JPH09179246A - 凝集色素含有写真要素 - Google Patents

凝集色素含有写真要素

Info

Publication number: JPH09179246A
Authority: JP; Japan
Prior art keywords: dye; dyes; absorption; dispersion; gelatin
Prior art date: 1995-11-30
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.): Pending

Application number

JP8321597A

Other languages

English (en)

Japanese (ja)

Other versions

JPH09179246A5 (2

Inventor

Margaret Jones Helber

ジョーンズヘルバーマーガレット

James Harrison William

ジェームスハリソンウィリアム

Ann Gallo Elizabeth

アンガルロエリザベス

Mary Christine Brick

クリスティーヌブリックマリー

Steven Wade Kortum

ウェイドコータムスティーブン

Norman Barber Gary

ノーマンバーバーガリー

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date 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 date listed.)

1995-11-30

Filing date

1996-12-02

Publication date

1997-07-11

1996-12-02 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1997-07-11 Publication of JPH09179246A publication Critical patent/JPH09179246A/ja

2004-11-18 Publication of JPH09179246A5 publication Critical patent/JPH09179246A5/ja

Status Pending legal-status Critical Current

Links

238000004040 coloring Methods 0.000 title abstract description 6
239000006185 dispersion Substances 0.000 claims abstract description 84
238000010521 absorption reaction Methods 0.000 claims abstract description 56
125000000217 alkyl group Chemical group 0.000 claims abstract description 12
125000003118 aryl group Chemical group 0.000 claims abstract description 12
125000001072 heteroaryl group Chemical group 0.000 claims abstract description 11
229910052717 sulfur Inorganic materials 0.000 claims abstract description 10
229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims abstract description 7
230000004931 aggregating effect Effects 0.000 claims description 15
125000000547 substituted alkyl group Chemical group 0.000 claims description 13
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
125000002252 acyl group Chemical group 0.000 claims description 9
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 8
239000011593 sulfur Chemical group 0.000 claims description 8
125000003107 substituted aryl group Chemical group 0.000 claims description 7
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
150000001767 cationic compounds Chemical class 0.000 claims description 6
150000002892 organic cations Chemical class 0.000 claims description 6
239000001301 oxygen Substances 0.000 claims description 6
238000012545 processing Methods 0.000 abstract description 22
230000008033 biological extinction Effects 0.000 abstract description 10
150000001768 cations Chemical class 0.000 abstract description 2
239000000758 substrate Substances 0.000 abstract 1
239000000975 dye Substances 0.000 description 246
239000010410 layer Substances 0.000 description 88
229920000159 gelatin Polymers 0.000 description 63
239000008273 gelatin Substances 0.000 description 63
108010010803 Gelatin Proteins 0.000 description 61
235000019322 gelatine Nutrition 0.000 description 61
235000011852 gelatine desserts Nutrition 0.000 description 61
239000000839 emulsion Substances 0.000 description 56
238000000034 method Methods 0.000 description 56
-1 silver halide Chemical class 0.000 description 46
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239000004332 silver Substances 0.000 description 41
230000005855 radiation Effects 0.000 description 29
239000007787 solid Substances 0.000 description 26
230000003595 spectral effect Effects 0.000 description 24
239000000463 material Substances 0.000 description 23
239000000084 colloidal system Substances 0.000 description 21
239000011248 coating agent Substances 0.000 description 20
238000000576 coating method Methods 0.000 description 20
230000003287 optical effect Effects 0.000 description 20
239000000203 mixture Substances 0.000 description 17
239000002245 particle Substances 0.000 description 16
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
238000005520 cutting process Methods 0.000 description 15
238000000862 absorption spectrum Methods 0.000 description 14
238000011160 research Methods 0.000 description 14
239000012736 aqueous medium Substances 0.000 description 13
239000002002 slurry Substances 0.000 description 11
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230000035945 sensitivity Effects 0.000 description 9
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239000000126 substance Substances 0.000 description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
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230000000052 comparative effect Effects 0.000 description 7
238000001228 spectrum Methods 0.000 description 7
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ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
238000001914 filtration Methods 0.000 description 6
230000031700 light absorption Effects 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
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239000013638 trimer Substances 0.000 description 6
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125000004432 carbon atom Chemical group C* 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000011229 interlayer Substances 0.000 description 5
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HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 5
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
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KAMCBFNNGGVPPW-UHFFFAOYSA-N 1-(ethenylsulfonylmethoxymethylsulfonyl)ethene Chemical compound C=CS(=O)(=O)COCS(=O)(=O)C=C KAMCBFNNGGVPPW-UHFFFAOYSA-N 0.000 description 2
JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 2
CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
229910021612 Silver iodide Inorganic materials 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 2
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235000013405 beer Nutrition 0.000 description 2
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238000004061 bleaching Methods 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
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125000002541 furyl group Chemical group 0.000 description 2
108010025899 gelatin film Proteins 0.000 description 2
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
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239000010931 gold Substances 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
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230000000873 masking effect Effects 0.000 description 2
239000000155 melt Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 0.000 description 2
BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
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239000005020 polyethylene terephthalate Substances 0.000 description 2
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239000004576 sand Substances 0.000 description 2
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
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235000002639 sodium chloride Nutrition 0.000 description 2
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238000003786 synthesis reaction Methods 0.000 description 2
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GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 description 1
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
MOXDGMSQFFMNHA-UHFFFAOYSA-N 2-hydroxybenzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1O MOXDGMSQFFMNHA-UHFFFAOYSA-N 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
XTBFKMDOQMQYPP-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine;hydron;chloride Chemical compound Cl.CCN(CC)C1=CC=C(N)C=C1 XTBFKMDOQMQYPP-UHFFFAOYSA-N 0.000 description 1
FFAJEKUNEVVYCW-UHFFFAOYSA-N 4-n-ethyl-4-n-(2-methoxyethyl)-2-methylbenzene-1,4-diamine Chemical compound COCCN(CC)C1=CC=C(N)C(C)=C1 FFAJEKUNEVVYCW-UHFFFAOYSA-N 0.000 description 1
LEVKCNAQSSPBTR-UHFFFAOYSA-N 5-(3-methoxyphenyl)-1,3-diazinane-2,4,6-trione Chemical compound COC1=CC=CC(C2C(NC(=O)NC2=O)=O)=C1 LEVKCNAQSSPBTR-UHFFFAOYSA-N 0.000 description 1
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ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
FCZYGJBVLGLYQU-UHFFFAOYSA-M sodium;2-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethoxy]ethanesulfonate Chemical compound [Na+].CC(C)(C)CC(C)(C)C1=CC=C(OCCOCCOCCS([O-])(=O)=O)C=C1 FCZYGJBVLGLYQU-UHFFFAOYSA-M 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
238000003892 spreading Methods 0.000 description 1
230000007480 spreading Effects 0.000 description 1
230000003068 static effect Effects 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
150000003457 sulfones Chemical class 0.000 description 1
239000000725 suspension Substances 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
229910052714 tellurium Inorganic materials 0.000 description 1
PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
125000004001 thioalkyl group Chemical group 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
238000012546 transfer Methods 0.000 description 1
ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
238000009966 trimming Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1

Classifications

- 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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
- G03C1/83—Organic dyestuffs therefor
- G03C1/832—Methine or polymethine dyes
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/008—Preparations of disperse dyes or solvent dyes

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Chemical Kinetics & Catalysis (AREA)
Organic Chemistry (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP8321597A 1995-11-30 1996-12-02 凝集色素含有写真要素 Pending JPH09179246A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US08/565,480 US6183944B1 (en)	1995-11-30	1995-11-30	Aggregated dyes for radiation-sensitive elements
US08/565480		1995-11-30

Publications (2)

Publication Number	Publication Date
JPH09179246A true JPH09179246A (ja)	1997-07-11
JPH09179246A5 JPH09179246A5 (2)	2004-11-18

Family

ID=24258795

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP8321597A Pending JPH09179246A (ja)	1995-11-30	1996-12-02	凝集色素含有写真要素

Country Status (5)

Country	Link
US (5)	US6183944B1 (2)
EP (1)	EP0778493B1 (2)
JP (1)	JPH09179246A (2)
CN (2)	CN1181394C (2)
DE (1)	DE69614231T2 (2)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2001348520A (ja) *	2000-04-03	2001-12-18	Fuji Photo Film Co Ltd	メチン化合物、固体微粒子分散物、インクジェット用記録液、およびインクジェット記録方法

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP3893425B2 (ja) *	1998-02-06	2007-03-14	富士フイルム株式会社	熱現像写真感光材料およびその製造方法
US6180295B1 (en) *	1998-09-11	2001-01-30	Eastman Kodak Company	Liquid crystalline filter dyes for imaging elements
US6214499B1 (en)	1998-09-11	2001-04-10	Eastman Kodak Company	Liquid crystalline filter dyes for imaging elements
JP2001194524A (ja) *	2000-01-13	2001-07-19	Fuji Photo Film Co Ltd	光学フィルター、これを用いた前面板及び画像表示装置
JP2003043628A (ja) *	2001-08-03	2003-02-13	Fuji Photo Film Co Ltd	熱現像感光材料
WO2003019289A1 (en) *	2001-08-27	2003-03-06	Axiom Biotechnologies, Inc.	Fluorescent dyes
BE1015271A3 (fr) *	2003-01-03	2004-12-07	Semika S A	Dispersion photosensible a viscosite ajustable pour le depot de metal sur un substrat isolant et son utilisation.
EP1719544A1 (en) *	2005-02-18	2006-11-08	L'oreal	Dye composition comprising an oxonol type methine direct dye, process for implementation and uses thereof
US7630128B2 (en) *	2007-02-02	2009-12-08	Sperian Eye & Face Protection Inc. a Delaware Corporation	Optical filter panel having a narrow-width selective-wavelength attenuation and high visible light transmission

Family Cites Families (55)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2983608A (en)	1958-10-06	1961-05-09	Eastman Kodak Co	Yellow-colored magenta-forming couplers
BE589419A (2)	1959-04-06
US3148062A (en)	1959-04-06	1964-09-08	Eastman Kodak Co	Photographic elements and processes using splittable couplers
US3247127A (en)	1960-04-14	1966-04-19	Eastman Kodak Co	Light-absorbing water-permeable colloid layer containing an oxonol dye
BE603213A (2)	1960-04-28
US3148022A (en)	1961-10-17	1964-09-08	Du Pont	Process for extracting beryllium values from ores
BE628098A (2)	1962-02-07
US3379529A (en)	1963-02-28	1968-04-23	Eastman Kodak Co	Photographic inhibitor-releasing developers
US3460883A (en)	1965-10-01	1969-08-12	Ibm	Total internal reflection deflector
US3617291A (en)	1967-10-10	1971-11-02	Eastman Kodak Co	Two-equivalent couplers for photography
BE730884A (2)	1968-04-01
GB1265485A (2)	1968-05-21	1972-03-01
US3542581A (en)	1968-11-05	1970-11-24	Eastman Kodak Co	Method of de-aggregating oxonol dye-containing gelatin layers
US3615506A (en)	1970-02-09	1971-10-26	Eastman Kodak Co	Silver halide emulsions containing 3-cyclicamino-5-pyrazolone color couplers
US3733201A (en)	1971-10-01	1973-05-15	Eastman Kodak Co	Photographic compositions and elements comprising coupling compounds which on development release silver halidecomplexing materials and dyes
JPS566540B2 (2)	1973-03-31	1981-02-12
GB1530272A (en)	1975-02-21	1978-10-25	Agfa Gevaert	2-pyrazolin-5-ones and their use as colour couplers for silver halide photography
GB1534711A (en)	1975-04-30	1978-12-06	Agfa Gevaert	Barbituric acid derivatives and their use as intermediates in the preparation of light-absorbing dyes
JPS5242121A (en)	1975-09-30	1977-04-01	Fuji Photo Film Co Ltd	Color photographic light sensitive material
GB1571506A (en)	1976-02-23	1980-07-16	Agfa Gevaert	4-phenyl azo - 2 - pyrazolin - 5 - one colour coupler and their use in photography
JPS52111717A (en) *	1976-03-16	1977-09-19	Fuji Photo Film Co Ltd	Silver halide photographic photosensitive material containing dyes
JPS52111618A (en)	1976-03-16	1977-09-19	Hitachi Kiden Kogyo Kk	Induction motor controller
FR2382325A1 (fr)	1977-03-02	1978-09-29	Kodak Pathe	Produit comprenant une couche d'enregistrement magnetique transparente
JPS53134430A (en)	1977-04-27	1978-11-24	Mitsubishi Paper Mills Ltd	Silver halide photosensitive materials for multiilayer color photograph
JPS5912169B2 (ja)	1980-07-04	1984-03-21	富士写真フイルム株式会社	ハロゲン化銀カラ−感光材料
US4420556A (en)	1980-09-11	1983-12-13	Eastman Kodak Company	Photographic silver halide materials
JPS57150845A (en)	1981-03-13	1982-09-17	Fuji Photo Film Co Ltd	Silver halide photographic material
JPH0234372B2 (ja)	1982-04-02	1990-08-02	Konishiroku Photo Ind	Harogenkaginkaraashashinkankozairyo
EP0096570B1 (en)	1982-06-05	1988-08-24	Olympus Optical Co., Ltd.	An optical system focus-state detector
JPS5950439A (ja)	1982-09-16	1984-03-23	Fuji Photo Film Co Ltd	ハロゲン化銀写真感光材料
US4543323A (en)	1982-12-18	1985-09-24	Konishiroku Photo Industry Co., Ltd.	Light-sensitive silver halide photographic material
CA1287765C (en)	1985-02-28	1991-08-20	Eastman Kodak Company	Dye-forming photographic material and process comprising bleach accelerator releasing compound
DE3530357A1 (de)	1985-08-24	1987-02-26	Agfa Gevaert Ag	Farbfotografisches aufzeichnungsmaterial
ES2014297B3 (es)	1986-07-08	1990-07-01	Agfa-Gevaert Nv	Elemento fotografico colorante para proyeccion cinematografica.
US4803150A (en)	1986-12-23	1989-02-07	Eastman Kodak Company	Radiographic element exhibiting reduced crossover
US4900652A (en)	1987-07-13	1990-02-13	Eastman Kodak Company	Radiographic element
JP2542858B2 (ja)	1987-07-27	1996-10-09	富士写真フイルム株式会社	ハロゲン化銀カラ―写真感光材料の処理方法
US4865956A (en)	1987-11-24	1989-09-12	Eastman Kodak Company	Photographic elements containing a bleach accelerator precursor
US4923784A (en)	1987-11-24	1990-05-08	Eastman Kodak Company	Photographic elements containing a bleach accelerator precursor
US4859578A (en)	1988-06-21	1989-08-22	Eastman Kodak Company	Photographic recording material providing improved granularity properties
US4912025A (en)	1988-06-21	1990-03-27	Eastman Kodak Company	Photographic recording material for accelerated development
US4988611A (en)	1988-06-30	1991-01-29	Eastman Kodak Company	Imaging utilizing a light-handleable photographic element having solid particle dispersion filter dye layer
DE69029676T2 (de)	1989-04-06	1997-05-07	Fuji Photo Film Co Ltd	Photographisches Silberhalogenidmaterial und Verarbeitungsmethode dafür
JP2867372B2 (ja) *	1991-07-04	1999-03-08	コニカ株式会社	ハロゲン化銀写真感光材料
US5274109A (en)	1991-12-20	1993-12-28	Eastman Kodak Company	Microprecipitated methine oxonol filter dye dispersions
DE69318863T2 (de)	1992-02-03	1998-09-24	Fuji Photo Film Co Ltd	Verfahren zur Dispergierung eines Farbstoffs und ein Farbstoff enthaltendes photographisches Silberhalogenidmaterial
EP0640225B1 (en)	1992-05-14	1998-10-14	Eastman Kodak Company	Aqueous mixtures of spectrally sensitizing dyes for photographic emulsions
EP0582000A1 (en)	1992-08-03	1994-02-09	Agfa-Gevaert N.V.	Photographic colour negative or colour intermediate film element
JPH06118565A (ja) *	1992-09-30	1994-04-28	Konica Corp	ハロゲン化銀写真感光材料
JP2832410B2 (ja)	1992-10-12	1998-12-09	富士写真フイルム株式会社	ハロゲン化銀写真感光材料
JP3124663B2 (ja)	1993-03-24	2001-01-15	富士写真フイルム株式会社	ハロゲン化銀写真感光材料
JP3222657B2 (ja)	1993-10-07	2001-10-29	富士写真フイルム株式会社	オキソノール化合物
EP0651030A1 (en) *	1993-10-29	1995-05-03	COOKSON MATTHEY CERAMICS & MATERIALS LIMITED	Pigmentary material
US5451494A (en)	1994-04-28	1995-09-19	Eastman Kodak Company	Photographic elements containing acyl substituted oxonol dyes
US5922523A (en)	1995-11-30	1999-07-13	Eastman Kodak Company	Filter dyes for photographic elements

1995
- 1995-11-30 US US08/565,480 patent/US6183944B1/en not_active Expired - Fee Related
1996
- 1996-11-15 DE DE69614231T patent/DE69614231T2/de not_active Expired - Fee Related
- 1996-11-15 EP EP96203193A patent/EP0778493B1/en not_active Expired - Lifetime
- 1996-11-30 CN CNB001309072A patent/CN1181394C/zh not_active Expired - Fee Related
- 1996-11-30 CN CN96121694A patent/CN1078902C/zh not_active Expired - Fee Related
- 1996-12-02 JP JP8321597A patent/JPH09179246A/ja active Pending
2000
- 2000-12-07 US US09/733,786 patent/US6342339B2/en not_active Expired - Fee Related
- 2000-12-07 US US09/731,448 patent/US6300046B1/en not_active Expired - Fee Related
- 2000-12-07 US US09/733,787 patent/US6291149B1/en not_active Expired - Fee Related
- 2000-12-07 US US09/731,447 patent/US6306567B1/en not_active Expired - Fee Related

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2001348520A (ja) *	2000-04-03	2001-12-18	Fuji Photo Film Co Ltd	メチン化合物、固体微粒子分散物、インクジェット用記録液、およびインクジェット記録方法

Also Published As

Publication number	Publication date
US6300046B1 (en)	2001-10-09
US6183944B1 (en)	2001-02-06
US6306567B1 (en)	2001-10-23
CN1313526A (zh)	2001-09-19
DE69614231D1 (de)	2001-09-06
US20010038979A1 (en)	2001-11-08
US6291149B1 (en)	2001-09-18
DE69614231T2 (de)	2002-05-08
EP0778493A1 (en)	1997-06-11
CN1157302A (zh)	1997-08-20
CN1181394C (zh)	2004-12-22
US6342339B2 (en)	2002-01-29
EP0778493B1 (en)	2001-08-01
CN1078902C (zh)	2002-02-06
US20010038978A1 (en)	2001-11-08

Legal Events

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2006-03-29

A131

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Effective date: 20060328

2006-11-22

A02

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Effective date: 20061121

Publication	Publication Date	Title
US4950586A (en)	1990-08-21	Solid particle dispersions of filter dyes for photographic elements
JP2000086928A (ja)	2000-03-28	分散物及びそれを含む写真要素
JP2000086927A (ja)	2000-03-28	分散物及びそれを含む写真要素
JPH09179246A (ja)	1997-07-11	凝集色素含有写真要素
US5783377A (en)	1998-07-21	Infrared absorber dyes
EP0751421B1 (en)	2002-10-23	Photographic materials comprising cyanine dyes with chain sulphone substituent
EP0679936B1 (en)	2000-08-09	Photographic elements containing particular sensitizing dyes
US5922523A (en)	1999-07-13	Filter dyes for photographic elements
JPH09185143A (ja)	1997-07-15	赤感性ハロゲン化銀乳剤層含有写真要素
JP2660421B2 (ja)	1997-10-08	ハロゲン化銀写真感光材料
EP0762198B1 (en)	2000-10-04	Photographic elements comprising filter dyes
EP0775938B1 (en)	2003-02-12	Combination of yellow filter dye and 4-equivalent pyrazolone magenta coupler
JP3452964B2 (ja)	2003-10-06	ハロゲン化銀写真要素及びその製造方法
JP2003261786A (ja)	2003-09-19	ベンゾチアジン色素
US5834173A (en)	1998-11-10	Filter dyes for photographic elements
EP0740200B1 (en)	2000-07-26	Photographic elements containing oxonol filter dye mixture and their preparation
JPH05197078A (ja)	1993-08-06	写真要素用フィルター色素固体粒子分散体
JP2003241342A (ja)	2003-08-27	ベンゾチアジン色素を含む画像形成要素
JPH02201352A (ja)	1990-08-09	ハロゲン化銀写真感光材料
JPH0235443A (ja)	1990-02-06	高感度で高コントラストな画像が得られるハロゲン化銀写真感光材料

JPH09179246A - 凝集色素含有写真要素 - Google Patents

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Classifications

Landscapes

Applications Claiming Priority (2)

Publications (2)

Family

ID=24258795

Family Applications (1)

Country Status (5)

Cited By (1)

Families Citing this family (9)

Family Cites Families (55)

Cited By (1)

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