Gw. Skelton et al., Terminal trifluoromethyl-alkoxy and -alkenyloxy nematic liquid crystals for LCDs with active matrix addressing, LIQ CRYST, 28(3), 2001, pp. 417-435
We have synthesized a new class of compounds suitable for LCD applications,
incorporating a trifluoromethyl group in the terminal alkoxy- or alkenylox
y-chain. These compounds appear to fulfil many of the requirements for use
in TN-LCDs. Core units containing a cyclohexyl ring, which tend to induce a
lower viscosity than that of the analogous aromatic materials, were synthe
sized. Systems containing several aromatic rings were also prepared with a
view to producing compounds of high birefringence. Compounds containing a l
ateral fluorosubstituent as well as a polar substituent in a terminal posit
ion were synthesized in order to generate a high positive value of the diel
ectric anisotropy. Molecules incorporating a bicyclo[2.2.2]octane ring were
also synthesized in order to produce a high nematic clearing point and to
influence the elastic constants. Compounds with three 1,4-disubstituted rin
gs were synthesized with a view to producing materials with a high nematic
clearing point and as low a melting point as possible. A series of compound
s with a carbon-carbon double bond in the terminal chain was prepared in an
attempt to produce compounds with appropriate values and ratios of the ela
stic constants.