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Updated: Jan 12, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Cationic-Catalyst Strategy Enabling Ultrafast and Controlled Polymerization and Efficient Depolymerization Toward a
Kang Chen1,2,3, Yueming Wu1,2,4, Minzhang Chen2,4
1State Key Laboratory of Bioreactor Engineering, East China University of Science and Technology, Shanghai, 200237, P.R. China.
Abstract:
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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