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(E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide
In the title compound, C(14)H(12)ClN(3)O(2), the acylhydrazone base [C(=O)—N—N=C] is essentially planar, with an r.m.s. deviation of 0.0095 Å, and makes a dihedral angle of 12.52 (10)°with the pyridine ring. In the crystal, molecules are linked via pairs of N—H⋯O hydrogen bonds, forming inversion d...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588333/ https://www.ncbi.nlm.nih.gov/pubmed/23476415 http://dx.doi.org/10.1107/S1600536812045989 |
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author | Rao, Xiao-jin Wu, Wen-Shi Li, Chuan-hui Huang, Yu-min |
author_facet | Rao, Xiao-jin Wu, Wen-Shi Li, Chuan-hui Huang, Yu-min |
author_sort | Rao, Xiao-jin |
collection | PubMed |
description | In the title compound, C(14)H(12)ClN(3)O(2), the acylhydrazone base [C(=O)—N—N=C] is essentially planar, with an r.m.s. deviation of 0.0095 Å, and makes a dihedral angle of 12.52 (10)°with the pyridine ring. In the crystal, molecules are linked via pairs of N—H⋯O hydrogen bonds, forming inversion dimers with an R (2) (2)(8) graph-set motif. The dimers are linked via C—H⋯π interactions forming chains along [101]. |
format | Online Article Text |
id | pubmed-3588333 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35883332013-03-08 (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide Rao, Xiao-jin Wu, Wen-Shi Li, Chuan-hui Huang, Yu-min Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(12)ClN(3)O(2), the acylhydrazone base [C(=O)—N—N=C] is essentially planar, with an r.m.s. deviation of 0.0095 Å, and makes a dihedral angle of 12.52 (10)°with the pyridine ring. In the crystal, molecules are linked via pairs of N—H⋯O hydrogen bonds, forming inversion dimers with an R (2) (2)(8) graph-set motif. The dimers are linked via C—H⋯π interactions forming chains along [101]. International Union of Crystallography 2012-12-08 /pmc/articles/PMC3588333/ /pubmed/23476415 http://dx.doi.org/10.1107/S1600536812045989 Text en © Rao et al. 2013 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 Rao, Xiao-jin Wu, Wen-Shi Li, Chuan-hui Huang, Yu-min (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title | (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title_full | (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title_fullStr | (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title_full_unstemmed | (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title_short | (E)-2-(4-Chlorophenoxy)-N′-(pyridin-4-ylmethylidene)acetohydrazide |
title_sort | (e)-2-(4-chlorophenoxy)-n′-(pyridin-4-ylmethylidene)acetohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588333/ https://www.ncbi.nlm.nih.gov/pubmed/23476415 http://dx.doi.org/10.1107/S1600536812045989 |
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