Abstract
The intramolecular Diels-Alder reactions of helicenes deform their π-conjugated screw-shaped skeletons. In particular, terminally tetrafluorinated [7]helicene (F4 -[7]helicene) undergoes a photoinduced Diels-Alder reaction followed by a photoinduced double fluorine atom transfer. Herein, we thoroughly investigated this photochemical domino process by decreasing the level of fluorine substitution. F3 -[7]Helicenes bearing two fluorine atoms at the dienophile terminal underwent photoinduced Diels-Alder reactions, but the whole domino process became slow. F2 -[7]Helicene, which is difluorinated only at the dienophile terminal, was also photolabile. As a result, two fluorine atoms were sufficient for the photochemical domino reaction to occur. X-ray crystallographic analysis revealed that F2 -[7]helicene was less compressed than F4 -[7]helicene, indicating that terminal polyfluorination enhanced the intramolecular arene-fluoroarene stacking interactions and thus promoted the transformations.
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