Gou Haibin, Ma Xifei, Su Qian, Liu Lei, Ying Ting, Qian Wei, Dong Li, Cheng Weiguo
CAS Key Laboratory of Green Process and Engineering, State Key Laboratory of Multiphase Complex Systems, Beijing Key Laboratory of Ionic Liquids Clean Process, Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100190, China.
Phys Chem Chem Phys. 2021 Jan 28;23(3):2005-2014. doi: 10.1039/d0cp06041k.
The development of metal-free, high effective and recyclable catalysts plays a pivotal role in transforming CO2 into high value-added products such as cyclic carbonates. In this paper, we introduced the hydrogen bond donor (HBD) groups into poly(ionic liquid)s via free radical polymerization, which successfully combined the HBD and ionic liquids (ILs) into one heterogeneous catalyst. The HBD could synergistically activate epoxides with hydroxyl functionalized ionic liquids and efficiently catalyze the cycloaddition of CO2 into cyclic carbonates. The yield of propylene carbonate (PC) reached 94% (at 105 °C, 2 MPa CO2, 3 h), which far exceeded poly(ionic liquid)s without HBDs functionalization (PC yield 72%), and even approached bulk ionic liquids (PC yield 95%). Moreover, HBD-functionalized poly(ionic liquid)s (HPILs) exhibited excellent recyclability after five runs and afforded wide substrate scope. According to the experimental results, 1H NMR spectra and density functional theory (DFT) calculations showed 2-hydroxyethyl methacrylate (HEMA) and the hydroxyl of ILs would form strong H-bonds with epoxides contributing to the ring-opening process of epoxides, and a possible HBD and nucleophilic anion synergistically catalytic mechanism was proposed. The method herein paved a brand new way for green technology and utilization of poly(ionic liquid)s.
无金属、高效且可回收催化剂的开发在将二氧化碳转化为环状碳酸酯等高附加值产品方面发挥着关键作用。在本文中,我们通过自由基聚合将氢键供体(HBD)基团引入聚离子液体中,成功地将HBD和离子液体(ILs)结合成一种多相催化剂。HBD可以与羟基官能化离子液体协同活化环氧化物,并有效地催化二氧化碳与环氧化物环加成生成环状碳酸酯。碳酸丙烯酯(PC)的产率达到94%(在105℃、2MPa二氧化碳、3小时的条件下),这远远超过了未进行HBD官能化的聚离子液体(PC产率72%),甚至接近本体离子液体(PC产率95%)。此外,HBD官能化聚离子液体(HPILs)在五次循环后表现出优异的可回收性,并且底物范围广泛。根据实验结果、1H NMR光谱和密度泛函理论(DFT)计算表明,甲基丙烯酸2-羟乙酯(HEMA)和离子液体的羟基会与环氧化物形成强氢键,促进环氧化物的开环过程,并提出了一种可能的HBD和亲核阴离子协同催化机理。本文所述方法为聚离子液体的绿色技术和利用开辟了一条全新的途径。