Issue 38, 2024

Ring-opening polymerization of cyclic esters mediated by base/(thio)urea binary catalysts toward sustainable polyesters

Abstract

Aliphatic polyesters prepared by the ring-opening polymerization (ROP) of cyclic esters have shown great promise as sustainable polymers due to the potential bio-renewable feedstock, biodegradability and good material performance. The recently developed base/(thio)urea binary catalysts have achieved great success for the “living”/controlled ROP of cyclic esters due to their high catalytic activity and selectivity. In this review, we will highlight the latest achievements in the synthesis of sustainable polyesters mediated by base/(thio)urea binary catalysts. We first introduce the mechanistic insight of base/(thio)urea catalysts, focusing on the discussion of the impact factors on the catalytic mechanism, catalytic activity and selectivity. The ROP of a variety of cyclic esters, especially those with closed-loop recyclability, will be highlighted based on the ring size. Furthermore, the current limitations and future directions of base/(thio)urea catalysts will be discussed.

Graphical abstract: Ring-opening polymerization of cyclic esters mediated by base/(thio)urea binary catalysts toward sustainable polyesters

Article information

Article type
Review Article
Submitted
13 aug 2024
Accepted
10 sep 2024
First published
10 sep 2024

Polym. Chem., 2024,15, 3832-3846

Ring-opening polymerization of cyclic esters mediated by base/(thio)urea binary catalysts toward sustainable polyesters

L. Wang, Y. Liu, Y. Shen and Z. Li, Polym. Chem., 2024, 15, 3832 DOI: 10.1039/D4PY00884G

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