Dinuclear and mononuclear manganese(iv)-radical complexes and their catalytic catecholase activity

Abstract

Seven o-aminophenol ligands based on aniline and m-phenylenediamine, which act as mono- and di-nucleating non-innocent ligands, respectively, together with their seven Mn(IV)-complexes, 1–7 are described. One of them, 1, is dinuclear and 2–7 are mononuclear, in which the ligands are coordinated in their oxidized o-iminobenzosemiquinone radical forms. The crystal structures of 1 and 3 were determined by X-ray diffraction and the electronic structures were established by various physical methods including EPR and variable-temperature (2–290 K) susceptibility measurements. Electrochemical measurements (CV and SQW) indicate primarily ligand-centered redox processes. The Mn(IV)-radical complexes, 1–7, catalyze the oxidation of 3,5-di-tert-butylcatechol with molecular oxygen as the sole oxidant to afford 3,5-di-tert-butylquinone quantitatively under mild conditions to mimic the function of the copper-containing enzyme catechol oxidase. An “on–off” mechanism of the radicals without redox participation of the metal center is proposed for the catalytic oxidation process. Complex 1 is found to be a good catalyst for oxidative C–C coupling of hindered phenols to diphenoquinones.