Cai Sheng, Zhu Dongliang, Zou Yan, Zhao Jing
State Key Laboratory of Coordination Chemistry, Institute of Chemistry and Biomedical Sciences, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Chemistry for Life Sciences, Nanjing University, Nanjing, 210093, China.
Research and Development Centre, China Tobacco Anhui Industrial Co., Ltd., 9 Tianda Road, Hefei, Anhui, 230088, China.
Nanoscale Res Lett. 2016 Dec;11(1):321. doi: 10.1186/s11671-016-1529-z. Epub 2016 Jul 1.
A series of porous polymers bearing functional quaternary ammonium salts were solvothermally synthesized through the free radical copolymerization of divinylbenzene (DVB) and functionalized quaternary ammonium salts. The obtained polymers feature highly cross-linked matrices, large surface areas, and abundant halogen anions. These polymers were evaluated as heterogeneous catalysts for the synthesis of cyclic carbonates from epoxides and CO2 in the absence of co-catalysts and solvents. The results revealed that the synergistic effect between the functional hydroxyl groups and the halide anion Br(-) afforded excellent catalytic activity to cyclic carbonates. In addition, the catalyst can be easily recovered and reused for at least five cycles without significant loss in activity.
通过二乙烯基苯(DVB)与功能化季铵盐的自由基共聚反应,溶剂热合成了一系列带有功能性季铵盐的多孔聚合物。所制备的聚合物具有高度交联的基体、大的表面积和丰富的卤素阴离子。在没有助催化剂和溶剂的情况下,评估了这些聚合物作为非均相催化剂由环氧化物和CO2合成环状碳酸酯的性能。结果表明,官能团羟基与卤化物阴离子Br(-)之间的协同作用赋予了环状碳酸酯优异的催化活性。此外,该催化剂易于回收且至少可重复使用五次,活性无明显损失。