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Sulfonium

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Thiols sulfides and sulfonium ions


A sulfonium ion, also known as sulphonium ion or sulfanium ion, is a positively charged ion (a "cation") featuring three organic substituents attached to sulfur. These organosulfur compounds have the formula [SR3]+. Together with a negatively charged counterion, they give sulfonium salts. They are typically colorless solids that are soluble in organic solvent.

Contents

Sulfonium FileSulfonium ion general structurepng Wikimedia Commons

Synthesis

Sulfonium Sulfonium Ion OChemPal

Sulfonium compounds are usually synthesized by the reaction of thioethers with alkyl halides. For example, the reaction of dimethyl sulfide with iodomethane yields trimethylsulfonium iodide:

CH
3
–S–CH
3
+ CH
3
–I
(CH
3
)
3
S+
+ I
Sulfonium Sulfonium Ylid Reactions

Before the above reaction, the sulfur atom has two lone electron pairs. One of these lone pairs links to the methyl group. At the same time, as part of a concerted nucleophilic substitution mechanism (SN2), the iodide leaving group departs. This leaves a positively charged trimethylsulfonium ion, whose charge is balanced by the iodide. The rate of reaction is even faster with stronger methylating agents, such as methyl trifluoromethanesulfonate.

Structure

Sulfonium Patent US6939658 Lithographic printing plate precursor Google

The compounds are pyramidal at sulfur. Thus, Me3S+ is isostructural and isoelectronic to trimethylphosphine. Sulfonium compounds wherein the three substituents differ are chiral and optically stable.

Biochemistry

Sulfonium FileSulfonium ion general structuresvg Wikimedia Commons

The sulfonium (more specifically methioninium) species S-adenosylmethionine occurs widely in nature, where it is used as a source of the adenosoyl radical. This radical participates in the biosynthesis of various compounds.

Another, sulfonium (methioninium) species found in nature is S-methylmethionine.

Organic synthesis

Sulfonium Illustrated Glossary of Organic Chemistry Sulfonium ion

Sulfonium salts are precursor to sulfur ylides, which are useful in C-C forming reactions. In a typical application, a R2S+CH2R′ center is deprotonated to give the ylide R2S+CHR.

Tris(dimethylamino)sulfonium difluorotrimethylsilicate [((CH3)2N)3S]+[F2Si(CH3)3] is a popular fluoridation agent.

Sulfonium FileStructure of sulfonium saltspng Wikimedia Commons

Some azo dyes are modified with sulfonium groups to give them a positive charge. The compound triphenylsulfonium triflate is a photoacid, a compound that under light converts to an acid.

Sulfonium Dimethylmethylthiosulfonium tetrafluoroborate 97 SigmaAldrich

References

Sulfonium Wikipedia