Abstract

A new angular trinuclear copper(II) complex [Cu 3L 1L 2(1-MeIm)(H 2O)](ClO 4) ( 1), where H 3L 1 and H 2L 2 are penta and tetra-dentate Schiff base ligands, is prepared from a reaction of [CuL 2] and [Cu 2L 1(μ-Br)] in the presence of 1-methylimidazole (1-MeIm) and isolated as a perchlorate salt. The complex which crystallizes in the monoclinic space group P2 1/ n shows the presence of a discrete angular trinuclear copper(II) core in which the monomeric precursor is linked with the dimeric precursor through phenoxo bridges. The core structure resembles well with the active site structure of blue multicopper oxidases. The Cu⋯Cu separations of ca. 3.3 Å in the angular unit is 0.4 Å shorter than those observed in the active site of the oxidized form of ascorbate oxidase. The complex displays a visible band at 620 nm ( ε=500 M −1 cm −1) in DMSO. It shows magnetic moment values of 3.07 and 2.18 μ B at 300 and 18 K, respectively, for the Cu 3 cluster. The complex models the structural and magnetic properties of the trinuclear active site of blue copper oxidases.

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