The synthesis of liquid crystalline materials for organic semiconductor device applications

Dixon, Mark S.

Abstract

This research is based on the synthesis and evaluation of novel photo- and chemically-reactive, liquid crystalline monomers (reactive mesogens) with improved charge-transporting properties. Low-molar-mass (LMM) liquid crystalline monomers, based on a series of substituted dibenzothiophenes, thiophenes, [2,2']-bithiophenes, thieno[3,2-b]thiophenes, benzo-2,1,3-thiadiazoles and fluorenes have been synthesised. These materials incorporate photo-polymerisable (non-conjugated diene and methacrylate) and chemically-polymerisable (oxetane) end-groups, attached by aliphatic spacer units of varying length to an aromatic core. These photo- and chemically-polymerisable end-groups are situated at the peripheries of the molecular structure, allowing the potential fabrication of multi-layer, organic semiconductor devices due to the insoluble, cross-linked polymer network obtained after polymerisation of the analogous reactive mesogens (RMs).

Citation

Dixon, M. S. (2009). The synthesis of liquid crystalline materials for organic semiconductor device applications. (Thesis). University of Hull. Retrieved from https://hull-repository.worktribe.com/output/4209106

• Thesis Type: Thesis
• Deposit Date: Aug 15, 2011
• Publicly Available Date: Feb 22, 2023
• Keywords: Chemistry
• Public URL: https://hull-repository.worktribe.com/output/4209106
• Additional Information: Department of Chemistry, The University of Hull
• Award Date: Jun 1, 2009