1,2-Bis(4-meth­oxy­phen­oxy)ethane

The whole mol­ecule of the title compound, C(16)H(18)O(4), is generated by twofold rotational symmetry; the twofold axis bis­ects the central C—C bond. The O—C—C—O torsion angle about the central C—C bond is 69.45 (16)°. Symmetry-related benzene rings are inclined to one another by 64.91 (8)°. In th...

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Detalles Bibliográficos
Autores principales: Ji, Jun, Zhang, XiuQin, Wang, Kai, Ju, ChaoFan, Chen, Qiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629599/
https://www.ncbi.nlm.nih.gov/pubmed/23634086
http://dx.doi.org/10.1107/S1600536813007009
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author Ji, Jun
Zhang, XiuQin
Wang, Kai
Ju, ChaoFan
Chen, Qiang
author_facet Ji, Jun
Zhang, XiuQin
Wang, Kai
Ju, ChaoFan
Chen, Qiang
author_sort Ji, Jun
collection PubMed
description The whole mol­ecule of the title compound, C(16)H(18)O(4), is generated by twofold rotational symmetry; the twofold axis bis­ects the central C—C bond. The O—C—C—O torsion angle about the central C—C bond is 69.45 (16)°. Symmetry-related benzene rings are inclined to one another by 64.91 (8)°. In the crystal, mol­ecules are connected by C—H⋯O hydrogen bonds, forming a three-dimensional network.
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spelling pubmed-36295992013-04-30 1,2-Bis(4-meth­oxy­phen­oxy)ethane Ji, Jun Zhang, XiuQin Wang, Kai Ju, ChaoFan Chen, Qiang Acta Crystallogr Sect E Struct Rep Online Organic Papers The whole mol­ecule of the title compound, C(16)H(18)O(4), is generated by twofold rotational symmetry; the twofold axis bis­ects the central C—C bond. The O—C—C—O torsion angle about the central C—C bond is 69.45 (16)°. Symmetry-related benzene rings are inclined to one another by 64.91 (8)°. In the crystal, mol­ecules are connected by C—H⋯O hydrogen bonds, forming a three-dimensional network. International Union of Crystallography 2013-03-16 /pmc/articles/PMC3629599/ /pubmed/23634086 http://dx.doi.org/10.1107/S1600536813007009 Text en © Ji et al. 2013 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
Ji, Jun
Zhang, XiuQin
Wang, Kai
Ju, ChaoFan
Chen, Qiang
1,2-Bis(4-meth­oxy­phen­oxy)ethane
title 1,2-Bis(4-meth­oxy­phen­oxy)ethane
title_full 1,2-Bis(4-meth­oxy­phen­oxy)ethane
title_fullStr 1,2-Bis(4-meth­oxy­phen­oxy)ethane
title_full_unstemmed 1,2-Bis(4-meth­oxy­phen­oxy)ethane
title_short 1,2-Bis(4-meth­oxy­phen­oxy)ethane
title_sort 1,2-bis(4-meth­oxy­phen­oxy)ethane
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629599/
https://www.ncbi.nlm.nih.gov/pubmed/23634086
http://dx.doi.org/10.1107/S1600536813007009
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