Abstract: Process for the production of leather using products obtainable by reacting (A) at least one cyclic organic carbonate with (B) at least one compound having at least two nucleophilic groups per molecule, selected from sulfonic acid, hydroxyl, primary or secondary amino or mercapto groups.

Abstract: Process for the production of leather using products obtainable by reacting (A) at least one cyclic organic carbonate with (B) at least one compound having at least two nucleophilic groups per molecule, selected from sulfo, hydroxyl, primary or secondary amino or mercapto groups.

Abstract: The invention relates to a method for vulcanizing caoutchouc or latex by adding a mixture M which contains a component a) from a1) 20 to 96% by weight of sulfur, a2) 4 to 80% by weight of a complexing agent, and optionally other additives b) to caoutchouc or latex and then vulcanizing the mixture. The inventive method is characterized in that the average particle size of the primary particles of component a) ranges from 0.05 to 20 ?m.

Abstract: The present invention provides dye preparations comprising, each percentage being based on the weight of the preparation, a) from 0.1% to 30% by weight of one or more anthraquinone, quinophthalone or azo dyes which are free of ionic groups as a component (A), b) from 0.1% to 20% by weight of a dispersant based on a naphthalenesulfonic acid-formaldehyde condensation product having an average molecular weight of at least 11 000 g/mol, as a component (B), c) from 0.1% to 90% by weight of one or more mono- or polyhydric alcohols as a component (C), d) from 0% to 5% by weight of customary assistants as a component (D), and e) optionally water ad 100% by weight.

Abstract: The invention relates to a method for vulcanizing caoutchouc or latex by adding a mixture M which contains a component a) from a1) 20 to 96% by weight of sulfur, a2) 4 to 80% by weight of a complexing agent, and optionally other additives b) to caoutchouc or latex and then vulcanizing the mixture. The inventive method is characterized in that the average particle size of the primary particles of component a) ranges from 0.05 to 20 ?m.

Abstract: Phthalocyanines of the formula where Me is twice hydrogen, twice lithium, magnesium, zinc, copper, nickel, VO, TiO, AlCl, AlOH, AlOCOCH3, AlOCOCF3, SiCl2 or Si(OH)2, at least four of the radicals R1 to R16 are each independently of the others a five- or six-membered saturated nitrogen-containing heterocyclic radical which is bonded to the phthalocyanine structure via a ring nitrogen atom and which can additionally contain further hetero atoms, and any remaining radicals R1 to R16 are each hydrogen, halogen, hydroxysulfonyl or C1-C4-dialkylsulfamoyl, subject to the proviso that tetrakispiperidinylphthalocyanine shall be excluded, and heterocyclyl-substituted phthalocyanines are useful for marking liquids, in particular mineral oils.

Abstract: Use of compounds from the class of the phthalocyanines, naphthalocyanines, nickel dithiolene complexes, aminium compounds of aromatic amines, methine dyes or azulenesquaric acid dyes which have their absorption maximum in the range from 600 to 1,200 nm and/or a fluorescence maximum in the range from 620 to 1,200 nm, as markers for liquids, a process for detecting markers in liquids, and a detector suitable for this purpose.

Abstract: Use of compounds from the class of the phthalocyanines, naphthalocyanines, nickel dithiolene complexes, aminium compounds of aromatic amines, methine dyes or azulenesquaric acid dyes which have their absorption maximum in the range from 600 to 1,200 nm and/or a fluorescence maximum in the range from 620 to 1,200 nm, as markers for liquids, a process for detecting markers in liquids, and a detector suitable for this purpose.

Abstract: Compounds of the general formula I ##STR1## where the A radicals are, independently of one another, ##STR2## where the rings B and C can also, independently of one another, be substituted by C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, nitro, hydroxysulfonyl, benzoyl or a fused-on benzo ring,R is hydrogen or methyl, and the two hydrogen atoms on the nitrogens Can be replaced by copper, nickel, vanadyl, magnesium, AlCl or zinc,are suitable as IR-absorbers.

Abstract: A process is described for preparing alkoxy-octasubstituted metal-free or metal-containing naphthalocyanines by etherification of 1,4-dihydroxy-2,3-dicyanonaphthalene and formation of the metal-free naphthalocyanine with or without subsequent metallization.

Abstract: Ink ribbons containing one or more compounds from the group comprising phthalocyanines, the naphthalocyanines, the nickel dithiolene complexes, the methine dyes and the azulene quaternary-acid dyes, all of which have their absorption maximum in the region from 700 to 1,200 nm.

Abstract: Crystalline molecular sieves useful as colorants contain one or more chromophores of the class of the mono- or polyazo dyes that are devoid of acidic groups.

Abstract: Compounds from the class consisting of the phthalocyanines, naphthalocyanines, the aminium compounds of aromatic amines, the methine dyes or the azulenesquaric acid dyes, which have their absorption maximum in the range from 600 to 1,200 nm and a fluorescence maximum in the range from 620 to 1,200 nm, are used as crack-detecting agents.

Abstract: Naphthalocyanines of the general formula I ##STR1## where the variables have the following meanings: R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.6, R.sup.7 and R.sup.8 are each independently of the others hydrogen, hydroxyl or C.sub.1 -C.sub.20 -alkyl or C.sub.1 -C.sub.20 -alkoxy, whose carbon chains may each be interrupted by from 1 to 4 oxygen atoms in ether function and which may be phenyl-substituted,R.sup.9, R.sup.10, R.sup.11 and R.sup.12 are each independently of the others hydrogen, halogen or C.sub.1 -C.sub.20 -alkyl or C.sub.1 -C.sub.20 -alkoxy, whose carbon chains may each be interrupted by from 1 to 4 oxygen atoms in ether function,Me is two hydrogen atoms, two univalent metal atoms or a bivalent metal atom with or without further substituents for valence saturation,are pigments with isometric particles and a particle size distribution from 10 to 300 nm.

Abstract: A photosensitive recording element comprises(A) a dimensionally stable substrate,(B) a photopolymerizable relief-forming recording layer and, if required, an adhesion-promoting layer arranged between (A) and (B), a release layer (C) applied to that side of the recording layer (B) which faces away from the substrate (A), and, if required, a cover sheet (D) applied thereon, the photopolymerizable relief-forming recording layer (B) containingb.sub.1) at least one polymeric binder,b.sub.2) at least one photopolymerizable olefinically unsaturated monomer which is compatible with b.sub.1),b.sub.3) at least one photopolymerization initiator andb.sub.4) at least one aryl alkyl ketone,and is suitable for the production of relief printing plates.

Abstract: In laked tris- or tetracationic polymethine dyes I ##STR1## the variables have the following meanings: A is the radical of a fused-on substituted or unsubstituted benzene or naphthalene nucleus,Y is nitrogen or phosphorus,Z is --NR.sup.1 --, --O--, --S--, --C(CH.sub.3).sub.2 -- or --CH.dbd.CH--, where R.sup.1 is a radical as defined for R,D is --CX.sup.1 .dbd., --CH.dbd.CX.sup.1 --CH.dbd., ##STR2## Het.sup.e is the equivalent of a heteropolyacid anion, m is from 1 to 10, andn is 3 or 4, where (R).sub.3, X.sup.1, and X.sup.2 have the meanings set out in the specification.

Abstract: There are described rhodamine derivatives of the formula ##STR1## where R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are each hydrogen or substituted or unsubstituted C.sub.1 -C.sub.4 -alkyl, or R.sup.2 is paired off with R.sup.5 or R.sup.4 with R.sup.6 to form 1,3-propylene, which can be substituted,R.sup.5, R.sup.6, R.sup.7 and R.sup.8 are each hydrogen or methyl,R.sup.9 is hydrogen, substituted or unsubstituted C.sub.1 -C.sub.4 -alkyl or a radical of the formula (C.sub.2 H.sub.4 O--).sub.n H, where n is 2 or 3, andAn.sup..crclbar. is the equivalent of an anion derived from an addition or condensation polymer that contains acid groups, novel cyclic rhodamine dyes, and the use of the novel rhodamine derivatives and cyclic rhodamine dyes for dyeing polyacrylonitrile fibers, for incorporation into polymers or for preparing inks.

Abstract: Methine dyes with a polyketo group I ##STR1## where A is ##STR2## R.sup.1 is a 5- or 6-membered cycloaliphatic radical which contains one or two hetero atoms from the group --NR.sup.4 --, --O-- and --S-- and which may be fused to an isoaromatic or heteroaromatic group, R.sup.2 and R.sup.3 are identical or different C.sub.1 -C.sub.10 -alkyl groups or together one of the radicals R.sup.1, and m and n are identical or different integers from 0 to 3, are useful as drugs, for producing singlet oxygen, as sensitizers in electrophotographic layers and for photopolymerizations and as laser light sensitive dyes in optical recording media; also novel triketo- and tetraketomethine dyes.

Abstract: Indolizinetrimethine dyes useful for laser-optical recording media have the formula ##STR1## where the variables are defined as follows: R.sup.1 is C.sub.1 -C.sub.22 -alkyl which may be substituted by halogen, hydroxyl, C.sub.1 -C.sub.6 -alkoxy, benzyloxy, C.sub.1 -C.sub.6 -alkanoyl, C.sub.1 -C.sub.6 -alkoxycarbonyl or phenyl, C.sub.3 -C.sub.7 -cycloalkyl, which may be substituted by halogen, C.sub.1 -C.sub.4 -alkyl or C.sub.1 -C.sub.4 -alkoxy, or phenyl which may be substituted by halogen, hydroxyl, cyano, C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -alkoxy, carboxyl, C.sub.1 -C.sub.6 -alkoxycarbonyl or hydroxysulfonyl,R.sup.2 has one of the meanings of R.sup.1, except than the carbon chain of C.sub.1 -C.sub.22 -alkyl may be interrupted by from one to five oxygen atoms in ether function,R.sup.3 is hydrogen, halogen or C.sub.1 -C.sub.6 -alkyl,Z is --O-- or --NH--, andAn.sup..crclbar. is one equivalent of an acid anion.

Abstract: A liquid useful as printing ink contains one or more dyes with their absorption maximum within the range from 700 to 1200 nm selected from the phthalocyanines, the naphthalocyanines, the nickel-dithiolene complexes, the aminium compounds of aromatic amines, the methine dyes or the azulenesquaric acid dyes, as well as solvent and binder.