Approximation multi-configuration

Kosloff R and Hammerich A D 1991 Nonadiabatic reactive routes and the applicability of multi configuration time dependent self consistent field approximations Feredey Discuss. Chem. Soc. 91 239-47... 

Many-body calculations which go beyond the Hartree-Fock model can be performed in two ways, i.e. using either a variational or a perturbational procedure. There are a number of variational methods which account for correlation effects superposition-of-configurations (or configuration interaction (Cl)), random phase approximation with exchange, method of incomplete separation of variables, multi-configuration Hartree-Fock (MCHF) approach, etc. However, to date only Cl and MCHF methods and some simple versions of perturbation theory are practically exploited for theoretical studies of many-electron atoms and ions. 

We have thus arrived at the expansion of the two-particle operator in terms of irreducible tensorial products having certain ranks in relation to the total and quasispin angular momenta of both subshells. This representation of two-particle operators can conveniently be used for the form of multi-configuration approximation in which the wave function of two subshells is constructed using the vectorial coupling scheme for quasispin angular momenta of individual subshells... 

Thus, the use of wave function in the form (23.67) and operators in the form (23.62)—(23.66) makes it possible to separate the dependence of multi-configuration matrix elements on the total number of electrons using the Wigner-Eckart theorem, and to regard this form of superposition-of-configuration approximation itself as a one-configuration approximation in the space of total quasispin angular momentum. 

Expressions (29.8) and (29.9) are the Hartree-Fock equations in a multi-configurational approximation [222], or the Hartree-Fock-Jucys equations. They must be solved together with the equations... 

The accurate calculation of these molecular properties requires the use of ab initio methods, which have increased enormously in accuracy and efficiency in the last three decades. Ab initio methods have developed in two directions first, the level of approximation has become increasingly sophisticated and, hence, accurate. The earliest ab initio calculations used the Hartree-Fock/self-consistent field (HF/SCF) methodology, which is the simplest to implement. Subsequently, such methods as Mpller-Plesset perturbation theory, multi-configuration self-consistent field theory (MCSCF) and coupled-cluster (CC) theory have been developed and implemented. Relatively recently, density functional theory (DFT) has become the method of choice since it yields an accuracy much greater than that of HF/SCF while requiring relatively little additional computational effort. 

The multi configuration time dependent self consistent field approximation (MCTDSCF)... 

An approximation which is convergent to the exact solution of the time-dependent Schrddinger equation can be generated with the multi configuration time dependent SCF scheme. Therein the summation in eq. (3) is truncated to a finite number N... 

Werner and co-workers [2, 21, 34] used internally-contracted multi-reference configuration-interaction (IC-MRCI) calculations, based on state-averaged (three-state) multi-configuration, self-consistent-field (MCSCF) calculations with large atomic orbital basis sets, to determine the three electronically adiabatic C1(F)+H2 PESs in the reactant arrangement L4, 2A, and lA. These all correlate with X( P) + H2. These three adiabatic electronic states are the IC-MRCI approximations to the three lowest eigenfunctions of Hgi, namely... 

A conceptually straightforward improvement on the CI approximation is to reoptimize the molecular orbitals for a truncated CI expansion. This approach is called multi-configuration self-consistent field method (MCSCF) and its most prominent variant is the complete active space SCF method (CASSCF) [64]. In the first generation of MCSCF methods [65, 66], the CI coefficients C/ in Eq. 

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