2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate

In the title compound, C(16)H(11)NO(2)·C(5)H(9)NO, the dihedral angles between the male­imide and phenyl rings are 34.7 (2) and 64.8 (2)°. In the crystal, the 2,3-di­phenyl­male­imide and 1-methyl­pyrrolidin-2-one mol­ecules form centrosymmetrical dimers via pairs of strong N—H⋯O hydrogen bonds and...

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Autores principales: Bulatov, Evgeny, Boyarskaya, Dina, 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/PMC3998429/
https://www.ncbi.nlm.nih.gov/pubmed/24764976
http://dx.doi.org/10.1107/S1600536814002372
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author Bulatov, Evgeny
Boyarskaya, Dina
Chulkova, Tatiana
Haukka, Matti
author_facet Bulatov, Evgeny
Boyarskaya, Dina
Chulkova, Tatiana
Haukka, Matti
author_sort Bulatov, Evgeny
collection PubMed
description In the title compound, C(16)H(11)NO(2)·C(5)H(9)NO, the dihedral angles between the male­imide and phenyl rings are 34.7 (2) and 64.8 (2)°. In the crystal, the 2,3-di­phenyl­male­imide and 1-methyl­pyrrolidin-2-one mol­ecules form centrosymmetrical dimers via pairs of strong N—H⋯O hydrogen bonds and π–π stacking inter­actions between the two neighboring male­imide rings [centroid–centroid distance = 3.495 (2) Å]. The dimers are further linked by weak C—H⋯O and C—H⋯π hydrogen bonds into a three-dimensional framework.
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spelling pubmed-39984292014-04-24 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate Bulatov, Evgeny Boyarskaya, Dina Chulkova, Tatiana Haukka, Matti Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(11)NO(2)·C(5)H(9)NO, the dihedral angles between the male­imide and phenyl rings are 34.7 (2) and 64.8 (2)°. In the crystal, the 2,3-di­phenyl­male­imide and 1-methyl­pyrrolidin-2-one mol­ecules form centrosymmetrical dimers via pairs of strong N—H⋯O hydrogen bonds and π–π stacking inter­actions between the two neighboring male­imide rings [centroid–centroid distance = 3.495 (2) Å]. The dimers are further linked by weak C—H⋯O and C—H⋯π hydrogen bonds into a three-dimensional framework. International Union of Crystallography 2014-02-08 /pmc/articles/PMC3998429/ /pubmed/24764976 http://dx.doi.org/10.1107/S1600536814002372 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
Boyarskaya, Dina
Chulkova, Tatiana
Haukka, Matti
2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title_full 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title_fullStr 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title_full_unstemmed 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title_short 2,3-Di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
title_sort 2,3-di­phenyl­male­imide 1-methyl­pyrrol­idin-2-one monosolvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998429/
https://www.ncbi.nlm.nih.gov/pubmed/24764976
http://dx.doi.org/10.1107/S1600536814002372
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AT haukkamatti 23diphenylmaleimide1methylpyrrolidin2onemonosolvate

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