Liu Xin, Hu Zhitao, Portela Brandon S, Rettner Emma M, Pineda Agustin, Miscall Joel, Rorrer Nicholas A, Krummel Amber T, Paton Robert S, Miyake Garret M
Department of Chemistry, Colorado State University, Center Ave, Fort Collins, CO 80523, United States.
School of Materials Science and Engineering, Colorado State University, Fort Collins, CO 80523, United States.
Angew Chem Int Ed Engl. 2025 Jan 27;64(5):e202418411. doi: 10.1002/anie.202418411. Epub 2024 Nov 21.
Herein, we report a selective photooxidation of commodity postconsumer polyolefins to produce polymers with in-chain ketones. The reaction does not involve the use of catalyst, metals, or expensive oxidants, and selectively introduces ketone functional groups. Under mild and operationally simple conditions, yields up to 1.23 mol % of in-chain ketones were achieved. Installation of in-chain ketones resulted in materials with improved adhesion of the materials and miscibility of mixed plastics relative to the unfunctionalized plastics. The introduction of ketone groups into the polymer backbone allows these materials to react with diamines, forming dynamic covalent polyolefin networks. This strategy allows for the upcycling of mixed plastic waste into reprocessable materials with enhanced performance properties compared to polyolefin blends. Mechanistic studies support the involvement of photoexcited nitroaromatics in consecutive hydrogen and oxygen atom transfer reactions.
在此,我们报道了一种将消费后商品聚烯烃选择性光氧化以生产含链内酮聚合物的方法。该反应不涉及使用催化剂、金属或昂贵的氧化剂,并且能选择性地引入酮官能团。在温和且操作简单的条件下,链内酮的产率高达1.23 mol %。相对于未官能化的塑料,链内酮的引入使材料具有更好的材料附着力和混合塑料的混溶性。将酮基引入聚合物主链使这些材料能够与二胺反应,形成动态共价聚烯烃网络。这种策略能够将混合塑料废料升级循环为与聚烯烃共混物相比具有增强性能的可再加工材料。机理研究支持光激发的硝基芳烃参与连续的氢和氧原子转移反应。