DE1925359A1 - Photographisches Aufzeichnungsmaterial - Google Patents
Photographisches AufzeichnungsmaterialInfo
- Publication number
- DE1925359A1 DE1925359A1 DE19691925359 DE1925359A DE1925359A1 DE 1925359 A1 DE1925359 A1 DE 1925359A1 DE 19691925359 DE19691925359 DE 19691925359 DE 1925359 A DE1925359 A DE 1925359A DE 1925359 A1 DE1925359 A1 DE 1925359A1
- Authority
- DE
- Germany
- Prior art keywords
- silver halide
- halide emulsion
- recording material
- couplers
- radical
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 68
- -1 silver halide Chemical class 0.000 claims description 178
- 239000000839 emulsion Substances 0.000 claims description 66
- 229910052709 silver Inorganic materials 0.000 claims description 62
- 239000004332 silver Substances 0.000 claims description 62
- 239000000975 dye Substances 0.000 claims description 38
- 239000003112 inhibitor Substances 0.000 claims description 32
- 150000003254 radicals Chemical class 0.000 claims description 32
- 230000035945 sensitivity Effects 0.000 claims description 16
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 14
- ZRHUHDUEXWHZMA-UHFFFAOYSA-N 1,4-dihydropyrazol-5-one Chemical compound O=C1CC=NN1 ZRHUHDUEXWHZMA-UHFFFAOYSA-N 0.000 claims description 11
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 5
- 125000005842 heteroatom Chemical group 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- 239000001301 oxygen Substances 0.000 claims description 5
- 229910052717 sulfur Inorganic materials 0.000 claims description 5
- 239000011593 sulfur Substances 0.000 claims description 5
- 125000004423 acyloxy group Chemical group 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 150000005840 aryl radicals Chemical class 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 238000005859 coupling reaction Methods 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000005605 benzo group Chemical group 0.000 claims description 3
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 3
- 239000001046 green dye Substances 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 125000005031 thiocyano group Chemical group S(C#N)* 0.000 claims description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 125000003368 amide group Chemical group 0.000 claims 1
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims 1
- 239000010410 layer Substances 0.000 description 86
- 238000004519 manufacturing process Methods 0.000 description 18
- 229920000159 gelatin Polymers 0.000 description 13
- 235000019322 gelatine Nutrition 0.000 description 13
- 108010010803 Gelatin Proteins 0.000 description 9
- 239000012298 atmosphere Substances 0.000 description 9
- 239000008273 gelatin Substances 0.000 description 9
- 235000011852 gelatine desserts Nutrition 0.000 description 9
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 8
- 229910052799 carbon Inorganic materials 0.000 description 7
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- 238000003384 imaging method Methods 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 150000003142 primary aromatic amines Chemical class 0.000 description 5
- 239000001828 Gelatine Substances 0.000 description 4
- 239000011230 binding agent Substances 0.000 description 4
- 229910052801 chlorine Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 229960001413 acetanilide Drugs 0.000 description 3
- 125000001309 chloro group Chemical group Cl* 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- RMHJJUOPOWPRBP-UHFFFAOYSA-N naphthalene-1-carboxamide Chemical compound C1=CC=C2C(C(=O)N)=CC=CC2=C1 RMHJJUOPOWPRBP-UHFFFAOYSA-N 0.000 description 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 2
- FEPBITJSIHRMRT-UHFFFAOYSA-N 4-hydroxybenzenesulfonic acid Chemical class OC1=CC=C(S(O)(=O)=O)C=C1 FEPBITJSIHRMRT-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 description 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical class [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 description 2
- 125000005337 azoxy group Chemical group [N+]([O-])(=N*)* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 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 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 125000006413 ring segment Chemical group 0.000 description 2
- 230000003595 spectral effect Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 239000001043 yellow dye Substances 0.000 description 2
- UUAQXLSKDAOPJC-UHFFFAOYSA-N (1-anilino-1,3-dioxo-3-phenylpropan-2-yl) thiocyanate Chemical compound C=1C=CC=CC=1C(=O)C(SC#N)C(=O)NC1=CC=CC=C1 UUAQXLSKDAOPJC-UHFFFAOYSA-N 0.000 description 1
- RQJVRTHWJHBYOM-UHFFFAOYSA-N 1-hydroxy-4-(1-phenyltetrazol-5-yl)sulfanyl-n-(2-tetradecoxyphenyl)naphthalene-2-carboxamide Chemical compound CCCCCCCCCCCCCCOC1=CC=CC=C1NC(=O)C1=CC(SC=2N(N=NN=2)C=2C=CC=CC=2)=C(C=CC=C2)C2=C1O RQJVRTHWJHBYOM-UHFFFAOYSA-N 0.000 description 1
- VGVRPFIJEJYOFN-UHFFFAOYSA-N 2,3,4,6-tetrachlorophenol Chemical class OC1=C(Cl)C=C(Cl)C(Cl)=C1Cl VGVRPFIJEJYOFN-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-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
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical group NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- 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 1
- ITELOYMXHDBNIE-UHFFFAOYSA-N 2-chloro-5-(hexadecylamino)naphthalen-1-ol Chemical compound ClC1=CC=C2C(NCCCCCCCCCCCCCCCC)=CC=CC2=C1O ITELOYMXHDBNIE-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- FTCOWMWIZNVSPP-UHFFFAOYSA-N 2-phenyl-4h-pyrazol-3-one Chemical compound O=C1CC=NN1C1=CC=CC=C1 FTCOWMWIZNVSPP-UHFFFAOYSA-N 0.000 description 1
- XIXWLPSLFASNLH-UHFFFAOYSA-N 3-oxo-n-[4-[(3-oxo-3-phenylpropanoyl)amino]phenyl]-3-phenylpropanamide Chemical compound C=1C=C(NC(=O)CC(=O)C=2C=CC=CC=2)C=CC=1NC(=O)CC(=O)C1=CC=CC=C1 XIXWLPSLFASNLH-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical group CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- OVBCQMARDRXVPA-UHFFFAOYSA-N 4-amino-5-(3-aminobenzoyl)-2-phenyl-4H-pyrazol-3-one Chemical compound C1(=CC=CC=C1)N1N=C(C(C1=O)N)C(C1=CC(=CC=C1)N)=O OVBCQMARDRXVPA-UHFFFAOYSA-N 0.000 description 1
- HCXJFMDOHDNDCC-UHFFFAOYSA-N 5-$l^{1}-oxidanyl-3,4-dihydropyrrol-2-one Chemical group O=C1CCC(=O)[N]1 HCXJFMDOHDNDCC-UHFFFAOYSA-N 0.000 description 1
- VFEXVJUZYQATIC-UHFFFAOYSA-N 5-octadecylimino-2-phenyl-4-(1-phenyltetrazol-5-yl)sulfanylpyrazolidin-3-one Chemical compound C1(=CC=CC=C1)N1N=C(C(C1=O)SC1=NN=NN1C1=CC=CC=C1)NCCCCCCCCCCCCCCCCCC VFEXVJUZYQATIC-UHFFFAOYSA-N 0.000 description 1
- WVDVPWSDGNQWPH-UHFFFAOYSA-N 5-oxo-3-pentadecyl-1-(2,4,6-trichlorophenyl)-4H-pyrazole-4-sulfonic acid Chemical compound ClC1=C(C(=CC(=C1)Cl)Cl)N1N=C(C(C1=O)S(=O)(=O)O)CCCCCCCCCCCCCCC WVDVPWSDGNQWPH-UHFFFAOYSA-N 0.000 description 1
- NEVPBGBSOYLFNQ-UHFFFAOYSA-N C1=CC(S(O)(=O)=O)=C(NC(C)=O)C(CCC)=C1C(=O)C1=CC=CC=C1 Chemical compound C1=CC(S(O)(=O)=O)=C(NC(C)=O)C(CCC)=C1C(=O)C1=CC=CC=C1 NEVPBGBSOYLFNQ-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- 101150052863 THY1 gene Proteins 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 241000358324 Viverricula indica Species 0.000 description 1
- MRQGLDBNQNEFAH-UHFFFAOYSA-N [3-(4-nitrophenyl)imino-5-oxo-1-(2,4,6-trichlorophenyl)pyrazolidin-4-yl] octadecanoate Chemical compound ClC1=C(C(=CC(=C1)Cl)Cl)N1N=C(C(C1=O)OC(CCCCCCCCCCCCCCCCC)=O)NC1=CC=C(C=C1)[N+](=O)[O-] MRQGLDBNQNEFAH-UHFFFAOYSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- DYRDKSSFIWVSNM-UHFFFAOYSA-N acetoacetanilide Chemical compound CC(=O)CC(=O)NC1=CC=CC=C1 DYRDKSSFIWVSNM-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000003931 anilides Chemical class 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
- 125000003118 aryl group Chemical group 0.000 description 1
- ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical compound C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 1
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical class C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000005521 carbonamide group Chemical group 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- JEVCWSUVFOYBFI-UHFFFAOYSA-N cyanyl Chemical compound N#[C] JEVCWSUVFOYBFI-UHFFFAOYSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000004470 heterocyclooxy group Chemical group 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000012216 imaging agent Substances 0.000 description 1
- 235000021190 leftovers Nutrition 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- AEHUQGGSYVUDEB-UHFFFAOYSA-N n-(1-hydroxy-5-phenoxynaphthalen-2-yl)acetamide Chemical compound C=1C=CC2=C(O)C(NC(=O)C)=CC=C2C=1OC1=CC=CC=C1 AEHUQGGSYVUDEB-UHFFFAOYSA-N 0.000 description 1
- FQEPWQOAOIVBFL-UHFFFAOYSA-N n-(2-hydroxy-4,6-dimethylphenyl)-4-(2-methylbutan-2-yl)-3-phenoxybenzamide Chemical compound CCC(C)(C)C1=CC=C(C(=O)NC=2C(=CC(C)=CC=2C)O)C=C1OC1=CC=CC=C1 FQEPWQOAOIVBFL-UHFFFAOYSA-N 0.000 description 1
- MIROIROPBNMABJ-UHFFFAOYSA-N n-(2-hydroxy-4,6-dimethylphenyl)benzamide Chemical compound OC1=CC(C)=CC(C)=C1NC(=O)C1=CC=CC=C1 MIROIROPBNMABJ-UHFFFAOYSA-N 0.000 description 1
- BNSRNYYTRWSNTD-UHFFFAOYSA-N n-(2-hydroxyphenyl)-4-(2-methylbutan-2-yl)-3-phenoxybenzamide Chemical compound CCC(C)(C)C1=CC=C(C(=O)NC=2C(=CC=CC=2)O)C=C1OC1=CC=CC=C1 BNSRNYYTRWSNTD-UHFFFAOYSA-N 0.000 description 1
- AWONMSRRUQBLCH-UHFFFAOYSA-N n-(5-hydroxynaphthalen-1-yl)-5,6,7,8-tetrahydronaphthalene-2-sulfonamide Chemical compound C1CCCC2=CC(S(=O)(=O)NC3=C4C=CC=C(C4=CC=C3)O)=CC=C21 AWONMSRRUQBLCH-UHFFFAOYSA-N 0.000 description 1
- FWCQMJCQJFTDKP-UHFFFAOYSA-N n-(5-hydroxynaphthalen-1-yl)benzenesulfonamide Chemical compound C1=CC=C2C(O)=CC=CC2=C1NS(=O)(=O)C1=CC=CC=C1 FWCQMJCQJFTDKP-UHFFFAOYSA-N 0.000 description 1
- CDFGHFVQQORMPR-UHFFFAOYSA-N n-(5-hydroxynaphthalen-1-yl)hexanamide Chemical compound C1=CC=C2C(NC(=O)CCCCC)=CC=CC2=C1O CDFGHFVQQORMPR-UHFFFAOYSA-N 0.000 description 1
- LLQNURAMZLUWIX-UHFFFAOYSA-N n-(6-chloro-5-hydroxynaphthalen-1-yl)benzenesulfonamide Chemical compound C1=CC=C2C(O)=C(Cl)C=CC2=C1NS(=O)(=O)C1=CC=CC=C1 LLQNURAMZLUWIX-UHFFFAOYSA-N 0.000 description 1
- XYEARSGGJVQUEC-UHFFFAOYSA-N n-[2-(2-cyanoacetyl)-1-benzofuran-5-yl]benzamide Chemical compound C=1C=C2OC(C(CC#N)=O)=CC2=CC=1NC(=O)C1=CC=CC=C1 XYEARSGGJVQUEC-UHFFFAOYSA-N 0.000 description 1
- ZRVDCNGCQDBZAL-UHFFFAOYSA-N n-[5-benzoyl-2-[benzyl(phenyl)sulfamoyl]phenyl]acetamide Chemical compound CC(=O)NC1=CC(C(=O)C=2C=CC=CC=2)=CC=C1S(=O)(=O)N(C=1C=CC=CC=1)CC1=CC=CC=C1 ZRVDCNGCQDBZAL-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- GLOJZKQUUVFNGA-UHFFFAOYSA-N nonyl 2-acetamido-4-benzoylbenzenesulfonate Chemical compound C(C1=CC=CC=C1)(=O)C1=CC(=C(C=C1)S(=O)(=O)OCCCCCCCCC)NC(=O)C GLOJZKQUUVFNGA-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 239000001047 purple dye Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical group O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000000191 radiation effect Effects 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 159000000000 sodium salts Chemical class 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
- 239000002904 solvent Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- HERSKCAGZCXYMC-UHFFFAOYSA-N thiophen-3-ol Chemical class OC=1C=CSC=1 HERSKCAGZCXYMC-UHFFFAOYSA-N 0.000 description 1
- 150000004992 toluidines Chemical class 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
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
-
- 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/46—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein having more than one photosensitive layer
-
- 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
- G03C2007/3034—Unit layer
-
- 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
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US73059368A | 1968-05-20 | 1968-05-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1925359A1 true DE1925359A1 (de) | 1970-09-10 |
Family
ID=24935967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19691925359 Pending DE1925359A1 (de) | 1968-05-20 | 1969-05-19 | Photographisches Aufzeichnungsmaterial |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US3620747A (enrdf_load_stackoverflow) |
| JP (1) | JPS493843B1 (enrdf_load_stackoverflow) |
| BE (1) | BE733342A (enrdf_load_stackoverflow) |
| DE (1) | DE1925359A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2008905A1 (enrdf_load_stackoverflow) |
| GB (1) | GB1275069A (enrdf_load_stackoverflow) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2421544A1 (de) * | 1973-05-04 | 1974-11-21 | Fuji Photo Film Co Ltd | Mehrschichtiges farbphotographisches lichtempfindliches material |
Families Citing this family (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS4917735B1 (enrdf_load_stackoverflow) * | 1970-12-26 | 1974-05-02 | ||
| US3839044A (en) * | 1971-03-25 | 1974-10-01 | Eastman Kodak Co | Silver halide emulsions containing 2-equivalent color couplers |
| US4003744A (en) * | 1972-12-07 | 1977-01-18 | Polaroid Corporation | Photographic products with photosensitive layers of same spectral sensitivity and different speed |
| JPS587987B2 (ja) * | 1973-04-13 | 1983-02-14 | 富士写真フイルム株式会社 | カラ−シヤシンカンコウザイリヨウ |
| JPS5939738B2 (ja) * | 1973-08-16 | 1984-09-26 | コニカ株式会社 | 多層カラ−写真感光材料 |
| US3960558A (en) * | 1974-04-29 | 1976-06-01 | Polaroid Corporation | Dye free, spectrally sensitive silver halide layers in diffusion transfer films |
| JPS51337A (enrdf_load_stackoverflow) * | 1974-06-20 | 1976-01-06 | Fuji Photo Film Co Ltd | |
| US4184876A (en) * | 1974-07-09 | 1980-01-22 | Eastman Kodak Company | Color photographic materials having increased speed |
| US4205990A (en) * | 1975-08-02 | 1980-06-03 | Konishiroku Photo Industry Co., Ltd. | Process for forming a cyan dye image by the use of a 2-equivalent cyan coupler |
| JPS5943736B2 (ja) * | 1976-01-26 | 1984-10-24 | 富士写真フイルム株式会社 | カラ−写真画像の形成方法 |
| JPS5352423A (en) * | 1976-10-23 | 1978-05-12 | Konishiroku Photo Ind Co Ltd | Color image formation method |
| WO1979001020A1 (en) * | 1978-05-02 | 1979-11-29 | Polaroid Corp | Photosensitive elements |
| US4391896A (en) * | 1978-09-20 | 1983-07-05 | Eastman Kodak Company | Mixture of nondiffusible redox dye-releasers for curve shape control |
| DE2855997A1 (de) * | 1978-12-23 | 1980-07-10 | Agfa Gevaert Ag | Fotografisches aufzeichnungsmaterial |
| DE3029209A1 (de) * | 1980-08-01 | 1982-03-18 | Agfa-Gevaert Ag, 5090 Leverkusen | Lichtempfindliches fotografisches aufzeichnungsmaterial und dessen verwendung zur herstellung fotografischer bilder |
| US4414308A (en) * | 1981-03-20 | 1983-11-08 | Konishiroku Photo Industry Co., Ltd. | Silver halide color photographic photosensitive material |
| JPS5850533A (ja) * | 1981-09-21 | 1983-03-25 | Fuji Photo Film Co Ltd | ハロゲン化銀カラー感光材料の処理方法 |
| JPS58140740A (ja) * | 1982-02-15 | 1983-08-20 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| JPS58143335A (ja) * | 1982-02-19 | 1983-08-25 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| JPS6066250A (ja) * | 1983-09-21 | 1985-04-16 | Konishiroku Photo Ind Co Ltd | ハロゲン化銀写真感光材料 |
| JPS60172040A (ja) * | 1984-02-17 | 1985-09-05 | Fuji Photo Film Co Ltd | カラ−反転写真感光材料 |
| US4963465A (en) * | 1989-01-12 | 1990-10-16 | Agfa-Gevaert Aktiengesellschaft | Color photographic negative recording material |
| FR2664399A1 (fr) * | 1990-07-04 | 1992-01-10 | Kodak Pathe | Produit inversible pour la photographie en couleurs avec sous-couche a grains fins. |
| JPH0553264A (ja) * | 1991-08-23 | 1993-03-05 | Konica Corp | ハロゲン化銀カラー写真感光材料 |
| JPH0743850A (ja) * | 1993-07-27 | 1995-02-14 | Konica Corp | 直接ポジハロゲン化銀カラー写真感光材料 |
| FR2723791B1 (fr) * | 1994-08-17 | 1997-01-03 | Kodak Pathe | Produit photographique au chlorure d'argent et procede de photographie utilisant ce produit |
| DE69517475T2 (de) * | 1994-08-17 | 2001-03-08 | Eastman Kodak Co., Rochester | Farbphotographisches Silberhalogenidmaterial |
| US7978925B1 (en) | 2005-04-16 | 2011-07-12 | Apple Inc. | Smoothing and/or locking operations in video editing |
| US8885978B2 (en) | 2010-07-05 | 2014-11-11 | Apple Inc. | Operating a device to capture high dynamic range images |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1066090B (enrdf_load_stackoverflow) * | 1956-09-26 | |||
| US3050391A (en) * | 1957-12-30 | 1962-08-21 | Gen Aniline & Film Corp | Photographic film with fine grain silver chloride underlayer |
| BE591444A (enrdf_load_stackoverflow) * | 1959-04-06 | |||
| US3148062A (en) * | 1959-04-06 | 1964-09-08 | Eastman Kodak Co | Photographic elements and processes using splittable couplers |
| BE603747A (enrdf_load_stackoverflow) * | 1960-05-13 | |||
| US3450536A (en) * | 1961-03-24 | 1969-06-17 | Eg & G Inc | Silver halide photographic film having increased exposure-response characteristics |
| US3227550A (en) * | 1962-09-07 | 1966-01-04 | Eastman Kodak Co | Photographic color reproduction process and element |
| US3364022A (en) * | 1963-04-01 | 1968-01-16 | Eastman Kodak Co | Direct positive photographic color reproduction process and element utilizing thio-substituted hydroquinones as development inhibitors |
| US3243294A (en) * | 1963-11-06 | 1966-03-29 | Eastman Kodak Co | Photographic direct-positive color process |
-
1968
- 1968-05-20 US US730593A patent/US3620747A/en not_active Expired - Lifetime
-
1969
- 1969-05-16 JP JP44037470A patent/JPS493843B1/ja active Pending
- 1969-05-16 GB GB25122/69A patent/GB1275069A/en not_active Expired
- 1969-05-19 DE DE19691925359 patent/DE1925359A1/de active Pending
- 1969-05-20 FR FR6916208A patent/FR2008905A1/fr not_active Withdrawn
- 1969-05-20 BE BE733342D patent/BE733342A/xx not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2421544A1 (de) * | 1973-05-04 | 1974-11-21 | Fuji Photo Film Co Ltd | Mehrschichtiges farbphotographisches lichtempfindliches material |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1275069A (en) | 1972-05-24 |
| FR2008905A1 (enrdf_load_stackoverflow) | 1970-01-30 |
| BE733342A (enrdf_load_stackoverflow) | 1969-11-03 |
| US3620747A (en) | 1971-11-16 |
| JPS493843B1 (enrdf_load_stackoverflow) | 1974-01-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| E77 | Valid patent as to the heymanns-index 1977 |