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2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one)
In the title compound, C(25)H(29)NO(6), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are oriented to allow for the formation of two intramolecular O—H⋯O hydrogen bonds. In the crystal, weak C—H⋯O hydrogen bonds are formed b...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414961/ https://www.ncbi.nlm.nih.gov/pubmed/22904948 http://dx.doi.org/10.1107/S1600536812032242 |
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author | Cha, Joo Hwan Cho, Yong Seo Lee, Jae Kyun Park, Junghwan Sato, Hiroyasu |
author_facet | Cha, Joo Hwan Cho, Yong Seo Lee, Jae Kyun Park, Junghwan Sato, Hiroyasu |
author_sort | Cha, Joo Hwan |
collection | PubMed |
description | In the title compound, C(25)H(29)NO(6), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are oriented to allow for the formation of two intramolecular O—H⋯O hydrogen bonds. In the crystal, weak C—H⋯O hydrogen bonds are formed between molecules, generating a two-dimensional supramolecular structure. |
format | Online Article Text |
id | pubmed-3414961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34149612012-08-17 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) Cha, Joo Hwan Cho, Yong Seo Lee, Jae Kyun Park, Junghwan Sato, Hiroyasu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(29)NO(6), each of the cyclohexenone rings adopts a half-chair conformation. The hydroxy and carbonyl O atoms face each other and are oriented to allow for the formation of two intramolecular O—H⋯O hydrogen bonds. In the crystal, weak C—H⋯O hydrogen bonds are formed between molecules, generating a two-dimensional supramolecular structure. International Union of Crystallography 2012-07-21 /pmc/articles/PMC3414961/ /pubmed/22904948 http://dx.doi.org/10.1107/S1600536812032242 Text en © Cha et al. 2012 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 Cha, Joo Hwan Cho, Yong Seo Lee, Jae Kyun Park, Junghwan Sato, Hiroyasu 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title | 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_full | 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_fullStr | 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_full_unstemmed | 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_short | 2,2′-[(E)-3-(4-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_sort | 2,2′-[(e)-3-(4-nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414961/ https://www.ncbi.nlm.nih.gov/pubmed/22904948 http://dx.doi.org/10.1107/S1600536812032242 |
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