Abstract:
Disclosed are polymeric dyes of formula (1a), (1b), or (1c); wherein A and B, independently from each other represent a polymer backbone; X1 and X2 independently from each other are a linkage group selected from —S—, —S—S—, —N—, —N═—, —N(R5)—, —S(O)—, —SO2—, —(CH2CH2—O)1-5—, —(CH2CH2CH2—O)1-5—, —C(O)—, —C(O)O—, —OCO—, (formula II) —CON(R1)—, —C(NR1R2)2—, —(R1)NC(O)—, —C(S)R1—; which may be interrupted and/or terminated at one or both ends by one or more than one —C1C30alkylene- or —C2-C12alkenylene-; or an optionally substituted, saturated or unsaturated, fused or non-fused aromatic or nonaromatic (heterocyclic) bivalent radical optionally comprising at least one heteroatom; a saturated or unsaturated, fused or non-fused aromatic or nonaromatic bivalent radical comprising at least one heteroatom, which is optionally substituted by C1-C30alkyl, C1-C30alkoxy, C2-C12alkenyl, C5-C10aryl, C5-C10cycloalkyl, C1-C10alkyl(C5-C10arylene), hydroxy or halogen; R1 and R2 independently from each other are hydrogen; unsubstituted or substituted, straight-chain or branched, monocyclic or polycyclic, interrupted or uninterrupted C1-C14alkyl; C2-C14alkenyl; C6-C10aryl; C6-C10aryl-C1-C10alkyl; or C5-C10alkyl(C5-C10aryl); Y1 and Y2 independently from each other are a residue of an organic dye selected from hydrazone dyes of formula (1d), wherein Z1, Z2 and Z3, independently from each other are —CR8— or —NR9+-; and at least one of Z1, Z2 or Z3 is —NR9+-; wherein at least one of Y1 and Y2 is a residue of an organic dye; R, R3, R4, R5, R6, R7, R8 and R9 independently from each other are hydrogen; hydroxy; C1-C5alkyl; hydroxy-C1C5alkyl; C1C5alkoxy; —NO2; —Cl; —Br; —COOH; —SO3H; —CN; NH2; or CH3—CO—NH—; An1, An2 and An3, independently from each other are an anion; a and b independently from each other are a number from 1 to 3; m is a number from 0 to 5000; n is a number from 0 to 5000; and p is a number from 1 to 5000; wherein the sum of m+n+p≧3. The dyes are distinguished by their depth of shade and their good fastness properties to washing, such as, for example, fastness to light, shampooing and rubbing.
Abstract:
There has been found1) a method for reducing the toxicity of spent liquors from dyeing with cationic dyes or mixtures thereof, characterized by the step of dyeing with cationic dyes having a computed electrostatic shielding energy (idealized hydration energy) of .gtoreq.50 kcal/mol,2) cationic, generally low toxicity dyes, their preparation and use for dyeing.
Abstract:
Chromogenic polycyclic azamethines of formula ##STR1## wherein T.sub.1 and T.sub.2 are each independently of the other lower alkyl, cycloalkyl, benzyl, or, when taken together, are alkylene,Q is --CH or, preferably, N,W is alkylene, alkenylene, 1,2-cycloalkylene or 1,2-arylene,R is hydrogen, lower alkyl, aryl or aralkyl, andY is alkyl or alkenyl, each unsubstituted or substituted by halogen, hydroxyl, cyano or lower alkoxy, or is aralkyl, and the ring A is unsubstituted or substituted by halogen, cyano, hydroxy, lower alkyl, lower alkoxy, lower alkylcarbonyl, lower alkylcarbonyloxy, lower alkylamino, di-lower alkylamino or lower alkylcarbonylamino, and the ring B is unsubstituted or substituted by halogen, cyano, C.sub.1 -C.sub.12 alkyl, C.sub.1 -C.sub.12 alkoxy, C.sub.2 -C.sub.12 alkoxyalkoxy or aralkoxy or a glycol ether group.These azamethines are particularly suitable for use as color formers in pressure-sensitive or heat-sensitive recording materials and give strong and lightfast yellow and orange colorations.
Abstract:
The preparation of hydrazone dyestuffs of the formula ##STR1## wherein R.sup.13 and R.sup.14 independently of one another represent hydrogen, C.sub.1 -- to C.sub.4 --alkyl, C.sub.1-- to C.sub.4-- alkoxy or halogen, in particular chlorine or bromine, andA.sup.- denotes an anionic radical,by reacting azo bases of the general formula ##STR2## wherein R.sup.13 and R.sup.14 have the above mentioned meaning andR.sup.15 represents hydrogen or the methyl group, with dimethyl sulphate in a mixture of water and an organic solvent and in the presence of an acid-binding agent, is characterized in that (a) aromatic or aliphatic chlorinated hydrocarbons are used as the organic solvents, (b) the reaction is carried out at a temperature of 10.degree.-60.degree. C., (c) a 5-90% excess of dimethyl sulphate is employed and (d) the reaction is allowed to proceed at a pH of 5-10.
Abstract:
Dyestuffs of the formula ##STR1## wherein R represents alkyl, alkenyl, cycloalkyl or aralkyl,R.sub.1 represents hydrogen, alkyl, alkenyl, cycloalkyl or aralkylR.sub.2 represents alkylene, of which the chain can be interrupted by O,Y represents -CO- or -O-CO-O-,A represents an aromatic ring andX.sup.- represents an anion,Are suitable for dyeing and printing of polyacrylonitrile and acid modified polyesters and polyamides.
Abstract:
Process for the preparation of heterocyclic compounds of the general formula ##SPC1##By condensation of an o-substituted amine of the general formula ##SPC2##With a carbonyl compound of the general formula ##EQU1## in the presence of a hydrazine of the general formula ##EQU2## followed by quaternization if appropriate. In the formulae the radicals have the meaning as indicated below.
Abstract:
A process for making yellow, basic azomethine dyes for paper, leather and textiles, and concentrated, stable solutions thereof; the process being an improvement in the process of reacting an azo dye base precursor of the formula ##SPC1##Wherein A is phenyl or substituted phenyl, with dimethyl sulfate in solution, and in the presence of an acid-binding agent,THE IMPROVEMENT COMPRISING EMPLOYING AN AQUEOUS SOLUTION HAVING AT LEAST 30 WEIGHT PERCENT WATER, EMPLOYING DIMETHYL SULFATE IN A MOLAR EXCESS OF FROM 100% TO 300%, AND EMPLOYING FROM 2.0 TO 3.5 MOLES OF MAGNESIUM OXIDE AS THE ACID-BINDING AGENT PER MOLE OF PRECURSOR.
Abstract:
A process for dyeing acid-modified polyester fibers comprising contacting the fibers with a dye bath containing a thiazoleazotype cationic dye of the formula (I);
wherein R1 and R3 are each a C1 - C2 alkyl group, R2 is a hydrogen atom, a C1 - C2 alkyl group or a C1 - C2 alkoxy group, R4 is a hydrogen atom or a C1 - C2 alkyl group, R5 is a hydroxyl group or a C1 - C2 alkoxy group, and X is an anion. The dye compounds of the formula (I) dye acid-modified polyester fibers a bright shade and with good light fastness. The dye compounds of the Formula (I) wherein R2 is a hydrogen atom or a methoxy or ethoxy group are novel dye compounds.
WHEREIN B IS PHENYL, TETRAHYDROPHENYL OR HEXAHYDROPHENYL;
=C IS DIHYDROINDOYL, PYRIMIDONYL, DIHYDROPYRIMIDONYL, BENZOTHIAZOLYL, DIHYDROQUINOXALYL, DIHYDROQUINOXALONYL, OR DIHYDROQUINAZOLYL; Y IS
-O-, -S-, OR -N(-R)-
WHERE R IS HYDROGEN, LOWER ALKYL, 2-CHLOROETHYL, 3-CHLOROPROPYL, BENZYL, B-PHENYLETHYL, Y-PHENYLPROPYL, PHENYLPROPYL-(2,2), 4-NITRONENZYL, PHENYL, LOWER ALKYLPHENYL, CHLOROPEHNYL, OR 4-AMINOPHENYL; R1 IS LOWER ALKYL, 2-CHLOROETHYL, 3-CHLOROPROPYL, LOWER ALKENYL, BENZYL, B-PHENYLETHYL, Y-PHENYLPROPYL, PHENYLPROPYL-(2,2), 4-NITROBENZYL, ETHOXYETHYL, OR ETHOXYCARBONYL-METHYL; R2 IS HYDROGEN, FLUORO, CHLORO, BROMO, LOWER ALKOXY, LOWER ALKYL, 2-CHLOROETHYL, 3-CHLOROPROPYL, HYDROXY, DIMETHYLAMINO, DIETHYLAMINO, DI-N-PROPYLAMINO, OR LOWER ALKANOYLAMINO; R3, WHEN RING B IS PHENYL, IS HYDROGEN, CHLORO, BROMO, LOWER ALKYL, 2-CHLOROETHYL, 3-CHLOROPROPYL, LOWER ALKOXY, HYDROXYL, DIEMTHYLAMINO, DIETHYLAMINO, DI-NPROPYLAMINO, OR LOWER ALKANOYLAMINO; R3, WHEN RING B IS TETRAHYDROPHENYL, OR HEXAHYDROPHENYL, IS HYDROGEN, CHLORO, OR LOWER ALKYL; R4 IS LOWER ALKYL, 2-CHLOROETHYL, 3-CHLOROPROPYL, CYCLOHEXYL, 4 - METHYLCYCLOHEXYL, BENZYL, B-PHENYLETHYL, Y-PHENYLPROPYL, PHENYLPROPYL-(2,2), 4-NITROBENZYL, PHENYL, LOWER ALKYLPHENYL, CHLOROPEHNYL, OR BROMOPHENYL; AND A- IS AN ANION.