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Intramolecular Cyclization Dominating Homopolymerization of Multivinyl Monomers toward Single-Chain Cyclized/Knotted Polymeric Nanoparticles

机译:分子内环化主导多乙烯基单体向单链环化/打结聚合物纳米粒子的均聚。

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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 Cu-0-mediated controlled/living radical polymerization in the presence of additional Cu-II, which enables the efficient promotion of intrarnolecular cydization 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.
机译:多官能单体的聚合可以产生具有不同官能度和新颖的大分子结构的聚合物。但是,控制多乙烯基单体(MVM)均聚的能力一直是一个挑战。在这里,我们证明了基于丙烯酸酯的MVM的均聚可以通过在额外的Cu-II存在下通过Cu-0介导的受控/活性自由基聚合进行动力学控制,从而能够有效地促进核内细胞化和抑制分子间交联。胶凝作用被有效地延迟了大约10分钟。浓缩聚合体系中的单体转化率为40%([M] = 40.9 wt%),远高于Flory-Stockmayer理论的预测。此外,对合成聚合物的仔细检查发现,由于单罐原位分子内反应和正在传播的聚合物链的自环化,形成了单链环化/打结的聚合物纳米粒子(SCKNPs)。这种简便的方法为多种新颖的单链环化/打结聚合物材料的设计和合成开辟了一条新途径。

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