Solvent tuning from normal to inverted marcus region of intramolecular electron transfer in ferrocene-based organic radicals.

The solvent dependence of spectroscopic data of two neutral paramagnetic donor-acceptor dyads, based on a polychlorinated triphenylmethyl radical acceptor unit linked through a vinylene pi-bridge to a ferrocene (compound 1) or a nonamethylferrocene donor (compound 2) unit, is described. Both compounds exhibit broad absorptions in the near-IR region, with band maxima appearing around 1000 and 1500 nm for 1 and 2, respectively. These bands correspond to the excitation of a neutral DA ground state to the charge-separated D+A- state, indicative of an intramolecular electron-transfer process. Compounds 1 and 2 show two reversible one-electron redox processes associated with the oxidation of the ferrocene and the reduction of the polychlorotriphenylmethyl radical subunits. The solvent dependence of the redox potentials was also investigated, allowing the determination of the redox asymmetries DeltaG degrees of both dyads. The latter values, along with the experimental Eopt spectroscopic data, allow us to estimate, using the total energy balance Eopt = lambda + DeltaG degrees , the reorganization energy values, lambda, and their solvent polarity dependence. Since DeltaG degrees and lambda are of the same order of magnitude but exhibit opposite trends in their solvent polarity dependence, a unique shift from the normal to the inverted Marcus region with the change in solvent polarity is found. The kinetics of the charge recombination step of the excited charge-separated D+A- state was studied by picosecond transient absorption spectroscopy, which allows us to observe and monitor for the first time the charge-separated D+A- state, thereby confirming unambiguously the photoinduced electron-transfer phenomena.