JP2000512627A - 黒色画像を生じることができるプロセスレスジアセチレン系塩フィルム - Google Patents
黒色画像を生じることができるプロセスレスジアセチレン系塩フィルムInfo
- Publication number
- JP2000512627A JP2000512627A JP09542334A JP54233497A JP2000512627A JP 2000512627 A JP2000512627 A JP 2000512627A JP 09542334 A JP09542334 A JP 09542334A JP 54233497 A JP54233497 A JP 54233497A JP 2000512627 A JP2000512627 A JP 2000512627A
- Authority
- JP
- Japan
- Prior art keywords
- image
- mixture
- color
- polyacetylene
- forming
- 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.)
- Ceased
Links
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- 229910052751 metal Inorganic materials 0.000 claims abstract description 155
- 239000002184 metal Substances 0.000 claims abstract description 155
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- 239000011701 zinc Substances 0.000 claims description 85
- 229910052725 zinc Inorganic materials 0.000 claims description 84
- -1 alkyl carboxylate anions Chemical class 0.000 claims description 73
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical group [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 71
- 239000003086 colorant Substances 0.000 claims description 43
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- 229910002651 NO3 Inorganic materials 0.000 claims description 3
- 125000005599 alkyl carboxylate group Chemical group 0.000 claims description 3
- 239000004327 boric acid Substances 0.000 claims description 3
- JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 claims description 3
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
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- FMXSYRBHGUMFBA-UHFFFAOYSA-N 6-amino-3-azaniumylidene-9-[2-carboxy-4-[6-[4-[4-[4-[4-[3-carboxy-6-[4-(trifluoromethyl)phenyl]naphthalen-1-yl]phenyl]piperidin-1-yl]butyl]triazol-1-yl]hexylcarbamoyl]phenyl]-5-sulfoxanthene-4-sulfonate Chemical compound Nc1ccc2c(-c3ccc(cc3C(O)=O)C(=O)NCCCCCCn3cc(CCCCN4CCC(CC4)c4ccc(cc4)-c4cc(cc5cc(ccc45)-c4ccc(cc4)C(F)(F)F)C(O)=O)nn3)c3ccc(=[NH2+])c(c3oc2c1S(O)(=O)=O)S([O-])(=O)=O FMXSYRBHGUMFBA-UHFFFAOYSA-N 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 125000005619 boric acid group Chemical group 0.000 claims 1
- 238000013329 compounding Methods 0.000 claims 1
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- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical class [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims 1
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- 239000004094 surface-active agent Substances 0.000 description 24
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- 235000019322 gelatine Nutrition 0.000 description 16
- 235000011852 gelatine desserts Nutrition 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
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- HQPMKSGTIOYHJT-UHFFFAOYSA-N ethane-1,2-diol;propane-1,2-diol Chemical compound OCCO.CC(O)CO HQPMKSGTIOYHJT-UHFFFAOYSA-N 0.000 description 1
- DUVOZUPPHBRJJO-UHFFFAOYSA-N ethyl 2-isocyanatoacetate Chemical compound CCOC(=O)CN=C=O DUVOZUPPHBRJJO-UHFFFAOYSA-N 0.000 description 1
- KNFXXAGQEUUZAZ-UHFFFAOYSA-N ethyl ethaneperoxoate Chemical compound CCOOC(C)=O KNFXXAGQEUUZAZ-UHFFFAOYSA-N 0.000 description 1
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- 150000004676 glycans Chemical class 0.000 description 1
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- 150000002823 nitrates Chemical class 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- QMQBZOVJDLTKAZ-UHFFFAOYSA-N nonadeca-4,6-diynoic acid Chemical compound CCCCCCCCCCCCC#CC#CCCC(O)=O QMQBZOVJDLTKAZ-UHFFFAOYSA-N 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- NHWNTDQMMIRLNS-UHFFFAOYSA-N pentacosa-10,12-diyne Chemical compound CCCCCCCCCCCCC#CC#CCCCCCCCCC NHWNTDQMMIRLNS-UHFFFAOYSA-N 0.000 description 1
- ZPUDRBWHCWYMQS-UHFFFAOYSA-N pentacosa-10,12-diynoic acid Chemical compound CCCCCCCCCCCCC#CC#CCCCCCCCCC(O)=O ZPUDRBWHCWYMQS-UHFFFAOYSA-N 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
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- 229920001282 polysaccharide Polymers 0.000 description 1
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- 229920000136 polysorbate Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- WVIICGIFSIBFOG-UHFFFAOYSA-N pyrylium Chemical compound C1=CC=[O+]C=C1 WVIICGIFSIBFOG-UHFFFAOYSA-N 0.000 description 1
- 238000005057 refrigeration Methods 0.000 description 1
- 150000003297 rubidium Chemical class 0.000 description 1
- 229910001419 rubidium ion Inorganic materials 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 229940047670 sodium acrylate Drugs 0.000 description 1
- BYKRNSHANADUFY-UHFFFAOYSA-M sodium octanoate Chemical compound [Na+].CCCCCCCC([O-])=O BYKRNSHANADUFY-UHFFFAOYSA-M 0.000 description 1
- JXKPEJDQGNYQSM-UHFFFAOYSA-M sodium propionate Chemical compound [Na+].CCC([O-])=O JXKPEJDQGNYQSM-UHFFFAOYSA-M 0.000 description 1
- 239000004324 sodium propionate Substances 0.000 description 1
- 235000010334 sodium propionate Nutrition 0.000 description 1
- 229960003212 sodium propionate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
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- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229910052713 technetium Inorganic materials 0.000 description 1
- GKLVYJBZJHMRIY-UHFFFAOYSA-N technetium atom Chemical compound [Tc] GKLVYJBZJHMRIY-UHFFFAOYSA-N 0.000 description 1
- JBQYATWDVHIOAR-UHFFFAOYSA-N tellanylidenegermanium Chemical compound [Te]=[Ge] JBQYATWDVHIOAR-UHFFFAOYSA-N 0.000 description 1
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 description 1
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- FRNOGLGSGLTDKL-UHFFFAOYSA-N thulium atom Chemical compound [Tm] FRNOGLGSGLTDKL-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- BIKXLKXABVUSMH-UHFFFAOYSA-N trizinc;diborate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]B([O-])[O-].[O-]B([O-])[O-] BIKXLKXABVUSMH-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- SRWMQSFFRFWREA-UHFFFAOYSA-M zinc formate Chemical compound [Zn+2].[O-]C=O SRWMQSFFRFWREA-UHFFFAOYSA-M 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- YVPVXCHUPLHHKP-UHFFFAOYSA-N zinc;hexahydrate Chemical compound O.O.O.O.O.O.[Zn] YVPVXCHUPLHHKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/18—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon triple bonds as unsaturation
- C07C57/24—Diacetylene or polyacetylene dicarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/18—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms with only carbon-to-carbon triple bonds as unsaturation
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
- G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
-
- 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
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/025—Non-macromolecular photopolymerisable compounds having carbon-to-carbon triple bonds, e.g. acetylenic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Materials Engineering (AREA)
- Engineering & Computer Science (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/652,144 US5731112A (en) | 1996-05-23 | 1996-05-23 | Processless diacetylenic salt films capable of developing a black image |
| US08/652,144 | 1996-05-23 | ||
| PCT/US1997/004688 WO1997044708A1 (en) | 1996-05-23 | 1997-03-07 | Processless diacetylenic salt films capable of developing a black image |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2000512627A true JP2000512627A (ja) | 2000-09-26 |
| JP2000512627A5 JP2000512627A5 (cg-RX-API-DMAC7.html) | 2004-12-02 |
Family
ID=24615681
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP09542334A Ceased JP2000512627A (ja) | 1996-05-23 | 1997-03-07 | 黒色画像を生じることができるプロセスレスジアセチレン系塩フィルム |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US5731112A (cg-RX-API-DMAC7.html) |
| EP (1) | EP0900409B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2000512627A (cg-RX-API-DMAC7.html) |
| AT (1) | ATE273530T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU2541597A (cg-RX-API-DMAC7.html) |
| DE (1) | DE69730210T2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO1997044708A1 (cg-RX-API-DMAC7.html) |
Cited By (2)
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| JP2007524718A (ja) * | 2003-04-01 | 2007-08-30 | アイエスピー インヴェストメンツ インコーポレイテッド | 放射線感受性フィラメントとしてのポリアセチレンのリチウム塩とその製法および使用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| US8120811B2 (en) | 2007-11-21 | 2012-02-21 | Quad/Graphics, Inc. | System and method for adding data to a printed publication |
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| EP2326753A2 (en) * | 2008-09-10 | 2011-06-01 | DataLase Ltd | Textile colouration with diacetylene compounds |
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Family Cites Families (56)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3501303A (en) * | 1966-06-06 | 1970-03-17 | Battelle Development Corp | Photosensitive crystalline polyacetylenic system and method of exposure |
| US3501308A (en) * | 1966-07-01 | 1970-03-17 | Battelle Development Corp | Photosensitive crystalline polyacetylenic sensitized with a pi-acid |
| US3723121A (en) * | 1970-11-03 | 1973-03-27 | Du Pont | Process for recording images with laser beams |
| US3810778A (en) * | 1971-05-03 | 1974-05-14 | Polaroid Corp | Method for production of a photographic film |
| US3743505A (en) * | 1971-06-14 | 1973-07-03 | Eastman Kodak Co | Direct-print process utilizing photosensitive polyacetylenic amine salts containing carboxylate moieties |
| US3844791A (en) * | 1971-06-14 | 1974-10-29 | Eastman Kodak Co | Photosensitive material comprising polyacetylenic amine salts |
| BE789476A (fr) * | 1971-10-01 | 1973-03-29 | Basf Ag | Procede de preparation de cliches |
| US3772011A (en) * | 1971-11-04 | 1973-11-13 | Eastman Kodak Co | Print-out elements and methods using photoconductors and polygnes |
| US3811895A (en) * | 1972-01-14 | 1974-05-21 | Eastman Kodak Co | Sensitized compounds and elements |
| US3822134A (en) * | 1972-01-17 | 1974-07-02 | Eastman Kodak Co | Vacuum deposited radiation-sensitive elements |
| US3772028A (en) * | 1972-02-02 | 1973-11-13 | Eastman Kodak Co | Sensitized photosensitive compounds and elements |
| US3772027A (en) * | 1972-02-04 | 1973-11-13 | Eastman Kodak Co | Photosensitive element containing a photosensitive crystalline polyacetylenic compound and a photoconductive inorganic metal salt |
| US3794491A (en) * | 1972-06-14 | 1974-02-26 | Eastman Kodak Co | Amplification of low-density polyyne images |
| US3954816A (en) * | 1972-12-14 | 1976-05-04 | Eastman Kodak Company | Photosensitive material comprising polyacetylenic amine salts |
| US4066676A (en) * | 1974-02-06 | 1978-01-03 | Eastman Kodak Company | Photosensitive material comprising polyacetylenic amine salts |
| US3999946A (en) * | 1976-02-23 | 1976-12-28 | Allied Chemical Corporation | Time-temperature history indicators |
| US4247613A (en) * | 1976-07-23 | 1981-01-27 | Eastman Kodak Company | Electric field sensitization of polyacetylenic materials |
| US4125534A (en) * | 1977-02-25 | 1978-11-14 | Allied Chemical Corporation | Carbazolyl diacetylenic compounds |
| US4208501A (en) * | 1977-02-25 | 1980-06-17 | Allied Chemical Corporation | Carbazolyl diacetylenic polymers |
| US4189399A (en) * | 1977-07-19 | 1980-02-19 | Allied Chemical Corporation | Co-crystallized acetylenic compounds |
| US4339951A (en) * | 1977-10-05 | 1982-07-20 | Allied Corporation | Tempeature measurement and display of indicia using thermochromic polyacetylenes |
| US4215208A (en) * | 1977-10-05 | 1980-07-29 | Allied Chemical Corporation | Thermochromic polyacetylenes containing urethane groups |
| US4452995A (en) * | 1978-08-30 | 1984-06-05 | Allied Corporation | Dialkoxycarbonylmethyleneurethane diynes |
| US4238352A (en) * | 1978-11-13 | 1980-12-09 | Allied Chemical Corporation | Co-polymerized acetylenic compositions |
| US4235108A (en) * | 1978-11-13 | 1980-11-25 | Allied Chemical Corporation | Device for measuring temperature using co-crystallized acetylenic compositions |
| US4242440A (en) * | 1979-04-30 | 1980-12-30 | Allied Chemical Corporation | Thermochromic polyacetylenes used in laser beam recording method |
| US4439514A (en) * | 1979-06-25 | 1984-03-27 | University Patents, Inc. | Photoresistive compositions |
| US4581315A (en) * | 1979-06-25 | 1986-04-08 | University Patents, Inc. | Photoresistive compositions |
| US4536450A (en) * | 1980-03-12 | 1985-08-20 | University Patents, Inc. | Nonlinear optical materials and processes employing diacetylenes |
| US4699997A (en) * | 1980-06-16 | 1987-10-13 | Allied Corporation | Metal salts of polyacetylenic compounds and uses thereof |
| US4452959A (en) * | 1980-11-19 | 1984-06-05 | Showa Denko K.K. | Process for producing a gel-like composition of a high polymer of acetylene, and process for molding said composition |
| US4562141A (en) * | 1982-09-29 | 1985-12-31 | Ciba Geigy Corporation | Polymerisable composition comprising conjugated diacetylenic compounds, material coated therewith and the use thereof |
| DE3473065D1 (en) * | 1983-11-26 | 1988-09-01 | Basf Ag | Process for the production of resist images and dry resist film for this process |
| US4705742A (en) * | 1985-09-23 | 1987-11-10 | Gaf Corporation | Processless multicolor imaging |
| US4863832A (en) * | 1985-12-16 | 1989-09-05 | Canon Kabushiki Kaisha | Optical recording employing diacetylene compound and dye to change color and form pits |
| US4705741A (en) * | 1986-03-14 | 1987-11-10 | Gaf Corporation | Processless color imaging and film therefor |
| US4698296A (en) * | 1986-03-14 | 1987-10-06 | Gaf Corporation | Processless color imaging and film therefor |
| US4784934A (en) * | 1986-12-15 | 1988-11-15 | Gaf Corporation | Sensitivity of processless recording media |
| US4867917A (en) * | 1986-12-24 | 1989-09-19 | Schnur Joel M | Method for synthesis of diacetylenic compounds |
| JPH0291106A (ja) * | 1988-09-28 | 1990-03-30 | Agency Of Ind Science & Technol | 多次元化高分子結晶の製造方法 |
| JPH02155689A (ja) * | 1988-12-08 | 1990-06-14 | Olympus Optical Co Ltd | 光記録方式 |
| GB9002360D0 (en) * | 1990-02-02 | 1990-04-04 | De La Rue Co Plc | Ink composition and components thereof |
| US5420000A (en) * | 1990-04-09 | 1995-05-30 | Jp Laboratories, Inc. | Heat fixable high energy radiation imaging film |
| US5149616A (en) * | 1990-10-23 | 1992-09-22 | Isp Investments Inc. | Processless imaging to maximize blue light absorption of an image |
| US5139928A (en) * | 1990-10-23 | 1992-08-18 | Isp Investments Inc. | Imageable recording films |
| US5149617A (en) * | 1990-10-23 | 1992-09-22 | Isp Investments Inc. | Imageable diacetylene ethers |
| US5095134A (en) * | 1990-10-23 | 1992-03-10 | Isp Investments Inc. | Thermochromic diacetylene ethers containing ester or urethane groups |
| US5215869A (en) * | 1990-10-23 | 1993-06-01 | Isp Investments Inc. | Process of forming a permanent yellow imaged light modulating film |
| US5215870A (en) * | 1990-10-23 | 1993-06-01 | Isp Investments Inc. | Process of forming a permanent yellow imaged light modulating film |
| US5139927A (en) * | 1990-10-23 | 1992-08-18 | Isp Investments Inc. | Permanent yellow imaged light modulating film |
| US5158862A (en) * | 1990-10-23 | 1992-10-27 | Isp Investments Inc. | Processless imaging to maximize blue light absorption of an image |
| US5153106A (en) * | 1991-03-11 | 1992-10-06 | Isp Investments Inc. | Direct color imaging with laser in a writing mode |
| US5232820A (en) * | 1991-03-18 | 1993-08-03 | Isp Investments Inc. | Process of directly imaging a thermosensitive polyacetylene salt dyes |
| US5137964A (en) * | 1991-03-18 | 1992-08-11 | Isp Investments Inc. | Visually imageable polyacetylene salt dyes |
| TW325477B (en) * | 1992-12-23 | 1998-01-21 | Ciba Sc Holding Ag | Thermochromic compounds, their preparation and the use thereof |
| US5731112A (en) * | 1996-05-23 | 1998-03-24 | Isp Investments Inc. | Processless diacetylenic salt films capable of developing a black image |
-
1996
- 1996-05-23 US US08/652,144 patent/US5731112A/en not_active Expired - Lifetime
-
1997
- 1997-03-07 AT AT97916931T patent/ATE273530T1/de not_active IP Right Cessation
- 1997-03-07 EP EP97916931A patent/EP0900409B1/en not_active Expired - Lifetime
- 1997-03-07 WO PCT/US1997/004688 patent/WO1997044708A1/en not_active Ceased
- 1997-03-07 DE DE69730210T patent/DE69730210T2/de not_active Expired - Lifetime
- 1997-03-07 JP JP09542334A patent/JP2000512627A/ja not_active Ceased
- 1997-03-07 AU AU25415/97A patent/AU2541597A/en not_active Abandoned
-
1998
- 1998-03-05 US US09/035,607 patent/US6177578B1/en not_active Expired - Fee Related
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002148790A (ja) * | 2000-09-04 | 2002-05-22 | Fuji Photo Film Co Ltd | 感熱性組成物、それを用いた平版印刷版原版及びスルホニウム塩化合物 |
| JP2007524718A (ja) * | 2003-04-01 | 2007-08-30 | アイエスピー インヴェストメンツ インコーポレイテッド | 放射線感受性フィラメントとしてのポリアセチレンのリチウム塩とその製法および使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| DE69730210T2 (de) | 2005-08-04 |
| AU2541597A (en) | 1997-12-09 |
| WO1997044708A1 (en) | 1997-11-27 |
| EP0900409B1 (en) | 2004-08-11 |
| US6177578B1 (en) | 2001-01-23 |
| ATE273530T1 (de) | 2004-08-15 |
| US5731112A (en) | 1998-03-24 |
| EP0900409A4 (en) | 2000-06-28 |
| EP0900409A1 (en) | 1999-03-10 |
| DE69730210D1 (de) | 2004-09-16 |
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