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N,N′,N′′-Tricyclohexylguanidinium iodide
In the title compound, C(19)H(36)N(3) (+)·I(−), the orientation of the cyclohexyl rings around the planar (sum of N—C—N angles = 360°) CN(3) (+) unit produces steric hindrance around the N—H groups. As a consequence of this particular orientation of the tricyclohexylguanidinium cation (hereafter...
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/PMC3239094/ https://www.ncbi.nlm.nih.gov/pubmed/22199942 http://dx.doi.org/10.1107/S1600536811049683 |
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author | Said, Farouq F. Ali, Basem F. Richeson, Darrin |
author_facet | Said, Farouq F. Ali, Basem F. Richeson, Darrin |
author_sort | Said, Farouq F. |
collection | PubMed |
description | In the title compound, C(19)H(36)N(3) (+)·I(−), the orientation of the cyclohexyl rings around the planar (sum of N—C—N angles = 360°) CN(3) (+) unit produces steric hindrance around the N—H groups. As a consequence of this particular orientation of the tricyclohexylguanidinium cation (hereafter denoted CHGH(+)), hydrogen bonding is restricted to classical N—H⋯I and non-clasical (cyclohexyl)C—H⋯I hydrogen bonds. The propeller CHGH(+) cation and the oriented hydrogen-bonding interactions lead to a three-dimensional supramolecular structure. |
format | Online Article Text |
id | pubmed-3239094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32390942011-12-23 N,N′,N′′-Tricyclohexylguanidinium iodide Said, Farouq F. Ali, Basem F. Richeson, Darrin Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(36)N(3) (+)·I(−), the orientation of the cyclohexyl rings around the planar (sum of N—C—N angles = 360°) CN(3) (+) unit produces steric hindrance around the N—H groups. As a consequence of this particular orientation of the tricyclohexylguanidinium cation (hereafter denoted CHGH(+)), hydrogen bonding is restricted to classical N—H⋯I and non-clasical (cyclohexyl)C—H⋯I hydrogen bonds. The propeller CHGH(+) cation and the oriented hydrogen-bonding interactions lead to a three-dimensional supramolecular structure. International Union of Crystallography 2011-11-30 /pmc/articles/PMC3239094/ /pubmed/22199942 http://dx.doi.org/10.1107/S1600536811049683 Text en © Said 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 Said, Farouq F. Ali, Basem F. Richeson, Darrin N,N′,N′′-Tricyclohexylguanidinium iodide |
title |
N,N′,N′′-Tricyclohexylguanidinium iodide |
title_full |
N,N′,N′′-Tricyclohexylguanidinium iodide |
title_fullStr |
N,N′,N′′-Tricyclohexylguanidinium iodide |
title_full_unstemmed |
N,N′,N′′-Tricyclohexylguanidinium iodide |
title_short |
N,N′,N′′-Tricyclohexylguanidinium iodide |
title_sort | n,n′,n′′-tricyclohexylguanidinium iodide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239094/ https://www.ncbi.nlm.nih.gov/pubmed/22199942 http://dx.doi.org/10.1107/S1600536811049683 |
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