Tetraphenylborate
| Names | |
|---|---|
| Preferred IUPAC name
Tetraphenylboranuide | |
| Other names
Tetraphenylborate(1−) (additive), tetraphenylboranuide
| |
| Identifiers | |
3D model (JSmol)
|
|
| ChEMBL | |
| ChemSpider | |
| MeSH | D013775 |
PubChem CID
|
|
| UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C24H20B | |
| Molar mass | 319.23 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
| |
Tetraphenylborate is an organoboron anion consisting of a central boron atom with four phenyl groups. It is a colorless anion that forms water-insoluble salts with a variety of cations. It was considered as a precipitant for caesium-137 ions in the context of radiowaste cleanup.[1]
Salts of tetraphenylborate have been used as uncouplers of oxidative phosphorylation.[2]
Oxidation of tetraphenylborate gives biphenyl and (C6H5)2BOH.[3]
See also
- Sodium tetraphenylborate
- Potassium tetraphenylborate
- Triphenylborane
- BARF and other fluorinated derivatives are used as non-coordinating anions
References
- ^ Fanning, James C. (1995). "The Solubilities of the Alkali Metal Salts and the Precipitation of Cs+ from Aqueous Solution". Coordination Chemistry Reviews. 140: 27–36. doi:10.1016/0010-8545(94)01123-S.
- ^ Utsumi, Kozo; Packer, Lester (1967). "Uncoupling of energy transfer reactions in mitochondria by tetraphenylboron". Archives of Biochemistry and Biophysics. 122 (2): 509–15. doi:10.1016/0003-9861(67)90226-3. PMID 4229179.
- ^ Abley, Peter; Halpern, Jack (1971). "Oxidation of tetraphenylborate by hexachloroiridate(IV)". Journal of the Chemical Society D: Chemical Communications (20): 1238. doi:10.1039/c29710001238.