![](https://upload.wikimedia.org/wikipedia/commons/thumb/1/1d/Generic-phosphinite-2D.png/150px-Generic-phosphinite-2D.png)
![](https://upload.wikimedia.org/wikipedia/commons/thumb/2/2d/Methyl-diphenylphosphinite-2D-skeletal.png/150px-Methyl-diphenylphosphinite-2D-skeletal.png)
In organic chemistry, phosphinites are organophosphorus compounds with the formula P(OR)R2. They are used as ligands in homogeneous catalysis and coordination chemistry.[1]
Preparation
[edit]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.
Reactions
[edit]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
[edit]- ^ D. E. C. Corbridge (1995). Phosphorus: An Outline of its Chemistry, Biochemistry, and Technology (5th ed.). Amsterdam: Elsevier. ISBN 0-444-89307-5.
- ^ Rajanbabu, T. V. Babu (2012). "Phosphinite and Phosphonite Ligands". Phosphorus(III) Ligands in Homogeneous Catalysis: Design and Synthesis. pp. 159–232. doi:10.1002/9781118299715.ch5. ISBN 9781118299715.
See also
[edit]- Phosphine - PR3
- Phosphine oxide - OPR3
- Phosphonite - P(OR)2R
- Phosphite - P(OR)3
- Phosphinate - OP(OR)R2
- Phosphonate - OP(OR)2R
- Phosphate - OP(OR)3