Azo Coupling
An azo coupling is an organic reaction between a
diazonium compound and another aromatic compound that produces an azo compound .
In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile and the activated arene is a nucleophile.
In most cases, including the examples below, the diazonium compound is also aromatic .
In most cases, including the examples below, the diazonium compound is also aromatic .
Diazotization
The process of conversion of primary aromatic amines into its diazonium salt is called diazotization. Diazonium salts are important synthetic intermediates that can undergo coupling reactions to form azo dyes and electrophilic substitution reactions to introduce functional groups .
Uses of the reaction
The product will absorb longer wavelengths of light (specifically they absorb in the visible region) than the reactants because of increased conjugation . Consequently, aromatic azo compounds tend to be brightly colored due to the extended conjugated systems . Many are used as dyes (see the extra azo dye reactions ). Important azo dyes include methyl red and pigment red 170 .Azo coupling is also used to produce prontosil and other sulfa drugs.
Examples of coupling reaction
Many procedures have been described. Phenol reacts with benzenediazonium chloride to give a yellow-orange azo compound . The reaction is base-catalysed.
The related dye called aniline yellow is produced from the reaction of aniline and the diazonium salt.
Similarly β-naphthol couples with phenyldiazonium
electrophile to produce an intense orange-red dye.
For exrta reaction
For video about the Azo coupling reactions
