ABSTRACT
Several oligomers (MWs > 1000 g mol−1) with highly rigid and conjugated aromatic cores, incorporating 1,4-disubstituted phenylene, 2,7-disubstituted fluorene, 1,4-disubstituted thiophene and/or 2,7-disubstituted carbazole rings with lateral and terminal substituents were synthesised as novel organic semiconductors. These novel liquid crystalline oligomers exhibit glass transition temperatures above room temperature, high clearing points and a broad nematic temperature range as well as electroluminescent behaviour in solution-processed devices.
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Acknowledgments
Huaiyin Institute of Technology, the China Scholarship Council and the University of Hull are thanked for their support for Dr Guang Hu.
Disclosure statement
There are no conflicts of interest to declare.