Addition homo- and copolymerization of 3-triethoxysilyltricyclo[4.2.1.02,5]non-7-ene
- Authors: Alentiev D.A.1, Korchagina S.A.1, Finkel’shtein E.S.1, Nechaev M.S.1,2, Asachenko A.F.1,3, Topchiy M.A.1, Gribanov P.S.1, Bermeshev M.V.1,4
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Affiliations:
- A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
- Department of Chemistry, M. V. Lomonosov Moscow State University
- Peoples’ Friendship University of Russia
- D. I. Mendeleev University of Chemical Technology of Russia
- Issue: Vol 67, No 1 (2018)
- Pages: 121-126
- Section: Article
- URL: https://ogarev-online.ru/1066-5285/article/view/241964
- DOI: https://doi.org/10.1007/s11172-018-2046-2
- ID: 241964
Cite item
Abstract
New norbornene type monomer bearing reactive triethoxysilyl group was synthesized, and its addition homo- and copolymerization with 3-trimethylsilyltricyclonon-7-ene was studied. The target monomer was obtained using regio- and stereospecific [2σ+2σ+2π] cyclo-addition of quadricyclane with vinyltrichlorosilane followed by the reaction of the formed cycloadduct with ethanol in the presence of triethylamine. Addition polymerization was investigated over the three-component Pd-containing catalytic system (Pd complex, Na+[B(3,5-(CF3)2C6H3)4]–(cocatalyst) and tricyclohexylphosphine). The N-heterocyclic carbene Pd complex (SIPrPd(cinn)Cl) with high activity and tolerance to the Si—O—C moieties was used as a catalyst. The yields of the homo- and copolymers were 24—68% depending on the monomer (comonomer): Pd: B: PCy3 ratio. The obtained addition polymers are high-molecular-weight amorphous products, the glass transition temperature of which exceeds 300 °C. The presence of reactive Si(OC2H5)3 groups in the homo- and copolymers made it possible to carry out a hard-to-realize cross-linking involving side substituents and followed by the formation of insoluble polymers.
About the authors
D. A. Alentiev
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991
S. A. Korchagina
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991
E. Sh. Finkel’shtein
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991
M. S. Nechaev
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science; Department of Chemistry, M. V. Lomonosov Moscow State University
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991; 1/3 Leninskie Gory, Moscow, 119991
A. F. Asachenko
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science; Peoples’ Friendship University of Russia
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991; 6 ul. Miklukho-Maklaya, Moscow, 117198
M. A. Topchiy
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991
P. S. Gribanov
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991
M. V. Bermeshev
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science; D. I. Mendeleev University of Chemical Technology of Russia
Author for correspondence.
Email: bmv@ips.ac.ru
Russian Federation, 29 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047
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