Controlled polymerization of levoglucosenone-derived enynes to give bio-based polymers with tunable degradation rates and high glass transition temperatures

通过控制左旋葡糖酮衍生的烯炔的聚合反应,制备出具有可调降解速率和高玻璃化转变温度的生物基聚合物。

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Abstract

In recent years, pollution from plastic waste has intensified the demand for sustainable polymers. Hence, biomass-derived degradable polymers offer a promising solution. For example, levoglucosenone, a readily available biomass product from cellulose pyrolysis, is an attractive building block for polymer synthesis. However, the metathesis polymerization of levoglucosenone-derived monomers has been difficult to control due to poor monomer reactivity, requiring an unstable but reactive ruthenium catalyst (C793). To facilitate the polymerization, we introduced a cascade motif to successfully demonstrate controlled polymerization of levoglucosenone-derived enynes using a commercially available 3rd-generation Grubbs catalyst. This living polymerization also enabled block copolymer synthesis. Furthermore, the degradation rates of these polymers can be adjusted over 2 orders of magnitude through monomer structural modifications. Notably, we observed higher glass transition temperatures of 152-198 °C by varying structural parameters.

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