作者：Yuanyuan Qu, Junyuan Hu, Fengzhen Guo, Dong Ji, Yuguang Li, Zhenjiang Li, Yunsheng Xu, Jin Huang, Li
关键字：开环聚合，协同催化，聚碳酸酯，理论计算
论文来源：期刊
具体来源：Macromolecules
发表时间：2023年
Control over polymerization thermodynamics and kinetics enables the generation of polymers with on-demand properties. This is exemplified by the ring-opening polymerization of tetraethylene glycol carbonate (4EGMC) using an alkali cation (M+)-based binary catalytic system at ambient temperature. By introducing a guanidine catalyst [(1,5,7-triazabicyclo[4.4.0]dec-5-ene), TBD], the alkali cation-assisted ring-opening polymerization of macrocyclic carbonate was ca. 120–270 times faster than the reaction without an alkali cation, M+ (0.16–0.36 min–1 with M+ vs 0.001 min–1 without M+). Moreover, the interaction between 4EGMC and M+ led to an increase in the ring strain, supported by both bench experiments and computational simulations. This interaction altered the driving force of polymerization from the change of entropy to enthalpy, which revealed the pivotal role of alkali cations in regulating the ring-opening polymerization of macrocyclic carbonate.