| 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 | 3,4-苝二酰亚胺衍生物及其制备方法和用途 | CN201911041398.2 | 2019-10-30 | CN110724104B | 2022-07-05 | 沈永嘉; 张伟; 张顺; 张永强; 张志刚; 沈羽 |
| 本发明主要涉及一种3,4‑苝二酰亚胺衍生物及其用途。所述3,4‑苝二酰亚胺衍生物为式I所示化合物。本发明提供的3,4‑苝二酰亚胺衍生物可用于制备适合水性涂料或油墨着色的苝系黑色颜料。式I中，R2为氢或C1～C3的烷氧基，p为1或2。 | ||||||
| 2 | 3,4-苝二酰亚胺衍生物及其制备方法和用途 | CN201911041398.2 | 2019-10-30 | CN110724104A | 2020-01-24 | 沈永嘉; 张伟; 张顺; 张永强; 张志刚; 沈羽 |
| 本发明主要涉及一种3,4-苝二酰亚胺衍生物及其用途。所述3,4-苝二酰亚胺衍生物为式I所示化合物。本发明提供的3,4-苝二酰亚胺衍生物可用于制备适合水性涂料或油墨着色的苝系黑色颜料。式I中，R2为氢或C1～C3的烷氧基，p为1或2。 | ||||||
| 3 | 含硼的二萘嵌苯单酰亚胺、其生产方法、其作为生产二萘嵌苯单酰亚胺衍生物的结构单元的用途、单酰亚胺衍生物及其在染料敏化太阳能电池中的用途 | CN201380041568.1 | 2013-07-24 | CN104520276A | 2015-04-15 | H·沃内博格; I·布鲁德; R·森德; G·巴塔格利亚林; C·李; K·米伦 |
| 本发明公开了通式I、II、III和IV的化合物：式(I)，其中各变量具有说明书中所给含义，以及一种制备通式I、II、III和IV的化合物的方法。公开了各自根据上述方法制备的通式II、III和IV的化合物以及通式II、III和IV的化合物本身在制备染料敏化太阳能电池中的用途；以及该类染料敏化太阳能电池本身。 | ||||||
| 4 | Boron containing perylene monoimides, process for their production, their use as building blocks for production of perylene monoimide derivatives, monoimide derivatives and their use in dye-sensitized solar cells | AU2013301239 | 2013-07-24 | AU2013301239A1 | 2015-02-05 | WONNEBERGER HENRIKE; BRUDER INGMAR; SEND ROBERT; BATTAGLIARIN GLAUCO; LI CHEN; MULLEN KLAUS |
| Compounds of general formula I, II, III and IV: Formula (I) wherein the variables have the meaning given in the description, and a process for the preparation of compounds of general formula I, II, III and IV are disclosed. The use of the compounds of general formulae II, III and IV each prepared according to the abovementioned processes and of compounds of general formulae II, III and IV per se for the preparation of dye-sensitized solar cells; and such dye-sensitized solar cells per se are disclosed. | ||||||
| 5 | Thermal transfer of Pyridonfarbstoffen | DE59500736 | 1995-04-22 | DE59500736D1 | 1997-11-06 | SENS RUEDIGER DR; ETZBACH KARL-HEINZ DR |
| 6 | Thermal transfer of pyridone dyes | US424098 | 1995-04-19 | US5545235A | 1996-08-13 | Rudiger Sens; Karl-Heinz Etzbach |
| A process for transferring dyes from a transfer to plastic-coated paper by diffusion or sublimation with the aid of an energy source comprises using a transfer on which there is or are one or more pyridone dyes of the formula ##STR1## where X is nitrogen or CH,R.sup.1 and R.sup.2 are each substituted or unsubstituted C.sub.1 -C.sub.10 -alkyl, C.sub.5 -C.sub.7 -cycloalkyl, C.sub.3 -C.sub.4 -alkenyl or substituted or unsubstituted phenyl, or R.sup.1 and R.sup.2 are together with the nitrogen atom joining them together a heterocyclic radical,R.sup.3 is C.sub.3 -C.sub.10 -alkyl or C.sub.5 -C.sub.7 -cycloalkyl,R.sup.4 is hydrogen, C.sub.1 -C.sub.4 -alkyl or substituted or unsubstituted phenyl,R.sup.5 is cyano, substituted or unsubstituted carbamoyl, carboxyl, C.sub.1 -C.sub.8 -alkoxycarbonyl or benzimidazolyl, andR.sup.6 is substituted or unsubstituted C.sub.1 -C.sub.10 -alkyl, C.sub.5 -C.sub.7 -cycloalkyl or substituted or unsubstituted phenyl. | ||||||
| 7 | New fluorescent compound and method for producing the same | JP2004308055 | 2004-10-22 | JP2006117593A | 2006-05-11 | MAETA HAJIME; MIZUNO KAZUHIKO; MAEDA TOMOHIRO |
| PROBLEM TO BE SOLVED: To develop a new fluorescent substance having various absorption wavelengths and luminescence wavelengths by introducing functional groups into a fluorescent organic compound. SOLUTION: The new fluorescent substance is represented by structural formula (1) [A-(ethynyl) m] n-B (wherein A is a trimethylsilyl, phenyl or tertiary butyl group; B is pyrene; m is an integer selected from 1-3; n is 3 or 4). The new fluorescent substance makes absorption wavelength longer and improves fluorescent quantum yield and thermal stability and enables control of solubility to organic solvents and water-based solvents and is applicable to fluorescent dyes, fluorescent probe molecules, etc., by introducing a plurality of [A-(ethynyl)m] groups into an aromatic compound. COPYRIGHT: (C)2006,JPO&NCIPI | ||||||
| 8 | 液体漂白剤組成物 | JP2018060875 | 2018-03-27 | JP2019172768A | 2019-10-10 | 山口 由佳; 小倉 弘嗣 |
| 【課題】色調安定性、液位視認性に優れるとともに、臭気を抑制した液体漂白剤組成物を提供すること。 【解決手段】(A)成分:過酸化水素と、(B)成分:キサンテン系色素、キノリン系色素、及びピレン系色素からなる群から選択される少なくとも1種の色素と、(C)成分:フェノール系ラジカルトラップ剤を液体漂白剤組成物の総質量に対して0〜0.2質量%と、を含む液体漂白剤組成物。 【選択図】なし |
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| 9 | Method for transferring dye on plastic-coated paper from transfer | JP10256195 | 1995-04-26 | JPH07304268A | 1995-11-21 | RIYUUDEIGAA ZENSU; KAARU HAINTSU ETSUTSUBATSUHA |
| PURPOSE: To obtain good light resistance and stability by using a transfer on which at least one specified pyridone dye exists in a process for transferring dyes to a plastic-coated paper by diffusion or sublimation with the aid of an energy source. CONSTITUTION: In a method for printing for transferring dyes to a plastic-coated paper by diffusion or sublimation with the aid of an energy source, a transfer on which there exists at least one pyridone dye of a separately described formula wherein X is nitrogen or CH; R 1 and R 2 are each a 1-4C alkoxy carbonyl, a 1-4C alkoxycarbonyloxy, etc.; R 3 is a 3-10C alkyl, a 5-7C cycloalkyl; R 4 is H, a 1-4C alkyl group, a 1-4C alkoxy, etc.; R 5 is cyano, carbamoyl, etc.; R 6 is a 1-10C alkyl group, a 5-7C cycloalkyl group, etc., is used. COPYRIGHT: (C)1995,JPO | ||||||
| 10 | NOUVELLES QUINONES, LEURS SYNTHESES ET UTILISATIONS | FR0853058 | 2008-05-09 | FR2930944B1 | 2016-12-30 | BUFFET NOEMIE; BOCK HARALD |
| 11 | NOUVELLES QUINONES, LEURS SYNTHESES ET UTILISATIONS | FR0853058 | 2008-05-09 | FR2930944A1 | 2009-11-13 | BUFFET NOEMIE; BOCK HARALD |
| Quinone de formule (Ia) ou (Ib) dans lesquellesR<1> et R<2> représentent chacun indépendamment- un atome d'hydrogène,- un groupe alkyle en C1-30, dans lequel un ou plusieurs chaînons -CH2-, à l'exception du chaînon de rattachement, peuvent être remplacés par un atome d'oxygène, un atome de soufre, un groupe NH, N(alkyle en C1-4) ou C=O, et qui est éventuellement substitué, ou- un groupe aryle en C6-10 ou hétéroaryle en C4-10, éventuellement substitué, chaque R<3> représente indépendamment- un atome d'hydrogène,- un groupe alkyle en C1-30, linéaire ou ramifié, dans lequel un ou plusieurs chaînons -CH2-peuvent être remplacés par un atome d'oxygène, un atome de soufre, un groupe NH, N(alkyle en C1-4) ou C=O, et qui est éventuellement substitué, ou- un groupe aryle en C6-10, hétéroaryle en C4-10, (aryle en C6-10)-carbonyle, (hétéroaryle en C4-10)-carbonyle, chacun des ces groupes étant éventuellement substitué,n est un nombre entier entre 0 et 5 inclus,avec la réserve que, lorsque n = 0 et les deux R<3> représentent chacun un atome d'hydrogène, alors R<1> et R<2> ne représentent pas tous les deux un atome d'hydrogène, un groupe 2-quinoléinyle ou un groupe 2,5-bis-(tertio-butyl)phényle.L'invention concerne également un procédé de synthèse de ces quinones ainsi que l'utilisation de ces quinones en tant que colorants, en particulier de colorants dichroïques, et/ou en tant que transporteurs de charges et/ou d'excitons dans des dispositifs photoélectriques. | ||||||
| 12 | Thermal transfer of Pyridonfarbstoffen | DE4415358 | 1994-05-02 | DE4415358A1 | 1995-11-09 | SENS RUEDIGER DR; ETZBACH KARL-HEINZ DR |
| 13 | Typewriter keyboard that learn of writing easier and the prerequisites for improving the education acquired | DE2322264 | 1973-05-03 | DE2322264A1 | 1974-11-14 | GUNKEL ERICH |
| 14 | BORON CONTAINING PERYLENE MONOIMIDES, PROCESS FOR THEIR PRODUCTION, THEIR USE AS BUILDING BLOCKS FOR PRODUCTION OF PERYLENE MONOIMIDE DERIVATIVES, MONOIMIDE DERIVATIVES AND THEIR USE IN DYE-SENSITIZED SOLAR CELLS | PCT/IB2013/056070 | 2013-07-24 | WO2014024074A1 | 2014-02-13 | WONNEBERGER, Henrike; BRUDER, Ingmar; SEND, Robert; BATTAGLIARIN, Glauco; LI, Chen; MÜLLEN, Klaus |
Compounds of general formula I, II, III and IV: Formula (I) wherein the variables have the meaning given in the description, and a process for the preparation of compounds of general formula I, II, III and IV are disclosed. The use of the compounds of general formulae II, III and IV each prepared according to the abovementioned processes and of compounds of general formulae II, III and IV per se for the preparation of dye-sensitized solar cells; and such dye-sensitized solar cells per se are disclosed. |
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| 15 | 9-시아노 치환된 페릴렌-3,4-디카르복실산 모노이미드 | KR1020117022802 | 2003-09-08 | KR1020110113217A | 2011-10-14 | 뵈흠아르노; 블라쉬카피터; 헬퍼윌리; 함멜디르크; 슈리히팅피터; 뮐렌클라우스 |
| 본 발명은 하기 화학식(I)의 9-시아노 치환된 페릴렌-3,4-디카르복실산 모노이미드에 관한 것으로, 식 중 변수는 다음과 같이 정의된다. 식 중에서, X는 화학 결합, 임의로 치환된 C
1 -C
30 -알킬렌, C
5 -C
8 -시클로알킬렌, 아릴렌, 헤테로아릴렌, C
1 -C
20 -알킬아릴렌, C
1 -C
20 -알킬헤테로아릴렌, 아릴-C
1 -C
20 -알킬렌 또는 헤테로아릴-C
1 -C
20 -알킬렌이고; Y는 작용기 Y' 또는 중합가능한 기 P이거나, 또는 XY는 함께 R기를 형성하며; Y'는 아미노, 히드록실, -COOH, -SO
3 H, 염소 또는 브롬이고; P는 화학식 (II)의 기이며; A, B는 각각 독립적으로 수소, C
1 -C
6 -알킬, 페닐이거나, 또는 함께 A와 B가 결합되어 있는 이중 결합을 함유하는 시클로펜텐 또는 시클로헥센 고리를 형성하고; Q는 화학 결합, -O-, -NR
2 -, -S-, -OCO-, -OCOO-, -OCONR
3 -, -NR
3 CO-, -NR
3 COO-, -NR
3 CONR
4 -, -CO-, -COO-, -CONR
3 -, -SO
2 -O-, -SO
2 NR
3 -, -O-SO
2 - 또는 -NR
3 SO
2 -기이며; n은 0, 1, 2 또는 3이고; R은 H, 임의로 치환된 C
1 -C
30 -알킬, C
5 -C
8 -시클로알킬, 아릴 또는 헤테로아릴이다.
화학식 (I) 화학식 (II) |
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| 16 | BORON CONTAINING PERYLENE MONOIMIDES, PROCESS FOR THEIR PRODUCTION, THEIR USE AS BUILDING BLOCKS FOR PRODUCTION OF PERYLENE MONOIMIDE DERIVATIVES, MONOIMIDE DERIVATIVES AND THEIR USE IN DYE-SENSITIZED SOLAR CELLS | EP13828249 | 2013-07-24 | EP2880018A4 | 2016-01-13 | WONNEBERGER HENRIKE; BRUDER INGMAR; SEND ROBERT; BATTAGLIARIN GLAUCO; LI CHEN; MÜLLEN KLAUS |
| 17 | BORON CONTAINING PERYLENE MONOIMIDES, PROCESS FOR THEIR PRODUCTION, THEIR USE AS BUILDING BLOCKS FOR PRODUCTION OF PERYLENE MONOIMIDE DERIVATIVES, MONOIMIDE DERIVATIVES AND THEIR USE IN DYE-SENSITIZED SOLAR CELLS | EP13828249.6 | 2013-07-24 | EP2880018A1 | 2015-06-10 | WONNEBERGER, Henrike; BRUDER, Ingmar; SEND, Robert; BATTAGLIARIN, Glauco; LI, Chen; MÜLLEN, Klaus |
| Compounds of general formula I, II, III and IV: Formula (I) wherein the variables have the meaning given in the description, and a process for the preparation of compounds of general formula I, II, III and IV are disclosed. The use of the compounds of general formulae II, III and IV each prepared according to the abovementioned processes and of compounds of general formulae II, III and IV per se for the preparation of dye-sensitized solar cells; and such dye-sensitized solar cells per se are disclosed. | ||||||
| 18 | NOUVELLES QUINONES, LEURS SYNTHESES ET UTILISATIONS. | EP09750043.3 | 2009-05-05 | EP2300407B1 | 2018-03-07 | BUFFET, Noémie; BOCK, Harald |
| 19 | NOUVELLES QUINONES, LEURS SYNTHESES ET UTILISATIONS. | EP09750043.3 | 2009-05-05 | EP2300407A2 | 2011-03-30 | BUFFET, Noémie; BOCK, Harald |
| The invention relates to quinones of formula (Ia) or (Ib), in which Formula (Ia) and Formula (Ib) R 1 and R 2 each independently represent - a hydrogen atom, - a C 1-3O alkyl group in which one or more -CH 2- linkages, apart from the attachment linkage, may be replaced by an oxygen atom, a sulphur atom, or an NH, N(C 1-4 alkyl) or C=O group, and which is optionally substituted, or - an optionally substituted C 6-10 aryl or C 4-1O heteroaryl group, each R 3 independently represents - a hydrogen atom, a linear or branched C 1-3O alkyl group, in which one or more -CH 2- linkages may be replaced by an oxygen atom, a sulphur atom, or an NH, N(C 1-4 alkyl) or C=O group, and which is optionally substituted, or - a C 6-1O aryl, C 4-1O heteroaryl, (C 6-10 aryl)carbonyl, or (C 4-10 heteroaryl)carbonyl group, each of these groups optionally being substituted, and n is an integer between 1 and 5 inclusive. The invention also relates to a method for synthesizing these quinones and also to the use of these quinones as dyes, in particular dichroic dyes, and/or as charge carriers and/or exciton carriers in photoelectric devices. | ||||||
| 20 | NOUVELLES QUINONES, LEURS SYNTHESES ET UTILISATIONS. | PCT/FR2009/050830 | 2009-05-05 | WO2009141562A3 | 2009-11-26 | BUFFET, Noémie; BOCK, Harald |
L' invention concerne des quinones de formule (Ia) ou (Ib) Formule (la) Formule (Ib) dans lesquelles R1 et R2 représentent chacun indépendamment - un atome d'hydrogène, - un groupe alkyle en C1-3O, dans lequel un ou plusieurs chaînons -CH2-, à l'exception du chaînon de rattachement, peuvent être remplacés par un atome d'oxygène, un atome de soufre, un groupe NH, N(alkyle en C1-4) ou C=O, et qui est éventuellement substitué, ou - un groupe aryle en C6-1O ou hétéroaryle en C4-1O, éventuellement substitué, chaque R3 représente indépendamment - un atome d'hydrogène, - un groupe alkyle en C1-3O, linéaire ou ramifié, dans lequel un ou plusieurs chaînons -CH2- peuvent être remplacés par un atome d'oxygène, un atome de soufre, un groupe NH, N(alkyle en C1-4) ou C=O, et qui est éventuellement substitué, ou - un groupe aryle en C6-1O, hétéroaryle en C4-1O, (aryle en C6-10)-carbonyle, (hétéroaryle en C4-10)-carbonyle, chacun des ces groupes étant éventuellement substitué, n est un nombre entier entre 1 et 5 inclus. L'invention concerne également un procédé de synthèse de ces quinones ainsi que l'utilisation de ces quinones en tant que colorants, en particulier de colorants dichroïques, et/ou en tant que transporteurs de charges et/ou d' excitons dans des dispositifs photoélectriques. |
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