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University of Hull

The synthesis of liquid crystalline materials for organic semiconductor device applications

Abstract

dc:description.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).

Degree

thesis:*
Name dc:type.qualificationname
PhD
Level dc:type.qualificationlevel
Doctoral
Grantor dc:publisher.institution
University of Hull
Year dc:date.issued
2009

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Dixon, Mark S.
Advisor dc:contributor.advisor
  • Kelly, S. M. (Stephen Malcolm)

Subjects

dc:subject × 1

Rights

Language dc:language
en

Identifiers

dc:identifier.*
Identifier
oai:hull-repository.worktribe.com:4209106
OAI identifier oai:identifier
oai:hull-repository.worktribe.com:4209106

Chain of custody

source
Harvested from
University of Hull
Base URL
hull-repository.worktribe.com/oaiprovider
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
related terms
citation

Dixon, Mark S.. The synthesis of liquid crystalline materials for organic semiconductor device applications. Doctoral thesis, University of Hull, 2009. https://hull-repository.worktribe.com/4209106/1/Thesis