原子转移自由基聚合
接触带电
分散性
聚合
材料科学
自由基聚合
光化学
激进的
化学工程
化学
聚合物
高分子化学
物理化学
有机化学
摩擦电效应
工程类
作者
Chen Wang,Ruoqing Zhao,Wenru Fan,Lei Li,Haoyang Feng,Zexuan Li,Ci Yan,Xiaoyang Shao,Krzysztof Matyjaszewski,Zhenhua Wang
标识
DOI:10.1002/anie.202309440
摘要
Traditional mechanochemically controlled reversible-deactivation radical polymerization (RDRP) utilizes ultrasound or ball milling to regenerate activators, which induce side reactions because of the high-energy and high-frequency stimuli. Here, we propose a facile approach for tribochemically controlled atom transfer radical polymerization (tribo-ATRP) that relies on contact-electro-catalysis (CEC) between titanium oxide (TiO2 ) particles and CuBr2 /tris(2-pyridylmethylamine (TPMA), without any high-energy input. Under the friction induced by stirring, the TiO2 particles are electrified, continuously reducing CuBr2 /TPMA into CuBr/TPMA, thereby conversing alkyl halides into active radicals to start ATRP. In addition, the effect of friction on the reaction was elucidated by theoretical simulation. The results indicated that increasing the frequency could reduce the energy barrier for the electron transfer from TiO2 particles to CuBr2 /TPMA. In this study, the design of tribo-ATRP was successfully achieved, enabling CEC (ca. 10 Hz) access to a variety of polymers with predetermined molecular weights, low dispersity, and high chain-end fidelity.
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