Solvent, isotope, and magnetic field effects in the geminate recombination of radical ion pairs

Publisher Website
Google Scholar
Abstract
The magnetic field dependence of the geminate recombination triplet yield of radical ion pairs generated via photoinduced electron transfer in polar solvents is investigated for the systems pyrene/N,N‐dimethylaniline (Py/DMA), pyrene/3,5‐dimethoxy‐N,N‐dimethylaniline (Py/DMDMA), and the perdeuterated system Py‐d10/DMA‐d11. The magnetic field dependence characterized through its B1/2 value is found to be dependent on the sum of the hyperfine coupling constants in the radical pair in agreement with previous theoretical predictions. A drastic reduction of the B1/2 value is observed with the perdeuterated system. By means of measurements of the radical ion and triplet absorption signals with nanosecond time resolution, the influence of the solvent on the geminate singlet and triplet recombination yields is investigated. Complementary measurements of exciplex lifetimes and quantum yields are carried out in a series of solvents with different polarities in order to determine the rate constants of fluorescence emission and intersystem crossing in the exciplexes.