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4,4′-Bipyridine–3-nitrobenzoic acid (1/2)
The title compound, C(10)H(8)N(2)·2C(7)H(5)NO(4),was obtained unintentionally as the harvested product of the hydrothermal reaction between Co(OAc)(2)·4H(2)O and 4,4′-bipyridine in the presence of 3-nitrophthalic acid. In the reaction, 3-nitrophthalic acid is transformed into 3-nitrobenzoic acid...
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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/PMC2983553/ https://www.ncbi.nlm.nih.gov/pubmed/21580317 http://dx.doi.org/10.1107/S1600536810003594 |
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author | Zhu, Zhen Wang, Feng-Qin Zhao, Yong-Nan |
author_facet | Zhu, Zhen Wang, Feng-Qin Zhao, Yong-Nan |
author_sort | Zhu, Zhen |
collection | PubMed |
description | The title compound, C(10)H(8)N(2)·2C(7)H(5)NO(4),was obtained unintentionally as the harvested product of the hydrothermal reaction between Co(OAc)(2)·4H(2)O and 4,4′-bipyridine in the presence of 3-nitrophthalic acid. In the reaction, 3-nitrophthalic acid is transformed into 3-nitrobenzoic acid by an in situ decarboxylation reaction, in which the carboxylate group is not deprotonated and is uncoordinated. In the crystal, the uncoordinated 3-nitrobenzoic acid and free 4,4′-bipyridine molecules are linked alternately by O—H⋯N hydrogen bonds into chains, which are assembled by C—H⋯O hydrogen bonds into a three-dimensional supramolecular network. |
format | Text |
id | pubmed-2983553 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29835532010-12-30 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) Zhu, Zhen Wang, Feng-Qin Zhao, Yong-Nan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(8)N(2)·2C(7)H(5)NO(4),was obtained unintentionally as the harvested product of the hydrothermal reaction between Co(OAc)(2)·4H(2)O and 4,4′-bipyridine in the presence of 3-nitrophthalic acid. In the reaction, 3-nitrophthalic acid is transformed into 3-nitrobenzoic acid by an in situ decarboxylation reaction, in which the carboxylate group is not deprotonated and is uncoordinated. In the crystal, the uncoordinated 3-nitrobenzoic acid and free 4,4′-bipyridine molecules are linked alternately by O—H⋯N hydrogen bonds into chains, which are assembled by C—H⋯O hydrogen bonds into a three-dimensional supramolecular network. International Union of Crystallography 2010-02-06 /pmc/articles/PMC2983553/ /pubmed/21580317 http://dx.doi.org/10.1107/S1600536810003594 Text en © Zhu et al. 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 Zhu, Zhen Wang, Feng-Qin Zhao, Yong-Nan 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title | 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title_full | 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title_fullStr | 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title_full_unstemmed | 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title_short | 4,4′-Bipyridine–3-nitrobenzoic acid (1/2) |
title_sort | 4,4′-bipyridine–3-nitrobenzoic acid (1/2) |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983553/ https://www.ncbi.nlm.nih.gov/pubmed/21580317 http://dx.doi.org/10.1107/S1600536810003594 |
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