Free-radical photoring-opening polymerization of cyclic allylic sulfide: From photocleavable photoinitiators to three components photoredox systems. (22nd February 2023)

• Record Type: Journal Article
• Authors: Ley, C.; Eicher, M.; Chaumeil, H.; Schuller, A.-S.; Halbardier, L.; Allonas, X.
• Is Part Of: Polymer. Volume 268(2023)
• Publication Date: 2023-02-22
• Subjects: CAS Cyclic Allylic Sulfides -- RROP Radical Ring Opening Polymerization; Polymers -- Periodicals; Polymerization -- Periodicals; Polymères -- Périodiques; Polymérisation -- Périodiques; 547.7
• DOI: 10.1016/j.polymer.2023.125691
• Languages: English
• ISSNs: 0032-3861

Abstract

Abstract: Photopolymers form a family of materials that have been developed to meet specific demands in fields such as coatings, varnishes, semiconductors, optical fibers, printing plates, holographic recording, etc. However, the multifunctional acrylate monomers currently used present an important volume contraction. A drawback for applications where little shrinkage during polymerization is mandatory to keep shapes and properties of the material. To overcome this problem, monomers reacting by ring opening polymerization can be used. Among possible monomers, cyclic allylic sulfides are very interesting candidates: they are highly reactive and their polymerization mechanism is almost not affected by the presence of oxygen. In this work the effects of the photoinitiating systems on the free radical ring opening photopolymerization kinetics of an eight-member cyclic allylic sulfide is studied. It is shown that cleavable type I, bimolecular type II and three components redox photoinitiating systems allow the formation of linear photopolymers with high polymerization rates and final conversions. The photopolymerization kinetics obtained show that the photopolymerization is not sensitive to oxygen which leads to reduced exposure time and higher sensitivity. This remarkable property should also extend the usage of such monomers in the coating applications where oxygen inhibition is a drawback. Finally, the benefit of ring opening polymerization process is demonstrated trough the volume contraction measurement which was found to be lower than 1.5%. Graphical abstract: Image 1 Highlights: Radical ring opening photopolymerization of cyclic allylic sulfides monomers. Low oxygen sensitivity of the cyclic allylic sulfides monomer photopolymerization. Lower volume contraction than acrylate monomer with a value of less than 1.5%.