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N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide
In the title compound, C(12)H(9)ClN(2)OS, the dihedral angle between the aromatic rings is 9.78 (11)°. In the crystal structure, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. Weak aromatic π–π stacking [centroid–centroid separations = 3.7210 (15) and...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983898/ https://www.ncbi.nlm.nih.gov/pubmed/21580733 http://dx.doi.org/10.1107/S1600536810010615 |
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author | Jiang, Jin-He |
author_facet | Jiang, Jin-He |
author_sort | Jiang, Jin-He |
collection | PubMed |
description | In the title compound, C(12)H(9)ClN(2)OS, the dihedral angle between the aromatic rings is 9.78 (11)°. In the crystal structure, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. Weak aromatic π–π stacking [centroid–centroid separations = 3.7210 (15) and 3.8706 (15) Å] also occurs. |
format | Text |
id | pubmed-2983898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29838982010-12-30 N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide Jiang, Jin-He Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(9)ClN(2)OS, the dihedral angle between the aromatic rings is 9.78 (11)°. In the crystal structure, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. Weak aromatic π–π stacking [centroid–centroid separations = 3.7210 (15) and 3.8706 (15) Å] also occurs. International Union of Crystallography 2010-03-27 /pmc/articles/PMC2983898/ /pubmed/21580733 http://dx.doi.org/10.1107/S1600536810010615 Text en © Jin-He Jiang 2010 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 Jiang, Jin-He N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title |
N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title_full |
N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title_fullStr |
N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title_full_unstemmed |
N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title_short |
N′-(4-Chlorobenzylidene)thiophene-2-carbohydrazide |
title_sort | n′-(4-chlorobenzylidene)thiophene-2-carbohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983898/ https://www.ncbi.nlm.nih.gov/pubmed/21580733 http://dx.doi.org/10.1107/S1600536810010615 |
work_keys_str_mv | AT jiangjinhe n4chlorobenzylidenethiophene2carbohydrazide |