2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate
In the title thiosemicarbazone derivative, C(9)H(10)N(4)OS·H(2)O, intramolecular N—H⋯N hydrogen bonds result in the formation of two nearly coplanar five- and six-membered rings, which are also almost coplanar with the adjacent phenyl ring. The oxime group has an E configuration and is involved in...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960784/ https://www.ncbi.nlm.nih.gov/pubmed/21201956 http://dx.doi.org/10.1107/S1600536808004947 |
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author | Sarıkavaklı, Nursabah Babahan, İknur Şahin, Ertan Hökelek, Tuncer |
author_facet | Sarıkavaklı, Nursabah Babahan, İknur Şahin, Ertan Hökelek, Tuncer |
author_sort | Sarıkavaklı, Nursabah |
collection | PubMed |
description | In the title thiosemicarbazone derivative, C(9)H(10)N(4)OS·H(2)O, intramolecular N—H⋯N hydrogen bonds result in the formation of two nearly coplanar five- and six-membered rings, which are also almost coplanar with the adjacent phenyl ring. The oxime group has an E configuration and is involved in intermolecular O—H⋯O hydrogen bonding as a donor. In the crystal structure, intramolecular O—H⋯S and N—H⋯N and intermolecular O—H⋯O and N—H⋯S hydrogen bonds generate edge-fused R (2) (2)(8) and R (4) (1)(11) ring motifs. The hydrogen-bonded motifs are linked to each other to form a three-dimensional supramolecular network. |
format | Text |
id | pubmed-2960784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29607842010-12-30 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate Sarıkavaklı, Nursabah Babahan, İknur Şahin, Ertan Hökelek, Tuncer Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title thiosemicarbazone derivative, C(9)H(10)N(4)OS·H(2)O, intramolecular N—H⋯N hydrogen bonds result in the formation of two nearly coplanar five- and six-membered rings, which are also almost coplanar with the adjacent phenyl ring. The oxime group has an E configuration and is involved in intermolecular O—H⋯O hydrogen bonding as a donor. In the crystal structure, intramolecular O—H⋯S and N—H⋯N and intermolecular O—H⋯O and N—H⋯S hydrogen bonds generate edge-fused R (2) (2)(8) and R (4) (1)(11) ring motifs. The hydrogen-bonded motifs are linked to each other to form a three-dimensional supramolecular network. International Union of Crystallography 2008-02-22 /pmc/articles/PMC2960784/ /pubmed/21201956 http://dx.doi.org/10.1107/S1600536808004947 Text en © Sarıkavaklı et al. 2008 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 Sarıkavaklı, Nursabah Babahan, İknur Şahin, Ertan Hökelek, Tuncer 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title | 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title_full | 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title_fullStr | 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title_full_unstemmed | 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title_short | 2-Hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
title_sort | 2-hydroxyimino-1-phenylethanone thiosemicarbazone monohydrate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960784/ https://www.ncbi.nlm.nih.gov/pubmed/21201956 http://dx.doi.org/10.1107/S1600536808004947 |
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