Diffusion-controlled rates of formation were found from the temperature dependence of apparent quenching rate constants for exciplexes, when the driving force of excited-state electron transfer -0.1 < deltaG(ET)* < +0.1 eV. This is inconsistent with the conventional mechanism of electron-transfer reactions, involving preliminary reorganisation of the medium and reactants, and provides strong support for the mechanism of medium reorganisation stimulated by strong electronic coupling of locally excited and charge-transfer states.

Exciplex emission spectra and rate constants of their decay via internal conversion and intersystem crossing are studied and discussed in terms of conventional radiationless transition approach. Exciplexes of 9-cyanophenanthrene with 1,2,3-trimethoxybenzene and 1,3,5-trimethoxybenzene were studied in heptane, toluene, butyl acetate, dichloromethane, butyronitrile, and acetonitrile. A better description of spectra and rate constants is obtained using 0-0 transition energy and Gauss broadening of vibrational bands rather than the free energy of electron transfer and reorganization energy. The coincidence of parameters describing exciplex emission spectra and dependence of exciplex decay rate constants on energy gap gives the evidence of radiationless quantum transition mechanism rather than thermally activated medium reorganization mechanism of charge recombination in exciplexes and excited charge transfer complexes (contact radical ion pairs) as well as in solvent separated radical ion pairs. Radiationless quantum transition mechanism is shown to provide an appropriate description also for the main features of exergonic excited-state charge separation reactions if fast mutual transformations of loose and tight pairs of reactants are considered. In particular, very fast electron transfer (ET) in tight pairs of reactants with strong electronic coupling of locally excited and charge transfer states can prevent the observation of an inverted region in bimolecular excited-state charge separation even for highly exergonic reactions.

Specific features of ultrafast photoinduced electron transfer (ET) in concentrated liquid solutions and in neat electron donating solvents are discussed in terms of continuous distribution of ET rate constants, related to electron tunneling with statistical distribution of electronic coupling matrix element and distances between reactant molecules. Available data on photoinduced electron transfer in solutions for several systems are analyzed. Electron tunneling approach is shown to provide global description of nonexponential kinetics of excited states decay at various concentrations of reactant and in neat solvents.

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