G. Elger et al., MODELS FOR PHOTOSYNTHESIS - EPR STUDIES OF CYCLOHEXYLENE-LINKED PORPHYRIN QUINONES, Acta chemica Scandinavica, 51(5), 1997, pp. 593-601
Time-resolved EPR spectra are reported for photoexcited cyclohexylene
bridged porphyrin-quinone diads and porphyrin-quinone-quinone triads i
n isotropic solutions and in the soft glass phase of liquid crystals.
Spin-polarized EPR spectra were observed for the charge-separated bira
dical states. The EPR polarization patterns are discussed in terms of
the favored decay channel of the photoexcited singlet state of the por
phyrin donor. The decay pathway may either be singlet electron transfe
r to the quinone(s) followed by singlet-triplet mixing to yield radica
l pairs (RP) with triplet character or, more likely, triplet electron
transfer after spin-orbit intersystem crossing, or a superposition of
both pathways. Using liquid crystals, information about the orientatio
n of the guest molecules in the liquid crystal matrix with respect to
the long axes of the liquid crystal molecules can be obtained. High fi
eld/high frequency (3.4 T, 95 GHz) EPR spectra of the transient porphy
rin-quinone RP state are reported for the first time. By comparing the
EPR measurements at different Zeeman fields, additional information a
bout the polarization mechanism can be obtained.