Quantum chemistry

Quantum chemistry is a branch of chemistry whose primary focus is the application of quantum mechanics in physical models and
experiments of chemical systems. It is also called molecular quantum mechanics.

Contents
Overview
History
Electronic structure
Wave model
Valence bond
Molecular orbital
Density functional theory
Chemical dynamics
Adiabatic chemical dynamics
Non-adiabatic chemical dynamics
See also
References
External links

Overview
Experimental quantum chemists rely heavily on spectroscopy, through which information regarding the quantization of energy on a
molecular scale can be obtained. Common methods are infra-red (IR) spectroscopy, nuclear magnetic resonance (NMR)
spectroscopy, and scanning probe microscopy.

Theoretical quantum chemistry, the workings of which also tend to fall under the category of computational chemistry, seeks to
calculate the predictions of quantum theory as atoms and molecules can only have discrete energies; as this task, when applied to
polyatomic species, invokes the many-body problem, these calculations are performed using computers rather than by analytical
"back of the envelope" methods.

It involves heavy interplay of experimental and theoretical methods. In these ways, quantum chemists investigate chemical
phenomena.

Quantum chemistry studies theground state of individual atoms and molecules, and the excited states, and transition states that occur
during chemical reactions.

On the calculations, quantum chemical studies use also semi-empirical and other methods based on quantum mechanical principles,
and deal with time dependent problems. Many quantum chemical studies assume the nuclei are at rest (Born–Oppenheimer
approximation). Many calculations involve iterative methods that include self-consistent field methods. Major goals of quantum
chemistry include increasing the accuracy of the results for small molecular systems, and increasing the size of large molecules that
can be processed, which is limited by scaling considerations—the computation time increases as a power of the number of atoms.

History
Some view the birth of quantum chemistry as starting with the discovery of the Schrödinger equation and its application to the
hydrogen atom in 1926. However, the 1927 article of Walter Heitler (1904-1981) and Fritz London, is often recognized as the first
milestone in the history of quantum chemistry. This is the first application of quantum mechanics to the diatomic hydrogen molecule,
and thus to the phenomenon of the chemical bond. In the following years much progress was accomplished by Edward Teller, Robert
S. Mulliken, Max Born, J. Robert Oppenheimer, Linus Pauling, Erich Hückel, Douglas Hartree, Vladimir Fock, to cite a few. The
history of quantum chemistry also goes through the 1838 discovery of cathode rays by Michael Faraday, the 1859 statement of the
black body radiation problem by Gustav Kirchhoff, the 1877 suggestion by Ludwig Boltzmann that the energy states of a physical
system could be discrete, and the 1900 quantum hypothesis by Max Planck that any energy radiating atomic system can theoretically
be divided into a number of discrete energy elements ε such that each of these energy elements is proportional to the frequency ν with
which they each individually radiate energy and a numerical value called Planck’s Constant. Then, in 1905, to explain the
photoelectric effect (1839), i.e., that shining light on certain materials can function to eject electrons from the material, Albert
Einstein postulated, based on Planck’s quantum hypothesis, that light itself consists of individual quantum particles, which later came
to be called photons (1926). In the years to follow, this theoretical basis slowly began to be applied to chemical structure, reactivity,
and bonding. Probably the greatest contribution to the field was made byLinus Pauling.

Electronic structure
The first step in solving a quantum chemical problem is usually solving the Schrödinger equation (or Dirac equation in relativistic
quantum chemistry) with the electronic molecular Hamiltonian. This is called determining the electronic structure of the molecule. It
can be said that the electronic structure of a molecule or crystal implies essentially its chemical properties. An exact solution for the
Schrödinger equation can only be obtained for the hydrogen atom (though exact solutions for the bound state energies of the
hydrogen molecular ion have been identified in terms of the generalized Lambert W function). Since all other atomic, or molecular
systems, involve the motions of three or more "particles", their Schrödinger equations cannot be solved exactly and so approximate
solutions must be sought.

Wave model
The foundation of quantum mechanics and quantum chemistry is the wave model, in which the atom is a small, dense, positively
charged nucleus surrounded by electrons. The wave model is derived from the wave function, a set of possible equations derived
from the time evolution of the Schrödinger equation which is applied to the wavelike probability distribution of subatomic particles.
Unlike the earlier Bohr model of the atom, however, the wave model describes electrons as "clouds" moving in orbitals, and their
positions are represented by probability distributions rather than discrete points. The strength of this model lies in its predictive
power. Specifically, it predicts the pattern of chemically similar elements found in the periodic table. The wave model is so named
because electrons exhibit properties (such as interference) traditionally associated with waves. See wave-particle duality. In this
model, when we solve the Schrödinger Equation for an Hydrogenoid Atom, we obtain a solution that depends on some numbers,
called quantum numbers, that describes the orbital, the most probable space where an electron can be. These are n, the principal
quantum number, for the energy, l, or secondary quantum number, which correlates to the angular momentum, ml, for the orientation,
and ms the spin. This model can explain the new lines that appeared in the spectroscopy of atoms. For multielectron atoms we must
introduce some rules as that the electrons fill orbitals in a way to minimize the energy of the atom, in order of increasing energy, the
Pauli exclusion principle, Hund's rule, and the aufbau principle.

Valence bond
Although the mathematical basis of quantum chemistry had been laid by Schrödinger in 1926, it is generally accepted that the first
true calculation in quantum chemistry was that of the German physicists Walter Heitler and Fritz London on the hydrogen (H2)
molecule in 1927. Heitler and London's method was extended by the American theoretical physicist John C. Slater and the American
theoretical chemist Linus Pauling to become the valence-bond (VB) [or Heitler–London–Slater–Pauling (HLSP)] method. In this
method, attention is primarily devoted to the pairwise interactions between atoms, and this method therefore correlates closely with
classical chemists' drawings of bonds. It focuses on how the atomic orbitals of an atom combine to give individual chemical bonds
when a molecule is formed, incorporating the two key concepts oforbital hybridization and resonance.
Molecular orbital
An alternative approach was developed in 1929 by Friedrich Hund and Robert S. Mulliken, in which electrons are described by
mathematical functions delocalized over an entire molecule. The Hund–Mulliken approach or molecular orbital (MO) method is less
intuitive to chemists, but has turned out capable of predicting spectroscopic properties better than the VB method. This approach is
the conceptional basis of theHartree–Fock method and further post Hartree–Fock methods.

Density functional theory

The Thomas–Fermi model was developed independently by Thomas and Fermi in 1927. This was the first attempt to describe many-
electron systems on the basis of electronic density instead of wave functions, although it was not very successful in the treatment of
entire molecules. The method did provide the basis for what is now known as density functional theory (DFT). Modern day DFT uses
the Kohn-Sham method, where the density functional is split into four terms; the Kohn-Sham kinetic energy, an external potential,
exchange and correlation energies. A large part of the focus on developing DFT is on improving the exchange and correlation terms.
Though this method is less developed than post Hartree–Fock methods, its significantly lower computational requirements (scaling
typically no worse than n3 with respect to n basis functions, for the pure functionals) allow it to tackle larger polyatomic molecules
and even macromolecules. This computational affordability and often comparable accuracy to MP2 and CCSD(T) (post-Hartree–
Fock methods) has made it one of the most popular methods incomputational chemistry.

Chemical dynamics
A further step can consist of solving the Schrödinger equation with the total molecular Hamiltonian in order to study the motion of
molecules. Direct solution of the Schrödinger equation is called quantum molecular dynamics, within the semiclassical
approximation semiclassical molecular dynamics, and within the classical mechanics framework molecular dynamics (MD).
Statistical approaches, using for exampleMonte Carlo methods, are also possible.

Adiabatic chemical dynamics

In adiabatic dynamics, interatomic interactions are represented by single scalar potentials called potential energy surfaces. This is the
Born–Oppenheimer approximationintroduced by Born and Oppenheimer in 1927. Pioneering applications of this in chemistry were
performed by Rice and Ramsperger in 1927 and Kassel in 1928, and generalized into the RRKM theory in 1952 by Marcus who took
the transition state theory developed by Eyring in 1935 into account. These methods enable simple estimates of unimolecular reaction
rates from a few characteristics of the potential surface.

Non-adiabatic chemical dynamics

Non-adiabatic dynamics consists of taking the interaction between several coupled potential energy surface (corresponding to
different electronic quantum states of the molecule). The coupling terms are called vibronic couplings. The pioneering work in this
field was done by Stueckelberg, Landau, and Zener in the 1930s, in their work on what is now known as theLandau–Zener transition.
Their formula allows the transition probability between two diabatic potential curves in the neighborhood of an avoided crossing to
be calculated. Spin-forbidden reactions are one type of non-adiabatic reactions where at least one change in spin state occurs when
progressing from reactant to product.

See also
Atomic physics
Computational chemistry
Condensed matter physics
Car–Parrinello molecular dynamics
Electron localization function
International Academy of Quantum Molecular Science
 Molecular modelling
Physical chemistry
List of quantum chemistry and solid-state physics software
QMC@Home
Quantum Aspects of Life
Quantum electrochemistry
Relativistic quantum chemistry
Theoretical physics
Spin forbidden reactions

References
Atkins, P.W.; Friedman, R. (2005).Molecular Quantum Mechanics(4th ed.). Oxford University Press.ISBN 978-0-
19-927498-7.
Atkins, P.W. Physical Chemistry. Oxford University Press.ISBN 0-19-879285-9.
Atkins, P.W.; Friedman, R. (2008).Quanta, Matter and Change: A Molecular Approach to Physical Change .
ISBN 978-0-7167-6117-4.
Pullman, Bernard; Pullman, Alberte (1963).Quantum Biochemistry. New York and London: Academic Press.
ISBN 90-277-1830-X.
Scerri, Eric R. (2006). The Periodic Table: Its Story and Its Significance. Oxford University Press.ISBN 0-19-530573-
6. Considers the extent to which chemistry and especially the periodic system has been reduced to quantum
mechanics.
Kostas Gavroglu, Ana Simões:NEITHER PHYSICS NOR CHEMISTRY.A History of Quantum Chemistry, MIT Press,
2011, ISBN 0-262-01618-4
McWeeny, R. Coulson's Valence. Oxford Science Publications.ISBN 0-19-855144-4.
Karplus M., Porter R.N. (1971).Atoms and Molecules. An introduction for students of physical chemistry , Benjamin–
Cummings Publishing Company, ISBN 978-0-8053-5218-4
Szabo, Attila; Ostlund, Neil S. (1996).Modern Quantum Chemistry: Introduction to Advanced Electronic Structure
Theory. Dover. ISBN 0-486-69186-1.
Landau, L.D.; Lifshitz, E.M.Quantum Mechanics:Non-relativistic Theory. Course of Theoretical Physic.3. Pergamon
Press. ISBN 0-08-019012-X.
Levine, I. (2008). Physical Chemistry (6th ed.). McGraw–Hill Science.ISBN 978-0-07-253862-5.
Pauling, L. (1954). General Chemistry. Dover Publications. ISBN 0-486-65622-5.
Pauling, L.; Wilson, E. B. (1963) [1935].Introduction to Quantum Mechanics with Applications to Chemistry . Dover
Publications. ISBN 0-486-64871-0.
Simon, Z. (1976). Quantum Biochemistry and Specific Interactions . Taylor & Francis. ISBN 978-0-85626-087-2.

External links
The Sherrill Group – Notes
ChemViz Curriculum Support Resources
Early ideas in the history of quantum chemistry
The Particle Adventure

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