Unique structural topologies involving metal–metal and metal–sulfur interactions: salts of [Ni(C3S5)2]x− with cis-anti-cis-dicyclohexyl-18-crown-6 complexed counter ions

Abstract

Preparation by electrocrystallisation has been carried out for the salts [Rb(anti-dchyl-18c6)]2[Ni(dmit)2] 1, [Rb(anti-dchyl-18c6)][Ni(dmit)2] 2, [Cs(anti-dchyl-18c6)]2[Ni(dmit)2] 3 and [Cs(anti-dchyl-18c6)1.5][Ni(dmit)2]64 (anti-dchyl-18c6 = cis-anti-cis-dicyclohexyl-18-crown-6, dmit = C3S5). Salts 1 and 3 involve the planar dianionic nickel complex sandwiched by two metal–crown units. This leads to short Rb+ ⋯ Ni and Rb+ ⋯ S interactions in 1 and the shortest recorded Cs+ ⋯ Ni distance of 3.47 A in 3, presumably stabilised by the four surrounding S atoms at 3.73–4.44 A. DFT calculations on the dianionic salts 1 and 3 indicate an essentially electrostatic interaction between the [Ni(dmit)2]2− complex and the Rb+ or Cs+ ion and show frontier orbitals qualitatively similar to those previously derived from EHMO calculations on molecular conductors containing [Ni(dmit)2]. Salt 2 consists of non-stacked nickel complexes arranged in chains linked by S ⋯ Rb+ interactions through the terminal sulfurs with the Rb+ ion placed exactly within the plane of the crown oxygens. Magnetic susceptibility measurement indicated weak antiferromagnetic interactions. Salt 4 shows a 2-D sheet of nickel complexes stacked in a herringbone arrangement separated by layers of counter ions complexed by the crowns in a disordered manner with the anion ∶ cation ratio of 6 ∶ 1 uniquely high among [Ni(dmit)2]x− salts. Salt 4 displays semiconductor behaviour with σRT = 10−2 S cm−1.