Wei Meng-Ge, Li Hong-Ru, He Liang-Nian
College of Pharmacy, Nankai University, 38 Tongyan Road, Tianjin, 300350, P. R. China.
State Key Laboratory and Institute of Elemento-Organic Chemistry, College of Chemistry, Nankai University, Tianjin, 300071, P. R. China.
Chempluschem. 2024 Jul;89(7):e202300778. doi: 10.1002/cplu.202300778. Epub 2024 Mar 19.
A series of KF/Mg-Fe oxides were fabricated via the solid-state reaction between KF and Mg-Fe oxides. Especially, when 20 wt % KF was supported on the Mg-Fe bi-metal oxides and calcined at 400-600 °C, the solid material with more basic sites than the support itself was obtained. When applied as catalyst to dimethyl carbonate (DMC) synthesis through transesterification of ethylene carbonate (EC) and methanol, this material can afforded up to 88 % yield and 97 % selectivity toward DMC in 2 h under reflux conditions with the molar ratio of methanol to ethylene carbonate set at 8. It is worth noting that the catalyst was easily separated and reused, retaining at least 89 % catalytic activity during the first four recycles. Although an attenuated activity was still observed due to the inevitable filtration loss and dissolution, this solid base can still provide clues to the development recyclable catalyst in green synthesis of DMC.
通过KF与Mg-Fe氧化物之间的固态反应制备了一系列KF/Mg-Fe氧化物。特别是,当20 wt%的KF负载在Mg-Fe双金属氧化物上并在400-600°C下煅烧时,得到了比载体本身具有更多碱性位点的固体材料。当将该材料用作通过碳酸亚乙酯(EC)和甲醇的酯交换反应合成碳酸二甲酯(DMC)的催化剂时,在甲醇与碳酸亚乙酯的摩尔比设定为8的回流条件下,该材料在2小时内可提供高达88%的产率和97%的DMC选择性。值得注意的是,该催化剂易于分离和重复使用,在前四次循环中至少保留89%的催化活性。尽管由于不可避免的过滤损失和溶解仍观察到活性减弱,但这种固体碱仍可为DMC绿色合成中可回收催化剂的开发提供线索。