原子转移自由基聚合
化学
单体
动力学
聚合
动链长度
光化学
自由基聚合
催化作用
高分子化学
聚合物
有机化学
物理
量子力学
作者
Andrew J. D. Magenau,Nicholas C. Strandwitz,Armando Gennaro,Krzysztof Aleksander Matyjaszewski
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2011-03-31
卷期号:332 (6025): 81-84
被引量:814
标识
DOI:10.1126/science.1202357
摘要
Atom transfer radical polymerization is a versatile technique for exerting precise control over polymer molecular weights, molecular weight distributions, and complex architectures. Here, we show that an externally applied electrochemical potential can reversibly activate the copper catalyst for this process by a one-electron reduction of an initially added air-stable cupric species (Cu(II)/Ligand). Modulation of polymerization kinetics is thereby tunable in real time by varying the magnitude of applied potential. Application of multistep intermittent potentials successfully triggers initiation of polymerization and subsequently toggles the polymerization between dormant and active states in a living manner. Catalyst concentrations down to 50 parts per million are demonstrated to maintain polymerization control manifested in linear first-order kinetics, a linear increase in polymer molecular weight with monomer conversion, and narrow polymer molecular weight distributions over a range of applied potentials.
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