Exploiting Molecular Symmetry Reduction to Enrich Liquid Crystal Phase Diversity

Peer reviewed: 
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Scholarly level: 
Faculty/Staff
Final version published as: 

David F. Ester & Vance E. Williams (2019) Exploiting molecular symmetry reduction to enrich liquid crystal phase diversity, Liquid Crystals, DOI: 10.1080/02678292.2019.1575991 

https://doi.org/10.1080/02678292.2019.1575991

Date created: 
2019-02-17
Identifier: 
DOI: 10.1080/02678292.2019.1575991
Keywords: 
Liquid crystals
Phase transitions
Symmetry
Abstract: 

The strategic tuning of liquid crystalline phase behaviour by adjusting molecular symmetry was investigated. A family of sixteen symmetrical and unsymmetrical 2,6-di(4’-n-alkoxybenzoyloxy) naphthalene derivatives were prepared and their liquid crystal properties examined by differential scanning calorimetry, polarised optical microscopy, and x-ray diffraction. All mesogens formed nematic phases, with longer-chain analogues also exhibiting smectic C phases at lower temperatures. Melting temperatures of the compounds strongly depend on molecular symmetry, whereas clearing transitions are relatively insensitive to this effect. A detailed analysis indicates that the clearing point can be predicted based on the nature of the terminal alkyl chains, with only a secondary effect from molecular symmetry. Moreover, low symmetry molecules showed a greater tendency to form smectic C phases, which was ascribed to the selective depression of the melting point versus the SmC-N transition. This demonstrates that molecular symmetry-breaking is a valuable tool both for tuning liquid crystalline phase range and for increasing a material’s polymorphism.

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Supplemental material is included with this paper.

Language: 
English
Document type: 
Article
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