Acta Cryst. (1999). B55, 380-388 [ doi:10.1107/S0108768198012968 ]
Abstract: The crystal structures of (1,5,9,13,20-pentamethyl-3,7,11,15,18,22-hexaazabicyclo[7.7.7]tricosane-
6N,N',N'',N''',N'''',N''''')nickel(II) diperchlorate-x(water) (x = 0.530), [Ni(C22H48N6)](ClO4)2.0.530H2O, and (1,5,9,13,20-pentamethyl-3,7,11,15,18,22-hexaazabicyclo[7.7.7]tricosane-
6N,N',N'',N''',N'''',N''''')zinc(II) diperchlorate-x(water) (x = 0.608), [Zn(C22H48N6)](ClO4)2.0.608H2O, are isomorphic and each is described as an intergrowth of four substructures, consistent with different modulations of an idealized parent structure of space group C2/c. Two substructures correspond to alternative orientations of a C1 structure for which x = 0 in the general formula [M(C22H48N6)](ClO4)2.xH2O, and two substructures correspond to alternative origins of a P21/n structure for which x = 1. Twinning also occurs. An analysis of the pseudosymmetry, a description of the refinement and a description of the refined structures are presented. The MN6 coordination geometry is essentially octahedral, in contrast to the trigonal-prismatic geometry observed for the CdII and HgII complexes of the same ligand.
Copyright © International Union of Crystallography
IUCr Webmaster