Kinetics of the Formation of an Active Oxo Species of µ-Carbidodimeric Water-Soluble Iron(IV) Sulfophthalocyanine in the Reaction with tert-Butyl Hydroperoxide
- Authors: Zaitseva S.V.1, Tyurin D.V.2, Zdanovich S.A.1, Koifman O.I.1,2
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Affiliations:
- Krestov Institute of Solution Chemistry
- Ivanovo State University of Chemistry and Technology
- Issue: Vol 64, No 6 (2019)
- Pages: 815-821
- Section: Physical Chemistry of Solutions
- URL: https://journals.rcsi.science/0036-0236/article/view/169400
- DOI: https://doi.org/10.1134/S0036023619060184
- ID: 169400
Cite item
Abstract
The kinetic characteristics were determined for the formation of a highly active oxo species of µ-carbidodimeric water-soluble iron(IV) sulfophthalocyanine under the action of tert-butyl hydroperoxide. The reaction rate was found, and a possible reaction mechanism was proposed. It was determined that the formation of a radical cation in the macrocycle of µ-carbidodimeric iron(IV) sulfophthalocyanine is preceded by coordination of the peroxide molecule with subsequent homolytic cleavage of the O-O bond. The oxo species formed in the reaction can oxidize organic peroxide and is readily regenerated in the presence of an organic base. The activity of the radical-cation species of the dimeric iron(IV) complex in the methyl orange oxidation reaction was shown.
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About the authors
S. V. Zaitseva
Krestov Institute of Solution Chemistry
Author for correspondence.
Email: svz@isc-ras.ru
Russian Federation, Ivanovo, 153045
D. V. Tyurin
Ivanovo State University of Chemistry and Technology
Email: svz@isc-ras.ru
Russian Federation, Ivanovo, 153000
S. A. Zdanovich
Krestov Institute of Solution Chemistry
Email: svz@isc-ras.ru
Russian Federation, Ivanovo, 153045
O. I. Koifman
Krestov Institute of Solution Chemistry; Ivanovo State University of Chemistry and Technology
Email: svz@isc-ras.ru
Russian Federation, Ivanovo, 153045; Ivanovo, 153000
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