JPH0823673B2 - ハロゲン化銀写真要素 - Google Patents

ハロゲン化銀写真要素

Info

Publication number: JPH0823673B2
Authority: JP; Japan
Prior art keywords: group; coupler; bleach accelerator; carbon atoms; layer
Prior art date: 1985-02-28
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 - Lifetime

Application number

JP61040486A

Other languages

English (en)

Japanese (ja)

Other versions

JPS61201247A (ja

Inventor

ルイスホールジエフリー

ノーマンキルミンスターケネス

フオツグロマネツトロバート

ピータースザジエウスキーリチヤード

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.)

1985-02-28

Filing date

1986-02-27

Publication date

1996-03-06

1986-02-27 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1986-09-05 Publication of JPS61201247A publication Critical patent/JPS61201247A/ja

1996-03-06 Publication of JPH0823673B2 publication Critical patent/JPH0823673B2/ja

2011-03-06 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

229910052709 silver Inorganic materials 0.000 title claims description 42
239000004332 silver Substances 0.000 title claims description 42
-1 Silver halide Chemical class 0.000 title claims description 35
239000007844 bleaching agent Substances 0.000 claims description 76
125000004432 carbon atom Chemical group C* 0.000 claims description 34
125000000217 alkyl group Chemical group 0.000 claims description 32
239000000839 emulsion Substances 0.000 claims description 32
125000002947 alkylene group Chemical group 0.000 claims description 6
239000002243 precursor Substances 0.000 claims description 5
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
125000005647 linker group Chemical group 0.000 claims description 3
150000001875 compounds Chemical class 0.000 description 38
238000004061 bleaching Methods 0.000 description 21
239000000975 dye Substances 0.000 description 18
239000008273 gelatin Substances 0.000 description 18
229920000159 gelatin Polymers 0.000 description 18
239000003795 chemical substances by application Substances 0.000 description 17
238000000034 method Methods 0.000 description 17
239000000047 product Substances 0.000 description 17
108010010803 Gelatin Proteins 0.000 description 16
235000019322 gelatine Nutrition 0.000 description 16
235000011852 gelatine desserts Nutrition 0.000 description 16
238000012545 processing Methods 0.000 description 16
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 12
239000000203 mixture Substances 0.000 description 12
239000000523 sample Substances 0.000 description 12
238000011161 development Methods 0.000 description 11
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 11
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
125000003118 aryl group Chemical group 0.000 description 10
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
230000015572 biosynthetic process Effects 0.000 description 9
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
125000003545 alkoxy group Chemical group 0.000 description 8
239000000463 material Substances 0.000 description 8
238000003786 synthesis reaction Methods 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
239000003112 inhibitor Substances 0.000 description 7
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
230000008878 coupling Effects 0.000 description 6
238000010168 coupling process Methods 0.000 description 6
238000005859 coupling reaction Methods 0.000 description 6
230000000694 effects Effects 0.000 description 6
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
238000000921 elemental analysis Methods 0.000 description 5
229910052739 hydrogen Inorganic materials 0.000 description 5
239000001257 hydrogen Substances 0.000 description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
238000000605 extraction Methods 0.000 description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
230000002411 adverse Effects 0.000 description 3
239000007795 chemical reaction product Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
229910052731 fluorine Inorganic materials 0.000 description 3
239000011737 fluorine Substances 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
150000002367 halogens Chemical class 0.000 description 3
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 3
150000002894 organic compounds Chemical class 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
238000011160 research Methods 0.000 description 3
230000035945 sensitivity Effects 0.000 description 3
238000003756 stirring Methods 0.000 description 3
125000000101 thioether group Chemical group 0.000 description 3
239000001043 yellow dye Substances 0.000 description 3
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical group NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000012634 fragment Substances 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 2
238000010898 silica gel chromatography Methods 0.000 description 2
230000003381 solubilizing effect Effects 0.000 description 2
239000002904 solvent Substances 0.000 description 2
238000004611 spectroscopical analysis Methods 0.000 description 2
125000001424 substituent group Chemical group 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
KYVBNYUBXIEUFW-UHFFFAOYSA-N 1,1,3,3-tetramethylguanidine Chemical compound CN(C)C(=N)N(C)C KYVBNYUBXIEUFW-UHFFFAOYSA-N 0.000 description 1
150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 1
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical group C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
BKZLVXLDRQUFHT-UHFFFAOYSA-N 3-(5-sulfanylidene-2h-tetrazol-1-yl)propanoic acid Chemical compound OC(=O)CCN1N=NN=C1S BKZLVXLDRQUFHT-UHFFFAOYSA-N 0.000 description 1
229940018563 3-aminophenol Drugs 0.000 description 1
DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 1
XRZDIHADHZSFBB-UHFFFAOYSA-N 3-oxo-n,3-diphenylpropanamide Chemical class C=1C=CC=CC=1NC(=O)CC(=O)C1=CC=CC=C1 XRZDIHADHZSFBB-UHFFFAOYSA-N 0.000 description 1
UPULOMQHYQDNNT-UHFFFAOYSA-N 5h-1,3-oxazol-2-one Chemical class O=C1OCC=N1 UPULOMQHYQDNNT-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
NIPMJVLJVGQZRB-UHFFFAOYSA-N Cl[IH]Br Chemical compound Cl[IH]Br NIPMJVLJVGQZRB-UHFFFAOYSA-N 0.000 description 1
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
229960000583 acetic acid Drugs 0.000 description 1
125000002015 acyclic group Chemical group 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
239000003086 colorant Substances 0.000 description 1
239000013068 control sample Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000002425 crystallisation Methods 0.000 description 1
230000008025 crystallization Effects 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
229910001873 dinitrogen Inorganic materials 0.000 description 1
230000005670 electromagnetic radiation Effects 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
239000010946 fine silver Substances 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
239000010931 gold Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
230000036571 hydration Effects 0.000 description 1
238000006703 hydration reaction Methods 0.000 description 1
239000000416 hydrocolloid Substances 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
238000005259 measurement Methods 0.000 description 1
NRVFDGZJTPCULU-UHFFFAOYSA-N meda Chemical compound Cl.CN(C)CCS NRVFDGZJTPCULU-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000000178 monomer Substances 0.000 description 1
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
238000000746 purification Methods 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical class N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
230000000717 retained effect Effects 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
125000004434 sulfur atom Chemical group 0.000 description 1
230000002194 synthesizing effect Effects 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
150000003536 tetrazoles Chemical group 0.000 description 1
QYSXJUFSXHHAJI-YRZJJWOYSA-N vitamin D3 Chemical compound C1(/[C@@H]2CC[C@@H]([C@]2(CCC1)C)[C@H](C)CCCC(C)C)=C\C=C1\C[C@@H](O)CCC1=C QYSXJUFSXHHAJI-YRZJJWOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30541—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the released group
- G03C7/30552—Mercapto

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP61040486A 1985-02-28 1986-02-27 ハロゲン化銀写真要素 Expired - Lifetime JPH0823673B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US70711585A	1985-02-28	1985-02-28
US707115		1985-02-28

Publications (2)

Publication Number	Publication Date
JPS61201247A JPS61201247A (ja)	1986-09-05
JPH0823673B2 true JPH0823673B2 (ja)	1996-03-06

Family

ID=24840404

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP61040486A Expired - Lifetime JPH0823673B2 (ja)	1985-02-28	1986-02-27	ハロゲン化銀写真要素

Country Status (4)

Country	Link
EP (1)	EP0193389B2 (fr)
JP (1)	JPH0823673B2 (fr)
CA (1)	CA1287765C (fr)
DE (1)	DE3675034D1 (fr)

Families Citing this family (66)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0820707B2 (ja) *	1986-09-11	1996-03-04	コニカ株式会社	ハロゲン化銀カラ−写真感光材料
JPS63121845A (ja) *	1986-11-12	1988-05-25	Fuji Photo Film Co Ltd	ハロゲン化銀写真感光材料及びその処理方法
JPS63301950A (ja) *	1987-01-19	1988-12-08	Konica Corp	ハロゲン化銀カラー写真感光材料
JPS63216048A (ja) *	1987-03-05	1988-09-08	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料
EP0287073B1 (fr) *	1987-04-14	1995-03-08	Fuji Photo Film Co., Ltd.	Procédé de traitement d'un matériau photographique à l'halogénure d'argent
JPH0192747A (ja) *	1987-06-15	1989-04-12	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料
JP2543705B2 (ja) *	1987-06-25	1996-10-16	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
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
JPH01131561A (ja) *	1987-08-13	1989-05-24	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料の処理方法
JPH0255A (ja) *	1987-10-02	1990-01-05	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料
JPH01108546A (ja)	1987-10-22	1989-04-25	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料
JP2553890B2 (ja) *	1987-10-29	1996-11-13	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
JPH01140153A (ja)	1987-11-27	1989-06-01	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料
JPH07117725B2 (ja) *	1987-11-30	1995-12-18	コニカ株式会社	粒状性に優れた色素画像が得られるハロゲン化銀カラー写真感光材料の処理方法
JPH0833628B2 (ja)	1987-12-15	1996-03-29	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
JP2684374B2 (ja) *	1988-01-20	1997-12-03	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
JP2528344B2 (ja) *	1988-02-10	1996-08-28	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
JPH01213650A (ja) *	1988-02-20	1989-08-28	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料の処理方法
JPH01223454A (ja) *	1988-03-03	1989-09-06	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料
JP2565368B2 (ja) *	1988-03-09	1996-12-18	富士写真フイルム株式会社	ハロゲン化銀カラー写真感光材料
US4912024A (en) *	1988-06-21	1990-03-27	Eastman Kodak Company	Photographic material having releasable compound
CA1338080C (fr) *	1988-06-21	1996-02-27	Drake Matthew Michno	Materiaux photographiques a substances volatiles
US4859578A (en) *	1988-06-21	1989-08-22	Eastman Kodak Company	Photographic recording material providing improved granularity properties
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1986
- 1986-02-18 CA CA 502070 patent/CA1287765C/fr not_active Expired - Fee Related
- 1986-02-26 DE DE8686301365T patent/DE3675034D1/de not_active Expired - Lifetime
- 1986-02-26 EP EP19860301365 patent/EP0193389B2/fr not_active Expired - Lifetime
- 1986-02-27 JP JP61040486A patent/JPH0823673B2/ja not_active Expired - Lifetime

Also Published As

Publication number	Publication date
EP0193389B2 (fr)	1995-03-15
EP0193389A3 (en)	1988-11-23
DE3675034D1 (de)	1990-11-29
EP0193389B1 (fr)	1990-10-24
CA1287765C (fr)	1991-08-20
JPS61201247A (ja)	1986-09-05
EP0193389A2 (fr)	1986-09-03

Legal Events

Date	Code	Title	Description
2004-03-09	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2005-03-08	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2006-02-27	EXPY	Cancellation because of completion of term

Publication	Publication Date	Title
JPH0823673B2 (ja)	1996-03-06	ハロゲン化銀写真要素
JP2656924B2 (ja)	1997-09-24	写真要素
US3928041A (en)	1975-12-23	Development inhibitor yielding compound for silver halide photography
JPS6145247A (ja)	1986-03-05	イエローｄｉｒカプラーを有するカラー写真記録材料
JP2774130B2 (ja)	1998-07-09	シアン色素生成カプラーを含有する写真材料
JPH0240647A (ja)	1990-02-09	改良された粒状度特性を与える写真記録材料
JPH06194796A (ja)	1994-07-15	写真記録材料
US4546073A (en)	1985-10-08	Photographic recording material containing a precursor of a photographically-active compound
JP3195426B2 (ja)	2001-08-06	Ｄｉｒカプラー含有写真要素
JPH0617997B2 (ja)	1994-03-09	蛍光色素−放出カプラー化合物を含有する像形成素子
JPS632103B2 (fr)	1988-01-16
JPH0743511B2 (ja)	1995-05-15	写真要素
JPH05694B2 (fr)	1993-01-06
JPS6326377B2 (fr)	1988-05-30
JPH0369935A (ja)	1991-03-26	写真的に活性な化合物を放出する能力のあるカツプラーを含むカラー写真記録材料
JPH08240892A (ja)	1996-09-17	酸化された現像主薬の掃去剤を含有する写真要素
EP0520496B1 (fr)	2000-08-09	Produit photographique et procédé comprenant un coupleur universel
JPH0659412A (ja)	1994-03-04	写真要素
JPH0239146A (ja)	1990-02-08	カラー写真要素
JPH05194437A (ja)	1993-08-03	ベンゾトリアゾール化合物の製造方法およびそれを含む写真感光材料および写真処理液
JP2511661B2 (ja)	1996-07-03	新規なカプラ−を含有するハロゲン化銀写真感光材料
JPH0651461A (ja)	1994-02-25	写真要素及び写真カプラー
JP3310044B2 (ja)	2002-07-29	ピラゾロトリアゾールカプラー、並びに写真要素及び色素画像形成方法
JPH08278615A (ja)	1996-10-22	酸化された現像主薬の掃去剤を含有する写真要素
JPH0651466A (ja)	1994-02-25	写真要素及び写真カプラー