Abstract

The reactivity of the hybrid phosphorus–sulfur proligands pr iPSH, phPS 2H 2 and ePS 2H 2 with iridium and rhodium precursors has been explored. By reacting IrCl 3 with pr iPSH in the presence of NEt 3 as base, the octahedral Ir(III) specie [Ir( pr iPS) 3] was obtained and its crystal structure determined. Reactions of the potentially tridentated proligands phPS 2H 2 and ePS 2H 2 with trans-[MF(CO)(PPh 3) 2] (M=Rh and Ir) were also investigated. Complexes of general formula [M(H)( phPS 2)(CO)(PPh 3)] were obtained with phPS 2H 2. A single crystal X-ray structure determination for [Rh(H)( phPS 2)(CO)(PPh 3)] showed the complex to be octahedral. Reactions with the aliphatic proligand ePS 2H 2 afforded analogous species to those with phPS 2H 2.

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