Fluorine-decorated ionic liquid salts used for the efficient transformation of low concentration CO2

Abstract

As a C1 feedstock, CO2 has the potential to be uniquely highly economical in both a chemical and a financial sense. Herein, through a precise design and controllable synthesis, a series of fluorine-modified ionic liquid salts composed of quaternary phosphonium cations or imidazolium cations with bromide anions were constructed. Their catalytic activity in the cycloaddition reaction of CO2 with epoxides to form cyclic carbonates was comprehensively investigated to illustrate the promotion effect of the functional fluorine group in the ionic liquid based catalysts. Our experimental results show that the obtained fluorine-modified ionic liquids exhibit much higher catalytic activity than the original ionic liquids with similar structure due to the high affinity of fluorine with CO2. The difference of catalytic activities was further amplified when the cycloaddition reactions were carried out under low CO2 concentration conditions and the fluorine-containing ionic liquids F-IL-TCP possessed the highest catalytic activity with a conversion of 76.4% in 96 h, which is much higher than the fluorine free ionic liquid IL-TCP. It is believed that this work paved a way for the development of novel catalysts for the efficient elimination and transformation of CO2.

Graphical abstract: Fluorine-decorated ionic liquid salts used for the efficient transformation of low concentration CO2

Supplementary files

Article information

Article type
Paper
Submitted
12 Feb 2025
Accepted
11 Mar 2025
First published
12 Mar 2025

New J. Chem., 2025, Advance Article

Fluorine-decorated ionic liquid salts used for the efficient transformation of low concentration CO2

H. Su, J. Han, C. Fang, T. Dai, Z. Wang, Z. Dai, H. Ni, Y. Xiong and X. Meng, New J. Chem., 2025, Advance Article , DOI: 10.1039/D5NJ00615E

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