解聚
聚合物
聚合
阳离子聚合
材料科学
催化作用
化学工程
高分子化学
纳米技术
原子经济
缩聚物
有机化学
化学
配位聚合
聚合物结构
作者
Kang Chen,Yueming Wu,Minzhang Chen,Xinqi Huang,Jingcheng Zou,Xin Chen,Runhui Liu
标识
DOI:10.1002/anie.202520392
摘要
The development of chemically recyclable polymers is considered one of the ideal solutions to alleviate the growing polymer waste. Fast, controlled synthesis and closed-loop recycling of amino acid (AA) polymers, as an important class of polyamides, are highly important for applications and circular polymer economy. Strong base-initiated N-carboxyanhydrides (NCAs) polymerization can prepare AA polymers very quickly, however, has the long-standing challenge of poor molecular weight controllability and numerous side reactions. Herein, we develop a highly efficient cationic-catalyst strategy that enables both "ultrafast, controlled AA polymer synthesis" and "closed-loop AA polymer recycling". This robust and easily scalable cationic-catalyst strategy is compatible with various organic strong bases as initiators, and enables the synthesis of molecular weight well-controlled AA polymers on a hectogram scale (∼120 g) within minutes. Moreover, the cationic catalyst facilitates the efficient depolymerization of AA polymers into environmentally friendly amino acids, with a recovery rate of 85.9%. In addition, the catalyst itself can be recycled quantitatively. In short, the highly efficient cationic-catalyst strategy implies practical and promising applications in polymerization and depolymerization chemistry, demonstrating great potential for the circular polymer economy and sustainable management of polymer waste.
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