Cyclodextrins in polymer synthesis: Free radical polymerization of methylated beta-cyclodextrin complexes of methyl methacrylate and styrene, controlled by dodecanethiol as the chain-transfer agent in aqueous medium
P. Glockner et H. Ritter, Cyclodextrins in polymer synthesis: Free radical polymerization of methylated beta-cyclodextrin complexes of methyl methacrylate and styrene, controlled by dodecanethiol as the chain-transfer agent in aqueous medium, MACRO CH P, 201(17), 2000, pp. 2455-2457
Methylated beta -cyclodextrin (me-beta -CD) was used to complex the hydroph
obic monomers methyl methacrylate (1) or styrene (2) yielding the water-sol
uble 1:1-host/guest complexes methyl methacrylate/me-beta -CD (1a) and styr
ene/me-beta -CD (2a), respectively. In addition, the hydrophobic chain-tran
sfer agent dodecanethiol (3) was complexed by two equivalents of me-beta -C
D yielding the water-soluble dodecanethiol/me-beta -CD (3a). The included m
onomers were polymerized in water by a free-radical mechanism in the presen
ce of 3a as the chain-transfer agent. The chain-transfer constants were det
ermined. In order to evaluate these results, the chain-transfer constants o
f 3 were also determined in the case of the corresponding uncomplexed monom
ers 1 and 2 in organic solution. It was found that the chain-transfer const
ants of 1a and 2a (Cs-1a = 0.5 +/- 0.2, Cs-2a = 2.2 +/- 0.3) are significan
tly tower compared with the values obtained from the polymerizations of the
corresponding uncomplexed monomers 1 and 2 in organic solution (Cs-1 = 3.1
+/- 0.3, Cs-2 = 3.4 +/- 0.3).