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Copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride and alkyl methacrylates

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Abstract

Radical copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride with methyl methacrylate and allyl methacrylate in the bulk and methanol solution in the presence of azobis-isobutyric acid dinitryle at 70–90°C has been studied. Copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride with methyl methacrylate or allyl methacrylate in the bulk proceeds with formation of random copolymers enriched in methacrylate units; in the copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidiny chloride with methyl methacrylate in methanol, the copolymerization constants of the monomers become close. The kinetic parameters of the reaction have been studied, the relative activities of the monomers have been determined. It has been found that 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride is copolymerized with allyl methacrylate or methylmethacrylate to form pyrrolidinium structures in the cyclolinear polymer chain. At high degrees of conversion of the copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride with allyl methacrylate, the viscosity increases and the side polymer chains are crosslinked by “allyl bonds” to form insoluble copolymers, swelling in benzene and DMSO.

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Authors and Affiliations

  1. Institute of Technical Chemistry, Russian Academy of Sciences, Ural Branch, Perm, 614013, Russia

    M. N. Gorbunova & I. A. Borisova

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  1. M. N. Gorbunova
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  2. I. A. Borisova
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Correspondence to M. N. Gorbunova.

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Original Russian Text © M.N. Gorbunova, I.A. Borisova, 2016, published in Vysokomolekulyarnye Soedineniya, Seriya B, 2016, Vol. 58, No. 6, pp. 440–449.

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Gorbunova, M.N., Borisova, I.A. Copolymerization of 2,2-diallyl-1,1,3,3-tetraethylguanidinium chloride and alkyl methacrylates. Polym. Sci. Ser. B 58, 650–658 (2016). https://doi.org/10.1134/S1560090416060075

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  • DOI: https://doi.org/10.1134/S1560090416060075

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