Crucial Roles of a Pendant Imidazole Ligand of a Cobalt Porphyrin Complex in the Stoichiometric and Catalytic Reduction of Dioxygen

Abstract

Abstract A cobalt porphyrin complex with a pendant imidazole base ([(L 1 )Co II ]) is an efficient catalyst for the homogeneous catalytic two‐electron reduction of dioxygen by 1,1′‐dimethylferrocene (Me 2 Fc) in the presence of triflic acid (HOTf), as compared with a cobalt porphyrin complex without a pendant imidazole base ([(L 2 )Co II ]). The pendant imidazole ligand plays a crucial role not only to provide an imidazolinium proton for proton‐coupled electron transfer (PCET) from [(L 1 )Co II ] to O 2 in the presence of HOTf but also to facilitate electron transfer (ET) from [(L 1 )Co II ] to O 2 in the absence of HOTf. The kinetics analysis and the detection of intermediates in the stoichiometric and catalytic reduction of O 2 have provided clues to clarify the crucial roles of the pendant imidazole ligand of [(L 1 )Co II ] for the first time.