33 results about "Rubrene" patented technology

One aspect of the present invention is a light-emitting element having a layer containing an aromatic hydrocarbon and a metal oxide between a pair of electrodes. There is no particular limitation on the kind of aromatic hydrocarbon; however, an aromatic hydrocarbon having a hole mobility of 1 x 10-6 cm2 / Vs or more is preferable. Examples of such aromatic hydrocarbons include 2-tert-butyl-9,10-bis(2-naphthyl)anthracene, anthracene, 9,10-diphenylanthracene, tetracene, rubrene, perylene, 2,5,8,11-tetra(tert-butyl)perylene and so on. As the metal oxide, a metal oxide exhibiting electron-accepting properties for aromatic hydrocarbons is preferable. As such metal oxides, for example, molybdenum oxide, vanadium oxide, ruthenium oxide, rhenium oxide and the like are given.

The present invention designs a preparation method for double-layer induced rubrene film growth, that is, the growth of rubrene film is induced by increasing the number of effective induction layers, and the epitaxial growth is highly ordered and high-quality on the high-quality double-layer induction layer. The crystalline rubrene film realizes the organic-organic epitaxial growth relationship by controlling the epitaxial layer growth behavior, crystallinity and film microstructure, and constructs a highly ordered and highly crystalline polycrystalline rubrene film to achieve to increase its mobility.

The invention relates to a method for preparing an NGAL (Neutrophil Gelatinase Associated Lipocalin) optical excitation chemiluminescence detection kit. The method comprises the following steps: activating a luminous microsphere, namely activating the luminous microsphere through prepared carbodiimide and Sulfo-NHS solutions in a PBS (Phosphate Buffer Saline) buffer solution, wherein the luminous microsphere is a carboxyl modified luminous microsphere, and the luminous microsphere is coated with dimethylthiophene, anthracene and rubrene and carried with an europium chelate; coupling the luminous microsphere with an anti-NGAL antibody, namely selecting the carboxyl modified luminous microsphere, carrying out mixing reaction on the anti-NGAL monoclonal antibody and the activated carboxyl modified luminous microsphere to couple the anti-NGAL antibody to the luminous microsphere, and adding freshly prepared carbodiimide at the same time while mixing the anti-NGAL antibody and the activated luminous microsphere; labeling the anti-NGAL antibody through biotin; and labeling a photosensitive microsphere through avidin. The invention also relates to preparation and use methods of the NGAL optical excitation chemiluminescence detection kit. The methods disclosed by the invention solve the problems that the sensitivity is low and the detection is easily interfered by the environment in a detection method in the prior art.

The present invention relates to a 2-substituted rubrene compound represented by formula (I), characterized in that R1 represented by formula (I) is a formyl group, which is 2-formylrubrene, and 2-formyl red Uses of fluorene, and method for synthesizing the same. Using 2-formylrubrene as raw material, other 2-substituted rubrene compounds were synthesized through oxidation, reduction and condensation reactions. As a novel red fluorescent material, the compound of the present invention has high fluorescence quantum efficiency, and can be used as a material for the light-emitting layer in an electroluminescent device.

The invention discloses method of preparing rubrene micro-nanowire of organic semiconductor materials, and the method is characterized by using rubrene as a raw material for vapor deposition, using naphthacene single crystal growing through clean slices of silicon or physics gas-phase transmission method as the substrate, adopting a vacuum vapor deposition method, and under a condition of controlling the deposition rate and the deposition time, forming rubrene micro-nanowire with a standard size through deposition on the substrate of the semiconductor.According to the invention, because of adopting a vacuum vapor deposition method capable of controlling the deposition rate and deposition time accurately, the size of the rubrene micro-nanowire can be controlled accurately and simultaneously the preparation technique can also be simplified.

The invention relates to a 6, 11 dibasic-5,12-naphthalene and naphthoquinone which is generated by implementing a Diels-Alder cycloaddition reaction through 1,3-dibasic benzofuran and benzene naphthoquinone, and then a rubrene derivative is generated by substituting addition reaction through the lithium alkylide, through a structural modification, the main rubrene body is introduced with a plurality of active conjugation radicals, so that the emission wavelength of the main body is in red shift, thereby a red light emission wavelength is realized, simultaneously, the steric hindrance between the molecules can be enlarged through introducing larger radicals; so the glass transition temperature can be raised; the concentration quenching effect can be lowered and the lightening property of material can be improved.