화학공학소재연구정보센터
Journal of Physical Chemistry B, Vol.114, No.11, 3791-3798, 2010
Optical and Conformational Studies on Benzobisthiazole Derivatives
2,6-Didodecyl-4,8-diphenyl-beiizo[1,2-d;4,5-d']bisthiazole (3) and 2,6-didodecyl-4,8-dipyrrole-2-yl-benzo[1,2-d;4,5-d']bisthiazole (5) were synthesized, and their optical properties were investigated in solution and in the solid state. Compounds 3 and 5 were excited with the 325 nm He-Cd laser line to produce blue and green luminescence, respectively. The luminescence of 5 (Phi = 14%) was more efficient than that of 3 (Phi = 5%). Structural and optical properties were further determined with DFT and ZINDO calculations. The planar Structure of 5 results in pi -> pi* electronic transitions from the pyrrole moiety to the benzobisthiazole frame, while the twisted geometry of 3 results in luminescence strongly associated with the pi -> pi* transitions within the benzothiazole frame. The effect of solvent oil the luminescence properties of 5 is summarized as competition between intra- and intermolecular NH center dot center dot center dot N hydrogen bonds.