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Crystal structure of tris[4-(dimethylamino)pyridinium] tris(oxalato-κ(2) O,O′)chromate(III) tetrahydrate
In the title hybrid salt, (C(7)H(11)N(2))(3)[Cr(C(2)O(4))(3)]·4H(2)O, the central Cr(III) ion of the complex anion (point group symmetry 2) is coordinated by six O atoms from three chelating oxalate(2−) ligands in a slightly distorted octahedral coordination sphere. The Cr—O bond lengths vary from...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4645054/ https://www.ncbi.nlm.nih.gov/pubmed/26594521 http://dx.doi.org/10.1107/S2056989015020113 |
Sumario: | In the title hybrid salt, (C(7)H(11)N(2))(3)[Cr(C(2)O(4))(3)]·4H(2)O, the central Cr(III) ion of the complex anion (point group symmetry 2) is coordinated by six O atoms from three chelating oxalate(2−) ligands in a slightly distorted octahedral coordination sphere. The Cr—O bond lengths vary from 1.9577 (11) to 1.9804 (11) Å, while the chelate O—Cr—O angles range from 82.11 (6) to 93.41 (5)°. The 4-(dimethylamino)pyridinium cations (one situated in a general position and one on a twofold rotation axis) are protonated at the pyridine N atoms. In the crystal, N—H⋯O and O—H⋯O hydrogen bonds link the cations and anions into a three-dimensional network. π–π interactions between the pyridine rings of adjacent cations provide additional stabilization of the crystal packing, with the closest centroid-to-centroid distances being 3.541 (1) and 3.575 (1) Å. |
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