Abstract:
The present invention relates to specific pentamethine cyanine azo complex dye compounds and their use as dyes in optical layers for optical data recording, preferably for optical data recording using a laser with a wavelength from 630 to 670 nm.The invention further relates to an optical layer comprising said dyes and to a write only read many (WORM) type optical recording medium capable of recording and reproducing information with radiation of a red laser, which employs said pentamethine cyanine azo complex type dye in the optical layer.
Abstract:
New azo compounds containing the radical of a 3-halogeno-6-hydroxy-pyridone-(2) of the formula ##STR1## wherein X represents halo, R and R' represent hydrogen aryl, cyclohexyl, alkyl or substituted alkyl and D represents the residue of a diazo component of the benzene series, said compounds useful as dyestuffs.
Abstract:
The present invention is to provide an optical recording medium which is capable of performing good recording and reproducing by using a laser having a wavelength of 300 to 900 nm, a novel azo metal chelate compound, and a novel azo compound. Furthermore, the present invention is to provide an optical recording medium having an azo metal chelate compound in a recording layer.
Abstract:
Azo dyestuffs which contain an acid substituent which confers solubility in water of the formula ##STR1## wherein D is the radical of a sulfo substituted benzene or naphthalene diazo component;R' is alkyl of 1 to 4 carbon atoms;Z is a fiber reactive group; andN is an integer of 1 to 4 are disclosed and are useful in dyeing nitrogen containing fibers such as polyamides, polyurethanes, silk, leather and wool as well as cellulose materials, in particular cotton.
Abstract:
A compound of the formula ##SPC1##Wherein R and R' each represent a hydrogen atom, an alkyl or aryl radical or a heterocyclic radical and X represents a sulphoalkyl group. These compounds are useful as coupling components for the manufacture of dyestuffs which are distinguished by high tinctorial strength.
Abstract:
Heavy metal complexes of azo compounds of the formula
WHERE D is the residue of a heterocyclic diazo component and is selected from pyridyl; benzthiazolyl that is unsubstituted or substituted by chloro, nitro or methoxy; indazolyl that is unsubstituted or substituted by chloro, methoxy or nitro; triazolyl; carboxytriazolyl; 4-phenyl-5-methyl-pyrazolyl; 1phenyl-2,3-dimethylpyrazolyl-5-one; benztriazolyl; benzimidazolyl; thiazolyl; methylthiazolyl; thiadiazolyl that is unsubstituted or substituted by phenyl, pyridyl, acetylamino, phenylsulphonyl, chloro, carbomethoxy, methylthio, ethylthio, phenylthio, cyclohexylthio, methylsulphonyl or methyl; quinolyl that is unsubstituted or substituted by sulfo, chloro, bromo, acetylamino, methyl, sulfophenylazo, or sulfophenylazo containing a fibre-reactive acylamino group, where acyl is selected from chloroacetyl, bromoacetyl, Beta chloropropyionyl, Beta -bromopropionyl, Alpha , Beta dichloropropionyl, Alpha , Beta -dibromopropionyl, chloromaleyl, acrylyl, Beta -chloroacrylyl, Beta bromoacrylyl, Alpha -chloroacrylyl, Alpha -bromoacrylyl, Alpha , Beta -dichloroacrylyl, Alpha , Beta -dibromoacrylyl, trichloroacrylyl, chlorocrotonyl and propiolyl; or benzisothiazolyl that is unsubstituted or substituted by methyl, ethyl, methoxy, chloro, bromo, cyano, nitro, Nmethylsulfonamido, N,N-dimethylsulfonamido or methylsulfonyl; or D is phenyl or naphthyl that contains an OH, NH2 or COOH group in the position orthho-to the azo bond, said phenyl or naphthyl being further unsubstituted or substituted by chloro, bromo, nitro, cyano, lower alkyl, lower alkoxy, lower alkylsulphonyl, sulfonic acid, carboxylic acid, sulphonamide, N-lower alkylsulphonamide, N-lower hydroxyalkyl-sulphonamide, N,Ndiethylsulphonamide, N,N-di( Beta -hydroxyethyl)-sulphonamide, phenylazo, naphthylazo, formylamino, acetylamino, benzoylamino, benzenesulphonamide, p-toluenesulphonylamino, methanesulphonylamino, carboxymethoxyamino, carboethoxyamino, dimethylaminosulphonylamino or isopropoxyamino, X is hydroxy, alkoxy of 1 to 4 carbon atoms, phenoxy, naphthoxy, Beta -hydroxyethylamino, gamma -methoxy-n-propylamino, isopropoxy-n-propylamino, N,N-diethylethylenediamine, cyclohexylamino, piperidyl, morpholyl, phenylamino, carboxyphenylamino, sulfonaphthylaminno, mercapto, methylthio, Beta -hydroxyethylthio, phenylthio, carboxyphenylthio, naphthylthio, thiazolylthio, methylsulphonyl, phenylsulphonyl, methyl-phenylsulphonyl, sulfo or fibre-reactive acrylaminno where acyl is selected from the group consisting of chloroacetyl, bromoacetyl, Beta -chloropropionyl, Beta bromopropionyl, Alpha , Beta -dichloropropionyl, Alpha , Beta -dibromopropionyl, chloromaleyl, acrylyl, Beta -chloroacrylyl, Beta -bromoacrylyl, Alpha -chloroacrylyl, Alpha bromoacrylyl, Alpha , Beta -dichloroacrylyl, Alpha , Beta dibromoacrylyl, trichloroacrylyl, chlorocrotonyl and propiolyl ARE USEFUL TO DYE SUCH FIBERS AS WOOL AND NYLON IN SHADES OF GREEN AND BLUE THAT ARE FAST TO ACID, ALKALI, LIGHT AND RUBBING.
Abstract:
Azo compounds of the formula ##STR1## wherein R represents a hydrogen atom, an alkyl or aryl radical, R' represents a hydrogen or halogen atom, a cyano, carboxylic amide, alkylsulphonyl, arylsulphonyl, nitro, nitroso, amino, or acylamino group, and D represents the radical of a diazo component, are valuable dyestuffs for the dyeing of textile materials.
Abstract:
Azo compounds of the formulaD-N=N-K (1)wherein D denotes the radical of an aromatic diazo component and K denotes the radical of a halogeno-2,3-dihydroxy-pyridine, as well as heavy metal complexes of azo compounds of the formula (1).
Abstract:
A dyestuff of the formula ##SPC1##Wherein m is 1, 2 or 3; R.sup.9 is ##SPC2##Wherein n is 0 or 1 and R" is hydrogen or lower alkyl or ##SPC3##Wherein p is 1, 2 or 3; R.sup.10 is C.sub.1.sub.-6 alkyl, benzyl, sulphobenzyl, phenyethyl, sulphophenylethyl, ##EQU1## wherein r is 2 to 6, ##SPC4##Or ##SPC5##Wherein R" has the meaning given above and the dyestuff as a whole contains only one group represented by Z, and Z is a cellulose-reactive group. The dyestuff is useful in dyeing and printing cellulose, polyamide and wool textile materials. Textile dyes with the above dyestuff exhibits good fastness to washing and to bleaching and good resistance to acids and alkalies.