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Semisynthetic roxburghin tetramethyl ether
The title molecule, (E)-2,3′,4,5-tetramethoxystilbene, C(18)H(20)O(4), is virtually planar. The angle between the two benzene rings is 4.06 (6)°. The intermolecular interactions present in the structure are weak. There are C—H⋯O hydrogen bonds and C—H⋯π-electron ring interactions. The molecul...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961722/ https://www.ncbi.nlm.nih.gov/pubmed/21202934 http://dx.doi.org/10.1107/S1600536808018266 |
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author | Saez, Alex Ramirez de Arellano, Carmen El Aouad, Noureddine Rodriguez, Silvia Otalvaro, Felipe Cortes, Diego Saez, Jairo |
author_facet | Saez, Alex Ramirez de Arellano, Carmen El Aouad, Noureddine Rodriguez, Silvia Otalvaro, Felipe Cortes, Diego Saez, Jairo |
author_sort | Saez, Alex |
collection | PubMed |
description | The title molecule, (E)-2,3′,4,5-tetramethoxystilbene, C(18)H(20)O(4), is virtually planar. The angle between the two benzene rings is 4.06 (6)°. The intermolecular interactions present in the structure are weak. There are C—H⋯O hydrogen bonds and C—H⋯π-electron ring interactions. The molecules are ordered into planes that are parallel to ([Image: see text]01). The distance between adjacent planes is about 3.3 Å and therefore π–π electron interactions between the aromatic planes are also plausible. |
format | Text |
id | pubmed-2961722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29617222010-12-30 Semisynthetic roxburghin tetramethyl ether Saez, Alex Ramirez de Arellano, Carmen El Aouad, Noureddine Rodriguez, Silvia Otalvaro, Felipe Cortes, Diego Saez, Jairo Acta Crystallogr Sect E Struct Rep Online Organic Papers The title molecule, (E)-2,3′,4,5-tetramethoxystilbene, C(18)H(20)O(4), is virtually planar. The angle between the two benzene rings is 4.06 (6)°. The intermolecular interactions present in the structure are weak. There are C—H⋯O hydrogen bonds and C—H⋯π-electron ring interactions. The molecules are ordered into planes that are parallel to ([Image: see text]01). The distance between adjacent planes is about 3.3 Å and therefore π–π electron interactions between the aromatic planes are also plausible. International Union of Crystallography 2008-06-19 /pmc/articles/PMC2961722/ /pubmed/21202934 http://dx.doi.org/10.1107/S1600536808018266 Text en © Saez et al. 2008 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 Saez, Alex Ramirez de Arellano, Carmen El Aouad, Noureddine Rodriguez, Silvia Otalvaro, Felipe Cortes, Diego Saez, Jairo Semisynthetic roxburghin tetramethyl ether |
title | Semisynthetic roxburghin tetramethyl ether |
title_full | Semisynthetic roxburghin tetramethyl ether |
title_fullStr | Semisynthetic roxburghin tetramethyl ether |
title_full_unstemmed | Semisynthetic roxburghin tetramethyl ether |
title_short | Semisynthetic roxburghin tetramethyl ether |
title_sort | semisynthetic roxburghin tetramethyl ether |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961722/ https://www.ncbi.nlm.nih.gov/pubmed/21202934 http://dx.doi.org/10.1107/S1600536808018266 |
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