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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2018 Volume 28, Issue 3, Pages 297–299 (Mi mendc1744)

This article is cited in 9 papers

Communications

Synthesis and properties of 1,3-diphenyl-5-(benzothiazol-2-yl)-6-R-verdazyls

T. G. Fedorchenkoa, G. N. Lipunovaa, A. V. Shchepochkina, A. N. Tsmokalyukb, P. A. Slepukhinab, O. N. Chupakhinab

a I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
b Institute of Chemical Engineering, Ural Federal University, Ekaterinburg, Russian Federation

Abstract: Novel 1,3-diphenyl-5-(benzothiazol-2-yl)-6-R-verdazyls, stable free radicals, were synthesized from the corresponding formazans by alkylation followed by cyclization and oxidation of the intermediate leucoverdazyls (yields 78–93%). The radicals were characterized by ESR, electronic and IR spectroscopy, mass spectrometry, X-ray diffraction (for one of them) and cyclic voltammetry. The resulting verdazyls are stable under ordinary conditions and are reduced more readily but more difficult to oxidize than the triphenylverdazyl analogue.

Language: English

DOI: 10.1016/j.mencom.2018.05.023



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