Micellar Effects on Dediazoniation and on Azo Coupling Reactions

✍ Scribed by Román Pazo-Llorente; Ma Carmen Rodriguez-Menacho; Elisa González-Romero; Carlos Bravo-Dı́az

• Book ID: 102585261
• Publisher: Elsevier Science
• Year: 2002
• Tongue: English
• Weight: 134 KB
• Volume: 248
• Category: Article
• ISSN: 0021-9797
• DOI: 10.1006/jcis.2001.8196

✦ Synopsis

The effects of a sodium dodecyl sulfate, SDS, micellar solution on the coupling rates of two arenediazonium ions, ArN(2)(+), with the hydrophobic 1-naphthylamine, 1NA and N-(1-naphthyl) ethylenediamine, NED, coupling agents and with the hydrophilic Na salt of 2-naphthol-6-sulfonic acid, 2N6S, have been studied. First, we explored the micellar effects on the thermal decomposition of the arenediazonium ions. The observed rate constants are slightly depressed or increased, depending on the nature of ArN(2)(+), compared to those in pure water upon increasing [SDS]. Estimations of the corresponding association constant to the micelle indicate that a significant fraction of the arenediazonium ions are incorporated into the micelles even at low surfactant concentrations. The sulfonate group in 2N6S prevents its incorporation into the micellar aggregate due to the electrostatic barrier imposed by the micelles and, in consequence, the coupling reaction is inhibited. In contrast, when employing the naphthylamine derivatives, the observed rate constant increase rapidly up to a maximum at [SDS]