Addition homo- and copolymerization of 3-triethoxysilyltricyclo[4.2.1.02,5]non-7-ene


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Resumo

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.

Sobre autores

D. Alentiev

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991

S. Korchagina

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991

E. Finkel’shtein

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991

M. 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
Rússia, 29 Leninsky prosp., Moscow, 119991; 1/3 Leninskie Gory, Moscow, 119991

A. Asachenko

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science; Peoples’ Friendship University of Russia

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991; 6 ul. Miklukho-Maklaya, Moscow, 117198

M. Topchiy

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991

P. Gribanov

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science

Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991

M. Bermeshev

A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science; D. I. Mendeleev University of Chemical Technology of Russia

Autor responsável pela correspondência
Email: bmv@ips.ac.ru
Rússia, 29 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047

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