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 sulfides. Examples of important sulfoxides are alliin, a precursor to the chemical that gives freshly crushed garlic its aroma, and DMSO, a common solvent.
Structure and bonding
Sulfoxides are characterized by pyramidal sulfur center with relatively short S-O distances.
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 molecular geometry as for sp³ carbon. When the two organic residues are dissimilar, the sulfur is a chiral center, for example, methylphenylsulfoxide.
Sulfoxides are typically prepared by oxidation of sulfides. Typical oxidants are hydrogen peroxide, being careful to avoid over oxidation to the sulfone. Dimethyl sulfide is oxidized to dimethyl sulfoxide and then to dimethyl sulfone. Many chiral sulfoxides are prepared from asymmetric catalytic oxidation of achiral sulfides with a transition metal and a chiral ligand.
Diaryl sulfoxides can be prepared by Friedel-Crafts arylation of sulfur dioxide using acid catalyst:
- 2 ArH + SO2 → Ar2SO + H2O
- CH3S(O)CH3 + NaH → CH3S(O)CH2Na + H2
Sulfoxides form complexes with transition metals.
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