Well-controlled Organocatalytic Ring-opening Polymerization of Seven-membered Cyclic Carbonates with Cyclohexyl Fusion

被引:1
|
作者
Zhang, Wei [1 ]
Shan, Si-Yi [2 ]
Dai, Jiang [2 ]
Cai, Zhongzheng [2 ]
Zhu, Jian-Bo [2 ]
机构
[1] Tianjin Univ Sci & Technol, Coll Chem Engn & Mat Sci, Tianjin Key Lab Brine Chem Engn & Resource Ecoutil, Tianjin 300457, Peoples R China
[2] Sichuan Univ, Coll Chem, Natl Engn Lab Ecofriendly Polymer Mat Sichuan, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; Organic catalyst; Living ring-opening polymerization; Aliphatic polycarbonate; KINETIC RESOLUTION POLYMERIZATION; RAC-LACTIDE;
D O I
10.1007/s40242-024-4094-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Developing green and well-controlled polymerization methods is of great significance for the preparation of biomedical polymer materials. In this contribution, an efficient organocatalytic ring-opening polymerization (ROP) of a class of seven-membered cyclic carbonates (T6DO, T6HDO, C6DO, C6HDO) containing cis- or trans-cyclohexane structure was established. Organic catalyst 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) promoted living polymerization of these cyclic carbonates to deliver polycarbonate and block copolymer products with predictable molecular weights and narrow dispersity. The robust TBD-mediated ROP at 90 degrees C showcased turnover frequency (TOF) up to 10(3) h(-1). The resulting amorphous polycarbonates displayed good thermal stability.
引用
收藏
页码:856 / 862
页数:7
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