JPH0528821B2 - - Google Patents
Info
- Publication number
- JPH0528821B2 JPH0528821B2 JP60098718A JP9871885A JPH0528821B2 JP H0528821 B2 JPH0528821 B2 JP H0528821B2 JP 60098718 A JP60098718 A JP 60098718A JP 9871885 A JP9871885 A JP 9871885A JP H0528821 B2 JPH0528821 B2 JP H0528821B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- compound
- layer
- groups
- coupler
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- -1 silver halide Chemical class 0.000 claims description 163
- 150000001875 compounds Chemical class 0.000 claims description 114
- 229910052709 silver Inorganic materials 0.000 claims description 59
- 239000004332 silver Substances 0.000 claims description 58
- 239000000839 emulsion Substances 0.000 claims description 50
- 238000011161 development Methods 0.000 claims description 48
- 239000003795 chemical substances by application Substances 0.000 claims description 37
- 239000000463 material Substances 0.000 claims description 35
- 239000003112 inhibitor Substances 0.000 claims description 30
- 239000002243 precursor Substances 0.000 claims description 16
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000010410 layer Substances 0.000 description 100
- 239000000975 dye Substances 0.000 description 44
- 125000001424 substituent group Chemical group 0.000 description 41
- 125000003118 aryl group Chemical group 0.000 description 37
- 125000004432 carbon atom Chemical group C* 0.000 description 36
- 238000000034 method Methods 0.000 description 31
- 125000000623 heterocyclic group Chemical group 0.000 description 24
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 23
- 238000012545 processing Methods 0.000 description 23
- 125000001931 aliphatic group Chemical group 0.000 description 22
- 230000000694 effects Effects 0.000 description 21
- 108010010803 Gelatin Proteins 0.000 description 19
- 125000004442 acylamino group Chemical group 0.000 description 19
- 125000000217 alkyl group Chemical group 0.000 description 19
- 239000008273 gelatin Substances 0.000 description 19
- 229920000159 gelatin Polymers 0.000 description 19
- 235000019322 gelatine Nutrition 0.000 description 19
- 235000011852 gelatine desserts Nutrition 0.000 description 19
- 125000000565 sulfonamide group Chemical group 0.000 description 18
- 125000003342 alkenyl group Chemical group 0.000 description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 16
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 15
- 125000004122 cyclic group Chemical group 0.000 description 15
- 125000003545 alkoxy group Chemical group 0.000 description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 12
- 125000005843 halogen group Chemical group 0.000 description 11
- 230000001235 sensitizing effect Effects 0.000 description 11
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
- 125000003277 amino group Chemical group 0.000 description 10
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 10
- 239000000084 colloidal system Substances 0.000 description 10
- 238000005406 washing Methods 0.000 description 10
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 9
- 125000002252 acyl group Chemical group 0.000 description 9
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 description 9
- 125000004104 aryloxy group Chemical group 0.000 description 9
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 9
- 238000005859 coupling reaction Methods 0.000 description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 239000002245 particle Substances 0.000 description 9
- 239000002253 acid Substances 0.000 description 8
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 8
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 8
- 239000000178 monomer Substances 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 8
- 125000004430 oxygen atom Chemical group O* 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 150000003839 salts Chemical class 0.000 description 8
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 8
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 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 7
- 229910021612 Silver iodide Inorganic materials 0.000 description 7
- 125000005110 aryl thio group Chemical group 0.000 description 7
- 125000004093 cyano group Chemical group *C#N 0.000 description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 7
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 7
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 7
- 229940045105 silver iodide Drugs 0.000 description 7
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
- 125000004414 alkyl thio group Chemical group 0.000 description 6
- 125000003710 aryl alkyl group Chemical group 0.000 description 6
- 238000003776 cleavage reaction Methods 0.000 description 6
- 125000006165 cyclic alkyl group Chemical group 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 6
- 230000000087 stabilizing effect Effects 0.000 description 6
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 6
- ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 5
- 206010070834 Sensitisation Diseases 0.000 description 5
- 125000004390 alkyl sulfonyl group Chemical group 0.000 description 5
- 125000004391 aryl sulfonyl group Chemical group 0.000 description 5
- 230000008878 coupling Effects 0.000 description 5
- 238000010168 coupling process Methods 0.000 description 5
- 230000002401 inhibitory effect Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- 230000035945 sensitivity Effects 0.000 description 5
- 230000008313 sensitization Effects 0.000 description 5
- 230000006641 stabilisation Effects 0.000 description 5
- 238000011105 stabilization Methods 0.000 description 5
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 5
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical group NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 4
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- 125000004423 acyloxy group Chemical group 0.000 description 4
- 125000003282 alkyl amino group Chemical group 0.000 description 4
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
- 125000001769 aryl amino group Chemical group 0.000 description 4
- 125000005116 aryl carbamoyl group Chemical group 0.000 description 4
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 4
- 239000007844 bleaching agent Substances 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 4
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000010413 mother solution Substances 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- 235000010265 sodium sulphite Nutrition 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 125000004434 sulfur atom Chemical group 0.000 description 4
- 239000004094 surface-active agent Substances 0.000 description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 4
- JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical group NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 3
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 description 3
- 125000004422 alkyl sulphonamide group Chemical group 0.000 description 3
- 125000002947 alkylene group Chemical group 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 150000001450 anions Chemical class 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 125000005129 aryl carbonyl group Chemical group 0.000 description 3
- 238000004061 bleaching Methods 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000002738 chelating agent Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- 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 3
- 230000001419 dependent effect Effects 0.000 description 3
- 238000000586 desensitisation Methods 0.000 description 3
- 125000004663 dialkyl amino group Chemical group 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 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 3
- 150000002148 esters Chemical class 0.000 description 3
- 125000002883 imidazolyl group Chemical group 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical group CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 3
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 3
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- 125000004076 pyridyl group Chemical group 0.000 description 3
- GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical class N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 3
- 125000005493 quinolyl group Chemical group 0.000 description 3
- 239000002516 radical scavenger Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 239000003381 stabilizer Substances 0.000 description 3
- 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 3
- 239000000126 substance Substances 0.000 description 3
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 2
- YLVACWCCJCZITJ-UHFFFAOYSA-N 1,4-dioxane-2,3-diol Chemical compound OC1OCCOC1O YLVACWCCJCZITJ-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
- XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 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 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical group CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- 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 2
- ZGTMUACCHSMWAC-UHFFFAOYSA-L EDTA disodium salt (anhydrous) Chemical compound [Na+].[Na+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O ZGTMUACCHSMWAC-UHFFFAOYSA-L 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- SWTHJRAOHKSITP-UHFFFAOYSA-M IBr.[Ag].[Ag]I Chemical compound IBr.[Ag].[Ag]I SWTHJRAOHKSITP-UHFFFAOYSA-M 0.000 description 2
- OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001299 aldehydes Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000005153 alkyl sulfamoyl group Chemical group 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 2
- XYXNTHIYBIDHGM-UHFFFAOYSA-N ammonium thiosulfate Chemical compound [NH4+].[NH4+].[O-]S([O-])(=O)=S XYXNTHIYBIDHGM-UHFFFAOYSA-N 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 150000001565 benzotriazoles Chemical class 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 150000001661 cadmium Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229910052804 chromium Inorganic materials 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 229910017052 cobalt Inorganic materials 0.000 description 2
- 239000010941 cobalt Substances 0.000 description 2
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- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical class SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 125000002112 pyrrolidino group Chemical group [*]N1C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 150000003236 pyrrolines Chemical class 0.000 description 1
- 150000003248 quinolines Chemical class 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 238000006462 rearrangement reaction Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- KIWUVOGUEXMXSV-UHFFFAOYSA-N rhodanine Chemical class O=C1CSC(=S)N1 KIWUVOGUEXMXSV-UHFFFAOYSA-N 0.000 description 1
- 150000003283 rhodium Chemical class 0.000 description 1
- 239000008237 rinsing water Substances 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 229910000077 silane Inorganic materials 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
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- DZCAZXAJPZCSCU-UHFFFAOYSA-K sodium nitrilotriacetate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CC([O-])=O DZCAZXAJPZCSCU-UHFFFAOYSA-K 0.000 description 1
- UWSAIOMORQUEHN-UHFFFAOYSA-L sodium;2-[2-[carboxylatomethyl(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(5+) Chemical compound [Na+].[Fe+5].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O UWSAIOMORQUEHN-UHFFFAOYSA-L 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
- 230000003595 spectral effect Effects 0.000 description 1
- 125000005156 substituted alkylene group Chemical group 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 125000005649 substituted arylene group Chemical group 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical group 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 150000003536 tetrazoles Chemical class 0.000 description 1
- 150000003475 thallium Chemical class 0.000 description 1
- JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical class SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 description 1
- 150000003557 thiazoles Chemical class 0.000 description 1
- 150000003549 thiazolines Chemical class 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000003441 thioacyl group Chemical group 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- 125000005031 thiocyano group Chemical group S(C#N)* 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 150000003585 thioureas Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000006276 transfer reaction Methods 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- NJPOTNJJCSJJPJ-UHFFFAOYSA-N tributyl benzene-1,3,5-tricarboxylate Chemical compound CCCCOC(=O)C1=CC(C(=O)OCCCC)=CC(C(=O)OCCCC)=C1 NJPOTNJJCSJJPJ-UHFFFAOYSA-N 0.000 description 1
- 150000003639 trimesic acids Chemical class 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 150000003751 zinc Chemical class 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
- G03C7/30594—Combination of substances liberating photographically active agents
-
- 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
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/156—Precursor compound
- Y10S430/158—Development inhibitor releaser, DIR
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60098718A JPS61255342A (ja) | 1985-05-09 | 1985-05-09 | ハロゲン化銀カラ−写真感光材料 |
| DE8686106347T DE3665226D1 (en) | 1985-05-09 | 1986-05-09 | Silver halide color photographic materials |
| EP86106347A EP0204175B1 (en) | 1985-05-09 | 1986-05-09 | Silver halide color photographic materials |
| US07/681,639 US5126236A (en) | 1985-05-09 | 1991-04-04 | Color photographic materials with DIR compound combinations |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60098718A JPS61255342A (ja) | 1985-05-09 | 1985-05-09 | ハロゲン化銀カラ−写真感光材料 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61255342A JPS61255342A (ja) | 1986-11-13 |
| JPH0528821B2 true JPH0528821B2 (en]) | 1993-04-27 |
Family
ID=14227300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60098718A Granted JPS61255342A (ja) | 1985-05-09 | 1985-05-09 | ハロゲン化銀カラ−写真感光材料 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US5126236A (en]) |
| EP (1) | EP0204175B1 (en]) |
| JP (1) | JPS61255342A (en]) |
| DE (1) | DE3665226D1 (en]) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62127734A (ja) * | 1985-11-27 | 1987-06-10 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| EP0271061B1 (en) * | 1986-12-09 | 1995-03-29 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material and method for processing the same |
| JPH0758387B2 (ja) * | 1987-03-03 | 1995-06-21 | 富士写真フイルム株式会社 | ハロゲン化銀写真感光材料 |
| JPS63254453A (ja) * | 1987-04-13 | 1988-10-21 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−写真感光材料及びその処理方法 |
| GB8716977D0 (en) * | 1987-07-17 | 1987-08-26 | Kodak Ltd | Benzoyl-acetanilide couplers |
| JPH07120003B2 (ja) * | 1988-02-22 | 1995-12-20 | 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の処理方法 |
| JP2559254B2 (ja) * | 1988-05-06 | 1996-12-04 | 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の処理方法 |
| US5476759A (en) * | 1990-03-12 | 1995-12-19 | Fuji Photo Film Co., Ltd. | Silver halide color photographic material |
| JPH03261948A (ja) * | 1990-03-13 | 1991-11-21 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
| JPH04445A (ja) | 1990-04-17 | 1992-01-06 | 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 |
| EP0476327B1 (en) | 1990-08-20 | 1999-11-17 | Fuji Photo Film Co., Ltd. | Data-retainable photographic film product and process for producing color print |
| US5272043A (en) * | 1991-06-28 | 1993-12-21 | Eastman Kodak Company | Photographic material and process comprising DIR coupler |
| US5286613A (en) * | 1992-06-24 | 1994-02-15 | Eastman Kodak Company | Photographic material comprising a combination of couplers forming washout and non-washout dyes |
| JPH06214354A (ja) * | 1993-01-14 | 1994-08-05 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料及びその処理方法 |
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|---|---|---|---|---|
| US2193015A (en) | 1939-05-24 | 1940-03-12 | Eastman Kodak Co | Developer containing sulphonamide groups |
| BE470936A (en]) | 1940-02-24 | |||
| US2343703A (en) | 1942-09-04 | 1944-03-07 | Eastman Kodak Co | Pyrazolone coupler for color photography |
| US2369929A (en) | 1943-03-18 | 1945-02-20 | Eastman Kodak Co | Acylamino phenol couplers |
| US2407210A (en) | 1944-04-14 | 1946-09-03 | Eastman Kodak Co | Color couplers |
| US2566271A (en) | 1947-05-23 | 1951-08-28 | Eastman Kodak Co | Photographic developer containing substituted sulfonamide groups |
| US2600788A (en) | 1949-06-07 | 1952-06-17 | Eastman Kodak Co | Halogen-substituted pyrazolone couplers for color photography |
| BE543745A (en]) | 1954-12-20 | |||
| BE543742A (en]) | 1954-12-20 | |||
| US2933390A (en) | 1955-10-12 | 1960-04-19 | Eastman Kodak Co | Supersensitization of photographic silver halide emulsions |
| US2895826A (en) | 1956-10-08 | 1959-07-21 | Eastman Kodak Co | Photographic color couplers containing fluoroalkylcarbonamido groups |
| BE619301A (en]) | 1959-04-06 | |||
| US3265506A (en) | 1964-05-04 | 1966-08-09 | Eastman Kodak Co | Yellow forming couplers |
| US3106621A (en) * | 1961-01-17 | 1963-10-08 | Bruno Angel | Fast current breaker switch |
| NL283102A (en]) | 1961-09-11 | |||
| US3152896A (en) | 1963-02-18 | 1964-10-13 | Eastman Kodak Co | Magenta-forming couplers |
| US3379529A (en) | 1963-02-28 | 1968-04-23 | Eastman Kodak Co | Photographic inhibitor-releasing developers |
| US3314794A (en) | 1964-05-13 | 1967-04-18 | Eastman Kodak Co | Ultraviolet absorbers |
| CH485782A (de) | 1964-06-23 | 1970-02-15 | Gevaert Photo Prod Nv | Verfahren zur Emulsionspolymerisation |
| GB1121034A (en) | 1965-09-13 | 1968-07-24 | Fuji Photo Film Co Ltd | Colour photographic light-sensitive elements containing an ultraviolet absorber |
| US3426010A (en) | 1965-12-01 | 1969-02-04 | Du Pont | Thiazole-pyrazolone azo yellow dyes |
| DE1547862C3 (de) | 1965-12-30 | 1974-02-07 | Fuji Shashin Film K.K., Kanagawa (Japan) | Spektral übersensibilisierte photographische Silberhalogenidemulsion |
| US3446622A (en) | 1966-01-11 | 1969-05-27 | Ferrania Spa | Process for the preparation of color images using 2 - ureido phenolic couplers |
| US3519429A (en) | 1966-05-16 | 1970-07-07 | Eastman Kodak Co | Silver halide emulsions containing a stabilizer pyrazolone coupler |
| BE707403A (en]) | 1966-12-03 | 1968-04-16 | ||
| DE1547640A1 (de) | 1967-04-10 | 1969-12-04 | Agfa Gevaert Ag | Verbessertes photographisches Material |
| JPS4831256B1 (en]) | 1969-09-05 | 1973-09-27 | ||
| BE757036A (fr) | 1969-10-07 | 1971-03-16 | Fuji Photo Film Co Ltd | Materiels photosensibles de photographie en couleurs ayant une meilleure solidite a la lumiere |
| GB1334515A (en) | 1970-01-15 | 1973-10-17 | Kodak Ltd | Pyrazolo-triazoles |
| DE2056177A1 (de) | 1970-11-14 | 1972-05-25 | Agfa Gevaert AG, 5090 Leverkusen | Photographische Schichten mit einem Gehalt an ultraviolettes Licht absorbie renden Verbindungen |
| US3758308A (en) | 1971-02-18 | 1973-09-11 | Eastman Kodak Co | Silver halide emulsion containing para fluoro phenols |
| JPS5512586B1 (en]) | 1971-03-11 | 1980-04-02 | ||
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| BE792265R (fr) | 1971-12-03 | 1973-06-04 | Eastman Kodak Co | Procede de traitement photographique en couleurs et composes chimiques utiles pour la mise en oeuvre de ce |
| GB1425020A (en) | 1971-12-17 | 1976-02-18 | Konishiroku Photo Ind | Photographic yellow coupler |
| DE2261361C2 (de) | 1971-12-17 | 1984-11-29 | Konishiroku Photo Industry Co., Ltd., Tokio/Tokyo | Farbfotografisches Aufzeichnungsmaterial und Farbentwickler für die Farbfotografie |
| US3932480A (en) | 1972-02-28 | 1976-01-13 | Polaroid Corporation | Benzylthiosulfuric acid salts |
| JPS5116141B2 (en]) | 1972-11-29 | 1976-05-21 | ||
| JPS5116142B2 (en]) | 1972-12-18 | 1976-05-21 | ||
| JPS5119987B2 (en]) | 1973-02-05 | 1976-06-22 | ||
| JPS5333846B2 (en]) | 1973-02-22 | 1978-09-18 | ||
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| JPS587987B2 (ja) | 1973-04-13 | 1983-02-14 | 富士写真フイルム株式会社 | カラ−シヤシンカンコウザイリヨウ |
| JPS541175B2 (en]) | 1973-04-21 | 1979-01-22 | ||
| JPS5125733B2 (en]) | 1973-07-16 | 1976-08-02 | ||
| JPS532728B2 (en]) | 1974-01-25 | 1978-01-31 | ||
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| US4138258A (en) | 1974-08-28 | 1979-02-06 | Fuji Photo Film Co., Ltd. | Multi-layered color photographic materials |
| US4045229A (en) | 1974-09-17 | 1977-08-30 | Eastman Kodak Company | Novel UV absorbing compounds and photographic elements containing UV absorbing compounds |
| CA1079432A (en) | 1974-09-17 | 1980-06-10 | Tsang J. Chen | Uniform, efficient distribution of hydrophobic materials through hydrophilic colloid layers, and products useful therefor |
| DE2509722C2 (de) * | 1975-03-06 | 1986-12-18 | Agfa-Gevaert Ag, 5090 Leverkusen | Farbphotographisches Aufzeichnungsmaterial |
| JPS5139853A (ja) | 1974-09-28 | 1976-04-03 | Aikoku Kogyo Kk | Aamusojugatakureen |
| US3993501A (en) | 1975-03-24 | 1976-11-23 | Union Carbide Corporation | Nonaqueous electrochemical cell |
| DE2540959C3 (de) | 1975-09-13 | 1981-12-10 | Agfa-Gevaert Ag, 5090 Leverkusen | Farbphotographisches Aufzeichnungsmaterial |
| JPS5814668B2 (ja) * | 1975-11-07 | 1983-03-22 | 富士写真フイルム株式会社 | シヤシンヨウゲンゾウヤク |
| JPS5269624A (en) | 1975-12-09 | 1977-06-09 | Fuji Photo Film Co Ltd | Photographic coupler |
| JPS589942B2 (ja) | 1975-12-29 | 1983-02-23 | 富士写真フイルム株式会社 | ゲンゾウヨクセイザイホウシユツガタカプラ− |
| JPS5943736B2 (ja) | 1976-01-26 | 1984-10-24 | 富士写真フイルム株式会社 | カラ−写真画像の形成方法 |
| DE2622923A1 (de) | 1976-05-21 | 1977-12-01 | Agfa Gevaert Ag | Farbphotographisches aufzeichnungsmaterial |
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| US4310612A (en) | 1978-10-10 | 1982-01-12 | Eastman Kodak Company | Blocked photographically useful compounds in photographic compositions, elements and processes employing them |
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| JPS5926016B2 (ja) | 1979-05-31 | 1984-06-23 | 富士写真フイルム株式会社 | 黄色カプラ− |
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| JPS57155537A (en) | 1981-03-20 | 1982-09-25 | Konishiroku Photo Ind Co Ltd | Color photographic sensitive silver halide material |
| JPS57201955A (en) | 1981-06-04 | 1982-12-10 | Toshiba Corp | Ticket issuing device |
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| DE3275761D1 (en) | 1981-08-25 | 1987-04-23 | Eastman Kodak Co | Photographic elements containing ballasted couplers |
| JPS5849964A (ja) | 1981-09-21 | 1983-03-24 | Asahi Optical Co Ltd | レンズ系を利用した複写機における数値制御モ−タ−の制御機構 |
| JPS5898731A (ja) | 1981-12-07 | 1983-06-11 | Fuji Photo Film Co Ltd | カラ−写真感光材料 |
| JPS58111941A (ja) * | 1981-12-16 | 1983-07-04 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| JPS58140740A (ja) * | 1982-02-15 | 1983-08-20 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| AU568488B2 (en) * | 1982-02-24 | 1988-01-07 | Konishiroku Photo Industry Co., Ltd. | Light-sensitive silver halide colour photographic material |
| JPS58205151A (ja) | 1982-05-24 | 1983-11-30 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−感光材料 |
| US4410618A (en) | 1982-06-11 | 1983-10-18 | Eastman Kodak Company | Blocked photographic reagents |
| JPS5933059A (ja) | 1982-08-17 | 1984-02-22 | Nippon Steel Corp | 双ロ−ル型鋳造圧延機とその制御方法 |
| US4463086A (en) | 1982-08-17 | 1984-07-31 | Konishiroku Photo Industry Co., Ltd. | Light-sensitive silver halide color photographic material |
| JPS5975475A (ja) | 1982-10-21 | 1984-04-28 | Toshiba Corp | 画像情報記憶検索装置 |
| JPH0239207B2 (ja) | 1982-12-10 | 1990-09-04 | Iseki Agricult Mach | Datsukokukinosokubanhokyokozo |
| US4543323A (en) | 1982-12-18 | 1985-09-24 | Konishiroku Photo Industry Co., Ltd. | Light-sensitive silver halide photographic material |
| JPS59131933A (ja) * | 1983-01-19 | 1984-07-28 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| JPS59162548A (ja) | 1983-02-15 | 1984-09-13 | Fuji Photo Film Co Ltd | 色画像形成方法 |
| JPS59160135A (ja) | 1983-03-02 | 1984-09-10 | Fuji Photo Film Co Ltd | ハロゲン化銀感光材料 |
| JPS59171956A (ja) | 1983-03-18 | 1984-09-28 | Fuji Photo Film Co Ltd | カラ−画像形成方法 |
| JPS59180555A (ja) | 1983-03-31 | 1984-10-13 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| JPS59184343A (ja) | 1983-04-04 | 1984-10-19 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料の処理方法 |
| JPS59204038A (ja) | 1983-05-06 | 1984-11-19 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| JPS59214854A (ja) * | 1983-05-20 | 1984-12-04 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−写真感光材料 |
| JPS6072379A (ja) | 1983-09-29 | 1985-04-24 | Toshiba Corp | 電子カメラ |
| JPS6078013A (ja) | 1983-10-06 | 1985-05-02 | Tenotsukusu:Kk | 地盤改良機における切削土の混合撹拌翼装置 |
| JPS60185950A (ja) | 1984-02-23 | 1985-09-21 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−感光材料 |
| JPS60249149A (ja) * | 1984-05-25 | 1985-12-09 | Fuji Photo Film Co Ltd | ハロゲン化銀カラ−写真感光材料 |
-
1985
- 1985-05-09 JP JP60098718A patent/JPS61255342A/ja active Granted
-
1986
- 1986-05-09 DE DE8686106347T patent/DE3665226D1/de not_active Expired
- 1986-05-09 EP EP86106347A patent/EP0204175B1/en not_active Expired
-
1991
- 1991-04-04 US US07/681,639 patent/US5126236A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US5126236A (en) | 1992-06-30 |
| DE3665226D1 (en) | 1989-09-28 |
| JPS61255342A (ja) | 1986-11-13 |
| EP0204175B1 (en) | 1989-08-23 |
| EP0204175A1 (en) | 1986-12-10 |
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