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(E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one
In the title compound, C(21)H(24)O(3), intermolecular O—H⋯O and C—H⋯O interactions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the molecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π interactions....
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050273/ https://www.ncbi.nlm.nih.gov/pubmed/21522676 http://dx.doi.org/10.1107/S1600536810052086 |
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author | Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun |
author_facet | Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun |
author_sort | Ngaini, Zainab |
collection | PubMed |
description | In the title compound, C(21)H(24)O(3), intermolecular O—H⋯O and C—H⋯O interactions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the molecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π interactions. |
format | Text |
id | pubmed-3050273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30502732011-04-26 (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(24)O(3), intermolecular O—H⋯O and C—H⋯O interactions form bifurcated acceptor bonds, generating R (2) (1)(6) ring motifs. These ring motifs link the molecules into extended chains along [010]. The crystal structure is further stabilized by C—H⋯π interactions. International Union of Crystallography 2010-12-18 /pmc/articles/PMC3050273/ /pubmed/21522676 http://dx.doi.org/10.1107/S1600536810052086 Text en © Ngaini 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 Ngaini, Zainab Fadzillah, Siti Muhaini Haris Hussain, Hasnain Razak, Ibrahim Abdul Fun, Hoong-Kun (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title | (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_full | (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_fullStr | (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_full_unstemmed | (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_short | (E)-1-[4-(Hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
title_sort | (e)-1-[4-(hexyloxy)phenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050273/ https://www.ncbi.nlm.nih.gov/pubmed/21522676 http://dx.doi.org/10.1107/S1600536810052086 |
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