Triethylphosphine

Triethylphosphine
Names
	Other names triethylphosphane
Identifiers
CAS Number	554-70-1;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:39971;
ChemSpider	25463;
EC Number	209-068-8
Gmelin Reference	2485
PubChem CID	27365;
UNII	5W435D16PM;
	InChI InChI=1S/C6H15P/c1-4-7(5-2)6-3/h4-6H2,1-3H3 Key: RXJKFRMDXUJTEX-UHFFFAOYSA-N;
	SMILES CCP(CC)CC;
Properties
Chemical formula	C6H15P
Molar mass	118.16 g·mol−1
Appearance	colorless liquid
Density	0.802 g/cm3
Boiling point	127–128 °C (261–262 °F; 400–401 K)
Hazards
GHS pictograms
GHS signal word	Danger
GHS hazard statements	H224, H225, H250, H314
GHS precautionary statements	P210, P222, P233, P240, P241, P242, P243, P260, P264, P280, P301+330+331, P302+334, P303+361+353, P304+340, P305+351+338, P310, P321, P363, P370+378, P403+235, P405, P422, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Triethylphosphine is the organophosphorus compound with the formula P(CH₂CH₃)₃, commonly abbreviated as PEt₃. It is a colorless liquid with an unpleasant odor characteristic of alkylphosphines. The compound is a common ligand in organometallic chemistry.

Structure and simple reactions

It is a pyramidal molecule with approximate C_3v symmetry.

PEt₃ is usually prepared using Grignard reagents:

3 CH₃CH₂MgCl + P(OC₆H₅)₃ → P(CH₂CH₃)₃ + 3 C₆H₅OMgCl

PEt₃ reacts with strong acids to give salts [HPEt₃]X.^[1] This reaction is reversible. Similarly, it is also easily alkylated to give phosphonium derivatives. PEt₃ is easily oxidised to the phosphine oxide with oxygen.

Coordination chemistry

Triethylphosphine is a highly basic ligand that forms complexes with most metals. As a ligand, triethylphosphine's Tolman cone angle is 132°.^[2] Being a relatively compact phosphine, several can bind to a single transition metal, as illustrated by the existence of Pt(PEt₃)₄.^[3] As a phosphine ligand, triethylphosphine gained acceptance earlier than did the simpler trimethylphosphine, as illustrated by the preparation of the hydride complex trans-PtHCl(PEt₃)₂.^[4]

Structure of Pt(PEt₃)₄.^[5]

Safety

PEt₃ is toxic. It converts to non-pyrophoric phosphine oxide upon treatment with bleach.

References

↑ Annette Schier and Hubert Schmidbaur "P-Donor Ligands" in Encyclopedia of Inorganic Chemistry 2006, Wiley-VCH, Weinheim. doi:10.1002/0470862106.ia177
↑ G. L. Miessler and D. A. Tarr Inorganic Chemistry, 3rd Ed, Pearson/Prentice Hall publisher, ISBN 0-13-035471-6.
↑ T. Yoshida T. Matsuda S. Otsuka (1990). "Tetrakis(Triethylphosphine)Platinum(0)". Inorg. Syntheses. 28: 122. doi:10.1002/9780470132593.ch32.
↑ Joseph Chatt (1968). "Hydride Complexes". Science. 160: 723–729. doi:10.1126/science.160.3829.723.
↑ Pospiech, S.; Bolte, M.; Lerner, H.-W.; Wagner, M. (2014). "Insertion Reactions into the Boron–Boron Bonds of Barrelene-Type 1,2-Diaminodiboranes(4)". Organometallics. 33: 6967–6974. doi:10.1021/om501087u.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[Schmidbaur-1] Annette Schier and Hubert Schmidbaur "P-Donor Ligands" in Encyclopedia of Inorganic Chemistry 2006, Wiley-VCH, Weinheim. doi:10.1002/0470862106.ia177

[2] G. L. Miessler and D. A. Tarr Inorganic Chemistry, 3rd Ed, Pearson/Prentice Hall publisher, ISBN 0-13-035471-6.

[3] T. Yoshida T. Matsuda S. Otsuka (1990). "Tetrakis(Triethylphosphine)Platinum(0)". Inorg. Syntheses. 28: 122. doi:10.1002/9780470132593.ch32.

[4] Joseph Chatt (1968). "Hydride Complexes". Science. 160: 723–729. doi:10.1126/science.160.3829.723.

[5] Pospiech, S.; Bolte, M.; Lerner, H.-W.; Wagner, M. (2014). "Insertion Reactions into the Boron–Boron Bonds of Barrelene-Type 1,2-Diaminodiboranes(4)". Organometallics. 33: 6967–6974. doi:10.1021/om501087u.