Synthesis, structure, spectroscopic and redox properties of copper(II)-N-3,5-Bu(2)(t)phenylsalicylaldinine complexes: Crystal and molecular structure of bis(N-3,5-Bu-2(t)-phenylsalicylaldininato) copper (II)


Kasumov V., Bulut A., Koksal F., Aslanoglu M., Ucar I., Kazak C.

POLYHEDRON, vol.25, no.5, pp.1133-1141, 2006 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 25 Issue: 5
  • Publication Date: 2006
  • Doi Number: 10.1016/j.poly.2005.08.048
  • Journal Name: POLYHEDRON
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Index Chemicus (IC)
  • Page Numbers: pp.1133-1141
  • Keywords: bulky salicylaldiminato-Cu(II) complexes, X-ray crystal structure, spectroscopy, electrochemistry, chemical redox behaviors, RADICAL COMPLEXES, BEHAVIOR, SERIES, FORM, EPR
  • Ondokuz Mayıs University Affiliated: No

Abstract

New bulky bis(N-3, 5-Bu(2)(t)phenyl-R-salicyaldiminato)copper(II) complexes X were synthesized and characterized by analytical, spectroscopic (IR, UV/Vis, EPR), electrochemical methods, and their chemical redox reactivity were studied. X-ray structural analysis of 1 revealed that the CuN2O2 coordination core forms a distorted square-planar geometry with a cis-N2O2 donor set which is not expected for analogous complexes. The UV/Vis and EPR results indicate that X complexes have a tetrahedrally distorted square-planar structure in the solid state and in solution. In the chemical oxidation of X by (NH4)(2)Ce(NO3)(6) along with disappearance of their EPR spectra, the appearance of new Cu(II) patterns at g = 2.169-2.189 for all X and radical signals in the cases of 5 and 6 were detected. The chemical reduction of some X complexes was accompanied by the disappearance of their EPR signals. The separation in peak potentials (Delta E-p) for complexes X are in order 4 < 3 < 2 < 1 < 6. The electrochemical results suggested that the complex 4 has the highest electrochemical rate assuming both the Cu(II) and Cu(I) forms appear in a similar geometrical configuration, so the electron transfer does not require larger reorganization of the complex in complex 4. (c) 2005 Elsevier Ltd. All rights reserved.