Chemical insights into the electronic structure of Fe( <scp>II</scp> ) porphyrin using <scp>FCIQMC</scp> , <scp>DMRG</scp> , and generalized active spaces
Oskar Weser, Leon Freitag, Kai Guther, Ali Alavi, Giovanni Li Manni
Abstract
Abstract Stochastic‐CASSCF and DMRG procedures have been utilized to quantify the role of the electron‐correlation mechanisms that, in an Fe‐porphyrin model system, are responsible for the differential stabilization of the 3 E g over the 5 A 1 g state. Orbital entanglement diagrams and CI coefficients of the wave function in a localized orbital basis allow for an effective interpretation of the role of charge‐transfer configurations. A preliminary version of the Stochastic Generalized Active Space Self‐Consistent Field method has been developed and is here introduced to further assess the π backdonation stabilizing effect. 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 π backdonation.