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N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide
In the title compound, C(14)H(10)I(2)N(2)O(2), the two aromatic rings are inclined at a dihedral angle of 16.72 (33)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, intermolecular N—H⋯O interactions link the molecules into chains running along t...
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/PMC3201245/ https://www.ncbi.nlm.nih.gov/pubmed/22064780 http://dx.doi.org/10.1107/S1600536811036488 |
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author | Thirugnanasundar, A. Suresh, J. Meenakshi, C. Chakkaravarthi, G. Rajagopal, G. |
author_facet | Thirugnanasundar, A. Suresh, J. Meenakshi, C. Chakkaravarthi, G. Rajagopal, G. |
author_sort | Thirugnanasundar, A. |
collection | PubMed |
description | In the title compound, C(14)H(10)I(2)N(2)O(2), the two aromatic rings are inclined at a dihedral angle of 16.72 (33)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, intermolecular N—H⋯O interactions link the molecules into chains running along the c axis. C—H⋯O interactions also occur. The crystal used for the structure determination was a non-merohedral twin with a domain ratio of 0.972 (2):0.028 (2). |
format | Online Article Text |
id | pubmed-3201245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32012452011-11-06 N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide Thirugnanasundar, A. Suresh, J. Meenakshi, C. Chakkaravarthi, G. Rajagopal, G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(10)I(2)N(2)O(2), the two aromatic rings are inclined at a dihedral angle of 16.72 (33)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, intermolecular N—H⋯O interactions link the molecules into chains running along the c axis. C—H⋯O interactions also occur. The crystal used for the structure determination was a non-merohedral twin with a domain ratio of 0.972 (2):0.028 (2). International Union of Crystallography 2011-09-14 /pmc/articles/PMC3201245/ /pubmed/22064780 http://dx.doi.org/10.1107/S1600536811036488 Text en © Thirugnanasundar 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 Thirugnanasundar, A. Suresh, J. Meenakshi, C. Chakkaravarthi, G. Rajagopal, G. N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title |
N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title_full |
N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title_fullStr |
N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title_full_unstemmed |
N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title_short |
N′-[(E)-2-Hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
title_sort | n′-[(e)-2-hydroxy-3,5-diiodobenzylidene]cyclohexane-1-carbohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201245/ https://www.ncbi.nlm.nih.gov/pubmed/22064780 http://dx.doi.org/10.1107/S1600536811036488 |
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