JPS5845696B2 - カラ−拡散転写法用写真フィルム単位 - Google Patents

カラ−拡散転写法用写真フィルム単位

Info

Publication number: JPS5845696B2
Authority: JP; Japan
Prior art keywords: group; nitroxyl; image; polymer; oxidant
Prior art date: 1973-11-02
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

Application number

JP49126127A

Other languages

English (en)

Japanese (ja)

Other versions

JPS5080131A (fr

Inventor

サルヴアトーレポンテイセロイグナチオ

アランキヤンプベルジエラルド

エルコヘンハイマン

グウエイリングハンス

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1973-11-02

Filing date

1974-11-02

Publication date

1983-10-12

1974-11-02 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1975-06-30 Publication of JPS5080131A publication Critical patent/JPS5080131A/ja

1983-10-12 Publication of JPS5845696B2 publication Critical patent/JPS5845696B2/ja

Status Expired legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims description 29
238000012546 transfer Methods 0.000 title claims description 19
238000009792 diffusion process Methods 0.000 title claims description 14
239000007800 oxidant agent Substances 0.000 claims description 41
-1 silver halide Chemical class 0.000 claims description 41
230000001590 oxidative effect Effects 0.000 claims description 30
229910052709 silver Inorganic materials 0.000 claims description 25
239000004332 silver Substances 0.000 claims description 25
239000000839 emulsion Substances 0.000 claims description 21
239000000463 material Substances 0.000 claims description 17
230000008569 process Effects 0.000 claims description 9
239000000203 mixture Substances 0.000 claims description 8
229920003169 water-soluble polymer Polymers 0.000 claims description 2
229920000642 polymer Polymers 0.000 description 67
ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical compound O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 54
239000000975 dye Substances 0.000 description 34
125000004432 carbon atom Chemical group C* 0.000 description 33
150000001875 compounds Chemical class 0.000 description 29
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 26
239000000243 solution Substances 0.000 description 23
238000002360 preparation method Methods 0.000 description 17
125000000217 alkyl group Chemical group 0.000 description 15
238000012545 processing Methods 0.000 description 15
230000003647 oxidation Effects 0.000 description 14
238000007254 oxidation reaction Methods 0.000 description 14
229910052757 nitrogen Inorganic materials 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 12
125000004433 nitrogen atom Chemical group N* 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 11
125000003118 aryl group Chemical group 0.000 description 10
229910052799 carbon Inorganic materials 0.000 description 10
125000003277 amino group Chemical group 0.000 description 9
125000000732 arylene group Chemical group 0.000 description 9
239000007787 solid Substances 0.000 description 9
GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
229920001577 copolymer Chemical compound 0.000 description 8
238000001914 filtration Methods 0.000 description 8
108010010803 Gelatin Proteins 0.000 description 7
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 7
125000002947 alkylene group Chemical group 0.000 description 7
150000001721 carbon Chemical group 0.000 description 7
229920000159 gelatin Polymers 0.000 description 7
239000008273 gelatin Substances 0.000 description 7
235000019322 gelatine Nutrition 0.000 description 7
235000011852 gelatine desserts Nutrition 0.000 description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 6
235000019270 ammonium chloride Nutrition 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
125000000623 heterocyclic group Chemical group 0.000 description 6
125000001424 substituent group Chemical group 0.000 description 6
CWNSVVHTTQBGQB-UHFFFAOYSA-N N,N-Diethyldodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CC)CC CWNSVVHTTQBGQB-UHFFFAOYSA-N 0.000 description 5
230000000694 effects Effects 0.000 description 5
239000000178 monomer Substances 0.000 description 5
150000003254 radicals Chemical class 0.000 description 5
DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 4
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 4
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 4
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
150000001412 amines Chemical class 0.000 description 4
125000004429 atom Chemical group 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
238000011161 development Methods 0.000 description 4
125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
238000001556 precipitation Methods 0.000 description 4
150000003839 salts Chemical group 0.000 description 4
125000003107 substituted aryl group Chemical group 0.000 description 4
150000003512 tertiary amines Chemical class 0.000 description 4
239000004408 titanium dioxide Substances 0.000 description 4
125000002373 5 membered heterocyclic group Chemical group 0.000 description 3
125000004070 6 membered heterocyclic group Chemical group 0.000 description 3
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical class ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 3
YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 3
239000002168 alkylating agent Substances 0.000 description 3
229940100198 alkylating agent Drugs 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
125000001841 imino group Chemical group [H]N=* 0.000 description 3
238000005259 measurement Methods 0.000 description 3
239000002243 precursor Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 3
239000000126 substance Substances 0.000 description 3
229940126062 Compound A Drugs 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
PEEHTFAAVSWFBL-UHFFFAOYSA-N Maleimide Chemical compound O=C1NC(=O)C=C1 PEEHTFAAVSWFBL-UHFFFAOYSA-N 0.000 description 2
239000004157 Nitrosyl chloride Substances 0.000 description 2
229920003060 Poly(vinyl benzyl chloride) Polymers 0.000 description 2
239000004793 Polystyrene Substances 0.000 description 2
206010070834 Sensitisation Diseases 0.000 description 2
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
230000002378 acidificating effect Effects 0.000 description 2
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
230000002411 adverse Effects 0.000 description 2
125000003545 alkoxy group Chemical group 0.000 description 2
230000002152 alkylating effect Effects 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000004202 carbamide Substances 0.000 description 2
125000005521 carbonamide group Chemical group 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
125000002091 cationic group Chemical group 0.000 description 2
125000000392 cycloalkenyl group Chemical group 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
238000001362 electron spin resonance spectrum Methods 0.000 description 2
YYXLGGIKSIZHSF-UHFFFAOYSA-N ethene;furan-2,5-dione Chemical compound C=C.O=C1OC(=O)C=C1 YYXLGGIKSIZHSF-UHFFFAOYSA-N 0.000 description 2
239000012467 final product Substances 0.000 description 2
230000006870 function Effects 0.000 description 2
150000004795 grignard reagents Chemical class 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
239000011159 matrix material Substances 0.000 description 2
VPCDQGACGWYTMC-UHFFFAOYSA-N nitrosyl chloride Chemical compound ClN=O VPCDQGACGWYTMC-UHFFFAOYSA-N 0.000 description 2
235000019392 nitrosyl chloride Nutrition 0.000 description 2
239000004014 plasticizer Substances 0.000 description 2
229920000139 polyethylene terephthalate Polymers 0.000 description 2
239000005020 polyethylene terephthalate Substances 0.000 description 2
239000004848 polyfunctional curative Substances 0.000 description 2
229920002223 polystyrene Polymers 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
238000011160 research Methods 0.000 description 2
230000008313 sensitization Effects 0.000 description 2
NDVLTYZPCACLMA-UHFFFAOYSA-N silver oxide Chemical compound [O-2].[Ag+].[Ag+] NDVLTYZPCACLMA-UHFFFAOYSA-N 0.000 description 2
159000000000 sodium salts Chemical class 0.000 description 2
125000000547 substituted alkyl group Chemical group 0.000 description 2
239000000758 substrate Substances 0.000 description 2
125000000565 sulfonamide group Chemical group 0.000 description 2
125000003944 tolyl group Chemical group 0.000 description 2
IBDVWXAVKPRHCU-UHFFFAOYSA-N 2-(2-methylprop-2-enoyloxy)ethyl 3-oxobutanoate Chemical compound CC(=O)CC(=O)OCCOC(=O)C(C)=C IBDVWXAVKPRHCU-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
ZNQOWAYHQGMKBF-UHFFFAOYSA-N 2-dodecylbenzene-1,4-diol Chemical compound CCCCCCCCCCCCC1=CC(O)=CC=C1O ZNQOWAYHQGMKBF-UHFFFAOYSA-N 0.000 description 1
LUQZKEZPFQRRRK-UHFFFAOYSA-N 2-methyl-2-nitrosopropane Chemical group CC(C)(C)N=O LUQZKEZPFQRRRK-UHFFFAOYSA-N 0.000 description 1
KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
MRIBCCHYZOSDOM-UHFFFAOYSA-N 3-(1-phenyltetrazol-5-yl)sulfanylpropanenitrile Chemical compound N#CCCSC1=NN=NN1C1=CC=CC=C1 MRIBCCHYZOSDOM-UHFFFAOYSA-N 0.000 description 1
KFNGWPXYNSJXOP-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propane-1-sulfonic acid Chemical compound CC(=C)C(=O)OCCCS(O)(=O)=O KFNGWPXYNSJXOP-UHFFFAOYSA-N 0.000 description 1
YNJSNEKCXVFDKW-UHFFFAOYSA-N 3-(5-amino-1h-indol-3-yl)-2-azaniumylpropanoate Chemical compound C1=C(N)C=C2C(CC(N)C(O)=O)=CNC2=C1 YNJSNEKCXVFDKW-UHFFFAOYSA-N 0.000 description 1
NYUTUWAFOUJLKI-UHFFFAOYSA-N 3-prop-2-enoyloxypropane-1-sulfonic acid Chemical compound OS(=O)(=O)CCCOC(=O)C=C NYUTUWAFOUJLKI-UHFFFAOYSA-N 0.000 description 1
XUXUHDYTLNCYQQ-UHFFFAOYSA-N 4-amino-TEMPO Chemical group CC1(C)CC(N)CC(C)(C)N1[O] XUXUHDYTLNCYQQ-UHFFFAOYSA-N 0.000 description 1
KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 description 1
125000003341 7 membered heterocyclic group Chemical group 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
REUKGNXLKLMNPH-UHFFFAOYSA-N CN(C)c1ccc(NC2C=CC(=O)C=C2)cc1 Chemical compound CN(C)c1ccc(NC2C=CC(=O)C=C2)cc1 REUKGNXLKLMNPH-UHFFFAOYSA-N 0.000 description 1
JFPVXVDWJQMJEE-QMTHXVAHSA-N Cefuroxime Chemical compound N([C@@H]1C(N2C(=C(COC(N)=O)CS[C@@H]21)C(O)=O)=O)C(=O)C(=NOC)C1=CC=CO1 JFPVXVDWJQMJEE-QMTHXVAHSA-N 0.000 description 1
LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
239000007818 Grignard reagent Substances 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
239000004642 Polyimide Substances 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
TZTCYKFMDLPFPV-UHFFFAOYSA-N [Br-].C(C1=CC=CC=C1)C1([NH2+]C=CC=C1)C Chemical compound [Br-].C(C1=CC=CC=C1)C1([NH2+]C=CC=C1)C TZTCYKFMDLPFPV-UHFFFAOYSA-N 0.000 description 1
150000001253 acrylic acids Chemical class 0.000 description 1
125000002252 acyl group Chemical group 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical class NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 1
238000010539 anionic addition polymerization reaction Methods 0.000 description 1
239000000987 azo dye Substances 0.000 description 1
235000019445 benzyl alcohol Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
229940047496 ceftin Drugs 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
150000001805 chlorine compounds Chemical group 0.000 description 1
125000000068 chlorophenyl group Chemical group 0.000 description 1
JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 1
125000004122 cyclic group Chemical group 0.000 description 1
238000000354 decomposition reaction Methods 0.000 description 1
125000005266 diarylamine group Chemical group 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
230000004907 flux Effects 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
230000005283 ground state Effects 0.000 description 1
239000000383 hazardous chemical Substances 0.000 description 1
125000005842 heteroatom Chemical group 0.000 description 1
238000003384 imaging method Methods 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
125000005647 linker group Chemical group 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
125000005395 methacrylic acid group Chemical group 0.000 description 1
XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
239000003607 modifier Substances 0.000 description 1
229910052750 molybdenum Inorganic materials 0.000 description 1
239000011733 molybdenum Substances 0.000 description 1
AJDUTMFFZHIJEM-UHFFFAOYSA-N n-(9,10-dioxoanthracen-1-yl)-4-[4-[[4-[4-[(9,10-dioxoanthracen-1-yl)carbamoyl]phenyl]phenyl]diazenyl]phenyl]benzamide Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2NC(=O)C(C=C1)=CC=C1C(C=C1)=CC=C1N=NC(C=C1)=CC=C1C(C=C1)=CC=C1C(=O)NC1=CC=CC2=C1C(=O)C1=CC=CC=C1C2=O AJDUTMFFZHIJEM-UHFFFAOYSA-N 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
150000002832 nitroso derivatives Chemical class 0.000 description 1
125000004043 oxo group Chemical group O=* 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
125000005496 phosphonium group Chemical group 0.000 description 1
150000004714 phosphonium salts Chemical class 0.000 description 1
IYDGMDWEHDFVQI-UHFFFAOYSA-N phosphoric acid;trioxotungsten Chemical compound O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.O=[W](=O)=O.OP(O)(O)=O IYDGMDWEHDFVQI-UHFFFAOYSA-N 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920001721 polyimide Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
150000003141 primary amines Chemical class 0.000 description 1
LYBIZMNPXTXVMV-UHFFFAOYSA-N propan-2-yl prop-2-enoate Chemical compound CC(C)OC(=O)C=C LYBIZMNPXTXVMV-UHFFFAOYSA-N 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
238000001226 reprecipitation Methods 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
229910001923 silver oxide Inorganic materials 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000005156 substituted alkylene group Chemical group 0.000 description 1
125000005649 substituted arylene group Chemical group 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium group Chemical group [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
238000010189 synthetic method Methods 0.000 description 1
238000012360 testing method Methods 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
230000009466 transformation Effects 0.000 description 1
229910052721 tungsten Inorganic materials 0.000 description 1
150000003657 tungsten Chemical class 0.000 description 1
229910052720 vanadium Inorganic materials 0.000 description 1
GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/42—Structural details
- G03C8/52—Bases or auxiliary layers; Substances therefor

Landscapes

Engineering & Computer Science (AREA)
Architecture (AREA)
Structural Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

JP49126127A 1973-11-02 1974-11-02 カラ−拡散転写法用写真フィルム単位 Expired JPS5845696B2 (ja)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US412081A US3868252A (en)	1973-11-02	1973-11-02	Photographic elements containing polymeric oxidants

Publications (2)

Publication Number	Publication Date
JPS5080131A JPS5080131A (fr)	1975-06-30
JPS5845696B2 true JPS5845696B2 (ja)	1983-10-12

Family

ID=23631534

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP49126127A Expired JPS5845696B2 (ja)	1973-11-02	1974-11-02	カラ−拡散転写法用写真フィルム単位

Country Status (7)

Country	Link
US (1)	US3868252A (fr)
JP (1)	JPS5845696B2 (fr)
BE (1)	BE821740A (fr)
CA (1)	CA1035898A (fr)
DE (1)	DE2451628C3 (fr)
FR (1)	FR2249908B1 (fr)
GB (1)	GB1481570A (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2541754C2 (de) *	1975-09-19	1986-01-09	Agfa-Gevaert Ag, 5090 Leverkusen	Photographische Silberhalogenidemulsion
JPS6021370B2 (ja) *	1979-11-05	1985-05-27	富士写真フイルム株式会社	写真感光材料
US4435502A (en)	1982-06-28	1984-03-06	Eastman Kodak Company	Use of ketal blocked quinones to reduce post-process D-min increase in positive redox dye-releasing image transfer systems
US4407928A (en) *	1982-06-28	1983-10-04	Eastman Kodak Company	Use of ketal blocked quinones to reduce post-process Dmin increase in positive redox dye-releasing image transfer systems
GB8326238D0 (en) *	1983-09-30	1983-11-02	Scott G	Stabilised thermo-plastic polymer compositions
US5620941A (en) *	1996-04-16	1997-04-15	Eastman Kodak Company	Stabilizers for dye-donor element used in thermal dye transfer

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2698798A (en) *	1949-05-21	1955-01-04	Polaroid Corp	Color photographic process and product
US3065074A (en) *	1958-08-20	1962-11-20	Polaroid Corp	1,4-benzoquinone oxidizing agents for color transfer processes
DE1175072B (de) *	1963-04-11	1964-07-30	Agfa Ag	Lichtempfindliches photographisches Material mit mindestens einer Halogensilber-emulsionsschicht
CA943694A (en) *	1968-03-01	1974-03-12	Hyman L. Cohen	Polymers and photographic elements containing same
US3698897A (en) *	1971-07-06	1972-10-17	Eastman Kodak Co	Diffusion transfer processes and film units comprising compounds which are cleavable upon oxidation in alkali media to produce diffusible dyes or dye precursors

1973
- 1973-11-02 US US412081A patent/US3868252A/en not_active Expired - Lifetime
1974
- 1974-10-03 CA CA210663A patent/CA1035898A/fr not_active Expired
- 1974-10-30 FR FR7436210A patent/FR2249908B1/fr not_active Expired
- 1974-10-30 DE DE2451628A patent/DE2451628C3/de not_active Expired
- 1974-10-31 BE BE150108A patent/BE821740A/fr not_active IP Right Cessation
- 1974-11-01 GB GB47395/74A patent/GB1481570A/en not_active Expired
- 1974-11-02 JP JP49126127A patent/JPS5845696B2/ja not_active Expired

Also Published As

Publication number	Publication date
FR2249908A1 (fr)	1975-05-30
DE2451628C3 (de)	1980-08-21
DE2451628A1 (de)	1975-05-07
GB1481570A (en)	1977-08-03
BE821740A (fr)	1975-04-30
CA1035898A (fr)	1978-08-01
US3868252A (en)	1975-02-25
FR2249908B1 (fr)	1976-10-22
JPS5080131A (fr)	1975-06-30
DE2451628B2 (de)	1979-09-27

Publication	Publication Date	Title
EP0056444B1 (fr)	1984-05-09	Eléments photographiques comprenant des réactifs photographiques bloqués et procédé les utilisant
EP0079056A2 (fr)	1983-05-18	Matériau photographique en couleurs développable à chaud
US4199354A (en)	1980-04-22	Positive-working immobile photographic compounds and photographic elements containing same
GB2081466A (en)	1982-02-17	Silver halide photographic elements
US4088488A (en)	1978-05-09	Photographic elements containing nitroxyl radical oxidants
JPS5845696B2 (ja)	1983-10-12	カラ−拡散転写法用写真フィルム単位
JPS5914739B2 (ja)	1984-04-05	カラ−拡散転写法
JPS5931062B2 (ja)	1984-07-31	拡散転写法用感光要素
US3928043A (en)	1975-12-23	Photographic elements containing iodoso or iodoxy oxidants
US4168976A (en)	1979-09-25	Photographic film units containing aza heterocyclic polymeric mordants
JPS593736B2 (ja)	1984-01-25	カラ−拡散転写法用写真感光シ−ト
US3998640A (en)	1976-12-21	Photographic elements containing N-oxide oxidants
US4987061A (en)	1991-01-22	Heat developable color photographic recording element
US4193795A (en)	1980-03-18	Photographic film units containing a polymeric mordant which covalently bonds with certain dyes
US4036643A (en)	1977-07-19	Diffusion transfer color process using lactone or sultone ring containing lipophilic non-diffusing color formers which yield diffusing dyes
CA1117348A (fr)	1982-02-02	Unites de pellicule photographique, contenant un mordant polymerique qui forme des liaisons covalentes avec certains colorants
JPS61269148A (ja)	1986-11-28	加熱工程を有する画像形成方法
EP0073245B1 (fr)	1985-01-09	Polymeres clivables et produits photographiques et procede les utilisant
US4689286A (en)	1987-08-25	Color photographic recording material developable by heat treatment
JPH0588819B2 (fr)	1993-12-24
US3998637A (en)	1976-12-21	Process for producing positive color diffusion transfer images using redox dye releasers
US4047952A (en)	1977-09-13	Imagewise soluble silver salt intensification of diffusion transfer silver images
US4201840A (en)	1980-05-06	Photographic film units containing a polymeric mordant which covalently bonds with certain dyes
GB2056104A (en)	1981-03-11	Dye Image Formation Process and Silver Halide Photographic Film Unit
US3909263A (en)	1975-09-30	5,5{40 ,6,6{40 -Tetrahydroxy-3,3,3{40 ,3{40 -tetramethyl-bis-spirohydrindene auxiliary developers