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1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea
The title compound, C(14)H(10)BrN(3)O(3)S, crystallizes as two concomitant polymorphs that differ in colour (one yellow and one colourless). Only the structure of the colourless form could be determined. The molecule exists in the thioamide form with an intramolecular N—H⋯O=C hydrogen bond across...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977201/ https://www.ncbi.nlm.nih.gov/pubmed/21583565 http://dx.doi.org/10.1107/S1600536809025884 |
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author | Saeed, Sohail Rashid, Naghmana Tahir, Arifa Jones, Peter G. |
author_facet | Saeed, Sohail Rashid, Naghmana Tahir, Arifa Jones, Peter G. |
author_sort | Saeed, Sohail |
collection | PubMed |
description | The title compound, C(14)H(10)BrN(3)O(3)S, crystallizes as two concomitant polymorphs that differ in colour (one yellow and one colourless). Only the structure of the colourless form could be determined. The molecule exists in the thioamide form with an intramolecular N—H⋯O=C hydrogen bond across the thiourea system. Molecules are linked into layers parallel to (120) by Br⋯O(nitro) contacts [3.103 (1) Å], classical hydrogen bonds from the other NH function to the S atom and N(nitro)⋯O=C contacts. The layers are linked by weak C—H⋯O(nitro) hydrogen bonds to produce the observed three-dimensional network. |
format | Text |
id | pubmed-2977201 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29772012010-12-30 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea Saeed, Sohail Rashid, Naghmana Tahir, Arifa Jones, Peter G. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(10)BrN(3)O(3)S, crystallizes as two concomitant polymorphs that differ in colour (one yellow and one colourless). Only the structure of the colourless form could be determined. The molecule exists in the thioamide form with an intramolecular N—H⋯O=C hydrogen bond across the thiourea system. Molecules are linked into layers parallel to (120) by Br⋯O(nitro) contacts [3.103 (1) Å], classical hydrogen bonds from the other NH function to the S atom and N(nitro)⋯O=C contacts. The layers are linked by weak C—H⋯O(nitro) hydrogen bonds to produce the observed three-dimensional network. International Union of Crystallography 2009-07-15 /pmc/articles/PMC2977201/ /pubmed/21583565 http://dx.doi.org/10.1107/S1600536809025884 Text en © Saeed et al. 2009 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 Saeed, Sohail Rashid, Naghmana Tahir, Arifa Jones, Peter G. 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title | 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title_full | 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title_fullStr | 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title_full_unstemmed | 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title_short | 1-(4-Bromophenyl)-1-(4-nitrobenzoyl)thiourea |
title_sort | 1-(4-bromophenyl)-1-(4-nitrobenzoyl)thiourea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977201/ https://www.ncbi.nlm.nih.gov/pubmed/21583565 http://dx.doi.org/10.1107/S1600536809025884 |
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