JPH02216147A - 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: JPH02216147A
Authority: JP; Japan
Prior art keywords: silver halide; sample; layer; sensitive; color
Prior art date: 1989-02-17
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

JP3804489A

Other languages

English (en)

Japanese (ja)

Inventor

Satomi Asano

浅野　里美

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.)

1989-02-17

Filing date

1989-02-17

Publication date

1990-08-29

1989-02-17 Application filed by Konica Minolta Inc filed Critical Konica Minolta Inc

1989-02-17 Priority to JP3804489A priority Critical patent/JPH02216147A/ja

1990-02-16 Priority to EP19900301714 priority patent/EP0383623A3/fr

1990-08-29 Publication of JPH02216147A publication Critical patent/JPH02216147A/ja

Status Pending legal-status Critical Current

Links

-1 Silver halide Chemical class 0.000 title claims abstract description 104
229910052709 silver Inorganic materials 0.000 title claims abstract description 64
239000004332 silver Substances 0.000 title claims abstract description 64
239000000463 material Substances 0.000 title claims abstract description 37
239000010410 layer Substances 0.000 claims abstract description 101
239000000839 emulsion Substances 0.000 claims abstract description 69
239000001043 yellow dye Substances 0.000 claims abstract description 17
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 claims abstract description 16
239000002356 single layer Substances 0.000 claims abstract description 14
150000001875 compounds Chemical class 0.000 claims abstract description 11
239000002245 particle Substances 0.000 abstract description 18
238000011161 development Methods 0.000 abstract description 17
238000012545 processing Methods 0.000 abstract description 17
125000003118 aryl group Chemical group 0.000 abstract description 15
125000000217 alkyl group Chemical group 0.000 abstract description 13
239000003112 inhibitor Substances 0.000 abstract description 9
125000001424 substituent group Chemical group 0.000 abstract description 7
125000003545 alkoxy group Chemical group 0.000 abstract description 5
239000000758 substrate Substances 0.000 abstract 1
239000000975 dye Substances 0.000 description 38
230000001235 sensitizing effect Effects 0.000 description 23
108010010803 Gelatin Proteins 0.000 description 21
239000008273 gelatin Substances 0.000 description 21
229920000159 gelatin Polymers 0.000 description 21
235000019322 gelatine Nutrition 0.000 description 21
235000011852 gelatine desserts Nutrition 0.000 description 21
238000003860 storage Methods 0.000 description 19
230000035945 sensitivity Effects 0.000 description 16
239000003795 chemical substances by application Substances 0.000 description 15
230000000694 effects Effects 0.000 description 15
238000000034 method Methods 0.000 description 14
238000006243 chemical reaction Methods 0.000 description 13
239000010408 film Substances 0.000 description 13
239000000203 mixture Substances 0.000 description 13
229910021645 metal ion Inorganic materials 0.000 description 11
229940090898 Desensitizer Drugs 0.000 description 9
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 9
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 9
238000004321 preservation Methods 0.000 description 9
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 6
238000009826 distribution Methods 0.000 description 6
125000004430 oxygen atom Chemical group 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
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
125000000753 cycloalkyl group Chemical group 0.000 description 5
125000000623 heterocyclic group Chemical group 0.000 description 5
230000015572 biosynthetic process Effects 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
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 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
125000004442 acylamino group Chemical group 0.000 description 3
125000003342 alkenyl group Chemical group 0.000 description 3
125000003710 aryl alkyl group Chemical group 0.000 description 3
239000013256 coordination polymer Substances 0.000 description 3
230000008878 coupling Effects 0.000 description 3
238000010168 coupling process Methods 0.000 description 3
238000005859 coupling reaction Methods 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
125000005843 halogen group Chemical group 0.000 description 3
230000006872 improvement Effects 0.000 description 3
229910052740 iodine Inorganic materials 0.000 description 3
239000011630 iodine Substances 0.000 description 3
NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical class C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 3
229910052757 nitrogen Inorganic materials 0.000 description 3
239000000243 solution Substances 0.000 description 3
230000003595 spectral effect Effects 0.000 description 3
239000000126 substance Substances 0.000 description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
108010002352 Interleukin-1 Proteins 0.000 description 2
108010002350 Interleukin-2 Proteins 0.000 description 2
101150004094 PRO2 gene Proteins 0.000 description 2
229960000583 acetic acid Drugs 0.000 description 2
150000008062 acetophenones Chemical class 0.000 description 2
239000002253 acid Substances 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 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
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 2
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 2
238000004061 bleaching Methods 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
238000007796 conventional method Methods 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
238000011033 desalting Methods 0.000 description 2
230000006866 deterioration Effects 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
230000006870 function Effects 0.000 description 2
UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 description 2
150000002367 halogens 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
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
125000004433 nitrogen atom Chemical group N* 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 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
150000003839 salts Chemical class 0.000 description 2
SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 2
230000000087 stabilizing effect Effects 0.000 description 2
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
125000004434 sulfur atom Chemical group 0.000 description 2
230000001629 suppression Effects 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
238000005406 washing Methods 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
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
LMSDCGXQALIMLM-UHFFFAOYSA-N 2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetic acid;iron Chemical compound [Fe].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O LMSDCGXQALIMLM-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
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
229920002284 Cellulose triacetate Polymers 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
MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 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
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
229910052777 Praseodymium Inorganic materials 0.000 description 1
229910052772 Samarium Inorganic materials 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 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
125000004423 acyloxy group Chemical group 0.000 description 1
239000000654 additive Substances 0.000 description 1
229960000643 adenine Drugs 0.000 description 1
125000004656 alkyl sulfonylamino group Chemical group 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
SWLVFNYSXGMGBS-UHFFFAOYSA-N ammonium bromide Chemical compound [NH4+].[Br-] SWLVFNYSXGMGBS-UHFFFAOYSA-N 0.000 description 1
150000003863 ammonium salts Chemical class 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
125000005161 aryl oxy carbonyl group Chemical group 0.000 description 1
125000005110 aryl thio group Chemical group 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
XNSQZBOCSSMHSZ-UHFFFAOYSA-K azane;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxymethyl)amino]acetate;iron(3+) Chemical compound [NH4+].[Fe+3].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O XNSQZBOCSSMHSZ-UHFFFAOYSA-K 0.000 description 1
150000003851 azoles Chemical class 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
239000011230 binding agent Substances 0.000 description 1
230000005540 biological transmission Effects 0.000 description 1
239000007844 bleaching agent Substances 0.000 description 1
229910052793 cadmium Inorganic materials 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
230000008859 change 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
238000010586 diagram Methods 0.000 description 1
125000005117 dialkylcarbamoyl group Chemical group 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
239000006081 fluorescent whitening agent Substances 0.000 description 1
239000012634 fragment Substances 0.000 description 1
235000011389 fruit/vegetable juice Nutrition 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
125000005842 heteroatom Chemical group 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
150000002473 indoazoles Chemical class 0.000 description 1
150000002475 indoles Chemical class 0.000 description 1
239000011229 interlayer Substances 0.000 description 1
229910052741 iridium 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
239000002932 luster Substances 0.000 description 1
239000006224 matting agent Substances 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
PZVFQOBASICMME-UHFFFAOYSA-N n-ethylmethanesulfonamide Chemical compound CCNS(C)(=O)=O PZVFQOBASICMME-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 compound C1=C(O)C=CC2=CC(O)=CC=C21 MNZMMCVIXORAQL-UHFFFAOYSA-N 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
125000001624 naphthyl group Chemical group 0.000 description 1
UOKZUTXLHRTLFH-UHFFFAOYSA-N o-phenylhydroxylamine Chemical class NOC1=CC=CC=C1 UOKZUTXLHRTLFH-UHFFFAOYSA-N 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
229910052762 osmium Inorganic materials 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
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
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
238000002360 preparation method 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
125000005493 quinolyl group Chemical group 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
238000006479 redox reaction Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
229910052706 scandium Inorganic materials 0.000 description 1
230000008313 sensitization 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
159000000000 sodium salts Chemical class 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
239000007787 solid Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
238000010186 staining Methods 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 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
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
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
- 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
- G03C7/30541—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the released group
- 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
- G03C7/3029—Materials characterised by a specific arrangement of layers, e.g. unit layers, or layers having a specific function
- G03C2007/3036—Single layer constitution
- 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
- G03C2200/00—Details
- G03C2200/19—Colour negative
- 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
- G03C7/3029—Materials characterised by a specific arrangement of layers, e.g. unit layers, or layers having a specific function

Landscapes

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

JP3804489A 1989-02-17 1989-02-17 ハロゲン化銀カラー写真感光材料 Pending JPH02216147A (ja)

Priority Applications (2)

Application Number	Priority Date	Filing Date	Title
JP3804489A JPH02216147A (ja)	1989-02-17	1989-02-17	ハロゲン化銀カラー写真感光材料
EP19900301714 EP0383623A3 (fr)	1989-02-17	1990-02-16	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP3804489A JPH02216147A (ja)	1989-02-17	1989-02-17	ハロゲン化銀カラー写真感光材料

Publications (1)

Publication Number	Publication Date
JPH02216147A true JPH02216147A (ja)	1990-08-29

Family

ID=12514533

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP3804489A Pending JPH02216147A (ja)	1989-02-17	1989-02-17	ハロゲン化銀カラー写真感光材料

Country Status (2)

Country	Link
EP (1)	EP0383623A3 (fr)
JP (1)	JPH02216147A (fr)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE69129389T2 (de) *	1990-06-28	1998-10-08	Fuji Photo Film Co Ltd	Photographische Silberhalogenidmaterialien
JP2832394B2 (ja) *	1990-06-28	1998-12-09	富士写真フイルム株式会社	ハロゲン化銀写真感光材料およびイミダゾール誘導体
JPH04152339A (ja) *	1990-10-17	1992-05-26	Fuji Photo Film Co Ltd	ハロゲン化銀カラー写真感光材料
US5399465A (en) *	1993-01-15	1995-03-21	Eastman Kodak Company	Method of processing reversal elements comprising selected development inhibitors and absorber dyes
US5561031A (en) *	1995-03-23	1996-10-01	Eastman Kodak Company	Color reversal elements with incorporated bleach accelerator

Family Cites Families (5)

* 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
US4420555A (en) *	1982-07-19	1983-12-13	Eastman Kodak Company	Photographic materials containing yellow filter dyes
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
EP0280252B1 (fr) *	1987-02-26	1994-01-12	Fuji Photo Film Co., Ltd.	Matériau photographique à l'halogénure d'argent et procédé pour former une image hautement contrastic avec ce matériau
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

1989
- 1989-02-17 JP JP3804489A patent/JPH02216147A/ja active Pending
1990
- 1990-02-16 EP EP19900301714 patent/EP0383623A3/fr not_active Withdrawn

Also Published As

Publication number	Publication date
EP0383623A3 (fr)	1991-06-19
EP0383623A2 (fr)	1990-08-22

Publication	Publication Date	Title
JPH0670709B2 (ja)	1994-09-07	増加した露出ラチチュードを有する写真プリント材料
EP0297804B1 (fr)	1993-08-18	Matériau photographique à l'halogénure d'argent sensible à la lumière
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
JPS5911094B2 (ja)	1984-03-13	ハロゲン化銀写真感光材料
EP0599383B1 (fr)	2001-02-28	Eléments photographiques à l' halogénure d'argent contenant composés colorants substitués par furanne ou pyrrole
JPH02216147A (ja)	1990-08-29	ハロゲン化銀カラー写真感光材料
US3764327A (en)	1973-10-09	Color photographic light sensitive material
JP3391599B2 (ja)	2003-03-31	写真要素および可視画像提供方法
JPH02214856A (ja)	1990-08-27	ハロゲン化銀カラー写真感光材料
JPH0558533B2 (fr)	1993-08-26
JPH0119571B2 (fr)	1989-04-12
JPS62196645A (ja)	1987-08-31	感度・保存性を改良したハロゲン化銀写真感光材料
JPS595238A (ja)	1984-01-12	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
JPH02219056A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH01198749A (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
JPH02219053A (ja)	1990-08-31	ハロゲン化銀カラー写真感光材料
JPH049942A (ja)	1992-01-14	ハロゲン化銀写真乳剤
JPH11133530A (ja)	1999-05-21	ハロゲン化銀写真感光材料及び画像形成方法
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
JPH0690479B2 (ja)	1994-11-14	カブリを低減したハロゲン化銀カラ−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
JPH032286B2 (fr)	1991-01-14
JPH06105344B2 (ja)	1994-12-21	ハロゲン化銀カラ−写真感光材料