Nitrosyl chloride
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Nitrosyl chloride | |
---|---|
IUPAC name | Nitrosyl chloride |
Other names | Nitrogen oxychloride Nitrosonium chloride |
Identifiers | |
CAS number | [2696-92-6] |
SMILES | O=N(Cl) |
Properties | |
Molecular formula | ClNO |
Molar mass | 65.46 g/mol |
Appearance | yellow gas, red liquid |
Density | 1.417 g/cm3, liquid @ -12 °C 2.99 g/L, gas |
Melting point |
-59.6 °C |
Boiling point |
-6.4 °C |
Solubility in water | decomposes |
Solubility in other solvents | chlorocarbons |
Structure | |
Molecular shape | sp2 at N |
Dipole moment | 1.90 D |
Hazards | |
Main hazards | highly toxic |
Related compounds | |
Related compounds | NO NOHSO4 NOBF4 SNCl |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
Nitrosyl chloride is the chemical compound NOCl. It is a yellow gas that is most commonly encountered as a decomposition product of aqua regia, a mixture of hydrochloric acid and nitric acid. The related nitrosyl halides nitrosyl fluoride, NOF, and nitrosyl bromide, NOBr, are also known.
Contents |
[edit] Structure and synthesis
Although its formula is written NOCl, the structure is better represented ONCl. A double bond exists between N and O (distance = 1.16 Å) and a single bond between N and Cl (distance = 1.69 Å). The O-N-Cl angle is 113°.[1]
NOCl can be prepared by the direct combination of chlorine and nitric oxide. Alternatively, nitrosylsulfuric acid and HCl also affords the compound:
- HCl + NOHSO4 → NOCl + H2SO4
It also arises from the combination of hydrochloric and nitric acids according to the following reaction:[2]
- HNO3 + 3 HCl → Cl2 + 2 H2O + NOCl
Although this mixture was used for dissolving gold for a long time the first description of the gas was done by Edmund Davy in 1831.[3]
[edit] Reactions
- NOCl reacts with halide acceptors to give the nitrosyl cation, [NO]+. This species is available as NOBF4.
- NOCl reacts with water to release HCl.
- Heating NOCl above 100 C gives back Cl2 and NO.
- In organic synthesis, NOCl is often employed. It adds to alkenes to afford α-chloro oximes.[4]
[edit] Safety
NOCl is toxic and irritating to the lungs.
[edit] References
- ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5.
- ^ L. J. Beckham, W. A. Fessler, M. A. Kise (1951). "Nitrosyl Chloride". Chemical Reviews 48: 319–396. doi: .
- ^ Edmund Davy (1830 - 1837). "Abstracts of the Papers Printed in the Philosophical Transactions of the Royal Society of London, Vol. 3.": 27–29.
- ^ Ohno, M,; Naruse, N.; Terasawa, I. (1973). "7-cyanoheptanal". Org. Synth.; Coll. Vol. 5: 266.