Role of the one-body Jastrow factor in the transcorrelated self-consistent field equation

2006 ◽  
Vol 106 (7) ◽  
pp. 1477-1486 ◽  
Author(s):  
Naoto Umezawa ◽  
Toyohiro Chikyow

1—The method of the self-consistent field for determining the wave functions and energy levels of an atom with many electrons was developed by Hartree, and later derived from a variation principle and modified to take account of exchange and of Pauli’s exclusion principle by Slater* and Fock. No attempt was made to consider relativity effects, and the use of “ spin ” wave functions was purely formal. Since, in the solution of Dirac’s equation for a hydrogen-like atom of nuclear charge Z, the difference of the radial wave functions from the solutions of Schrodinger’s equation depends on the ratio Z/137, it appears that for heavy atoms the relativity correction will be of importance; in fact, it may in some cases be of more importance as a modification of Hartree’s original self-nsistent field equation than “ exchange ” effects. The relativistic self-consistent field equation neglecting “ exchange ” terms can be formed from Dirac’s equation by a method completely analogous to Hartree’s original derivation of the non-relativistic self-consistent field equation from Schrodinger’s equation. Here we are concerned with including both relativity and “ exchange ” effects and we show how Slater’s varia-tional method may be extended for this purpose. A difficulty arises in considering the relativistic theory of any problem concerning more than one electron since the correct wave equation for such a system is not known. Formulae have been given for the inter-action energy of two electrons, taking account of magnetic interactions and retardation, by Gaunt, Breit, and others. Since, however, none of these is to be regarded as exact, in the present paper the crude electrostatic expression for the potential energy will be used. The neglect of the magnetic interactions is not likely to lead to any great error for an atom consisting mainly of closed groups, since the magnetic field of a closed group vanishes. Also, since the self-consistent field type of approximation is concerned with the interaction of average distributions of electrons in one-electron wave functions, it seems probable that retardation does not play an important part. These effects are in any case likely to be of less importance than the improvement in the grouping of the wave functions which arises from using a wave equation which involves the spins implicitly.


2020 ◽  
Author(s):  
Oskar Weser ◽  
Leon Freitag ◽  
Kai Guther ◽  
Ali Alavi ◽  
Giovanni Li Manni

<div>Stochastic-CASSCF and DMRG procedures have been utilized to quantify the role of the electron correlation mechanisms that in a Fe-porphyrin model system are responsible for the differential stabilization of the triplet over the quintet state. Orbital entanglement diagrams and CI-coefficients of the wave function in a localised orbital basis allow for an effective interpretation of the role of charge-transfer configurations. A preliminary version of the <i>Stochastic Generalized Active Space Self-Consistent Field</i> method has been developed and is here introduced to further assess the pi-backdonation stabilizing effect.</div><div>By the new method excitations between metal and ligand orbitals can selectively be removed from the complete CI expansion. It is demonstrated that these excitations are key to the differential stabilization of the triplet, effectively leading to a quantitative measure of the correlation enhanced pi-backdonation.</div><div><br></div>


1983 ◽  
Vol 61 (10) ◽  
pp. 2310-2315 ◽  
Author(s):  
Danial D. M. Wayner ◽  
Russell J. Boyd ◽  
Donald R. Arnold

The nature of the one-electron two-centre bond in the cyclopropane and 1,2-divinylcyclopropane radical cations is elucidated by use of abinitio self consistent field (SCF) molecular orbital (MO) calculations. The charge and spin distributions in the 90,90 and 90,0 conformations are compared at the STO-3G and 4-31G basis set levels. From energy differences between the radical cations in the 90,90 conformation and the 90,0 (transition state) conformation, the activation barriers for cis–trans isomerization in the 2A1 state of C3H6,+ and of the 1,2-divinylcyclopropane radical cation are estimated. These results are compared to previous calculations and experimental data where possible.


2015 ◽  
Vol 17 (18) ◽  
pp. 12356-12364
Author(s):  
Martina Zámečníková ◽  
Dana Nachtigallová

The role of the bridging water molecules has been studied during the excited state photodynamics of a N-methylformamide dimer in complex with water molecules employing the complete active space self-consistent field (CASSCF) and CAS perturbation theory (CASPT2) methods.


1997 ◽  
Vol 11 (32) ◽  
pp. 3733-3750 ◽  
Author(s):  
Akihiro Sano ◽  
Mikio Eto ◽  
Hiroshi Kamimura

In this paper we first describe the multi-configuration self-consistent field method with configuration interaction (MCSCF-CI) which is a variational method most suitable for strongly-correlated cluster systems. Then the calculated results of CuO 6 cluster embedded in hole-doped La 2-x Sr x CuO 4 and of CuO 4 cluster in the electron-doped Nd 2-x Ce x CuO 4 are reviewed. Finally the calculated results on the electronic structure of CuO 5 pyramid embedded in the insulating YBa 2 Cu 3 O 6 and superconducting YBa2Cu3O7 are newly presented. In the latter case we will clarify an important role of the Cu-O chain in the electronic and superconducting state of YBa2Cu3O7 .


1999 ◽  
Vol 576 ◽  
Author(s):  
Anna C. Balazs ◽  
Chandralekha Singh ◽  
Valeriy V. Ginzburg

ABSTRACTWe analyze the thermodynamics of polymer-clay mixtures within the framework of density functional theory (DFT). The interaction potential between clay particles is calculated using the self-consistent field (SCF) method and is strongly dependent on the length and density of grafted short-chain organic modifiers. By combining the DFT and SCF techniques, we determine the role of the grafted chains on the equilibrium phase behavior of the mixtures.


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