The University of Southampton
University of Southampton Institutional Repository

Molecular flexibility in the design of low molar mass liquid crystals

Molecular flexibility in the design of low molar mass liquid crystals
Molecular flexibility in the design of low molar mass liquid crystals

This Thesis investigates the influence of molecular flexibility on the meso-genic behaviour and in particular, the properties of dimeric liquid crystals and their relationship to molecular structure. Dimers possess two semi-rigid anisometric units linked through a flexible alkyl spacer, this increased overall flexibility was thought to suppress smectic behaviour. In Chapter 2, however, the properties of several series of a,u-bis (4-alkylanilinebenzylidine-4'-oxy)alkanes are presented a rich smectic polymorphism. Chapter 3 introduces a new class of dimer, the asymmetric dimeric liquid crystal, in which two different mesogenic groups are linked through a flexible spacer, and as examples, the a-(4-cyanobiphenyl- 4'-oxy)-w-(4-alkylaniline-benzylidine-4'-oxy)alkanes were synthesised. The dependence of the thermal stability of the smectic phase on the length of the terminal alkyl chain is very unusual because it does not simply increase on increasing chain length but instead passes through a minimum. This novel behaviour is rationalised by proposing that the structure of the smectic phase changes from being intercalated to interdigitated on increasing chain length. Chapter 4 investigates the properties of dimers and their relationship to molecular structure via the synthesis of a range of new compounds. In Chapter 5, the effect of a flexible core is examined in compounds which possess a mesogenic group linked via an alkyl chain to a small anisometric group. Finally, Chapter 6 presents the transitional properties of several series of mesogens which possess lateral alkyl chains; the observation of liquid- crystalline behaviour for this class of compound is rationalised by proposing that the lateral chain lies parallel to the molecular long axis and so is not in its all-trans conformation.

University of Southampton
Imrie, Corrie Thomas
3120b047-9dab-4cfa-96a0-c94ee7ef8fdc
Imrie, Corrie Thomas
3120b047-9dab-4cfa-96a0-c94ee7ef8fdc

Imrie, Corrie Thomas (1988) Molecular flexibility in the design of low molar mass liquid crystals. University of Southampton, Doctoral Thesis.

Record type: Thesis (Doctoral)

Abstract

This Thesis investigates the influence of molecular flexibility on the meso-genic behaviour and in particular, the properties of dimeric liquid crystals and their relationship to molecular structure. Dimers possess two semi-rigid anisometric units linked through a flexible alkyl spacer, this increased overall flexibility was thought to suppress smectic behaviour. In Chapter 2, however, the properties of several series of a,u-bis (4-alkylanilinebenzylidine-4'-oxy)alkanes are presented a rich smectic polymorphism. Chapter 3 introduces a new class of dimer, the asymmetric dimeric liquid crystal, in which two different mesogenic groups are linked through a flexible spacer, and as examples, the a-(4-cyanobiphenyl- 4'-oxy)-w-(4-alkylaniline-benzylidine-4'-oxy)alkanes were synthesised. The dependence of the thermal stability of the smectic phase on the length of the terminal alkyl chain is very unusual because it does not simply increase on increasing chain length but instead passes through a minimum. This novel behaviour is rationalised by proposing that the structure of the smectic phase changes from being intercalated to interdigitated on increasing chain length. Chapter 4 investigates the properties of dimers and their relationship to molecular structure via the synthesis of a range of new compounds. In Chapter 5, the effect of a flexible core is examined in compounds which possess a mesogenic group linked via an alkyl chain to a small anisometric group. Finally, Chapter 6 presents the transitional properties of several series of mesogens which possess lateral alkyl chains; the observation of liquid- crystalline behaviour for this class of compound is rationalised by proposing that the lateral chain lies parallel to the molecular long axis and so is not in its all-trans conformation.

Text
334740.pdf - Version of Record
Available under License University of Southampton Thesis Licence.
Download (12MB)

More information

Published date: 1988

Identifiers

Local EPrints ID: 460859
URI: http://eprints.soton.ac.uk/id/eprint/460859
PURE UUID: f4e09ad7-3ece-412b-ab8d-d8e5e4ec2742

Catalogue record

Date deposited: 04 Jul 2022 18:31
Last modified: 16 Mar 2024 18:43

Export record

Contributors

Author: Corrie Thomas Imrie

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.

×