JP2778702B2 - 色素像形成性カプラー化合物を含む写真記録材料 - Google Patents

色素像形成性カプラー化合物を含む写真記録材料

Info

Publication number: JP2778702B2
Authority: JP; Japan
Prior art keywords: group; dye; coupler; compound; carbon atoms
Prior art date: 1987-09-21
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

Application number

JP63233816A

Other languages

English (en)

Japanese (ja)

Other versions

JPH01101549A (ja

Inventor

バレットマーケルポール

ジェイムズギアチェリオデビッド

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.)

1987-09-21

Filing date

1988-09-20

Publication date

1998-07-23

1988-09-20 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1989-04-19 Publication of JPH01101549A publication Critical patent/JPH01101549A/ja

1998-07-23 Application granted granted Critical

1998-07-23 Publication of JP2778702B2 publication Critical patent/JP2778702B2/ja

2013-07-23 Anticipated expiration legal-status Critical

Status Expired - Fee Related legal-status Critical Current

Links

239000000463 material Substances 0.000 title claims abstract description 15
150000001875 compounds Chemical class 0.000 title abstract description 32
-1 silver halide Chemical class 0.000 claims abstract description 56
229940124530 sulfonamide Drugs 0.000 claims abstract description 28
229910052709 silver Inorganic materials 0.000 claims abstract description 22
239000004332 silver Substances 0.000 claims abstract description 22
238000010521 absorption reaction Methods 0.000 claims abstract description 20
239000003795 chemical substances by application Substances 0.000 claims abstract description 10
230000003595 spectral effect Effects 0.000 claims abstract description 6
239000000975 dye Substances 0.000 claims description 39
239000000839 emulsion Substances 0.000 claims description 23
125000000217 alkyl group Chemical group 0.000 claims description 19
125000004432 carbon atom Chemical group C* 0.000 claims description 18
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
239000001043 yellow dye Substances 0.000 claims description 10
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 claims description 9
125000005843 halogen group Chemical group 0.000 claims description 5
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 3
238000006243 chemical reaction Methods 0.000 abstract description 3
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 18
125000003118 aryl group Chemical group 0.000 description 7
239000002904 solvent Substances 0.000 description 7
239000000203 mixture Substances 0.000 description 6
125000003277 amino group Chemical group 0.000 description 5
239000000460 chlorine Substances 0.000 description 5
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 4
108010010803 Gelatin Proteins 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
125000003710 aryl alkyl group Chemical group 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
125000002843 carboxylic acid group Chemical group 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 4
229920000159 gelatin Polymers 0.000 description 4
239000008273 gelatin Substances 0.000 description 4
235000019322 gelatine Nutrition 0.000 description 4
235000011852 gelatine desserts Nutrition 0.000 description 4
150000002367 halogens Chemical group 0.000 description 4
125000000623 heterocyclic group Chemical group 0.000 description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
125000001931 aliphatic group Chemical group 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
239000000123 paper Substances 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
239000000654 additive Substances 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
125000006267 biphenyl group Chemical group 0.000 description 2
238000004061 bleaching Methods 0.000 description 2
125000001309 chloro group Chemical group Cl* 0.000 description 2
239000000084 colloidal system Substances 0.000 description 2
238000005859 coupling reaction Methods 0.000 description 2
125000004663 dialkyl amino group Chemical group 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 2
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
125000004417 unsaturated alkyl group Chemical group 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
239000004711 α-olefin Substances 0.000 description 2
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 1
BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
XRZDIHADHZSFBB-UHFFFAOYSA-N 3-oxo-n,3-diphenylpropanamide Chemical compound C=1C=CC=CC=1NC(=O)CC(=O)C1=CC=CC=C1 XRZDIHADHZSFBB-UHFFFAOYSA-N 0.000 description 1
ZNBNBTIDJSKEAM-UHFFFAOYSA-N 4-[7-hydroxy-2-[5-[5-[6-hydroxy-6-(hydroxymethyl)-3,5-dimethyloxan-2-yl]-3-methyloxolan-2-yl]-5-methyloxolan-2-yl]-2,8-dimethyl-1,10-dioxaspiro[4.5]decan-9-yl]-2-methyl-3-propanoyloxypentanoic acid Chemical compound C1C(O)C(C)C(C(C)C(OC(=O)CC)C(C)C(O)=O)OC11OC(C)(C2OC(C)(CC2)C2C(CC(O2)C2C(CC(C)C(O)(CO)O2)C)C)CC1 ZNBNBTIDJSKEAM-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
125000004442 acylamino group Chemical group 0.000 description 1
125000005036 alkoxyphenyl group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
239000000908 ammonium hydroxide Substances 0.000 description 1
XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 1
150000001491 aromatic compounds Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
XNSQZBOCSSMHSZ-UHFFFAOYSA-K azane;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(3+) Chemical compound [NH4+].[Fe+3].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O XNSQZBOCSSMHSZ-UHFFFAOYSA-K 0.000 description 1
125000000751 azo group Chemical group [*]N=N[*] 0.000 description 1
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000005392 carboxamide group Chemical group NC(=O)* 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
230000008878 coupling Effects 0.000 description 1
238000010168 coupling process Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000006310 cycloalkyl amino group Chemical group 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical compound C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
229910000378 hydroxylammonium sulfate Inorganic materials 0.000 description 1
125000002960 margaryl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000000873 masking effect Effects 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000003801 milling Methods 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
QVJDYYAGYLLMMU-UHFFFAOYSA-N n-ethylaniline;sulfuric acid;hydrate Chemical compound O.OS(O)(=O)=O.CCNC1=CC=CC=C1 QVJDYYAGYLLMMU-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
125000006501 nitrophenyl group Chemical group 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
238000005691 oxidative coupling reaction Methods 0.000 description 1
230000001590 oxidative effect Effects 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
BHZRJJOHZFYXTO-UHFFFAOYSA-L potassium sulfite Chemical compound [K+].[K+].[O-]S([O-])=O BHZRJJOHZFYXTO-UHFFFAOYSA-L 0.000 description 1
235000019252 potassium sulphite Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical class [H]N([H])* 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000001429 visible spectrum Methods 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
- G03C7/392—Additives
- G03C7/39208—Organic compounds
- G03C7/39236—Organic compounds with a function having at least two elements among nitrogen, sulfur or oxygen

Landscapes

Physics & Mathematics (AREA)
Spectroscopy & Molecular Physics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Mechanical Pencils And Projecting And Retracting Systems Therefor, And Multi-System Writing Instruments (AREA)

JP63233816A 1987-09-21 1988-09-20 色素像形成性カプラー化合物を含む写真記録材料 Expired - Fee Related JP2778702B2 (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US9917687A	1987-09-21	1987-09-21
US099176		1987-09-21

Publications (2)

Publication Number	Publication Date
JPH01101549A JPH01101549A (ja)	1989-04-19
JP2778702B2 true JP2778702B2 (ja)	1998-07-23

Family

ID=22273328

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP63233816A Expired - Fee Related JP2778702B2 (ja)	1987-09-21	1988-09-20	色素像形成性カプラー化合物を含む写真記録材料

Country Status (4)

Country	Link
EP (1)	EP0309159B1 (de)
JP (1)	JP2778702B2 (de)
AT (1)	ATE87378T1 (de)
DE (1)	DE3879597T2 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2876075B2 (ja) *	1989-05-25	1999-03-31	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
JPH03160438A (ja) *	1989-11-20	1991-07-10	Konica Corp	ハロゲン化銀カラー写真感光材料
JP3089579B2 (ja) *	1993-01-11	2000-09-18	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及びカラー画像形成方法
JPH06230534A (ja) *	1993-02-05	1994-08-19	Konica Corp	ハロゲン化銀カラー写真感光材料
EP2455431B1 (de)	2003-10-23	2013-08-21	Fujifilm Corporation	Tinte und Tintensatz zur Tintenstrahlaufzeichnung
JP5785799B2 (ja)	2010-07-30	2015-09-30	富士フイルム株式会社	新規なアゾ化合物、水溶液、インク組成物、インクジェット記録用インク、インクジェット記録方法、インクジェット記録用インクカートリッジ、及びインクジェット記録物
JP5866150B2 (ja)	2010-07-30	2016-02-17	富士フイルム株式会社	新規なアゾ化合物、水溶液、インク組成物、インクジェット記録用インク、インクジェット記録方法、インクジェット記録用インクカートリッジ、及びインクジェット記録物
JP2014198816A (ja)	2012-09-26	2014-10-23	富士フイルム株式会社	アゾ化合物、水溶液、インク組成物、インクジェット記録用インク、インクジェット記録方法、インクジェット記録用インクカートリッジ、及びインクジェット記録物

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US4882267A (en)	1986-12-02	1989-11-21	Konica Corporation	Silver halide photographic light-sensitive material with excellent color reproducibility

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DD231664A1 (de) *	1984-12-17	1986-01-02	Wolfen Filmfab Veb	Lichtempfindliches fotografisches gelatinehaltiges silberhalogenidmaterial mit plastifikatoren
JPS62215272A (ja) *	1986-02-17	1987-09-21	Fuji Photo Film Co Ltd	カラ−画像形成方法
JPS6341853A (ja) *	1986-08-07	1988-02-23	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料
JPS6396656A (ja) *	1986-10-13	1988-04-27	Konica Corp	色再現性にすぐれたハロゲン化銀写真感光材料

1988
- 1988-09-16 EP EP88308568A patent/EP0309159B1/de not_active Expired - Lifetime
- 1988-09-16 AT AT88308568T patent/ATE87378T1/de not_active IP Right Cessation
- 1988-09-16 DE DE88308568T patent/DE3879597T2/de not_active Expired - Fee Related
- 1988-09-20 JP JP63233816A patent/JP2778702B2/ja not_active Expired - Fee Related

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US4882267A (en)	1986-12-02	1989-11-21	Konica Corporation	Silver halide photographic light-sensitive material with excellent color reproducibility

Also Published As

Publication number	Publication date
DE3879597T2 (de)	1993-10-07
EP0309159A1 (de)	1989-03-29
DE3879597D1 (de)	1993-04-29
EP0309159B1 (de)	1993-03-24
JPH01101549A (ja)	1989-04-19
ATE87378T1 (de)	1993-04-15

Legal Events

Date	Code	Title	Description
2004-05-11	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2005-04-26	R250	Receipt of annual fees	Free format text: JAPANESE INTERMEDIATE CODE: R250
2006-05-08	LAPS	Cancellation because of no payment of annual fees

Publication	Publication Date	Title
US3933500A (en)	1976-01-20	Color photographic light-sensitive material
US4009038A (en)	1977-02-22	Silver halide color photographic materials
US3935016A (en)	1976-01-27	Silver halide color photographic materials containing 3-anilino-5-pyrazolone couplers
US3948663A (en)	1976-04-06	Multi-layer color photographic light-sensitive material
JPH01554A (ja)	1989-01-05	ピラゾロアゾール型シアンカプラーを含有するハロゲン化銀カラー写真感光材料
US5147764A (en)	1992-09-15	Photographic element with 2-equivalent 5-pyrazolone and competitor for oxidized developing agent
EP0309159B1 (de)	1993-03-24	Photographisches Eintragungsmaterial, enthaltend farbbildende Kupplerverbindungen
US4935321A (en)	1990-06-19	Photographic recording material comprising a dye image-forming compound
US4973535A (en)	1990-11-27	Photographic recording material comprising a dye image-forming coupler compound
JPH0234372B2 (ja)	1990-08-02	Harogenkaginkaraashashinkankozairyo
EP0309158B1 (de)	1993-02-10	Photographisches Eintragungsmaterial mit einer ein purpurrotes Farbbild bildenden Kupplerverbindung
US4199361A (en)	1980-04-22	Color photographic light-sensitive element
EP0309160A1 (de)	1989-03-29	Photographisches Eintragungsmaterial, enthaltend eine farbbildbildende Kupplerverbindung
US4254213A (en)	1981-03-03	Process for forming black dye images
EP0459340A1 (de)	1991-12-04	Photographisches Element
US5302500A (en)	1994-04-12	Silver halide color photographic light-sensitive material offering excellent hue reproduction
US3859095A (en)	1975-01-07	Color-photographic material with improved color reproduction
US4808502A (en)	1989-02-28	Photographic recording material comprising a magenta dye image forming coupler compound
EP0543921B1 (de)	1995-03-08	Photographisches material
JP3282065B2 (ja)	2002-05-13	ハロゲン化銀カラー写真感光材料
JPS63256952A (ja)	1988-10-24	形成される色素の分光吸収特性が良好なハロゲン化銀写真感光材料
JPH04238347A (ja)	1992-08-26	ハロゲン化銀カラー写真感光材料
JPH04233536A (ja)	1992-08-21	カラー反転写真要素
JPH05150429A (ja)	1993-06-18	ハロゲン化銀カラー写真感光材料
JPH0667382A (ja)	1994-03-11	ハロゲン化銀カラー写真感光材料