Issue 5, 2020

Introducing the Tishchenko reaction into sustainable polymer chemistry

Abstract

Taking advantage of the structural characteristics of lignin-derived phenolic compounds, a combination of the Williamson and Tishchenko reactions produced a series of new α,ω-diene functionalized carboxylic ester monomers from both petrochemical and renewable resources, which were applicable in subsequent thiol–ene click and acyclic diene metathesis (ADMET) polymerizations, providing a series of poly(thioether esters) and unsaturated aromatic–aliphatic polyesters with high molecular weights.

Graphical abstract: Introducing the Tishchenko reaction into sustainable polymer chemistry

Supplementary files

Article information

Article type
Communication
Submitted
14 Kas 2019
Accepted
23 Ara 2019
First published
23 Ara 2019

Green Chem., 2020,22, 1542-1547

Introducing the Tishchenko reaction into sustainable polymer chemistry

T. Ren, Q. Chen, C. Zhao, Q. Zheng, H. Xie and M. North, Green Chem., 2020, 22, 1542 DOI: 10.1039/C9GC03926K

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