The synthesis, X-ray molecular structure, physico-chemical characterization and dual antioxidant activity (catalase and superoxide dismutase) of a new polymeric mixed valence Mn(III)Mn(II) complex, containing the ligand H₂BPClNOL (N-(2-hydroxybenzyl)-N-(2-pyridylmethyl)[(3-chloro)(2-hydroxy)] propylamine) is described. The monomeric unit is composed of a dinuclear Mn(II)Mn(III) moiety, [Mn(III)(μ-HBPClNOL)(μ-BPClNOL)Mn(II)(Cl)](ClO₄)·2H₂O, 1, in which the Mn ions are connected by two different bridging groups provided by two molecules of the ligand H₂BPClNOL, a phenoxide and an alkoxide group. In the solid state, this mixed valence dinuclear unit is connected to its neighbors through chloro bridges. Magnetic measurements indicated the presence of ferromagnetic [J = +0.076(13) cm^-1] and antiferromagnetic [J = -5.224(13) cm^-1] interactions. The compound promotes O 2 • - dismutation in aqueous solution (IC₅₀ = 0.370 μmol dm^-3, k _cat = 3.6x10⁶ M^-1 s^-1). EPR studies revealed that a high-valent Mn(III)-O-Mn(IV) species is involved in the superoxide dismutation catalytic cycle. Complex 1 shows catalase activity only in the presence of a base, e.g., piperazine or triethylamine. Kinetic studies were carried out in the presence of piperazine and employing two different methods, resulting in k _cat values of 0.58 ± 0.03 s^-1 (detection of O₂ production employing a Clark electrode) and 2.59 ± 0.12 s^-1 (H₂O₂ consuption recorded via UV-Vis). EPR and ESI-(+)-MS studies indicate that piperazine induces the oxidation of 1, resulting in the formation of the catalytically active Mn(III)-O-Mn(IV) species.

Crystiane A. Pereira

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