Transition metal complexes of acetamidomalondihydroxamate: Synthesis, spectral, thermal and electrochemical studies


Yilmaz F. , YILMAZ V., TOPCU S.

JOURNAL OF COORDINATION CHEMISTRY, vol.57, no.6, pp.525-534, 2004 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 57 Issue: 6
  • Publication Date: 2004
  • Doi Number: 10.1080/00958970410001696843
  • Title of Journal : JOURNAL OF COORDINATION CHEMISTRY
  • Page Numbers: pp.525-534

Abstract

Acetamidomalondihydroxamate (K(2)AcAMDH) and its manganese(II), iron(II), cobalt(II), nickel(II), copper(II) and zinc(II) complexes were synthesized and characterized by elemental analysis, UV-VIS, IR and magnetic susceptibility. The pK(a1) and pK(a2) values of the dihydroxamic acid in aqueous solution were found to be 8.0 +/- 0.1 and 9.7 +/- 0.1. The dihydroxamate anion AcAMDH behaves as a tetradentate bridging ligand through both hydroxamate groups, forming complexes with a metal to ligand ratio of 1:1 in the solid state. The FTIR spectra and thermal decompositions of the ligand and its metal complexes were recorded. The redox behavior of the complexes was investigated in aqueous solution by square wave voltammetry and cyclic voltammetry at neutral pH. In contrast to the solid state, in solution the copper(II) and zinc(II) ions form stable complex species with a metal to ligand ratio of 1 : 2. The iron(II) and nickel(II) complexes show a two-electron irreversible reduction behavior, while the copper(II) and zinc(II) complexes undergo reversible electrode reactions. The stability constants of the complexes were determined by square wave voltammetry.