Grant James Strachan
Liquid crystal trimers containing tertiary benzanilide groups.
Strachan, Grant James; Majewska, Magdalena M.; Cruickshank, Ewan; Pociecha, Damian; Gorecka, Ewa; Storey, John M.D.; Imrie, Corrie T.
Authors
Magdalena M. Majewska
Dr Ewan Cruickshank e.cruickshank2@rgu.ac.uk
Lecturer
Damian Pociecha
Ewa Gorecka
John M.D. Storey
Corrie T. Imrie
Abstract
The rational design of new liquid crystal materials relies on an understanding of the relationship between molecular structure and the formation of liquid crystalline phases. The development of new materials can benefit from the use of a wide range of functional groups, but some groups prove challenging to combine with liquid crystallinity. Tertiary benzanilide groups are a clear example of this, as their strong conformational preferences disrupt liquid crystallinity when included in typical liquid crystalline structures. This means that it has not been possible to harness the molecular design possibilities offered by amide N-substitution. However, designing flexible structures to accommodate the conformation of tertiary benzanilides has allowed us to synthesise a variety of liquid crystal trimers forming nematic and smectic phases, and investigate the effect of lateral and N-substitution on their phase behaviour. Trimers with large (benzyl and decyl) N-substituents favour the formation of an orthogonal smectic (SmA) phase, and, unusually, exhibit pronounced negative thermal expansion.
Citation
STRACHAN, G.J., MAJEWSKA, M.M., CRUICKSHANK, E., POCIECHA, D., GORECKA, E., STOREY, J.M. and CORRIE, T.I. 2025. Liquid crystal trimers containing tertiary benzanilide groups. Journal of materials chemistry C [online], Advanced Article. Available from: https://doi.org/10.1039/D5TC01532D
Journal Article Type | Article |
---|---|
Acceptance Date | May 30, 2025 |
Online Publication Date | May 30, 2025 |
Deposit Date | Jun 4, 2025 |
Publicly Available Date | Jun 20, 2025 |
Journal | Journal of materials chemistry C |
Print ISSN | 2050-7526 |
Publisher | Royal Society of Chemistry |
Peer Reviewed | Peer Reviewed |
DOI | https://doi.org/10.1039/d5tc01532d |
Keywords | Molecular structures; Liquid crystalline phases; Tertiary benzanilide groups |
Public URL | https://rgu-repository.worktribe.com/output/2872712 |
Files
STRACHAN 2025 Liquid crystal trimers (AAM)
(2.8 Mb)
PDF
Publisher Licence URL
https://creativecommons.org/licenses/by/3.0/
Copyright Statement
© The Royal Society of Chemistry 2025.
You might also like
The influence of methyl groups on the formation of the ferroelectric nematic phase.
(2025)
Journal Article
Sulfur-linked cyanoterphenyl-based liquid crystal dimers and the twist-bend nematic phase.
(2025)
Journal Article
The role of fluorine substituents in the formation of the ferroelectric nematic phase.
(2024)
Journal Article
A design approach to obtaining highly polar liquid crystal dimers.
(2024)
Journal Article
Downloadable Citations
About OpenAIR@RGU
Administrator e-mail: publications@rgu.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2025
Advanced Search