Phosphine Oxide

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).

Structure and bonding

Tertiary phosphine oxides

Tertiary phosphine oxides are the most commonly encountered phosphine oxides. With the formula R₃PO, they are tetrahedral compounds. They are usually prepared by oxidation of tertiary phosphines. 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. 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.

Secondary phosphine oxides

Secondary phosphine oxides (SPOs), formally derived from secondary phosphines (R₂PH), are again tetrahedral at phosphorus. One commercially available example of a secondary phosphine oxide is diphenylphosphine oxide. SPOs are used in the formulation of catalysts for cross coupling reactions.

Unlike tertiary phosphine oxides, SPOs often undergo further oxidation, which enriches their chemistry:
:R₂P(O)H + H₂O₂ → R₂P(O)OH + H₂O
These reactions are preceded by tautomerization to the phosphinous acid (R₂POH):
:R₂P(O)H R₂POH

Primary phosphine oxides

Primary phosphine oxides, formally oxidized derivatives of primary phosphines, are again tetrahedral at phosphorus. With four different substituents (O, OH, H, R) they are chiral. The primary phosphine oxides subject to tautomerization, which leads to racemization, and further oxidation, analogous to the behavior of SPOs. Additionally, primary phosphine oxides are susceptible to disproportionation to the phosphinic acid and the primary phosphine:
:2RP(O)H₂ → RP(O)(H)OH + 2RPH₂

Syntheses

Phosphine oxide are typically produced by oxidation of organophosphines. The oxygen in air is often sufficiently oxidizing to fully convert trialkylphosphines to their oxides at room temperature:
:R₃P + 1/2 O₂ → R₃PO
This conversion is usually undesirable. In order to suppress this reaction, air-free techniques are often employed when handling say, trimethylphosphine.

Less basic phosphines, such as methyldiphenylphosphine are converted to their oxides by treatment with hydrogen peroxide:
: PMePh₂ + H₂O₂ → OPMePh₂ + H₂O

Phosphine oxides are generated as a by-product of the Wittig reaction:
:R₃PCR'₂ + R"₂CO → R₃PO + R'₂C=CR"₂
Another albeit unconventional route to phosphine oxides is the thermolysis of phosphonium hydroxides:
: Ph₄l + NaOH → Ph₃PO + NaCl + PhH

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

Deoxygenation

The deoxygenation of phosphine oxides has been extensively developed because many useful stoichiometric reactions convert tertiary phosphines to the corresponding oxides. Regeneration of the tertiary phosphine requires cheap oxophilic reagents, which are usually silicon-based. These deoxygenation reactions can be subdivided into stoichiometric and catalytic processes.

Stoichiometric processes

Use of trichlorosilane is a standard laboratory method. Industrial routes use phosgene or equivalent reagents, which produce chlorotriphenylphosphonium chloride, which is separately reduced.
For chiral phosphine oxides, deoxygenation can proceed with retention or inversion of configuration. Classically, inversion is favored by a combination of trichlorosilane and triethylamine, whereas in the absence of the Lewis base, the reaction proceeds with retention.
:HSiCl₃ + Et₃N ⇋ SiCl₃⁻ + Et₃NH⁺
:R₃PO + Et₃NH⁺ ⇋ R₃POH⁺ + Et₃N
:SiCl₃⁻ + R₃POH⁺ → 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 has been effected with boranes and alanes.

Catalytic processes

Phosphoric acids ((RO)₂PO₂H) catalyze the deoxygenation of phosphine oxides by hydrosilanes.

Use

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.

Parent compound

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).

Phosphine oxide is reported as an intermediate in the room-temperature polymerization of phosphine and nitric oxide to solid P_xH_y.

References

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Functional groups
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