Artificial light-harvesting system with sequential energy transfer in photocatalytic C-P coupling based on supramolecular organic framework of triphenylamine

被引:0
作者
Yang, Xuan-Zong [1 ]
Zhang, Zhao-Gao [2 ]
Xin, Cheng-Long [3 ]
Liu, Hui [1 ]
Yu, Shengsheng [1 ]
Xing, Ling-Bao [1 ]
机构
[1] Shandong Univ Technol, Sch Chem & Chem Engn, Zibo 255000, Peoples R China
[2] Jiangsu Weunite Fine Chem Co Ltd, Xuzhou 221424, Peoples R China
[3] Shandong Ctr Dis Control & Prevent, Jinan 255014, Peoples R China
基金
中国国家自然科学基金;
关键词
Supramolecular organic framework; Light-harvesting systems; Sequential energy transfer; Photocatalysis; C-P bond coupling; PHOTOSYNTHESIS; CAGES;
D O I
10.1016/j.jcis.2024.11.028
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Porous structures exhibit an increased access surface area, thereby promoting the efficient transportation of active oxygen species. Reinforcing the development of artificial light-harvesting systems (LHSs) with porous structured supramolecular organic frameworks (SOFs) as the energy donor can significantly enhance its photocatalytic performance, thereby facilitating efficient organic transformation via photocatalysis. In this investigation, we have successfully fabricated a supramolecular organic framework (MT-SOF) composed of cucurbit[8] uril (CB[8]) and triphenylamine derivative (MeTPPA). Because of the framework structure and large ring restriction in MT-SOF, its fluorescence emission shows a significant increase when compared to that of the individual MeTPPA molecule. By harnessing the remarkable fluorescence emission characteristics of MT-SOF, it was employed as an energy donor in conjunction with Sulforhodamine 101 (SR101) and Cyanine 5 (Cy5) as acceptors to fabricate sequential energy transfer LHS. MT-SOF-SR101-Cy5 has the ability to act as a photosensitizer, facilitating the C-P bond coupling with broad applicability. It is important to mention that when compared to MeTPPA, MT-SOF and MT-SOF-SR101, the photocatalytic performance of MT-SOF-SR101-Cy5, featuring
引用
收藏
页码:587 / 595
页数:9
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