离子液体
催化作用
二乙烯基苯
单体
聚合
化学
溶剂
环加成
氢键
产量(工程)
化学工程
无机化学
离子键合
多孔性
高分子化学
离子
材料科学
有机化学
聚合物
分子
共聚物
苯乙烯
工程类
冶金
作者
Quanlan Liao,Xiaoqing Wang,Fangfang Zhao,Tiaxniang Zhao,Jianxin Cao
标识
DOI:10.1016/j.mcat.2023.113684
摘要
Ionic liquids have widely been recognized as highly effective catalysts for the synthesis of cyclic carbonates from CO2 and epoxides. However, the cumbersome separation process hinders the practical application of these catalysts. In this study, a strategy involving free radical polymerization was employed to successfully co-polymerized monomers of ionic liquid and divinylbenzene (DVB), resulting in the fabrication of anion-rich porous poly(ionic liquid)s (PILs) that incorporated a hydrogen bonding site of -NH2-+. The texture properties of the as-prepared PILs were characterized in detail, and they were then utilized as catalysts for the cycloaddition of CO2 and epoxides to form cyclic carbonates. Remarkably, the reaction exhibited a remarkable yield of up to 99 % under solvent- and metal-free conditions. It is noteworthy that PIL-2 demonstrated easy recoverability, with a slight reduction in catalytic activity of about 7 % after five cycles. Additionally, a mechanism based on hydrogen bond synergistic for the conversion of CO2 by anion-rich porous PILs was proposed. This study offers a valuable insight for the development of recyclable poly(ionic liquid)s catalysts for CO2 conversion.
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