Skip to main content

Synthesis of 4-Alkyl-2′′, 3′′ difluoro terphenyl nitrile using coupling reactions

Lewis, Robert; Kayani, Zohra N.; Lewis, Robert A.; Naseem, Shahzad

Authors

Robert Lewis R.A.Lewis@hull.ac.uk

Zohra N. Kayani

Robert A. Lewis

Shahzad Naseem



Abstract

Study of chirality in liquid crystals is one of the most interesting areas of liquid crystal science. Liquid crystallineterphenyls with two lateral fluoro substituent and alkyl substituent in the 4- have been synthesised. Convergentapproach was applied which involved the use of arylboronic acids and aryl halides in palladium-catalysedcross-coupling reactions. All the diifluoroterphenyls generate the smectic C phase. Mixture of 4-Alkyl-2′′,3difluoro terphenyl nitrile in achiral host mixture HM1 generates ferroelectric liquid crystal properties.Ferroelectric properties were found to be highly dependent upon the relative lengths of the alkyl chainattached to chiral dopant. The compounds were studied using optical polarisation microscopy, differentialscanning calorimetric, nuclear magnetic resonance, and Instec elecro-optical device to find ferroelectric liquidcrystal properties.

Journal Article Type Article
Publication Date 2012-11
Journal Journal of Molecular Liquids
Print ISSN 0167-7322
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 175
Pages 72-84
APA6 Citation Kayani, Z. N., Lewis, R. A., & Naseem, S. (2012). Synthesis of 4-Alkyl-2′′, 3′′ difluoro terphenyl nitrile using coupling reactions. Journal of Molecular Liquids, 175, (72-84). doi:10.1016/j.molliq.2012.08.012. ISSN 0167-7322
DOI https://doi.org/10.1016/j.molliq.2012.08.012
Keywords Terphenyls; Convergent approach; Host mixture; Chiral dopant; Ferroelectric liquid crystal
Publisher URL http://www.sciencedirect.com/science/article/pii/S016773221200298X
;