Photoelectron spectroscopy of molecular systems and quantum-chemical calculations in terms of the density functional theory: Iron π complexes L-Fe(CO)3

Abstract

The HeI and NeI photoelectron spectra of irontricarboniyl complexes with cyclic diene ligands—αmethylstyrene, orthoquinodimethane, and cyclooctatetraene—were obtained. The results of quantum-chemical calculations of the molecules of these compounds in the approximation of the density functional theory (B3LYP/6-31G*) are presented. It is shown that this approximation describes well the excited ionic states of the π complexes under study. The relative ionization cross sections σπ and σ3d , which characterize the probability of removal of electrons from the molecular π-ligand and 3d-metal orbitals, are estimated. The mechanism of the selective coordination of the Fe(CO)3 groups to corresponding organic ligands is discussed. The energies of the L-Fe(CO)3 chemical bond are calculated.