Rigid molecular cylinders with a 1 nm diameter were synthesized by assembling arylene panels with Pt-mediated macrocylization. Chrysenylene panels that previously participated in tetrameric macrocyclization were contorted by the addition of two benzo groups on the sides to form dibenzochrysenylene, which allowed for a reduction in the numbers of participating panels to three. Consequently, narrowed cyclochrysenylene congeners were obtained. The narrowed chiral cylinders possessed width-dependent chiroptical properties. The magnetic transition dipole moment was dictated by the radius of a ring-current-like circle that was formed by local electric transition dipole moments on the cylinder.
Keywords: chirality; circular dichroism; cylinders; macrocycles; nanotubes.
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