PULSED-EPR ON THE PHOTOEXCITED TRIPLET-STATE OF C60 IN FLUID SOLUTION- ELECTRON-TRANSFER FROM END-CAPPED QUATERTHIOPHENE AND C60-RADICAL ANION FORMATION
M. Bennati et al., PULSED-EPR ON THE PHOTOEXCITED TRIPLET-STATE OF C60 IN FLUID SOLUTION- ELECTRON-TRANSFER FROM END-CAPPED QUATERTHIOPHENE AND C60-RADICAL ANION FORMATION, Chemical physics, 185(2), 1994, pp. 221-227
The photoexcited triplet state of C60 in fluid toluene solution was in
vestigated by pulsed-EPR spectroscopy in a temperature range T = 200-3
00 K. The time evolution of the triplet EPR signal is found to be dete
rmined by the spin-lattice relaxation time T1 and the triplet decay. I
n the presence of the electron donor end-capped quaterthiophene the C6
0-triplet decay is quenched by electron transfer reaction. The tempera
ture dependence of the triplet quenching rate k(q) suggests the format
ion of an exciplex intermediate. Moreover we observe the formation of
the C60-radical anion following electron transfer. The kinetics and po
larization of the C60- EPR signal are discussed.