Copper(II) complexes of symmetrical and unsymmetrical tetradentate Schiff base ligands incorporating 1-benzoylacetone: Synthesis, crystal structures and electrochemical behavior

Abstract

Three new copper(II) complexes [CuL 1] 2(ClO 4) 2 ( 1), [CuL 2]ClO 4 ( 2) and [CuL 3] ( 3) with three Schiff base ligands [HL 1 = 1-phenyl-3-{3-[(pyridin-2-ylmethylene)-amino]-propylimino}-butan-1-one, HL 2 = 1-phenyl-3-[3-(1-pyridin-2-yl-ethylideneamino)-propylimino]-butan-1-one and H 2L 3 = 3-[3-(1-methyl-3-oxo-3-phenyl-propylideneamino)-propylimino]-1-phenyl-butan-1-one] have been synthesized and structurally characterized by X-ray crystallography. The mono-negative tetradentate asymmetric Schiff base ligands (L 1) − and (L 2) − are chelated in complexes 1 and 2 to form square planar copper(II) complexes. In complex 1, the two units are associated weakly through ketonic oxygen of benzoylacetone fragment to form the dimeric entity. The square planar geometry of complex 3 is unusually distorted towards tetrahedral one. All three complexes exhibit reversible cyclic voltammetric responses in acetonitrile solution corresponding to the Cu II/Cu I redox process. The E 1/2 (−0.47 V versus SCE) of 3 shows significant anodic shift due to the tetrahedral distortion around Cu(II) compare to that of 1 and 2 (−0.82 and −0.87 V versus SCE, respectively).