Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one

The title chalcone derivative, C(14)H(10)Cl(2)O(3), is almost planar, with a dihedral angle of 7.0 (2) ° between the 3,5-di­chloro-2-hy­droxy­phenyl and 5-methyl­furan rings. There is an intra­molecular O—H⋯O hydrogen bond present forming an S(6) ring motif. In the crystal, mol­ecules are linked by...

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Autores principales: Sreenatha, N. R., Lakshminarayana, B. N., Ganesha, D. P., Gnanendra, C. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2018
Materias:
Research Communications
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176444/
https://www.ncbi.nlm.nih.gov/pubmed/30319799
http://dx.doi.org/10.1107/S2056989018012173
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author Sreenatha, N. R.
Lakshminarayana, B. N.
Ganesha, D. P.
Gnanendra, C. R.
author_facet Sreenatha, N. R.
Lakshminarayana, B. N.
Ganesha, D. P.
Gnanendra, C. R.
author_sort Sreenatha, N. R.
collection PubMed
description The title chalcone derivative, C(14)H(10)Cl(2)O(3), is almost planar, with a dihedral angle of 7.0 (2) ° between the 3,5-di­chloro-2-hy­droxy­phenyl and 5-methyl­furan rings. There is an intra­molecular O—H⋯O hydrogen bond present forming an S(6) ring motif. In the crystal, mol­ecules are linked by bifurcated C—H/H⋯O hydrogen bonds, enclosing an R (1) (2)(6) ring motif, forming a 2(1) helix propagating along the b-axis direction. The inter­molecular inter­actions were qu­anti­fied using Hirshfeld surface analysis.
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spelling pubmed-61764442018-10-12 Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one Sreenatha, N. R. Lakshminarayana, B. N. Ganesha, D. P. Gnanendra, C. R. Acta Crystallogr E Crystallogr Commun Research Communications The title chalcone derivative, C(14)H(10)Cl(2)O(3), is almost planar, with a dihedral angle of 7.0 (2) ° between the 3,5-di­chloro-2-hy­droxy­phenyl and 5-methyl­furan rings. There is an intra­molecular O—H⋯O hydrogen bond present forming an S(6) ring motif. In the crystal, mol­ecules are linked by bifurcated C—H/H⋯O hydrogen bonds, enclosing an R (1) (2)(6) ring motif, forming a 2(1) helix propagating along the b-axis direction. The inter­molecular inter­actions were qu­anti­fied using Hirshfeld surface analysis. International Union of Crystallography 2018-09-18 /pmc/articles/PMC6176444/ /pubmed/30319799 http://dx.doi.org/10.1107/S2056989018012173 Text en © Sreenatha et al. 2018 http://creativecommons.org/licenses/by/2.0/uk/ 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/2.0/uk/
spellingShingle Research Communications
Sreenatha, N. R.
Lakshminarayana, B. N.
Ganesha, D. P.
Gnanendra, C. R.
Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title_full Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title_fullStr Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title_full_unstemmed Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title_short Crystal structure and Hirshfeld surface analysis of (E)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
title_sort crystal structure and hirshfeld surface analysis of (e)-1-(3,5-di­chloro-2-hy­droxy­phen­yl)-3-(5-methyl­furan-2-yl)prop-2-en-1-one
topic Research Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6176444/
https://www.ncbi.nlm.nih.gov/pubmed/30319799
http://dx.doi.org/10.1107/S2056989018012173
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