Synthesis and characterization of planar five-ring-fused dithiophene-dione
Document Type
Article
Publication Date
3-1-2012
Abstract
A series of new organic semiconductors based on s-indaceno[1,2-b:5,6- b′]dithiophene-4,9-dione was successfully synthesized and characterized. The electron withdrawing carbonyl group lowers the LUMO energy levels, leading to increased electronegativities, which is beneficial for high photo-stability in air. The n-alkyl substituted compounds, 1c and 1d, crystallize with the rigid coplanar systems packed into slipped face-to-face π-stacks. Interestingly, 1c and 1d also show liquid crystalline behaviors, which give highly ordered molecular packing over large area. © 2012 SIOC, CAS, Shanghai, & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Publication Source (Journal or Book title)
Chinese Journal of Chemistry
First Page
681
Last Page
688
Recommended Citation
Wang, J., Zeng, W., Xu, H., Li, B., Cao, X., & Zhang, H. (2012). Synthesis and characterization of planar five-ring-fused dithiophene-dione. Chinese Journal of Chemistry, 30 (3), 681-688. https://doi.org/10.1002/cjoc.201100141