Abstract
Abstract Liquid crystals (LCs) containing a trifluoromethylamino group are prepared by the cross-coupling reaction of p-bromo-substituted-(hetero)aryl(trifluoromethyl)amines that are derived from the corresponding dithiocarbamates through oxidative desulfurization–fluorination. The novel LCs are shown to exhibit mainly a smectic phase over a wide range of temperatures. Their electro-optical properties as a component of nematic LCs are compared with those of the corresponding methylamines.
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