Amplification of Dissymmetry Factors in π-Extended [7]- and [9]Helicenes

π-Extended helicenes constitute an important class of polycyclic aromatic hydrocarbons with intrinsic chirality. Herein, we report the syntheses of π-extended [7]helicene <b>4</b> and π-extended [9]helicene <b>6</b> through regioselective cyclodehydrogenation in high yields, where a "prefusion" strategy plays a key role in preventing undesirable aryl rearrangements. The unique helical structures are unambiguously confirmed by X-ray crystal structure analysis. Compared to the parent pristine [7]helicene and [9]helicene, these novel π-extended helicenes display significantly improved photophysical properties, with a quantum yield of 0.41 for <b>6</b>. After optical resolution by chiral high-performance liquid chromatography, the chiroptical properties of enantiomers <b>4</b>-<i>P</i>/<i>M</i> and <b>6</b>-<i>P</i>/<i>M</i> are investigated, revealing that the small variation in helical length from [7] to [9] can cause an approximately 10-fold increase in the dissymmetry factors. The circularly polarized luminescence brightness of <b>6</b> reaches 12.6 M^-1 cm^-1 as one of the highest among carbohelicenes.