Influence of the counter-anions on the [Ni(Him)6]2+ complex cation (Him = imidazole)
A. Koščíková *, L. Krešáková, J. Černák
Department of Inorganic Chemistry, Institute of Chemistry, P. J. Šafárik University, Moyzesova 11, 041 54 Košice, Slovakia
E-mail: * andrea.koscikova@student.upjs.sk
Abstract: Four ionic Ni(II) complexes containing the [Ni(Him)6]2+ (Him = imidazole) complex cation were prepared: [Ni(Him)6](CO3)·5H2O (1), [Ni(Him)6](ac)2·H2O (2, ac = acetate), [Ni(Him)6](NO3)2 (3), and [Ni(Him)6]SiF6 (4); complexes 2 and 4 are new. The prepared complexes were characterized chemically and spectroscopically. Results of X-ray single crystal studies have shown that all four complexes exhibit ionic crystal structures comprising [Ni(Him)6]2+ complex cations, the respective anion(s), and in case of 1 and 2, additional solvate water molecules. Ni(II) central atoms in all complexes 1-4 are hexa-coordinated by six N-atoms originating from monodentate Him ligands. While in 1 and 4 the NiN6 chromophore is quite a regular octahedron with only one independent Ni-N bond, as imposed by local symmetry, in 2 and 3 the octahedra are slightly deformed. On the other hand, significant differences were observed in the orientation of Him rings within the respective coordination polyhedra.
Keywords: Crystal structure, hexa-coordination, imidazole, nickel(II)
Acta Chimica Slovaca, Vol. 19, No. 1, 2026, pp. 1—9, DOI: 10.2478/acs-2026-0001