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The synthesis of poly(trifluoropropylmethyl)siloxane (PTFPMS) by anionic ring-opening polymerization of 1,3,5-tris(trifluoropropylmethyl)cyclotrisiloxane (F 3 ) was studied in miniemulsion using didodecyldimethylammonium bromide (DDDBr) as emulsifier and sodium hydroxide as initiator. This new process of polymerization produced well-defined α,ω-dihydroxylated polymer in very high yields and with molar masses ranging from 2000 to 30 000 g mol -1 . A kinetic study showed that polymerization occurs in two stages. During the first stage, which corresponds to the anionic kinetically controlled ring-opening polymerization of F 3, the maximum nonequilibrium yield is close to 100%. The second stage involves condensation and backbiting reactions. The delay between these steps offers a broad “termination window” for achieving high polymer yield.
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Barrère et al. (2001) studied this question.
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