Face-to-face pacman-type porphyrin-fullerene dyads: design, synthesis, charge-transfer interactions, and photophysical studies

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Authors
D'Souza, Francis
Maligaspe, Eranda
Karr, Paul A.
Schumacher, Amy Lea
El Ojaimi, Maya
Gros, Claude P.
Barbe, Jean-Michel
Ohkubo, Kei
Fukuzumi, Shunichi
Issue Date
2008-01-01
Type
Article
Language
eng
Keywords
Research Support, Non-U.S. Gov't
Research Projects
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Abstract

Pacman-type face-to-face zinc-porphyrin-fullerene dyads have been newly synthesized and studied. Owing to the close proximity of the donor and acceptor entities, strong pi-pi intramolecular interactions between the porphyrin and fullerene entities resulted in modulating the spectral and electrochemical properties of the dyads. New absorption and emission bands that correspond to the charge-transfer interactions were observed in the near-IR region. Time-resolved transient absorption studies revealed efficient photoinduced electron transfer from the singlet excited porphyrin to the fullerene entity. The rate constants for photoinduced electron transfer are analyzed in terms of the Marcus theory of electron transfer, which afforded a large electron coupling matrix element (V=140 cm(-1)) for the face-to-face dyads. As a consequence of the large charge-recombination driving force in the Marcus inverted region, a relatively long lifetime of the charge-separated state has been achieved.

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Citation
Chemistry (Weinheim an der Bergstrasse, Germany). 2008; 14(2): 674-81.
Publisher
John Wiley and Sons
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ISSN
0947-6539
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