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4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate
In the structure of the title molecular salt, C(5)H(7)N(2) (+)·C(8)H(11)O(4) (−), the cis monoanions associate through short O—H⋯O hydrogen bonds in the carboxylic acid groups [graph set C(7)], forming zigzag chains which extend along the c axis. These are interlinked through pyridinium and amine...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201255/ https://www.ncbi.nlm.nih.gov/pubmed/22058823 http://dx.doi.org/10.1107/S1600536811039547 |
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author | Smith, Graham Wermuth, Urs D. |
author_facet | Smith, Graham Wermuth, Urs D. |
author_sort | Smith, Graham |
collection | PubMed |
description | In the structure of the title molecular salt, C(5)H(7)N(2) (+)·C(8)H(11)O(4) (−), the cis monoanions associate through short O—H⋯O hydrogen bonds in the carboxylic acid groups [graph set C(7)], forming zigzag chains which extend along the c axis. These are interlinked through pyridinium and amine N—H⋯O hydrogen bonds, giving a three-dimensional network structure. |
format | Online Article Text |
id | pubmed-3201255 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32012552011-11-06 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate Smith, Graham Wermuth, Urs D. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the structure of the title molecular salt, C(5)H(7)N(2) (+)·C(8)H(11)O(4) (−), the cis monoanions associate through short O—H⋯O hydrogen bonds in the carboxylic acid groups [graph set C(7)], forming zigzag chains which extend along the c axis. These are interlinked through pyridinium and amine N—H⋯O hydrogen bonds, giving a three-dimensional network structure. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201255/ /pubmed/22058823 http://dx.doi.org/10.1107/S1600536811039547 Text en © Smith and Wermuth 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 Smith, Graham Wermuth, Urs D. 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title | 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title_full | 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title_fullStr | 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title_full_unstemmed | 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title_short | 4-Aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
title_sort | 4-aminopyridinium cis-2-carboxycyclohexane-1-carboxylate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201255/ https://www.ncbi.nlm.nih.gov/pubmed/22058823 http://dx.doi.org/10.1107/S1600536811039547 |
work_keys_str_mv | AT smithgraham 4aminopyridiniumcis2carboxycyclohexane1carboxylate AT wermuthursd 4aminopyridiniumcis2carboxycyclohexane1carboxylate |