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(E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions
In the title compound, C(10)H(13)N(3)OS, the azomethine C=N double bond has an E configuration. The phenyl ring and methylhydrazine carbothioamide moiety [maximum deviation = 0.008 (2) Å] are twisted slightly with a dihedral angle of 14.88 (10)°. In the crystal, molecules are linked into sheets...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505611/ https://www.ncbi.nlm.nih.gov/pubmed/31110788 http://dx.doi.org/10.1107/S2056989019004444 |
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author | Arafath, Md. Azharul Kwong, Huey Chong Adam, Farook |
author_facet | Arafath, Md. Azharul Kwong, Huey Chong Adam, Farook |
author_sort | Arafath, Md. Azharul |
collection | PubMed |
description | In the title compound, C(10)H(13)N(3)OS, the azomethine C=N double bond has an E configuration. The phenyl ring and methylhydrazine carbothioamide moiety [maximum deviation = 0.008 (2) Å] are twisted slightly with a dihedral angle of 14.88 (10)°. In the crystal, molecules are linked into sheets parallel to the ab plane via N—H⋯S hydrogen bonds and C—H⋯π interactions. |
format | Online Article Text |
id | pubmed-6505611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-65056112019-05-20 (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions Arafath, Md. Azharul Kwong, Huey Chong Adam, Farook Acta Crystallogr E Crystallogr Commun Research Communications In the title compound, C(10)H(13)N(3)OS, the azomethine C=N double bond has an E configuration. The phenyl ring and methylhydrazine carbothioamide moiety [maximum deviation = 0.008 (2) Å] are twisted slightly with a dihedral angle of 14.88 (10)°. In the crystal, molecules are linked into sheets parallel to the ab plane via N—H⋯S hydrogen bonds and C—H⋯π interactions. International Union of Crystallography 2019-04-05 /pmc/articles/PMC6505611/ /pubmed/31110788 http://dx.doi.org/10.1107/S2056989019004444 Text en © Arafath et al. 2019 http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Research Communications Arafath, Md. Azharul Kwong, Huey Chong Adam, Farook (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title | (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title_full | (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title_fullStr | (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title_full_unstemmed | (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title_short | (E)-2-(2-Hydroxy-3-methylbenzylidene)-N-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by N—H⋯S and C—H⋯π interactions |
title_sort | (e)-2-(2-hydroxy-3-methylbenzylidene)-n-methylhydrazine-1-carbothioamide: supramolecular assemblies in two-dimensions mediated by n—h⋯s and c—h⋯π interactions |
topic | Research Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6505611/ https://www.ncbi.nlm.nih.gov/pubmed/31110788 http://dx.doi.org/10.1107/S2056989019004444 |
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