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The synthesis and liquid crystal properties of some 4-n-nonylphenyl esters of 3-(4'-n-alkoxybiphenylyl)- and 3-(4'-n-alkoxybiphenylyl)-3-methyl-propanoic acids and their laterally fluorinated analogues
Authors:A W Hall  D Lacey  G W Gray  J Benson
Institution:  a The School of Chemistry, The University, Hull, England b R&D Administration, Merck Ltd, Poole, Dorset, England c Courtaulds Research, Spondon, Derbyshire, England
Abstract:A number of 4-n-nonylphenyl esters and mono- and di-fluorinated 4-n-nonylphenyl esters derived from 3-(4'-n-alkoxybiphenylyl)propanoic acids (II) have been synthesized and their thermotropic liquid crystal properties assessed with a view to obtaining tilted smectic phases for possible use in ferroelectric display devices. Many of these compounds exhibit wide temperature range SC and SI/F phases, but none gave the ideal phase sequence SC-SA-N-I mainly because the structure of these compounds was not conducive to the formation of the nematic phase. To try to alleviate this problem a series of 4-n-nonylphenyl esters based on 3-(4'-n-alkoxybiphenylyl)-3-methylpropanoic acid was prepared, where a lateral methyl group was incorporated in the β-position of the -CH2CH2CO2- linkage. Incorporation of the lateral methyl group encouraged the formation of a nematic phase at the expense of both the smectic A phase and tilted smectic phases.
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