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3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide

The asymmetric unit of the title compound, C(16)H(12)N(2)O(2)S, contains three independent mol­ecules. Intra­molecular N—H⋯O hydrogen bonds in the three mol­ecules lead to very similar conformations: the thio­pene ring and naphthalene ring system in the three mol­ecules form dihedral angles of 10.3 ...

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Detalles Bibliográficos
Autores principales: Wu, Qingkun, Yin, Handong, Wang, Daqi
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051446/
https://www.ncbi.nlm.nih.gov/pubmed/21522969
http://dx.doi.org/10.1107/S160053681005405X
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author Wu, Qingkun
Yin, Handong
Wang, Daqi
author_facet Wu, Qingkun
Yin, Handong
Wang, Daqi
author_sort Wu, Qingkun
collection PubMed
description The asymmetric unit of the title compound, C(16)H(12)N(2)O(2)S, contains three independent mol­ecules. Intra­molecular N—H⋯O hydrogen bonds in the three mol­ecules lead to very similar conformations: the thio­pene ring and naphthalene ring system in the three mol­ecules form dihedral angles of 10.3 (2), 9.1 (2) and 9.3 (3)°. In the crystal structure, inter­molecular O—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [031].
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spelling pubmed-30514462011-04-26 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide Wu, Qingkun Yin, Handong Wang, Daqi Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(16)H(12)N(2)O(2)S, contains three independent mol­ecules. Intra­molecular N—H⋯O hydrogen bonds in the three mol­ecules lead to very similar conformations: the thio­pene ring and naphthalene ring system in the three mol­ecules form dihedral angles of 10.3 (2), 9.1 (2) and 9.3 (3)°. In the crystal structure, inter­molecular O—H⋯O hydrogen bonds link the mol­ecules into chains propagating in [031]. International Union of Crystallography 2011-01-08 /pmc/articles/PMC3051446/ /pubmed/21522969 http://dx.doi.org/10.1107/S160053681005405X Text en © Wu et al. 2011 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
Wu, Qingkun
Yin, Handong
Wang, Daqi
3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title_full 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title_fullStr 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title_full_unstemmed 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title_short 3-Hy­droxy-N′-[(E)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
title_sort 3-hy­droxy-n′-[(e)-2-thienyl­methyl­idene]-2-naphtho­hydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051446/
https://www.ncbi.nlm.nih.gov/pubmed/21522969
http://dx.doi.org/10.1107/S160053681005405X
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