Addition polymerization of functionalized norbornenes as a powerful tool for assembling molecular moieties of new polymers with versatile properties

被引:118
作者
Bermeshev, M. V. [1 ]
Chapala, P. P. [1 ]
机构
[1] RAS, AV Topchiev Inst Petrochem Synth, 29 Leninskiy Pr, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
Vinyl/addition polymerization; Functional polymers; Rigid polymers; Post-polymerization modification; Norbornene; Tricyclononene; Substituted norbornenes; Pd Catalysts; Ni Catalysts; Gas permeability; Membranes; Photoresists; Pervaporation; PD(II) COMPLEXES BEARING; GAS-TRANSPORT PROPERTIES; NM RESIST APPLICATIONS; POLYNORBORNENE POLYCATIONIC LATEXES; PD(ACAC)(2)/BF3OET2 CATALYST SYSTEM; VINYL-TYPE POLYNORBORNENES; EMISSIVE LAYER MATERIAL; ALPHA-DIIMINE LIGANDS; PALLADIUM COMPLEXES; CHAIN TRANSFER;
D O I
10.1016/j.progpolymsci.2018.06.003
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
This comprehensive review surveys recent research trends in the addition polymerization of functionalized norbornenes for the macromolecular design of high performance materials in terms of catalyst activity, monomer reactivity, modifications and potential applications of addition polynorbornenes bearing functional groups. The structure of addition polynorbornene backbones is responsible for their high thermal resistance and chemical stability. In order to impart desired properties to the polymers, various functional side groups can be incorporated into the monomer units by the Ti-, Ni-, or Pd-catalyzed polymerization of norbornenes, which are available via cycloaddition reactions or norbornadiene-2,5 modifications. Based on the use of different substituents in the norbornene monomer units and different polymer compositions, the addition polynorbornenes have been successfully developed for the preparation of pervaporation, gas-separation, and proton-conducting membranes, sensors, catalyst supports, and for applications as photoresist, electrooptical, and dielectric materials etc. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 46
页数:46
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