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Utilizing Self-Immolative ATRP Initiators To Prepare Stimuli-Responsive Polymeric Films from Nonresponsive Polymers

机译:利用自我灭活的ATRP引发剂从非反应聚合物制备刺激响应性聚合物膜

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摘要

Stimuli-responsive polymers were synthesized by atom transfer radical polymerization (ATRP) using a photoresponsive self-immolative bifunctional initiator. The photoactivated self-immolative junctions allow transforming nonresponsive polymers into photocleavable polymers that can be split into two equally sized fragments when exposed to the stimulation. We demonstrate this modular approach by preparing a series of photoresponsive poly(benzyl methacrylate) and polystyrene polymers of various molecular weights. Taking advantage of the well-defined architecture of the polymers, we studied their photoresponse as thin films and examined the effect of irradiation time and solvent addition on the degree of response and splitting. The results show that the polymers can be split in the solid phase, confirming that the self-immolative quinone methide elimination can occur in solid phase. Importantly, we could also obtain insights into the role of the mobility of the polymer chains in the solid phase and in the presence of solvent molecules on the responsiveness of the films and degree of splitting. The potential to introduce such modular self-immolative units into different types of widely used of polymers will allow the utilization of this approach to create wide range of responsive materials that can undergo vast structural changes by relatively minor synthetic modifications.
机译:通过使用光反应自我牺牲的双官能引发剂通过原子传递自由基聚合(ATRP)合成刺激性聚合物。光活化的自侵略性结允许将非响应聚合物转化为光可释放的聚合物,当暴露于刺激时可以将其分成两个等大小的片段。我们通过制备一系列光反应聚(甲基丙烯酸苄酸酯)和各种分子量的聚苯乙烯聚合物来证明这种模块化方法。利用聚合物的明确定义架构,我们将光响应视为薄膜,并检查了照射时间和溶剂添加对响应程度和分裂的影响。结果表明,聚合物可以在固相中分开,证实自我侵略性的醌甲基除去可在固相中发生。重要的是,我们还可以获得对固相中聚合物链的迁移率和溶剂分子在薄膜的反应性上的作用中的见解以及分裂程度的溶剂分子。将这种模块化自我牺牲单位引入不同类型的聚合物的可能性将允许利用这种方法来创造各种响应材料,可以通过相对较小的合成修饰进行巨大的结构性变化。

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