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4-(o-Tolyl)piperazin-1-ium chloride
In the title molecular salt, C(11)H(17)N(2) (+)·Cl(−), the piperazin-1-ium ring adopts a chair conformation with the aromatic ring in a pseudo-equatorial orientation. The dihedral angle between the benzene ring and the mean plane of the piperazin-1-ium ring is 51.22 (6)°. In the crystal, N—H⋯Cl hyd...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247500/ https://www.ncbi.nlm.nih.gov/pubmed/22220118 http://dx.doi.org/10.1107/S1600536811044394 |
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author | Fun, Hoong-Kun Asik, Safra Izuani Jama Chandrakantha, B. Isloor, Arun M. Shetty, Prakash |
author_facet | Fun, Hoong-Kun Asik, Safra Izuani Jama Chandrakantha, B. Isloor, Arun M. Shetty, Prakash |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title molecular salt, C(11)H(17)N(2) (+)·Cl(−), the piperazin-1-ium ring adopts a chair conformation with the aromatic ring in a pseudo-equatorial orientation. The dihedral angle between the benzene ring and the mean plane of the piperazin-1-ium ring is 51.22 (6)°. In the crystal, N—H⋯Cl hydrogen bonds link the molecules into chains propagating in [100]. Weak C—H⋯π interactions also ocur. |
format | Online Article Text |
id | pubmed-3247500 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32475002012-01-04 4-(o-Tolyl)piperazin-1-ium chloride Fun, Hoong-Kun Asik, Safra Izuani Jama Chandrakantha, B. Isloor, Arun M. Shetty, Prakash Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecular salt, C(11)H(17)N(2) (+)·Cl(−), the piperazin-1-ium ring adopts a chair conformation with the aromatic ring in a pseudo-equatorial orientation. The dihedral angle between the benzene ring and the mean plane of the piperazin-1-ium ring is 51.22 (6)°. In the crystal, N—H⋯Cl hydrogen bonds link the molecules into chains propagating in [100]. Weak C—H⋯π interactions also ocur. International Union of Crystallography 2011-10-29 /pmc/articles/PMC3247500/ /pubmed/22220118 http://dx.doi.org/10.1107/S1600536811044394 Text en © Fun 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 Fun, Hoong-Kun Asik, Safra Izuani Jama Chandrakantha, B. Isloor, Arun M. Shetty, Prakash 4-(o-Tolyl)piperazin-1-ium chloride |
title | 4-(o-Tolyl)piperazin-1-ium chloride |
title_full | 4-(o-Tolyl)piperazin-1-ium chloride |
title_fullStr | 4-(o-Tolyl)piperazin-1-ium chloride |
title_full_unstemmed | 4-(o-Tolyl)piperazin-1-ium chloride |
title_short | 4-(o-Tolyl)piperazin-1-ium chloride |
title_sort | 4-(o-tolyl)piperazin-1-ium chloride |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247500/ https://www.ncbi.nlm.nih.gov/pubmed/22220118 http://dx.doi.org/10.1107/S1600536811044394 |
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