Difference between revisions of "Triphenylphosphine"
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===Physical=== | ===Physical=== | ||
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==Availability== | ==Availability== | ||
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==Projects== | ==Projects== | ||
*Make triphenylphosphine oxide | *Make triphenylphosphine oxide | ||
+ | *Make PPh3 complexes ([Co(PPh<sub>3</sub>)<sub>2</sub>]Cl<sub>2</sub> e.g.) | ||
==Handling== | ==Handling== |
Latest revision as of 14:18, 6 October 2019
Triphenylphosphine sample and original bottle.
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Names | |
---|---|
IUPAC name
Triphenylphosphane
| |
Other names
TPP
| |
Properties | |
C18H15P P(C6H5)3 PPh3 Ph3P | |
Molar mass | 262.292 g/mol |
Appearance | White solid |
Odor | Nearly odorless |
Density | 1.194 g/cm3 (at 20 °C) |
Melting point | 80 °C (176 °F; 353 K) |
Boiling point | 377 °C (711 °F; 650 K) |
0.0017 g/100 ml (at 22 °C) | |
Solubility | Soluble in glacial acetic acid, benzene, CCl4, chloroform, diethyl ether, THF Slightly soluble in alcohols |
Vapor pressure | 1.1·10-4 mmHg |
Acidity (pKa) | 7.64 (pKa of conjugate acid in acetonitrile) |
Hazards | |
Safety data sheet | Sigma-Aldrich |
Flash point | 180 °C (356 °F; 453 K) |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
700 mg/kg (rat, oral) |
Related compounds | |
Related compounds
|
Phosphine |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 - often abbreviated to PPh3 or Ph3P.
Contents
Properties
Chemical
Triphenylphosphine is a weak base, but does form stable salts with strong acids such as HCl and HBr.
Triphenylphosphine undergoes slow oxidation by air to give triphenylphosphine oxide, Ph3PO:
- 2 PPh3 + O2 → 2 Ph3PO
Triphenylphosphine abstracts sulfur from polysulfide compounds, episulfides, and elemental sulfur, forming triphenylphosphine sulfide, Ph3PS. Simple organosulfur compounds such as thiols and thioethers are unreactive, however.
Physical
Triphenylphosphine is a white solid, soluble in organic solvents.
Availability
Triphenylphosphine is sold by lab suppliers.
Preparation
Can be made by reacting phosphorus trichloride with phenylmagnesium bromide or phenyllithium.
Projects
- Make triphenylphosphine oxide
- Make PPh3 complexes ([Co(PPh3)2]Cl2 e.g.)
Handling
Safety
Triphenylphosphine is irritant.
Storage
In closed plastic or glass bottles, away from oxidizers.
Disposal
Controlled oxidation/incineration will suffice.