2,4-Dinitro-1-phenoxy­benzene

The title compound, C(12)H(8)N(2)O(5), was obtained by the reaction of 1-chloro-2,4-dinitro­benzene and phenol in the presence of potassium carbonate. The nitro-substituted benzene ring lies on a mirror plane, with one NO(2) group in the same plane and the other disordered across this plane. The phe...

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Detalles Bibliográficos
Autores principales: Du, Zhen-Ting, Xu, Yan, Yu, Hong-Rui, Li, Yong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979788/
https://www.ncbi.nlm.nih.gov/pubmed/21579833
http://dx.doi.org/10.1107/S1600536810001911
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author Du, Zhen-Ting
Xu, Yan
Yu, Hong-Rui
Li, Yong
author_facet Du, Zhen-Ting
Xu, Yan
Yu, Hong-Rui
Li, Yong
author_sort Du, Zhen-Ting
collection PubMed
description The title compound, C(12)H(8)N(2)O(5), was obtained by the reaction of 1-chloro-2,4-dinitro­benzene and phenol in the presence of potassium carbonate. The nitro-substituted benzene ring lies on a mirror plane, with one NO(2) group in the same plane and the other disordered across this plane. The phenoxy­benzene unit is placed perpendicular to this mirror, resulting in an exact orthogonal relationship between the phenyl and benzene rings in the mol­ecule. The crystal packing exhibits no significantly short inter­molecular contacts.
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spelling pubmed-29797882010-12-30 2,4-Dinitro-1-phenoxy­benzene Du, Zhen-Ting Xu, Yan Yu, Hong-Rui Li, Yong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(8)N(2)O(5), was obtained by the reaction of 1-chloro-2,4-dinitro­benzene and phenol in the presence of potassium carbonate. The nitro-substituted benzene ring lies on a mirror plane, with one NO(2) group in the same plane and the other disordered across this plane. The phenoxy­benzene unit is placed perpendicular to this mirror, resulting in an exact orthogonal relationship between the phenyl and benzene rings in the mol­ecule. The crystal packing exhibits no significantly short inter­molecular contacts. International Union of Crystallography 2010-01-20 /pmc/articles/PMC2979788/ /pubmed/21579833 http://dx.doi.org/10.1107/S1600536810001911 Text en © Du et al. 2010 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
Du, Zhen-Ting
Xu, Yan
Yu, Hong-Rui
Li, Yong
2,4-Dinitro-1-phenoxy­benzene
title 2,4-Dinitro-1-phenoxy­benzene
title_full 2,4-Dinitro-1-phenoxy­benzene
title_fullStr 2,4-Dinitro-1-phenoxy­benzene
title_full_unstemmed 2,4-Dinitro-1-phenoxy­benzene
title_short 2,4-Dinitro-1-phenoxy­benzene
title_sort 2,4-dinitro-1-phenoxy­benzene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979788/
https://www.ncbi.nlm.nih.gov/pubmed/21579833
http://dx.doi.org/10.1107/S1600536810001911
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AT xuyan 24dinitro1phenoxybenzene
AT yuhongrui 24dinitro1phenoxybenzene
AT liyong 24dinitro1phenoxybenzene

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