Mechanistic Insight into Dioxygen Evolution from Diastereomeric μ‑Peroxo Dinuclear Co(III) Complexes Based on Stoichiometric Electron-Transfer Oxidation

Stoichiometric electron-transfer (ET) oxidation of two diastereomeric μ-peroxo-μ-hydroxo dinuclear Co­(III) complexes with tris­(2-pyridylmethyl)­amine (TPA) was examined to scrutinize the reaction mechanism of O2 evolution from the peroxo complexes, as seen in the final step in water oxidation by a Co­(III)–TPA complex. The two isomeric Co­(III)-peroxo complexes were synthesized and selectively isolated by recrystallization under different conditions. Although cyclic voltammograms of the two isomers in aqueous solutions showed one reversible wave at 1.1 V vs NHE at pH 2.0, two oxidation waves were observed at 1.0 and 1.4 V at pH 7.0 in the aqueous solutions, the latter of which is responsible for the O2-releasing process. At pH 7, one diastereomer showed higher reactivity than the other in O2 evolution, indicating the importance of structures of the μ-peroxo complexes in the reaction. In order to clarify the O2-evolving mechanism, we performed electron paramagnetic resonance (EPR) and resonance Raman (RR) measurements for characterizing one-electron oxidized species: The observed EPR and RR signals supported the formation of μ-superoxo-μ-hydroxo dinuclear Co­(III) complexes; however, no characteristic difference was observed between two isomers in the EPR parameters including g values and superhyperfine coupling constants. ET-oxidation rate constants of the isomers were determined to be much faster than the O2-evolving rate constants, indicating that the O2-releasing step is the rate-determining step in the O2 evolution through the stoichiometric ET oxidation of the dinuclear Co­(III)−μ-peroxo complexes. Therefore, the difference of reactivity in the O2 evolution for the two isomers should be derived from the thermodynamic stability of two-electron oxidized species of the dinuclear Co­(III)-μ-peroxo complexes, μ-dioxygen-μ-hydroxo dinuclear Co­(III) intermediates