2002Journal of Polymer Science Part A Polymer ChemistryRequires access

Preparation of functionalized block copolymers based on a polysiloxane backbone by anionic ring‐opening polymerization

Josef Bauer, Nicola Hüsing, Guido Kickelbick

Open publisher page 26 citations

Abstract

Abstract Polysiloxane diblock copolymers containing a pure polysiloxane backbone were prepared by the functionalization of poly(dimethylsiloxane)‐b‐poly(methylvinylsiloxane) copolymers. The copolymers were obtained by the sequential anionic copolymerization of either 1,3,5,7‐tetramethyl‐1,3,5,7‐tetravinylcyclotetrasiloxane or 1,3,5‐trimethyl‐1,3,5‐trivinylcyclotrisiloxane with hexamethylcyclotrisiloxane. The two vinyl monomers showed large differences in the propagation rates, but both could be used for the formation of polysiloxane block copolymers. Differences in the polymerization sequences were investigated and revealed that better control was obtained if the slower propagating monomer was polymerized first. The method permitted the synthesis of block copolymers with molecular weight distributions around 1.4 and lower and high block purities. The vinyl groups of the block copolymers were quantitatively and selectively functionalized by hydrosilation or epoxidation reactions. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1539–1551, 2002

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Abstract Polysiloxane diblock copolymers containing a pure polysiloxane backbone were prepared by the functionalization of poly(dimethylsiloxane)‐b‐poly(methylvinylsiloxane) copolymers. The copolymers were obtained by the sequential anionic copolymerization of either 1,3,5,7‐tetramethyl‐1,3,5,7‐tetravinylcyclotetrasiloxane or 1,3,5‐trimethyl‐1,3,5‐trivinylcyclotrisiloxane with hexamethylcyclotrisiloxane. The two vinyl monomers showed large differences in the propagation rates, but both could be used for the formation of polysiloxane block copolymers. Differences in the polymerization sequences were investigated and revealed that better control was obtained if the slower propagating monomer was polymerized first. The method permitted the synthesis of block copolymers with molecular weight distributions around 1.4 and lower and high block purities. The vinyl groups of the block copolymers were quantitatively and selectively functionalized by hydrosilation or epoxidation reactions. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1539–1551, 2002

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Available abstract

Abstract Polysiloxane diblock copolymers containing a pure polysiloxane backbone were prepared by the functionalization of poly(dimethylsiloxane)‐b‐poly(methylvinylsiloxane) copolymers. The copolymers were obtained by the sequential anionic copolymerization of either 1,3,5,7‐tetramethyl‐1,3,5,7‐tetravinylcyclotetrasiloxane or 1,3,5‐trimethyl‐1,3,5‐trivinylcyclotrisiloxane with hexamethylcyclotrisiloxane. The two vinyl monomers showed large differences in the propagation rates, but both could be used for the formation of polysiloxane block copolymers. Differences in the polymerization sequences were investigated and revealed that better control was obtained if the slower propagating monomer was polymerized first. The method permitted the synthesis of block copolymers with molecular weight distributions around 1.4 and lower and high block purities. The vinyl groups of the block copolymers were quantitatively and selectively functionalized by hydrosilation or epoxidation reactions. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 1539–1551, 2002

Key concepts: Copolymer, Polymer chemistry, Monomer, Polymerization, Materials science, Ring-opening polymerization, Anionic addition polymerization, Polymer

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