Issue 45, 2016

Poly(thioacrylate)s: expanding the monomer toolbox of functional polymers

Abstract

Radically polymerizable monomers such as acrylates, acrylamides, and styrenes have been investigated because of their corresponding polymers for many years. However, thioacrylates are a forgotten class of monomers and have not been studied for decades. Herein, we present a simple synthetic approach to prepare various thioacrylate monomers as well as their controlled radical polymerization for the first time. Four different thioacrylate (TA) monomers namely, ethyl thioacrylate, phenyl thioacrylate, n-propyl thioacrylate and isopropyl thioacrylate have been polymerized via RAFT polymerization. A trithiocarbonate chain transfer agent was utilized to control the molar mass and dispersity of thioacrylate polymers. Homopolymers of thioacrylates with different degrees of polymerizations were prepared and their block copolymerizations were studied with ethylacrylate and thioacrylates. All obtained polymers were analyzed in detail using GPC, NMR, TGA, DSC and water contact angle.

Graphical abstract: Poly(thioacrylate)s: expanding the monomer toolbox of functional polymers

Supplementary files

Article information

Article type
Paper
Submitted
02 Oct 2016
Accepted
24 Oct 2016
First published
25 Oct 2016
This article is Open Access
Creative Commons BY-NC license

Polym. Chem., 2016,7, 7011-7018

Poly(thioacrylate)s: expanding the monomer toolbox of functional polymers

S. Aksakal and C. Remzi Becer, Polym. Chem., 2016, 7, 7011 DOI: 10.1039/C6PY01721E

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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