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3,4-Bis(4-bromophenyl)-N-phenylmaleimide
In the title molecule, C(22)H(13)Br(2)NO(2), the three benzene rings are arranged in a propeller-like fashion around the central malemide ring, making dihedral angles of 48.2 (4), 30.2 (4) and 34.8 (4)° with the malemide ring. The C—C single-bond lengths connecting benzene groups and maleimide are...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089159/ https://www.ncbi.nlm.nih.gov/pubmed/21754500 http://dx.doi.org/10.1107/S1600536811014152 |
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author | Liu, Yong Zheng, Shuai Zhou, Jing Gao, Dongmei Du, Zhen-Ting |
author_facet | Liu, Yong Zheng, Shuai Zhou, Jing Gao, Dongmei Du, Zhen-Ting |
author_sort | Liu, Yong |
collection | PubMed |
description | In the title molecule, C(22)H(13)Br(2)NO(2), the three benzene rings are arranged in a propeller-like fashion around the central malemide ring, making dihedral angles of 48.2 (4), 30.2 (4) and 34.8 (4)° with the malemide ring. The C—C single-bond lengths connecting benzene groups and maleimide are significantly shorter [C—C = 1.468 (9) and 1.478 (9) Å] than a typical Csp (3)—Csp (3) single bond, indicating partial conjugation between the benzene and the maleimide. A weak nonclassical C—H⋯O hydrogen bond helps to stabilize the crystal structure. |
format | Text |
id | pubmed-3089159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30891592011-07-13 3,4-Bis(4-bromophenyl)-N-phenylmaleimide Liu, Yong Zheng, Shuai Zhou, Jing Gao, Dongmei Du, Zhen-Ting Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecule, C(22)H(13)Br(2)NO(2), the three benzene rings are arranged in a propeller-like fashion around the central malemide ring, making dihedral angles of 48.2 (4), 30.2 (4) and 34.8 (4)° with the malemide ring. The C—C single-bond lengths connecting benzene groups and maleimide are significantly shorter [C—C = 1.468 (9) and 1.478 (9) Å] than a typical Csp (3)—Csp (3) single bond, indicating partial conjugation between the benzene and the maleimide. A weak nonclassical C—H⋯O hydrogen bond helps to stabilize the crystal structure. International Union of Crystallography 2011-04-22 /pmc/articles/PMC3089159/ /pubmed/21754500 http://dx.doi.org/10.1107/S1600536811014152 Text en © Liu et al. 2011 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 Liu, Yong Zheng, Shuai Zhou, Jing Gao, Dongmei Du, Zhen-Ting 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title | 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title_full | 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title_fullStr | 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title_full_unstemmed | 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title_short | 3,4-Bis(4-bromophenyl)-N-phenylmaleimide |
title_sort | 3,4-bis(4-bromophenyl)-n-phenylmaleimide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089159/ https://www.ncbi.nlm.nih.gov/pubmed/21754500 http://dx.doi.org/10.1107/S1600536811014152 |
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