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March 19, 2026Journal of the American Chemical Society4 citations

Perfectly Alternating Copolymerizations of Methacrylates and Coumarin to Robust C–C Main-Chain Polymers with Full Degradability and Depolymerizability

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ZLZicheng LiangYSYangyang SunTRThayalan Rajeshkumar

Key Points

  • The aim is to achieve perfectly alternating copolymerization of methacrylates and coumarin to create robust and degradable polymers.
  • Utilized a novel Al(C6F5)3/PnBu3 Lewis pair cooperative catalyst for copolymerization.
  • Conducted computational studies to assess sequence control mechanisms.
  • Synthesized a range of alternating vinyl copolymers from various monomers and feed ratios.
  • Achieved high molecular weight copolymers up to 330.8 kg/mol.
  • Polymers exhibited high transparency and thermal resistance (Tg: 130-190 °C).
  • Demonstrated complete degradability in strong bases and thermal depolymerizability in specific solvents.

Abstract

This contribution reports the first copolymerization of methacrylates with simple, commercially available, and biorenewable coumarin (CM). The key to this achievement lies in the rational design of a new Al(C6F5)3/PnBu3 Lewis pair cooperative catalyst, which possesses several unique features, including high efficiency, living nature, and, more strikingly, perfectly alternating sequence control. Computational studies elucidate that kinetic control, enabled by different attractive London dispersion interactions between enolaluminate active species and two monomer substrates, is a decisive factor for alternating sequence control. Accordingly, a series of alternating vinyl copolymers with a high molecular weight (Mn) of up to 330.8 kg/mol can be synthesized directly from commercial/general vinyl monomers regardless of monomer structures and feed ratios. These copolymers have been determined to be highly transparent materials with high heat resistance (Tg: 130-190 °C), good thermal stability (Td up to 300 °C), and good durability and are meanwhile fully degradable at room temperature under a strong base and completely thermal depolymerizable in the presence of a strong donating solvent (e.g., DMF), thus affording a new class of robust, durable, yet fully degradable, depolymerizable C-C main-chain polymers, which are generally unachievable due to an inherent performance/degradability (depolymerizability) trade-off.

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Cite This Study

Liang et al. (2026) studied this question.

synapsesocial.com/papers/69bb91c7496e729e6297f322https://doi.org/10.1021/jacs.6c01713
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