Abstract
We report the efficient
synthesis of electron-acceptors based on cationic P-doped PAHs (Polycyclic
Aromatic Hydrocarbons). Both
endo- and exo-skeletal modifications of the p-core
allow fine-tuning their optical and
redox properties. Combined experimental (spectrolectrochemical and Electron Paramagnetic Resonance) and theoretical studies provide an in-depth
characterization of the reduced species and specifically of the stable radical
cations formed. Finally, electrochemical modulation of
fluorescence highlights the potential of these intrinsically switchable electroactive
fluorophores.
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