Detection of Superoxide Anion and Singlet Oxygen in the Decomposition of Several Peroxovanadium(V) Complexes

  • Kanamori, Kan (Department of Chemistry, Faculty of Science, Toyama University) ;
  • Hata, Kaori (Department of Chemistry, Faculty of Science, Toyama University) ;
  • Shimoyama, Toshiyuki (Department of Chemistry, Faculty of Science, Toyama University) ;
  • Hayakawa, Shingo (Department of Applied Chenistry & Biotechnology, Faculty of Engeneering, Yamanashi Uniyersity) ;
  • Tajima, Hirotaka (Department of Applied Chenistry & Biotechnology, Faculty of Engeneering, Yamanashi Uniyersity) ;
  • Matsugo, Seiichi (Department of Applied Chenistry & Biotechnology, Faculty of Engeneering, Yamanashi Uniyersity)
  • Published : 2002.08.01

Abstract

Several peroxovanadium(V) complexes with an organic chelate ligand decompose spontaneously, depending on the nature of the chelate ligand. The self-decomposition reactions of the dinuclear peroxovanadium(V) complex with 2-oxo-l,3-diaminopropane-N,N,N',N'-tetraacetate (dpot) and the peroxovanadium(V) complexes with N-carboxymethylhistidinate (cmhist) and histamine-N,N-diacetate (histada) accompany the reduction of vanadium(V) to vanadium(IV). This implies that the peroxide anion acts as a reducing agent and thus the peroxide is oxidized in the decomposition process of the peroxovanadium(V) complexes. The oxidized dioxygen species have been characterized spectrophotometrically. Superoxide anion has been detected in 2-3 % yields using the reduction of cytochrome c method and chemiluminescence method utilized MCLA as a fluorescer. Singlet oxygen has also been detected in higher yields on the basis of chemiluminescence of tryptophan.

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