278176-07-1

Novel bolaamphiphiles containing two α-cyanostilbene units interconnected with 2,7-substituted-9,9-dialkylated fluorene as the central core and a diol unit at each terminal have been synthesized efficiently by a palladium catalyzed Suzuki coupling reaction and the Knoevenagel condensation reaction as key steps. POM, DSC and XRD investigation reveals that these compounds can organize into single wall triangular honeycomb columnar phases. A unique packing model was established in which the twisted π-conjugated backbones stacked alternatively into the walls and were connected through the end diol groups to form a triangular honeycomb, and the almost perpendicularly distributed alkyl side chains filled the cells. Such packing was additionally stabilized by the local anti-parallel dipole interactions of α-cyanostilbene and the H-bonding between CN?H. These compounds showed the AIEE effect and emitted yellow luminescence which could be further utilized to generate white light emission by coating on a commercially available blue LED lamp. Additionally, light-emitting liquid crystal display (LE-LCD) device could be obtained by dissolution of such AIE active distinctive luminogens in commercially available nematic LCs.

A new and efficient synthetic approach for the one-pot construction of benzofluorene fused aromatic hydrocarbons was developed via a transient-directing group strategy. The palladium-catalyzed cascade reaction proceeded via consecutive arylation, cyclization and aromatization steps. Moderate to good yields along with broad functional group tolerance were achieved under mild reaction conditions.