Ring-Opening Metathesis Polymerization of Nitrile Substituted cis-Cyclooctenes

被引:11
|
作者
Schneider, Martin F. [1 ]
Gantner, Carola [1 ]
Obrecht, Werner [2 ]
Nuyken, Oskar [1 ]
机构
[1] Tech Univ Munich, Wacker Lehrstuhl Makromol Chem, D-85748 Garching, Germany
[2] LANXESS Deutschland GmbH, Business Unit TRP, Intellectual Property Strategy, D-51369 Leverkusen, Germany
关键词
cyclooctene; cyclopolymerization; nitrile; ring-opening; metathesis polymerization (ROMP); ruthenium catalyst; CROSS-METATHESIS; CATALYSTS; ROMP;
D O I
10.1002/marc.201000301
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
New nitrile-containing polymers have been synthesized by ring-opening metathesis polymerization of cis-cyanocyclooct-4-ene and cis-1,2- dicyanocyclooct-5-ene with a 2nd generation Grubbs catalyst [(H 2IMes)(PCy3)Cl2Ru=CHPh] (H2IMes=N,N0- bis(mesityl)-4,5-dihydroimidazol-2-ylidene). With increasing content of nitrile moieties on the cyclooctene ring the reaction rates decrease from cis-cyclooctene to cis-cyanocyclooct-4-ene and cis-1,2-dicyanocyclooct-5-ene. Contrary to commercially available nitrile rubbers (unhydrogenated and hydrogenated butadiene/acrylonitrile copolymers) in which double bonds, nitrile moieties, and methylene bridges are randomly distributed along the main chain, the new polymers show a regular distribution of structural entities. © 2010 WILEY-VCH Verlag GmbH & Co. KGa.
引用
收藏
页码:1731 / 1735
页数:5
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