Tris(trimethylsilyl)phosphine

Tris(trimethylsilyl)phosphine
Names
	Preferred IUPAC name Tris(trimethylsilyl)phosphane
Identifiers
CAS Number	15573-38-3 ;
3D model (JSmol)	Interactive image;
ChemSpider	239909;
ECHA InfoCard	100.154.516
EC Number	626-081-8;
PubChem CID	272683;
CompTox Dashboard (EPA)	DTXSID70297687 ;
	InChI InChI=1S/C9H27PSi3/c1-11(2,3)10(12(4,5)6)13(7,8)9/h1-9H3 Key: OUMZKMRZMVDEOF-UHFFFAOYSA-N;
	SMILES C[Si](C)(C)P([Si](C)(C)C)[Si](C)(C)C;
Properties
Chemical formula	C9H27PSi3
Molar mass	250.544 g·mol−1
Appearance	colorless liquid
Density	0.863 g/cm3
Melting point	24 °C (75 °F; 297 K)
Boiling point	243–244 °C (469–471 °F; 516–517 K)
Hazards
	Occupational safety and health (OHS/OSH):
Main hazards	poison, inflammable
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H250, H252, H315, H319, H335
Precautionary statements	P210, P222, P235+P410, P261, P264, P271, P280, P302+P334, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, P407, P413, P420, P422, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Tris(trimethylsilyl)phosphine is the organophosphorus compound with the formula P(SiMe₃)₃ (Me = methyl). It is a colorless liquid that ignites in air and hydrolyses readily.^[1]

Synthesis

Tris(trimethylsilyl)phosphine is prepared by treating trimethylsilyl chloride, white phosphorus, and sodium-potassium alloy:^[2]

1/4 P₄ + 3 Me₃SiCl + 3 K → P(SiMe₃)₃ + 3 KCl

Several other methods exist.^[1]

Reactions

The compound hydrolyzes to give phosphine:

P(SiMe₃)₃ + 3 H₂O → PH₃ + 3 HOSiMe₃

Treatment of certain acyl chlorides with tris(trimethylsilyl)phosphine gives phosphaalkynes, one example being tert-butylphosphaacetylene.^[4]

Synthesis of a phosphaalkyne using tris(trimethylsilyl)phosphine.

Reaction with potassium tert-butoxide cleaves one P-Si bond, giving the phosphide salt:^[5]

P(SiMe₃)₃ + KO-t-Bu → KP(SiMe₃)₂ + Me₃SiO-t-Bu

It is a reagent in the preparation of metal phosphido clusters by reaction with metal halides or carboxylates. In such reactions the silyl halide or silyl carboxylate is liberated as illustrated in this idealized reaction:

P(SiMe₃)₃ + 3 CuCl → Cu₃P + 3 ClSiMe₃

Safety

Tris(trimethylsilyl)phosphine spontaneously ignites in air, thus it is handled using air-free techniques.

References

^ ^a ^b Kosarev, Sergey A.; Collier, Steven J. (2011). "Tris(trimethylsilyl)phosphine". Handbook of Reagents for Organic Synthesis. Vol. Reagents for Silicon-Mediated Organic Synthesis. pp. 422–427. doi:10.1002/047084289X.rn01332. ISBN 978-0-471-93623-7.
^ Becker, Gerd; Schmidt, Helmut; Uhl, Gudrun; Uhl, Werner (1990). "Tris(Trimethylsilyl)Phosphine and Lithium Bis(Trimethylsilyl)Phosphide.Bis-(Tetrahydrofuran)". Inorganic Syntheses. Vol. 27. pp. 243–9. doi:10.1002/9780470132586.ch48. ISBN 978-0-470-13258-6.
^ Fenske, D.; Holstein, W. (1994). "[Cu₉₆P₃₀{P(SiMe₃)₂}₆(PEt₃)₁₈], a New Phosphorus-Bridged Copper Cluster". Angew. Chem. Int ed. Engl. 33 (12): 1290–1292. doi:10.1002/anie.199412901.
^ M. Regitz (1990). "Phosphaalkynes: new building blocks in synthetic chemistry". Chem. Rev. 90: 191–213. doi:10.1021/cr00099a007..
^ Russell, Christopher A.; Townsend, Nell S. (2012). "Phosphaalkynes". In Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M (eds.). Phosphorus(III) Ligands in Homogeneous Catalysis. Wiley-VCH. pp. 343–354. doi:10.1002/9781118299715.ch11. ISBN 978-1-118-29971-5.

[eEROS-1] Kosarev, Sergey A.; Collier, Steven J. (2011). "Tris(trimethylsilyl)phosphine". Handbook of Reagents for Organic Synthesis. Vol. Reagents for Silicon-Mediated Organic Synthesis. pp. 422–427. doi:10.1002/047084289X.rn01332. ISBN 978-0-471-93623-7.

[2] Becker, Gerd; Schmidt, Helmut; Uhl, Gudrun; Uhl, Werner (1990). "Tris(Trimethylsilyl)Phosphine and Lithium Bis(Trimethylsilyl)Phosphide.Bis-(Tetrahydrofuran)". Inorganic Syntheses. Vol. 27. pp. 243–9. doi:10.1002/9780470132586.ch48. ISBN 978-0-470-13258-6.

[3] Fenske, D.; Holstein, W. (1994). "[Cu₉₆P₃₀{P(SiMe₃)₂}₆(PEt₃)₁₈], a New Phosphorus-Bridged Copper Cluster". Angew. Chem. Int ed. Engl. 33 (12): 1290–1292. doi:10.1002/anie.199412901.

[4] M. Regitz (1990). "Phosphaalkynes: new building blocks in synthetic chemistry". Chem. Rev. 90: 191–213. doi:10.1021/cr00099a007..

[5] Russell, Christopher A.; Townsend, Nell S. (2012). "Phosphaalkynes". In Kamer, Paul C. J.; Van Leeuwen, Piet W. N. M (eds.). Phosphorus(III) Ligands in Homogeneous Catalysis. Wiley-VCH. pp. 343–354. doi:10.1002/9781118299715.ch11. ISBN 978-1-118-29971-5.

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