CA1320657C - Materiau a halogenure d'argent pour la photographie en couleurs et methode de production d'images en couleurs au moyen de ce materiau - Google Patents

Materiau a halogenure d'argent pour la photographie en couleurs et methode de production d'images en couleurs au moyen de ce materiau

Info

Publication number: CA1320657C
Authority: CA; Canada
Prior art keywords: gamma; group; silver halide; color; photographic material
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.): Expired - Lifetime

Application number

CA000587510A

Other languages

English (en)

Inventor

Noboru Sasaki

Jun Arakawa

Yasushi Nozawa

Katsumi Makino

Youichi Suga

Katsumi Hirano

Norihiko Sakata

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

1989-01-04

Publication date

1993-07-27

1989-01-04 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1993-07-27 Application granted granted Critical

1993-07-27 Publication of CA1320657C publication Critical patent/CA1320657C/fr

2010-07-27 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 98
229910052709 silver Inorganic materials 0.000 title claims abstract description 83
239000004332 silver Substances 0.000 title claims abstract description 83
239000000463 material Substances 0.000 title claims abstract description 61
238000004519 manufacturing process Methods 0.000 title claims abstract description 5
239000000839 emulsion Substances 0.000 claims abstract description 120
230000035945 sensitivity Effects 0.000 claims abstract description 46
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims abstract description 41
150000004820 halides Chemical class 0.000 claims abstract description 30
239000010410 layer Substances 0.000 claims description 181
230000000694 effects Effects 0.000 claims description 41
239000011229 interlayer Substances 0.000 claims description 41
229910021612 Silver iodide Inorganic materials 0.000 claims description 32
238000011161 development Methods 0.000 claims description 32
239000003112 inhibitor Substances 0.000 claims description 15
239000003795 chemical substances by application Substances 0.000 claims description 14
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 claims description 8
230000003647 oxidation Effects 0.000 claims description 8
238000007254 oxidation reaction Methods 0.000 claims description 8
229940045105 silver iodide Drugs 0.000 claims description 8
230000008878 coupling Effects 0.000 claims description 6
238000010168 coupling process Methods 0.000 claims description 6
238000005859 coupling reaction Methods 0.000 claims description 6
239000002243 precursor Substances 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 claims description 3
238000000034 method Methods 0.000 description 54
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 38
125000000217 alkyl group Chemical group 0.000 description 37
230000001965 increasing effect Effects 0.000 description 37
230000003247 decreasing effect Effects 0.000 description 32
230000018109 developmental process Effects 0.000 description 29
125000001424 substituent group Chemical group 0.000 description 28
125000003118 aryl group Chemical group 0.000 description 27
125000000623 heterocyclic group Chemical group 0.000 description 25
125000004432 carbon atom Chemical group C* 0.000 description 23
239000000975 dye Substances 0.000 description 22
238000002360 preparation method Methods 0.000 description 21
108010010803 Gelatin Proteins 0.000 description 20
239000008273 gelatin Substances 0.000 description 20
229920000159 gelatin Polymers 0.000 description 20
235000019322 gelatine Nutrition 0.000 description 20
235000011852 gelatine desserts Nutrition 0.000 description 20
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 20
230000003595 spectral effect Effects 0.000 description 20
125000005843 halogen group Chemical group 0.000 description 19
238000009826 distribution Methods 0.000 description 18
125000003545 alkoxy group Chemical group 0.000 description 17
125000001931 aliphatic group Chemical group 0.000 description 13
101100501963 Caenorhabditis elegans exc-4 gene Proteins 0.000 description 12
230000009102 absorption Effects 0.000 description 12
238000010521 absorption reaction Methods 0.000 description 12
125000004442 acylamino group Chemical group 0.000 description 12
150000001875 compounds Chemical class 0.000 description 12
239000000203 mixture Substances 0.000 description 12
125000003342 alkenyl group Chemical group 0.000 description 11
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 10
125000004093 cyano group Chemical group *C#N 0.000 description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 description 10
239000000654 additive Substances 0.000 description 9
125000004453 alkoxycarbonyl group Chemical group 0.000 description 9
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 9
230000002401 inhibitory effect Effects 0.000 description 9
125000004104 aryloxy group Chemical group 0.000 description 8
239000003086 colorant Substances 0.000 description 8
239000013078 crystal Substances 0.000 description 8
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 8
238000011160 research Methods 0.000 description 8
125000004390 alkyl sulfonyl group Chemical group 0.000 description 7
125000004414 alkyl thio group Chemical group 0.000 description 7
125000003710 aryl alkyl group Chemical group 0.000 description 7
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 7
125000005110 aryl thio group Chemical group 0.000 description 7
239000011248 coating agent Substances 0.000 description 7
238000000576 coating method Methods 0.000 description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
238000012545 processing Methods 0.000 description 7
239000002253 acid Substances 0.000 description 6
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 6
125000004391 aryl sulfonyl group Chemical group 0.000 description 6
125000000753 cycloalkyl group Chemical group 0.000 description 6
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
125000003277 amino group Chemical group 0.000 description 5
125000002029 aromatic hydrocarbon group Chemical group 0.000 description 5
238000009835 boiling Methods 0.000 description 5
125000004122 cyclic group Chemical group 0.000 description 5
125000000392 cycloalkenyl group Chemical group 0.000 description 5
230000007547 defect Effects 0.000 description 5
230000002708 enhancing effect Effects 0.000 description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
229910052740 iodine Inorganic materials 0.000 description 5
229910052751 metal Inorganic materials 0.000 description 5
239000002184 metal Substances 0.000 description 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
229910052757 nitrogen Inorganic materials 0.000 description 5
230000001235 sensitizing effect Effects 0.000 description 5
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 5
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
206010070834 Sensitisation Diseases 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
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 4
239000011258 core-shell material Substances 0.000 description 4
210000004209 hair Anatomy 0.000 description 4
125000005842 heteroatom Chemical group 0.000 description 4
229910052739 hydrogen Inorganic materials 0.000 description 4
239000011630 iodine Substances 0.000 description 4
230000000873 masking effect Effects 0.000 description 4
239000003960 organic solvent Substances 0.000 description 4
125000005493 quinolyl group Chemical group 0.000 description 4
230000008313 sensitization Effects 0.000 description 4
239000000243 solution Substances 0.000 description 4
125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 description 4
239000004094 surface-active agent Substances 0.000 description 4
125000003396 thiol group Chemical group [H]S* 0.000 description 4
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical group O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 description 3
DBTDEFJAFBUGPP-UHFFFAOYSA-N Methanethial Chemical compound S=C DBTDEFJAFBUGPP-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
150000007513 acids Chemical class 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
125000004423 acyloxy group Chemical group 0.000 description 3
230000000996 additive effect Effects 0.000 description 3
125000003368 amide group Chemical group 0.000 description 3
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 3
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 3
230000008859 change Effects 0.000 description 3
239000000084 colloidal system 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
125000004663 dialkyl amino group Chemical group 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
CTXKDHZPBPQKTD-UHFFFAOYSA-N ethyl n-(carbamoylamino)carbamate Chemical compound CCOC(=O)NNC(N)=O CTXKDHZPBPQKTD-UHFFFAOYSA-N 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 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
229910021645 metal ion Inorganic materials 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
230000003287 optical effect Effects 0.000 description 3
125000004430 oxygen atom Chemical group O* 0.000 description 3
229920000120 polyethyl acrylate Polymers 0.000 description 3
239000004848 polyfunctional curative Substances 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
230000002829 reductive effect Effects 0.000 description 3
239000007787 solid Substances 0.000 description 3
238000001228 spectrum Methods 0.000 description 3
239000003381 stabilizer 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
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
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
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
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
101100221809 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cpd-7 gene Proteins 0.000 description 2
229910019142 PO4 Inorganic materials 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
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
125000005422 alkyl sulfonamido group Chemical group 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
125000001769 aryl amino group Chemical group 0.000 description 2
125000005116 aryl carbamoyl group Chemical group 0.000 description 2
125000005421 aryl sulfonamido group Chemical group 0.000 description 2
125000004429 atom Chemical group 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 2
125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 2
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
229940000425 combination drug Drugs 0.000 description 2
239000013256 coordination polymer Substances 0.000 description 2
230000009034 developmental inhibition Effects 0.000 description 2
FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
125000002541 furyl group Chemical group 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 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
239000003446 ligand Substances 0.000 description 2
238000002156 mixing Methods 0.000 description 2
125000001624 naphthyl group Chemical group 0.000 description 2
239000002667 nucleating agent Substances 0.000 description 2
125000002971 oxazolyl group Chemical group 0.000 description 2
229910052760 oxygen Inorganic materials 0.000 description 2
239000001301 oxygen Substances 0.000 description 2
239000002245 particle Substances 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
ZJAOAACCNHFJAH-UHFFFAOYSA-N phosphonoformic acid Chemical compound OC(=O)P(O)(O)=O ZJAOAACCNHFJAH-UHFFFAOYSA-N 0.000 description 2
229920003229 poly(methyl methacrylate) Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000004926 polymethyl methacrylate Substances 0.000 description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 2
239000011241 protective layer Substances 0.000 description 2
230000005070 ripening Effects 0.000 description 2
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
238000001179 sorption measurement Methods 0.000 description 2
230000006641 stabilisation Effects 0.000 description 2
238000011105 stabilization Methods 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
239000000126 substance Substances 0.000 description 2
125000004434 sulfur atom Chemical group 0.000 description 2
238000012360 testing method Methods 0.000 description 2
JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-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
JLHMJWHSBYZWJJ-UHFFFAOYSA-N 1,2-thiazole 1-oxide Chemical compound O=S1C=CC=N1 JLHMJWHSBYZWJJ-UHFFFAOYSA-N 0.000 description 1
YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 1
GLFGFXDDVYKLKP-UHFFFAOYSA-N 1,3-benzothiazol-2-yl acetate Chemical compound C1=CC=C2SC(OC(=O)C)=NC2=C1 GLFGFXDDVYKLKP-UHFFFAOYSA-N 0.000 description 1
SBXXBWUBUAZTKV-UHFFFAOYSA-N 1,3-benzoxazol-2-yl acetate Chemical compound C1=CC=C2OC(OC(=O)C)=NC2=C1 SBXXBWUBUAZTKV-UHFFFAOYSA-N 0.000 description 1
UVRFNSBXRRNDRU-UHFFFAOYSA-N 1h-benzimidazol-2-yl acetate Chemical compound C1=CC=C2NC(OC(=O)C)=NC2=C1 UVRFNSBXRRNDRU-UHFFFAOYSA-N 0.000 description 1
YQTCQNIPQMJNTI-UHFFFAOYSA-N 2,2-dimethylpropan-1-one Chemical group CC(C)(C)[C]=O YQTCQNIPQMJNTI-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
KYRRAGIOAZNKGO-UHFFFAOYSA-N 2-(1,3-benzoxazol-2-yl)acetamide Chemical compound C1=CC=C2OC(CC(=O)N)=NC2=C1 KYRRAGIOAZNKGO-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
UUNIOFWUJYBVGQ-UHFFFAOYSA-N 2-amino-4-(3,4-dimethoxyphenyl)-10-fluoro-4,5,6,7-tetrahydrobenzo[1,2]cyclohepta[6,7-d]pyran-3-carbonitrile Chemical compound C1=C(OC)C(OC)=CC=C1C1C(C#N)=C(N)OC2=C1CCCC1=CC=C(F)C=C12 UUNIOFWUJYBVGQ-UHFFFAOYSA-N 0.000 description 1
125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 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
BRUJXXBWUDEKCK-UHFFFAOYSA-N 3h-pyrazolo[5,1-c][1,2,4]triazole Chemical class C1=NN2CN=NC2=C1 BRUJXXBWUDEKCK-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
125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
CLENKVQTZCLNQS-UHFFFAOYSA-N 9-propylheptadecan-9-yl dihydrogen phosphate Chemical compound CCCCCCCCC(CCC)(OP(O)(O)=O)CCCCCCCC CLENKVQTZCLNQS-UHFFFAOYSA-N 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
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
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 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
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Natural products CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 1
IYXGSMUGOJNHAZ-UHFFFAOYSA-N Ethyl malonate Chemical compound CCOC(=O)CC(=O)OCC IYXGSMUGOJNHAZ-UHFFFAOYSA-N 0.000 description 1
ZLSWBLPERHFHIS-UHFFFAOYSA-N Fenoprop Chemical compound OC(=O)C(C)OC1=CC(Cl)=C(Cl)C=C1Cl ZLSWBLPERHFHIS-UHFFFAOYSA-N 0.000 description 1
101000913968 Ipomoea purpurea Chalcone synthase C Proteins 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
BXUURYQQDJGIGA-UHFFFAOYSA-N N1C=NN2N=CC=C21 Chemical compound N1C=NN2N=CC=C21 BXUURYQQDJGIGA-UHFFFAOYSA-N 0.000 description 1
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
101000907988 Petunia hybrida Chalcone-flavanone isomerase C Proteins 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
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
229910006069 SO3H Inorganic materials 0.000 description 1
FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
239000004902 Softening Agent Substances 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
HPCNGJIHSHCKAQ-UHFFFAOYSA-N [cyano(nitrosulfonyl)amino]urea Chemical compound N(C(=O)N)N(S(=O)(=O)[N+](=O)[O-])C#N HPCNGJIHSHCKAQ-UHFFFAOYSA-N 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
229960001413 acetanilide Drugs 0.000 description 1
150000001242 acetic acid derivatives Chemical class 0.000 description 1
230000009471 action Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
239000003513 alkali Substances 0.000 description 1
239000012670 alkaline solution Substances 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
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
239000002216 antistatic agent Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 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
230000008901 benefit Effects 0.000 description 1
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 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
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
235000010290 biphenyl Nutrition 0.000 description 1
239000004305 biphenyl Substances 0.000 description 1
125000006267 biphenyl group Chemical group 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
238000004061 bleaching Methods 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
229910021538 borax Inorganic materials 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
239000000872 buffer Substances 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
150000001721 carbon Chemical group 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
125000002843 carboxylic acid group Chemical group 0.000 description 1
125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 description 1
239000008199 coating composition Substances 0.000 description 1
230000021615 conjugation Effects 0.000 description 1
238000010276 construction Methods 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
238000001739 density measurement Methods 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
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
150000005690 diesters Chemical class 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000009792 diffusion process Methods 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
239000003623 enhancer Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 1
125000004705 ethylthio group Chemical group C(C)S* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
229960005102 foscarnet Drugs 0.000 description 1
239000000417 fungicide Substances 0.000 description 1
230000004927 fusion Effects 0.000 description 1
230000037308 hair color Effects 0.000 description 1
239000008233 hard water Substances 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
238000005286 illumination Methods 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
230000006872 improvement Effects 0.000 description 1
LOCAIGRSOJUCTB-UHFFFAOYSA-N indazol-3-one Chemical compound C1=CC=C2C(=O)N=NC2=C1 LOCAIGRSOJUCTB-UHFFFAOYSA-N 0.000 description 1
229910052738 indium Inorganic materials 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
150000002500 ions Chemical class 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
229910000464 lead oxide Inorganic materials 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
WRIRWRKPLXCTFD-UHFFFAOYSA-N malonamide Chemical compound NC(=O)CC(N)=O WRIRWRKPLXCTFD-UHFFFAOYSA-N 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000004674 methylcarbonyl group Chemical group CC(=O)* 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
150000002763 monocarboxylic acids Chemical class 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
BECUBVOEPSAYDH-UHFFFAOYSA-N n-(1h-benzimidazol-2-yl)acetamide Chemical compound C1=CC=C2NC(NC(=O)C)=NC2=C1 BECUBVOEPSAYDH-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
230000007935 neutral effect Effects 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
125000004365 octenyl group Chemical group C(=CCCCCCC)* 0.000 description 1
VECVSKFWRQYTAL-UHFFFAOYSA-N octyl benzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1 VECVSKFWRQYTAL-UHFFFAOYSA-N 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
150000002989 phenols Chemical class 0.000 description 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
125000006678 phenoxycarbonyl group Chemical group 0.000 description 1
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 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
229910052700 potassium Inorganic materials 0.000 description 1
230000008569 process Effects 0.000 description 1
150000003217 pyrazoles Chemical class 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
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical compound N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 1
238000009877 rendering Methods 0.000 description 1
230000002441 reversible effect Effects 0.000 description 1
239000008237 rinsing water 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
239000011734 sodium Substances 0.000 description 1
239000004328 sodium tetraborate Substances 0.000 description 1
235000010339 sodium tetraborate Nutrition 0.000 description 1
CMXPERZAMAQXSF-UHFFFAOYSA-M sodium;1,4-bis(2-ethylhexoxy)-1,4-dioxobutane-2-sulfonate;1,8-dihydroxyanthracene-9,10-dione Chemical compound [Na+].O=C1C2=CC=CC(O)=C2C(=O)C2=C1C=CC=C2O.CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC CMXPERZAMAQXSF-UHFFFAOYSA-M 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
125000000565 sulfonamide group Chemical group 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
125000000542 sulfonic acid group Chemical group 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 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
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
239000006097 ultraviolet radiation absorber Substances 0.000 description 1
JOYRKODLDBILNP-UHFFFAOYSA-N urethane group Chemical group NC(=O)OCC JOYRKODLDBILNP-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)

CA000587510A 1988-01-14 1989-01-04 Materiau a halogenure d'argent pour la photographie en couleurs et methode de production d'images en couleurs au moyen de ce materiau Expired - Lifetime CA1320657C (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP4946/88		1988-01-14
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
CA1320657C true CA1320657C (fr)	1993-07-27

Family

ID=11597738

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000587510A Expired - Lifetime CA1320657C (fr)	1988-01-14	1989-01-04	Materiau a halogenure d'argent pour la photographie en couleurs et methode de production d'images en couleurs au moyen de ce materiau

Country Status (3)

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

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 (fr) *	1994-05-20	2001-02-28	Eastman Kodak Company	Pellicule à contraste bas
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 (fr) *	2005-02-18	2006-08-23	Fuji Photo Film B.V.	Matériau photographique couleur à l' halogénure d' argent sensible à la lumière
DE102024109114A1 (de)	2024-03-28	2025-10-02	Adidas Ag	Schuh, der mit Boden- und Seitenlandebereichen geformt ist, um Bewegung zu führen

Family Cites Families (4)

* 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
JPH07117718B2 (ja) *	1985-02-26	1995-12-18	富士写真フイルム株式会社	カラー写真感光材料
JPH0690463B2 (ja) *	1986-01-08	1994-11-14	富士写真フイルム株式会社	カラ−写真感光材料
JPH0638158B2 (ja) *	1986-05-01	1994-05-18	富士写真フイルム株式会社	ハロゲン化銀カラ−写真感光材料

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

Also Published As

Publication number	Publication date
EP0324471A3 (en)	1990-05-30
JPH01182847A (ja)	1989-07-20
EP0324471A2 (fr)	1989-07-19

Legal Events

Date	Code	Title	Description
2010-07-27	MKEX	Expiry	Effective date: 20100727

Publication	Publication Date	Title
US4626498A (en)	1986-12-02	Color reversal photographic light-sensitive material
US5053324A (en)	1991-10-01	Color photographic light-sensitive materials having red color saturation and improved discrimination of green colors
JPH0347490B2 (fr)	1991-07-19
US5037728A (en)	1991-08-06	Photographic material package unit
JPS62160449A (ja)	1987-07-16	カラ−写真感光材料
US5024925A (en)	1991-06-18	Method of forming color image from a color reversal photographic material comprising a specified iodide content and spectral distribution
US4599301A (en)	1986-07-08	Silver halide color photographic material
US4678743A (en)	1987-07-07	Silver halide color photographic material
US5063146A (en)	1991-11-05	Silver halide photographic material
CA1320657C (fr)	1993-07-27	Materiau a halogenure d'argent pour la photographie en couleurs et methode de production d'images en couleurs au moyen de ce materiau
US4741994A (en)	1988-05-03	Silver halide color photographic material
US5085979A (en)	1992-02-04	Silver halide color photographic materials and processing method
US5166042A (en)	1992-11-24	Silver halide photographic material suitable for use under varying light conditions
US4725529A (en)	1988-02-16	Developing inhibitor arrangment in light-sensitive silver halide color photographic materials
EP0606952A2 (fr)	1994-07-20	Elément d'inversion photographique couleur avec une reproduction en couleur améliorée
US5079132A (en)	1992-01-07	Method for forming a color positive having improved color reproduction
US5578436A (en)	1996-11-26	Silver halide color photographic material
JP2514054B2 (ja)	1996-07-10	カラ―感光材料
US5514527A (en)	1996-05-07	Silver halide color photographic material
JPH0521219B2 (fr)	1993-03-23
EP0428899B1 (fr)	1997-10-01	Utilisation de coupleurs magenta moins tachant
JPH0521218B2 (fr)	1993-03-23
JP2881330B2 (ja)	1999-04-12	色相再現に優れたカラー写真感光材料
JPH01237652A (ja)	1989-09-22	ハロゲン化銀写真感光材料
JPH01237649A (ja)	1989-09-22	ハロゲン化銀カラー写真感光材料