Sulfonium

Sulfonium ion

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.

Synthesis

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)
3S+
+ I−

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 (S_N2), 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

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.^[1]

Applications and occurrence

Biochemistry

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.^[2][3]

Structure of S-adenosylmethionine.

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

Organic synthesis

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⁻.^[4]

Structure of tris(dimethylamino)sulfonium difluorotrimethylsilicate.

Tris(dimethylamino)sulfonium difluorotrimethylsilicate [((CH₃)₂N)₃S]⁺[F₂Si(CH₃)₃]⁻ is a popular fluoridation agent.^[5]

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.

See also

• Sulfenate R–S–O–R
• Sulfide R–S–R
• Sulfate R–SO₄–R
• Sulfite R–SO₃–R
• Sulfonate R–SO−
  3
• Onium compounds

References

1. ↑ March, J. “Advanced Organic Chemistry” 5th Ed. J. Wiley and Sons, 1992: New York. ISBN 0-471-60180-2.
2. ↑ Layer, G.; Heinz, D. W.; Jahn, D.; Schubert, W.-D. "Structure and function of radical SAM enzymes" Current Opinion in Chemical Biology 2004, volume 8, 468-476. doi:10.1016/j.cbpa.2004.08.001
3. ↑ Perry A. Frey, Olafur Th. Magnusson "S-Adenosylmethionine:  A Wolf in Sheep's Clothing, or a Rich Man's Adenosylcobalamin?" Chem. Rev., 2003, 103 (6), pp 2129–2148. doi:10.1021/cr020422m
4. ↑ Mitchell J. Bogdanowicz, Barry M. Trost (1988). "Cyclopropylphenylsulfonium Tetrafluoroborate". Org. Synth. ; Coll. Vol., 6, p. 364 
5. ↑ W. J. Middleton (1990). "Tris(dimethylamino)sulfonium difluorotrimethylsilicate". Org. Synth. ; Coll. Vol., 7, p. 528 

External links

• IUPAC definition (short pdf)