“…[2] Indeed, their inherent helical chirality confers to carbo-and heterohelicenes, [3] as well as to metal containing derivatives of the latter, [4] excellent chiroptical properties, such as huge optical rotations and strong circular dichroism activity, [5] making them valuable functional precursors for applications such as nonlinear optics, [6] luminescent materials, [4b,7] or, possibly, chiral wave guides. [8] Moreover, much effort is currently devoted toward the modulation of the chiroptical properties of helicenes upon irradiation or redox processes in the case where photo- [9] or electroactive [10] units are present in their structure, yet in these both reported systems the helicenic unit is not preserved in one of the commutable states. For example, in the latter, [10] a chiroptical redox switch was achieved between dihydro[5]helicenes and dicationic binaphtyl species upon reversible breaking of a C-C bond triggered by electron transfer.…”