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March 21, 2026Journal of the American Chemical Society5 citations

Isoselective Ring-Opening Polymerization to Access High-Performance Poly(α-Substituted-β-Propiolactone)s

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JLJun-Ming LiuQCQing CaoQFQianrong Fang

Key Points

  • This research aims to synthesize isotactic poly(α-substituted-β-propiolactone) using ring-opening polymerization to explore its properties.
  • Utilized a salalen yttrium complex catalyst for polymerization.
  • Focused on preparing isotactic forms of poly(α-substituted-β-propiolactone).
  • Analyzed the thermal and mechanical properties of the resulting products.
  • Achieved highly isotactic P(αRPL) with a melting temperature of 165 °C.
  • Demonstrated that the isotactic P(n-BuPL) is strong and ductile, comparable to high-density polyolefins.
  • Confirmed that the synthesized products can undergo clean depolymerization into recyclable materials.

Abstract

Poly(α-substituted-β-propiolactone), P(αRPL), is attractive since it is closely related in structure to the biodegradable natural polyhydroxyalkanoates (PHAs). However, the chemical synthesis of isotactic P(αRPL) via ring-opening polymerization has yet to be explored. Herein, we exploited a robust salalen yttrium complex (Y2) as the catalyst to successfully prepare highly isotactic P(αRPL) with Pm > 0.95. These P(αRPL) products exhibited tacticity-dependent thermal and mechanical properties. Remarkably, the highly isotactic P(BPL) containing a benzyl side chain showcased a high melting transition temperature (Tm) of 165 °C. The highly isotactic P(n-BuPL) containing alkyl side chain served as a strong and ductile material comparable to the commercial high-density polyolefins. More importantly, these P(αRPL) products could undergo clean depolymerization to their starting material, α-substituted acrylic acids, offering a closed-loop recycling pathway. This synthetic system allowed access to isotactic P(αRPL), establishing a powerful platform for the discovery of sustainable plastics.

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Cite This Study

Liu et al. (2026) studied this question.

synapsesocial.com/papers/69be386a6e48c4981c678d3chttps://doi.org/10.1021/jacs.6c01637
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