Photoredox Catalysts Based on <i>N</i> ‐(Hexyl)benzothioxanthene‐3,4‐dicarboximide for Photopolymerization and 3D Printing Under Visible Light

B Bin Song Y Yijun Zhang Z Zheng Liu P Pierre Boulay (Université de Haute Alsace, CNRS, IS2M UMR 7361 Mulhouse F‐68100 France) C Céline Dietlin (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France) F Fabrice Morlet‐Savary (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France) M Michael Schmitt D Didier Gigmes J Jean‐Michel Becht (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France) F Frédéric Dumur (Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France) J Jacques Lalevée (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France)

Abstract

Abstract Photoredox catalytic systems are widely used in free radical polymerization as an important photoinitiating approach. However, many reported photoredox catalytic systems are limited by their low stabilities, high excitation powers, and low initiating efficiencies upon excitation in the visible region. Therefore, it is still a great challenge to develop efficient photoinitiating systems for photopolymerization under visible light. In this work, three new effective photosensitizers from N ‐(hexyl)benzothioxanthene‐3,4‐dicarboximide derivatives, namely 2‐hexyl‐1 H ‐thioxantheno[2,1,9‐ def ]isoquinoline‐1,3(2 H )‐dione (BTXI), 5‐bromo‐2‐hexyl‐1 H ‐thioxantheno[2,1,9‐ def ]isoquinoline‐1,3(2 H )‐dione (BTXI‐Br) and 2‐hexyl‐1 H ‐thioxantheno[2,1,9‐ def ]isoquinoline‐1,3(2 H )‐dione 6,6‐dioxide (BTXIO), were designed by density functional theory calculation and synthesized as photoredox catalysts for visible light induced photopolymerization. When combined with initiators such as oxidants, that is, bis (4‐ tert ‐butylphenyl)iodonium hexafluorophosphate or sulfonium salts (i.e., thianthrenium salts, phenoxathiinium salt, phenothiazinium salt, dibenzothiophenium salt) and the reductant ethyl dimethylaminobenzoate to form three‐component initiating systems, they showed good to high performance in visible light photo polymerizations with LED@405 nm and LED@450 nm. In addition, these photoinitiating systems enable the successful digital light processing and direct laser writing of 3D structures with high resolution, demonstrating a promising strategy for 3D printing applications.

Article Details

Volume / Issue Vol. 64, Issue 30
Published July 21, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (11)

B

Bin Song

Y

Yijun Zhang

Z

Zheng Liu

P

Pierre Boulay

Université de Haute Alsace, CNRS, IS2M UMR 7361 Mulhouse F‐68100 France

C

Céline Dietlin

Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France

F

Fabrice Morlet‐Savary

Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France

M

Michael Schmitt

D

Didier Gigmes

J

Jean‐Michel Becht

Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France

F

Frédéric Dumur

Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France

J

Jacques Lalevée

Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France