Catalysis of Cycloaddition of Carbon Dioxide and Epoxides Using a Bifunctional Schiff Base Iron(III) Catalyst

被引:28
作者
Al-Qaisi, Feda'a M. [1 ]
Nieger, Martin [1 ]
Kemell, Marianna L. [1 ]
Repo, Timo J. [1 ]
机构
[1] Univ Helsinki, Inorgan Chem Lab, Dept Chem, POB 55, FIN-00014 Helsinki, Finland
关键词
CO2; activation; cyclic carbonate; epoxide coupling; iron catalyst; bifunctional; CYCLIC CARBONATES; ORGANIC CARBONATES; MILD CONDITIONS; IONIC LIQUIDS; ALTERNATING COPOLYMERIZATION; CHEMICAL FIXATION; COUPLING REACTION; HIGHLY EFFICIENT; PROPYLENE-OXIDE; CO2; FIXATION;
D O I
10.1002/slct.201600162
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cyclic carbonates are solvents with high boiling points and low toxicity. For synthesis of cyclic carbonates we report on bifunctional Schiff base iron(III) complex for catalytic coupling reaction of propylene oxide and CO2. Due to the presence of two imidazole groups in the ligand framework it facilitates the coupling reaction in the absence of co-catalyst with good activity reaching TON value 225 within 4 h. Among various solvents used, the catalyst gives the highest activity in dichloromethane. Moreover, the complex catalyses also the cycloaddition reactions of CO2 and epichlorohydrin, styrene, 1-hexene and cyclohexene oxides. The iron catalysed coupling reaction was followed with in situ infrared spectroscopy giving an apparent first order reaction (n approximate to 1) towards catalyst concentration. Accordingly, a monomolecular mechanism involving imidazole carbamate is proposed.
引用
收藏
页码:545 / 548
页数:4
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