Zhong Wei, Bobbink Felix D, Fei Zhaofu, Dyson Paul J
College of Biological, Chemical Sciences and Engineering, Jiaxing University, Jiaxing, 314001, P. R. China.
Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015, Lausanne, Switzerland.
ChemSusChem. 2017 Jul 10;10(13):2728-2735. doi: 10.1002/cssc.201700570. Epub 2017 Jun 1.
There is a growing interest in sustainable heterogeneous catalysts based on organic polymers. Here, we describe a series of polyimidazolium salt catalysts, prepared from the direct reaction of arene-bridged bis- and tris-alkyl halides with trimethylsilylimidazole. The polyimidazolium salts were characterized by spectroscopic and analytical techniques and it was found that their morphology and porosity could be controlled by adjusting the steric parameters of the spacer in the alkyl-halide starting materials. Moreover, the polymers are excellent heterogeneous organocatalysts for the cycloaddition of CO to epoxides to afford cyclic carbonates at atmospheric pressure under solvent-free conditions. The polymer catalysts exhibit long-term stability and may be recycled and reused at least 10 times.
基于有机聚合物的可持续多相催化剂正受到越来越多的关注。在此,我们描述了一系列聚咪唑鎓盐催化剂,它们是由芳烃桥连的双卤代烃和三卤代烃与三甲基硅基咪唑直接反应制备而成。通过光谱和分析技术对聚咪唑鎓盐进行了表征,发现可以通过调整卤代烃起始原料中间隔基的空间参数来控制其形态和孔隙率。此外,这些聚合物是优异的多相有机催化剂,可在无溶剂条件下于大气压下催化CO与环氧化物环加成生成环状碳酸酯。聚合物催化剂表现出长期稳定性,并且可以循环再利用至少10次。