Abstract
Radical copolymerization of styrene with tert-butyl acrylate is studied under different conditions. It is found that the addition of tri-n-butylborane or tri-n-butylborane along with p-quinones (2,3-dimethylbenzoquinone, 2,5-di-tert-butylbenzoquinone) results in changes in the relative activities of monomers. Copolymerization in the presence of tri-n-butylborane and p-quinones proceeds via the mechanism of reversible inhibition and is characterized by the linear increase in number-average molecular weight with conversion and by the capacity of copolymers of reinitiation. The hydrolyzed copolymer samples form more stable films compared to copolymers prepared via conventional radical copolymerization.
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Original Russian Text © D.V. Ludin, Yu.L. Kuznetsova, O.G. Zamyshlyaeva, S.D. Zaitsev, 2017, published in Vysokomolekulyarnye Soedineniya, Seriya B, 2017, Vol. 59, No. 1, pp. 3–11.
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Ludin, D.V., Kuznetsova, Y.L., Zamyshlyaeva, O.G. et al. Controlled radical copolymerization of styrene and tert-butyl acrylate in the presence of tri-n-butylborane–p-quinone catalytic system. Polym. Sci. Ser. B 59, 7–15 (2017). https://doi.org/10.1134/S1560090417010109
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DOI: https://doi.org/10.1134/S1560090417010109