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
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.