Syntheses and crystal structures of mono-, di- and trinuclear cobalt complexes of a salen type ligand

Abstract

Three cobalt complexes containing the salen type ligand, bis(salicylidene)-meso-1,2-diphenylethylenediaminato (mdpSal 2−), are reported. The complexes differ in nuclearity and include the mononuclear, Co(mdpSal) ( 1), which contains a Co(II) metal center bound to one mdpSal −2 ligand frame in a square planar geometry. The second complex is the dinuclear [Co(mdpSal)Cl] 2 ( 2) in which both cobalt ions have been oxidized to the +3 oxidation state. The overall geometry of complex 2 is an edge-sharing bioctahedron with the coordination sphere around each cobalt metal center consisting of one mdpSal −2 ligand and one Cl − ion. The shared edge between the Co(III) ions contains two bridging phenolate groups, one from each ligand frame. Complex 3 is a linear, mixed valence, trinuclear species, [Co(mdpSal)(OAc)(μ-OAc)] 2Co, with the oxidation states of the metal centers assigned as Co(III)–Co(II)–Co(III). The terminal Co(III) centers are equivalent with the central Co(II) lying on the inversion center of the molecule. Each cobalt ion in 3 adopts an octahedral geometry with the terminal Co(III) ions being bound to one mdpSal 2− ligand each. All phenolate groups bridge to the central Co(II). The coordination sphere about each metal center in the trinuclear complex is completed by four acetate groups, two of which bind in a μ-fashion bridging from the terminal Co(III) metal centers to the central Co(II). The complexes have been characterized by X-ray crystallography as well as UV–Vis and IR spectroscopy.