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4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph
The title compound, C(17)H(15)N(3)O(4)S, is a monoclinic polymorph with space group P2(1)/c of the previously reported triclinic form in P [Image: see text] [Subashini et al. (2009 ▶). J. Chem. Crystallogr. 39, 112–116]. In both polymorphs, intramolecular O—H⋯N hydrogen bonds and dimer formation vi...
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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/PMC2983326/ https://www.ncbi.nlm.nih.gov/pubmed/21587557 http://dx.doi.org/10.1107/S1600536810036585 |
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author | Ebenezer, Samuel Muthiah, Packianathan Thomas |
author_facet | Ebenezer, Samuel Muthiah, Packianathan Thomas |
author_sort | Ebenezer, Samuel |
collection | PubMed |
description | The title compound, C(17)H(15)N(3)O(4)S, is a monoclinic polymorph with space group P2(1)/c of the previously reported triclinic form in P [Image: see text] [Subashini et al. (2009 ▶). J. Chem. Crystallogr. 39, 112–116]. In both polymorphs, intramolecular O—H⋯N hydrogen bonds and dimer formation via a pair of intermolecular N—H⋯N hydrogen bonds with an R (2) (2)(8) motif are observed. The two polymorphs differ in the next level of supramolecular organization involving C—H⋯O hydrogen bonds with varied packing and different conformations. |
format | Text |
id | pubmed-2983326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29833262010-12-30 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph Ebenezer, Samuel Muthiah, Packianathan Thomas Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(17)H(15)N(3)O(4)S, is a monoclinic polymorph with space group P2(1)/c of the previously reported triclinic form in P [Image: see text] [Subashini et al. (2009 ▶). J. Chem. Crystallogr. 39, 112–116]. In both polymorphs, intramolecular O—H⋯N hydrogen bonds and dimer formation via a pair of intermolecular N—H⋯N hydrogen bonds with an R (2) (2)(8) motif are observed. The two polymorphs differ in the next level of supramolecular organization involving C—H⋯O hydrogen bonds with varied packing and different conformations. International Union of Crystallography 2010-09-18 /pmc/articles/PMC2983326/ /pubmed/21587557 http://dx.doi.org/10.1107/S1600536810036585 Text en © Ebenezer and Muthiah 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 Ebenezer, Samuel Muthiah, Packianathan Thomas 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title | 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title_full | 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title_fullStr | 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title_full_unstemmed | 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title_short | 4-[(2-Hydroxybenzylidene)amino]-N-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
title_sort | 4-[(2-hydroxybenzylidene)amino]-n-(5-methylisoxazol-3-yl)benzenesulfonamide: a monoclinic polymorph |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983326/ https://www.ncbi.nlm.nih.gov/pubmed/21587557 http://dx.doi.org/10.1107/S1600536810036585 |
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