序号 | 专利名 | 申请号 | 申请日 | 公开(公告)号 | 公开(公告)日 | 发明人 |
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41 | Kationische Triazenfarbstoffe und ihre Verwendung | EP81109833.4 | 1981-11-23 | EP0053751B1 | 1984-08-29 | Fürstenwerth, Hauke, Dr. |
42 | An optical recording material having a high storage density | JP2002580321 | 2002-03-12 | JP3989846B2 | 2007-10-10 | 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 |
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. | ||||||
43 | Cationic triazacyclononane trimethinecyanine dye | JP11664893 | 1993-04-21 | JP3518613B2 | 2004-04-12 | アルフレート・ブラク; カール−ハインリヒ・ランゲ; ハウケ・フユルステンベルト; ロデリツヒ・ラウエ |
44 | New and known cationic 4,5-dihydro-1h-1,2,3-triazolium compound as dye and dyeing or printing method using new cationic 4,5-dihydro-1h-1,2,3-triazolium compound | JP18801996 | 1996-07-01 | JPH0912913A | 1997-01-14 | TOMASU BETSUKAA; HORUSUTO BERUNETO; HENRI GIIRA |
PROBLEM TO BE SOLVED: To provide a new triazolium compound useful e.g. as a material for ink-jet recording ink capable of dyeing and printing a cation-dyeable fiber, tannin-treated cellulose material, paper, silk, leather, etc., in high affinity and extremely high fastness to light, water and abrasion. SOLUTION: Dyeing and printing are performed by using a 4,5-dihydro-1 H-1,2,3-triazolium compound of the formula I (R 1 and R 2 are each independently a 6-14C aryl or a ≤3-cyclic heterocyclic group having ≤4 hetero-atoms selected from O, S and N; R 3 and R 4 are each independently H, a 1-12C alkyl, a 2-12C alkenyl, a 4-8C cycloalkyl, etc.; X - is an anion). Especially suitable compound of the formula I is a 4,5-dihydro-1H-1,2,3-triazolium compound of the formula II (R 3 and R 4 are each independently H, a 1-4C alkyl which may be substituted with hydroxyl, halogen, cyano, etc., etc.; R 5 to R 12 are each independently H, a 6C arylazo, an aminocarbonyl, etc.). COPYRIGHT: (C)1997,JPO | ||||||
45 | Dye and dye-donor element for thermal dye transfer recording | JP25822695 | 1995-09-12 | JPH08104819A | 1996-04-23 | RIYUKU BANMEERU |
PROBLEM TO BE SOLVED: To provide the subject element for use in a thermal dye sublimation transfer process and comprising, on a support, a dye layer containing a polymeric binder and a dye represented by a specified formula. SOLUTION: The objective element comprising, on a support, a dye layer containing a polymeric binder and a dye of formula I {wherein Z is H or a substituent; and X is N-R [wherein R is NR 3R 4 or an aromatic coupling compound E-Q (wherein Q is a group which may be replaced by a diazotized amine; and R 3 and R 4 together with the atoms to which they are bonded represent the necessary atoms or like to form a ring] or formula II [wherein R 1 is NR 3R 4, OR 12, or SR 12; R 2 is H, cyano, COR 13, CO 2R 12 (wherein R 12 and R 13 are each H, an alkyl, an alkenyl, or the like), or the like; Y is a substituent; and n is 0 or 1-4]}, is provided. It is suitable that a dye of formula I is obtained, for example, by dissolving a dye of formula III and NH 4SCN in THF, refluxing the solution, adding H 2Cl 2 to the system, and subjecting the mixture to suitable subsequent operations. COPYRIGHT: (C)1996,JPO | ||||||
46 | Preparation of dye | JP11663193 | 1993-04-21 | JPH0649375A | 1994-02-22 | RODERITSUHI RAUE; KAARUUHAINRIHI RANGE; ARUFUREETO BURAKU |
PURPOSE: To prepare a stable dye soln. without using an expensive process such as pressure permeation or reverse osmosis. CONSTITUTION: The objective dye of the formula; D-N=N-Z [where D is an arom. or heterocyclic diazo and Z is an arylamino or heterocyclic imino of the formula; -N=Het (where Het is a heterocyclic divalent group)] is prepd. by an economically and ecologically especially preferable method by which an arom. or heteocyclic diazo component of the formula; D-NH 2 is reacted with a compd. of the formula; H-Z 1 (where Z 1 is an arylamino or hetarylamino) in an aq. medium in the presence of a material giving nitrous acid and in the presence of CO 2 at 5-100 bar pressure and at 0-125°C. COPYRIGHT: (C)1994,JPO | ||||||
47 | Cationic triazene dyes, manufacture and use | JP19187381 | 1981-12-01 | JPS57121056A | 1982-07-28 | HAUKE FUYURUSUTENBUERUTO |
48 | Die Verwendung von kationischen 4,5-Dihydro-1H-1,2,3-triazoliumverbindungen als Farbstoffe | EP96109919.9 | 1996-06-20 | EP0752451B1 | 2001-10-17 | Böcker, Thomas, Dr.; Berneth, Horst, Dr.; Giera, Henry, Dr. |
49 | Dye donor element for use in thermal transfer printing | EP96200512.0 | 1996-02-27 | EP0792757A1 | 1997-09-03 | Vanmaele, Luc |
The present invention provides a dye-donor element for use according to thermal dye sublimation transfer, said dye-donor element comprising a support having thereon a dye layer comprising a polymeric binder and at least one dye, wherein said at least one dye corresponds to the following general formula (I) :
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50 | Die Verwendung von neuen und bekannten kationischen 4,5-Dihydro-1H-1,2,3-triazoliumverbindungen als Farbstoffe und neue kationische 4,5-Dihydro-1H-1,2,3-Triazoliumverbindungen | EP96109919.9 | 1996-06-20 | EP0752451A1 | 1997-01-08 | Böcker, Thomas, Dr.; Berneth, Horst, Dr.; Giera, Henry, Dr. |
4,5-Dihydro-1H-1,2,3-triazoliumverbindungen der Formel (I)
Neue 4,5-Dihydro-1H-1,2,3-triazoliumverbindungen entsprechen der Formel (I) mit den Maßgaben, daß wenn R3 und R4 jeweils Wasserstoff bedeuten, im Fall von R1 = 4-Methylphenyl R2 nicht für 4-Nitrophenyl, 4-Methoxyphenyl oder Phenyl steht und R1 und R2 nicht beide gleichzeitig für 4-Methylphenyl, 4-Nitrophenyl, 4-Methoxyphenyl oder Phenyl stehen. |
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51 | Kationische Triazatrimethinfarbstoffe | EP93106053.7 | 1993-04-14 | EP0567846B1 | 1996-12-04 | Fürstenwerth, Hauke, Dr.; Lange, Karl-Heinrich, Dr.; Raue, Roderich, Dr.; Brack, Alfred, Dr. |
52 | Dyes and dye-donor elements for thermal dye transfer recording | EP94202634.5 | 1994-09-13 | EP0701906A1 | 1996-03-20 | Vanmaele, Luc |
The present invention provides a dye-donor element for use according to thermal dye sublimation transfer. The dye-donor element comprises a support having thereon a dye layer comprising a polymeric binder and a dye corresponding to the following general formula (I):
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53 | Kationische Triazenfarbstoffe und ihre Verwendung | EP81109833.4 | 1981-11-23 | EP0053751A1 | 1982-06-16 | Fürstenwerth, Hauke, Dr. |
Die kationischen Triazenfarbstoffe der allgemeinen Formel
und worin die cyclischen und acyclischen Reste nichtionogene Substituenten und/oder eine Carboxylgruppe enthalten können, könpen zum Färben und Bedrucken natürlicher und synthetischer Materialien verwendet werden. |
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54 | 자외선 흡수제들 및 청색광 발색단들의 조합을 이용한 인공수정체들 | KR1020127028243 | 2011-04-27 | KR101869746B1 | 2018-06-21 | 러레이도,월터알.; 아키나이,알리이. |
향상된광 투과특성을가진안과용장치재료들을개시한다. 상기재료들은특정자외선흡수제들및 청색광을흡수하는발색단들의조합을포함한다. | ||||||
55 | 자외선 흡수제들 및 청색광 발색단들의 조합을 이용한 인공수정체들 | KR1020127028243 | 2011-04-27 | KR1020130094692A | 2013-08-26 | 러레이도,월터알.; 아키나이,알리이. |
향상된 광 투과 특성을 가진 안과용 장치 재료들을 개시한다. 상기 재료들은 특정 자외선 흡수제들 및 청색광을 흡수하는 발색단들의 조합을 포함한다.
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56 | 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. |