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作 者:Jingxuan Yang Run Shi Liang-Liang Mao Hongyan Xiao Yi Zeng Guohong Liao Yuxiang Weng Xu-Bing Li Jiaqi Zhao Yunxuan Zhao Tierui Zhang Chen-Ho Tung Li-Zhu Wu Huan Cong
机构地区:[1]Key Laboratory of Photochemical Conversion and Optoelectronic Materials,Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Beijing 100190 [2]Key Laboratory of Bio-Inspired Materials and Interfacial Science,Technical Institute of Physics and Chemistry,Chinese Academy of Sciences,Beijing 100190 [3]Beijing National Laboratory for Condensed Matter Physics,Laboratory of Soft Matter Physics,Institute of Physics,Chinese Academy of Sciences,Beijing 100190 [4]University of Chinese Academy of Sciences,Beijing 100049 [5]Binzhou Institute of Technology,Weiqiao-UCAS Science and Technology Park,Binzhou City,Shandong 256606 [6]Songshan Lake Materials Laboratory,Dongguan,Guangdong 523808
出 处:《CCS Chemistry》2024年第8期1920-1928,共9页中国化学会会刊(英文)
基 金:supported by Beijing Natural Science Foundation(grant no.2234089);the National Natural Science Foundation of China(grant nos.92356307,21922113,22088102,21988102,and 22071257);the National Key Research and Development Program of China(grant no.2022YFA1207600);the Strategic Priority Research Program of Chinese Academy of Sciences(grant no.XDB33000000);TIPC Director’s Fund.
摘 要:Designing and creating molecular structures with precisely organized organic chromophores as donors and acceptors are critical for exploring photo-induced charge transfer properties.Donor and acceptor moieties can be incorporated to the confined skeletons of organic cages,thereby offering opportunities tomanipulate excited state characters for the development of novel photofunctional molecules.Herein,we present the convergent synthesis and photophysical characterizations of an organic cage with anisotropic skeleton.The strained and rigid cage can be concisely prepared by connecting two distinct macrocycles through axial stacking strategy,featuring triarylamine and amide moieties as separate donors and acceptors,respectively.Steady-state and time-resolved spectra reveal photo-induced through-space intramolecular charge transfer and long-lived charge separation,thereby verifying the cage’s photocatalytic utility for efficient hydrogen production.
关 键 词:organic cage macrocycles photoinduced charge transfer THROUGH-SPACE photocatalytic hydrogen evolution
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