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Trimethylphosphine

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Related compounds
  
NMe3 PH3 PPh3

Molar mass
  
76.08 g/mol

Density
  
748 kg/m³

Appearance
  
Colorless liquid

Formula
  
C3H9P

Boiling point
  
38 °C

Melting point
  
-86 °C

Trimethylphosphine wwwsigmaaldrichcomcontentdamsigmaaldrichstr

Trimethylphosphine is the organophosphorus compound with the formula P(CH3)3, commonly abbreviated as PMe3. This colorless liquid has a strongly unpleasant odor, which is characteristic of alkylphosphines. The compound is a common ligand in coordination chemistry.

Contents

Trimethylphosphine Trimethylphosphine C3H9P ChemSpider

Structure and bonding

Trimethylphosphine ChlorotrimethylphosphinegoldI 99 SigmaAldrich

It is a pyramidal molecule with approximate C3v symmetry — the molecular point group of ammonia (NH3) and phosphine (PH3). The C–P–C bond angles are approximately 98.6°.

Trimethylphosphine Trimethylphosphine Wikiwand

The C–P–C bond angles are consistent with the notion that phosphorus predominantly uses the 3p orbitals for forming bonds and that there is little sp hybridization of the phosphorus atom. The latter is a common feature of the chemistry of phosphorus because the gap between the 3s and 3p orbital is large compared to the corresponding gap for the 2s and 2p orbitals that are in the valence shell for carbon, nitrogen, and oxygen (elements for which sp-mixing is strong). As a result, the lone pair of trimethylphosphine has predominantly s-character as is the case for phosphine, PH3.

PMe3 is usually prepared by the treatment of triphenyl phosphite with methylmagnesium chloride:

3 CH3MgCl + P(OC6H5)3 → P(CH3)3 + 3 C6H5OMgCl

The synthesis is conducted in dibutyl ether, from which the more volatile PMe3 can be distilled.

Acid-base reactions

With a pKa of 8.65, PMe3 reacts with strong acids to give salts [HPMe3]X. This reaction is reversible. WIth strong bases, such as alkyl lithium compounds, a methyl group undergoes deprotonation to give PMe2CH2Li.

PMe3 is easily oxidised to the phosphine oxide with oxygen. It is also easily alkylated to give phosphonium derivatives RPMe3+. The compound is stable to water.

Coordination chemistry

Trimethylphosphine is a highly basic ligand that forms complexes with most metals. As a ligand, trimethylphosphine's Tolman cone angle is 118°. This angle is an indication of the amount of steric protection that this ligand provides to the metal that to which it is bound.

Being a relatively compact ligand, several can bind to a single transition metal, as illustrated by this Fe(0) complex:

2 PMe3 + Fe(CO)5 → Fe(CO)3(PMe3)2 + 2 CO

Its complex with silver iodide, AgI(PMe3) is an air-stable solid that releases PMe3 upon heating.

Safety

PMe3 is potentially pyrophoric as well as toxic. PMe3 converts to non-pyrophoric phosphine oxide by treatment with dilute bleach.

Trimethylphosphine

References

Trimethylphosphine Wikipedia