Effects of electronic coherence transfer after photoexcitation of excitonic complexes and their manifestation in optical spectroscopy are discussed. Temperature dependence of the absorption band maximum of a simple excitonic dimer is interpreted in terms of coherence transfer between two excited states. The role of reorganization energy of the transitions in the magnitude of the effect is discussed.
A large reorganization energy difference between the two states is found to induce significant band shift. As an example of a time-dependent spectroscopic method sensitive to coherences and possibly to their transfer, we present recent two-dimensional photon echo measurements of energy relaxation in the so-called Fenna-Matthews-Olson complex of Chlorobium tepidum, where distinct oscillatory patters predicted to be signatures of electronic coherence have been observed.