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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1994 Volume 4, Issue 3, Pages 109–110 (Mi mendc5177)

This article is cited in 6 papers

Intermediates in the Reactions of Chloranil and 2,6-Dichloro-1,4-benzoquinone with Pyrrolidine

S. V. Chapysheva, T. Ibatab

a Institute of Problems of Chemical Physics, Russian Academy of Sciences, Chernogolovka, Moscow Region, Russian Federation
b Institute of Chemistry, College of General Education, Osaka University, Toyonaka, Osaka, Japan

Abstract: Although the intermediates in the reactions of chloranil and 2,6-dichloro-1,4-benzoquinone with pyrrolidine are the corresponding monoaminated chloroquinones, these compounds exhibit a pronounced tendency to form molecular complexes; thus, the spectral characteristics of 2,3,5-trichloro-6-pyrrolidino-1,4-benzoquinone indicate its partial self-complexation into the corresponding biradical dimer. 2,6-Dichloro-3-pyrrolidino-1,4-benzoquinone forms a stable quinhydrone complex with 2,6-dichlorohydroquinone.

Language: English

DOI: 10.1070/MC1994v004n03ABEH000373



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