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Mendeleev Communications, 1998, Volume 8, Issue 2, Pages 59–60
DOI: https://doi.org/10.1070/MC1998v008n02ABEH000901
(Mi mendc4654)
 

This article is cited in 1 scientific paper (total 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
Full-text PDF (174 kB) Citations (1)
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.
Document Type: Article
Language: English


Citation: M. F. Budyka, O. D. Laukhina, T. N. Gavrishova, “Self-quenching in the stepwise photocyclization of 1,4-bis(diphenylamino)butane to 1,4-dicarbazolylbutane”, Mendeleev Commun., 8:2 (1998), 59–60
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  • This publication is cited in the following 1 articles:
    1. M. F. Budyka, O. V. Chashchikhin, “Spectral and photochemical properties of hybrid organic—inorganic nanosystems based on CdS quantum dots and a styrylquinoline ligand”, High Energy Chem, 50:5 (2016), 349  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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