A concise review of computational studies of the carbon dioxide-epoxide copolymerization reactions

被引:113
作者
Darensbourg, Donald J. [1 ]
Yeung, Andrew D. [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77843 USA
基金
美国国家科学基金会;
关键词
RING-OPENING POLYMERIZATION; COMPLEX-MEDIATED FORMATION; PROPYLENE-OXIDE; ALTERNATING COPOLYMERIZATION; CYCLIC CARBONATES; FUNCTIONAL POLYCARBONATES; TIN(II) INITIATORS; GLYCEROL CARBONATE; CHEMISTRY RELEVANT; CATALYTIC-ACTIVITY;
D O I
10.1039/c4py00299g
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The production of polycarbonates from carbon dioxide and epoxides is an important route by which CO2, a waste product with harmful environmental effects, is converted into useful products. Some of these polymers have been commercialized as binders, adhesives, and coatings; low molecular weight polycarbonate polyols are used to prepare polyurethanes and ABA triblock polymers. Of current interest is poly(glycerol carbonate) that may consume excess glycerol that is generated from biodiesel production. This review surveys the use of computational chemistry toward answering questions pertaining to the CO2-epoxide copolymerization. Emphasis is placed on the thermodynamics of polymer formation, and the kinetics of polymer growth and degradation.
引用
收藏
页码:3949 / 3962
页数:14
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