| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 161 | Compounds for electronic devices | US13574004 | 2010-12-17 | US09133119B2 | 2015-09-15 | Amir Hossain Parham; Christof Pflumm; Constanze Brocke |
| The present invention relates to compounds of the formula (I) and to the use thereof in organic electronic devices, and to organic electronic devices which comprise compounds of the formula (I), preferably as hole-transport materials and/or as matrix materials, in particular in combination with a further matrix material. | ||||||
| 162 | Sulfonamide derivatives of polycyclic dyes used for analytical applications | US10563079 | 2004-07-02 | US09035042B2 | 2015-05-19 | Alexander Zilles; Jutta Arden-Jacob; Karl-Heinz Drexhage; Norbert Uwe Kemnitzer; Monika Hamers-Schneider |
| The invention concerns the production of quinoline compounds containing sulfonic acid groups, the said quinoline compounds and their conversion into dyes containing sulfonic acid groups. The dyes according to the invention are used especially to label analytes, for example to label biomolecules. | ||||||
| 163 | ORGANIC MATERIAL FOR DEPOSITION, AND ORGANIC PHOTOELECTRIC CONVERSION ELEMENT, IMAGING ELEMENT, DEPOSITION METHOD, AND MANUFACTURING METHOD FOR ORGANIC PHOTOELECTRONIC ONVERSION ELEMENT OBTAINED USING THE SAME | US14604486 | 2015-01-23 | US20150129861A1 | 2015-05-14 | Mitsumasa HAMANO; Eiji FUKUZAKI |
| An organic material for deposition that is used for dry deposition of an organic layer included in an organic photoelectric conversion element is provided in which the organic material contains an organic composition of the organic layer as a principal component, and a residual solvent content of the organic material for deposition is equal to or less than 3 mol %. | ||||||
| 164 | DIAMINOPHENOTHIAZINIUM DERIVATIVES FOR LABELLING BIOMOLECULES, METHOD AND SUBSTRATE FOR LABELLING OLIGONUCLEOTIDES, AND OLIGONUCLEOTIDES OBTAINED | US14379417 | 2013-02-21 | US20150011712A1 | 2015-01-08 | Carole Chaix; Gabriel De Crozals |
| The present invention relates to diaminophenothiazinium derivatives of formula (I); in which R1, R2, R3, R4, R5, R6 and X− are as defined in Claim 1, and also the methods for labelling oligonucleotides using such a derivative, labeling substrates and the oligonucleotides which can be obtained by means of such methods or from such labelling substrates. | ||||||
| 165 | Polymeric Compounds And Methods Of Making And Using The Same | US14100785 | 2013-12-09 | US20140308317A1 | 2014-10-16 | Xiaodong Fan; Yongjiang Xu; Dahui Liu; Michael J. Costanzo |
| The present disclosure provides compounds, or pharmaceutically acceptable salts thereof, for inhibiting the growth of a microbe; treating a mammal having a microbial infection, malaria, mucositis, an ophthalmic infection, an otic infection, a cancer, or a Mycobacterium infection; killing or inhibiting the growth of a Plasmodium species; inhibiting the growth of a Mycobacterium species; modulating an immune response in a mammal; or antagonizing unfractionated heparin, low molecular weight heparin, or a heparin/low molecular weight heparin derivative. | ||||||
| 166 | METHOD FOR HYDROGEN SULFIDE DETECTION | US14240755 | 2012-08-30 | US20140302546A1 | 2014-10-09 | Gal Winter Ziv; Christopher Daniel Curtin |
| A method for detecting H2S produced by a microorganism comprising providing a thiazine dye to a culture medium; culturing a microorganism in the culture medium; and detecting H2S produced by the microorganism by determining a colour change of the culture medium from an interaction of the thiazine dye with H2S present in the culture medium. | ||||||
| 167 | Difluoro benzotriazolyl solar cell material, preparation method and use thereof | US14126896 | 2011-09-23 | US08816043B2 | 2014-08-26 | Mingjie Zhou; Ping Wang; Zhenhua Zhang; Hui Huang |
| The present invention relates to solar cells and discloses a difluoro benzotriazolyl solar cell material and preparation method and use thereof. The solar cell material is represented by formula (I), wherein both R1 and R2, are C1 to C20 alkyl, and n is an integer from 10 to 50. In the difluoro benzotriazolyl solar cell material, since the 1,2,3-benzotriazole solar cell material contains two fluorine atoms, the HOMO energy level is reduced by 0.11 eV, while the fluorine-substituted 1,2,3-benzotriazole has two imido groups with electron-withdrawing ability; the fluorine-substituted 1,2,3-benzotriazole is a heterocyclic compound with strong electron-withdrawing ability, and an alkyl chain can be easily introduced to the N-position of the N—H bond of the benzotriazole. The functional group of the alkyl chain can improve the solar energy conversion efficiency, thus solving the low efficiency problem of solar cells made of the solar cell material. | ||||||
| 168 | Stabilizer of color former and use thereof | US12933569 | 2009-03-18 | US08758648B2 | 2014-06-24 | Satoshi Yonehara; Norio Inamura |
| The present invention provides a stabilizer that can stabilize a salt of 10-(carboxymethylaminocarbonyl)-3,7-bis(dimethylamino)phenothiazine or a derivative thereof even under the existence of moisture or under light irradiation. A compound described in at least one of (1) and (2) below is used as the stabilizer of the salt of 10-(carboxymethylaminocarbonyl)-3,7-bis(dimethylamino)phenothiazine or the derivative thereof. (1) a surfactant having an alkyl group with a carbon number of 8 to 16 (2) at least one pigment substance selected from the group consisting of a compound represented by the following formula (I), a compound represented by the following formula (II), and a flavonoid pigment | ||||||
| 169 | ELECTROLUMINESCENT DEVICE USING ELECTROLUMINESCENT COMPOUND AS LUMINESCENT MATERIAL | US13813420 | 2011-07-29 | US20140054564A1 | 2014-02-27 | Chi-Sik Kim; Soo-Young Lee; Young-Gil Kim; Hyo-Jung Lee; Su-Hyun Lee; Hyun Kim; Young-Jun Cho; Hyuck-Joo Kwon; Kyung-Joo Lee; Bong-Ok Kim; Sung-Min Kim |
| Provided is an organic electroluminescent device that exhibits an efficient host-dopant energy transfer mechanism, and thus, expresses a certain high-efficiency electroluminescent performance, based on improved electron density distribution. The organic electroluminescent device also overcomes low initial efficiency and short operation life property, and secures high-performance electroluminescent performance with high efficiency and long life property for each color. | ||||||
| 170 | 3,6-disubstituted xanthylium salts and use thereof in treatment of tauopathies | US13133868 | 2009-12-10 | US08658665B2 | 2014-02-25 | Scott Clunas; John Mervyn David Storey; Janet Elizabeth Rickard; David Horsley; Charles Robert Harrington; Claude Michel Wischik |
| This invention pertains generally to processes, uses, methods and materials utilizing particular xanthylium compounds, including compounds of formula (I) and (II), as further defined herein. These compounds are useful as drugs, for example, in the treatment of tauopathies, such as Alzheimer's disease. | ||||||
| 171 | PHOTOPOLYMER FORMULATION FOR PRODUCING HOLOGRAPHIC MEDIA HAVING HIGHLY CROSSLINKED MATRIX POLYMERS | US13883008 | 2011-11-04 | US20130224634A1 | 2013-08-29 | Horst Berneth; Thomas Rölle; Friedrich-Karl Bruder; Thomas Fäcke; Marc-Stephan Weiser; Dennis Hönel |
| The invention relates to a photopolymer formulation comprising a polyol component, a polyisocyanate component, a writing monomer, and a photoinitiator, containing a coinitiator and a dye having the formula F An, where F stands for a cationic dye and An″ stands for an anion, wherein the dye having the formula F An comprises a water absorption of =5%. The invention further relates to a holographic medium, in particular in the form of a film, containing a photopolymer formulation according to the invention, to the use of such a medium for recording holograms, and to a special dye that can be used in the photopolymer formulation according to the invention. | ||||||
| 172 | Oxidative dye composition and indicator | US11222335 | 2005-09-08 | US08481331B2 | 2013-07-09 | Tricia Cregger; Randal W. Eveland; Antoinette Bower |
| An oxidative dye indicator composition comprising an indicator dye that has been pre-reacted with a reducing agent prior to use in an oxidizing or disinfectant sterilizing system. The pre-reacted dye, when subjected to an oxidizing disinfection or sterilization agent, such as peracetic acid or hydrogen peroxide, under goes a visible color change and thus can serve as a chemical, process, or chemical integrator, indicator. The dyes include various azines, thiazines, and oxazines compounds and the reducing agents include alkali metal alkoxides and alkaline earth metal alkoxide compounds. | ||||||
| 173 | COMPOUNDS FOR ELECTRONIC DEVICES | US13574004 | 2010-12-17 | US20120292576A1 | 2012-11-22 | Amir Hossain Parham; Christof Pflumm; Constanze Brocke |
| The present invention relates to compounds of the formula (I) and to the use thereof in organic electronic devices, and to organic electronic devices which comprise compounds of the formula (I), preferably as hole-transport materials and/or as matrix materials, in particular in combination with a further matrix material. | ||||||
| 174 | PHENOLIC COMPOUND AND RECORDING MATERIAL | US13261234 | 2010-09-28 | US20120204763A1 | 2012-08-16 | Toshio Aihara; Hiroshi Sakai; Shuntaro Kinoshita; Satoshi Kodama; Tadahiro Kondo; Kazumi Jyujyo |
| An object of the present invention is to provide a recording material that is excellent in color-developing properties and background and image stabilities, and a compound used therein. The present invention relates to a compound represented by the formula (I) [wherein R11 to R14 each independently represent a halogen atom or the like; n, p, q, and r each independently represent 0 or any integer of 1 to 4; m represents 0 or any integer of 1 to 2; a represents any integer of 1 to 10; R2 represents a hydrogen atom or the like; R3 represents an OR51 group or the like; and R41 and R42 each independently represent a hydrogen atom or the like], a composition containing the compound, a method for producing the compound, a recording material containing at least one compound represented by the formula (I), and a recording sheet having the recording material. | ||||||
| 175 | 3,6-DISUBSTITUTED XANTHYLIUM SALTS | US13133868 | 2009-12-10 | US20110300074A1 | 2011-12-08 | Scott Clunas; John Mervyn David Storey; Janet Elizabeth Rickard; David Horsley; Charles Robert Harrington; Claude Michel Wischik |
| This invention pertains generally to processes, uses, methods and materials utilising particular xanthylium compounds, including compounds of formula (I) and (II), as further defined herein. These compounds are useful as drugs, for example, in the treatment of tauopathies, such as Alzheimer's disease. | ||||||
| 176 | Arsenical Fluorescent Agents and Assays | US13053206 | 2011-03-21 | US20110229929A1 | 2011-09-22 | Laura Ellen Downs Beaulieu; Mary J. Tanga |
| The invention provides methods and compositions for labeling dithiol-containing analytes. | ||||||
| 177 | 3,7-diamino-10H-phenothiazine salts and their use | US12294599 | 2007-03-28 | US07888350B2 | 2011-02-15 | Claude Michel Wischik; Janet Elizabeth Rickard; Charles Robert Harrington; David Horsley; John Mervyn David Storey; Colin Marshall; James Peter Sinclair; Thomas Craven Baddeley |
| This invention pertains generally to the field of phenothiazine compounds, and more particularly to certain stably reduced phenothiazine compounds, specifically, certain 3,7 diamino-10H-phenothiazine (DAPTZ) compounds of the following formula wherein: each of R1 and R9 is independently selected from: —H; C1-4alkyl; C2-4alkenyl; and halogenated C1-4alkyl; each of R3NA and R3NB is independently selected from: —H; C1-4alkyl; C2-4alkenyl; and halogenated C1-4alkyl; each of R7NA and R7NB is independently selected from: —H; C1-4alkyl; C2-4alkenyl; and halogenated C1-4alkyl; each of HX1 and HX2 is independently a protic acid; and pharmaceutically acceptable salts, solvates, and hydrates thereof. These compounds are useful as drugs, for example, in the treatment of tauopathies, such as Alzheimer's disease, and also as prodrugs for the corresponding oxidized thioninium drugs (for example, methythioninium chloride, MTC). | ||||||
| 178 | Doped semiconductor material and process for production thereof | US10489131 | 2003-02-20 | US07858967B2 | 2010-12-28 | Martin Pfeiffer; Leo Karl; Ansgar Werner; Torsten Fritz |
| 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. | ||||||
| 179 | Method for quantitatively determining cholesterol in high density lipoproteins and reagents therefor | US10531315 | 2003-10-16 | US07851174B2 | 2010-12-14 | Yuki Katayama; Mayumi Fujinaka |
| A method for quantitatively determining cholesterol in high-density lipoprotein in a sample, which comprises: reacting a sample with i) cholesterol esterase and cholesterol oxidase or ii) cholesterol esterase, an oxidized coenzyme and cholesterol dehydrogenase in an aqueous medium comprising i) nonionic surfactant, polyanion and albumin or ii) a combination of a surfactant selected from the group consisting of polyoxyethylene alkylamine or polyoxyethylene alkenylamine and a surfactant selected from the group consisting of polyoxyethylene polycyclic phenyl ether sulfate and an anionic bile acid derivative, and measuring the formed hydrogen peroxide or a reduced coenzyme; and a reagent used therefor. | ||||||
| 180 | DISPLAY ELEMENT AND METHOD OF DRIVING THE SAME | US12519663 | 2007-12-06 | US20100091353A1 | 2010-04-15 | Noriyuki Kokeguchi; Kaori Ono |
| Provided is a novel electrochemical display element which performs bright white display, high contrast black/white display and full-color display with a simple member configuration. A method for driving such display element is also provided. The display element contains an electrochromic compound, which is colored or has its color disappear due to oxidation or reduction, a metallic salt compound, an electrolyte and a white scattered material, between opposing electrodes. The display element substantially performs multiple color display of three colors or more, i.e., black display, white display and colored display other than black, by driving operation of the opposing electrodes. | ||||||
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