FLÜSSIGKRISTALLINE ALKENYLVERBINDUNGEN DIE EINEN FÜNFGLIEDRIGEN HETEROCYCLISCHEN RING ENTHALTEN

Liquid crystal mixtures comprising at least one of the compounds of formula (I) containing a heterocyclic five-membered ring and with a carbon-carbon double bond in the termninal group are new.RJ=CnH2n+1CH=CHCmH2mZ1; n=1-5; m=0-5; and q=0, 1 or 2; A1 and A2=2,5-disubstituted furan, 2,5-disubstituted...

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Bibliographische Detailangaben
Hauptverfasser:	TUFFIN, PATRICIA, DUFFY, LEE, KELLY, MALCOLM, WILD, HELEN, CAMPBELL, NEIL
Format:	Patent
Sprache:	ger
Schlagworte:	ADHESIVES CHEMISTRY DEVICES OR ARRANGEMENTS, THE OPTICAL OPERATION OF WHICH ISMODIFIED BY CHANGING THE OPTICAL PROPERTIES OF THE MEDIUM OF THEDEVICES OR ARRANGEMENTS FOR THE CONTROL OF THE INTENSITY,COLOUR, PHASE, POLARISATION OR DIRECTION OF LIGHT, e.g.SWITCHING, GATING, MODULATING OR DEMODULATING DYES FREQUENCY-CHANGING HETEROCYCLIC COMPOUNDS MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NATURAL RESINS NON-LINEAR OPTICS OPTICAL ANALOGUE/DIGITAL CONVERTERS OPTICAL LOGIC ELEMENTS OPTICS ORGANIC CHEMISTRY PAINTS PHYSICS POLISHES TECHNIQUES OR PROCEDURES FOR THE OPERATION THEREOF
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Beschreibung
Zusammenfassung:	Liquid crystal mixtures comprising at least one of the compounds of formula (I) containing a heterocyclic five-membered ring and with a carbon-carbon double bond in the termninal group are new.RJ=CnH2n+1CH=CHCmH2mZ1; n=1-5; m=0-5; and q=0, 1 or 2; A1 and A2=2,5-disubstituted furan, 2,5-disubstituted thiophene, 2,5-disubstituted oxazole, 2,5-disubstituted thiazole, 2,5-disubstituted 1,3,4-oxadiazole, 2,5-disubstituted 1,3,4-thiadiazole, 1,4-disubstituted benzene, 2,5-disubstituted pyrimidine, 2,5-disubstituted pyridine, 2,6-disubstituted naphthalene; laterally substituted 1,4-disubstituted benzene, laterally substituted 2,5-disubstituted pyrimidine, laterally substituted 2,5-disubstituted pyridine or laterally substituted 2,6-disubstituted naphthalene (lateral substituents=F, Cl, Br or CN); A3=any A1 or 1,4-disubstituted bicyclo(2.2.2)octane, trans-1,4-disubstituted cyclohexane, trans-2,5-disubstituted dioxane or 1,4-disubstituted piperidine; Z1=O, COO or OOC; Z2 and Z3=direct bond, COO, OOC, C2H4, CH2O, OCH2, C4H8, C3H6O, (E)-CH=CHC2H4, (Z)-CH2CH=CHCH2, (E)-CH=CHCH2O or -C equivalent to C-; R=1-20C alkyl, alkoxy, alkenyl, alkenyloxy, alkanoyloxy, alkenoyloxy or OCpF2p+1; and p=1-20. When Z1=O and m=1, 3 or 5 the carbon-carbon double bond configuration in RJ is E. When Z1=O and m=2 or 4 the carbon-carbon double bond configuration in RJ is Z. When Z1=COO or OOC and m=0, 2 or 4 the carbon-carbon double bond configuration in RJ is E. When Z1=COO or OOC and m=1, 3 or 5 the carbon-carbon double bond configuration in RJ is Z.