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 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.

2 Verfahren zum Färben und Bedrucken von hydrophoben, synthetischen, organischen Fasermaterialien mit wasserunlöslichen Azofarbstoffen EP80100538.0 1980-02-04 EP0014451A1 1980-08-20 Hoyer, Ernst, Dr.; Steckelberg, Willi, Dr.; Deucker, Walter, Dr.; Schickfluss, Rudolf, Dr.

Verfahren zum Färben oder Bedrucken von hydrophoben, synthetischen, organischen Fasermaterialien, dadurch gekennzeichnet, daß wasserunlösliche Azofarbstoffe der allgemeinen Formel verwendet werden, worin X eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen oder die Phenylgruppe bedeutet, weiche durch Alkylgruppen mit 1 bis 4 Kohlenstoffatomen, Alkoxygruppen mit 1 bis 4 Kohlenstoffatomen, Halogenatome und- /oder Nitrogruppen substituiert sein kann, und D für den Rest einer aromatischen Diazokomponente steht.

Bei der Anwendung der Azofarbstoffe der vorstehend genannten Formel lassen sich auf den genannten Fasermaterialien, wie solchen aus Celluloseestern, Polyestern, Polyurethanen, Polyolefinen oder Polyamiden lebhafte und klare grünstichig gelbe bis gelbstichig orange Färbungen erzielen, die sehr gut naß-, wach-, abgasund lichtecht sind.

3 Pyrazolone derivatives, their preparation and use as coupling components EP82107108 1982-08-06 EP0072508A3 1983-03-16 Kunde, Klaus, Dr.
Verbindungen der allgemeinen Formel worin
R C₁-C₄-Alkyl,
R₁ Wasserstoff oder ein nichtionischer Substituent,
n 0, 1 oder 2,
4 Verfahren zum Färben und Bedrucken von hydrophoben, synthetischen, organischen Fasermaterialien mit wasserunlöslichen Azofarbstoffen EP80100538.0 1980-02-04 EP0014451B1 1982-12-22 Hoyer, Ernst, Dr.; Steckelberg, Willi, Dr.; Deucker, Walter, Dr.; Schickfluss, Rudolf, Dr.
5 Dyes and dye-donor elements for thermal dye transfer recording EP94202634 1994-09-13 EP0701906B1 1997-12-29 VANMAELE LUC
6 Pyrazolonderivate, ihre Herstellung und ihre Verwendung als Kupplungskomponenten EP82107108.1 1982-08-06 EP0072508A2 1983-02-23 Kunde, Klaus, Dr.

Verbindungen der allgemeinen Formel worin

  • R C1-C4-Alkyl,
  • R, Wasserstoff oder ein nichtionischer Substituent,
  • n 0, 1 oder 2,
  • R2 und R3 unabhängig voneinander Wasserstoff, C1-C4-Alkyl, β-Hydroxy-C2-C4-alkyl oder Benzyl,
  • R4 und R5 unabhängig voneinander Wasserstoff, C1-C4-Alkyl oder β-Hydroxy-C2-C4-alkyl und
  • An(-) ein Anion sind, werden als Kupplungskomponenten bei der Herstellung von Azofarbstoffen verwendet.

7 Cumarinic pigments, process for their preparation and their use EP80100135.5 1980-01-11 EP0015361A1 1980-09-17 Battisti, Ruggero; Bausani, Giovanni; Casagrande, Francesco; Mazzaferro, Nicola

The present invention concerns a new class of pigments derived from cumarin and, more particularly, of bis- iminocumarinic and bis-cumarinic pigments having the following formula I described herein before. The present invention also includes novel processes for making the cumarinic pigments of the invention. Also, the invention relates to the use of the novel pigments of the invention for the preparation of paints, storing enamels, inks and pastes for the printing of fabrics. Also, included in this invention is the dyeing of plastic materials with the novel cumarinic pigments.

8 Chemosensors Based on Quantum Dots and Oxazine Compounds US12158213 2006-12-19 US20080305047A1 2008-12-11 Francisco M. Raymo; Massimiliano Tomasulo; Ibrahim Yildiz
We identified a mechanism to detect chemical changes with a modified semiconductor nanoparticle (e.g., an oxazine-adsorbed CdSe—ZnS core-shell quantum dot). Our strategy is based on the chemical transformation of chromo-genie ligands adsorbed on the surface of a quantum dot. This activates an energy transfer pathway from the quantum dot to the adsorbed chromogenic ligands, which causes a change (e.g., increase or decrease) in a characteristic of fluorescent emission (e.g., intensity or lifetime). Thus, modified quantum dots acting through this mechanism can efficiently transduce a chemical event or occurrence into a change in optical signal. Our design can be adapted to signal chemical changes by a diversity of target analytes and, thus, it can be used to develop other fluorescent chemosensors based on the unique properties of quantum dots.
9 Process and intermediates for preparing fiber-reactive phthalocyanine dyes US944641 1978-09-21 US4204056A 1980-05-20 Rolf Muller; Joachim Ribka
Process for preparing fiber-reactive water-soluble phthalocyanine azo dyes, using the following conversion stages ##STR1## followed by the diazonium coupling of the fiber-reactive group to the pyrazole ring. The novel intermediates are desirable products.
10 Spiro compounds US528620 1974-12-02 US3950403A 1976-04-13 Paul Rys; Rolf Vogelsanger
Compounds which contain a group bonded directly to an aromatic nucleus of the formula--(CH.sub.2 --).sub.n --X 1.in which n is a positive integer having a value of at least 2 and X represents a removable substituent.
11 Triazolopyrimido isoquinolinone derivatives US30717372 1972-11-16 US3847919A 1974-11-12 KNOWLES P; WOOLDRIDGE K; MARSHALL S; PAIN D
1. AN ISOQUINOLINE DERIVATIVE OF THE FORMULA:

8-(O=),R1-11-H-1,2,3-TRIAZOLO(5,4-B)-BENZO(H)-PYRIDO(1,2-

A)PYRIMIDINE

WHEREIN R1 REPRESENTS HYDROGEN, OR ALKYL OR ALKOXY OF 1 THROUGH 10 CARBON ATOMS OR BENZYL ON THE CARBON ATOM IN THE 1-, 2-, 3-, 4- AND 5-POSITION OF THE FORMULA, AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF.
12 Azo dyestuffs containing a phenylpiperidine coupling component US3663529D 1969-06-13 US3663529A 1972-05-16 KUBBA VED PARKASH; RAMANATHAN VISVANATHAN; JENNY WALTER
AZO DYESTUFFS WHICH CONTAIN AT LEAST ONE RESIDUE OF A COUPLING COMPONENT OF FORMULA

-(1,4-PHENYLENE)-N<(-CH2-CH2-C(<)-CH2-CH2-)

WHEREIN THE CARBON ATOM WHICH IS LOCATED IN THE 4-POSITION OF THE AZACYCLOHEXANE RING IS BONDED TO 1 TO PREFERABLY 2 IDENTICAL OR MUTUALLY DIFFERENT POSITISING GROUPS WHICH ARE CAPABLE OF RENDERING AN ADJACENT METHYLENE GROUP ACID.
13 Tris(arylazoaryl)-s-triazine 2,4,6(1h,3h,5h) trione and trithione as toxicants US3437729D 1967-09-27 US3437729A 1969-04-08 CORNELL JOHN H JR
14 Iron complexes of pyrazolone monoazo dyes and method of preparation US3423393D 1965-03-17 US3423393A 1969-01-21 KLEIN KARL J
15 Nu-aralkyl- and nu-aryl derivatives of tetrahydro-oxathiazine-(1, 4, 5)-dioxide-(4, 4) and process for preparing them US24043762 1962-11-27 US3202657A 1965-08-24 RUDOLF KUHNE; FRITZ MEININGER; WILHELM PFIRRMANN ROLF
16 Certain 3-phenylhydrazono-2-amino-1,1,3-propene tricarbonitrile US294253 1981-08-18 US4401600A 1983-08-30 Robert Portmann
The invention relates to a process for the preparation of azo dyes of the formula ##STR1## or mixtures thereof, in which Ar is a substituted or unsubstituted phenyl, naphthyl or aromatic heterocyclic radical and Y is a group of the formula --O--R, --S--R or ##STR2## in which R is a substituted or unsubstituted alkyl, aryl or heterocyclic radical and R.sub.1 and R.sub.2 independently of one another are hydrogen or a substituted or unsubstituted alkyl, aryl or heterocyclic radical, and the groups R.sub.1 and R.sub.2, together with the nitrogen atom to which they are bonded, can form a ring.The process comprises first coupling dimeric malonodinitrile with a diazo component and cyclizing the resulting intermediate with an alcohol, thioalcohol or amine.
17 Process for the preparation of azo dyes US42696 1979-05-25 US4243583A 1981-01-06 Robert Portmann
The invention relates to a process for the preparation of azo dyes of the formula ##STR1## or mixtures thereof, in which Ar is a substituted or unsubstituted phenyl, naphthyl or aromatic heterocyclic radical and Y is a group of the formula --O-R, --S-R or ##STR2## in which R is a substituted or unsubstituted alkyl, aryl or heterocyclic radical and R.sub.1 and R.sub.2 independently of one another are hydrogen or a substituted or unsubstituted alkyl, aryl or heterocyclic radical, and the groups R.sub.1 and R.sub.2, together with the nitrogen atom to which they are bonded, can form a ring.The process comprises first coupling dimeric malonodinitrile with a diazo component and cyclizing the resulting intermediate with an alcohol, thioalcohol or amine.
18 Polycyclic compounds US587478 1975-06-16 US4084053A 1978-04-11 Nalin Binduprasad Desai; Visvanathan Ramanathan
Polycyclic compounds of the general formula I ##STR1## in which the nucleus A can be further substituted, Y is a hydrogen atom or an optionally substituted hydrocarbon radical, and R.sub.1 and R.sub.2 each denote hydrogen, aryl, aralkyl, cycloalkyl or an aliphatic radical, and R.sub.1 and R.sub.2 can form a ring containing the amine nitrogen and mixtures thereof with one another. The dyestuffs dye natural and synthetic fibres in fast yellow and orange shades.
19 Spiro compounds US638573 1975-12-08 US4042635A 1977-08-16 Paul Rys; Rolf Vogelsanger
Compounds which contain a group bonded directly to an aromatic nucleus of the formula--(CH.sub.2 --).sub.n --X (1)in which n is a positive integer having a value of at least 2 and X represents a removable substituent.
20 Polycyclic N-hetero dyestuffs US45892474 1974-04-08 US3929785A 1975-12-30 RAMANATHAN VISVANATHAN
Polycyclic compounds of the general formula I

in which the nucleus A can be substituted yet further, amongst Z1 and Z2 one Z is a nitrogen atom -N and one Z is a group of the formulae

both Y are identical or different optionally substituted amino groups of the formulae

or groups of the formulae -S-R3 or -O-R4, and Y2 can be an alkyl or aryl radical, preferably a methyl radical, R1, R2, R3 and R4 each denoting hydrogen, aryl, aralkyl, cycloalkyl or an acyclic aliphatic radical and R1 and R2 being able to form a ring containing the amine nitrogen, and their mixtures with one another. The dyestuffs give fast yellow shades on polyester or polyacrylic fibers or on wool and synthetic polyamides.
QQ群二维码
意见反馈