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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1998 Volume 8, Issue 2, Pages 59–60 (Mi mendc4654)

This article is cited in 1 paper

Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane

M. F. Budyka, O. D. Laukhina, T. N. Gavrishova

Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation

Abstract: The quantum yields of stepwise cyclization of the first and second diphenylamino groups in 1,4-bis(diphenylamino)butane are 0.3 and 0.02, respectively, which indicates quenching of the excited diphenylamino group by a carbazole unit in the asymmetric semicyclized compound.

Language: English

DOI: 10.1070/MC1998v008n02ABEH000901



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