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Counting loops in sidechain-crosslinked polymers from elastic solids to single-chain nanoparticles

机译:计算从弹性固体到单链纳米粒子的侧链交联聚合物中的环

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摘要

The vast differences in material properties accessible via crosslinking of sidechain-functionalized polymers are driven by topology. For example, vulcanized rubbery networks feature intermolecular connections and loop topologies of various orders while single-chain nanoparticles (SCNPs) are comprised, in principle, entirely of primary loops. Despite this fact, precise quantification of loops in sidechain crosslinked polymers has not been accomplished. Here, it is demonstrated that by introducing cleavable linkers and mass labels onto the pendant functional groups of reactive polymers, the number of primary loops in sidechain crosslinked materials ranging from rubbery networks (gels) to soluble SCNPs can be precisely quantified. This study sheds new light on the topology of sidechain-crosslinked networks, providing design principles for augmenting the properties of this industrially and academically important class of materials through topological control.
机译:通过侧链官能化的聚合物的交联可达到的材料性能的巨大差异是由拓扑结构驱动的。例如,硫化橡胶网络具有分子间连接和各种顺序的环拓扑结构,而单链纳米颗粒(SCNP)原则上完全由初级环组成。尽管有这个事实,但尚未完成对侧链交联聚合物中环的精确定量。在此证明,通过将可裂解的接头和质量标记引入反应性聚合物的侧基官能团上,可以精确定量侧链交联材料中主要环的数量,从橡胶状网络(凝胶)到可溶性SCNP,不等。这项研究为侧链交联网络的拓扑结构提供了新的思路,提供了通过拓扑控制来增强这种在工业和学术上重要的材料类别的性能的设计原理。

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