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Synthesis of naturally-derived macromolecules through simplified electrochemically mediated ATRP

机译:通过简化的电化学介导的ATRP合成天然来源的大分子

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摘要

The flavonoid-based macroinitiator was received for the first time by the transesterification reaction of quercetin with 2-bromoisobutyryl bromide. In accordance with the “grafting from” strategy, a naturally-occurring star-like polymer with a polar 3,3',4',5,6-pentahydroxyflavone core and hydrophobic poly(tert-butyl acrylate) (PtBA) side arms was synthesized via a simplified electrochemically mediated ATRP (seATRP), utilizing only 78 ppm by weight (wt) of a catalytic CuII complex. To demonstrate the possibility of temporal control, seATRP was carried out utilizing a multiple-step potential electrolysis. The rate of the polymerizations was well-controlled by applying optimal potential values during preparative electrolysis to prevent the possibility of intermolecular coupling of the growing polymer arms. This appears to be the first report using on-demand seATRP for the synthesis of QC-(PtBA-Br)5 pseudo-star polymers. The naturally-derived macromolecules showed narrow MWDs (Đ = 1.08–1.11). 1H NMR spectral results confirm the formation of quercetin-based polymers. These new flavonoid-based polymer materials may find applications as antifouling coatings and drug delivery systems.
机译:槲皮素与2-溴异丁酰溴的酯交换反应是首次获得基于类黄酮的大分子引发剂。根据“嫁接自”策略,天然存在的星形聚合物具有极性3,3',4',5,6-五羟基黄酮核和疏水性聚丙烯酸叔丁酯(PtBA)侧臂通过简化的电化学介导的ATRP(seATRP)合成,仅使用78 ppm重量(wt)的催化Cu II 配合物。为了证明时间控制的可能性,利用多步电势电解进行了seATRP。通过在制备性电解过程中施加最佳电势值来很好地控制聚合速率,以防止生长中的聚合物臂发生分子间偶联的可能性。这似乎是第一个使用按需seATRP合成QC-(PtBA-Br)5假星型聚合物的报告。天然来源的大分子显示出狭窄的MWD(Đ= 1.08–1.11)。 1 1 H NMR光谱结果证实了槲皮素基聚合物的形成。这些新的基于类黄酮的聚合物材料可能会用作防污涂料和药物输送系统。

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