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Bis(2-amino-6-methyl­pyridinium) trans-diaqua­bis­(pyrazine-2,3-dicarboxyl­ato)cuprate(II) hexa­hydrate

The title compound, (C(6)H(9)N(2))(2)[Cu(C(6)H(2)N(2)O(4))(2)(H(2)O)(2)]·6H(2)O, was obtained by the reaction of CuCl(2)·2H(2)O with pyrazine-2,3-dicarb­oxy­lic acid (pyzdcH(2)) and 2-amino-6-methyl­pyridine (2a-6mpy) in aqueous solution. The Cu(II) atom is located on an inversion centre and has an...

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Detalles Bibliográficos
Autores principales: Eshtiagh-Hosseini, Hossein, Hassanpoor, Azam, Mirzaei, Masoud, Szymańska-Buzar, Teresa, Kochel, Andrzej
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3100057/
https://www.ncbi.nlm.nih.gov/pubmed/21753974
http://dx.doi.org/10.1107/S1600536811008981
Descripción
Sumario:The title compound, (C(6)H(9)N(2))(2)[Cu(C(6)H(2)N(2)O(4))(2)(H(2)O)(2)]·6H(2)O, was obtained by the reaction of CuCl(2)·2H(2)O with pyrazine-2,3-dicarb­oxy­lic acid (pyzdcH(2)) and 2-amino-6-methyl­pyridine (2a-6mpy) in aqueous solution. The Cu(II) atom is located on an inversion centre and has an overall octa­hedral coordination environment. Two N and two O atoms from (pyzdc)(2−) ligands define the equatorial plane and two water mol­ecules are in axial positions, resulting in a typical tetra­gonally Jahn–Teller-distorted environment. Extensive classical O—H⋯O, O—H⋯N and N—H⋯O and non-classical C—H⋯O hydrogen bonds, as well as π–π stacking inter­actions between aromatic rings of the cations [centroid–centroid distance = 3.58 (9) Å], lead to the formation of a three-dimensional supra­molecular structure.