C5R5–iron complexes (R = H or Me) of polyaromatic hydrocarbons: stabilization of the monoreduced state and large variation of spin distribution as a function of the ligand structures

Abstract

Several new polyaromatic iron complexes have been synthesized with C₅H₅ or C₅Me₅ ligands and the synthesis of others is much improved using molten components; cyclic voltammetry shows a considerable stabilization of the Fe^I state by permethylation of the C₅H₅ ligand, and a wide range of spin distribution on the polyaromatic ligand: biphenyl triphenylene naphthalene < phenanthrene < pyrene < perylene corronene, is found for the C₅H₅ complexes only.