US3870523A - Heat developable photographic material containing azo dyes as sensitizers - Google Patents
Heat developable photographic material containing azo dyes as sensitizers Download PDFInfo
- Publication number
- US3870523A US3870523A US434453A US43445374A US3870523A US 3870523 A US3870523 A US 3870523A US 434453 A US434453 A US 434453A US 43445374 A US43445374 A US 43445374A US 3870523 A US3870523 A US 3870523A
- Authority
- US
- United States
- Prior art keywords
- group
- heat developable
- developable photographic
- photographic material
- groups
- 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
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- 239000000463 material Substances 0.000 title claims abstract description 103
- 239000000987 azo dye Substances 0.000 title description 2
- -1 SILVER HALIDE Chemical class 0.000 claims abstract description 50
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- 229910052709 silver Inorganic materials 0.000 claims abstract description 43
- 239000004332 silver Substances 0.000 claims abstract description 43
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- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 21
- 230000001235 sensitizing effect Effects 0.000 claims abstract description 21
- 239000011230 binding agent Substances 0.000 claims abstract description 18
- 125000003118 aryl group Chemical group 0.000 claims abstract description 11
- 230000003197 catalytic effect Effects 0.000 claims abstract description 9
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 8
- 150000001340 alkali metals Chemical group 0.000 claims abstract description 8
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims abstract description 8
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- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 235000010724 Wisteria floribunda Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- TUYRNAGGIJZRNM-LBHUVFDKSA-N [(2s)-2-[(2r)-4-hexadecanoyloxy-3-hydroxy-5-oxo-2h-furan-2-yl]-2-hydroxyethyl] hexadecanoate Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](O)[C@H]1OC(=O)C(OC(=O)CCCCCCCCCCCCCCC)=C1O TUYRNAGGIJZRNM-LBHUVFDKSA-N 0.000 description 1
- FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
- NZHXEWZGTQSYJM-UHFFFAOYSA-N [bromo(diphenyl)methyl]benzene Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Br)C1=CC=CC=C1 NZHXEWZGTQSYJM-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- CODQAJUDLCXKOA-UHFFFAOYSA-O azanium;silver;nitrate Chemical compound [NH4+].[Ag].[O-][N+]([O-])=O CODQAJUDLCXKOA-UHFFFAOYSA-O 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-M behenate Chemical compound CCCCCCCCCCCCCCCCCCCCCC([O-])=O UKMSUNONTOPOIO-UHFFFAOYSA-M 0.000 description 1
- 229940116224 behenate Drugs 0.000 description 1
- 229940116226 behenic acid Drugs 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 229910052790 beryllium Inorganic materials 0.000 description 1
- ATBAMAFKBVZNFJ-UHFFFAOYSA-N beryllium atom Chemical compound [Be] ATBAMAFKBVZNFJ-UHFFFAOYSA-N 0.000 description 1
- ZDZHCHYQNPQSGG-UHFFFAOYSA-N binaphthyl group Chemical group C1(=CC=CC2=CC=CC=C12)C1=CC=CC2=CC=CC=C12 ZDZHCHYQNPQSGG-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229910052797 bismuth Inorganic materials 0.000 description 1
- JCXGWMGPZLAOME-UHFFFAOYSA-N bismuth atom Chemical compound [Bi] JCXGWMGPZLAOME-UHFFFAOYSA-N 0.000 description 1
- FQUNFJULCYSSOP-UHFFFAOYSA-N bisoctrizole Chemical compound N1=C2C=CC=CC2=NN1C1=CC(C(C)(C)CC(C)(C)C)=CC(CC=2C(=C(C=C(C=2)C(C)(C)CC(C)(C)C)N2N=C3C=CC=CC3=N2)O)=C1O FQUNFJULCYSSOP-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- HKQOBOMRSSHSTC-UHFFFAOYSA-N cellulose acetate Chemical compound OC1C(O)C(O)C(CO)OC1OC1C(CO)OC(O)C(O)C1O.CC(=O)OCC1OC(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC1C(OC(C)=O)C(OC(C)=O)C(OC(C)=O)C(COC(C)=O)O1.CCC(=O)OCC1OC(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C1OC1C(OC(=O)CC)C(OC(=O)CC)C(OC(=O)CC)C(COC(=O)CC)O1 HKQOBOMRSSHSTC-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011247 coating layer Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229960000956 coumarin Drugs 0.000 description 1
- 235000001671 coumarin Nutrition 0.000 description 1
- 238000007766 curtain coating Methods 0.000 description 1
- OPTDDWCXQQYKGU-UHFFFAOYSA-N diphenyldichloromethane Chemical compound C=1C=CC=CC=1C(Cl)(Cl)C1=CC=CC=C1 OPTDDWCXQQYKGU-UHFFFAOYSA-N 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000007765 extrusion coating Methods 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 150000005204 hydroxybenzenes Chemical class 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- BEJNERDRQOWKJM-UHFFFAOYSA-N kojic acid Chemical compound OCC1=CC(=O)C(O)=CO1 BEJNERDRQOWKJM-UHFFFAOYSA-N 0.000 description 1
- 229960004705 kojic acid Drugs 0.000 description 1
- WZNJWVWKTVETCG-UHFFFAOYSA-N kojic acid Natural products OC(=O)C(N)CN1C=CC(=O)C(O)=C1 WZNJWVWKTVETCG-UHFFFAOYSA-N 0.000 description 1
- 229910052746 lanthanum Inorganic materials 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical compound [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 239000006224 matting agent Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N methyl monoether Natural products COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000004780 naphthols Chemical class 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 150000002896 organic halogen compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 150000002941 palladium compounds Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920006289 polycarbonate film Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229940065287 selenium compound Drugs 0.000 description 1
- 150000003343 selenium compounds Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 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
- NGBNXJUWQPLNGM-UHFFFAOYSA-N silver;azane Chemical compound N.[Ag+] NGBNXJUWQPLNGM-UHFFFAOYSA-N 0.000 description 1
- OIZSSBDNMBMYFL-UHFFFAOYSA-M silver;decanoate Chemical compound [Ag+].CCCCCCCCCC([O-])=O OIZSSBDNMBMYFL-UHFFFAOYSA-M 0.000 description 1
- LTYHQUJGIQUHMS-UHFFFAOYSA-M silver;hexadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCC([O-])=O LTYHQUJGIQUHMS-UHFFFAOYSA-M 0.000 description 1
- ORYURPRSXLUCSS-UHFFFAOYSA-M silver;octadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCC([O-])=O ORYURPRSXLUCSS-UHFFFAOYSA-M 0.000 description 1
- OHGHHPYRRURLHR-UHFFFAOYSA-M silver;tetradecanoate Chemical compound [Ag+].CCCCCCCCCCCCCC([O-])=O OHGHHPYRRURLHR-UHFFFAOYSA-M 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- RKSOPLXZQNSWAS-UHFFFAOYSA-N tert-butyl bromide Chemical compound CC(C)(C)Br RKSOPLXZQNSWAS-UHFFFAOYSA-N 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
- 229910052716 thallium Inorganic materials 0.000 description 1
- BKVIYDNLLOSFOA-UHFFFAOYSA-N thallium Chemical compound [Tl] BKVIYDNLLOSFOA-UHFFFAOYSA-N 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 229930007845 β-thujaplicin Natural products 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
- G03C1/00—Photosensitive materials
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
- G03C1/49836—Additives
- G03C1/49845—Active additives, e.g. toners, stabilisers, sensitisers
- G03C1/49854—Dyes or precursors of dyes
Definitions
- ABSTRACT Heat developable photographic materials having at least one photosensitive layer on a support. This layer containing the following components:
- Ar N NAr (1) sensitizing effect.
- a photographic process using silver halides is the process which has heretofore been most widely utilized due to the. excellent photographic properties thereof, such as high sensitivity and good gradation over any of the other processes such as an electrophotographic process or a diazo-photographic process.
- silver halide photographic materials used in this process are developed with a developer after image-wise exposure thereof, and then, they are subjected to several after-treatments such as stopping,f1xation, washing with water or stabilization so that the developed images are not discolored or deteriorated under normal light or so that the non-developed part (hereunder referred to as background) is not blackened. Accordingly, these treatments require time and labor.
- a first method is the so-called one-bath development and fixation method as described in, for example, U.S. Pat. No. 2,875,048, British Pat. No. 954,453 and German Pat. No. 1,163,142, where the two operations of development and fixation in the conventional silver halide photographic process are carried out in one bath.
- a second method is to try to change the wet-type treatment which has been employed in the present silver halide photographic process, to adry-type treatment, for example as described in German Pat. No. 1,174,159, British Pat. Nos. 943,476 and 951,644, etc.
- a third method is to try to use, as photosensitive elements, a combination of a main component of a long chain aliphatic carboxylic acid silver salt such as silver behenate, or another silver salt such as silver saccharin or silver benzotriazole, and a catalytic amount of a silver halide, for example as described in Japanese Pat. Publication Nos. 26582/69 and 22185/70, British Pat. No. 1,205,500, and US. Pat. Nos. 3,152,904, 3,457,075, 3,635,719, and 3,645,739, etc.
- This invention relates to the third approach among the above described three types of methods.
- An object of this invention is to provide heat developable photographic materials having at least one sensitized light-sensitive layer.
- the present inventors have conducted various research in an effort to obtain such sensitizers which are effective for heat developable photographic materials, and have at last found that the compounds of formulae (1) (II) as described herein have excellent sensitizing effects for the heat developable photographic materials of this invention.
- This invention therefore relates to heat developable photographic materials having at least one layer on a support, which layer contains the following components:
- Suitable aryl group represented by Ar,, Ar Ar and Ar,-, in the above formulae includes phenyl, oz-naphthyl and B-naphthyl groups, which can be unsubstituted or substituted.
- Suitable arylene groups represented by Ar includes phenylene, biphenylene and naphthylene groups, which can be unsubstituted or substituted.
- Suitable substituents of these aryl and arylene groups include alkyl groups (e.g., methyl groups, ethyl groups, t-butyl groups, etc), halogen atoms (e.g., chloride atoms, bromine atoms, iodine atoms), hydroxyl groups, SO;,M groups, -COOM groups, aryl groups (e.g., phenyl groups, tolyl groups, xylyl groups, etc.), nitro groups, amino groups, alkylamino groups, arylamino groups, acyl groups (e.g., acetyl groups, propionyl groups, etc.), alkoxy groups (e.g., methoxy groups, ethoxy groups, propoxy groups, etc.), arylsulfonyloxy groups, alkylsulfonyloxy groups, etc. as representative examples.
- alkyl groups e.g., methyl groups, ethyl
- alkyl, alkoxy and acyl groups suitably can have 1 to 8 carbon atoms, preferably l to 4 carbon atoms.
- Preferred alkali metals are Li, Na, K, Pb, etc.
- Preferred alkaline earth metals are Ca, Ba, Mg, etc. (1+)
- the arylene group bonding can be at any position. Nao 5 Representative examples of preferred compounds of 3v this invention are as follows:
- the amount of the component (e) which is added is suitably about 10' to 10 mole per 1 mole of the organic silver salt. This amount can be varied, depending upon the kind of the compound used, the kind of the organic silver salt, the kind of the catalytic amount of the silver halide, the kind of the reducing agent, the treating temperature, etc. If the amount of the component (e) exceeds the above described range, the degree of coloration of lightsensitive layer increases very often, which is disadvantageous in some uses. However, when the material is applied to such uses where coloration is not a problem or when compounds giving rise to less coloration are used as the component (e), the amount of the component (e) which can be used can exceed this range.
- organic silver salts are suitable for use in the present invention, for example, the silver salts of organic compounds containing imino, mercapto or carboxyl groups, for example, as disclosed in US. Pat. Nos. 3,457,075 and 3,152,904.
- organic silver salts are silver benzotriazole, silver saccharin, silver phthaladionone, the silver salt of 3-mercapto-4-phenyl-l,2,4- triazole, the silver salt or 4-hydroxy-6-methyl-l ,3,3a,7- tetrazaindene, the silver salt of Z-(S-ethylthioglycolamido)-benzothiazole, silver caprate, silver laurate, silver myristate, silver palmitate, silver stearate, silsver behenate, silver akipate, silver sebacate, etc.
- the component (b) of the present invention is (la compound which reacts with the silver salt of the component (a) to form a silver halide, or is (2) a silver halide.
- Representative examples of the compound (1 are inorganic compounds of the formula MX,,; where M represents a hydrogen atom, an ammonium group or a metal atom (such as strontium, cadmium, zinc, tin, chromium, sodium, barium, iron, cesium, lanthanum, copper, calcium, nickel, magnesium, potassium, aluminum, antimony, gold, cobalt, mercury, lead, beryllium, lithium, manganese, gallium, indium, rhodium, ruthenium, palladium, iridium, platinum, thallium, bismuth, etc.), X represents a halogen atom (such as chlorine, bromine, iodine),and when M is a hydrogen atom or an ammonium group n is l, but when M is a metal atom
- organic halogen compounds such as triphenylmethyl chloride, triphenylmethyl bromide, 2-bromo-2-methylpropane, 2-bromobutyric acid, 2- bromoethanol, benzophenone dichloride, iodoformy carbon tetrachloride, etc. can also be included within the scope of compound(l).
- Suitable silver halides of the latter (2) include silver chloride, silver bromide, silver iodobromide, silver iodobromochloride, silver bromochloride and silver iodide.
- Suitable examples of components (b) above, are disclosed in US. Pat. No. 3,457,075.
- the photosensitive silver halide can be in any form,
- a suitable particle size can range from about 0.002 M to 2 u preferably 0.006 p. to 0.5 ,u.
- the emulsion containing the photosensitive silver halide can be optionally prepared according to any of the methods which are known in the field of photography.
- the emulsion can be prepared by the single-jet process, by the double-jet process, for example, a Lippmann emulsion, an ammonia process emul sion, a thiocyanate or thioether digested emulsion; for example, the emulsions as described in US. Pat. Nos. 2,222,264 and 3,320,069 and 3,271,157.
- the silver halide which can used in this invention can be sensitized with conventional chemical sensitizers which are generally used for silver halide emulsions, for example, with reducing agents, sulfur or selenium compounds, gold, platinum or palladium compounds or a mixture thereof. Suitable methods for sensitization are described, for example, in US. Pat. Nos. 2,623,499; 2,399,083; 3,297,447 and 3,297,446.
- the compound of the above described component (b) can be used alone or as a mixture of two or more kinds of compounds.
- the amount of component (b) which can be added is suitably in the range of about 0.00] to 0.5 mole, preferably 0.01 to 0.2 mol, per 1 mole of organic silver salt. If the amount of the component (b) is lower than this range, the sensitivity of the material is reduced, but on the contrary, if the amount thereof exceeds this range, the presence of too large an amount of component (b) causes such an unfavorable phenomenon that when the material is left exposed to room light after the heat development thereof, the nonimage part gradually blackens, resulting in a decrease in the contrast between the non-image part and the image part.
- the reducing agent of the component (c) of the present invention must be one suitable for the reduction of the organic silver salt to form silver images, when heated in the presence of the exposed silver halide catalyst.
- a suitable reducing agent is determined in accordance-with the combination of the organic silver salt used, and, for example, substituted phenols, substituted or unsubstituted bisphenols, substituted or unsubstituted naphthols, dior poly-hydroxy benzenes, dior poly-hydroxy naphthalenes, hydroquinone monoethers, ascorbic acid or derivatives thereof, 3- pyrazolidones, pyrazol-S-ones, reducing sugars, kojic acid, hinokitiol, etc. can be rised.
- Hydroquinone methylhydroquinone, chlorohydroquinone, bromohydroquinone, phenylhydroquinone, hydroquinone-monosulfonate, t-octylhydroquinone, t-butylhydroquinone, ,2,S-dimethylhydroquinone, 2,6-dimethylhydroquinone, methoxyhydroquinone, ethoxyhydroquinone, p-methoxyphenol, pethoxyphenol, hydroquinone-monobenzylether, catechol, pyrogallol, resorcin, p-aminophenol, o-
- bisphenol A bisphenol A, l,1-bis-(2-hydroxy-3,S-dimethylphenyl)- 3,-5,5-trimethylhexane, 2,4,4-trimethylpentyl-bis-(2- hydroxy-3,S-dimethylphenyl)methane, bis(Z-hydroxy- 3-t-butyl-5-methylphenyl)-methane, bis(2-hydroxy- 4,4-methylenebis(3- methyl-S-t-butylphenol), 4,4'-methylenebis(2,6-di-tbutylphenol), 2,2'-methylenebis(2-t-butyl-4- ethylphenol), 2,6-dimethylenebis(2-hydroxy-3-t-butyldimethylamine, a,a'-(3,5-di-t-butyl-4-hydroxyphenyl)- dimethylether, etc.
- reducing agents can be used in the form of a mixture of two or more of them.
- a suitable reducing agent is selected in combination with the organic silver salt.
- the higher fatty acid silver salts such as silver behenate are relatively difficultly reduced, and therefore relatively strong reducing agents, for example, the bisphenols such as 4,4'-methylenebis(3- methyl--t-butylphenol) are suitable therefor.
- relatively weak reducing agents for example, the substituted phenols such as p-phenylphenol, are suitable for silver salts which are relatively easily reduced, such as silver laurate.
- strong reducing agents such as ascorbic acid type reducing agents are suitable for silver salts which are extremely difficultly reduced, such as silver benzotriazole.
- the amount of reducing agent which is used in this invention as described above will vary depending upon the organic silver salt used and the kind of reducing agent used, and therefore, the amount cannot unequivocally set forth, but in general, the amount suitably ranges from about 0.1 to 5 moles, preferably 0.6 to 2 moles per 1 mole of organic silver salt.
- an appropriate reducing agent can be selected and used in combination with a specific organic silver salt, and therefore it is unnecessary to specifically define the organic silver salt and reducing agent used.
- the components (a), (b), (c) and (e) are preferably dispersed in a binder and applied on a support.
- all of the components (a) to (e) are completely dispersed in the binder and applied on a support as one layer, or alternatively, these components (a) to (e) can be separated into groups and dispersed separately in the binder and then the respective dispersions are applied on a support as individual layers.
- the binder component (d) any and every conventional binder which has heretofore been used in this field can be used. In general, hydrophobic binders are preferred, but hydrophilic binders can also be used.
- binders are preferably transparent or semi-transparent, and suitable binders are, for example, natural substances, such as gelatin, gelatin derivatives or mixtures thereof with latex type vinyl polymers, cellulose derivatives, and synthetic polymer sub-- stances, etc.
- binders are as follows: gelatin, gelatin phthalide, acrylamide, polyvinyl butyral, cellulose acetate-butyrate, cellulose acetatepropionate, polymethylmethacrylate', polyvinyl pyrrolidone, polystyrene, ethyl-cellulose, polyvinyl chloride, chlorinated rubber, polyisobutylene, butadienestyrene copolymers, vinyl chloride-vinyl acetate copolymers, vinyl acetate-vinyl chloride-maleic acid copolymers, polyvinyl alcohol, polyvinyl acetate, benzyl cellulose, cellulose acetate, cellulose propionate, cellulose acetate-phthalate, etc.
- the amount of binder is suitably in a ratio (by weight) of about 0.1:1 to 5:1,preferably 0.2:1 to 3:1 on the basis of the amount of the organic silver salt.
- the component (a) or (c) is a high molecular weight substance which has the function of a binder, the use of binder can be omitted.
- supports in a broad range can be used.
- Representative supports are, for example, cellulose nitrate films, cellulose ester films, poly(- vinylacetal) films, polystyrene films, poly(ethyleneterephthalate) films, polycarbonate films, and glass, paper, metal, etc. supports a suitable coating amo unt ranges from 0.1 to 3 g/m preferably 0.3 to 2 g/m
- An antistatic layer or a conductive layer can be provided in the heat developing photographic materials of this invention.
- an anti-halation material and an anti-halation dye can also be incorporated therein.
- the heat developable photographic materials of this invention can optionally contain matting agents such as starch, titanium dioxide, zinc oxide and silica.
- matting agents such as starch, titanium dioxide, zinc oxide and silica.
- fluorescent whitening agents such as stilbene, triazine, oxazole, and coumarin type fluorescent whitening agents can also be contained therein.
- the heat developable photosensitive layer(s) of this invention can be applied to a support using various coating methods, for example, the dip method the airknife method, the curtain coating method as well as the extrusion coating method with a hopper as described in US. Pat. No. 2,681,294. If necessary, two or more layers can be simultaneously applied.
- optical sensitizing dyes which have heretofore been used for silver halide emulsions can advantageously be used in the heat developing-out photographic material of the present invention for imparting additional sensitivity thereto.
- the cyanine dyes and merocyanine dyes as disclosed in US. Pat. Nos. 3,457,075 and 3,761,279, are suitable as the optical sensitizing dyes which can be used in the present invention.
- . 2 5 ca-ca n N x (L S H 2 5 C 11 s l k a 0 N S C 11 v 7 2% s (1 011 on s N l A 1 o n s C H 11 CH N N (Hi-CRT- S o u /L 5 ll N ⁇ N developable photographic material.
- the thickness of this over-coating polymer layer film is suit- 5 S ably 1 to 20 .1..
- Suitable polymers for this layer are, for example, as T follows: polyvinyl chloride, polyvinyl acetate, vinyl C 11 chloridevinyl acetate copolymers, polyvinyl butyral,
- polystyrene polymethylmethacryate
- polyurethane 2 5 5 rubbers polyurethane 2 5 5 rubbers
- xylene resins polystyrene, polymethylmethacryate, polyurethane 2 5 5 rubbers, xylene resins, .benzylcellulose, ethyl cellulose,
- the tem- L H c H perature generally employed in the heating is suitably 2 5 2 5 in the range of 100 to 160C, more preferably 110 to 140C.
- the time for the development is in general about 1 to 60 seconds. Higher temperatures or lower temperatures can be selected within the above described range, by prolonging or reducing the heating time.
- the photographic material can be brought into contact with a simple hot plate or the like,
- s or can be brought into contact with a heated drum, or as the case may be, can also be passed through a heated f .zone.
- high frequency induction heating or ON laser beam heating can also be utilized.
- sensitizing dyes are preferably added to photographic materials in the form of a solution or dispersion dissolved or dispersed in an organic solvent.
- the use of the optical sensitizing dye together with the sensitizer component (e) of this invention causes an increase of sensitivity of the resulting heat.
- EXAMPLE 1 3.4 g of behenic acid were dissolved in ml of toluene at 60C and the resulting solution was adjusted to 60C. While stirring with a stirrer, 100 ml of a diluted nitric acid aqueous solution (pH 2.0 at 25C) were added and mixed therewith.
- the resulting mixture solution was kept at 60C, and while continuously stirring with a stirrer, an aqueous solution containing a silverammonium complex is added thereto.
- This complex solution was prepared as follows. Aqueous ammonia was added to about 80 ml of an aqueous solution containing 1 .7 g of silver nitrate to form a silver-ammonium complex, and water was added thereto to make the total volume of the aqueous solution 100 ml.) Thus, a dispersion containing fine crystals of silver behenate was obtained. This dispersion was left at room temperature (about C) for 20 minutes, whereby an aqueous layer and a toluene layer were separated from each other.
- each of these photographic materials (A) (C) was further over-coated a 15 wt percent tetrahydro-furan solution of a vinyl chloride-vinyl acetate copolymer (consisting of 95 wt percent of vinyl chloride and 5 wt percent of vinyl acetate), to form a over-coating film of a thickness of 10 ,u (after drying).
- a vinyl chloride-vinyl acetate copolymer consisting of 95 wt percent of vinyl chloride and 5 wt percent of vinyl acetate
- EXAMPLE 2 In this Example, the same amount of merocyanine dye of Example 1 was used together with Compound (3), in place of the use of Compound (3) only, and others materials were the same as in Example 1.
- Material Material Material Material B (C Relative Sensitivity 9,300 100 600 The effect of the present sensitizer is similar to that of the Example 1.
- EXAMPLE A solution of l l g of lauric acid dissolved in 100 ml of isoamyl acetate was kept at 5C, and, while stirring, 100 ml of a diluted nitric acid aqueous solution (pH 2.0 at 25C) were added thereto and admixed, and then while further continuously stirring, 50 ml of a silver nitrate-ammonium complex aqueous solution containing 8.5 g of silver nitrate were added thereto over the course of 1 minute thereby to react the lauric acid and silver ion.
- Theaqueous phase wasfirst removed, and 400 ml of water were added again to the remaining phase to wash the same by the decantation method. This operation was repeated three times, and then 400 ml of methanol were added to separate the silver benzotriazole by centrifuging. Thus, .8 g of silver benzotriazole were obtained.
- the particles of the silver benzotriazole were of a nearly spherical form, having a particle size diameter of about 1 u.
- a heat developable photographic material having at least one photosensitive layer on a support, said layer containing the following components:
- Ar Ar and Ar,- each represents an aryl group and Ar, represents an arylene group, with the proviso that at least one of Ar, and Ar and at least one of Ar;,, Ar and Ar is substituted with a SO M group.
- M being a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, or a Nl-l, group.
- sensitizer (e) is selected from the group consisting of the following com-. pounds coon NaO S COONa SO Na Mao;
- optical sensitizing dye is a cyanine dye or a merocyanine dye.
Abstract
Heat developable photographic materials having at least one photosensitive layer on a support, this layer containing the following components: A. AN ORGANIC SILVER SALT, B. A CATALYTIC AMOUNT OF A PHOTOSENSITIVE SILVER HALIDE OR A COMPOUND WHICH REACTS WITH THE ORGANIC SILVER SALT (A) TO PRODUCE A PHOTOSENSITIVE SILVER HALIDE, C. A REDUCING AGENT, D. A BINDER, AND E. AS A SENSITIZER, AT LEAST ONE OF THE FOLLOWING COMPOUNDS (I) and (II): Ar1 - N N - Ar2 (I) Ar3 - N N - Ar4 - N N - Ar5 (II) wherein Ar1, Ar2Ar3 and Ar5 each represents an aryl group and Ar4 represents an arylene group, with the proviso that at least one of Ar1 and Ar2, and at least one of Ar3, Ar4 and Ar5 are substituted with -SO3M or -COOM, M being a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, or a -NH4 group. The sensitizer (e) has a particularly excellent sensitizing effect.
Description
United States Patent 1 Ikenoue et a1.
\ HEAT DEVELOPABLE PHOTOGRAPHIC MATERIAL CONTAINING AZO DYES AS SENSITIZERS [75] Inventors: Shinpei Ikenoue; Takao Masuda,
both of Asaka, Japan [73] Assignee: Fuji Photo Film Co., Ltd.,
Kanagawa, Japan [22] Filed: Jan. 17, 1974 [2]] Appl. No.: 434,453
[30] Foreign Application Priority Data Jan. 17, 1973 Japan 48-7624 [52] U.S. Cl 96/l14.1, 96/67, 96/139 [51] Int. Cl G03c 1/02 [58] Field of Search 96/l14.1, 114.6, 109, 107, 96/108; 117/367, 36.8
Primary Examiner-Norman G. Torchin Assistant Examiner-Judson R. Hightower Attorney, Agent, or Firm-Sughrue, Rothwell, Mion,
Zinn & Macpeak [111 3,870,523 1 Mar. 11, 1975 [57] ABSTRACT Heat developable photographic materials having at least one photosensitive layer on a support. this layer containing the following components:
a. an organic silver salt,
b. a catalytic amount of a photosensitive silver halide or a compound which reacts with the organic silver salt (a) to produce a photosensitive silver halide,
c. a reducing agent,
d. a binder, and
e. as a sensitizer, at least one of the following compounds (I) and (II):
Ar N=NAr (1) sensitizing effect.
12 Claims, No Drawings HEAT DEVELOPABLE PHOTOGRAPHIC MATERIAL CONTAINING AZO DYES AS SENSITIZERS BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates to heat developable photographic materials, in particular, to those having at least one photosensitive layer of an especially high sensitivity.
2. Description of the Prior Art A photographic process using silver halides is the process which has heretofore been most widely utilized due to the. excellent photographic properties thereof, such as high sensitivity and good gradation over any of the other processes such as an electrophotographic process or a diazo-photographic process. However, silver halide photographic materials used in this process are developed with a developer after image-wise exposure thereof, and then, they are subjected to several after-treatments such as stopping,f1xation, washing with water or stabilization so that the developed images are not discolored or deteriorated under normal light or so that the non-developed part (hereunder referred to as background) is not blackened. Accordingly, these treatments require time and labor. In addition, there are the danger to working personnel due to contact with the chemicals and the difficulties in that the interior of the treating room and the hands and clothes of operators are stained. Therefore, in the photographic process using silver halides, it is extremely desired to improve the treatment thereof so that the treatment can be carried out in a dry state without solution treatment and that the treated image can be kept stable.
For this, various efforts have heretofore been made. A first method is the so-called one-bath development and fixation method as described in, for example, U.S. Pat. No. 2,875,048, British Pat. No. 954,453 and German Pat. No. 1,163,142, where the two operations of development and fixation in the conventional silver halide photographic process are carried out in one bath. A second method is to try to change the wet-type treatment which has been employed in the present silver halide photographic process, to adry-type treatment, for example as described in German Pat. No. 1,174,159, British Pat. Nos. 943,476 and 951,644, etc. A third method is to try to use, as photosensitive elements, a combination of a main component of a long chain aliphatic carboxylic acid silver salt such as silver behenate, or another silver salt such as silver saccharin or silver benzotriazole, and a catalytic amount of a silver halide, for example as described in Japanese Pat. Publication Nos. 26582/69 and 22185/70, British Pat. No. 1,205,500, and US. Pat. Nos. 3,152,904, 3,457,075, 3,635,719, and 3,645,739, etc.
This invention relates to the third approach among the above described three types of methods.
However, sufficient photosensitivity can not as yet be attained in the conventional heat developing-out photographic materials, for example those comprising compositions ofa fatty acid silver salt, a reducing agent and a catalytic amount of silver halide.
Regarding conventional techniques for sensitization of conventional heat developing photographicmaterials, the description, for example, in the above described U.S. Pat. No. 3,457,075 which belongs to the third method, is that known merocyanine-dyes are effective as so-called optical sensitizers for silver halide emulsions. However, every optical sensitizer which is effective for silver halide emulsions is, in general, not always effective for every. heat developable photographic material, and it is difficult to predict what kind of sensitizer of what structure is effective for heat developable photographic materials of this invention.
SUMMARY OF THE INVENTION An object of this invention is to provide heat developable photographic materials having at least one sensitized light-sensitive layer.
The present inventors have conducted various research in an effort to obtain such sensitizers which are effective for heat developable photographic materials, and have at last found that the compounds of formulae (1) (II) as described herein have excellent sensitizing effects for the heat developable photographic materials of this invention.
This invention therefore relates to heat developable photographic materials having at least one layer on a support, which layer contains the following components:
a. an-organic silver salt,
b. a catalytic amount of a photosensitive silver halide or a compound which reacts with the organic silver salt (a) to produce a photosensitive silver halide,
c. a reducing agent,
d. a binder, and
e. as a sensitizer, at least one of the following com pounds (I) and (II);
Ar -N=NAr,N=N=Ar (11) wherein An, Ar Ar and Ar each represents an aryl group and Ar, represents an arylene group, with the proviso that at least one of Ar and Ar and at least one of Ar Ar, and Ar are substituted with a -SO M or COOM group with M being a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, or a -NH, group.
DETAILED DESCRIPTION OF THE INVENTION Suitable aryl group represented by Ar,, Ar Ar and Ar,-, in the above formulae includes phenyl, oz-naphthyl and B-naphthyl groups, which can be unsubstituted or substituted. Suitable arylene groups represented by Ar includes phenylene, biphenylene and naphthylene groups, which can be unsubstituted or substituted. Suitable substituents of these aryl and arylene groups include alkyl groups (e.g., methyl groups, ethyl groups, t-butyl groups, etc), halogen atoms (e.g., chloride atoms, bromine atoms, iodine atoms), hydroxyl groups, SO;,M groups, -COOM groups, aryl groups (e.g., phenyl groups, tolyl groups, xylyl groups, etc.), nitro groups, amino groups, alkylamino groups, arylamino groups, acyl groups (e.g., acetyl groups, propionyl groups, etc.), alkoxy groups (e.g., methoxy groups, ethoxy groups, propoxy groups, etc.), arylsulfonyloxy groups, alkylsulfonyloxy groups, etc. as representative examples.
Of these substituents, the alkyl, alkoxy and acyl groups suitably can have 1 to 8 carbon atoms, preferably l to 4 carbon atoms.
Preferred alkali metals are Li, Na, K, Pb, etc.
Preferred alkaline earth metals are Ca, Ba, Mg, etc. (1+) The arylene group bonding can be at any position. Nao 5 Representative examples of preferred compounds of 3v this invention are as follows:
5 -N=N- NH (1) I NaO S COONa NaO S- .N=N l0 -N=N OH a v on 5 v on 3N( H v NaO s SO Na (8) j NaO s SO Naon NaO S--N=N N N (1o) S0 Na H3 on CH5 CH3 on O Na SO Na ca on on M =N -N=N S0 Na NaO S- -N=N-/ CH3 cu O Na l on
/\ N- I Inn SO Na S0 Na on H so Na m The amount of the component (e), which is the compound effective as a sensitizer of the present invention,
which is added is suitably about 10' to 10 mole per 1 mole of the organic silver salt. This amount can be varied, depending upon the kind of the compound used, the kind of the organic silver salt, the kind of the catalytic amount of the silver halide, the kind of the reducing agent, the treating temperature, etc. If the amount of the component (e) exceeds the above described range, the degree of coloration of lightsensitive layer increases very often, which is disadvantageous in some uses. However, when the material is applied to such uses where coloration is not a problem or when compounds giving rise to less coloration are used as the component (e), the amount of the component (e) which can be used can exceed this range.
The following organic silver salts (component a) are suitable for use in the present invention, for example, the silver salts of organic compounds containing imino, mercapto or carboxyl groups, for example, as disclosed in US. Pat. Nos. 3,457,075 and 3,152,904.
Representative examples of these organic silver salts are silver benzotriazole, silver saccharin, silver phthaladionone, the silver salt of 3-mercapto-4-phenyl-l,2,4- triazole, the silver salt or 4-hydroxy-6-methyl-l ,3,3a,7- tetrazaindene, the silver salt of Z-(S-ethylthioglycolamido)-benzothiazole, silver caprate, silver laurate, silver myristate, silver palmitate, silver stearate, silsver behenate, silver akipate, silver sebacate, etc.
The component (b) of the present invention is (la compound which reacts with the silver salt of the component (a) to form a silver halide, or is (2) a silver halide. Representative examples of the compound (1 are inorganic compounds of the formula MX,,; where M represents a hydrogen atom, an ammonium group or a metal atom (such as strontium, cadmium, zinc, tin, chromium, sodium, barium, iron, cesium, lanthanum, copper, calcium, nickel, magnesium, potassium, aluminum, antimony, gold, cobalt, mercury, lead, beryllium, lithium, manganese, gallium, indium, rhodium, ruthenium, palladium, iridium, platinum, thallium, bismuth, etc.), X represents a halogen atom (such as chlorine, bromine, iodine),and when M is a hydrogen atom or an ammonium group n is l, but when M is a metal atom, n is a number corresponding to the valence of the metal. Y
In addition, organic halogen compounds such as triphenylmethyl chloride, triphenylmethyl bromide, 2-bromo-2-methylpropane, 2-bromobutyric acid, 2- bromoethanol, benzophenone dichloride, iodoformy carbon tetrachloride, etc. can also be included within the scope of compound(l). Suitable silver halides of the latter (2) include silver chloride, silver bromide, silver iodobromide, silver iodobromochloride, silver bromochloride and silver iodide. Suitable examples of components (b) above, are disclosed in US. Pat. No. 3,457,075.
The photosensitive silver halide can be in any form,
such as crude particles or fine particles, and in particular, emulsions of extremely fine particles are especially useful. A suitable particle size can range from about 0.002 M to 2 u preferably 0.006 p. to 0.5 ,u.
The emulsion containing the photosensitive silver halide can be optionally prepared according to any of the methods which are known in the field of photography. For example, the emulsion can be prepared by the single-jet process, by the double-jet process, for example, a Lippmann emulsion, an ammonia process emul sion, a thiocyanate or thioether digested emulsion; for example, the emulsions as described in US. Pat. Nos. 2,222,264 and 3,320,069 and 3,271,157.
The silver halide which can used in this invention can be sensitized with conventional chemical sensitizers which are generally used for silver halide emulsions, for example, with reducing agents, sulfur or selenium compounds, gold, platinum or palladium compounds or a mixture thereof. Suitable methods for sensitization are described, for example, in US. Pat. Nos. 2,623,499; 2,399,083; 3,297,447 and 3,297,446.
The compound of the above described component (b) can be used alone or as a mixture of two or more kinds of compounds. The amount of component (b) which can be added is suitably in the range of about 0.00] to 0.5 mole, preferably 0.01 to 0.2 mol, per 1 mole of organic silver salt. If the amount of the component (b) is lower than this range, the sensitivity of the material is reduced, but on the contrary, if the amount thereof exceeds this range, the presence of too large an amount of component (b) causes such an unfavorable phenomenon that when the material is left exposed to room light after the heat development thereof, the nonimage part gradually blackens, resulting in a decrease in the contrast between the non-image part and the image part.
The reducing agent of the component (c) of the present invention must be one suitable for the reduction of the organic silver salt to form silver images, when heated in the presence of the exposed silver halide catalyst.
A suitable reducing agent is determined in accordance-with the combination of the organic silver salt used, and, for example, substituted phenols, substituted or unsubstituted bisphenols, substituted or unsubstituted naphthols, dior poly-hydroxy benzenes, dior poly-hydroxy naphthalenes, hydroquinone monoethers, ascorbic acid or derivatives thereof, 3- pyrazolidones, pyrazol-S-ones, reducing sugars, kojic acid, hinokitiol, etc. can be rised.
Representativeexamples of these compounds are ex-' emplified in the following:
Hydroquinone, methylhydroquinone, chlorohydroquinone, bromohydroquinone, phenylhydroquinone, hydroquinone-monosulfonate, t-octylhydroquinone, t-butylhydroquinone, ,2,S-dimethylhydroquinone, 2,6-dimethylhydroquinone, methoxyhydroquinone, ethoxyhydroquinone, p-methoxyphenol, pethoxyphenol, hydroquinone-monobenzylether, catechol, pyrogallol, resorcin, p-aminophenol, o-
.aminophenol, N-methyl-p-aminophenol, 2-methoxy-4- ynaphthalene, l-hydroxy-4-aminonaphthalene, l,S-dihydroxynaphthalene, l-hydroxy-2-phenyl14- 'methoxynaphthalene, 1-hydroxy-2-methyl-4- methoxynaphthalene, a-naphthol, B-naphthol, 1,1- dihydroxy-Z,2-binaphthyl, 4,4-dimethoxy-l ,l dihydroxy-2,2, binaphthyl, 6 ,6'-dibromo-2,2-dihyl,l-binaphthyl, bis(2-hydroxy-l-naphthyl)-methane,
' 3,S-di-t-butylphenyl)methane,
bisphenol A, l,1-bis-(2-hydroxy-3,S-dimethylphenyl)- 3,-5,5-trimethylhexane, 2,4,4-trimethylpentyl-bis-(2- hydroxy-3,S-dimethylphenyl)methane, bis(Z-hydroxy- 3-t-butyl-5-methylphenyl)-methane, bis(2-hydroxy- 4,4-methylenebis(3- methyl-S-t-butylphenol), 4,4'-methylenebis(2,6-di-tbutylphenol), 2,2'-methylenebis(2-t-butyl-4- ethylphenol), 2,6-dimethylenebis(2-hydroxy-3-t-butyldimethylamine, a,a'-(3,5-di-t-butyl-4-hydroxyphenyl)- dimethylether, etc.
These reducing agents can be used in the form of a mixture of two or more of them. A suitable reducing agent is selected in combination with the organic silver salt. For example, the higher fatty acid silver salts such as silver behenate are relatively difficultly reduced, and therefore relatively strong reducing agents, for example, the bisphenols such as 4,4'-methylenebis(3- methyl--t-butylphenol) are suitable therefor. On the other hand, relatively weak reducing agents, for example, the substituted phenols such as p-phenylphenol, are suitable for silver salts which are relatively easily reduced, such as silver laurate. In addition, strong reducing agents such as ascorbic acid type reducing agents are suitable for silver salts which are extremely difficultly reduced, such as silver benzotriazole.
The amount of reducing agent which is used in this invention as described above will vary depending upon the organic silver salt used and the kind of reducing agent used, and therefore, the amount cannot unequivocally set forth, but in general, the amount suitably ranges from about 0.1 to 5 moles, preferably 0.6 to 2 moles per 1 mole of organic silver salt.
As is evident from the above explanation, in the formation of heat developable photographic materials of the present invention, an appropriate reducing agent can be selected and used in combination with a specific organic silver salt, and therefore it is unnecessary to specifically define the organic silver salt and reducing agent used.
In the present invention, the components (a), (b), (c) and (e) are preferably dispersed in a binder and applied on a support. In this instance, all of the components (a) to (e) are completely dispersed in the binder and applied on a support as one layer, or alternatively, these components (a) to (e) can be separated into groups and dispersed separately in the binder and then the respective dispersions are applied on a support as individual layers. As the binder component (d) any and every conventional binder which has heretofore been used in this field can be used. In general, hydrophobic binders are preferred, but hydrophilic binders can also be used. These binders are preferably transparent or semi-transparent, and suitable binders are, for example, natural substances, such as gelatin, gelatin derivatives or mixtures thereof with latex type vinyl polymers, cellulose derivatives, and synthetic polymer sub-- stances, etc.
Representative example of these binders are as follows: gelatin, gelatin phthalide, acrylamide, polyvinyl butyral, cellulose acetate-butyrate, cellulose acetatepropionate, polymethylmethacrylate', polyvinyl pyrrolidone, polystyrene, ethyl-cellulose, polyvinyl chloride, chlorinated rubber, polyisobutylene, butadienestyrene copolymers, vinyl chloride-vinyl acetate copolymers, vinyl acetate-vinyl chloride-maleic acid copolymers, polyvinyl alcohol, polyvinyl acetate, benzyl cellulose, cellulose acetate, cellulose propionate, cellulose acetate-phthalate, etc.
The amount of binder is suitably in a ratio (by weight) of about 0.1:1 to 5:1,preferably 0.2:1 to 3:1 on the basis of the amount of the organic silver salt.
1f the component (a) or (c) is a high molecular weight substance which has the function of a binder, the use of binder can be omitted.
With respect to the support to be used in the present invention, various kinds of supports in a broad range can be used. Representative supports are, for example, cellulose nitrate films, cellulose ester films, poly(- vinylacetal) films, polystyrene films, poly(ethyleneterephthalate) films, polycarbonate films, and glass, paper, metal, etc. supports a suitable coating amo unt ranges from 0.1 to 3 g/m preferably 0.3 to 2 g/m An antistatic layer or a conductive layer can be provided in the heat developing photographic materials of this invention. In addition, an anti-halation material and an anti-halation dye can also be incorporated therein.
In addition, the heat developable photographic materials of this invention can optionally contain matting agents such as starch, titanium dioxide, zinc oxide and silica. Further, fluorescent whitening agents such as stilbene, triazine, oxazole, and coumarin type fluorescent whitening agents can also be contained therein.
The heat developable photosensitive layer(s) of this invention can be applied to a support using various coating methods, for example, the dip method the airknife method, the curtain coating method as well as the extrusion coating method with a hopper as described in US. Pat. No. 2,681,294. If necessary, two or more layers can be simultaneously applied.
Some types of optical sensitizing dyes which have heretofore been used for silver halide emulsions can advantageously be used in the heat developing-out photographic material of the present invention for imparting additional sensitivity thereto. For examaple, the cyanine dyes and merocyanine dyes, as disclosed in US. Pat. Nos. 3,457,075 and 3,761,279, are suitable as the optical sensitizing dyes which can be used in the present invention.
Example of suitable merocyanine dyes are as follows:
. 2 5 =ca-ca n N x (L S H 2 5 C 11 s l k a 0 N S C 11 v 7 2% s (1 011 on s N l A 1 o n s C H 11 CH N N (Hi-CRT- S o u /L 5 ll N\N developable photographic material. The content of the optical sensitizing dye in the photographic material of this invention is about 10 to 10 mole per 1 mole of the organic silver salt component (a). If the sensitizer of the present invention is effective also as an optical sensitizer, the optical sensitizing dye need not necessar- J: =CH-CH=CH-CH s 5 l o 11 s 5 y a ily be used. In addition, an over-coating polymer layer I 11 o I CH=CCH= !I 2 5 2 5 can optionally be provided on the photosensitive layer S of the heat developable photographic material of this 3-614 -=CH I invention, for the purpose of increasing the transpar- N ency of the photosensitive layer, increasing the density of image formed and improving the storability of the H c H freshness of said material (that is, the ability to main- 2 5 a 5 tain the original photographic properties, or those ex- 1 isting immediately after the preparation of the photographic material, .even after storage thereof). The thickness of this over-coating polymer layer film is suit- 5 S ably 1 to 20 .1..
CH CH CH CH=CH Suitable polymers for this layer are, for example, as T follows: polyvinyl chloride, polyvinyl acetate, vinyl C 11 chloridevinyl acetate copolymers, polyvinyl butyral,
polystyrene, polymethylmethacryate, polyurethane 2 5 5 rubbers, xylene resins, .benzylcellulose, ethyl cellulose,
cellulose acetate-butyrate, cellulose acetate, polyvinyl- I idene chloride, chlorinated polypropylene, polyvinyl pyrrolidone, cellulose propionate, polyvinyl formal, c B 0 11 cellulose acetate-phthalate, polycarbonate, cellulose 5 l acetatepropionate, etc. (11 N N The above described heat developable photographic materials can be developed merely by heating. the 4- same, after exposure to a light source such as a xenon C1 N v C1 lamp, a tungsten lamp, a mercury lamp, etc. The tem- L H c H perature generally employed in the heating is suitably 2 5 2 5 in the range of 100 to 160C, more preferably 110 to 140C. The time for the development is in general about 1 to 60 seconds. Higher temperatures or lower temperatures can be selected within the above described range, by prolonging or reducing the heating time.
Various means can be employed for the heat development of the photograpahic materials of this invena tion, for example, the photographic material can be brought into contact with a simple hot plate or the like,
. s or can be brought into contact with a heated drum, or as the case may be, can also be passed through a heated f .zone. In addition, high frequency induction heating or ON laser beam heating can also be utilized.
Now, the present invention will be explained in greater detail by reference to the following Examples. I Unless otherwise indicated, all parts, percents, ratios and the like are by weight.
These sensitizing dyes are preferably added to photographic materials in the form of a solution or dispersion dissolved or dispersed in an organic solvent. In this invention, the use of the optical sensitizing dye together with the sensitizer component (e) of this invention causes an increase of sensitivity of the resulting heat EXAMPLE 1 3.4 g of behenic acid were dissolved in ml of toluene at 60C and the resulting solution was adjusted to 60C. While stirring with a stirrer, 100 ml of a diluted nitric acid aqueous solution (pH 2.0 at 25C) were added and mixed therewith. The resulting mixture solution was kept at 60C, and while continuously stirring with a stirrer, an aqueous solution containing a silverammonium complex is added thereto. This complex solution was prepared as follows. Aqueous ammonia was added to about 80 ml of an aqueous solution containing 1 .7 g of silver nitrate to form a silver-ammonium complex, and water was added thereto to make the total volume of the aqueous solution 100 ml.) Thus, a dispersion containing fine crystals of silver behenate was obtained. This dispersion was left at room temperature (about C) for 20 minutes, whereby an aqueous layer and a toluene layer were separated from each other.
The aqueous layer was first removed, and 400 ml of water were added again to the remaining toluene layer, which was then washed therewith according to the decantation method. This operation was repeated three times, and then 400 ml of toluene were added to separate the silver behenate by centrifing. 4 g of silver behenate were obtained in the form of spindle-shaped crystals (lone side: about 1 a, short side: about 0.005
2.5 g of the obtained silver behenate were added to 20 ml of an isopropyl alcohol solution containing 2 g of polyvinyl butyral and subjected to ball-milling for 1 hour to form a polymer dispersion. To 20 ml of the thus formed silver salt-polymer dispersion were added the following components to prepare a heat developable photographic composition, which was then applied to a polyethylene terephthalate film support in an amount of 1.5 g (silver content)/m (support) to produce heat developable photograpahic material (A).
Ammonium Bromide 1 ml (2.5 wt7r methanol solution) Compound (3) (0.025 wt% methyl 5 ml cellosolve solution) 2,2'-Methylenebis(6-t-butyl-4- 3 ml methyl-phenol) (2.5 wt% methyl cellosolve solution) Phthaladinone l ml (2.5 wt7r methyl cellosolve solution) A part from this; two other kinds heat developable photograpahic materials (B) and (C) are prepared in a similar manner for comparison: the former (B) not containing the sensitizer Compound (30f the present invention, and the latter (C) containing, as a sensitizing dy'e, the same amount of the following merocyanine dye in place of Compound (3).
Merocyanine Dye Used in Material (C):
On the photosensitive layer of each of these photographic materials (A) (C) was further over-coated a 15 wt percent tetrahydro-furan solution of a vinyl chloride-vinyl acetate copolymer (consisting of 95 wt percent of vinyl chloride and 5 wt percent of vinyl acetate), to form a over-coating film of a thickness of 10 ,u (after drying).
These three kinds of photographic materials were exposed to a tungsten light source in an amount of exposure of 240,000 luc.sec through an optical wedge, and thereafter heated for 10 seconds at 120C for develop- Material Material Material (A Relative Sensitivity 14,000 600 From the above results, it can be understood that the sensitizer of the present invention has an extremely high sensitizing effect, in a comparison of the material (A) with the other material (B) or (C).
EXAMPLE 2 In this Example, the same amount of merocyanine dye of Example 1 was used together with Compound (3), in place of the use of Compound (3) only, and others materials were the same as in Example 1.
The results obtained are shown in the following Table. It can be understood therefrom that the sensitizer of the present invention displays a very excellent sensitizing effect due to the joint use with the merocyanine dye.
Material Material Material 7 (A) (B) (C Relative Sensitivity 21,000 100 600 EXAMPLE 3 In this Example, the same amount of the above described Compound (2) was used in place of Compound (3), and others materials were the same as in Example 1.
The results obtained are shown in the following Table. The effect of the present sensitizer is similar to that of Example 1.
Material Material Material (A) B) Relative Sensitivity 12,000 100 600 EXAMPLE 4 The same amount of the above described Compound (15) was used in place of Compound (3), and others materials were the same as in Example 1.
The results obtained are shown in the following Table.
Material Material Material B (C Relative Sensitivity 9,300 100 600 The effect of the present sensitizer is similar to that of the Example 1.
EXAMPLE A solution of l l g of lauric acid dissolved in 100 ml of isoamyl acetate was kept at 5C, and, while stirring, 100 ml of a diluted nitric acid aqueous solution (pH=2.0 at 25C) were added thereto and admixed, and then while further continuously stirring, 50 ml of a silver nitrate-ammonium complex aqueous solution containing 8.5 g of silver nitrate were added thereto over the course of 1 minute thereby to react the lauric acid and silver ion.
Spindle-shaped crystals of silver laurate were obtained (long side: about 0.8 t, short side: about 0.04 a). After the thus prepared silver salt was washed with water and then with methanol, 3.0 g of polyvinyl butyral and 20 ml of isopropyl alcohol (per 2.7 g of silver laurate) were added thereto to disperse the silver salt in a ball-mill, whereby a silver salt-polymer dispersion was prepared.
To 20 ml of the silver salt-polymer dispersion were added the following components to prepare a heat developable photographic composition, which was then applied to a polyethylene terephthalate film support in an amount of 1.7 g (silver content)/m (support) to produce a heat developable photographic material (A).
l,3-Dibromo-5,S-dimethylhydantoin 1 ml (2.5 1% methyl eellosolve solution) Ammonium Bromide l ml (2.5 wt% methanol solution) Compound (3) 1 5 ml (0.025 wt% methyl cellosolve solution) p-Phenylphenol 3 ml (70 wt% methyl cellosolve solution) Phthaladinone (2.5 wt% methyl 1 ml cellosolve solution) Anhydrous Tetrachlorophthalic Acid 1 ml (0.6 wt% methanol solution) of 95 wt percent of vinyl chloride and 5 wt percent of 1 vinyl acetate), to form an over-coating'film of a thickness of ,u (after drying).
These three kinds of photographic materials (A) to (C) were exposed to a tungsten light source in an amount of exposure of 200,000 lux.sec through an optical wedge, and thereafter heated for 7 seconds at 120C for development. In each case, the photographic transmission density was measured and the relative sensitivity was calculated in a similar manner to Example 1. The results obtained are shown in the following Table.
Material Material Material (C) Relative Sensitivity 18,700 100 500 From the above results, it can be understood that the sensitizer of this invention displays an extremely excellent sensitizing effect.
EXAMPLE 6 20 Material Material Mate rial Relative Sensitivity 7,200 100 500 It was noted that Compound (6) has an excellent sensitizing effect similar to Compound (3) of the Example 5.
EXAMPLE 7 In the same manner of Example 5, the same amount of the above described Compound (13) was used in place of Compound (3). The results obtained are shown in the following Table.
Material Material Material Relative Sensitivity 6,300 100 500 Compound (13) also was effective as a sensitizer, similar to Compound (3) of Example 5.
EXAMPLE 8 6 g of benzotriazole were dissolved in 100 ml of isoamyl acetate at 50C and then cooled and adjusted to l5C. While stirring with a stirrer, a solution of 8.5 g of silver nitrate dissolved in 100 ml of a diluted nitric acid aqueous solution (pl- =20 at 25C), which was adjusted to 3C, was added thereto. Thus, a dispersion containing fine crystals of silver benzotriazole was prepared. The resulting dispersion was left at normal temperature for 20 minutes, whereupon an aqueous phase and an isoamyl acetate phase were separated from each other. Theaqueous phase wasfirst removed, and 400 ml of water were added again to the remaining phase to wash the same by the decantation method. This operation was repeated three times, and then 400 ml of methanol were added to separate the silver benzotriazole by centrifuging. Thus, .8 g of silver benzotriazole were obtained. The particles of the silver benzotriazole were of a nearly spherical form, having a particle size diameter of about 1 u. 2.5 g of the thus formed silver benzotriazole were added to 40 ml of an isopropyl alcohol solution containing 4 g of polyvinyl butyral and subjected to ball-milling for 4 hours to disperse the same, whereby a silver salt-polymer dispersion was prepared.
Ammonium lodide (8.5 wt% methanol 1 ml solution) Solution Containing 2 g of Ascorbic ml Acid Monopalmitate and 2 g of Ascorbic Acid Dipalmitate in 10 ml of Methyl Ccllosolve Compound (5) (0.2 wt'/: methyl ccllosolvc l ml solution) N-Ethyl-N'-dodccylurca 2 ml (2.5 wl7t mcthyl ccllosolvc solution) A part from this, two other kinds of heat developable photographic materials (B) and (C) were prepared in a similar manner for comparison, the former (B) not containing sensitizer of the present invention, the above Compound (5), and the latter (C) containing, as sensitizing dye, the same amount of the merocyanine dye (of the Example 1) in place of Compound (5).
On the photosensitive layer of each of the thus produced photographic materials (A) to (C) was further over-coated a wt percent tetrahydrofuran solution of a vinyl chloride-vinyl acetate copolymer (consisting of 95 wt percent of vinyl chloride and 5 wt percent of vinyl acetate), to form an over-coating film a thickness of 8 pt (after drying).
Small pieces of these three kinds of photographic materials (A) to (C) were exposed to a tungsten light source in an amount of exposure of 1,200,000 lux.sec through an optical wedge, and thereafter heated for 30 seconds at 130C for development. In each case, the photographic transmission density was measured and the relative sensitivity was calculated in a similar manner to Example 1. The results obtained are shown in the following Table.
Material Material Material (A) Relative Sensitivity 4,300 lOO 200 From the above results, it can be understood that the sensitizer of this invention displays an extremely excellent sensitizing effect.
EXAMPLE 9 Material Material Material (A) (B) (C) Relative Sensitivity 3,800 100 200 It is noted that Compound (1 1) has an excellent sensitizing effect similar to the Compound (5) of Example 8.
EXAMPLE 10 In the same manner of Example 8, the same amount of the above described Compound (12) was used in place of Compound (5). The results obtained are shown in the following Table.
Material Material Material (A Relative Sensitivity 3,200 200 Compound (l2) also was effective as a sensitizer, similar to Compound (5) of Example 8.
EXAMPLE 11 In the same manner of Example 1, the same amount of the following cyanine dye was used together with Compound (1), in place of Compound (1) only.
Material Material Material (A) Relative Sensitivity 19,000 100 600 While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
What is claimed is:
l. A heat developable photographic material having at least one photosensitive layer on a support, said layer containing the following components:
a. an organic silver salt,
b. a catalytic amount of a photosensitive silver halide or a compound capable of reacting with said organic silver salt (a) to produce a photosensitive silver halide,
c. a reducing agent,
d. a binder, and
e. as a sensitizer, at least one of the following Compounds (I) and (ll):
Ar N N Al wherein An, Ar Ar and Ar,-, each represents an aryl group and Ar, represents an arylene group, with the proviso that at least one of Ar, and Ar and at least one of Ar;,, Ar and Ar is substituted with a SO M group.
or a COOM group, M being a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, or a Nl-l, group.
2. The heat developable photographic material as claimed in claim 1, wherein said Ar Ar Ar and Ar groups are substituted or unsubstituted phenyl groups, a-naphthyl groups or B-naphthyl groups, and said Ar, group is a substituted or unsubstituted phenylene group, biphenylene group or a naphthylene group. 3. The heat developable photographic material as claimed in claim 2, wherein said aryl and arylene groups are substituted with an alkyl group, a halogen atom, a hydroxyl group, an SO M group, a COOM group, an aryl group, a nitro group, an amino group, an alkylamino group, an arylamino group, an acry group, an alkoxy group, an arylsulfonyloxy group, or an alkylsulfonyloxy group.
4. The heat developable photographic material as claimed in claim 3, wherein said alkyl, alkoxy and acyl groups have 1 to 8 carbon atoms.
5. The heat developable photographic material as claimed in claim 4, wherein said alkyl, alkoxy and acyl groups have 1 to 4 carbon atoms.
6. The heat developable photographic material as claimed in claim 1, wherein said alkali metal is Li, Na, K or Rb.
7. The heat developable photographic materials as claimed in claim 1, wherein said alkaline earth metal is Ca. Ba, or Mg.
8. The heat developable photographic material as claimed in claim 1, wherein said sensitizer (e) is selected from the group consisting of the following com-. pounds coon NaO S COONa SO Na Mao;
CH OH -N=N- OH OONa O Na H SO Na CH CH 3 H H -N=IL N=N 5 K0 S- N=N SO3N8 and H HO NaO S- -N=N =N- 5 Q Q 0 S- -N=N- 2 2 2 N=N-N=N 3 SOQNa c1 9. The heat developable photographic material as OH claimed in claim 1, wherein said sensitizer (e) is present in an amount ranging from about 10 to 10' per 1 mole of said organic silver salt.
10. The heat developable photographic material as l claimed in claim 1, which further contains an optical 5 SOBNa sensitizing dye in an amount of about 10 to 10 per 1 mole of said organic silver salt.
3 OH H0 11. The heat developable photographic material as claimed in claim 1, wherein said optical sensitizing dye is a cyanine dye or a merocyanine dye. v
12. The heat developable photographic material as claimed in claim 1, including an over-coating layer on said photosensitive layer.
Claims (12)
1. A HEAT DEVELOPABLE PHOTOGRAPHIC MATERIAL HAVING AT LEAST ONE PHOTOSENSITIVE LAYER ON A SUPPORT, SAID LAYER CONTAINING THE FOLLOWING COMPONENTS: A. AN ORGANIC SILVER SALT, B. A CATALYTIC AMOUNT OG A PHOTOSENSITIVE SILVER HALIDE OR A COMPOUND CAPABLE OF REACTING WITH SAID ORGANIC SILVER SALT (A) TO PRODUCE A PHOTOSENSITIVE SILVER HALIDE, C. REDUCING AGENT, D. A BINDER, AND E. AS A SENSITIZER, AT LEAST ONE OF THE FOLLOWING COMPOUNDS (I) AND (II)AR1 - N = N - AR2 AR3 - N = N - AR4 - N = N - AR5 WHEREIN AR1, AR2, AR3 AND AR5 EACH REPRESENTS AN ARYL GROUP AND AR4 REPRESENTS AN ARYLENE GROUP, WITH THE PROVISO THAT AT LEAST ONE OF AR1 AND AR2 AND AT LEAST ONE OF AR3, AR4 AND AR5 IS SUBSTITUTED WITH A -SO3M GROUP AR A - COOM GROUP, M BEING A HYDROGEN ATOM, AN ALKALI METAL ATOM, AN ALKALINE EARTH METAL ATOM, OR A -NH4 GROUP.
1. A heat developable photographic material having at least one photosensitive layer on a support, said layer containing the following components: a. an organic silver salt, b. a catalytic amount of a photosensitive silver halide or a compound capable of reacting with said organic silver salt (a) to produce a photosensitive silver halide, c. a reducing agent, d. a binder, and e. as a sensitizer, at least one of the following Compounds (I) and (II): Ar1 - N N - Ar2 (I) AR3 - N N - Ar4 - N N - Ar5 (II) wherein Ar1, Ar2, Ar3 and Ar5 each represents an aryl group and Ar4 represents an arylene group, with the proviso that at least one of Ar1 and Ar2, and at least one of Ar3, Ar4 and Ar5 is substituted with a -SO3M group or a -COOM group, M being a hydrogen atom, an alkali metal atom, an alkaline earth metal atom, or a -NH4 group.
2. The heat developable photographic material as claimed in claim 1, wherein said Ar1, Ar2, Ar3 and Ar5 groups are substituted or unsubstituted phenyl groups, Alpha -naphthyl groups or Beta -naphthyl groups, and said Ar4 group is a substituted or unsubstituted phenylene group, biphenylene group or a naphthylene group.
3. The heat developable photographic material as claimed in Claim 2, wherein said aryl and arylene groups are substituted with an alkyl group, a halogen atom, a hydroxyl group, an -SO3M group, a COOM group, an aryl group, a nitro group, an amino group, an alkylamino group, an arylamino group, an acry group, an alkoxy group, an arylsulfonyloxy group, or an alkylsulfonyloxy group.
4. The heat developable photographic material as claimed in Claim 3, wherein said alkyl, alkoxy and acyl groups have 1 to 8 carbon atoms.
5. The heat developable photographic material as claimed in claim 4, wherein said alkyl, alKoxy and acyl groups have 1 to 4 carbon atoms.
6. The heat developable photographic material as claimed in claim 1, wherein said alkali metal is Li, Na, K or Rb.
7. The heat developable photographic materials as claimed in claim 1, wherein said alkaline earth metal is Ca, Ba, or Mg.
8. The heat developable photographic material as claimed in claim 1, wherein said sensitizer (e) is selected from the group consisting of the following compounds
9. The heat developable photographic material as claimed in claim 1, wherein said sensitizer (e) is present in an amount ranging from about 10 6 to 10 2 per 1 mole of said organic silver salt.
10. The heat developable photographic material as claimed in claim 1, which further contains an optical sensitizing dye in an amount of about 10 6 to 10 2 per 1 mole of said organic silver salt.
11. The heat developable photographic material as claimed in claim 1, wherein said optical sensitizing dye is a cyanine dye or a merocyanine dye.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP48007624A JPS4996717A (en) | 1973-01-17 | 1973-01-17 |
Publications (1)
Publication Number | Publication Date |
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US3870523A true US3870523A (en) | 1975-03-11 |
Family
ID=11670963
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US434453A Expired - Lifetime US3870523A (en) | 1973-01-17 | 1974-01-17 | Heat developable photographic material containing azo dyes as sensitizers |
Country Status (5)
Country | Link |
---|---|
US (1) | US3870523A (en) |
JP (1) | JPS4996717A (en) |
DE (1) | DE2401982A1 (en) |
FR (1) | FR2324025A1 (en) |
GB (1) | GB1424643A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2379833A1 (en) * | 1977-02-07 | 1978-09-01 | Eastman Kodak Co | THERMODEVELOPABLE PHOTOGRAPHIC PRODUCT |
US4128428A (en) * | 1974-04-10 | 1978-12-05 | Fuji Photo Film Co., Ltd. | Heat developable light-sensitive material |
US4142901A (en) * | 1976-11-12 | 1979-03-06 | Eastman Kodak Company | Photographic materials comprising azo sensitizing dyes |
US4173478A (en) * | 1977-10-28 | 1979-11-06 | Eastman Kodak Company | Photographic materials comprising azo sensitizing dyes |
US4187108A (en) * | 1977-02-07 | 1980-02-05 | Eastman Kodak Company | Heat developable material and process |
US4207108A (en) * | 1976-11-04 | 1980-06-10 | Eastman Kodak Company | Silver halide photothermographic element, composition and process |
US4237213A (en) * | 1976-01-30 | 1980-12-02 | Canon Kabushiki Kaisha | Image forming method |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5151933A (en) * | 1974-11-01 | 1976-05-07 | Fuji Photo Film Co Ltd | NETSUGENZOKANKOZAIRYO |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3457075A (en) * | 1964-04-27 | 1969-07-22 | Minnesota Mining & Mfg | Sensitized sheet containing an organic silver salt,a reducing agent and a catalytic proportion of silver halide |
US3645739A (en) * | 1966-02-21 | 1972-02-29 | Fuji Photo Film Co Ltd | Thermally developable light-sensitive elements |
US3700457A (en) * | 1970-04-09 | 1972-10-24 | Eastman Kodak Co | Use of development inhibitor releasing compounds in photothermographic elements |
US3770448A (en) * | 1970-04-29 | 1973-11-06 | Agfa Gevaert Ag | Lightsensitive photographic material |
-
1973
- 1973-01-17 JP JP48007624A patent/JPS4996717A/ja active Pending
-
1974
- 1974-01-10 FR FR7400839A patent/FR2324025A1/en active Granted
- 1974-01-14 GB GB165974A patent/GB1424643A/en not_active Expired
- 1974-01-16 DE DE2401982A patent/DE2401982A1/en active Pending
- 1974-01-17 US US434453A patent/US3870523A/en not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3457075A (en) * | 1964-04-27 | 1969-07-22 | Minnesota Mining & Mfg | Sensitized sheet containing an organic silver salt,a reducing agent and a catalytic proportion of silver halide |
US3645739A (en) * | 1966-02-21 | 1972-02-29 | Fuji Photo Film Co Ltd | Thermally developable light-sensitive elements |
US3700457A (en) * | 1970-04-09 | 1972-10-24 | Eastman Kodak Co | Use of development inhibitor releasing compounds in photothermographic elements |
US3770448A (en) * | 1970-04-29 | 1973-11-06 | Agfa Gevaert Ag | Lightsensitive photographic material |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4128428A (en) * | 1974-04-10 | 1978-12-05 | Fuji Photo Film Co., Ltd. | Heat developable light-sensitive material |
US4237213A (en) * | 1976-01-30 | 1980-12-02 | Canon Kabushiki Kaisha | Image forming method |
US4207108A (en) * | 1976-11-04 | 1980-06-10 | Eastman Kodak Company | Silver halide photothermographic element, composition and process |
US4142901A (en) * | 1976-11-12 | 1979-03-06 | Eastman Kodak Company | Photographic materials comprising azo sensitizing dyes |
FR2379833A1 (en) * | 1977-02-07 | 1978-09-01 | Eastman Kodak Co | THERMODEVELOPABLE PHOTOGRAPHIC PRODUCT |
US4187108A (en) * | 1977-02-07 | 1980-02-05 | Eastman Kodak Company | Heat developable material and process |
US4173478A (en) * | 1977-10-28 | 1979-11-06 | Eastman Kodak Company | Photographic materials comprising azo sensitizing dyes |
Also Published As
Publication number | Publication date |
---|---|
JPS4996717A (en) | 1974-09-12 |
DE2401982A1 (en) | 1974-07-18 |
FR2324025B1 (en) | 1978-03-10 |
GB1424643A (en) | 1976-02-11 |
FR2324025A1 (en) | 1977-04-08 |
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