Miao Cheng-Xia, Wang Jin-Quan, Wu Ying, Du Ya, He Liang-Nian
State Key Laboratory, Institute of Elemento-Organic Chemistry, Nankai University, Tianjin, China.
ChemSusChem. 2008;1(3):236-41. doi: 10.1002/cssc.200700133.
A bifunctional cobalt-salen complex containing a Lewis acidic metal center and a quaternary phosphonium salt unit anchored on the ligand effectively catalyzes the synthesis of cyclic carbonates from CO2 and epoxides under mild conditions without the utilization of additional organic solvents or co-catalysts. The effects of various reaction variables on the catalytic performance were studied in detail and indicate an optimized reaction temperature of about I00 degrees C and CO2 pressure of around 4 MPa, although the reaction proceeds smoothly even at pressures as low as 2 MPa. The catalyst is applicable to a variety of epoxides, producing the corresponding cyclic carbonates in good yields in most cases. Furthermore, the catalyst can be easily recovered and reused several times without significant loss of its catalytic activity. This process thus represents a greener pathway for the environmentally benign chemical fixation of CO2 to produce cyclic carbonates.
一种双功能钴-萨伦配合物,其含有一个路易斯酸性金属中心和一个锚定在配体上的季鏻盐单元,能够在温和条件下有效地催化由二氧化碳和环氧化物合成环状碳酸酯,无需使用额外的有机溶剂或共催化剂。详细研究了各种反应变量对催化性能的影响,结果表明,尽管在低至2 MPa的压力下反应也能顺利进行,但优化的反应温度约为100℃,二氧化碳压力约为4 MPa。该催化剂适用于多种环氧化物,在大多数情况下能以良好的产率生成相应的环状碳酸酯。此外,该催化剂易于回收并可重复使用多次,而其催化活性不会有显著损失。因此,该过程代表了一种更绿色的途径,用于将二氧化碳进行环境友好型化学固定以生产环状碳酸酯。