Nitrosonium tetrafluoroborate
Names | |
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IUPAC name
nitrosonium tetrafluoroborate | |
Other names
nitrosyl tetrafluoroborate | |
Identifiers | |
14635-75-7 | |
ChemSpider | 9312255 |
Jmol interactive 3D | Image |
PubChem | 151929 |
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Properties | |
BF4NO | |
Molar mass | 116.81 g·mol−1 |
Appearance | colourless crystalline solid |
Density | 2.185 g cm−3 |
Melting point | 250 °C (482 °F; 523 K) (sublimes) |
decomposes | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Nitrosonium tetrafluoroborate, also called nitrosyl tetrafluoroborate, is a chemical compound with the chemical formula NOBF4. This colourless solid finds use in organic synthesis as a nitrosating agent.[1]
NOBF4 is the nitrosonium salt of fluoroboric acid, and is composed of a nitrosonium cation, [NO]+, and a tetrafluoroborate anion, [BF4]−.
Reactions
Nitrosonium tetrafluoroborate may be used to prepare metal salts of the type [MII(CH3CN)x][BF4]2 (M = Cr, Mn, Fe, Co, Ni, Cu). The nitrosonium cation acts as the oxidizer, itself being reduced to nitric oxide gas:[2]
- M + NOBF4 + xCH3CN → [M(CH3CN)x](BF4)2 + NO
With ferrocene the ferrocenium tetrafluoroborate is formed.[3]
References
- ↑ "A15806 Nitrosonium tetrafluoroborate, 98%". Alfa Aesar website. Retrieved 2010-09-04.
- ↑ Robert A. Heintz, Jennifer A. Smith, Paul S. Szalay, Amy Weisgerber, And Kim R. Dunbar. "11. Homoleptic Transition Metal Acetonitrile Cations with Tetrafluoroborate or Trifluoromethanesulfonate Anions". Inorg. Synth. 33: 75–83. doi:10.1002/0471224502.ch2.
- ↑ Roger M. Nielson, George E. McManis, Lance K. Safford, Michael J. Weaver (1989). "Solvent and electrolyte effects on the kinetics of ferrocenium-ferrocene self-exchange. A reevaluation". J. Phys. Chem. 93 (5): 2152. doi:10.1021/j100342a086.
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