Dyes and Pigments 92 (2011) 573e579

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Dyes and Pigments

journal homepage: www.elsevier.com/locate/dyepig

Synthesis, optical properties and ultrafast dynamics of a 2,1,3-benzothiadiazole-

based red emitter with intense fluorescence and large two-photon absorption
cross-section
Yaochuan Wang a, b, Ju Huang c, Hui Zhou a, Guohong Ma d, Shixiong Qian a, *, Xu-hui Zhu c, **
a
Surface Physics Laboratory (State Key Laboratory), Physics Department, Fudan University, Shanghai 200433, People’s Republic of China
b
State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
c
State Key Laboratory of Physics and Chemistry of Luminescence and Institute of Polymer Optoelectronic Materials and Devices, South China University of Technology (SCUT),
Guangzhou 510640, People’s Republic of China
d
Physics Department, Shanghai University, Shanghai 200000, People’s Republic of China

a r t i c l e i n f o a b s t r a c t

Article history: A new 2,1,3-benzothiadiazole-based red fluorescent compound with a DeAeD type structure was
Received 31 October 2010 synthesized and characterized. The central 2,1,3-benzothiadiazole core was symmetrically connected via
Received in revised form the 4,7-positions with two donor groups in which the 7-position of a fluorenyl ring was substituted with
25 June 2011
a carbazol-9-yl moiety and the 2-position was substituted by a 5-thienyl moiety. The carbazol moieties
Accepted 27 June 2011
Available online 3 July 2011
were further derivatized by two 2-naphthyl moieties at the 3,6-positions. Femtosecond laser spectro-
scopic techniques including excited state fluorescence and pump-probe technique investigations,
together with steady state absorption and one-photon fluorescence spectra, were employed to
Keywords:
Two-photon absorption
systematically investigate the optical properties and ultrafast dynamics of the new compound in tetra-
Two-photon fluorescence hydrofuran solution. It shows a large two-photon absorption cross-section and high fluorescence
Excited state dynamics quantum yield, indicating potential application in two-photon fluorescence imaging field. The ultrafast
Intramolecular charge transfer dynamics results reveal competition between a pure excited state relaxation process and stimulated
Benzothiadiazole radiation in the red wavelength region.
Red emitter Ó 2011 Published by Elsevier Ltd.

1. Introduction 600w800 nm wavelength region, a window widely recognized as

being attractive for bio-analysis and in-vivo imaging, has become
Materials with large two-photon absorption (TPA) properties one of the major obstacles for these applications [13,14].
find a wide range of potential applications such as two-photon The 2,1,3-benzothiadiazole unit has been shown to be a conve-
fluorescence (TPF) imaging, optical limiting, optical data storage, nient electron acceptor and used to construct p-conjugated func-
phototherapy and up-conversion lasing [1e6]. Among them, TPF tional organic materials in organic optoelectronic devices [15e22].
imaging, which is usually under the excitation of picosend/femto- However, there are few reports about TPA materials using 2,1,3-
second pulses in the near infrared region, makes possible fluo- benzothiadiazole as an electron acceptor [10e12]. The TPA appli-
sescence images of living cells, biological tissue and other objects cations will greatly benefit from large TPA cross-section and
with high three-dimensional spatial resolution, reduced photo- excellent fluorescent properties of the active compound. Various
damage and low background fluorescence interference [7]. strategies for the design and synthesis of highly efficient two-
However, the commonly used fluorophores are mainly blue or photon active compounds have been proposed by manipulating
green emitters. Until now, investigations focused on the design and electron donor (D) and/or acceptor (A) properties and their incor-
synthesis of efficient red emitters are quite limited [8e12], and poration in a molecular architecture [23e26]. Two-photon excited
their applications are restricted by small TPA cross-sections or low fluorescence, Z-scan, degenerate four-wave mixing technique and
fluorescence quantum yields. The scarcity of excellent fluorophores many other techniques were employed to measure the TPA cross-
showing a large TPA cross-section and efficient TPF emission in section of materials [27e29].
In order to design and synthesize active compounds with large
TPA/TPF activities and to understand the intrinsic mechanisms,
* Corresponding author. Tel.: þ86 21 65642084; fax: þ86 21 65641344. a detailed investigation of the excited states is of great importance.
** Corresponding author. Tel.: þ86 20 87114346 15, fax: þ86 20 87110606. In the past years, we investigated the TPA properties and ultrafast
E-mail addresses: [email protected] (S. Qian), [email protected] (X.-h. Zhu). dynamics of several compounds [29,30].

0143-7208/$ e see front matter Ó 2011 Published by Elsevier Ltd.

doi:10.1016/j.dyepig.2011.06.032
574 Y. Wang et al. / Dyes and Pigments 92 (2011) 573e579

In this work, we report on the interesting TPA and TPF proper- (4 g, 12.3 mmol) in toluene (130 mL), aqueous Na2CO3 (2 M,
ties of a new 2,1,3-benzothiadiazole-based red emitter (Z) con- 52 mL) and ethanol (26 mL) under a nitrogen atmosphere. The
sisting of a DeAeD molecular structure (Fig. 1a). The n-octyl reaction was heated to reflux at 90  C for 24 h. After being cooled to
moieties at the 9,9-positions of the fluorenyl groups are used to room temperature, the mixture was diluted with distilled water.
improve the solubility of the resulting compound. The branched The organic layer was separated, dried over anhydrous MgSO4,
molecular structure could be useful to reduce intermolecular filtered and concentrated under reduced pressure. The residue was
interaction at a high solution concentration for instance in TPF purified by column chromatography with petroleum ether/
measurements, thus improving the fluorescence yield. dichloromethane (3:1) to afford a white solid after washing in
ethanol under reflux. Yield: 4.7 g (91%). TLC Rf (3:1 petroleum
2. Material and experimental section ether/dichloromethane v/v): 0.34. 1H NMR (300 MHz, CDCl3)
d (ppm): 7.46e7.56 (m, 6H), 7.82e89.00 (m, 10H), 8.13e8.18 (m,
2.1. Synthesis 3H), 8.55 (m, 2H). m.p. ¼ 265.4  C. Td ¼ >400  C (with 5% loss). IR
(KBr): 3420 cm1 (NeH stretch), 3046 cm1 (]CeH stretch), 1602,
Compound Z was readily synthesized by reaction of the Suzuki 1493 cm1 (eC]Ce stretch).
reagent 3 [31] with 4,7-bis(5-bromothiophen-2-yl)-2,1,3-
benzothiadiazole 4 via a conventional Suzuki coupling reaction 2.1.2. 9-(2-Bromo-9,9-dioctylfluoren-7-yl)-3,6-bis(2-naphthyl)
(Scheme 1). The 1H NMR spectrum was shown in Fig. 1b. carbazole (2)
A mixture of CuI (0.12 g, 0.67 mmol), 18-Crown-6 (0.058 g,
2.1.1. 3,6-Bis(2-naphthyl)carbazole (1) 0.22 mmol), K2CO3 (1.84 g, 13.36 mmol), 1,3-dimethyl-3,4,5,6-
Pd(PPh3)4 (224 mg, 0.19 mmol) was added to a mixture of 2- tetrahydro-2(1H)-pyrimidinone (DMPU) (2 mL), 2,7-dibromo- 9,9-
naphthylboronic acid (4.44 g, 25.8 mmol), 3,6-dibromocarbazole dioctylfluorene (5.4 g, 10.1 mmol) and compound 1 (2.8 g,

Fig. 1. a) Molecular structure of compound Z; b) 1H NMR spectrum.

 Y. Wang et al. / Dyes and Pigments 92 (2011) 573e579 575

Scheme 1. Synthetic route to compound Z. i) Pd(PPh3)4, 2M Na2CO3 aqueous solution, toluene, ethanol, reflux; ii) DMPU, 18-crown-6, CuI, K2CO3; iii) n-BuLi, THF, 78  C, iv)
2-isopropoxy-4,4,5,5- tetramethyl-1,3,2-dioxaboralane.

6.68 mmol) was heated at 170  C for 24 h under nitrogen. After being 2.1.4. Compound Z
cooled to room temperature, the mixture was quenched with 1N HCl Synthesized from compound 3 and 4,7-bis(5-bromothiophen-
and extracted with dichloromethane. The combined organic phase 2-yl)-2,1,3-benzothiadiazole (4) according to the procedure
was washed with water, dried over anhydrous MgSO4, filtered and described for 1. TLC Rf (4:1 petroleum ether/dichloromethane v/v):
concentrated under reduced pressure. The crude product was purified 0.23. 1H NMR (300 MHz, CDCl3) d (ppm): 0.8e0.93 (m, 20H),
by column chromatography with petroleum ether/dichloromethane 1.1e1.26 (m, 40H), 2.10e2.15 (m, 8H), 7.47e8.00 (m, 48H),
to afford a white solid. Yield: 3.66 g (64%). TLC Rf (6:1 petroleum ether/ 8.19e8.21 (m, 6H), 8.61e8.62 (m, 4H). Elemental analysis (%) calcd.
dichloromethane v/v): 0.32. 1H NMR (300 MHz, CDCl3) d (ppm): for C136H126N4S3: C, 85.40; H, 6.64; N, 2.93; S, 5.03. found: C,
0.78e0.89 (m, 10H), 1.15e1.27 (m, 20H), 1.99e2.01 (m, 4H), 7.45e8.00 85.00; H, 6.66; N, 2.62; S, 4.94. Tg ¼ 116  C (observed in the first
(m, 22H), 8.20 (s, 2H), 8.60 (d, 2H, J ¼ 1.6 Hz). Td ¼ >220  C (with 5% heating run), m.p. ¼ 250  C. IR (KBr): 3051 cm1(]CeH stretch),
loss). IR (KBr): 3044 cm1 (]CeH stretch), 2923, 2851 cm1 2923, 2851 cm1 (eCH2e, eCH3 stretch), 1474 cm1(eC]Ce).
(eCH2e, eCH3 stretch), 1487 cm1(eC]Ce).
2.2. Experimental methods
2.1.3. 7-(3,6-Bis(2-naphthyl)carbazol-9-yl)-9,9-dioctylfluoren-2-
ylboronic pinacol ester (3) The UVevisible absorption spectra of compound Z in tetrahy-
A solution of n-BuLi in hexanes (2.5 M, 2.1 ml, 5.2 mmol) was drofuran (THF) and in the solid state were obtained on a HP 8453
slowly added to a solution of. compound 2 (3.5 g, 4 mmol) in dry THF spectrophotometer. One-photon fluorescence spectra were
(35 mL) at 78  C under nitrogen. The mixture was stirred for measured by using a JobineYvon spectrofluorometer JY Fluorolog-
30 min at this temperature, and then 2-isopropoxy-4,4,5,5- 3 spectrofluorometer.
tetramethyl- 1,3,2-dioxaborolane (1.08 mL, 5.2 mmol) was added. The TPA spectrum was obtained by using the TPF method with
The reaction mixture was stirred for 12 h under nitrogen whilst Rhodamine B as the reference [32]. The ultrafast dynamics were
gradually warming to room temperature. A portion of distilled water measured by using a femtosecond (fs) pump-probe technique
was added. The organic phase was extracted into dichloromethane, which was described in the previous work [33,34]. The TPF spectra
dried over anhydrous MgSO4, filtered and concentrated under were recorded by a fiber spectrometer (TRISTAN). Femtosecond
reduced pressure. The residue was purified by silica chromatog- pulses employed for TPA measurement were generated by a mode-
raphy using petroleum ether/dichloromethane (4:1 v/v) as the locked Ti-sapphire laser system (OPA, Spectra-physics), with the
eluent to afford a white solid. Yield: 2.98 g (81%). TLC Rf (4:1 repetition rate of 1 kHz, the pulse duration of 150 fs, and the
petroleum ether/dichloromethane v/v): 0.52. 1H NMR (300 MHz, wavelength from 650 nm to 810 nm. Pulses employed for ultrafast
CDCl3) d (ppm): 0.76e0.91 (m,10H), 1.01e1.27 (m, 20H),1.42 (s, 12H), dynamics measurements were generated by spitfire stage of a fs
2.02e2.19 (m, 4H), 7.48e8.01 (m, 22H), 8.20 (s, 2H), 8.60 (d, 2H). system, with 140 fs pulse duration, 1 kHz repetition rate and about
576 Y. Wang et al. / Dyes and Pigments 92 (2011) 573e579

300 mW average output power. All the measurements were carried Table 1
out at room temperature. Optical properties of compound Z in THF solution and as film.

labsa (nm) lflub Dsc fd lTPEe s810f smaxg

(nm) (nm) (nm) (GM) (GM)
3. Results and discussions
340/373/515 625 90 0.36 477/645 310 2103
(solution)
3.1. Linear absorption and one-photon fluorescence spectra 342/374/530 671 141
(solid)
The linear absorption spectra and one-photon fluorescence a
Peak wavelengths of absorption spectra.
emission spectra of compound Z in THF solution and in the solid b
The peak wavelength of one-photon fluorescence.
c
state are shown in Fig. 2. The solid state film on quartz was spin- Stokes shift are calculated from the absorption and one photon fluorescence
spectra.
cast from tolunene solution [31]. The relevant properties are d
Fluorescence quantum yield measured in THF.
summarized in Table 1. When dissolved in THF solution (ca. e
The peak wavelength of fluorescence by two-photon exciting.
105 mol L1), the absorption band at 515 nm could be attributed to f
TPA cross section measured by TPF methods at wavelength of 810 nm.
the charge-transfer transition between the terminal electron-donor g
Peak two-photon absorptivity in GM (1050 cm4 s photon1).
moieties and the central electron-accepting 2,1,3-benzothiadiazole
core [11]. The emission peak is at 625 nm. However, the absorption
and emission maxima are red-shifted to 530 nm and 671 nm in the TPA cross-section of sample can be calculated by Equation (1), in
solid film, respectively, which could be caused by the increased which the subscripts s and r stand for the sample and reference
intermolecular interaction and the structural rigidification of the compound, respectively.
chromorphore molecule [19,35].
ss ¼ sr ðSs =Sr ÞðFr =Fs Þðfr =fs Þðcr =cs Þ (1)
S is the integral area of the detected two-photon induced fluores-
3.2. Two-photon fluorescence and two-photon cross-section
cence signal, F is the fluorescence quantum yield. f is the overall
fluorescence collection efficiency, c is the molar concentration. In
Compound Z emits intense red up-conversion fluorescence
the measurement, the collection efficiencies of sample and refer-
under the excitation of fs pulses at wavelength of 800 nm. Fig. 3a
ence compounds were nearly the same. The two-photon fluores-
shows the fluorescence spectra of compound Z in THF solution
cence excitation spectrum of compound Z is shown in Fig. 3b. The
under different excitation power densities of fs pulses, the inset
TPA cross-section at wavelength of 810 nm was determined to be
being the fluorescence intensity versus the square of the excitation
310 GM. When the wavelength was tuned to shorter wavelength,
power density, confirming that the strong fluorescence emission is
the value of the TPA cross-section increased gradually. The TPA
indeed generated by the TPA process. It should be noticed that, the
cross-section at 650 nm was measured to be 2103 GM. Due to the
TPF spectrum of compound Z features two emission peaks. The
wavelength limitation of the fs laser system, we cannot measure
shorter wavelength peak located at 477 nm should be attributed to
the values at the region shorter than 650 nm. Even though, the
the transition from the first excited state S1 to the ground state S0.
measured value of the TPA cross-section of our compound at
The longer emission peak located at 645 nm shows a 20 nm red-
650 nm is much larger than those of 2,1,3-benzothiadiazole based
shift in comparison to that in one-photon fluorescence spectrum.
derivatives reported recently in literature [10e12], indicating that
This red shift would be attributed to the reabsorption effect [36], as
our molecular design for the improvement of the TPF property is
we used a much higher concentration (0.01 M) of Z in the TPF
effective.
measurement than that used in one-photon experiment.
The fluorescence quantum yield was determined to be 0.36 in
THF solution using Rhodamine B as reference (F ¼ 0.64 in ethanol, 3.3. Ultrafast excited state dynamics
excited at 510 nm), similar to those of the analogue emitters
reported earlier [31]. We measured the TPA cross-section of In order to investigate the excited state relaxation process as
compound Z determined by the TPF method uses fs pulses at well as the nature of the ICT properties, a femtosecond pump-probe
650e810 nm with Rhodamine B in ethanol as the reference. The experiment was carried out. A portion of the 800 nm laser beam
was used to generate a white-light supercontinuum to provide the
probe pulses, another portion was frequency-doubled to 400 nm by
a 0.5 mm thick beta-barium borate crystal to generate pump pulses.

Fig. 3. a) TPF spectra of compound Z under different excitation power densities. Inset
Fig. 2. The linear absorption and steady-state fluorescence spectra of compound Z, is TPF intensity versus the square of the excitation power density. b) Two-photon
including the solution in THF solution and thin film. absorption spectrum of compound Z in 650e810 nm region.
 Y. Wang et al. / Dyes and Pigments 92 (2011) 573e579 577

The polarization of the pump beam was set to be perpendicular

with respect to that of the probe beam in order to sample pure
depopulation dynamics. The evolution of fs transient absorption
spectra of compound Z in THF solution pumped by 400 nm pulses is
shown in Fig. 4a, and the transient absorption spectra at time
delays of 0 ps and 100 ps between pump and probe pulse are
shown in Fig. 4b.
At an initial time delay of 0 ps, a transient photobleaching region
around 450e675 nm and a transient photoabsorption region
beyond 675 nm are observed. The photoabsorption region is
attributed to the absorption of the excited state, and the photo-
bleaching region is mainly caused by stimulated emission of fluo-
rescence. At the delay time of 100 ps, in the wavelength regions of
45e575 nm, 625e700 nm and below 425 nm, the compound
shows photobleaching behavior, whereas a photoabsorption signal
is observed in the other wavelength regions, for instance, between
575 and 625 nm.
Fig. 5 shows the decay traces at several representative probe
wavelengths. The calculated time constants are summarized in
Table 2. Very different decay properties were observed at different
probe wavelengths. At a wavelength of 400 nm, the dynamics of
compound Z is dominated by a very long photoabsorption process.
When the probe wavelength was tuned to 435 nm, a weak
bleaching peak emerged, together with a long (>1000 ps) and
relatively weak photoabsorption component. When the probe
pulses were tuned to even longer wavelength, the photobleaching
peak was firstly strengthened, and finally evolved into a sharp
photoabsorption peak at wavelength longer than 670 nm. The
long process shows a photobleaching feature in wavelength range
of 450e700 nm (except 560e610 nm). When the probe wave-
length was tuned from 700 to 800 nm, the long photoabsorption
process of dynamics was strengthened gradually. It has been
Fig. 4. a) The evolution of fs transient absorption spectra of compound Z in THF noted in literature that the rise and decay dynamics of the fluo-
solution pumped by 400 nm pulses; b) transient absorption spectra at time delays of rescence (photobleaching signal) show obvious wavelength
0 ps and 100 ps between pump and probe pulse.

Fig. 5. Dynamics decay traces for compound Z in THF at different probe wavelengths.
578 Y. Wang et al. / Dyes and Pigments 92 (2011) 573e579

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