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Polycyclic rod-shaped azo dyes based on aminophenylpyrimidines Full article

Journal Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353
Output data Year: 1996, Volume: 32, Number: 5, Pages: 596-604 Pages count : 9 DOI: 10.1007/BF01164793
Authors Sedova V.F. 1 , Borovik V.P. 1 , Mikhaleva M.A. 1 , Shkurko O.P. 1
Affiliations
1 (Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Division, Russian Academy of Sciences, Novosibirsk 630090, Russian Federation

Abstract: We have synthesized rod-shaped tricydic monoazo and bisazo dyes based on amino derivatives of arylpyrimidines and N, N-dialkylanilines or p-nitroso-N, N-dialkylanilines. We have shown that the process of azo coupling of the diazonium salt obtained from 2,5-bis(p-aminophenyl)pyrimidine is accompanied by dediazoniation, with substitution of the diazonium group by hydrogen or an aryl group. The monoazo dyes obtained display mesomorphic properties which are absent in the bisazo dyes. ©1996 Plenum Publishing Corporation.
Cite: Sedova V.F. , Borovik V.P. , Mikhaleva M.A. , Shkurko O.P.
Polycyclic rod-shaped azo dyes based on aminophenylpyrimidines
Chemistry of Heterocyclic Compounds. 1996. V.32. N5. P.596-604. DOI: 10.1007/BF01164793 Scopus РИНЦ OpenAlex
Dates:
Published print: May 1, 1996
Identifiers:
Scopus: 2-s2.0-25644452070
Elibrary: 13244548
OpenAlex: W2013843869
Citing: Пока нет цитирований
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