Copper(II) complexes of tridentate selenobisphenolate ligand in mixed ligand environments: Synthesis, crystal structure, EPR and electrochemical studies

Abstract

A series of square-pyramidal copper(II) complexes, [Cu(L Se)( N ∧ N)] (H 2L Se = seleno-bisphenolate; N ∧ N = bipyridyl, phenanthroline or N, N-dimethylethylenediamine) have been synthesized and characterized by elemental analyses, magnetic measurements, IR, EPR, and electronic spectral studies. Single crystal X-ray structures of [Cu(L Se)(bpy)]·H 2O ( 2), [Cu(L Se)(phen)]·CH 2Cl 2 ( 3) and [Cu(L Se)( N, N-Me 2en)] ( 4) showed that all the complexes have approximately square-pyramidal geometry. In complexes 2 and 3, the square plane is occupied by O(1), O(2), N(1) and N(2) and the apical position by Se atom of L Se 2− ligand. The asymmetric unit of complex 4 contains two crystallographically independent discrete molecules A and B with CuN 2OSe chromophore comprising the square plane and the axial position being occupied by another phenolate oxygen atom. Complexes 2, 3 and 4 are found to be paramagnetic and EPR parameters extracted are: g ∥ = 2.232, g ⊥ = 2.069; 〈 g eff〉 = 1.95; and g ∥ = 2.232, g ⊥ = 2.083 for complexes 2, 3 and 4, respectively. Both the complexes 2 and 4 show three reduction processes: (a) a quasi-reversible reduction of Cu II to Cu I, (b) an irreversible reduction of Cu I to Cu 0 with the release of free ligand, and (c) a reduction process occurs at this coordinated ligand. They also show a well-defined quasi-reversible oxidation of Cu II to Cu III and an irreversible oxidation peak at ∼1.30 and 1.40 V vs. Ag/AgCl for 4 and 2, respectively, with no cathodic counterpart, and were attributed to the oxidation of the metal coordinated ligand.