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Acta Cryst. (2007). E63, m2468-m2469  [ doi:10.1107/S1600536807042651 ]

catena-Poly[piperazindiium [zincate(II)-bis([mu]-pyridine-2,3-dicarboxylato)-[kappa]3N,O2:O3;[kappa]3O3:N,O2] tetrahydrate]

H. Aghabozorg, S. Daneshvar, E. Motyeian, M. Ghadermazi and J. Attar Gharamaleki

Abstract: The centrosymmetric title compound, {(C4H12N2)[Zn(C14H6N2O8)2]·4H2O}n or {(pipzH2)[Zn(py-2,3-dc)2]·4H2O}n, where py-2,3-dcH2 is pyridine-2,3-dicarboxylic acid and pipz is piperazine, was obtained by the reaction of zinc(II) nitrate tetrahydrate with (pipzH2)(py-2,3-dc) as a proton-transfer compound in aqueous solution. Each ZnII (site symmetry {\\overline 1}) is coordinated in a distorted octahedral geometry by four O atoms and two N atoms from two bidentate (py-2,3-dc)2- ligands, which also act as bridging ligands between ZnII atoms. The four donor atoms of the two coplanar (py-2,3-dc)2- anions form a square-planar arrangement around the ZnII centre. In the crystal structure, extensive O-H...O, N-H...O and C-H...O hydrogen bonds, as well as ion pairing and [pi]-[pi] stacking [with a distance of 3.8693 (8) Å between two aromatic rings] between different fragments, play an important role in the stabilization of the supramolecular structure.

Online 8 September 2007


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