Exploration of metal sulfide syntheses and the dissolution process of antimony sulfide in phosphonium-based ionic liquids.

Ionic liquids (ILs), especially task-specific ILs, are capable of dissolving various solids at moderate temperatures without the need for special reaction vessels. Direct synthesis of binary sulfides of B, Bi, Ge, Mo, Cu, Au, Sn, In, Ti, V, Fe, Co, Ga, Ni, Al, Zn, and Sb in [P]Cl was tested at 100 °C, below the melting point of sulfur. Under these conditions, substantial sulfide formation occurred only for nickel (NiS, NiS, NiS) and copper (CuS, CuS). Sb showed no formation of crystalline sulfide, but after addition of EtOH, an orange material precipitated which was identified as amorphous metastibnite. Subsequently, the dissolution of antimony sulfide (SbS), the main source of antimony production, in the phosphonium-based ILs [P][OAc] and [P]Cl at 100 °C was studied in detail. The dissolution proceeds without HS evolution, and amorphous SbS can be precipitated from these solutions. Heating SbS in the Lewis-acidic IL [BMIm]Cl·4.7AlCl led to the crystallization of [SbSCl][AlCl], which contains a new quadruple heterocubane cation.