Kinetic characteristics of the destruction of β,β-annelated porphyrazines in a nitrogen-containing base–dimethylsulfoxide system
- Authors: Petrov O.A.1, Osipova G.V.1, Gornukhina O.V.1
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Affiliations:
- Ivanovo State University of Chemistry and Technology
- Issue: Vol 91, No 3 (2017)
- Pages: 476-481
- Section: Chemical Kinetics and Catalysis
- URL: https://journals.rcsi.science/0036-0244/article/view/169321
- DOI: https://doi.org/10.1134/S0036024417030219
- ID: 169321
Cite item
Abstract
The state of tetra(1,2,5-thiadiazolo)porphyrazine in a dimethyl sulfoxide medium is investigated. Relatively high stability is observed for the resulting proton-transfer complex, and a chemical structure is proposed for it. It is shown that the nature of the substituent in the porphyrazine macrocycle influences the kinetic parameters of the destruction of tetra(1,2,5-thiadiazolo)porphyrazine, tetra(5-tert-butylpyrazino) porphyrazine, octaethyltetrapyrazinoporphyrazine, and octaphenyltetrapyrazinoporphyrazine in a nitrogen-containing base–dimethylsulfoxide system. The effect the NH acidity of the porphyrazine macrocycle and the nature of the nitrogenous bases have on the reaction rate and activation parameters of the destruction of β,β-annelated porphyrazine proton-transfer complexes is established.
About the authors
O. A. Petrov
Ivanovo State University of Chemistry and Technology
Author for correspondence.
Email: poa@isuct.ru
Russian Federation, Ivanovo, 153000
G. V. Osipova
Ivanovo State University of Chemistry and Technology
Email: poa@isuct.ru
Russian Federation, Ivanovo, 153000
O. V. Gornukhina
Ivanovo State University of Chemistry and Technology
Email: poa@isuct.ru
Russian Federation, Ivanovo, 153000