Charge migration in polycyclic norbornadiene cations: Winning the race against decoherence.

The observation of electronic motion remains a key target in the development of the field of attoscience. However, systems in which long-lived oscillatory charge migration may be observed must be selected carefully, particularly because it has been shown that nuclear spatial delocalization leads to a loss of coherent electron density oscillations. Here we demonstrate electron dynamics in norbornadiene and extended systems where the hole density migrates between two identical chromophores. By studying the effect of nuclear motion and delocalization in these example systems, we present the physical properties that must be considered in candidate molecules in which to observe electron dynamics. Furthermore, we also show a key contribution to nuclear delocalization arises from motion in the branching plane of the cation. For the systems studied, the dephasing time increases with system size while the energy gap between states, and therefore the frequency of the density oscillation, decreases with size (obeying a simple exponential dependence on the inter-chromophore distance). We present a system that balances these two effects and shows several complete oscillations in the spin density before dephasing occurs.