Tetraphenylphosphonium chloride
Tetraphenylphosphonium chloride is the chemical compound with the formula Template:Chem2, abbreviated Template:Chem2 or Template:Chem2 or Template:Chem2, where Ph stands for phenyl. 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, Template:Chem2 is useful as a phase-transfer catalyst, again because it allows inorganic anions to dissolve in organic solvents.
Structure and basic properties
The structure of this salt is Template:Chem2. It consists of tetraphenylphosphonium cations Template:Chem2 and chloride anions Template:Chem2. The Template:Chem2 cation is tetrahedral around the phosphorus atom.
PPh4Cl crystallises as the anhydrous salt,[1] which is the normal item of commerce, as well as a monohydrate[2] and a dihydrate.[3]
In X-ray crystallography, Template:Chem2 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.
| File:Tetraphenylphosphonium-chloride-from-xtal-3D-SF.png | File:Tetraphenylphosphonium-chloride-xtal-3D-SF.png | File:Tetraphenylphosphonium-chloride-xtal-3D-balls.png |
| constituent ions in the solid | space-filling model of part of the crystal structure |
ball-and-stick model of part of the crystal structure |
Preparation
Template:Chem2 and many analogous compounds can be prepared by the reaction of chlorobenzene with triphenylphosphine catalysed by nickel salts:[4]
The compound was originally prepared as the corresponding bromide salt (CAS No. 2751-90-8), which in turn was synthesized by passing dry oxygen through the reaction of phenylmagnesium bromide and triphenylphosphine.[5] The synthesis probably proceeds via the reaction of the Grignard reagent with triphenylphosphine oxide.
Use in synthesis
Tetraphenylphosphonium salts of inorganic or organometallic anions are often sought because they are easily crystallized. They also tend to be soluble in polar organic solvents such as acetonitrile and dimethylformamide. Examples include the tetraphenylphosphonium perrhenate (Template:Chem2)[6] and various thiomolybdates.[7] Complexes of maleonitriledithiolate are also isolated as their Template:Chem2 salts.[8]
References
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