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(E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one
In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent molecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O intermolecular interactions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs....
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969075/ https://www.ncbi.nlm.nih.gov/pubmed/21582591 http://dx.doi.org/10.1107/S160053680901054X |
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author | Razak, Ibrahim Abdul Fun, Hoong-Kun Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain |
author_facet | Razak, Ibrahim Abdul Fun, Hoong-Kun Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain |
author_sort | Razak, Ibrahim Abdul |
collection | PubMed |
description | In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent molecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O intermolecular interactions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs. These intermolecular interactions link the molecules into one-dimensional chains along the [10[Image: see text]] direction. The crystal structure is further stabilized by C—H⋯π interactions. |
format | Text |
id | pubmed-2969075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29690752010-12-30 (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one Razak, Ibrahim Abdul Fun, Hoong-Kun Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(32)O(3), the asymmetric unit contains two crystallographically independent molecules: both enone groups adopt an s-cis configuration. In the crystal, O—H⋯O and C—H⋯O intermolecular interactions form bifurcated hydrogen bonds, which generate R (1) (2)(6) ring motifs. These intermolecular interactions link the molecules into one-dimensional chains along the [10[Image: see text]] direction. The crystal structure is further stabilized by C—H⋯π interactions. International Union of Crystallography 2009-03-28 /pmc/articles/PMC2969075/ /pubmed/21582591 http://dx.doi.org/10.1107/S160053680901054X Text en © Razak et al. 2009 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 Razak, Ibrahim Abdul Fun, Hoong-Kun Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title | (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_full | (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_fullStr | (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_full_unstemmed | (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_short | (E)-1-(4-Decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_sort | (e)-1-(4-decyloxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969075/ https://www.ncbi.nlm.nih.gov/pubmed/21582591 http://dx.doi.org/10.1107/S160053680901054X |
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