[HTML version][PDF version][CIF][3d view][Structure Factors][Supplementary Material][CIF check Report][Issue contents]  [Open access]

[Contents scheme]

Acta Cryst. (2009). E65, m1507-m1508  [ doi:10.1107/S1600536809045565 ]

Di-[mu]-chlorido-bis(chlorido{2,2'-[3-(1H-imidazol-4-ylmethyl)-3-azapentane-1,5-diyl]diphthalimide}copper(II))

Z.-P. Qi, A.-D. Wang, H. Zhang and X.-X. Wang

Abstract: The centrosymmetric dinuclear CuII complex, [Cu2Cl4(C24H21N5O4)2], was synthesized by the reaction of CuCl2·2H2O with the tripodal ligand 2,2'-[3-(1H-imidazol-4-ylmethyl)-3-azapentane-1,5-diyl]diphthalimide (L). Each of the CuII ions is coordinated by two N atoms from the ligand, two bridging Cl atoms and one terminal Cl atom. The CuII coordination can be best be described as a transition state between four- and five-coordination, since one of the bridging Cl atoms has a much longer Cu-Cl bond distance [2.7069 (13) Å] than the other [2.2630 (12) Å]. In addition, the Cu...Cu distance is 3.622 (1) Å. The three-dimensional structrure is generated by N-H...O, C-H...O and C-H...Cl hydrogen bonds and [pi]-[pi] interactions [centroid-centroid distances = 3.658 (4) and 4.020 (4) Å].

Online 4 November 2009


Copyright © International Union of Crystallography
IUCr Webmaster