Theoretical study of the electronic structure of MCH2+(M=Fe,Co,Ni)

摘要

State of the art coupled cluster (CC) methods are applied to accurately characterize the ground state electronic structure and photoelectron spectra of transition metal carbene ions MCH2+ (M=Fe, Co, and Ni). The geometries and energies of the lowest energy quartet, triplet, and doublet electronic states as well as several low-lying vertical excitation energies of FeCH2+, CoCH2+, and NiCH2+ are reported. The excitation energies are computed using the equation-of-motion CC and for states of different symmetries, by the energy differences of single reference ground and excited states (Delta-CC). The latter employ several reference states; the unrestricted Hartree-Fock, restricted open shell Hartree-Fock, and unrestricted Kohn-Sham. We conclude that the (2)A(1) electronic ground state of NiCH2+ is separated by about 30.0 kJ/mol from the next highest state, and the lowest B-4(1) and B-4(2) states of FeCH2+ as well as the (3)A(2) and (3)A(1) states of CoCH2+ are nearly degenerate. The presence of metal-pi(*)(MCH2) charge transfer states with significant oscillator strengths in the visibleear-UV energy domain of the theoretical spectra of FeCH2+ and CoCH2+ are at the origin of the photofragmentation of these compounds observed after irradiation between 310 and 360 nm. (c) 2007 American Institute of Physics.