ESR spectra of electrochemically generated free anion radicals of hetaryl-substituted trichloro-1,4-benzoquinones

Authors

  • Я. Страдынь Latvian Institute of Organic Synthesis, Riga LV-1006
  • P. Гаварс Latvian Institute of Organic Synthesis, Riga LV-1006
  • Л. Баумане Latvian Institute of Organic Synthesis, Riga LV-1006
  • P. Валтерс Riga Technical University, Riga LV-1658

Abstract

The ESR method was used to confirm the formation of free anion radicals in the source of electrochemical reduction of 5-thiazolyl-substituted 1,4-benzoquinones and related compounds, as well as the ability of the unpaired electron to become delocalized over the system of π electrons not only of the benzoquinone nucleus but also of the hetaryl substituent added to it.

How to Cite
Stradyn', Ya.; Gavars, R.; Baumane, L.; Valters, R. Chem. Heterocycl. Compd. 1995, 31, 227. [Khim. Geterotsikl. Soedin. 1995, 258.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169685

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Published

1995-02-25

Issue

No. 2 (1995)

Section

Original Papers