Issue 35, 2020

Effect of anethole on the copolymerization of vinyl monomers

Abstract

Anethole, a monomer that can be extracted from bioresources, cannot homopolymerize. Its ability to copolymerize with other vinyl monomers depends on both steric hindrance and the electronic nature of the comonomer. Its copolymerization behaviour with acrylic acid, 2-ethylhexyl acrylate, styrene and methyl methacrylate was investigated. Reactivity ratios were determined by the nonlinear least squares method. Even though the presence of anethole strongly retards the rate of consumption of the comonomer, its incorporation in copolymer chains can be improved with semi batch polymerization. Finally, the side reactions that occur during the copolymerizations – e.g. formation of branches or low molecular weight chains – were investigated. We observed that anethole not only acted as a comonomer, but also as a chain transfer agent, likely due to the presence of labile hydrogen.

Graphical abstract: Effect of anethole on the copolymerization of vinyl monomers

Supplementary files

Article information

Article type
Paper
Submitted
09 Jun 2020
Accepted
26 Jul 2020
First published
28 Jul 2020

Polym. Chem., 2020,11, 5630-5641

Effect of anethole on the copolymerization of vinyl monomers

J. Lena, A. M. van Herk and S. Jana, Polym. Chem., 2020, 11, 5630 DOI: 10.1039/D0PY00833H

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