Interaction of N-substituted phenothiazines with halogen-containing solvents

Authors

  • О. Б. Томилин N. P. Ogarev Mordovian State University, Saransk 430000
  • E. П. Коновалова N. P. Ogarev Mordovian State University, Saransk 430000
  • B. H. Южалкин N. P. Ogarev Mordovian State University, Saransk 430000
  • А. H. Клякин N. P. Ogarev Mordovian State University, Saransk 430000
  • Э. П. Санаева N. P. Ogarev Mordovian State University, Saransk 430000

Abstract

ESR spectroscopy was used to study the interaction of several N-substituted phenothiazines with halogencontaining solvents (CCl4, CHCl3, CH2Br2). The dissolution of phenothiazines in these solvents was found to be associated with an ESR signal indicating the presence of an oxidation-reduction reaction in which the halogen-containing compounds act as acceptors, and the phenothiazines act as electron donors. The HFS of the ESR spectra of the cation radicals obtained was studied.

How to Cite
Tomilin, O. B.; Konovalova, E. P.; Yuzhalkin, V. N.; Klyakin, A. N.; Sanaeva, E. P. Chem. Heterocycl. Compd. 1996, 32, 246. [Khim. Geterotsikl. Soedin. 1996, 274.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165458

Downloads

Published

1996-02-25

Issue

No. 2 (1996)

Section

Original Papers