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Single crystals of a triclinic polymorphic form of mer-[mu]-oxalato-bis­[chloridotripyridine­cobalt(II)] pyridine disolvate, [Co2(C2O4)Cl2(C5H5N)6]·2C5H5N, have been prepared by solvothermal methods. The structure and geometric parameters strongly resemble those of the previously reported monoclinic polymorph [Bolte (2006). Acta Cryst. E62, m597-m598]. In both polymorphic forms, the dinuclear complex mol­ecules are located on a crystallographic centre of inversion, with the CoII cations in a distorted octa­hedral environment consisting of a chloride ligand, three pyridine ligands and a chelating bis-bidentate oxalate ligand. This last serves as a bridging ligand between two CoII cations. The polymorphs differ in the mutual orientation of their pyridine ligands in the dinuclear mol­ecules and in their inter­molecular connectivity. In the triclinic polymorph, C-H...O, C-H...Cl, C-H...[pi] and [pi]-[pi] inter­actions link the dinuclear mol­ecules into a three-dimensional structure. Pyridine solvent mol­ecules are attached to this structure via weak inter­actions.
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