Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state

This is the first report of phase properties and photoisomerization behaviour of a series of amphiphilic azobenzene-imidazolium derivatives. The cationic imidazolium moiety was functionalised with varying alkyl chain length (C10-C18) and connected to an azobenzene via a flexible ether spacer. Their...

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Main Authors: Babamale, Halimah Funmilayo, Ng, Si Ling, Tang, Wai Kit, Yam, WanSinn
Format: Article
Published: Elsevier 2024
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Online Access:http://eprints.um.edu.my/44753/
https://doi.org/10.1016/j.molstruc.2024.137494
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spelling my.um.eprints.447532024-07-11T05:39:25Z http://eprints.um.edu.my/44753/ Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state Babamale, Halimah Funmilayo Ng, Si Ling Tang, Wai Kit Yam, WanSinn QD Chemistry This is the first report of phase properties and photoisomerization behaviour of a series of amphiphilic azobenzene-imidazolium derivatives. The cationic imidazolium moiety was functionalised with varying alkyl chain length (C10-C18) and connected to an azobenzene via a flexible ether spacer. Their phase transitional properties and photoisomerization in solution were modulated by the alkyl chains in the imidazolium moiety. C14 was the shortest chain length to induce the formation of a liquid crystal phase, wherein compounds having C14-C18 exhibited stable smectic A phase. All compounds photo switched from trans-to-cis isomers in solution when illuminated with UV radiation. DFT calculations revealed that the trans isomers could adopt two geometries, however, folded geometry (global minima) was thermodynamically more stable than the open chain structure. The long conjugate (C16) had a higher trans-cis isomerization barrier due to the multilayer folding geometry that reduced its structural flexibility as compared to the C10 homologue. The photo conversion efficiency (CE) was alkyl chain length dependent. The C10 salt had a larger CE than C16 homologue due to the transition gap between S1 excited state and ground surface is smaller in the former (0.211 eV) than that in the latter (0.278 eV), thus resulting in efficient photoisomerization in the former. © 2024 Elsevier 2024-05-05 Article PeerReviewed Babamale, Halimah Funmilayo and Ng, Si Ling and Tang, Wai Kit and Yam, WanSinn (2024) Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state. Journal of Molecular Structure, 1303. ISSN 0022-2860, DOI https://doi.org/10.1016/j.molstruc.2024.137494 <https://doi.org/10.1016/j.molstruc.2024.137494>. https://doi.org/10.1016/j.molstruc.2024.137494 10.1016/j.molstruc.2024.137494
institution Universiti Malaya
building UM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaya
content_source UM Research Repository
url_provider http://eprints.um.edu.my/
topic QD Chemistry
spellingShingle QD Chemistry
Babamale, Halimah Funmilayo
Ng, Si Ling
Tang, Wai Kit
Yam, WanSinn
Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
description This is the first report of phase properties and photoisomerization behaviour of a series of amphiphilic azobenzene-imidazolium derivatives. The cationic imidazolium moiety was functionalised with varying alkyl chain length (C10-C18) and connected to an azobenzene via a flexible ether spacer. Their phase transitional properties and photoisomerization in solution were modulated by the alkyl chains in the imidazolium moiety. C14 was the shortest chain length to induce the formation of a liquid crystal phase, wherein compounds having C14-C18 exhibited stable smectic A phase. All compounds photo switched from trans-to-cis isomers in solution when illuminated with UV radiation. DFT calculations revealed that the trans isomers could adopt two geometries, however, folded geometry (global minima) was thermodynamically more stable than the open chain structure. The long conjugate (C16) had a higher trans-cis isomerization barrier due to the multilayer folding geometry that reduced its structural flexibility as compared to the C10 homologue. The photo conversion efficiency (CE) was alkyl chain length dependent. The C10 salt had a larger CE than C16 homologue due to the transition gap between S1 excited state and ground surface is smaller in the former (0.211 eV) than that in the latter (0.278 eV), thus resulting in efficient photoisomerization in the former. © 2024
format Article
author Babamale, Halimah Funmilayo
Ng, Si Ling
Tang, Wai Kit
Yam, WanSinn
author_facet Babamale, Halimah Funmilayo
Ng, Si Ling
Tang, Wai Kit
Yam, WanSinn
author_sort Babamale, Halimah Funmilayo
title Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
title_short Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
title_full Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
title_fullStr Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
title_full_unstemmed Azobenzene-Imidazolium ionic liquid crystals: Phase properties and photoisomerization in solution state
title_sort azobenzene-imidazolium ionic liquid crystals: phase properties and photoisomerization in solution state
publisher Elsevier
publishDate 2024
url http://eprints.um.edu.my/44753/
https://doi.org/10.1016/j.molstruc.2024.137494
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