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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...

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Detalles Bibliográficos
Autores principales: Makon ma Houga, Noé, Capet, Frédéric, Nenwa, Justin, Bebga, Gouet, Foulon, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2015
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
Descripción
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.