| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 较重卤原子取代的斯夸苷基染料,其制备方法及其在光动力的治疗和工业应用中作为敏化剂用途 | CN00137291.2 | 2000-12-29 | CN1361205A | 2002-07-31 | 拉迈亚·达纳博伊纳; 阿伦·泰扎特威蒂尔·卡利亚特; 苏雷什·达斯; 贝恩德·埃佩 |
| 本发明涉及如下面分子式1的较重卤原子取代斯夸苷基染料及其药学可接受的衍生物,以及其制备方法,其中X是较重卤原子,它们可被用于光动力的治疗和工业应用中。 | ||||||
| 2 | 增强荧光的方法 | CN200480013569.6 | 2004-03-25 | CN100587010C | 2010-02-03 | 詹姆斯·亚历山大·麦金托士; 邓肯·亚当·维尔; 彼得·海尔莫斯·克鲁索; 丹尼尔·理查德·考夫兰; 崔弘仑 |
| 本发明描述了增强荧光染料的荧光的方法和/或使荧光染料产生斯托克斯频移的方法，该方法包括使染料与碱和/或去污剂结合。该方法适合于使用荧光染料的化学技术和/或生物化学技术，尤其适合于诸如电泳等需要对有机分子进行染色或标记的技术。 | ||||||
| 3 | 增强荧光的方法 | CN200480013569.6 | 2004-03-25 | CN1791644A | 2006-06-21 | 詹姆斯·亚历山大·麦金托士; 邓肯·亚当·维尔; 彼得·海尔莫斯·克鲁索; 丹尼尔·理查德·考夫兰; 崔弘仑 |
| 本发明描述了增强荧光染料的荧光的方法和/或使荧光染料产生斯托克斯频移的方法，该方法包括使染料与碱和/或去污剂结合。该方法适合于使用荧光染料的化学技术和/或生物化学技术，尤其适合于诸如电泳等需要对有机分子进行染色或标记的技术。 | ||||||
| 4 | 核壳染料、感光性树脂组合物、感光性树脂膜、彩色滤光片以及CMOS图像传感器 | CN202211191861.3 | 2022-09-28 | CN115873420A | 2023-03-31 | 杨叡知; 金善大; 郑义树; 金二柱; 朴白晟; 李连洙; 李英; 赵明镐 |
| 本发明提供一种核壳染料、包含其的感光性树脂组合物、使用感光性树脂组合物制造的感光性树脂膜、彩色滤光片以及CMOS图像传感器，且核壳染料由以下组成：由化学式1表示的核；和由化学式2表示且围绕核的壳。(在化学式1和化学式2中，每一取代基如说明书中所定义。)[化学式1][化学式2] | ||||||
| 5 | 较重卤原子取代的斯夸苷基染料,其制备方法及其在光动力的治疗和工业应用中作为敏化剂的用途 | CN00137291.2 | 2000-12-29 | CN100341948C | 2007-10-10 | 拉迈亚·达纳博伊纳; 阿伦·泰扎特威蒂尔·卡利亚特; 苏雷什·达斯; 贝恩德·埃佩 |
| 本发明涉及如下面分子式1的较重卤原子取代斯夸苷基染料及其药学可接受的衍生物，以及其制备方法，分子式1其中X是较重卤原子，它们可被用于光动力的治疗和工业应用中。 | ||||||
| 6 | 带有背印的显示元件 | CN200310119852.4 | 2003-11-20 | CN1502479A | 2004-06-09 | K·W·威廉斯; H·D·陈; 王瑞贞 |
| 本发明涉及一种卤化银照片显示元件，它包含载体，具有至少一种卤化银乳液层的正面，以及背面，所述的正面和背面位于载体相对的两面；其中所述的照片元件进一步包含一种被印在背面的印刷油墨组合物，该组合物包含凝聚的疏水性高分子粒子，所述粒子具有一种红外吸收染料与之相结合。 | ||||||
| 7 | METHOD OF ENHANCING FLUORESCENCE | EP04723131.1 | 2004-03-25 | EP1611208A1 | 2006-01-04 | MACKINTOSH, James, Alexander; VEAL, Duncan, Adam; KARUSO, Peter, Helmuth; COGHLAN, Daniel, Richard; CHOI, Hung-Yoon |
| A method of enhancing the fluorescence of and/or producing an increased Stokes' shift in a fluorescent dye comprising combining the dye with a base and/or a detergent is described. The method is suitable in chemical or biochemical techniques using fluorescent dyes, particularly techniques requiring staining or labelling of organic molecules, such as electrophoresis. | ||||||
| 8 | METHOD OF ENHANCING FLUORESCENCE | EP04723131 | 2004-03-25 | EP1611208A4 | 2011-07-27 | MACKINTOSH JAMES ALEXANDER; VEAL DUNCAN ADAM; KARUSO PETER HELMUTH; COGHLAN DANIEL RICHARD; CHOI HUNG-YOON |
| 9 | 벤조 디푸라논계 화합물 함유 조성물 및 이를 사용한 소수성 재료의 착색 방법 | KR1019930023858 | 1993-11-11 | KR1019940011586A | 1994-06-21 | 가쓰다노부유끼; 야부시따신이찌; 하시즈메슈헤이 |
| 10 | Pyrrolidone derivatives, oligomers and polymers | US15510862 | 2015-09-14 | US10420849B2 | 2019-09-24 | Donald A Tomalia; David M Hedstrand; Linda S Nixon |
| Simple organic structures, organic/inorganic polymers, and other substrates have been made, all of which have at least one pyrrolidone moiety present, and found to exhibit low toxicity, low complement activation features and may be used to reduce protein interactions with drug conjugates while enhancing in vivo residency times for these conjugates when used as an injectable composition; thus these compounds can be used as substitutes for PEG in PEGaylation. Surprisingly, these compounds also exhibit unique intrinsic fluorescence (IF) or non-traditional fluorescence (NTF) properties that currently cannot be explained by traditional photochemistry and fluorescence paradigms are described. These compounds have a variety of applications such as in cellular imaging, gene transfection, bio-diagnostics, biosensing, fluorescence directed surgical resections, drug delivery, forensics, environmental diagnostics, mineral/gemstone characterization, counterfeit goods detection, tracer studies related to liquid/water flow, oil field enhancements and diagnostics, prevention of photo-bleaching, and LED display enhancements and others. | ||||||
| 11 | Phenyl xanthene dyes | US14741258 | 2015-06-16 | US09493656B2 | 2016-11-15 | Joe Y. L. Lam; Steven M. Menchen; Ruiming Zou; Scott C. Benson |
| Fluorescent phenyl xanthene dyes are described that comprise any fluorescein, rhodamine or rhodol comprising a particular C9 phenyl ring. One or both of the ortho groups on the lower C9 phenyl ring is ortho substituted with a group selected from alkyl, heteroalkyl, alkoxy, halo, haloalkyl, amino, mercapto, alkylthio, cyano, isocyano, cyanato, mercaptocyanato, nitroso, nitro, azido, sulfeno, sulfinyl, and sulfino. In one embodiment, halo and/or hydroxy groups are used. Optimal dyes contain a lower C9 phenyl ring in which both ortho groups are the same and the lower ring exhibits some form a symmetry relative to an imaginary axis running from the phenyl rings point of attachment to the remainder of the xanthene dye through a point para to the point of attachment. The phenyl xanthene dyes may be activated. Furthermore, the phenyl xanthene dyes may be conjugated to one or more substances including other dyes. The phenyl xanthene dyes are useful for a number of purposes, including labels for use in automated DNA sequencing as well the formation of fluorescent “bar codes” for polymeric particles used in the multiplexed analysis of analytes. | ||||||
| 12 | Benzodioxepin-3-one compounds as dyes or as fluorescent emitters | US14351645 | 2012-09-17 | US08907110B2 | 2014-12-09 | Thomas Rudolph; Philipp Buehle; Ralf Rosskopf |
| The invention relates to specific benzodioxepin-3-one compounds, to a process for the preparation thereof and to the use thereof as dyes or as fluorescent emitters for organic electroluminescent devices (OLEDs) or for organic light-emitting electrochemical cells (OLECs), and to corresponding electronic devices. | ||||||
| 13 | BENZODIOXEPIN-3-ONE COMPOUNDS AS DYES OR AS FLUORESCENT EMITTERS | US14351645 | 2012-09-17 | US20140234238A1 | 2014-08-21 | Thomas Rudolph; Philipp Buehle; Ralf Rosskopf |
| The invention relates to specific benzodioxepin-3-one compounds, to a process for the preparation thereof and to the use thereof as dyes or as fluorescent emitters for organic electroluminescent devices (OLEDs) or for organic light-emitting electrochemical cells (OLECs), and to corresponding electronic devices. | ||||||
| 14 | Heterocyclic polynuclear pigments and process for preparing same | US663151 | 1976-03-02 | US4048173A | 1977-09-13 | Giuseppe Ribaldone; Giampiero Borsotti |
| New compounds are disclosed having the general formula: ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 may be the same or different and are selected from the class consisting of H, Cl and OCH.sub.3. They are useful as pigments. They are prepared by reacting a substituted or unsubstituted 1-aza-2-hydroxybenzanthrone with 2,3-dichloro-1,4-naphthoquinone, in the presence of pyridine, at a temperature between 80.degree. and about 120.degree. C. | ||||||
| 15 | Naphthoquinone derivatives | US613336 | 1975-09-15 | US4033963A | 1977-07-05 | Bansi Lal Kaul |
| The present invention relates to naphthoquinone derivatives of formula I, ##STR1## in which R.sub.1 signifies a halogen atom, a nitro group or an unsubstituted or substituted alkoxy or amino group,R.sub.2 signifies the atoms necessary to form an unsaturated ring system, which ring system has 1 or 2 nuclei and is unsubstituted or substituted,R.sub.3 signifies an unsubstituted or substituted 5-triazinyl or pyrimidyl radical, andn is 0, 1 or 2,Which compounds are free from sulphonic acid groups are useful as pigments or disperse dyes. | ||||||
| 16 | Naphthoxidine dyestuffs and process for making same | US3422111D | 1964-08-06 | US3422111A | 1969-01-14 | BOSSHARD HANS; BOSSARD WERNER |
| 17 | PYRROLIDONE DERIVATIVES, OLIGOMERS AND POLYMERS | US15510862 | 2015-09-14 | US20170246323A1 | 2017-08-31 | Donald A Tomalia; David M Hedstrand; Linda S Nixon |
| Simple organic structures, organic/inorganic polymers, and other substrates have been made, all of which have at least one pyrrolidone moiety present, and found to exhibit low toxicity, low complement activation features and may be used to reduce protein interactions with drug conjugates while enhancing in vivo residency times for these conjugates when used as an injectable composition; thus these compounds can be used as substitutes for PEG in PEGaylation. Surprisingly, these compounds also exhibit unique intrinsic fluorescence (IF) or non-traditional fluorescence (NTF) properties that currently cannot be explained by traditional photochemistry and fluorescence paradigms are described. These compounds have a variety of applications such as in cellular imaging, gene transfection, bio-diagnostics, biosensing, fluorescence directed surgical resections, drug delivery, forensics, environmental diagnostics, mineral/gemstone characterization, counterfeit goods detection, tracer studies related to liquid/water flow, oil field enhancements and diagnostics, prevention of photo-bleaching, and LED display enhancements and others. | ||||||
| 18 | Phenyl Xanthene Dyes | US14188309 | 2014-02-24 | US20140242665A1 | 2014-08-28 | Joe Y. LAM; Steven MENCHEN; Ruiming ZOU; Scott BENSON |
| Fluorescent phenyl xanthene dyes are described that comprise any fluorescein, rhodamine or rhodol comprising a particular C9 phenyl ring. One or both of the ortho groups on the lower C9 phenyl ring is ortho substituted with a group selected from alkyl, heteroalkyl, alkoxy, halo, haloalkyl, amino, mercapto, alkylthio, cyano, isocyano, cyanato, mercaptocyanato, nitroso, nitro, azido, sulfeno, sulfinyl, and sulfino. In one embodiment, halo and/or hydroxy groups are used. Optimal dyes contain a lower C9 phenyl ring in which both ortho groups are the same and the lower ring exhibits some form a symmetry relative to an imaginary axis running from the phenyl rings point of attachment to the remainder of the xanthene dye through a point para to the point of attachment. The phenyl xanthene dyes may be activated. Furthermore, the phenyl xanthene dyes may be conjugated to one or more substances including other dyes. The phenyl xanthene dyes are useful for a number of purposes, including labels for use in automated DNA sequencing as well the formation of fluorescent “bar codes” for polymeric particles used in the multiplexed analysis of analytes. | ||||||
| 19 | Process for dyeing hair with hydroxyquinone dyes and metal salts | US418932 | 1989-10-06 | US4971596A | 1990-11-20 | Jean F. Grollier |
| Process for dyeing human keratinous fibres, characterized in that there are applied on these fibres, in separate stages, a composition (A) containing a metal salt chosen from copper, iron, cobalt, magnesium, and silver salts, or mixtures thereof, in a cosmetically acceptable medium, and, before or after the application of the composition (A), a composition (B) containing, in a cosmetically acceptable medium, at least one dye corresponding to the formulae: ##STR1## in which formulae R.sub.1 denotes hydrogen or hydroxy, R.sub.2 and r.sub.3 denote hydrogen, alkyl, alkoxy; R.sub.4 denotes hydrogen, hydroxy, alkoxy, alkyl, chlorine; R.sub.5 denotes hydrogen, chlorine, alkoxy, hydroxy; and R.sub.6, R.sub.7 and R.sub.8 denote hydrogen or hydroxy. | ||||||
| 20 | Use of benzoquinones for the direct dyeing of keratin fibres | US682475 | 1984-12-17 | US4867751A | 1989-09-19 | Gerard Lang; Alain Malaval; Jean-Francois Grollier; Georges Rosenbaum |
| The invention relates to the use, for dyeing keratin fibres, and in particular human hair, of benzoquinone derivatives of the formula: ##STR1## in which R.sub.1 and R.sub.3 independently of one another denote hydrogen, a hydroxyl group, an alkoxy group or an optionally hydroxylated alkyl group, and R.sub.2 and R.sub.4 independently of one another denote hydrogen, hydroxyl, alkoxy, alkyl, or phenyl optionally substituted by OH, these compounds having at most two alkyl or alkoxy groups on the quinone ring; if one of the radicals R.sub.1, R.sub.2, R.sub.3 or R.sub.4 denotes a methyl, hydroxyl or methoxy group, at least one of the other substituents is different from hydrogen, and if two of these substituents R.sub.1, R.sub.2, R.sub.3 or R.sub.4 are identical and located in the para-position relative to one another and denote hydroxyl or methoxy, at least one of the other two substituents is different from hydrogen. | ||||||
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