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2-(2,4-Difluorophenyl)-5-nitropyridine
In the title molecule, C(11)H(6)F(2)N(2)O(2), the benzene and pyridine rings form a dihedral angle of 32.57 (6)°. The nitro group is tilted with respect to the pyridine ring by 12.26 (9)°. An intramolecular C—H⋯F hydrogen bond is present. In the crystal, molecules interact through π–π stacking i...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393273/ https://www.ncbi.nlm.nih.gov/pubmed/22807830 http://dx.doi.org/10.1107/S1600536812024713 |
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author | Sun, Feng Shen, Xuan Zhao, Rui Wang, Xin Zhu, Dun-Ru |
author_facet | Sun, Feng Shen, Xuan Zhao, Rui Wang, Xin Zhu, Dun-Ru |
author_sort | Sun, Feng |
collection | PubMed |
description | In the title molecule, C(11)H(6)F(2)N(2)O(2), the benzene and pyridine rings form a dihedral angle of 32.57 (6)°. The nitro group is tilted with respect to the pyridine ring by 12.26 (9)°. An intramolecular C—H⋯F hydrogen bond is present. In the crystal, molecules interact through π–π stacking interactions [centroid–centroid distances = 3.7457 (14) Å], forming columnar arrangements along the b axis. The crystal packing is further enforced by intermolecular C—H⋯O and C—H⋯N hydrogen bonds. |
format | Online Article Text |
id | pubmed-3393273 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33932732012-07-17 2-(2,4-Difluorophenyl)-5-nitropyridine Sun, Feng Shen, Xuan Zhao, Rui Wang, Xin Zhu, Dun-Ru Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecule, C(11)H(6)F(2)N(2)O(2), the benzene and pyridine rings form a dihedral angle of 32.57 (6)°. The nitro group is tilted with respect to the pyridine ring by 12.26 (9)°. An intramolecular C—H⋯F hydrogen bond is present. In the crystal, molecules interact through π–π stacking interactions [centroid–centroid distances = 3.7457 (14) Å], forming columnar arrangements along the b axis. The crystal packing is further enforced by intermolecular C—H⋯O and C—H⋯N hydrogen bonds. International Union of Crystallography 2012-06-02 /pmc/articles/PMC3393273/ /pubmed/22807830 http://dx.doi.org/10.1107/S1600536812024713 Text en © Sun et al. 2012 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 Sun, Feng Shen, Xuan Zhao, Rui Wang, Xin Zhu, Dun-Ru 2-(2,4-Difluorophenyl)-5-nitropyridine |
title | 2-(2,4-Difluorophenyl)-5-nitropyridine |
title_full | 2-(2,4-Difluorophenyl)-5-nitropyridine |
title_fullStr | 2-(2,4-Difluorophenyl)-5-nitropyridine |
title_full_unstemmed | 2-(2,4-Difluorophenyl)-5-nitropyridine |
title_short | 2-(2,4-Difluorophenyl)-5-nitropyridine |
title_sort | 2-(2,4-difluorophenyl)-5-nitropyridine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393273/ https://www.ncbi.nlm.nih.gov/pubmed/22807830 http://dx.doi.org/10.1107/S1600536812024713 |
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