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Optically active bimesogens incorporating branched central spacers

In the current fascination with liquid crystalline dimers, bimesogens and oligomers the role of the central spacer in these systems has perhaps been somewhat neglected. In compound 1, a phenyl 4-cyanobenzoate bimesogen, the central spacer incorporates a methyl group at the 2-position and is therefor...

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Detalles Bibliográficos
Autores principales: Mandle, Richard J., Goodby, John W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080582/
https://www.ncbi.nlm.nih.gov/pubmed/35541138
http://dx.doi.org/10.1039/c8ra02075b
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author Mandle, Richard J.
Goodby, John W.
author_facet Mandle, Richard J.
Goodby, John W.
author_sort Mandle, Richard J.
collection PubMed
description In the current fascination with liquid crystalline dimers, bimesogens and oligomers the role of the central spacer in these systems has perhaps been somewhat neglected. In compound 1, a phenyl 4-cyanobenzoate bimesogen, the central spacer incorporates a methyl group at the 2-position and is therefore chiral. The helical twisting power of 1, measured in both 5CB and E7, was found to be 0.36 and 0.35 μm(−1) wt%(−1) respectively. Compound 1 exhibited a monotropic chiral nematic phase, however no twist-bend modulated phase was observed. We prepared a number of analogues of 1 incorporating different mesogenic units and observe that those with a small aspect ratio are non mesogenic, whereas those with larger aspect ratios variously exhibit chiral nematic, TB, SmC and SmB phases.
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spelling pubmed-90805822022-05-09 Optically active bimesogens incorporating branched central spacers Mandle, Richard J. Goodby, John W. RSC Adv Chemistry In the current fascination with liquid crystalline dimers, bimesogens and oligomers the role of the central spacer in these systems has perhaps been somewhat neglected. In compound 1, a phenyl 4-cyanobenzoate bimesogen, the central spacer incorporates a methyl group at the 2-position and is therefore chiral. The helical twisting power of 1, measured in both 5CB and E7, was found to be 0.36 and 0.35 μm(−1) wt%(−1) respectively. Compound 1 exhibited a monotropic chiral nematic phase, however no twist-bend modulated phase was observed. We prepared a number of analogues of 1 incorporating different mesogenic units and observe that those with a small aspect ratio are non mesogenic, whereas those with larger aspect ratios variously exhibit chiral nematic, TB, SmC and SmB phases. The Royal Society of Chemistry 2018-05-22 /pmc/articles/PMC9080582/ /pubmed/35541138 http://dx.doi.org/10.1039/c8ra02075b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Mandle, Richard J.
Goodby, John W.
Optically active bimesogens incorporating branched central spacers
title Optically active bimesogens incorporating branched central spacers
title_full Optically active bimesogens incorporating branched central spacers
title_fullStr Optically active bimesogens incorporating branched central spacers
title_full_unstemmed Optically active bimesogens incorporating branched central spacers
title_short Optically active bimesogens incorporating branched central spacers
title_sort optically active bimesogens incorporating branched central spacers
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9080582/
https://www.ncbi.nlm.nih.gov/pubmed/35541138
http://dx.doi.org/10.1039/c8ra02075b
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AT goodbyjohnw opticallyactivebimesogensincorporatingbranchedcentralspacers