Structure–Reactivity Relationships of Oxime–Oxalate/Glyoxylate/Ester Derivatives: Dual Photo/Thermal Initiators for Visible Light Polymerization and Composite Preparation

T Tong Gao T Thybault De Monfreid (Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France) J Ji Feng J Jing Zhang F Fabrice Morlet‐Savary (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France) C Céline Dietlin (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France) M Michael Schmitt F Frédéric Dumur (Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France) J Jean‐Patrick Joly (Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France) M Malek Nechab (Aix Marseille Univ CNRS ICR UMR 7273 Marseille F‐13397 France) P Pu Xiao J Jacques Lalevée (Université De Haute‐Alsace CNRS, IS2M UMR 7361 Mulhouse France)

Abstract

Abstract In this study, we reported the design, synthesis, and comprehensive evaluation of a series of nitro carbazole‐based oxime photoinitiators (OPIs, OP1: oxime oxalate, OP2: oxime glyoxylate), as a series of efficient Type I photoinitiators (PIs) for the free radical photopolymerization (FRP) of trimethylolpropane triacrylate (TMPTA) and ethoxylated trimethylolpropane triacrylate (ETPTA) under blue light‐emitting diodes and sunlight irradiation. Computational molecular modeling was employed to predict the effect of OPIs structures on the photoinitiation properties. The predictions suggest that OP1 had a higher propensity for decarboxylation and therefore a better photoinitiation behavior. Compared to OP2, OP3, and commercial benchmark photoinitiator TPO, OP1 exhibits exceptional photoinitiation performance when exposed to LED@405 nm, LED@450 nm, and sunlight. OP1 undergoes decarboxylation to efficiently produce CO 2 and free radicals, thereby initiating the photopolymerization reaction. Remarkably, OP1 is successfully applied in 3D printing, producing complete morphology with high‐resolution structure, showcasing its potential for advanced manufacturing applications. The photochemical mechanism of OPIs is comprehensively elucidated using the monitoring of the CO 2 , steady state photolysis, UV–vis absorption spectroscopy, fluorescence spectroscopy, and electron spin resonance techniques. These experimental investigations are supported by data OP1 from the molecular modelling carried out. Additionally, thermal polymerization shows that OP1 had a high thermal initiation capability, and the composites are successfully prepared together with carbon fibers. The cytotoxicity of the synthesized oxime oxalate and TPO on human umbilical vein endothelial cells (HUVECs) results in a lower cytotoxicity for the oxalate than for TPO. Therefore, OP1, which has never been reported before, can be used as a highly efficient and low cytotoxic dual photo/thermal initiator. This research not only provides theoretical and practical insights into the design and development of new efficient Type I PIs, but also opens up new perspectives for curing applications that require scalability, cost‐effectiveness, environmental sustainability, and green chemistry.

Article Details

Volume / Issue Vol. 65, Issue 4
Published January 22, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

T

Tong Gao

T

Thybault De Monfreid

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

J

Ji Feng

J

Jing Zhang

F

Fabrice Morlet‐Savary

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

C

Céline Dietlin

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

M

Michael Schmitt

F

Frédéric Dumur

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

J

Jean‐Patrick Joly

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

M

Malek Nechab

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

P

Pu Xiao

J

Jacques Lalevée

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