Copolymerization of CO2 and meso epoxides using enantioselective β-diiminate catalysts: a route to highly isotactic polycarbonates

被引:115
|
作者
Ellis, W. Chadwick [1 ]
Jung, Yukyung [1 ]
Mulzer, Michael [1 ]
Di Girolamo, Rocco [1 ]
Lobkovsky, Emil B. [1 ]
Coates, Geoffrey W. [1 ]
机构
[1] Cornell Univ, Baker Lab, Dept Chem & Chem Biol, Ithaca, NY 14853 USA
基金
美国国家科学基金会;
关键词
ASYMMETRIC ALTERNATING COPOLYMERIZATION; RING-OPENING POLYMERIZATION; CARBON-DIOXIDE; CYCLOHEXENE OXIDE; ZINC CATALYSTS; COMPLEXES; DEPOLYMERIZATION; REACTIVITY; MECHANISM; ACID;
D O I
10.1039/c4sc01686f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report a new class of catalysts for the enantioselective copolymerization of CO2 and alicyclic meso epoxides. C-1-Symmetric beta-diiminate zinc catalysts were designed on the basis of mechanistic information and subsequently optimized using structure-activity relationships and iterative ligand design. The optimized catalysts yield highly isotactic poly(cyclohexene carbonate) and poly(cyclopentene carbonate) with units of up to 94% ee under mild conditions. A diblock copolymer of CO2/cyclohexene oxide and CO2/cyclopentene oxide was synthesized, demonstrating the controlled behaviour of the catalyst. Solid-state structures and solution-state dynamics of the catalyst were studied to explain trends in enantioselectivities and turnover frequencies. A strong correlation between the isotacticity of the polymer and its melting temperature was observed. X-ray powder diffraction was used to measure crystallinity and study the changes in morphology observed upon annealing.
引用
收藏
页码:4004 / 4011
页数:8
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