Reaction of PR3, R=cyclohexyl (Cy), cyclopentyl (Cy-p) or phenyl, with [InH
3(NMe3)] affords the 1:1 indium trihydride complexes, [InH3(PR3)]. The stab
ilities and spectroscopic properties of these complexes are described in te
rms of the phosphine ligands' steric bulk and nucleophilicity. Reaction of
two equivalents of PCy3 with [InH3(NMe3)] yields the complex [InH3(PCy3)(2)
] which has been characterised by X-ray crystallography. The first phosphid
o-indium hydride complex, [{InH2(PCy2)}(3)], has been prepared by a novel s
ynthetic route which involves treatment of [InH3(NMe3)] with LiPCy2. Its cr
ystal structure shows it to exist as a cyclic trimer in the solid state. Th
e complex, [InH3(PCy3)] has been used to prepare a range of monomeric indiu
m chalcogenolato complexes, [In(EPh)(3)(PCy3)], E=S, Se or Te, all of which
have been structurally characterised.