Reactivities and Electronic Structures of μ-1,2-Peroxo and μ-1,2-Superoxo CoIIICoIII Complexes: Electrophilic Reactivity and O2 Release Induced by Oxidation.

Abstract

Peroxo complexes are key intermediates in water oxidation catalysis (WOC). Cobalt plays an important role in WOC, either as oxides CoOx or as {CoIII(μ-1,2-peroxo)CoIII} complexes, which are the oldest peroxo complexes known. The oxidation of {CoIII(μ-1,2-peroxo)CoIII} complexes had usually been described to form {CoIII(μ-1,2-superoxo)CoIII} complexes; however, recently the formation of {CoIV(μ-1,2-peroxo)CoIII} species were suggested. Using a bis(tetradentate) dinucleating ligand, we present here the synthesis and characterization of {CoIII(μ-1,2-peroxo)(μ-OH)CoIII} and {CoIII(μ-OH)2CoIII} complexes. Oxidation of {CoIII(μ-1,2-peroxo)(μ-OH)CoIII} at -40 °C in CH3CN provides the stable {CoIII(μ-1,2-superoxo)(μ-OH)CoIII} species and activates electrophilic reactivity. Moreover, {CoIII(μ-1,2-peroxo)(μ-OH)CoIII} catalyzes water oxidation, not molecularly but rather via CoOx films. While {CoIII(μ-1,2-peroxo)(μ-OH)CoIII} can be reversibly deprotonated with DBU at -40 °C in CH3CN, {CoIII(μ-1,2-superoxo)(μ-OH)CoIII} undergoes irreversible conversions upon reaction with bases to a new intermediate that is also the decay product of {CoIII(μ-1,2-superoxo)(μ-OH)CoIII} in aqueous solution at pH > 2. Based on a combination of experimental methods, the new intermediate is proposed to have a {CoII(μ-OH)CoIII} core formed by the release of O2 from {CoIII(μ-1,2-superoxo)(μ-OH)CoIII} confirmed by a 100% yield of O2 upon photocatalytic oxidation of {CoIII(μ-1,2-peroxo)(μ-OH)CoIII}. This release of O2 by oxidation of a peroxo intermediate corresponds to the last step in molecular WOC.