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

Author:

Yamanaka Ken-ichi12,Fujitsuka Mamoru2,Araki Yasuyuki2,Tashiro Kentaro3,Sato Azumi3,Yuzawa Tetsuro3,Aida Takuzo34

Affiliation:

1. Toyota Central R & D Laboratories, Inc., Nagakute, Aichi 480-1192, Japan

2. Institute of Multidisciplinary Research for Advanced Materials, Tohoku University, 2-1-1 Katahira, Sendai 980-8577, Japan

3. Department of Chemistry and Biotechnology, School of Engineering, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8656, Japan

4. ERATO Nanospace Project, Japan Science and Technology Corporation, 2-41 Aomi, Koto-ku, Tokyo 135-0064, Japan

Abstract

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 fluorescence lifetime and transient absorption measurements revealed that photoinduced charge-separation takes place via the excited singlet state (1 ZnP *) with the rate constant of (1-2) × 1010 s −1. For the charge recombination, about a half of the radical-ion pair decayed quickly with 2.9 × 109 s −1 as evaluated from picosecond transient absorption measurements, whereas the remaining half was long-lived with slow decay (1.6 × 106 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.

Publisher

World Scientific Pub Co Pte Lt

Subject

General Chemistry

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