C3-symmetric zinc complexes as sustainable catalysts for transforming carbon dioxide into mono- and multi-cyclic carbonates

被引:74
作者
Naveen, Kanagaraj [1 ]
Ji, Hoon [1 ]
Kim, Tea Soon [1 ]
Kim, Dongwoo [1 ]
Cho, Deug-Hee [1 ]
机构
[1] Korea Res Inst Chem Technol, Ctr Adv Specialty Chem, 45 Jongga Ro, Ulsan 44412, South Korea
关键词
Carbon dioxide fixation; Multi-cyclic carbonates; Zinc complexes; Bifunctional catalysts; Counter anions; EFFICIENT CATALYSTS; ALUMINUM CATALYST; CO2; FIXATION; EPOXIDES; CONVERSION; CYCLOADDITION; POLYURETHANES; CHALLENGES; PORPHYRIN; CHEMICALS;
D O I
10.1016/j.apcatb.2020.119395
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, we report a single-step preparation method for the synthesis of a series of C-3-symmetric zinc complexes containing both a Lewis acidic zinc center and a nucleophilic halide counter ion for coupling CO2 with epoxides. The Zn-complexes were shown to be effective one-component bifunctional catalysts and displayed high catalytic activity and selectivity for the transformation of CO2 into cyclic carbonates under mild conditions. This strategy is simple, efficient, environmentally benign, and does not require an additional cocatalyst or solvent, and the catalyst can be easily recovered and reused several times without significant loss in catalytic activity. The CO2 coupling reaction proceeded on broad range of substrates and exhibited good tolerance to functional groups, and the cyclic carbonate products were isolated in high yields. On the basis of the experimental results, a plausible reaction mechanism was proposed, and the high catalytic activity was explained.
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页数:9
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