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2,3-Diaminopyridinium benzoate benzoic acid solvate
In the title compound, C(5)H(8)N(3) (+)·C(7)H(5)O(2) (−)·C(7)H(6)O(2), the carboxyl and carboxylate groups are twisted away from their attached benzene rings by 10.75 (7) and 20.33 (6)°, respectively. In the crystal structure, the 2,3-diaminopyridinium cations, benzoate anions and benzoic acid mol...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979855/ https://www.ncbi.nlm.nih.gov/pubmed/21579888 http://dx.doi.org/10.1107/S1600536810001443 |
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author | Hemamalini, Madhukar Fun, Hoong-Kun |
author_facet | Hemamalini, Madhukar Fun, Hoong-Kun |
author_sort | Hemamalini, Madhukar |
collection | PubMed |
description | In the title compound, C(5)H(8)N(3) (+)·C(7)H(5)O(2) (−)·C(7)H(6)O(2), the carboxyl and carboxylate groups are twisted away from their attached benzene rings by 10.75 (7) and 20.33 (6)°, respectively. In the crystal structure, the 2,3-diaminopyridinium cations, benzoate anions and benzoic acid molecules are linked into a two-dimensional network parallel to (001) by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds and π–π interactions between the pyridinium rings [centroid–centroid distance = 3.4981 (7) Å]. |
format | Text |
id | pubmed-2979855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29798552010-12-30 2,3-Diaminopyridinium benzoate benzoic acid solvate Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(5)H(8)N(3) (+)·C(7)H(5)O(2) (−)·C(7)H(6)O(2), the carboxyl and carboxylate groups are twisted away from their attached benzene rings by 10.75 (7) and 20.33 (6)°, respectively. In the crystal structure, the 2,3-diaminopyridinium cations, benzoate anions and benzoic acid molecules are linked into a two-dimensional network parallel to (001) by O—H⋯O, N—H⋯O and C—H⋯O hydrogen bonds and π–π interactions between the pyridinium rings [centroid–centroid distance = 3.4981 (7) Å]. International Union of Crystallography 2010-01-30 /pmc/articles/PMC2979855/ /pubmed/21579888 http://dx.doi.org/10.1107/S1600536810001443 Text en © Hemamalini and Fun 2010 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 Hemamalini, Madhukar Fun, Hoong-Kun 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title | 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title_full | 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title_fullStr | 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title_full_unstemmed | 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title_short | 2,3-Diaminopyridinium benzoate benzoic acid solvate |
title_sort | 2,3-diaminopyridinium benzoate benzoic acid solvate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979855/ https://www.ncbi.nlm.nih.gov/pubmed/21579888 http://dx.doi.org/10.1107/S1600536810001443 |
work_keys_str_mv | AT hemamalinimadhukar 23diaminopyridiniumbenzoatebenzoicacidsolvate AT funhoongkun 23diaminopyridiniumbenzoatebenzoicacidsolvate |