Lemniscular carbon nanohoops with contiguous conjugation from planar chiral [2.2]paracyclophane: influence of the regioselective synthesis on topological chirality

We report herein the regioselective synthesis of all-carbon lemniscular nanohoops bis-po -CC and bis-pm -TC by the rational control of ring closures at the different positions of planar chiral tetrasubstituted [2.2]paracyclophane. Topological analyses reveal that bis-pm -TC is topologically chiral while bis-po -CC is topologically achiral. X-ray crystal analysis demonstrates that bis-pm -TC adopts a lemniscular conformation with a contiguous conjugation. CD and CPL measurements further reveal that the chiroptical properties of bis-pm -TC are obviously different from those of bis-po -CC due to their different topological chiralities. We report herein two lemniscular carbon nanohoops bis-po -CC and bis-pm -TC with contiguous conjugation from planar chiral [2.2]paracyclophane, and elucidate the influence of the regioselective synthesis on their topological chirality.