聚合
单体
离子强度
聚合物
高分子化学
材料科学
化学工程
树枝状大分子
离子聚合
磺酸盐
苯乙烯
自由基聚合
化学
钠
共聚物
有机化学
复合材料
水溶液
工程类
作者
Chendan Li,José Rodrigo Magana,Fabian H. Sobotta,Junyou Wang,Martien A. Cohen Stuart,Bas G. P. van Ravensteijn,Ilja K. Voets
标识
DOI:10.1002/anie.202206780
摘要
Abstract We report a switchable, templated polymerization system where the strength of the templating effect can be modulated by solution pH and/or ionic strength. The responsiveness to these cues is incorporated through a dendritic polyamidoamine‐based template of which the charge density depends on pH. The dendrimers act as a template for the polymerization of an oppositely charged monomer, namely sodium styrene sulfonate. We show that the rate of polymerization and maximum achievable monomer conversion are directly related to the charge density of the template, and hence the environmental pH. The polymerization could effectively be switched “ON” and “OFF” on demand, by cycling between acidic and alkaline reaction environments. These findings break ground for a novel concept, namely harnessing co‐assembly of a template and growing polymer chains with tunable association strength to create and control coupled polymerization and self‐assembly pathways of (charged) macromolecular building blocks.
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