4.7 Article

Efficient Synthesis of Itaconate Polyesters with Amine-Triggered Rapid Degradation and Outstanding Mechanical Properties: An Experimental and Theoretical Study on Degradation Mechanisms

Journal

MACROMOLECULES
Volume -, Issue -, Pages -

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.macromol.2c00971

Keywords

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Funding

  1. National Key Research and Development Program of China [2021YFB3700300, 2018FYA0901200]
  2. National Natural Science Foundation of China [U21B2093, 52103015, 51773218, 31970041]
  3. China Postdoctoral Science Foundation [2020M681963]
  4. Ningbo Natural Science Foundation [2021J207]
  5. Public Welfare Science and Technology Projects of Ningbo [2021S071]

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A series of PBXI copolyesters with outstanding mechanical properties were successfully synthesized, showing good degradation performance in experiments,providing a new strategy for the synthesis of potentially biodegradable copolymers.
A range of degradable polyesters have been developed as sustainable alternatives for commercial plastics; however, limitations of composting facilities and uncontrolled degradation in the environment hindered their viability. In this study, biobased itaconic acid was selected as an active site to control the degradation of polyesters. A series of PBXI copolyesters with Mw's ranging from 4.86 to 8.31 x 10(4) g/mol and high intrinsic viscosities of more than 1.15 dL/g were successfully synthesized without any cross linking by selecting appropriate reaction conditions, including condensation temperature and vacuum, effective inhibitor, and catalyst. The obtained copolyesters were semicrystalline, and their T-m's could be regulated from 42.5 to 179.5 degrees C. They exhibited outstanding elastic modulus (120-598 MPa) and tensile strength (17.9-51.4 MPa) among degradable polymers. Degradation experiments demonstrated that the incorporation of itaconate segments could facilitate both the hydrolysis and enzymatic degradation of polyesters. The state-of-the-art computation and analysis via molecular dynamics (MD) simulations of PBXI-CALB complexes elucidated the enzymatic degradation mechanism. Experimental results proved that, at room temperature, the degradation could be stimulated and regulated by amines without a catalyst and the Mn's of lactamization products rapidly decreased to less than 5000 g/mol within 24 h. Moreover, the copolymerized structure of copolyesters and solvent factors could influence the aza-Michael addition between amines and itaconate units. This work provides a strategy to synthesize biodegradable copolymers with the potential to undergo controlled and rapid in vivo degradation with outstanding mechanical properties.

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