ABSTRACT
The asymmetric unit of the title salt, (C12H11BrN)2[Ni(C4N2S2)2], consists of one 1-(4-bromo-benz-yl)pyridinium cation and one half of a complex [Ni(mnt)2](2-) (mnt(2-) is the maleo-nitrile-dithiol-ate dianion). The Ni(2+) ion is located on an inversion centre and is coordinated by four S atoms from two mnt(2-) ligands, exhibiting a square-planar coordination environment. In the cation, the planes of the pyridinium and benzene rings make a dihedral angle of 69.86â (19)°. The cations and anions are alternately arranged in layers parallel to (001) and are held together by non-classical C-Hâ¯N hydrogen bonds.
ABSTRACT
The title ion-pair complex, (C(25)H(20)ClFP)(2)[Ni(C(2)N(2)S(3))(2)], was obtained by the direct reaction of (4-F,2-ClBzTPP)(+)·Br(-) [4-F,2-ClBzTPP(+) is (2-chloro-4-fluoro-benz-yl)triphenyl-phos-pho-nium], NiCl(2)·6H(2)O and Na(2)tdas (tdas(2-) is 1,2,5-thia-diazole-3,4-dithiol-ate) in methanol. The asymmetric unit of the title structure comprises one (4-F,2-ClBzTPP)(+) cation and half of an [Ni(tdas)(2)](2-) complex anion, with the Ni(II) ion situated on a center of symmetry, leading to a slightly distorted square-planar coordination of the latter. In the cation, the tetra-hedral angles around the P atom are nearly undistorted. In the crystal, the cations and anions are linked by C-Hâ¯S, C-Hâ¯N and C-Hâ¯Cl hydrogen bonds.