Tris(4-bromophenyl)ammoniumyl hexachloroantimonate
 | |
| Identifiers | |
|---|---|
| 24964-91-8 salt 37881-41-7 cation | |
| Properties | |
| C18H12Br3Cl6NSb | |
| Molar mass | 816.47 g·mol−1 |
| Appearance | blue solid |
| Melting point | 141 to 142 °C (286 to 288 °F; 414 to 415 K) |
| acetonitrile | |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Tris(4-bromophenyl)ammoniumyl hexachloroantimonate is the organic compound with the formula [(4-BrC6H4)3N]SbCl6. Commonly known as magic blue, it is the hexachloroantimonate salt of an amine radical cation. It is a blue solid that reacts with many solvents but is soluble in acetonitrile. The compound is a popular oxidizing agent in organic and organometallic chemistry, with a reduction potential of 0.7 V vs. ferrocene/ferrocenium (MeCN solution).[1]
The structure of the cation consists of a three-bladed propeller structure with a planar amine. It is nearly identical to the parent triphenylamine. The weakly coordinating anion is SbCl6-, which is octahedral.[2]
References
- ↑ Connelly, N. G.; Geiger, W. E. (1996). "Chemical Redox Agents for Organometallic Chemistry". Chem. Rev. 96 (2): 877–910. doi:10.1021/cr940053x. PMID 11848774.
- ↑ Quiroz-Guzman, Mauricio; Brown, Seth N. (2010). "Tris(4-bromophenyl)aminium hexachloridoantimonate ('Magic Blue'): A strong oxidant with low inner-sphere reorganization". Acta Crystallographica Section C Crystal Structure Communications. 66 (7): m171. doi:10.1107/S0108270110019748.
This article is issued from Wikipedia - version of the 11/5/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.