专利检索_ 由其他偶氮化合物制备的偶氮染料专利检索_ 由其他偶氮化合物制备的偶氮染料专利检索查询

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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	极性染料	CN200680007770.2	2006-03-09	CN101137735A	2008-03-05	亚历山大·A·加尔
本发明涉及新型极性荧光和猝灭剂染料，以及具有增强极性的小沟结合体。本发明还涉及自动化合成条件下制备标记有极性胂酸酯染料的探针的方法和使用这些探针的方法。
2	아조 화합물, 경화성 조성물, 컬러 필터 및 그 제조 방법	KR1020080090149	2008-09-12	KR1020090028456A	2009-03-18	미즈카와유키; 다카쿠와히데키; 후지모리도루
An azo compound is provided to ensure good fastness, elution resistance and great mole adsorption coefficient, and to obtain a color filter capable of thinning, having excellent fastness. An azo compound is represented by the general equation (I), the general equation (II) or the general equation (III). A curable composition comprises the azo compound represented by the general equation (I), the general equation (II) or the general equation (III). The azo compound has the maximum absorption wavelength of the visible part of 500nm-600nm and the second absorption wavelength of the visible part of 400nm-500nm. The curable composition more includes a polymeric monomer and a radiation-sensitive compound. A color filter is obtained by forming a curable composition layer by applying the curable composition on a support and forming patterns through mask, exposure and development.
3	음이온 화합물	KR1019910012228	1991-07-18	KR100164610B1	1999-01-15	피터그레고리; 로얼드와인포드케넌; 프라하레드매니브하이미스트리
본 발명은 다음 일반식 (1)의 유리산 형태의 음이온성 아조 화합물들에 관한 것이다. 식중, 일반식(1) 화합물이 -COOH 와 -COSH 에서 선택된 그룹을 최소한 -SO ₃ H 그룹만큼 많이 갖는다는 조건을 만족한다면, J는 Ar ¹ 및 Ar ² 는 이둘중 최소한 하나가 COOH 와 COSH 로부터 선택된 최소한 하나의 치환체를 갖는다면 이들 각각은 서로 무관하게 아릴 또는 치환된 아릴; 각각의 R ¹ 과 R ² 는 서로 무관하게 H, 알킬, 치환된 알킬, 알케닐 또는 치환된 알케닐,; L 은 2가의 유기 결합 그룹 ; n 은 0 또는 1 ; 각각의 X 는 서로 무관하게 카보닐 또는 다음 일반식 (2), (3) 또는 (4) 그룹 : 각각의 Z 는 서로 무관하게 NR ³ R ⁴ , SR ⁵ 또는 OR ⁵ ; 각각의 Y 는 서로 무관하게 H, Cl, Z, SR ⁶ 또는 OR ⁶ ; 각각의 E 는 서로 무관하게 Cl 또는 CN ; R ³ , R ⁴ , R ⁵ 및 R ⁶ 은 서로 무관하게는 H , 알킬, 치환된 알킬, 알케닐, 치환된 알케닐, 아릴, 치환된 아릴, 아랄킬, 치환된 아랄킬 또는 R ³ 와 R ⁴ 가 이들이 연결되어 있는 질소원자와 합쳐져 5 - 또는 6 - 원 고리를 형성한다. 이 화합물들은 잉크분사식 인쇄에 사용하기위한 잉크를 제조하는데 사용할 수 있다.
4	POLAR DYES	EP06737586.5	2006-03-09	EP1866387B1	2013-05-08	GALL, Alexander A.

5	Utilisation de composés azoïques polycationiques en teinture des fibres kératiniques	EP05292243.2	2005-10-24	EP1738799B1	2008-08-20	Lagrange, Alain; David, Hervé; Greaves, Andrew

6	Additionsprodukte von acryloylamino-substituierten Farbstoffen, deren Herstellung und deren Verwendung	EP00810806.0	2000-09-07	EP1085056A3	2002-01-30	Lehmann, Urs; Frick, Marcel
Monoazo-, Polyazo-, Metallkomplexazo-, Anthrachinon-, Phthalocyanin-, Formazan- oder Dioxazin-Farbstoffe, die mindestens eine Struktureinheit der Formel (1) enthalten, worin Z gegebenenfalls im Alkylteil substituiertes oder durch Sauerstoff unterbrochenes C₁-C₂₄-Alkoxy, gegebenenfalls im Phenylring substituiertes Phenoxy, gegebenenfalls im Alkylteil substituiertes C₁-C₄-Alkylthio, gegebenenfalls im Phenylring substituiertes Phenylthio, Amino, gegebenenfalls im Alkylteil substituiertes oder durch Sauerstoff oder einen Rest - NR₁- unterbrochenes N-Mono- oder N,N-Di-C₁-C₂₄-Alkylamino, wobei R₁ Wasserstoff oder C₁-C₄-Alkyl bedeutet, C₁₀-C₂₀-Terpenamino, gegebenenfalls im Cycloalkylring substituiertes C₅-C₇-Cycloalkylamino, gegebenenfalls im Arylteil substituiertes Phenyl- oder Naphthylamino oder N-C₁-C₄-Alkyl-N-phenyl- oder N-C₁-C₄-Alkyl-N-naphthylamino, Morpholino, Piperazin-1-yl oder Piperidin-1-yl ist, und X Wasserstoff, Hydroxy, Chlor oder Brom bedeutet, oder X die Bedeutung von Z hat, ergeben Färbungen oder Drucke mit guten Lichtechtheiten und hoher Farbbrillanz.
7	SOLUBLE CHROMOPHORES HAVING IMPROVED SOLUBILISING GROUPS	EP98904092.8	1998-01-17	EP0968250A1	2000-01-05	HALL-GOULLE, Véronique; BIZE, Aline
Compounds of formula (I): A(B)x wherein x is an integer from 1 to 8; A is the radical of a chromophore of the quinacridone, anthraquinone, perylene, indigo, quinophthalone, indanthrone, isoindolinone, isoindoline, dioxazine, azo, phthalocyanine or diketopyrrolopyrrole series that is bonded to x groups B via one or more hetero atoms, those hetero atoms being selected from the group consisting of N, O and S and forming part of the radical A; each group B independently of any other(s) is hydrogen or a group of formula α, at least one group B being a group of said formula, wherein Q is p, q-C2-C12alkylene that is unsubstituted or mono- or poly-substituted by C1-C12alkoxy, C1-C12alkylthio or by C2-C24dialkylamino, p and q being different position numbers; X is a hetero atom selected from the group consisting of N, O and S, m being the number 0 when X is O or S and m being the number 1 when X is N, and L1 and L2 are each independently of the other [-(p',q'-C2-C12alkylene)-Z-]n-C1-C12alkyl or C1-C12alkyl that is unsubstituted or mono- or poly-substituted by C1-C12alkoxy, C1-C12alkylthio, C2-C24dialkylamino, C6-C12aryloxy, C6-C12arylthio, C7-C24arylalkylamino or by C12-C24diarylamino, wherein n is a number from 1 to 1000, p' and q' are different position numbers, each Z independently of any other(s) is a hetero atom O, S or C1-C12alkyl-substituted N, and C2-C12alkylene in the repeating units [-C2-C12alkylene-Z-] may be identical or different; and L1 and L2 may be saturated or one- to ten-fold unsaturated, uninterrupted or interrupted at any desired points by from 1 to 10 groups selected from the group consisting of -(C=O)- and -C6H4-, and may carry no substituents or may carry from 1 to 10 further substituents selected from the group consisting of halogen, cyano and nitro; with the proviso that when -Q- is -(CH2)r-, wherein r is a number from 2 to 12, and X is S, L2 may not be unsubstituted, saturated and uninterrupted C1-C4alkyl. The compounds according to the invention are used in high-molecular-weight organic materials, thermo-, photo- or chemo-sensitive recording materials, light-sensitive negative or positive resist compositions, ink compositions for ink-jet printing and colour tapes for thermal transfer printing.
8	Verfahren zur Herstellung von Aminoazofarbstoffen	EP95107162.0	1995-05-11	EP0684288B1	1997-02-12	Bermes, Rudolf, Dr.; Keilhauer, Heinz

9	Ink compositions	EP93300017.6	1993-01-04	EP0559310B1	1996-04-03	Gregory, Peter; Kenyon, Ronald Wynford; Mistry, Prahalad Manibhai; Taylor, John Anthony

10	Verfahren zur Herstellung von Aminoazofarbstoffen	EP95107162.0	1995-05-11	EP0684288A1	1995-11-29	Bermes, Rudolf, Dr.; Keilhauer, Heinz
Verfahren zur Herstellung von Aminoazofarbstoffen durch wäßrigsaure Hydrolyse der entsprechenden N-sulfomethylierten Aminoazofarbstoffe in Gegenwart von Amidosulfonsäure, Harnstoff oder deren Gemischen.
11	Azofarbstoffe, Verfahren zu deren Herstellung und deren Verwendung	EP91810025.6	1991-01-15	EP0439423B1	1995-05-31	Schaetzer, Jürgen, Dr.; Adam, Jean-Marie, Dr.

12	Azofarbstoffe, Verfahren zu deren Herstellung und deren Verwendung	EP91810025.6	1991-01-15	EP0439423A3	1991-12-18	Schaetzer, Jürgen, Dr.; Adam, Jean-Marie, Dr.
Die Erfindung betrifft Azofarbstoffe der Formel worin R₁ Wasserstoff, C₁-C₄-Alkyl, R₂ C₂-C₄-Alkyl, R₃ Wasserstoff, C₁-C₄-Alkyl oder gegebenenfalls substituiertes C₅-C₇-Cycloalkyl oder Phenyl sind und dir Benzringe I und II gegebenenfalls substituiert sind. Die Azofarbstoffe eignen sich zum Färben oder Bedrucken von natürlichen oder synthetischen Polyamidmaterialien, besonders in Kombination mit anderen Farbstoffen und insbesondere aus Kurzflotten. Die Azofarbstoffe zeichnen sich durch allgemein gute Eigenschaften insbesondere gutes Aufziehverhalten aus.
13	Ink-jet printing inks	EP89311303.5	1989-11-01	EP0369643A2	1990-05-23	Pawlowski, Norman E.; Norton, Kenneth A.
Ink compositions for ink-jet printing comprise water, a water-miscible solvent, and a water-soluble dye comprising an aromatic dye molecule having attached to the aromatic nucleus thereof from 2 to 10 alkylamino groups having the formula selected from the group consisting of: (a) -(CH₂)_n-NH₂, (b) -NH-(CH₂)_n-NH₂, (c) -CH₂-NH-(CH₂)_n-NH₂, where n = 2 to 5, and (d) -NH-(C₂H₄NH)_xC₂H₄NH₂, where x = 0 to large. These dyes have good water solubility at near neutral pH and interact well with paper. Certain of the dyes are novel per se.
14	Silver halide color photographic material	EP85110769.8	1985-08-27	EP0173302B1	1989-05-10	Ichijima, Seiji; Mihayashi, Keiji; Ono, Mitsunori; Tamoto, Koji; Itoh, Isamu; Nakamura, Yoshisada

15	Fotografisches Aufzeichnungsmaterial und hierfür geeignete Verbindungen mit fotografisch wirksamem, abspaltbarem Rest	EP81102517.0	1981-04-03	EP0037985B1	1983-06-15	Renner, Günter, Dr.; Wolff, Erich, Dr.

16	화합물 및 이것을 포함하는 조성물	KR1020177024231	2016-02-17	KR1020170128257A	2017-11-22	히다노리유키; 오카와하루키
파장 350 nm ∼ 510 nm 의범위에극대흡수를갖는, 이색성색소로서기능하는신규화합물인, 이하의식 (1) 로나타내는화합물.(식중, R은, 수소원자, 탄소수 1 ∼ 20 의알킬기등을나타내고, R∼ R는, 수소원자이외의치환기이고, 각각독립적으로탄소수 1 ∼ 4 의알킬기등을나타내고, n, m, p 는, 각각독립적으로 0 ∼ 2 의정수이고, Ar은, N 이페닐렌기에결합하고있는함질소포화헤테로고리기이고, 당해함질소포화헤테로고리기의적어도일방의β 위치가산소원자또는황 원자인 5 ∼ 8 원자고리를나타낸다.)
17	아조 화합물, 경화성 조성물, 컬러 필터 및 그 제조 방법	KR1020080090149	2008-09-12	KR101536317B1	2015-07-13	미즈카와유키; 다카쿠와히데키; 후지모리도루
본발명에의하면, 하기일반식(I), 일반식(Ⅱ), 또는일반식(Ⅲ)으로표시되는아조화합물이제공된다. (식중, R, R는각각독립적으로수소원자, 또는치환기를나타내고, D, D는각각독립적으로커플러잔기(coupler residue)를나타낸다. Z, Z는각각독립적으로, -C(R)=, 또는 -N=를나타내고, R은, 수소원자, 또는치환기를나타낸다)
18	특정 양이온성 디아조 화합물, 이를 직접 염료로 함유하는조성물, 케라틴 섬유의 염색 방법 및 이를 위한 장치	KR1020050054706	2005-06-23	KR1020060066608A	2006-06-16	그레아베앙드르; 다비드에르베
The present disclosure relates to cationic diazo dye compounds of formula (I): Dye1-LK-Dye2 (I): it also relates to dye compositions comprising the direct dye compounds, and also to a process for dyeing fibers using this composition and a multi-component kit.
19	음이온 화합물	KR1019910012227	1991-07-18	KR100153007B1	1998-11-02	피터그레고리; 도널드윈포드케년
본 발명은 다음 구조식(1)을 갖는 유리산 형태의 음이온 아조 화합물에 관한 것이다. 본 화합물은 잉크 분사식 인쇄에 사용되는 잉크를 제조하는데 유용하다.
20	POLAR DYES	PCT/US2006008425	2006-03-09	WO2006099050A3	2007-03-01	GALL ALEXANDER A
The present invention relates to novel polar fluorescent and quenchers dyes, and minor groove binder with enhanced polarity. The present invention further relates to methods of preparing oligonucleotide probes labeled with polar arsonate dyes under the condition of automated synthesis and method of using such probes.

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