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

Cyclophane-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.

Bis(triarylmethylium)-type Macrocyclic Dications: Mechanochromic Emission Extending to the Red Region.

Macrocyclic dications 2 composed of two triarylmethylium units were designed and synthesized. In contrast to the reference monocations 1 , macrocyclic dications 2 exhibited mechanochromic emission extending to the red region (-900 nm), since the luminescence color in a solid state can reversibly change due to their constrained structures granted by alkylene linkers and the choice of a proper counterion. X-ray diffraction and spectroscopic analyses revealed that such mechanochromic behavior was induced by the crystal-to-amorphous transition.