5-Imino-3,4-diphenyl-1H-pyrrol-2-one

The title compound, C(16)H(12)N(2)O, exists in the crystalline state as the 5-imino-3,4-di­phenyl­-1H-pyrrol-2-one tautomer. The dihedral angles between the pyrrole and phenyl rings are 35.3 (2) and 55.3 (2)°. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate a graph-...

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Detalles Bibliográficos
Autores principales: Bulatov, Evgeny, Chulkova, Tatiana, Haukka, Matti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998320/
https://www.ncbi.nlm.nih.gov/pubmed/24764881
http://dx.doi.org/10.1107/S1600536814001032
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author Bulatov, Evgeny
Chulkova, Tatiana
Haukka, Matti
author_facet Bulatov, Evgeny
Chulkova, Tatiana
Haukka, Matti
author_sort Bulatov, Evgeny
collection PubMed
description The title compound, C(16)H(12)N(2)O, exists in the crystalline state as the 5-imino-3,4-di­phenyl­-1H-pyrrol-2-one tautomer. The dihedral angles between the pyrrole and phenyl rings are 35.3 (2) and 55.3 (2)°. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate a graph-set motif of R (2) (2)(8) via N—H⋯N hydrogen bonds.
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spelling pubmed-39983202014-04-24 5-Imino-3,4-diphenyl-1H-pyrrol-2-one Bulatov, Evgeny Chulkova, Tatiana Haukka, Matti Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(12)N(2)O, exists in the crystalline state as the 5-imino-3,4-di­phenyl­-1H-pyrrol-2-one tautomer. The dihedral angles between the pyrrole and phenyl rings are 35.3 (2) and 55.3 (2)°. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds generate a graph-set motif of R (2) (2)(8) via N—H⋯N hydrogen bonds. International Union of Crystallography 2014-01-18 /pmc/articles/PMC3998320/ /pubmed/24764881 http://dx.doi.org/10.1107/S1600536814001032 Text en © Bulatov et al. 2014 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Organic Papers
Bulatov, Evgeny
Chulkova, Tatiana
Haukka, Matti
5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title 5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title_full 5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title_fullStr 5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title_full_unstemmed 5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title_short 5-Imino-3,4-diphenyl-1H-pyrrol-2-one
title_sort 5-imino-3,4-diphenyl-1h-pyrrol-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998320/
https://www.ncbi.nlm.nih.gov/pubmed/24764881
http://dx.doi.org/10.1107/S1600536814001032
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AT chulkovatatiana 5imino34diphenyl1hpyrrol2one
AT haukkamatti 5imino34diphenyl1hpyrrol2one

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