期刊
MOLECULAR CATALYSIS
卷 450, 期 -, 页码 39-45出版社
ELSEVIER
DOI: 10.1016/j.mcat.2018.02.018
关键词
CO2 cycloaddition; DBU-based ionic liquids; Epoxide; Cyclic carbonate
资金
- National Natural Science Foundation of China [21673060]
- Fund for Research and Development of Science and Technology in Shenzhen [JCYJ20160427184531017]
- State Key Lab of Urban Water Resource and Environment of Harbin Institute of Technology [HIT2017DX10]
The cycloaddition of CO2 to epoxides is an important reaction and has got increasing attention. In this work, a series of DBU-based ionic liquids (DILs) were synthesized via facile neutralization of superbase 1,8-Diazabicyclo [5.4.0]undec-7-ene (DBU) with corresponding hydrogen bond donor acids, such as D(-)-tartaric acid (TA), malic acid (MA) and succinic acid (SA). The DILs cooperated with ZnI2 were first evaluated in detail for catalyzing the coupling reaction of CO2 with propylene oxide (PO), and DIL-1 exhibited obviously enhanced catalytic activity under 80 degrees C, 3 MPa and solvent-free conditions. The effects of reaction parameters on the activity for propylene carbonate (PC) synthesis were thoroughly investigated, and a possible synergistic catalytic mechanism was proposed. The catalytic system reported here could be separated by simple centrifugation from the products after reaction and then reused efficiently. Moreover, the catalytic system showed the advantages of simple synthesis, high catalytic activity, low cost, and substrate versatility for CO2 conversion to cyclic carbonates.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据