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 使用特定的偶氮化合物的打印方法 CN03819007.9 2003-04-11 CN100374516C 2008-03-12 R·布拉德布里; A·迪金逊; P·J·杜布尔; P·格雷戈里; M·S·哈吉索特里欧; T·保罗; A·H·波帕特; N·J·汤普森; P·怀特
一种用于在基体上打印图像的方法,包括在其上施用含有液体介质和式(1)化合物的组合物:T-Q-N=N-L-T,其中各个T独立地为偶氮基团;Q为任选取代的、任选金属化的1,8-二羟基基;和L为二价有机连接基。还公开了组合物和染料。
2 浓缩染料溶液 CN200580016565.8 2005-05-17 CN1961045A 2007-05-09 M·奥伯霍尔策
包含一种或多种可阳离子化的染料、有机酸的浓缩染料水溶液及其在染色和/或印刷有机基体以及制备喷墨打印用油墨中的用途(式I),其中各个A独立地为-NH-或-O-,B为多价基团或原子,n’和n”为自然数且n’和n”的总和≥2,m为式(c1)或(c2)基团。
3 用于喷墨印刷油墨的三偶氮染料 CN200380108631.5 2003-11-13 CN1738868A 2006-02-22 D·P·德沃纳尔德
在基材上印刷图像的方法,所述方法包括在基材上涂覆含液体介质和式(1)的三偶氮化合物或其盐的组合物:其中:A为任选被取代的链烯基、环或杂环基团;L1和L2各自独立为任选被取代的芳基或杂芳基;和m和n各自独立为0或1,使得m+n为1或2;其中:(i)式(1)的化合物任选为金属螯合物形式;和(ii)L1和L2中至少一个带有至少一个选自磺基、羧基、C1-4-烷基和C1-4-烷氧基-OH的取代基。还要求保护含有式(1)的组合物和化合物。
4 纤维-活性络合的双偶氮染料 CN201080005263.1 2010-01-18 CN102292400B 2016-01-20 J·艾希霍恩; A·施莱尔
纤维-活性络合的双偶氮染料本发明涉及具有式(I)的染料其中R1至R4,D1,f,以及M的定义如权利要求1所述,以及制备它们的过程以及它们在含羟基-和/或酰胺基-材料上染色和印花的用途。
5 用于喷墨印刷油墨的三偶氮染料 CN200380108631.5 2003-11-13 CN1738868B 2010-07-14 D·P·德沃纳尔德
在基材上印刷图像的方法,所述方法包括在基材上涂覆含液体介质和式(1)的三偶氮化合物或其盐的组合物:其中:A为任选被取代的链烯基、环或杂环基团;L1和L2各自独立为任选被取代的芳基或杂芳基;和m和n各自独立为0或1,使得m+n为1或2;其中:(i)式(1)的化合物任选为金属螯合物形式;和(ii)L1和L2中至少一个带有至少一个选自磺基、羧基、C1-4-烷基和C1-4-烷氧基-OH的取代基。还要求保护含有式(1)的组合物和化合物。
6 纤维-活性络合的双偶氮染料 CN201080005263.1 2010-01-18 CN102292400A 2011-12-21 J·艾希霍恩; A·施莱尔
纤维-活性络合的双偶氮染料本发明涉及具有式(I)的染料其中R1至R4,D1,f,以及M的定义如权利要求1所述,以及制备它们的过程以及它们在含羟基-和/或酰胺基-材料上染色和印花的用途。
7 使用特定的偶氮化合物的打印方法 CN03819007.9 2003-04-11 CN1675322A 2005-09-28 R·布拉德布里; A·迪金逊; P·J·杜布尔; P·格雷戈里; M·S·哈吉索特里欧; T·保罗; A·H·波帕特; N·J·汤普森; P·怀特
一种用于在基体上打印图像的方法,包括在其上施用含有液体介质和式(1)化合物的组合物:T-Q-N=N-L-T,其中各个T独立地为偶氮基团;Q为任选取代的、任选金属化的1,8-二羟基基;和L为二价有机连接基。还公开了组合物和染料。
8 잉크 젯 프린팅 잉크용 트리스아조 염료 KR1020057008665 2003-11-13 KR101023261B1 2011-03-21 드보날드데이비드필립
<화학식 1> 본 발명은 액체 매질 및 화학식 1의 트리스-아조 화합물 또는 그 염을 포함하는 조성물을 기재에 도포하는 단계를 포함하는 기재 상에 이미지를 인쇄하는 방법을 제공한다: 상기 식에서, A는 선택적으로 치환된 알케닐, 동소환 또는 복소환기; L 1 및 L 2 는, 각각 독립적으로, 선택적으로 치환된 아릴 또는 헤테로아릴; 및 m 및 n은, 각각 독립적으로, 0 또는 1 이고, m+n은 1 또는 2이고: 상기 식에서, (i) 화학식 1의 화합물은 선택적으로 금속 킬레이트의 형태이고; (ii) L 1 및 L 2 중 적어도 하나는 술포, 카르복시, C 1-4 -알콕시 및 C 1-4 -알콕시-OH로부터 선택된 적어도 하나의 치환기를 갖는다. 또한 화학식 1을 포함하는 조성물 및 화합물을 청구한다.
9 아조 화합물을 이용한 인쇄 방법 KR1020047020219 2003-04-11 KR1020050019131A 2005-02-28 브래드버리로이; 딕킨슨알렌; 더블필립존; 그레고리피터; 하지소테리오우마리아소테리; 폴토마스; 포팻애자이하리다스; 톰슨네일제임스; 이트폴
본 발명은 액체 매질 및 하기 화학식 1의 화합물을 포함하는 조성물을 기판에 도포하는 단계를 포함하는, 기판 상에 화상을 인쇄하는 방법에 관한 것이다: <화학식 1> TQN=NLT 상기 화학식 1 중, T는 독립적으로, 아조기이고; Q는 선택적으로 치환되며, 선택적으로 금속화된 1,8-디히드록시나프틸기이고; L은 2가 유기 연결기이다. 또한, 조성물 및 염료에도 관한 것이다.
10 염료함유편광필름 KR1019940026273 1994-10-13 KR100341162B1 2003-01-09 오기노가즈야; 하야시나루또시; 야마모또세쓰꼬; 오무라다까시
A polarizing film which comprises, in a film substrate, at least one dye selected from: 1) a dye of formula (1): Q<1>-N=N-Q<2>-X-Q<3>-N=N-Q<4> (1) wherein: Q<1> and Q<4>, which are the same or different, are each unsubstituted or substituted phenyl or naphthyl; Q<2> and Q<3>, which are the same or different, are each unsubstituted or substituted phenylene; and X is -N=N- or <CHEM> provided that, when X is -N=N- and both of Q<2> and Q<3> are unsubstituted phenylene, at least one of Q<1> and Q<4> is not phenyl which is substituted only by an alkyl-substituted amino or is not phenyl substituted by an alkyl-substituted amino and by methyl; and 2) a dye of formula (2): <CHEM> wherein: each Me, which are the same or different, is a transition metal selected from copper, nickel, zinc and iron; Q<5> and Q<6>, which are the same or different, are each an unsubstituted or substituted 1,2-naphthalene group; Y is -N=N- or <CHEM> and R<1> and R<2>, which are the same or different, are each hydrogen, lower alkyl, lower alkoxy or sulfo.
11 염료 함유 편광 필름 KR1019920015537 1992-08-28 KR100220494B1 1999-09-15 오기노가즈야; 아오키세츠코; 히가시고지
편광 필름 물질 및 하기 일반식(Ⅰ)의 금속-함유 염료를 포함하는 염료-함유 편광 필름은 요오드를 사용한 필름과 비교하여 편광 활성이 높고 내구성이 우수하다. 상기식에서, Me는 구리, 니켈, 아연 및 철로부터 선택된 전이 금속이며; Z는 수소, 저급 아킬, 저급 알콕시, 설포 또는 비치환되거나 치환된 아미노이고; Q는 비치환되거나 치환된 1-나프톨 또는 2-나프톨 잔기이며, 비치환되거나 치환된 페닐아조 또는 나프틸아조 그룹을 함유하지 않거나 추가로 함유할 수 있고, 나프톨 그룹의 하이드록시 그룹은 Z를 포함하는 벤젠환에 결합된 아조 그룹에 인접하며, 착물을 형성하기 위해 Me로 나타낸 전이 금속과 결합하고; Q가 아조 그룹을 추가로 함유하지 않는 나프톨 잔기인 경우, T는 비치환되거나 치환된 나프틸이며; Q가 아조 그룹을 추가로 함유하는 나프톨 잔기인 경우, T는 비치환되거나 치환된 페닐 또는 나프틸 그룹이다.
12 섬유-반응성 구리 착물 디스아조 염료 KR1020117017588 2010-01-18 KR101699989B1 2017-01-26 아이히호른요하임; 슈렐안드레아스
본발명은식 (I)의염료및 이들의제조방법및 히드록실및/또는카르복사미도함유재료를염색하고날염하기위한이들의용도에관한것이다:[식중, R내지 R, D, f, 및 M 은제 1 항에제시된바와같이정의됨].
13 농축 염료 용액 KR1020067024734 2005-05-17 KR1020070024538A 2007-03-02 오베르홀저마틴
Concentrated aqueous dye solutions comprising one or more cationizable dyes, an organic acid and water and their use for dyeing and/or printing organic substrates and for producing inkjet printing inks (Formula I), where each A is independently -NH- or - O-, B is a polyvalent group or atom, n' and n'' are natural numbers and the surn total of n' and n'' is >= 2, m is a group having the formula (c1) or (c2). ® KIPO & WIPO 2007
14 염료계 편광 필름 및 염료계 편광자 KR1020040010113 2004-02-16 KR1020040074939A 2004-08-26 하야시나루또시
PURPOSE: A dye type polarizing film of a polyvinyl alcohol film and a dye type polarizer are provided to improve the color reproductivity of a liquid-crystalline display by using the dye type polarizer. CONSTITUTION: A polarizing film includes a dichroic dye. The dichroic dye is adsorbed and oriented in the polarizing film. A hue angle H is in a range of 105 degrees to 150 degrees and a chroma C* is 7 or smaller when a parallel hue is expressed on a chromaticity coordinate of (a*,b*). In the polarizing film, a chroma C* is 3 or smaller when an orthogonal hue is expressed on the chromaticity coordinate of (a*,b*).
15 수용성 아조 화합물의 제조방법 KR1019820005411 1982-12-02 KR1019840002877A 1984-07-21 오또다께사또시; 마쯔나가료오조; 후루자와마사오
내용없음
16 COMPOSITIONS AND INKS CONTAINING DISAZO DYES PCT/GB0302438 2003-06-05 WO03104332A8 2005-02-17 DICKINSON ALAN; THOMPSON NEIL JAMES; WIGHT PAUL; GREGORY PETER; DOUBLE PHILIP JOHN; BRADBURY ROY
A process for printing an image on a substrate comprising applying thereto a composition comprising a liquid medium and a compound of Formula (1) A-N=N-L-N=N-A wherein: each A independently is optionally substituted aryl or heteroaryl; and L is an optionally substituted, optionally metallised 1,8-dihydroxynaphthylene group; provided that: (i) at most one of the groups represented by A has a hydroxy substituent ortho to the -N=N- groups shown in Formula (1); and (ii) Formula (1) is not: Also claimed are compositions for printing, compounds and processes for making the compounds.
17 BLACK TRIS AZO METAL COMPLEX DYES PCT/EP0102487 2001-03-06 WO0172906A3 2002-03-14 GEISENBERGER JOSEF; WUZIK ANDREAS
The present invention relates to the metal complexes of tris azo dyes of general formula (4), wherein R<1> represents an aryl radical that is mono- or poly-, e.g. 2-, 3-, 4- or 5-fold, substituted with OH, O(C1-C6)-alkyl, O(C1-C6)-alkyl-COOM, O(C1-C6)-alkyl-SO3M, O(hydroxy(C1-C6)-alkyl, (C1-C6)-alkyl, COOM, SO3M, SO2NH2, SO2N(hydroxy(C1-C6)-alkyl)2, SO2NH(C1-C6)-alkyl, SO2N((C1-C6)-alkyl)2, NH2, NH(C1-C6)-alkyl, NHacyl, NHaryl, N(hydroxy(C1-C6)-alkyl)2, N((C1-C6)-alkyl)2 and/or halogen; R<2> stands for OH, O(C1-C6)-alkyl, COOM or SO3M; R<3>, R<4> and R<5> are hydrogen or a substituent; R<6> stands for a non-substituted or a mono- or poly-substituted, mononuclear or binuclear, carbocycli or heterocyclic aromatic, an equally substituted pyrazole radical or an equally substituted pyridone radical. The dyes can be used for dyeing and imprinting natural and synthetic fibre materials, recording liquids, especially according to the ink jet method, liquid adjustments for colouring paper pulp and as a colouring agent for electrophotographic toners, powder lacquers and colour filters which contain the inventive dyes.
18 FIBER-REACTIVE COPPER COMPLEX DISAZO DYES PCT/EP2010050495 2010-01-18 WO2010086243A3 2010-10-21 EICHHORN JOACHIM; SCHRELL ANDREAS
The present invention relates to dyes of the formula (I), in which R1 to R4, D1, f, and M are defined as indicated in claim 1, to processes for preparing them, and to their use for dyeing and printing hydroxyl- and/or carboxamido-containing materials.
19 Water-soluble complex dye, recording fluid and recording method US11005021 2004-12-07 US07025815B2 2006-04-11 Wataru Shimizu; Mio Ishida; Hideo Sano; Yukichi Murata
A water-soluble complex dye capable of forming an image having light resistance, ozone resistance and high saturation; a water-based recording fluid, particularly an ink jet recording fluid, employing such a dye; an ink set employing such a recording fluid; and an ink jet recording method, are presented.
20 Black trisazo metal complex dyes US09816180 2001-03-23 US06749674B2 2004-06-15 Josef Geisenberger; Andreas Wuzik
Disclosed are metal complexes of trisazo dyes of the general formula 4 wherein R1 through R6 are as defined in the specification. The dyes are useful for dyeing and printing natural and synthetic fiber materials, recording fluids, especially for the inkjet process, liquid formulations for paper pulp dyeing, and also as colorants for electrophotographic toners, powder coatings and color filters including the dyes of the invention.
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