聚合
差向异构体
单体
催化作用
立体选择性
化学
过程(计算)
材料科学
纳米技术
化学工程
组合化学
高分子科学
化学过程
可持续生产
化工产品
化学合成
化学工业
块(置换群论)
反应条件
化学改性
化学反应
精细化工
有机化学
作者
Yuting Huang,Hao‐Yi Huang,Min Xie,Jiuwei Cui,Zhijie Wu,Da‐Gang Yu,Haifeng Xiang,Zhongzheng Cai,Jian‐Bo Zhu
摘要
Although poly(l-lactic acid) (PLLA) has attracted broad interest as a sustainable plastic, its chemical recycling to a monomer has been an elusive endeavour. A major obstacle for this process is that the epimerization of l-lactide (l-LA) to meso-LA has led to a loss of the original material performance of PLLA. Our robust spirosalen-scandium complexes (Sc) showcased outstanding heteroselectivity towards ring-opening polymerization of rac-LA and syndioselectivity for the polymerization of meso-LA. Herein we report a strategy to circumvent the inevitable epimerization by exploiting an Sc catalytic system, which promoted stereoselective and sequence-controlled polymerization of l-LA in the presence of meso-LA and gave rise to the stereogradient block PLA P(meso-LA-grad-LLA) without compromising the material properties of the original PLLA. This epimerization-tolerant strategy for chemical recycling of PLLA provides an innovative pathway for the next generation of chemical recyclable polymers.
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