中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Facile Functionalization of Polyethylene via Click Chemistry

文献类型:期刊论文

作者Hong M ; Liu JY ; Li BX ; Li YS
刊名macromolecules
出版日期2011
卷号44期号:14页码:5659-5665
关键词LIVING RADICAL POLYMERIZATION REPEATED 1 PALLADIUM-CATALYZED COPOLYMERIZATION 2-INSERTION TRANSITION-METAL-COMPLEXES REGIOSELECTIVE COPOLYMERIZATION TITANIUM COMPLEXES MATERIALS SCIENCE BLOCK-COPOLYMERS CHELATE LIGANDS POLAR MONOMERS
ISSN号0024-9297
通讯作者li ys
中文摘要a series of well-defined functional polyethylene graft copolymers with high molecular weights have been conveniently synthesized via the combination of ethylene/5-norbornene-2-methyl propargyl ether (nmpe) copolymerization using bis(beta-enaminoketonato)titanium catalysts and following click coupling reaction. bis(beta-enaminoketonato)titanium catalysts have been proved to be the potent catalysts for ethylene/nmpe copolymerization, producing high molecular weight copolymers with unimodal molecular weight distributions. (13)c nmr (dept) and (1)h nmr spectra reveal the copolymerization proceeds in a regioselective way with allcynyl group retained near the main chain. the following click coupling reactions between ethylene/nmpe copolymer and azido-terminated polymer (peo-n(3), ps-n(3)) have been achieved under mild conditions independent of the chemical structure and molecular weight of azido-terminated polymer, providing functional polyethylene with well-defined structure and high molecular weight.
收录类别SCI收录期刊论文
语种英语
WOS记录号WOS:000292850100016
公开日期2012-06-08
源URL[http://ir.ciac.jl.cn/handle/322003/44455]  
专题长春应用化学研究所_长春应用化学研究所知识产出_期刊论文
推荐引用方式
GB/T 7714
Hong M,Liu JY,Li BX,et al. Facile Functionalization of Polyethylene via Click Chemistry[J]. macromolecules,2011,44(14):5659-5665.
APA Hong M,Liu JY,Li BX,&Li YS.(2011).Facile Functionalization of Polyethylene via Click Chemistry.macromolecules,44(14),5659-5665.
MLA Hong M,et al."Facile Functionalization of Polyethylene via Click Chemistry".macromolecules 44.14(2011):5659-5665.

入库方式: OAI收割

来源:长春应用化学研究所

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