Switchable catalytic processes involving the copolymerization of epoxides and carbon dioxide for the preparation of block polymers

被引:29
|
作者
Darensbourg, Donald J. [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
来源
INORGANIC CHEMISTRY FRONTIERS | 2017年 / 4卷 / 03期
基金
美国国家科学基金会;
关键词
SELECTIVE POLYMERIZATION CATALYSIS; PROPYLENE-OXIDE; CO2/EPOXIDE COPOLYMERIZATION; STEREOCHEMISTRY CONTROL; TRIBLOCK COPOLYMERS; ONE-POT; CO2; COMPLEX; POLYCARBONATES; PORPHYRIN;
D O I
10.1039/c7qi00013h
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
This minireview's primary focus is to review recent studies from my research program on the development of one-pot, two-step processes for the synthesis of di- and tri-block polymers. In all of these prepared polymeric materials at least one component is a polycarbonate derived from the copolymerization of CO2 and epoxides. Synthetic methodology for the preparation of polycarbonate diols of well-defined molecular weights with narrow polydispersities are presented using (salen) CoX/onium salt catalyst systems. These polyols were subsequently utilized in the synthesis of di-and tri- block polylactide/polycarbonate or polyphosphoester/polycarbonate polymers employing organocatalysts. In addition, the introduction of these polyols to a second epoxide/CO2 copolymerization process provided block polycarbonate materials. Of particular interest, the first or second epoxide monomer incorporated into the copolymer can possess vinyl groups for postpolymerization modification by thiol-ene chemistry. These degradable polymeric materials have significant potential for use in biomedical applications.
引用
收藏
页码:412 / 419
页数:8
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