The University of Southampton
University of Southampton Institutional Repository

The effects of structural complexity on the properties of low molar mass liquid crystals

The effects of structural complexity on the properties of low molar mass liquid crystals
The effects of structural complexity on the properties of low molar mass liquid crystals

This thesis investigates the effect of molecular flexibility on the mesogenic behaviour of dimeric and trimeric liquid crystals. Chapter 1 describes the structures and properties of mesogenic materials and the experimental techniques by which they are studied. In chapter 2 the mesogenic properties of a series of benzene-1,3,5-tri(4-carboxyhexyloxybenzylidene-4'-n-alkylanilines) in which three rod-like mesogenic units are attached to a disc-like core via flexible spacers are examined. A complex and unusual smectic polymorphism is noted for this series. Optical and X-ray diffraction studies reveal that the phases formed are calamitic rather than discotic or columnar. One possible explanation for this behaviour is that the flexible spacer chains preferentially adopt conformations that give a high molecular length to breadth ratio in the liquid crystal phase.

In chapter 3 the properties of homologous series of novel structurally isomeric trimeric liquid crystals are presented. These molecules have a phenyl diester core and two pendant Schiff's bases attached via flexible spacers. The mesophase behaviour has a strong dependence on spacer chain parity, particularly at short terminal chain lengths. Ortho disubstituted derivatives have been shown by X-ray diffraction to form bilayer smectic phases whilst meta and para disubstituted derivatives form monolayer smectic phases.

In chapter 4 a 1,1'-ferrocene unit replaces the disubstituted benzene as the core of a trimeric molecule. These materials form nematic and smectic phases as a function of terminal chain length. The spacer chain parity has little effect on the mesophase stability which is reduced by incorporation of the ferrocene.

The dependence of the odd-even behaviour for dimeric liquid crystals on the geometry of the linkage between the spacer and mesogenic units is studied in chapter 5. The orientational order of cyanobiphenyl dimers with methylene or ether links is probed by NMR spectroscopy via an anthracene-d10 solute. The enhanced odd-even effect observed for methylene linked dimers relative to those with ether links is shown to be in accord with theoretical predictions.

University of Southampton
Douglass, Andrew Gordon
Douglass, Andrew Gordon

Douglass, Andrew Gordon (1993) The effects of structural complexity on the properties of low molar mass liquid crystals. University of Southampton, Doctoral Thesis.

Record type: Thesis (Doctoral)

Abstract

This thesis investigates the effect of molecular flexibility on the mesogenic behaviour of dimeric and trimeric liquid crystals. Chapter 1 describes the structures and properties of mesogenic materials and the experimental techniques by which they are studied. In chapter 2 the mesogenic properties of a series of benzene-1,3,5-tri(4-carboxyhexyloxybenzylidene-4'-n-alkylanilines) in which three rod-like mesogenic units are attached to a disc-like core via flexible spacers are examined. A complex and unusual smectic polymorphism is noted for this series. Optical and X-ray diffraction studies reveal that the phases formed are calamitic rather than discotic or columnar. One possible explanation for this behaviour is that the flexible spacer chains preferentially adopt conformations that give a high molecular length to breadth ratio in the liquid crystal phase.

In chapter 3 the properties of homologous series of novel structurally isomeric trimeric liquid crystals are presented. These molecules have a phenyl diester core and two pendant Schiff's bases attached via flexible spacers. The mesophase behaviour has a strong dependence on spacer chain parity, particularly at short terminal chain lengths. Ortho disubstituted derivatives have been shown by X-ray diffraction to form bilayer smectic phases whilst meta and para disubstituted derivatives form monolayer smectic phases.

In chapter 4 a 1,1'-ferrocene unit replaces the disubstituted benzene as the core of a trimeric molecule. These materials form nematic and smectic phases as a function of terminal chain length. The spacer chain parity has little effect on the mesophase stability which is reduced by incorporation of the ferrocene.

The dependence of the odd-even behaviour for dimeric liquid crystals on the geometry of the linkage between the spacer and mesogenic units is studied in chapter 5. The orientational order of cyanobiphenyl dimers with methylene or ether links is probed by NMR spectroscopy via an anthracene-d10 solute. The enhanced odd-even effect observed for methylene linked dimers relative to those with ether links is shown to be in accord with theoretical predictions.

This record has no associated files available for download.

More information

Published date: 1993

Identifiers

Local EPrints ID: 462492
URI: http://eprints.soton.ac.uk/id/eprint/462492
PURE UUID: 0b44ea76-65b6-4418-adca-e5ae561a811b

Catalogue record

Date deposited: 04 Jul 2022 19:09
Last modified: 04 Jul 2022 19:09

Export record

Contributors

Author: Andrew Gordon Douglass

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×