Issue 12, 2023

Functional group polarity-modulated formation of liquid crystals of amphiphilic cyclodextrins

Abstract

Cyclodextrins (CDs) constitute a unique class of D-glucose-based macrocycles that possess a truncated cone-shaped central cavity. They are non-toxic and biodegradable. The presence of pseudo face-to-face symmetry in the native CDs represents a distinctive advantage to design amphiphilic materials capable of self-assembly into liquid crystals. In this work, a new family of amphiphilic β-CD derivatives possessing 14 stearoyl chains (non-polar) and 7 functionalized tetraethylene glycols were synthesized using an improved design and more efficient chemistry, and the synthetic targets showed excellent ability to form stable hexagonal columnar mesophases over wide temperature ranges. We demonstrated that the polarity and sizes of introduced functional groups can further affect the temperature ranges of formed LC phases. Moreover, variable temperature solid-state nuclear magnetic resonance spectroscopy studies of a lithium composite with compound 2 revealed fast local Li-ion exchange processes with very low activation energies, suggesting the benefit of using these materials as potential electrolytes for high ionic conductions. The results from this work can provide guidance for the design of future generations of CD-based LC materials for ion conduction.

Graphical abstract: Functional group polarity-modulated formation of liquid crystals of amphiphilic cyclodextrins

Supplementary files

Article information

Article type
Paper
Submitted
26 Nov 2022
Accepted
01 Mar 2023
First published
06 Mar 2023

J. Mater. Chem. C, 2023,11, 4153-4163

Functional group polarity-modulated formation of liquid crystals of amphiphilic cyclodextrins

A. Che, C. O. Zellman, D. Sarkar, S. Trudel-Lachance, J. Espejo, V. K. Michaelis, V. E. Williams and C. Ling, J. Mater. Chem. C, 2023, 11, 4153 DOI: 10.1039/D2TC05024B

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements