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Frémy's salt

Chemical compound From Wikipedia, the free encyclopedia

Frémy's salt
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Frémy's salt is a chemical compound with the formula (K4[ON(SO3)2]2), sometimes written as (K2[NO(SO3)2]). It is a bright yellowish-brown solid, but its aqueous solutions are bright violet.[1][2] The related sodium salt, disodium nitrosodisulfonate (NDS, Na2ON(SO3)2, CAS 29554-37-8) is also referred to as Frémy's salt.[3]

Quick Facts Names, Identifiers ...

Regardless of the cations, the salts are distinctive because aqueous solutions contain the radical [ON(SO3)2]2−.

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Applications

Frémy's salt, being a long-lived free radical, is used as a standard in electron paramagnetic resonance (EPR) spectroscopy, e.g. for quantitation of radicals. Its intense EPR spectrum is dominated by three lines of equal intensity with a spacing of about 13 G (1.3 mT).[4][5][6]

The inorganic aminoxyl group is a persistent radical, akin to TEMPO.

It has been used in some oxidation reactions, such as for oxidation of some anilines and phenols[7][8][9][10][11] allowing polymerization and cross-linking of peptides and peptide-based hydrogels.[12][13]

It can also be used as a model for peroxyl radicals in studies that examine the antioxidant mechanism of action in a wide range of natural products.[14]

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Preparation

Frémy's salt is prepared from hydroxylaminedisulfonic acid. Oxidation of the conjugate base gives the purple dianion:

HON(SO3H)2 → [HON(SO3)2]2− + 2 H+
2 [HON(SO3)2]2− + PbO2 → 2 [ON(SO3)2]2− + PbO + H2O

The synthesis can be performed by combining nitrite and bisulfite to give the hydroxylaminedisulfonate. Oxidation is typically conducted at low-temperature, either chemically or by electrolysis.[3][2]

Other reactions:

HNO2 + 2 HSO
3
HON(SO
3
)2−
2
+ H2O
3 HON(SO
3
)2−
2
+ MnO
4
+ H+ → 3 ON(SO
3
)2−
2
+ MnO2 + 2 H2O
2 ON(SO
3
)2−
2
+ 4 K+ → K4[ON(SO3)2]2
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History

Frémy's salt was discovered in 1845 by Edmond Frémy (1814–1894).[15] Its use in organic synthesis was popularized by Hans Teuber, such that an oxidation using this salt is called the Teuber reaction.[9][10]

References

Further reading

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