Sulfonium Explained

In organic chemistry, 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 . Together with a negatively-charged counterion, they give sulfonium salts. They are typically colorless solids that are soluble in organic solvent.[1] [2]

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:

+ →

The reaction proceeds by a nucleophilic substitution mechanism (SN2). Iodide is the leaving group departs. The rate of methylation is faster with more electrophilic methylating agents, such as methyl trifluoromethanesulfonate.

Inversion

Sulfonium ions with three different substituents are chiral owing to their pyramidal structure. Unlike the isoelectronic oxonium ions (R3O+), chiral sulfonium ions are resolvable into optically stable enantiomers.[3] [Me(Et)SCH<sub>2</sub>CO<sub>2</sub>H]+ is the first chiral sulfonium cation to be resolved into enantiomers.[4] The barrier to inversion ranges from 100 to 130 kJ/mol.[2]

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 or methyl radicals. These radicals participate in the biosynthesis of many compounds.[5] [6]

Other naturally-occurring sulfonium species are S-methylmethionine (methioninium) and the related dimethylsulfoniopropionate (DMSP).

Organic synthesis

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

Tris(dimethylamino)sulfonium difluorotrimethylsilicate [((CH<sub>3</sub>)<sub>2</sub>N)<sub>3</sub>S]+[F<sub>2</sub>Si(CH<sub>3</sub>)<sub>3</sub>] is a popular fluoridation agent.

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

References

  1. Book: The Sulphonium Group: Part 1, Volume 1. 1981. C. J. M. Stirling. 9780470771648. 10.1002/9780470771648. John Wiley & Sons. PATAI'S Chemistry of Functional Groups. Book: The Sulphonium Group: Part 2, Volume 2. 1981. C. J. M. Stirling. 9780470771655. 10.1002/9780470771655. John Wiley & Sons. PATAI'S Chemistry of Functional Groups.
  2. 10.1002/ejic.202000249. Synthetic Applications of Sulfonium Salts. 2020. Kozhushkov. Sergei I.. Alcarazo. Manuel. European Journal of Inorganic Chemistry. 2020. 26. 2486–2500. 32742188. 7386937.
  3. March, J. “Advanced Organic Chemistry” 5th Ed. J. Wiley and Sons, 1992: New York.
  4. Book: 10.1016/B978-0-12-507704-0.50007-6. Asymmetric Synthesis. 1984. 227–261. Optical Activation and Utilization of Compounds Containing Chiral Sulfur Centers. Michael R.. Barbachyn. Carl R.. Johnson. 9780125077040.
  5. 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.
  6. 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.

External links