序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
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) : wherein :

  • X represents N-R or
  • R represents NR3R4 or the residue of an aromatic coupling compound R-Q wherein Q is a group displaceable by a diazotised amine;
  • R1 represents NR3R4, OR12 or SR12;
  • R2 represents hydrogen, cyano, COR13, CO2R13, CONR14R15 or SO2R16;
  • R3 and R4 each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic group or R3 and R4 together with the nitrogen atom to which they are attached represent the atoms necessary to complete a ring or R3 and/or R4 and one of the Y-substituents together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6- membered, fused-on heterocyclic ring ;
  • Y represents a substituent, e.g. SH, OH, an amino group, a halogen, CN, NO2, an alkyl group, an alkenyl group, an alkynyl group, an alkoxy group, a thioalkoxy group, a carbamoyl group, a sulfamoyl group, an acylamino group, a sulfonylamino group or a carboxylic ester;
  • n represents 0, 1, 2, 3 or 4, the substituents being the same or different when n is greater than 1 or two or more Y substituents can form an annelated ring system;
  • R12, R13, R14 and R15 each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic ring or R14 and R15 together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered ring or R12 or R13 or R14 or R15 together with one of the Y-substituents and the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered fused-on heterocyclic ring;
  • R16 represents hydroxy, an alkoxy group, an aryloxy group, NR17R18, an aryl group, an alkyl group, an alkenyl group, an alkynyl group, or R16 together with one of the Y-substituents and the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered fused-on heterocyclic ring;
  • R17 and R18 each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic ring or R17 and R18 together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered ring;
  • A represents an alkyl group, an alkenyl group, an alkynyl group or an aryl group;
  • G represents hydrogen, CN or R19-C=B;
  • Z represents hydrogen, halogen, CN, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an amino group, an alkoxy group, a thioalkoxy group, a sulphone group, or G and Z together with the atoms to which they are attached represent the atoms necessary to form an alicyclic, aromatic or heteroaromatic ring;
  • B represents O, N-R20, CR21R22;
  • R19 represents hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an aryloxy group, an alkoxy group, such as methoxy or ethoxy, a alkylthio group, an amino group, an electron withdrawing group, e.g. CN, a halogen, a carboxylic ester, an amide e.g. carboxylamide, a sulphonate, a phosphonate, a carbonyl group, a nitro group or R19 and R21, R22 or R20 together with the atoms to which they are attached represent the necessary atoms to form a ring;
  • R20 represents H, CN, NR23R24, OR23, OCOR23, OCO2R23, OCONR23R24, OSO2R23, OP(O)(OR23)(OR24), an alkyl group, an alkenyl group, an alkynyl group or an aryl group;
  • R21 and R22 independently represent a heterocyclic ring, e.g. thiazolyl, benzothiazolyl, isothiazolyl, benzoisothiazolyl, thienyl, pyridinyl, imidazolyl, benzimidazolyl, pyrazolyl, oxazolyl, thiadiazolyl, triazolyl, quinolyl, isoquinolyl, pyridoisothiazolyl, benzoxazolyl, isoxazolyl, benzoisoxazolyl, pyrrolyl and isothiadiazolyl or an electron withdrawing group. e.g. CN, a carboxylic ester, an amide e.g. carboxylamide, a sulphonate, a phosphonate, a carbonyl group, a nitro group or R21 and R22 together with the atoms to which they are attached represent the necessary atoms to form a ring;
  • R23 and R24 independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic ring e.g. as defined hereinbefore, or R23 and R24 together with the atoms to which they are attached represent the atoms necessary to form a heterocyclic ring.

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) in der

R1 und R2
unabhängig voneinander C6-C14-Aryl oder einen heterocyclischen Rest mit bis zu 3 Ringen und bis zu 4 Heteroatomen aus der Reihe O, S und N bedeuten,
R3 und R4
unabhängig voneinander Wasserstoff, C1-C12-Alkyl, C2-C12-Alkenyl, C4-C8-Cycloalkyl, C7-C17-Aralkyl, C6-C14-Aryl oder Nitril bedeuten oder
R3 und R4
gemeinsam eine 2- bis 5-gliedrige C-Brücke bedeuten, die gegebenenfalls von bis zu zwei Sauerstoff- und/oder Stickstoffatomen unterbrochen sein kann und
X-
ein Anion bedeutet,
wobei alle vorhandenen Alkyl-, Alkenyl-, Cycloalkyl-, Aralkyl- und Arylreste, sowie annelierte und heterocyclische Reste gegebenenfalls mit nichtionogenen Substituenten, Carboxylgruppen, Ammoniumgruppen und/oder Pyridiniumgruppen substituiert sein können, werden als Farbstoffe verwendet.

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.

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):

wherein :

Z represents hydrogen or a substituent,

X represents N-R or

R represents NR³R⁴ or the residue of an aromatic coupling compound E-Q wherein Q is a group displaceable by a diazotised amine;

R¹ represents NR³R⁴, OR¹² or SR¹²;

R² represents hydrogen, cyano, COR¹³, CO₂R¹³, CONR¹⁴R¹⁵, SO₂R¹⁶;

R³ and R⁴ each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, an a heterocyclic group or R³ and R⁴ together with the atoms to which they are attached represent the atoms necessary to complete a ring;

Y represents a substituent;

n represents 0, 1, 2, 3 or 4, the substituents being the same or different when n is greater than 1 or two or more Y substituents can form an annelated ring system;

R¹², R¹³, R¹⁴ and R¹⁵ each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic ring or R³ and R⁴ together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered ring or R³ and/or R⁴ together with the atoms to which they are attached and one of the Y-substituents represent the necessary atoms to form a 5- or 6- membered, fused-on heterocyclic ring or R¹⁴ and R¹⁵ together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6- membered ring or R¹³ or R¹⁴ or R¹⁵ or R¹⁴ and R¹⁵ together with one of the Y-substituents and the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered fused-on heterocyclic ring;

R¹⁶ represents hydroxy, an alkoxy group, an aryloxy group, NR¹⁷R¹⁸, an aryl group or an alkyl group, an alkenyl group, an alkynyl group, or R¹⁶ together with one of the Y-substituents and the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered fused-on heterocyclic ring;

R¹⁷ and R¹⁸ each independently represent hydrogen, an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic ring or R¹⁷ and R¹⁸ together with the atoms to which they are attached represent the necessary atoms to form a 5- or 6-membered ring.

The present invention further provides a method for making an image using the aforementioned dye donor element.

53 Kationische Triazenfarbstoffe und ihre Verwendung EP81109833.4 1981-11-23 EP0053751A1 1982-06-16 Fürstenwerth, Hauke, Dr.

Die kationischen Triazenfarbstoffe der allgemeinen Formel worin

  • B Alkylmercapto, Arylmercapto oder einen Rest der Formel
  • R Wasserstoff, einen Alkyl-, Alkenyl-, Acyl-, Cycloalkyl-, Aryl-, Aralkyl-, Amino-, Alkylamino-, Dialkylamino-, Arylamino-, Aralkylamino- oder heterocyclischen Rest und
  • R, Wasserstoff, einen Alkyl-, Alkenyl- oder Aralkylrest bedeuten, oder
  • R und R, zu einem Heterocyclus verbunden sind,
  • R2, R3 einen Alkyl-, Alkenyl-, Alkinyl oder Aralkylrest oder einer der Reste R2 oder R3 auch Wasserstoff bedeuten, oder
  • R3 mit der o-Stellung von A verbunden ist,
  • A einen Arylrest und
  • An(-) ein Anion bedeuten,


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.

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.
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.
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