Addition homo- and copolymerization of 3-triethoxysilyltricyclo[4.2.1.02,5]non-7-ene
- 作者: 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
-
隶属关系:
- 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
- 期: 卷 67, 编号 1 (2018)
- 页面: 121-126
- 栏目: Article
- URL: https://bakhtiniada.ru/1066-5285/article/view/241964
- DOI: https://doi.org/10.1007/s11172-018-2046-2
- ID: 241964
如何引用文章
详细
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.
作者简介
D. Alentiev
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
俄罗斯联邦, 29 Leninsky prosp., Moscow, 119991
S. Korchagina
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 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
俄罗斯联邦, 29 Leninsky prosp., Moscow, 119991
P. Gribanov
A. V. Topchiev Institute of Petrochemical Synthesis of Russian Academy of Science
Email: bmv@ips.ac.ru
俄罗斯联邦, 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
编辑信件的主要联系方式.
Email: bmv@ips.ac.ru
俄罗斯联邦, 29 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047
补充文件
