Kubota Koji, Toyoshima Naoki, Miura Daiyo, Jiang Julong, Maeda Satoshi, Jin Mingoo, Ito Hajime
Division of Applied Chemistry, Graduate School of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Institute for Chemical Reaction Design and Discovery (WPI-ICReDD), Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Angew Chem Int Ed Engl. 2021 Jul 12;60(29):16003-16008. doi: 10.1002/anie.202105381. Epub 2021 Jun 9.
Herein, we report a novel strategy for introducing a luminophore into generic polymers facilitated by mechanical stimulation. In this study, polymeric mechanoradicals were formed in situ under ball-milling conditions to undergo radical-radical coupling with a prefluorescent nitroxide-based reagent in order to incorporate a luminophore into the polymer main chains via a covalent bond. This method allowed the direct and conceptually simple preparation of luminescent polymeric materials from a wide range of generic polymers such as polystyrene, polymethyl methacrylate, and polyethylene. These results indicate that the present mechanoradical coupling strategy may help to transform existing commodity polymers into more valuable functional materials.
在此,我们报道了一种通过机械刺激将发光团引入通用聚合物的新策略。在本研究中,聚合物机械自由基在球磨条件下原位形成,与基于预荧光氮氧化物的试剂进行自由基-自由基偶联,以便通过共价键将发光团引入聚合物主链。该方法允许从多种通用聚合物(如聚苯乙烯、聚甲基丙烯酸甲酯和聚乙烯)直接且概念上简单地制备发光聚合物材料。这些结果表明,目前的机械自由基偶联策略可能有助于将现有的商品聚合物转化为更有价值的功能材料。