Acta Crystallographica Section E (Jun 2009)

Redetermination of (2,2′-bipyridine-κ2N,N′)dichloridopalladium(II) dichloromethane solvate

  • Nam-Ho Kim,
  • In-Chul Hwang,
  • Kwang Ha

DOI
https://doi.org/10.1107/S1600536809016262
Journal volume & issue
Vol. 65, no. 6
pp. m615 – m616

Abstract

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In the title compound, [PdCl2(C10H8N2)]·CH2Cl2, the Pd2+ ion is four-coordinated in a slightly distorted square-planar environment by two N atoms of the 2,2′-bipyridine (bipy) ligand and two chloride ions. The compound displays intramolecular C—H...Cl hydrogen bonds and pairs of complex molecules are connected by intermolecular C—H...Cl hydrogen bonds. Intermolecular π–π interactions are present between the pyridine rings of the ligand, the shortest centroid–centroid distance being 4.096 (3) Å. As a result of the electronic nature of the chelate ring, it is possible to create π–π interactions to its symmetry-related counterpart [3.720 (2) Å] and also with a pyridine ring [3.570 (3) Å] of the bipy unit. The present structure is a redetermination of a previous structure [Vicente et al. (1997). Private communication (refcode PYCXMN02). CCDC, Cambridge, England]. In the new structure refinement all H atoms were located in a difference Fourier synthesis. Their coordinates were refined freely, together with isotropic displacement parameters.