Frozen localized molecular orbitals in electron correlation calculations – Exploiting the Hartree–Fock density matrix

Abstract

The Hartree–Fock density matrix is used to generate occupied and virtual molecular orbitals localized on a selected (active) region within a molecule. The orbitals are well suited for high level description of electron correlation in the active site. Orbitals outside the active site are not constructed explicitly, they provide a frozen core for the correlation calculation. Standard correlation methods are straightforward to apply and result local correlation energies. Transforming to locally canonical orbitals facilitates an iteration-free evaluation of local Møller–Plesset(MP n) energies. Selection of active orbitals does not produce dangling bonds since no chemical bonds are cut at the boundary.