Xinquan Wang, Zecong Ye, Hui Liang, Shaomin Ji, Yanping Huo, Yingxiao Mu
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引用次数: 0
Abstract
In this work, anthrone-based donor-acceptor-donor type photoinitiators (DXD and DTD) were synthesized and introduced into a two-component system with diphenylIodonium hexafluorophosphate (Iod) for radical photopolymerization of acrylic resin monomers. At the photoinitiator concentration of 0.5 wt%, under irradiation with LED@365 nm at the power of 20 mW cm - 2 , the double bond conversion of monomer initiated by DXD, DTD were 63%, 64%, respectively, showing more excellent photoinitiation activities in comparison with that of the commercial photoinitiator (2-isopropylthioxine, ITX) of 52%. DTD and DXD even achieved 75% and 71% conversion rates at lower power (10mW cm -2 ), respectively. Moreover, DXD (7%) and DTD (8%) exhibited rather lower mobility than ITX (37%) in light-curable films. Remarkably, triplet states were revealed to have an important effect on photopolymerization. The relevant mechanisms were scientifically understood by means of steady-state photolysis, fluorescence quenching, laser flash photolysis and electron spin resonance spin trapping technologies.
本文合成了基于蒽酮的给体-受体-给体型光引发剂(DXD和DTD),并将其引入到六氟二苯硫鎓(Iod)的双组分体系中,用于丙烯酸树脂单体的自由基光聚合。在光引发剂浓度为0.5 wt%、功率为20 mW cm - 2的LED@365 nm照射下,DXD、DTD引发单体的双键转化率分别为63%、64%,表现出比商用光引发剂(2-异丙基硫辛,ITX) 52%的更优异的光引发活性。DTD和DXD甚至在较低功率(10mW cm -2)下分别实现了75%和71%的转换率。此外,DXD(7%)和DTD(8%)在光固化膜中的迁移率远低于ITX(37%)。值得注意的是,三重态对光聚合有重要影响。通过稳态光解、荧光猝灭、激光闪光光解和电子自旋共振自旋捕获技术,科学地了解了相关机理。
期刊介绍:
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.