Abstract
Triarylamine-perchlorotriphenylmethyl radicals (TARA-PCTM) may be viewed as open-shell mixed valence donor−acceptor compounds that exhibit strong charge-transfer (CT) bands in the visible to NIR spectral region. While open-shell molecules generally do not fluoresce at RT, we observed a surprisingly strong fluorescence from the highly polar excited CT state of the TARA-PCTM radicals in the visible and NIR spectral region. The fluorescence quantum yield is enhanced by a factor of up to 150 compared to the unsubstituted perchlorotriphenylmethyl radical. The enhancement depends on the donor strength of the TARA moiety which was tuned by small substituents (OMe, Me, Cl, CN, and NO2) attached to the phenyl groups, thus forming a series of donor−acceptor species that mainly differ by the free energy difference of the excited CT state and the ground state. The reorganization parameters of the CT process were extracted by Bixon−Jortner fits to either the absorption or the fluorescence bands. The dynamics of the no...
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