Issue 4, 2016

Lewis acid–base bifunctional aluminum–salen catalysts: synthesis of cyclic carbonates from carbon dioxide and epoxides

Abstract

Two Lewis acid–base bifunctional monometallic aluminum–salen complexes were prepared based on a new type of salen ligand with two N-methylhomopiperazine moieties at the 3,3′-position. The Al(salen) complexes proved to be efficient and recyclable homogeneous catalysts towards the organic solvent-free synthesis of cyclic carbonates from epoxides and CO2 in the absence of a co-catalyst, in which >90% yield of cyclic carbonate could be obtained under relatively mild conditions. The catalysts can be easily recovered and reused five times without significant loss of activity and selectivity. Furthermore, the Lewis acid–base cooperative activation mechanism by the bifunctional Al(salen) complexes was proposed according to experimental data.

Graphical abstract: Lewis acid–base bifunctional aluminum–salen catalysts: synthesis of cyclic carbonates from carbon dioxide and epoxides

Supplementary files

Article information

Article type
Paper
Submitted
20 Nov 2015
Accepted
15 Dec 2015
First published
18 Dec 2015

RSC Adv., 2016,6, 3243-3249

Author version available

Lewis acid–base bifunctional aluminum–salen catalysts: synthesis of cyclic carbonates from carbon dioxide and epoxides

Y. Ren, O. Jiang, H. Zeng, Q. Mao and H. Jiang, RSC Adv., 2016, 6, 3243 DOI: 10.1039/C5RA24596F

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