Intramolecular photoinduced electron-transfer processes in buta-1,3-diynyl-benzene-linked porphyrin-fullerene dyad

被引:15
|
作者
Yamanaka, Ken-ichi [1 ]
Fujitsuka, Mamoru
Araki, Yasuyuki
Tashiro, Kentaro
Sato, Azumi
Yuzawa, Tetsuro
Aida, Takuzo
机构
[1] Toyota Cent Res & Dev Labs Inc, Nagakute, Aichi 4801192, Japan
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Sendai, Miyagi 9808577, Japan
[3] Univ Tokyo, Sch Engn, Dept Chem & Biotechnol, Bunkyo Ku, Tokyo 1138656, Japan
[4] Japan Sci & Technol Corp, ERATO, Nanospace Project, Koto Ku, Tokyo 1350064, Japan
关键词
photoinduced electron transfer; zinc porphyrin; fullerene; bridge;
D O I
10.1142/S108842460700045X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Intramolecular electron-transfer process of porphyrin-fullerene dyad linked by phenyl buta-1,3-diynyl-phenyl unit (ZnP-sp-C-60) was studied by laser flash photolysis. Picosecond fluores- cence lifetime And transient absorption measurements revealed that photoinduced charge-separation takes place via the excited singlet state ('ZnP*) with the rate constant of (1-2) x 10(10) s(-1). For the charge recombination, about a half of the radical-ion pair decayed quickly with 2.9 x 10(9) s(-1) as evaluated from picosecond transient absorption measurements, whereas the remaining half was long-lived with slow 106 decay (1.6 x 10(6)s(-1)) as estimated from nanosecond transient absorption measurements. The lifetime of the radical-ion pair of ZnP-SP-C-60 was longer than those of directly connected dyads with a buta- 1,3-diynyl bridge and buta- 1,3-diynyl-phenyl bridge by the insertion of an extra phenyl group in addition to the pyrrodino ring. Copyright (C) 2007 Society of Porphyrins & Phthalocyanines.
引用
收藏
页码:397 / 405
页数:9
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