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-66614]Cl was tested at 100 degrees C, i.e. below the melting point of sulfur. Under these conditions, substantial sulfide formation occurred only for nickel (Ni3S4, Ni3S2, NiS) and copper (Cu2S, 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 (Sb2S3), the main source of antimony production, in the phosphonium-based ILs [P-66614][OAc] and [P-66614]Cl at 100 degrees C was studied in detail. The dissolution proceeds without H2S evolution, and amorphous Sb2S3 can be precipitated from these solutions. Heating Sb2S3 in the Lewis-acidic IL [BMIm]Cl center dot 4.7AlCl(3) led to the crystallization of [Sb13S16Cl2][AlCl4](5), which contains a new quadruple heterocubane cation.

Automated summary

Ionic liquids (ILs), including task-specific ILs, have the ability to dissolve various solids at moderate temperatures without special reaction vessels. This study investigated the synthesis of sulfides of various elements in ILs as well as the dissolution of antimony sulfide in ILs. Additionally, a new quadruple heterocubane cation was discovered through the crystallization of Sb2S3 in a Lewis-acidic IL.