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Synthesis of novel star polymers with vinyl-functionalized hyperbranched core via 'arm-first' strategy

机译:通过“臂先”策略合成具有乙烯基官能化超支化核的新型星形聚合物

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Star polymers bearing vinyl-functionalized hyperbranched cores were successfully prepared at moderate-to-high monomer conversions (ca. 80%) via a modified "arm-first" strategy. This was achieved by reversible addition-fragmentation chain transfer polymerization of a methacrylate type asymmetrical divinyl monomer with thiobenzoate-capped polystyrenes as macro-chain-transfer agents (Macro-CTAs). Neither intermolecular nor intramolecular cross-linking occurred up to high levels of monomer conversion. The molecular weights (MWs) of Macro-CTAs significantly influence the structures of the resultant star polymers. A lower-MW Macro-CTA favors the formation of a star copolymer bearing big core and multiple short arms, whereas a higher-MW one is confined to the architecture bearing small core with only a few long arms. Moreover, the ca. 70% pendant vinyl groups remained in the hyperbranched core can be directly modified using reactions such as epoxidation and UV initiated thiol-ene addition reactions, resulting in star polymers with various functional groups in the core.
机译:通过改良的“臂先”策略,成功以中等到高的单体转化率(约80%)成功制备了带有乙烯基官能化超支化核的星形聚合物。这是通过甲基丙烯酸酯型不对称二乙烯基单体与硫代苯甲酸酯封端的聚苯乙烯作为大链转移剂(Macro-CTA)的可逆加成-断裂链转移聚合来实现的。在高水平的单体转化率下,分子间和分子内交联都没有发生。 Macro-CTA的分子量(MWs)显着影响所得星形聚合物的结构。较低分子量的Macro-CTA有利于形成带有大核和多个短臂的星形共聚物,而具有较高分子量的Macro-CTA则局限于带有小核且只有几个长臂的结构。此外,ca。残留在超支化核中的70%侧基乙烯基可以使用环氧化和UV引发的硫醇-烯加成反应等反应直接改性,从而在核中形成具有各种官能团的星形聚合物。

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