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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.
Afiliação
  • Fang Z; School of Chemistry, Biomedical Sciences Research Complex, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, United Kingdom.
  • Al-Maharik N; School of Chemistry, Biomedical Sciences Research Complex, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, United Kingdom.
  • Kirsch P; Department of Chemistry, Faculty of Science, An Najah National University, Nablus, Palestine.
  • Bremer M; Merck KGaA, Liquid Crystal R&D Chemistry, Frankfurter Str. 250, 64293 Darmstadt, Germany.
  • Slawin AMZ; Merck KGaA, Liquid Crystal R&D Chemistry, Frankfurter Str. 250, 64293 Darmstadt, Germany.
  • O'Hagan D; School of Chemistry, Biomedical Sciences Research Complex, University of St Andrews, North Haugh, St Andrews, Fife KY16 9ST, United Kingdom.
Beilstein J Org Chem ; 16: 674-680, 2020.
Article em En | MEDLINE | ID: mdl-32362945
ABSTRACT
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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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Beilstein J Org Chem Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Reino Unido