Cargando…
5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone
The molecule of the title compound, C(8)H(8)BrN(3)OS, is close to being planar, with maximum deviations of −0.127 (3) and 0.135 (5) Å for the N atoms of the –NH– and NH(2)– groups, respectively. Intramolecular N—H⋯N and O—H⋯N hydrogen bonds to the same acceptor N atom generate S(5) and S(6) ring m...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009273/ https://www.ncbi.nlm.nih.gov/pubmed/21589160 http://dx.doi.org/10.1107/S1600536810043357 |
_version_ | 1782194648492539904 |
---|---|
author | Kargar, Hadi Kia, Reza Akkurt, Mehmet Büyükgüngör, Orhan |
author_facet | Kargar, Hadi Kia, Reza Akkurt, Mehmet Büyükgüngör, Orhan |
author_sort | Kargar, Hadi |
collection | PubMed |
description | The molecule of the title compound, C(8)H(8)BrN(3)OS, is close to being planar, with maximum deviations of −0.127 (3) and 0.135 (5) Å for the N atoms of the –NH– and NH(2)– groups, respectively. Intramolecular N—H⋯N and O—H⋯N hydrogen bonds to the same acceptor N atom generate S(5) and S(6) ring motifs. In the crystal structure, molecules are connected into [010] chains by pairs of N—H⋯S hydrogen bonds with R (2) (2)(8) graph-set motifs. The crystal used for data collection was found to be an inversion twin. |
format | Text |
id | pubmed-3009273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30092732010-12-30 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone Kargar, Hadi Kia, Reza Akkurt, Mehmet Büyükgüngör, Orhan Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(8)H(8)BrN(3)OS, is close to being planar, with maximum deviations of −0.127 (3) and 0.135 (5) Å for the N atoms of the –NH– and NH(2)– groups, respectively. Intramolecular N—H⋯N and O—H⋯N hydrogen bonds to the same acceptor N atom generate S(5) and S(6) ring motifs. In the crystal structure, molecules are connected into [010] chains by pairs of N—H⋯S hydrogen bonds with R (2) (2)(8) graph-set motifs. The crystal used for data collection was found to be an inversion twin. International Union of Crystallography 2010-10-31 /pmc/articles/PMC3009273/ /pubmed/21589160 http://dx.doi.org/10.1107/S1600536810043357 Text en © Kargar et al. 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 Kargar, Hadi Kia, Reza Akkurt, Mehmet Büyükgüngör, Orhan 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title | 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title_full | 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title_fullStr | 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title_full_unstemmed | 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title_short | 5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone |
title_sort | 5-bromo-2-hydroxybenzaldehyde thiosemicarbazone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009273/ https://www.ncbi.nlm.nih.gov/pubmed/21589160 http://dx.doi.org/10.1107/S1600536810043357 |
work_keys_str_mv | AT kargarhadi 5bromo2hydroxybenzaldehydethiosemicarbazone AT kiareza 5bromo2hydroxybenzaldehydethiosemicarbazone AT akkurtmehmet 5bromo2hydroxybenzaldehydethiosemicarbazone AT buyukgungororhan 5bromo2hydroxybenzaldehydethiosemicarbazone |