Luo Xiongfei, Wan Jianyong, Meckbach Nicolai, Strehmel Veronika, Li Shujun, Chen Zhijun, Strehmel Bernd
Northeast Forestry University, Key Laboratory of Bio-based Material Science and Technology of Ministry of Education, Hexing Road 26, 150040, Harbin, China.
Department of Chemistry, Institute for Coatings and Surface Chemistry, Niederrhein University of Applied Sciences, Adlerstr. 1, 47798, Krefeld, Germany.
Angew Chem Int Ed Engl. 2022 Oct 4;61(40):e202208180. doi: 10.1002/anie.202208180. Epub 2022 Sep 1.
Sustainable carbon dots (CDs) based on furfuraldehyde (F-CD) resulted in a photosensitive material after pursuing the Alder-Longo reaction. The porphyrin moiety formed connects the F-CDs in a covalent organic network. This heterogeneous material (P-CD) was characterized by XPS indicating incorporation of the respective C, N and O moieties. Time resolved fluorescence including global analysis showed contribution of three linked components to the overall dynamics of the excited state. Electrochemical and photonic properties of this heterogeneous material facilitated photopolymerization in a photo-ATRP setup where either CuBr /TPMA, FeBr /Br or a metal free reaction setup activated controlled polymerization. Chain extension experiments worked in all three cases showing end group fidelity for activation of controlled block copolymerization using MMA and styrene as monomers. Traditional radical polymerization using a diaryl iodonium salt as co-initiator failed.
基于糠醛的可持续碳点(F-CD)在进行阿尔德-隆戈反应后生成了一种光敏材料。形成的卟啉部分在共价有机网络中连接F-CD。这种异质材料(P-CD)通过X射线光电子能谱(XPS)表征,表明各自的碳、氮和氧部分已掺入。包括全局分析在内的时间分辨荧光显示,三个相连的组分对激发态的整体动力学有贡献。这种异质材料的电化学和光子性质促进了在光原子转移自由基聚合(photo-ATRP)装置中的光聚合反应,其中使用CuBr/TPMA、FeBr/Br或无金属反应装置激活可控聚合。在所有三种情况下,链延伸实验均有效,表明使用甲基丙烯酸甲酯(MMA)和苯乙烯作为单体激活可控嵌段共聚时端基具有保真度。使用二芳基碘鎓盐作为共引发剂的传统自由基聚合失败。