DE69401682T2 - Farbphotographisches Silberhalogenidmaterial - Google Patents
Farbphotographisches SilberhalogenidmaterialInfo
- Publication number
- DE69401682T2 DE69401682T2 DE69401682T DE69401682T DE69401682T2 DE 69401682 T2 DE69401682 T2 DE 69401682T2 DE 69401682 T DE69401682 T DE 69401682T DE 69401682 T DE69401682 T DE 69401682T DE 69401682 T2 DE69401682 T2 DE 69401682T2
- Authority
- DE
- Germany
- Prior art keywords
- group
- aryl
- alkyl
- heterocyclic
- silver halide
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- -1 silver halide Chemical class 0.000 title claims description 244
- 229910052709 silver Inorganic materials 0.000 title claims description 77
- 239000004332 silver Substances 0.000 title claims description 77
- 239000000463 material Substances 0.000 title claims description 74
- 239000000839 emulsion Substances 0.000 claims description 73
- 125000004432 carbon atom Chemical group C* 0.000 claims description 71
- 125000003118 aryl group Chemical group 0.000 claims description 66
- 125000000217 alkyl group Chemical group 0.000 claims description 64
- 150000001875 compounds Chemical class 0.000 claims description 61
- 125000000623 heterocyclic group Chemical group 0.000 claims description 41
- 125000001424 substituent group Chemical group 0.000 claims description 34
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 125000004429 atom Chemical group 0.000 claims description 13
- 125000005843 halogen group Chemical group 0.000 claims description 13
- 125000003545 alkoxy group Chemical group 0.000 claims description 10
- 230000003647 oxidation Effects 0.000 claims description 10
- 238000007254 oxidation reaction Methods 0.000 claims description 10
- 125000004104 aryloxy group Chemical group 0.000 claims description 9
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 6
- 229910052755 nonmetal Inorganic materials 0.000 claims description 6
- 125000004450 alkenylene group Chemical group 0.000 claims description 5
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 5
- 238000005859 coupling reaction Methods 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000003808 silyl group Chemical class [H][Si]([H])([H])[*] 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003368 amide group Chemical group 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 125000004185 ester group Chemical group 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims description 3
- 229910052710 silicon Inorganic materials 0.000 claims description 3
- 150000002843 nonmetals Chemical group 0.000 claims description 2
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 2
- 125000004442 acylamino group Chemical group 0.000 claims 4
- 125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 claims 4
- 125000004423 acyloxy group Chemical group 0.000 claims 3
- 125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 claims 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 3
- 125000000565 sulfonamide group Chemical group 0.000 claims 3
- 125000004149 thio group Chemical group *S* 0.000 claims 3
- 125000002252 acyl group Chemical group 0.000 claims 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 2
- 125000001769 aryl amino group Chemical group 0.000 claims 2
- 125000003943 azolyl group Chemical group 0.000 claims 2
- 125000005499 phosphonyl group Chemical group 0.000 claims 2
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims 2
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 claims 1
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims 1
- 125000005200 aryloxy carbonyloxy group Chemical group 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000010410 layer Substances 0.000 description 106
- 239000003381 stabilizer Substances 0.000 description 40
- 239000000975 dye Substances 0.000 description 37
- 239000002904 solvent Substances 0.000 description 35
- 239000000203 mixture Substances 0.000 description 33
- 239000003795 chemical substances by application Substances 0.000 description 32
- 229920000159 gelatin Polymers 0.000 description 25
- 235000019322 gelatine Nutrition 0.000 description 25
- 238000000034 method Methods 0.000 description 25
- 108010010803 Gelatin Proteins 0.000 description 22
- 239000008273 gelatin Substances 0.000 description 22
- 235000011852 gelatine desserts Nutrition 0.000 description 22
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 16
- 230000001235 sensitizing effect Effects 0.000 description 16
- 238000012545 processing Methods 0.000 description 13
- 150000003254 radicals Chemical class 0.000 description 13
- 238000009826 distribution Methods 0.000 description 12
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 10
- 229910021612 Silver iodide Inorganic materials 0.000 description 10
- 229920001577 copolymer Polymers 0.000 description 10
- 238000002156 mixing Methods 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 229940045105 silver iodide Drugs 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- 229910021607 Silver chloride Inorganic materials 0.000 description 8
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 8
- 238000004040 coloring Methods 0.000 description 8
- 238000002845 discoloration Methods 0.000 description 8
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 8
- 238000009835 boiling Methods 0.000 description 7
- 239000002612 dispersion medium Substances 0.000 description 7
- 239000003960 organic solvent Substances 0.000 description 7
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 7
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 6
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 150000005840 aryl radicals Chemical class 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 6
- 238000005406 washing Methods 0.000 description 6
- 101100221809 Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) cpd-7 gene Proteins 0.000 description 5
- 239000004698 Polyethylene Substances 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 229920000573 polyethylene Polymers 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 4
- 238000005562 fading Methods 0.000 description 4
- 239000004816 latex Substances 0.000 description 4
- 229920000126 latex Polymers 0.000 description 4
- 239000011591 potassium Substances 0.000 description 4
- 229910052700 potassium Inorganic materials 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 4
- KKFDJZZADQONDE-UHFFFAOYSA-N (hydridonitrato)hydroxidocarbon(.) Chemical compound O[C]=N KKFDJZZADQONDE-UHFFFAOYSA-N 0.000 description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 3
- 239000001828 Gelatine Substances 0.000 description 3
- 206010070834 Sensitisation Diseases 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000008033 biological extinction Effects 0.000 description 3
- ZEUDGVUWMXAXEF-UHFFFAOYSA-L bromo(chloro)silver Chemical compound Cl[Ag]Br ZEUDGVUWMXAXEF-UHFFFAOYSA-L 0.000 description 3
- OIPQUBBCOVJSNS-UHFFFAOYSA-L bromo(iodo)silver Chemical compound Br[Ag]I OIPQUBBCOVJSNS-UHFFFAOYSA-L 0.000 description 3
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 239000000084 colloidal system Substances 0.000 description 3
- 230000001808 coupling effect Effects 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000000539 dimer Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 3
- 235000019341 magnesium sulphate Nutrition 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000002994 raw material Substances 0.000 description 3
- 230000008313 sensitization Effects 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical group O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000012463 white pigment Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 description 2
- WMVJWKURWRGJCI-UHFFFAOYSA-N 2,4-bis(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC=C(O)C(C(C)(C)CC)=C1 WMVJWKURWRGJCI-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- CWNSVVHTTQBGQB-UHFFFAOYSA-N N,N-Diethyldodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CC)CC CWNSVVHTTQBGQB-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 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 2
- ZFOZVQLOBQUTQQ-UHFFFAOYSA-N Tributyl citrate Chemical compound CCCCOC(=O)CC(O)(C(=O)OCCCC)CC(=O)OCCCC ZFOZVQLOBQUTQQ-UHFFFAOYSA-N 0.000 description 2
- IEIREBQISNYNTN-UHFFFAOYSA-K [Ag](I)(Br)Cl Chemical compound [Ag](I)(Br)Cl IEIREBQISNYNTN-UHFFFAOYSA-K 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 230000002421 anti-septic effect Effects 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 2
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- FKRCODPIKNYEAC-UHFFFAOYSA-N ethyl propionate Chemical compound CCOC(=O)CC FKRCODPIKNYEAC-UHFFFAOYSA-N 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- PANJMBIFGCKWBY-UHFFFAOYSA-N iron tricyanide Chemical compound N#C[Fe](C#N)C#N PANJMBIFGCKWBY-UHFFFAOYSA-N 0.000 description 2
- 150000002688 maleic acid derivatives Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 239000011241 protective layer Substances 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- OLRJXMHANKMLTD-UHFFFAOYSA-N silyl Chemical class [SiH3] OLRJXMHANKMLTD-UHFFFAOYSA-N 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- VXUYXOFXAQZZMF-UHFFFAOYSA-N titanium(IV) isopropoxide Chemical compound CC(C)O[Ti](OC(C)C)(OC(C)C)OC(C)C VXUYXOFXAQZZMF-UHFFFAOYSA-N 0.000 description 2
- 125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 2
- 125000001425 triazolyl group Chemical group 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- IAUKWGFWINVWKS-UHFFFAOYSA-N 1,2-di(propan-2-yl)naphthalene Chemical compound C1=CC=CC2=C(C(C)C)C(C(C)C)=CC=C21 IAUKWGFWINVWKS-UHFFFAOYSA-N 0.000 description 1
- AMBLIDWNRBBNHW-UHFFFAOYSA-N 1,3-dichloro-5-hydroxy-1,3,5-triazinane;sodium Chemical compound [Na].ON1CN(Cl)CN(Cl)C1 AMBLIDWNRBBNHW-UHFFFAOYSA-N 0.000 description 1
- VDFVNEFVBPFDSB-UHFFFAOYSA-N 1,3-dioxane Chemical group C1COCOC1 VDFVNEFVBPFDSB-UHFFFAOYSA-N 0.000 description 1
- OZFIGURLAJSLIR-UHFFFAOYSA-N 1-ethenyl-2h-pyridine Chemical compound C=CN1CC=CC=C1 OZFIGURLAJSLIR-UHFFFAOYSA-N 0.000 description 1
- ALAVMPYROHSFFR-UHFFFAOYSA-N 1-methyl-3-[3-(5-sulfanylidene-2h-tetrazol-1-yl)phenyl]urea Chemical compound CNC(=O)NC1=CC=CC(N2C(=NN=N2)S)=C1 ALAVMPYROHSFFR-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
- ZFYKDNCOQBBOST-UHFFFAOYSA-N 1-phenylbut-3-en-1-one Chemical compound C=CCC(=O)C1=CC=CC=C1 ZFYKDNCOQBBOST-UHFFFAOYSA-N 0.000 description 1
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 description 1
- RWKSBJVOQGKDFZ-UHFFFAOYSA-N 16-methylheptadecyl 2-hydroxypropanoate Chemical compound CC(C)CCCCCCCCCCCCCCCOC(=O)C(C)O RWKSBJVOQGKDFZ-UHFFFAOYSA-N 0.000 description 1
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 1
- ATCRIUVQKHMXSH-UHFFFAOYSA-M 2,4-dichlorobenzoate Chemical compound [O-]C(=O)C1=CC=C(Cl)C=C1Cl ATCRIUVQKHMXSH-UHFFFAOYSA-M 0.000 description 1
- AXCGIKGRPLMUDF-UHFFFAOYSA-N 2,6-dichloro-1h-1,3,5-triazin-4-one;sodium Chemical compound [Na].OC1=NC(Cl)=NC(Cl)=N1 AXCGIKGRPLMUDF-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
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- 230000003746 surface roughness Effects 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- NJPOTNJJCSJJPJ-UHFFFAOYSA-N tributyl benzene-1,3,5-tricarboxylate Chemical compound CCCCOC(=O)C1=CC(C(=O)OCCCC)=CC(C(=O)OCCCC)=C1 NJPOTNJJCSJJPJ-UHFFFAOYSA-N 0.000 description 1
- IELLVVGAXDLVSW-UHFFFAOYSA-N tricyclohexyl phosphate Chemical compound C1CCCCC1OP(OC1CCCCC1)(=O)OC1CCCCC1 IELLVVGAXDLVSW-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- OHRVKCZTBPSUIK-UHFFFAOYSA-N tridodecyl phosphate Chemical compound CCCCCCCCCCCCOP(=O)(OCCCCCCCCCCCC)OCCCCCCCCCCCC OHRVKCZTBPSUIK-UHFFFAOYSA-N 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ZOPCDOGRWDSSDQ-UHFFFAOYSA-N trinonyl phosphate Chemical compound CCCCCCCCCOP(=O)(OCCCCCCCCC)OCCCCCCCCC ZOPCDOGRWDSSDQ-UHFFFAOYSA-N 0.000 description 1
- APVVRLGIFCYZHJ-UHFFFAOYSA-N trioctyl 2-hydroxypropane-1,2,3-tricarboxylate Chemical compound CCCCCCCCOC(=O)CC(O)(C(=O)OCCCCCCCC)CC(=O)OCCCCCCCC APVVRLGIFCYZHJ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical group OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- 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
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
- G03C7/38—Couplers containing compounds with active methylene groups in rings
- G03C7/381—Heterocyclic compounds
- G03C7/382—Heterocyclic compounds with two heterocyclic rings
- G03C7/3825—Heterocyclic compounds with two heterocyclic rings the nuclei containing only nitrogen as hetero atoms
- G03C7/383—Heterocyclic compounds with two heterocyclic rings the nuclei containing only nitrogen as hetero atoms three nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Claims (19)
1. Farbphotographisches Silberhalogenidmaterial mit einem
Träger und mindestens einer darauf aufgebrachten Schicht, die
mindestens einen Cyankuppler enthält, dargestellt durch
Formel (I)
worin R&sub1; und R&sub2; jeweils einen Substituenten außer einer
Methylgruppe bedeuten
R&sub3;, R&sub4;, R&sub5; und R&sub6; bedeuten jeweils ein Wasserstoffatom oder
einen Substituenten,
Z bedeutet ein Nichtmetallatom oder eine Gruppe aus
Nichtmetallatomen, die erforderlich sind, um einen Ring zu
bilden, und die Gruppe aus Nichtmetallatomen von Z kann
wahlweise mit mindestens einem Substituenten substituiert sein,
und
X bedeutet ein Wasserstoffatom oder eine Gruppe, die von
der Verbindung bei einer Kupplungsreaktion mit einem
Oxidationsprodukt eines Farbentwicklers auf der Basis eines
aromatischen primären Amins abgespalten werden kann.
2. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin R&sub1; und R&sub2; jeweils ein Halogenatom, eine
aliphatische Gruppe mit 2 bis 30 Kohlenstoffatomen, eine
Arylgruppe,
eine heterocyclische Gruppe, eine Alkoxygruppe, eine
Aryloxygruppe, eine heterocyclische Oxygruppe, eine Alkyl-,
Aryl- oder heterocyclische Thiogruppe, eine Alkyl-,
Aryloder heterocyclische Acyloxygruppe, eine
Carbamoyloxygruppe, eine Silyloxygruppe, eine Alkyl-, Aryl- oder
heterocyclische Sulfonyloxygruppe, eine Acylaminogruppe, eine
Alkylaminogruppe, eine Arylaminogruppe, eine Ureidogruppe,
eine Sulfamoylaminogruppe, eine Alkenyloxygruppe, eine
Formylgruppe, eine Alkyl-, Aryl- oder heterocyclische
Acylgruppe, eine Alkyl-, Aryl- oder heterocyclische
Sulfonylgruppe, eine Alkyl-, Aryl- oder heterocyclische
Sulfinylgruppe, eine Alkyl-, Aryl- oder heterocyclische
Oxycarbonylgruppe, eine Alkyl-, Aryl- oder heterocyclische
Oxycarbonylaminogruppe, eine Alkyl-, Aryl- oder
heterocydische Sulfonamidgruppe, eine Carbamoylgruppe, eine
Sulfamoylgruppe, eine Phosphonylgruppe, eine Sulfamidogruppe,
eine Imidogruppe, eine Azolylgruppe, eine Alkyl- oder
Arylsubstituierte Silylgruppe, eine Hydroxylgruppe, eine
Cyanogruppe, eine Carboxylgruppe, eine Nitrogruppe, eine
Sulfogruppe oder eine unsubstituierte Aminogruppe bedeuten.
3. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin R&sub1; und R&sub2; jeweils eine aliphatische Gruppe mit 2
bis 30 Kohlenstoffatomen, eine Arylgruppe mit 6 bis 30
Rohlenstoffatomen, eine Alkoxygruppe mit 1 bis 30
Kohlenstoffatomen, eine Aryloxygruppe mit 6 bis 30
Kohlenstoffatomen, ein Halogenatom, eine Alkyl- oder
Aryloxycarbonylgruppe, eine Carbamoylgruppe oder eine
Alkyloder Aryl-substituierte Silylgruppe bedeuten.
4. Farbphotographisches Silberhalogenidmaterial nach
Anspruch 1, worin R&sub1; und R&sub2; jeweils eine verzweigte
Alkylgruppe mit 3 bis 30 Kohlenstoffatomen bedeuten.
5. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin R&sub3;, R&sub4;, R&sub5; und R&sub6; jeweils ein Wasserstoffatom, ein
Halogenatom, eine aliphatische Gruppe, eine Arylgruppe,
eine heterocyclische Gruppe, eine Alkoxygruppe, eine
Aryloxygruppe, eine heterocyclische Oxygruppe, eine Alkyl-,
Aryl-
oder heterocyclische Thiogruppe, eine Alkyl-, Aryl- oder
heterocyclische Acyloxygruppe, eine Carbamoyloxygruppe,
eine Silyloxygruppe, eine Alkyl-, Aryl- oder heterocyclische
Sulfonyloxygruppe, eine Acylaminogruppe, eine
Alkylaminogruppe, eine Arylaminogruppe, eine Ureidogruppe, eine
Sulfamoylaminogruppe, eine Alkenyloxygruppe, eine
Formylgruppe, eine Alkyl-, Aryl- oder heterocyclische Acylgruppe,
eine Alkyl-, Aryl- oder heterocyclische Sulfonylgruppe,
eine Alkyl-, Aryl- oder heterocyclische Sulfinylgruppe, eine
Alkyl-, Aryl- oder heterocyclische Oxycarbonylgruppe, eine
Alkyl-, Aryl- oder heterocyclische Oxycarbonylaminogruppe,
eine Alkyl-, Aryl- oder heterocyclische Sulfonamidgruppe,
eine Carbamoylgruppe, eine Sulfamoylgruppe, eine
Phosphonylgruppe, eine Sulfamidogruppe, eine Imidogruppe, eine
Azolylgruppe, eine Alkyl- oder Aryl-substituierte
Silylgruppe, eine Hydroxylgruppe, eine Cyanogruppe, eine
Carboxylgruppe, eine Nitrogruppe, eine Sulfogruppe oder eine
unsubstituierte Aminogruppe bedeuten
6. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin R&sub3;, R&sub4; und R&sub5; jeweils ein Wasserstoffatom, eine
Alkylgruppe mit 1 bis 30 Kohlenstoffatomen, eine
Arylgruppe, eine Alkoxygruppe, eine Aryloxygruppe, ein Halogenatom
oder eine Gruppe, die an die Verbindung über eine
Estergruppe, eine Amidogruppe oder ein Siliziumatom gebunden
ist, bedeuten.
7. Farbphotographisches Silberhalogenidmaterial nach Anspruch
11 worin R&sub3;, R&sub4; und R&sub5; jeweils ein Wasserstoffatom
bedeuten.
8. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin R&sub6; eine Alkylgruppe, eine Arylgruppe, eine
heterocyclische Gruppe, eine Carbamoylgruppe, eine
Acylaminogruppe oder eine Ureidogruppe ist.
9. Farbphotographisches Silberhalogenidmaterial nach Anspruch
5, worin R&sub6; durch
dargestellt ist, worin Rx und Ry jeweils einen
Substituenten bedeuten und m bedeutet eine ganze Zahl von 0 bis 4.
10. Farbphotographisches Silberhalogenidmaterial nach Anspruch
9, worin RX eine Alkoxygruppe mit 1 bis 40
Kohlenstoffatomen oder eine Aryloxygruppe mit 6 bis 46 Kohlenstoffatomen
ist.
11. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin Z ein Atom oder eine Atomgruppe bedeutet, die
erforderlich ist, um einen 5-, 6-, 7- oder 8-gliedrigen Ring
zu bilden.
12. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin Z eine zweiwertige Aminogruppe, eine Etherbindung,
eine Thioetherbindung, eine Alkylengruppe, eine
Alkenylengruppe, eine Iminogruppe, eine Sulfonylgruppe oder eine
Carbonylgruppe ist.
13. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin Z eine Alkylengruppe oder eine Alkenylengruppe
ist.
14. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin Z eine Alkylengruppe ist.
15. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin die Gruppe
dargestellt ist durch
worin R&sub8; bis R&sub1;&sub3; jeweils ein Wasserstoffatom oder einen
Substituenten bedeuten.
16. Farbphotographisches silberhalogenidmaterial nach Anspruch
1, worin X ein Wasserstoffatom, ein Halogenatom, eine
Alkoxygruppe, eine Aryloxygruppe, eine heterocyclische
Oxygruppe, eine Alkyl-, Aryl- oder heterocyclische
Acyloxygruppe, eine Alkyl-, Aryl- oder heterocyclische
Sulfonyloxygruppe, eine Dialkyl- oder Diarylphosphonoxygruppe,
eine Dialkyl- oder Diarylphosphinoxygruppe, eine
Alkoxycarbonyloxygruppe, eine Aryloxycarbonyloxygruppe, eine
heterocyclische Oxycarbonyloxygruppe, eine Alkyl-, Aryl- oder
heterocyclische Sulfonylgruppe, eine Alkyl-, Aryl- oder
heterocyclische Sulfinylgruppe, eine Alkyl-, Aryl- oder
heterocyclische Carbonylgruppe, eine Alkyl-, Aryl- oder
heterocyclische Acylaminogruppe, eine Alkyl-, Aryl- oder
heterocyclische Sulfonamidgruppe, eine Carbamoylaminogruppe,
eine Alkyl-, Aryl- oder heterocyclische Thiogruppe, eine
Imidogruppe, eine Arylazogruppe und eine 5-gliedrige oder
6-gliedrige Stickstoff enthaltende heterocyclische Gruppe
bedeutet, die über ihr Stickstoffatom an die
Kupplungsposition der Verbindung gebunden ist.
17. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin X ein Chloratom ist.
18. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin der Cyankuppler in eine rotempfindliche
Silberhalogenidemulsionsschicht eingebracht ist.
19. Farbphotographisches Silberhalogenidmaterial nach Anspruch
1, worin der Gehalt des Cyankupplers im Bereich von
1 x 10 Mol bis 1 Mol pro Mol des Silberhalogenids in der
Schicht, die den Cyankuppler enthält, liegt.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP5163254A JP3026243B2 (ja) | 1993-06-08 | 1993-06-08 | ハロゲン化銀カラー写真感光材料 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE69401682D1 DE69401682D1 (de) | 1997-03-20 |
DE69401682T2 true DE69401682T2 (de) | 1997-05-28 |
Family
ID=15770305
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE69401682T Expired - Lifetime DE69401682T2 (de) | 1993-06-08 | 1994-06-07 | Farbphotographisches Silberhalogenidmaterial |
Country Status (4)
Country | Link |
---|---|
US (1) | US5384236A (de) |
EP (1) | EP0628867B1 (de) |
JP (1) | JP3026243B2 (de) |
DE (1) | DE69401682T2 (de) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH07140612A (ja) * | 1993-11-16 | 1995-06-02 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー感光材料 |
JP3505241B2 (ja) * | 1994-10-12 | 2004-03-08 | 富士写真フイルム株式会社 | 1H−1,2,4−トリアゾール誘導体及び1H−ピロロ−〔1,2−b〕〔1,2,4〕トリアゾール誘導体 |
JP3438966B2 (ja) * | 1994-10-12 | 2003-08-18 | 富士写真フイルム株式会社 | ハロゲン化銀カラー感光材料 |
EP0720981B1 (de) * | 1995-01-05 | 1998-10-14 | Fuji Photo Film Co., Ltd. | Cyclohexyloxycarbonylacetohydrazide, und ihre Verwendung für die Herstellung von 1H-1,2,4-Triazolen |
JPH0980712A (ja) * | 1995-09-12 | 1997-03-28 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JP3584119B2 (ja) | 1996-04-05 | 2004-11-04 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
JPH11119393A (ja) * | 1997-10-14 | 1999-04-30 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
DE19819830A1 (de) | 1998-05-04 | 1999-11-11 | Agfa Gevaert Ag | Farbfotografisches Kopiermaterial |
US6391533B1 (en) | 1998-10-14 | 2002-05-21 | Fuji Photo Film Co., Ltd. | Silver halide color photosensitive material and color image forming method using the same |
JP4265863B2 (ja) * | 2000-03-27 | 2009-05-20 | 富士フイルム株式会社 | ハロゲン化銀カラー写真感光材料、ピロロトリアゾール化合物および色素形成用化合物 |
CN1276301C (zh) | 2000-09-28 | 2006-09-20 | 富士胶片株式会社 | 卤化银彩色照相感光材料、吡咯并三唑化合物和成色化合物 |
CN100354751C (zh) * | 2001-11-22 | 2007-12-12 | 富士胶片株式会社 | 提高卤化银彩色光敏材料感光速率的方法 |
WO2005073804A1 (en) | 2004-01-30 | 2005-08-11 | Fuji Photo Film Co., Ltd. | Silver halide color photographic light-sensitive material and color image-forming method |
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BE470936A (de) | 1940-02-24 | |||
US3645801A (en) | 1968-12-20 | 1972-02-29 | Bethlehem Steel Corp | Method of producing rolled steel having high-strength and low-impact transition temperature |
CA1079432A (en) | 1974-09-17 | 1980-06-10 | Tsang J. Chen | Uniform, efficient distribution of hydrophobic materials through hydrophilic colloid layers, and products useful therefor |
BE833512A (fr) | 1974-09-17 | 1976-03-17 | Nouvelle composition de latex charge par un compose hydrophobe, sa preparation et son application photographique | |
GB1504949A (en) | 1974-09-17 | 1978-03-22 | Eastman Kodak Co | Aqueous polymer latexes containing hydrophobic materials |
CA1141637A (en) | 1979-10-10 | 1983-02-22 | Erma C. Cameron | Cofactor indicator compositions |
GB8426447D0 (en) | 1984-10-19 | 1984-11-28 | Kodak Ltd | Photographic colour couplers |
US4818672A (en) | 1986-06-13 | 1989-04-04 | Konishiroku Photo Industry Co., Ltd. | Silver halide color photographic light-sensitive material improved in cyan image characteristics |
DE3750631T2 (de) | 1986-07-10 | 1995-02-09 | Fuji Photo Film Co Ltd | Farbphotographisches silberhalidmaterial. |
US4873183A (en) * | 1986-11-25 | 1989-10-10 | Konica Corporation | Silver halide color photographic light-sensitive material containing pyrazoloazole type cyan coupler |
CA1338796C (en) | 1987-01-28 | 1996-12-17 | Nobuo Furutachi | Color photographs, a process for preparing them and color photographic materials employed therefor |
JP2601272B2 (ja) | 1987-04-28 | 1997-04-16 | コニカ株式会社 | 迅速処理においても感度、カブリの写真性能の劣化がなく、さらにバクテリア、カビ等による腐敗、分解作用が良好に防止されるハロゲン化銀写真感光材料 |
JPH01158431A (ja) | 1987-09-16 | 1989-06-21 | Fuji Photo Film Co Ltd | カラーポジ画像形成法 |
US4880726A (en) | 1987-11-12 | 1989-11-14 | Fuji Photo Film Co., Ltd. | Method of forming a color image |
JP2604208B2 (ja) | 1988-01-27 | 1997-04-30 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
EP0337490B1 (de) | 1988-04-15 | 1995-12-20 | Fuji Photo Film Co., Ltd. | Lichtempfindliches photographisches Silberhalogenidmaterial |
DE68924683T2 (de) | 1988-08-15 | 1996-03-28 | Fuji Photo Film Co Ltd | Farbphotographisches Silbenhalogenidmaterial. |
JP2537079B2 (ja) | 1988-09-28 | 1996-09-25 | 富士写真フイルム株式会社 | 直接ポジ写真感光材料 |
JPH0293641A (ja) | 1988-09-30 | 1990-04-04 | Fuji Photo Film Co Ltd | ハロゲン化銀写真感光材料 |
JPH03194539A (ja) | 1989-12-22 | 1991-08-26 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料 |
JPH0434548A (ja) | 1990-05-31 | 1992-02-05 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー反転写真感光材料の処理方法 |
JP2950431B2 (ja) | 1990-10-08 | 1999-09-20 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
JP2684267B2 (ja) * | 1990-11-28 | 1997-12-03 | 富士写真フイルム株式会社 | シアン画像形成方法及びハロゲン化銀カラー写真感光材料 |
JP2684265B2 (ja) | 1990-11-30 | 1997-12-03 | 富士写真フイルム株式会社 | シアン画像形成方法及びハロゲン化銀カラー写真感光材料 |
JP2782565B2 (ja) | 1990-12-07 | 1998-08-06 | 富士写真フイルム株式会社 | カラー画像安定化処理液、安定液、安定補充液、調整液、漂白液及びハロゲン化銀カラー写真感光材料の処理方法 |
JP2729542B2 (ja) | 1991-02-22 | 1998-03-18 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料用の処理液及びそれを用いた処理方法 |
JPH04270344A (ja) | 1991-02-26 | 1992-09-25 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー写真感光材料の処理方法 |
JP2729545B2 (ja) | 1991-06-05 | 1998-03-18 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料用の処理液及びそれを用いた処理方法 |
EP0903350B1 (de) * | 1991-06-07 | 2003-03-12 | Fuji Photo Film Co., Ltd. | Pyrrolotriazolderivat |
US5250402A (en) | 1991-06-26 | 1993-10-05 | Fuji Photo Film Co., Ltd. | Photographic bleaching composition and a processing method therewith |
JP2889999B2 (ja) | 1991-09-05 | 1999-05-10 | 富士写真フイルム株式会社 | 写真用処理組成物及び処理方法 |
JPH05134351A (ja) | 1991-11-14 | 1993-05-28 | Fuji Photo Film Co Ltd | 直接ポジカラー写真感光材料および画像形成方法 |
JP2699237B2 (ja) * | 1991-11-27 | 1998-01-19 | 富士写真フイルム株式会社 | ハロゲン化銀カラー写真感光材料 |
-
1993
- 1993-06-08 JP JP5163254A patent/JP3026243B2/ja not_active Expired - Fee Related
-
1994
- 1994-06-07 EP EP94108697A patent/EP0628867B1/de not_active Expired - Lifetime
- 1994-06-07 DE DE69401682T patent/DE69401682T2/de not_active Expired - Lifetime
- 1994-06-08 US US08/257,189 patent/US5384236A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JPH06347960A (ja) | 1994-12-22 |
JP3026243B2 (ja) | 2000-03-27 |
US5384236A (en) | 1995-01-24 |
DE69401682D1 (de) | 1997-03-20 |
EP0628867B1 (de) | 1997-02-05 |
EP0628867A1 (de) | 1994-12-14 |
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