Abstract: A fluorinated phenyl compound having the general formula [1]: wherein each of s, v and x=0 or 1, each of t and u=1, 2 or 3, and each of y and z=0, 1 or 2; A, B and C are independently selected from conjugated cyclic moieties including heterorings and fused rings; R1 and R3 may be independently cyano, or (C1-C12)alkyl, (C1-C12)alkoxy, (C1-C11) alkoxycarbonyl or (C1-C11)alkylcarbonyloxy which may be fluoro- and/or cyano-substituted; R2=H or F; R4=H or F; and R5=H or F. Such compounds have high transverse dipole moments and are potentially useful in liquid crystal compositions and in devices including same.

Abstract: A liquid crystalline compounds:

Abstract: Liquid crystal compounds of formula (I) are described, where formula (I) is given as R1—A—(X)m—(B)n—R2 where A is selected from naphthyl, fluorinated naphthyl, brominated naphthyl, B is selected from phenyl, methylated phenyl, brominated phenyl, fluorinated phenyl, thiophene, pyrimidine and pyridine. R1 and R2 are independently selected from alkyl, alkoxy, akynyl, thioalkyl, Br, CN, SCN, NCS, perfluoroalkyl, perfluoroalkoxy and hydrogen, X is selected from C≡C, COO and C≡C, m is 0 or 1, n is 0 or 1 where m is 1 and n is 0 where m is 0; provided that where A is naphthyl, n is 1 and m is 0 then B is selected from methylated phenyl, brominated phenyl, thiophene, pyrimidine and pyridine; and further provided that where A is naphthyl, X is C≡C, m is 1 and n is 1, then B is selected from thiophene, pyrimidine and pyridine.

Abstract: The synthesis of novel compound (I) is described: 5-bromo-2-iodopyrimidine may be used for the synthesis of a range of chemical compounds both known and novel. The synthesis of a number of novel liquid crystalline compounds is described.

Abstract: 5-Bromo-2-iodopyrimidine is used to synthesize a range of chemical compounds including liquid crystalline compounds.

Abstract: This invention describes compounds of formula (I) ##STR1## wherein R is C.sub.1-16 alkyl or alkoxy; X is selected from F and Cl and indicates that one or more of the phenyl rings may be laterally substituted; x is selected from 0-3; A and B are independently selected from CO.sub.2, OCO, .tbd.C and single bond; R.sub.1 and R.sub.2 are independently selected from H and C.sub.1-16 alkyl provided that R.sub.1 and R.sub.2 are different; n is 0 or 1 provided that if n is zero then B is single bond. These compounds may be used as dopants suitable for use in ferroelectric liquid crystal mixtures.

Abstract: The present invention describes liquid crystal compounds which are suitable for use in liquid crystal devices including those which exploit the electroclinic effect.

Abstract: R.sub.1 --A--(X).sub.m --(B).sub.n --R.sub.2 (I)R.sub.3 --J--(Y).sub.p --(Z).sub.q --R.sub.4 (II)Liquid crystal compounds of formula (I) are described, where formula (I) is given as R.sub.1 --A--(X).sub.m --(B).sub.n --R.sub.2 where A is selected from nathyl, fluorinated naphthyl, brominated naphthyl, B is selected from phenyl, methylated phenyl, brominated phenyl, fluorinated phenyl, thiophene, pyrimidine and pyridine, R.sub.1 and R.sub.2 are independently selected from alkyl, alkoxy, alkynyl, thioalkyl, Br, CN, SCN, NCS, perfluoroalkyl, perfluoroalkoxy and hydrogen, X is selected from C.tbd.C, COO and C.tbd.C, m is 0 or 1, n is 0 or 1 where m is 1 and n is 0 where m is 0; provided that where A is naphthyl, n is 1 and m is 0 then B is selected from methylated phenyl, brominated phenyl, thiophene, pyrimidine and pyridine; and further provided that where A is naphthyl, X is C.tbd.C, m is 1 and n is 1, then B is selected from thiophene, pyrimidine and pyridine.

Abstract: Compounds of formula (I) which are suitable for use in liquid crystal devices including those devices which exploit the electroclinic effect. The compounds of formula (I) may also be used as chiral dopoants suitable for use with ferroelectric liquid crystals or they may be used as chiral nematic dopants.