Abstract

Abstract The reactions of the chloromanganese(III) complexes of the Schiff bases derived from salicylaldehydes or β-diketones and diamines or monoamines with superoxide ion, O2−, in dimethyl sulfoxide were investigated. The complexes were found to react to give either the oxygenated Mn Schiff base complexes or the reduced Mn(II) Schiff base complexes. The difference in the reactivity toward O2− was correlated to the polarographic half-wave potentials corresponding to the reduction of Mn(III) to Mn(II) of the complexes. Some oxygenated complexes were isolated and characterized.

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