![[HTML version]](/e/graphics/htmlborder.gif)
![[PDF version]](/e/graphics/pdfborder.gif)
![[CIF]](/e/graphics/cifborder.gif)
![[3d view]](/e/graphics/3dviewborder.gif)
![[Structure Factors]](/e/graphics/structurefactorsborder.gif)
![[Supplementary Material]](/e/graphics/supplementarymaterialsborder.gif)
![[CIF check Report]](/e/graphics/checkcifborder.gif)
![[Issue contents]](/e/graphics/issuecontentsborder.gif)
![[Open access]](/e/graphics/free.gif)
![[Contents scheme]](rn2079contents.gif)
Acta Cryst. (2011). E67, m457 [ doi:10.1107/S1600536811008798 ]
![[eta]](/logos/entities/eta_rmgif.gif)
3-Allyl)bromido(1-phenyl-1H-imidazole-![[kappa]](/logos/entities/kappa_rmgif.gif)
N3)palladium(II)Abstract: The title compound, [PdBr(C3H5)(C9H8N2)], was synthesized by the reaction of the allylpalladium(II) bromide dimer and 1-phenyl-1H-imidazole. The Pd atom is coordinated by one allyl group [in 3 mode, the central CH group of the allyl group is disordered over two sets of sites in a 0.668 (5):0.332 (5) ratio], one bromide anion and a 1-phenyl-1H-imidazole ligand. Intramolecular face-to-face ![[pi]](/logos/entities/pi_rmgif.gif)
- stacking interactions occur between adjacent phenyl or imidazole groups, with centroid-centroid distances in the range 3.877 (1)-3.6596 (6) Å, forming a supramolecular chain along [100].
Online 15 March 2011
Copyright © International Union of Crystallography
IUCr Webmaster