Assessment of semiempirical methods for the photoisomerisation of a protonated Schiff base

摘要

The potential energy surfaces and non-adiabatic dynamics of the C5H6NH 2 + protonated Schiff base (PSB3) have been investigated using the OM2 semiempirical Hamiltonian with GUGA configuration interaction. Three approaches to selecting the GUGA-CI active space are evaluated using closed-shell and open-shell molecular orbitals. Energy minima and minimum energy crossing points (MECPs) have been compared with ab initio CASSCF and CASPT2 results. Only the open-shell calculations give a qualitatively correct MECP. Minimum energy path (MEP) calculations demonstrate that a minimal active space gives a barrierless path from the planar S1 minimum to the ground state, whereas larger active spaces result in a small barrier to torsional motion. Surface hopping dynamics calculations indicate that this barrier induces bi-exponential dynamics. The comparable CASSCF S1 energy surface is barrierless, but the CASPT2 surface features an energy plateau, which may also lead to more complex dynamics.