Sulfenic acid

Short description: Organosulfur compound of the form R–SOH

While sulfenic acids have the potential of exhibiting tautomerism, spectroscopic measurements as well as theoretical studies indicate that the structure on the left predominates almost exclusively.

In chemistry, a sulfenic acid is an organosulfur compound and oxoacid with the general formula R–S–OH. It is the first member of the family of organosulfur oxoacids, which also include sulfinic acids (R–S(=O)OH) and sulfonic acids (R–S(=O)
2OH), respectively. The base member of the sulfenic acid series with R = H is hydrogen thioperoxide.

## Contents

* 1 Properties
* 2 Formation and occurrence
* 2.1 Peroxiredoxins
* 2.2 Garlic and onions
* 2.3 Organic and inorganic chemistry
* 3 Other sulfenyl compounds
* 4 References

## Properties

In contrast to sulfinic and sulfonic acids, simple sulfenic acids, such as methanesulfenic acid, CH3SOH, are highly reactive and cannot be isolated in solution. In the gas phase the lifetime of methanesulfenic acid is about one minute. The gas phase structure of methanesulfenic acid was found by microwave spectroscopy (rotational spectroscopy) to be CH3–S–O–H.[1] Sulfenic acids can be stabilized through steric effects, which prevent the sulfenic acid from condensing with itself to form thiosulfinates, RS(O)SR, such as allicin from garlic. Through the use of X-ray crystallography, the structure of such stabilized sulfenic acids were shown to be R–S–O–H.[2][3] The stable, sterically hindered sulfenic acid 1-triptycenesulfenic acid has been found to have a pKa of 12.5 and an O–H bond-dissociation energy (bde) of 71.9 ± 0.3 kcal/mol, which can be compared to a pKa of ≥14 and O–H BDE of ~88 kcal/mol for the (valence) isoelectronic hydroperoxides, ROOH.[4]

## Formation and occurrence

### Peroxiredoxins

Peroxiredoxins are ubiquitous and abundant enzymes that detoxify peroxides. They function by the conversion of a cysteine residue to a sulfenic acid. The sulfenic acid then converts to a disulfide by reaction with another residue of cysteine.[5]

### Garlic and onions

Sulfenic acids are produced by the enzymatic decomposition of alliin and related compounds following tissue damage to garlic, onions, and other plants of the genus Allium. 1-Propenesulfenic acid, formed when onions are cut, is rapidly rearranged by a second enzyme, the lachrymatory factor synthase, giving syn-propanethial-S-oxide.[6] 2-Propenesulfenic acid, formed from allicin, is thought to be responsible for garlic’s potent antioxidant activity.[7] Mass spectrometry with a DART ion source were used to identify 2-propenesulfenic formed when garlic is cut or crushed and to demonstrate that this sulfenic acid has a lifetime of less than one second.[8] The pharmacological activity of certain drugs, such as omeprazole, esomeprazole, ticlopidine, clopidogrel, and prasugrel is proposed to involve sulfenic acid intermediates.[9] Oxidation of cysteine residues in protein to the corresponding protein sulfenic acids is suggested to be important in redox-mediated signal transduction.[10][11]

Sulfenic acid forms part of the series of chemical reactions that occur when cutting onions. The lachrymal glands are irritated by the end product of the reactions, syn-Propanethial-S-oxide, causing tears.[12]

### Organic and inorganic chemistry

Dioctadecyl 3,3'-thiodipropanoate: Oxidation to the sulfoxide and subsequent Ei elimination generates a sulfenic acid. This material is used as a polymer stabilizer where it protects against long term heat ageing

Sulfoxides can undergo thermal elimination via an Ei mechanism to yield vinyl alkenes and sulfenic acids:[13][14]

R−S(O)CHA2CHA2−RA′⟶R−SOH+CHA2=CH−RA′

Compounds which react in this manner are used as polymer stabilizers where they protects against long term heat ageing,[15] structures based on thiodipropionate esters are popular.[16]

Sulfenate-based ligands are found at the active site of the nitrile hydratases. The S=O group is proposed as the nucleophile that attacks the nitrile.[17]

## Other sulfenyl compounds

Cyclohexylthiophthalimide is an example of a sulfenamide, yet another derivative of sulfenic acid.

The prefix sulfenyl in organic nomenclature denotes the RS group (R ≠ H). One example is methanesulfenyl chloride, CH3SCl.[18]

Sulfenate esters have the formula RSOR′. They arise by the reaction of sulfenyl chlorides on alcohols.[19] Sulfenate esters are intermediates in the Mislow-Evans rearrangement of allyl sulfoxides.[13] Sulfenamides have the formula RSNR′2.

## References

1. ↑ "Methanesulfenic Acid". Journal of the American Chemical Society 100 (11): 3622–3624. 1978. doi:10.1021/ja00479a068.
2. ↑ "Synthesis, Structure, and Reactions of a Sulfenic Acid Bearing a Novel Bowl-Type Substituent: The First Synthesis of a Stable Sulfenic Acid by Direct Oxidation of a Thiol". Journal of the American Chemical Society 119 (6): 1460–1461. 1997. doi:10.1021/ja962994s.
3. ↑ "Synthesis of a Stable Sulfenic Acid by Oxidation of a Sterically Hindered Thiol (Thiophenetriptycene-8-thiol)1 and Its Characterization". Journal of the American Chemical Society 118 (50): 12836–12837. 1996. doi:10.1021/ja962995k.
4. ↑ "The redox chemistry of sulfenic acids". Journal of the American Chemical Society 132 (47): 16759–16761. 2010. doi:10.1021/ja1083046. PMID 21049943.
5. ↑ Rhee, Sue Goo; Kil, In Sup (2017). "Multiple Functions and Regulation of Mammalian Peroxiredoxins". Annual Review of Biochemistry 86: 749–775. doi:10.1146/annurev-biochem-060815-014431. PMID 28226215.
6. ↑ Block, E. (2010). Garlic and Other Alliums: The Lore and the Science. Royal Society of Chemistry. ISBN 978-0-85404-190-9. https://books.google.com/books?id=6AB89RHV9ucC.
7. ↑ "Garlic: Source of the Ultimate Antioxidants – Sulfenic Acids". Angewandte Chemie International Edition 48 (1): 157–60. 2009. doi:10.1002/anie.200804560. PMID 19040240.
8. ↑ "Applications of Direct Analysis in Real Time–Mass Spectrometry (DART-MS) in Allium Chemistry. 2-Propenesulfenic and 2-Propenesulfinic Acids, Diallyl Trisulfane S-Oxide and Other Reactive Sulfur Compounds from Crushed Garlic and Other Alliums". Journal of Agricultural and Food Chemistry 58 (8): 4617–4625. 2010. doi:10.1021/jf1000106. PMID 20225897.
9. ↑ "Sulfenic acids as reactive intermediates in xenobiotic metabolism". Archives of Biochemistry and Biophysics 507 (1): 174–185. 2011. doi:10.1016/j.abb.2010.09.015. PMID 20869346. https://zenodo.org/record/898058.
10. ↑ Kettenhofen, NJ, Wood, MJ (2010). "Formation, Reactivity, and Detection of Protein Sulfenic Acids". Chem. Res. Toxicol. 23 (11): 1633–1646. doi:10.1021/tx100237w. PMID 20845928.
11. ↑ Gupta, Vinayak; Kate S. Carroll (February 2014). "Sulfenic acid chemistry, detection and cellular lifetime". Biochimica et Biophysica Acta (BBA) - General Subjects 1840 (2): 847–875. doi:10.1016/j.bbagen.2013.05.040. PMID 23748139.
12. ↑ "Why does chopping an onion make you cry?". The Library of Congress. https://www.loc.gov/rr/scitech/mysteries/onion.html.
13. ↑ 13.0 13.1 Braverman, S., "Rearrangements involving sulfenic acids and their derivatives," in Sulfenic Acids and Derivatives, 1990, John Wiley & Sons. doi:10.1002/9780470772287.ch8
14. ↑ Michael Carrasco, Robert J. Jones, Scott Kamel, H. Rapoport, Thien Truong (1992). "N-(Benzyloxycarbonyl)-L-Vinylglycine Methyl Ester". Organic Syntheses 70: 29. doi:10.15227/orgsyn.070.0029.
15. ↑ Kröhnke, C. (2016). "Polymer Stabilization". Reference Module in Materials Science and Materials Engineering. doi:10.1016/B978-0-12-803581-8.01487-9. ISBN 978-0-12-803581-8.
16. ↑ Armstrong, C.; Plant, M.A.; Scott, G. (February 1975). "Mechanisms of antioxidant action: the nature of the redox behaviour of thiodipropionate esters in polypropylene". European Polymer Journal 11 (2): 161–167. doi:10.1016/0014-3057(75)90141-X.
17. ↑ Harrop, Todd C.; Mascharak, Pradip K. (2004). "Fe(III) and Co(III) Centers with Carboxamido Nitrogen and Modified Sulfur Coordination: Lessons Learned from Nitrile Hydratase". Accounts of Chemical Research 37 (4): 253–260. doi:10.1021/ar0301532. PMID 15096062.
18. ↑ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (2006-) "sulfenyl groups". doi:10.1351/goldbook.S06098
19. ↑ Petrovic, Goran; Saicic, Radomir N.; Cekovic, Zivorad (2005). "Phenylsulfenylation of Nonactivated Carbon Atom by Photolysiis of Alkyl Benzenesulfenated: Preparation of 2-Phenylthio-5-heptanol". Organic Syntheses 81: 244. doi:10.15227/orgsyn.081.0244.

* v
* t
* e

Functional groups

| Only carbon,
hydrogen,
and oxygen|

| Hydrocarbons|

* Allene
* Alkene (Allyl group

|

Other|

* Acetoxy
* Acetyl
* Acryloyl
* Acyl
* Aldehyde
* Alkoxy (Methoxy)
* Benzoyl
* Carbonyl
* Carboxyl
* Carboxylic anhydride
* Dioxirane
* Epoxide
* Ester
* Ether
* Ethylenedioxy
* Hydroxy
* Ketone
* Methylenedioxy
* Peroxide (Organic)
* Ynone

Only one
element
apart from
C, H, O|

| Nitrogen|

* Amine
* Azo compound
* Cyanate
* Hydrazone
* Imide
* Imine
* Isocyanate
* Isonitrile
* Nitrene
* Nitrile
* Nitro compound
* Nitroso compound
* Organic amide
* Oxime

|

Phosphorus|

* Phosphonate
* Phosphonous

Sulfur|

* Disulfide
* Sulfone
* Sulfonic acid
* Sulfoxide
* Thial
* Thioester
* Thioether
* Thioketone
* Thiol

Selenium|

* Selenol
* Selenonic acid
* Seleninic acid
* Selenenic acid
* Selone

Tellurium|

* Tellurol
* Telluroketone

Other|

* Isothiocyanate
* Phosphoramide
* Sulfenyl chloride
* Sulfonamide
* Thiocyanate

See also chemical classification, chemical nomenclature ([[Chemistry:IUPAC nomenclature of inorganic, IUPAC nomenclature of organic chemistry|organic]])

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