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https://doi.org/10.1039/d4sc01042f
Copy DOIJournal: Chemical science | Publication Date: Jan 1, 2024 |
License type: CC BY-NC 3.0 |
Macrocyclic molecules have characteristic properties different from linear ones, such as high symmetry and guest-inclusion ability. To bring drastic changes to these properties, direct introduction of many substituents is a challenging but effective tool. Herein, we attain direct installation of ten six-membered-ring aromatic π-units into both rims of a pillar[5]arene. In contrast to previous pillar[n]arenes with less hindered five-membered-ring units, which showed conformational complexity and crushed crystal structures, the per-phenyl-substituted pillar[5]arene has a cylinder-shaped crystal structure with a dichloromethane inside the cavity and is obtained as a single pair of D 5-symmetric enantiomers. The average dihedral angles between the core and peripheral benzene rings sharply increase from 38° to 66°. These differences indicate the importance of local steric repulsion on both rims for determining the structures and properties of macrocycles.
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