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3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate
In the title salt, C(5)H(8)N(3) (+)·C(7)H(3)N(2)O(7) (−), the pyridine N atom of the 3,4-diaminopyridine molecule is protonated. The 3,5-dinitrosalicylate anion shows whole-molecule disorder over two orientations with a refined occupancy ratio of 0.875 (4): 0.125 (4). In the crystal, the cations...
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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/PMC3009103/ https://www.ncbi.nlm.nih.gov/pubmed/21588952 http://dx.doi.org/10.1107/S1600536810038936 |
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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 salt, C(5)H(8)N(3) (+)·C(7)H(3)N(2)O(7) (−), the pyridine N atom of the 3,4-diaminopyridine molecule is protonated. The 3,5-dinitrosalicylate anion shows whole-molecule disorder over two orientations with a refined occupancy ratio of 0.875 (4): 0.125 (4). In the crystal, the cations and anions are connected by intermolecular N—H⋯O and C—H⋯O hydrogen bonds, forming a three-dimensional network. |
format | Text |
id | pubmed-3009103 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30091032010-12-30 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate Hemamalini, Madhukar Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title salt, C(5)H(8)N(3) (+)·C(7)H(3)N(2)O(7) (−), the pyridine N atom of the 3,4-diaminopyridine molecule is protonated. The 3,5-dinitrosalicylate anion shows whole-molecule disorder over two orientations with a refined occupancy ratio of 0.875 (4): 0.125 (4). In the crystal, the cations and anions are connected by intermolecular N—H⋯O and C—H⋯O hydrogen bonds, forming a three-dimensional network. International Union of Crystallography 2010-10-09 /pmc/articles/PMC3009103/ /pubmed/21588952 http://dx.doi.org/10.1107/S1600536810038936 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 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title | 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title_full | 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title_fullStr | 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title_full_unstemmed | 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title_short | 3,4-Diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
title_sort | 3,4-diaminopyridinium 2-carboxy-4,6-dinitrophenolate |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009103/ https://www.ncbi.nlm.nih.gov/pubmed/21588952 http://dx.doi.org/10.1107/S1600536810038936 |
work_keys_str_mv | AT hemamalinimadhukar 34diaminopyridinium2carboxy46dinitrophenolate AT funhoongkun 34diaminopyridinium2carboxy46dinitrophenolate |