| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 81 | 3,6-DISUBSTITUTED XANTHYLIUM SALTS | US15373224 | 2016-12-08 | US20170088534A1 | 2017-03-30 | Scott CLUNAS; John Mervyn Davd STOREY; Janet Elizabeth RICKARD; David HORSLEY; Charles Robert HARRINGTON; Claude Michel WISCHIK |
| Described are a compound of formula (II) or (III): The compounds are effective in the treatment of disease, including a tauopathy condition or a disease of tau protein aggregation. | ||||||
| 82 | GREEN COLORING COMPOSITION FOR USE IN COLOR FILTER, COLORED FILM, COLOR FILTER, AND SOLID-STATE IMAGING ELEMENT | US15215656 | 2016-07-21 | US20160327860A1 | 2016-11-10 | Satoru MURAYAMA; Kazuto SHIMADA |
| The present invention provides a green coloring composition for use in a color filter, which can form a green colored film having low incident-angle dependence and improves the color-separation properties of a solid-state imaging device including the colored film; and a colored film, a color filter, and a solid-state imaging device. The green coloring composition for use in a color filter of the present invention is a green coloring composition for use in a color filter, containing a green colorant, a near-infrared absorbent, and a polymerizable compound, in which when the green coloring composition for use in a color filter is used to form a colored film having a film thickness of 0.8 μm, the maximum value of the transmittance at a wavelength from 400 nm to 450 nm of the colored film is 5% or less, the maximum value of the transmittance at a wavelength from 500 nm to 600 nm of the colored film is 70% or more, the minimum value of the transmittance at a wavelength from 650 nm to less than 700 nm of the colored film is 20% or less, and the minimum value of the transmittance at a wavelength from 700 nm to 900 nm of the colored film is 30% or less. | ||||||
| 83 | Substrates and methods for staining live stem cells | US13985559 | 2012-02-14 | US09334523B2 | 2016-05-10 | Uma Lakshmipathy; Upinder Singh; Scott Grecian; Rene Quintanilla; Kyle Gee; Mahendra Rao |
| The invention relates to novel substrates and methods for staining live stem cells. The stain may be used to identify induced pluripotent stem cell colonies during the process of somatic cell reprogramming. | ||||||
| 84 | Permanent attachment of agents to surfaces containing C-H functionality | US14124045 | 2012-07-12 | US09315628B2 | 2016-04-19 | Jason J. Locklin |
| An embodiment of the present disclosure can include a compound, a structure bonded to the compound, and the like. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a dye or a pigment and the structure can be a fiber, hair, or another structure. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a fluorinated compound and the structure can be a counter top, metal, or the like. | ||||||
| 85 | COMPOUNDS FOR ELECTRONIC DEVICES | US14814994 | 2015-07-31 | US20150340613A1 | 2015-11-26 | AMIR H. 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. | ||||||
| 86 | Electronic Device | US14648409 | 2013-11-04 | US20150336959A1 | 2015-11-26 | Junyou Pan; Amir Hossain Parham; Rene Peter Scheurich; Thomas Rudolph |
| The present application relates to an electronic device comprising a heteroaromatic compound of a formula (I) as functional material, in particular as electron-transport material and as matrix material for emitter compounds. | ||||||
| 87 | Organic light-emitting device | US14537862 | 2014-11-10 | US09172046B1 | 2015-10-27 | Seul-Ong Kim; Youn-Sun Kim; Dong-Woo Shin; Jung-Sub Lee; Naoyuki Ito |
| An organic light-emitting device includes a first electrode; a second electrode; and an organic layer between the first electrode and the second electrode and including an emission layer. The emission layer includes at least one first material represented by any one of Formulae 1-1 and 1-2 and at least one second material represented by Formula 2: | ||||||
| 88 | Terminally Activated Delayed Fluorescence Material, A Method Of Synthesizing The Same and An OLED Device Using The Same | US14347618 | 2014-01-13 | US20150270494A1 | 2015-09-24 | Shidang Xu; Zhenguo Chi; Yi Zhang; Jiarui Xu; Yifan Wang; Qinghua Zou |
| The present invention provides a thermally activated delayed fluorescence material, a method of synthesizing the same and an OLED device using the same. The thermally activated delayed fluorescence material includes a structure formula 1 as wherein the group Ar1 is identical to or different from the group Ar2, and the group Ar1 and the group Ar2 are consisted of carbazole and/or phenothiazine. The thermally activated delayed fluorescence material has a higher glass transition temperature, high thermal stability and excellent luminous efficiency. The method of synthesizing the same has simplified steps, easily purified product, high yield, and luminous and thermal properties of the product can be adjusted by connecting to differentiated functional groups. The OLED device using the same has a light emitting layer of high fluorescence efficiency and long-term stability, so that luminous efficiency and service life of the OLED device can meet practical demand. | ||||||
| 89 | Camouflage Pattern With Extended Infrared Reflectance Separation | US14594502 | 2015-01-12 | US20150192392A1 | 2015-07-09 | Dale R. Wendel |
| Fabrics containing camouflage patterns are produced from dyes wherein at least certain of the colors contained in the pattern contain a low reflectance dye. The low reflectance dye is added to one or more colors in the pattern in order to preserve the camouflage pattern when viewed through night vision goggles as relatively long wavelengths, such at wavelengths greater than 900 nm. In one embodiment, the low reflectance dye comprises a thiazine. The low reflectance dye is blended with other dyes to produce colors in the pattern. By altering the concentration of the low reflectance dye in each of the colors, the colors contained in the camouflage pattern remain separate and distinct even at relatively long wavelengths. | ||||||
| 90 | SOLAR CELL MATERIALS | US14281196 | 2014-05-19 | US20150144198A1 | 2015-05-28 | Michael D. Irwin; Robert D. Maher, III; Jerred A. Chute; Vivek V. Dhas |
| A photovoltaic cell of improved construction may include an active layer comprising first and second active material, and a dye. Either of the first and second active material may include a copper-oxide compound. The active layer may further include a thin-coat interfacial layer, which may coat at least a portion of either of the first and second active material. The dye may include a primary electron donor moiety, a core moiety, and an electron-withdrawing moiety. | ||||||
| 91 | METHOD FOR MEASURING COMPONENT TO BE MEASURED IN SPECIMEN | US14391885 | 2013-04-18 | US20150079620A1 | 2015-03-19 | Hideyuki Kuwata; Tomoko Aratake; Kenta Kinjo |
| Provided is a measuring method of a component to be measured in a specimen while suppressing an influence of bilirubin. A measuring method of a component to be measured, comprising converting the component to be measured in the specimen to hydrogen peroxide through an enzymatic reaction, reacting the formed hydrogen peroxide with an oxidative-coloring chromogen in the presence of a peroxidase, and measuring an absorbance of the colored reaction solution to thereby determine the component to be measured, wherein a fatty acid or a salt thereof coexists. The measuring method of a component to be measured in a specimen according to the present invention is useful in clinical diagnosis. | ||||||
| 92 | Sulfonamide derivatives of polycyclic dyes used for analytical applications | US13071901 | 2011-03-25 | US08846924B2 | 2014-09-30 | 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. | ||||||
| 93 | TRICYCLIC COMPOUNDS AS ANTICANCER AGENTS | US14238511 | 2012-08-16 | US20140213578A1 | 2014-07-31 | Michael Ohlmeyer; Goutham Narla; Neil Dhawan; David Kastrinsky |
| Tricyclic chemical modulators of FOXO transcription factor proteins are disclosed. The compounds are useful to treat cancer, age-onset proteotoxicity, stress-induced depression, inflammation, and acne. The compounds are of the following phenothiazine, dibenzoazepine and annulene and similar genera: | ||||||
| 94 | PERMANENT ATTACHMENT OF AGENTS TO SURFACES CONTAINING C-H FUNCTIONALITY | US14124045 | 2012-07-12 | US20140121333A1 | 2014-05-01 | Jason J. Locklin |
| An embodiment of the present disclosure can include a compound, a structure bonded to the compound, and the like. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a dye or a pigment and the structure can be a fiber, hair, or another structure. In an embodiment, the compound can be a linker between an agent and a structure, where the agent can be a fluorinated compound and the structure can be a counter top, metal, or the like. | ||||||
| 95 | COMPOUNDS FOR ELECTRONIC DEVICES | US14115107 | 2012-04-12 | US20140070146A1 | 2014-03-13 | Amir Hossain Parham; Arne Buesing; Christof Pflumm; Teresa Mujica-Fernaud; Philipp Stoessel; Thomas Eberle |
| The present application relates to a compound of a formula (I), to the use of this compound in an electronic device, and to an electronic device comprising one or more compounds of the formula (I). The invention furthermore relates to the preparation of the compound of the formula (I) and to a formulation comprising one or more compounds of the formula (I). | ||||||
| 96 | Dye for a dye-sensitised solar cell, and a solar cell comprising the same | US12866347 | 2009-02-05 | US08629269B2 | 2014-01-14 | Kwang-Yol Kay; Kang-Jin Kim; Jong-Hyung Kim; Young-Jin Kwon |
| The present invention relates to a dye for a dye-sensitized solar cell. The dye according to the present invention has a high degree of light absorbency and can improve the photoelectric current conversion efficiency when employed in a light-absorbing layer for a solar cell. Chemical Formula 1 illustrates the present invention. wherein X1, X2, N, Z1, and A1 are described herein. | ||||||
| 97 | Sulfonamide derivatives of polycyclic dyes used for analytical applications | US13071921 | 2011-03-25 | US08614317B2 | 2013-12-24 | 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. | ||||||
| 98 | SUBSTRATES AND METHODS FOR STAINING LIVE STEM CELLS | US13985559 | 2012-02-14 | US20130323770A1 | 2013-12-05 | Uma Lakshmipathy; Upinder Singh; Scott Grecian; Rene Quintanilla; Kyle Gee; Mahendra Rao |
| The invention relates to novel substrates and methods for staining live stem cells. The stain may be used to identify induced pluripotent stem cell colonies during the process of somatic cell reprogramming. | ||||||
| 99 | METHOD FOR MEASURING COMPONENT TO BE MEASURED | US13991652 | 2011-12-12 | US20130288283A1 | 2013-10-31 | Tomomi Murakami |
| The present invention provides a method for measuring a component to be measured in a sample, comprising converting the component to be measured in the sample into hydrogen peroxide and measuring the formed hydrogen peroxide in the presence of an α-keto acid using an oxidative-coloring chromogen. The present invention also provides a method for suppressing the influence of a peroxide on a method of converting a component to be measured in a sample into hydrogen peroxide and measuring the formed hydrogen peroxide using an oxidative-coloring chromogen, the suppression method comprising using an α-keto acid. The measuring method and the suppression method of the present invention using an α-keto acid suppress the influence of a peroxide to give an accurate measurement of the component to be measured in the sample. | ||||||
| 100 | PHOTOELECTRIC CONVERSION MATERIAL, FILM CONTAINING THE MATERIAL, PHOTOELECTRIC CONVERSION DEVICE, METHOD FOR PREPARING PHOTOELECTRIC CONVERSION DEVICE, METHOD FOR USING PHOTOELECTRIC CONVERSION DEVICE, PHOTOSENSOR AND IMAGING DEVICE | US13789537 | 2013-03-07 | US20130181202A1 | 2013-07-18 | Katsuyuki YOFU; Kimiatsu NOMURA; Eiji FUKUZAKI; Yuki HIRAI; Mitsumasa HAMANO; Tetsuro MITSUI |
| There is provided a compound represented by a specific formula, which has an absorption maximum at 400 nm or more and less than 720 nm in a UV-visible absorption spectrum, wherein a molar extinction coefficient is 10,000 mol−1·l·cm−1 or more at the absorption maximum wavelength, and a difference between a melting point and a deposition temperature (a melting point−a deposition temperature) is 31° C. or more. | ||||||
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