丙烯酸酯
自由基聚合
高分子化学
光致聚合物
3D打印
化学
光引发剂
聚合
光化学
材料科学
动力学
本体聚合
激进的
丙烯酸酯聚合物
钴介导的自由基聚合
活性自由基聚合
聚合物
可逆加成-断裂链转移聚合
自由基反应
咔唑
反应机理
作者
Chenzhi Yao,Qike Sun,Hui Deng,Gongyang Chen,Heng Xia,Zhengjiang Liu,Timur Borjigin,Jiansong Yin,Jacques Lalevée,Yangyang Xu
出处
期刊:Macromolecules
[American Chemical Society]
日期:2026-01-28
卷期号:59 (3): 1145-1155
标识
DOI:10.1021/acs.macromol.5c02921
摘要
Photoinduced radical chemistry is pivotal for synthesizing polymeric materials under light irradiation. In this study, carbazole moieties were incorporated at distinct positions within the aza-boron-dipyrromethene (aza-BODIPY) scaffold, yielding three novel push–pull dyes that function as high-performance photoinitiators for the free radical polymerization of acrylates upon exposure to visible-light LED irradiation. When combined with iodonium salts or amines as co-initiators, these aza-BODIPY derivatives form efficient two-component photoinitiating systems that exhibit outstanding initiation performance. Notably, distinct polymerization kinetics were observed for two benchmark acrylate monomers. Through a combination of experimental investigations and theoretical calculations, a comprehensive photochemical mechanism has been elucidated. Furthermore, these newly developed carbazole-substituted aza-BODIPY-based photoinitiating systems enable the fabrication of high-resolution three-dimensional macroscale architectures via 3D printing. This work advances the fundamental understanding and practical application of visible-light-induced free radical polymerization.
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