Photoinduced Triplet-Triplet Energy Transfer in a 2-Ureido-4(1H)-Pyrimidinone-Bridged, Quadruply Hydrogen-Bonded Ferrocene-Fullerene Assembly

被引:26
作者
Feng, Ke [1 ]
Yu, Mao-Lin [1 ]
Wang, Su-Min [1 ]
Wang, Ge-Xia [1 ]
Tung, Chen-Ho [1 ]
Wu, Li-Zhu [1 ]
机构
[1] Chinese Acad Sci, Key Lab Photochem Convers & Optoelect Mat, Tech Inst Phys & Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
energy transfer; fullerenes; hydrogen bonds; metallocenes; self-assembly; INTRAMOLECULAR ELECTRON-TRANSFER; MODIFIED CURTIUS REACTION; CONVENIENT REAGENT; CHARGE SEPARATION; SYSTEM; DYADS; STATE; NORBORNADIENE; TRIAD; PORPHYRIN)-FULLERENE;
D O I
10.1002/cphc.201200818
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
2-Ureido-4(1H)-pyrimidinone-bridged ferrocenefullerene assembly I is designed and synthesized for elaborating the photoinduced electron-transfer processes in self-complementary quadruply hydrogen-bonded modules. Unexpectedly, steady-state and time-resolved spectroscopy reveal an inefficient electron-transfer process from the ferrocene to the singlet or triplet excited state of the fullerene, although the electron-transfer reactions are thermodynamically feasible. Instead, an effective intra-assembly triplettriplet energy-transfer process is found to be operative in assembly I with a rate constant of 9.2 x 105 s(-1) and an efficiency of 73% in CH2Cl2 at room temperature.
引用
收藏
页码:198 / 203
页数:6
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