中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
RAFT polymerization of a novel allene-derived asymmetrical divinyl monomer: A facile strategy to alkene-functionalized hyperbranched vinyl polymers with high degrees of branching

文献类型:期刊论文

作者Bao YM ; Shen GR ; Liu XH ; Li YS
刊名journal of polymer science part a-polymer chemistry
出版日期2013
卷号51期号:13页码:2959-2969
关键词LIVING COORDINATION POLYMERIZATION PI-ALLYLNICKEL CATALYST TRANSFER RADICAL POLYMERIZATION ALLYL METHACRYLATE BLOCK-COPOLYMERS DENDRITIC MACROMOLECULES MOLECULAR-PARAMETERS METHYL-METHACRYLATE DERIVATIVES DENDRIMERS
ISSN号0887-624x
通讯作者li ys
中文摘要hyperbranched vinyl polymers with high degrees of branching (dbs) up to 0.43 functionalized with numerous pendent allene groups have been successfully prepared via reversible addition fragmentation chain transfer polymerization of a state-of-art allene-derived asymmetrical divinyl monomer, allenemethyl methacrylate (amma). the gelation did not occur until high monomer conversions (above 90%), as a result of the optimized reactivity difference between the two vinyl groups in amma. the branched structure was confirmed by a combination of a triple-detection size exclusion chromatography (light scattering, refractive index, and viscosity detectors) and detailed 1h nmr analyses. a two-step mechanism is proposed for the evolution of branching according to the dependence of molecular weight and db on monomer conversion. controlled radical polymerization proceeds until moderate conversions, mainly producing linear polymers. subsequent initiation and propagation on the polymerizable allene side chains as well as the coupling of macromolecular chains generate numerous branches at moderate-to-high monomer conversions, dramatically increasing the molecular weight of the polymer. amma was also explored as a new branching agent to construct poly(methyl methacrylate)-type hyperbranched polymers by its copolymerization with methyl methacrylate. the db can be effectively tuned by the amount of amma, showing a linear increase trend. the pendent allene groups in the side chains of the copolymers were further functionalized by epoxidation and thiol-ene chemistry in satisfactory yields. (c) 2013 wiley periodicals, inc. j. polym. sci., part a: polym. chem. 2013, 51, 2959-2969
收录类别SCI收录期刊论文
语种英语
WOS记录号WOS:000319681900023
公开日期2014-04-15
源URL[http://ir.ciac.jl.cn/handle/322003/49768]  
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
Bao YM,Shen GR,Liu XH,et al. RAFT polymerization of a novel allene-derived asymmetrical divinyl monomer: A facile strategy to alkene-functionalized hyperbranched vinyl polymers with high degrees of branching[J]. journal of polymer science part a-polymer chemistry,2013,51(13):2959-2969.
APA Bao YM,Shen GR,Liu XH,&Li YS.(2013).RAFT polymerization of a novel allene-derived asymmetrical divinyl monomer: A facile strategy to alkene-functionalized hyperbranched vinyl polymers with high degrees of branching.journal of polymer science part a-polymer chemistry,51(13),2959-2969.
MLA Bao YM,et al."RAFT polymerization of a novel allene-derived asymmetrical divinyl monomer: A facile strategy to alkene-functionalized hyperbranched vinyl polymers with high degrees of branching".journal of polymer science part a-polymer chemistry 51.13(2013):2959-2969.

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来源:长春应用化学研究所

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