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(E)-2,2′-[3-(2-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. Each of the pairs of hydroxy and carbonyl O atoms are oriented to allow for the formation of intramolecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives. The nitro group is...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238826/ https://www.ncbi.nlm.nih.gov/pubmed/22199679 http://dx.doi.org/10.1107/S1600536811043686 |
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author | Cha, Joo Hwan Kim, Young Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun |
author_facet | Cha, Joo Hwan Kim, Young Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun |
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. Each of the pairs of hydroxy and carbonyl O atoms are oriented to allow for the formation of intramolecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives. The nitro group is rotationally disordered over two orientations in a 0.544 (6):0.456 (6) ratio. In the crystal, weak intermolecualr C—H⋯O hydrogen bonds link molecules into layers parallel to the ab plane. |
format | Online Article Text |
id | pubmed-3238826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32388262011-12-23 (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) Cha, Joo Hwan Kim, Young Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun 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. Each of the pairs of hydroxy and carbonyl O atoms are oriented to allow for the formation of intramolecular O—H⋯O hydrogen bonds, which are typical of xanthene derivatives. The nitro group is rotationally disordered over two orientations in a 0.544 (6):0.456 (6) ratio. In the crystal, weak intermolecualr C—H⋯O hydrogen bonds link molecules into layers parallel to the ab plane. International Union of Crystallography 2011-11-02 /pmc/articles/PMC3238826/ /pubmed/22199679 http://dx.doi.org/10.1107/S1600536811043686 Text en © Cha 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 Cha, Joo Hwan Kim, Young Hee Min, Sun-Joon Cho, Yong Seo Lee, Jae Kyun (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title | (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_full | (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_fullStr | (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_full_unstemmed | (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_short | (E)-2,2′-[3-(2-Nitrophenyl)prop-2-ene-1,1-diyl]bis(3-hydroxy-5,5-dimethylcyclohex-2-en-1-one) |
title_sort | (e)-2,2′-[3-(2-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/PMC3238826/ https://www.ncbi.nlm.nih.gov/pubmed/22199679 http://dx.doi.org/10.1107/S1600536811043686 |
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