{"title":"Comprehensive Study of the Synergistic Effect in Photocyclic Three-Component Initiating System for Radical Polymerization","authors":"Julien Christmann, Christian Ley, Xavier Allonas","doi":"10.1021/acs.macromol.5c00392","DOIUrl":null,"url":null,"abstract":"In radical photopolymerization, synergistic three-component initiating systems lead to far better radical polymerization performances compared with the corresponding two-component systems. The third component is able to produce additional initiating radicals, regenerate the photoinitiator, thus forming a photocyclic initiating system, and consume terminating photoproducts that occur in two-component photoinitiators. However, the respective roles of these reactions are not well-defined. Kinetic modeling is applied to a synergistic photocyclic initiating system to provide insights into the synergistic effects observed in a system based on an organic dye (Rose Bengal), a triazine derivative, and a tertiary amine as the third component. From kinetic modeling, the low polymerization performances of the dye-triazine system are attributed to back electron transfer but mainly to termination reactions by the oxidized dye photoproduct. Introduction of the amine greatly improves the polymerization performances. From time-resolved experiments, this is explained by its reaction with oxidized Rose Bengal to regenerate the dye and produce additional initiating radicals. It is also shown that the combination of these three components leads to dual photocyclic behavior. Kinetic modeling of the three-component system shows good agreement with the experimental data. Finally, a theoretical study using the kinetic model developed here highlights that the consumption of the oxidized dye terminating agent by the tertiary amine is the main reason for the improved polymerization kinetics.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00392","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
In radical photopolymerization, synergistic three-component initiating systems lead to far better radical polymerization performances compared with the corresponding two-component systems. The third component is able to produce additional initiating radicals, regenerate the photoinitiator, thus forming a photocyclic initiating system, and consume terminating photoproducts that occur in two-component photoinitiators. However, the respective roles of these reactions are not well-defined. Kinetic modeling is applied to a synergistic photocyclic initiating system to provide insights into the synergistic effects observed in a system based on an organic dye (Rose Bengal), a triazine derivative, and a tertiary amine as the third component. From kinetic modeling, the low polymerization performances of the dye-triazine system are attributed to back electron transfer but mainly to termination reactions by the oxidized dye photoproduct. Introduction of the amine greatly improves the polymerization performances. From time-resolved experiments, this is explained by its reaction with oxidized Rose Bengal to regenerate the dye and produce additional initiating radicals. It is also shown that the combination of these three components leads to dual photocyclic behavior. Kinetic modeling of the three-component system shows good agreement with the experimental data. Finally, a theoretical study using the kinetic model developed here highlights that the consumption of the oxidized dye terminating agent by the tertiary amine is the main reason for the improved polymerization kinetics.
期刊介绍:
Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.