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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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):
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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
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. |
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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, |
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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
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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. |
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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. |
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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. |
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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. |