Synthesis of [2.2]Paracyclophane/9-Alkylfluorene Hybrids and the Discovery of a Solvent-assisted Rearrangement.

Work on the synthesis of [2.2]paracyclophane/9-alkylfluorene hybrids led to the discovery of the rearrangement of cyclopentadienone 7 to cyclophane 6. A DFT computational study revealed that this formal 1,3-alkyl shift occurs in two steps, but requires the participation of a solvent molecule (ethanol). The rearrangement could be avoided by generating 7 under mild conditions and using benzynes as dienophiles to afford the targeted cyclophanes 14 and 16, the latter of which exhibits dual fluorescence emission.