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5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone
In the title Schiff base compound, C(10)H(12)BrN(3)OS, the C—N—N—C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648288/ https://www.ncbi.nlm.nih.gov/pubmed/23723908 http://dx.doi.org/10.1107/S1600536813008787 |
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author | Li, Zhaoyang Sato, Osamu |
author_facet | Li, Zhaoyang Sato, Osamu |
author_sort | Li, Zhaoyang |
collection | PubMed |
description | In the title Schiff base compound, C(10)H(12)BrN(3)OS, the C—N—N—C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers. |
format | Online Article Text |
id | pubmed-3648288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-36482882013-05-30 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone Li, Zhaoyang Sato, Osamu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title Schiff base compound, C(10)H(12)BrN(3)OS, the C—N—N—C torsion angle is 172.07 (11)°. An intramolecular hydrogen bond exists between the hydroxy H atom and the azomethine N atom. In the crystal, pairs of hydrogen bonds involving the imino H atom and the S atom give rise to supramolecular dimers. International Union of Crystallography 2013-04-20 /pmc/articles/PMC3648288/ /pubmed/23723908 http://dx.doi.org/10.1107/S1600536813008787 Text en © Li and Sato 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 Li, Zhaoyang Sato, Osamu 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title | 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title_full | 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title_fullStr | 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title_full_unstemmed | 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title_short | 5-Bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
title_sort | 5-bromo-2-hydroxybenzaldehyde 4-ethylthiosemicarbazone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648288/ https://www.ncbi.nlm.nih.gov/pubmed/23723908 http://dx.doi.org/10.1107/S1600536813008787 |
work_keys_str_mv | AT lizhaoyang 5bromo2hydroxybenzaldehyde4ethylthiosemicarbazone AT satoosamu 5bromo2hydroxybenzaldehyde4ethylthiosemicarbazone |