| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 41 | 电子器件 | CN201380061758.X | 2013-11-04 | CN104813496B | 2017-08-08 | 潘君友; 埃米尔·侯赛因·帕勒姆; 勒内·彼得·朔伊里奇; 托马斯·鲁道夫 |
| 本发明涉及包含式(I)的杂芳族化合物作为功能材料、特别是作为电子传输材料和作为发光体化合物的基质材料的电子器件。 | ||||||
| 42 | 氨基酸类双光子荧光染料 | CN201410667110.3 | 2014-11-20 | CN104479396B | 2016-08-24 | 仉华; 蒋涛; 聂亚敏; 陈粤华; 王魁; 蒋凯 |
| 氨基酸类双光子荧光染料，所述荧光染料具有通式I的结构。该类双光子荧光染料在肿瘤活细胞中非核酸区域以及非肿瘤细胞内具有较低的荧光背景，在肿瘤活细胞中核酸区域内具有较强的荧光信号，且对肿瘤活细胞内核酸具有很强的专一性标记。这类化合物具有一定水平的水溶性，同时具有良好的细胞膜通透性。并且还具有较大的有效的双光子吸收截面。本发明的这类化合物同时还具有较低的生物毒性、光毒性、光漂白性。其光谱范围与生物样品的光谱范围有足够大的差异。。 | ||||||
| 43 | 作为荧光参考标准品的DDAO化合物 | CN201180066331.X | 2011-12-28 | CN103597093A | 2014-02-19 | S·C·本森; C·莫尼和蒂; S·M·凯普夫 |
| 根据本教导，提供了利用至少一种式(I)的参比染料的方法和组合物：在一些实施方案中，方法包括测量报告染料和至少一种式(I)的参比染料的检测信号。在一些实施方案中，组合物包含式(I)的参比染料、缓冲剂、核苷酸和蛋白的选择物。 | ||||||
| 44 | 新型有机染料及其制造方法 | CN201080027068.9 | 2010-06-18 | CN102803394A | 2012-11-28 | 裵镐基; 安贤哲; 李钟灿 |
| 本发明涉及一种新型染料增感光电转换元件用有机染料及其制造方法，根据本发明的有机染料在染料敏化太阳能电池(dye-sensitized solar cell，DSSC)中作为染料增感光电转换元件而使用，显示比以往的染料更高的摩尔吸光系数、Jsc(短路光电流密度)和光电转换效率，从而可以大大提高太阳能电池的效率。 | ||||||
| 45 | 噻嗪靛颜料分散剂、和利用所述分散剂的颜料组合物、着色组合物和滤色器 | CN200710100974.7 | 2007-04-28 | CN101063005A | 2007-10-31 | 藤木雅之; 后藤祥子 |
| 由式(1)或(2)代表的噻嗪靛颜料分散剂，其中，E代表碱性基团。包含颜料材料和所述噻嗪靛颜料分散剂的颜料组合物。包含所述颜料组合物和颜料载体的着色组合物。包括由所述着色组合物制备的滤色器节的滤色器。 | ||||||
| 46 | 喹吖啶酮有机颜料制备工艺 | CN98112387.2 | 1998-03-12 | CN1229107A | 1999-09-22 | 王庆河; 张水生; 张惠茹; 苏志利; 胡碧云; 孙海青; 张利华 |
| 一种喹吖啶酮系列有机颜料制备工艺。本发明属喹吖啶酮有机染料制备技术领域。采用2,5－二芳胺基对苯二甲酸,在聚磷酸[PPA]中闭环制喹吖啶酮的工艺,制备系列有机颜料C.I.PV19(γ)、C.I.PV19(β)、C.I.PR122。工艺合理可行。产品收率高、质量稳定。 | ||||||
| 47 | REGENERATION OF SYMMETRICAL NONAQUEOUS ORGANIC REDOX FLOW BATTERIES | PCT/US2023013670 | 2023-02-23 | WO2023164025A1 | 2023-08-31 | GIANETTI THOMAS; MOUTET JULES |
| A method of regenerating a symmetrical redox flow battery includes: a first discharge process having a duration in which a capacity of the redox flow battery in a first polarity and comprising a membrane decreases from a first to a second capacity, the process comprising: flowing a catholyte through a catholyte compartment in the first polarity; flowing an anolyte through an anolyte compartment in the first polarity; wherein: the first polarity of the redox flow battery includes a membrane having a first face in fluid communication with the catholyte compartment and a second face in fluid communication with the anolyte compartment; and the first and the second faces of the membrane being opposing surfaces of the membrane; and a second discharge process comprising: reversing the polarity of the catholyte and anolyte compartments wherein: the redox flow battery in the second polarity exhibits an initial increased capacity compared to the second capacity from the first discharge process. | ||||||
| 48 | N-(2-AMINOETHYL)MORPHOLINE-BASED RNA ANALOGS, METHOD FOR THE PREPARATION AND USE THEREOF | PCT/PL2022050013 | 2022-03-10 | WO2022191725A1 | 2022-09-15 | MAMOT ADAM; SIKORSKI PAWEŁ; KOWALSKA JOANNA; JEMIELITY JACEK |
| The subject of the invention is RNA analogs of formula 1, their preparation and application, inter alia, in microscopic observations, study of the gene expression process and monitoring of enzyme activity. wherein R1 is an (oligo)nucleotide containing group, R2 is a nucleobase, R3 is a functional group. | ||||||
| 49 | FLUORENYL CYANINE DYES | PCT/US2021036201 | 2021-06-07 | WO2021252368A1 | 2021-12-16 | MAO FEI; LEUNG WAI-YEE; MCGARRAUGH PATRICK |
| The present invention relates to fluorescent dyes in general. The present invention provides a wide range of fluorescent dyes and kits containing the same, which are applicable for labeling a variety of biomolecules, cells and microorganisms. The present invention also provides various methods of using the fluorescent dyes for research and development, forensic identification, environmental studies, diagnosis, prognosis, and/or treatment of disease conditions. | ||||||
| 50 | NEUE FLUORESZENZFARBSTOFFE UND NEUE ANALYSEVERFAHREN FÜR DIE GLYCAN-ANALYTIK | PCT/EP2019/075940 | 2019-09-25 | WO2020069945A1 | 2020-04-09 | BERNDT, Daniel; NIZAMOV, Shamil; KASTRUP, Lars |
Die Erfindung betrifft einen Fluoreszenzmarker nach der folgenden Formel I, wobei Fluo ausgesucht ist aus der Gruppe bestehend aus den Fluorophoren nach den Formeln ll-IV L ein Linker und die Gruppe X entweder eine -SO2- oder eine -PO(OH)- Gruppe ist. Des Weiteren betrifft die vorliegende Erfindung die Verwendung der erfindungsgemäßen Fluoreszenzmarker insbesondere auch als Standard in der Glycan-Analyse, Konjugate aus Fluoreszenzmarker und Glycanen, sowie ein Kit-of-Parts enthaltend die erfindungsgemäßen Fluoreszenzmarker. |
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| 51 | ASSAY | PCT/IB2019/055896 | 2019-07-10 | WO2020012391A1 | 2020-01-16 | SITTON, Gregory W. |
Method of assaying for an analyte in a sample, and kits for performing the assay. |
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| 52 | SMALL-MOLECULE ORGANIC DYES | PCT/EP2018/073151 | 2018-08-28 | WO2019057451A1 | 2019-03-28 | SPARR, Christof; FISCHER, Christian |
The present invention relates to compounds of formula (A), wherein Z is NR10 or O. These compounds represent novel acridinium and xanthylium salts having an unprecedented substituted heterocyclic core. They are useful as fluorescent dyes or precursors thereof in different applications including various imaging and sensing techniques, and, in particular, as photosensitizers and hereby preferably as photocatalysts. The present invention further relates to processes for preparing the inventive compounds via 1,5-organodimetallic reagents from double directed ortho-metalation reactions or combined halogen-metal exchange/ directed ortho-metalation reactions. |
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| 53 | 신규한 유기염료 및 이의 제조방법 | PCT/KR2010/003947 | 2010-06-18 | WO2010147425A2 | 2010-12-23 | 배호기; 안현철; 이종찬 |
본 발명은 신규한 염료증감 광전변환소자용 유기염료 및 이의 제조방법에 관한 것으로, 본 발명에 따른 유기염료는 염료감응태양전지(dye-sensitized solar cell, DSSC)에 염료증감 광전변환소자로서 사용되어 종래의 염료보다 향상된 몰흡광계수, Jsc(단회로 광전류 밀도) 및 광전기 변환효율을 나타내어 태양전지의 효율을 크게 향상시킬 수 있다. |
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| 54 | QUINACRIDONE LABELLING REAGENTS FOR FLUORESCENCE DETECTION OF BIOLOGICAL MATERIALS | PCT/GB0202537 | 2002-05-30 | WO02099432A3 | 2003-05-01 | SMITH JOHN ANTHONY |
| Disclosed are new quinacridone dye derivatives having characteristic fluorescence lifetimes. Also disclosed are methods for labelling target biological materials employing the quinacridone dyes and use of the labelled materials in biological assays. The quinacridone derivatives have the structure (I), in which Z<1> and Z<2> independently represent the atoms necessary to complete one ring, two fused ring, or three fused ring aromatic or heteroaromatic systems, each ring having five or six atoms selected from carbon atoms and optionally no more than two atoms selected from oxygen, nitrogen and sulphur; R<3>, R<4>, R<5>, R<6>, R<7> and R<8> are independently selected from hydrogen, halogen, amide, hydroxyl, cyano, nitro, mono- or di-nitro-substituted benzyl, amino, mono- or di-C1-C4 alkyl-substituted amino, sulphydryl, carbonyl, carboxyl, C1-C6 alkoxy, acrylate, vinyl, styryl, aryl, heteroaryl, C1-C20 alkyl, aralkyl, sulphonate, sulphonic acid, quaternary ammonium, the group -E-F and the group -(CH2-)nY; R<1> and R<2> are independently selected from hydrogen, mono- or di-nitro-substituted benzyl, C1-C20 alkyl, aralkyl, the group -E-F and the group -(CH2-)nY; E is a spacer group, F is a target bonding group; Y is selected from sulphonate, sulphate, phosphonate, phosphate, quaternary ammonium and carboxyl; and n is an integer from 1 to 6. The invention also relates to a set of different fluorescent quinacridone dye derivatives, each dye having a different fluorescence lifetime, the set of dyes being particularly useful for multiparameter analysis. | ||||||
| 55 | CHEMILUMINESCENT ENERGY TRANSFER CONJUGATES AND THEIR USES AS LABELS IN BINDING ASSAYS | PCT/IB1998/000831 | 1998-05-29 | WO98054574A2 | 1998-12-03 | |
| A new class of chemiluminescent acridinium or benzacridinium compounds is disclosed by virtue of forming an intramolecular energy transfer conjugate (ETC) between the acridinium or benzacridinium compound and a luminophore. A method of extending the emission wavelengths of acridinium or benzacridinium esters in order to further reduce or eliminate the emission spectral overlap between the parent polysubstituted aryl Acridinium Esters (DMAE) and Benzacridinium Esters (LEAE) is disclosed. The ETC's retain the unique desired properties of acridinium or benzacridinium compounds including complete light emission in very short period of time, monophasic emission spectrum, simplicity of triggering mechanism, ability of labeling the biological molecules of interest to form a tracer, and good stability. Additionally, the range of the emission spectrum of an acridinium or benzacridinium compound can now be shifted at will and at longer leap through the choice of a luminophore as the integral part of an ETC molecule. Disclosed are chemiluminescent labeled conjugates comprising an acridinium or benzacridinium moiety convalently attached to a luminophore via a spacer, said moiety further conjugated to a biological molecule of interest, wherein said spacer is of an appropriate length to allow the excited species generated from said moiety to transfer energy efficiently to said luminophore, resulting in the emission of light in the spectral region of said luminophore. Also disclosed are binding assays using said conjugates, test kits comprising said conjugates and methods of preparing the conjugates. | ||||||
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