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Abstract: Three new tetraphenylethylene based oligomers bearing triphenylethylene moiety were synthesized utilizing Suzuki coupling reaction and their aggregation-induced emission properties were studied. They show excellent solubility in common organic solvents and emit light in blue region (440−504nm). AIE effect is predominant for tetra-substituted TPE (20.1-fold) than mono-substituted one (4.5-fold). [Copyright &y& Elsevier]

Abstract: A new series of V-shaped pyridine-cored π-conjugated oligomers are synthesized utilizing two-fold Heck/Suzuki coupling reactions. Optical properties of these compounds (λ max=390–449 nm, Φ fl=79–5%, in solutions) are discussed. They are shown to be thermally stable and soluble in common organic solvents. Stilbenoid oligomers exhibited much higher fluorescence quantum yields than tri- and tetra-phenylethylene substituted oligomers in solutions. [Copyright &y& Elsevier]

Abstract: Two novel star-shaped π-conjugated oligomers bearing a triphenylpyridine moiety as peripheral units and triphenylamine as a core have been synthesized via the threefold Heck/Sonogoshira coupling reaction protocol and their absorption and fluorescence properties have been examined. These oligomers showed excellent solubility in common organic solvents, emit light in blue and violet regions, and have high thermal stability. [Copyright &y& Elsevier]

Abstract: Two new conjugated dendrimers bearing a tetraphenylethylene moiety as dendrons and triphenylamine as a core have been synthesized through a convergent synthetic strategy using threefold Heck/threefold Sonogashira coupling reaction. These dendrimers showed excellent solubility in common organic solvents and emit light in the blue and violet regions. [Copyright &y& Elsevier]