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Polysiloxane/Polystyrene Thermo-Responsive and Self-Healing Polymer Network via Lewis Acid-Lewis Base Pair Formation

机译:通过路易斯酸-路易斯碱对形成的聚硅氧烷/聚苯乙烯热响应和自愈聚合物网络

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摘要

The use of thermo-reversible Lewis Pair (LP) interactions in the formation of transient polymer networks is still greatly underexplored. In this work, we describe the synthesis and characterization of polydimethylsiloxane/polystyrene (PDMS/PS) blends that form dynamic Lewis acid-Lewis base adducts resulting in reversible crosslinks. Linear PS containing 10 mol % of di-2-thienylboryl pendant groups randomly distributed was obtained in a two-step one-pot functionalization reaction from silyl-functionalized PS, while ditelechelic PDMS with pyridyl groups at the chain-termini was directly obtained via thiol-ene “click” chemistry from commercially available vinyl-terminated PDMS. The resulting soft gels, formed after mixing solutions containing the PDMS and PS polymers, behave at room temperature as elastomeric solid-like materials with very high viscosity (47,300 Pa·s). We applied rheological measurements to study the thermal and time dependence of the viscoelastic moduli, and also assessed the reprocessability and self-healing behavior of the dry gel.
机译:在瞬态聚合物网络的形成中使用热可逆路易斯对(LP)相互作用的研究仍大大不足。在这项工作中,我们描述了聚二甲基硅氧烷/聚苯乙烯(PDMS / PS)共混物的合成和表征,这些共混物形成了动态的路易斯酸-路易斯碱加合物,导致可逆交联。从甲硅烷基官能化的PS通过两步一锅功能化反应获得线性分布的PS,该线性PS包含10 mol%的二-2-噻吩基硼烷基侧基,而通过硫醇直接获得在末端带有吡啶基的二telechelic PDMS商购可得的乙烯基封端的PDMS中的“烯”“点击”化学物质。在混合包含PDMS和PS聚合物的溶液后形成的软凝胶,在室温下表现为具有很高粘度(47,300 Pa·s)的弹性固体状材料。我们应用流变学方法研究了粘弹性模量的热和时间依赖性,并评估了干凝胶的可再加工性和自愈性能。

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