Cation‐Stacking Approach Enabling Interconversion between Bis(xanthylium) and its Reduced Species

Abstract

AbstractCyclophane‐type dications with two units of xanthylium were designed, with the expectation that intramolecular interaction between cation units could induce changes in absorption and redox behavior. The desired dications were synthesized via the macrocyclic diketone as a key intermediate, which was efficiently obtained by a stepwise etherification. X‐ray and UV/Vis measurements revealed that the cyclophane‐type dications adopt a stacking structure in both the crystal and solution. Due to the intramolecular interaction caused by π–π stacking of the xanthylium units, a considerable blue shift compared to the corresponding monocations and a two‐stage one‐electron reduction process were observed in the dications. Furthermore, upon electrochemical reduction of dications, the formation of biradicals via radical cation species was demonstrated by UV/Vis spectroscopy with several isosbestic points at both stages. Therefore, the cation‐stacking approach is a promising way to provide novel properties due to perturbation of their molecular orbitals and to stabilize the reduced species even though they have open‐shell characters.