| 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 | 偶氮直接染料和使用这些染料用于染发的方法 | CN201580059822.X | 2015-10-29 | CN107075266B | 2020-06-02 | 海克·格特鲁克·阿贝尔; 阿明·奥桑; 马库斯·施佩克巴切尔; 英戈·赖因霍尔德·韦伯 |
| 式(I)或(II)或(III)的化合物，其中R5、R6、R7、R8’、R8”和R8”’是如本文定义的。此化合物可以用在用于纤维染色的组合物中。 | ||||||
| 2 | 在信息层中含有三氮菁染料作为吸光性化合物的光学数据存储介质 | CN02810907.4 | 2002-03-20 | CN1513176A | 2004-07-14 | H·伯内斯; F·-K·布鲁德; W·黑泽; R·哈根; K·哈森吕克; S·科斯特罗米尼; P·兰登伯格; R·奥泽尔; T·索默曼; J·-W·施塔维茨; T·比林格尔 |
| 本发明因此涉及含有优选透明的基材的光学数据存储介质，该基材任选已涂敷了一层或多层的反射层和在其表面上施涂光可记录的信息层，任选的一层或多层反射层和任选的保护层或附加的基材或覆盖层，该数据存储介质能够利用蓝光或红光，优选激光来记录和读，其中信息层含有吸光性化合物和任选的粘结剂。本发明数据载体进一步的特征在于至少一种三氮菁染料用作该吸光性化合物。 | ||||||
| 3 | 偶氮直接染料和使用这些染料用于染发的方法 | CN201580059822.X | 2015-10-29 | CN107075266A | 2017-08-18 | 海克·格特鲁克·阿贝尔; 阿明·奥桑; 马库斯·施佩克巴切尔; 英戈·赖因霍尔德·韦伯 |
| 式(I)或(II)或(III)的化合物，其中R5、R6、R7、R8’、R8”和R8”’是如本文定义的。此化合物可以用在用于纤维染色的组合物中。 | ||||||
| 4 | 2,2′-双(2-羟基-4-磺酸基-1-萘氨偶氮基)-5,5′-二甲基-4,4′-联噻唑及其制备方法 | CN201110292383.0 | 2011-10-03 | CN102311404B | 2013-10-30 | 王君玲; 张殿龙; 樊月琴; 王科伟; 贾治芳 |
| 本发明涉及一种双杂环三氮烯化合物，具体为2,2＇-双(2-羟基-4-磺酸基-1-萘氨偶氮基)-5,5＇-二甲基-4,4＇-联噻唑及其制备方法。包括下列步骤：（1）2,5-二溴己二酮的制备，（2）2,2＇-二氨基-5,5＇-二甲基-4，4＇-联噻唑的制备，（3）5,5＇-二甲基-4，4＇-联噻唑-2，2＇-双重氮盐的制备，（4）目标产物BHSNAADMBT的制备。本发明技术方案将双噻唑杂环和具有荧光性质的萘环衍生物通过三氮烯结构连接起来，合成具有双分析官能团和较大空间位阻的试剂，不但与金属离子反应有较高的灵敏度，而且具有较好的选择性。该试剂是良好的光度分析显色剂，也是灵敏度高、选择性好的新型荧光分析试剂。 | ||||||
| 5 | 2,2′-双(2-羟基-4-磺酸基-1-萘氨偶氮基)-5,5′-二甲基-4,4′-联噻唑及其制备方法 | CN201110292383.0 | 2011-10-03 | CN102311404A | 2012-01-11 | 王君玲; 张殿龙; 樊月琴; 王科伟; 贾治芳 |
| 本发明涉及一种双杂环三氮烯化合物，具体为2,2＇-双(2-羟基-4-磺酸基-1-萘氨偶氮基)-5,5＇-二甲基-4,4＇-联噻唑及其制备方法。包括下列步骤：（1）2,5-二溴己二酮的制备，（2）2,2＇-二氨基-5,5＇-二甲基-4，4＇-联噻唑的制备，（3）5,5＇-二甲基-4，4＇-联噻唑-2，2＇-双重氮盐的制备，（4）目标产物BHSNAADMBT的制备。本发明技术方案将双噻唑杂环和具有荧光性质的萘环衍生物通过三氮烯结构连接起来，合成具有双分析官能团和较大空间位阻的试剂，不但与金属离子反应有较高的灵敏度，而且具有较好的选择性。该试剂是良好的光度分析显色剂，也是灵敏度高、选择性好的新型荧光分析试剂。 | ||||||
| 6 | Optical recording material having high memory density | JP2007154383 | 2007-06-11 | JP2007290401A | 2007-11-08 | LEHMANN URS; BUDRY JEAN-LUC; SCHMIDHALTER BEAT; SPAHNI HEINZ; SUTTER PETER |
| PROBLEM TO BE SOLVED: To provide a new compound usable for a recording layer of an optical recording medium. SOLUTION: The optical recoding medium containing a base material, the recording layer and a reflection layer makes the recording layer contain compounds of the formula (I), the formula (II), the formula (III) or the formula (IV). In the formula (I), the formula (II), the formula (III) or the formula (IV), A 1 and A 2 are mutually independent, C(C 1-C 5alkyl)2, C(C 4-C 5alkylene), N(R 15), O, S, Se or non-substitution, Q is the formula (12), and (in the formula (12), R 17 is hydrogen, cyano and non-substitution), X - is an inorganic anion, organic anion having a negative electric charge, or preferably organic metal anion or x pieces (x is a number of 2-4) having a negative charge, organic anion or 1/x pieces of organic metal anion or a mixture thereof. Further, R 1, R 2, R 7 and R 8 are mutually independent, respectively non-substituent, R 3, R 4, R 5, R 6, R 9, R 10, R 11, R 12, R 13 and R 14 are mutually independent and respectively non-substituted. COPYRIGHT: (C)2008,JPO&INPIT | ||||||
| 7 | Optical recording material with high recording density | JP2007003155 | 2007-01-11 | JP2007197726A | 2007-08-09 | LEHMANN URS; BUDRY JEAN-LUC; SCHMIDHALTER BEAT; SPAHNI HEINZ; SUTTER PETER |
| PROBLEM TO BE SOLVED: To provide a new compound usable as a recording layer of an optical recording medium. SOLUTION: The invention relates to the compounds having a specific benzothiazole structure applicable to short wave length laser beam, and having structures represented by formula (I)-(IV). In the formula X - is an anionic compound. COPYRIGHT: (C)2007,JPO&INPIT | ||||||
| 8 | Photorecording medium and amine compound | JP2002153756 | 2002-05-28 | JP2003342487A | 2003-12-03 | ISHIDA TSUTOMU; SHIOZAKI HIROYOSHI; OGISO AKIRA; KOIKE MASASHI |
| <P>PROBLEM TO BE SOLVED: To provide a photorecording medium which enables good photorecording and regeneration by a laser having a wavelength of 300-500 nm, and a novel amine compound. <P>SOLUTION: The photorecording medium contains at least one recording medium having at least one compound selected from the amine compound to be represented by the formula (1): A<SB>1</SB>-NH-X<SB>1</SB>=X<SB>2</SB>-A<SB>2</SB>(wherein A<SB>1</SB>and A<SB>2</SB>are each independently a substituted or nonsubstituted aryl group or a substituted or nonsubstituted metallocenyl group provided that at least one of A<SB>1</SB>and A<SB>2</SB>is an aryl group to which a metallocenyl group or a metallocene residue is bonded; and X<SB>1</SB>and X<SB>2</SB>are each independently a nitrogen atom or a substituted or nonsubstituted methine group) as one of tautomerizable structures. <P>COPYRIGHT: (C)2004,JPO | ||||||
| 9 | Photosensitive compositions | JP14016785 | 1985-06-28 | JPH0644149B2 | 1994-06-08 | HIRAO AKIKO; ONISHI KIYONOBU; ISORI KUNIHIRO |
| 10 | JPS6043382B2 - | JP6945083 | 1983-04-20 | JPS6043382B2 | 1985-09-27 | KOIBUCHI SHIGERU; ISOBE ASAO; MAKINO DAISUKE |
| 11 | Method of coloring hair made from the reaction of the capped diazonium compound and the hair, and related compositions and compounds | JP2006530175 | 2004-05-05 | JP2007500735A | 2007-01-18 | ポール エリウ，ビクター; カフマン，ドミニク; フローリング，ベアーテ |
| 【課題】キャップされたジアゾニウム化合物と毛髪の反応からなる毛髪の着色方法、及び関連する組成物及び化合物の提供。
【解決手段】多孔質材料の着色方法であって、該方法は、ａ）着色される材料に少なくとも１種のキャップされたジアゾニウム化合物を適用すること、及びｂ）その後、前記材料上に存在する前記キャップされたジアゾニウム化合物を毛髪と反応させることからなる方法。 更に、新規染色化合物及びそれらの組成物が請求される。 【選択図】なし |
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| 12 | An optical recording material having a high storage density | JP2002580321 | 2002-03-12 | JP2004532141A | 2004-10-21 | シュパーニ，ハインツ; シュミッドハルター，ベアト; ズター，ペーター; ブードリー，ジャン−リュク; レーマン，ウルス |
| 本発明は、基板、反射層及び式（Ｉ）、（II）、（III）又は（IV）の化合物に基づく記録層を含む光学記録媒体に関する。 置換基の正確な意味の記述が注目される。 記録及び再生は、たとえば青色レーザを使用して、特に３５０〜５００nmの波長で実施される。 記録再生の質は秀逸であり、高い記憶密度を可能にする。 同じく特許請求されるものは、式（Ｉ）、（II）、（III）又は（IV）の新規な化合物ならびに以下の配置で、ａ）反射金属又は好ましくは反射金属層を有するポリマーからなる支持材料、ｂ）光学記録層、ｃ）金属、架橋した有機金属又は誘電性無機物質からなる分離層、及びｃ）カバー層を含む光学記録媒体である。 | ||||||
| 13 | Coloring matter-donor element used in thermal transfer printing method | JP5115997 | 1997-02-20 | JPH09234964A | 1997-09-09 | RIYUKU BANMEERU |
| PROBLEM TO BE SOLVED: To easily transfer a coloring matter of a coloring matter-donor element by forming a coloring matter layer containing a polymer bonding agent and a coloring matter represented by a specified formula on a substrate. SOLUTION: In forming an image by transferring a coloring matter from an area in which a coloring matter-donor element is heated selectively, a substrate having a coloring matter layer containing a polymer bonding agent and at least one kind of coloring matter formed on the substrate is contained in a coloring matter-donor element, and as at least one kind of coloring matter, the coloring matter represented by the formula I is used. In the formula, X is presented by N-R or the formula II, R 2 represents NR 3R 4 or the like, R 1 represents NR 3R 4 or the like, R 2 represents hydrogen or the like, Y represents a substituent, for example, SH, OH or the like, A represents alkyl or the like, G represents CN, R 19-C=B or the like, Z represents halogen or the like, G and Z together with the atoms bonded with them represent atoms required for forming alicyclic, aromatic or aromatic heterocyclic ring. COPYRIGHT: (C)1997,JPO | ||||||
| 14 | Triazene dye for use in thermal transfer printing | JP12434394 | 1994-05-13 | JPH0753885A | 1995-02-28 | RIYUKU BUANMAERU |
| PURPOSE: To provide a novel triazene dye which has a specific structure and is useful for thermal transfer printing by dye sublimation. CONSTITUTION: A dye layer contg. a dye of formula I (wherein A is the residue of a diazotizable heteroarom. amine; and R 1 and R 2 are each H, alkyl or the like) is formed on a substrate (pref. one contg. polyethylene terephthalate), giving a thermal transfer printing material. Among dyes represented by formula I, a dye of formula II (wherein R 1 is C 4H 9 or C 6H 4PCH 3; R 3 is CHO; and R 4 is Cl) is a novel compd. and is prepd. e.g. by adding nitrosylsulfuric acid to a compd. of formula III in phosphoric acid and adding the resultant syrup to a compd. of formula IV in THF, acetic acid, and ice to cause the reaction. The thermal transfer printing material is prepd. pref. by dissolving or dispersing the dye, a binder medium, etc., in a solvent and applying the resultant compsn. to a substrate. Cellulose acetate butyrate is an example of a pref. binder. COPYRIGHT: (C)1995,JPO | ||||||
| 15 | Cationic triazatrimethine dye | JP11664893 | 1993-04-21 | JPH0688036A | 1994-03-29 | HAUKE FUYURUSUTENBERUTO; KAARUUHAINRIHI RANGE; RODERITSUHI RAUE; ARUFUREETO BURAKU |
| PURPOSE: To prepare the subject dye excellent in durability and affinity to fibers, which is useful for dyeing polyacrylonitrile, acid-modified polyester and polyamide fibers by selecting a particular triazamethine dye. CONSTITUTION: The selected triazamethine dye is expressed by formula I {Z is a group of formula II (R 3 is H, an alkyl, alkenyl or aralkyl; X is remaining members of a five-membered, optionally substituted or optionally fused partly unsaturated heterocyclic ring which contains 1-3 hetero atoms selected from the group consisting of O, S and N; B is an alkylmercapto, arylmercapto or a group of formula; -NR(R 1) [R is R 3, an acyl, cycloalkyl, aryl, amino, (di) alkylamino, arylamino, aralkylamino and heterocycle; R 1 is R 3; R, R 1 together with N may form heterocyclic group]; R 2 is R 3 or an alkynyl; A n (-) is anion: (acyclic)cyclic group may contain non-ionic substituents and/or COOH}, e.g. the compound of formula III. COPYRIGHT: (C)1994,JPO | ||||||
| 16 | DYES WITH CHANGEABLE SOLUBILITIES, AND METHODS FOR THEIR USE | PCT/US2010/061803 | 2010-12-22 | WO2012087310A1 | 2012-06-28 | MILLER, Seth, Adrian |
Disclosed herein are solubility changeable dye compositions, methods of preparing such compositions and methods of using them. The composition includes a dye component linked via a linker moiety to a stimulus responsive hydrophobic moiety which modulates the solubility of the dye, wherein the hydrophobic moiety is configured to be de-linked from the dye component on exposure to a stimulus and render the dye component more hydrophilic. |
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| 17 | OPTICAL RECORDING MATERIALS HAVING HIGH STORAGE DENSITY | PCT/EP0202707 | 2002-03-12 | WO02082438A3 | 2003-08-28 | LEHMANN URS; BUDRY JEAN-LUC; SCHMIDHALTER BEAT; SPAHNI HEINZ; SUTTER PETER |
| This invention relates to an optical recording medium, comprising a substrate, a reflecting layer and a recording layer based on compounds of formula (I), (II), (III) or (IV). Attention is drawn to the description for the precise meanings of the substituents. Recording and playback are carried out especially at a wavelength of from 350 to 500 nm, for example using a blue laser. The recording and playback quality is excellent and allows high storage density. Likewise claimed are some novel compounds of formula (I), (II), (III) or (IV), as well as an optical recording medium comprising, in the following arrangement, a) a supporting material consisting of a reflecting metal or, preferably, of a polymer having a reflection metallic layer; b) an optical recording layer; c) a separating layer consisting of a metallic, crosslinked organometallic or dielectric inorganic substance; and c) a covering layer. | ||||||
| 18 | 포스포노 하이드로 카르빌 아미노 트리아지닐 염료의 제조방법 | KR1019760000926 | 1976-04-15 | KR100008623B1 | 1980-09-18 | 데이비드윌리암프랜트; 데이비드죤윌리암스 |
| 19 | PROTECTED TRIAZABUTADIENE COMPOSITIONS FOR CELLULAR STUDIES IN INTACT BIOLOGICAL SYSTEMS | US17751474 | 2022-05-23 | US20220274931A1 | 2022-09-01 | John C. Jewett; Natasha Cornejo; Bismark Amofah; Lindsay E. Guzman; W Mudiyanselage Anjalee Wijetunge; Abigail Shepard; Danielle Johnson |
| Protected triazabutadiene molecules, such as those according to Formula D or variations thereof, as probes for cellular studies in intact biological systems. The protected triazabutadiene probes selectively release benzene diazonium ions (BDIs) intracellularly, providing a tool for accessing and/or labeling intracellular proteins or molecules prior to cell lysis. The present invention also includes methods for synthesizing the protected triazabutadienes, the protected triazabutadienes themselves, and methods of use. | ||||||
| 20 | Triazabutadienes as cleavable cross-linkers | US16321605 | 2017-07-31 | US11339129B2 | 2022-05-24 | John C. Jewett; Flora W. Kimani; Lindsay E. Guzman; Brandon M. Cornali |
| Triazabutadiene molecules as cleavable cross-linkers adapted to cross-link components with click chemistry, e.g., clickable triazabutadienes. For example, in some embodiments, the triazabutadienes feature alkyne handles attached to the imidazole portion or the aryl portion of the triazabutadienes, wherein the alkyne handles can link to azide handles (e.g., azide handles disposed on other components) via click chemistry. Also described are methods of producing said clickable triazabutadienes and methods of use of said clickable triazabutadienes. The present invention also features methods of cleaving said clickable triazabutadienes, e.g., for liberating the diazonium species for further chemical reactions. | ||||||
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