Zuolun Zhang, Robert M Edkins, Jörn Nitsch, Katharina Fucke, Antonius Eichhorn, Andreas Steffen, Yue Wang, Todd B Marder
The push-pull character of a series of donor-bithienyl-acceptor compounds has been tuned by adopting triphenylamine or 1,1,7,7-tetramethyljulolidine as a donor and B(2,6-Me2 -4-RC6 H2)2 (R=Me, C6 F5 or 3,5-(CF3)2 C6 H3) or B[2,4,6-(CF3 )3 C6 H2]2 as an acceptor. Ir-catalyzed C-H borylation was utilized in the derivatization of the boryl acceptors and the tetramethyljulolidine donor. The donor and acceptor strengths were evaluated by electrochemical and photophysical measurements. In solution, the compound with the strongest acceptor, B[2,4,6-(CF3)3 C6 H2]2 ((FMes)2 B), has strongly quenched emission, while all other compounds show efficient green to red (ΦF =0...
January 2, 2015: Chemistry: a European Journal