Phosphinite

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Structural formula of a generic phosphinite. R represents a side chain.
Skeletal formula of methyl diphenylphosphinite.

Phosphinites are organophosphorus compounds with the formula P(OR)R2. They are used as ligands in homogeneous catalysis and coordination chemistry.[1]

Preparation

Phosphinites are prepared by alcoholysis of organophosphinous chlorides. For example, treatment of chlorodiphenylphosphine with methanol and base give methyl diphenylphosphonite:

ClPPh2 + CH3OH → CH3OPPh2 + HCl

Although they are esters of phosphinous acids (R2POH), phosphinites are not made via such intermediates.

Reactions

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]

References

  1. D. E. C. Corbridge "Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology" 5th Edition Elsevier: Amsterdam 1995. ISBN 0-444-89307-5.
  2. Pryjomska, I.; Bartosz-Bechowski, H.; Ciunik, Z.; Trzeciak, A.M., Ziółkowski, J. J. "Chemistry of palladium phosphinite (PPh2(OR)) and phosphonite (P(OPh)2(OH)) complexes: catalytic activity in methoxycarbonylation and Heck coupling reactions" Dalton Trans. 2006, pp. 213-20. doi:10.1039/B512835H

See also

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