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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...

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Autores principales: Saez, Alex, Ramirez de Arellano, Carmen, El Aouad, Noureddine, Rodriguez, Silvia, Otalvaro, Felipe, Cortes, Diego, Saez, Jairo
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
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.
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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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