Unlike most simple, monomeric cobalt porphyrins, the cobalt tetramethylporphyrin identified in the title catalyzes the electroreduction of O 2 to H 2 O instead of H 2 O 2 . On graphite electrodes, coatings of the porphyrin prepared by irreversible adsorption from chloroform solutions catalyze the electroreduction of O 2 in aqueous HClO 4 at unusually positive potentials. Both the title porphyrin and the corresponding unsubstituted cobalt porphine are argued to derive their activity as four-electron reduction catalysts from their propensity to form dimers (or higher aggregates) in solution and, presumptively, on the surface of graphite electrodes.
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Shi et al. (1998) studied this question.
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