Tetraphenylphosphonium chloride
| Tetraphenylphosphonium chloride | |
|---|---|
| 200px | |
| IUPAC name | Tetraphenylphosphonium chloride |
| Identifiers | |
| CAS number | |
| Properties | |
| Molecular formula | C24H20ClP |
| Molar mass | 374.84 g/mol |
| Appearance | colourless solid |
| Density | 1.27 |
| Melting point |
272-274 |
| Solubility in water | organic solvents |
| Hazards | |
| R-phrases | 36/37/38 |
| S-phrases | 26-36 |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
Tetraphenylphosphonium chloride is the chemical compound with the formula (C6H5)4PCl, abbreviated Ph4PCl or PPh4Cl. Tetraphenylphosphonium and especially tetraphenylarsonium salts were formerly of interest in gravimetric analysis of perchlorate and related oxyanions. This colourless salt is used to generate lipophilic salts from inorganic and organometallic anions. Thus, Ph4P+ is useful as a phase-transfer catalyst, again because it allows inorganic anions to dissolve in organic solvents.
Structure and basic properties
The cation is tetrahedral. PPh4Cl crystallises as the anhydrous salt,[1] which is normal item of commerce, as well as a monohydrate[2] and a dihydrate.[3]
In X-ray crystallography, PPh4+ salts are of interest as they often crystallise easily. The rigidity of the phenyl groups facilitates packing and elevates the melting point relative to alkyl-based quaternary ammonium salts. Also, since these salts are soluble in organic media, a wide range of solvents can be employed for their crystallisation.
Preparation
The compound was first reported in 1928, when it was prepared via the corresponding bromide salt (CAS# 2751-90-8), which in turn was synthesized by passing dry oxygen through the reaction of phenylmagnesium bromide and triphenylphosphine[4] The synthesis probably proceeds via the the reaction of the Grignard reagent with triphenylphosphine oxide.
- PhMgBr + Ph3PO → Ph4POMgBr
- Ph4POMgBr + HBr → Ph4PBr + “Mg(OH)Br”
PPh4Cl can also be prepared by the high temperature (>190 °C) reaction of chlorobenzene with triphenylphosphine catalysed by nickel acetylacetonate and by aluminium trichloride.
References
- ↑ J. F. Richardson, J. M. Ball, P. M. Boorman “Structure of Tetraphenylphosphonium Chloride” Acta Crystallographica 1986, volume C42, pp. 1271-1272. doi:10.1107/S0108270186092612.
- ↑ E. E. Schweizer, C. J. Baldacchini, A. L. Rheingold “Tetraphenylphosphonium Chloride Monohydrate, Tetraphenylphosphonium Bromide and Tetraphenylphosphonium Iodide” Acta Crystallographica 1989. volume C45, page 1236-1239. doi:10.1107/S0108270189000363.
- ↑ A. J. Blake, C. D. Garner, J. M. Tunney “Tetraphenylphosphonium Chloride Dihydrate ” Acta Crystallographica 2003, volume E59, o9-o10. doi:10.1107/S1600536802021682
- ↑ Dodonow, J.; Medox, H. “Zur Kenntnis der Grignardschen Reaktion: Über die Darstellung von Tetraphenyl-phosphoniumsalzen” Berichte der deutschen chemischen Gesellschaft 1928, volume 61, pp. 907-911. doi:10.1002/cber.19280610505 10.1002/cber.19280610505.
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