| Abstract: | Methyl methacrylate (MMA) was polymerized by thiophenol without oxidants. Hydroquinone had no effect on the polymerization, indicating that the polymerization proceeded via a non-radical process. Since other monomers with an x,β-unsaturated carbonyl group polymerized similarly, the initiation and propagation were explained by the Michael addition. Radical scavengers such as 1,1-diphenyl-2-picrylhydrazyl(DPPH) and galvinoxyl enhanced the polymerization because of an accompanying radical polymerization initiated by radical species formed by the reaction of them with thiophenol. Aluminium acetylacetonate, which has no effect on radical polymerization, accelerated the thiophenol-initiated polymerization supporting the postulated mechanism. |
