A sulfoxide is a chemical compound containing a sulfinyl (SO) functional group attached to two carbon atoms. It is a polar functional group. Sulfoxides are the oxidized derivatives of sulfides. Examples of important sulfoxides are alliin, a precursor to the compound that gives freshly crushed garlic its aroma, and DMSO, a common solvent.
Structure and bonding
Sulfoxides feature a pyramidal sulfur center with relatively short S-O distances. In DMSO, the S-O distance is 1.531 Å.
Sulfoxides are generally represented with the structural formula R–S(=O)–R', where R and R' are organic groups. The bond between the sulfur and oxygen atoms is intermediate of a dative bond and a polarized double bond. The S–O interaction has an electrostatic aspect, resulting in significant dipolar character, with negative charge centered on oxygen. A lone pair of electrons resides on the sulfur atom giving it tetrahedral geometry if one considers the lone pair or trigonal pyramidal if the lone pair is ignored.(See VSEPR theory) When the two organic residues are dissimilar, the sulfur is a chiral center, for example, methylphenylsulfoxide.
Sulfoxides are typically prepared by oxidation of sulfides. A typical oxidant is hydrogen peroxide. Oxidation of thioanisole can be effected with periodate. In these oxidations, care is required to avoid over oxidation to the sulfone. Dimethyl sulfide is oxidized to dimethyl sulfoxide and then to dimethyl sulfone. Unsymmetrical sulfides are prochiral, thus their oxidation gives chiral sulfoxides. Certain reagents or catalysts effect enantioselective oxidations.
Diaryl sulfoxides can be prepared by Friedel-Crafts arylation of sulfur dioxide using acid catalyst:
- 2 ArH + SO2 → Ar2SO + H2O
Sulfoxides, such as DMSO, have basic character, being excellent ligands and readily alkylated. Similarly, they can be oxidized to sulfones.
- CH3S(O)CH3 + NaH → CH3S(O)CH2Na + H2
Sulfoxides form complexes with transition metals.
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