JPH02217847A - 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: JPH02217847A
Authority: JP; Japan
Prior art keywords: silver halide; group; general formula; layer; photosensitive
Prior art date: 1989-02-20
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

JP3955089A

Other languages

English (en)

Japanese (ja)

Inventor

Yoshiro Ito

伊東　義郎

Yukio Oya

大矢　行男

Masashi Matsuzaka

松坂　昌司

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.)

Konica Minolta Inc

Original Assignee

Konica Minolta Inc

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.)

1989-02-20

Filing date

1989-02-20

Publication date

1990-08-30

1989-02-20 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1989-02-20 Priority to JP3955089A priority Critical patent/JPH02217847A/ja

1990-02-16 Priority to EP19900301715 priority patent/EP0384671A3/de

1990-08-30 Publication of JPH02217847A publication Critical patent/JPH02217847A/ja

Status Pending legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 95
229910052709 silver Inorganic materials 0.000 title claims abstract description 68
239000004332 silver Substances 0.000 title claims abstract description 67
239000000463 material Substances 0.000 title claims abstract description 33
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims abstract description 66
239000010410 layer Substances 0.000 claims abstract description 65
239000000839 emulsion Substances 0.000 claims abstract description 54
239000002516 radical scavenger Substances 0.000 claims abstract description 14
239000002356 single layer Substances 0.000 claims abstract description 13
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 claims abstract description 5
238000011161 development Methods 0.000 abstract description 23
239000003795 chemical substances by application Substances 0.000 abstract description 16
238000012545 processing Methods 0.000 abstract description 15
238000006243 chemical reaction Methods 0.000 abstract description 11
239000000837 restrainer Substances 0.000 abstract 2
239000007800 oxidant agent Substances 0.000 abstract 1
230000001590 oxidative effect Effects 0.000 abstract 1
239000000975 dye Substances 0.000 description 26
125000000217 alkyl group Chemical group 0.000 description 23
238000000034 method Methods 0.000 description 16
239000002245 particle Substances 0.000 description 16
125000001424 substituent group Chemical group 0.000 description 16
125000004435 hydrogen atom Chemical group [H]* 0.000 description 15
125000003118 aryl group Chemical group 0.000 description 14
239000007864 aqueous solution Substances 0.000 description 13
125000000623 heterocyclic group Chemical group 0.000 description 13
230000035945 sensitivity Effects 0.000 description 12
150000001875 compounds Chemical class 0.000 description 11
239000000243 solution Substances 0.000 description 11
239000007789 gas Substances 0.000 description 10
239000003112 inhibitor Substances 0.000 description 10
229910021645 metal ion Inorganic materials 0.000 description 10
238000004321 preservation Methods 0.000 description 10
125000000753 cycloalkyl group Chemical group 0.000 description 9
230000000694 effects Effects 0.000 description 9
108010010803 Gelatin Proteins 0.000 description 8
239000008273 gelatin Substances 0.000 description 8
229920000159 gelatin Polymers 0.000 description 8
235000019322 gelatine Nutrition 0.000 description 8
235000011852 gelatine desserts Nutrition 0.000 description 8
125000004430 oxygen atom Chemical group O* 0.000 description 8
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 8
239000000203 mixture Substances 0.000 description 7
230000001235 sensitizing effect Effects 0.000 description 7
229940090898 Desensitizer Drugs 0.000 description 6
125000003342 alkenyl group Chemical group 0.000 description 6
239000012298 atmosphere Substances 0.000 description 6
238000009826 distribution Methods 0.000 description 6
125000005843 halogen group Chemical group 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
238000003860 storage Methods 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
125000003545 alkoxy group Chemical group 0.000 description 5
125000003710 aryl alkyl group Chemical group 0.000 description 5
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 5
239000011248 coating agent Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
230000008878 coupling Effects 0.000 description 5
238000010168 coupling process Methods 0.000 description 5
238000005859 coupling reaction Methods 0.000 description 5
PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
206010034972 Photosensitivity reaction Diseases 0.000 description 4
125000004414 alkyl thio group Chemical group 0.000 description 4
125000004429 atom Chemical group 0.000 description 4
125000004432 carbon atom Chemical group C* 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
230000036211 photosensitivity Effects 0.000 description 4
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
125000004442 acylamino group Chemical group 0.000 description 3
125000004453 alkoxycarbonyl group Chemical group 0.000 description 3
125000004390 alkyl sulfonyl group Chemical group 0.000 description 3
125000003277 amino group Chemical group 0.000 description 3
125000005110 aryl thio group Chemical group 0.000 description 3
125000004104 aryloxy group Chemical group 0.000 description 3
125000004093 cyano group Chemical group *C#N 0.000 description 3
125000005842 heteroatom Chemical group 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 3
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 3
230000003595 spectral effect Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
125000004434 sulfur atom Chemical group 0.000 description 3
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
150000008062 acetophenones Chemical class 0.000 description 2
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 2
125000002947 alkylene group Chemical group 0.000 description 2
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
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 2
230000006866 deterioration Effects 0.000 description 2
238000010586 diagram Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000005516 engineering process Methods 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
235000011187 glycerol Nutrition 0.000 description 2
UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
125000002883 imidazolyl group Chemical group 0.000 description 2
150000003949 imides Chemical class 0.000 description 2
QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical class C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 2
239000011630 iodine Substances 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
239000007788 liquid Substances 0.000 description 2
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 2
238000002156 mixing Methods 0.000 description 2
NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical class C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 2
229910052762 osmium Inorganic materials 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
238000001556 precipitation Methods 0.000 description 2
229910052703 rhodium Inorganic materials 0.000 description 2
230000005070 ripening Effects 0.000 description 2
229910052707 ruthenium Inorganic materials 0.000 description 2
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
150000003852 triazoles Chemical class 0.000 description 2
125000001425 triazolyl group Chemical group 0.000 description 2
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
YXIWHUQXZSMYRE-UHFFFAOYSA-N 1,3-benzothiazole-2-thiol Chemical class C1=CC=C2SC(S)=NC2=C1 YXIWHUQXZSMYRE-UHFFFAOYSA-N 0.000 description 1
YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical class C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical class SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 1
LOIUBRXCXMKWFZ-UHFFFAOYSA-J 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;iron(4+) Chemical compound [Fe+4].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O LOIUBRXCXMKWFZ-UHFFFAOYSA-J 0.000 description 1
QPKNFEVLZVJGBM-UHFFFAOYSA-N 2-aminonaphthalen-1-ol Chemical class C1=CC=CC2=C(O)C(N)=CC=C21 QPKNFEVLZVJGBM-UHFFFAOYSA-N 0.000 description 1
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 description 1
CBHTTYDJRXOHHL-UHFFFAOYSA-N 2h-triazolo[4,5-c]pyridazine Chemical class N1=NC=CC2=C1N=NN2 CBHTTYDJRXOHHL-UHFFFAOYSA-N 0.000 description 1
OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical class SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 description 1
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical class NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 1
QGNQEODJYRGEJX-UHFFFAOYSA-N 4h-isoquinoline-1,3-dione Chemical class C1=CC=C2C(=O)NC(=O)CC2=C1 QGNQEODJYRGEJX-UHFFFAOYSA-N 0.000 description 1
GFFGJBXGBJISGV-UHFFFAOYSA-N Adenine Chemical compound NC1=NC=NC2=C1N=CN2 GFFGJBXGBJISGV-UHFFFAOYSA-N 0.000 description 1
229930024421 Adenine Natural products 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-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
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
101150004094 PRO2 gene Proteins 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
241000557758 Tribeles Species 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
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
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
229960000643 adenine Drugs 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Natural products N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 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
229940101006 anhydrous sodium sulfite Drugs 0.000 description 1
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000004391 aryl sulfonyl group Chemical group 0.000 description 1
150000003851 azoles Chemical class 0.000 description 1
QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
229910001864 baryta Inorganic materials 0.000 description 1
150000001556 benzimidazoles Chemical class 0.000 description 1
IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 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
AXMKEYXDFDKKIO-UHFFFAOYSA-N bilane Chemical compound C=1C=C(CC=2NC(CC=3NC=CC=3)=CC=2)NC=1CC1=CC=CN1 AXMKEYXDFDKKIO-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
229910052797 bismuth Inorganic materials 0.000 description 1
125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
125000004181 carboxyalkyl group Chemical group 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
230000001112 coagulating effect Effects 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
238000012937 correction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
238000010612 desalination reaction Methods 0.000 description 1
238000011033 desalting Methods 0.000 description 1
KYQODXQIAJFKPH-UHFFFAOYSA-N diazanium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [NH4+].[NH4+].OC(=O)CN(CC([O-])=O)CCN(CC(O)=O)CC([O-])=O KYQODXQIAJFKPH-UHFFFAOYSA-N 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000006073 displacement reaction Methods 0.000 description 1
239000006081 fluorescent whitening agent Substances 0.000 description 1
125000004005 formimidoyl group Chemical group [H]\N=C(/[H])* 0.000 description 1
239000012634 fragment Substances 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
150000002366 halogen compounds Chemical class 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
125000001183 hydrocarbyl group Chemical group 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
AKCUHGBLDXXTOM-UHFFFAOYSA-N hydroxy-oxo-phenyl-sulfanylidene-$l^{6}-sulfane Chemical class SS(=O)(=O)C1=CC=CC=C1 AKCUHGBLDXXTOM-UHFFFAOYSA-N 0.000 description 1
150000002473 indoazoles Chemical class 0.000 description 1
150000002475 indoles Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
229910052741 iridium Inorganic materials 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000006224 matting agent Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
125000002950 monocyclic group Chemical group 0.000 description 1
LDEGHVGGILPJGN-UHFFFAOYSA-N n'-phenylpropanediamide Chemical class NC(=O)CC(=O)NC1=CC=CC=C1 LDEGHVGGILPJGN-UHFFFAOYSA-N 0.000 description 1
PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical class C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 description 1
MNZMMCVIXORAQL-UHFFFAOYSA-N naphthalene-2,6-diol Chemical class C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
150000007523 nucleic acids Chemical class 0.000 description 1
102000039446 nucleic acids Human genes 0.000 description 1
108020004707 nucleic acids Proteins 0.000 description 1
UOKZUTXLHRTLFH-UHFFFAOYSA-N o-phenylhydroxylamine Chemical class NOC1=CC=CC=C1 UOKZUTXLHRTLFH-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical class SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 1
150000003232 pyrogallols Chemical class 0.000 description 1
GZTPJDLYPMPRDF-UHFFFAOYSA-N pyrrolo[3,2-c]pyrazole Chemical class N1=NC2=CC=NC2=C1 GZTPJDLYPMPRDF-UHFFFAOYSA-N 0.000 description 1
125000005493 quinolyl group Chemical group 0.000 description 1
238000006479 redox reaction Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052706 scandium Inorganic materials 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
HAAYBYDROVFKPU-UHFFFAOYSA-N silver;azane;nitrate Chemical compound N.N.[Ag+].[O-][N+]([O-])=O HAAYBYDROVFKPU-UHFFFAOYSA-N 0.000 description 1
HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 1
AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
235000019345 sodium thiosulphate Nutrition 0.000 description 1
NASFKTWZWDYFER-UHFFFAOYSA-N sodium;hydrate Chemical compound O.[Na] NASFKTWZWDYFER-UHFFFAOYSA-N 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
125000005504 styryl group Chemical group 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
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
229920001059 synthetic polymer Polymers 0.000 description 1
JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical class SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000005323 thioketone group Chemical group 0.000 description 1
229910052727 yttrium Inorganic materials 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/392—Additives
- G03C7/39208—Organic compounds
- 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

Landscapes

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

JP3955089A 1989-02-20 1989-02-20 ハロゲン化銀カラー写真感光材料 Pending JPH02217847A (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP3955089A JPH02217847A (ja)	1989-02-20	1989-02-20	ハロゲン化銀カラー写真感光材料
EP19900301715 EP0384671A3 (de)	1989-02-20	1990-02-16	Lichtempfindliches farbphotographisches Silberhalogenidmaterial

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP3955089A JPH02217847A (ja)	1989-02-20	1989-02-20	ハロゲン化銀カラー写真感光材料

Publications (1)

Publication Number	Publication Date
JPH02217847A true JPH02217847A (ja)	1990-08-30

Family

ID=12556168

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP3955089A Pending JPH02217847A (ja)	1989-02-20	1989-02-20	ハロゲン化銀カラー写真感光材料

Country Status (2)

Country	Link
EP (1)	EP0384671A3 (de)
JP (1)	JPH02217847A (de)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0566531A (ja) *	1991-09-05	1993-03-19	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH04256954A (ja) *	1991-02-08	1992-09-11	Konica Corp	色相再現性にすぐれたハロゲン化銀カラー写真感光材料

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5810738A (ja) *	1981-07-13	1983-01-21	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−感光材料
JPS6254259A (ja) *	1985-05-13	1987-03-09	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料とその処理方法
JPS63259650A (ja) *	1987-04-17	1988-10-26	Konica Corp	色素汚染等が改良されたハロゲン化銀写真感光材料

1989
- 1989-02-20 JP JP3955089A patent/JPH02217847A/ja active Pending
1990
- 1990-02-16 EP EP19900301715 patent/EP0384671A3/de not_active Withdrawn

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0566531A (ja) *	1991-09-05	1993-03-19	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料

Also Published As

Publication number	Publication date
EP0384671A3 (de)	1991-07-17
EP0384671A2 (de)	1990-08-29

Publication	Publication Date	Title
US4472496A (en)	1984-09-18	Process for preparing silver halide emulsion
JPH0654375B2 (ja)	1994-07-20	カラ−画像形成法
JPH0656483B2 (ja)	1994-07-27	カラ−画像形成法
JPH01105940A (ja)	1989-04-24	ハロゲン化銀写真感光材料
JPS6365441A (ja)	1988-03-24	ハロゲン化銀カラ−写真感光材料の処理方法
JPS59109055A (ja)	1984-06-23	ハロゲン化銀写真感光材料
US4780403A (en)	1988-10-25	Silver halide color photographic material containing disulfide type bleach accelerator
JPH0754404B2 (ja)	1995-06-07	カラ−画像形成方法
JPS63234244A (ja)	1988-09-29	ハロゲン化銀写真感光材料
US4741990A (en)	1988-05-03	Method for processing silver halide photographic light-sensitive materials
JPH0786666B2 (ja)	1995-09-20	ハロゲン化銀写真感光材料
US5011768A (en)	1991-04-30	Silver halide photographic material
JPH02217847A (ja)	1990-08-30	ハロゲン化銀カラー写真感光材料
US4952488A (en)	1990-08-28	Silver halide color photographic material and processing process therefor
US4946772A (en)	1990-08-07	Silver halide emulsions and photographic materials
JPH0786664B2 (ja)	1995-09-20	ハロゲン化銀写真感光材料
EP0204530B1 (de)	1991-09-11	Verfahren zur Herstellung eines direkt positiven Farbbildes
JPH02216147A (ja)	1990-08-29	ハロゲン化銀カラー写真感光材料
JPH02217846A (ja)	1990-08-30	ハロゲン化銀カラー写真感光材料
JPH02220051A (ja)	1990-09-03	ハロゲン化銀カラー写真感光材料の処理方法
JPH10307363A (ja)	1998-11-17	ポリ（アルキレンオキシド）を含むハロゲン化銀写真要素
JPH02214856A (ja)	1990-08-27	ハロゲン化銀カラー写真感光材料
US5376514A (en)	1994-12-27	Silver halide photosensitive materials
JPH02219053A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH0652412B2 (ja)	1994-07-06	迅速処理可能なハロゲン化銀カラ−写真感光材料

JPH02217847A - ハロゲン化銀カラー写真感光材料 - Google Patents

Info

Links

Classifications

Landscapes

Priority Applications (2)

Applications Claiming Priority (1)

Publications (1)

Family

ID=12556168

Family Applications (1)

Country Status (2)

Cited By (1)

Families Citing this family (1)

Family Cites Families (3)

Cited By (1)

Also Published As

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