Abstract:
Materials for optical recording media are disclosed. Specifically, the materials are metal chelate compounds of azo dyes, which are formed from sulfamoylated m-diaminobenzene compounds and benzene ring-containing azo compounds. Further, the invention provides an optical recording medium, characterized in that said metal chelate compounds of azo dyes are employed onto the optical recording medium to form a recording layer. The invention also discloses a process for the production of an optical recording medium.
Abstract:
Materials for optical recording media are disclosed. Specifically, the materials are metal chelate compounds of azo dyes, which are formed from sulfamoylated m-diaminobenzene compounds and benzene ring-containing azo compounds. Further, the invention provides an optical recording medium, characterized in that said metal chelate compounds of azo dyes are employed onto the optical recording medium to form a recording layer. The invention also discloses a process for the production of an optical recording medium.
Abstract:
Novel metal complexes for optical data carriers comprising a preferably transparent substrate which may, if desired, have previously been coated with one or more reflection layers and to whose surface a light-writable information layer, if desired one or more reflection layers and if desired a protective layer or a further substrate or a covering layer have been applied, which can be written on or read by means of blue or red light, preferably laser light, where the information layer comprises a light-absorbent compound and, if desired, a binder, characterized in that at least one such metal complex is used as light-absorbent compound, have been found.
Abstract:
The azo-metal chelate dye to which the present invention is applied is a compound formed as follows: for example, 1,3,4-thiadiazole ring is selected as the diazo component; the diazo component is combined with a coupler component having condensed rings including a fluorine-substituted alkylsulfonylamino group and an amino group, to form an azo dye compound; and the azo dye compound forms chelate bonds with at least one metal selected from the group consisting of Co, Ni, Cu and Pd. Here, two absorption bands (OD1 and OD2) are seen in the absorption spectrum, which is measured in a range of 400 to 800 nm wavelengths. The azo-metal chelate dye is characterized in that the optical density ratio (OD2/OD1) of the two absorption bands is greater than 1.25. By using this azo-metal chelate dye, an optical recording medium capable of high-speed recording is provided.
Abstract:
An optical recording medium dye is described. The optical recording medium dye is an azo metal chelate compound, wherein the azo metal chelate compound comprises the following structure: 1 wherein R1 is a hydrogen atom, a C1-6 straight chain or branched alkyl group, an amino group, an alkylamino group or a tolylamino group; R2 is a hydrogen atom, a hydroxyl group, a halogen atom, an ether group, a C1-6 straight chain or branched alkyl group; R3 is a hydrogen atom, a C1-6 straight chain or branched alkyl group; R4 is a hydrogen atom, a C1-6 straight chain or branched alkyl group or a halogen atom; A3 is a residue forming a heterocyclic ring derivative together with a carbon atom and a nitrogen atom.
Abstract:
An azo metal chelate compound of an azo compound of the formula (I) with a metal: ##STR1## wherein A is a residue forming a heterocyclic ring together with the carbon atom and the nitrogen atom to which it is bonded, X is a residue forming an aromatic group together with the two carbon atoms to which it is bonded, R.sup.1 is an alkyl group which may be substituted, an aryl group which may be substituted, an alkenyl group which may be substituted, or a cycloalkyl group which may be substituted, Y is a hydrogen atom or a cation, and n is an integer of from 1 to 3.
Abstract:
New inclusion compound, intercalation compounds or solid solutions which are the nickel salts or nickel complexes of a compound which, in one of its tauteromeric structures, corresponds to the formula ##STR1## which contain at least one other included compound, except for one composition of matter which consists of 45 to 82% by weight of azobarbituric acid/nickel 1:1 complex, 3 to 15% by weight of benzene-sulphonamide, 5 to 20% by weight of nickel acetate and 10 to 20% by weight of water and the use of these materials as pigments are disclosed.
Abstract:
2:1-chromium complex dyes of the formula: ##STR1## in which: A is the radical of a carbocyclic diazo component with a complex-forming hydroxy or carboxy group adjacent to the azo bridge;B is the radical of a carbocyclic, heterocyclic or open-chain coupling component with a complex-forming hydroxy or amino group adjacent to the azo bridge;D is the radical of a carbocyclic aldehyde with a complex-forming hydroxy group adjacent to the azomethine bond;E is an aliphatic radical with a complex-forming amino group; and n is the number of carboxy groups not participating in the formation of the complex and the sulfonic acid groups.The dyes are eminently suitable for dyeing natural and synthetic polyamides, clear shades with good fastness properties being obtained.
Abstract:
It has been found that nickel-containing polyolefins can be dyed and printed in deep colors and with very good to excellent fastness properties when a thiazole-azo-(3-cyano-2,6-dihydroxypyridine) dyestuff is used.
Abstract:
Sulphonated, sulphocarboxylated or polycarboxylated metallisable dyes are pasted with water and an anionic dispersant, the pH of the paste being such that the dye is practically in the undissolved state at room temperature and the dye particles have a size not greater than 5 microns. The pastes may then be dried, e.g. spray dried, to form a dry powder. The pastes and powders so obtained may be employed to dye animal or superpolyamide fibres by known after-chroming or simultaneous chroming (monochrome or metachrome) processes even with very hard water using a bath-circulating apparatus. In the examples the following aniomic dispersants are employed: (1) dinaphthylmethane disulphonate together with sodium diheptyl sulphosuccinate, (3) as in (1) plus sodium sulphoricinoleate, (4) sodium lignin sulphonate and sulphated lauryl alcohol, (5) as in (1) plus diheptyl sulphosuccinate. Specifications 976,417 and 1,001,181 are referred to.