EPR INVESTIGATION OF PHOTOINDUCED RADICAL PAIR FORMATION AND DECAY TOA TRIPLET-STATE IN A CAROTENE-PORPHYRIN-FULLERENE TRIAD

Citation
D. Carbonera et al., EPR INVESTIGATION OF PHOTOINDUCED RADICAL PAIR FORMATION AND DECAY TOA TRIPLET-STATE IN A CAROTENE-PORPHYRIN-FULLERENE TRIAD, Journal of the American Chemical Society, 120(18), 1998, pp. 4398-4405
Citations number
48
Categorie Soggetti
Chemistry
ISSN journal
00027863
Volume
120
Issue
18
Year of publication
1998
Pages
4398 - 4405
Database
ISI
SICI code
0002-7863(1998)120:18<4398:EIOPRP>2.0.ZU;2-Q
Abstract
The photochemistry of a molecular triad consisting of a porphyrin (P) covalently linked to a carotenoid polyene (C) and a fullerene derivati ve (C-60) has been studied at 20 K by time-resolved EPR spectroscopy f ollowing laser excitation. Excitation of the porphyrin moiety yields C -P-1-C-60, which decays by photoinduced electron transfer to yield C-P .+-C-60(.-). This state rapidly evolves into a final charge-separated state C.+-P-C-60(.-), whose spin-polarized EPR signal was observed and simulated. There is a weak exchange interaction between the electrons in the radical pair (J = 1.2 G). The C.+-P-C-60(.-) state decays to g ive the carotenoid triplet in high yield with a time constant of 1.2 m u s. The spin polarization of C-3-P-C-60 is characteristic of a triple t formed by charge recombination of a singlet-derived radical pair. Th e kinetics of the decay of C-3-P-C-60 to the ground state were also de termined. The photoinduced electron transfer from an excited singlet s tate at low temperature and the high yield of charge recombination to a spin-polarized triplet mimic similar processes observed in photosynt hetic reaction centers.