DE69707951T2 - Diazoverbindungen für Laser-induzierte massenübertragende Bildaufzeichnungsmaterialien - Google Patents
Diazoverbindungen für Laser-induzierte massenübertragende BildaufzeichnungsmaterialienInfo
- Publication number
- DE69707951T2 DE69707951T2 DE69707951T DE69707951T DE69707951T2 DE 69707951 T2 DE69707951 T2 DE 69707951T2 DE 69707951 T DE69707951 T DE 69707951T DE 69707951 T DE69707951 T DE 69707951T DE 69707951 T2 DE69707951 T2 DE 69707951T2
- Authority
- DE
- Germany
- Prior art keywords
- diazo
- compound
- layer
- donor
- mass transfer
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000012546 transfer Methods 0.000 title claims description 130
- 239000000463 material Substances 0.000 title claims description 117
- 150000008049 diazo compounds Chemical class 0.000 title claims description 47
- 238000003384 imaging method Methods 0.000 title description 23
- 150000001875 compounds Chemical class 0.000 claims description 72
- 238000000354 decomposition reaction Methods 0.000 claims description 36
- 239000000758 substrate Substances 0.000 claims description 31
- 238000000034 method Methods 0.000 claims description 25
- 239000006100 radiation absorber Substances 0.000 claims description 21
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims description 20
- 125000000524 functional group Chemical group 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 4
- 125000006732 (C1-C15) alkyl group Chemical group 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 125000006527 (C1-C5) alkyl group Chemical group 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 126
- 239000010410 layer Substances 0.000 description 90
- 239000000975 dye Substances 0.000 description 66
- -1 azidomethyl Chemical group 0.000 description 53
- 239000000243 solution Substances 0.000 description 48
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- 239000000203 mixture Substances 0.000 description 26
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- 230000035945 sensitivity Effects 0.000 description 22
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 21
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- 238000000576 coating method Methods 0.000 description 18
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- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 17
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- PXIPVTKHYLBLMZ-UHFFFAOYSA-N Sodium azide Chemical compound [Na+].[N-]=[N+]=[N-] PXIPVTKHYLBLMZ-UHFFFAOYSA-N 0.000 description 14
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 14
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- 229910052751 metal Inorganic materials 0.000 description 11
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- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 10
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- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
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- 239000011780 sodium chloride Substances 0.000 description 7
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000012954 diazonium Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 241000356539 Aquis Species 0.000 description 5
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- 238000006243 chemical reaction Methods 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 150000001989 diazonium salts Chemical class 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- 230000008018 melting Effects 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 238000005065 mining Methods 0.000 description 5
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 4
- WROAPMIYFGUNPW-UHFFFAOYSA-N 3-diazonio-5,8,8-trimethyl-2-oxobicyclo[3.2.1]oct-3-en-4-olate Chemical compound O=C1C(=[N+]=[N-])C(=O)C2(C)CCC1C2(C)C WROAPMIYFGUNPW-UHFFFAOYSA-N 0.000 description 4
- KUXKACNMIDMZAB-UHFFFAOYSA-N 5-diazonio-2-methyl-6-oxo-2-(2-phenylethyl)-1,3-dioxin-4-olate Chemical compound C=1C=CC=CC=1CCC1(C)OC(=O)C(=[N+]=[N-])C(=O)O1 KUXKACNMIDMZAB-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 229920000877 Melamine resin Polymers 0.000 description 4
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
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- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine group Chemical group N1=CCC2=CC=CC=C12 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
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- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
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- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 3
- PSINDLUNOGABJV-UHFFFAOYSA-N (z)-2-diazonio-1,3-diethoxy-3-oxoprop-1-en-1-olate Chemical compound CCO\C([O-])=C(/[N+]#N)C(=O)OCC PSINDLUNOGABJV-UHFFFAOYSA-N 0.000 description 3
- RXYMTVAHQNMICF-UHFFFAOYSA-N 2-diazonio-1,3-bis[(2-methylpropan-2-yl)oxy]-3-oxoprop-1-en-1-olate Chemical compound CC(C)(C)OC([O-])=C([N+]#N)C(=O)OC(C)(C)C RXYMTVAHQNMICF-UHFFFAOYSA-N 0.000 description 3
- CYYVRGUWUAFEDN-UHFFFAOYSA-N 2-diazonio-3-oxo-1-phenylbut-1-en-1-olate Chemical compound CC(=O)C([N+]#N)=C([O-])C1=CC=CC=C1 CYYVRGUWUAFEDN-UHFFFAOYSA-N 0.000 description 3
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- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 3
- 241000723346 Cinnamomum camphora Species 0.000 description 3
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- 230000003647 oxidation Effects 0.000 description 1
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- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 1
- JGTNAGYHADQMCM-UHFFFAOYSA-N perfluorobutanesulfonic acid Chemical compound OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F JGTNAGYHADQMCM-UHFFFAOYSA-N 0.000 description 1
- 125000005007 perfluorooctyl group Chemical group FC(C(C(C(C(C(C(C(F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)F)(F)* 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical group [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical group [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 239000011941 photocatalyst Substances 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
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- 229920002285 poly(styrene-co-acrylonitrile) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920005668 polycarbonate resin Polymers 0.000 description 1
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- 229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 description 1
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- 229920001721 polyimide Polymers 0.000 description 1
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- 229920001855 polyketal Polymers 0.000 description 1
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- LRIBRUAEJSZTFO-UHFFFAOYSA-M potassium;1,2,2,3,3,4,5,5,6,6-decafluoro-4-(1,1,2,2,2-pentafluoroethyl)cyclohexane-1-sulfonate Chemical compound [K+].[O-]S(=O)(=O)C1(F)C(F)(F)C(F)(F)C(F)(C(F)(F)C(F)(F)F)C(F)(F)C1(F)F LRIBRUAEJSZTFO-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
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- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
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- 230000008022 sublimation Effects 0.000 description 1
- 125000004964 sulfoalkyl group Chemical group 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
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- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000000979 synthetic dye Substances 0.000 description 1
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- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 238000010345 tape casting Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical compound FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
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- 150000003568 thioethers Chemical class 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
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- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/26—Thermography ; Marking by high energetic means, e.g. laser otherwise than by burning, and characterised by the material used
- B41M5/382—Contact thermal transfer or sublimation processes
- B41M5/392—Additives, other than colour forming substances, dyes or pigments, e.g. sensitisers, transfer promoting agents
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41C—PROCESSES FOR THE MANUFACTURE OR REPRODUCTION OF PRINTING SURFACES
- B41C1/00—Forme preparation
- B41C1/10—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme
- B41C1/1091—Forme preparation for lithographic printing; Master sheets for transferring a lithographic image to the forme by physical transfer from a donor sheet having an uniform coating of lithographic material using thermal means as provided by a thermal head or a laser; by mechanical pressure, e.g. from a typewriter by electrical recording ribbon therefor
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
- C07C245/12—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom
- C07C245/14—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton
- C07C245/18—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F3/00—Colour separation; Correction of tonal value
- G03F3/10—Checking the colour or tonal value of separation negatives or positives
- G03F3/108—Checking the colour or tonal value of separation negatives or positives using a non-impact printing method, e.g. ink jet, using duplicating or marking methods covered by B41M5/00, e.g. by ablation or by thermographic means
Landscapes
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Optics & Photonics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- General Physics & Mathematics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Photosensitive Polymer And Photoresist Processing (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/627,160 US5691098A (en) | 1996-04-03 | 1996-04-03 | Laser-Induced mass transfer imaging materials utilizing diazo compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69707951D1 DE69707951D1 (de) | 2001-12-13 |
| DE69707951T2 true DE69707951T2 (de) | 2002-07-25 |
Family
ID=24513455
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69707951T Expired - Fee Related DE69707951T2 (de) | 1996-04-03 | 1997-03-26 | Diazoverbindungen für Laser-induzierte massenübertragende Bildaufzeichnungsmaterialien |
Country Status (4)
| Country | Link |
|---|---|
| US (2) | US5691098A (https=) |
| EP (1) | EP0799716B1 (https=) |
| JP (1) | JPH1036331A (https=) |
| DE (1) | DE69707951T2 (https=) |
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| US7071913B2 (en) | 1995-07-20 | 2006-07-04 | E Ink Corporation | Retroreflective electrophoretic displays and materials for making the same |
| US7106296B1 (en) | 1995-07-20 | 2006-09-12 | E Ink Corporation | Electronic book with multiple page displays |
| US6262706B1 (en) | 1995-07-20 | 2001-07-17 | E Ink Corporation | Retroreflective electrophoretic displays and materials for making the same |
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| US6120839A (en) | 1995-07-20 | 2000-09-19 | E Ink Corporation | Electro-osmotic displays and materials for making the same |
| US5747217A (en) * | 1996-04-03 | 1998-05-05 | Minnesota Mining And Manufacturing Company | Laser-induced mass transfer imaging materials and methods utilizing colorless sublimable compounds |
| US6037085A (en) * | 1996-06-19 | 2000-03-14 | Printing Development Inc. | Photoresists and method for making printing plates |
| US5908731A (en) * | 1996-07-04 | 1999-06-01 | Agfa-Gevaert, N.V. | Heat sensitive imaging element and a method for producing lithographic plates therewith |
| US5945517A (en) * | 1996-07-24 | 1999-08-31 | Tokyo Ohka Kogyo Co., Ltd. | Chemical-sensitization photoresist composition |
| US6067185A (en) | 1997-08-28 | 2000-05-23 | E Ink Corporation | Process for creating an encapsulated electrophoretic display |
| US7242513B2 (en) | 1997-08-28 | 2007-07-10 | E Ink Corporation | Encapsulated electrophoretic displays having a monolayer of capsules and materials and methods for making the same |
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| US7002728B2 (en) | 1997-08-28 | 2006-02-21 | E Ink Corporation | Electrophoretic particles, and processes for the production thereof |
| US6839158B2 (en) | 1997-08-28 | 2005-01-04 | E Ink Corporation | Encapsulated electrophoretic displays having a monolayer of capsules and materials and methods for making the same |
| CA2320788A1 (en) | 1998-03-18 | 1999-09-23 | Joseph M. Jacobson | Electrophoretic displays and systems for addressing such displays |
| AU3552699A (en) | 1998-04-10 | 1999-11-01 | E-Ink Corporation | Electronic displays using organic-based field effect transistors |
| AU3987299A (en) | 1998-05-12 | 1999-11-29 | E-Ink Corporation | Microencapsulated electrophoretic electrostatically-addressed media for drawing device applications |
| USD485294S1 (en) | 1998-07-22 | 2004-01-13 | E Ink Corporation | Electrode structure for an electronic display |
| WO2000020923A1 (en) | 1998-10-07 | 2000-04-13 | E Ink Corporation | Illumination system for nonemissive electronic displays |
| AU6293499A (en) | 1998-10-07 | 2000-04-26 | E-Ink Corporation | Capsules for electrophoretic displays and methods for making the same |
| DE60003281T2 (de) | 1999-01-15 | 2004-05-06 | 3M Innovative Properties Co., Saint Paul | Thermisches Übertragungsverfahren. |
| US6168903B1 (en) * | 1999-01-21 | 2001-01-02 | Presstek, Inc. | Lithographic imaging with reduced power requirements |
| GB9904326D0 (en) * | 1999-02-26 | 1999-04-21 | Ici Plc | Improvements in or relating to mass transfer printing |
| WO2000059625A1 (en) | 1999-04-06 | 2000-10-12 | E Ink Corporation | Methods for producing droplets for use in capsule-based electrophoretic displays |
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| US7038655B2 (en) | 1999-05-03 | 2006-05-02 | E Ink Corporation | Electrophoretic ink composed of particles with field dependent mobilities |
| GB9917676D0 (en) * | 1999-07-09 | 1999-09-29 | Ici Plc | Improvements in or relating to mass transfer printing |
| DE19937478B4 (de) * | 1999-08-07 | 2004-08-19 | Man Roland Druckmaschinen Ag | Thermotransferfolie zur laserinduzierten Beschichtung einer Metalloberfläche |
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| US6716629B2 (en) * | 2000-10-10 | 2004-04-06 | Biotrove, Inc. | Apparatus for assay, synthesis and storage, and methods of manufacture, use, and manipulation thereof |
| DE10063819B4 (de) * | 2000-12-21 | 2006-02-02 | Man Roland Druckmaschinen Ag | Maskenerstellung zur Herstellung einer Druckform |
| JP2002248874A (ja) * | 2001-02-27 | 2002-09-03 | Konica Corp | レーザー熱転写用インクシート及びその製造方法並びに画像記録方法 |
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-
1996
- 1996-04-03 US US08/627,160 patent/US5691098A/en not_active Expired - Lifetime
-
1997
- 1997-03-26 DE DE69707951T patent/DE69707951T2/de not_active Expired - Fee Related
- 1997-03-26 EP EP97105097A patent/EP0799716B1/en not_active Expired - Lifetime
- 1997-04-03 JP JP9084776A patent/JPH1036331A/ja active Pending
- 1997-05-19 US US08/858,307 patent/US5756689A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0799716A3 (en) | 1998-02-04 |
| EP0799716A2 (en) | 1997-10-08 |
| JPH1036331A (ja) | 1998-02-10 |
| US5756689A (en) | 1998-05-26 |
| DE69707951D1 (de) | 2001-12-13 |
| EP0799716B1 (en) | 2001-11-07 |
| US5691098A (en) | 1997-11-25 |
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| Date | Code | Title | Description |
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| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |