In organic chemistry, phosphinites are organophosphorus compounds with the formula . They are used as ligands in homogeneous catalysis and coordination chemistry.[1]
Phosphinites are prepared by alcoholysis of organophosphinous chlorides. For example, treatment of chlorodiphenylphosphine with methanol and base gives methyl diphenylphosphinite:
ClPPh2 + CH3OH → CH3OPPh2 + HCl
Although they are esters of phosphinous acids (R2POH), phosphinites are not made via such intermediates.
Oxidation of phosphinites gives phosphinates:
2 P(OR)R2 + O2 → 2 OP(OR)R2
Phosphinites are ligands, giving derivatives similar to metal phosphine complexes. They are stronger pi-acceptors than typical phosphine ligands.[2]