Simple inorganic base promoted C-N and C-C formation: synthesis of benzo[4,5]imidazo[1,2-]pyridines as functional AIEgens used for detecting picric acid

Metal-free catalyzed intermolecular tandem Michael addition/cyclization has been developed for the synthesis of benzo[4,5]imidazo[1,2- a ]pyridines from α-bromocinnamaldehyde and 2-substituted benzimidazoles. The reaction promoted by a simple inorganic base displays moderate to good yields and good functional group tolerance. The optical properties of some typical products have been investigated. We found that, due to the presence of the benzene ring at the C1-position of benzo[4,5]imidazo[1,2- a ]pyridines which restricts intramolecular motion, as a new type of aggregation-induced emission (AIE) luminogen (AIEgen), they show very good solid-state fluorescence with quantum yields up to 88.80%. Importantly, the AIE performance of compound 3b can be useful to detect the nitroaromatic explosive picric acid (PA) with a detection limit and quenching constant of 42.5 nM and 7.27 × 10 4 M −M , respectively. Metal-free catalyzed intermolecular tandem Michael addition/cyclization is developed for the synthesis of benzo[4,5]imidazo[1,2- a ]pyridines from α-bromocinnamaldehyde. The RIM of the benzene ring at the C1-position makes them a new class of AIE molecules.