Issue 2, 2018

Protic pyrazolium ionic liquids for efficient chemical fixation of CO2: design, synthesis, and catalysis

Abstract

The conversion of carbon dioxide into organic products under benign conditions is still challenging. Ionic liquids are regarded as efficient and “green” catalysts from a sustainability view point. However, little attention has been focused on pyrazolium ILs although they are structural isomers of imidazolium ILs. Even fewer studies have been performed on protic pyrazolium ILs. In this work, three new protic pyrazolium ILs, HTMPzBr, HMM3PzBr, and HMM5PzBr, have been synthesized to explore their catalytic activity for the coupling reaction of carbon dioxide and propylene oxide. Both theoretical calculations and experimental characterization have verified that HTMPzBr and HMM5PzBr have similar catalytic activity, which is higher than that of HMM3PzBr. The role of various weak interactions, especially hydrogen bonds, in the reaction is elucidated by detailed theoretical analysis. The sequence of catalytic activity predicted by the Double-IL theoretical model is totally consistent with the experimental result. It is reasonable to design ionic liquids from a molecular level if a suitable theoretical model is applied, and this would provide some guidance for further experimental study.

Graphical abstract: Protic pyrazolium ionic liquids for efficient chemical fixation of CO2: design, synthesis, and catalysis

Supplementary files

Article information

Article type
Paper
Submitted
31 Jul 2017
Accepted
15 Dec 2017
First published
15 Dec 2017

Mol. Syst. Des. Eng., 2018,3, 348-356

Protic pyrazolium ionic liquids for efficient chemical fixation of CO2: design, synthesis, and catalysis

D. Zheng, T. Wang, X. Zhu, C. Chen, T. Ren, L. Wang and J. Zhang, Mol. Syst. Des. Eng., 2018, 3, 348 DOI: 10.1039/C7ME00068E

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements