Ultrafast Energy Transfer Dynamics in a Squaraine Heterotriad.

ABSTRACT

A squaraine heterotriad consisting of three different covalently linked squaraine chromophores was synthesized, and its absorption spectra were interpreted in terms of Kasha's exciton coupling theory. Using the exciton couplings derived from model dyads (ca. 700 cm-1) as the input, we were able to predict the exciton state energies of the heterotriad. Transient absorption spectroscopy with femtosecond time resolution showed that excitation of the highest exciton state populates a state mainly localized at one terminal squaraine chromophore, and energy transfer to the lowest exciton state localized at the other terminal squaraine occurs within 30 fs. Field-induced surface hopping dynamics simulations support the assumption of ultrafast energy transfer. Moreover, they show the close relationship between internal conversion and energy transfer in the intermediate to weak coupling regime. The latter is a consequence of excitation localization caused by molecular vibrations.