidine 关5470-07-0兴
共275–314兲 45.2⫾0.4 共294兲 GS 关98/12兴
共275–314兲 44.9⫾0.4 共298兲 GS 关98/12兴
C8 H17NO butyric acid, N,N-diethylamide 关1114-76-7兴
共298 –373兲 38.7 共313兲 A 关87/5兴
C8 H17NO caprylaldehyde oxime 关929-55-5兴
共313– 400兲 71.3 共328兲 A 关87/5兴
C8 H17NO 2-octanone oxime 关7207-49-0兴
共293– 487兲 67.5 共308兲 A 关87/5兴
C8 H17NO 3-octanone oxime 关7207-50-3兴
共293– 400兲 67.2 共308兲 A 关87/5兴
C8 H17NO 4-octanone oxime 关7207-51-4兴
共293– 400兲 68.8 共308兲 A 关87/5兴
C8 H17NO2 2,4,4-trimethyl-2-nitropentane
共288 –324兲 54.2⫾0.8 共298兲 GS 关97/5兴
C8 H17NO2 lactic acid, N-isopentylamide
共386 – 433兲 77.9 共401兲 A 关87/5兴
C8 H17NO2 lactic acid, N-pentylamide
共373– 448兲 81.8 共388兲 A 关87/5兴
C8 H17NO2 共l兲 leucine ethyl ester 关2743-60-4兴
共333– 449兲 43.5 共348兲 A 关87/5兴
C8 H17NO2 ethyl 2-共N,N-dimethylamino兲-2-methylpropionate
55.6⫾0.4 共283兲 DSC 关93/15兴
C8 H17NO2 共1-methylheptyl兲nitrite
共303–338兲 44.9 共318兲 A 关87/5兴
C8 H18 2,2-dimethylhexane 关590-73-8兴
37.3 共298兲 关71/28兴
共243–380兲 39.7 共258兲 关47/5兴
37.3⫾0.1 共298兲 C 关47/7兴
共302–381兲 36.6 共317兲 A, MM 关87/5兴关45/2兴
C8 H18 2,3-dimethylhexane 关584-94-1兴
38.8 共298兲 关71/28兴
共250–388兲 41.4 共265兲 关47/5兴
38.8⫾0.1 共298兲 C 关47/7兴
共310–390兲 37.6 共325兲 A, MM 关87/5兴关45/2兴
C8 H18 2,4-dimethylhexane 关589-43-5兴
37.8 共298兲 关71/28兴
共246 –382兲 41.0 共261兲 关47/5兴
37.8⫾0.1 共298兲 C 关47/7兴
共305–385兲 36.9 共320兲 A, MM 关87/5兴关45/2兴
C8 H18 2,5-dimethylhexane 关592-13-2兴
37.9 共298兲 关71/28兴
共246 –382兲 41.1 共261兲 关47/5兴
37.9⫾0.1 共298兲 C 关47/7兴
共307–383兲 36.9 共322兲 A, MM 关87/5兴关45/2兴
C8 H18 3,3-dimethylhexane 关563-16-6兴
共247–385兲 41.2 共262兲 关47/5兴
37.5⫾0.1 共298兲 C 关47/7兴
共308 –386兲 36.6 共323兲 A, MM 关87/5兴关45/2兴
C8 H18 3,4-dimethylhexane 关583-48-2兴
共251–390兲 41.3 共266兲 关47/5兴
39.0⫾0.1 共298兲 C 关47/7兴
共313–392兲 37.7 共328兲 A, MM 关87/5兴关45/2兴
关99/16兴
C9 H7 N isoquinoline 关119-65-3兴
共439–517兲 51.0 共454兲 A, EB 关87/5兴关61/10兴
C9 H7 N quinoline 关91-22-5兴
共573– 668兲 46.9 共588兲 DSC 关96/10兴
共504 – 616兲 46.5 共519兲 关92/1兴
共463–794兲 46.1 共478兲 A 关87/5兴
共286 –309兲 58.1 共298兲 GS 关80/6兴
共433–511兲 49.2 共448兲 EB 关87/5兴关61/10兴
C9 H8 indene 关95-13-6兴
共369– 457兲 45.3 共384兲 A 关87/5兴
共289– 455兲 43.6 共304兲 A 关87/5兴关47/5兴
共329– 454兲 43.9 共392兲 关42/3兴
C9 H8 Cl2 O3 2,4-dichlorophenoxyacetic acid, methyl ester 关1928-38-7兴
共403–548兲 68.0 共418兲 A 关87/5兴关99/16兴
C9 H8 Cl3 NO3 2,2,4-trichloro-5-共4-morpholinyl兲-4-cyclopentene-1,3-dione 关75907-45-8兴
共453– 483兲 79.6 共468兲 GC 关80/25兴
C9 H8 N2 1-phenylpyrazole 关1126-00-7兴
70.2⫾3.4 共298兲 C 关00/1兴
C9 H8 N2 1-phenylimidazole 关7164-98-9兴
84.6⫾3.7 共298兲 C 关00/1兴
C9 H8 O 1-indanone 关83-33-0兴
共318 –348兲 60.3⫾0.4 GS 关98/3兴
C9 H8 O 3-phenyl-2-propenal 共cinnamaldehyde兲 关14371-10-9兴
62.4 共298兲 GC 关02/37兴
共408 – 482兲 51.7 共444兲 TGA 关02/40兴
共349–519兲 58.2 共364兲 A 关87/5兴关47/5兴
共353–373兲 72.7 共363兲 A 关87/5兴
C9 H8 O2 trans cinnamic acid 关140-10-3兴
共430–573兲 73.9 共445兲 A 关87/5兴
C9 H8 O2 7,7-dimethoxynorborane 关39869-70-0兴
共321–357兲 49.0 共339兲 EB 关94/16兴
C9 H9 F6 NO5 共l兲 N,O-bis共trifluoroacetal兲-threonine methyl ester 关1548-45-4兴
共323– 413兲 72.5 共338兲 A 关87/5兴关99/16兴
C9 H9 N 3-methylindole 共skatole兲 关83-34-1兴
共368 –540兲 64.5 共383兲 A 关87/5兴关47/5兴
C9 H9 N ␣-methylbenzylcyanide 关1823-91-2兴
共284 –318兲 60.8⫾0.7 共301兲 GS 关00/2兴
共284 –318兲 60.9⫾0.7 共298兲 GS 关00/2兴
C9 H9 NO4 3-nitrobenzoic acid, ethyl ester 关618-98-4兴
共381–571兲 65.1 共396兲 A 关87/5兴关47/5兴
C9 H10 indane 关496-11-7兴
共374 – 466兲 44.0 共389兲 A 关87/5兴
49.0 共298兲 C 关81/10兴
共355– 482兲 45.0 共370兲 关76/26兴
C9 H10 2-methylstyrene 关611-15-4兴
共305–385兲 47.9 共320兲 A 关87/5兴关53/13兴
C9 H10 3-methylstyrene 关100-80-1兴
共314 –385兲 47.5 共329兲 A 关87/5兴关53/13兴
C9 H10 4-methylstyrene 关622-97-9兴
共304 –390兲 47.6 共319兲 A 关87/5兴关53/13兴
C9 H10 ␣-methylstyrene 关98-83-9兴
共274 –314兲 49.2⫾0.3 共294兲 GS 关99/21兴
48.9⫾0.3 共298兲 关99/21兴
共331– 467兲 48.6⫾0.4 共298兲 EB 关97/6兴
共343– 493兲 44.3 共358兲 A 关87/5兴
共353– 413兲 44.8 共368兲 A 关87/5兴
C9 H10 cis -methylstyrene 关766-90-5兴
共348 – 498兲 44.8 共363兲 A 关87/5兴
C9 H10 trans -methylstyrene 关873-66-5兴
共291– 452兲 46.4 共306兲 A 关87/5兴关47/5兴
C9 H10 allylbenzene 关300-57-2兴
共274 –313兲 46.5⫾0.2 共294兲 GS 关99/21兴
46.3⫾0.2 共298兲 关99/21兴
C9 H10Cl2 O4 2,6-dichlorosyringaldehyde
共293–323兲 82.2 共308兲 CGC 关99/13兴
C9 H10F2 1,1-difluoro-3-phenylpropane
共278 –318兲 53.3⫾0.4 共298兲 GS 关97/14兴
C9 H10O allyl phenyl ether 关1746-13-0兴
共349– 456兲 49.4 共364兲 A 关87/5兴
C9 H10O cinnamyl alcohol 关104-54-1兴
共295–325兲 68.1⫾0.1 共310兲 TG,DTA 关02/3兴
共310–328兲 79.8 共319兲 A 关87/5兴
共373–523兲 56.2 共388兲 A 关87/5兴
C9 H10O 2,4-dimethylbenzaldehyde 关15764-16-6兴
共358 – 489兲 57.4 共373兲 A 关87/5兴
C9 H10O 5-hydroxyindane 关1470-94-6兴
共393–524兲 55.4 共408兲 A 关87/5兴
C9 H10O 4⬘-methylacetophenone 关122-00-9兴
共288 –333兲 59.6 共303兲 A 关87/5兴
C9 H10O 2-phenylpropionaldehyde 关93-53-8兴
共364 –517兲 52.3⫾0.2 共360兲 EB 关02/21兴
共364 –517兲 49.4⫾0.2 共400兲 EB 关02/21兴
共364 –517兲 46.6⫾0.3 共440兲 EB 关02/21兴
共364 –517兲 43.4⫾0.5 共480兲 EB 关02/21兴
C9 H10O 3-phenylpropionaldehyde 关104-53-0兴
共330–363兲 67.5 共345兲 A 关87/5兴
C9 H10O benzyl methyl ketone 关103-79-7兴
共343–383兲 56.1 共298兲 CGC 关95/21兴
共343–383兲 55.0 共298兲 CGC 关95/21兴
共273–328兲 53.5⫾0.3 共298兲 关54/8兴
C9 H10O ethyl phenyl ketone 共propiophenone兲 关93-55-0兴
共388 – 623兲 52.1 共403兲 A 关87/5兴
共391– 454兲 44.4 共406兲 EB, GS 关65/7兴
C9 H10O 2-vinylanisole 关612-15-7兴
共314 – 467兲 56.7 共329兲 A 关87/5兴关47/5兴
C9 H10O 3-vinylanisole 关626-20-0兴
共316 – 471兲 55.9 共331兲 A 关87/5兴关47/5兴
C9 H10O 4-vinylanisole 关637-69-4兴
共318 – 478兲 54.9 共333兲 A 关87/5兴关47/5兴
C9 H10O2 methyl o-toluate 关89-71-4兴
57.3⫾0.2 共293兲 C 关98/6兴
C9 H10O2 methyl m-toluate 关99-36-5兴
60.3⫾0.2 共296兲 C 关98/6兴
53.5 共388兲 关74/1兴
C9 H10O2 acetic acid, 3-tolyl ester 关122-46-3兴
共385– 480兲 55.7 共400兲 A, EB 关87/5兴关69/13兴
C9 H10O2 acetic acid, 4-tolyl ester 关140-39-6兴
共385– 480兲 55.9 共400兲 A, EB 关87/5兴关69/13兴
C9 H10O2 2-acetylanisole 关579-74-8兴
56.5 关86/10兴
C9 H10O2 4-acetylanisole 关100-06-1兴
共311–334兲 66.5 共322兲 A, ME 关87/5兴关54/9兴
C9 H10O2 3,4-dihydro-2H-1,5-benzodioxepin 关7216-18-4兴
55.6 关58/25兴
C9 H10O2 benzyl acetate 关140-11-4兴
共283– 490兲 55.5 共298兲 A 关87/5兴
共283–328兲 60.4 共305兲 ME 关54/10兴
C9 H10O2 ethylbenzoate 关93-89-0兴
共369–531兲 52.5⫾0.2 共380兲 EB 关02/15兴
共369–531兲 49.6⫾0.2 共420兲 EB 关02/15兴
共369–531兲 46.7⫾0.3 共460兲 EB 关02/15兴
共369–531兲 43.6⫾0.5 共500兲 EB 关02/15兴
共344 – 440兲 57.0 共356兲 BG 关88/2兴
共344 – 440兲 50.5 共419兲 BG 关88/2兴
共288 –333兲 55.9 共303兲 A 关87/5兴
共358 – 487兲 50.4 共373兲 A 关87/5兴
共317– 486兲 51.9 共332兲 关47/5兴
C13H28O 3,3,6-trimethyl-4-propyl-4-heptanol
共383–513兲 60.1 共398兲 关73/26兴
C13H28O 2,2,5-trimethyl-3-tert-butyl-3-hexanol 关32579-70-7兴
共377–513兲 57.6 共392兲 关73/26兴
C13H28O4 tripropylene glycol, monobutyl ether 关57499-93-1兴
共374 –543兲 67.1 共389兲 A 关87/5兴关47/5兴
C13H28S 1-tridecanethiol 关19484-26-5兴
共433–598兲 64.7 共448兲 关99/16兴
C13H29N tridecylamine 关2869-34-3兴
共458 –562兲 60.1 共473兲 A, EST 关87/5兴关56/17兴
C14H8 Cl4 p,p⬘-DDE 关72-55-9兴
共343– 453兲 87.2 共398兲 GC 关90/2兴
C14H8 O2 9,10-anthraquinone 关84-65-1兴
共559– 660兲 64.3 共574兲 A 关87/5兴
C14H8 O4 1,4-dihydroxy-9,10-anthraquinone 关81-64-1兴
共469– 633兲 74.0 共484兲 A 关87/5兴关47/5兴
C14H9 Cl5 1,1,1-trichloro-2,2-bis共4-chlorophenyl兲ethane 共p,p⬘DDT兲 关50-29-3兴
106.1⫾1.3 共398兲 GS 关01/1兴
共343– 453兲 93.2 共398兲 GC 关90/2兴
C14H9 Cl5 1,1,1-trichloro-2-共4-chlorophenyl兲2-共2-chlorophenyl兲ethane 共p,o⬘DDT兲 关789-02-6兴
共343– 453兲 88.6 共398兲 GC 关90/2兴
C14H9 Cl5 DDT
共313–363兲 83.7 共338兲 关49/3兴
C14H10 anthracene 关120-12-7兴
共323– 473兲 72.4 共398兲 GC 关02/18兴
79.1 共298兲 CGC 关01/1兴
79.8 共298兲 CGC 关98/11兴
共453–503兲 79.6 共298兲 CGC 关95/21兴
共343– 453兲 69.7 共398兲 GC 关90/2兴
共504 – 615兲 58.6 共519兲 A 关87/5兴
共500– 616兲 59.2 共558兲 I 关23/1兴
共500– 616兲 60.3 共515兲 I 关23/1兴关84/9兴
共496 – 614兲 59.6 共555兲 I 关22/1兴
共496 – 614兲 60.7 共511兲 I 关22/1兴关84/9兴
C14H10 phenanthrene 关85-01-8兴
共323– 473兲 72.2 共398兲 GC 关02/18兴
78.7 共298兲 CGC 关98/11兴
共403– 453兲 78.5 共298兲 CGC 关95/21兴
共343– 453兲 71.2 共398兲 GC 关90/2兴
共391– 613兲 58.2 共406兲 A 关87/5兴
共373– 423兲 69.6 共388兲 A 关87/5兴关75/11兴
71.2 共372兲 关77/22兴
共476 – 620兲 57.2 共548兲 I 关23/1兴
共476 – 620兲 61.2 共491兲 I 关23/1兴关84/9兴
共505– 614兲 59.3 共560兲 I 关22/1兴
共505– 614兲 61.2 共520兲 I 关22/1兴关84/9兴
C14H10 diphenylacetylene 关501-65-5兴
共439–517兲 63.8⫾0.2 共440兲 EB 关02/17兴
共439–517兲 60.9⫾0.2 共480兲 EB 关02/17兴
共439–517兲 58.1⫾0.3 共520兲 EB 关02/17兴
C14H10Cl4 1,1-dichloro-2,2-bis共4-chlorophenyl兲ethane p,p⬘-DDD 关72-54-8兴
共343– 453兲 88.5 共398兲 GC 关90/2兴
C14H10Cl4 共2,2⬘,4,6⬘-tetrachloro-5-methyldiphenyl兲methane 关121107-48-0兴
98.6 共298兲 GC 关96/24兴
C14H10Cl4 共2,2⬘,4,5⬘-tetrachloro-5-methyldiphenyl兲methane 关121107-46-8兴
101.0 共298兲 GC 关96/24兴
C14H10Cl4 共2,2⬘,5,5⬘-tetrachloro-4-methyldiphenyl兲methane 关121107-54-8兴
101.2 共298兲 GC 关96/24兴
C14H10Cl4 共2,2⬘,4,4⬘-tetrachloro-5-methyldiphenyl兲methane 关121107-44-6兴
101.3 共298兲 GC 关96/24兴
C14H10Cl4 共2,2⬘,4,6⬘-tetrachloro-3-methyldiphenyl兲methane 关121107-47-9兴
100.1 共298兲 GC 关96/24兴
C14H10Cl4 共2⬘,3,4,6⬘-tetrachloro-6-methyldiphenyl兲methane 关121107-83-5兴
101.1 共298兲 GC 关96/24兴
C15H9 N3 pyrido关2,3-f兴关1,7兴phenanthroline
共648 –707兲 65.1 共663兲 A 关87/5兴
C15H9 N3 pyrido关3,2-f兴关1,7兴phenanthroline
共648 –706兲 67.4 共663兲 A 关87/5兴
C15H10N2 O2 2,2⬘-diisocyanatodiphenylmethane 关2536-05-2兴
共343– 413兲 90.1 共358兲 A 关87/5兴
C15H10N2 O2 2,4⬘-diisocyanatodiphenylmethane 关5873-54-1兴
共343– 413兲 89.3 共358兲 A 关87/5兴
C15H10N2 O2 4,4⬘-diisocyanatodiphenylmethane 关101-68-8兴
共343– 413兲 90.5 共358兲 A 关87/5兴
共442–530兲 93.8 共457兲 A 关87/5兴
共442–530兲 90.6 共483兲 A 关66/28兴
C15H11NO2 1-methylamino-9,10-anthraquinone 关82-38-2兴
共433– 493兲 103.5 共448兲 A 关87/5兴
C15H12 2-methylanthracene 关613-12-7兴
共323– 473兲 76.1 共398兲 GC 关02/18兴
C15H12 9-methylanthracene 关779-02-0兴
共354 – 402兲 98.9 共369兲 A 关87/5兴
共423–587兲 58.5 共465兲 关83/4兴
共423–515兲 58.1 共515兲 关83/4兴
共423–515兲 56.5 共555兲 关83/4兴
C15H12 1-methylphenanthrene 关832-69-9兴
共323– 473兲 76.3 共398兲 GC 关02/18兴
C15H12O dibenzosuberone 关1210-35-1兴
共314 –338兲 90.0⫾1.5 GS 关98/4兴
C15H12O2 1,3-diphenyl-1,3-propanedione 关120-46-7兴
共368 –383兲 60.1 共375兲 A 关87/5兴
C15H14Cl3 O2 PS 共chloromethyl兲thiophosphnic acid, O,O-bis共2-chloro-4-methylphenyl兲 ester 关57875-65-7兴
共343–365兲 93.2 共354兲 A 关87/5兴关99/16兴
C15H14O 1,3-diphenylacetone 关102-04-5兴
共398 – 604兲 65.7 共413兲 A 关87/5兴关47/5兴
C15H14O2 2,2-diphenyl-1,3-dioxolane 关4359-34-6兴
共331–370兲 84.6⫾0.6 共298兲 GS 关02/32兴
共331–370兲 81.2⫾0.6 GS 关98/21兴
C15H14O2 1-biphenyloxy-2,3-epoxypropane 关7144-65-2兴
共408 – 613兲 80.0 共423兲 A 关87/5兴
C15H14O3 2-hydroxy-4-ethoxybenzophenone 关15889-70-0兴
共373– 433兲 90.7 共403兲 ME 关84/1兴
C15H14O5 2,2⬘-dihydroxy-4,4⬘-dimethoxybenzophenone 关131-54-4兴
共406 – 497兲 77.4 共423兲 A, UV 关87/5兴关60/2兴
C15H15Cl chloro-di-4-tolylmethane 关13389-70-3兴
共406 – 453兲 75.2 共421兲 A 关87/5兴
C15H16 ditolylmethane 关1335-47-3兴
共573– 673兲 51.8 共588兲 关64/11兴
C15H16 1,1-diphenylpropane 1530-03-6兴
共298 –343兲 71.4⫾0.4 共321兲 GS 关99/8兴
共298 –343兲 72.8⫾0.4 共298兲 GS 关99/8兴
C15H16 1,3-diphenylpropane 关1081-75-0兴
共342–577兲 61.5 共357兲 A 关87/5兴
C15H16N4 O2 3-methyl-3⬘-nitro-4-N,N-dimethylaminoazobenzene
共370–388兲 98.6 共379兲 A 关87/5兴
C15H16O di-共4-tolyl兲methanol 关885-77-8兴
共413– 478兲 81.7 共428兲 A 关87/5兴
C15H16O 1-isovaleronaphthone
共409–593兲 76.2 共424兲 A 关87/5兴关47/5兴
C15H16O2 Bisphenol A 关80-05-7兴
共466 – 634兲 102.2 共481兲 A 关87/5兴关47/5兴
C15H17NO2 N-共2-hydroxy-3-phenoxypropyl兲phenylamine
共343–373兲 113.9 共358兲 A 关87/5兴
C15H18 1-pentylnaphthalene 关86-89-5兴
共415–535兲 62.7 共430兲 A 关87/5兴
C15H18O 2,4,6-triallylphenol 关20490-22-6兴
共423–571兲 61.0 共438兲 A 关87/5兴
C15H19Cl3 O3 2,4,5-trichlorophenoxyacetic acid, heptyl ester
关70/14兴
C16H33I 1-iodohexadecane 关544-77-4兴
共475– 673兲 73.0 共490兲 A, EST 关87/5兴关61/13兴
关70/14兴
C16H34 hexadecane 关544-76-3兴
81.8⫾1.3 共298兲 CGC 关00/9兴
共453–503兲 81.4 共298兲 CGC 关95/21兴
共423– 473兲 81.4 共298兲 CGC 关95/21兴
共363– 413兲 81.2 共298兲 CGC 关95/21兴
共393–583兲 68.5 共408兲 关94/14兴
81.4 共298兲 关94/12兴
共505–589兲 59.8 共520兲 关92/2兴
共323– 423兲 74.9 共338兲 A 关87/5兴
66.9 共343兲 GC 关77/34兴
66.2 共353兲 GC 关77/34兴
65.6 共363兲 GC 关77/34兴
64.9 共373兲 GC 关77/34兴
64.2 共383兲 GC 关77/34兴
81.4⫾0.4 共298兲 C 关72/29兴
81.1 共298兲 关71/28兴
共467–563兲 61.7 共482兲 A, MM 关87/5兴关54/7兴
共299–324兲 93.4 共311兲 ME 关49/14兴
共293–308兲 80.2 共300兲 ME 关49/17兴
共442– 469兲 65.7 共455兲 ME 关38/8兴
C16H34 2-methylpentadecane 关1560-93-6兴
共417–554兲 62.0 共432兲 A 关87/5兴
C16H34 3-methylpentadecane 关2882-96-4兴
共417–555兲 61.0 共432兲 A 关87/5兴
C16H34 4-methylpentadecane 关2801-87-8兴
共411–553兲 57.8 共426兲 A 关87/5兴
C16H34 5-methylpentadecane 关25117-33-3兴
共408 –551兲 57.3 共423兲 A 关87/5兴
C16H34 7-methylpentadecane 关6165-40-8兴
共355– 410兲 66.3 共370兲 A 关87/5兴
C16H34 2,3-dimethyltetradecane 关18435-23-9兴
共412–554兲 57.4 共427兲 A 关87/5兴
C16H34 2,4-dimethyltetradecane 关61868-06-2兴
共404 –539兲 60.6 共419兲 A 关87/5兴
C16H34 2,4,6-trimethyltridecane
共395–521兲 59.1 共410兲 A 关87/5兴
C16H34 2,2,4,4,6,8,8-heptamethylnonane 关4390-04-9兴
共423–545兲 52.4 共438兲 关88/8兴
C16H34 3,3.6,6-tetraethyloctane
共301–330兲 73.0⫾1.9 共308兲 HSA 关95/27兴
74.3⫾1.9 共298兲 关95/27兴
72.3⫾1.8 共298兲 CGC 关95/27兴
C16H34N2 bis共1,1,3,3-tetramethylbutyl兲diazene 关39198-34-0兴
66.5⫾0.6 共298兲 C 关76/3兴
C16H34O 1-hexadecanol 关36653-82-4兴
共328 –362兲 100.4 共347兲 GS 关01/3兴
共328 –362兲 108.8 共298兲 GS 关01/3兴
112.5 共298兲 CGC 关00/10兴
共343– 463兲 88.2 共403兲 关92/14兴
共509–569兲 68.9 共524兲 A 关87/5兴
共415– 487兲 83.2 共430兲 A 关87/5兴关74/13兴
共323–376兲 112.3 共338兲 关73/26兴
共418 – 463兲 78.8 共423兲 关73/26兴
共498 –569兲 70.0 共513兲 A, EB 关87/5兴关70/2兴
共445–598兲 77.3 共460兲 DTA 关69/5兴
共323–335兲 109.5 共329兲 ME 关65/15兴
C16H34O 2-hexadecanol 关14852-31-4兴
共333– 453兲 102.2 共348兲 关99/11兴
C16H34O3 2关2-共dodecyloxy兲ethoxy兴ethanol 关3055-93-4兴
共448 – 489兲 82.1 共463兲 A 关87/5兴
关99/16兴
C20H32 1,2,3,4-tetrahydro-5,8-dimethyl-1-octylnaphthalene 关55255-58-8兴
共419– 481兲 78.6 共434兲 关63/24兴关84/9兴
关99/16兴
C20H34 9-cyclohexyltetradecahydroanthracene 关55255-70-4兴
共419– 488兲 74.5 共434兲 A 关87/5兴
C20H34 tetradecylbenzene 关1459-10-5兴
共485– 665兲 74.5 共500兲 关99/16兴
99.6 共298兲 关71/28兴
C20H34O2 ethyl linolenate 关1191-41-9兴
共447– 491兲 72.7 共462兲 A 关87/5兴
C20H34O11 diethylene glycol dicarboxylic acid, di关1-共butoxycarbonyl兲ethyl兴 ester
共433–525兲 103.6 共448兲 A 关87/5兴
C20H34O11 diethylene glycol dicarboxylic acid, di关1-共sec-butoxycarbonyl兲ethyl兴 ester
共418 –513兲 103.1 共433兲 A 关87/5兴
C20H34O11 diethylene glycol dicarboxylic acid, di关1-共isobutoxycarbonyl兲ethyl兴 ester
共415–513兲 103.1 共430兲 A 关87/5兴
C20H36O2 ethyl linoleate 关544-35-4兴
共448 – 497兲 72.6 共463兲 A 关87/5兴
C20H36O6 共syn-cis/anti-cis兲 dicyclohexano-18-crown-6
124.2⫾4.0 共298兲 CGC 关00/9兴
C20H38 2-butyl-3-hexyldecahydronaphthalene 关66455-55-8兴
共407– 472兲 76.9 共422兲 关63/24兴关84/9兴
关99/16兴
C20H38 7-butyl-1-hexyldecahydronaphthalene 关66455-54-7兴
共407– 467兲 80.0 共422兲 关63/24兴关84/9兴
关99/16兴
C20H38 1,4-dimethyl-5-octyldecahydronaphthalene 关54964-83-9兴
共404 – 466兲 73.9 共419兲 关63/24兴关84/9兴
关99/16兴
C20H38 2,6-dimethyl-3-octyldecahydronaphthalene 关54964-85-1兴
共406 – 469兲 76.4 共421兲 关63/24兴关84/9兴
C20H38 3,4-dicyclohexyl-3,4-dimethylhexane 关26527-76-4兴
共343–365兲 78.4 共359兲 关99/16兴关80/16兴
C20H38 1-eicosyne 关765-27-5兴
共473– 651兲 68.9 共488兲 关99/16兴
C20H38 2-eicosyne 关61847-99-2兴
共480– 661兲 69.8 共495兲 关99/16兴
C20H38 3-eicosyne 关61886-66-6兴
共470– 648兲 68.4 共485兲 关99/16兴
C20H38O 3,7,11,15-tetramethyl-1-hexadecyn-3-ol 关29171-23-1兴
共403– 457兲 43.8⫾1.9 共430兲 关88/4兴
C20H38O2 ethyl oleate 关111-62-6兴
共384 – 481兲 92.4 共399兲 A 关87/5兴
C20H38O2 hexadecyl methacrylate 关2495-27-4兴
共431–541兲 73.1 共446兲 A 关87/5兴
C20H38O2 共Z兲 3-octadecenyl acetate
共393– 438兲 108.7 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共E兲 3-octadecenyl acetate
共393– 438兲 109.3 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共Z兲 9-octadecenyl acetate 关693-80-1兴
共393– 438兲 107.8 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共E兲 9-octadecenyl acetate 关22147-38-2兴
共393– 438兲 108.7 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共Z兲 11-octadecenyl acetate 关6186-98-7兴
共393– 438兲 108.4 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共E兲 11-octadecenyl acetate 关69282-64-0兴
共393– 438兲 109.1 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共Z兲 13-octadecenyl acetate 关60037-58-3兴
共393– 438兲 108.7 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共E兲 13-octadecenyl acetate
共393– 438兲 109.8 共298兲 GC 关97/13兴关00/10兴
C20H38O2 共Z兲 15-octadecenyl acetate
共393– 438兲 110.2 共298兲 GC 关97/13兴关00/10兴
C27H56 10-hexyl-10-methyleicosane
129.9⫾1.8 共298兲 CGC 关95/27兴
C27H56 5-ethyl-5-methyltetracosane
133.8⫾1.8 共298兲 CGC 关95/27兴
C27H56S 1-heptacosanethiol 关66291-85-8兴
共471–727兲 118.3 共486兲 EST 关99/16兴
C28H14 phenanthro关1,10,9,8-opqra兴perylene 关190-39-6兴
共580– 630兲 180.5 共595兲 A 关87/5兴
C28H22 9,9⬘-dimethyl-9,9⬘-bifluorenyl
共368 – 403兲 94.6 B 关94/4兴
C28H32 1,7-diphenyl-4-共3-phenylpropyl兲-3-heptene 关55282-03-6兴
共488 –556兲 98.0 共503兲 A, MG 关87/5兴关55/11兴
C28H34 1,7-diphenyl-4-共3-phenylpropyl兲heptane 关55282-64-9兴
共490–557兲 100.3 共505兲 A, MG 关87/5兴关55/11兴
C28H44O ergosterol 关57-87-4兴
共421– 454兲 118.7 共436兲 A 关87/5兴
C28H46O4 diisodecyl phthalate 关26761-40-0兴
共371– 496兲 79.3 共386兲 A 关87/5兴
C28H50 docosylbenzene 关5634-22-0兴
共453–715兲 110.8 共468兲 关99/16兴
C28H50 2-decyl-1-phenyldodecane 关55334-72-0兴
共497–532兲 102.5 共512兲 A 关87/5兴
C28H50O11 di关1-共2-ethylhexyl兲oxycarbonyl兴ethyl diethylene glycol dicarboxylate
共463–553兲 116.6 共478兲 A 关87/5兴
C28H50O11 di关1-共octyloxycarbony兲ethyl兴 diethylene glycol dicarboxylate
共463–564兲 112.5 共478兲 A 关87/5兴
C28H52 1,7-dicyclohexyl-4-共3-cyclohexylpropyl兲heptane 关55334-73-1兴
共482–549兲 98.7 共497兲 A, MG 关87/5兴关55/11兴
C28H54 1-cyclohexyl-2-共cyclohexylmethyl兲pentadecane 关55255-74-8兴
共501–536兲 105.4 共516兲 A, MG 关87/5兴关55/11兴
C28H56 docosylcyclohexane 关61828-07-7兴
共452–715兲 110.0 共467兲 关99/16兴
C28H56 1-octacosene 关18835-34-2兴
共448 –703兲 111.0 共463兲 关99/16兴
C28H56 11-共cyclohexylmethyl兲heneicosane
共499–538兲 94.2 共514兲 A, MG 关87/5兴关55/11兴
C28H56 2,2,4,10,12,12-hexamethyl-7-共3,5,5-trimethylhexyl兲-6-tridecene 关55255-73-7兴
共426 – 488兲 83.8 共441兲 A, MG 关87/5兴关55/11兴
C28H58 2-methylheptacosane 关1561-00-8兴
共448 –700兲 111.9 共463兲 关99/16兴
C28H58 2,2,4,10,12,12-hexamethyl-7-共3,5,5-trimethylhexyl兲tridecane 关3035-75-4兴
共308 –393兲 98.5 共323兲 A 关87/5兴关64/12兴
共429– 491兲 84.9 共444兲 A, MG 关87/5兴关55/11兴
C28H58 7-hexyldocosane 关55373-86-9兴
共506 –531兲 100.7 共518兲 A 关87/5兴
C28H58 octacosane 关630-02-4兴
150.8⫾0.5 共298兲 CGC 关02/44兴
150.7⫾1.7 共298兲 CGC 关00/9兴
152.4⫾2.9 共298兲 CGC 关97/17兴
共483–588兲 100.5 共498兲 关94/14兴
共407– 456兲 135⫾3 共431兲 TE 关94/2兴
共426 – 493兲 105.5 共441兲 TE, ME, GS 关91/9兴
共473–515兲 103.1⫾3.0 共494兲 GS 关90/14兴
共450–575兲 100.6 共500兲 EB, IPM 关89/1兴
共450–575兲 98.1 共560兲 EB, IPM 关89/1兴
共300–390兲 131.7 共315兲 A 关87/5兴
共481–705兲 106.6 共496兲 A, EST 关87/5兴关66/8兴
C28H58 9-octyleicosane 关13475-77-9兴
共460–530兲 106.8 共475兲 A 关87/5兴
C28H58S 1-octacosanethiol 关16331-26-3兴
共477–736兲 120.2 共492兲 EST 关99/16兴
C29H50 11-共2,5-dimethylphenyl兲-10-heneicosene
共471–534兲 99.2 共486兲 A, MG 关87/5兴关55/11兴
C29H52 tricosylbenzene 关61828-04-4兴
Al
C3 H9 Al trimethylaluminum 关75-24-1兴
共336 – 400兲 39.8 共351兲 关63/5兴
63.2⫾1.7 关63/34兴关82/15兴
41.1 BG 关46/13兴
C4 H10AlCl diethylaluminum chloride 关96-10-6兴
共278 –318兲 50.5 共293兲 关91/1兴
共273– 473兲 53.9 共373兲 关91/1兴
C4 H11Al diethylaluminum hydride 关871-27-2兴
57.7⫾2.1 关67/33兴关82/15兴
关65/27兴
46.9 关65/27兴
C6 H15Al triethylaluminum 关97-93-8兴
73.2⫾2.1 关67/33兴关82/15兴
关65/27兴
60.2 关65/27兴
54.1 BG 关46/13兴
C6 H15AlO diethylaluminum ethoxide 关1586-92-1兴
共403– 463兲 48.7⫾0.8 共433兲 关74/16兴
C7 H17AlO diethylaluminum propoxide
共398 – 463兲 51.0⫾0.8 共430兲 关74/16兴
C8 H19Al diisobutylaluminum hydride 关1191-15-7兴
42.3⫾2.1 关67/33兴关82/15兴
关65/27兴
35.6 关65/27兴
C9 H21Al tripropylaluminum 关102-67-0兴
42.5⫾1.2 关67/33兴关82/15兴
C9 H21AlO3 aluminum isopropoxide 关555-31-7兴
共353–399兲 48.1⫾6.3 共376兲 关72/18兴
C12H27Al triisobutylaluminum 关100-99-2兴
共273–322兲 38.3 共298兲 关64/20兴
C12H27AlO3 tributoxyaluminum 关3085-30-1兴
共503–533兲 104.1 共518兲 A, I 关87/5兴关57/26兴
C12H27AlO3 triisobutoxyaluminum 关3453-79-0兴
共500–550兲 139.4 共515兲 A, I 关87/5兴关57/26兴
C12H27AlO3 tri-sec-butoxyaluminum 关2269-22-9兴
共425– 469兲 81.5 共440兲 A, I 关87/5兴关57/26兴
C15H12AlF9 O6 tris共1,1,1-trifluoro-2,4-pentanedionato兲aluminum共III兲 关14354-59-7兴
共349– 411兲 58.7⫾0.7 共380兲 BG 关88/18兴
共392– 484兲 69.6⫾0.5 共438兲 关78/10兴
C15H21AlO6 tris共pentane-2,4-dionato兲aluminum共III兲 关13963-57-0兴
共430–530兲 78.7⫾0.9 共298兲 T 关86/11兴
AlB3 H12 aluminum borohydride
共231–290兲 30.0 共260兲 关40/13兴
As
CAsCl2 F3 S dichloro 共trifluoromethylthio兲arsine
共293–373兲 37.1 共333兲 关60/25兴
CH3 AsBr2 methyl dibromoarsine 关676-70-0兴
共293–333兲 49.9 共313兲 关48/12兴
CH3 AsCl2 methyl dichloroarsine 关593-89-5兴
共273–313兲 41.0 共293兲 关48/12兴
CH3 AsF2 methyl difluorarsine
共244 –350兲 35.5 共297兲 MM 关46/15兴
C2 AsClF6 S2 chloro bis共trifluoromethylthio兲arsine
共293–373兲 39.6 共333兲 关60/25兴
C2 H2 AsCl3 -chlorovinyldichloroarsine
共339–383兲 U88.3 共354兲 关47/3兴
C2 H2 AsCl3 cis-2-chlorovinyldichloroarsine
共341–382兲 48.5 共356兲 关48/4兴
C2 H2 AsCl3 trans-2-chlorovinyldichloroarsine
共323– 423兲 54.5 共338兲 关50/1兴
C2 H2 AsCl3 2-chlorovinyldichloroarsine 关541-25-3兴
共293–333兲 53.4 共313兲 关48/12兴
C3 H9 BS dimethyl共methylthio兲borane 关19163-05-4兴
共227–304兲 31.6 共265兲 关99/16兴
C3 H9 BS2 methylbis共methylthio兲borane 关19163-08-7兴
共300–373兲 44.7 共315兲 关99/16兴
C3 H9 BS3 tris共methylthio兲borane 关997-49-9兴
共325– 462兲 44.9 共394兲 关99/16兴
共303– 493兲 51.6 共398兲 关67/8兴
共303– 493兲 54.0⫾0.8 共298兲 关67/8兴
C3 H9 B3 O3 methylboric acid anhydride
共273–327兲 37.4 共288兲 关40/4兴
C3 H12BN borine trimethylamine
共136 –195兲 19.9 共180兲 关37/6兴
C3 H15B5 1-isopropylpentaborane 共9兲
共273–398兲 37.2 共335兲 关63/26兴
C4 BClF6 bis共perfluorovinyl兲chloroborine
共280–322兲 35.6 共301兲 T 关60/12兴
C4 H6 BF divinylfluoroborane
共193–273兲 25.8 共233兲 T 关60/10兴
C4 H6 BCl divinylchloroborane
共275–298兲 33.0 共286兲 T 关60/10兴
C5 H10O-BF3 tetrahydopyran—boron trifluoride complex
共323–368兲 60.9 共345兲 关60/8兴
C4 H10O-BF3 diethyl ether—boron trifluoride complex
共283–353兲 55.1 共318兲 关60/7兴
C4 H10BClO2 diethoxychloroborane
38.9⫾0.8 共298兲 关31/3兴关70/31兴
C4 H12BClN2 bis共dimethylamino兲chloroborane
41.8⫾2.1 共298兲 关51/14兴关70/31兴
C4 H11N-C3 H9 B N,N-dimethylethylamine—trimethylborane complex
共303–339兲 58.2 共321兲 关60/9兴
C4 H12B2 O4 tetramethoxydiboron
共273–348兲 44.0 共310兲 关60/13兴
44.7 关72/32兴
C4 H17B5 1-sec-butylpentaborane 共9兲
共299– 428兲 41.4 共364兲 关63/26兴
C5 H16B10 isopropenyl-o-carborane
共323– 473兲 36.7 共398兲 关63/46兴
C5 H16B10O2 1-acetoxymethyl-o-carborane 关19528-60-0兴
56.5 共569兲 关74/31兴
C5 H19B5 1-methyl-2-sec-butylpentaborane
共301– 423兲 41.0 共362兲 关63/26兴
C6 BF9 tris共perfluorovinyl兲borine
共297–335兲 41.1 共316兲 T 关60/12兴
C6 H5 BBr2 phenylboron dibromide
共391– 433兲 43.9⫾2.1 共412兲 T 关67/1兴
C6 H5 BCl2 phenylboron dichloride
共273–318兲 33.7⫾0.8 共296兲 T 关67/1兴
C6 H12BCl3 O3 tris共2-chloroethyl兲 orthoborate
共390– 448兲 57.7 共419兲 关46/9兴
C6 H13BO2 1-butaneboronic acid, cyclic ethylene ester 关10173-39-4兴
40.2 共329兲 关70/29兴
C6 H15B triethylborane 关97-94-9兴
33.6 共293兲 关83/1兴
36.8⫾0.4 关63/32兴关82/15兴
C6 H15BO3 triethylborate 关150-46-9兴
共302–382兲 41.0 共317兲 关67/2兴
共302–382兲 38.2 共391兲 关67/2兴
C6 H15BS3 triethylthioborane
61.5⫾2.1 关66/27兴关70/31兴
C6 H15B3 O3 triethylboroxin
共347– 424兲 46.0 共362兲 EB 关90/19兴
C6 H16BN 共N-ethylamino兲diethylborane
60.7⫾0.8 关67/32兴关82/15兴
C6 H17B5 Br2 Si2 2,4-bis共bromodimethylsilyl兲-2,4-dicarbo-closo-heptaborane 共7兲 关66798-29-6兴
55.2⫾1.3 关52/20兴关82/15兴
C6 H14Hg diisopropyl mercury 关1071-39-2兴
53.6⫾1.7 关52/20兴关82/15兴
C12H30Ge2 Hg bis共triethylgermyl兲mercury 关4149-28-4兴
共383– 403兲 64.8 共393兲 关72/15兴
C12H30HgSi2 bis共triethylsilyl兲mercury 关4149-29-5兴
共383– 433兲 64.0 共398兲 关72/15兴
C18H42Ge2 Hg bis共triisopropylgermyl兲mercury 关24004-54-4兴
共373– 483兲 68.7 共388兲 关72/15兴
HgI2 mercuric iodide 关7774-29-0兴
共537– 610兲 147.4 共574兲 UV 关02/7兴
Ho
C33H57HoO6 tris共2,2,6,6-tetramethylheptane-3,5-dionato兲holmium共III兲 关15522-73-3兴
共458 –500兲 84.6 BG 关69/28兴
I
HI hydrogen iodide 关10034-85-2兴
19.8 共238兲 C 关29/4兴
In
C6 H15In triethyl indium 关923-34-2兴
共326 –376兲 45.0⫾0.7 共351兲 关01/9兴关01/24兴
C9 H21In tripropyl indium 关3015-98-3兴
共400– 483兲 52.0 共441兲 关99/16兴
C9 H21In triisopropyl indium 关17144-80-8兴
共318 –366兲 52.3⫾0.7 共342兲 关01/9兴
共394 – 478兲 51.0 共336兲 关99/16兴
C12H27In tributyl indium 关15676-66-1兴
共444 –539兲 58.5 共459兲 A 关87/5兴
C15H12F9 InO6 tris共1,1,1-trifluoro-2,4-pentanedionato兲indium共III兲 关15453-87-9兴
共398 – 478兲 77.4⫾0.6 共438兲 关78/10兴
Li
C4 H9 Li butyl lithium 关109-72-8兴
107.1⫾2.9 关61/24兴关82/15兴
关Note: Authors of 关61/24兴 noted that the experimental data was not
very reproducible, and subject to considerable error.兴
Lu
C33H57LuO6 tris共2,2,6,6-tetramethylheptane-3,5-dionato兲lutetium共III兲 关15497-45-2兴
共448 – 490兲 83.6 BG 关69/28兴
Mn
C5 H3 MnO5 Si silyl pentacarbonyl manganese 关15770-61-3兴
共294 –391兲 39.6 共343兲 T 关69/37兴关67/40兴
C10H10Mn bis共cyclopentadienyl兲manganese 关1271-27-8兴
共378 – 435兲 58.0 共393兲 A 关87/5兴
C10O10MnRe manganese rhenium decacarbonyl 关14693-30-2兴
共440– 463兲 56.5 共451兲 关71/14兴
C10O10Mn2 dimanganese decacarbonyl 关10170-69-1兴
共428 – 463兲 60.7⫾1.3 共446兲 关71/14兴
Mo
MoF6 molybdenum hexafluoride 关7783-77-9兴
共318 –363兲 27.4 共340兲 关68/27兴
N
BrClFN bromochlorofluoroammonia
共240–310兲 30.2 共275兲 关96/31兴
BrF2 N bromodifluoroammonia 关15605-95-5兴
共180–250兲 23.2 共215兲 关96/31兴
Br2 FN dibromofluoroammonia 关145543-67-5兴
共280–350兲 33.6 共315兲 关96/31兴
Br3 N nitrogen tribromide 关15162-90-0兴
共380– 450兲 44.1 共415兲 关96/31兴
Cl2 FN dichlorofluoroammonia
共200–280兲 25.7 共240兲 关96/31兴
Cl3 N nitrogen trichloride 关10025-85-1兴
共280– 440兲 32.9 共360兲 关96/31兴
HNO3 nitric acid 关7697-37-2兴
共273–356兲 38.6 共312兲 关66/30兴
32.1 关58/27兴
F4 N4 P4 tetrameric phosphonitrilic fluoride
37.3 关58/27兴
F6 NP3 tris共difluorophosphino兲amine
31.2 关75/38兴
PH3 phosphine 关7803-51-2兴
14.6⫾0.1 共186兲 关39/5兴
14.6 共185兲 关37/15兴
F5 P phosphorous pentafluoride 关7647-19-0兴
共179–189兲 17.2 共184兲 QM 关37/16兴
Pb
C2 H8 Pb dimethylplumbane
共173–223兲 25.5 共198兲 关60/26兴
C3 H10Pb trimethylplumbane
共193–243兲 31.1 共218兲 关60/26兴
C4 H12Pb tetramethyllead 关75-74-1兴
38.1⫾0.4 关59/17兴关82/15兴
共298 –308兲 35.7 共303兲 关29/6兴
C5 H9 F5 Pb 共pentafluoroethyl兲trimethyllead
共295–329兲 39.1 共312兲 T 关60/11兴
C8 H20Pb tetraethyllead 关78-00-2兴
56.6⫾1.0 共298兲 C 关80/4兴
共311– 456兲 57.3 共326兲 关47/5兴
56.9⫾2.5 关56/22兴关82/15兴
共273–343兲 56.3 共308兲 关36/9兴
共351– 423兲 56.7 共387兲 关35/7兴
Pr
C33H57O6 Pr tris共2,2,6,6-tetramethylheptane-3,5-dionato兲praseodymium共III兲 关15492-48-5兴
共495–530兲 109.2 BG 关69/28兴
Re
C10O10MnRe manganese rhenium decacarbonyl 关14693-30-2兴
共440– 463兲 56.5 共451兲 关71/14兴
C10O10 Re2 dirhenium decacarbonyl 关14285-68-8兴
共454 – 483兲 68.7 共468兲 关71/14兴
Ru
C5 O5 Ru ruthenium pentacarbonyl
共243–323兲 42.2 共283兲 关91/16兴
C10H10Ru ruthenocene 关1287-13-4兴
共479–544兲 53.6⫾1.4 共511兲 关84/11兴
S
Br2 OS thionyl bromide 关507-16-4兴
共313– 439兲 43.6 共330兲 关99/16兴
Br2 S2 disulfur dibromide 关13172-31-1兴
共365–503兲 53.9 共380兲 关99/16兴
Br2 FO2 S sulfuryl bromide fluoride 关13536-61-3兴
共236 –333兲 32.0 共251兲 关99/16兴
ClF2 NO2 S difluoroamidosulfuryl chloride
共232–290兲 31.2 共261兲 关71/19兴
ClFOS thionyl chloride fluoride 关14177-25-4兴
共212–304兲 27.7 共227兲 关99/16兴
ClFO2 S sulfuryl chloride fluoride 关13637-84-8兴
共211–300兲 29.0 共226兲 关99/16兴
ClFO5 S2 pyrosulfuryl chloride fluoride 关13637-85-9兴
共284 –396兲 40.8 共299兲 关99/16兴
ClHO3 S chlorosulfonic acid 关7790-94-5兴
共324 – 454兲 45.8 共339兲 关99/16兴
Cl2 OS thionyl chloride 关7719-09-7兴
共257–372兲 32.4 共272兲 关99/16兴
Cl2 O2 S sulfuryl chloride 关7791-25-5兴
共357–365兲 34.5 共272兲 关99/16兴
Cl2 O5 S2 pyrosulfuryl dichloride 关7791-27-7兴
共325– 450兲 44.7 共340兲 关99/16兴
Cl2 S sulfur chloride 关10545-99-0兴
共265–348兲 43.8 共280兲 关99/16兴
C6 H11NSi2 N-phenyldisilazane
共298 –356兲 34.9 共327兲 T 关69/33兴
C6 H12Si2 1,1,3,3-tetramethyl-1,3-disilacyclobutane 关1627-98-1兴
39.5 共391兲 关75/31兴
C6 H12Si 1-methyl-1-vinylsilacyclobutane
33.1 共298兲 C 关91/4兴
C6 H14Si 1,1,2-trimethylsilacyclobutane 关30681-90-4兴
36.0 共298兲 C 关91/4兴
C6 H14Si 1,1-dimethylsilacyclopentane
37.7⫾2.1 关72/30兴关82/15兴
C6 H14Si 1,1,3-trimethylsilacyclobutane 关2295-13-8兴
35.5 共298兲 C 关91/4兴
C6 H15ClSi chlorotriethylsilane 关994-30-9兴
共268 – 419兲 42.9 共419兲 关47/5兴
C6 H15FO3 Si triethoxyfluorosilane
共291–373兲 40.3 共332兲 I 关49/26兴
C6 H15NOSi2 pentamethyldisilanyl isocyanate
共320–377兲 44.2 共348兲 关63/40兴
C6 H16OSi propoxytrimethylsilane 关1825-63-4兴
34.3⫾0.6 共298兲 C 关88/15兴
34.3⫾0.3 共298兲 C 关85/13兴
C6 H16OSi isopropoxytrimethylsilane 关1825-64-5兴
31.8⫾0.6 共298兲 C 关88/15兴
31.8⫾0.4 共298兲 EB 关85/13兴
C6 H16OSi triethylsilanol 关597-52-4兴
共298 – 413兲 50.6 共355兲 I 关53/15兴
C6 H16O2 Si diethoxydimethylsilane 关78-62-6兴
43.1⫾0.7 共298兲 C 关88/15兴
43.1⫾0.3 共298兲 EB 关85/13兴
共254 –386兲 43.3 共269兲 关47/5兴
C6 H16O3 SSi trimethoxy关2-共methylthio兲ethyl兴silane 关66785-19-1兴
45.2⫾0.7 共298兲 C 关89/11兴
C6 H16O3 SSi 关共ethylthio兲methyl兴trimethoxysilane 关53696-79-0兴
41.4⫾0.6 共298兲 C 关89/11兴
C6 H16Si dimethyldiethylsilane 关756-81-0兴
38.9⫾0.6 共298兲 C 关88/15兴
C6 H16Si triethylsilane 关617-86-7兴
37.4⫾0.6 共298兲 C 关88/15兴
共303–373兲 33.5 EB, I 关75/34兴
36.4⫾1.3 关72/30兴关82/15兴
C6 H16Si2 1,1,3,3-tetramethyl-1,3-disilacyclobutane 关1627-98-1兴
36.7⫾1.1 共298兲 I 关74/23兴
41.0⫾2.1 关72/30兴关82/15兴
C6 H17B5 Br2 Si2 2,4-bis共bromodimethylsilyl兲-2,4-dicarbo-closo-heptaborane 共7兲 关66798-29-6兴
共388 – 463兲 53.1 共403兲 I 关79/25兴
C6 H17B5 Cl2 Si2 2,4-bis共chlorodimethylsilyl兲-2,4-dicarbo-closo-heptaborane 共7兲 关28699-83-4兴
共359– 439兲 46.2 共374兲 I 关79/25兴
C6 H18Cl2 O2 Si3 1,5-dichlorohexamethyltrisiloxane
共299– 457兲 49.8 共314兲 关47/5兴
C6 H18OSi2 hexamethyldisiloxane 关107-46-0兴
共300–383兲 36.9 共315兲 EB 关86/4兴
共293–361兲 33.1 共327兲 关71/15兴
37.2⫾1.7 关64/26兴关82/15兴
共309– 411兲 36.0 共324兲 EB 关61/15兴
34.6⫾0.1 共332兲 C 关61/15兴
33.1⫾0.1 共351兲 C 关61/15兴
31.3⫾0.1 共373兲 C 关61/15兴
37.2⫾1.7 关47/5兴
C6 H18O3 Si3 hexamethylcyclotrisiloxane 关541-05-9兴
共342– 419兲 40.8 共357兲 EB 关86/4兴
共353– 403兲 39.7 共368兲 关74/18兴
共339– 407兲 39.0 共373兲 关71/15兴
共343–388兲 39.7 共365兲 关53/20兴
C6 H18Si2 hexamethyldisilane 关1450-14-2兴
1882 26/9 H. Sinozaki, R. Hara, and S. Mitsukuri, Bull. Chem. Soc. Jpn. 1,
82/1 F. Kraft, Ber. 15, 1687 共1882兲. 59– 61 共1926兲.
1883 1927
83/1 G. W. A. Kahlbaum, Ber. 16, 2476 –2484 共1883兲. 27/1 W. H. Rinkenbach, Ind. Eng. Chem. 19, 474 – 476 共1927兲.
1886 27/2 J. H. Perry, J. Phys. Chem. 31, 1737–1741 共1927兲.
86/1 A. Richardson, J. Chem. Soc. 共London兲 49, 761–776 共1886兲. 27/3 N. N. Nagornov, Ann. Inst. Anal. Phys. Chem. 共Leningrad兲 3,
1894 562–583 共1927兲; Chem. Zentr. II, 2668 共1927兲; Chem. Abstracts 22,
94/1 G. W. A. Kahlbaum, Z. Phys. Chem. 13, 14 –55 共1894兲. 4298 共1928兲.
1898 27/4 O. E. May, J. F. T. Berliner, and D. F. J. Lynch, J. Am. Chem. Soc.
98/1 G. W. A. Kahlbaum, Z. Phys. Chem. 26, 577 共1898兲. 49, 1012–1016 共1927兲.
98/2 W. Louguinine, Ann. Chim. 共Paris兲 7, 334 –377 共1898兲. 27/5 S. Klosky, L. P. L. Woo, and R. J. Flanigan, J. Am. Chem. Soc. 49,
1901 1280–1281 共1927兲.
01/1 M. De Forgrand, Comp. Rend. 132, 688 共1901兲. 1928
1903 28/1 O. A. Nelson, Ind. Eng. Chem. 20, 1382–1384 共1928兲.
03/1 J. Dewar and H. O. Jones, Proc. Roy. Soc. London 71A, 427 28/2 O. A. Nelson, Ind. Eng. Chem. 20, 1380–1382 共1928兲.
共1903兲. 28/3 M. Roland, Bull. Soc. Chim. Belg. 37, 117–140 共1928兲.
1904 28/4 W. F. Giauque and R. Wiebe, J. Am. Chem. Soc. 50, 101–122
04/1 A. Jaquerod and E. Wassmer, Ber. 3, 2531–2535 共1904兲. 共1928兲.
1906 28/5 G. S. Parks and B. Barton, J. Am. Chem. Soc. 50, 24 –27 共1928兲.
06/1 A. Rex, Z. Physik. Chem. 55, 355–370 共1906兲. 28/6 W. F. Giauque and R. Wiebe, J. Am. Chem. Soc. 50, 2193–2202
1910 共1928兲.
10/1 E. C. Bingham, Am. Chem. J. 43, 287–309 共1910兲. 1929
1912 29/1 J. N. Pearce and P. E. Peters, J. Phys. Chem. 33, 873– 878 共1929兲.
12/1 W. Herz and W. Rathmann, Chem.-Ztg. 36, 1417–1418 共1912兲. 29/2 C. P. Smyth and E. W. Engel, J. Am. Chem. Soc. 51, 2646 –2660
1914 共1929兲.
14/1 A. Stock and E. Willfroth, Ber. 47, 144 –154 共1914兲. 29/3 H. L. Johnston and W. F. Giauque, J. Am. Chem. Soc. 51, 3194 –
1915 3215 共1929兲.
15/1 J. M. Crafts, J. Chim. Phys. Phys.-Chim. Biol. 13, 105–161 共1915兲. 29/4 W. F. Giauque and R. Wiebe, J. Am. Chem. Soc. 51, 1441–1449
1919 共1929兲.
19/1 E. Moles and T. Batuecas, J. Chim. Phys. Phys.-Chim. Biol. 17, 29/5 C. F. Haggerty and J. F. Weiler, J. Am. Chem. Soc. 51, 1623–1626
537–588 共1919兲. 共1929兲.
1921 29/6 Y. Tanaka and Y. Nagai, Proc. Imp. Acad. 共Japan兲 5, 78 –79 共1929兲;
21/1 A. Stock, F. Henning, and E. Kuss, Ber. 54, 1119–1129 共1931兲. Chem. Abstracts 23, 2622 共1929兲.
21/2 O. Maas and C. H. Wright, J. Am. Chem. Soc. 43, 1098 –1111 1930
共1921兲. 30/1 O. A. Nelson, Ind. Eng. Chem. 22, 971–972 共1930兲.
21/3 O. Maas and C. H. Wright, J. Am. Chem. Soc. 43, 1098 –1111 30/2 R. H. Bullard and A. C. Haussman, J. Phys. Chem. 34, 743–747
共1921兲. 共1930兲.
1922 30/3 M. A. Zmaczynski, J. Chim. Phys. 27, 503–517 共1930兲.
22/1 O. A. Nelson and C. E. Senseman, Ind. Eng. Chem. 14, 58 – 62 30/4 G. B. Cunningham, Power 72, 374 –377 共1930兲.
共1922兲. 30/5 R. Livingston and G. B. Heisig, J. Am. Chem. Soc. 52, 2409–2410
22/2 R. S. Taylor and L. B. Smith, J. Am. Chem. Soc. 44, 2450–2463 共1930兲.
共1922兲. 30/6 H. A. Schuette and R. W. Thomas, J. Am. Chem. Soc. 52, 2028 –
1923 2030 共1930兲.
23/1 F. S. Mortimer and R. V. Murphy, Ind. Eng. Chem. 15, 1140–1142 30/7 J. H. Simons, J. Am. Chem. Soc. 52, 3488 –3493 共1930兲.
共1923兲. 30/8 A. S. Coolidge, J. Am. Chem. Soc. 52, 1874 –1887 共1930兲.
23/2 C. E. Senseman and O. A. Nelson, Ind. Eng. Chem. 15, 382–383 1931
共1923兲. 31/1 H. A. Scheulte and M. A. Cowley, J. Am. Chem. Soc. 53, 3485–
1924 3489 共1931兲.
24/1 J. Simons, J. Am. Chem. Soc. 46, 2179–2183 共1924兲. 31/2 O. Ruff and W. Menzel, Z. Anorg. Allgem. Chem. 202, 49– 61
24/2 O. Maas and P. G. Hiebert, J. Am. Chem. Soc. 46, 2693–2700 共1931兲.
共1924兲. 31/3 E. Wiberg and W. Sütterlin, Z. Anorg. Allgem. Chem. 202, 1–21
1925 共1931兲.
25/1 J. H. Perry, J. Am. Chem. Soc. 47, 2629–2632 共1925兲. 1932
1926 32/1 W. E. Vaughan, J. Am. Chem. Soc. 54, 3863–3876 共1932兲.
26/1 H. Sinozaki, R. Hara, and S. Mitsukuri, Bull Chem. Soc. Jpn. 1, 32/2 L. M. Ellis, Jr. and E. E. Reid, J. Am. Chem. Soc. 54, 1674 –1687
59– 61 共1926兲. 共1932兲.
26/2 A. G. Loomis and J. E. Walters, J. Am. Chem. Soc. 48, 2051–2055 32/3 J. O. Clayton and W. F. Giauque, J. Am. Chem. Soc. 54, 2610–2626
共1926兲. 共1932兲.
26/3 F. Straus, Ber. 59, 1664 –1681 共1926兲. 32/4 W. J. Jones, W. J. C. Dyke, G. Davies, D. C. Griffiths, and J. H. E.
26/4 W. V. Evans and M. B. Aylesworth, Ind. Eng. Chem. 18, 24 –27 Webb, J. Chem. Soc. 2285–2293 共1932兲.
共1926兲. 1933
26/5 C. A. Taylor and W. H. Rinkenbach, J. Chem. Soc. 48, 1305–1309 33/1 W. Menzel and F. Mohry, Z. Anorg. Allgem. Chem. 210, 257–263
共1926兲. 共1933兲.
26/6 G. W. C. Yates, Philos. Mag. 817– 826 共1926兲. 33/2 G. B. Heisig and O. D. Murd, J. Am. Chem. Soc. 55, 3485–3487
26/7 W. A. Felsing and S. A. Durban, J. Am. Chem. Soc. 48, 2885–2893 共1933兲.
共1926兲. 33/3 H. S. Booth, P. E. Burchfield, E. M. Bixly, and J. B. MacKelvey, J.
26/8 J. H. Perry and F. Porter, J. Am. Chem. Soc. 48, 299–302 共1926兲. Am. Chem. Soc. 53, 2231–2235 共1933兲.
33/4 F. Hovorka and F. E. Geiger, J. Am. Chem. Soc. 55, 4759– 4761 37/2 J. D. Kemp and W. F. Giauque, J. Am. Chem. Soc. 59, 79– 84
共1933兲. 共1937兲.
33/5 O. A. Nelson and H. D. Young, J. Am. Chem. Soc. 55, 2429–2431 37/3 H. W. Thompson and F. S. Dainton, Trans. Faraday Soc. 33,
共1933兲. 1546 –1555 共1937兲.
33/6 M. A. Cowley and H. A. Schuelte, J. Am. Chem. Soc. 55, 387–391 37/4 A. Guyer, W. Schutze, and M. Weidenmann, Helv. Chim. Acta 20,
共1933兲. 936 –949 共1937兲.
33/7 A. Taylor and E. T. Layng, J. Chem. Phys. 1, 798 – 808 共1933兲. 37/5 C. J. Egan and J. D. Kemp, J. Am. Chem. Soc. 59, 1264 –1268
33/8 H. S. Booth, P. E. Burchfield, E. M. Bixly, and J. B. MacKelvey, J. 共1937兲.
Am. Chem. Soc. 53, 2231–2235 共1933兲. 37/6 A. B. Burg and W. I. Schlesinger, J. Am. Chem. Soc. 59, 780–787
33/9 F. Hovorka, H. P. Lankelma, and C. K. Naujoks, J. Am. Chem. Soc. 共1937兲.
53, 4820– 4822 共1933兲. 37/7 V. G. Moor, E. K. Kanep, and I. E. Dobkin, Trans. Exptl. Research
33/10 H. Tannelberger, Ber. 66B, 484 – 486 共1933兲; Chem. Abstracts 27, Lab. Khemgas, Materials on Cracking and Chemical Treatment of
3374 共1933兲. Cracking Products U.S.S.R. 3, 320–328 共1937兲; Chem. Abstracts 31,
33/11 G. B. Heisig, J. Am. Chem. Soc. 55, 2304 –2311 共1933兲. 6072 共1937兲.
33/12 E. G. V. Barrett and L. J. Burrage, J. Phys. Chem. 37, 1029–1035 37/8 A. V. Grosse and V. N. Ipatieff, J. Org. Chem. 2, 447– 458 共1937兲.
共1933兲. 37/9 J. C. Rintelen, Jr., J. H. Saylor, and P. M. Gross, J. Am. Chem. Soc.
33/13 F. T. Miles and A. W. C. Menzies, J. Phys. Chem. 37, 435– 430 59, 1129–1130 共1937兲.
共1933兲. 37/10 J. G. Aston, C. W. Siller, and G. H. Messerly, J. Am. Chem. Soc.
33/14 C. A. Kraus and F. E. Toonder, Proc. Natl. Acad. Sci. 共USA兲 19, 59, 1743–1751 共1937兲.
292–298 共1933兲; Chem. Abstracts 27, 2646 共1933兲. 37/11 G. S. Gardner and J. E. Brewer, Ind. Eng. Chem. 29, 179–181
33/15 M. T. Toral and E. Moles, Anales Soc. Espan. Fis. Quim. 31, 共1937兲.
735–745 共1933兲; Chem. Abstracts 28, 954 共1934兲. 37/12 R. H. Purcell and F. D. Zahoorbux, J. Chem. Soc. 1029–1035
33/16 W. F. Giauque and J. O. Clayton, J. Am. Chem. Soc. 55, 4875– 共1937兲.
4889 共1933兲.
37/13 R. Overstreet and W. F. Giauque, J. Am. Chem. Soc. 59, 254 –259
1934 共1937兲.
34/1 W. Mehl, Z. Physik. Chem. A164, 312–313 共1934兲.
37/14 R. K. Witt and J. D. Kemp, J. Am. Chem. Soc. 59, 273–276
34/2 W. Hieber and A. Woerner, Z. Elektrochem. 40, 252–256 共1934兲. 共1937兲.
34/3 N. E. Rigler, W. A. Felsing, and H. R. Henze, J. Am. Chem. Soc. 37/15 C. C. Stephenson and W. F. Giauque, J. Chem. Phys. 5, 149–158
56, 1499 共1934兲. 共1937兲.
34/4 W. C. Schumb and F. A. Bickford, J. Am. Chem. Soc. 56, 852– 858 37/16 R. Linke and W. Rohrmann, Z. Physik. Chem. B35, 256 –260
共1934兲. 共1937兲.
34/5 G. N. Lewis and P. W. Schultz, J. Am. Chem. Soc. 56, 1002 共1934兲. 1938
34/6 J. W. Goodeve, Trans. Faraday Soc. 30, 501–504 共1934兲. 关Vapor
38/1 J. D. Brandner, Ind. Eng. Chem. 30, 681– 684 共1938兲.
pressure data are presented graphically in paper as log P versus 1/T.]
38/2 M. Linhard, Z. Anorg. Allgem. Chem. 236, 200–208 共1938兲.
34/7 S. Oguri, S. Anjo and Y. Kuwabara, Bull. Waseda Appl. Chem. Soc.
38/3 C. G. Egan and J. D. Kemp, J. Am. Chem. Soc. 60, 2097–2101
22, 1– 4 共1934兲; Chem. Abstracts 28, 4298 共1934兲.
共1938兲.
34/8 A. N. Campbell and A. J. R. Campbell, Trans. Faraday Soc. 30,
38/4 L. Reidel, Z. Ges. Kalte-Ind. 45, 221 共1938兲.
1109–1114 共1934兲.
38/5 G. Scatchard and C. L. Raymond, J. Am. Chem. Soc. 60, 1278 –
1935
1287 共1938兲 关Erratum 60, 3099 共1938兲兴.
35/1 R. Spence and W. Wild, J. Chem. Soc. 138, 506 –509 共1935兲.
38/6 D. Radalescu and M. Alexa, Bull. Chem. Soc. Romania 20A,
35/2 H. W. Thompson and J. W. Linnett, Trans. Faraday Soc. 31,
89–113 共1938兲.
1743–1747 共1935兲.
38/7 K. Kuchinskaya, Sbornik Trudov. Opytnogo Zavoda im. Akad. S. V.
35/3 H. Bauer and K. Burschkies, Ber. 68, 1238 –1243 共1935兲.
Lebedeva 27–30 共1938兲; Chem. Abstracts 34, 3147 共1940兲.
35/4 H. Schierholtz and M. L. Staples, J. Am. Chem. Soc. 57, 2709–
2711 共1935兲. 38/8 A. R. Ubbelohde, Trans. Faraday Soc. 34, 283–292 共1938兲.
35/5 V. A. Kireev and A. A. Popov, J. Gen. Chem. 共U.S.S.R.兲 5, 1399– 38/9 E. Levin and I. Shtern, Zh. Prikl. Khim. 共Moscow兲 11, 426 – 441
1401 共1935兲; Chem. Abstracts 30, 2441 共1936兲. 共1938兲.
35/6 J. A. V. Butler, C. N. Ramchandani, and D. W. Thompson, J. Chem. 38/10 F. Hovorka, H. P. Lankelma, and S. C. Stanford, J. Am. Chem.
Soc. 280–285 共1935兲. Soc. 60, 820– 827 共1938兲.
35/7 W. J. Jones, D. P. Evans, T. Gulwell, and D. C. Griffiths, J. Chem. 38/11 W. F. Giauque and C. C. Stephenson, J. Am. Chem. Soc. 60,
Soc. 39– 47 共1935兲. 1389–1394 共1938兲.
1936 38/12 E. Eftring, Dissertation, University of Lund, 1938; as quoted in
36/1 H. W. Thompson and J. W. Linnett, Trans. Faraday Soc. 32, 关56/25兴.
681– 685 共1936兲. 1939
36/2 M. Ewert, Bull. Soc. Chim. Belg. 45, 493–515 共1936兲. 39/1 J. G. Aston, M. L. Eidinoff, and W. S. Forster, J. Am. Chem. Soc.
36/3 H. E. Bent, G. R. Cuthbertson, M. Dorfman, and R. E. Leary, J. 61, 1539–1543 共1939兲.
Am. Chem. Soc. 58, 165–170 共1936兲. 39/2 T. M. Powell and W. F. Giauque, J. Am. Chem. Soc. 61, 2366 –2370
36/4 K. Kearby, J. Am. Chem. Soc. 58, 374 –375 共1936兲. 共1939兲.
36/5 H. Merten and H. Schlüter, Chem. Ber. 69B, 1364 –1366 共1936兲. 39/3 F. H. Verhoek and A. L. Marshall, J. Am. Chem. Soc. 61, 2736 –
36/6 F. Hovorka, R. A. Schaefer, and D. Dreisback, J. Am. Chem. Soc. 2742 共1939兲.
58, 2264 共1936兲. 39/4 K. B. Goldblum, R. W. Martin, and R. B. Young, Ind. Eng. Chem.
36/7 G. R. Negishi, J. Am. Chem. Soc. 58, 2293–2296 共1936兲. 39, 1474 –1476 共1947兲.
36/8 J. G. Aston and G. H. Messerly, J. Am. Chem. Soc. 58, 2354 –2361 39/5 A. Frank and K. Clusius, Z. Phys. Chem. 42B, 395– 421 共1939兲.
共1936兲. 39/6 W. Patnode and W. J. Scheiber, J. Am. Chem. Soc. 61, 3449–3451
36/9 E. J. Buckler and R. G. W. Norrish, J. Chem. Soc. 1567–1569 共1939兲.
共1936兲. 39/7 L. Reidel, Bull. Intern. Inst. Refrig. 20, 1–10 共1939兲.
1937 1940
37/1 A. Klemenc and G. Wagner, Ber. 70B, 1880–1882 共1937兲; Chem. 40/1 A. F. Benning and R. C. McHarness, Ind. Eng. Chem. 32, 497– 499
Abstracts 31, 8412 共1937兲. 共1940兲.
40/2 G. H. Messerly and J. C. Aston, J. Am. Chem. Soc. 62, 886 – 890 43/4 J. G. Aston, H. L. Finke, and S. C. Schumann, J. Am. Chem. Soc.
共1940兲. 65, 341–346 共1943兲.
40/3 A. B. Lamb and E. E. Roper, J. Am. Chem. Soc. 62, 806 – 814 43/5 J. G. Aston, G. J. Szasz, and H. L. Finke, J. Am. Chem. Soc. 65,
共1940兲. 1135–1139 共1943兲.
40/4 A. B. Burg, J. Am. Chem. Soc. 62, 2228 –2234 共1940兲. 43/6 W. P. Hall and E. E. Reid, J. Am. Chem. Soc. 65, 1466 –1468
40/5 J. M. Stuckey and J. H. Saylor, J. Am. Chem. Soc. 62, 2922–2955 共1943兲.
共1940兲. 43/7 J. S. N. Cramer, Rec. Trav. Chem. 62, 606 – 610 共1943兲; Chem.
40/6 K. S. Pitzer, J. Am. Chem. Soc. 62, 1224 –1227 共1940兲. Zentr. II, 2234 共1943兲; Chem. Abstracts 38, 6148 共1944兲.
40/7 F. Hovorka, H. P. Lankelma, and W. R. Smith, J. Am. Chem. Soc. 43/8 G. Holst and L. Melander, Svensk. Kem. Tid. 55, 131–135 共1943兲;
62, 2372–2374 共1940兲. Chem. Abstracts 40, 2706 共1946兲.
40/8 F. Hovorka, H. P. Lankelma, and A. E. Axelrod, J. Am. Chem. Soc. 1944
62, 187–189 共1940兲. 44/1 H. J. McDonald, J. Phys. Chem. 48, 47–50 共1944兲.
40/9 F. Hovorka, H. P. Lankelma, and I. Schneider, J. Am. Chem. Soc. 44/2 T. R. Rubin, B. D. Levedahl, and D. M. Yost, J. Am. Chem. Soc.
62, 1096 –1098 共1940兲. 66, 279–282 共1944兲.
40/10 J. G. Aston and G. H. Messerly, J. Am. Chem. Soc. 62, 1917– 44/3 H. Russell, Jr., D. R. V. Golding, and D. M. Yost, J. Am. Chem.
1923 共1940兲. Soc. 66, 16 –20 共1944兲.
40/11 J. G. Aston, R. M. Kennedy, and S. C. Schumann, J. Am. Chem. 44/4 G. Milazzo, Gazz. Chim. Ital. 74, 49–57 共1944兲.
Soc. 62, 2059 共1940兲; 62, 2063 共1940兲. 44/5 I. I. Ioffe and E. S. Yamp’olskaya, Zh. Prikl. Khim. 17, 527–528
40/12 A. A. Zil’berman-Granovskaya and E. A. Shugam, J. Phys. Chem. 共1944兲; Chem. Abstracts 39, 3986 共1945兲.
共USSR兲 14, 759–767 共1940兲. 44/6 J. G. Aston, M. L. Sagenkahn, G. J. Szasz, G. W. Moessen, and H.
40/13 H. I. Schlesinger, R. T. Sanderson, and A. B. Burg, J. Am. Chem. F. Zuhr, J. Am. Chem. Soc. 66, 1171–1177 共1944兲.
Soc. 62, 3421–3425 共1940兲. 44/7 P. M. Althouse and H. O. Triebold, Ind. Eng. Chem., Anal. Ed. 16,
40/14 E. R. Smith, J. Res. National Bureau Stand. 24, 229–234 共1940兲. 605– 606 共1944兲.
40/15 G. H. Messerly and R. M. Kennedy, J. Am. Chem. Soc. 62, 44/8 R. B. Scott, W. J. Ferbuson, and F. G. Brickwedde, J. Res. National
2988 –2991 共1940兲.
Bureau Stand. 33, 1–20 共1944兲.
1941
44/9 H. J. Emeleus and A. G. Maddock, J. Chem. Soc. 293–296 共1944兲.
41/1 A. F. Belyaev, Acta Physicochem. U.S.S.R. 14, 523 共1941兲.
1945
41/2 D. M. Youst, C. S. Garner, D. W. Osborne, T. R. Rubin, and H.
45/1 E. S. Swift, Jr. and H. P. Hochanadel, J. Am. Chem. Soc. 67,
Russell, Jr., J. Am. Chem. Soc. 63, 2267–2272 共1941兲.
880– 881 共1945兲.
41/3 R. M. Kennedy, M. Sagenkahn, and J. G. Aston, J. Am. Chem. Soc.
45/2 C. B. Willingham, W. J. Taylor, J. M. Pignocco, and F. D. Rossini,
63, 2267–2272 共1941兲.
J. Res. National Bureau Stand. 35, 219–224 共1945兲.
41/4 D. W. Osborne, C. S. Garner, R. N. Doecher, and D. M. Yost, J.
45/3 L. Guttman and K. S. Pitzer, J. Am. Chem. Soc. 67, 324 –327
Am. Chem. Soc. 63, 3496 –3499 共1941兲.
共1945兲.
41/5 J. G. Aston, R. M. Kennedy, and G. H. Messerly, J. Am. Chem.
45/4 R. C. Wackher, C. B. Linn, and A. V. Grosse, Ind. Eng. Chem. 37,
Soc. 63, 2243–2348 共1941兲.
464 – 468 共1945兲.
41/6 M. W. Lister, J. Am. Chem. Soc. 63, 143–149 共1941兲.
45/5 H. J. Hoge, J. Res. National Bureau Stand. 34, 281–293 共1945兲.
41/7 V. A. Kireev and I. P. Sitnikov, J. Appl. Chem. 共USSR兲 14,
483– 485 共1941兲; Chem. Abstracts 36, 2189 共1942兲. 45/6 H. S. Davis and O. F. Wiedeman, Ind. Eng. Chem. 37, 482– 485
共1945兲.
41/8 C. B. Heisig, J. Am. Chem. Soc. 63, 1698 –1699 共1941兲.
41/9 E. R. Smith, J. Res. National Bureau Stand. 26, 129–134 共1941兲. 45/7 E. J. Prosen and F. D. Rossini, J. Res. National Bureau Stand. 34,
59– 63 共1945兲.
41/10 J. W. Stout and L. H. Fisher, J. Chem. Phys. 9, 163–168 共1941兲.
41/11 H. Russell, Jr., R. E. Rundle, and D. M. Yost, J. Am. Chem. Soc. 45/8 F. S. Fawcett and H. E. Rasmussen, J. Am. Chem. Soc. 67,
1705–1709 共1945兲.
63, 2825–2828 共1941兲.
1946
41/12 L. O. Brockway and N. R. Davidson, J. Am. Chem. Soc. 63, 3287
共1941兲. 46/1 R. A. Ruehrkein and T. M. Powell, J. Am. Chem. Soc. 68, 1063–
41/13 L. Riedel, Z. Ges Kalte-Ind. 48, 9–13 共1941兲. 1066 共1946兲.
1942 46/2 J. E. Kilpatrick and K. S. Pitzer, J. Am. Chem. Soc. 68, 1066 –1072
42/1 H. Russell, Jr., D. W. Osborne, and D. M. Yost, J. Am. Chem. Soc. 共1946兲.
64, 165–169 共1942兲. 46/3 F. H. Field and J. H. Saylor, J. Am. Chem. Soc. 68, 2649–2650
42/2 D. W. Osborne, R. W. Doescher, and D. M. Yost, J. Am. Chem. 共1946兲.
Soc. 64, 169–172 共1942兲. 46/4 G. W. Thompson, Chem. Rev. 38, 1–39 共1946兲.
42/3 P. E. Burchfield, J. Am. Chem. Soc. 64, 2501 共1942兲. 46/5 C. R. Patrick and G. S. Prosser, Trans. Faraday Soc. 60, 700–704
42/4 G. E. Williams and E. C. Gilbert, J. Am. Chem. Soc. 64, 2776 – 共1946兲.
2777 共1942兲. 46/6 H. Gilman and R. G. Jones, J. Am. Chem. Soc. 68, 517–520
42/5 S. C. Schumann, J. G. Aston, and M. Sagenkahn, J. Am. Chem. 共1946兲.
Soc. 64, 1039–1043 共1942兲 关Erratum 64, 30690 共1942兲兴. 46/7 J. G. Aston, H. L. Finke, A. B. Bestul, E. L. Pace, and G. J. Szasz,
42/6 J. A. Beattie, H. G. Ingersoll, and W. H. Stockmayer, J. Am. Chem. J. Am. Chem. Soc. 68, 52–57 共1946兲.
Soc. 64, 546 –548 共1942兲. 46/8 R. B. Scott and R. G. Brickwedde, J. Res. National Bureau Stand.
42/7 S. W. Benson and G. B. Kistiakowsky, J. Am. Chem. Soc. 64, 35, 501–512 共1946兲.
80– 86 共1942兲. 46/9 W. J. Jones, L. H. Thomas, E. H. Pritchard, and S. T. Bowden, J.
42/8 S. W. Benson, Ind. Eng. Chem., Anal. Ed. 13, 189–191 共1942兲. Chem. Soc. 824 – 827 共1946兲.
42/9 B. Suginuma and K. Satozaki, Rikagaku Kenkyusho Iho 41, 432 46/10 K. S. Pitzer, L. Guttman, and E. F. Westrum, Jr., J. Am. Chem.
共1942兲. Soc. 68, 2209–2212 共1946兲.
1943 46/11 R. Spitzer and K. S. Pitzer, J. Am. Chem. Soc. 68, 2537–2538
43/1 K. S. Pitzer and D. W. Scott, J. Am. Chem. Soc. 65, 803– 811 共1946兲.
共1943兲. 46/12 J. W. Knowlton, N. C. Schieltz, and D. MacMillan, J. Am. Chem.
43/2 D. R. Stevens, Ind. Eng. Chem. 35, 655– 660 共1943兲. Soc. 68, 208 –210 共1946兲.
43/3 J. F. Lemons and W. A. Felsing, J. Am. Chem. Soc. 65, 46 – 48 46/13 C. H. Bamford, D. L. Levi, and D. M. Newitt, J. Chem. Soc.
共1943兲. 468 – 471 共1946兲.
46/14 H. J. Emeleus and A. G. Maddock, J. Chem. Soc. 1131–1134 49/1 R. R. Dreisbach and S. A. Shrader, Ind. Eng. Chem. 41, 2879–2880
共1946兲. 共1949兲; R. R. Dreisbach and R. A. Martin, Ind. Eng. Chem. 41, 2875–
46/15 L. H. Long, H. J. Emeleus, and H. V. A. Briscoe, J. Chem. Soc. 2878 共1949兲.
1123–1126 共1946兲 49/2 E. Nicolini and P. Laffitte, Comptes Rend. 229, 757–759 共1949兲;
46/16 D. A. Crooks and F. M. Feetham, J. Chem. Soc. 899–901 共1946兲. 229, 935–936 共1949兲.
46/17 L. S. Dzung, Brown Boveri Rev. 33, 158 –163 共1946兲. 49/3 W. Kuhn and P. Massini, Helv. Chim. Acta 32, 1530–1542 共1949兲.
1947 49/4 W. F. Giauque and J. Gordon, J. Am. Chem. Soc. 71, 2176 –2181
47/1 J. Beersmans and J. C. Jungers, Bull. Soc. Chim. Belg. 56, 238 –250 共1949兲.
共1947兲. 49/5 C. B. Kretschmer and R. Wiebe, J. Am. Chem. Soc. 71, 1793–1797
47/2 D. J. G. Ives, R. W. Pittman, and W. Wardlaw, J. Chem. Soc. 共1949兲.
1080–1083 共1947兲. 49/6 A. F. Forziati, W. R. Norris, and F. D. Rossini, J. Res. National
47/3 C. Gould, G. Holzman, and C. Niemann, Anal. Chem. 19, 204 –206 Bureau Stand. 43, 555–563 共1949兲.
共1947兲. 49/7 G. Waddinton, J. W. Knowlton, D. W. Scott, S. D. Oliver, S. S.
47/4 J. A. A. Ketalaar, P. F. Van Velden, and J. S. Zalm, Rec. Trav. Chim. Todd, W. N. Hubbard, J. C. Smith, and H. M. Huffman, J. Am. Chem.
66, 721–732 共1947兲. Soc. 71, 797– 808 共1949兲.
47/5 D. R. Stull, Ind. Eng. Chem. 39, 517–540 共1947兲. 49/8 G. Waddington, J. C. Smith, D. W. Scott, and H. M. Huffman, J.
47/6 E. W. Balson, K. G. Denbigh, and N. K. Adam, Trans. Faraday Soc. Am. Chem. Soc. 71, 3902–3906 共1949兲.
43, 42– 48 共1947兲. 49/9 E. S. Perry and W. H. Weber, J. Am. Chem. Soc. 71, 3726 –3730
47/7 N. S. Osborne and D. C. Ginnings, J. Res. National Bureau Stand. 共1949兲.
39, 453– 477 共1947兲. 49/10 T. Higuchi, N. Endow, and J. E. Willard, J. Am. Chem. Soc. 71,
47/8 F. H. Stross, C. M. Gable, and G. C. Rounds, J. Am. Chem. Soc. 365–366 共1949兲.
69, 1629–1630 共1947兲. 49/11 G. W. Sears and E. R. Hopke, J. Am. Chem. Soc. 71, 2575–2576
47/9 F. H. Stross, J. M. Monger, and H. De V. Finch, J. Am. Chem. Soc. 共1949兲.
69, 1627–1628 共1947兲. 49/12 D. W. Scott, G. Waddington, J. C. Smith, and H. M. Huffman, J.
47/10 G. Waddington, S. S. Todd, and H. M. Huffman, J. Am. Chem. Am. Chem. Soc. 71, 2767–2773 共1949兲.
Soc. 69, 22–30 共1947兲. 49/13 D. W. Scott, G. D. Oliver, M. E. Gross, W. N. Hubbard, and H. M.
47/11 W. M. Jones and W. F. Giauque, J. Am. Chem. Soc. 69, 983–987 Huffman, J. Am. Chem. Soc. 71, 2293–2297 共1949兲.
共1947兲. 49/14 G. S. Parks and G. E. Moore, J. Chem. Phys. 17, 1151–1153
47/12 G. Waddington and D. R. Douslin, J. Am. Chem. Soc. 69, 共1949兲.
2275–2279 共1947兲. 49/15 J. Birks and R. S. Bradley, Proc. Roy. Soc. 共London兲 A198,
47/13 J. G. Aston and G. J. Szasz, J. Am. Chem. Soc. 69, 3108 –3114 226 –239 共1949兲.
共1947兲. 49/16 E. S. Perry, W. H. Weber, and B. F. Baubert, J. Am. Chem. Soc.
47/14 R. D. Fowler, J. M. Hamilton, Jr., J. S. Kasper, C. E. Weber, W. B. 71, 3720–3726 共1949兲.
Burford III, and H. C. Anderson, Ind. Eng. Chem. 39, 375–378 共1947兲. 49/17 R. S. Bradley and A. D. Shellard, Trans. Faraday Soc. 45,
47/15 J. M. Blocher, Jr. and I. E. Campbell, J. Am. Chem. Soc. 69, 501–507 共1949兲.
2100–2101 共1947兲. 49/18 F. R. Buck, K. F. Coles, G. T. Kennedy, and F. Morton, J. Chem.
1948 Soc. 2377–2383 共1949兲.
48/1 K. B. Kellogg and G. H. Cady, J. Am. Chem. Soc. 70, 3986 –3990 49/19 J. C. Nicholson, J. Chem. Soc. 1553–1555 共1949兲.
共1948兲.
49/20 N. L. Yarym-Agaev, N. N. Fedos’ev, and K. G. Skorikov, Zh. Fiz.
48/2 W. F. Giauque and W. M. Jones, J. Am. Chem. Soc. 70, 120–124 Khim. 11, 1257–1265 共1949兲.
共1948兲.
49/21 A. S. Carson, K. Hartley, and H. A. Skinner, Trans. Faraday Soc.
48/3 E. L. Pace and J. G. Aston, J. Chem. Soc. 566 –570 共1948兲.
45, 1159–1167 共1949兲.
48/4 G. H. Whiting, J. Chem. Soc. 1209–1210 共1948兲.
49/22 A. S. Carson, K. Hartley, and H. A. Skinner, Proc Royal Soc.
48/5 J. F. Ganeff and J. C. Jungers, Bull. Soc. Chim. Belg. 57, 82– 87
共London兲 A195, 500–512 共1949兲.
共1948兲.
49/23 D. W. Scott, M. E. Gross, G. D. Oliver, and H. M. Huffman, J.
48/6 J. Gordon and W. F. Giauque, J. Am. Chem. Soc. 70, 1506 –1510
共1948兲. Am. Chem. Soc. 71, 1634 –1636 共1949兲.
48/7 A. A. Banks, H. J. Emeleus, R. N. Haszeldine, and V. Kerrigan, J. 49/24 J. R. Partington and A. L. Wynes, J. Phys. Chem. 53, 500–503
Chem. Soc. 2188 –2190 共1948兲. 共1949兲.
48/8 C. E. Bonhorst and P. M. Athouse, Ind. Eng. Chem. 40, 2379–2384 49/25 L. F. Hatch, G. Sutherland, and W. J. Ross, J. Org. Chem. 14,
共1948兲. 1130–1136 共1949兲; vapor pressure data presented graphically as log P
versus 1/T in paper.
48/9 C. E. Redemann, S. W. Chaikin, and R. B. Fearing, J. Am. Chem.
Soc. 70, 631– 634 共1948兲. 49/26 H. J. Emeleus and H. G. Heal, J. Chem. Soc. 1696 –1699 共1949兲.
48/10 P. A. Small, K. W. Small, and P. Cowley, Trans. Faraday Soc. 44, 49/27 J. Thompson and H. J. Emeleus, J. Chem. Soc. 3080 共1949兲.
810– 816 共1948兲. 49/28 L. O. Winstrom and L. Kulp, Ind. Eng. Chem. 41, 2584 –2586
48/11 H. E. Bent and R. J. Francel, J. Am. Chem. Soc. 70, 634 – 637 共1949兲.
共1948兲. 1950
48/12 C. E. Redemann, S. W. Chaiken, R. B. Fearing, and D. Benedict, 50/1 J. B. Matthews, J. F. Sumner, and E. A. Moellyn-Hughes, Trans.
J. Am. Chem. Soc. 70, 637– 639 共1948兲. Faraday Soc. 46, 797– 803 共1950兲.
48/13 C. E. Redemann, S. W. Chaikin, and R. B. Fearing, J. Am. Chem. 50/2 R. M. Noyes, W. A. Noyes, and H. Steinmetz, J. Am. Chem. Soc.
Soc. 70, 1648 –1650 共1948兲. 72, 33–34 共1950兲.
48/14 C. E. Redemann, S. W. Chaikin, R. B. Fearing, G. J. Rotariu, J. 50/3 A. Michels and T. Wassennar, Physica 共Amsterdam兲 16, 221–224
Savit, and D. Van Hoesen, J. Am. Chem. Soc. 70, 3604 –3606 共1948兲. 共1950兲.
48/15 A. Michels and T. Wassenaar, Physica 共Amsterdam兲 14, 104 –110 50/4 K. F. Coles and F. Popper, Ind. Eng. Chem. 42, 1434 –1438 共1950兲.
共1948兲. 50/5 D. W. Scott, H. L. Finke, M. E. Gross, G. B. Guthrie, and H. M.
48/16 O. Glemser and V. Haüser, Z. Naturforsch. 3B, 159–163 共1948兲. Huffman, J. Am. Chem. Soc. 72, 2424 –2430 共1950兲.
48/17 H. J. Emeleus and J. F. Wood, J. Chem. Soc. 2183–2188 共1948兲. 50/6 A. F. Forziati, D. L. Camin, and F. D. Rossini, J. Res. Natl. Bur.
1949 Standards 45, 406 – 410 共1950兲.
50/7 D. W. Scott, H. L. Finke, W. N. Hubbard, J. P. McCullough, M. E. 52/12 D. W. Scott, H. L. Finke, J. P. McCullough, M. E. Gross, R. E.
Gross, K. D. Williamson, G. Waddington, and H. M. Huffman, J. Am. Pennington, and G. Waddington, J. Am. Chem. Soc. 74, 2478 –2848
Chem. Soc. 72, 4664 – 4666 共1950兲. 共1952兲.
50/8 D. W. Scott and G. Waddington, J. Am. Chem. Soc. 72, 4310– 4311 52/13 T. A. Scott, Jr., D. MacMillan, and E. H. Melvin, Ind. Eng. Chem.
共1950兲. 44, 172–175 共1952兲.
50/9 H. O. Day and W. A. Felsing, J. Am. Chem. Soc. 72, 1698 –1699 52/14 E. T. G. Fuge, S. T. Bowden, and W. J. Jones, J. Phys. Chem. 56,
共1950兲. 1013–1016 共1952兲.
50/10 J. G. Aston, S. V. R. Mastrangelo, and G. W. Moessen, J. Am. 52/15 G. Edwards, Trans. Faraday Soc. 48, 513–515 共1952兲.
Chem. Soc. 72, 5287–5291 共1950兲. 52/16 J. H. Simons and J. W. Hausteller, J. Chem. Phys. 20, 1516 –1519
50/11 A. Z. Conner, P. J. Elving, J. Benischeck, P. E. Tobias, and S. 共1952兲.
Steingiser, Ind. Eng. Chem. 42, 106 –110 共1950兲. 52/17 G. B. Guthrie, D. W. Scott, W. N. Hubbard, C. Katz, J. P.
50/12 K. Hartley, H. O. Pritchard, and H. A. Skinner, Trans. Faraday McCullough, M. E. Gross, K. D. Williamson, and G. Waddington, J. Am.
Soc. 46, 1019–1025 共1950兲. Chem. Soc. 74, 4662– 4669 共1952兲.
1951 52/18 I. Brown, Austr. J. Sci. Research 5, 530–540 共1952兲.
51/1 J. G. Aston, H. L. Fink, G. J. Janz, and K. E. Russell, J. Am. Chem. 52/19 G. D. Oliver and J. W. Grisard, J. Am. Chem. Soc. 74, 2705–2707
Soc. 73, 1939–1943 共1951兲. 共1952兲.
51/2 J. P. McCullough, W. B. Person, and R. Spitzer, J. Am. Chem. Soc. 52/20 C. T. Mortimer, H. O. Pritchard, and H. A. Skinner, Trans. Faraday
73, 4069– 4071 共1951兲. Soc. 48, 220–228 共1952兲.
51/3 D. G. Flom, N. Alpert, and P. J. Elving, Ind. Eng. Chem. 43, 52/21 L. Kaplan, W. L. Kester, and J. J. Katz, J. Am. Chem. Soc. 75,
1178 –1181 共1951兲. 5531–5532 共1952兲.
51/4 D. W. Scott, H. L. Finke, J. P. McCullough, M. E. Gross, K. D. 52/22 G. A. R. Brandt, H. J. Emeleus, and R. N. Haszeldine, J. Chem.
Williamson, G. Waddington, and H. M. Huffman, J. Am. Chem. Soc. 73, Soc. 2198 –2205 共1952兲.
261–265 共1951兲. 1953
51/5 D. Bryce-Smith and K. E. Howlett, J. Chem. Soc. 1141–1142 53/1 J. A. Barker, I. Brown, and F. Smith, Disc. Faraday Soc. 15,
共1951兲. 142–150 共1953兲.
51/6 G. D. Oliver and J. W. Grisard, J. Am. Chem. Soc. 73, 1688 –1690 53/2 G. T. Furukawa, R. E. McCoskey, and M. L. Reilly, J. Res. Natl.
共1951兲. Bur. Standards 51, 69–72 共1953兲.
51/7 G. M. Barrow and A. L. McClellan, J. Am. Chem. Soc. 73, 53/3 J. G. Aston, J. L. Wood, and T. P. Zolki, J. Am. Chem. Soc. 75,
573–575 共1951兲. 6202– 6204 共1953兲.
51/8 T. F. Smith and R. F. Bonner, Ind. Eng. Chem. 43, 1169–1173 53/4 E. F. G. Herington and J. F. Martin, Trans. Faraday Soc. 49,
共1951兲. 154 –162 共1953兲.
51/9 J. C. Potter and J. H. Saylor, J. Am. Chem. Soc. 73, 90–91 共1951兲. 53/5 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Zh. Fiz.
51/10 A. C. Egerton, W. Emte, and G. J. Minkoff, Diss. Faraday Soc. Khim. 27, 1032–1038 共1953兲; Chem. Abstracts 49, 3594e 共1955兲.
278 –282 共1951兲. 53/6 S. Kardon and J. H. Saylor, J. Am. Chem. Soc. 75, 1997 共1953兲.
51/11 J. W. Grisard, H. A. Bernhardt, and G. D. Oliver, J. Am. Chem. 53/7 J. P. McCullough, D. W. Scott, H. L. Finke, W. N. Hubbard, M. E.
Soc. 73, 5725–5727 共1951兲. Gross, C. Katz, R. E. Pennington, J. F. Messerly, and G. Waddington, J.
Am. Chem. Soc. 75, 1818 –1824 共1953兲.
51/12 K. Hartley, H. O. Pritchard, and H. A. Skinner, Trans. Faraday
Soc. 47, 254 –263 共1951兲. 53/8 D. W. Scott, H. L. Finke, W. N. Hubbard, J. P. McCullough, C.
Katz, M. E. Gross, J. F. Messerly, R. E. Pennington, and G. Waddington,
51/13 W. H. Johnson, M. V. Kilday, and E. J. Prosen, J. Res. Nat. Bur.
J. Am. Chem. Soc. 75, 2795–2800 共1953兲.
Stand. 65A, 215–219 共1961兲.
53/9 H. Stage, E. Müller, and P. Faldix, Erdöle und Kohle 6, 375–380
51/14 A. B. Burg and C. L. Randolph, J. Am. Chem. Soc. 73, 953–957
共1953兲. 关Enthalpies of vaporization were calculated by fitting published
共1951兲.
vapor pressure data, taken from various sources to the Antoine equation.
51/15 J. G. Aston, G. J. Janz, and K. E. Russell, J. Am. Chem. Soc. 73,
Some of the references are to unpublished data measured by chemical
1943–1945 共1951兲.
companies.兴
1952 53/10 R. T. Davis, Jr. and R. W. Schiessler, J. Phys. Chem. 57, 966 –968
52/1 V. E. Stiles and G. H. Cady, J. Am. Chem. Soc. 74, 3771–3773 共1953兲.
共1952兲. 53/11 H. A. Skinner and T. F. S. Tees, J. Chem. Soc. 3378 –3383 共1953兲.
52/2 L. C. Leitch and A. T. Morse, Can. J. Chem. 30, 924 –932 共1952兲. 53/12 G. W. Rathjens and W. D. Gwinn, J. Am. Chem. Soc. 75, 5629–
52/3 G. B. Guthrie, D. W. Scott, Jr., and G. Waddington, J. Am. Chem. 5633 共1953兲.
Soc. 74, 2795–2800 共1952兲. 53/13 H. E. Clements, K. V. Wise, and S. E. Johnson, J. Am. Chem. Soc.
52/4 G. E. Coates, F. Glocling, and N. D. Huck, J. Chem. Soc. 4496 – 75, 1593–5395 共1953兲.
4501 共1952兲. 53/14 K. A. Walsh, U. S. Atom. Energy Comm. Report LA-1649, 1953,
52/5 W. S. Jones and W. S. Tamplin, 共glycols兲 American Chemical Chem. Abstracts 55, 19391c 共1961兲.
Society’s Series of Chemistry monographs 共1952兲. 53/15 W. T. Grubb and R. C. Osthoff, J. Am. Chem. Soc. 75, 2230–2232
52/6 J. P. McCullough, D. W. Scott, H. L. Finke, M. E. Gross, K. D. 共1953兲.
Williamson, R. E. Pennington, G. Waddington, and H. M. Huffman, J. 53/16 T. Charnley, C. T. Mortimer, and H. A. Skinner, J. Chem. Soc.
Am. Chem. Soc. 74, 2801–2804 共1952兲. 1181–1184 共1953兲.
52/7 G. H. Whipple, Ind. Eng. Chem. 44, 1664 –1667 共1952兲. 53/17 A. Michels, T. Wassenaar, P. Louwerse, R. J. Lunbeck, and G. W.
52/8 H. L. Finke, D. W. Scott, M. E. Gross, G. Waddington, and H. M. Wolkers, Physica 19, 287–289 共1953兲.
Huffman, J. Am. Chem. Soc. 74, 2804 –2806 共1952兲. 53/18 G. D. Oliver, H. T. Milton, and J. W. Grisard, J. Am. Chem. Soc.
52/9 P. T. White, D. G. Bernard-Smith, and F. A. Fidler, Ind. Eng. Chem. 75, 2827–2829 共1953兲.
44, 1430–1438 共1952兲. 53/19 H. Schaefer and F. Zeppernick, Z. Anorg. Allgem. Chem. 272,
52/10 W. N. Hubbard, H. L. Finke, D. W. Scott, J. P. McCullough, C. 274 –278 共1953兲.
Katz, M. E. Gross, J. F. Messerly, R. E. Pennington, and G. Waddington, 53/20 R. C. Osthoff, W. T. Grubb, and C. A. Burkhard, J. Am. Chem.
J. Am. Chem. Soc. 74, 6025– 6030 共1952兲. Soc. 75, 2227–2229 共1953兲.
52/11 D. W. Scott, H. L. Finke, W. N. Hubbard, J. P. MuCullough, G. D. 1954
Oliver, M. E. Gross, C. Katz, K. D. Williamson, G. Waddington, and H. 54/1 A. C. Jenkins and G. F. Chambers, Ind. Eng. Chem. 46, 2367–2369
M. Huffman, J. Am. Chem. Soc. 74, 4656 – 4662 共1952兲. 共1954兲.
54/2 J. P. McCullough, D. W. Scott, R. E. Pennington, I. A. Hossenlopp, 55/19 R. H. Sherman and W. F. Giauque, J. Am. Chem. Soc. 77,
and G. Waddington, J. Am. Chem. Soc. 76, 4791– 4796 共1954兲. 2154 –2160 共1955兲.
54/3 A. E. Potter, Jr. and H. L. Ritter, J. Phys. Chem. 58, 1040–1042 55/20 W. H. Mears, R. F. Stahl, S. R. Orfeo, R. C. Shair, L. F. Kells, W.
共1954兲. Thompson, and H. McCann, Ind. Eng. Chem. 47, 1449–1454 共1955兲.
54/4 M. Davies and D. G. Jenkin, J. Chem. Soc. 2374 –2377 共1954兲. 55/21 A. T. Morse, P. B. Ayscough, and L. C. Leitch, Can. J. Chem. 33,
54/5 G. T. Furukawa, R. E. McCoskey, and M. L. Reilly, J. Research 453– 457 共1955兲.
Natl. Bureau Standards 52, 11–16 共1954兲. 55/22 R. Dreyer, W. Martin, and U. von Weber, J. Prakt. Chem. 273,
54/6 T. I. Bowell and G. L. Jones, Jr., J. Phys. Chem. 58, 666 – 667 324 –328 共1955兲.
共1954兲. 55/23 J. Fischer and J. Bingle, J. Am. Chem. Soc. 77, 6511– 6512
54/7 D. L. Camin, A. F. Forziati, and F. D. Rossini, J. Phys. Chem. 58, 共1955兲.
440– 442 共1954兲. 1956
54/8 G. R. Nicholson, M. Szarc, and J. W. Taylor, J. Chem. Soc. 56/1 D. Ambrose, Trans. Faraday Soc. 52, 772–781 共1956兲.
2767–2769 共1954兲. 56/2 J. C. M. Li and K. S. Pitzer, J. Am. Chem. Soc. 78, 1077–1080
54/9 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Zh. Fiz. 共1956兲.
Khim. 28, 1969–1974 共1954兲; Chem. Abstracts 50, 4573i 共1956兲. 56/3 P. Gray, M. W. T. Pratt, and M. J. Larkin, J. Chem. Soc. 210–212
共1956兲.
54/10 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Zh. Fiz.
56/4 J. C. M. Li, J. Am. Chem. Soc. 78, 1081–1083 共1956兲.
Khim. 28, 810– 813 共1954兲; Chem. Abstracts 49, 6677c 共1955兲.
56/5 G. Milazzo, Ann. Chim. 共Rome兲 46, 1105–1111 共1956兲; Chem.
54/11 W. H. Hubbard and G. Waddington, Rec. Trav. Chim. 910–913
Abstracts 51, 7791c 共1957兲.
共1954兲.
56/6 J. Pick, V. Fried, E. Hala, and O. Vilim, Collect. Czech. Chem.
54/12 M. Bukala, J. Majewski, and W. Rodzinski, Przemysl Chem. 10,
Commun. 21, 260–261 共1956兲.
6 –11 共1954兲.
56/7 R. E. Pennington, D. W. Scott, H. L. Finke, J. P. McCullough, J. F.
54/13 R. C. Osthoff and W. T. Grubb, J. Am. Chem. Soc. 76, 399– 401
Messerly, I. A. Hossenlopp, and G. Waddington, J. Am. Chem. Soc. 78,
共1954兲.
3266 –3272 共1956兲.
54/14 G. Lord and A. A. Wolf, J. Chem. Soc. 2546 –2551 共1954兲.
56/8 A. Von Brockhaus and E. Jenckel, Macromol. Chem. 18Õ19,
54/15 V. Fried, J. Pick, E. Hala, and O. Vilim, Chem. Listy 48, 774 –775 262–293 共1956兲.
共1954兲.
56/9 D. L. Camin and F. D. Rossini, J. Phys. Chem. 60, 1446 –1451
54/16 K. A. Sense, M. J. Snyder, and J. W. Clegg, J. Phys. Chem. 58, 共1956兲.
223–224 共1954兲. 56/10 E. J. Barber and G. H. Cady, J. Phys. Chem. 60, 504 –505 共1956兲.
54/17 K. V. Wise, J. Am. Chem. Soc. 76, 3094 –3095 共1954兲. 56/11 F. Fromm and M. C. Loeffler, J. Phys. Chem. 60, 252–253 共1956兲.
54/18 L. H. Long and J. F. Sackman, Trans. Faraday Soc. 50, 1177–1182 56/12 R. H. Capps and W. M. Jackson, J. Phys. Chem. 60, 811– 812
共1954兲. 共1956兲.
1955 56/13 D. W. Scott, J. P. McCullough, W. N. Hubbard, J. F. Messerly, I.
55/1 J. G. Aston, P. E. Wills, and T. P. Zolki, J. Am. Chem. Soc. 77, A. Hossenlopp, F. R. Frow, and G. Waddington, J. Am. Chem. Soc. 78,
3939–3941 共1955兲. 5463–5468 共1956兲.
55/2 J. J. Jasper and G. B. Miller, J. Phys. Chem. 59, 441– 442 共1955兲. 56/14 D. N. Glew and L. W. Reeves, J. Phys. Chem. 60, 615 共1956兲.
55/3 G. A. N. Cummings and E. McLaughlin, J. Chem. Soc. 1391–1392 56/15 E. M. Toops, Jr., J. Phys. Chem. 60, 304 –306 共1956兲.
共1955兲. 56/16 Manufacturing Chemists Association Research Project 1956, Tables
55/4 O. R. Foz Gazulla, J. Morcilio, A. Perez-Masia, and A. Mendes, 23-9-2共2.0111兲-k and 23-9-2共2.0112兲-k; Tables 23-10-2共2.0111兲-k and
Anales Real Soc. Espan. Fis. Quim. 共Madrid兲 50B, 23–34 共1955兲. 23-10-2共2.0112兲-k; Tables 23-11-2共2.0111兲-k and 23-11-2共2.0112兲-k. The
55/5 G. H. Kosolapoff, J. Chem. Soc. 2964 –2965 共1955兲. authors suspect that the tabulated Antoine Constants for the various
55/6 J. G. Aston, T. P. Zolki, and J. L. Wood, J. Am. Chem. Soc. 77, compounds were generated in the manner discussed in Ref. 关61/13兴.
281–284 共1955兲. 56/17 Manufacturing Chemists Association Research Project 1956, Tables
55/7 D. L. Camin and F. D. Rossini, J. Phys. Chem. 59, 1173–1179 23-18-2共1.01111兲-k and 23-18-2共1.01112兲-k. The authors suspect that the
共1955兲. tabulated Antoine Constants for the various compounds were generated in
55/8 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Zh. Fiz. the manner discussed in Ref. 关61/13兴.
Khim. 29, 653– 657 共1955兲; Chem. Abstracts 50, 16231e 共1956兲. 56/18 D. Garvin and C. Schubert, J. Phys. Chem. 60, 807– 808 共1956兲.
55/9 E. Von Terres, F. Gebert, H. Hulsemann, H. Petereit, H. Toepsch, 56/19 D. W. Scott, J. P. McCullough, W. D. Good, J. F. Messerly, R. E.
and W. Ruppert, Brennst.-Chem. 36, 272–274 共1955兲. Pennington, T. C. Kincheloe, I. A. Hossenlopp, D. R. Douslin, and G.
55/10 O. Ya. Tsypikina, J. Appl. Chem. 共U.S.S.R.兲 28, 167–172 共1955兲; Waddington, J. Am. Chem. Soc. 78, 5457–5463 共1956兲.
Chem. Abstracts 49, 9967h 共1955兲. 56/20 H. L. Finke, D. W. Scott, M. E. Gross, J. F. Messerly, and G.
55/11 R. W. Schiessler and F. C. Whitmore, Ind. Eng. Chem. 47, Waddington, J. Am. Chem. Soc. 78, 5469–5476 共1956兲.
1660–1665 共1955兲; data are deposited as supplementary material, 56/21 M. T. Rogers and J. L. Speirs, J. Phys. Chem. 60, 1462–1463
Document No. 4597. 共1956兲.
55/12 J. P. McCullough, H. L. Finke, J. F. Messerly, R. E. Pennington, I. 56/22 W. D. Good, D. W. Scott, and G. Waddington, J. Phys. Chem. 60,
A. Hossenlopp, and G. Waddington, J. Am. Chem. Soc. 77, 6119– 6125 1090–1095 共1956兲.
共1955兲. 56/23 E. Neale, L. T. D. Williams, and V. T. Moores, J. Chem. Soc.
55/13 D. W. Scott, H. L. Finke, J. P. McCullough, M. E. Gross, J. F. 422– 427 共1956兲.
Messerly, R. E. Pennington, and G. Waddington, J. Am. Chem. Soc. 77, 56/24 L. H. Long and J. F. Sackman, Trans. Faraday Soc. 52, 1201–1206
4993– 4998 共1955兲. 共1956兲.
55/14 G. T. Furukawa, R. E. McCoskey, M. L. Reilly, and A. W. 56/25 F. W. Kirkbride, J. Appl. Chem. 6, 11–21 共1956兲.
Herman, J. Res. Natl. Bur. Standards 55, 201–207 共1955兲. 56/26 D. Brennan and A. R. Ubbelohde, J. Chem. Soc. 3011–3016
55/15 L. H. Long and J. F. Sackman, Trans. Faraday Soc. 51, 1062–1064 共1956兲.
共1955兲. 1957
55/16 F. Brown and P. L. Robinson, J. Chem. Soc. 3147–3151 共1955兲. 57/1 F. Call, J. Sci. Food Agric. 8, 81– 85 共1957兲.
55/17 J. E. Spice, L. A. K. Staveley, and G. A. Harrow, J. Chem. Soc. 57/2 P. Gray and M. W. T. Pratt, J. Chem. Soc. 2163–2168 共1957兲.
100–104 共1955兲. 57/3 I. Brown and F. Smith, Aust. J. Chem. 10, 423– 428 共1957兲.
55/18 C. A. Brown and A. W. Laubengayer, J. Am. Chem. Soc. 77, 57/4 T. C. Bissot, R. W. Parry, and D. H. Campbell, J. Am. Chem. Soc.
3699–3700 共1955兲. 79, 796 – 800 共1957兲.
57/5 W. K. Hall and L. Alexander, J. Phys. Chem. 61, 240–242 共1957兲. 58/11 A. B. Burg and F. J. Slota, Jr., J. Am. Chem. Soc. 80, 1107–1109
57/6 J. Dykyj, M. Seprakova, and J. Paulech, Chem. Zvesti 11, 461– 466 共1958兲.
共1957兲. 58/12 R. D. Dunlap, C. J. Murphy, Jr., and R. C. Bedford, J. Am. Chem.
57/7 D. W. Scott, H. L. Finke, J. P. McCullough, J. F. Messerly, R. E. Soc. 80, 83– 85 共1958兲.
Pennington, I. A. Hossenlopp, and G. Waddington, J. Am. Chem. Soc. 58/13 D. C. Bradley and J. D. Swanwick, J. Chem. Soc. 3207–3214
79, 1062–1068 共1957兲. 共1958兲.
57/8 A. Dobry and R. Keller, J. Phys. Chem. 61, 1448 –1449 共1957兲. 58/14 F. Feher and G. Hitzemann, Z. Anorg. Allgem. Chem. 294, 50– 62
57/9 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Zh. Fiz. 共1958兲.
Khim. 31, 1278 –1284 共1957兲; Chem. Abstracts 52, 3270f 共1958兲. 58/15 C. B. Colburn and A. Kennedy, J. Am. Chem. Soc. 80, 5004
57/10 J. P. McCullough, W. N. Hubbard, F. R. Frow, I. A. Hossenlopp, 共1958兲.
and G. Waddington, J. Am. Chem. Soc. 79, 561–566 共1957兲. 58/16 K. A. Sense and R. W. Stone, J. Phys. Chem. 62, 453– 457 共1958兲.
57/11 J. P. McCullough, D. R. Douslin, J. F. Messerly, I. A. Hossenlopp, 58/17 A. V. Novoselova, K. N. Semenenko, and O. Ya. Turova, Vestnik
T. C. Kincheloe, and G. Waddington, J. Am. Chem. Soc. 79, 4289– 4295 Moskov. Univ. Ser. Mekh., Astron. Fiz. Khim. 13, 139–147 共1958兲.
共1957兲. 58/18 L. H. Long and J. F. Sackman, Trans. Faraday Soc. 54, 1797–1803
57/12 F. Glaser and H. Ruland, Chemie Ing. Tech. 29, 772 共1957兲. 共1958兲.
57/13 B. C. Easton, M. K. Hargreaves, and R. K. S. Mitchell, J. Appl. 58/19 P. Gray and M. W. T. Pratt, J. Chem. Soc. 3403–3412 共1958兲.
Chem. 共London兲 7, 198 –204 共1957兲. 58/20 P. A. Fowell and C. T. Mortimer, J. Chem. Soc. 3734 –3736
57/14 J. S. Rowlinson and R. I. Thacker, Trans. Faraday Soc. 53, 1– 8 共1958兲.
共1957兲. 58/21 H. J. Emeleus and J. D. Smith, J. Chem. Soc. 527–528 共1958兲.
57/15 L. Maier, O. Seyforth, F. C. A. Stone, and E. Rochov, J. Am. 58/22 R. C. Cass, S. E. Fletcher, C. T. Mortimer, P. G. Quincey, and H.
Chem. Soc. 79, 5884 –5889 共1957兲. D. Springall, J. Chem. Soc. 958 –963 共1958兲.
57/16 A. Rose, J. A. Acciari, R. C. Johnson, and W. W. Sanders, Ind. 58/23 R. C. Cass, S. E. Fletcher, C. T. Mortimer, H. D. Springall, and T.
Eng. Chem. 49, 104 –109 共1957兲. R. White, J. Chem. Soc. 1406 –1410 共1958兲.
57/17 W. S. Barnhart, R. J. Seffl, R. F. Wade, F. W. West, and J. L. 58/24 E. A. V. Ebsworth and H. J. Emeleus, J. Chem. Soc. 2150–2156
Zollinger, J. Chem. Eng. Data 2, 80– 83 共1957兲. 共1958兲.
58/25 R. C. Cass, S. E. Fletcher, C. T. Mortimer, P. G. Quincey, and H.
57/18 E. F. Neilson and D. White, J. Am. Chem. Soc. 79, 5618 –5621
共1957兲. D. Springall, J. Chem. Soc. 2595–2599 共1958兲.
58/26 D. C. Bradley, L. J. Kay, J. D. Swanick, and W. Wardlaw, J.
57/19 J. W. Frazer and R. H. Sanborn, U. S. Atomic Energy Commission,
Chem. Soc. 3656 –3659 共1958兲.
Report UCRL-4978, 1957; Chem. Abstracts 52, 8936a 共1958兲.
58/27 C. P. Haber and R. K. Uenishi, Chem. Eng. Data Ser. 3, 323–324
57/20 J. Aylett, J. Chem. Soc. 4152– 4154 共1957兲.
共1958兲; Chem. Abstracts 53, 16781b 共1959兲.
57/21 K. D. Williamson and R. H. Harrison, J. Chem. Phys. 26, 1409–
58/28 H. Bloom and B. J. Welch, J. Phys. Chem. 62, 1594 –1595 共1958兲.
1411 共1957兲.
1959
57/22 J. B. Pedley, H. A. Skinner, and C. L. Chernick, Trans. Faraday
59/1 R. A. McDonald, S. A. Shrader, and D. R. Stull, J. Chem. Eng. Data
Soc. 53, 1612–1617 共1957兲.
4, 311–313 共1959兲.
57/23 L. H. Long and J. F. Sackman, Trans. Faraday Soc. 53, 1606 –1611
59/2 D. L. Hildenbrand and R. A. McDonald, J. Phys. Chem. 68,
共1957兲.
1521–1523 共1959兲.
57/24 A. K. Fischer, F. A. Cotton, and J. Wilkinson, J. Am. Chem. Soc.
59/3 Kh. A. Aronovich, L. P. Kastorskii, and K. F. Fedorova, Zh. Fiz.
79, 2044 –2046 共1957兲.
Khim. 41, 20 共1959兲.
57/25 S. D. Beskov, L. I. Kochetkova, and R. M. Golubeva, Uchenye 59/4 J. P. McCullough, D. R. Douslin, W. N. Hubbard, S. S. Todd, J. F.
Zapiski Moskov. Gosudarst. Pedagog. Inst. Im. V. I. Lenina 99, 147–149 Messerly, I. A. Hossenlopp, F. R. Frow, J. P. Dawson, and G.
共1957兲; Chem. Abstracts 53, 20993d 共1959兲.
Waddington, J. Am. Chem. Soc. 81, 5884 –5890 共1959兲.
57/26 R. C. Wilhoit, J. Phys. Chem. 61, 114 –116 共1957兲. 59/5 M. Seprakova, J. Paulech, and J. Dykyj, Chem. Zvesti 313–316
57/27 H. D. Kaesz and F. G. A. Stone, J. Chem. Soc. 1433–1435 共1957兲. 共1959兲.
57/28 J. W. Dale, H. J. Emeleus, R. N. Haszeldine, and J. H. Moss, J. 59/6 A. B. Burg and L. R. Grant, J. Am. Chem. Soc. 81, 1–5 共1959兲.
Chem. Soc. 3708 –3713 共1957兲. 59/7 D. W. Scott, D. R. Douslin, J. F. Messerly, S. S. Todd, I. A.
1958 Hossenlopp, T. C. Kincheloe, and J. P. McCullough, J. Am. Chem. Soc.
58/1 L. Molard, Mem. Poudres 40, 13 共1958兲; as quoted in 关77/6兴. 81, 1015–1020 共1959兲.
58/2 A. Rose, B. T. Paphronis, and E. T. Williams, J. Chem. Eng. Data 3, 59/8 J. P. McCullough, R. E. Pennington, J. C. Smith, I. A. Hossenlopp,
216 –219 共1958兲. and G. Waddington, J. Am. Chem. Soc. 81, 5880–5883 共1959兲.
58/3 R. E. Frost and E. G. Rochow, J. Inorg. Nucl. Chem. 52, 201–206 59/9 M. Usanovich and A. I. Dembitskii, Zh. Obshch. Khim. 29,
共1958兲; Chem. Abstracts 52, 6999c 共1958兲. 1781–1785 共1959兲.
58/4 J. A. Brown and W. H. Mears, J. Phys. Chem. 62, 960–962 共1958兲. 59/10 D. L. Hildenbrand, G. C. Sinke, R. A. McDonald, and W. R.
58/5 J. K. Koehler and W. F. Giauque, J. Am. Chem. Soc. 80, 2659– Kramer, J. Chem. Phys. 31, 650– 654 共1959兲.
2662 共1958兲. 59/11 I. Brown and F. Smith, Aust. J. Chem. 12, 407– 412 共1959兲.
58/6 D. W. Scott, J. P. McCullough, J. F. Messerly, R. E. Pennington, I. 59/12 W. D. Good, D. R. Douslin, D. W. Scott, A. George, J. L. Lacina,
A. Hossenlopp, H. L. Finke, and G. Waddington, J. Am. Chem. Soc. 80, J. P. Dawson, and G. Waddington, J. Phys. Chem. 63, 1133–1138 共1959兲.
55–59 共1958兲. 59/13 M. Usanovich and A. I. Dembitskii, Zh. Obshch. Khim. 29,
58/7 J. P. McCullough, H. L. Finke, D. W. Scott, R. E. Pennington, M. 1771–1781 共1959兲.
E. Gross, J. F. Messerly, and G. Waddington, J. Am. Chem. Soc. 80, 59/14 A. J. Leadbetter and J. E. Spice, Can. J. Chem. 37, 1923–1929
4786 – 4793 共1958兲. 共1959兲.
58/8 W. N. Hubbard, D. R. Douslin, J. P. McCullough, D. W. Scott, S. S. 59/15 E. Terres, L. Brinkmann, D. Fischer, D. Hüllstrung, W. Loz, and
Todd, J. F. Messerly, I. A. Hossenlopp, A. George, and G. Waddington, J. G. Weisbrod, Brennstoff-Chem. 40, 279–280 共1959兲.
Am. Chem. Soc. 80, 3547–3554 共1958兲. 59/16 J. B. Pedley and H. A. Skinner, Trans. Faraday Soc. 55, 544 –547
58/9 V. V. Serpinskii, S. A. Voitkevich, and N. Yu. Lyuboshits, Trudy 共1959兲.
Vsesoyuz. Nauch.- Issledovatel. Inst. Sintet. I. Natural. Dushistykh 59/17 W. D. Good, D. W. Scott, J. L. Lacina, and J. P. McCullough, J.
Veshchestv 4, 125–130 共1958兲. Phys. Chem. 63, 1139–1142 共1959兲.
58/10 W. Mahler and A. B. Burg, J. Am. Chem. Soc. 80, 6161– 6167 59/18 F. A. Cotton, A. K. Fischer, and J. Wilkinson, J. Am. Chem. Soc.
共1958兲. 81, 800– 803 共1959兲.
59/19 L. J. Paridon, G. E. MacWood, and J.-H. Hu, J. Phys. Chem. 63, 61/1 J. E. Griffiths and M. Onyszchuk, Can. J. Chem. 39, 339–347
1998 –1999 共1959兲. 共1961兲.
59/20 K. Mödritzer, Chem. Ber. 92, 2637–2640 共1959兲; Chem. Abstracts 61/2 E. L. Pace and R. J. Bobka, J. Chem. Phys. 35, 454 – 457 共1961兲.
54, 3180e 共1960兲. 61/3 J. Heinrich, J. Ilavsky, and J. Surovy, Chem. Zvesti 15, 414 – 418
59/21 H. J. Emeleus and J. D. Smith, J. Chem. Soc. 375–381 共1959兲. 共1961兲.
59/22 W. R. Cullen and H. J. Emeleus, J. Chem. Soc. 372–375 共1959兲. 61/4 H. Grosse-Ruyken and R. Kleesaat, Z. Anorg. Allgem. Chem. 308,
59/23 S. E. Fletcher, C. T. Mortimer, and H. D. Springall, J. Chem. Soc. 122–132 共1961兲.
580–584 共1959兲. 61/5 B. Sternback and A. G. MacDiarmid, J. Am. Chem. Soc. 83,
59/24 P. A. Folwell and C. T. Mortimer, J. Chem. Soc. 2913–2918 3384 –3388 共1961兲.
共1959兲. 61/6 A. Rose and W. R. Supina, J. Chem. Eng. Data 6, 173–179 共1961兲.
59/25 E. Amberger, Angew. Chem. 71, 372–373 共1959兲; Chem. Abstracts 61/7 W. T. Berg, D. W. Scott, W. N. Hubbard, S. S. Todd, J. F. Messerly,
53, 16780c 共1959兲. I. A. Hossenlopp, A. Osborn, D. R. Douslin, and J. P. McCullough, J.
59/26 H. Suga and S. Seki, Bull. Chem. Soc. Jpn. 32, 1088 共1959兲. Phys. Chem. 65, 1425–1430 共1961兲.
59/27 P. Chaiyavech and M. Van Winkle, J. Chem. Eng. Data 4, 53–57 61/8 J. P. McCullough, H. L. Finke, W. N. Hubbard, S. S. Todd, J. F.
共1959兲. Messerly, D. R. Douslin, and G. Waddington, J. Phys. Chem. 65,
59/28 L. C. Yen and T. M. Reed III, J. Chem. Eng. Data 4, 102–107 784 –791 共1961兲.
共1959兲. 61/9 R. E. Banks, A. E. Ginsberg, and R. N. Haszeldine, J. Chem. Soc.
59/29 F. P. Pike and C. F. Foster, Jr., J. Chem. Eng. Data 4, 305–306 1740–1743 共1961兲.
共1959兲. 61/10 S. Malanowski, Bull. Acad. Pol Sci. Ser. Sci. Chim. 9, 71–76
1960 共1961兲.
60/1 A. Aihara, Bull. Chem. Soc. Jpn. 33, 194 –200 共1960兲. 61/11 S. Malanowski, Bull. Acad. Pol. Sci. Ser. Sci. Chim. 9, 83 共1961兲.
60/2 R. G. Schmitt and R. C. Hirt, J. Polym. Sci. 45, 35– 47 共1960兲. 61/12 J. Dykvy, M. Seprakova, and J. Paulech, Chem. Zvesti 15,
60/3 C. R. Mueller and J. Ignatowski, J. Chem. Phys. 32, 1430–1434 465– 468 共1961兲; Chem. Abstracts 56, 10930b 共1962兲.
共1960兲. 61/13 J. C. M. Li and F. D. Rossini, J. Chem. Eng. Data 6, 268 –270
60/4 R. J. L. Andon, D. P. Biddiscombe, J. D. Cox, R. Handley, D. 共1961兲.
Harrop, E. F. G. Herington, and J. F. Martin, J. Chem. Soc. 5246 –5254 61/14 A. B. Burg and J. E. Griffiths, J. Am. Chem. Soc. 83, 4333– 4335
共1960兲. 共1961兲.
60/5 M. L. Klyueva, K. P. Mischenko, and M. K. Fedorov, Zh. Prikl. 61/15 D. W. Scott, J. F. Messerly, S. S. Todd, G. B. Gutherie, I. A.
Khim. 33, 473– 475 共1960兲; Chem. Abstracts 54, 11616g 共1960兲. Hosenlopp, R. T. Moore, A. Osborn, W. T. Berg, and J. P. McCullough, J.
60/6 L. G. L. Ward and A. G. MacDiarmid, J. Am. Chem. Soc. 82, Phys. Chem. 65, 1320–1326 共1961兲.
2151–2153 共1960兲. 61/16 H. M. Huffman, M. E. Gross, D. W. Scott, and J. P. McCullough,
60/7 D. E. McLaughlin and M. Tamres, J. Am. Chem. Soc. 82, 5618 – J. Phys. Chem. 65, 495–503 共1961兲.
5621 共1960兲. 61/17 J. K. Nickerson, K. A. Kobe, and J. J. McKetta, J. Phys. Chem.
60/8 D. E. McLaughlin, M. J. Tamres, and S. Searless, Jr., J. Am. Chem. 65, 1037–1043 共1961兲.
Soc. 82, 5621–5625 共1960兲. 61/18 J. F. Mathews and J. J. McKetta, J. Phys. Chem. 65, 758 –762
60/9 H. D. Kaesz and F. G. A. Stone, J. Am. Chem. Soc. 82, 6213– 6218 共1961兲.
共1960兲. 61/19 A. F. Frolov, M. A. Loginova, and M. M. Kiseleva, Zh. Phys.
60/10 F. E. Brinckman and F. G. A. Stone, J. Am. Chem. Soc. 82, Khim. 35, 1784 –1788 共1961兲.
6218 – 6223 共1960兲. 61/20 E. J. Smutny and A. Bondi, J. Phys. Chem. 65, 546 –550 共1961兲.
60/11 H. D. Kaesz, J. P. Phillips, and F. G. A. Stone, J. Am. Chem. Soc. 61/21 J. R. Case, N. H. Ray, and H. L. Roberts, J. Chem. Soc. 2070–
82, 6228 – 6232 共1960兲. 2075 共1961兲.
60/12 S. L. Stafford and F. G. A. Stone, J. Am. Chem. Soc. 82, 6238 – 61/22 J. R. Case, N. H. Ray, and H. L. Roberts, J. Chem. Soc. 2066 –
6240 共1960兲. 2070 共1961兲.
60/13 R. J. Brotherton, A. L. McCloskey, J. L. Boone, and H. M. 61/23 I. M. Schiopu, O. Bot, and V. Onu, Bul. Inst. Politeh. Iasi. 7,
Manasevit, J. Am. Chem. Soc. 82, 6245– 6248 共1960兲. 115–118 共1961兲; Chem. Abstracts 58, 10793c 共1963兲.
60/14 R. J. Brotherton, A. L. McCloskey, L. L. Petterson, and H. 61/24 P. A. Fowell and C. T. Mortimer, J. Chem. Soc. 3793–3796
Steinberg, J. Am. Chem. Soc. 82, 6242– 6245 共1960兲. 共1961兲.
60/15 W. P. Van Meter and G. H. Cady, J. Am. Chem. Soc. 82, 6005– 61/25 W. D. Good, J. L. Lacina, and J. P. McCullough, J. Phys. Chem.
6008 共1960兲. 65, 2229–2231 共1961兲.
60/16 D. N. Glew, Can. J. Chem. 38, 208 –211 共1960兲. 61/26 H. Zimmerman and H. Greisenfelder, Z. Electrochem. 65, 368 –371
60/17 J. Novak, J. Matous, and J. Pick, Collect. Czech. Chem. Commun. 共1961兲.
25, 2405–2413 共1960兲. 61/27 E. Amberger and H. Boeters, Angew. Chem. 73, 114 共1961兲;
60/18 E. J. Lynch and C. R. Wilke, J. Chem. Eng. Data 5, 300 共1960兲. Chem. Abstracts 55, 16403h 共1961兲.
60/19 J. W. Frazer, J. Inorg. Nucl. Chem. 16, 63– 66 共1960兲. 61/28 E. Amberger, Chem. Ber. 94, 1447–1452 共1961兲; Chem. Abstracts
60/20 D. L. Camin and F. D. Rossini, J. Chem. Eng. Data 5, 368 –372 56, 8279e 共1962兲.
共1960兲. 61/29 J. F. Ditter, J. C. Perrine, and I. Shapiro, J. Chem. Eng. Data 6,
60/21 R. A. McKay and B. H. Sage, J. Chem. Eng. Data 5, 21–24 271 共1961兲.
共1960兲. 61/30 A. Labbauf, J. B. Greenshields, and F. D. Rossini, J. Chem. Eng.
60/22 F. M. Trent, F. D. Miller, and G. H. Brown, J. Chem. Eng. Data 5, Data 6, 261–263 共1961兲.
110–111 共1960兲. 61/31 P. Hestermans and D. White, J. Phys. Chem. 65, 362–365 共1961兲.
60/23 A. P. Claydon, P. A. Fowell, and C. T. Mortimer, J. Chem. Soc. 1962
3284 –3287 共1960兲. 62/1 R. H. Valentini, G. E. Brodale, and W. R. Giauque, J. Phys. Chem.
60/24 H. J. Emeleus and S. N. Nabi, J. Chem. Soc. 1103–1108 共1960兲. 66, 392–395 共1962兲.
60/25 H. J. Emeleus and H. Pugh, J. Chem. Soc. 1108 –1112 共1960兲. 62/2 G. Waddington, J. C. Smith, K. D. Williamson, and D. W. Scott, J.
60/26 E. Amberger, Angew. Chem. 72, 494 共1960兲; Chem. Abstracts 55, Phys. Chem. 66, 1074 –1077 共1962兲.
22103f 共1961兲; 60, 4171d 共1964兲. 62/3 A. J. Von Arvia, P. J. Aymoning, and H. J. Schumacher, Z. Anorg.
60/27 R. M. Yarrington and W. B. Kay, J. Chem. Eng. Data 5, 24 –29 Allgem. Chem. 316, 325–334 共1962兲.
共1960兲. 62/4 A. Kreglewski, Bull. Acad. Pol. Sci., Ser. Sci. Chem. 10, 629– 633
1961 共1962兲.
62/5 H.-J. Bittrich, E. Kauer, M. Kraft, G. Schoeppe, W. Soell, and A. 63/6 H. Hiraoka and J. H. Hildebrand, J. Phys. Chem. 67, 916 –918
Ullrich, J. Prakt. Chem. 17, 250–262 共1962兲. 共1963兲.
62/6 A. D. Craig and A. G. MacDiarmid, J. Inorg. Nucl. Chem. 24, 63/7 G. A. Bottomley and G. H. F. Seiflow, J. Appl. Chem. 13, 399– 409
161–164 共1962兲. 共1963兲.
62/7 W. E. Hatton, D. R. Douslin, G. C. Sinke, and D. R. Stull, J. Chem. 63/8 D. P. Biddiscombe, R. R. Collerson, R. Handley, E. F. G. Herington,
Eng. Data 7, 229–231 共1962兲. J. F. Martin, and C. H. S. Sprake, J. Chem. Soc. 1954 –1957 共1963兲.
62/8 A. D. Craig, J. Chem. Soc. 548 –553 共1962兲. 63/9 W. D. Good, D. R. Douslin, and J. P. McCullough, J. Phys. Chem.
62/9 D. W. Scott, W. D. Good, S. S. Todd, J. F. Messerly, W. T. Berg, I. 67, 1312–1314 共1963兲.
A. Hossenlop, J. L. Lucina, A. G. Osborn, and J. P. McCullough, J. 63/10 D. P. Biddiscombe, R. Handley, D. Harrop, A. J. Head, G. B.
Chem. Phys. 36, 406 – 412 共1962兲. Lewis, J. F. Martin, and C. H. S. Sprake, J. Chem. Soc. 5764 –5768
62/10 D. W. Scott, D. R. Douslin, H. L. Finke, W. N. Hubbard, J. F. 共1963兲.
Messerly, I. A. Hossenlopp, and J. P. McCullough, J. Phys. Chem. 66, 63/11 D. W. Scott, W. N. Hubbard, J. F. Messerly, S. S. Todd, I. A.
1334 –1341 共1962兲. Hossenlopp, W. D. Good, D. R. Douslin, and J. P. McCullough, J. Am.
62/11 M. Mansson and S. Sunner, Acta Chem. Scand. 16, 1863–1869 Chem. Soc. 67, 680– 685 共1963兲.
共1962兲. 63/12 D. W. Scott, W. D. Good, G. B. Gutherie, S. S. Todd, I. A.
62/13 W. D. Good, D. R. Douslin, and J. P. McCullough, J. Phys. Chem. Hossenlopp, A. G. Osborn, and J. P. McCullough, J. Am. Chem. Soc. 67,
66, 958 –959 共1962兲. 685– 689 共1963兲.
62/14 J. H. Stern and F. H. Dorer, J. Phys. Chem. 66, 97–99 共1962兲. 63/13 M. Kraus, L. Beranek, K. Kochloefl, and V. Bazant, Chem.
62/15 N. S. Berman and J. J. McKetta, J. Phys. Chem. 66, 1444 –1448 Prumysl 12, 649– 652 共1962兲; Chem. Abstracts 58, 10746d 共1963兲.
共1962兲. 63/14 R. J. Best, J. Chem. Eng. Data 8, 267–270 共1963兲.
62/16 H. Mackle and R. G. Mayrick, Trans. Faraday Soc. 58, 238 –243 63/15 J. G. Wojtasinski, J. Chem. Eng. Data 8, 381–385 共1963兲.
共1962兲. 63/16 A. Rose and V. N. Schrodt, J. Chem. Eng. Data 8, 9–13 共1963兲.
62/17 H. Mackle and R. G. Mayrick, Trans. Faraday Soc. 58, 230–237 63/17 W. P. Gilbreath and G. H. Cady, Inorg. Chem. 2, 496 – 499 共1963兲.
共1962兲. 63/18 E. T. Benyon, Jr. and J. J. McKetta, J. Phys. Chem. 67, 2761–2765
62/18 G. R. Ross and W. G. Heideger, J. Chem. Eng. Data 7, 505–507 共1963兲.
共1962兲. 63/19 W. D. Good, S. S. Todd, J. F. Messerly, J. L. Lacina, J. P. Dawson,
62/19 S. M. Williamson and G. H. Cady, Inorg. Chem. 1, 673– 677 D. W. Scott, and J. P. McCullough, J. Phys. Chem. 67, 1306 –1311
共1962兲. 共1963兲.
62/20 H. Mackle and R. G. Mayrick, Trans. Faraday Soc. 58, 33–39 63/20 D. Ambrose and R. Townsend, J. Chem. Soc. 3614 –3625 共1963兲.
共1962兲. 63/21 A. Capkova and V. Fried, Collect. Czech. Chem. Commun. 28,
62/21 J. E. Griffiths and A. B. Burg, J. Am. Chem. Soc. 84, 3442–3450 2235–2239 共1963兲.
共1962兲. 63/22 C. G. Vinson, Jr. and J. J. Martin, J. Chem. Eng. Data 8, 74 –75
62/22 J. J. Martin, J. Chem. Eng. Data 7, 68 –72 共1962兲. 共1963兲.
62/23 H.-J. Bittrich and E. Kauer, Z. Phys. Chem. 共Frankfurt/Main兲 219, 63/23 D. W. Scott, J. F. Messerly, S. S. Todd, I. A. Hossenlopp, A.
224 –238 共1962兲. Osborn, and J. P. McCullough, J. Chem. Phys. 38, 532–539 共1963兲.
62/24 G. J. Pasek and G. Thodes, J. Chem. Eng. Data 7, 21–26 共1962兲. 63/24 J. A. Dixon, G. R. Yarnell, and J. A. Mountain, J. Chem. Eng.
62/25 A. Bauder and H. Guenthard, Helv. Chim. Acta 45, 1698 –1702 Data 8, 572–573 共1963兲.
共1962兲. 63/25 V. V. Sokolov, L. P. Zhilina, and K. P. Mischenko, Zh. Prikl Khim.
62/26 P. Sellers and S. Sunner, Acta Chem. Scand. 16, 46 –52 共1962兲. 36, 750–754 共1963兲.
62/27 J. P. Oliver and L. G. Stevens, J. Inorg. Nucl. Chem. 24, 953–960 63/26 M. A. Greenbaum, J. N. Foster, M. L. Arin, and M. Farber, J.
共1962兲. Phys. Chem. 67, 36 – 40 共1963兲.
62/28 G. C. Sinke and D. L. Hildenbrand, J. Chem. Eng. Data 7, 74 63/27 E. J. Spanier and A. G. MacDiarmid, Inorg. Chem. 2, 214 –215
共1962兲. 共1963兲.
62/29 S. P. Vohra, T. L. Kang, K. A. Kobe, and J. J. McKetta, J. Chem. 63/28 M. Lustig and G. H. Cady, Inorg. Chem. 2, 388 –390 共1963兲.
Eng. Data 7, 150–155 共1962兲. 63/29 R. R. Holmes and R. P. Wagner, Inorg. Chem. 2, 384 –388 共1963兲.
62/30 G. Geiseler, K. Quitzsch, J. Hoffmann, and W. Moeschler, Z. 63/30 M. Abedini and A. G. MacDiarmid, Inorg. Chem. 2, 608 – 613
Physik. Chem. 共Leipzig兲 220, 391–396 共1962兲. 共1963兲.
62/31 E. A. V. Ebsworth, H. J. Emeleus, and N. Welcman, J. Chem. Soc. 63/31 S. B. Hartley, W. S. Holmes, J. K. Jaques, M. F. Mole, and J. C.
2290–2293 共1962兲. McCoubrey, Quat. Rev. Chem. Soc. 17, 204 共1973兲.
62/32 H. J. Emeleus, K. H. Packer, and N. Welcman, J. Chem. Soc. 63/32 A. E. Pope and H. A. Skinner, J. Chem. Soc. 3704 –3712 共1963兲.
2529–2531 共1962兲. 63/33 G. L. Gal’chenko and R. M. Varushchenko, Zh. Fiz. Khim. 37,
62/33 A. J. Downs, J. Chem. Soc. 4361– 4366 共1962兲. 2513–2519 共1963兲.
62/34 E. Amberger and H. Boeters, Angew. Chem. 74, 293 共1962兲; 63/34 C. T. Mortimer and P. Sellers, J. Chem. Soc. 1978 –1981 共1963兲.
Chem. Abstracts 57, 4276f 共1962兲. 63/35 I. B. Rabinovich, V. I. Tel’noi, N. V. Karyakin, and G. A.
62/35 E. Amberger and H. Boeters, Angew. Chem. 74, 32–33 共1962兲; Razuvaev, Dokl. Akad. Nauk. SSSR 149, 324 –326 共1963兲.
Chem. Abstracts 57, 12522e 共1962兲. 63/36 J. V. Davies, A. E. Pope, and H. A. Skinner, Trans. Faraday Soc.
62/36 B. Cohen and A. G. MacDiarmid, Inorg. Chem. 1, 754 –756 59, 2233–2242 共1963兲.
共1962兲. 63/37 W. F. Lautsch, A. Tröber, W. Zimmer, L. Mehner, W. Linck, H. M.
62/37 J. Tjebbes, Acta Chem. Scand. 16, 916 –921 共1962兲. Lehman, H. Brandenberger, H. Korner, H.-J. Metschker, K. Wagner, and
1963 R. Kaden, Z. Chem. 3, 415– 421 共1963兲.
63/1 R. H. Boyd, J. Chem. Phys. 38, 2529–2535 共1963兲. 63/38 J. L. Hales, J. D. Cox, and E. B. Lees, Trans. Faraday Soc. 59,
63/2 K. G. McCurdy and K. J. Laidler, Can. J. Chem. 41, 1867–1871 1544 –1554 共1963兲.
共1963兲. 63/39 E. A. V. Ebsworth and S. G. Frankiss, J. Chem. Soc. 661– 665
63/3 I. Shapiro, B. Keilin, R. E. Williams, and C. D. Good, J. Am. 共1963兲.
Chem. Soc. 85, 3167–3171 共1963兲. 63/40 J. V. Urenovitch and A. G. MacDiarmid, J. Chem. Soc. 1091–1095
63/4 J. A. Brown, J. Chem. Eng. Data 8, 106 –108 共1963兲. 共1963兲.
63/5 J. P. McCullough, J. F. Messerly, R. T. Moore, and S. S. Todd, J. 63/41 H. J. Emeleus and N. Welcman, J. Chem. Soc. 1268 –1271 共1963兲.
Phys. Chem. 67, 677– 679 共1963兲. 63/42 H. J. Emeleus and A. Haas, J. Chem. Soc. 1272–1275 共1963兲.
63/43 D. C. Abercromby and P. F. Tiley, J. Chem. Soc. 4902– 4903 65/4 I. I. Serebryannaya and S. Sh. Byk, Khim. Prom. 23, 828 – 829
共1963兲. 共1965兲.
63/44 E. Amberger and H. Boeters, Z. Naturforsch. 18B, 157 共1963兲; 65/5 L. A. McDougall and J. E. Kilpatrick, J. Chem. Phys. 42, 2311–
Chem. Abstracts 59, 5194g 共1963兲. 2321 共1965兲.
63/45 G. Pass and H. L. Roberts, Inorg. Chem. 2, 1016 –1019 共1963兲. 65/6 I. V. Kudryashov and R. I. Savechenko, Izv. Vysh. Ucheb. Zav.
63/46 M. M. Fein, J. Bobinski, N. Mayes, N. Schwartz, and M. S. Khim. Khim. Tekhnol. 8, 602 共1965兲.
Cohen, Inorg. Chem. 2, 1111–1115 共1963兲. 65/7 R. R. Collerson, J. F. Counsell, R. Handley, J. F. Martin, and C. H.
1964 S. Sprake, J. Chem. Soc. 3697–3700 共1965兲.
64/1 J. V. Enstein, L. I. Duronina, and A. S. Pashinkin, Zh. Prikl. Khim. 65/8 D. R. Douslin and A. Osborn, J. Sci. Instrum. 42, 369–373 共1965兲.
37, 2543–2545 共1964兲. 65/9 A. N. Marinichev and M. P. Susarev, Zh. Prikl. Khim. 38, 378 –383
64/2 A. V. Kletskii, Inzh. Fiz. Zh. Akad. Nauk. Beldrussk. SSR 7, 40– 43 共1965兲.
共1964兲. 65/10 N. V. Lutugina, V. N. Kolbina, and L. I. Reshetova, Zh. Prikl.
64/3 G. Fisher and A. S. Buchanan, Aust. J. Chem. 17, 481 共1964兲. Khim. 38, 1541–1546 共1965兲.
64/4 L. K. Peterson and A. B. Burg, J. Am. Chem. Soc. 86, 2587–2591 65/11 P. A. Naro, J. Chem. Eng. Data 10, 86 共1965兲.
共1964兲. 65/12 I. Wadso, Acta Chem. Scand. 19, 1079–1087 共1965兲.
64/5 G. Geiseler and W. Konig, Z. Physik. Chem. 共Leipzig兲 227, 81–90 65/13 R. E. Rondeau and L. A. Harrah, J. Chem. Eng. Data 10, 84 – 85
共1964兲. 共1965兲.
64/6 K. P. Murphy, J. Chem. Eng. Data 9, 259–260 共1964兲. 65/14 H. L. Finke, I. A. Hossenlopp, and W. T. Berg, J. Phys. Chem. 69,
64/7 A. N. Gubkov, N. A. Fermor, and N. I. Smirnov, Zh. Prikl. Khim. 3030–3031 共1965兲.
37, 2204 –2210 共1964兲. 65/15 M. Davies and B. Kybett, Trans. Faraday Soc. 61, 1608 –1617
64/8 A. Capkova and V. Fried, Coll. Czech. Chem. Commun. 29, 共1965兲.
336 –340 共1964兲. 65/16 J. F. Counsell, J. L. Hales, and J. F. Martin, Trans. Faraday Soc.
64/9 N. N. Sevrugova, V. A. Sokorskii, and N. M. Zhavoronkov, Zh. 61, 1869–1875 共1965兲.
Prikl. Khim. 共Leningrad兲 37, 1989–1993 共1964兲. 65/17 J. Linek, V. Fried, and J. Pick, Collect. Czech. Chem. Commun.
64/10 N. A. Goldberg, V. A. Gorbushchenkov, and Z. G. Teplova, Zh. 30, 1358 –1365 共1965兲.
Prikl. Khim. 37, 745–747 共1964兲. 65/18 R. Noftle and G. H. Cady, Inorg. Chem. 4, 1010–1012 共1965兲.
64/11 E. G. Mangalin, Khim. Prom. 4, 304 –306 共1964兲. 65/19 J. M. Shreeve, L. C. Duncan, and G. H. Cady, Inorg. Chem. 4,
64/12 D. W. Morecroft, J. Chem. Eng. Data 9, 488 – 490 共1964兲. 1516 –1517 共1965兲.
64/13 A. Rose and V. Schrodt, J. Chem. Eng. Data 9, 12–16 共1964兲. 65/20 L. A. Nisel’son and I. I. Lapivus, Russ. J. Phys. Chem. 39, 80– 83
共1965兲.
64/14 R. Handley, D. Harrop, J. F. Martin, and C. H. S. Sprake, J. Chem.
65/21 I. G. Gakh and E. P. Babin, Russ. J. Phys. Chem. 39, 924 共1965兲.
Soc. 4404 – 4406 共1964兲.
65/22 L. A. Nisel’son and I. I. Lapidus, Russ. J. Phys. Chem. 39,
64/15 D. Ambrose and R. Townsend, Trans. Faraday Soc. 60, 1025–1029
931–932 共1965兲.
共1964兲.
65/23 G. W. Fraser and J. M. Shreeve, Inorg. Chem. 4, 1497–1498
64/16 C. R. Patrick and G. S. Prosser, Trans. Faraday Soc. 60, 700–704
共1965兲.
共1964兲.
65/24 H. Kilian and H. J. Bittrich, Z. Phys. Chem. 230, 383 共1965兲.
64/17 H. Mackle and R. T. B. McClean, Trans. Faraday Soc. 60,
65/25 J. Heinrich, J. Surovy, and J. Dojcansky, Chem. Zvesti 19,
817– 821 共1964兲.
462– 464 共1965兲.
64/18 L. C. Duncan and G. H. Cady, Inorg. Chem. 3, 850– 852 共1964兲.
65/26 J. Linek, V. Fried, and J. Pick, Collect. Czech. Chem. Commun.
64/19 L. C. Duncan and G. H. Cady, Inorg. Chem. 3, 1045–1047 共1964兲.
30, 1358 –1365 共1965兲.
64/20 Yu. Kh. Shaulov, V. S. Tubyanskaya, E. V. Evstegneeva, and G. O.
65/27 Yu. Kh. Shaulov, G. O. Schmyreva, and V. S. Tubyanskaya, Zh.
Shmyreva, Russ. J. Phys. Chem. 38, 967–970 共1964兲.
Fiz. Khim. 39, 105–109 共1965兲.
64/21 L. A. Serafimov, V. S. Timofeev, M. P. Strukova, and S. V. L’vov,
65/28 H. S. Hull, A. F. Reid, and A. G. Turnbull, Austr. J. Chem. 18,
Russ. J. Phys. Chem. 38, 1018 –1019 共1964兲. 249–252 共1965兲.
64/22 C. T. Ratcliffe and J. M. Shreeve, Inorg. Chem. 3, 631– 633 65/29 B. J. Aylett and L. K. Peterson, J. Chem. Soc. 4043– 4048 共1965兲.
共1964兲.
1966
64/23 N. S. Berman, C. W. Larkam, and J. J. McKetta, J. Chem. Eng.
66/1 A. W. Laubengayer and C. W. J. Scaife, J. Chem. Eng. Data 11,
Data 9, 218 –219 共1964兲.
172–174 共1966兲.
64/24 V. Kliment, V. Fried, and J. Pick, Collect. Czech. Chem. Commun. 66/2 I. Wadso, Acta Chem. Scand. 20, 544 –552 共1966兲.
29, 2008 –2015 共1964兲.
66/3 T. R. Bott and H. N. Adler, J. Chem. Eng. Data 11, 25–30 共1966兲.
64/25 F. S. Fawcett and R. D. Lipscomb, J. Am. Chem. Soc. 86,
66/4 W. H. Mears, E. Rosenthal, and J. V. Sinka, J. Chem. Eng. Data 11,
2576 –2579 共1964兲.
338 –342 共1966兲.
64/26 W. D. Good, J. L. Lacina, B. L. De Prater, and J. P. McCullough,
66/5 A. N. Osborn and D. R. Douslin, J. Chem. Eng. Data 11, 502–509
J. Phys. Chem. 68, 579–586 共1964兲. 共1966兲.
64/27 J. L. Bills and F. A. Cotton, J. Phys. Chem. 68, 806 – 810 共1964兲. 66/6 N. E. Miller, M. D. Murphy, and D. L. Reznicek, Inorg. Chem. 5,
64/28 A. E. Pope and H. A. Skinner, Trans. Faraday Soc. 60, 1404 –1407 1832–1834 共1966兲.
共1964兲. 66/7 G. Geiseler, J. Fruwert, and R. Huetting, Chem. Ber. 99, 1594 –1601
64/29 B. J. Aylett and L. K. Peterson, J. Chem. Soc. 3429–3436 共1964兲. 共1966兲.
64/30 R. G. Cavell, J. Chem. Soc. 1992–1995 共1964兲. 66/8 A. P. Kudchadker and B. J. Zwolinski, J. Chem. Eng. Data 11,
64/31 R. G. Cavell and H. J. Emeleus, J. Chem. Soc. 5825–5832 共1964兲. 253–255 共1966兲.
64/32 R. G. Cavell and H. J. Emeleus, J. Chem. Soc. 5896 –5897 共1964兲. 66/9 H. L. Morris, M. Tamres, and S. Searles, Inorg. Chem. 5, 2156 –
64/33 H. Mackle and P. A. G. O’Hare, Trans. Faraday Soc. 60, 506 –509 2160 共1966兲.
共1964兲. 66/10 W. D. Good and B. L. DePrater, J. Phys. Chem. 70, 3606 –3609
1965 共1966兲.
65/1 S. J. Price and M. G. Jacko, Can. J. Chem. 43, 3481–3482 共1965兲. 66/11 F. D. Evans and P. F. Tiley, J. Chem. Soc. B 134 –136 共1966兲.
65/2 W. E. Putnam, D. M. McEachern, and J. E. Kiplatrick, J. Chem. 66/12 E. F. Meyer and R. E. Wagner, J. Phys. Chem. 70, 3162–3168
Phys. 42, 749–755 共1965兲. 共1966兲.
65/3 I. Mertl and J. Polak, Collect. Czech. Chem. Commun. 30, 3526 – 66/13 M. F. Zimmer, R. A. Robb, and G. A. Carpenter, J. Chem. Eng.
3528 共1965兲. Data 11, 577–579 共1966兲.
66/14 V. A. Branzhan, S. V. Semenenko, and O. G. Kirillova, Zh. Prikl. 67/19 D. W. Scott, W. T. Berg, I. A. Hossenlopp, W. N. Hubbard, J. F.
Khim. 39, 1399–1403 共1966兲; Chem. Abstracts 65, 9820f 共1966兲. Messerly, S. S. Todd, D. R. Douslin, J. P. McCullough, and G.
66/15 D. D. DesMarteau and G. H. Cady, Inorg. Chem. 5, 169–171 Waddington, J. Phys. Chem. 71, 2263–2270 共1967兲.
共1966兲. 67/20 A. Ribner and E. F. Westrum, Jr., J. Phys. Chem. 71, 1208 –1215
66/16 M. Abedini and A. G. MacDiarmid, Inorg. Chem. 5, 2040–2042 共1967兲.
共1966兲. 67/21 A. J. B. Cruickshank and A. J. B. Cutler, J. Chem. Eng. Data 12,
66/17 J. J. Delfino and J. M. Shreeve, Inorg. Chem. 5, 308 –309 共1966兲. 326 –329 共1967兲.
66/18 B. L. Earl, B. K. Hill, and J. M. Shreeve, Inorg. Chem. 5, 67/22 M. M. Omar, J. Chem. Soc. C 2038 –2040 共1967兲.
2184 –2186 共1966兲. 67/23 D. Reedy and G. Urry, Inorg. Chem. 6, 2117–2118 共1967兲.
66/19 B. Börjesson, Y. Nakase, and S. Sunner, Acta Chem. Scand. 20, 67/24 L. L. Lapidus, L. A. Nisel’son, and A. A. Karateeva, Russ. J. Phys.
803– 810 共1966兲. Chem. 41, 241–243 共1967兲.
66/20 D. C. Bradley and M. J. Hillyer, Trans. Faraday Soc. 62, 2374 – 67/25 E. A. Miroshnichenko, Yu. A. Lebedev, S. A. Shevelev, V. I.
2381 共1966兲. Gulevskaya, A. A. Fainzil’berg, and A. Ya. Apin, Russ. J. Phys. Chem.
66/21 R. C. Dobbie, J. Chem. Soc. A 1555–1556 共1966兲. 41, 783–785 共1967兲.
66/22 A. E. Beezer and C. T. Mortimer, J. Chem. Soc. A 514 –516 67/26 Yu. V. Golubkov, I. I. Lapidus, and L. A. Nisel’son, Russ. J. Phys.
共1966兲. Chem. 41, 1122–1123 共1967兲.
66/23 M. A. Ring, H. E. O’Neal, A. H. Kadhim, and F. Jappe, J. 67/27 T. M. Lesteva, S. K. Ogorodnikov, and A. I. Morozova, Zh. Prikl.
Organomet. Chem. 5, 124 –129 共1966兲. Khim. 共Leningrad兲 40, 891– 894 共1967兲.
66/24 D. J. Coleman and H. A. Skinner, Trans. Faraday Soc. 62, 67/28 M. Lustig, Inorg. Chem. 6, 1064 –1065 共1967兲.
1721–1755 共1966兲. 67/29 M. L. Anderson and R. N. Hammer, J. Chem. Eng. Data 12,
66/25 V. I. Tel’noi and I. B. Rabinovich, Russ. Zh. Fiz Khim. 40, 442– 447 共1967兲.
1556 –1563 共1966兲.
67/30 V. Fried, P. Gallant, and G. B. Schneier, J. Chem. Eng. Data 12,
66/26 G. Gattow and M. Dräger, Z. Anorg. Allg. Chem. 343, 232–243 504 –508 共1967兲.
共1966兲.
67/31 O. Glemser, U. Biermann, and M. Fild, Chem. Ber. 100, 1082–
66/27 A. Finch, P. J. Gardner, and E. J. Pearn, Trans. Faraday Soc. 62, 1086 共1967兲.
1072–1081 共1966兲.
67/32 N. K. Smith and W. D. Good, J. Chem. Eng. Data 12, 570–572
66/28 A. A. Zalykin and Yu. A. Strepikheev, J. Appl. Chem. USSR 39, 共1967兲.
2448 共1966兲.
67/33 S. Pawlenko, Chem. Ber. 100, 3591–3598 共1967兲.
66/29 G. P. Luchinskii, Zh. Fiz. Khim. 40, 593–598 共1966兲.
67/34 J. C. Baldwin, M. F. Lappert, J. B. Pedley, and J. A. Treverton, J.
66/30 I. Holeci, Chem. Prumysl 16, 267–270 共1966兲.
Chem. Soc. A 1980–1984 共1967兲.
66/31 D. H. Brown, G. W. Fraser, and D. W. A. Sharp, J. Chem. Soc. A
67/35 S. M. Danov and Yu. D. Golubev, Tr. Khim. Khim. Tekhnol.
171–174 共1966兲.
52–55 共1967兲; Chem. Abstracts 68, 95253a 共1968兲.
66/32 R. C. Dobbie and H. J. Emeleus, J. Chem. Soc. A 933–936 共1966兲.
67/36 T. L. Charlton and R. G. Cavell, Inorg. Chem. 6, 2204 –2208
66/33 H. J. Emeleus and T. Onak, J. Chem. Soc. A 1291–1292 共1966兲.
共1967兲.
66/34 J. L. Carson, R. C. Stewart, and A. G. Williamson, J. Chem. Eng.
67/37 K. Pihlaja and J. Heikkila, Acta Chem. Scand. 21, 2430–2434
Data 11, 231–233 共1966兲.
共1967兲.
66/35 M. Mansson and S. Sunner, Acta Chem. Scand. 20, 845– 848
67/38 M. Hirata and S. Suda, Kagaku Kogaku 31, 339–342 共1967兲.
共1966兲.
67/39 J. L. Hales, E. B. Lees, and D. Ruxton, J. Trans. Faraday Soc. 63,
1967
1876 –1879 共1967兲.
67/1 A. Finch, P. J. Gardner, E. J. Pearn, and G. B. Watts, Trans. Faraday
67/40 B. J. Aylett and J. M. Campbell, Inorg. Nucl. Chem. Letters 3,
Soc. 63, 1880–1888 共1967兲.
137–139 共1967兲.
67/2 P. M. Christopher and A. Shilman, J. Chem. Eng. Data 12, 333–335
67/41 V. R. Paetzold, R. Kurze, and G. Engelhardt, Z. Anorg. Allgem.
共1967兲.
Chem. 353, 62–71 共1967兲.
67/3 J. Murto and A. Kivinen, Suomen Kemistil. B 40, 258 –264 共1967兲.
67/42 M. P. Edejer and G. Thodos, J. Chem. Eng. Data 12, 206 –209
67/4 A. C. Meeks and I. J. Goldfarb, J. Chem. Eng. Data 12, 196 共1967兲.
共1967兲.
67/5 E. L. Pace and A. C. Plaush, J. Chem. Phys. 47, 38 – 43 共1967兲.
1968
67/6 K. H. Goebel, J. Schaffenger, and G. Opel, Chem. Tech. 19,
68/1 I. Wadso, Acta Chem. Scand. 22, 2438 –2444 共1968兲.
307–308 共1967兲.
67/7 R. L. Shak, J. Chem. Eng. Data 12, 474 – 480 共1967兲. 68/2 E. L. Cherkasskaya, A. M. Tur, Z. F. Petrenkova, and V. I.
Lyubomilov, Zh. Prikl. Khim. 41, 2553–2554 共1968兲.
67/8 A. Finch, P. J. Gardner, and G. B. Watts, Trans. Faraday Soc. 63,
1603–1607 共1967兲. 68/3 F. Gopal and S. A. Rizvi, J. Indian Chem. Soc. 45, 13–16 共1968兲.
67/9 A. C. Plaush and E. L. Pace, J. Chem. Phys. 47, 44 – 48 共1967兲. 68/4 A. G. Osborn and D. R. Douslin, J. Chem. Eng. Data 13, 534 –537
67/10 H. C. Van Ness, C. A. Soczek, G. L. Peloquin, and R. L. Machado, 共1968兲.
J. Chem. Eng. Data 12, 217–223 共1967兲. 68/5 P. F. Malbrunot, P. A. Meunier, G. M. Scatena, W. H. Mears, K. P.
67/11 M. Haccuria and M. P. Mathieu, Ind. Chim. Belg. 32, 165–167 Murphy, and J. V. Sinka, J. Chem. Eng. Data 13, 16 –21 共1968兲.
共1967兲. 68/6 W. J. Gaw and F. L. Swinton, Trans. Faraday Soc. 64, 637– 647
67/12 H. A. Berman and E. D. West, J. Chem. Eng. Data 12, 197–199 共1968兲.
共1966兲. 68/7 E. Z. Zhuravlev and I. I. Konstantinov, Zh. Prikl. Khim. 41,
67/13 W. A. Van Hook, J. Chem. Phys. 46, 1907–1918 共1967兲. 1170–1172 共1968兲.
67/14 A. B. Kletshii and L. E. Petric, Zh. Fiz. Khim. 41, 1183–1184 68/8 J. O. Hill and I. Wadso, Acta Chem. Scand. 22, 1590–1594 共1968兲.
共1967兲. 68/9 E. Morawetz, Acta Chem. Scand. 22, 1509–1531 共1968兲.
67/15 G. A. Crowder, Z. H. Taylor, T. M. Reed, and J. A. Young, J. 68/10 D. Ambrose, J. Chem. Soc. 1381–1383 共1968兲.
Chem. Eng. Data 12, 481– 485 共1967兲. 68/11 L. Fowler, W. N. Trump, and C. E. Vogler, J. Chem. Eng. Data 13,
67/16 E. F. Westrum and A. Ribner, J. Phys. Chem. 71, 1216 –1224 209–210 共1968兲.
共1967兲. 68/12 E. E. Baroody, G. A. Carpenter, R. A. Robb, and M. F. Zimmer, J.
67/17 I. I. Konstantinov, E. Z. Zhuravlev, and Z. G. Teplova, Zh. Prikl. Chem. Eng. Data 13, 215–217 共1968兲.
Khim. 40, 1084 –1087 共1967兲. 68/13 I. I. Lapidus and L. A. Nisel’son, Russ. J. Phys. Chem. 42,
67/18 N. V. Ermakov and V. P. Skripov, Zh. Fiz. Khim. 41, 77– 81 733–734 共1968兲.
共1967兲. 68/14 Yu. Ya. Maksimov, Russ. J. Phys. Chem. 42, 1550–1552 共1968兲.
68/15 C. Ratcliffe and J. M. Shreeve, J. Am. Chem. Soc. 90, 5403–5408 69/20 S. M. Danov, V. B. Matin, P. V. Jefremov, and N. K. Slashtshina,
共1968兲. Zh. Fiz. Khim. 43, 733–736 共1969兲; Chem. Abstracts 71, 6729g 共1969兲.
68/16 R. V. Kachalova and M. S. Nemcov, Zh. Prikl. Khim. 共Leningrad兲 69/21 J. Vojtko, M. Cihova, and M. Hrusovsky, Zb. Pr. Chem.-Tech. Fak.
41, 2315–2319 共1968兲. Svst. 179 共1969/1970兲; Chem. Abstracts 76, 76492b 共1972兲.
68/17 R. D. Place and S. M. Williamson, J. Am. Chem. Soc. 90, 69/22 O. Glemser and S. P. Von Halasz, Inorg. Nucl. Chem. Lett. 5,
2550–3556 共1968兲. 393–398 共1969兲.
68/18 N. Welcman and M. Wulf, Israel J. Chem. 6, 37– 41 共1968兲. 69/23 R. Lamantine and R. Perrin, Bull. Soc. Chim. France 443– 445
68/19 M. Mansson, Y. Nakase, and S. Sunner, Acta Chem. Scand. 22, 共1969兲.
171–174 共1968兲. 69/24 H. Mackle, D. V. McNally, and W. V. Steele, Trans. Faraday Soc.
68/20 D. P. Baccanari, J. A. Novinski, Y.-C. Pan, M. M. Yevitz, and H. 65, 2060–2068 共1969兲.
A. Swain, Jr., Trans. Faraday Soc. 64, 1201–1205 共1968兲. 69/25 S. Meszaros, Period. Poltech. Chem. Eng. 共Budapest兲 13, 79– 88
68/21 O. Glemser and S. P. von Halasz, Z. Naturforsch. 23B, 743–745 共1969兲; Chem. Abstracts 72, 66308z 共1970兲.
共1968兲. 69/26 O. Glemser, R. Mews, and H. W. Roesky, J. Chem. Soc., Chem.
68/22 O. Glemser, S. P. von Halasz, and U. Biermann, Z. Naturforsch. Commun. 914, 共1969兲.
23B, 1381–1382 共1968兲. 69/27 Y. K. Shaulov, A. K. Federov, and V. G. Genchel, Zh. Fiz Khim.
68/23 W. J. Gaw and F. L. Swinton, Trans. Faraday. Soc. 64, 2023–2034 185, 1336 –1337 共1969兲.
共1968兲. 69/28 J. E. Sicre, J. T. Dubois, K. J. Eisentraut, and R. E. Sievers, J. Am.
68/24 V. V. Kushchenko and K. Mishchenko, P. Zh. Prikl. Khim. 41, Chem. Soc. 91, 3476 –3481 共1969兲.
646 – 648 共1968兲; Chem. Abstracts 68, 117314a 共1968兲. 69/29 M. A. Soulie, P. Goursot, A. Peneloux, and J. Metzger, J. Chim.
68/25 B. M. Kuadzhe, G. P. Ustyugov, and A. A. Kudryavtsev, Tr. Mosk. Phys. Physicochim. Biol. 66, 607– 610 共1969兲.
Khim. Tekhnol. Inst. 58, 27–28 共1968兲; Chem. Abstracts 71, 6728 69/30 M. Ya. Agarunov and S. N. Hajiev, Dokl. Akad. Nauk. SSSR 185,
共1969兲. 221 共1969兲.
68/26 R. J. L. Andon, J. F. Counsell, J. L. Hales, E. B. Lees, and J. F.
69/31 T. Melia and R. Merrifield, J. Appl. Chem. 共London兲 19, 79– 82
Martin, J. Chem. Soc. 2357–2361 共1968兲. 共1969兲.
68/27 L. A. Nisel’son, R. K. Nikolaev, T. D. Sokolova, V. I. Stolyarov, 69/32 J. Mason, J. Chem. Soc. A 1587–1592 共1969兲.
and Yu. M. Korolev, Izv. Sib. Otd. Akad. Nauk. SSSR, Ser. Khim. Nauk
69/33 B. J. Aylett and M. J. Hakim, J. Chem. Soc. A 800– 803 共1969兲.
109–114 共1968兲; Chem. Abstracts 69, 69834s 共1969兲.
69/34 B. J. Aylett and M. J. Hakim, J. Chem. Soc. A 636 – 638 共1969兲.
68/28 G. Geiseler and J. Hoffmann, Z. Phys. Chem. 共Frankfurt am Main兲
69/35 B. J. Aylett and M. J. Hakim, J. Chem. Soc. A 639– 642 共1969兲.
57, 318 –330 共1968兲.
69/36 B. J. Aylett and J. M. Campbell, J. Chem. Soc. A 1910–1916
68/29 M. Cihova, J. Vojtko, and M. Hrusovsky, Zb. Pr. Chemickotechnol.
共1969兲.
Fak. SVST 共Slov. Vys. SK. Tech.兲 135–138 共1968兲; Chem. Abstracts 72,
69/37 B. J. Aylett and J. M. Campbell, J. Chem. Soc. A 1916 –1920
136676u 共1970兲.
共1969兲.
68/30 W. B. Fox, J. S. MacKenzie, E. R. McCarthy, J. R. Holmes, R. F.
Stahl, and R. Juurik, Inorg. Chem. 7, 2064 –2067 共1968兲. 69/38 B. J. Aylett, J. M. Campbell, and A. Walton, J. Chem. Soc. A
2110–2113 共1969兲.
68/31 A. S. Khorevskaya and S. Sh. Byk, Zh. Prikl. Khim. 共Leningrad兲
41, 2566 –2568 共1968兲; Chem. Abstracts 70, 61317a 共1969兲. 69/39 R. D. George and K. M. Mackay, J. Chem. Soc. A 2122–2126
1969 共1969兲.
69/1 Zh. V. Davydova, I. A. Makolkin, and P. S. Bataev, Zh. Obshch. 1970
Khim. 39, 1668 –1669 共1969兲. 70/1 A. J. Valerga, Dissertation Abstracts 31, 3316-B 共1970–1971兲.
69/2 I. Wadso, Acta Chem. Scand. 23, 2061–2064 共1969兲. 70/2 D. Ambrose and C. H. S. Sprake, J. Chem. Thermodyn. 2, 631– 645
69/3 J. A. Devore and H. E. O’Neal, J. Phys. Chem. 73, 2644 –2648 共1970兲.
共1969兲. 70/3 J. Polak, S. Murakami, V. T. Lam, and G. C. Benson, J. Chem. Eng.
69/4 M. A. Soulie, P. Goursot, A. Peneloux, and J. Metzger, J. Chim. Data 15, 323–328 共1970兲.
Phys. Physicochim. Biol. 66, 603– 606 共1969兲. 70/4 D. Ambrose, J. F. Counsell, and A. J. Davenport, J. Chem.
69/5 R. H. Kemme and S. I. Kreps, J. Chem. Eng. Data 14, 98 –102 Thermodyn. 2, 283–294 共1970兲.
共1969兲. 70/5 E. D. Smith and W. L. Thornsberry, J. Chem. Eng. Data 15,
69/6 J. H. Smith and E. L. Pace, J. Phys. Chem. 73, 4232– 4236 共1969兲. 296 –297 共1970兲.
69/7 B. G. Rueben, J. Chem. Eng. Data 14, 235–236 共1969兲. 70/6 R. M. Varushchenko, N. A. Belikova, S. M. Skuratov, and A. F.
69/8 T. M. Lesteva, A. I. Morozova, V. I. Morozova, S. K. Ogorodnikov, Plate, Zh. Fiz. Khim. 44, 3022–3025 共1970兲.
and T. M. Tyvina, Zh. Prikl. Khim. 42, 533–538 共1969兲. 70/7 D. N. Andreevskii and M. M. Brazhnikov, Vestn. Beloruss. Univ. 2,
69/9 T. J. V. Findlay, J. Chem. Eng. Data 14, 229–231 共1969兲. 14 –18 共1970兲; Chem. Abstracts 76, 158651s 共1972兲.
69/10 G. C. Calero, M. M. Valle, and C. G. Losa, Rev. Acad. Cienc. Fis. 70/8 J. Konicek and I. Wadso, Acta Chem. Scand. 24, 2612–2616
Quim. Nat. Zaragoza 24, 137–158 共1969兲. 共1970兲.
69/11 A. L. Woodman and A. Adicoff, J. Chem. Eng. Data 14, 479– 480 70/9 R. J. Irving and I. Wadso, Acta Chem. Scand. 24, 589–593 共1970兲.
共1969兲. 70/10 G. A. Carpenter, M. F. Zimmer, E. E. Baroody, and R. A. Robb, J.
69/12 A. G. Osborn and D. R. Douslin, J. Chem. Eng. Data 14, 208 –209 Chem. Eng. Data 15, 150–153 共1970兲.
共1969兲. 70/11 W. D. Good and R. T. Moore, J. Chem. Eng. Data 15, 150–153
69/13 R. J. Sheehan and S. H. Langer, J. Chem. Eng. Data 14, 248 –250 共1970兲.
共1969兲. 70/12 A. K. Goncharov, M. Kh. Karapet’yants, and G. M. Kol’yakova,
69/14 J. Konicek, M. Prochazka, V. Krestanova, and M. Smisek, Collect. Russ. J. Phys. Chem. 44, 466 – 467 共1970兲.
Czech. Chem. Commun. 34, 2249–2257 共1969兲. 70/13 J. E. Smith and G. H. Cady, Inorg. Chem. 9, 1293–1294 共1970兲.
69/15 J. Cidlinsky and J. Polak, Collect. Czech. Chem. Commun. 34, 70/14 J. Dykyj and A. Vanko, Petrochemica 10, 3–22 共1970兲.
1317–1321 共1969兲. 70/15 L. M. Zaborowski and J. M. Shreeve, J. Am. Chem. Soc. 92,
69/16 F. Franks and B. Watson, Trans. Faraday Soc. 65, 2339–2349 3665–3668 共1970兲.
共1969兲. 70/16 J. Dykyj, Petrochemica 10, 51–59 共1970兲; 123–146 共1970兲; 10,
69/17 N. G. Krokhin, Russ. J. Phys. Chem. 43, 1342–1343 共1969兲. 187–206 共1970兲.
69/18 M. Mansson, J. Chem. Thermodyn. 1, 141–151 共1969兲. 70/17 K. Kusano and I. Wadso, Acta Chem. Scand. 24, 2037–2042
69/19 I. Brown, W. Fock, and F. Smith, J. Chem. Thermodyn. 1, 共1970兲.
273–291 共1969兲. 70/18 P. Sellers, J. Chem. Thermodyn. 2, 211–219 共1970兲.
70/19 D. Harrop, A. J. Head, and G. B. Lewis, J. Chem. Thermodyn. 2, 71/16 I. I. Skorokhodov, V. E. Ditsent, N. A. Teret’eva, and M. N.
203–210 共1970兲. Zolotarev, Russ. J. Phys. Chem. 45, 902 共1971兲.
70/20 J. F. Counsell, J. O. Fenwick, and E. B. Lees, J. Chem. 71/17 F. Swindell, L. M. Zaborowski, and J. M. Shreeve, Inorg. Chem.
Thermodyn. 2, 367–372 共1970兲. 10, 1635–1638 共1971兲.
70/21 M. Prochazka, V. Krestanova, J. Konicek, and M. Smisek, Collect. 71/18 R. A. De Marco and J. M. Shreeve, Inorg. Chem. 10, 911–913
Czech. Chem. Commun. 35, 727–732 共1970兲. 共1971兲.
70/22 E. Koizumi and S. Ouchi, Nippon Kagaku Zasshi 91, 501–503 71/19 L. M. Zaborowski and J. M. Shreeve, Inorg. Chem. 10, 407– 409
共1970兲. 共1971兲.
70/23 D. W. Scott, J. Chem. Thermodyn. 2, 833– 837 共1970兲. 71/20 D. T. Sauer and J. M. Shreeve, Inorg. Chem. 10, 358 –362 共1971兲.
70/24 O. Eisen and A. Orav, Eesti Tead. Akad. Toim., Keem. Geol. 19, 71/21 J. Dykyj, Petrochemia 11, 27– 45 共1971兲.
202–205 共1970兲.
71/22 Z. I. Geller, V. D. Simonov, M. V. Lyubarskii, E. A. Brakhfogel, L.
70/25 A. J. Valerja and J. E. Kilpatrick, J. Chem. Phys. 52, 4545– 4549
M. Meizler, and I. A. Paramonov, Izv. Uyssh. Ucheb. Zaved., Nept. Gaz
共1970兲.
7, 71–74 共1971兲.
70/26 A. B. Burg and D.-K. Kang, J. Am. Chem. Soc. 92, 1901–1908
共1970兲. 71/23 I. Mita, I. Imai, and I. Kambe, Thermochimica Acta 2, 337–344
共1971兲.
70/27 S. P. Von Halasz and O. Glemser, Chem. Ber. 103, 553–560
共1970兲. 71/24 L. A. Nisel’son, K. V. Tret’yakova, E. P. Paremuzov, and E. N.
70/28 J. Vojtko, M. Cihova, and M. Hrusovsky, Chem. Zvesti 24, Torbina, Izv. Akad. Nauk SSSR, Neorg. Mater. 7, 792–794 共1971兲;
173–176; Chem. Abstracts 74, 46115x 共1971兲. Chem. Abstracts 75, 67746q 共1971兲.
70/29 A. Finch, P. J. Gardner, P. McNamara, and G. R. Wellum, J. Chem. 71/25 B. Ringner, S. Sunner, and H. Watanabe, Acta Chem. Scand. 25,
Soc. A 3339–3345 共1970兲. 141–146 共1971兲.
70/30 S.-J. Chang, D. McNally, S. Sharry-Tehrany, M. J. Hickey, and R. 71/26 K. Pihlaja and M.-L. Tuomi, Acta Chem. Scand. 25, 465– 469
H. Boyd, J. Am. Chem. Soc. 92, 3109–3118 共1970兲. 共1971兲.
70/31 J. D. Cox and G. Pilcher, Thermochemistry of Organic and 71/27 J. Polak and G. C. Benson, J. Chem. Thermodyn. 3, 235–242
Organometallic Compounds 共Academic, London, 1970兲. 共1971兲.
70/32 Y. K. Shaulov, A. K. Federov, G. Y. Zueva, G. V. Borisyuk, and V. 71/28 R. C. Wihoit and B. J. Zwolinski, Handbook of Vapor Pressures
G. Genchen, Russ. J. Phys. Chem. 44, 1181–1182 共1970兲; Zh. Fiz. Khim. and Heats of Vaporization of Hydrocarbons and Related Compounds, API
44, 2081–2083; Chem. Abstracts 74, 7230m 共1971兲. 44-TRC 共Publications in Science and Engineering, College Station, TX,
70/33 M. G. Barlow, R. N. Haszeldine, and R. Hubbard, J. Chem. Soc. C 1971兲.
1232–1237 共1970兲. 71/29 I. B. Rabinovich, E. G. Kiparisov, and Y. A. Aleksandrov, Dokl.
70/34 F. I. Mullayanov, G. V. Galagan, M. F. Buz’ko, Yu. V. Churkin, Akad. Nauk. SSSR 200, 1116 –1118 共1971兲.
and A. A. Shiryaeva, Tr. Nauch-Issled. Inst. Neftekhim. Proizvod. 95–97 71/30 G. M. Kol’yakova, I. B. Rabinovich, and N. S. Vyazankin, Dokl.
共1970兲; Chem. Abstracts 74, 91930v 共1971兲. Akad. Nauk. SSSR 200, 111–113 共1971兲.
70/35 A. K. Baev, Obshch. Prikl. Khim. 146 –160 共1970兲; Chem. 71/31 P. Sellers, Acta Chem. Scand. 25, 2099–2102 共1971兲.
Abstracts 74, 91934z 共1971兲. 71/32 I. E. Nakhutin, N. M. Smirnova, V. I. Krivenko, and G. A.
70/36 V. D. Moisev and N. D. Antonova, Zh. Fiz. Khim. 44, 2912–2913 Loshakov, Zh. Obshch. Khim. 41, 940–943 共1971兲; Chem. Abstracts 75,
共1970兲; Chem. Abstracts 69, 80487e 共1971兲. 122154x 共1971兲.
70/37 V. B. Sokolov, M. Kh. Karapet’yants, and A. K. Goncharov, Tr. 71/33 S. A. Voitkevich, M. M. Shchedrina, N. P. Solov’eva, and T. A.
Mosk. Khim.-Tekhnol. Inst. 67, 37–39 共1970兲; Chem. Abstracts 75, Rudol’fi, Maslo-Zhir. Prom. 37, 27–30 共1971兲.
122149z 共1971兲. 71/34 D. T. Sauer and J. M. Shreeve, J. Fluorine Chem. 1, 1–11 共1971兲.
70/38 P. Sellers, Acta Chem. Scand. 24, 2453–2458 共1970兲. 71/35 D. W. Osborne, F. Schreiner, and H. Selig, J. Chem. Phys. 54,
1971 3790–3798 共1971兲.
71/1 J. K. Choi and M. J. Joncich, J. Chem. Eng. Data 16, 87–90 共1971兲. 71/36 W. D. Good and R. T. Moore, J. Chem. Thermodyn. 3, 701–705
71/2 H. K. Hall, Jr. and J. H. Baldt, J. Am. Chem. Soc. 93, 140–145 共1971兲.
共1971兲. 71/37 F. E. Rodgers, J. Phys. Chem. 75, 1734 –1737 共1971兲.
71/3 C. Eon, C. Pommier, and G. Guiochon, J. Chem. Eng. Data 16,
1972
408 – 410 共1971兲.
72/1 M. Colomina, J. L. Laynez, R. Perez-Ossorio, and C. Turrion, J.
71/4 E. F. Meyer, T. A. Renner, and K. S. Stec, J. Phys. Chem. 76,
Chem. Thermodyn. 4, 499–506 共1972兲.
642– 648 共1971兲.
71/5 K. Kusano and I. Wadso, Acta Chem. Scand. 25, 219–224 共1971兲. 72/2 E. L. Pace and P. E. Hodge, J. Chem. Thermodyn. 4, 441– 447
共1972兲.
71/6 Yu. N. Matyushin, V. I. Pepekin, S. P. Golova, T. I. Godovikova,
and L. I. Khmelnitskii, Bull Acad. Sci. USSR, Div. Chem. Sci. 162–164 72/3 M. Mansson, J. Chem. Thermodyn. 4, 865– 871 共1972兲.
共1971兲. 72/4 J. F. Counsell and D. A. Lee, J. Chem. Thermodyn. 4, 915–917
71/7 E. Morawetz, Chem. Scripta 1, 103–111 共1971兲. 共1972兲.
71/8 P. Sellers, Acta Chem. Scand. 25, 2189–2193 共1971兲. 72/5 R. Prydz and R. D. Goodwin, J. Chem. Thermodyn. 4, 123–127
71/9 K. Kusano and I. Wadso, Bull. Chem. Soc. Jpn. 44, 1705–1707 共1972兲.
共1971兲. 72/6 T. Boublik and K. Aim, Collect. Czech. Chem. Commun. 37, 3513
71/10 N. D. Lebedeva, Yu. A. Katin, and G. Ya. Akhmedova, Russ. J. 共1972兲.
Phys. Chem. 45, 1192–1193 共1971兲. 72/7 R. M. Varuschenko and A. I. Druzhinina, Zh. Fiz. Khim. 46, 1313
71/11 V. B. Sokolov, M. Kh. Karapet’yants, N. D. Rumyantseva, and V. 共1972兲.
A. Drozdov, Russ. J. Phys. Chem. 45, 1332–1333 共1971兲. 72/8 G. Jakli and W. A. Van Hook, J. Chem. Thermodyn. 4, 857– 864
71/12 A. K. Goncharov, M. Kh. Karapet’yants, and T. K. Gar, Russ. J. 共1972兲.
Phys. Chem. 45, 104 –105 共1971兲. 72/9 D. Ambrose, C. H. S. Sprake, and R. Townsend, J. Chem.
71/13 N. D. Lebedeva, Yu. A. Katin, and G. Ya. Akhmedova, Russ. J. Thermodyn. 4, 247–254 共1972兲.
Phys. Chem. 45, 771–772 共1971兲. 72/10 A. K. Goncharov and M. Kh. Karapet’yants, Zh. Fiz. Khim. 46,
71/14 A. K. Baev, V. V. Dem’yanchuk, G. Girzoev, G. I. Novikov, and N. 228 –230 共1972兲.
E. Kolobova, Russ. J. Phys. Chem. 45, 777–778 共1971兲. 72/11 W. D. Good, J. Chem. Eng. Data 17, 158 –162 共1972兲.
71/15 V. E. Ditsent, I. I. Skorokhodov, N. A. Terent’eva, and M. N. 72/12 W. C. Neely and T. D. Hall, J. Chem. Eng. Data 17, 294 –295
Zolotareva, Russ. J. Phys. Chem. 45, 901–902 共1971兲. 共1972兲.
72/13 V. B. Sokolov, M. Kh. Karapet’yants, S. P. Kolesnikov, B. L. 73/3 J. F. Counsell and D. A. Lee, J. Chem. Thermodyn. 5, 583–589
Perl’mutter, and O. M. Nefedov, Tr. Mosk. Khim.-Tekhnol. Inst. 71, 6 –7 共1973兲.
共1972兲; Chem. Abstracts 80, 100456y 共1974兲. 73/4 G. R. De Mare, T. Lehman, and M. Termonia, J. Chem. Thermodyn.
72/14 V. B. Sokolov, G. P. Bragin, and M. Kh. Karapet’yants, Tr. Mosk. 5, 829– 832 共1973兲.
Khim.-Tekhnol. Inst. 71, 8 –9 共1972兲; Chem. Abstracts 80, 100457z 73/5 D. H. Rochester and J. R. Symonds, J. Chem. Soc., Faraday Trans.
共1974兲. 1, 1267–1273 共1973兲.
72/15 G. P. Brajin, M. Kh. Karapet’yants, A. K. Goncharov, and G. M. 73/6 J. Konicek, Acta Chem. Scand. 27, 1496 –1502 共1973兲.
Kol’yakova, Tr. Mosk. Khim.-Tekhnol. Inst. 71, 10–12 共1972兲; Chem. 73/7 D. Ambrose, C. H. S. Sprake, and R. Townsend, J. Chem. Soc.,
Abstracts 80, 100458a 共1974兲. Faraday Trans. 1 69, 839– 841 共1975兲.
72/16 V. E. Ditsent, I. I. Skorokhodov, N. A. Terent’eva, and M. N. 73/8 H.-J. Rauh, W. Geyer, H. Schmidt, and G. Z. Geiseler, Phys. Chem.
Zolotareva, Russ. J. Phys. Chem. 46, 317–318 共1972兲; Zh. Fiz. Khim. 共Leipzig兲 253, 43– 48 共1973兲.
46, 544 共1972兲; Chem. Abstracts 77, 9812p 共1972兲. 73/9 F. A. Gothard, D. C. Mentianu, D. G. Breban, and C. I. Cristea, J.
72/17 E. A. Volchkova, D. D. Smol’yaminova, V. G. Genchel, I. L. Chem. Eng. Data 18, 381–384 共1973兲.
Lopatkina, and Yu. Kh. Shaulova, Russ. J. Phys. Chem. 46, 1053–1054 73/10 E. A. Dietz and D. R. Martin, J. Inorg. Nucl. Chem. 35, 3681–
共1972兲. 3684 共1973兲.
72/18 R. H. T. Bleyerveld and W. Fieggen, Recl. Trav. Chim. Pays-Bas 73/11 G. F. Carruth and R. Kobayashi, J. Chem. Eng. Data 18, 115–126
91, 477– 482 共1972兲; Chem. Abstracts 76, 145167p 共1972兲. 共1973兲.
72/19 V. E. Ditsent, I. I. Skorokhodov, N. A. Terent’eva, and M. N. 73/12 E. F. Meyer and R. D. Hotz, J. Chem. Eng. Data 18, 359–362
Zolotareva, Russ. J. Phys. Chem. 46, 1088 共1972兲; Zh. Fiz. Khim. 46, 共1973兲.
1887–1888 共1972兲; Chem. Abstracts 77, 106168r 共1972兲; 77, 106166p 73/13 V. Svoboda, F. Vesely, R. Holub, and J. Pick, Collect. Czech.
共1972兲. Chem. Commun. 38, 3539–3543 共1973兲.
72/20 J. Dykyj, Petrochemia 12, 13–31 共1972兲; 12, 34 – 63 共1972兲. 73/14 J. Linek and I. Wichterle, Collect. Czech. Chem. Commun. 38,
72/21 R. F. Swindell and J. M. Shreeve, J. Am. Chem. Soc. 94, 5713– 1846 –1852 共1973兲.
5718 共1972兲. 73/15 I. N. Fel’dman, V. V. Savko, U. I. Mamai, and M. F. Finkel’shtein,
72/22 S. G. Metcalf and J. M. Shreeve, Inorg. Chem. 11, 1631–1634 Russ. J. Phys. Chem. 47, 1531 共1973兲.
共1972兲.
73/16 N. N. D’yachkova, E. N. Vigdorovich, and L. A. Ivanyutin, Russ.
72/23 S. R. O’Neill and J. M. Shreeve, Inorg. Chem. 11, 1629–1631
J. Phys. Chem. 47, 258 –259 共1973兲.
共1972兲.
73/17 G. L. Gal’chenko, E. P. Brykina, R. M. Varushchenko, L. S.
72/24 R. F. Swindell, D. P. Babb, T. J. Ouellette, and J. M. Shreeve,
Vasil’ev, and B. N. Mikhailov, Russ. J. Phys. Chem. 47, 914 共1973兲.
Inorg. Chem. 11, 242–245 共1972兲.
73/18 J. Kkykj and M. Repas, Petrochemia 13, 179–198 共1973兲.
72/25 D. T. Sauer and J. M. Shreeve, Inorg. Chem. 11, 238 –242 共1972兲.
73/19 C. J. Schack, D. Pilipovich, and J. F. Hon, Inorg. Chem. 12,
72/26 Ya. A. Strepikheev, O. P. Novikova, and A. L. Chimishkyan, Khim.
897–900 共1973兲.
Prom. 共Moscow兲 48, 230–231 共1972兲; Chem. Abstracts 69, 145717t
73/20 A. Majid and J. M. Shreeve, J. Org. Chem. 38, 4028 – 4031 共1973兲.
共1972兲.
72/27 G. Geiseler and J. Sawitowsky, Z. Phys. Chem. 共Leipzig兲 250, 73/21 G. H. Sprenger, K. J. Wright, and J. M. Shreeve, Inorg. Chem. 12,
43– 48 共1972兲. 2890–2893 共1973兲.
72/28 E. Morawetz, J. Chem. Thermodyn. 4, 455– 460 共1972兲. 73/22 R. A. De Marco and J. M. Shreeve, Inorg. Chem. 12, 1896 –1899
共1973兲.
72/29 E. Morawetz, J. Chem. Thermodyn. 4, 139–144 共1972兲.
73/23 K. J. Wright and J. M. Shreeve, Inorg. Chem. 12, 77– 80 共1973兲.
72/30 J. B. Pedley and B. S. Iseard, CATCH Tables, Silicon Compounds
共University of Sussex Press, Brighton, 1972兲. 73/24 C. S.-C. Wang and J. M. Shreeve, Inorg. Chem. 12, 81– 83 共1973兲.
72/31 G. M. Kol’yakova, I. B. Rabinovich, E. N. Gladyshev, and N. S. 73/25 V. I. Pepekin, Yu. A. Lebedev, and A. Ya. Apin, Dokl. Phys. Chem.
Vyazankin, Dokl. Akad. Nauk. SSSR 204, 356 –358 共1972兲. 208, 35–37 共1973兲.
72/32 A. Finch, P. J. Gardner, and A. F. Webb, J. Chem. Thermodyn. 4, 73/26 R. C. Wilhoit and B. J. Zwolinski, J. Phys. Chem. Ref. Data
495– 498 共1972兲. 共Suppl. 1兲 2, 1-1–1-420 共1973兲. 关Note: The authors report Antoine
72/33 R. Sabbah, R. Chastel, and M. Laffitte, Thermochimica Acta 5, constants for numerous alcohols that were calculated from vapor pressure
117–127 共1972兲. data taken from the published literature. For several of the alcohols, the
72/34 L. A. Nisel’son, T. D. Sokolova, and R. K. Nikolaev, Vestn. Mosk. authors had only a very limited number of experimental data points that
Univ. Khim. 13, 432– 434 共1972兲; Chem. Abstracts 78, 8069k 共1973兲. were pooled from several sources.兴
72/35 M. Nishimura, M. Hakayama, and T. Yano, J. Chem. Eng. Jpn. 5, 73/27 W. Waradzin and P. Skubla, Chem. Prum. 23, 556 –557 共1973兲;
223–226 共1972兲; Chem. Abstracts 78, 48659j 共1973兲. Chem. Abstracts 80, 112780n 共1974兲.
72/36 G. K. Johnson, P. A. G. O’Hare, and E. H. Appelman, Inorg. 73/28 P. D. Dawson, Jr., I. M. Silberberg, and J. J. McKetta, J. Chem.
Chem. 11, 800– 802 共1972兲. Eng. Data 18, 7–15 共1973兲.
72/37 V. A. Granzhan and E. A. Salganikov, Tr. Nauch.-Issled. Proekt. 73/29 D. V. S. Jain and O. P. Yadav, Indian J. Chem. 11, 28 –30 共1973兲.
Inst. Azotn. Prom. Prod. Org. Sin. 85– 87 共1972兲; Chem. Abstracts 79, 73/30 H.-D. Beckhaus and C. Rüchardt, Tetrahedron Lett. 1971–1974
118908m 共1973兲. 共1973兲.
72/38 K. Nakanishi and O. Toyama, Bull. Chem. Soc. Jpn. 45, 3210– 73/31 G. M. Kol’yakova, I. B. Rabinovich, and E. N. Zorina, Dokl.
3211 共1972兲. Akad. Nauk. SSSR 209, 616 – 617 共1973兲.
72/39 D. E. J. Arnold, E. A. V. Ebsworth, H. F. Jessep, and D. W. H. 73/32 V. I. Tel’noi, I. B. Rabinovich, and V. A. Umilin, Dokl. Akad.
Rankin, J. Chem. Soc., Dalton Trans. 1681–1687 共1972兲. Nauk. SSSR 209, 127–129 共1973兲.
72/40 R. A. De Marco and J. M. Shreve, J. Fluorine Chem. 1, 269–276 73/33 D. S. Barnes and C. T. Mortimer, J. Chem. Thermodyn. 5,
共1972兲. 371–377 共1973兲.
72/41 J. Laynez and I. Wadso, Acta Chem. Scand. 26, 3148 –3152 73/34 B. J. Aylett, I. A. Ellis, and C. J. Porritt, J. Chem. Soc., Dalton
共1972兲. Trans. 83– 87 共1973兲.
72/42 M. Mansson, Acta Chem. Scand. 26, 1707–1708 共1972兲. 73/35 B. J. Aylett, I. A. Ellis, and J. R. Richmond, J. Chem. Soc., Dalton
72/43 F. E. Rogers, J. Phys. Chem. 75, 1734 –1737 共1971兲. Trans. 981–987 共1973兲.
1973 73/36 A. Blair and H. Ihle, J. Inorg. Nucl. Chem. 35, 3795–3803 共1973兲.
73/1 H. K. Hall, Jr., C. D. Smith, and J. H. Bald, J. Am. Chem. Soc. 95, 73/37 P. A. Bernstein and D. D. Desmarteau, J. Fluorine Chem. 2,
3197–3201 共1973兲. 315–321 共1973兲.
73/2 J. W. Wilson and J. T. F. Fenurck, J. Chem. Thermodyn. 5, 341–345 73/38 T. Abe and J. M. Shreeve, J. Fluorine Chem. 3, 17–26 共1973/
共1973兲. 1974兲.
75/26 A. Hoepfner, N. Parekh, Ch. Hoerner, and A. Abdel-Hamid, Ber. 76/16 G. K. Borisov and S. G. Chugunova, Russ. J. Phys. Chem. 50,
Bunsenges Phys. Chem. 79, 216 –222 共1975兲. 1791 共1976兲.
75/27 D. Ambrose, J. W. Ellender, C. H. S. Sprake, and R. I. Townsend, 76/17 G. O. Shmyreva, V. G. Shlyakova, R. M. Golosova, A. B.
J. Chem. Soc., Faraday Trans. 71, 35– 41 共1975兲. Petrunin, D. B. Bekker, and A. F. Zhigach, Russ. J. Phys. Chem. 50, 478
75/28 Kh. I. Geidarov, O. I. Dzhafarov, and K. A. Karasharli, Russ. J. 共1976兲.
Phys. Chem. 49, 197–198 共1975兲. 76/18 C. A. Burton and J. M. Shreeve, J. Am. Chem. Soc. 98, 6545–
75/29 V. B. Sokolov, M. Kh. Karapet’yants, T. N. Sergeeva, S. P. 6547 共1976兲.
Kolesnikov, and B. L. Perl’mutter, Izv. Vyssh. Uchebn. Zaved., Khim. 76/19 K. Steele, B. E. Poling, and D. B. Manley, J. Chem. Eng. Data 21,
Khim. Teknol. 18, 1319–1321 共1975兲; Chem. Abstracts 84, 22433e 399– 403 共1976兲.
共1976兲. 76/20 M. M. Brazhnikov, A. D. Peshchenko, and O. V. Ral’ko, Zh. Prikl.
75/30 V. B. Sokolov, M. Kh. Karapet’yants, T. N. Sergeeva, S. P. Khim. 共Leningrad兲 49, 1041–1044 共1976兲.
Kolesnikov, and B. L. Perl’mutter, Izv. Vyssh. Uchebn. Zaved., Khim. 76/21 V. P. Kuznetsova, E. A. Miroshnichenko, A. N. Zelenetskii, G. V.
Khim. Teknol. 18, 1234 –1237 共1975兲; Chem. Abstracts 84, 9167b Rakova, Yu. A. Lebedev, and N. S. Enikolopyan, Dokl. Phys. Chem. 226,
共1976兲. 147–150 共1976兲.
75/31 Z. A. Guseinov, K. A. Karasharli, O. I. Dzharfarov, G. G. 76/22 E. G. Kiparisova, L. Ya. Tsvetkova, and B. V. Lebedev, Russ. J.
Nurullaev, N. S. Nametkin, L. E. Gusel’nikov, F. A. Volinina, E. N. Phys. Chem. 50, 638 共1976兲.
Burdasov, and V. N. Vdovin, Dokl. Akad. Nauk 共SSSR兲 222, 1369–1372 76/23 D. L. S. Brown, J. A. Connor, M. L. Leung, M. I. Paz-Andrade,
共1975兲. and H. A. Skinner, J. Organomet. Chem. 110, 79– 89 共1976兲.
75/32 Ch. Hoerner, A. Hoepfner, and B. Schmeiser, Ber. Bunsenges Phys. 76/24 V. E. Ditsent, I. I. Skorokhodov, N. A. Terent’eva, M. N.
Chem. 79, 222–225 共1975兲. Zolotareva, Z. V. Belyakova, and Z. V. Belikova, Zh. Fiz. Khim. 50,
75/33 F. Rivenq, Bull. Soc. Chim. France 共Pt. 1兲 2433–2434 共1975兲. 1905–1906 共1976兲; Chem. Abstracts 85, 166806x 共1976兲.
75/34 G. P. Bragin and M. Kh. Karapet’yants, Tr. Khim. Khim. Tekhnol. 76/25 Z. A. Guseimov, A. A. Kuliev, K. A. Karasharli, and O. I.
78 –79 共1975兲; Chem. Abstracts 85, 83381d 共1976兲. Dzhafarov, Azerb. Khim. Zh. 72–74 共1975兲; Chem. Abstracts 84, 65359c
75/35 K. W. Chun, J. C. Drummond, W. H. Smith, and R. R. Davison, J. 共1976兲.
Chem. Eng. Data 20, 58 – 61 共1975兲. 76/26 D. Ambrose and C. H. S. Sprake, J. Chem. Thermodyn. 8,
75/36 M. E. Anthoney, A. S. Carson, and P. G. Laye, 4th Conference 601– 602 共1976兲.
International Thermodynamics Chim., 关C.R.兴, Vol. 1, pp. 99–103; Chem. 76/27 W. S. Hamilton, P. Thompson, and S. Pustejovsky, J. Chem. Eng.
Abstracts 84, 163961n 共1976兲. Data 21, 428 – 429 共1976兲.
75/37 J. F. Masi and R. B. Scott, J. Res. National Bureau Stand., Sect. A 76/28 E. R. Falardeau and D. D. Desmarteau, J. Fluorine Chem. 7,
79A, 619– 628 共1975兲. 185–195 共1976兲.
75/38 D. E. J. Arnold and D. W. H. Rankin, J. Chem. Soc., Dalton Trans.
76/29 I. Stahl, R. Mews, and O. Glemser, J. Fluorine Chem. 7, 55– 64
889– 894 共1975兲. 共1976兲.
75/39 R. Vilcu, S. Perisanu, and I. Ciocazanu, 4th Conference
76/30 E. R. Falardeau and D. D. Desmarteau, J. Fluorine Chem. 7,
International Thermodynamics, Chim. 关C.R.兴 Vol. 1, pp. 105–112. 409– 414 共1976兲.
75/40 M. Gambaruto, J. E. Sicre, and H. J. Schumacher, J. Fluorine
76/31 M. J. Hopkinson and D. D. Desmarteau, J. Fluorine Chem. 7,
Chem. 5, 175–179 共1975兲. 501–510 共1976兲.
75/41 R. A. De Marco, T. A. Kovacina, and W. B. Fox, J. Fluorine
1977
Chem. 6, 93–104 共1975兲.
77/1 M. Mansson, P. Sellers, G. Stridh, and S. Sunner, J. Chem.
75/42 K. E. Peterman and J. M. Shreeve, J. Fluorine Chem. 6, 83–92
Thermodyn. 9, 91–97 共1976兲.
共1975兲.
77/2 P. Sellers, J. Chem. Thermodyn. 9, 139–142 共1977兲.
75/43 R. A. De Marco, T. A. Kovacina, and W. B. Fox, J. Fluorine
Chem. 5, 221–230 共1975兲. 77/3 A. S. Carson, P. G. Laye, and M. Yurkeli, J. Chem. Thermodyn. 9,
827– 829 共1977兲.
1976
76/1 G. Stridh, J. Chem. Thermodyn. 8, 193–194 共1976兲. 77/4 W. V. Steele and I. Watt, J. Chem. Thermodyn. 9, 843– 849 共1977兲.
76/2 D. Ambrose, J. H. Ellender, C. H. S. Sprake, and R. Townsend, J. 77/5 G. Stridh, S. Sunner, and Ch. Svenson, J. Chem. Thermodyn. 9,
Chem. Thermodyn. 8, 165–178 共1976兲. 1005–1010 共1977兲.
76/3 P. S. Engel, R. A. Melaugh, M. Mansson, J. W. Timberlake, A. W. 77/6 P. A. Pella, J. Chem. Thermodyn. 9, 301–305 共1977兲.
Garner, and F. D. Rossini, J. Chem. Thermodyn. 8, 607– 621 共1976兲. 77/7 L. A. Peacock and R. Fuchs, J. Am. Chem. Soc. 99, 5524 –5525
76/4 R. A. Melaugh, M. Mansson, and F. D. Rossini, J. Chem. 共1977兲.
Thermodyn. 8, 623– 626 共1976兲. 77/8 V. Svoboda, V. Majer, F. Vesely, and J. Pick, Collect. Czech. Chem.
76/5 G. Stridh, J. Chem. Thermodyn. 8, 895– 899 共1976兲. Commun. 42, 1755–1760 共1977兲.
76/6 G. Stridh, J. Chem. Thermodyn. 8, 901–906 共1976兲. 77/9 N. I. Boldenkov and Yu. Ya Maksimov, Zh. Fiz. Khim. 51, 1502–
76/7 V. P. Kolesov, G. M. Slavutskaya, and L. N. Dityat’eva, J. Chem. 1504 共1977兲.
Thermodyn. 8, 907–914 共1976兲. 77/10 E. F. Meyer and T. H. Gens, J. Chem. Eng. Data 22, 30–31
76/8 J. E. Connett, J. F. Counsell, and D. A. Lee, J. Chem. Thermodyn. 共1977兲.
8, 1199–1203 共1976兲. 77/11 H. K. Cammenga, F. W. Schulze, and W. Theuerl, J. Chem. Eng.
76/9 M. E. Anthoney, A. S. Carson, and P. G. Laye, J. Chem. Soc., Data 22, 131–134 共1977兲.
Perkin Trans. 2 1032–1036 共1976兲. 77/12 V. Svoboda, F. Vesely, R. Holub, and J. Pick, Collect. Czech.
76/10 E. F. Meyer and C. A. Hotz, J. Chem. Eng. Data 21, 274 –279 Chem. Commun. 42, 943–951 共1977兲.
共1976兲. 77/13 R. M. Varushchenko, M. M. Ammar, and L. L. Bulgakova, Russ. J.
76/11 S. J. Ascroft, J. Chem. Eng. Data 21, 397–398 共1976兲. Phys. Chem. 51, 167–168 共1977兲.
76/12 K. V. Rao and C. Chiranjivi, J. Chem. Eng. Data 21, 393–394 77/14 V. V. Pisarev, A. M. Rozhnov, and A. G. Sarkisov, Russ. J. Phys.
共1976兲. Chem. 51, 323–324 共1977兲.
76/13 H. C. Hon, R. P. Singh, and A. P. Kudchadker, J. Chem. Eng. Data 77/15 T. Kitazume and J. M. Shreeve, J. Am. Chem. Soc. 99, 3690–3695
21, 430– 431 共1976兲. 共1977兲.
76/14 J. Cihlar, V. Hynek, V. Svoboda, and R. Holub, Collect. Czech. 77/16 T. Kitazume and J. M. Shreeve, J. Am. Chem. Soc. 99, 4194 – 4196
Chem. Commun. 41, 1– 6 共1976兲. 共1977兲.
76/15 M. M. Ammar, L. L. Bulgakova, and R. M. Varushchenko, Russ. J. 77/17 C. A. Burton and J. M. Shreeve, Inorg. Chem. 16, 1039–1042
Phys. Chem. 50, 1466 –1467 共1976兲. 共1977兲.
77/18 C. A. Burton and J. M. Shreeve, Inorg. Chem. 16, 1408 –1411 78/17 B. V. Lebedev, L. Ya. Tsvetkova, I. B. Rabinovich, E. Sh.
共1977兲. Finkel’shtein, and B. S. Strel’chick, Termodin. Org. Soedin. 7, 3–7
77/19 T. Kitazume and J. M. Shreeve, Inorg. Chem. 16, 1818 –1819 共1978兲; Chem. Abstracts 92, 83507u 共1980兲.
共1977兲. 78/18 M. A. V. Ribeiro da Silva and R. G. Irving, Rev. Port. Quim. 20,
77/20 R. M. Varushchenko, M. M. Ammar, and L. L. Bulgakova, Zh. Fiz. 36 – 46 共1978兲; Chem. Abstracts 90, 211054s 共1979兲.
Khim. 51, 278 –279 共1977兲. 78/19 V. P. Kolesov and L. N. Dityat’eva, Termodin. Org. Soedin. 7,
77/21 E. Z. Zhuravlev, T. L. Melent’eva, P. V. Mulyanov, A. I. 44 – 47 共1978兲; Chem. Abstracts 92, 75657c 共1980兲.
Kormushechkina, T. M. Bogdanova, and I. I. Konstantinov, Zh. Prikl 78/20 S. D. Cave, A. Chainese, and A. Prantera, J. Chem. Eng. Data 23,
Khim. 共Leningrad兲 50, 2032–2035 共1977兲. 279–281 共1978兲.
77/22 H. L. Finke, J. F. Messerly, S. H. Lee, A. G. Osborn, and D. R. 78/21 S. Sundaram and D. S. Viswanath, J. Chem. Eng. Data 23, 63– 64
Douslin, J. Chem. Thermodyn. 9, 937–956 共1977兲. 共1978兲.
77/23 J. B. Pedley and J. Rylance, N. P. L. Computer Analyzed 78/22 I. Stahl, R. Mews, and O. Glemser, J. Fluorine Chem. 11, 455– 465
Thermochemical Data: Organic and Organometallic Compounds 共School 共1978兲.
of Molecular Sciences, University of Sussex Press, Brighton, UK, 1977兲. 78/23 R. A. De Marco and W. B. Fox, J. Fluorine Chem. 12, 137–151
77/24 B. C. Kim and D. H. Kim, Hwahak Kwa Hwahak Kongop 20, 共1978兲.
232–234 共1977兲; Chem. Abstracts 88, 95565s 共1978兲. 1979
77/25 N. D. Lebedeva, V. L. Ryadnenko, N. N. Kiseleva, and L. F. 79/1 S. Sunner, Ch. Svensson, and A. S. Zelepuga, J. Chem. Thermodyn.
Nazarova, Vses. Konf. Kalorim. 关Rasshir. Tezisy Dokl.兴 7th 1, 91–95 11, 491– 495 共1979兲.
共1977兲; Chem. Abstracts 92, 75617q 共1980兲. 79/2 S. Sunner and Ch. Svensson, J. Chem. Soc., Faraday Trans. 1 75,
77/26 M. V. Lyubarskii and R. I. Smolyanets, Vses. Konf. Kalorim. 2359–2365 共1979兲.
关Rasshir. Tezisy Dokl.兴 7th 1, 119–121 共1977兲; Chem. Abstracts 92, 79/3 T. M. Letcher, S. W. Orchard, and M. Albers, J. Chem. Thermodyn.
75619s 共1980兲. 11, 173–175 共1979兲.
77/27 V. A. Aleshina, M. P. Kozina, and G. L. Gal’chenko, Vses. Konf. 79/4 C. G. De Kruif and H. A. Oonk, J. Chem. Thermodyn. 11, 287–290
Kalorim. 关Rasshir. Tezisy Dokl.兴 7th 1, 85–91 共1977兲; Chem. Abstracts 共1979兲.
92, 94582r 共1980兲. 79/5 S. H. Lee-Bechtold, I. A. Hossenlop, D. W. Scott, A. G. Osborn,
77/28 L. N. Dityat’eva and V. P. Kolesov, Vses. Konf. Kalorim. 关Rasshir. and W. D. J. Good, Chem. Thermodyn. 11, 469– 482 共1979兲.
Tezisy Dokl.兴 7th 1, 95–97 共1977兲; Chem. Abstracts 92, 58009a 共1980兲. 79/6 Ch. Sevensson, J. Chem. Thermodyn. 11, 593–596 共1979兲.
77/29 T. F. Vasil’eva and V. I. Kotov, Vses. Konf. Kalorim. 关Rasshir. 79/7 P. P. S. Saluja, L. A. Peacock, and R. Fuchs, J. Am. Chem. Soc.
Tezisy Dokl.兴 7th 1, 102–106 共1977兲; Chem. Abstracts 92, 58010u 101, 1958 –1962 共1979兲.
共1980兲. 79/8 L. Petros, V. Majer, J. Koubek, V. Svoboda, and J. Pick, Collect.
77/30 J. J. Rao and D. S. Viuswanath, J. Chem. Eng. Data 22, 36 –38 Czech. Chem. Commun. 44, 3533–3540 共1979兲.
共1977兲. 79/9 V. Majer, V. Svoboda, J. Koubek, and J. Pick, Collect. Czech.
77/31 T. R. Das, C. O. Reed, Jr., and P. T. Eubank, J. Chem. Eng. Data Chem. Commun. 44, 3521–3528 共1979兲.
22, 3–9 共1977兲. 79/10 M. Balish and V. Fried, J. Chem. Eng. Data 24, 91–92 共1979兲.
77/32 T. R. Das, C. O. Reed, Jr., and P. T. Eubank, J. Chem. Eng. Data 79/11 A. B. Macknick and J. M. Prausnitz, J. Chem. Eng. Data 24,
22, 9–15 共1977兲. 175–178 共1979兲.
77/33 T. R. Das, C. O. Reed, Jr., and P. T. Eubank, J. Chem. Eng. Data 79/12 A. P. Kudchadker, S. A. Kudchadker, R. P. Shukla, and P. R.
22, 16 –21 共1977兲. Patnaik, J. Phys. Chem. Ref. Data 8, 499–513 共1979兲.
77/34 N. Novakova and J. Novak, J. Chromatogr. 135, 13–24 共1977兲. 79/13 V. Majer, V. Svoboda, S. Hala, and J. Pick, Collect. Czech. Chem.
1978 Commun. 44, 637– 651 共1979兲.
78/1 W. V. Steele, J. Chem. Thermodyn. 10, 919–927 共1978兲. 79/14 G. Berthon, V. Angot, V. Beden, and O. Enea, J. Chem.
78/2 R. B. Cundall, T. F. Palmer, and C. E. C. Wood, J. Chem. Soc., Thermodyn. 11, 539–546 共1979兲.
Faraday Trans. 1 74, 1339–1345 共1978兲. 79/15 V. S. Markovnik, A. I. Sachek, A. D. Peshchenko, O. V. Shvaro, D.
78/3 P. S. Engel, R. L. Mongomery, M. Mansson, R. A. Leckonby, H. L. N. Andreevskii, and N. M. Olizarevich, Termodin. Org. Soedin. 107–110
Foyt, and F. D. Rossini, J. Chem. Thermodyn. 10, 205–211 共1978兲. 共1979兲.
78/4 D. G. McCormick and W. S. Hamilton, J. Chem. Thermodyn. 10, 79/16 L. H. Thomas, R. Meatyard, H. Smith, and G. H. Davies, J. Chem.
275–278 共1978兲. Eng. Data 24, 159–161 共1979兲.
78/5 B. V. Lebedev, L. Ya. Tsvetkova, and I. B. Rabinovich, J. Chem. 79/17 R. Fuchs and L. A. Peacock, Can. J. Chem. 57, 2302–2304 共1979兲.
Thermodyn. 10, 809– 815 共1978兲. 79/18 S. I. Sukhova, O. N. Vlasov, and L. V. Li, Nov. Khim. Sredstva
78/6 D. Indritz, J. Stone, and F. Williams, J. Chem. Eng. Data 23, 6 –7 Azsch Rast. 51–52 共1979兲; Chem. Abstracts 92, 83359x 共1980兲.
共1978兲. 79/19 W. F. Spencer, T. D. Shoup, M. M. Cliath, W. J. Farmer, and R.
78/7 R. L. Montgomery, F. D. Rossini, and M. Mansson, J. Chem. Eng. Haque, J. Agric. Food Chem. 27, 273–278 共1979兲.
Data 23, 125–129 共1978兲. 79/20 I. K. Igumenov, Yu. V. Chumachenko, and S. V. Zemskov, Khim.
78/8 A. H. N. Mousa, J. Chem. Eng. Data 23, 133–134 共1978兲. Termodin. Termokhim. 65– 66 共1979兲; Chem. Abstracts 91, 217803c
78/9 W. S. Hamilton, S. Benton, J. French, D. McCormick, S. 共1979兲.
Pustejovsky, and P. Thomspon, J. Chem. Eng. Data 23, 201–203 共1978兲. 79/21 V. I. Bludilina, A. K. Baev, V. K. Matveev, I. L. Gaidym, and E. I.
78/10 I. K. Igumenov, Yu. V. Chumanchenko, and S. V. Zemskov, Russ. Shcherbina, Zh. Fiz. Khim. 53, 1052–1053 共1979兲; Chem. Abstracts 91,
J. Phys. Chem. 52, 1531–1532 共1978兲. 9585f 共1979兲.
78/11 Yu. V. Chumachenko, I. K. Igumenov, and S. V. Zemskov, Russ. J. 79/22 D. Das, S. R. Dhawadkar, and M. S. Chandraekharaiah,
Phys. Chem. 52, 1393–1394 共1978兲. Thermochimica Acta 30, 371–376 共1979兲.
78/12 G. O. Shmyreva, V. G. Shlyakova, and R. M. Golosova, Russ. J. 79/23 P. J. Maher and B. D. Smith, J. Chem. Eng. Data 24, 16 –22
Phys. Chem. 52, 135–136 共1978兲. 共1979兲.
78/13 T. D. Grabik, S. G. Konstantinov, G. P. Dudchik, and O. G. 79/24 M. Zander and W. Thomas, J. Chem. Eng. Data 24, 1–2 共1979兲.
Polyachenok, Russ. J. Phys. Chem. 52, 894 – 895 共1978兲. 79/25 R. M. Golosova, G. O. Shmyreva, V. G. Shlyakova, A. B.
78/14 T. Kitazume and J. M. Shreeve, Inorg. Chem. 17, 2173–2176 Petrunin, D. B. Bekker, and A. F. Zhigach, Zh. Fiz. Khim. 53, 766 –767
共1978兲. 共1979兲.
78/15 R. P. Corbally, M. J. Perkins, A. S. Carson, P. G. Laye, and W. V. 79/26 P. Shul’tse, R. M. Varushchenko, G. L. Gal’chenko, T. V. Klimova,
Steele, J. Chem. Soc., Chem. Commun. 778 –779 共1978兲. and V. I. Stanko, J. Gen. Chem. USSR 50, 1482–1488 共1979兲; Zh.
78/16 R. Fuch and L. A. Peacock, Can J. Chem. 56, 2493–2498 共1978兲. Obshch. Khim. 50, 1818 –1825 共1979兲.
79/27 J. Carre, P. Claudy, J. M. Letoffe, M. Kollmannsberger, and J. 81/8 I. A. Hossenlopp and D. W. Scott, J. Chem. Thermodyn. 13,
Bousquet, J. Fluorine Chem. 14, 139–152 共1979兲. 405– 414 共1981兲.
79/28 A. Sekiya and D. D. Desmarteau, J. Fluorine Chem. 14, 289–297 81/9 I. A. Hossenlopp and D. W. Scott, J. Chem. Thermodyn. 13,
共1979兲. 415– 421 共1981兲.
1980 81/10 I. A. Hossenlopp and D. W. Scott, J. Chem. Thermodyn. 13,
80/1 V. Majer, L. Svab, and V. Svoboda, J. Chem. Thermodyn. 12, 423– 428 共1981兲.
843– 847 共1980兲. 81/11 D. Ambrose, J. H. Ellender, H. A. Gundry, D. A. Lee, and R.
80/2 R. H. Davies, A. Finch, and P. G. Gardner, J. Chem. Thermodyn. Townsend, J. Chem. Thermodyn. 13, 795– 802 共1981兲.
12, 291–296 共1980兲. 81/12 M. Shimizu, Y. Saito, and K. Kusano, Preprints 17th Conference
80/3 V. Majer, Z. Wanger, V. Svoboda, and V. Cadek, J. Chem. on Chemical Thermodynic Thermal Analysis, Japan 1981, p. 50; as
Thermodyn. 12, 387–391 共1980兲. quoted in 关85/6兴.
80/4 M. H. Abraham and R. J. Irving, J. Chem. Thermodyn. 12, 539–544 81/13 V. Majer, V. Svoboda, A. Posta, and J. Pick, Collect. Czech. Chem.
共1980兲. Commun. 46, 817– 822 共1981兲.
80/5 R. Fuchs and L. A. Peacock, Can. J. Chem. 58, 2796 –2799 共1980兲. 81/14 V. Svoboda, V. Charvatova, V. Majer, and J. Pick, Collect. Czech.
80/6 C. Van de Rostyne and J. M. Prausnitz, J. Chem. Eng. Data 25, 1–3 Chem. Commun. 46, 2983–2988 共1981兲.
共1980兲. 81/15 T. Abe and J. M. Shreeve, Inorg. Chem. 20, 2894 –2899 共1981兲.
80/7 M. Urbani, R. Gigli, and V. Picente, J. Chem. Eng. Data 25, 97–100 81/16 T. Abe and J. M. Shreeve, Inorg. Chem. 20, 2432–2434 共1981兲.
共1980兲. 81/17 D. Ambrose and D. J. Hall, J. Chem. Thermodyn. 13, 61– 66
80/8 E. F. Meyer, M. J. Awe, and R. E. Wagner, J. Chem. Eng. Data 25, 共1981兲.
371–374 共1980兲. 81/18 G. N. D’yakova, G. L. Korichev, A. D. Korkhova, T. F. Vasil’eva,
80/9 V. Mayer, V. Svoboda, A. Posta, and J. Pick, Collect. Czech. Chem. and I. A. Vasil’ev, Zh. Prikl. Khim. 共Leningrad兲 54, 1644 –1646 共1981兲.
Commun. 45, 3063–3069 共1980兲. 81/19 J. S. Chickos, A. S. Hyman, L. H. Ladon, and J. F. Liebman, J.
80/10 T. Abe and J. M. Shreeve, Inorg. Chem. 19, 3063–3067 共1980兲. Org. Chem. 46, 4294 – 4296 共1981兲.
80/11 A. G. Osborn and D. W. Scott, J. Chem. Thermodyn. 12, 429– 438 81/20 S. N. Guseinova, V. V. Kas’yanov, and Yu. V. Politanskii, Khim.
共1980兲. Prom-st. Ser., Khlornaya Prom-st. 28 –30 共1981兲; Chem. Abstracts 95,
80/12 N. K. Smith, R. C. Stewart, Jr., A. G. Osborn, and D. W. Scott, J. 225804b 共1981兲.
Chem. Thermodyn. 12, 919–926 共1980兲. 81/21 G. M. Wilson, R. H. Johnston, S.-C. Hwang, and C. Tsonopoulos,
80/13 V. Svoboda, V. Uchtyilova, V. Majer, and J. Pick, Collect. Czech. Ind. Eng. Chem., Process Des. Dev. 20, 94 –104 共1981兲.
Chem. Commun. 45, 3233–3240 共1980兲. 81/22 D. Ferro, V. Piacente, and M. Pelino, Rev. Roum. Chim. 26, 9–15
共1981兲.
80/14 J. A. Jonsson, L. Mathiasson, and A.-M. Olsson, Acta Chem.
81/23 R. M. Varushchenko, L. L. Bulgakova, P. S. Minzabekyants, and
Scand. 34A, 147–150 共1980兲.
K. N. Makarov, Russ. J. Phys. Chem. 55, 1480–1482 共1981兲.
80/15 L. H. Thomas, H. Smith, and G. H. Davis, J. Chem. Tech.
81/24 V. E. Ditsent, I. I. Skorokhodov, M. N. Zolotareva, V. I. Savuskina,
Biotechnol. 30, 476 – 480 共1980兲.
and B. N. Tabenko, Zh. Prikl. Khim. 共Leningrad兲 54, 1617–1619 共1981兲.
80/16 H.-D. Beckhaus, G. Kratt, K. Lay, J. Greiselmann, C. Rüchardt, B.
1982
Kitschke, and H. J. Lindner, Chem. Ber. 113, 3441–3455 共1980兲.
82/1 B. T. Grayson and L. A. Fosbraey, Pestic. Sci. 13, 269–278 共1982兲.
80/17 P. Nasir, S. C. Hwang, and R. Kobayashi, J. Chem. Eng. Data 25,
82/2 F. L. Rook, J. Chem. Eng. Data 27, 72–73 共1982兲.
298 –301 共1980兲.
82/3 C. Castellari, R. Francesconi, and F. Comelli, J. Chem. Eng. Data
80/18 R. Francesconi, C. Castellari, A. Arcelli, and F. Comelli, Can. J.
27, 156 –158 共1982兲.
Chem. Eng. 58, 113–115 共1980兲.
82/4 G. C. De Kruif, R. C. F. Schaake, J. C. Van Meltenburg, K. Van der
80/19 J. A. Roth and M. Orchin, J. Organometal. Chem. 187, 103–105
Klauw, and J. G. Blok, J. Chem. Thermodyn. 14, 791–798 共1982兲.
共1980兲.
82/5 R. Fuchs, J. H. Hallman, and M. O. Perlman, Can. J. Chem. 60,
80/20 N. D. Lebedeva, L. F. Nazarov, and Yu. A. Katin, Zh. Prikl. Khim. 1832–1835 共1982兲.
共Leningrad兲 53, 1394 –1395 共1980兲. 82/6 R. Fuchs, L. A. Peacock, and W. K. Stephenson, Can. J. Chem. 60,
80/21 A. Aihara, Denki Tsushin. Daigaku Gakuho 31, 65– 68 共1980兲; 1953–1958 共1982兲.
Chem. Abstracts 94, 174045z 共1981兲. 82/7 B. Gutsche and H. Knapp, Fluid Phase Equilib. 8, 285–300 共1982兲.
80/22 W. Gombler and H.-U. Weiler, J. Fluorine Chem. 15, 279–288 82/8 G. S. Hong, R. Wakslak, H. Finston, and V. Fried, J. Chem. Eng.
共1980兲. Data 27, 146 –148 共1982兲.
80/23 C. R. Patrick and F. Tomes, J. Fluorine Chem. 15, 267–278 82/9 K. Bystrom and M. J. Mansson, J. Chem. Soc., Perkin Trans. II
共1980兲. 565–569 共1982兲.
80/24 V. S. Pityugin, T. L. Kislitsyna, R. F. Shakirov, L. N. 82/10 V. Svoboda, V. Charvatova, V. Majer, and V. Hynek, Collect.
Sharif’yanova, and E. N. Maslennikov, Khim. Prom-st., Ser.: Khlornaya Czech. Chem. Commun. 47, 543–549 共1982兲.
Prom-st. 11–14 共1980兲. 82/11 C. Invernizzi, Termotecnica 4, 78 – 85 共1982兲.
80/25 L. N. Sharif’yanova, F. M. Sadykova, and S. G. Akhmerova, 82/12 R. M. Varushchenko, S. S. Puchkov, and A. I. Druzinina, Zh. Fiz.
Khim. Prom-st., Ser.: Khlornaya Prom-st. 16 –18 共1980兲. Khim. 56, 2934 –2937 共1982兲.
1981 82/13 A. I. Sachek, A. D. Peshenenko, V. S. Markovnik, O. V. Ral’ko, D.
81/1 S. A. Wieczorek and P. Kobayashi, J. Chem. Eng. Data 26, 8 –11, N. Andreevskii, and A. A. Leont’eva, Termodin. Org. Soedin. 94 –98
共1981兲; 26, 11–13 共1981兲. 共1982兲.
81/2 D. R. Edwards and J. M. Prausnitz, J. Chem. Eng. Data 26, 82/14 P. Reche and M.-F. Grenier-Loustalot, J. Chromatogr. 238,
121–124 共1981兲. 317–334 共1982兲.
81/3 K. G. De Kruif, J. M. Herman, and P. J. Van den Berg, J. Chem. 82/15 G. Pilcher and H. A. Skinner, in The Chemistry of the
Eng. Data 26, 359–362 共1981兲. Metal-Carbon Bond, edited by F. R. Hartley and S. Patai 共Wiley, New
81/4 V. Tekac, V. Majer, V. Svoboda, and V. Hynek, J. Chem. York, 1982兲, Chap. 2.
Thermodyn. 13, 659– 662 共1981兲. 82/16 B. E. Gammon, J. E. Callanan, I. A. Hossenlopp, A. G. Osborn,
81/5 T. S. Papina, P. A. Erastov, and V. P. Kolevsov, J. Chem. and W. D. Good, Proc. Symp. Thermophys. Prop. 8, 402– 408 共1982兲.
Thermodyn. 13, 683– 689 共1981兲. 82/17 D. J. Wren and A. C. Vikis, J. Chem. Thermodyn. 14, 435– 437
81/6 C. G. De Kruif, T. Kuipers, J. C. van Miltenburg, R. C. F. Schaake, 共1982兲.
and G. Stevens, J. Chem. Thermodyn. 13, 1081–1086 共1981兲. 82/18 J. Furukawa, M. Sakiyama, S. Seki, Y. Saito, and K. Kusano, Bull.
81/7 K. Bystrom, J. Chem. Thermodyn. 13, 139–145 共1981兲. Chem. Soc. Jpn. 55, 3329–3330 共1982兲.
82/19 R. A. De Marco and W. B. Fox, J. Org. Chem. 47, 3772–3773 84/15 M.-A. Michou-Saucet, J. Jose, C. Michou-Saucet, and J. C. Merlin,
共1982兲. Thermochimica Acta 75, 85–106 共1984兲.
1983 84/16 A. H. N. Mousa, J. Fluorine Chem. 25, 165–168 共1984兲.
83/1 J. E. House, Jr., Thermochimica Acta 71, 215–218 共1983兲. 84/17 M. P. Kozina, L. P. Timofeeva, G. L. Gal’chenko, E. S. Balenkova,
83/2 V. Machat, thesis, Utzcht, Prague, 1983. and M. D. Ordubadi, Vestn. Mosk. Univ., Ser. 2: Khim. 25, 364 –368
83/3 V. Uchytilova, V. Majer, V. Svoboda, and V. Hynek, J. Chem. 共1984兲; Chem. Abstracts 101, 190955q 共1984兲.
Thermodyn. 15, 853– 858 共1983兲. 84/18 A. E. Shcherbina, L. M. Kaporovskii, and E. A. Shcherbina, Zh.
83/4 A. Sivaraman and R. Kobayashi, J. Chem. Thermodyn. 15, 1127– Prikl. Khim. 共Leningrad兲 57, 1910–1912 共1984兲; Chem. Abstracts 101,
1135 共1983兲. 177895a 共1984兲.
83/5 X.-W. An and M. Mansson, J. Chem. Thermodyn. 15, 287–293 84/19 C. Castellari, R. Francesconi, and F. Comelli, J. Chem. Eng. Data
共1983兲. 29, 90–93 共1984兲.
83/6 R. Fuchs and J. H. Hallman, Can. J. Chem. 61, 503–505 共1983兲. 84/20 C. Castellari, R. Francesconi, and F. Comelli, J. Chem. Eng. Data
83/7 J. H. Hallman, W. K. Stepenson, and R. Fuchs, Can. J. Chem. 61, 29, 126 –128 共1984兲.
20-44 –2047 共1983兲. 84/21 S. Putcha, R. V. Ivanturi, and R. Machiraju, J. Chem. Eng. Data
83/8 C. Tsonopoulos and G. M. W. Wilson, AIChE J. 29, 990–999 29, 135–136 共1984兲.
共1983兲. 84/22 S. R. Bosco and A. G. Turner, J. Chem. Eng. Data 29, 242–243
83/9 D. Ferro, V. Piacente, and P. Scardala, Thermochimica Acta 68, 共1984兲.
329–339 共1983兲. 84/23 C. Castellari, R. Francesconi, F. Comelli, and S. Ottani, J. Chem.
83/10 A.-M. Olsson, J. A. Jonsson, B. Thelin, and T. Liljefors, J. Chem. Eng. Data 29, 283–284 共1984兲.
Ecol. 9, 375–385 共1983兲. 84/24 H. Katayama and Y. Harada, J. Chem. Eng. Data 29, 373–375
83/11 Yu. Ya. Van-Chin-Syan, N. S. Kachurina, G. A. Petrovskaya, and S. 共1984兲.
K. Chuchmarev, Russ. J. Phys. Chem. 57, 1751–1752 共1983兲. 84/25 A. Sivaraman and R. Kobayashi, J. Chem. Eng. Data 29, 375–379
83/12 G. Natarajan and D. S. Viswanath, Rev. Sci. Instrum. 54, 1175– 共1984兲.
1179 共1983兲. 84/26 I. Cervenkova and T. Boublik, J. Chem. Eng. Data 29, 425– 427
83/13 A. Tamir, C. Dragoescu, A. Apelblat, and J. Wisniak, Fluid Phase 共1984兲.
Equilib. 10, 9– 42 共1983兲. 84/27 J. T. Sipowska and S. A. Wieczorek, J. Chem. Thermodyn. 16,
83/14 T. Schmeling and R. Strey, Ber. Bunsenges. Phys. Chem. 87, 693– 699 共1984兲.
871– 874 共1983兲. 84/28 N. D. Lebedeva, N. M. Gutner, Yu. A. Katin, N. M. Kozlova, N.
83/15 J. E. House, Jr., J. Fluorine Chem. 22, 299–303 共1983兲. N. Kiseleva, E. F. Makhina, and S. L. Dobychin, J. Appl. Chem. 共USSR兲
83/16 R. M. Clay, S. Corr, G. Keenan, and W. V. Steele, J. Am. Chem. 57, 2118 –2122 共1984兲.
Soc. 105, 2070–2071 共1983兲. 84/29 P. T. Eubank, L. E. Cediel, J. C. Holste, and K. R. Hall, J. Chem.
83/17 A. Sivaraman, R. J. Martin, and R. Kobayashi, Fluid Phase Eng. Data 29, 389–393 共1984兲.
Equilib. 12, 175–188 共1983兲. 84/30 R. Eng and S. I. Sandler, J. Chem. Eng. Data 29, 156 –161 共1984兲.
1984
84/31 D. M. Hull and B. C.-Y. Lu, J. Chem. Eng. Data 29, 417– 419
84/1 E. Surova, Chem. Zvesti 38, 83–99 共1984兲. 共1984兲.
84/2 V. Majer, V. Uchytilova, V. Svoboda, and A. Posta, J. Chem. 84/32 A. K. Baev, A. A. Barkatin, and L. M. Dyagileva, Vestsi Akad.
Thermodyn. 16, 761–766 共1984兲. Navuk BSSR, Ser. Khim. 60– 62 共1984兲.
84/3 S. C. Mraw and C. F. Keweshan, J. Chem. Thermodyn. 16,
84/33 A. K. Baev, V. E. Mikhailov, and A. A. Baev, Vestsi Akad. Navuk
873– 883 共1984兲.
BSSR, Ser. Khim. Navuk 75–77 共1984兲.
84/4 V. Majer, V. Svoboda, and M. Lencka, J. Chem. Thermodyn. 16,
84/34 A. E. Sokolovskii and A. K. Baev, Vestsi Akad. Navuk BSSR, Ser.
1019–1024 共1984兲.
Khim. Navuk 115–117 共1984兲.
84/5 V. Majer, V. Svoboda, and V. Hynek, J. Chem. Thermodyn. 16,
1059–1066 共1984兲. 1985
84/6 P. Starzewski, I. Wadso, and W. Zielenkiewicz, J. Chem. 85/1 V. Majer, V. Svoboda, and M. Lencka, J. Chem. Thermodyn. 17,
365–370 共1985兲.
Thermodyn. 16, 331–334 共1984兲.
84/7 V. Uchytilova, V. Majer, V. Svoboda, and I. Hemer, J. Chem. 85/2 K. Kusano, Thermochimica Acta 88, 109–120 共1985兲.
Thermodyn. 16, 475– 479 共1984兲. 85/3 V. Majer, V. Svoboda, V. Uchytilova, and M. Finke, Fluid Phase
84/8 V. Majer, V. Svoboda, J. Pechacek, and S. Hala, J. Chem. Equilibr. 20, 111–118 共1985兲.
Thermodyn. 16, 567–572 共1984兲. 85/4 A. Raviprasad and K. V. Rao, J. Chem. Thermodyn. 17, 117–121
84/9 T. Boublik, V. Fried, and E. Hala, The Vapor Pressures of Pure 共1985兲.
Substances: Selected Values of the Temperature Dependence of the Vapor 85/5 S. A. Wieczorek and J. T. Sipowska, J. Chem. Thermodyn. 17,
Pressures of Some Pure Substances in the Normal and Low Pressure 255–261 共1985兲.
Region, 2nd revised edition 共Elsevier, Amsterdan, The Netherlands, 85/6 V. Majer and V. Svoboda, Enthalpies of Vaporization of Organic
1984兲. The vaporization enthalpies were calculated from the vapor Compounds: A Critical Review and Data Compilation 共Blackwell
pressures obtained from the Antoine constants reported in this Scientific, Oxford, U.K., 1985兲.
compendium. In cases where the Antoine constant C⫽0, the Antoine 85/7 G. Barone, G. Castronuovo, G. Della Gatta, V. Elia, and A. Iannone,
Equation (log10 P⫽A⫺B/(C⫹T)) reduces to the integrated form of the Fluid Phase Equilib. 21, 157–164 共1985兲.
Clausius Clapeyron equation directly. This was the case for many 85/8 A. E. Sokolovski and A. K. Baev, Vestsi Akad. G. Emii Navuk
vaporization enthalpies. In those cases where C⫽0, the vaporization BSSR, Ser. Khim. Navuk 112–114 共1985兲.
enthalpy was calculated as ⌬H V ⫽2.303RB 关 T/(T⫹C) 兴 2 . 85/9 A. G. R. Scholz and E. Brunner, J. Chem. Eng. Data 30, 72–74
84/10 A. I. Sachek, V. S. Markovnik, A. D. Peshchenko, A. V. Shvaro, 共1985兲.
and D. N. Andreevskii, Khim. Prom.-St. 共Moscow兲 337–340 共1984兲. 85/10 G. Natarajan and D. S. Viswanath, J. Chem. Eng. Data 30,
84/11 A. K. Baev and A. A. Barkatin, Russ. J. Phys. 58, 195–198 共1984兲. 137–140 共1985兲.
84/12 H.-D. Beckhaus, C. Rüchardt, and M. Smisek, Thermochimica 85/11 V. Piacente, P. Scardala, D. Ferro, and R. Gigli, J. Chem. Eng.
Acta 79, 149–159 共1984兲. Data 30, 372–376 共1985兲.
84/13 A. Sokolovskii and A. K. Baev, Russ. J. Phys. Chem. 58, 195–198 85/12 K. D. Reddy, M. V. P. Rao, and M. Ramakrishna, J. Chem. Eng.
共1984兲. Data 30, 394 –397 共1985兲.
84/14 G. G. Nurullaev, S. A. Mekhtiev, K. A. Karasharli, N. F. Musaeva, 85/13 V. A. Klyuchnikov, T. F. Danilova, M. G. Voronkov, and V. M.
and M. S. Salakhov, Azerb. Khim. Zh. 132–135 共1984兲. D’yakov, Dokl. Phys. Chem. 281, 373–377 共1985兲.
85/14 S. N. Kondrat’ev and B. V. Strizhov, Zh. Fiz. Khim. 59, 2933– 87/12 R. M. Varushchenko, O. L. Loseva, and A. I. Druzhinina, Zh. Fiz.
2938 共1985兲. Khim. 61, 638 – 642 共1987兲.
85/15 A. H. N. Mousa, J. Fluorine Chem. 30, 29–35 共1985兲. 87/13 H. Yan, J. Gu, X. An, and R.-H. Hu, Huaxue Xuebao 45, 1184 –
85/16 E. H. Appelman, M. H. Mendelsohn, and H. Kim. J. Am. Chem. 1187 共1987兲.
Soc. 107, 6515– 6518 共1985兲. 87/14 Yu. Ya. Van-Chin-Syan and N. S. Kachurina, Russ. J. Phys. Chem.
85/17 C. J. Wormald and T. K. Yerlett, J. Chem. Thermodyn. 17, 61, 622– 624 共1987兲.
1171–1186 共1985兲. 87/15 F. Garcia-Sanchez and A. Trejo, J. Chem. Thermodyn. 19,
1986 359–361 共1987兲.
86/1 E. F. Meyer and J. J. Meyer, J. Chem. Eng. Data 31, 273–274 87/16 T. Treszczanowicz and B. C.-Y. Lu, J. Chem. Thermodyn. 19,
共1986兲. 391–394 共1987兲.
86/2 B. Wisniewska, M. Lencka, and M. Rogalski, J. Chem. Thermodyn. 87/17 E. C. Azandegbe, Analusis 15, 370–373 共1987兲.
18, 703–708 共1986兲. 87/18 H. Al-Najjar and D. Al-Sammerrai, J. Chem. Tech. Biotechnol. 37,
86/3 P. J. Achorn, W. G. Haseltine, and J. K. Miller, J. Chem. Eng. Data 145–152 共1987兲.
31, 385–387 共1986兲. 87/19 O. An, R. Hu, H. Wang, M. Wu, and Y. Zou, Acta Physico-Chim.
86/4 O. L. Flaningan, J. Chem. Eng. Data 31, 266 –277 共1986兲. Sinica 3, 668 – 671 共1987兲.
86/5 R. M. Varushchenko, Zh. Fiz. Khim. 60, 291–294 共1986兲. 1988
86/6 N. Allemand, J. Jose, and J. C. Merlin, Thermochimica Acta 105, 88/1 V. I. Tel’noi, V. N. Larina, E. N. Karataev, and E. N. Deryagina, Zh.
79–90 共1986兲. Fiz. Khim. 62, 3108 –3109 共1988兲.
86/7 V. S. Tsvetkov, A. G. Nazmutdinov, K. G. Sharonov, and A. M. 88/2 H. Katayama, J. Chem. Eng. Data 33, 75–77 共1988兲.
Rozhnov, Termodin. Org. Soedin. 71–73 共1986兲. 88/3 C. F. Askonas and T. E. Daubert, J. Chem. Eng. Data 33, 225–229
86/8 Yu. G. Dmitriev, N. S. Kachurina, C. H. Wang, and V. V. 共1988兲.
Kouchukei, Vestn. L’vov. Politekh. Inst. 201, 29–30 共1986兲. 88/4 A. K. Baglay, L. L. Gurarly, and G. G. Kuleshov, J. Chem. Eng.
86/9 M.-A. Michou-Saucet, J. Jose, and C. Michou-Saucet, Data 33, 512–518 共1988兲.
Thermochimica Acta 102, 271–279 共1986兲. 88/5 D. Ambrose and N. B. Ghiassee, J. Chem. Thermodyn. 20, 765–766
86/10 V. Baliah and K. Gnanasekaran, Indian J. Chem. 25A, 673– 674 共1988兲.
共1986兲. 88/6 D. Ambrose, N. B. Ghiassee, and R. Tuckerman, J. Chem.
86/11 Ya. Kh. Grinberg, V. B. Lazarev, A. Yu. Zavernyaev, V. A. Thermodyn. 20, 767–768 共1988兲.
Shreider, and S. D. Chepik, Zh. Fiz. Khim. 60, 1386 –1389 共1986兲; 88/7 I. A. Hossenlopp and D. G. Archer, J. Chem. Thermodyn. 20,
Chem. Abstracts 105, 86041k 共1986兲. 1061–1068 共1988兲.
86/12 S. Takagi, M. Ishikawa, M. Kumada, T. Kimura, and R. Fujishiro, 88/8 D. Ambrose and N. B. Ghiassee, J. Chem. Thermodyn. 20, 1231–
Thermochimica Acta 109, 55– 61 共1986兲. 1232 共1988兲.
86/13 H.-I. Paul, J. Krug, and H. Knapp, Thermochimica Acta 108, 9–27 88/9 T. M. Letcher, J. Sewry, and S. W. Orchard, J. Chem. Thermodyn.
共1986兲. 20, 1231–1232 共1988兲.
86/14 V. M. Vorotyntsev, V. V. Balabanov, and D. A. Shamrakov, Zh. Fiz. 88/10 M. Bastos, S. O. Nilsson, M. D. M. C. Ribeiro da Silva, M. A. V.
Khim. 60, 234 –235 共1986兲; Chem. Abstracts 104, 96047k 共1986兲. Ribeiro da Silva, and I. Wadso, J. Chem. Thermodyn. 20, 1353–1359
86/16 C. M. White, J. Chem. Eng. Data 31, 198 –203 共1986兲. 共1988兲.
86/17 T. K. Yerlett and C. J. Wormald, J. Chem. Thermodyn. 18, 88/11 R. M. Varushchenko, O. L. Loseva, A. I. Druzhinina, and E. F.
719–726 共1986兲. Zorina, Zh. Fiz. Khim. 62, 1776 –1780 共1988兲.
86/18 T. K. Yerlett and C. J. Wormald, J. Chem. Thermodyn. 18, 88/12 K. Sasse, J. Jose, and J.-C. Merlin, Fluid Phase Equilib. 42,
371–379 共1986兲. 287–304 共1988兲.
1987 88/13 R. H. Shay, B. N. Diel, D. M. Schubert, and A. D. Norman, Inorg.
87/1 X.-W. An, H.-P. Zhu, and R.-H. Hu, Thermochimica Acta 121, Chem. 27, 2378 –2382 共1988兲.
473– 477 共1987兲. 88/14 P. Knauth and R. Sabbah, Bull. Soc. Chem. Fr. 834 – 836 共1988兲.
87/2 P. Kneisi and J. W. Zondio, J. Chem. Eng. Data 21, 11–13 共1987兲. 88/15 M. G. Voronkov, V. P. Baryshok, V. A. Klyuchnikov, T. F.
87/3 P. L. Mills, R. L. Fenton, and F. G. Schaefer, J. Chem. Eng. Data Danilova, V. I. Pepekin, A. N. Korchagina, and Yu. I. Khudobin, J.
32, 251–265 共1987兲. Organomet. Chem. 345, 27–38 共1988兲.
87/4 R. Fuchs, E. J. Chambers, and W. K. Stepenson, Can. J. Chem. 65, 88/16 J. F. Messerly, H. L. Finke, W. D. Good, and B. Gammon, J.
2624 –2627 共1987兲. Chem. Thermodyn. 20, 485–501 共1988兲.
87/5 R. M. Stephenson and S. Malanowski, Handbook of the 88/17 H. Katayama, Bull. Chem. Soc. Jpn. 61, 3326 –3328 共1988兲.
Thermodynamics of Organic Compounds 共Elsevier: New York, 1987兲. 88/18 V. B. Lazarev, Ya. Kh. Grinberg, Z. P. Ozerova, and G. A.
The data in this listing were obtained directly from this compendium Sharpataya, J. Thermal Anal. 33, 797–799 共1988兲.
which does not contain literature references. The vaporization enthalpies 88/19 J.-Q. Dong, R.-S. Lin, and W.-H. Yen, Can. J. Chem. 66, 783–790
were calculated from the vapor pressures obtained from the Antoine 共1988兲.
constants reported in this compendium. Vapor pressures were calculated 88/20 D. R. Davies, M. B. Ewing, J. A. Hugill, and M. L. McGlashan,
over a 30 K temperature range closest to 298 K and the temperature Can. J. Chem. 66, 760–762 共1988兲.
dependence was reformulated in terms of the integrated form of the 1989
Clausius Clapeyron equation. 89/1 R. D. Chirico, A. Nguyen, W. V. Steele, M. M. Strube, and C. J.
87/6 D. Ambrose and N. B. Ghiassee, J. Chem. Thermodyn. 19, 911–913 Tsonopoulos, Chem. Eng. Data 34, 149–156 共1989兲.
共1987兲. 89/2 B. Varughese and J. T. Sommerfeld, J. Chem. Eng. Data 34, 25–26
87/7 D. Ambrose and N. B. Ghiassee, J. Chem. Thermodyn. 19, 903–909 共1989兲.
共1987兲. 89/3 H. S. Wu and S. I. Sandler, J. Chem. Eng. Data 34, 209–213
87/8 Z. Atik, Y. Saito, and K. Kusano, J. Chem. Thermodyn. 19, 99–102 共1989兲.
共1987兲. 89/4 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and W. V. Steele, J.
87/9 D. Ambrose and N. B. Ghiassee, J. Chem. Thermodyn. 19, 505–519 Chem. Thermodyn. 21, 1307–1331 共1989兲.
共1987兲. 89/5 M. Kato and M. Tanaka, J. Chem. Eng. Data 34, 206 –209 共1989兲.
87/10 P. L. Mills and R. L. Fenton, J. Chem. Eng. Data 32, 266 –273 89/6 E. Cepeda, C. Gonzalez, and J. M. Resa, J. Chem. Eng. Data 34,
共1987兲. 270–273 共1989兲.
87/11 R. M. Varushchenko, O. L. Loseva, and A. I. Druzhinina, Zh. Fiz. 89/7 S. J. Park and J. Gmehling, J. Chem. Eng. Data 34, 399– 401
Khim. 61, 31–35 共1987兲. 共1989兲.
89/8 K. Wang, X.-G. Ying, M.-S. Xia, J.-Z. Xia, and Y. Hu, J. Chem. 91/6 M. G. Voronkov, V. A. Klyuchnikov, L. I. Marenkova, T. F.
Eng. Data 34, 126 –130 共1989兲. Danilova, G. N. Shvets, S. I. Tsvetnitskaya, and Yu. I. Khudobin, J.
89/9 A. Sakoguichi, Y. Iwai, and J. Takenaka, Kagaku Kogaku Organomet. Chem. 406, 99–104 共1991兲.
Ronbunshu 15, 166 共1989兲. 91/7 K. B. Wiberg and R. F. Waldron, J. Am. Chem. Soc. 113, 7697–
89/10 X. An and H. Hu, Wuli Huaxue Xuebao 5, 565–571 共1989兲; 7705 共1991兲.
Chem. Abstracts 112, 118206f 共1990兲. 91/8 K. B. Wiberg and S. Hao, J. Org. Chem. 56, 5108 –5110 共1991兲.
89/11 M. G. Voronkov, M. S. Sorokin, V. A. Klyuchnikov, G. N. Shvetz, 91/9 V. Piacente, T. Pompili, P. Scardala, and D. Ferro, J. Chem.
and V. I. Pepekin, J. Organomet. Chem. 359, 301–313 共1989兲. Thermodyn. 23, 379–396 共1991兲.
89/12 M. G. Voronkov, V. A. Klyuchnikov, S. N. Kolabin, G. N. Shvets, 91/10 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and W. V. Steele, J.
P. I. Varushin, E. N. Deryagina, N. A. Korchevin, and S. I. Tsvetnitskaya, Chem. Thermodyn. 23, 431– 450 共1991兲.
Dokl. Phys. Chem. 307, 650– 653 共1989兲. 91/11 A. M. Rozhnov, V. V. Safronov, S. P. Verevkin, K. G. Sharonov,
89/13 R. M. Varushchenko and L. L. Pashchenko, Russ. J. Phys. Chem. and V. I. Alenin, J. Chem. Thermodyn. 23, 629– 635 共1991兲.
63, 964 –967 共1989兲. 91/12 K. G. Sharonov, Y. B. Mishentseva, A. M. Rozhnov, E. A.
89/14 K. Sasse, J. N’Guimbi, J. Jose, and J. C. Merlin, Thermochimica Miroshnichenko, and L. I. Korchatova, J. Chem. Thermodyn. 23,
Acta 146, 53– 61 共1989兲. 637– 642 共1991兲.
89/15 M. D. Vine and C. J. Wormald, J. Chem. Thermodyn. 21, 1151– 91/13 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and W. V. Steele, J.
1157 共1989兲. Chem. Thermodyn. 23, 759–779 共1991兲.
89/16 E. C. Azandegbe, Analusis 17, 285–289 共1989兲. 91/14 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
1990 Chem. Thermodyn. 23, 957–977 共1991兲.
90/1 M. L. P. Leitao, G. Pilcher, Y. Meng-Yan, J. M. Brown, and A. D. 91/15 M. B. Ewing and A. R. H. Goodwin, J. Chem. Thermodyn. 23,
Conn, J. Chem. Thermodyn. 22, 885– 891 共1990兲. 1163–1168 共1991兲.
91/16 R. Koelliker and G. Bor, Inorg. Chem. 30, 2236 –2237 共1991兲.
90/2 D. A. Hinckley, T. F. Bidleman, W. T. Foreman, and J. R. Tuschall,
J. Chem. Eng. Data 35, 232–237 共1990兲. 91/17 V. V. Dikii and G. Ya. Kabo, Dokl. Akad. Nauk BSSR 35,
158 –162 共1991兲; Chem. Abstracts 114, 206233j 共1981兲.
90/3 N. O. Smith, J. Chem. Eng. Data 35, 387–389 共1990兲.
1992
90/4 H.-D. Beckhaus, B. Dogan, J. Pakusch, S. Verevkin, and C.
92/1 C.-H. Lee, Q. Chen, R. S. Mohamed, and G. D. Holder, J. Chem.
Rüchardt, Chem. Ber. 123, 2153–2159 共1990兲.
Eng. Data 37, 179–183 共1992兲.
90/5 T. N. Nesterova, A. G. Nazmutdinov, V. S. Tsvetkov, A. M.
92/2 C.-H. Lee, D. M. Dempsey, R. S. Mohamed, and G. D. Holder, J.
Rozhnov, and I. Yu. Roshchupkina, J. Chem. Thermodyn. 22, 365–377
Chem. Eng. Data 37, 183–186 共1992兲.
共1990兲.
92/3 R. Jadot and M. Fraiha, J. Chem. Eng. Data 37, 509–511 共1992兲.
90/6 M. Lenka, J. Chem. Thermodyn. 22, 473– 480 共1990兲.
92/4 J. S. Chickos, D. G. Hesse, S. Y. Panshin, D. W. Rogers, M.
90/7 D. Ambrose, M. B. Ewing, N. B. Ghiassee, and J. C. S. Ochoa, J.
Saunders, P. M. Uffer, and J. F. Liebman, J. Org. Chem. 57, 1897–1899
Chem. Thermodyn. 22, 589– 605 共1990兲.
共1992兲.
90/8 M. Sohda, M. Okazaki, Y. Iwai, Y. Arai, A. Sakoguchi, R. Ueoka, 92/5 M. Gazicki, H. Schalko, P. Svasek, F. Olcaytug, and F. Kohl, J. Vac.
and Y. Kato, J. Chem. Thermodyn. 22, 607– 608 共1990兲. Sci. Technol. A 10, 51–58 共1992兲.
90/9 N. V. K. Dutt, A. P. Kahol, P. J. Reddy, and K. S. Raghunandanan, 92/6 A. A. Kozyro, G. Ya. Kabo, V. S. Kruck, M. S. Sheiman, I. A.
J. Chem. Eng. Data 35, 114 –117 共1990兲. Yursa, V. V. Simirskii, A. P. Krasulin, V. M. Sevruk, and V. I.
90/10 J. Ortego, P. Susial, and C. de Alfonso, J. Chem. Eng. Data 35, Gogolinskii, J. Chem. Thermodyn. 24, 883– 895 共1992兲.
216 –218 共1990兲. 92/7 J. He, X.-W. An, and R.-H. Hu, Acta Chim. Sinica 50, 943–947
90/11 X. An, J. He, and R.-H. Hu, Thermochimica Acta 169, 331–337 共1992兲.
共1990兲. 92/8 V. Svoboda, V. Kubes, and P. Basarova, J. Chem. Thermodyn. 24,
90/12 R. H. Davies, A. Finch, and K. Salem, Thermochimica Acta 170, 333–336 共1992兲.
213–216 共1990兲. 92/9 M. Gracia, F. Sanchez, P. Perez, J. Valero, and C. Gutierrez Losa, J.
90/13 T. Pompili and V. Piacente, Thermochimica Acta 170, 289–291 Chem. Thermodyn. 24, 463– 471 共1992兲.
共1990兲. 92/10 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
90/14 V. Piacente and P. Scardala, Thermochimica Acta 159, 193–200 Chem. Thermodyn. 24, 499–529 共1992兲.
共1990兲. 92/11 V. Svoboda, V. Kubes, and P. Basarova, J. Chem. Thermodyn. 24,
90/15 A. M. Rozhnov, V. I. Barkov, K. G. Sharonov, and V. S. Tsvetkov, 555–558 共1992兲.
J. Chem. Thermodyn. 22, 327–333 共1990兲. 92/12 M. Salvi-Narkhede, B.-H. Wang, J. L. Adcock, and W. H. Van
90/16 G. Barone, G. Della Gatta, D. Ferro, and V. Piacente, J. Chem. Hook, J. Chem. Thermodyn. 24, 1065–1075 共1992兲.
Soc. Faraday Trans. 86, 75–79 共1990兲. 92/13 S. P. Verevkin, H.-D. Beckhaus, and C. Rüchardt, Thermochimica
90/17 B. Dogan, H.-D. Beckhaus, J. Schaetzer, S. Hellmann, and C. Acta 197, 27–39 共1992兲.
Rüchardt, Chem. Ber. 123, 137–144 共1990兲. 92/14 J. N’Guimbi, H. Kasehgari, I. Mokbel, and J. Jose, Thermochimica
90/18 M. I. Lopez and J. E. Sicre, J. Phys. Chem. 94, 3860–3863 共1990兲. Acta 196, 367–377 共1992兲.
90/19 A. Sprozynski and J. Gregorowicz, Main Group Met. Chem. 13, 92/15 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
1– 6 共1990兲. Chem. Thermodyn. 24, 245–271 共1992兲.
1991 92/16 M.-S. Zhu, J. Wu, and Y.-D. Fu, Fluid Phase Equilib. 80, 99–105
91/1 N. I. Buchan, R. M. Potemski, and T. F. Kuech, J. Chem. Eng. Data 共1992兲.
36, 372–374 共1991兲. 92/17 L. A. Weber, Fluid Phase Equilib. 80, 141–148 共1992兲.
91/2 P. Basarova and V. Svoboda, Fluid Phase Equilib. 68, 13–34 共1992兲. 92/18 W. Kimizuka and J. Szydlowski, Fluid Phase Equilib. 77, 261–267
91/3 H. S. Wu, K. A. Pividal, and S. I. Sandler, J. Chem. Eng. Data 36, 共1992兲.
418 – 421 共1991兲. 92/19 K. Oguchi, M. Yamagishi, and A. Murano, Fluid Phase Equilib. 80,
91/4 M. G. Voronkov, V. A. Klyuchnikov, E. V. Sokolova, T. F. Danilova, 131–140 共1992兲.
G. N. Shvets, A. N. Korchagina, L. E. Gussel’nikov, and V. V. Volkova, 92/20 T. S. Papina, S. M. Pimenova, V. Yu. Zakharov, and V. P. Kolesov,
J. Organomet. Chem. 401, 245–248 共1991兲. Zh. Khim. Termodin. Termodin. 1, 207–211 共1992兲.
91/5 M. G. Voronkov, V. A. Klyuchnikov, E. V. Mironenko, G. N. Shvets, 92/21 D. C. Hawker, Chemosphere 25, 427– 436 共1992兲.
T. F. Danilova, and Yu. I. Khudobin, J. Organomet. Chem. 406, 91–97 1993
共1991兲. 93/1 X.-W. An and Y.-D. Xie, Thermochimica Acta 220, 17–25 共1993兲.
93/2 A. Aucejo, J. B. Monton, R. Munoz, and M. Sanchotello, J. Chem. 94/16 K. B. Wiberg, K. M. Morgan, and H. Maltz, J. Am. Chem. Soc.
Eng. Data 38, 160–162 共1993兲. 116, 11067–11077 共1994兲.
93/3 C.-H. Lee and G. D. Holder, J. Chem. Eng. Data 38, 320–323 94/17 W. V. Steele, R. D. Chirico, A. Nguyen, and S. E. Knipmeyer, J.
共1993兲. Chem. Thermodyn. 26, 515–544 共1994兲.
93/4 R. Reich and V. Sanhueza, J. Chem. Eng. Data 38, 341–343 共1993兲. 94/18 K. Aim, J. Chem. Thermodyn. 26, 977–986 共1994兲.
93/5 P. Susial and J. Ortego, J. Chem. Eng. Data 38, 434 – 436 共1993兲. 94/19 A. S. Carson, P. G. Laye, J. B. Pedley, A. M. Welsby, J. S.
93/6 A. M. Silva and L. A. Weber, J. Chem. Eng. Data 38, 644 – 646 Chickos, and S. Hosseini, J. Chem. Thermodyn. 26, 1103–1109 共1994兲.
共1993兲. 94/20 V. V. Diky, G. J. Kabo, A. A. Kozyro, A. P. Krasulin, and V. M.
93/7 P. Susial and J. Ortego, J. Chem. Eng. Data 38, 647– 649 共1993兲. Sevruk, J. Chem. Thermodyn. 26, 1001–1013 共1994兲.
93/8 J. Farkova and I. Wichterle, Fluid Phase Equilib. 90, 143–148 94/21 L. Terenzi and V. Piacenti, Thermochimica Acta 235, 61– 66
共1993兲. 共1994兲.
93/9 S. Husain, P. N. Sarma, G. Y. S. K. Swamy, and K. S. Devi, J. Am. 94/22 W. Spieksma, R. Luijk, and H. A. J. Govers, J. Chromatog. A 672,
Oil Chem. Soc. 70, 149–155 共1993兲. 141–148 共1994兲.
93/10 H. Kasehgari, I. Mokbel, C. Viton, and J. Jose, Fluid Phase 94/23 K. Liu and R. M. Dickhut, Chemosphere 29, 581–589 共1994兲.
Equilib. 87, 133–152 共1993兲. 1995
93/11 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and W. V. Steele, J. 95/1 M. A. V. Ribeiro da Silva, M. A. R. Matos, and L. M. P. F. Amaral,
Chem. Thermodyn. 25, 1461–1494 共1993兲. J. Chem. Thermodyn. 27, 565–574 共1995兲.
93/12 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, N. K. Smith, and W. 95/2 H. M. A. Al-Maydama, A. Finch, P. J. Gardner, and A. J. Head, J.
V. Steele, J. Chem. Thermodyn. 25, 729–761 共1993兲. Chem. Thermodyn. 27, 173–279 共1995兲.
93/13 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J. 95/3 J.-L. M. Abboud, P. Jimenez, M. V. Roux, C. Turrion, C.
Chem. Thermodyn. 25, 965–992 共1993兲. Lopez-Mardomingo, A. Podosenin, D. W. Rogers, and J. F. Liebman, J.
93/14 S. V. Syoev, A. N. Golubenko, L. D. Nikulina, and T. N. Phys. Org. 8, 15–20 共1995兲.
Martynova, Thermochimica Acta 225, 137–139 共1993兲. 95/4 A. Sakoguchi, R. Ueoka, Y. Kato, and Y. Arai, Kagaku Kogaku
93/15 R. Schulze, H.-D. Beckhaus, and C. Rüchardt, Chem. Ber. 126, Ronbunshu, 21, 219–222 共1995兲.
1031–1038 共1993兲. 95/5 A. K. Baev, V. E. Mikhailov, and I. N. Chernyak, Russ. J. Gen.
93/16 P. S. Engel, C. Wang, Y. Chen, C. Rüchardt, and H.-D. Beckhaus, Chem. 65, 977–980 共1995兲.
J. Am. Chem. Soc. 115, 65–74 共1993兲. 95/6 M. A. V. Ribeiro da Silva, M. L. C. C. H. Ferrao, and F. Jiye, J.
93/17 V. V. Diky, G. J. Kabo, A. A. Kozyro, A. P. Krasulin, and V. M. Chem. Eng. Data 40, 426 – 428 共1995兲.
Sevruk, J. Chem. Thermodyn. 25 1169–1181 共1993兲. 95/7 K. Rakus, S. P. Verevkin, W.-H. Peng, H.-D. Beckhaus, and C.
93/18 J. He, X. An, and R. Hu, Huaxue Xuebao 51, 1059–1065 共1993兲; Rüchardt, Liebigs Ann. 2059–2067 共1995兲.
Chem. Abstracts 120, 87930w 共1994兲.
95/8 K. Rakus, S. P. Verevkin, M. Keller, H.-D. Beckhaus, and C.
93/19 J.-L. M. Abboud, P. Jimenez, M. V. Roux, C. Turrion, and C.
Rüchardt, Liebigs Ann. 1483–1493 共1995兲.
Lopez-Mardomingo, Calor. Anal. Therm. 24, 181–183 共1993兲.
95/9 H. P. Diogo, R. C. Santos, P. M. Nunes, and M. E. Minas da
93/20 V. V. Ovchinnikov, A. A. Sobanov, and A. N. Pudovik, Dokl. Phys.
Piedade, Thermochimica Acta 249, 113–120 共1995兲.
Chem. 333, 483– 485 共1993兲.
95/10 M. G. M. Van der Vis and E. H. P. Cordfunke, Thermochimica
93/21 N. C. Ferreira, C. A. Moreira dos Santos, and I. C. C. Calegao,
Acta 265, 129–134 共1995兲.
Ecl. Quim., Sao Paulo 18, 49–54 共1993兲.
95/11 S. P. Verevkin, H.-D. Beckhaus, and C. Rüchardt, Thermochimica
93/22 H. Wolff, W. Kimizuka, and J. Szydlowski, Fluid Phase Equilib.
Acta 249, 1–11 共1995兲.
90, 163–175 共1993兲.
95/12 C. Gabaldon, P. Marzal, and J. B. Monton, J. Chem. Eng. Data 40,
1994
190–193 共1995兲.
94/1 R. Sabbah, D. Tabet, and S. Belaadi, Thermochimica Acta 247,
95/13 A. Dejoz, M. C. Burguet, R. Munoz, and M. Sanchotello, J. Chem.
193–199 共1994兲.
Eng. Data 40, 290–292 共1995兲.
94/2 V. Piacente, D. Fontana, and P. Scardala, J. Chem. Eng. Data 39,
95/14 A. Aucejo, V. Gonzalez-Alfaro, J. B. Monton, and M. I. Vazquez,
231–237 共1994兲.
J. Chem. Eng. Data 40, 332–335 共1995兲.
94/3 F. Welle, S. P. Verevkin, M. Keller, H.-D. Beckhaus, and C.
Rüchardt, Chem. Ber. 127, 697–710 共1994兲. 95/15 G.-H. Chen, Q. Wang, Z.-M. Ma, X.-H. Yan, and S.-J. Han, J.
Chem. Eng. Data 40, 361–366 共1995兲.
94/4 K. Rakus, S. P. Verevkin, J. Schatzer, H.-D. Beckhaus, and C.
Rüchardt, Chem. Ber. 127, 1095–1103 共1994兲. 95/16 A. Arce, A. Blanco, J. Martinez-Ageitos, and A. Soto, J. Chem.
94/5 K. Rakus, S. P. Verevkin, H.-D. Beckhaus, and C. Rüchardt, Chem. Eng. Data 40, 515–518 共1995兲.
Ber. 127, 2225–2234 共1994兲. 95/17 J. Ortego and S. Galvan, J. Chem. Eng. Data 40, 699–703 共1995兲.
94/6 R. L. Falconer and T. F. Bidleman, Atmosph. Environ. 28, 547–554 95/18 A. Xu-Wu and G. Da-Jun, Thermochimica Acta 253, 235–242
共1994兲. 共1995兲.
94/7 A. Aucejo, M. C. Burguet, J. B. Monton, R. Munoz, M. Sanchotello, 95/19 V. A. Luk’yanova and M. P. Kozina, Russ. J. Phys. Chem. 69,
and M. I. Vazquez, J. Chem. Eng. Data 39, 578 –580 共1994兲. 1906 –1907 共1995兲.
94/8 K. Aim, J. Chem. Eng. Data 39, 591–594 共1994兲. 95/20 R. M. Varushchenko and A. I. Droujinina, J. Chem. Thermodyn.
94/9 U. Karlson, W. T. Frankenberger, Jr., and W. F. Spencer, J. Chem. 27, 355–368 共1995兲.
Eng. Data 39, 608 – 610 共1994兲. 95/21 J. S. Chickos, S. Hosseini, and D. G. Hesse, Thermochimica Acta
94/10 M. A. Krähenbühl and J. Gmehling, J. Chem. Eng. Data 39, 249, 41– 62 共1995兲.
759–762 共1994兲. 95/22 W. V. Steele, R. D. Chirico, A. Nguyen, and S. E. Knipmeyer, J.
94/11 V. Ruzicka, Jr., M. Zabransky, K. Ruzicka, and V. Majer, Chem. Thermodyn 27, 311–334 共1995兲.
Thermochimica Acta 245, 121–144 共1994兲. 95/23 H. P. Diogo, M. E. Minas de Piedade, J. A. Martinho Simoes, and
94/12 K. Ruzicka and V. Majer, J. Phys. Chem. Ref. Data 23, 1–39 Y. Nagana, J. Chem. Thermodyn. 27, 597– 604 共1995兲.
共1994兲. 95/24 W. V. Steele, R. D. Chirico, A. B. Cowell, A. Nguyen, and S. E.
94/13 B. Koutek, M. Hoskovec, P. Vrkova, K. Konecny, and L. Feltl, J. Knipmeyer, J. Chem. Thermodyn. 27, 1407–1428 共1995兲.
Chromatog. A 679, 307–317 共1994兲. 95/25 S. P. Verevkin, B. Dogan, J. Hadrich, H.-D. Beckhaus, and C.
94/14 D. L. Morgan and R. Kobayashi, Fluid Phase Equilib. 97, 211–242 Rüchardt, J. Prakt. Chem. 337, 93–98 共1995兲.
共1994兲. 95/26 E. F. S. Vieira, J. C. de Queiroz, and F. S. Dias, Thermochimica
94/15 J. Ortega and S. Galvan, J. Chem. Eng. Data 39, 907–910 共1994兲. Acta 256, 249–260 共1995兲.
95/27 J. S. Chickos, D. G. Hesse, S. Hosseini, J. F. Liebman, G. D. 96/28 V. S. Ushakov, S. M. Sedov, B. A. Knyazev, and B. I. Kuchkaev,
Mendenhall, S. P. Verevkin, K. Rakus, H.-D. Beckhaus, and C. Rüchardt, Zh. Fiz. Khim. 70, 1573–1577 共1996兲.
J. Chem. Thermodyn. 27, 693–705 共1995兲. 96/29 A. K. Baev, A. I. Podkovirov, and V. I. Kosirkin, Izv. Vyssh.
95/28 M. Nolke, S. P. Verevkin, H.-D. Beckhaus, and C. Rüchardt, Uchebn. Zaved., Khim. Khim. Tekhnol. 39, 10–14 共1996兲.
Liebigs Ann. 41–51 共1995兲. 96/30 M. G. M. Van der Vis, E. H. P. Cordfunke, R. J. M. Konings, and
95/29 J. P. Guthrie and Z. Liu, Can. J. Chem. 73, 1395–1398 共1995兲. A. Oskam, J. Chem. Soc., Faraday Trans. 92, 973–978 共1996兲.
95/30 T. S. Papina, S. M. Pimenova, V. A. Luk’yanova, and V. P. 96/31 I. B. Sladkov and N. Yu. Novikova, Zh. Prikl. Khim.
Kolesov, Zh. Fiz. Khim. 69, 2148 –2151 共1995兲; Chem. Abstracts 124, 共S.-Peterburg兲 96, 1840–1844 共1996兲.
68148p. 共1996兲. 1997
95/31 V. A. Luk’yanova and M. P. Kozina, Zh. Fiz. Khim. 69, 2094 – 97/1 S. P. Verevkin, J. Chem. Thermodyn. 29, 1495–1501 共1997兲.
2095 共1995兲; Chem. Abstracts 124, 68127f 共1996兲. 97/2 M. A. V. Ribeiro da Silva, J. M. Goncalves, and G. Pilcher, J.
1996 Chem. Thermodyn. 29, 253–260 共1997兲.
96/1 M. A. V. Ribeiro da Silva, M. D. M. C. Ribeiro da Silva, M. F. B. 97/3 M. A. V. Ribeiro da Silva, M. A. R. Matos, and L. M. P. F. Amaral,
M. Monteiro, M. L. A. C. N. Gomes, J. S. Chickos, A. P. Smith, and J. F. J. Chem. Thermodyn. 29, 1545–1551 共1997兲.
Liebman, Struct. Chem. 7, 367–373 共1996兲. 97/4 M. A. V. Ribeiro da Silva, M. A. R. Matos, and L. M. P. F. Amaral,
96/2 M. A. V. Ribeiro da Silva, V. M. F. Morais, M. A. R. Matos, C. M. J. Chem. Thermodyn. 29, 1535–1543 共1997兲.
A. Rio, and C. M. G. S. Piedade, Struct. Chem. 7, 329–336 共1996兲. 97/5 S. P. Verevkin, Thermochimica Acta 307, 17–25 共1997兲.
96/3 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J. 97/6 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
Chem. Eng. Data 41, 1255–1268 共1996兲. Chem. Eng. Data 42, 1008 –1020 共1997兲.
96/4 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, A. Nguyen, N. K. 97/7 W. V. Steele, R. D. Chiricio, S. E. Knipmeyer, A. Nguyen, and N.
Smith, and I. R. Tasker, J. Chem. Eng. Data 41, 1269–1284 共1996兲. K. Smith, J. Chem. Eng. Data 42, 1037–1052 共1997兲.
96/5 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and N. K. 97/8 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
Smith, J. Chem. Eng. Data 41, 1285–1302 共1996兲. Chem. Eng. Data 42, 1021–1036 共1997兲.
96/6 L. A. Weber and D. R. Defibaugh, J. Chem. Eng. Data 41, 382–385 97/9 S. P. Verekin, J. Mogenthaler, and C. Rüchardt, J. Chem.
共1996兲. Thermodyn. 29, 1175–1183 共1997兲.
96/7 A. G. de Souza, M. G. A. Brasilino, and C. Airoldi, J. Chem. 97/10 F. W. Welle, S. P. Verevkin, H.-D. Beckhaus, and C. Rüchardt,
Thermodyn. 28, 1359–1367 共1996兲. Liebigs Ann./Recueil 155–163 共1997兲.
96/8 Yu. Ya. Van-Chin-Syan, V. V. Kochubei, V. V. Sergeev, Yu. A. 97/11 P. Hernández and J. Ortega, J. Chem. Eng. Data 42, 1090–1100
Raevskii, S. I. Gerasimchuk, and Kh. Z. Kotovich, Sov. J. Phys. Chem. 共1997兲.
共Eng. Trans.兲 70, 1789–1794 共1996兲. 97/12 L. M. G. Minier and R. Behrens, Jr., Propellants, Explos. Pyrotech.
96/9 P. Ulbig, M. Klüppel, and S. Schulz, Thermochimica Acta 271, 22, 23–33 共1997兲.
9–21 共1996兲. 97/13 B. Koutek, M. Hoskovec, P. Vrkocova, and L. Feltl, J. Chromatogr.
96/10 D. D. Back, L. R. Grzyll, and M. Corrigan, Thermochimica Acta A 759, 93–109 共1997兲.
272, 53– 63 共1996兲. 97/14 F. Schaffer, S. P. Verevkin, H.-J. Rieger, H.-D. Beckhaus, and C.
96/11 S. P. Verevkin, H.-D. Beckhaus, R. S. Belen’kaya, K. Rakus, and Rüchardt, Liebigs Ann./Recueil 1333–1344 共1997兲.
C. Rüchardt, Thermochimica Acta 279, 47– 64 共1996兲. 97/15 H. Artigas, C. Lafuente, P. Cea, F. M. Royo, and J. S. Urieta, J.
96/12 J. Linek, I. Wichterle, and K. Marsh, J. Chem. Eng. Data 41, Chem. Eng. Data 42, 132–136 共1997兲.
1212–1218 共1996兲. 97/16 T. Sako, S. Horiguchi, H. Ichimaru, and S. Nakagawa, J. Chem.
96/13 N. F. Giles, H. L. Wilson, and W. V. Wilding, J. Chem. Eng. Data Eng. Data 42, 169–717 共1997兲.
41, 1223–1238 共1996兲. 97/17 J. S. Chickos and J. A. Wilson, J. Chem. Eng. Data 42, 190–197
96/14 L. A. Weber and D. R. Defibaugh, J. Chem. Eng. Data 41, 共1997兲.
1477–1480 共1996兲. 97/18 W. V. Steele, R. D. Chirico, A. B. Cowell, S. E. Knipmeyer, and
96/15 M. F. Rodrigues and M. G. Bernardo-Gil, J. Chem. Eng. Data 41, A. Nguyen, J. Chem. Eng. Data 42, 1053–1066 共1997兲.
581–585 共1996兲. 97/19 J. C. G. Calado, E. J. M. Filipe, and J. N. C. Lopes, J. Chem.
96/16 S. R. Susay, M. A. Smith, and G. G. Lockwood, Anesth. Analg. Thermodyn. 29, 1435–1438 共1997兲.
83, 864 – 866 共1996兲. 97/20 A. V. Blokhin, G. J. Kabo, A. A. Kozyro, L. S. Ivashkevich, A. P.
96/17 B. Koutek, M. Hoskovec, P. Vrkocova, K. Konecny, L. Feltl, and J. Krasulin, V. V. Diky, and Yu. V. Maksimuk, Thermochimica Acta 292,
Vrkoc, J. Chromatogr. A 719, 391– 400 共1996兲. 19–29 共1997兲.
96/18 R. M. Varushchenko, L. L. Pashchenko, and A. I. Druzhinina, 97/21 S. P. Verevkin, J. Chem. Thermodyn. 29, 891– 899 共1997兲.
Russ. J. Phys. Chem. 70, 208 –211 共1996兲. 97/22 D. R. Defibaugh, E. Carrillo-Nava, J. J. Hurly, M. R. Moldover, J.
96/19 M. Polednicek, T. Guetachew, J. Jose, V. Ruzicka, V. Rohac, and W. Schmidt, and L. A. Weber, J. Chem. Eng. Data 42, 488 – 496 共1997兲.
M. Zabransky, ELDATA: Intl. Electron. J. Phys.-Chem. Data 2, 41–50 97/23 Yu. V. Maksimuk, G. J. Kabo, A. A. Kozyro, V. V. Simirsky, A. P.
共1996兲. Krasulin, and V. M. Sevruk, J. Chem. Thermodyn. 29, 687– 699 共1997兲.
96/20 S. P. Verevkin, S. Züffle, H.-D. Beckhaus, and C. Rüchardt, 97/24 M. Hallquist, I. Wangberg, and E. Ljungstrom, Environ. Sci.
Thermochimica Acta 285, 1–10 共1996兲. Technol. 31, 3166 –3172 共1997兲.
96/21 E. A. Miroshinchenko, Yu. D. Orlov, L. I. Korchatova, V. P. 97/25 H. A. Duarte-Garza, C.-A. Hwang, S. A. Kellerman, R. C. Miller,
Vorob’eva, and Yu. A. Lebedev, Zh. Fiz. Khim. 70, 1583–1586 共1996兲. K. R. Hall, J. C. Holste, K. N. Marsh, and G. E. Gammon, J. Chem.
96/22 C. Viton, M. Chavret, and J. Jose, ELDATA: Int. Electron. J. Eng. Data 42, 497–501 共1997兲.
Phys.-Chem. Data 2, 103–110 共1996兲. 97/26 B. L. Korsounskii and T. A. Apina, Int. Annu. Conf. ICT 46.1–
96/23 V. V. Ovchinnikov, T. B. Makeeva, L. I. Lapteva, and A. I. 46.7 共1997兲; Chem. Abstracts 127, 163997k 共1997兲.
Konovalov, Thermochim. Acta 277, 145–150 共1996兲. 97/27 L.-T. Lim and M. A. Tung, J. Food Sci. 62, 1061–1066 共1997兲.
96/24 A. G. van Haelst, F. W. M. van der Wielen, and H. A. J. Govers, J. 97/28 H. B. Krop, M. J. M. Velzen, J. R. Parsons, and H. A. J. Govers, J.
Chromatog. A 727, 265–273 共1996兲. Am. Oil Chem. Soc. 74, 309–315 共1997兲.
96/25 R. D. Chirico, W. V. Steele, A. Nguyen, T. D. Klots, and S. E. 97/29 S. P. Verevkin, M. Nölke, H.-D. Beckhaus, and C. Rüchardt, J.
Knipmeyer, J. Chem. Thermodyn. 28, 797– 818 共1996兲. Org. Chem. 62, 4683– 4686 共1997兲.
96/26 R. M. Varushchenko, A. I. Druzhinina, and L. L. Pashchenko, 97/30 A. K. Baev, Russ. J. Inorg. Chem. 42, 587–596 共1997兲.
Fluid Phase Equilibria 126, 93–104 共1996兲. 1998
96/27 O. Dahmani, I. Wichterle, and A. Ait-Kaci, Fluid Phase Equilib. 98/1 S. P. Verevkin, H.-D. Beckhaus, U. Schüle, and C. Rüchardt, Struct.
124, 135–146 共1996兲. Chem. 9, 1–7 共1998兲.
98/2 S. P. Verevkin and F. M. Welle, Struct. Chem. 9, 215–221 共1998兲. 99/12 D. E. G. Jones, H. T. Feng, R. A. Austen, and R. C. Fouchard, J.
98/3 R. Gudino, L. A. Torres, R. L. Santillan, and N. Farfan, J. Chem. Therm. Anal. Calorim. 55, 9–19 共1999兲; Chem. Abstracts 132, 182729u
Thermodyn. 30, 671– 679 共1998兲. 共2000兲.
98/4 S. P. Verevkin, Thermochimica Acta 310, 229–235 共1998兲. 99/13 Y. D. Lei, F. Wania, W. Y. Shiu, and D. G. B. Boocock, J. Chem.
98/5 M. A. George, K. M. Young, E. A. Robertson III, S. E. Beck, and Eng. Data 44, 200–202 共1999兲.
G. Voloshin, J. Chem. Eng. Data 43, 60– 64 共1998兲. 99/14 R. Garriga, A. C. Andres, P. Perez, and M. Gracia, J. Chem. Eng.
98/6 Y. V. Maksimuk, G. J. Kabo, V. V. Simirsky, A. A. Kozyro, and V. Data 44, 296 –302 共1999兲.
M. Sevruk, J. Chem. Eng. Data 43, 293–398 共1998兲. 99/15 G. N. Escobedo-Alvarado and S. I. Sandler, J. Chem. Eng. Data
98/7 M. A. Abdi and A. Meisen, J. Chem. Eng. Data 43, 133–137 44, 319–322 共1999兲.
共1998兲. 99/16 J. Dykyj, J. Svoboda, R. C. Wilhoit, M. L. Frenkel, and K. R.
98/8 V. Rohac, V. Ruzicka, K. Ruzicka, and K. Aim, J. Chem. Eng. Data Hall, Vapor Pressure of Chemicals: Part A. Vapor Pressure and Antoine
43, 770–775 共1998兲. Constants for Hydrocarbons and Sulfur, Selenium, Tellurium and
98/9 A. Aucejo, S. Loras, R. Munoz, P. Reich, and H. Segura, J. Chem. Hydrogen Containing Organic Compounds 共Springer, Berlin, 1999兲. The
Eng. Data 43, 973–977 共1998兲. vaporization enthalpies were calculated from the vapor pressures obtained
98/10 S. P. Verevkin, Thermochimica Acta 316, 131–136 共1998兲. from the Antoine constants reported in this compendium. In cases where
the Antoine constant C⫽0, the Antoine Equation (log10 P⫽A⫺B/(C
98/11 J. S. Chickos, D. Hesse, S. Hosseini, G. Nichols, and P. Webb,
⫹T)) reduces to the integrated form of the Clausius Clapeyron equation
Thermochimica Acta 313, 101–110 共1998兲.
directly. This was the case for many vaporization enthalpies. In those
98/12 S. P. Verevkin, Struct. Chem. 9, 113–119 共1998兲. cases where this condition was not met the vaporization enthalpy was
98/13 S. P. Verevkin, J. Chem. Thermodyn. 30, 1069–1079 共1998兲. calculated as ⌬H V ⫽2.303RB 关 T/(T⫹C) 兴 2 .
98/14 K. M. Morgan and D. A. Kopp, J. Chem. Soc., Perkin Trans. 2 99/17 V. N. Dibrivnyl, Z. E. Pistun, Yu. Ya. Van-Chin-Syan, A. P.
2759–2763 共1998兲. Yuvchenko, and T. D. Zvereva, Russ. J. Phys. Chem. 73, 2043–2045
98/15 J. D. Olson, Fluid Phase Equilib. 150Õ151, 713–720 共1998兲. 共1999兲.
98/16 V. Svoboda, V. Hynek, and B. Koutek, J. Chem. Thermodyn. 30, 99/18 S. P. Verevkin, J. Chem. Thermodyn. 31, 559–585 共1999兲.
1411–1417 共1998兲. 99/19 S. P. Verevkin, J. Chem. Thermodyn. 31, 1397–1416 共1999兲.
98/17 V. P. Kolesov, S. M. Pimenova, V. A. Lukyanova, T. S. 99/20 V. Rohac, V. Ruzicka, K. Ruzicka, M. Polednicek, K. Aim, J. Jose,
Kuznetsova, and M. P. Kozina, J. Chem. Thermodyn. 30, 1455–1464 and M. Zabransky, Fluid Phase Equilibra 157, 121–142 共1999兲.
共1998兲. 99/21 S. P. Verevkin, Thermochimica Acta 326, 17–25 共1999兲.
98/18 M. B. Ewing and J. C. Sanchez Ochoa, J. Chem. Thermodyn. 30, 99/22 V. A. Titov, L. N. Zelenina, and T. P. Chusova, Russ. J. Phys.
189–198 共1998兲. Chem. 73, 835– 837 共1999兲.
98/19 S. P. Verevkin, J. Chem. Thermodyn. 30, 1029–1040 共1998兲. 99/23 V. N. Dibrivnyl, G. V. Lusiv, Yu. Ya. Van-Chin-Syan, A. P.
98/20 K. G. Drouillard, G. T. Tomy, D. C. G. Muir, and K. J. Friesen, Yuvchenko, and E. A. Dikusar, Russ. J. Phys. Chem. 73, 2040–3042
Environ. Toxicol. Chem. 17, 1252–1260 共1998兲. 共1999兲.
98/21 S. P. Verevkin, W.-H. Peng, H.-D. Beckhaus, and C. Rüchardt, Eur. 99/24 R. D. Chirico, S. E. Knipmeyer, A. Nguyen, and W. V. Steele, J.
J. Org. Chem. 2323–2332 共1998兲. Chem. Thermodyn. 31, 339–378 共1999兲.
98/22 S. P. Verevkin, M. Kümmerlin, H.-D. Beckhaus, C. Galli, and C. 99/25 V. Rohac, J. E. Musgrove, K. Ruzicka, V. Ruzicka, M. Zabransky,
Rüchardt, Eur. J. Org. Chem. 579–584 共1998兲. and K. Aim. J. Chem. Thermodyn. 31, 971–986 共1999兲.
98/23 X. Zhang, H. Mo, K. Yang, and F. An, Huanjing Huaxue 17, 99/26 F. Weber, PTB-Mitteilungen 109, 469– 471 共1999兲.
50–54 共1998兲; Chem. Abstracts 128, 318311d 共1998兲 共value is referred to 99/27 M. A. E. Diaz, T. Guetachew, P. Landy, J. Jose, and A. Voilley,
as a vaporization enthalpy兲. Fluid Phase Equilib. 109, 469– 471 共1999兲.
98/24 W. Blanke, G. Klingenberg, and F. Weber, Int. J. Thermophys. 19, 99/28 S. Loras, A. Aucejo, and R. Munoz, Fluid Phase Equilib. 156,
653– 662 共1998兲. 185–195 共1999兲.
98/25 L. D. Stockton, T. L. Ng, N. Maung, I. B. Poole, J. O. Williams, 99/29 J. S. Lim, J.-Y. Park, B.-G. Lee, Y.-W. Lee, and J.-D. Kim, J.
A. C. Wright, D. F. Foster, and D. J. Cole-Hamilton, J. Cryst. Growth Chem. Eng. Data 44, 1226 –1230 共1999兲.
183, 95–98 共1998兲. 99/30 A. Aucejo, S. Loras, R. Munoz, and L. M. Ordonez, Fluid Phase
1999 Equilib. 156, 173–178 共1999兲.
99/1 M. A. V. Ribeiro da Silva, M. D. M. C. Ribeiro da Silva, M. A. R. 99/31 A. Keys, S. G. Bott, and A. R. Barron, Chem. Mater. 11, 3578 –
Matos, P. Jimenez, M. V. Roux, J. Elguero, R. Claramunt, P. Cabildo, and 3587 共1999兲.
A. Sanchez-Migallon, J. Chem. Thermodyn. 31, 129–138 共1999兲. 99/32 D. Fatu, J. Thermal. Anal. Calor. 56, 739–747 共1999兲.
99/2 S. P. Verevkin, Thermochimica Acta 332, 27–32 共1999兲. 99/33 M. I. Zaretskii, E. M. Chartov, L. A. Pushkina, and V. V. Elkin,
99/3 S. P. Verevkin, J. Chem. Eng. Data 44, 1245–1251 共1999兲. Russ. J. Appl. Chem. 72, 1702–1705 共1999兲.
99/4 S. P. Verevkin and A. Heintz, J. Chem. Eng. Data 44, 1240–1244 2000
共1999兲. 00/1 M. A. V. Ribeiro da Silva, M. D. M. C. Ribeiro da Silva, M. A. R.
99/5 O. Mo, M. Yanez, M. V. Roux, P. Jimenez, J. Z. Davalos, M. A. V. Matos, P. Jimenez, M. V. Roux, M. A. Martin-Luengo, J. Elguero, R.
Ribeiro da Silva, M. D. M. C. Ribeiro da Silva, M. A. R. Matos, L. M. Claramut, and P. Cabildo, J. Chem. Thermodyn. 32, 237–245 共2000兲.
P. F. Amaral, A. Sanchez-Migallon, P. Cabildo, R. Claramunt, J. Elguero, 00/2 S. P. Verevkin, J. Chem. Thermodyn. 32, 207–216 共2000兲.
and J. F. Liebman, J. Phys. Chem. 103, 9336 –9344 共1999兲. 00/3 M. A. V. Ribeiro da Silva, M. A. R. Matos, C. A. Rio, V. M. F.
99/6 F. S. Costa, M. E. Eusebio, J. S. Redinha, and M. L. P. Leitao, J. Morais, J. Wang, G. Nichols, and J. S. Chickos, J. Phys. Chem. A 104,
Chem. Thermodyn. 31, 895–903 共1999兲. 1774 –1778 共2000兲.
99/7 M. A. V. Ribeiro da Silva, M. A. R. Matos, V. M. F. Morais, and M. 00/4 I. Mokbel, K. Ruzicka, V. Majer, V. Ruzicka, M. Ribeiro, J. Jose,
S. Miranda, J. Org. Chem. 64, 8816 – 8820 共1999兲. and M. Zabransky, Fluid Phase Equilib. 169, 191–207 共2000兲.
99/8 S. P. Verevkin, J. Chem. Eng. Data 44, 175–179 共1999兲. 00/5 S. P. Verevkin and C. Schick, J. Chem. Eng. Data 45, 946 –952
99/9 Y. D. Lei, F. Wania, and W. Y. Shiu, J. Chem. Eng. Data 44, 共2000兲.
577–582 共1999兲. 00/6 S. P. Verevkin, J. Chem. Eng. Data 45, 953–960 共2000兲.
99/10 J. B. Monton, J. de la Torre, M. C. Burguet, R. Munoz, and S. 00/7 S. P. Verevkin, D. Wandschneder, and A. Heintz, J. Chem. Eng.
Loras, J. Chem. Eng. Data 44, 1158 –1162 共1999兲. Data 45, 618 – 625 共2000兲.
99/11 J. N’Guimbi, C. Berro, I. Mokbel, E. Rauzy, and J. Jose, Fluid 00/8 J. M. Resa, C. Gonzalez, S. Ortiz de Landaluce, and J. Lanz, J.
Phase Equilib. 162, 143–158 共1999兲. Chem. Eng. Data 45, 867– 871 共2000兲.
00/9 G. Nichols, J. Orf, S. M. Reiter, J. S. Chickos, and G. W. Gokel, 01/16 S. P. Verevkin and A. Heintz, J. Chem. Eng. Data 46, 984 –990
Thermochimica Acta 346, 15–28 共2000兲. 共2001兲.
00/10 P. V. Ova, B. Koultek, and M. Hoskovec, in Practice Oriented 01/17 K. Chylinski, Z. Fras, and S. K. Malanowski, J. Chem. Eng. Data
Results on Use and Production of Neem Ingredients and Pheromones VI; 46, 29–33 共2001兲.
edited by H. Kleeberg and C. P. W. Zebitz 共Druck and Graphic, Giessen, 01/18 S. P. Verevkin and A. Heintz, J. Chem. Eng. Data 46, 41– 46
2000兲, pp. 211–218. 共2001兲.
00/11 Y.-H. Liang and P.-S. Ma, Shiyou Huagong 29, 939–941 共2000兲. 01/19 S. Horstmann, H. Gardeler, K. Fischer, F. Köster, and J. Gmehling,
00/12 S. Rodriguez, H. Artigas, C. Lafuente, A. M. Mainar, and F. M. J. Chem. Eng. Data 46, 337–345 共2001兲.
Royo, Thermochimica Acta 362, 153–160 共2000兲. 01/20 K. Chatterjee, D. Dollimore, and K. Alexander, Instrum. Sci.
00/13 R. Reich, M. Cartes, H. Segura, and J. Wisniak, Phys. Chem. Liq. Technol. 29, 133–144 共2001兲; Chem. Abstracts 135, 16629t 共2001兲
38, 217–232 共2000兲. 共reported values are referred to as enthalpies of vaporization兲.
00/14 S. P. Verevkin, J. Chem. Thermodyn. 32, 247–259 共2000兲. 01/21 J. O. Lalah, K.-W. Schramm, D. Lenoir, B. Henkelmann, N.
00/15 S. P. Verevkin and A. Heintz, J. Chem. Thermodyn. 32, 1169–1182 Hertkorn, G. Matuschek, A. Kettrup, and K. Günther, Chem. Eur. J. 7,
共2000兲. 4790– 4795 共2001兲.
00/16 V. Rohac, M. Censky, D. Zala, V. Ruzicka, K. Ruzicka, K. Sporka, 01/22 I. Kul, D. D. DesMarteau, and A. L. Beyerlein, Fluid Phase
and K. Aim, J. Chem. Eng. Data 45, 1205–1210 共2000兲. Equilib. 185, 241–253 共2001兲.
00/17 M. Palczewska-Tulinska and A. M. Szafranski, J. Chem. Eng. Data 01/23 A. K. Baev and V. E. Mikhailov, Russ. J. Appl. Chem. 74,
1435–1438 共2001兲.
45, 988 –990 共2000兲.
01/24 A. K. Baev and I. N. Chernyak, Russ. J. Inorg. Chem. 46,
00/18 E. Bourret-Courchesne, Q. Ye, D. W. Peters, J. Arnold, M. Ahmed,
310–316; 共2001兲 Zh. Neorg. Khim. 46, 361–367 共2001兲; enthalpies of
S. J. C. Irvine, R. Kanjolia, L. M. Smith, and S. A. Rushworth, J. Cryst.
vaporization are presented graphically in paper for binary mixtures.
Growth 217, 47–54 共2000兲.
2002
00/19 B. Sztaray and T. Baer, J. Am. Chem. Soc. 122, 9219–9226
02/1 R. M. Varushchenko and A. I. Druzhinina, Fluid Phase Equilib. 199,
共2000兲.
109–119 共2002兲.
00/20 C. J. Wormald and D. P. Fennell, Int. J. Thermophys. 21, 767–779 02/2 D. Deng, H. Li, and S. Han, J. Chem. Thermodyn. 34, 1431–1437
共2000兲. 共2002兲.
00/21 A. I. Druzhinina, R. M. Varushchenko, V. S. Sarisova, and A. A. 02/3 T. V. Sorokina, D. Dollimore, and K. S. Alexander, Thermochimica
Pimerzin, Zh. Fiz. Khim. 74, 404 – 411 共2000兲. Acta 392Õ393, 315–321 共2002兲.
00/22 S. V. Melkhanova, S. M. Pimenova, V. P. Kolesov, A. A. Pimerzin, 02/4 A. Valtz, C. Coquelet, A. Baba-Ahmed, and D. Richon, Fluid Phase
and V. S. Sarkisova, J. Chem. Thermodyn. 32, 1311–1317 共2000兲. Equilib. 202, 29– 47 共2002兲.
00/23 S. Bobbo, R. Camporese, and R. Stryjek, J. Chem. Thermodyn. 32, 02/5 J.-P. Pokki, P. Uusi-Kyyny, J. Aittamaa, and S. Liukkonen, J. Chem.
1647–1656 共2000兲. Eng. Data 47, 371–375 共2002兲.
00/24 C. J. Wormald and M. D. Vine, J. Chem. Thermodyn. 32, 329–339 02/6 S. Bobbo, L. Fedele, M. Scattolini, and R. Camporese, J. Chem.
共2000兲. Eng. Data 47, 179–182 共2002兲.
00/25 C. J. Wormald and M. D. Vine, J. Chem. Thermodyn. 32, 659– 669 02/7 C.-H. Su, S. Zhu, N. Ramachandran, and A. Burger, J. Cryst.
共2000兲. Growth 235, 313–319 共2002兲.
00/26 C. J. Wormald and G. F. James, J. Chem. Eng. Data 45, 348 –352 02/8 H. Segura, J. Wisniak, G. Galindo, and R. Reich, Phys. Chem. Liq.
共2000兲. 40, 67– 81 共2002兲.
2001 02/9 B. E. Swiatek and S. K. Malanowski, J. Chem. Eng. Data 47,
01/1 S. Puri, J. S. Chickos, and W. J. Welsh, Anal. Chem. 73, 1480–1484 478 – 481 共2002兲.
共2001兲. 02/10 R. M. Varuschenko, L. L. Pashchenko, A. I. Druzhinina, A. Yu.
01/2 A. Wong, Y. D. Lei, M. Alaee, and F. Wania, J. Chem. Eng. Data Churkina, I. I. Vorob’ev, and S. N. Kravhun, Russ. J. Phys. Chem. 76,
46, 239–242 共2001兲. 546 –551 共2002兲.
01/3 D. Kilikov, S. P. Verevkin, and A. Heintz, Fluid Phase Equilib. 192, 02/11 R. M. Varuschenko, C. A. Aitkeeva, A. I. Druzhinina, Y. A.
187–206 共2001兲. Myshenseva, and L. L. Pashchenko, Russ. J. Phys. Chem. 76, 724 –728
01/4 R. M. Varushchenko, L. L. Paschenko, A. I. Druzhinina, A. V. 共2002兲.
Abramenkov, and A. A. Pimersin, J. Chem. Thermodyn. 33, 733–744 02/12 I. M. Marrucho, N. S. Oliveira, and R. Dohrn, J. Chem. Eng. Data
共2001兲. 47, 554 –558 共2002兲.
01/5 A. K. Baev, Russ. J. Appl. Chem. 74, 162–163 共2001兲. 02/13 I. Batiu, Fluid Phase Equilib. 198, 111–121 共2002兲.
01/6 S. Bernatova and I. Wichterle, Fluid Phase Equilib. 189, 111–118 02/14 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
共2001兲. Chem. Eng. Data 47, 648 – 666 共2002兲.
01/7 D. Kulikov, S. P. Verevkin, and A. Heintz, J. Chem. Eng. Data 46, 02/15 W. V. Steele, R. D. Chirico, A. B. Cowell, S. E. Knipmeyer, and
1593–1600 共2001兲. A. Nguyen, J. Chem. Eng. Data 47, 667– 688 共2002兲.
01/8 J. G. Blok, A. C. G. van Genderen, P. R. van der Linde, and H. A. 02/16 W. V. Steele, R. D. Chirico, A. B. Cowell, S. E. Knipmeyer, and
G. Oonk, J. Chem. Thermodyn. 33, 1097–1106 共2001兲. A. Nguyen, J. Chem. Eng. Data 47, 700–714 共2002兲.
01/9 A. K. Baev, Izv. Vyssh. Uchebn. Zaved., Khim. Khim. Tekhnol. 44, 02/17 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
3–13 共2001兲. Chem. Eng. Data 47, 689– 699 共2002兲.
01/10 N. Bureau, J. Jose, I. Mokbel, and J.-C. de Hemptinne, J. Chem. 02/18 Y. D. Lei, R. Chankalal, A. Chan, and F. Wania, J. Chem. Eng.
Thermodyn. 33, 1485–1498 共2001兲. Data 47, 801– 806 共2002兲.
01/11 S. A. Tittlemier and G. T. Tomy, Environ. Toxicol. Chem. 20, 02/19 J. Murata, S. Yamashita, M. Akiyama, S. Katayama, T. Hiaki, and
146 –148 共2001兲. A. Sekiya, J. Chem. Eng. Data 47, 911–915 共2002兲.
01/12 H. Segura, E. Lam, R. Reich, and J. Wisniak, Phys. Chem. Liq. 39, 02/20 W. V. Steele, R. D. Chirico, A. B. Cowell, S. E. Knipmeyer, and
43–54 共2001兲. A. Nguyen, J. Chem. Eng. Data 47, 725–739 共2002兲.
01/13 L. Zhu, H. Li, C. Wang, and S. Han, J. Chem. Eng. Data 46, 02/21 W. V. Steele, R. D. Chirico, S. E. Knipmeyer, and A. Nguyen, J.
1231–1234 共2001兲. Chem. Eng. Data 47, 715–724 共2002兲.
01/14 P. Uusi-Kyyny, J.-P. Pokki, J. Aittaman, and S. Liukkonen, J. 02/22 R. M. Varushchenko, L. L. Pashchenko, A. Y. Churkina, and A. V.
Chem. Eng. Data 46, 1244 –1248 共2001兲. Shabanova, Russ. J. Phys. Chem. 76, 915–921 共2002兲.
01/15 L. A. L. Munoz and M. A. Krahenbuhl, J. Chem. Eng. Data 46, 02/23 A. Rodriquez, J. Canosa, A. Dominquez, and J. Tojo, Fluid Phase
120–124 共2001兲. Equilib. 198, 95–109 共2002兲.
02/24 S. Bobbo, G. Artico, L. Fedele, M. Scattolini, and R. Camporese, G. Nichols, J. Orf, S. Reiter, J. S. Chickos, and G. W. Gokel, Thermochim.
J. Chem. Eng. Data 47, 839– 842 共2002兲. Acta 346, 15–28 共2000兲; J. S. Chickos and J. Wilson, J. Chem. Eng. Data
02/25 G. Di Nicola and G. Passerini, J. Chem. Eng. Data 47, 882– 886 42, 190–197 共1997兲, and references cited therein.
共2002兲. 4
J. S. Chickos, W. E. Acree, Jr., and J. F. Liebman, Estimating Phase
02/26 H. Segura, G. Galindo, R. Reich, J. Wisniak, and S. Loras, Phys. Change Entropies and Enthalpies, edited by D. Frurip and K. Irikura, ACS
Chem. Liq. 40, 277–294 共2002兲. Symposium Series 677 Computational Thermochemistry, Prediction and
02/27 A. C. G. van Genderen, J. C. van Miltenburg, J. G. Blok, M. J. Estimation of Molecular Thermodynamics 共American Chemical Society,
van Bommel, P. J. van Ekeren, G. J. K. van den Berg, and H. A. J. Washington, DC, 1998兲, pp. 63–93, and references cited therein.
5
Oonk, Fluid Phase Equilib. 202, 109–120 共2002兲. R. Sabbah, A. Xu-wu, J. S. Chickos, M. L. Planas Leitao, M. V. Roux, and
02/28 S. P. Verevkin, J. Chem. Thermodyn. 34, 263–275 共2002兲. L. A. Torres, Thermochim. Acta 331, 93–204 共1999兲.
6
02/29 E. L. Krasnykh, T. V. Vasiltsova, S. P. Verevkin, and A. Heintz, J. J. S. Chickos, W. Acree, Jr., and J. F. Liebman, J. Chem. Phys. Ref. Data
Chem. Eng. Data 47, 1372–1378 共2002兲. 28, 1535–1673 共1999兲.
7
02/30 S. Loras, A. Aucejo, J. B. Monton, J. Wisniak, and H. Segura, J. J. S. Chickos and W. Acree, Jr., J. Phys. Chem. Ref. Data 31, 537– 698
Chem. Eng. Data 47, 1256 –1262 共2002兲. 共2002兲.
8
02/31 A. Rodriquez, J. Canosa, A. Dominquez, and A. Tojo, J. Chem. M. Zabransky, V. Ruzicka, Jr., V. Majer, and E. S. Domalski, J. Phys.
Eng. Data 47, 1098 –1102 共2002兲. Chem. Ref. Data, Monograph No. 6, 1–1596 共1996兲; E. S. Domalski and
02/32 S. P. Verevkin, J. Chem. Eng. Data 47, 1071–1097 共2002兲. E. D. Hearing, J. Phys. Chem. Ref. Data 25, 1–533 共1996兲.
9
S. W. Benson, Thermochemical Kinetics, 2nd ed. 共Wiley-Interscience,
02/33 J. W. Goodrum and D. P. Geller, Bioresource Technol. 84, 75– 80
New York, 1976兲.
共2002兲. 关Note: The calculated values in the article had to be multiplied 10
W. J. Lyman, W. F. Reehl, and D. H. Rosenblatt, Handbook of Chemical
by 1,000 共personal communication兲.兴
Property Estimation Methods 共American Chemical Society, Washington,
02/34 O. Pfohl, C. Riebesell, and R. Dohrn, Fluid Phase Equilib. 202,
DC, 1982兲, Chap. 23.
289–306 共2002兲. 11
J. S. Chickos, S. Hosseini, D. G. Hesse, and J. F. Liebman, Struct. Chem.
02/35 M. D. M. C. Ribeiro da Silva, L. M. N. B. F. Santos, A. L. R.
4, 261–269 共1993兲; 4, 271–278 共1993兲.
Silva, O. Fernandes, and W. E. Acree, Jr., J. Chem. Thermodyn. 12
V. Majer and V. Svoboda, Enthalpies of Vaporization of Organic Com-
共submitted for publication兲. pounds: A Critical Review and Data Compilation, IUPAC Chemical Data
02/36 K. Clou, J. F. Janssens, N. Blaton, A. T. H. Lenstra, and H. O. Series No. 32 共Blackwell, Oxford, 1985兲.
Desseyn, Thermochimica Acta 共in press兲. 13
R. Ruzika and V. Majer, J. Phys. Chem. Ref. Data 23, 1–39 共1994兲.
02/37 A. van Roon, J. R. Parsons, and H. A. J. Govers, J. Chromatogr. A 14
E. S. Domalski and E. D. Hearing, J. Phys. Chem. Ref. Data 25, 1–525
955, 105–115 共2002兲. 共1996兲.
02/38 S. P. Verevkin and A. Heintz, J. Chem. Soc., Perkin Trans. 2 15
C. E. Rechsteiner, Jr., in Ref. 10, Chap. 13.
728 –733 共2002兲. 16
V. Svoboda and H. Smolova, Fluid Phase Equilibria 97, 1–11 共1994兲; P.
02/39 A. K. Baev and M. A. Shiskho, Russ. J. Appl. Chem. 75, 156 –158 Basarova and V. Svoboda, ibid. 105, 27– 47 共1995兲.
共2002兲. 17
A. Vetere, Fluid Phase Equilibria 106, 1–10 共1995兲.
02/40 A. Hazra, D. Dollimore, and K. Alexander, Thermochimica Acta 18
W. F. An, J. Y. Li, W. W. Cheng, and J. D. Gao, Chem. Eng. J. Biochem.
392Õ393, 221–229 共2002兲. Eng. J. 59, 101–109 共1995兲.
02/41 C. Wang, H. Li, L. Ma, and S. Han 共unpublished data兲. 19
C.-H. Tu and C. P. Liu, Fluid Phase Equilibria 121, 45– 65 共1996兲.
02/42 A. Dahmani, I. Mokbel, and J. Jose, Fluid Phase Equilib. 203, 20
P, Ulbig, M. Kluppel, and S. Schulz, Thermochim. Acta 271, 9–21 共1996兲.
193–204 共2002兲. 21
L. Coniglio, L. Trassy, and E. Rauzy, Ind. Eng. Chem. Res. 39, 5037–
02/43 A. K. Baev and M. A. Shishko, Russ. J. Appl. Chem. 75, 25–28 5048 共2000兲.
共2002兲. 22
Z. Y. Liu, Chem. Eng. Commun. 184, 221–228 共2001兲.
23
02/44 J. S. Chickos, P. Webb, G. Nichols, T. Kiyobayashi, P.-C. Cheng, N. Gopinathan and D. N. Saraf, Fluid Phase Equilibria 179, 277–284
and L. Scott, J. Chem. Thermodyn. 34, 1195–1206 共2002兲. 共2001兲.
02/45 M. Lubomska, A. Banas, and S. K. Malanowski, J. Chem. Eng.
24
K. Laidler, Can. J. Chem. 34, 626 – 48 共1956兲.
25
Data 47, 1466 –1471 共2002兲. M. Ducros, J. F. Greison, and H. Sannier, Thermochim. Acta 36, 39– 65
Unpublished Data 共1980兲; M. Ducros, J. F. Greison, H. Sannier, and I. Velasco, ibid. 44,
U/1 R. H. Fuchs 共unpublished data兲. 131– 40 共1981兲; M. Ducros and H. Sannier, ibid. 54, 153–157 共1982兲; M.
U/2 S. P. Verevkin, E. Krasnykh, T. Vasiltsova, and A. Heintz Ducros and H. Sannier, ibid. 75, 329–340 共1984兲.
26
J. P. Guthrie and K. F. Taylor, Can. J. Chem. 61, 602– 607 共1983兲.
共unpublished data as quoted in 关02/32兴兲. 27
J. S. Chickos, A. S. Hyman, L. H. Ladon, and J. F. Liebman, J. Org.
Chem. 46, 4294 – 4296 共1981兲; J. S. Chickos, D. G. Hesse, J. F. Liebman,
8. Acknowledgment and S. Y. Panshin, ibid. 53, 3424 –3429 共1988兲; J. S. Chickos, D. G.
Hesse, and J. F. Liebman, ibid. 54, 5250–5256 共1989兲.
28
K. H. Myers and R. P. Danner, J. Chem. Eng. Data 38, 175–200 共1993兲.
J.S.C. would like to thank the past and present students in 29
L. Constantinou, S. E. Prickett, and M. L. Mavrovouniotis, Ind. Eng.
Chemistry 202, Introduction to the Chemical Literature, who Chem. Res. 32, 1734 –1746 共1993兲; 33, 395– 402 共1994兲.
30
L. Constantinou and R. Gani, AIChE J. 40, 1697–1710 共1994兲.
have contributed to this compilation through their term pa- 31
C. H. Tu and C. P. Liu, Fluid Phase Equilibria 121, 45– 65 共1996兲.
pers. 32
K. Sivaji and D. H. L Prasad, Trans I. Chem. E. A76, 970–972 共1998兲.
33
K. U. Goss and R. P. Schwarzenbach, Environ. Sci. Techn. 33, 3390–3393
共1999兲.
9. References for Introductory Material 34
I. B. Golovanov and I. G. Tsygankova, Russ. J. Gen. Chem. 69, 1227–
1233 共1999兲.
1
J. B. Pedley, R. D. Naylor, and S. P. Kirby, Thermochemical Data of 35
J. Marrero and R. Gani, Fluid Phase Equilibria 183 共Special Issue兲, 183–
Organic Compounds, 2nd ed. 共Chapman and Hall, London, 1986兲. 208, 共2001兲.
2
W.-Y. Shiu and K.-C. Ma, J. Phys. Chem. Ref. Data 29, 1–130 共2000兲; 29, 36
A. P. Kudchadker and B. J. Zwolinski, J. Chem. Eng. Data 11, 253–255
387– 462 共2000兲; A. J. Delle Site, ibid. 26, 157–193 共1997兲. 共1966兲.
3
S. Puri, J. S. Chickos, and W. Welsh, Anal. Chem. 73, 1480–1484 共2001兲; 37
J. C. M. Li and F. D. Rossini, J. Chem. Eng. Data 6, 268 –270 共1961兲.