Photoinduced radical addition fragmentation chain transfer (PET-RAFT) polymerization typically requires high light intensity (>5 mW cm−2), limiting energy efficiency, and scalability. We demonstrate that adding a base to PET-RAFT systems drastically enhances the reactivity of acidic chain transfer agents (CTAs) with Zn-based photocatalysts (Zn porphyrin and Zn phthalocyanine). This approach enables complete polymerization under microwatt light intensity (0.25 mW cm−2), a significant improvement over traditional PET-RAFT, which showed no conversion under the same conditions. Both acrylates and methacrylates polymerized efficiently with excellent chain-end fidelity. Reactivity was triggered chemically (via base addition) or electrochemically (via electrolytic reduction). Mechanistic studies reveal that base addition promotes a CTA-Zn photocatalyst complex, shifting the activation from bimolecular to more efficient unimolecular PET-RAFT.

Photo-RAFT Polymerization Under Microwatt Irradiation via Unimolecular Photoinduced Electron Transfer

Lissandrini, Giovanni;Zeppilli, Davide;Lorandi, Francesca;Isse, Abdirisak A.
;
Orian, Laura;Fantin, Marco
2025

Abstract

Photoinduced radical addition fragmentation chain transfer (PET-RAFT) polymerization typically requires high light intensity (>5 mW cm−2), limiting energy efficiency, and scalability. We demonstrate that adding a base to PET-RAFT systems drastically enhances the reactivity of acidic chain transfer agents (CTAs) with Zn-based photocatalysts (Zn porphyrin and Zn phthalocyanine). This approach enables complete polymerization under microwatt light intensity (0.25 mW cm−2), a significant improvement over traditional PET-RAFT, which showed no conversion under the same conditions. Both acrylates and methacrylates polymerized efficiently with excellent chain-end fidelity. Reactivity was triggered chemically (via base addition) or electrochemically (via electrolytic reduction). Mechanistic studies reveal that base addition promotes a CTA-Zn photocatalyst complex, shifting the activation from bimolecular to more efficient unimolecular PET-RAFT.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11577/3553207
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