Abstract
The crystal structures and magnetic properties for two ion-pair complexes, [MG][Ni(dmit)2] (1) and [RhB][Ni(dmit)2] (2) (MG+ = N-(4-((4-(dimethylamino)phenyl)(phenyl)methylene)cyclohexa-2,5-dienylidene)-N-methylmethanaminium, RhB+ = 9-(2-carboxyphenyl)-3,6-bis(diethylamino)xanthylium; dmit2− = 1,3-dithiole-2-thione-4,5-dithiolate), have been investigated. Complex 1 crystallizes in the monoclinic space group P21/c, the stacking interactions between the GM+ and [Ni(dmit)2]− lead to the anion exhibiting a banana-shaped molecular geometry; the neighboring anions form a 1-D alternating chain along the crystallographic [1 1 0] direction via intermolecular lateral-to-lateral and head-to-head S ··· S contacts. The temperature dependence of magnetic susceptibility from 2–350 K does not display the magnetic character of a 1-D chain; the magnetic susceptibility data were fit to the Curie–Weiss equation to give C = 0.351(15) emu K mol−1, θ = −3.51(28) K, and χ 0 = 8.00(3) × 10−5 emu mol−1. Complex 2 belongs to the triclinic space group P-1 with two crystallographic inequivalent [Ni(dmit)2]− anions, which exhibit perfect planar geometry. Two ethyl groups of RhB+ are disordered over two positions at 296 K, and one becomes ordered at 150 K. The [Ni(dmit)2]− anions form a 2-D molecular layer via intermolecular lateral-to-lateral and head-to-lateral S ··· S interactions with the anionic layer parallel to the crystallographic (0 1 −1) plane. The temperature variation of magnetic susceptibility from 2 to 350 K shows that antiferromagnetic coupling dominates in the anionic layer, and the disorder–order changes of cationic structure are not coupled to magnetic property.
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