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submitted on 27.02.2020 and posted on 28.02.2020by wei xiong, Wenying Chang, Dong Shi, Lijiang Yang, Ziyou Tian, Hao Wang, Zhengchu Zhang, Xuhao Zhou, Erqiang Chen, HUA LU
To access infinitely
recyclable plastics, one key is to design thermodynamically neutral systems
based on dynamic bonds for easy manipulation of the polymerization and the
reverse depolymerization under low energy cost. Here, we present the controlled
ring-opening polymerization of various penicillamine-derived β-thiolactones and
the highly specific depolymerization of the resultant polythioesters (PNR-PenTE)
for complete monomer recycling. The gem-dimethyl
group confers better ROP control by reducing the activity of the chain-end
thiolate groups and stabilizing the thioester linkages in the polymer backbone.
High molar mass and narrow dispersity PNR-PenTE are conveniently
accessible at room temperature bearing well-defined end groups and tunable side
chains. PNR-PenTE can be tailored with water solubility, and/or be
easily fabricated into persistent films or fibers with interesting thermal and
mechanical properties. Most importantly, PNR-PenTE can be recycled
to pristine enantiopure β-thiolactones at >95% conversion in a
well-controlled unzipping fashion within min to hours at room temperature.
Overall, this work may streamline the rapid development of a wide range of polythioesters
with immense application potential as self-immolative building blocks, high
value biomaterials, and sacrificial domain for nanolithography.
This work is supported by the National Natural Science Foundation of China (21722401 for H.L. and 21634001 for E.Q.C.). The computation was supported by High-performance Computing Platform of Peking University. We thank Prof. Suwei Dong and Prof. Zichen Li for inspiring discussions.