(2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone

In the title compound, C(12)H(12)ClN(3)O(5), the piperidine ring adopts a chair conformation. One of the nitro groups is almost coplanar with the aromatic ring [O—N—C—C = −1.4 (2)°], whereas the other one is significantly twisted out of the ring plane [O—N—C—C = 34.7 (2)°]. The crystal packing is st...

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Detalles Bibliográficos
Autores principales: Luo, Xun, Huang, Yun-Chuang, Gao, Chao, Yu, Luo-Ting
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089352/
https://www.ncbi.nlm.nih.gov/pubmed/21754392
http://dx.doi.org/10.1107/S1600536811011469
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author Luo, Xun
Huang, Yun-Chuang
Gao, Chao
Yu, Luo-Ting
author_facet Luo, Xun
Huang, Yun-Chuang
Gao, Chao
Yu, Luo-Ting
author_sort Luo, Xun
collection PubMed
description In the title compound, C(12)H(12)ClN(3)O(5), the piperidine ring adopts a chair conformation. One of the nitro groups is almost coplanar with the aromatic ring [O—N—C—C = −1.4 (2)°], whereas the other one is significantly twisted out of the ring plane [O—N—C—C = 34.7 (2)°]. The crystal packing is stabilized by inter­molecular π–π stacking inter­actions with centroid–centroid distances of 3.579 (3) Å.
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spelling pubmed-30893522011-07-13 (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone Luo, Xun Huang, Yun-Chuang Gao, Chao Yu, Luo-Ting Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(12)ClN(3)O(5), the piperidine ring adopts a chair conformation. One of the nitro groups is almost coplanar with the aromatic ring [O—N—C—C = −1.4 (2)°], whereas the other one is significantly twisted out of the ring plane [O—N—C—C = 34.7 (2)°]. The crystal packing is stabilized by inter­molecular π–π stacking inter­actions with centroid–centroid distances of 3.579 (3) Å. International Union of Crystallography 2011-04-07 /pmc/articles/PMC3089352/ /pubmed/21754392 http://dx.doi.org/10.1107/S1600536811011469 Text en © Luo et al. 2011 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
Luo, Xun
Huang, Yun-Chuang
Gao, Chao
Yu, Luo-Ting
(2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title_full (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title_fullStr (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title_full_unstemmed (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title_short (2-Chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
title_sort (2-chloro-3,5-dinitro­phen­yl)(piperidin-1-yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089352/
https://www.ncbi.nlm.nih.gov/pubmed/21754392
http://dx.doi.org/10.1107/S1600536811011469
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AT huangyunchuang 2chloro35dinitrophenylpiperidin1ylmethanone
AT gaochao 2chloro35dinitrophenylpiperidin1ylmethanone
AT yuluoting 2chloro35dinitrophenylpiperidin1ylmethanone

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