Chemically Recyclable, Hydroxycinnamic Acid‐Derived Semi‐Aromatic Polycarbonates

ABSTRACT Polycarbonate polymers find widespread use for a variety of applications. Driven by the need to transition away from fossil‐based resources, there is increasing interest in exploring bio‐based monomers for the synthesis of polycarbonates. One interesting class of molecules that can be isolated from a variety of biological resources, including lignin, are hydroxycinnamic acids. This paper reports the synthesis of a library of aromatic diols using p ‐coumaric acid, ferulic acid, and sinapic acid as starting materials. Using dimethyl carbonate, these diols can be polymerized to generate a variety of semi‐aromatic polycarbonate homo‐ and copolymers. These polycarbonates can be depolymerized via an organocatalyzed process to afford the starting diols in essentially quantitative yield. The monomers obtained from this depolymerization process could subsequently be repolymerized, with no purification needed, to regenerate the original polymer with essentially identical molecular weight, providing a pathway to the chemical recycling of these materials.

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Publication Details

Journal
Journal of Polymer Science
Published
2025-04-09
DOI
https://doi.org/10.1002/pol.20250028
Primary Topic
Lignin and Wood Chemistry
Type
article
Field-Weighted Citation Impact
0.00

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article

Chemically Recyclable, Hydroxycinnamic Acid‐Derived Semi‐Aromatic Polycarbonates

Pascal Schouwink, Harm‐Anton Klok, Ghezae Tekleab
Journal of Polymer Science
Lignin and Wood Chemistry
article

Chemically Recyclable, Hydroxycinnamic Acid‐Derived Semi‐Aromatic Polycarbonates

Pascal Schouwink, Harm‐Anton Klok, Ghezae Tekleab
article en

Abstract

ABSTRACT Polycarbonate polymers find widespread use for a variety of applications. Driven by the need to transition away from fossil‐based resources, there is increasing interest in exploring bio‐based monomers for the synthesis of polycarbonates. One interesting class of molecules that can be isolated from a variety of biological resources, including lignin, are hydroxycinnamic acids. This paper reports the synthesis of a library of aromatic diols using p ‐coumaric acid, ferulic acid, and sinapic acid as starting materials. Using dimethyl carbonate, these diols can be polymerized to generate a variety of semi‐aromatic polycarbonate homo‐ and copolymers. These polycarbonates can be depolymerized via an organocatalyzed process to afford the starting diols in essentially quantitative yield. The monomers obtained from this depolymerization process could subsequently be repolymerized, with no purification needed, to regenerate the original polymer with essentially identical molecular weight, providing a pathway to the chemical recycling of these materials.

Journal of Polymer ScienceVol. 63(10)
École Polytechnique Fédérale de Lausanne (CH)
Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung
Openalex Percentile: Top 93%
Lignin and Wood Chemistry
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