US3615533A - Heat and light sensitive layers containing hydrazones - Google Patents
Heat and light sensitive layers containing hydrazones Download PDFInfo
- Publication number
- US3615533A US3615533A US711868A US3615533DA US3615533A US 3615533 A US3615533 A US 3615533A US 711868 A US711868 A US 711868A US 3615533D A US3615533D A US 3615533DA US 3615533 A US3615533 A US 3615533A
- Authority
- US
- United States
- Prior art keywords
- radical
- group
- silver
- carbocyclic aryl
- lower alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 150000007857 hydrazones Chemical class 0.000 title claims abstract description 40
- -1 silver halide Chemical class 0.000 claims abstract description 272
- 239000004332 silver Substances 0.000 claims abstract description 78
- 229910052709 silver Inorganic materials 0.000 claims abstract description 78
- 230000005855 radiation Effects 0.000 claims abstract description 35
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 claims description 48
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 34
- 150000003254 radicals Chemical class 0.000 claims description 30
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 claims description 28
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 230000008569 process Effects 0.000 claims description 25
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 22
- 229910044991 metal oxide Inorganic materials 0.000 claims description 22
- 150000004706 metal oxides Chemical class 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 17
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 17
- 150000003378 silver Chemical class 0.000 claims description 14
- 229910001961 silver nitrate Inorganic materials 0.000 claims description 14
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 11
- 239000004408 titanium dioxide Substances 0.000 claims description 11
- 230000005670 electromagnetic radiation Effects 0.000 claims description 9
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 8
- CQLFBEKRDQMJLZ-UHFFFAOYSA-M silver acetate Chemical compound [Ag+].CC([O-])=O CQLFBEKRDQMJLZ-UHFFFAOYSA-M 0.000 claims description 8
- 229940071536 silver acetate Drugs 0.000 claims description 8
- LMEWRZSPCQHBOB-UHFFFAOYSA-M silver;2-hydroxypropanoate Chemical compound [Ag+].CC(O)C([O-])=O LMEWRZSPCQHBOB-UHFFFAOYSA-M 0.000 claims description 8
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 7
- DPUIBGVQGAFCEL-UHFFFAOYSA-N n-(anthracen-1-ylmethylideneamino)aniline Chemical compound C=1C=CC2=CC3=CC=CC=C3C=C2C=1C=NNC1=CC=CC=C1 DPUIBGVQGAFCEL-UHFFFAOYSA-N 0.000 claims description 7
- AQRYNYUOKMNDDV-UHFFFAOYSA-M silver behenate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCCCCCC([O-])=O AQRYNYUOKMNDDV-UHFFFAOYSA-M 0.000 claims description 7
- XNGYKPINNDWGGF-UHFFFAOYSA-L silver oxalate Chemical compound [Ag+].[Ag+].[O-]C(=O)C([O-])=O XNGYKPINNDWGGF-UHFFFAOYSA-L 0.000 claims description 7
- SIEWBPYSALLVGO-UHDJGPCESA-M silver;(e)-3-phenylprop-2-enoate Chemical compound [Ag+].[O-]C(=O)\C=C\C1=CC=CC=C1 SIEWBPYSALLVGO-UHDJGPCESA-M 0.000 claims description 5
- 238000012545 processing Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 3
- 239000003638 chemical reducing agent Substances 0.000 abstract description 7
- 230000003595 spectral effect Effects 0.000 abstract description 5
- 150000001299 aldehydes Chemical class 0.000 abstract description 4
- 150000002576 ketones Chemical class 0.000 abstract description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 36
- 238000000576 coating method Methods 0.000 description 24
- 239000011248 coating agent Substances 0.000 description 22
- 239000000243 solution Substances 0.000 description 18
- 239000000839 emulsion Substances 0.000 description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- 238000006722 reduction reaction Methods 0.000 description 11
- 239000000463 material Substances 0.000 description 10
- 230000009467 reduction Effects 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 238000011161 development Methods 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000002131 composite material Substances 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 108010010803 Gelatin Proteins 0.000 description 4
- 239000012153 distilled water Substances 0.000 description 4
- 229920000159 gelatin Polymers 0.000 description 4
- 239000008273 gelatin Substances 0.000 description 4
- 235000019322 gelatine Nutrition 0.000 description 4
- 235000011852 gelatine desserts Nutrition 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- WKFCGJZYIWAEEX-NJKRNUQASA-N n-[(e)-[(e)-3-phenylprop-2-enylidene]amino]aniline Chemical compound C=1C=CC=CC=1N\N=C\C=C\C1=CC=CC=C1 WKFCGJZYIWAEEX-NJKRNUQASA-N 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 4
- 229910052721 tungsten Inorganic materials 0.000 description 4
- 239000010937 tungsten Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 229910021607 Silver chloride Inorganic materials 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000005840 aryl radicals Chemical class 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000007654 immersion Methods 0.000 description 3
- 229910021645 metal ion Inorganic materials 0.000 description 3
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 3
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Natural products OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- BZORFPDSXLZWJF-UHFFFAOYSA-N N,N-dimethyl-1,4-phenylenediamine Chemical compound CN(C)C1=CC=C(N)C=C1 BZORFPDSXLZWJF-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000010908 decantation Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- OKJPEAGHQZHRQV-UHFFFAOYSA-N iodoform Chemical compound IC(I)I OKJPEAGHQZHRQV-UHFFFAOYSA-N 0.000 description 2
- 238000007540 photo-reduction reaction Methods 0.000 description 2
- 239000004848 polyfunctional curative Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- WQGWDDDVZFFDIG-UHFFFAOYSA-N pyrogallol Chemical compound OC1=CC=CC(O)=C1O WQGWDDDVZFFDIG-UHFFFAOYSA-N 0.000 description 2
- 230000001603 reducing effect Effects 0.000 description 2
- 230000004044 response Effects 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- ORYURPRSXLUCSS-UHFFFAOYSA-M silver;octadecanoate Chemical compound [Ag+].CCCCCCCCCCCCCCCCCC([O-])=O ORYURPRSXLUCSS-UHFFFAOYSA-M 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical group [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 2
- 235000019345 sodium thiosulphate Nutrition 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- CCDRPBGPIXPGRW-JNKODXNQSA-N (4as,6ar,6as,6br,8ar,9r,10s,12ar,14bs)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid Chemical compound O([C@H]1CC[C@]2(C)[C@H]3CC=C4[C@@]([C@@]3(CC[C@H]2[C@@]1(CO)C)C)(C)CC[C@]1(CCC(C[C@H]14)(C)C)C(O)=O)C1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O CCDRPBGPIXPGRW-JNKODXNQSA-N 0.000 description 1
- 150000005206 1,2-dihydroxybenzenes Chemical class 0.000 description 1
- 150000005208 1,4-dihydroxybenzenes Chemical class 0.000 description 1
- ZENKESXKWBIZCV-UHFFFAOYSA-N 2,2,4,4-tetrafluoro-1,3-benzodioxin-6-amine Chemical group O1C(F)(F)OC(F)(F)C2=CC(N)=CC=C21 ZENKESXKWBIZCV-UHFFFAOYSA-N 0.000 description 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 1
- REFDOIWRJDGBHY-UHFFFAOYSA-N 2-bromobenzene-1,4-diol Chemical compound OC1=CC=C(O)C(Br)=C1 REFDOIWRJDGBHY-UHFFFAOYSA-N 0.000 description 1
- GKQZDIPRXDPUTL-UHFFFAOYSA-N 2-chloro-3-methylbenzene-1,4-diol Chemical compound CC1=C(O)C=CC(O)=C1Cl GKQZDIPRXDPUTL-UHFFFAOYSA-N 0.000 description 1
- CSDSSGBPEUDDEE-UHFFFAOYSA-N 2-formylpyridine Chemical compound O=CC1=CC=CC=N1 CSDSSGBPEUDDEE-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- BGNGWHSBYQYVRX-UHFFFAOYSA-N 4-(dimethylamino)benzaldehyde Chemical compound CN(C)C1=CC=C(C=O)C=C1 BGNGWHSBYQYVRX-UHFFFAOYSA-N 0.000 description 1
- ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 description 1
- CTHSUUAWAJXBSU-UHFFFAOYSA-N 5-amino-2-sulfanylidene-1h-pyrimidin-4-one Chemical compound NC1=CN=C(S)N=C1O CTHSUUAWAJXBSU-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CIWBSHSKHKDKBQ-DUZGATOHSA-N D-isoascorbic acid Chemical compound OC[C@@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-DUZGATOHSA-N 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical class [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- FOIXSVOLVBLSDH-UHFFFAOYSA-N Silver ion Chemical compound [Ag+] FOIXSVOLVBLSDH-UHFFFAOYSA-N 0.000 description 1
- PALNVYHUKHRDOP-UHFFFAOYSA-N UNPD162310 Natural products COC(=O)C1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(OC6OC(CO)C(O)C(OC7OC(CO)C(O)C(O)C7O)C6O)C(C)(C)C5CCC34C)C2C1)C(=O)O PALNVYHUKHRDOP-UHFFFAOYSA-N 0.000 description 1
- 206010047571 Visual impairment Diseases 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
- HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
- 239000011358 absorbing material Substances 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 235000011126 aluminium potassium sulphate Nutrition 0.000 description 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001727 cellulose butyrate Polymers 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 1
- 229940125782 compound 2 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125898 compound 5 Drugs 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 150000005205 dihydroxybenzenes Chemical class 0.000 description 1
- QCPTVXCMROGZOL-UHFFFAOYSA-L dipotassium;oxalate;hydrate Chemical compound O.[K+].[K+].[O-]C(=O)C([O-])=O QCPTVXCMROGZOL-UHFFFAOYSA-L 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000007606 doctor blade method Methods 0.000 description 1
- 235000010350 erythorbic acid Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940026239 isoascorbic acid Drugs 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical compound C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 description 1
- TYQCGQRIZGCHNB-JLAZNSOCSA-N l-ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(O)=C(O)C1=O TYQCGQRIZGCHNB-JLAZNSOCSA-N 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- WSFSSNUMVMOOMR-NJFSPNSNSA-N methanone Chemical compound O=[14CH2] WSFSSNUMVMOOMR-NJFSPNSNSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 150000004989 p-phenylenediamines Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229940050271 potassium alum Drugs 0.000 description 1
- GRLPQNLYRHEGIJ-UHFFFAOYSA-J potassium aluminium sulfate Chemical compound [Al+3].[K+].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O GRLPQNLYRHEGIJ-UHFFFAOYSA-J 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
- QJZUKDFHGGYHMC-UHFFFAOYSA-N pyridine-3-carbaldehyde Chemical compound O=CC1=CC=CN=C1 QJZUKDFHGGYHMC-UHFFFAOYSA-N 0.000 description 1
- BGUWFUQJCDRPTL-UHFFFAOYSA-N pyridine-4-carbaldehyde Chemical compound O=CC1=CC=NC=C1 BGUWFUQJCDRPTL-UHFFFAOYSA-N 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 229940079877 pyrogallol Drugs 0.000 description 1
- 150000003232 pyrogallols Chemical class 0.000 description 1
- 239000001397 quillaja saponaria molina bark Substances 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 239000012266 salt solution Substances 0.000 description 1
- 229930182490 saponin Natural products 0.000 description 1
- 150000007949 saponins Chemical class 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
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003567 thiocyanates Chemical class 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 150000004764 thiosulfuric acid derivatives Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
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- 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
- G03C1/4989—Photothermographic systems, e.g. dry silver characterised by a thermal imaging step, with or without exposure to light, e.g. with a thermal head, using a laser
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- 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
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- 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
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- 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
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
- G03C1/28—Sensitivity-increasing substances together with supersensitising substances
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- 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
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- 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
- G03C1/675—Compositions containing polyhalogenated compounds as photosensitive substances
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- 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
- G03C1/705—Compositions containing chalcogenides, metals or alloys thereof, as photosensitive substances, e.g. photodope systems
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
- G03G5/0616—Hydrazines; Hydrazones
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0618—Acyclic or carbocyclic compounds containing oxygen and nitrogen
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/062—Acyclic or carbocyclic compounds containing non-metal elements other than hydrogen, halogen, oxygen or nitrogen
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
- G03G5/0637—Heterocyclic compounds containing one hetero ring being six-membered containing one hetero atom
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0644—Heterocyclic compounds containing two or more hetero rings
- G03G5/0646—Heterocyclic compounds containing two or more hetero rings in the same ring system
- G03G5/065—Heterocyclic compounds containing two or more hetero rings in the same ring system containing three relevant rings
Definitions
- Kline, J. R. Frederick and D. M. DeLeo ABSTRACT Certain ketone and aldehyde organic hydrazones exhibit utility in radiation-sensitive layers and elements as a spectral sensitizer for silver halide and as a selective reducing agent in photographic, lhermographic and photothermographic layers.
- This invention relates to the production of images, and more particularly, to the production of images by thermographic or photographic means or combinations thereof using heat or light-sensitive layers containing organic hydrazone compounds.
- Yet another object of this invention is to provide new, spectrally sensitized photographic layers and elements.
- Yet another object of this invention is to provide, for imageforming purposes, new layers and elements capable of reproducing images by thermographic and photothermographic means.
- Another object of the present invention is to provide novel image-forming processes.
- R and R are each either a hydrogen atom, a lower alkyl radical or a carbocyclic aryl radical,
- R is either a carbocyclic aryl radical, an aralkyl radical, an
- R is either a lower alkyl radical, a carbocyclic aryl radical or a heterocyclic radical, and an image-promoting component that includes radiationsensitive silver salts, radiation-sensitive metal oxides and mixtures thereof.
- lower alkyl radicals include straight and branched chain aliphatic radicals having from one to six carbon atoms and preferably from one to four carbon atoms. Typical lower alkyl radicals are methyl, ethyl, chloroethyl, isopropyl and the like.
- Carbocyclic aryl radicals of the subject invention are deemed to include monoand polycyclic, carbocyclic aryl radicals, preferably having from six to 18 atoms in the aryl nucleus.
- aryl radicals are phenyl, anthracenyl, aminophenyl, diethoxyphenyl, triacetylphenyl, pdimethylaminophenyl, p-sulfophenyl, etc.
- Aralkyl radicals are such radicals as phenethyl and include radicals having both an aryl moiety, such as the described aryl radicals, and an alkyl moiety which is preferably a lower alkyl radical as noted herein.
- Aralkenyl radicals include radicals like phenethenyl and additional radicals having an aryl moiety such as those aryl radicals mentioned herein and an alkenyl moiety that includes unsaturated aliphatic radicals having from two to four carbon atoms such as ethenyl and 1,3-butadienyl.
- Heterocyclic radicals useful herein include monoand polycyclic heterocyclic radicals having from five to about l4 atoms and typically having from five to six atoms including hetero atoms in each cyclic nucleus. Exemplary of such heterocyclic radicals are pyridyl, quinolyl, julolidinyl, etc.
- Particularly preferred organic hydrazone compounds of this invention include ketone and aldehyde hydrazones such as:
- the subject hydrazone compounds are utilized in the presence of or in combination with certain radiation-sensitive, image-promoting components.
- radiation-sensitive refers broadly to electromagnetic radiation and includes both heat and light rays.
- Advantageous electromagnetic waves are, for example, gamma rays, ultraviolet radiation, visible light and infrared radiation.
- hydrazones suitable for use in the present invention can also be utilized as photoconductors in electrophotographic systems; this is particularly true for the com pound 4aminobenzaldehyde methylphenylhydrazone.
- the hydrazone compounds of this invention can be used in conjunction with a polyhalogen compound such as iodoform or carbon tetrachloride to produce printout images.
- the radiation-sensitive silver salts of the present invention are those silver salts that can be reduced to metallic silver by exposure to electromagnetic radiation, typically heat or light rays. More particularly, the radiation-reducible silver salts of this invention comprehend primarily heat-sensitive substantially water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms such as silver oxalate, silver stearate and silver behenate. Additionally, light-sensitive silver halides are advantageously employed herein, as are light-sensitive, water-soluble silver salts like silver nitrate, silver acetate and silver lactate. Other silver salts useful in the practice of this invention, that are reduced to metallic silver by the impingement of electromagnetic rays are known to those skilled in the art.
- Radiation-sensitive metal oxides useful in this invention are those metal oxides, both photoconductors and nonphotoconductors, which will transfer and donate electrons when activated by exposure to suitable electromagnetic radiation, typically rays of shorter wavelengths like X-rays as well as ultraviolet and actinic radiation.
- suitable electromagnetic radiation typically rays of shorter wavelengths like X-rays as well as ultraviolet and actinic radiation.
- Typical such oxides are aluminum oxide, zinc oxide, titanium dioxide and antimony trioxide, but still additional radiation-sensitive metal oxides are known to those skilled in the art.
- mixtures of radiation-sensitive silver salts and metal oxides are advantageously employed.
- the subject hydrazones are advantageously admixed with a light-sensitive silver halide salt. More particularly, in photographic elements having a support coated with at least one light-sensitive layer comprising a silver halide emulsion and a sensitizing amount of at least one of the hydrazone compounds described herein.
- the silver halide is spectrally sensitized to longer wavelengths by the organic hydrazone.
- Preferred as a spectral sensitizer for silver halide such as silver chloride, silver bromide, silver bromoiodide, silver chloroiodide and the like, is the hydrazone 4-(dimethylamino)benzaldehyde quinol-2-ylhydrazone.
- silver halide emulsions are spectrally sensitized in this fashion, such as gelatinosilver halide emulsions and silver halide emulsions containing other hydrophilic colloid binders such as polyvinyl alcohol, cellulose acetate and the like binder materials. Additionally, other addenda such as hardeners, antifoggants. coating aids and other typical ingredients can be present in the silver halide emulsions that are spectrally sensitized as described herein.
- the subject hydrazones are typically added to silver halide emulsions in extremely small sensitizing amounts, generally varying between about I mg. and about 3 3 per gram of silver. More highly varying amounts can also be employed in accordance with conventional practice without detrimental effects.
- a silver halide emulsion containing at least one ofthe organic hydrazone compounds of this invention is coated on a support material and dried. Coating thickness is susceptible of somewhat wide variation, but typically wet thicknesses of from about 0.001 inch 3 mg. 0.006 inch are employed. More extensive variations can be used where desired for particular coating techniques or sensitometric characteristics.
- the method of coating can be any of those known in the coating art, including such means as dipping, whirler coating and flow coating, except that hopper-coating or doctor blade coating means are preferred since they offer a higher degree of precision as regards coating thickness.
- Support materials which are advantageous in preparing these spectrally sensitized silver halide photographic elements are susceptible of extensive interchange and typically include cellulose esters such as cellulose acetate, cellulose butyrate, cellulose nitrate and cellulose acetate butyrate as well as other polymeric materials like polystyrene and poly(ethylene terephthalate). Additionally, papers including polyethylene and polypropylene coated paper are advantageous supports, as is baryta pigmented and other pigmented papers. Other support materials are well known in the art.
- the composite photographic element can be imagewise exposed and processed to yield a visible photographic silver image.
- the exposing means can be either a source of actinic radiation or a source of longer wavelength visible light to which the emulsion is sensitized by the subject organic hydrazone.
- a spectrally sensitized silver halide photographic element as described herein can be processed in a conventional silver halide photographic developing composition to produce a silver image.
- a silver halide developing agent typically a hydroxylated aryl compound, such as dihydroxybenzenes like hydroquinones, catechols and pyrogallols, as well as other polyhydroxylated compounds such as ascorbic acid.
- Additional developing agents include aminophenols, p-phenylene-diamines and 3-pyrazolidones.
- silver halide developing agents that are advantageously used herein are compounds like 2-methyl-3- chlorohydroquinone, bromohydroquinone, catechol, S-phenylcatechol, pyrogallol monomethylether(l-methoxy-2,3- dihydroxy benzene), S-methylpyrogallol monomethyl-ether isoascorbic acid, N-methyl-p-aminophenol, dimethyl-p-phenylene diamine, 4-amino-N,N-di(n-propyl)anilene and 6- amino'l-ethyl-l,2,3,4-tetrahydr0quinoline.
- Conventional fixing agents or silver halide solubilizing agents include water-soluble thiosulfates,
- a particularly preferred fixing agent is sodium thiosulfate. Stabilization is generally accomplished by treatment with a composite fixing bath that incorporates a fixing agent such as those mentioned hereinabove.
- the subject hydrazones function as heat and light activated selective reducing agents for metal ions, silver ions for example, in photographic, thermographic and photothermographic image-forming systems.
- Selective photo or photothermal reduction advantageously occurs subsequent to the formation of a metallic or other latent image which catalyzes the reduction of metal ions by the organic hydrazone compounds of this invention to form a visible image.
- an imagewiseexposed silver halide element such as is described hereinabove and containing at least one of the organic hydrazones of this invention.
- a visible photographic silver image can be produced on such an imagewise-exposed element merely by treatment with a conventional fixing agent and simultaneously exposing the element to visible light radiation.
- thermographic elements having a support such as those described herein coated with at least one of the hydrazones described herein and at least one substantially water-insoluble silver slat, typically of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms, such as silver cinnamate, silver behenate, silver stearate and silver oxalate.
- Coating techniques can be any of those noted hereinabove.
- the amount of hydrazone included in such element need only be sufiicient to advantageously reduce the silver salt to metallic silver upon a suitable exposure, and in like fashion the silver salt need only be present in an amount that provides a reduced silver image of a desirable density for viewing purposes.
- the hydrazone and silver salt are included in weight ratios of from about l;2 to about I24, but wider ratios can be used if desired.
- the water-insoluble silver salts are primarily heat sensitive and do not exhibit an excessive sensitivity to light radiation, exposure to ultraviolet and actinic light radiation can produce discoloration, and a suitable stabilizer such as a difunctional alkylene imine like N,N- bis-l,2-ethyleneisophthalimide can be included in the heatsensitive layer to prevent undesired photoreduction of silver.
- a solely thermographic element such as this type, an imagewise thermal reduction is obtained without a preexisting latent image by effecting an imagewise concentration of heat radiation to selectively trigger the reduction reaction in only image areas.
- Such a pattern is typically produced by contacting the image-forming element, during the application of heat by such means as infrared radiation, with an original bearing an imagewise distribution of a heat-absorbing material like an infrared-absorbing carbon base printing ink.
- Such images can be stabilized against further printing out by suitable treatment with a conventional fixing bath such as those described above.
- Other means of image stabilization can be utilized if desired.
- At least one water-soluble silver salt such as silver nitrate, silver acetate and silver lactate, or any other light-sensitive, water-soluble silver salt, can be advantageously incorporated into the element already having a hydrazone compound and a water-insoluble silver salt in the radiationsensitive layer.
- the water-soluble silver salt renders the element desirably light sensitive, and after an imagewise exposure to activating light radiation such as actinic light and the simultaneous formation of a metallic silver latent image by photoreduction of silver ions of the water-soluble silver salt, a visible metallic silver image can be produced by treatment with either heat or light radiation.
- a metallic silver image is produced by selective reduction in only those areas corresponding to the latent image area.
- a water-soluble silver salt need only be present in an amount sufficient to provide a metallic silver latent image that will promote the reduction of the water-insoluble silver salt upon development.
- amounts by weight of from about 0.5 part to about two parts per part of hydrazone are used.
- selective reduction produced by the subject hydrazone compounds can be encouraged or catalyzed by latent images obtained from the irradiation of photosensitive species other than silver halide, photoactivatable metal oxides for example, such as those described hereinabove.
- An element incorporating a support having coated thereon a light-sensitive layer including a hydrazone compound of this invention and a photoactivatable metal oxide can be imagewise exposed to light radiation and treated with a water-soluble silver salt solution such as aqueous silver nitrate to produce a visible metallic silver image in those areas corresponding to the imagewise exposure.
- a preferred light-sensitive metal oxide is titanium dioxide.
- the light-sensitive layer can also contain components like a hydrophilic colloid binder material such as gelatin or polyvinyl alcohol as well as other typical emulsion addenda such as spectral-sensitizing dyes, hardeners, coating aidsand the like.
- the light exposure can be to actinic light rays or to longer wavelength visible light radiation if the titanium dioxide or other photoactivatable metal oxide is spectrally sensitized to such longer wavelengths.
- the choice of both a support material and a coating technique can be any of those described elsewhere herein.
- metal oxide and hydrazone need only be sufficient to effect an adequate reduction of metal ion in the processing medium, and typically, ratios of from about 20 parts to about 40 parts by weight of metal oxide per part of hydrazone compound are used. Wider ratios can be employed if desired.
- the described elements containing a photosensitive metal oxide can also incorporate, in the light-sensitive layer, at least one reducible silver salt.
- the silver salt can be either a waterinsoluble or a water-soluble salt like those described herein, and subsequent to an imagewise exposure to produce a photographic latent image a variable conductivity in the photoactivatable metal oxide, it can be developed by various techniques to produce a visible silver metal image.
- the reducible silver salt is present in an amount sufficient to provide a visible silver image of a density adequate for viewing purposes. Conventionally, amounts by weight of from about two parts to about four parts per part of hydrazone compound are used.
- Treatment with a photographic developing agent such as those described elsewhere herein produces a photographic silver image, but such processing does not utilize the advantageous selective reducing properties of the subject hydrazones.
- it can be processed as either a wholly photographic printout element or as a photothermographic element, since treatment with longer periods of intense light irradiation such as a 5-second exposure at a distance of 12 inches with a 500- watt tungsten lamp or heating to temperatures of about 190 F. effect advantageous selective reduction of silver ion to produce a dense metallic silver image in those areas corresponding to the latent image.
- the substantially water-insoluble silver salts are preferred, however, since they exhibit both a susceptibility to advantageous reduction during image development and a higher resistance to undesired degradation during storage.
- EXAMPLE I To 100 ml. of 5 percent gelatin is added 2.0 ml. of 10 percent formaldehyde, 2.0 ml. of a 7%percent saponin solution, 5 20 ml. of a silver chloride emulsion which contains 1 mole of silver and l2 g. of gelatin in 0.52 kg. of emulsion. To separate ml. portions of this mixture is added [.0 ml. of a l percent acetone solution of the following hydrazones as spectral sensitizers for the silver halide.
- 300-500 my with a peak at 410 mp 300-540 up with I peak II 500 mu 300-580 mp with a peak at 540 mp 420-600 muwith a peak at Slt) mu 4 l0-540 mpwith a peak at 450 mu 4 l0-530 muwith a peak at 500 mp 400-560 muwith a broad peak over this entire range.
- Photographic elements are prepared as in example 1. After an imagewise exposure as in example 1 to form a latent silver image, the elements are immersed in the fixing bath described in example 1 and simultaneously exposed to white light rays, whereupon a dense silver image is produced in the previously imagewise-exposed areas.
- the hydrazone compound functions as a selective reducing agent in those areas bearing a latent silver image.
- thermographic element is prepared by coating a paper support with a composition containing:
- the coated element After drying, the coated element is contacted to a typewritten page and while in contact, the two are heated to about 190 F. A dense deposit of metallic silver is produced in those areas of the element corresponding to the image areas of the typewritten page.
- EXAMPLE 4 A silver oxalate-silver iodide precipitate is prepared as described in U.S. Pat. No. 3,143,419 by mixing:
- the silver nitrate solution is added to solution A and the resulting silver oxalate precipitate is washed by decantation.
- Solution C is then added and the resulting mixed precipitate is washed by decantation.
- the wet slurry is then mixed l:l with a 1 percent acetone solution of cinnamaldehyde phenylhydrazone and the mixture is flow coated on filter paper.
- a photothermographic paper results. Exposure of the coating on a wedge spectrograph for l0 seconds at a l-mm. slit width followed by thermal development at 120 C. for seconds produces a heat-developed silver image in the exposed areas.
- the element can be developed to produce a silver image by printout techniques using higher levels of an imagewise light exposure.
- a photographic element is prepared by coating a paper support material with a 0.004 wet thickness coating ofa formulation having the composition:
- the titanium dioxide element is flow coated with a 1 percent solution of 4aminobenzaldehyde methylphenylhydrazone dissolved in cc. of acetone.
- the dried coating is then exposed to a SOD-watt tungsten photoflood lamp through a line image for a period of about 1 second. This exposure produces a latent image that is made visible by immersing the exposed layer in 0.5 percent aqueous silver nitrate, since the hydrazone compound functionsas a selective reducing agent.
- the permanence of the image is improved by treatment with a sodium thiosulfate fixing bath to remove undeveloped silver salt.
- a titanium dioxide photographic element is prepared according to the procedure of example 5, except that the flow coating contains 2 cc. of a 1 percent acetone solution of cinnamaldehyde phenylhydrazone, 2 cc. of a 1 percent aqueous silver nitrate solution and sufficient acetone to dissolve any precipitate.
- the composite photographic element is dried and then exposed through a line original for 5 seconds to the tungsten light of a 500-watt photoflood lamp at a distance of 12 inches from the exposing plane.
- a dense silver printout image is formed in the exposed areas directly upon exposure, since the hydrazone acts as a selective reducing agent in those areas bearing a latent image.
- a second element is prepared in like fashion, except that the exposure time is shortened to onetenth of a second. No visible printout is observed; however, when the exposed coating is immersed in a black-and-white developer solution as in example i, a dense silver image is produced in the exposed areas.
- a third element is also prepared in like fashion and imagewise exposed for one-tenth second as with the second element. Image development is obtained by heating the paper on a hot plate at I F which produces a dense visible deposit of metallic silver in the exposed areas by photothermographic means.
- EXAMPLE 7 A slurry of 0. 15 g. ofsilver einnamate is prepared in 3 ml. of acetone. To this slurry is added 0.05 g. of anthracenealdehyde phenylhydrazone in 1 ml. of acetone, followed by the addition of 5 drops of the following solution:
- the resulting mixture is flow coated onto a titanium dioxide photographic element prepared as in example 5.
- the entire preparation is carried out under gold-colored fluorescent lamps.
- the composite element is exposed to produce a wedge spectrogram which shows a sensitivity from 280-560 mp. when the element is heated to l90-200 F. over a hotplate.
- a similar element is exposed for 1% seconds through a line original in a Photocopier (model 107 marketed by the Minnesota Mining and Manufacturing Company). A very faint tan image becomes visible in the exposed areas.
- the element is then heated by pressing it in contact with a hotplate at F. for about 2 seconds whereupon a dark reddish-brown image appears in the exposed areas.
- the background remains the yellow color of the original coating.
- the latent image can be intensified by photographic developing solutions, for example, by immersion in a black-and-white developer composition as in example I.
- the image may be fixed in thiosulfate solutions such as the fixing bath described in example I.
- EXAMPLE 8 A paper support material coated with silver behenate is flow coated with a solution containing 2 cc. of a 1 percent acetone solution of cinnamaldehyde phenylhydrazone, 2 cc. of a l percent aqueous silver nitrate solution and sufficient acetone to dissolve any precipitate. The coating is then dried. Exposure and development by printout, photographic or photothermographic means as in example 6 produces a dense silver image in the exposed areas.
- An element for recording image comprising a support having coated thereon a radiation-sensitive composition
- a radiation-sensitive composition comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
- reducible silver salt is selected from the group consisting of substantially water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
- reducible, water-insoluble silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
- reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- reducible silver salt radiation-sensitive component comprises the admixture of:
- a silver salt selected from the group consisting of waterinsoluble salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms, and
- a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- An element for recording images comprising a support having coated thereon a light-sensitive layer comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
- hydrazone is selected from the group consisting of:
- An element for recording images comprising a support having coated thereon a light-sensitive layer comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbo cyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
- reducible silver slat is selected from the group consisting of water-insoluble silver salts of vmonocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
- silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
- reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- An element for recording images comprising a support having coated thereon a light-sensitive layer comprising:
- a process for producing images on an element comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical and a heterocyclic radical
- a reducible silver salt which process comprises imagewise exposing said element to electromagnetic radiation for a period of time sufficient to produce a metallic silver image in the irradiated areas.
- a process for producing images on an imagcwise-exposed element comprising a support having coated thereon a light-sensitive layer comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
- process comprises treating said imagewise-exposed element with a processing medium selected from the group consisting of a silver halide developing composition and a silver halide fixing agent for a period of time sufficient to produce a metallic silver image in the exposed areas.
- a processing medium selected from the group consisting of a silver halide developing composition and a silver halide fixing agent for a period of time sufficient to produce a metallic silver image in the exposed areas.
- a process for producing images on an image light exposed element comprising:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and 4.
- R is selected from the group consisting of a lower alkyl wherein:
- R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R, is an aralkenyl radical, a lower alkyl radical,
- R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
- R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
- a reducible silver salt which process comprises treating said element with a developing means for a period oftime sufficient to produce a metallic silver image in the exposed areas.
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Abstract
Certain ketone and aldehyde organic hydrazones exhibit utility in radiation-sensitive layers and elements as a spectral sensitizer for silver halide and as a selective reducing agent in photographic, thermographic and photothermographic layers.
Description
United States Patent [72] Inventors Frederick J. Rauner;
Paul B. Gilman, both of Rochester, N.Y. 21 Appl. No. 71 1,868 [22] Filed Mar. 11, 1968 [45] Patented Oct. 26, 1971 [73] Assignee Eastman Kodak Company Rochester, N.Y.
[54] HEAT AND LIGHT SENSITIVE LAYERS CONTAINING HYDRAZONES 24 Claims, No Drawings [52] US. Cl 96/67, 96/95, 250/65 [51] 1nt.Cl G034: 1/76 [50] Fieldof Search 96/95, 107, 67, 102; 250/65 [5 6] References Cited UNITED STATES PATENTS 3,457,075 7/1969 Morgan et al 96/67 FOREIGN PATENTS 1,109,963 5/1966 Great Britain 96/53 1,397,549 3/1965 France OTHER REFERENCES P. S. & E., Vol.9, 6, Nov.- Dec. 1965, p, 364- 370. Laridon, Delzenne, Conix.
P. S. & E., Vol.7, 1963, p. 364- 370. D. W. Woodward, V. C. Chambers & A. B. Cohen.
Primary Examiner- Norman G. Torchin Assistant Examiner-John L. Goodrow Attorneys-W. 11.]. Kline, J. R. Frederick and D. M. DeLeo ABSTRACT: Certain ketone and aldehyde organic hydrazones exhibit utility in radiation-sensitive layers and elements as a spectral sensitizer for silver halide and as a selective reducing agent in photographic, lhermographic and photothermographic layers.
HEAT AND LIGHT SENSITIVE LAYERS CONTAINING IIYDRAZONES This invention relates to the production of images, and more particularly, to the production of images by thermographic or photographic means or combinations thereof using heat or light-sensitive layers containing organic hydrazone compounds.
It is known in the photographic art to utilize certain hydrazone compounds in conjunction with the production of images. For example, US. Pat. No. 2,423,710, describes the use in photographic emulsions of p-dialkylaminocinnamic aldehyde phenylhydrazones as chemical supersensitizers for 2'- cyanine or oxacarbocyanine spectral-sensitizing dyes. However, the range and variety of utility of hydrazones heretofore known for image-forming operations are of limited scope.
Accordingly, it is an object of this invention to provide, for photographic image-forming purposes, new light-sensitive layers and elements which contain organic hydrazone compounds.
It is another object of the present invention to provide, for image-forming purposes, new heat-sensitive layers and elements which contain organic hydrazone compounds.
Yet another object of this invention is to provide new, spectrally sensitized photographic layers and elements.
Yet another object of this invention is to provide, for imageforming purposes, new layers and elements capable of reproducing images by thermographic and photothermographic means.
Another object of the present invention is to provide novel image-forming processes.
Yet additional objects will become apparent from a consideration of the following specification and appended claims.
The objects of this invention are accomplished with imagerecording elements that have a support coated with a radiation-sensitive composition containing organic hydrazone compounds having the formula:
wherein:
R and R are each either a hydrogen atom, a lower alkyl radical or a carbocyclic aryl radical,
R is either a carbocyclic aryl radical, an aralkyl radical, an
aralkenyl radical or a heterocyclic radical, and
R is either a lower alkyl radical, a carbocyclic aryl radical or a heterocyclic radical, and an image-promoting component that includes radiationsensitive silver salts, radiation-sensitive metal oxides and mixtures thereof.
As defined herein, lower alkyl radicals include straight and branched chain aliphatic radicals having from one to six carbon atoms and preferably from one to four carbon atoms. Typical lower alkyl radicals are methyl, ethyl, chloroethyl, isopropyl and the like. Carbocyclic aryl radicals of the subject invention are deemed to include monoand polycyclic, carbocyclic aryl radicals, preferably having from six to 18 atoms in the aryl nucleus. Exemplary of aryl radicals are phenyl, anthracenyl, aminophenyl, diethoxyphenyl, triacetylphenyl, pdimethylaminophenyl, p-sulfophenyl, etc. Aralkyl radicals are such radicals as phenethyl and include radicals having both an aryl moiety, such as the described aryl radicals, and an alkyl moiety which is preferably a lower alkyl radical as noted herein. Aralkenyl radicals include radicals like phenethenyl and additional radicals having an aryl moiety such as those aryl radicals mentioned herein and an alkenyl moiety that includes unsaturated aliphatic radicals having from two to four carbon atoms such as ethenyl and 1,3-butadienyl. Heterocyclic radicals useful herein include monoand polycyclic heterocyclic radicals having from five to about l4 atoms and typically having from five to six atoms including hetero atoms in each cyclic nucleus. Exemplary of such heterocyclic radicals are pyridyl, quinolyl, julolidinyl, etc.
Particularly preferred organic hydrazone compounds of this invention include ketone and aldehyde hydrazones such as:
benzaldehyde phenylhydrazone benzaldehyde methylphenylhydrazone 2-thiophenaldehyde phenylhydrazone 2-pyridylaldehyde phenylhydrazone 4-pyridylaldehyde phenylhydrazone 3-pyridylaldehyde phenylhydrazone 4-aminobenzaldehyde methylhydrazone salicylaldehyde phenylhydrazone diethoxybenzaldehyde phenylhydrazon glyoxal diphenylhydrazone cinnamaldehyde phenylhydrazone cinnamylideneacetaldehyde methylphenylhydrazone triacetylbenzene triphenylhydrazone 4-aminobenzaldehyde methylphenylhydrazone anthracenealdehyde phenylhydrazone dimethylaminobenzaldehyde-4-sulfophenylhydrazone dimethylaminocinnamaldehyde-4-sulfophenylhydrazone julolidine aldehyde-4-sulfophenylhydrazone 4-(dimethylamino)benzaldehyde Z-quinolylhydrazone The hydrazone compounds of the general formula noted above can be prepared by known procedures. They are generally obtained in a simple manner by the condensation of equimolar quantities ofa hydrazine with compounds containing a carbonyl function, for example, aldehydes, ketones and quinones, in an organic solvent such as ethanol.
As noted herein, the subject hydrazone compounds are utilized in the presence of or in combination with certain radiation-sensitive, image-promoting components. The term radiation-sensitive, as used herein, refers broadly to electromagnetic radiation and includes both heat and light rays. Advantageous electromagnetic waves are, for example, gamma rays, ultraviolet radiation, visible light and infrared radiation.
The types of hydrazones suitable for use in the present invention can also be utilized as photoconductors in electrophotographic systems; this is particularly true for the com pound 4aminobenzaldehyde methylphenylhydrazone. Alternatively, the hydrazone compounds of this invention can be used in conjunction with a polyhalogen compound such as iodoform or carbon tetrachloride to produce printout images.
The radiation-sensitive silver salts of the present invention are those silver salts that can be reduced to metallic silver by exposure to electromagnetic radiation, typically heat or light rays. More particularly, the radiation-reducible silver salts of this invention comprehend primarily heat-sensitive substantially water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms such as silver oxalate, silver stearate and silver behenate. Additionally, light-sensitive silver halides are advantageously employed herein, as are light-sensitive, water-soluble silver salts like silver nitrate, silver acetate and silver lactate. Other silver salts useful in the practice of this invention, that are reduced to metallic silver by the impingement of electromagnetic rays are known to those skilled in the art.
Radiation-sensitive metal oxides useful in this invention are those metal oxides, both photoconductors and nonphotoconductors, which will transfer and donate electrons when activated by exposure to suitable electromagnetic radiation, typically rays of shorter wavelengths like X-rays as well as ultraviolet and actinic radiation. Typical such oxides are aluminum oxide, zinc oxide, titanium dioxide and antimony trioxide, but still additional radiation-sensitive metal oxides are known to those skilled in the art. In the radiation-sensitive compositions and elements described herein, mixtures of radiation-sensitive silver salts and metal oxides are advantageously employed.
As mentioned previously, the subject hydrazones are advantageously admixed with a light-sensitive silver halide salt. More particularly, in photographic elements having a support coated with at least one light-sensitive layer comprising a silver halide emulsion and a sensitizing amount of at least one of the hydrazone compounds described herein. The silver halide is spectrally sensitized to longer wavelengths by the organic hydrazone. Preferred as a spectral sensitizer for silver halide, such as silver chloride, silver bromide, silver bromoiodide, silver chloroiodide and the like, is the hydrazone 4-(dimethylamino)benzaldehyde quinol-2-ylhydrazone.
A wide variety of silver halide emulsions are spectrally sensitized in this fashion, such as gelatinosilver halide emulsions and silver halide emulsions containing other hydrophilic colloid binders such as polyvinyl alcohol, cellulose acetate and the like binder materials. Additionally, other addenda such as hardeners, antifoggants. coating aids and other typical ingredients can be present in the silver halide emulsions that are spectrally sensitized as described herein.
The subject hydrazones are typically added to silver halide emulsions in extremely small sensitizing amounts, generally varying between about I mg. and about 3 3 per gram of silver. More highly varying amounts can also be employed in accordance with conventional practice without detrimental effects. To produce a composite, sensitized photographic element, a silver halide emulsion containing at least one ofthe organic hydrazone compounds of this invention is coated on a support material and dried. Coating thickness is susceptible of somewhat wide variation, but typically wet thicknesses of from about 0.001 inch 3 mg. 0.006 inch are employed. More extensive variations can be used where desired for particular coating techniques or sensitometric characteristics.
The method of coating can be any of those known in the coating art, including such means as dipping, whirler coating and flow coating, except that hopper-coating or doctor blade coating means are preferred since they offer a higher degree of precision as regards coating thickness. Support materials which are advantageous in preparing these spectrally sensitized silver halide photographic elements are susceptible of extensive interchange and typically include cellulose esters such as cellulose acetate, cellulose butyrate, cellulose nitrate and cellulose acetate butyrate as well as other polymeric materials like polystyrene and poly(ethylene terephthalate). Additionally, papers including polyethylene and polypropylene coated paper are advantageous supports, as is baryta pigmented and other pigmented papers. Other support materials are well known in the art.
Subsequent to drying the silver halide containing layer, the composite photographic element can be imagewise exposed and processed to yield a visible photographic silver image. Since the hydrazone spectrally sensitizes the silver halide emulsion to visible light rays, the exposing means can be either a source of actinic radiation or a source of longer wavelength visible light to which the emulsion is sensitized by the subject organic hydrazone.
After an imagewise exposure, a spectrally sensitized silver halide photographic element as described herein can be processed in a conventional silver halide photographic developing composition to produce a silver image. Such developing compositions incorporate a silver halide developing agent, typically a hydroxylated aryl compound, such as dihydroxybenzenes like hydroquinones, catechols and pyrogallols, as well as other polyhydroxylated compounds such as ascorbic acid. Additional developing agents include aminophenols, p-phenylene-diamines and 3-pyrazolidones. Exemplary of silver halide developing agents that are advantageously used herein are compounds like 2-methyl-3- chlorohydroquinone, bromohydroquinone, catechol, S-phenylcatechol, pyrogallol monomethylether(l-methoxy-2,3- dihydroxy benzene), S-methylpyrogallol monomethyl-ether isoascorbic acid, N-methyl-p-aminophenol, dimethyl-p-phenylene diamine, 4-amino-N,N-di(n-propyl)anilene and 6- amino'l-ethyl-l,2,3,4-tetrahydr0quinoline. After image development, the image is stabilized by treatment with a photographic fixing agent. Conventional fixing agents or silver halide solubilizing agents include water-soluble thiosulfates,
and thiocyanates, and mercaptans, such as ammonium thiosulfate sodium thiocyanate, and the disodium salt of 2- mercapto-4-hydroxy-5-aminopyrimidine. hydroxy-S- aminopyrimidine. A particularly preferred fixing agent is sodium thiosulfate. Stabilization is generally accomplished by treatment with a composite fixing bath that incorporates a fixing agent such as those mentioned hereinabove.
In another aspect, the subject hydrazones function as heat and light activated selective reducing agents for metal ions, silver ions for example, in photographic, thermographic and photothermographic image-forming systems. Selective photo or photothermal reduction advantageously occurs subsequent to the formation of a metallic or other latent image which catalyzes the reduction of metal ions by the organic hydrazone compounds of this invention to form a visible image. illustrative of this capability is an alternative development procedure for an imagewiseexposed silver halide element such as is described hereinabove and containing at least one of the organic hydrazones of this invention. A visible photographic silver image can be produced on such an imagewise-exposed element merely by treatment with a conventional fixing agent and simultaneously exposing the element to visible light radiation. Although the particular reaction mechanism is not unequivocally known, it is speculated that the overall expo sure of the incorporated hydrazone produces a reducing agent in the coating which selectively reduces the silver ions of the solubilized silver halide onto the latent image specks produced by the first, imagewise exposureof the silver halide photographic clement. Continued exposure of the silver halide layer when it is immersed in the fixing bath produces no additional latent image.
Advantageous selective reduction is also accomplished with thermographic elements having a support such as those described herein coated with at least one of the hydrazones described herein and at least one substantially water-insoluble silver slat, typically of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms, such as silver cinnamate, silver behenate, silver stearate and silver oxalate. Coating techniques can be any of those noted hereinabove. The amount of hydrazone included in such element need only be sufiicient to advantageously reduce the silver salt to metallic silver upon a suitable exposure, and in like fashion the silver salt need only be present in an amount that provides a reduced silver image of a desirable density for viewing purposes. Typically, the hydrazone and silver salt are included in weight ratios of from about l;2 to about I24, but wider ratios can be used if desired. Although the water-insoluble silver salts are primarily heat sensitive and do not exhibit an excessive sensitivity to light radiation, exposure to ultraviolet and actinic light radiation can produce discoloration, and a suitable stabilizer such as a difunctional alkylene imine like N,N- bis-l,2-ethyleneisophthalimide can be included in the heatsensitive layer to prevent undesired photoreduction of silver. in a solely thermographic element such as this type, an imagewise thermal reduction is obtained without a preexisting latent image by effecting an imagewise concentration of heat radiation to selectively trigger the reduction reaction in only image areas. Such a pattern is typically produced by contacting the image-forming element, during the application of heat by such means as infrared radiation, with an original bearing an imagewise distribution of a heat-absorbing material like an infrared-absorbing carbon base printing ink. Such images can be stabilized against further printing out by suitable treatment with a conventional fixing bath such as those described above. Other means of image stabilization can be utilized if desired.
Additionally, at least one water-soluble silver salt such as silver nitrate, silver acetate and silver lactate, or any other light-sensitive, water-soluble silver salt, can be advantageously incorporated into the element already having a hydrazone compound and a water-insoluble silver salt in the radiationsensitive layer. The water-soluble silver salt renders the element desirably light sensitive, and after an imagewise exposure to activating light radiation such as actinic light and the simultaneous formation of a metallic silver latent image by photoreduction of silver ions of the water-soluble silver salt, a visible metallic silver image can be produced by treatment with either heat or light radiation. Upon suitable exposure to either heat rays or an imagewise pattern of light exposure such as intense tungsten radiation, the latent image catalyzes the hydrazones reducing action a metallic silver image is produced by selective reduction in only those areas corresponding to the latent image area. Such a water-soluble silver salt need only be present in an amount sufficient to provide a metallic silver latent image that will promote the reduction of the water-insoluble silver salt upon development. Typically, amounts by weight of from about 0.5 part to about two parts per part of hydrazone are used.
Alternatively, selective reduction produced by the subject hydrazone compounds can be encouraged or catalyzed by latent images obtained from the irradiation of photosensitive species other than silver halide, photoactivatable metal oxides for example, such as those described hereinabove. An element incorporating a support having coated thereon a light-sensitive layer including a hydrazone compound of this invention and a photoactivatable metal oxide can be imagewise exposed to light radiation and treated with a water-soluble silver salt solution such as aqueous silver nitrate to produce a visible metallic silver image in those areas corresponding to the imagewise exposure. A preferred light-sensitive metal oxide is titanium dioxide. The light-sensitive layer can also contain components like a hydrophilic colloid binder material such as gelatin or polyvinyl alcohol as well as other typical emulsion addenda such as spectral-sensitizing dyes, hardeners, coating aidsand the like. The light exposure can be to actinic light rays or to longer wavelength visible light radiation if the titanium dioxide or other photoactivatable metal oxide is spectrally sensitized to such longer wavelengths. Additionally in the preparation of a light radiation sensitive element containing a metal oxide like those noted herein, the choice of both a support material and a coating technique can be any of those described elsewhere herein. The respective amounts of metal oxide and hydrazone need only be sufficient to effect an adequate reduction of metal ion in the processing medium, and typically, ratios of from about 20 parts to about 40 parts by weight of metal oxide per part of hydrazone compound are used. Wider ratios can be employed if desired.
The described elements containing a photosensitive metal oxide can also incorporate, in the light-sensitive layer, at least one reducible silver salt. The silver salt can be either a waterinsoluble or a water-soluble salt like those described herein, and subsequent to an imagewise exposure to produce a photographic latent image a variable conductivity in the photoactivatable metal oxide, it can be developed by various techniques to produce a visible silver metal image. The reducible silver salt is present in an amount sufficient to provide a visible silver image of a density adequate for viewing purposes. Conventionally, amounts by weight of from about two parts to about four parts per part of hydrazone compound are used. Treatment with a photographic developing agent such as those described elsewhere herein produces a photographic silver image, but such processing does not utilize the advantageous selective reducing properties of the subject hydrazones. Alternatively, it can be processed as either a wholly photographic printout element or as a photothermographic element, since treatment with longer periods of intense light irradiation such as a 5-second exposure at a distance of 12 inches with a 500- watt tungsten lamp or heating to temperatures of about 190 F. effect advantageous selective reduction of silver ion to produce a dense metallic silver image in those areas corresponding to the latent image.
Although either type of reducible silver salt can be used advantageously, the substantially water-insoluble silver salts are preferred, however, since they exhibit both a susceptibility to advantageous reduction during image development and a higher resistance to undesired degradation during storage.
The following examples are included for a further understanding of the invention.
EXAMPLE I To 100 ml. of 5 percent gelatin is added 2.0 ml. of 10 percent formaldehyde, 2.0 ml. of a 7%percent saponin solution, 5 20 ml. of a silver chloride emulsion which contains 1 mole of silver and l2 g. of gelatin in 0.52 kg. of emulsion. To separate ml. portions of this mixture is added [.0 ml. of a l percent acetone solution of the following hydrazones as spectral sensitizers for the silver halide.
l. 4-aminobenzaldehyde methylphenylhydrazone 2. anthracenealdehyde phenylhydrazone 3. diethoxybenzaldehyde phenylhydrazone 4. dimethylaminobenzaldehyde-4-sulfophenylhydrazone 5. dimethylaminocinnamaldehyde-4-sulfophenylhydrazone 6. julolidinealdehyde-4-sulfophenylhydrazone 7. dimethylaminobenzaldehyde quinol-2-ylhydrazone Coatings of the above compounds are made at 0.004-inch wet thickness and dried. Wedge spectrograms show an extension of the spectral response as follows, when the strips are processed by immersion in a silver halide developing solution having the formula:
Water 500 cc. Elon 3 g. Sodium sulfite (desiccated) 45 g. Hydroquinone 12 g. Sodium carbonate (monohydrute) 80 g. Potassium bromide 2 g. Water to make L000 cc.
and immersion in a photographic fixing bath having the formula:
Water 600 cc. Sodium lhiosulfate 240 g. Sodium sulfite (desiccated) 15 g. Acetic acid (28% aqueous) 48 cc. Boric acid (crystals) 7.5 g. Potassium alum l5 g. Water to make L000 cc.
after WhlCl'l they are washed and dried:
Material Response A. Control (silver chloride) B. Control plus compound I. C. Control plus compound 2. D. Control plus compound 3. E. Control plus compound 4. F. Control plus compound 5. G. Control plus compound 6. H. Control plus compound 7.
300-500 my with a peak at 410 mp 300-540 up with I peak II 500 mu 300-580 mp with a peak at 540 mp 420-600 muwith a peak at Slt) mu 4 l0-540 mpwith a peak at 450 mu 4 l0-530 muwith a peak at 500 mp 400-560 muwith a broad peak over this entire range.
EXAMPLE 2 Photographic elements are prepared as in example 1. After an imagewise exposure as in example 1 to form a latent silver image, the elements are immersed in the fixing bath described in example 1 and simultaneously exposed to white light rays, whereupon a dense silver image is produced in the previously imagewise-exposed areas. The hydrazone compound functions as a selective reducing agent in those areas bearing a latent silver image.
EXAMPLE 3 A thermographic element is prepared by coating a paper support with a composition containing:
silver cinnumate 0.l5 g. anthracenealdehyde phenylhydrazone 0.05 g. acetone 4.00 ml solution of 36 g. ethyl acetate 240 ml. acetone and 60 ml.
alcohol (95:5 ethanol and methanol) 0.5 ml.
After drying, the coated element is contacted to a typewritten page and while in contact, the two are heated to about 190 F. A dense deposit of metallic silver is produced in those areas of the element corresponding to the image areas of the typewritten page.
EXAMPLE 4 A silver oxalate-silver iodide precipitate is prepared as described in U.S. Pat. No. 3,143,419 by mixing:
A. Potassium oxalate monohydrate 54.2 g.
Distilled Water 200 ml.
B. Silver nitrate 13.5 g.
Distilled water I50 ml.
C. Potassium iodide 5.6 g.
Distilled water 150 ml.
The silver nitrate solution is added to solution A and the resulting silver oxalate precipitate is washed by decantation. Solution C is then added and the resulting mixed precipitate is washed by decantation. The wet slurry is then mixed l:l with a 1 percent acetone solution of cinnamaldehyde phenylhydrazone and the mixture is flow coated on filter paper. A photothermographic paper results. Exposure of the coating on a wedge spectrograph for l0 seconds at a l-mm. slit width followed by thermal development at 120 C. for seconds produces a heat-developed silver image in the exposed areas. Alternatively, the element can be developed to produce a silver image by printout techniques using higher levels of an imagewise light exposure.
EXAMPLE 5 A photographic element is prepared by coating a paper support material with a 0.004 wet thickness coating ofa formulation having the composition:
A. Distilled water 25 cc. 8. Titanium dioxide 3 g. C. l0; gelatin 20 cc. D. 791' saponin 2 cc. E. I0; formaldehyde 0.5 cc.
After drying, the titanium dioxide element is flow coated with a 1 percent solution of 4aminobenzaldehyde methylphenylhydrazone dissolved in cc. of acetone. The dried coating is then exposed to a SOD-watt tungsten photoflood lamp through a line image for a period of about 1 second. This exposure produces a latent image that is made visible by immersing the exposed layer in 0.5 percent aqueous silver nitrate, since the hydrazone compound functionsas a selective reducing agent. The permanence of the image is improved by treatment with a sodium thiosulfate fixing bath to remove undeveloped silver salt.
EXAMPLE 6 A titanium dioxide photographic element is prepared according to the procedure of example 5, except that the flow coating contains 2 cc. of a 1 percent acetone solution of cinnamaldehyde phenylhydrazone, 2 cc. of a 1 percent aqueous silver nitrate solution and sufficient acetone to dissolve any precipitate. The composite photographic element is dried and then exposed through a line original for 5 seconds to the tungsten light of a 500-watt photoflood lamp at a distance of 12 inches from the exposing plane. A dense silver printout image is formed in the exposed areas directly upon exposure, since the hydrazone acts as a selective reducing agent in those areas bearing a latent image. A second element is prepared in like fashion, except that the exposure time is shortened to onetenth of a second. No visible printout is observed; however, when the exposed coating is immersed in a black-and-white developer solution as in example i, a dense silver image is produced in the exposed areas. A third element is also prepared in like fashion and imagewise exposed for one-tenth second as with the second element. Image development is obtained by heating the paper on a hot plate at I F which produces a dense visible deposit of metallic silver in the exposed areas by photothermographic means.
EXAMPLE 7 A slurry of 0. 15 g. ofsilver einnamate is prepared in 3 ml. of acetone. To this slurry is added 0.05 g. of anthracenealdehyde phenylhydrazone in 1 ml. of acetone, followed by the addition of 5 drops of the following solution:
Ethyl acetate 36.0 g. Acetone 240.0 ml. Alcohol ethanol.
5% methanol) 60.0 ml.
The resulting mixture is flow coated onto a titanium dioxide photographic element prepared as in example 5. The entire preparation is carried out under gold-colored fluorescent lamps. The composite element is exposed to produce a wedge spectrogram which shows a sensitivity from 280-560 mp. when the element is heated to l90-200 F. over a hotplate. A similar element is exposed for 1% seconds through a line original in a Photocopier (model 107 marketed by the Minnesota Mining and Manufacturing Company). A very faint tan image becomes visible in the exposed areas. The element is then heated by pressing it in contact with a hotplate at F. for about 2 seconds whereupon a dark reddish-brown image appears in the exposed areas. The background remains the yellow color of the original coating. At high levels of exposure, coatings prepared in this way print out directly. Alternatively, the latent image can be intensified by photographic developing solutions, for example, by immersion in a black-and-white developer composition as in example I. For permanence. the image may be fixed in thiosulfate solutions such as the fixing bath described in example I.
EXAMPLE 8 A paper support material coated with silver behenate is flow coated with a solution containing 2 cc. of a 1 percent acetone solution of cinnamaldehyde phenylhydrazone, 2 cc. of a l percent aqueous silver nitrate solution and sufficient acetone to dissolve any precipitate. The coating is then dried. Exposure and development by printout, photographic or photothermographic means as in example 6 produces a dense silver image in the exposed areas.
The invention has been described in detail with particular reference to certain preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
We claim:
1. An element for recording image, said element comprising a support having coated thereon a radiation-sensitive composition comprising:
a. a hydrazone having the formula:
wherein:
1. R is selected from the group consisting ofa hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
2. R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
3. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
wherein:
. R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
2. R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
4. R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
b. a reducible silver salt.
3. An element as described in claim 2 wherein the reducible silver salt is selected from the group consisting of substantially water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
4. An element as described in claim 3 wherein said reducible, water-insoluble silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
5. An element as described in claim 2 wherein the reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
6. An element as described in claim 2 wherein said reducible silver salt radiation-sensitive component comprises the admixture of:
a. a silver salt selected from the group consisting of waterinsoluble salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms, and
b. a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
7. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising:
a. a hydrazone having the formula:
wherein:
l. R, is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
2. R, is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
3. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
4. R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
b. a silver halide. 5 8. An element as described in claim 7 wherein the hydrazone is selected from the group consisting of:
a. 4-aminobenzaldehyde methylphenylhydrazone,
b. anthracenealdehyde phenylhydrazone,
c. diethoxybenzaldehyde phenylhydrazone,
d. dimethylaminobenzaldehyde-4-sulfophenylhydrazone,
e. dimethylaminocinnamaldehyde-4-sulfophenylhydrazone,
f. julolidinealdehyde-4-sulfophenylhydrazone, and
g. dimethylaminobenzaldehyde-quinol-Z-ylhydrazone.
9. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising:
a. a hydrazone having the formula:
wherein:
1. R is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
2. R, is selected from the group consisting of a carbo cyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
. R is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
b. a light-activatable metal oxide.
10. An element as described in claim 9 wherein said lightactivatable metal oxide is titanium dioxide.
11. An element as described in claim 9 wherein the lightsensitive layer also contains at least one reducible silver salt.
12. An element as described in claim 11 wherein the reducible silver slat is selected from the group consisting of water-insoluble silver salts of vmonocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
13. An element as described in claim 12 wherein the silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
14. An element as described in claim ll wherein the reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
15. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising:
a. a hydrazone selected from the group consisting of:
l. 4-aminobenzaldehyde methylphenylhydrazone,
2. anthracenealdehyde phenylhydrazone,
3. diethoxybenzaldehyde phenylhydrazone,
4. dimethylaminobenzaldehyde-4-sulfophenylhydrazone,
5. dimethylaminocinnamaldehyde-4-sulfophenylhydrazone,
6. julolidinealdehyde-4-sulfophenylhydrazone, and
7. dimethylaminobenzaldehyde-quinol-2-ylhydrazone.
b. titanium dioxide, and
c. a reducible silver salt.
16. A process for producing images on an element comprismg:
a. a hydrazone having the formula:
wherein:
. R, is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
R, is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
4. R, is selected from the group consisting of a lower alkyl radical and a heterocyclic radical, and
b. a reducible silver salt, which process comprises imagewise exposing said element to electromagnetic radiation for a period of time sufficient to produce a metallic silver image in the irradiated areas.
17. A process as described in claim 16 wherein the electromagnetic radiation comprises heat radiation.
18. A process as described in claim 16 wherein the electromagnetic radiation comprises light radiation.
19. A process for producing images on an imagcwise-exposed element comprising a support having coated thereon a light-sensitive layer comprising:
a. a hydrazone having the formula:
wherein:
l. R, is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
. R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
. R, is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
b. a silver halide,
which process comprises treating said imagewise-exposed element with a processing medium selected from the group consisting of a silver halide developing composition and a silver halide fixing agent for a period of time sufficient to produce a metallic silver image in the exposed areas.
20. A process for producing images on an image light exposed element comprising:
a. a hydrazone having the formula:
wherein:
l. R, is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R is an aralkenyl radical, a lower alkyl radical,
2. R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
3. R is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and 4. R, is selected from the group consisting of a lower alkyl wherein:
l. R, is selected from the group consisting of a hydrogen atom, a carbocyclic aryl radical and, when R, is an aralkenyl radical, a lower alkyl radical,
. R is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and l,3-butadienyl and a heterocyclic radical,
. R is selected from the group consisting ofa hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
. R, is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and
b. a light-activatable metal oxide, and
c. a reducible silver salt, which process comprises treating said element with a developing means for a period oftime sufficient to produce a metallic silver image in the exposed areas.
22. A process as described in claim 21 wherein said developing means comprises heat.
23. A process as described in claim 21 wherein said developing means comprises light irradiation corresponding to the original imagewise exposure.
24. A process as described in claim 21 wherein said developing means comprises a photographic silver halide developer.
Claims (55)
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. An element for recording images, said element comprising a support having coated thereon a radiation-sensitive layer comprising: a. a hydrazone having the formula: wherein:
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. anthracenealdehyde phenylhydrazone,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. R2 is selected from the group consisting of a carbocyclic aryl radical, an aralkyl radical, an aralkenyl radical selected from the group consisting of ethenyl and 1,3-butadienyl and a heterocyclic radical,
- 2. A radiation-sensitive metal oxide, and
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. diethoxybenzaldehyde phenylhydrazone,
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. An element as described in claim 2 wherein the reducible silver salt is selected from the group consisting of substantially water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 3. mixtures thereof.
- 3. R3 is selected from the group consisting of a hydrogen atom, a lower alkyl radical and a carbocyclic aryl radical, and
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. an image-promoting component selected from the group consisting of:
- 4. An element as described in claim 3 wherein said reducible, water-insoluble silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a reducible silver salt.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a silver halide.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a light-activatable metal oxide.
- 4. dimethylaminobenzaldehyde-4-sulfophenylhydrazone,
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a reducible silver salt, which pRocess comprises imagewise exposing said element to electromagnetic radiation for a period of time sufficient to produce a metallic silver image in the irradiated areas.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a silver halide, which process comprises treating said imagewise-exposed element with a processing medium selected from the group consisting of a silver halide developing composition and a silver halide fixing agent for a period of time sufficient to produce a metallic silver image in the exposed areas.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a light-activatable metal oxide, which process comprises treating said imagewise exposed element with a solution of a reducible, water-soluble silver salt for a period of time sufficient to produce a metallic silver image in the exposed areas.
- 4. R4 is selected from the group consisting of a lower alkyl radical, a carbocyclic aryl radical and a heterocyclic radical, and b. a light-activatable metal oxide, and c. a reducible silver salt, which process comprises treating said element with a developing means for a period of time sufficient to produce a metallic silver image in the exposed areas.
- 5. dimethylaminocinnamaldehyde-4-sulfophenylhydrazone,
- 5. An element as described in claim 2 wherein the reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- 6. An element as described in claim 2 wherein said reducible silver salt radiation-sensitive component comprises the admixture of: a. a silver salt selected from the group consisting of water-insoluble salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms, and b. a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- 6. julolidinealdehyde-4-sulfophenylhydrazone, and
- 7. dimethylaminobenzaldehyde-quinol-2-ylhydrazone. b. titanium dioxide, and c. a reducible silver salt.
- 7. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising: a. a hydrazone having the formula: wherein:
- 8. An element as described in claim 7 wherein the hydrazone is selected from the group consisting of: a. 4-aminobenzaldehyde methylphenylhydrazone, b. anthracenealdehyde phenylhydrazone, c. diethoxybenzaldehyde phenylhydrazone, d. dimethylaminobenzaldehyde-4-sulfophenylhydrazone, e. dimethylaminocinnamaldehyde-4-sulfophenylhydrazone, f. julolidinealdehyde-4-sulfophenylhydrazone, and g. dimethylaminobenzaldehyde-quinol-2-ylhydrazone.
- 9. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising: a. a hydrazone having the formula: wherein:
- 10. An element as described in claim 9 wherein said light-activatable metal oxide is titanium dioxide.
- 11. An element as described in claim 9 wherein the light-sensitive layer also contains at least one reducible silver salt.
- 12. An element as described in claim 11 wherein the reducible silver salt is selected from the group consisting of water-insoluble silver salts of monocarboxylic and dicarboxylic acids having from two to about 22 carbon atoms.
- 13. An element as described in claim 12 wherein the silver salt is selected from the group consisting of silver cinnamate, silver behenate and silver oxalate.
- 14. An element as described in claim 11 wherein the reducible silver salt is a water-soluble silver salt selected from the group consisting of silver nitrate, silver acetate and silver lactate.
- 15. An element for recording images, said element comprising a support having coated thereon a light-sensitive layer comprising: a. a hydrazone selected from the group consisting of:
- 16. A process for producing images on an element comprising: a. a hydrazone having the formula: wherein:
- 17. A process as described in claim 16 wherein the electromagnetic radiation comprises heat radiation.
- 18. A process as described in claim 16 wherein the electromagnetic radiation comprises light radiation.
- 19. A process for producing images on an imagewise-exposed element comprising a support having coated thereon a light-sensitive layer comprising: a. a hydrazone having the formula: wherein:
- 20. A process for producing images on an image light exposed element comprising: a. a hydrazone having the formula: wherein:
- 21. A process for producing images on an imagewise light exposed element comprising: a. a hydrazone having the formula: wherein:
- 22. A process as described in claim 21 wherein said developing means comprises heat.
- 23. A process as described in claim 21 wherein said develOping means comprises light irradiation corresponding to the original imagewise exposure.
- 24. A process as described in claim 21 wherein said developing means comprises a photographic silver halide developer.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US71186868A | 1968-03-11 | 1968-03-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3615533A true US3615533A (en) | 1971-10-26 |
Family
ID=24859866
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US711868A Expired - Lifetime US3615533A (en) | 1968-03-11 | 1968-03-11 | Heat and light sensitive layers containing hydrazones |
Country Status (4)
Country | Link |
---|---|
US (1) | US3615533A (en) |
BE (1) | BE729669A (en) |
FR (1) | FR2003646A1 (en) |
GB (1) | GB1263134A (en) |
Cited By (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4013473A (en) * | 1974-08-24 | 1977-03-22 | Agfa-Gevaert N.V. | Recording materials and image receiving materials for producing copies in a dry way |
JPS54150128A (en) * | 1978-05-17 | 1979-11-26 | Mitsubishi Chem Ind | Electrophotographic photosensitive member |
FR2437645A1 (en) * | 1978-09-29 | 1980-04-25 | Ricoh Kk | ELECTROPHOTOGRAPHIC PHOTOCONDUCTOR |
FR2438858A1 (en) * | 1978-10-13 | 1980-05-09 | Ricoh Kk | ELECTROPHOTOGRAPHIC ELEMENT CONTAINING PHENYLHYDRAZONES |
FR2462732A1 (en) * | 1979-07-30 | 1981-02-13 | Eastman Kodak Co | Silver halide photothermographic materials - contg. a heterocyclic hydrazone reducing agent whose oxidn. prod. reacts with a dye-forming coupler to form an image dye |
FR2462731A1 (en) * | 1979-07-30 | 1981-02-13 | Eastman Kodak Co | Silver halide photothermographic materials - contg. a heterocyclic hydrazone reducing agent whose oxidn. prod. reacts with a dye-forming coupler to form an image dye |
US4525722A (en) * | 1984-02-23 | 1985-06-25 | International Business Machines Corporation | Chemical heat amplification in thermal transfer printing |
US4659644A (en) * | 1983-12-22 | 1987-04-21 | Ricoh Company, Ltd. | Diazo-type thermosensitive recording material with hydrazone coupler and chelating metal compound |
US5128227A (en) * | 1990-03-27 | 1992-07-07 | Agfa-Gevaert, N.V. | Electrophotographic recording material having a julolidine hydrazone compound |
US5318939A (en) * | 1990-09-17 | 1994-06-07 | Ciba-Geigy Corporation | Pressure-sensitive or heat-sensitive recording material |
US5409798A (en) * | 1991-08-30 | 1995-04-25 | Canon Kabushiki Kaisha | Plate blank, process for producing printing plate from plate blank, and printing method and apparatus using plate |
US5529896A (en) * | 1993-06-22 | 1996-06-25 | Fuji Photo Film Co., Ltd. | Silver halide photographic material |
US5599648A (en) * | 1990-08-03 | 1997-02-04 | Canon Kabushiki Kaisha | Surface reforming method, process for production of printing plate, printing plate and printing process |
US5882837A (en) * | 1994-11-25 | 1999-03-16 | Fuji Photo Film Co., Ltd. | Heat-developable color light-sensitive material |
EP1186949A1 (en) * | 2000-09-11 | 2002-03-13 | Agfa-Gevaert | Photothermographic materials |
US6576415B2 (en) | 2000-09-11 | 2003-06-10 | Agfa-Gevaert | Photothermographic materials with increa sed photosensitivity |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4150987A (en) * | 1977-10-17 | 1979-04-24 | International Business Machines Corporation | Hydrazone containing charge transport element and photoconductive process of using same |
JPS5584943A (en) * | 1978-12-21 | 1980-06-26 | Ricoh Co Ltd | Laminated type electrophotographic photoreceptor |
JPH08146577A (en) * | 1994-11-25 | 1996-06-07 | Fuji Photo Film Co Ltd | Heat developing color photosensitive material |
-
1968
- 1968-03-11 US US711868A patent/US3615533A/en not_active Expired - Lifetime
-
1969
- 1969-03-06 GB GB01946/69A patent/GB1263134A/en not_active Expired
- 1969-03-10 BE BE729669D patent/BE729669A/xx unknown
- 1969-03-10 FR FR6906683A patent/FR2003646A1/fr not_active Withdrawn
Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4013473A (en) * | 1974-08-24 | 1977-03-22 | Agfa-Gevaert N.V. | Recording materials and image receiving materials for producing copies in a dry way |
JPS6140104B2 (en) * | 1978-05-17 | 1986-09-08 | Mitsubishi Chem Ind | |
JPS54150128A (en) * | 1978-05-17 | 1979-11-26 | Mitsubishi Chem Ind | Electrophotographic photosensitive member |
FR2426281A1 (en) * | 1978-05-17 | 1979-12-14 | Mitsubishi Chem Ind | ELECTROPHOTOGRAPHIC PLATE |
FR2437645A1 (en) * | 1978-09-29 | 1980-04-25 | Ricoh Kk | ELECTROPHOTOGRAPHIC PHOTOCONDUCTOR |
FR2438858A1 (en) * | 1978-10-13 | 1980-05-09 | Ricoh Kk | ELECTROPHOTOGRAPHIC ELEMENT CONTAINING PHENYLHYDRAZONES |
FR2462732A1 (en) * | 1979-07-30 | 1981-02-13 | Eastman Kodak Co | Silver halide photothermographic materials - contg. a heterocyclic hydrazone reducing agent whose oxidn. prod. reacts with a dye-forming coupler to form an image dye |
FR2462731A1 (en) * | 1979-07-30 | 1981-02-13 | Eastman Kodak Co | Silver halide photothermographic materials - contg. a heterocyclic hydrazone reducing agent whose oxidn. prod. reacts with a dye-forming coupler to form an image dye |
US4659644A (en) * | 1983-12-22 | 1987-04-21 | Ricoh Company, Ltd. | Diazo-type thermosensitive recording material with hydrazone coupler and chelating metal compound |
EP0152795A2 (en) * | 1984-02-23 | 1985-08-28 | International Business Machines Corporation | Thermal transfer printing |
US4525722A (en) * | 1984-02-23 | 1985-06-25 | International Business Machines Corporation | Chemical heat amplification in thermal transfer printing |
EP0152795A3 (en) * | 1984-02-23 | 1987-05-20 | International Business Machines Corporation | Thermal transfer printing |
US5128227A (en) * | 1990-03-27 | 1992-07-07 | Agfa-Gevaert, N.V. | Electrophotographic recording material having a julolidine hydrazone compound |
US5599648A (en) * | 1990-08-03 | 1997-02-04 | Canon Kabushiki Kaisha | Surface reforming method, process for production of printing plate, printing plate and printing process |
US5318939A (en) * | 1990-09-17 | 1994-06-07 | Ciba-Geigy Corporation | Pressure-sensitive or heat-sensitive recording material |
US5409798A (en) * | 1991-08-30 | 1995-04-25 | Canon Kabushiki Kaisha | Plate blank, process for producing printing plate from plate blank, and printing method and apparatus using plate |
US5529896A (en) * | 1993-06-22 | 1996-06-25 | Fuji Photo Film Co., Ltd. | Silver halide photographic material |
US5882837A (en) * | 1994-11-25 | 1999-03-16 | Fuji Photo Film Co., Ltd. | Heat-developable color light-sensitive material |
EP1186949A1 (en) * | 2000-09-11 | 2002-03-13 | Agfa-Gevaert | Photothermographic materials |
US6576415B2 (en) | 2000-09-11 | 2003-06-10 | Agfa-Gevaert | Photothermographic materials with increa sed photosensitivity |
Also Published As
Publication number | Publication date |
---|---|
GB1263134A (en) | 1972-02-09 |
BE729669A (en) | 1969-08-18 |
FR2003646A1 (en) | 1969-11-14 |
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