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2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate
The title Schiff base compound, C(13)H(9)BrClN(3)O(2)·CH(4)O, was derived from the condensation reaction of 3-bromo-5-chlorosalicylaldehyde with isonicotinohydrazide. The dihedral angle between the benzene and pyridine rings is 5.9 (2)°. In the crystal structure, molecules are linked through N—H⋯O...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962014/ https://www.ncbi.nlm.nih.gov/pubmed/21203101 http://dx.doi.org/10.1107/S1600536808019648 |
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author | Tang, Chun-Bao |
author_facet | Tang, Chun-Bao |
author_sort | Tang, Chun-Bao |
collection | PubMed |
description | The title Schiff base compound, C(13)H(9)BrClN(3)O(2)·CH(4)O, was derived from the condensation reaction of 3-bromo-5-chlorosalicylaldehyde with isonicotinohydrazide. The dihedral angle between the benzene and pyridine rings is 5.9 (2)°. In the crystal structure, molecules are linked through N—H⋯O, O—H⋯O, and O—H⋯Br intermolecular hydrogen bonds, forming dimers and chains. There is also an intramolecular O—H⋯N hydrogen bond. |
format | Text |
id | pubmed-2962014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29620142010-12-30 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate Tang, Chun-Bao Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(13)H(9)BrClN(3)O(2)·CH(4)O, was derived from the condensation reaction of 3-bromo-5-chlorosalicylaldehyde with isonicotinohydrazide. The dihedral angle between the benzene and pyridine rings is 5.9 (2)°. In the crystal structure, molecules are linked through N—H⋯O, O—H⋯O, and O—H⋯Br intermolecular hydrogen bonds, forming dimers and chains. There is also an intramolecular O—H⋯N hydrogen bond. International Union of Crystallography 2008-07-05 /pmc/articles/PMC2962014/ /pubmed/21203101 http://dx.doi.org/10.1107/S1600536808019648 Text en © Chun-Bao Tang 2008 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 Tang, Chun-Bao 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title | 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title_full | 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title_fullStr | 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title_full_unstemmed | 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title_short | 2′-(3-Bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
title_sort | 2′-(3-bromo-5-chloro-2-hydroxybenzylidene)isonicotinohydrazide methanol solvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962014/ https://www.ncbi.nlm.nih.gov/pubmed/21203101 http://dx.doi.org/10.1107/S1600536808019648 |
work_keys_str_mv | AT tangchunbao 23bromo5chloro2hydroxybenzylideneisonicotinohydrazidemethanolsolvate |