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...

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Autores principales: Sarıkavaklı, Nursabah, Babahan, İknur, Şahin, Ertan, Hökelek, Tuncer
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
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.
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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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