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4,4′-Bipyridine–2-hydroxypropane-1,2,3-tricarboxylic acid (3/2)
The combination of 2-hydroxypropane-1,2,3-tricarboxylic acid (H(3)hypta, also called citric acid) and 4,4′-bipyridine (4,4′-bipy) in a 1:1.5 molar ratio leads to the formation of the title molecular cocrystal, 1.5C(10)H(8)N(2)·C(6)H(8)O(7). The asymmetric unit contains one and a half 4,4′-bipy uni...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968425/ https://www.ncbi.nlm.nih.gov/pubmed/21582193 http://dx.doi.org/10.1107/S1600536809004607 |
Sumario: | The combination of 2-hydroxypropane-1,2,3-tricarboxylic acid (H(3)hypta, also called citric acid) and 4,4′-bipyridine (4,4′-bipy) in a 1:1.5 molar ratio leads to the formation of the title molecular cocrystal, 1.5C(10)H(8)N(2)·C(6)H(8)O(7). The asymmetric unit contains one and a half 4,4′-bipy units, with one lying across a centre of inversion, and one H(3)hypta molecule. The significant differences in the C—O bond distances support the existence of the un-ionized acid molecule and confirm the formation of a cocrystal. There are π–π and C—H⋯π stacking interactions between the aromatic rings of 4,4′-bipy [with interplanar distances of 3.7739 (8) and 3.7970 (8) Å] and between CH groups of H(3)hypta [with an H⋯π distance of 2.63 Å]. In the crystal structure, intermolecular O—H⋯N hydrogen bonds occur and an O—H⋯O hydrogen bond occurs within the citric acid moiety. |
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