| Abstract: | 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. |
