JPH02214856A - 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: JPH02214856A
Authority: JP; Japan
Prior art keywords: group; silver halide; dsr; sample; layer
Prior art date: 1989-02-16
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

JP3699589A

Other languages

English (en)

Japanese (ja)

Inventor

Hiroshi Okusa

洋大草

Shigeto Hirabayashi

茂人平林

Yukio Oya

大矢　行男

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.)

1989-02-16

Filing date

1989-02-16

Publication date

1990-08-27

1989-02-16 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1989-02-16 Priority to JP3699589A priority Critical patent/JPH02214856A/ja

1990-02-16 Priority to EP19900301756 priority patent/EP0383637A3/de

1990-08-27 Publication of JPH02214856A publication Critical patent/JPH02214856A/ja

Status Pending legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 112
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 31
239000010410 layer Substances 0.000 claims abstract description 97
239000000839 emulsion Substances 0.000 claims abstract description 82
150000001875 compounds Chemical class 0.000 claims abstract description 39
239000003795 chemical substances by application Substances 0.000 claims abstract description 30
239000002356 single layer Substances 0.000 claims abstract description 15
239000002243 precursor Substances 0.000 claims abstract description 9
230000003647 oxidation Effects 0.000 claims abstract description 4
238000007254 oxidation reaction Methods 0.000 claims abstract description 4
230000002000 scavenging effect Effects 0.000 claims abstract description 4
230000035945 sensitivity Effects 0.000 abstract description 26
238000012545 processing Methods 0.000 abstract description 22
230000008859 change Effects 0.000 abstract description 4
239000000758 substrate Substances 0.000 abstract 1
239000000975 dye Substances 0.000 description 42
108010010803 Gelatin Proteins 0.000 description 25
239000008273 gelatin Substances 0.000 description 25
229920000159 gelatin Polymers 0.000 description 25
235000019322 gelatine Nutrition 0.000 description 25
235000011852 gelatine desserts Nutrition 0.000 description 25
125000000217 alkyl group Chemical group 0.000 description 22
125000003118 aryl group Chemical group 0.000 description 21
238000011161 development Methods 0.000 description 20
230000001235 sensitizing effect Effects 0.000 description 20
238000006243 chemical reaction Methods 0.000 description 16
238000000034 method Methods 0.000 description 16
239000002245 particle Substances 0.000 description 15
230000000694 effects Effects 0.000 description 14
239000000203 mixture Substances 0.000 description 14
229940090898 Desensitizer Drugs 0.000 description 13
238000005859 coupling reaction Methods 0.000 description 12
239000010408 film Substances 0.000 description 12
125000000623 heterocyclic group Chemical group 0.000 description 11
238000003860 storage Methods 0.000 description 11
125000004442 acylamino group Chemical group 0.000 description 10
239000007864 aqueous solution Substances 0.000 description 10
239000003112 inhibitor Substances 0.000 description 10
229910021645 metal ion Inorganic materials 0.000 description 10
125000004432 carbon atom Chemical group C* 0.000 description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 description 9
238000004321 preservation Methods 0.000 description 9
125000003545 alkoxy group Chemical group 0.000 description 8
230000008878 coupling Effects 0.000 description 8
238000010168 coupling process Methods 0.000 description 8
125000001424 substituent group Chemical group 0.000 description 8
101000749364 Rattus norvegicus V-type proton ATPase subunit e 1 Proteins 0.000 description 7
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 7
125000005843 halogen group Chemical group 0.000 description 7
125000004430 oxygen atom Chemical group O* 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
238000009826 distribution Methods 0.000 description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 6
125000000565 sulfonamide group Chemical group 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 5
239000011248 coating agent Substances 0.000 description 5
238000000576 coating method Methods 0.000 description 5
125000004093 cyano group Chemical group *C#N 0.000 description 5
125000000753 cycloalkyl group Chemical group 0.000 description 5
239000002516 radical scavenger Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
125000003342 alkenyl group Chemical group 0.000 description 4
125000004453 alkoxycarbonyl group Chemical group 0.000 description 4
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 4
238000004040 coloring Methods 0.000 description 4
238000004519 manufacturing process Methods 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
238000006479 redox reaction Methods 0.000 description 4
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 4
239000003381 stabilizer Substances 0.000 description 4
239000006097 ultraviolet radiation absorber Substances 0.000 description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
125000003277 amino group Chemical group 0.000 description 3
238000004061 bleaching Methods 0.000 description 3
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
230000006866 deterioration Effects 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000011630 iodine Substances 0.000 description 3
125000004433 nitrogen atom Chemical group N* 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000007639 printing Methods 0.000 description 3
239000002904 solvent Substances 0.000 description 3
230000003595 spectral effect Effects 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
JVXHQHGWBAHSSF-UHFFFAOYSA-L 2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate;hydron;iron(2+) Chemical compound [H+].[H+].[Fe+2].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O JVXHQHGWBAHSSF-UHFFFAOYSA-L 0.000 description 2
108010002352 Interleukin-1 Proteins 0.000 description 2
108010002350 Interleukin-2 Proteins 0.000 description 2
DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical group NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 description 2
101150004094 PRO2 gene Proteins 0.000 description 2
206010070834 Sensitisation Diseases 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 2
125000004390 alkyl sulfonyl group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
125000005281 alkyl ureido group Chemical group 0.000 description 2
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
125000003710 aryl alkyl group Chemical group 0.000 description 2
125000001769 aryl amino group Chemical group 0.000 description 2
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
239000003638 chemical reducing agent Substances 0.000 description 2
239000000470 constituent Substances 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
239000013256 coordination polymer Substances 0.000 description 2
238000011033 desalting Methods 0.000 description 2
238000001035 drying Methods 0.000 description 2
238000005516 engineering process Methods 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
125000005842 heteroatom Chemical group 0.000 description 2
229910052741 iridium Inorganic materials 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
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 2
150000007523 nucleic acids Chemical class 0.000 description 2
102000039446 nucleic acids Human genes 0.000 description 2
108020004707 nucleic acids Proteins 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
230000008569 process Effects 0.000 description 2
239000011241 protective layer Substances 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
230000008313 sensitization Effects 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000004434 sulfur atom Chemical group 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
230000002747 voluntary effect Effects 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
ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical class O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 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
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
CNGYZEMWVAWWOB-VAWYXSNFSA-N 5-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-[(e)-2-[4-[[4-anilino-6-[bis(2-hydroxyethyl)amino]-1,3,5-triazin-2-yl]amino]-2-sulfophenyl]ethenyl]benzenesulfonic acid Chemical compound N=1C(NC=2C=C(C(\C=C\C=3C(=CC(NC=4N=C(N=C(NC=5C=CC=CC=5)N=4)N(CCO)CCO)=CC=3)S(O)(=O)=O)=CC=2)S(O)(=O)=O)=NC(N(CCO)CCO)=NC=1NC1=CC=CC=C1 CNGYZEMWVAWWOB-VAWYXSNFSA-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
VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
101100129750 Arabidopsis thaliana MDN1 gene Proteins 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
101000622010 Crotalus atrox Snake venom metalloproteinase atrolysin-B Proteins 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
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
241001024304 Mino Species 0.000 description 1
125000005118 N-alkylcarbamoyl group Chemical group 0.000 description 1
229910002651 NO3 Inorganic materials 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
101100049029 Rattus norvegicus Atp6v0e1 gene Proteins 0.000 description 1
101100327317 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CDC1 gene Proteins 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-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
241000557758 Tribeles Species 0.000 description 1
229910052769 Ytterbium Inorganic materials 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
150000008062 acetophenones Chemical class 0.000 description 1
239000008186 active pharmaceutical agent Substances 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
239000000654 additive Substances 0.000 description 1
229960000643 adenine Drugs 0.000 description 1
239000012670 alkaline solution Substances 0.000 description 1
125000004422 alkyl sulphonamide group Chemical group 0.000 description 1
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
235000011114 ammonium hydroxide 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
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
125000005264 aryl amine group Chemical group 0.000 description 1
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000004421 aryl sulphonamide group Chemical group 0.000 description 1
125000005110 aryl thio group Chemical group 0.000 description 1
125000004429 atom 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
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical class C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
229910052797 bismuth 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
229920002301 cellulose acetate Polymers 0.000 description 1
238000003776 cleavage reaction Methods 0.000 description 1
230000001112 coagulating effect Effects 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
230000000052 comparative effect Effects 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
238000009792 diffusion process Methods 0.000 description 1
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000010419 fine particle Substances 0.000 description 1
239000012634 fragment Substances 0.000 description 1
230000006870 function Effects 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
239000012362 glacial acetic acid Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
150000004820 halides Chemical class 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
125000002883 imidazolyl group Chemical group 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
230000006872 improvement Effects 0.000 description 1
150000002473 indoazoles Chemical class 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000011229 interlayer Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
230000000873 masking effect Effects 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
238000002156 mixing Methods 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
NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical class C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-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
UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
238000007344 nucleophilic reaction Methods 0.000 description 1
238000010534 nucleophilic substitution reaction Methods 0.000 description 1
125000002971 oxazolyl group Chemical group 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
230000000737 periodic effect Effects 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000005328 phosphinyl group Chemical group [PH2](=O)* 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 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
239000004848 polyfunctional curative Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
LUMVCLJFHCTMCV-UHFFFAOYSA-M potassium;hydroxide;hydrate Chemical compound O.[OH-].[K+] LUMVCLJFHCTMCV-UHFFFAOYSA-M 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 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
238000011160 research Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000007017 scission Effects 0.000 description 1
229910001961 silver nitrate 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
230000000087 stabilizing effect Effects 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical group O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 1
125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000725 suspension Substances 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
239000010409 thin film Substances 0.000 description 1
125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 description 1
125000005323 thioketone group Chemical group 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
238000005406 washing Methods 0.000 description 1
229910052727 yttrium 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
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30594—Combination of substances liberating photographically active agents
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers

Landscapes

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

JP3699589A 1989-02-16 1989-02-16 ハロゲン化銀カラー写真感光材料 Pending JPH02214856A (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP3699589A JPH02214856A (ja)	1989-02-16	1989-02-16	ハロゲン化銀カラー写真感光材料
EP19900301756 EP0383637A3 (de)	1989-02-16	1990-02-16	Lichtempfindliches farbphotographisches Silberhalogenidmaterial

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP3699589A JPH02214856A (ja)	1989-02-16	1989-02-16	ハロゲン化銀カラー写真感光材料

Publications (1)

Publication Number	Publication Date
JPH02214856A true JPH02214856A (ja)	1990-08-27

Family

ID=12485318

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP3699589A Pending JPH02214856A (ja)	1989-02-16	1989-02-16	ハロゲン化銀カラー写真感光材料

Country Status (2)

Country	Link
EP (1)	EP0383637A3 (de)
JP (1)	JPH02214856A (de)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5932407A (en) *	1997-04-30	1999-08-03	Eastman Kodak Company	Color photographic element containing oxidized developer-scavenging naphtholic coupler forming wash-out dye
US6130032A (en) *	1997-09-26	2000-10-10	Eastman Kodak Company	Photographic elements containing improved yellow dye-forming couplers
WO2020102195A1 (en)	2018-11-13	2020-05-22	Biotheryx, Inc.	Substituted isoindolinones

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2708466A1 (de) *	1977-02-26	1978-08-31	Agfa Gevaert Ag	Emulsionsabmischungen fuer colorumkehr-(aufsichts-)material
JP2530164B2 (ja) *	1987-02-05	1996-09-04	コニカ株式会社	鮮鋭性及び粒状性の改良されたハロゲン化銀カラ−写真感光材料
JPH0192747A (ja) *	1987-06-15	1989-04-12	Fuji Photo Film Co Ltd	ハロゲン化銀カラ−写真感光材料
EP0297836A3 (en) *	1987-06-30	1990-01-10	Konica Corporation	Silver halide light-sensitive color photographic material excellent in the color reproducibility and method for processing the same

1989
- 1989-02-16 JP JP3699589A patent/JPH02214856A/ja active Pending
1990
- 1990-02-16 EP EP19900301756 patent/EP0383637A3/de not_active Withdrawn

Also Published As

Publication number	Publication date
EP0383637A3 (de)	1991-06-12
EP0383637A2 (de)	1990-08-22

Publication	Publication Date	Title
JPH07119976B2 (ja)	1995-12-20	迅速処理可能でカブリ防止効果等にすぐれるハロゲン化銀カラ−写真感光材料
JPH01131555A (ja)	1989-05-24	ネガ型ハロゲン化銀カラー写真感光材料
JPH02214856A (ja)	1990-08-27	ハロゲン化銀カラー写真感光材料
JPH02216147A (ja)	1990-08-29	ハロゲン化銀カラー写真感光材料
JP2517294B2 (ja)	1996-07-24	湿度変化による感度の変動が改良されたハロゲン化銀写真感光材料
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
JPS63292126A (ja)	1988-11-29	高感度かつ階調性が改良されたハロゲン化銀写真乳剤の製造方法
JP3485210B2 (ja)	2004-01-13	ハロゲン化銀乳剤
JP2603066B2 (ja)	1997-04-23	ハロゲン化銀写真感光材料
JPS63142352A (ja)	1988-06-14	粒状性及び鮮鋭性の改良されたハロゲン化銀カラ−写真感光材料
JP2514325B2 (ja)	1996-07-10	粒状性、保存性の改良されたハロゲン化銀写真感光材料
JP3408251B2 (ja)	2003-05-19	ハロゲン化銀写真感光材料
JP2896937B2 (ja)	1999-05-31	ハロゲン化銀写真用カブリ抑制剤
JPH02217846A (ja)	1990-08-30	ハロゲン化銀カラー写真感光材料
JP2694069B2 (ja)	1997-12-24	ハロゲン化銀写真感光材料
JPH02219048A (ja)	1990-08-31	撮影機能を賦与した写真感光材料包装ユニット
JP2663349B2 (ja)	1997-10-15	カブリ抑制剤を含有するハロゲン化銀写真感光材料
JPH02219053A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH02219047A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH02219054A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH06175258A (ja)	1994-06-24	ハロゲン化銀写真感光材料
JPH07111557B2 (ja)	1995-11-29	ハロゲン化銀写真感光材料
JPH0785167B2 (ja)	1995-09-13	ハロゲン化銀カラ−写真感光材料の処理方法
JPH05333468A (ja)	1993-12-17	ハロゲン化銀写真感光材料
JPH01198753A (ja)	1989-08-10	ハロゲン化銀カラー反転反射プリント感光材料