(E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate

In the title compound, C(15)H(12)O(4)·H(2)O, the two benzene rings are not coplanar, making a dihedral angle of 7.24 (16)°. An intra­molecular hy­droxy–carbonyl O—H⋯O hydrogen bond occurs. In the crystal, four inter­molecular O—H⋯O hydrogen bonds involving the hy­droxy residues, the carbonyl group a...

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Detalles Bibliográficos
Autores principales: Wang, Jian-Guo, Wu, Lin, Zhong, Chan-Juan, Ouyang, Zhao-Hui, Yi, De-Lian
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052009/
https://www.ncbi.nlm.nih.gov/pubmed/21522472
http://dx.doi.org/10.1107/S1600536811006271
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author Wang, Jian-Guo
Wu, Lin
Zhong, Chan-Juan
Ouyang, Zhao-Hui
Yi, De-Lian
author_facet Wang, Jian-Guo
Wu, Lin
Zhong, Chan-Juan
Ouyang, Zhao-Hui
Yi, De-Lian
author_sort Wang, Jian-Guo
collection PubMed
description In the title compound, C(15)H(12)O(4)·H(2)O, the two benzene rings are not coplanar, making a dihedral angle of 7.24 (16)°. An intra­molecular hy­droxy–carbonyl O—H⋯O hydrogen bond occurs. In the crystal, four inter­molecular O—H⋯O hydrogen bonds involving the hy­droxy residues, the carbonyl group and the water mol­ecule lead to the formation of a three-dimensional network. The supra­molecular structure is further stabilized by weak C—H⋯O inter­actions.
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spelling pubmed-30520092011-04-26 (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate Wang, Jian-Guo Wu, Lin Zhong, Chan-Juan Ouyang, Zhao-Hui Yi, De-Lian Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(12)O(4)·H(2)O, the two benzene rings are not coplanar, making a dihedral angle of 7.24 (16)°. An intra­molecular hy­droxy–carbonyl O—H⋯O hydrogen bond occurs. In the crystal, four inter­molecular O—H⋯O hydrogen bonds involving the hy­droxy residues, the carbonyl group and the water mol­ecule lead to the formation of a three-dimensional network. The supra­molecular structure is further stabilized by weak C—H⋯O inter­actions. International Union of Crystallography 2011-02-26 /pmc/articles/PMC3052009/ /pubmed/21522472 http://dx.doi.org/10.1107/S1600536811006271 Text en © Wang 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
Wang, Jian-Guo
Wu, Lin
Zhong, Chan-Juan
Ouyang, Zhao-Hui
Yi, De-Lian
(E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title_full (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title_fullStr (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title_full_unstemmed (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title_short (E)-1-(2,4-Dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
title_sort (e)-1-(2,4-dihy­droxy­phen­yl)-3-(4-hydroxy­phen­yl)prop-2-en-1-one monohydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052009/
https://www.ncbi.nlm.nih.gov/pubmed/21522472
http://dx.doi.org/10.1107/S1600536811006271
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