Study of binary complexes of nickel(II), copper(II), and vanadium(V) with acetazolamide in aqueous medium by voltammetry


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Bulut I.

TURKISH JOURNAL OF CHEMISTRY, vol.33, no.4, pp.507-520, 2009 (SCI-Expanded) identifier

  • Publication Type: Article / Article
  • Volume: 33 Issue: 4
  • Publication Date: 2009
  • Doi Number: 10.3906/kim-0812-16
  • Journal Name: TURKISH JOURNAL OF CHEMISTRY
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus, TR DİZİN (ULAKBİM)
  • Page Numbers: pp.507-520
  • Keywords: Acetazolamide, Copper, Nickel, Vanadium, Binary complexes, Electronic Spectra, Voltammetry, CRYSTAL-STRUCTURE, 5-ACETAMIDO-1,3,4-THIADIAZOLE-2-SULFONAMIDE COMPLEXES, METAL-COMPLEXES, NI(II), CO(II), BEHAVIOR, ZN(II), HG(II), CD(II), CU(II)
  • Ondokuz Mayıs University Affiliated: No

Abstract

The voltammetric behaviour of acetazolamide, the systemic carbonic anhydrase inhibitor, in the presence of some metal ions (Cu(II), Ni(II), and V(V)) were investigated using square-wave and cyclic voltammetry in physiological pH (pH 7.4). Square-wave voltammogram of acetazolamide in the absence of metal ions gave only 1 reduction peak at -1.65 V attributed to a catalytic hydrogen peak. Three reversible peaks at -0.068, -0.262, and -0.434 V were observed for the solutions containing both copper(II) ions and acetazolamide in the SWV. The peak at -0.434 V was attributed to Cu(II)-acetazolamide complex. In the presence of acetazolamide, copper-acetazolamide complex formation was proved by a reversible peak with 2 electron transfers at -0.450 V. Complex formation of an adduct of trioxovanadate(V) with acetazolamide onto dropping mercury electrode was followed by a reduction peak at -0.480 V. Ni(II)-acetazolamide complex was observed to reduce at the more positive potential (-0.830 V) than that of the hydrated Ni(II) ions (-1.200 V) implying that acetazolamide is a catalyst for Ni(II) reduction at a mercury electrode. The UV-vis spectra of all the acetazolamide complexes were also discussed.