Abstract:
Anthraquinone dyes of the general formula: ##STR1## wherein R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are selected from the group consisting of H, OH, OCH.sub.3, NO.sub.2, NH.sub.2 and NHCH.sub.3 ; R.sup.2 and R.sup.5 are selected from the group consisting of:(a) alkyl-, aryl-, alkaryl-, alkoxyaryl-, aminoaryl-, alkylaminoaryl-, dialkylamino-, arylaminoaryl- or ##STR2## wherein R.sup.7 is selected from the group consisting of alkyl-, aryl-, amino-, alkylamino-, dialkylamino-, arylamino-, alkyloxy-, and aryloxy radicals,along with their syntheses routes are disclosed. The dyes are particularly useful in liquid crystal displays which function with a "guest host" effect or in other electrooptical display devices having a medium therein switchable between different ordering states.
Abstract:
Anthraquinone dyes of the general formula: ##STR1## wherein R.sup.1, R.sup.3, R.sup.4 and R.sup.6 are selected from the group consisting of H, OH, OCH.sub.3, NO.sub.2, NH.sub.2 and NHCH.sub.3 ; R.sup.2 and R.sup.5 are selected from the group consisting of: ##STR2## wherein R.sup.7 is selected from the group consisting of alkyl-, aryl-, amino-, alkylamino-, dialkylamino-, arylamino-, alkyloxy-, and aryloxy radicals, along with their syntheses routes are disclosed. The dyes are particularly useful in liquid crystal displays which function with a "guest host" effect or in other electrooptical display devices having a medium therein switchable between different ordering states.
Abstract:
N-substituted anthraquinones in which the substituent group is at least partially cyclic, either cyclohexyl or aromatic, and including anils of 1,4- and 1,8-diaminoanthraquinone with p-alkyl- and p-alkoxybenzaldehyde, are pleochroic and form guest-host combinations with dielectrically positive anisotropic nematic liquid crystals. These combinations are of value in electro-optical display devices.
Abstract:
Anthraquinone-azomethine compounds of the formula ##STR1## or of the tautomeric formula ##STR2## or of the tautomeric formula ##STR3## in which A denotes an anthraquinone radical which is free from sulphonic acid groups and optionally further substituted and which preferably consists of at most 5 fused rings,R.sub.1 denotes hydrogen, C.sub.1 -C.sub.4 -alkyl, hydroxy-C.sub.1 -C.sub.4 -alkyl, optionally substituted phenyl, carboxyl, carboxylic acid, C.sub.1 -C.sub.4 -alkyl ester or hydroxyl,R.sub.2 denotes hydrogen, halogen, nitro, cyano, optionally substituted carbamoyl or optionally substituted sulphamoyl, sulphonic acid C.sub.1 -C.sub.4 -alkyl ester, sulphonic acid aryl ester, C.sub.1 -C.sub.4 - alkylcarbonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, optionally substituted benzoyl, alkyl or optionally substituted phenyl sulphone, or a hetero-aromatic radical, for example a radical of the formula ##STR4## or of the formula ##STR5## or of the formula ##STR6## R.sub.3 denotes optionally substituted aryl or hetero-aryl, cycloalkyl or C.sub.1 -C.sub.12 -alkyl, it being possible for the alkyl chain to be interrupted by oxygen or sulphur and /or substituted by hydroxyl, N(R.sub.5).sub.2 -- or --N(R.sub.5).sub.3.sup..sym. X.sup..crclbar. groups,R.sub.4 denotes a substituent,R.sub.5 denotes hydrogen, C.sub.1 -C.sub.4 -alkyl, cycloalkyl or optionally substituted aryl,X denotes an anion,m denotes 1, 2, 3 or 4 andn denotes 0, 1, 2, 3 or 4,processes for their preparation and processes for dyeing synthetic fibre materials and for pigmenting organic macromolecular substances using the new anthraquinone-azomethine compounds.
Abstract:
Production of aldimino- and ketimino- -nitroaryl ethers of the formula
IN WHICH R1 is (m+n) -valent aryl, R2 and R3 each individually is selected from the group consisting of hydrogen, alkyl of up to eight carbon atoms, cycloalkyl, aralkyl, aryl and heterocyclic, with the proviso that R2 and R3 when taken together with the adjacent carbon atom to which they are attached form a ring selected from the group consisting of a 5- to 7-membered isocyclic and heterocyclic ring, m and n each individually is a number from one to two, R4 is (z+l) -valent aryl, and z is an number from one to two, by reacting the corresponding Schiff''s base of the formula
IN WHICH R1, R2, R3, m and n are the same as defined above with an aromatic halo-nitro compound of the formula X -R4 (-NO2)z IN WHICH X is fluoro, chloro or bromo, and R4 and z are the same as defined above, e.g. at about -20* to +200* C., in the presence of an acid acceptor; said ethers being intermediates for producing plant protection agents, e.g. fungicides, dyes and plastics auxiliaries, e.g. for preparing polyimide molded bodies.
Abstract:
Anthraquinone-azomethine compounds of the formula ##STR1## or of the tautomeric formula ##STR2## or of the tautomeric formula ##STR3## in which A denotes an anthraquinone radical which is free from sulphonic acid groups and optionally further substituted and which preferably consists of at most 5 fused rings,R.sub.1 denotes hydrogen, C.sub.1 -C.sub.4 -alkyl, hydroxy-C.sub.1 -C.sub.4 -alkyl, optionally substituted phenyl, carboxyl, carboxylic acid, C.sub.1 -C.sub.4 -alkyl ester or hydroxyl,R.sub.2 denotes hydrogen, halogen, nitro, cyano, optionally substituted carbamoyl or optionally substituted sulphamoyl, sulphonic acid C.sub.1 -C.sub.4 -alkyl ester, sulphonic acid aryl ester, C.sub.1 -C.sub.4 -alkylcarbonyl, C.sub.1 -C.sub.4 -alkoxycarbonyl, optionally substituted benzoyl, alkyl or optionally substituted phenyl sulphone, or a hetero-aromatic radical, for example a radical of the formula ##STR4## or of the formula ##STR5## or of the formula ##STR6## R.sub.3 denotes optionally substituted aryl or hetero-aryl, cycloalkyl or C.sub.1 -C.sub.12 -alkyl, it being possible for the alkyl chain to be interrupted by oxygen or sulphur and/or substituted by hydroxyl, N(R.sub.5).sub.2 --or--N(R.sub.5).sub.3.sup..sym. X.sup..crclbar. groups,R.sub.4 denotes a substituent,R.sub.5 denotes hydrogen, C.sub.1 -C.sub.4 -alkyl, cycloalkyl or optionally substituted aryl,X denotes an anion,m denotes 1, 2, 3 or 4 andn denotes 0, 1, 2, 3 or 4,processes for their preparation and processes for dyeing synthetic fibre materials and for pigmenting organic macromolecular substances using the new anthraquinone-azomethine compounds.
Abstract:
Anthraquinone-azomethine compounds of the formula ##STR1## or of the tautomeric formula ##STR2## in which A denotes an anthraquinone radical which is free from sulphonic acid groups and is optionally further substituted and which preferably consists of at most 5 fused rings,R.sub.1 denotes hydrogen, optionally substituted aryl, preferably ##STR3## hetero-aryl, cycloalkyl or C.sub.1 -C.sub.12 -alkyl, it being possible for the alkyl chain to be interrupted by oxygen or sulphur and/or to be substituted by hydroxyl groups or N(R.sub.3).sub.2 groups, --N(R.sub.3).sub.2 or ##STR4## R.sub.2 denotes a substituent, R.sub.3 denotes hydrogen, C.sub.1 -C.sub.4 -alkyl, cycloalkyl oroptionally substituted aryl,m denotes 1, 2, 3 or 4 andn denotes 0, 1, 2, 3, 4 or 5, processes for their preparation and processes for pigmenting organic macromolecular substances using the new anthraquinone-azomethine compounds.
Abstract:
THIS INVENTION CONCERNS ANTHRAQUINONE DYESTUFFS OF THE FORMULA
A(-NH-CH=C(-CN)-CO-N(-R1)-R2)N
WHEREIN A IS AN ANTHRAQUINONE RADICAL, N IS AN INTEGER FROM 1 TO 4 AND R1 AND R2 COMPLETE THE RESIDUE OF ALIPHATIC OF HETEROCYCLIC AMINES. THE DYESTUFFS ARE PREPARED BY REACTION OF THE APPROPRIATE CYANOACETIC ACID AMIDE WITH N-ANTHRAQUINONYL-N-FORMAMIDIUM SALTS. THESE DYESTUFFS ARE USEFUL FOR DYING OR PRINTING OF TEXTILES.