单体
丙烯酸酯
分子内力
聚合
高分子化学
聚合物
分子间力
自由基聚合
化学
丙烯酸酯聚合物
材料科学
分子
有机化学
作者
Yongsheng Gao,Dezhong Zhou,Tianyu Zhao,Xuan Wei,Seán McMahon,Jonathan O’Keeffe Ahern,Wei Wang,Udo Greiser,Brian J. Rodriguez,Wenxin Wang
出处
期刊:Macromolecules
[American Chemical Society]
日期:2015-09-23
卷期号:48 (19): 6882-6889
被引量:42
标识
DOI:10.1021/acs.macromol.5b01549
摘要
Polymerization of multifunctional monomers could produce polymers with different functionalities and novel macromolecular architectures. However, the ability to control the homopolymerization of multivinyl monomers (MVMs) has always been a challenge. Here we demonstrate that the homopolymerization of acrylate based MVMs can be kinetically controlled via Cu0-mediated controlled/living radical polymerization in the presence of additional CuII, which enables the efficient promotion of intramolecular cyclization and suppression of intermolecular cross-linking. The gelation is effectively delayed over ca. 40% monomer conversion in the concentrated polymerization system ([M] = 40.9 wt %), which is far higher than the Flory–Stockmayer theory predicts. Moreover, closer inspection of the synthesized polymers reveals that single-chain cyclized/knotted polymeric nanoparticles (SCKNPs) are formed due to the nature of one-pot in situ intramolecular reaction and self-cyclization of the propagating polymer chains. This facile method opens a new avenue to the design and synthesis of a broad range of novel single-chain cyclized/knotted polymeric materials.
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