Dinuclear copper complexes with cyanamide derivatives as bridging ligands

Abstract

Three mixed-valence copper complexes [{Cu(phen) 2} 2(μ-L)](PF 6) 2 (where phen = 1,10-phenanthroline, L = 1,4-dicyanamidobenzene (dicyd)), 1,4-dicyanamido-2,5-dimethylbenzene (Me 2dicyd) and 1,4-dicyanamido-2,5-dichlorobenzene (Cl 2dicyd), and one dinuclear Cu(II) complex [{Cu(phen) 2} 2(μ-apc)](PF 6) 3 (where apc = monoanion of 4-azo(phenylcyanamido)benzene) have been prepared and characterized by elemental analysis, IR and electronic absorption spectroscopies and cyclic voltammetry. [{Cu(phen) 2} 2(μ-apc)](PF 6) 3 · 2CH 3COCH 3 crystallized in the triclinic system and both five-coordinate Cu(II) ions in the dinuclear unit are linked through a bridging 4-azo(phenylcyanamido)benzene (apc) ligand. The cyanamide group (NCN) of the bridging ligand is coordinated to Cu(II) ions through the cyano-nitrogen and amido-nitrogen. The bond length between Cu(1) and cyano-nitrogen is slightly larger than that formed by Cu(2) and amido-nitrogen. The angular structural index parameters, τ, for Cu(1) and Cu(2) are 0.9 and 0.5, respectively. The copper(II) atoms display a different geometry with a N 5 chromophore group. The intra Cu⋯Cu separation is 5.156(1) Å. All of the dicyd dinuclear copper complexes show radical anion absorption.