| 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 | 包括光伏电池和基于二酮的聚合物在内的有机电子装置及聚合物 | CN201080049031.6 | 2010-09-01 | CN102812016A | 2012-12-05 | 埃琳娜·E·舍伊娜; 克里斯托弗·T·布朗; 克里斯托弗·勒内·加斯顿·格雷涅尔; 查德·兰迪斯; 阿塔·盖伊 |
| 本发明涉及可用于有机电子装置及光伏电池的p型材料中的聚合物。本发明还涉及包含式(I)的化合物、单体、二聚体、三聚体及聚合物。可达到良好的光伏效率及寿命。R基团可提供溶解性、环境稳定性以及光谱性质和/或电子性质的微调。可制备促成多个能带隙以及宽且强的吸收的不同聚合物微观结构。羰基可与邻近的噻吩环相互作用以为主链提供刚性，诱导平面性且降低和/或消除分子间链的扭曲缺陷。包含苯并二噻吩和/或苯并噻二唑结构的聚合物可显示尤其高的性能。 | ||||||
| 82 | 含芴芳香族化合物、有机电致发光元件用材料及使用其的有机电致发光元件 | CN201080033813.0 | 2010-10-14 | CN102471320A | 2012-05-23 | 吉田圭; 西村和树; 伊藤光则; 河村祐一郎; 荻原俊成; 岩隈俊裕 |
| 下述通式(1)所示的含芴芳香族化合物。(式(1)中，Nr1表示取代或无取代的、成环碳原子数2～5的单环含氮芳香族环或成环碳原子数2～9的二环含氮芳香族环，Ar表示芳香族环等，Fl1、Fl2表示芴基，Cz1、Cz2表示咔唑基。其中，上述通式(1)所示的含芴芳香族化合物之中，不包含以下式(2)所示的化合物。) | ||||||
| 83 | 硅石类颗粒组合物 | CN201080029695.6 | 2010-06-28 | CN102471078A | 2012-05-23 | 布鲁斯·A·凯泽; 蒂莫西·S·凯泽; 詹姆斯·H·阿代尔 |
| 本发明涉及一种形成由硅石类材料、活性物、存在或者不存在表面改性剂构成的硅石类颗粒或者复合材料的方法以及相关的组合物。该硅石类颗粒用化学式(SiO2)x(OH)yRzSt示例，其中R为活性物，例如包括标识剂类、胺类、硫醇类、环氧树脂类、有机硅氧烷类、有机硅烷类和水溶性溶剂类的有机或者无机分子，以及可选的表面改性剂S，可为有机的、聚合物的或者无机的。表面改性材料的实例为铝和硼的无机盐，或者有机材料例如有机硅烷类或者低分子量聚合物类。因此，该颗粒可用于包括在酸性、中性或者碱性pH、或者压力环境下的多种高温中的任何一种的多种应用中。该复合材料具有多种应用，例如造纸、水处理、化学示踪、个人护理、微生物控制以及聚合物类的供应。对于造纸，颗粒在输送漂白剂或者OBA、其它功能添加剂的同时，提供保留滤水性能，并服务添加剂跟踪器。 | ||||||
| 84 | 通过二氧化硅致密化改进的荧光二氧化硅纳米颗粒 | CN201080026346.9 | 2010-04-15 | CN102459062A | 2012-05-16 | U·B·维斯纳; E·赫兹; H·奥 |
| 本发明涉及一种具有致密二氧化硅壳的核-壳二氧化硅纳米颗粒。该纳米颗粒具备改进的性质，如提高了光致发光性和稳定性。本发明还提供了该纳米颗粒的制备方法。 | ||||||
| 85 | 有机发光介质 | CN201080003397.X | 2010-12-15 | CN102232106A | 2011-11-02 | 河村昌宏; 水木由美子 |
| 本发明提供含有下述式(1)所表示的芳香族胺衍生物和下述式(I)所表示的蒽衍生物的有机发光介质。 | ||||||
| 86 | 具有改进的颜料分散体的滤色片元件 | CN200980147840.8 | 2009-10-20 | CN102227655A | 2011-10-26 | 托米·李·小罗伊斯特; P·J·阿莱西; 唐纳德·理查德·戴尔 |
| 一种具有滤光层的滤色片，所述滤光层包含氟化酞菁颜料和至少一种第二颜料。在一个实施方式中，所述第二颜料在400nm～500nm的波长具有最大吸收以形成绿色滤色片。 | ||||||
| 87 | 高分子化合物、由该高分子化合物交联而得到的网状高分子化合物、有机场致发光元件用组合物、有机场致发光元件、有机EL显示器及有机EL照明 | CN200980110914.0 | 2009-04-01 | CN101981086A | 2011-02-23 | 饭田宏一朗; 远藤恭子; 李延军; 冈部一毅; 矢部昌义 |
| 本发明的目的在于提供一种空穴传输能力高、电化学稳定性优异、且适于利用湿式成膜法成膜的高分子化合物。此外，本发明的另一目的在于提供一种电流效率高、驱动电压低、且驱动寿命长的有机场致发光元件。为此，本发明提供一种高分子化合物，该高分子化合物具有交联性基团，且在该高分子化合物中，由重复单元中所含的芳胺部位隔着至少一个单键具有交联性基团。 | ||||||
| 88 | 有色的有机聚硅氧烷 | CN200780026899.2 | 2007-09-20 | CN101490136A | 2009-07-22 | 维尔纳·鲁斯; 罗克萨娜·伯尔别鲁; 斯特凡·埃伦贝格; 甘特·格利茨; 克里斯蒂安·奥克斯; 丹尼尔·席尔德巴赫 |
| 本发明涉及有色的有机聚硅氧烷，其包含下式的单元R1a(RO)bAcR2dSiO(4－a－b－c－d)/2(I)，其中R、R1、R2、A、a、b、c和d如权利要求1所定义，本发明还涉及该有色的有机聚硅氧烷的制备方法及其用途。 | ||||||
| 89 | 结合光捕获阵列的太阳能电池 | CN01813169.7 | 2001-07-20 | CN1457515A | 2003-11-19 | J·S·林西; G·J·梅耶 |
| 一种结合光捕获阵列的太阳能电池，包含：(a)包含第一电极的第一基材；和(b)一层电气连接到第一电极上的光捕获棒，每根光捕获棒包含式I的聚合物，其中m至少是1，并且可以是从2、3或4到20或更多；X1是一个电荷分离基团(优选卟啉大环，它可以是双层夹心化合物的一种配体)，其激发态能量等于或低于X2的激发态能量；并且X2到Xm+1是生色团(优选的还是卟啉大环)。 | ||||||
| 90 | Color conversion in LCD displays with silica nanoparticles | US15785443 | 2017-10-17 | US10072153B2 | 2018-09-11 | Daniel Szwarcman; Elad Cohen; Mor Shmuel Armon; Evgenia Liel (Jeny) Kuks; Rony Schwarz; Elena Eisurovich; Daniel Aronov; Eran Sella |
| Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. For example, rhodamine-based fluorescent compounds are used in matrices produced by sol gel processes and/or UV (ultraviolet) curing processes which are configured to stabilize the compounds and extend their lifetime—to provide the required emission specifications of the color conversion films. Film integration and display configurations further enhance the display performance with color conversion films utilizing various color conversion elements. | ||||||
| 91 | SECOND-ORDER NONLINEAR OPTICAL COMPOUND AND NONLINEAR OPTICAL ELEMENT COMPRISING THE SAME | US15944019 | 2018-04-03 | US20180224577A1 | 2018-08-09 | Akira OTOMO; Isao AOKI; Hideki MIKI; Hidehisa TAZAWA; Shiyoshi YOKOYAMA |
| Problem to Be Solved: to provide a chromophore having a far superior nonlinear optical activity to conventional chromophores and to provide a nonlinear optical element comprising said chromophore.Solution: a chromophore comprising a donor structure D, a π-conjugated bridge structure B, and an acceptor structure A, the donor structure D comprising an aryl group substituted with a substituted oxy group; and a nonlinear optical element comprising said chromophore. | ||||||
| 92 | Organic electronic material and organic electroluminescent device | US14404609 | 2013-06-05 | US10026901B2 | 2018-07-17 | Jinhai Huang; Lei Dai; Jinxin Chen; Lifei Cai |
| An organic light-emitting material having the structure of formula (I) or (II) as described below and an organic light-emitting device (OLED) are disclosed. The OLED adopts the compound containing fluoranthene group as the electron transport material possessing good electron transport and injection ability. The material also enhances the luminous efficiency and lifetime of the device because of its excellent thermal stability and film-forming properties. At the same time, the high triplet energy and excellent electron transport capacity of the material containing fluoranthene group make it suitable to be used as the host for phosphorescent devices, increasing the number of electrons in the light-emitting layer and the efficiency of the device. | ||||||
| 93 | Fused heterocyclic aromatic derivative, organic electroluminescence element material, and organic electroluminescence element using same | US14234533 | 2012-09-11 | US09978952B2 | 2018-05-22 | Yuki Nakano; Kei Yoshida; Hideaki Nagashima; Ryohei Hashimoto |
| A compound represented by the following formula (1). In the formula, A1 is O, S, Si(Ar1)(Ar2), P(═O)(Ar3)(Ar4), a substituted or unsubstituted arylene group including 6 to 30 ring carbon atoms, or a substituted or unsubstituted heteroarylene group including 5 to 30 ring atoms. | ||||||
| 94 | Organic metal complex, light emitting material, delayed fluorescent material, and organic light emitting device | US14910791 | 2014-06-23 | US09957260B2 | 2018-05-01 | Yumi Sakai; Hiroshi Miyazaki; Chihaya Adachi; Naoto Noutsuka |
| An organic metal complex represented by the following general formula is useful as a light emitting material for an organic electroluminescent device and others. X represents O, S or —N(R7)—; Y represents O, S or —N(—SO2—R8)—; R1 to R8 represent H, an alkyl group or an aryl group; at least one of Z1 and Z2 represents a phenoxazin-10-yl group, a phenothiazin-10-yl group, a phenazin-10-yl group, etc.; M represents an element of the group 1 except for hydrogen, the group 2, the group 11, the group 12, or the group 13 of the periodic table; L represents a ligand; n is 1 to 3; and m is 0 to 2: | ||||||
| 95 | Azetidine-substituted fluorescent compounds | US15301270 | 2015-04-01 | US09933417B2 | 2018-04-03 | Luke D. Lavis; Jonathan B. Grimm; Jiji Chen; Timothee Lionnet; Zhengjian Zhang; Andrey Revyakin; Joel Slaughter |
| The presently-disclosed subject matter includes azetidine-substituted fluorescent compounds, where the compounds may be used as probes, dyes, tags, and the like. The presently-disclosed subject matter also includes kits comprising the same as well as methods for using the same to detect a target substance. | ||||||
| 96 | CONDENSED CYCLIC COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE INCLUDING THE SAME | US15665703 | 2017-08-01 | US20180083196A1 | 2018-03-22 | Hiroaki ITOI |
| A condensed cyclic compound and an organic light-emitting device including the same, the condensed cyclic compound being represented by Formula 1: | ||||||
| 97 | MODIFICATIONS OF THE SOL-GEL AND PROCESS THEREOF | US15691774 | 2017-08-31 | US20180072892A1 | 2018-03-15 | Mor Shmuel ARMON; Elad COHEN; Evgenia Liel (Jeny) KUKS; Rony SCHWARZ; Eran SELLA; Daniel SZWARCMAN |
| Color conversion films for a LCD (liquid crystal display) having RGB (red, green, blue) color filters, as well as such displays, formulations, precursors and methods are provided, which improve display performances with respect to color gamut, energy efficiency, materials and costs. The color conversion films absorb backlight illumination and convert the energy to green and/or red emission at high efficiency, specified wavelength ranges and narrow emission peaks. The color conversion films may comprise at least one of: polydimethylsiloxane hydroxy terminated, dendritic polyol or polyvinylpyrrolidone. | ||||||
| 98 | Fluorogenic calcium ion indicators and methods of using the same | US15610184 | 2017-05-31 | US09810700B1 | 2017-11-07 | Zhenjun Diwu; Haitao Guo; Ruogu Peng; Qin Zhao; Jinfang Liao; Feng Liu |
| The present disclosure provides fluorogenic compounds useful for preparing fluorescent calcium ion indicators, the fluorescent indicators themselves, and the use of the fluorescent indicators in methods of detection, discrimination and quantification of metal ions. The subject fluorogenic compounds and fluorescent ion indicators can include a chelating group based on a 2-aminophenoxyethylene glycol 2-aminoethyl ether, N,N,N′,N′-tetraacetic acid (PEGTA) moiety or precursor thereof where the phenyl group of the PEGTA is substituted with or fused with a fluorophore moiety of interest. The subject methods find use in the detection of intracellular calcium ions. Also provided are kits for use in practicing the subject methods. | ||||||
| 99 | ALKOXYSILYL GROUP-CONTAINING ORGANIC EL DYE AND A METHOD FOR PRODUCING THE SAME | US15522121 | 2015-10-30 | US20170313885A1 | 2017-11-02 | Shinichiro ISOBE; Shuntaro MATAKA |
| Provided is an alkoxysilyl group-containing organic EL dye that can be used for the production of fluorescent silica particles that do not fade. This alkoxysilyl group-containing organic EL dye is represented by the general formula X—Y-Q-Z—Si(R1)n(OR2)3-n, wherein X is an organic EL dye, Y is a direct bond or —(CH2)p— (p represents an integer from 1 to 10) or —(O—CH2CH2)q— (q represents an integer from 1 to 10), Q is a bond selected from the group consisting of amide bond, ether bond, thioether bond, thioester bond, thiourea bond, disulfide bond, and polyoxyethylene bond, Z is —(CH2)3— or —(CH2)2NH(CH2)3—, R1 and R2 represent an alkyl group having 1 to 7 carbon atoms, and n represents 0 or 1. | ||||||
| 100 | RHODAMINE DERIVATIVES DYES AND USES THEREOF | US15622158 | 2017-06-14 | US20170283616A1 | 2017-10-05 | Evgenia Liel KUKS; Rony Schwarz; Eran Sella; Mor Shmuel Armon; Daniel Szwarcman |
| This invention is directed to photoluminescent compounds based on rhodamine dyes with red-shifted absorption and emission maxima and uses thereof for photoluminescence based devices. | ||||||
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