当前位置: X-MOL 学术J. Mol. Catal. A Chem. › 论文详情
Our official English website, www.x-mol.net, welcomes your feedback! (Note: you will need to create a separate account there.)
Facile synthesis of [urea-Zn]I2 eutectic-based ionic liquid for efficient conversion of carbon dioxide to cyclic carbonates
Journal of Molecular Catalysis A: Chemical Pub Date : 2016 , DOI: 10.1016/j.molcata.2015.11.017
Mengshuai Liu , Xin Li , Xiaoli Lin , Lin Liang , Xiangxiang Gao , Jianmin Sun

Several environmentally benign eutectic-based ionic liquids (ILs) were developed as novel homogeneous catalysts for efficient conversion of carbon dioxide to cyclic carbonates. Propylene oxide (PO) was selected as a benchmark substrate to optimize the catalytic activity, and on account of the catalytic cooperativity between the cation and anion in the [urea-Zn]I2 catalyst, excellent yield (95%) and selectivity (98%) to propylene carbonate (PC) was obtained under the optimized reaction conditions of 120 °C and 1.5 MPa for 3.0 h in the absence of cocatalyst and solvent. Also [urea-Zn]I2 was proved to be an efficient and versatile catalyst, and could realize catalytic conversion of CO2 with various epoxides. Moreover, the synergistic reaction mechanism involving cation structure and halogen anion for CO2 conversion was proposed, and the eutectic-based ILs were easily recyclable with high activity. The eutectic-based ILs that possessing low cost, moisture-stability, facile synthesis and efficiently bifunctional properties reported herein displayed the exceptionally outstanding features for efficient conversion of CO2 to cyclic carbonates.

中文翻译:

轻松合成基于[urea-Zn] I 2的共晶离子液体,可有效地将二氧化碳转化为环状碳酸酯

几种环境友好的基于共晶的离子液体(IL)被开发为新型的均相催化剂,用于有效地将二氧化碳转化为环状碳酸酯。选择环氧丙烷(PO)作为基准底物以优化催化活性,并考虑到[脲-Zn] I 2催化剂中阳离子与阴离子之间的催化协同作用,极佳的收率(95%)和选择性(98)在没有助催化剂和溶剂的情况下,在120℃和1.5 MPa的最佳反应条件下反应3.0小时,获得了碳酸亚丙酯(PC)的收率。还证明了[脲-Zn] I 2是一种高效且用途广泛的催化剂,可以实现CO 2的催化转化。与各种环氧化物。此外,提出了阳离子结构和卤素阴离子协同转化CO 2的协同反应机理,基于共晶的离子液体易于回收利用,具有较高的活性。本文报道的具有低成本,湿气稳定性,易于合成和有效的双功能性质的基于共晶的IL表现出将CO 2有效转化为环状碳酸酯的异常突出的特征。
更新日期:2017-01-31
down
wechat
bug