Sulfene

Sulfene

Skeletal formula of sulfene with both explicit hydrogens added Spacefill model of sulfene
Names
Other names Thioformaldehyde-S,S-dioxide
Identifiers
CAS Number	917-73-7 N
ChemSpider	10645700 Y
Jmol 3D model	Interactive image
PubChem	12244237
InChI InChI=1S/CH2O2S/c1-4(2)3/h1H2 Y Key: LZOZLBFZGFLFBV-UHFFFAOYSA-N Y InChI=1/CH2O2S/c1-4(2)3/h1H2 Key: LZOZLBFZGFLFBV-UHFFFAOYAF
SMILES C=S(=O)=O
Properties
Chemical formula	CH 2SO 2
Molar mass	78.090 g mol−1
Structure
Molecular shape	trigonal planar at C and S
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)
Infobox references

Sulfene is an extremely reactive chemical compound with the formula H₂C=SO₂. It is the simplest member of the sulfenes, the group of compounds which are S,S-dioxides of thioaldehydes and thioketones, and have the general formula R₂C=SO₂.

Preparation

The first general method for preparation of sulfene as an intermediate, reported simultaneously in 1962 by Gilbert Stork and by Günther Optiz, involved removal of hydrogen chloride from methanesulfonyl chloride using triethylamine in the presence of an enamine as trapping agent. The formation of a thietane 1,1-dioxide derivative was taken as evidence for the intermediacy of sulfene. Because of the highly electrophilic character of sulfene, the use of amines presents difficulties, since they can intercept the sulfene to form complexes, which may display reduced activity in trapping reactions compared to sulfene itself. A simple alternative which avoids the use of amines involves desilylation of trimethylsilylmethanesulfonyl chloride with cesium fluoride in the presence of trapping agents.

(CH₃)₃SiCH₂SO₂Cl + CsF → [CH₂=SO₂] + (CH₃)₃SiF + CsCl

Reactions

Sulfenes react with enamines, ynamines, and 1,3-cyclopentadienes to give thietanes, thietes and Diels-Alder adducts, respectively. In the presence of a chiral tertiary amine complex, several sulfenes could be trapped with trichloroacetaldehyde (chloral) in a catalytic asymmetric synthesis of β-sultones (four-membered ring sulfonate esters). Sulfene can also undergo insertion into metal-hydrogen bonds.