1,4-Phenyl­ene diallyl bis­(carbonate)

The title mol­ecule, C(14)H(14)O(6), is based on a benzene core di-substituted by allyl carbonate groups in the para positions. The mol­ecule is placed on an inversion centre, and the substituents are twisted with respect to the central benzene ring plane. The crystal structure does not include sign...

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Autores principales: López-Velázquez, Delia, Núñez-Méndez, Irma, Bernès, Sylvain, Martínez-de la Luz, Isabel, Pérez-Cruz, María Ana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2023
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993898/
https://www.ncbi.nlm.nih.gov/pubmed/36911076
http://dx.doi.org/10.1107/S2414314623001335
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author López-Velázquez, Delia
Núñez-Méndez, Irma
Bernès, Sylvain
Martínez-de la Luz, Isabel
Pérez-Cruz, María Ana
author_facet López-Velázquez, Delia
Núñez-Méndez, Irma
Bernès, Sylvain
Martínez-de la Luz, Isabel
Pérez-Cruz, María Ana
author_sort López-Velázquez, Delia
collection PubMed
description The title mol­ecule, C(14)H(14)O(6), is based on a benzene core di-substituted by allyl carbonate groups in the para positions. The mol­ecule is placed on an inversion centre, and the substituents are twisted with respect to the central benzene ring plane. The crystal structure does not include significant inter­molecular inter­actions other than weak C—H⋯O contacts between CH groups in the benzene ring and carbonate O atoms. [Image: see text]
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spelling pubmed-99938982023-03-09 1,4-Phenyl­ene diallyl bis­(carbonate) López-Velázquez, Delia Núñez-Méndez, Irma Bernès, Sylvain Martínez-de la Luz, Isabel Pérez-Cruz, María Ana IUCrdata Data Reports The title mol­ecule, C(14)H(14)O(6), is based on a benzene core di-substituted by allyl carbonate groups in the para positions. The mol­ecule is placed on an inversion centre, and the substituents are twisted with respect to the central benzene ring plane. The crystal structure does not include significant inter­molecular inter­actions other than weak C—H⋯O contacts between CH groups in the benzene ring and carbonate O atoms. [Image: see text] International Union of Crystallography 2023-02-21 /pmc/articles/PMC9993898/ /pubmed/36911076 http://dx.doi.org/10.1107/S2414314623001335 Text en © López-Velázquez et al. 2023 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
López-Velázquez, Delia
Núñez-Méndez, Irma
Bernès, Sylvain
Martínez-de la Luz, Isabel
Pérez-Cruz, María Ana
1,4-Phenyl­ene diallyl bis­(carbonate)
title 1,4-Phenyl­ene diallyl bis­(carbonate)
title_full 1,4-Phenyl­ene diallyl bis­(carbonate)
title_fullStr 1,4-Phenyl­ene diallyl bis­(carbonate)
title_full_unstemmed 1,4-Phenyl­ene diallyl bis­(carbonate)
title_short 1,4-Phenyl­ene diallyl bis­(carbonate)
title_sort 1,4-phenyl­ene diallyl bis­(carbonate)
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9993898/
https://www.ncbi.nlm.nih.gov/pubmed/36911076
http://dx.doi.org/10.1107/S2414314623001335
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AT nunezmendezirma 14phenylenediallylbiscarbonate
AT bernessylvain 14phenylenediallylbiscarbonate
AT martinezdelaluzisabel 14phenylenediallylbiscarbonate
AT perezcruzmariaana 14phenylenediallylbiscarbonate

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