Abstract: The invention relates to thermoplastic molding compositions comprising (A) from 34 to 99.99% by weight of at least one thermoplastic polymer selected from (i) polyarylene ethers, (ii) polyetherimides, (iii) polyarylene sulfides, and (iv) polycarbonates with glass transition temperature of at least 145° C., or else copolymers of the abovementioned polymers (i) to (iv), (B) from 0.01 to 10% by weight of at least one organic black pigment which is transparent in the range from 1000 nm to 1600 nm and which has thermal stability up to at least 300° C. to DIN EN 12877-1, (C) from 0 to 6% by weight of at least one mold-release agent selected from fatty acids, or from esters and amides, (D) from 0 to 50% by weight of one or more additives, where the total of the % by weight figures from (A), (B), (C) and (D) gives 100% by weight. The invention further relates to a process for preparation of the thermoplastic molding compositions, and to the moldings obtainable therefrom.

Abstract: The invention relates to thermoplastic molding compositions comprising (A) from 34 to 99.99% by weight of at least one thermoplastic polymer selected from (i) polyarylene ethers, (ii) polyetherimides, (iii) polyarylene sulfides, and (iv) polycarbonates with glass transition temperature of at least 145° C., or else copolymers of the abovementioned polymers (i) to (iv), (B) from 0.01 to 10% by weight of at least one organic black pigment which is transparent in the range from 1000 nm to 1600 nm and which has thermal stability up to at least 300° C. to DIN EN 12877-1, (C) from 0 to 6% by weight of at least one mold-release agent selected from fatty acids, or from esters and amides, (D) from 0 to 50% by weight of one or more additives, where the total of the % by weight figures from (A), (B), (C) and (D) gives 100% by weight. The invention further relates to a process for preparation of the thermoplastic molding compositions, and to the moldings obtainable therefrom.

Abstract: A process for converting perylene-3,4:9,10-tetracarboximides of the general formula I in which R1 and R2 are each unbranched, branched or cyclic C1-C8-alkyl to a form suitable for use as fluorescent dyes, which comprises a) dissolving or suspending the perylene-3,4:9,10-tetracarboximides whose molecules have a molecular volume of ?230 ?3 in an organic or inorganic solvent at from 0 to 250° C.

Abstract: A process for preparing quaterrylene-3,4:13,14-tetracarboximides of the general formula I in which R, R? are each independently hydrogen or optionally substituted C1-C30-alkyl, C5-C8-cycloalky or aryl or hetaryl; which comprises reacting a perylene-3,4-dicarboximide of the general formula IIa in the presence of a base-stable, high-boiling, organic solvent and of an alkali metal base or alkaline earth metal base, with a perylene-3,4-dicarboximide of the general formula IIb in which X is hydrogen, bromine or chlorine.

Abstract: The current invention relates to a perylene-3,4-dicarboxylic anhydride, substituted in the 9-position, of the general formula III wherein Z is bromine or cyano, and processes for preparing 9-bromoperylene-3,4-dicarboxylic anhydride and 9-cyanoperylene-3,4-dicarboxylic anhydride.

Abstract: Use of luster pigments based on a platelet-shaped metallic substrate coated with a low refractive dielectric layer which does not absorb visible light, for pigmenting macromolecular materials.

Abstract: A fluorescence conversion solar cell based on one or more panels composed of polymer doped with at least one fluorescent dye and/or glass panels coated with the doped polymer and photovoltaic cells mounted on the edges of the panels, which comprise one or more fluorescent dyes based on terrylenecarboxylic acid derivatives or a combination of these fluorescent dyes with further fluorescent dyes.

Abstract: Use of luster pigments based on a platelet-shaped metallic substrate coated with a low refractive dielectric layer which does not absorb visible light, for pigmenting macromolecular materials.

Abstract: Rylene derivatives of the general formula I in which the variables are each defined as follows: Rylene is a polycyclic conjugated ring system which comprises at least one perylene unit may comprise heteroatoms as ring atoms, may be functionalized by moieties comprising —CO— groups and/or may bear further substituents other than the A radicals; A is a radical of the formula X is oxygen or sulfur; R are identical or different radicals: optionally substituted alkyl, cycloalkyl, aryl, hetaryl, —U-aryl where U is an —O—, —S—, —NR2—, —CO—, —SO— or —SO2— moiety, or C1-C12-alkoxy, C1-C6-alkylthio, —C?CR2, —CR2?CR22, hydroxy, mercapto, halogen, cyano, nitro, —NR3R4, —NR3COR4, —CONR3R4, —SO2NR3R4, —COOR3 or —SO3R3; R? are identical or different radicals: hydrogen or one of the R radicals; R2 is hydrogen or alkyl, where the R2 radicals may be the same or different when they occur more than once; R3, R4 are each independently hydrogen; optionally substituted alkyl, aryl or hetaryl; n is from 1 to

Abstract: A process for preparing perylene-3,4:9,10-tetracarboxylic dianhydride, comprising: dimerizing a naphthalene-1,8-dicarboximide of the formula IIa; reoxidizing the resulting alkali metal salt of the leuco form of the perylene-3,4:9,10-tetracarboxylic diimide of the formula Ia; hydrolyzing the diimide to the tetraalkali metal salt of perylene-3,4:9,10-tetracarboxylic acid in the presence of an inert organic solvent, of an alkali metal base and of water; and subjecting the tetraalkali metal salt of perylene-3,4:9,10-tetracarboxylic acid to the action of an aqueous inorganic acid to convert it into perylene-3,4:9,10-tetracarboxylic dianhydride; wherein R3 is cyclohexyl or phenyl which may each be substituted by up to three C1-C4-alkyl radicals, and the dimerizing is in a substantially homogeneous reaction medium consisting essentially of an apolar aprotic organic solvent and an alkali metal base.

Abstract: The invention relates to a liquid crystal display comprising a multi-layered display unit (1) which is introduced into a housing (20). Said unit comprises, in a successive manner from the visible side to the rear side, a front polarisation filter (11), a liquid crystal layer (12), a rear polarisation filter (13) and a diffusion layer (14) or retro-reflection layer, optionally, with additional layers (15, 16). High luminosity is achieved by virtue of the fact that the diffusion layer or the retro-reflection layer are provided with fluorescent colours (14.1).

Abstract: Disclosed is a method for welding together plastic parts with the aid of laser radiation having a wavelength outside the visible range. According to the inventive method, the joining zone of one of the plastic parts that are to be joined together is provided with a substantially colorless material that is transparent in the visible range of the electromagnetic spectrum while absorbing the laser radiation. The inventive method is characterized in that at least one non-ionic, laser radiation-resistant compound that has a minimum thermal resistance of 300° C. and is selected among the group comprising the polycyclic organic compounds, doped tin oxides, and hexaborides MB6 of lanthanide metals and alkaline earth metals M is used as the laser radiation-absorbent material.

Abstract: Aqueous polymer dispersions comprising effect substance and having an average particle diameter of the dispersed particles of <500 nm, where the polymer particles comprise a polymer matrix constructed from at least one ethylenically unsaturated monomer as core, on the surface of which is arranged at least partially an effect substance which is soluble in the monomers which form the polymer matrix of the particles, methods for producing such polymer dispersions by miniemulsion polymerization of ethylenically unsaturated monomers, wherein a miniemulsion with an average particle size of the emulsified particles of <500 nm is prepared by emulsifying ethylenically unsaturated monomers in water in the presence of at least one effect substance and a surface-active agent, and it is polymerized in such a way in the presence of at least one free-radical polymerization initiator that initially only at most 50% of the monomers which are situated in the polymerization zone polymerize and where the effect substances

Abstract: Black perylene pigments which comprise one of the isomers of the formula Ia or Ib in which R1, R2 are each independently phenylene, naphthylene or pyridylene, each of which may be mono- or polysubstituted by C1-C12-alkyl, C1-C6-alkoxy, hydroxyl, nitro, and/or halogen; X is halogen; n Is from 0 to 4, or comprises a mixture of both isomers and has a blackness value ?210 in an alkyd/melamine baking varnish.

Abstract: A process for preparing terylene-3,4:11,12-tetracarboximides I where the variables are each defined as follows: R, R? are each independently hydrogen; if desired substituted alkyl or cycloalkyl; R1 is hydrogen or alkyl; R2 is hydrogen; alkyl; if desired substituted aryl or hetaryl, by reacting a perylene-3,4-dicarboximide II in the presence of a base-stable, high-boiling organic solvent and of an alkali metal or alkaline earth metal base, with a naphthalene-1,8-dicarboximide III in which X is hydrogen, bromine or chlorine.

Abstract: A description is given of the use of naphthalene-1,8-dicarboxylic monoimides of the formula (I), in which R1 is hydrogen, alkyl, alkenyl, cycloalkyl, cycloalkenyl, heterocycloalkyl, aryl or heteroaryl and R2 is a radical containing at least one ? electron system containing a carbon atom and at least one further atom selected from carbon, oxygen, and nitrogen, with the proviso that the radical contains at least one atom other than carbon; to protect organic material from the damaging effects of light, of compositions which comprise at least one naphthalene-1,8-dicarboxylic monoimide of the formula (I) in an amount which provides protection from the damaging effects of light, and at least one organic material, and of new naphthalene-1,8-dicarboxylic monoimides (I).

Abstract: Use of luster pigments based on a platelet-shaped metallic substrate coated with a low refractive dielectric layer which does not absorb visible light, for pigmenting macromolecular materials.

Abstract: Rylene dyes of the general formula I where the variables are defined as follows: R is hydrogen; optionally substituted C1-C30-alkyl, C5-C8-cycloalkyl, aryl or hetaryl; R? is bromine; cyano; —NR32; optionally substituted aryloxy, arylthio, hetaryloxy or hetarylthio; optionally substituted C3-C18-alk-1-ynyl; X, Y are both hydrogen or together are a radical of the formula Ia n is 2, 3, 4 or additionally 1 when X and Y are a radical of the formula Ia; n? is from 1 to 4; m is from 0 to 6.

Abstract: Rylene derivatives of the general formula I where the variables have the following meanings: R is hydrogen or substituted or unsubstituted C1-C30-alkyl, aryl or hetaryl; R1 is hydrogen or bromine; R2 is hydrogen or C1-C6-alkyl; R3 is hydrogen, C1-C18-alkyl or substituted or unsubstituted aryl or hetaryl; and n is 2 or 3.

Abstract: A process for converting perylene-3,4:9,10-tetracarboximides of the general formula I in which R1 and R2 are each unbranched, branched or cyclic C1-C8-alkyl to a form suitable for use as fluorescent dyes, which comprises a) dissolving or suspending the perylene-3,4:9,10-tetracarboximides in an organic or inorganic solvent whose molecules have a molecular volume of ?230 ?3 at from 0 to 250° C.