JPH01182847A - ハロゲン化銀カラー写真感光材料 - Google Patents

ハロゲン化銀カラー写真感光材料

Info

Publication number: JPH01182847A
Authority: JP; Japan
Prior art keywords: group; layer; coupler; color; silver halide
Prior art date: 1988-01-14
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

JP494688A

Other languages

English (en)

Japanese (ja)

Inventor

Noboru Sasaki

登佐々木

Jun Arakawa

純荒河

Yasushi Nozawa

野沢　靖

Katsumi Makino

槙野　克美

Yoichi Suga

陽一須賀

Katsumi Hirano

平野　克己

Norihiko Sakata

坂田　憲彦

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.)

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

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.)

1988-01-14

Filing date

1988-01-14

Publication date

1989-07-20

1988-01-14 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1988-01-14 Priority to JP494688A priority Critical patent/JPH01182847A/ja

1989-01-04 Priority to CA000587510A priority patent/CA1320657C/en

1989-01-12 Priority to EP89100479A priority patent/EP0324471A3/en

1989-07-20 Publication of JPH01182847A publication Critical patent/JPH01182847A/ja

Status Pending legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 128
229910052709 silver Inorganic materials 0.000 title claims abstract description 71
239000004332 silver Substances 0.000 title claims abstract description 71
239000000463 material Substances 0.000 title claims abstract description 38
239000000839 emulsion Substances 0.000 claims abstract description 93
230000035945 sensitivity Effects 0.000 claims abstract description 47
239000010410 layer Substances 0.000 claims description 168
230000000694 effects Effects 0.000 claims description 51
239000011229 interlayer Substances 0.000 claims description 11
239000000203 mixture Substances 0.000 abstract description 9
230000008859 change Effects 0.000 abstract description 5
BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 abstract 4
229940084388 gammar Drugs 0.000 abstract 4
238000000034 method Methods 0.000 description 49
230000001965 increasing effect Effects 0.000 description 35
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 35
125000003118 aryl group Chemical group 0.000 description 33
238000011161 development Methods 0.000 description 30
125000000217 alkyl group Chemical group 0.000 description 27
125000001424 substituent group Chemical group 0.000 description 26
239000011248 coating agent Substances 0.000 description 24
238000000576 coating method Methods 0.000 description 24
125000000623 heterocyclic group Chemical group 0.000 description 23
230000002829 reductive effect Effects 0.000 description 22
125000004432 carbon atom Chemical group C* 0.000 description 21
108010010803 Gelatin Proteins 0.000 description 19
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 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
229910021612 Silver iodide Inorganic materials 0.000 description 18
239000002245 particle Substances 0.000 description 17
125000003342 alkenyl group Chemical group 0.000 description 16
230000003595 spectral effect Effects 0.000 description 16
238000009826 distribution Methods 0.000 description 15
239000000975 dye Substances 0.000 description 15
125000005843 halogen group Chemical group 0.000 description 15
125000003545 alkoxy group Chemical group 0.000 description 14
239000003795 chemical substances by application Substances 0.000 description 14
101100501963 Caenorhabditis elegans exc-4 gene Proteins 0.000 description 13
125000004442 acylamino group Chemical group 0.000 description 13
230000000052 comparative effect Effects 0.000 description 13
239000003112 inhibitor Substances 0.000 description 13
125000001931 aliphatic group Chemical group 0.000 description 11
150000001875 compounds Chemical class 0.000 description 11
125000004093 cyano group Chemical group *C#N 0.000 description 10
125000004122 cyclic group Chemical group 0.000 description 10
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 9
238000010521 absorption reaction Methods 0.000 description 9
125000004453 alkoxycarbonyl group Chemical group 0.000 description 9
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 9
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 9
238000004040 coloring Methods 0.000 description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 description 9
125000001997 phenyl group Chemical class [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
238000002360 preparation method Methods 0.000 description 9
229940045105 silver iodide Drugs 0.000 description 9
125000005110 aryl thio group Chemical group 0.000 description 8
125000004104 aryloxy group Chemical group 0.000 description 8
238000005859 coupling reaction Methods 0.000 description 8
125000004435 hydrogen atom Chemical group [H]* 0.000 description 8
125000004414 alkyl thio group Chemical group 0.000 description 7
125000003277 amino group Chemical group 0.000 description 7
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 7
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 7
230000008878 coupling Effects 0.000 description 7
238000010168 coupling process Methods 0.000 description 7
230000003247 decreasing effect Effects 0.000 description 7
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 7
238000011160 research Methods 0.000 description 7
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 6
239000000654 additive Substances 0.000 description 6
125000004390 alkyl sulfonyl group Chemical group 0.000 description 6
125000003710 aryl alkyl group Chemical group 0.000 description 6
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 6
239000013078 crystal Substances 0.000 description 6
238000005516 engineering process Methods 0.000 description 6
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 6
238000012545 processing Methods 0.000 description 6
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 6
125000000565 sulfonamide group Chemical group 0.000 description 6
125000004391 aryl sulfonyl group Chemical group 0.000 description 5
230000000873 masking effect Effects 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
125000004433 nitrogen atom Chemical group N* 0.000 description 5
230000008569 process Effects 0.000 description 5
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
125000004466 alkoxycarbonylamino 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
238000009835 boiling Methods 0.000 description 4
239000011258 core-shell material Substances 0.000 description 4
125000006165 cyclic alkyl group Chemical group 0.000 description 4
230000007423 decrease Effects 0.000 description 4
125000004663 dialkyl amino group Chemical group 0.000 description 4
238000009792 diffusion process Methods 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
230000006872 improvement Effects 0.000 description 4
229910052740 iodine Inorganic materials 0.000 description 4
239000011630 iodine Substances 0.000 description 4
229910052751 metal Inorganic materials 0.000 description 4
239000002184 metal Substances 0.000 description 4
238000002156 mixing Methods 0.000 description 4
230000003287 optical effect Effects 0.000 description 4
125000004430 oxygen atom Chemical group O* 0.000 description 4
125000005493 quinolyl group Chemical group 0.000 description 4
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 4
239000000126 substance Substances 0.000 description 4
125000003396 thiol group Chemical group [H]S* 0.000 description 4
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 4
238000005406 washing Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
125000004423 acyloxy group Chemical group 0.000 description 3
239000000084 colloidal system Substances 0.000 description 3
239000003086 colorant Substances 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
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
230000002708 enhancing effect Effects 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
230000002209 hydrophobic effect Effects 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
125000002883 imidazolyl group Chemical group 0.000 description 3
239000004816 latex Substances 0.000 description 3
229920000126 latex Polymers 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
229910021645 metal ion Inorganic materials 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
229920000120 polyethyl acrylate Polymers 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
125000004076 pyridyl group Chemical group 0.000 description 3
230000001235 sensitizing effect Effects 0.000 description 3
238000001179 sorption measurement Methods 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
230000006641 stabilisation Effects 0.000 description 3
238000011105 stabilization Methods 0.000 description 3
230000001629 suppression Effects 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical group N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 2
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 2
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 2
YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-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
206010070834 Sensitisation Diseases 0.000 description 2
229910021607 Silver chloride Inorganic materials 0.000 description 2
YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
239000006096 absorbing agent Substances 0.000 description 2
125000002252 acyl group Chemical group 0.000 description 2
230000000996 additive effect Effects 0.000 description 2
125000004422 alkyl sulphonamide group Chemical group 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
125000003368 amide group Chemical group 0.000 description 2
125000001769 aryl amino group Chemical group 0.000 description 2
125000005116 aryl carbamoyl group Chemical group 0.000 description 2
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 2
125000004421 aryl sulphonamide group Chemical group 0.000 description 2
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 2
239000002131 composite material Substances 0.000 description 2
230000007547 defect Effects 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
150000005690 diesters Chemical class 0.000 description 2
239000003623 enhancer Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
125000002541 furyl group Chemical group 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
239000003446 ligand Substances 0.000 description 2
239000012528 membrane Substances 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
239000002667 nucleating agent Substances 0.000 description 2
150000002989 phenols Chemical class 0.000 description 2
ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 2
239000004848 polyfunctional curative Substances 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000002243 precursor Substances 0.000 description 2
238000007639 printing Methods 0.000 description 2
239000011241 protective layer Substances 0.000 description 2
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical compound N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 2
229920006395 saturated elastomer Polymers 0.000 description 2
230000008313 sensitization Effects 0.000 description 2
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
239000000243 solution Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
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 2
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
125000004434 sulfur atom Chemical group 0.000 description 2
238000012360 testing method Methods 0.000 description 2
230000004580 weight loss Effects 0.000 description 2
NJYFRQQXXXRJHK-UHFFFAOYSA-N (4-aminophenyl) thiocyanate Chemical compound NC1=CC=C(SC#N)C=C1 NJYFRQQXXXRJHK-UHFFFAOYSA-N 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 description 1
150000004782 1-naphthols Chemical class 0.000 description 1
KPVMVJXYXFUVLR-UHFFFAOYSA-N 12-ethyltetradecan-1-amine Chemical compound CCC(CC)CCCCCCCCCCCN KPVMVJXYXFUVLR-UHFFFAOYSA-N 0.000 description 1
MSSJNZSBWUFRGZ-UHFFFAOYSA-N 1h-benzimidazole;2,3-dihydro-1,3-thiazole Chemical compound C1NC=CS1.C1=CC=C2NC=NC2=C1 MSSJNZSBWUFRGZ-UHFFFAOYSA-N 0.000 description 1
SIMWFXSMDQBKED-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)acetamide Chemical compound C1=CC=C2SC(CC(=O)N)=NC2=C1 SIMWFXSMDQBKED-UHFFFAOYSA-N 0.000 description 1
ZOAYQTSFMDZTQA-UHFFFAOYSA-N 2-(1,3-benzothiazol-2-yl)acetic acid Chemical compound C1=CC=C2SC(CC(=O)O)=NC2=C1 ZOAYQTSFMDZTQA-UHFFFAOYSA-N 0.000 description 1
GFTPLFVZKMIYAP-UHFFFAOYSA-N 2-(1h-benzimidazol-1-ium-2-yl)acetate Chemical compound C1=CC=C2NC(CC(=O)O)=NC2=C1 GFTPLFVZKMIYAP-UHFFFAOYSA-N 0.000 description 1
STRDCKXOEFPOCT-UHFFFAOYSA-N 2-(1h-benzimidazol-2-yl)acetamide Chemical compound C1=CC=C2NC(CC(=O)N)=NC2=C1 STRDCKXOEFPOCT-UHFFFAOYSA-N 0.000 description 1
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 1
MGADZUXDNSDTHW-UHFFFAOYSA-N 2H-pyran Chemical compound C1OC=CC=C1 MGADZUXDNSDTHW-UHFFFAOYSA-N 0.000 description 1
125000004207 3-methoxyphenyl group Chemical class [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 description 1
XVEPKNMOJLPFCN-UHFFFAOYSA-N 4,4-dimethyl-3-oxo-n-phenylpentanamide Chemical compound CC(C)(C)C(=O)CC(=O)NC1=CC=CC=C1 XVEPKNMOJLPFCN-UHFFFAOYSA-N 0.000 description 1
YLNKRLLYLJYWEN-UHFFFAOYSA-N 4-(2,2-dibutoxyethoxy)-4-oxobutanoic acid Chemical compound CCCCOC(OCCCC)COC(=O)CCC(O)=O YLNKRLLYLJYWEN-UHFFFAOYSA-N 0.000 description 1
NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
MFGQIJCMHXZHHP-UHFFFAOYSA-N 5h-imidazo[1,2-b]pyrazole Chemical class N1C=CC2=NC=CN21 MFGQIJCMHXZHHP-UHFFFAOYSA-N 0.000 description 1
125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical compound CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
230000005457 Black-body radiation Effects 0.000 description 1
DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical compound [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 1
CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
125000005118 N-alkylcarbamoyl group Chemical group 0.000 description 1
MTJLUBFRVYWORM-UHFFFAOYSA-N N1=NC=C2C1=CC=N2.N2N=CCC2=O Chemical compound N1=NC=C2C1=CC=N2.N2N=CCC2=O MTJLUBFRVYWORM-UHFFFAOYSA-N 0.000 description 1
101100221809 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cpd-7 gene Proteins 0.000 description 1
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
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 1
JZFICWYCTCCINF-UHFFFAOYSA-N Thiadiazin Chemical compound S=C1SC(C)NC(C)N1CCN1C(=S)SC(C)NC1C JZFICWYCTCCINF-UHFFFAOYSA-N 0.000 description 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
235000010724 Wisteria floribunda Nutrition 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
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
238000000862 absorption spectrum Methods 0.000 description 1
150000003869 acetamides Chemical group 0.000 description 1
125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000012190 activator Substances 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
150000008431 aliphatic amides Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical group 0.000 description 1
125000005115 alkyl carbamoyl group Chemical group 0.000 description 1
125000004448 alkyl carbonyl group Chemical group 0.000 description 1
125000005153 alkyl sulfamoyl group Chemical group 0.000 description 1
125000004691 alkyl thio carbonyl group Chemical group 0.000 description 1
125000005281 alkyl ureido group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
235000019270 ammonium chloride Nutrition 0.000 description 1
229910000148 ammonium phosphate Inorganic materials 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 1
229910052921 ammonium sulfate Inorganic materials 0.000 description 1
235000011130 ammonium sulphate Nutrition 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
239000007864 aqueous solution Substances 0.000 description 1
125000005098 aryl alkoxy carbonyl group Chemical group 0.000 description 1
125000005129 aryl carbonyl group Chemical group 0.000 description 1
CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 description 1
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 1
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
150000001558 benzoic acid derivatives Chemical class 0.000 description 1
125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 description 1
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
ZJRCIQAMTAINCB-UHFFFAOYSA-N benzoylacetonitrile Chemical compound N#CCC(=O)C1=CC=CC=C1 ZJRCIQAMTAINCB-UHFFFAOYSA-N 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
125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
239000000872 buffer Substances 0.000 description 1
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 1
COPHVUDURPSYBO-UHFFFAOYSA-N butyl dioctyl phosphate Chemical compound CCCCCCCCOP(=O)(OCCCC)OCCCCCCCC COPHVUDURPSYBO-UHFFFAOYSA-N 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
229910052799 carbon Inorganic materials 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
150000001735 carboxylic acids Chemical class 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 description 1
125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 description 1
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
230000009849 deactivation Effects 0.000 description 1
239000000645 desinfectant Substances 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
NZZIMKJIVMHWJC-UHFFFAOYSA-N dibenzoylmethane Chemical compound C=1C=CC=CC=1C(=O)CC(=O)C1=CC=CC=C1 NZZIMKJIVMHWJC-UHFFFAOYSA-N 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
239000000539 dimer Substances 0.000 description 1
XWVQUJDBOICHGH-UHFFFAOYSA-N dioctyl nonanedioate Chemical compound CCCCCCCCOC(=O)CCCCCCCC(=O)OCCCCCCCC XWVQUJDBOICHGH-UHFFFAOYSA-N 0.000 description 1
ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
230000008030 elimination Effects 0.000 description 1
238000003379 elimination reaction Methods 0.000 description 1
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
229960005102 foscarnet Drugs 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
230000037308 hair color Effects 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
PTFYQSWHBLOXRZ-UHFFFAOYSA-N imidazo[4,5-e]indazole Chemical class C1=CC2=NC=NC2=C2C=NN=C21 PTFYQSWHBLOXRZ-UHFFFAOYSA-N 0.000 description 1
HOBCFUWDNJPFHB-UHFFFAOYSA-N indolizine Chemical compound C1=CC=CN2C=CC=C21 HOBCFUWDNJPFHB-UHFFFAOYSA-N 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000009830 intercalation Methods 0.000 description 1
230000002687 intercalation Effects 0.000 description 1
CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 1
230000001788 irregular Effects 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000005956 isoquinolyl group Chemical group 0.000 description 1
238000005304 joining Methods 0.000 description 1
229910000464 lead oxide Inorganic materials 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
230000003211 malignant effect Effects 0.000 description 1
WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
238000005259 measurement Methods 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
125000002004 n-butylamino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QJQAMHYHNCADNR-UHFFFAOYSA-N n-methylpropanamide Chemical group CCC(=O)NC QJQAMHYHNCADNR-UHFFFAOYSA-N 0.000 description 1
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
FZERHIULMFGESH-QBZHADDCSA-N n-phenylacetamide Chemical group CC(=O)[15NH]C1=CC=CC=C1 FZERHIULMFGESH-QBZHADDCSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
230000003647 oxidation Effects 0.000 description 1
238000007254 oxidation reaction Methods 0.000 description 1
YEXPOXQUZXUXJW-UHFFFAOYSA-N oxolead Chemical compound [Pb]=O YEXPOXQUZXUXJW-UHFFFAOYSA-N 0.000 description 1
125000000913 palmityl 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])[H] 0.000 description 1
125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
125000005936 piperidyl group Chemical group 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([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
VNAUDIIOSMNXBA-UHFFFAOYSA-N pyrazolo[4,3-c]pyrazole Chemical class N1=NC=C2N=NC=C21 VNAUDIIOSMNXBA-UHFFFAOYSA-N 0.000 description 1
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 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
230000009467 reduction Effects 0.000 description 1
230000005070 ripening Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000001953 sensory effect Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000004328 sodium tetraborate Substances 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
230000003068 static effect Effects 0.000 description 1
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
125000005031 thiocyano group Chemical group S(C#N)* 0.000 description 1
229930192474 thiophene Natural products 0.000 description 1
238000012549 training 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

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
- G03C7/3041—Materials with specific sensitometric characteristics, e.g. gamma, density

Landscapes

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

JP494688A 1988-01-14 1988-01-14 ハロゲン化銀カラー写真感光材料 Pending JPH01182847A (ja)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
JP494688A JPH01182847A (ja)	1988-01-14	1988-01-14	ハロゲン化銀カラー写真感光材料
CA000587510A CA1320657C (en)	1988-01-14	1989-01-04	Silver halide color photographic material and method for production of color image using the same
EP89100479A EP0324471A3 (en)	1988-01-14	1989-01-12	Silver halide color photographic material and method for producing of color image using the same

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP494688A JPH01182847A (ja)	1988-01-14	1988-01-14	ハロゲン化銀カラー写真感光材料

Publications (1)

Publication Number	Publication Date
JPH01182847A true JPH01182847A (ja)	1989-07-20

Family

ID=11597738

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP494688A Pending JPH01182847A (ja)	1988-01-14	1988-01-14	ハロゲン化銀カラー写真感光材料

Country Status (3)

Country	Link
EP (1)	EP0324471A3 (de)
JP (1)	JPH01182847A (de)
CA (1)	CA1320657C (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5212054A (en) *	1990-02-02	1993-05-18	Konica Corporation	Silver halide color photographic light-sensitive material
JP3041724B2 (ja) *	1991-01-25	2000-05-15	コニカ株式会社	色相再現性に優れたハロゲン化銀カラー写真感光材料
EP0684511B1 (de) *	1994-05-20	2001-02-28	Eastman Kodak Company	Niedrigkontrastfilm
US5576128A (en) *	1994-12-05	1996-11-19	Eastman Kodak Company	Color negative films with low mid-scale contrast for telecine transfer applications
US5561012A (en) *	1994-12-05	1996-10-01	Eastman Kodak Company	Process of forming a telecine transfer image having enhanced shadow detail
US5750320A (en) *	1996-02-16	1998-05-12	Eastman Kodak Company	Color motion picture print films for telecine transfer applications
EP1693702A1 (de) *	2005-02-18	2006-08-23	Fuji Photo Film B.V.	Farbphotographisches lichtempfindliches Silberhalogenidmaterial
DE102024109114A1 (de)	2024-03-28	2025-10-02	Adidas Ag	Schuh, der mit Boden- und Seitenlandebereichen geformt ist, um Bewegung zu führen

Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62954A (ja) *	1985-02-26	1987-01-06	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62160448A (ja) *	1986-01-08	1987-07-16	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62258453A (ja) *	1986-05-01	1987-11-10	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5763531A (en) *	1980-10-03	1982-04-17	Konishiroku Photo Ind Co Ltd	Multilayer color photographic material

1988
- 1988-01-14 JP JP494688A patent/JPH01182847A/ja active Pending
1989
- 1989-01-04 CA CA000587510A patent/CA1320657C/en not_active Expired - Lifetime
- 1989-01-12 EP EP89100479A patent/EP0324471A3/en not_active Withdrawn

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS62954A (ja) *	1985-02-26	1987-01-06	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62160448A (ja) *	1986-01-08	1987-07-16	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62258453A (ja) *	1986-05-01	1987-11-10	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料

Also Published As

Publication number	Publication date
EP0324471A3 (en)	1990-05-30
EP0324471A2 (de)	1989-07-19
CA1320657C (en)	1993-07-27

Publication	Publication Date	Title
US5053324A (en)	1991-10-01	Color photographic light-sensitive materials having red color saturation and improved discrimination of green colors
US4952485A (en)	1990-08-28	Silver halide color negative photographic materials
JPS62160449A (ja)	1987-07-16	カラ−写真感光材料
JPH0364056B2 (de)	1991-10-03
JPH0667372A (ja)	1994-03-11	異なったカラー記録層間のアキュータンスをぴったりと合わせたカラーフィルム
US5399468A (en)	1995-03-21	Color photographic silver halide duplicating element and process
JPS62206543A (ja)	1987-09-11	新規な層構成のハロゲン化銀カラ−写真感光材料
JPH01182847A (ja)	1989-07-20	ハロゲン化銀カラー写真感光材料
JPH07175183A (ja)	1995-07-14	反転カラー写真要素及びその処理方法
CA1039556A (en)	1978-10-03	Hybrid color photographic elements and processes for developing same
US4806459A (en)	1989-02-21	Color photographic material yellow and cyan dye forming couplers and compound which produces a diffusible development inhibitor or a precursor in a blue sensitive layer
JPH0658514B2 (ja)	1994-08-03	写真感光材料
JPH01237652A (ja)	1989-09-22	ハロゲン化銀写真感光材料
JPH01237655A (ja)	1989-09-22	ハロゲン化銀写真感光材料
JPH01237650A (ja)	1989-09-22	ハロゲン化銀カラー写真感光材料
JPH01237649A (ja)	1989-09-22	ハロゲン化銀カラー写真感光材料
JP2581950B2 (ja)	1997-02-19	ハロゲン化銀カラー写真感光材料
JPH01237653A (ja)	1989-09-22	ハロゲン化銀カラー写真感光材料
DE69210101T2 (de)	1996-12-12	Photographisches Element sowie Verfahren mit einem einen Entwicklungsinhibitor freisetzenden Kuppler und einem einen gelben Farbstoff bildenden Kuppler
JPH0521218B2 (de)	1993-03-23
JPH01237651A (ja)	1989-09-22	ハロゲン化銀カラー写真感光材料
JP2533338B2 (ja)	1996-09-11	カラ―画像形成方法
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