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1,3-Bis(2-cyanobenzyl)imidazolium bromide
In the title salt, C(19)H(15)N(4) (+)·Br(−), the central imidazole ring makes dihedral angles of 83.1 (2) and 87.6 (2)° with the terminal benzene rings. The dihedral angle between the terminal benzene rings is 6.77 (19)°; the cyanide substituents have an anti orientation. In the crystal, the cations...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239090/ https://www.ncbi.nlm.nih.gov/pubmed/22199938 http://dx.doi.org/10.1107/S1600536811048951 |
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author | Haque, Rosenani A. Ahmed, Safaa A. Zetty, Zulikha H. Hemamalini, Madhukar Fun, Hoong-Kun |
author_facet | Haque, Rosenani A. Ahmed, Safaa A. Zetty, Zulikha H. Hemamalini, Madhukar Fun, Hoong-Kun |
author_sort | Haque, Rosenani A. |
collection | PubMed |
description | In the title salt, C(19)H(15)N(4) (+)·Br(−), the central imidazole ring makes dihedral angles of 83.1 (2) and 87.6 (2)° with the terminal benzene rings. The dihedral angle between the terminal benzene rings is 6.77 (19)°; the cyanide substituents have an anti orientation. In the crystal, the cations and anions are linked via C—H⋯N and C—H⋯Br hydrogen bonds, forming sheets lying parallel to the ac plane. |
format | Online Article Text |
id | pubmed-3239090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32390902011-12-23 1,3-Bis(2-cyanobenzyl)imidazolium bromide Haque, Rosenani A. Ahmed, Safaa A. Zetty, Zulikha H. Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title salt, C(19)H(15)N(4) (+)·Br(−), the central imidazole ring makes dihedral angles of 83.1 (2) and 87.6 (2)° with the terminal benzene rings. The dihedral angle between the terminal benzene rings is 6.77 (19)°; the cyanide substituents have an anti orientation. In the crystal, the cations and anions are linked via C—H⋯N and C—H⋯Br hydrogen bonds, forming sheets lying parallel to the ac plane. International Union of Crystallography 2011-11-30 /pmc/articles/PMC3239090/ /pubmed/22199938 http://dx.doi.org/10.1107/S1600536811048951 Text en © Haque 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 Haque, Rosenani A. Ahmed, Safaa A. Zetty, Zulikha H. Hemamalini, Madhukar Fun, Hoong-Kun 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title | 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title_full | 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title_fullStr | 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title_full_unstemmed | 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title_short | 1,3-Bis(2-cyanobenzyl)imidazolium bromide |
title_sort | 1,3-bis(2-cyanobenzyl)imidazolium bromide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239090/ https://www.ncbi.nlm.nih.gov/pubmed/22199938 http://dx.doi.org/10.1107/S1600536811048951 |
work_keys_str_mv | AT haquerosenania 13bis2cyanobenzylimidazoliumbromide AT ahmedsafaaa 13bis2cyanobenzylimidazoliumbromide AT zettyzulikhah 13bis2cyanobenzylimidazoliumbromide AT hemamalinimadhukar 13bis2cyanobenzylimidazoliumbromide AT funhoongkun 13bis2cyanobenzylimidazoliumbromide |