This article relies largely or entirely on a single source .(October 2023) |
| Names | |
|---|---|
| IUPAC name | |
| Other names | |
| Identifiers | |
3D model (JSmol) | |
| Abbreviations | NOF[ citation needed ] |
| ChemSpider | |
| ECHA InfoCard | 100.029.230 |
| EC Number |
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PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| NOF | |
| Molar mass | 49.0045 g mol−1 |
| Appearance | Colourless gas |
| Density | 2.657 mg mL−1(gas) 1.326 g/cm3(liquid) |
| Melting point | −166 °C (−267 °F; 107 K) |
| Boiling point | −72.4 °C (−98.3 °F; 200.8 K) |
| Reacts | |
| Related compounds | |
Related compounds | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Nitrosyl fluoride ( N O F ) is a covalently bonded nitrosyl compound.
The compound is a colorless gas, with bent molecular shape. [1] The VSEPR model explains this geometry via a lone-pair of electrons on the nitrogen atom.
Nitrosyl fluoride is typically produced by direct reaction of nitric oxide and fluorine, although halogenation with a perfluorinated metal salt is also possible. The compound is a highly reactive fluorinating agent that converts many metals to their fluorides, releasing nitric oxide in the process:
For this reason, aqueous NOF solutions are, like aqua regia, powerful solvents for metals. [1]
Absent an oxidizable metal, NOF reacts with water to form nitrous acid, which then disproportionates to nitric acid:
These reactions occur in both acidic and basic solutions. [1]
Nitrosyl fluoride also forms salt-like adducts with Lewis-acidic fluorides; for example, BF3 reacts to give NOBF4. Similarly, the compound nitrosylates compounds with a free proton; thus alcohols convert to nitrites: [1]
Nitrosyl fluoride is used as a solvent and as a fluorinating and nitrating [ dubious – discuss ] agent in organic synthesis.[ citation needed ]