Specific Discrimination Polymerization for Highly Isotactic Polyesters Synthesis

被引:18
作者
Guo, Xuanhua [1 ,2 ,3 ,4 ]
Xu, Guangqiang [1 ,2 ,3 ,4 ]
Yang, Rulin [1 ,2 ,3 ]
Wang, Qinggang [1 ,2 ,3 ,4 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Key Lab Biobased Mat, Qingdao 266101, Peoples R China
[2] Shandong Energy Inst, Qingdao 266101, Peoples R China
[3] Qingdao New Energy Shandong Lab, Qingdao 266101, Peoples R China
[4] Univ Chinese Acad Sci, Ctr Mat Sci & Optoelect Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
RING-OPENING POLYMERIZATION; KINETIC RESOLUTION; RAC-LACTIDE; CATALYST; EPOXIDES;
D O I
10.1021/jacs.3c14091
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Isotactic polymers have emerged with unique and excellent properties in material sciences. Specific discrimination polymerization provides an ideal pathway to achieve highly isotactic polymers from their racemic monomers, which is of great significance and a challenge in polymeric chemistry. Although an enantioselective catalyst-mediated asymmetric kinetic resolution polymerization (AKRP) process makes it possible, a general and well-defined strategy for catalyst design is still rarely reported. Here, based on a novel dual-ligand strategy, a new type of chiral (BisSalen)Al complex with high enantioselectivity has been described, in which perfect AKRP of racemic phenethylglycolide (Pegl) is achieved for the first time. The more confined asymmetric microenvironment formed by a dual ligand is the key to improve the enantioselectivity of the original catalyst. To illustrate the generality of this strategy, a series of (BisSalen)Al complexes with homo- or heterodual ligands were designed for the AKRP of Pegl.
引用
收藏
页码:9084 / 9095
页数:12
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