Phosphine oxides are phosphorus compounds with the formula OPX3. When X = alkyl or aryl, these are organophosphine oxides. Triphenylphosphine oxide is an example. An inorganic phosphine oxide is phosphoryl chloride (POCl3). Such compounds are thermally stable, decomposing only above 450 °C. Phosphoryl refers to a functional group drawn with a phosphorus-oxygen double bond.
Structure and bonding
Phosphine oxides feature tetrahedral phosphorus centers. The P-O bond is short and polar. According to molecular orbital theory, the short P–O bond is attributed to the donation of the lone pair electrons from oxygen p-orbitals to the antibonding phosphorus-carbon bonds; This proposal, which is supported by ab initio calculations, has gained consensus in the chemistry community.
The nature of the P–O bond was once hotly debated. Some discussions invoked a role for phosphorus-centered d-orbitals in bonding, but this analysis is not supported by computational analyses. In terms of simple Lewis structure, the bond is more accurately represented as a dative bond, as is currently used to depict an amine oxide.
Phosphine oxides are generated as a by-product of the Wittig reaction:
- R3PCR'2 + R"2CO → R3PO + R'2C=CR"2
Another route to phosphine oxides is the thermolysis of phosphonium hydroxides:
- [PPh4]Cl + NaOH → Ph3PO + NaCl + PhH
In the laboratory, phosphine oxides are usually generated by the oxidation, often accidentally, of tertiary phosphines:
- R3P + 1/2 O2 → R3PO
Basic phosphines, such as trialkyl derivatives, are prone to this reaction.
The hydrolysis of phosphorus(V) dihalides also affords the oxide:
- R3PCl2 + H2O → R3PO + 2 HCl
A special nonoxidative route is applicable secondary phosphine oxides, which arise by the hydrolysis of the chlorophosphine. An example is the hydrolysis of chlorodiphenylphosphine to give diphenylphosphine oxide:
- Ph2PCl + H2O → Ph2P(O)H + HCl
The deoxygenation of phosphine oxides has been extensively developed. Trichlorosilane is a standard laboratory method. Industrial routes use phosgene or trichloromethylchloroformate, which produce chlorotriphenylphosphonium chloride, which is separately reduced.
For chiral phosphine oxides, deoxygenation can proceed with retention or inversion of configuration. Inversion is favored by a combination of trichlorosilane and triethylamine. In the absence of the base, the reaction proceeds with retention. The stereochemical course is explained mechanistically by complexation followed by intramolecular hydride transfer. On the other hand, the inversion of configuration in the presence of triethylamine is explained by complexation followed by intermolecular hydride transfer from a 1:1 triethylamine-trichlorosilane complex in an SN2 reaction. Based on these observations, it is thought that complexation of OPR3 by trichlorosilane occurs with retention of configuration.
- HSiCl3 + Et3N ⇋ −SiCl3 + Et3N+H
- R3PO + Et3NH+ ⇋ R3P+OH + Et3N
- −SiCl3 + R3P + OH → PR3 + HOSiCl3
The popularity of this method is partly attributable to the availability of inexpensive trichlorosilane. Instead of HSiCl3, other perchloropolysilanes, e.g. hexachlorodisilane (Si2Cl6), can also be used. In comparison, using the reaction of the corresponding phosphine oxides with perchloropolysilanes such as Si2Cl6 or Si3Cl8 in benzene or chloroform, phosphines can be prepared in higher yields.
- R3PO + Si2Cl6 → R3P + Si2OCl6
- 2 R3PO + Si3Cl8 → 2 R3P + Si3O2Cl8
Deoxygenation with perchloropolysilanes or trichlorosilane requires longer reaction times and is often problematic with sterically hindered or electron-deficient phosphine oxides. To counter this problem Ph3P or (EtO)3P along with trichlorosilane can be used.
Phosphine oxides are ligands in various applications of homogeneous catalysis. In coordination chemistry, they are known to have labilizing effects to CO ligands cis to it in organometallic reactions. The cis effect describes this process.
The parent compound phosphine oxide (H3PO) is unstable. It has been detected with mass spectrometry as a reaction product of oxygen and phosphine, by means of FT-IR in a phosphine-ozone reaction  and in matrix isolation with a reaction of phosphine, vanadium oxytrichloride and chromyl chloride. It has also been reported relatively stable in a water-ethanol solution by electrochemical oxidation of white phosphorus, where it slowly disproportionates into phosphine and hypophosphorous acid. Secondary phosphine oxides (R2P(O)H) are tautomers of phosphinous acids (R2POH).
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