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Synergy of Macrocycles and Macromolecular Topologies: An Efficient [3(4)]Triazolophane-Based Synthesis of Cage-Shaped Polymers

机译:宏细胞和大分子拓扑的协同作用:高效[3(4)]基于笼形聚合物的三唑烷基合成

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摘要

The development of complex topologies such as macromolecular cages constitutes a fascinating aspect of polymer chemistry. In the present work, a novel strategy involving self-closing bifunctional end-groups, which under specific conditions, are allowed to assemble themselves into a predefined thermodynamically favored macrostructure, was designed to fulfill the x degrees c topological conversion of star-shaped polymers to their respective cage-shaped polymers. A series of four different well-defined four-arm star-shaped poly(epsilon-caprolactone) polymers varying in molar masses were successfully synthesized, end-functionalized, and closed into cage-shaped polymers by formation of [3(4)]-triazolophane macrocycle units. The obtained cage-shaped polymers feature interesting properties that depend drastically on the chain length of the arms and seem to differ from previous reported polymer cages.
机译:诸如大分子笼等复杂拓扑的发展构成了聚合物化学的迷人方面。 在本作本作中,允许在特定条件下的自闭交双官能端组的新型策略被允许自己将自己组装成预定义的热力学上有利的宏观结构,以满足星形聚合物的X型C拓扑转化 它们各自的笼形聚合物。 一系列四种不同明确的四臂星形聚(ε-己内酯)聚合物在摩尔质量中改变,结束官能化,并通过形成[3(4)] - 三唑烷烷杏子单位。 所获得的笼形聚合物具有有趣的性质,这些特性依赖于臂的链长而差异,似乎与先前报道的聚合物笼不同。

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    《ACS Macro Letters》 |2020年第5期|共6页
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  • 正文语种 eng
  • 中图分类 有机化学;
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