sulfone
Sign in to saveAlso known as sulfones
thumb|150px|right|The structure of a sulfone thumb|Methylsulfonylmethane|Dimethyl sulfone, an example of a sulfone
Research
273,499 papers- A review of cardiovascular effects and underlying mechanisms of legacy and emerging per- and polyfluoroalkyl substances (PFAS).Archives of toxicology · 2023
- Environmental Exposure to Emerging Alternatives of Per- and Polyfluoroalkyl Substances and Polycystic Ovarian Syndrome in Women Diagnosed with Infertility: A Mixture Analysis.Environmental health perspectives · 2023
- Anticoagulant Sulfonate Polyamide/Poly(ether sulfone) Membrane Barrier for Efficient Blood Oxygenation.ACS nano · 2025
- High-performance sulfonated polyether sulfone/chitosan membrane on creatinine transport improved by lithium chloride.International journal of biological macromolecules · 2024
- Microbial desulfonation.FEMS microbiology reviews · 1998
via PubMed
~4 min read
Encyclopedic overview
9 sectionsContents
- Synthesis and reactions
- By oxidation of thioethers and sulfoxides
- From preformed SO<sub>2</sub> moieties
- Reactions
- Applications
- Polymers
- Pharmacology
- See also
- References
thumb|150px|right|The structure of a sulfone thumb|Methylsulfonylmethane|Dimethyl sulfone, an example of a sulfone
In organic chemistry, a sulfone is a organosulfur compound containing a sulfonyl () functional group attached to two carbon atoms. The central hexavalent sulfur atom is double-bonded to each of two oxygen atoms and has a single bond to each of two carbon atoms, usually in two separate hydrocarbon substituents.
Excerpted from Wikipedia’s “sulfone” article, available under the CC BY-SA 4.0 licence.