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E-BookEPUB2 - DRM Adobe / EPUBE-Book
240 Seiten
Englisch
John Wiley & Sonserschienen am03.08.20161. Auflage
The first book to aid in the understanding of multiconfigurational quantum chemistry, Multiconfigurational Quantum Chemistry demystifies a subject that has historically been considered difficult to learn. Accessible to any reader with a background in quantum mechanics and quantum chemistry, the book contains illustrative examples showing how these methods can be used in various areas of chemistry, such as chemical reactions in ground and excited states, transition metal and other heavy element systems. The authors detail the drawbacks and limitations of DFT and coupled-cluster based methods and offer alternative, wavefunction-based methods more suitable for smaller molecules.

Björn O. Roos received his PhD inTheoretical Physics and is Professor Emeritus at Lund University. He is a former board member of the Swedish National Research Foundation, a member of the Swedish Royal Academy of Sciences, the Nobel Committee for Chemistry, the International Academy of Quantum Molecular Sciences, and is on the advisory editorial board for Chemical Physics Letter, Molecular Physics, International Journal of Quantum Chemistry, and Chemical Physics Physical Chemistry. Dr. Roos is the author of approximately 300 peer-reviewed articles in international journals, various book chapters, and is editor and co-author of text books for the European Summer School in Quantum Chemistry.mehr
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Produkt

KlappentextThe first book to aid in the understanding of multiconfigurational quantum chemistry, Multiconfigurational Quantum Chemistry demystifies a subject that has historically been considered difficult to learn. Accessible to any reader with a background in quantum mechanics and quantum chemistry, the book contains illustrative examples showing how these methods can be used in various areas of chemistry, such as chemical reactions in ground and excited states, transition metal and other heavy element systems. The authors detail the drawbacks and limitations of DFT and coupled-cluster based methods and offer alternative, wavefunction-based methods more suitable for smaller molecules.

Björn O. Roos received his PhD inTheoretical Physics and is Professor Emeritus at Lund University. He is a former board member of the Swedish National Research Foundation, a member of the Swedish Royal Academy of Sciences, the Nobel Committee for Chemistry, the International Academy of Quantum Molecular Sciences, and is on the advisory editorial board for Chemical Physics Letter, Molecular Physics, International Journal of Quantum Chemistry, and Chemical Physics Physical Chemistry. Dr. Roos is the author of approximately 300 peer-reviewed articles in international journals, various book chapters, and is editor and co-author of text books for the European Summer School in Quantum Chemistry.
Details
Weitere ISBN/GTIN9781119277880
ProduktartE-Book
EinbandartE-Book
FormatEPUB
Format Hinweis2 - DRM Adobe / EPUB
FormatFormat mit automatischem Seitenumbruch (reflowable)
Erscheinungsjahr2016
Erscheinungsdatum03.08.2016
Auflage1. Auflage
Seiten240 Seiten
SpracheEnglisch
Dateigrösse15770 Kbytes
Artikel-Nr.3263183
Rubriken
Genre9201

Inhalt/Kritik

Leseprobe
Chapter 1
Introduction

How do we define multiconfigurational (MC) methods? It is simple. In Hartree-Fock (HF) theory and density functional theory (DFT), we describe the wave function with a single Slater determinant. Multiconfigurational wave functions, on the other hand, are constructed as a linear combination of several determinants, or configuration state functions (CSFs)-each CSF is a spin-adapted linear combination of determinants. The MC wave functions also go by the name Configuration Interaction (CI) wave function. A simple example illustrates the situation. The molecule (centers denoted A and B) equilibrium is well described by a single determinant with a doubly occupied orbital:

1.1

where is the symmetric combination of the atomic hydrogen orbitals (; the antisymmetric combination is denoted as ). However, if we let the distance between the two atoms increase, the situation becomes more complex. The true wave function for two separated atoms is

1.2

which translates to the electronic structure of the homolytic dissociation products of two radical hydrogens. Two configurations, and , are now needed to describe the electronic structure. It is not difficult to understand that at intermediate distances the wave function will vary from Eq. 1.1 to Eq. 1.2, a situation that we can describe with the following wave function:

1.3

where and , the so-called CI-coefficients or expansion coefficients, are determined variationally. The two orbitals, and , are shown in Figure 1.1, which also gives the occupation numbers (computed as and ) at a geometry close to equilibrium. In general, Eq. 1.3 facilitates the description of the electronic structure during any bond dissociation, be it homolytic, ionic, or a combination of the two, by adjusting the variational parameters and accordingly.

Figure 1.1 The and orbitals and associated occupation numbers in the molecule at the equilibrium geometry.

This little example describes the essence of multiconfigurational quantum chemistry. By introducing several CSFs in the expansion of the wave function, we can describe the electronic structure for a more general situation than those where the wave function is dominated by a single determinant. Optimizing the orbitals and the expansion coefficients, simultaneously, defines the approach and results in a wave function that is qualitatively correct for the problem we are studying (e.g., the dissociation of a chemical bond as the example above illustrates). It remains to describe the effect of dynamic electron correlation, which is not more included in this approach than it is in the HF method.

The MC approach is almost as old as quantum chemistry itself. Maybe one could consider the Heitler-London wave function [1] as the first multiconfigurational wave function because it can be written in the form given by Eq. 1.2. However, the first multiconfigurational (MC) SCF calculation was probably performed by Hartree and coworkers [2]. They realized that for the state of the oxygen atom, there where two possible configurations, and , and constructed the two configurational wave function:

1.4

The atomic orbitals were determined (numerically) together with the two expansion coefficients. Similar MCSCF calculations on atoms and negative ions were simultaneously performed in Kaunas, Lithuania, by Jucys [3]. The possibility was actually suggested already in 1934 in the book by Frenkel [4]. Further progress was only possible with the advent of the computer. Wahl and Das developed the Optimized Valence Configuration (OVC) Approach, which was applied to diatomic and some triatomic molecules [5, 6].

An important methodological step forward was the formulation of the Extended Brillouin's (Brillouin, Levy, Berthier) theorem by Levy and Berthier [7]. This theorem states that for any CI wave function, which is stationary with respect to orbital rotations, we have

1.5

where is an operator (see Eq. 9.32) that gives a wave function where the orbitals and have been interchanged by a rotation. The theorem is an extension to the multiconfigurational regime of the Brillouin theorem, which gives the corresponding condition for an optimized HF wave function. A forerunner to the BLB theorem can actually be found already in Löwdin's 1955 article [8, 9].

The early MCSCF calculations were tedious and often difficult to converge. The methods used were based on an extension of the HF theory formulated for open shells by Roothaan [10]. An important paradigm change came with the Super-CI method, which was directly based on the BLB theorem [11]. One of the first modern formulations of the MCSCF optimization problem was given by Hinze [12]. He also introduced what may be called an approximate second-order (Newton-Raphson) procedure based on the partitioning: , where is the unitary transformation matrix for the orbitals and is an anti-Hermitian matrix. This was later to become . The full exponential formulation of the orbital and CI optimization problem was given by Dalgaard and Jørgensen [13]. Variations in orbitals and CI coefficients were described through unitary rotations expressed as the exponential of anti-Hermitian matrices. They formulated a full second-order optimization procedure (Newton-Raphson, NR), which has since then become the standard. Other methods (e.g., the Super-CI method) can be considered as approximations to the NR approach.

One of the problems that the early applications of the MCSCF method faced was the construction of the wave function. It was necessary to keep it short in order to make the calculations feasible. Thus, one had to decide beforehand which where the most important CSFs to include in the CI expansion. Even if this is quite simple in a molecule like , it quickly becomes ambiguous for larger systems. However, the development of more efficient techniques to solve large CI problems made another approach possible. Instead of having to choose individual CSFs, one could choose only the orbitals that were involved and then make a full CI expansion in this (small) orbital space. In 1976, Ruedenberg introduced the orbital reaction space in which a complete CI expansion was used (in principle). All orbitals were optimized-the Fully Optimized Reaction Space-FORS [14].

An important prerequisite for such an approach was the possibility to solve large CI expansions. A first step was taken with the introduction of the Direct CI method in 1972 [15]. This method solved the problem of performing large-scale SDCI calculations with a closed-shell reference wave function. It was not useful for MCSCF, where a more general approach is needed that allows an arbitrary number of open shells and all possible spin-couplings. The generalization of the direct CI method to such cases was made by Paldus and Shavitt through the Graphical Unitary Group Approach (GUGA). Two papers by Shavitt explained how to compute CI coupling coefficients using GUGA [16, 17]. Shavitt's approach was directly applicable to full CI calculations. It formed the basis for the development of the Complete Active Space (CAS) SCF method, which has become the standard for performing MCSCF calculations [18, 19].

However, an MCSCF calculation only solves part of the problem-it can formulate a qualitatively correct wave function by the inclusion of the so-called static electron correlation. This determines the larger part of the wave function. For a quantitative correct picture, we need also to include dynamic electron correlation and its contribution to the total electronic energy. We devote a substantial part of the book to describe different methods that can be used. In particular, we concentrate on second-order perturbation theory with a CASSCF reference function (CASPT2). This method has proven to be accurate in many applications also for large molecules where other methods, such as MRCI or coupled cluster, cannot be used. The combination CASSCF/CASPT2 is the main computational tool to be discussed and illustrated in several applications.

This book mainly discusses the multiconfigurational approach in quantum chemistry; it includes discussions about the modern computational methods such as Hartree-Fock theory, perturbation theory, and various configuration interaction methods. Here, the main emphasis is not on technical details but the aim is to describe the methods, such that critical comparisons between the various approaches can be made. It also includes sections about the mathematical tools that are used and many different types of applications. For the applications presented in the last chapter of this book, the emphasis is on the practical problems associated with using the CASSCF/CASPT2 methods. It is hoped that the reader after finishing the book will have arrived at a deeper understanding of the CASSCF/CASPT2 approaches and will be able to use them with a critical mind.
1.1 References
[1] Heitler W, London F. Wechselwirkung neutraler Atome und homopolare Bindung nach der Quantenmechanik. Z Phys 1927;44:455-472.
[2] Hartree DR, Hartree W, Swirles B. Self-consistent field, including exchange and superposition of configurations, with some results for oxygen. Philos Trans R Soc London, Ser A 1939;238:229-247.
[3] Jucys A. Self-consistent field with exchange for carbon. Proc R Soc London, Ser A...
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