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Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes

This paper describes the synthesis of a series of organic liquid crystals (LCs) containing selectively fluorinated cyclopropanes at their termini. The syntheses used difluorocarbene additions to olefin precursors, an approach which proved straightforward such that these liquid crystal candidates cou...

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Detalles Bibliográficos
Autores principales: Fang, Zeguo, Al-Maharik, Nawaf, Kirsch, Peer, Bremer, Matthias, Slawin, Alexandra M Z, O’Hagan, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176930/
https://www.ncbi.nlm.nih.gov/pubmed/32362945
http://dx.doi.org/10.3762/bjoc.16.65
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author Fang, Zeguo
Al-Maharik, Nawaf
Kirsch, Peer
Bremer, Matthias
Slawin, Alexandra M Z
O’Hagan, David
author_facet Fang, Zeguo
Al-Maharik, Nawaf
Kirsch, Peer
Bremer, Matthias
Slawin, Alexandra M Z
O’Hagan, David
author_sort Fang, Zeguo
collection PubMed
description This paper describes the synthesis of a series of organic liquid crystals (LCs) containing selectively fluorinated cyclopropanes at their termini. The syntheses used difluorocarbene additions to olefin precursors, an approach which proved straightforward such that these liquid crystal candidates could be efficiently prepared. Their physical and thermodynamic properties were evaluated and depending on individual structures, they either displayed positive or negative dielectric anisotropy. The study gives some guidance into effective structure–property relationships for the design of LCs containing selectively fluorinated cyclopropane motifs.
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spelling pubmed-71769302020-05-01 Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes Fang, Zeguo Al-Maharik, Nawaf Kirsch, Peer Bremer, Matthias Slawin, Alexandra M Z O’Hagan, David Beilstein J Org Chem Full Research Paper This paper describes the synthesis of a series of organic liquid crystals (LCs) containing selectively fluorinated cyclopropanes at their termini. The syntheses used difluorocarbene additions to olefin precursors, an approach which proved straightforward such that these liquid crystal candidates could be efficiently prepared. Their physical and thermodynamic properties were evaluated and depending on individual structures, they either displayed positive or negative dielectric anisotropy. The study gives some guidance into effective structure–property relationships for the design of LCs containing selectively fluorinated cyclopropane motifs. Beilstein-Institut 2020-04-14 /pmc/articles/PMC7176930/ /pubmed/32362945 http://dx.doi.org/10.3762/bjoc.16.65 Text en Copyright © 2020, Fang et al. https://creativecommons.org/licenses/by/4.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0). Please note that the reuse, redistribution and reproduction in particular requires that the authors and source are credited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Fang, Zeguo
Al-Maharik, Nawaf
Kirsch, Peer
Bremer, Matthias
Slawin, Alexandra M Z
O’Hagan, David
Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title_full Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title_fullStr Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title_full_unstemmed Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title_short Synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
title_sort synthesis of organic liquid crystals containing selectively fluorinated cyclopropanes
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7176930/
https://www.ncbi.nlm.nih.gov/pubmed/32362945
http://dx.doi.org/10.3762/bjoc.16.65
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