1,4-Di-n-hept­yloxy-2,5-dinitro­benzene

The complete molecule of the title compound, C(20)H(32)N(2)O(6), is generated by crystallographic inversion symmetry. The two mutually trans nitro substituents are hence in fully eclipsed conformation and also twisted by 43.2 (2)° with respect to the phenyl ring plane. The benzene-connected portions...

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Detalles Bibliográficos
Autores principales: Blackburn, Octavia A., Coe, Benjamin J., Futhey, Robert, Helliwell, Madeleine
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980120/
https://www.ncbi.nlm.nih.gov/pubmed/21580141
http://dx.doi.org/10.1107/S160053680905123X
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author Blackburn, Octavia A.
Coe, Benjamin J.
Futhey, Robert
Helliwell, Madeleine
author_facet Blackburn, Octavia A.
Coe, Benjamin J.
Futhey, Robert
Helliwell, Madeleine
author_sort Blackburn, Octavia A.
collection PubMed
description The complete molecule of the title compound, C(20)H(32)N(2)O(6), is generated by crystallographic inversion symmetry. The two mutually trans nitro substituents are hence in fully eclipsed conformation and also twisted by 43.2 (2)° with respect to the phenyl ring plane. The benzene-connected portions of the alk­oxy substituents lie almost coplanar with the ring [C—O—C—C torsion angle = 2.0 (2)°]. In the crystal, weak C—H⋯O interactions link the molecules.
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spelling pubmed-29801202010-12-30 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene Blackburn, Octavia A. Coe, Benjamin J. Futhey, Robert Helliwell, Madeleine Acta Crystallogr Sect E Struct Rep Online Organic Papers The complete molecule of the title compound, C(20)H(32)N(2)O(6), is generated by crystallographic inversion symmetry. The two mutually trans nitro substituents are hence in fully eclipsed conformation and also twisted by 43.2 (2)° with respect to the phenyl ring plane. The benzene-connected portions of the alk­oxy substituents lie almost coplanar with the ring [C—O—C—C torsion angle = 2.0 (2)°]. In the crystal, weak C—H⋯O interactions link the molecules. International Union of Crystallography 2009-12-04 /pmc/articles/PMC2980120/ /pubmed/21580141 http://dx.doi.org/10.1107/S160053680905123X Text en © Blackburn 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
Blackburn, Octavia A.
Coe, Benjamin J.
Futhey, Robert
Helliwell, Madeleine
1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title_full 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title_fullStr 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title_full_unstemmed 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title_short 1,4-Di-n-hept­yloxy-2,5-dinitro­benzene
title_sort 1,4-di-n-hept­yloxy-2,5-dinitro­benzene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980120/
https://www.ncbi.nlm.nih.gov/pubmed/21580141
http://dx.doi.org/10.1107/S160053680905123X
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AT coebenjaminj 14dinheptyloxy25dinitrobenzene
AT futheyrobert 14dinheptyloxy25dinitrobenzene
AT helliwellmadeleine 14dinheptyloxy25dinitrobenzene

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