Issue 28, 2021

Novel imino- and aryl-sulfonate based photoacid generators for the cationic ring-opening polymerization of ε-caprolactone

Abstract

Photoinduced polymerization is a useful tool in many industrial applications such as coatings, adhesives and 3D printing. However, the use of light to promote polymerization has been almost exclusively used for radical photopolymerization, thus excluding a wide variety of monomers. In this context, the use of light irradiation to trigger other polymerizations to produce degradable polymers has scarcely been studied. Herein, we investigate the use of six novel photoacid generators based on anthrone and anthraquinone chromophores capable of producing triflic, para-toluensulfonic and methanesulfonic acids upon 365 nm LED light irradiation to trigger the ROP of cyclic esters. The efficiency of the catalyst is shown to be strongly related to the chromophore and the sulfonate substituent. After characterizing the photodissociation process using UV-Visible and NMR spectroscopy, DFT calculations were carried out in order to understand the photodissociation mechanism. Their use as effective catalysts for the cationic ring-opening polymerization of ε-Cl is confirmed by 1H NMR and SEC analysis either in solution or in bulk, obtaining fast polymerization rates at 100 °C. This catalyst family shows the ability to form polyester based coatings using light, expanding the number of coatings that may be prepared by photopolymerization processes.

Graphical abstract: Novel imino- and aryl-sulfonate based photoacid generators for the cationic ring-opening polymerization of ε-caprolactone

Supplementary files

Article information

Article type
Paper
Submitted
31 Maijs 2021
Accepted
28 Jūn. 2021
First published
30 Jūn. 2021

Polym. Chem., 2021,12, 4035-4042

Novel imino- and aryl-sulfonate based photoacid generators for the cationic ring-opening polymerization of ε-caprolactone

X. Lopez de Pariza, E. Cordero Jara, N. Zivic, F. Ruipérez, T. E. Long and H. Sardon, Polym. Chem., 2021, 12, 4035 DOI: 10.1039/D1PY00734C

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