Abstract:
Die vorliegende Erfindung betrifft die Verwendung von Oxokohlenstoff-, Pseudooxokohlenstoff- und Radialenverbindungen als Ladungsinjektionsschicht, sowie deren Verwendung in elektronischen Bauelementen.
Abstract:
A red leuco dye demonstrates unusually good thermal and photo stability. The red dye may be used with developers and wax carries for microencapsulation to form thermochromic pigments for use in inks, coatings and the like. This pigment is particularly desirable for use in metal-deco coatings, such as those used in aluminum cans in high beverage canning operations.
Abstract:
A red leuco dye demonstrates unusually good thermal and photo stability. The red dye may be used with developers and wax carries for microencapsulation to form thermochromic pigments for use in inks, coatings and the like. This pigment is particularly desirable for use in metal-deco coatings, such as those used in aluminum cans in high beverage canning operations.
Abstract:
Sulfonated diarylrhodamine compounds are useful as fluorescent labels of nucleosides, nucleotides, polynucleotides, and polypeptides. The compounds find particular application in the area of fluorescent nucleic acid analysis, e.g., automated DNA sequencing and fragment analysis, detection of probe hybridization in hybridization arrays, detection of nucleic acid amplification products, and the like.
Abstract:
Die vorliegende Erfindung betrifft Oxokohlenstoff-, Pseudooxokohlenstoff- und Radialenverbindungen sowie deren Verwendung als Dotand zur Dotierung eines organischen halbleitenden Matrixmaterials, als Blockermaterial, als Ladungsinjektionsschicht, als Elektrodenmaterial sowie als organischer Halbleiter, sowie diese verwendende elektronische Bauelemente und organische halbleitende Materialien.
Abstract:
The invention relates to a doped organic semiconductor material with increased charge carrier density and more effective charge carrier mobility, which may be obtained by doping an organic semiconductor material with a chemical compound comprising one or several organic molecular groups (A) and at least one further compound partner (B). The desired doping effect is achieved after cleavage of at least one organic molecular group (A) from the chemical compound by means of at least one organic molecular group (A) or by means of the product of a reaction of at least one molecular group (A) with another atom or molecule. A method for production thereof is disclosed.
Abstract:
A latent additive represented by general formula (1): wherein A is a 5- or 6-membered aromatic or heterocyclic ring; R 1 and R 2 are each hydrogen, halogen, cyano, hydroxyl, nitro, carboxyl, optionally substituted C1-C40 alkyl, C6-C20 aryl, C7-C20 arylalkyl, or C2-C20 heterocyclic ring-containing group; and R 4 is C1-C20 alkyl, C2-C20 alkenyl, C6-C20 aryl, C7-C20 arylalkyl, C2-C20 heterocyclic ring-containing group, or trialkylsilyl.
Abstract:
Provided are various compounds comprising the formula Also provided are fluorescent dyes comprising the above compound. Additionally, a fluorescence energy transfer system is provided that comprises the above-described fluorescent dye and a second dye, wherein the second dye is capable of energy transfer with the fluorescent dye. Further provided is a kit for labeling a target molecule, where the kit comprises the above-described fluorescent dye with additional reagents useful for labeling the target molecule. Additionally provided is a target molecule labeled with the above-described fluorescent dye. Methods of labeling a target molecule with the above-described fluorescent dye are also provided.
Abstract:
The present invention relates to compounds represented by the following Formulas (I) and (II), Ring-A of Formulas I and II can be, for example, an aryl group, and Q′ and Q′″ can each be independently selected from groups, such as, halogen, —OH, —CN, amine groups, amide groups, carboxylic acid ester groups, carboxylic acid groups, alkenyl groups, alkynyl groups, carbonate groups, sulfide groups, and sulfonic acid ester groups. The present invention also relates to photochromic compositions and photochromic articles that include one or more photochromic compounds, such as represented by Formula II.