Rule-Based Trial Wave Functions for Generalized Valence Bond Theory
Jean-Marc Langlois, Terumasa Yamasaki, Richard P. Muller, William A. Goddard III
Abstract
We present a general method suitable for automatic generation of trial wave functions for generalized valence bond (GVB) descriptions of large molecules. This method uses pseudo-Hartree-Fock (P-HF) molecular orbitals formed from HF atomic orbitals but without Fock matrix diagonalization. The occupied P-HF orbitals are projected onto atomic basis functions to obtain GVB first natural orbitals, and the unoccupied HF orbitals are projected to obtain GVB second natural orbitals. This method (denoted GVB-INIT) is fast because no HF wave functions need be calculated and because the localization is piecewise atomic. In conjunction with the recently developed GVB-DIIS method for converging GVB wave functions and the new pseudospectral programs (PS-GVB) for the Fock matrix elements, GVB-INIT makes calculation of highly correlated GVB wave functions quite practical. The efficacy of GVB-INIT is illustrated by application to several cases including GVB wave functions with up to 26 correlated pairs.
Group Members
Langlois, J., Yamasaki, T., Muller, R. P., & III, W. A. G. (1994). Rule-Based Trial Wave Functions for Generalized Valence Bond Theory. *J. Phys. Chem.*, *98*(51), 13498-13505. https://doi.org/10.1021/j100102a012