Roger, Maxime; Amro, Kassem; Rault-Berthelot, Joelle; Quiot, Mathias; Van der Lee, Arie; Poriel, Cyril; Richeter, Sebastien; Clement, Sebastien; Gerbier, Philippe published the artcile< Synthesis, photophysical and electropolymerization properties of thiophene-substituted 2,3-diphenylbuta-1,3-dienes>, Application In Synthesis of 3480-11-3, the main research area is thiophene diphenylbutadiene synthesis photophys electropolymerization property.
A series of 2,3-diphenylbuta-1,3-dienes (DPBs) bearing thiophene (T-DPB), bithiophene (BT-DPB) and ethylenedioxythiophene (EDOT-DPB) electropolymerizable units were prepared through desilylation reactions of the corresponding 3,4-diphenylsilole derivatives These DPB derivatives exhibit remarkably different aggregation induced emission (AIE) or aggregation enhanced emission (AEE) behavior depending on the strength of the mol. interactions occurring in the solid state. Indeed, T-DPB and EDOT-DPB were found to be good AIEgens while BT-DPB exhibited AEE behavior. Finally, the electrochem. properties of these new materials were investigated revealing for all DPBs the occurrence of electropolymerization processes leading potentially to low band gap polymers.
New Journal of Chemistry published new progress about Aggregation-induced emission. 3480-11-3 belongs to class bromides-buliding-blocks, and the molecular formula is C8H5BrS2, Application In Synthesis of 3480-11-3.
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary