CA1144412A - Element qui renferme une couche de colorant a base de o-dialdehyde aromatique, une composition de visualisation photosensible, et une couche surimposee de polymere - Google Patents

Element qui renferme une couche de colorant a base de o-dialdehyde aromatique, une composition de visualisation photosensible, et une couche surimposee de polymere

Info

Publication number: CA1144412A
Authority: CA; Canada
Prior art keywords: polymer; layer; dialdehyde; same; atoms
Prior art date: 1978-12-20
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

CA000323824A

Other languages

English (en)

Inventor

Anthony Adin

Richard C. Sutton

Joseph A. Verdone

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.)

1978-12-20

Filing date

1979-03-20

Publication date

1983-04-12

1979-03-20 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1983-04-12 Application granted granted Critical

1983-04-12 Publication of CA1144412A publication Critical patent/CA1144412A/fr

Status Expired legal-status Critical Current

Links

229920000642 polymer Polymers 0.000 title claims abstract description 41
125000003118 aryl group Chemical group 0.000 title claims abstract description 12
239000000203 mixture Substances 0.000 title claims description 32
230000005855 radiation Effects 0.000 title claims description 10
238000003384 imaging method Methods 0.000 claims abstract description 21
230000007935 neutral effect Effects 0.000 claims abstract description 20
ZNZYKNKBJPZETN-WELNAUFTSA-N Dialdehyde 11678 Chemical compound N1C2=CC=CC=C2C2=C1[C@H](C[C@H](/C(=C/O)C(=O)OC)[C@@H](C=C)C=O)NCC2 ZNZYKNKBJPZETN-WELNAUFTSA-N 0.000 claims abstract description 9
ZWLUXSQADUDCSB-UHFFFAOYSA-N phthalaldehyde Chemical compound O=CC1=CC=CC=C1C=O ZWLUXSQADUDCSB-UHFFFAOYSA-N 0.000 claims description 32
125000004432 carbon atom Chemical group C* 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
108010010803 Gelatin Proteins 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
239000008273 gelatin Substances 0.000 claims description 8
229920000159 gelatin Polymers 0.000 claims description 8
235000019322 gelatine Nutrition 0.000 claims description 8
235000011852 gelatine desserts Nutrition 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 5
125000004429 atom Chemical group 0.000 claims description 5
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
239000005977 Ethylene Substances 0.000 claims description 3
125000002947 alkylene group Chemical group 0.000 claims description 3
229910052799 carbon Inorganic materials 0.000 claims description 3
125000000623 heterocyclic group Chemical group 0.000 claims description 3
125000006413 ring segment Chemical group 0.000 claims description 3
229920006395 saturated elastomer Polymers 0.000 claims description 3
QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 claims description 2
229910052753 mercury Inorganic materials 0.000 claims description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 2
125000004433 nitrogen atom Chemical group N* 0.000 claims 2
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical group O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 2
238000011161 development Methods 0.000 abstract description 3
-1 poly(vinyl-pyrrolidone) Polymers 0.000 description 22
JAWGVVJVYSANRY-UHFFFAOYSA-N cobalt(3+) Chemical compound [Co+3] JAWGVVJVYSANRY-UHFFFAOYSA-N 0.000 description 19
239000010410 layer Substances 0.000 description 19
239000000463 material Substances 0.000 description 15
150000001412 amines Chemical class 0.000 description 13
239000011230 binding agent Substances 0.000 description 13
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 9
239000011248 coating agent Substances 0.000 description 9
238000000576 coating method Methods 0.000 description 9
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
238000000034 method Methods 0.000 description 7
150000004053 quinones Chemical class 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
VZVHUBYZGAUXLX-UHFFFAOYSA-N azane;azanide;cobalt(3+) Chemical compound N.N.N.[NH2-].[NH2-].[NH2-].[Co+3] VZVHUBYZGAUXLX-UHFFFAOYSA-N 0.000 description 5
238000006243 chemical reaction Methods 0.000 description 5
230000000052 comparative effect Effects 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
230000014759 maintenance of location Effects 0.000 description 5
238000011160 research Methods 0.000 description 5
239000002904 solvent Substances 0.000 description 5
BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 4
WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
238000002360 preparation method Methods 0.000 description 4
239000000047 product Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
125000001424 substituent group Chemical group 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000003638 chemical reducing agent Substances 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
GXWORUBZHJHIGI-UHFFFAOYSA-K cobalt(3+);triperchlorate Chemical compound [Co+3].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O GXWORUBZHJHIGI-UHFFFAOYSA-K 0.000 description 3
229920001577 copolymer Chemical group 0.000 description 3
238000004519 manufacturing process Methods 0.000 description 3
229940054441 o-phthalaldehyde Drugs 0.000 description 3
229920000139 polyethylene terephthalate Polymers 0.000 description 3
239000005020 polyethylene terephthalate Substances 0.000 description 3
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
230000003213 activating effect Effects 0.000 description 2
125000003342 alkenyl group Chemical group 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
XLJKHNWPARRRJB-UHFFFAOYSA-N cobalt(2+) Chemical compound [Co+2] XLJKHNWPARRRJB-UHFFFAOYSA-N 0.000 description 2
QSQUFRGBXGXOHF-UHFFFAOYSA-N cobalt(iii) nitrate Chemical compound [Co].O[N+]([O-])=O.O[N+]([O-])=O.O[N+]([O-])=O QSQUFRGBXGXOHF-UHFFFAOYSA-N 0.000 description 2
238000004132 cross linking Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
230000009977 dual effect Effects 0.000 description 2
KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 2
239000000499 gel Substances 0.000 description 2
230000006872 improvement Effects 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 2
239000000178 monomer Substances 0.000 description 2
229910000069 nitrogen hydride Inorganic materials 0.000 description 2
229920002451 polyvinyl alcohol Polymers 0.000 description 2
238000012545 processing Methods 0.000 description 2
230000004044 response Effects 0.000 description 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
229920002554 vinyl polymer Polymers 0.000 description 2
QDNPCYCBQFHNJC-UHFFFAOYSA-N 1,1'-biphenyl-3,4-diol Chemical compound C1=C(O)C(O)=CC=C1C1=CC=CC=C1 QDNPCYCBQFHNJC-UHFFFAOYSA-N 0.000 description 1
ZAMUDYFFFFHBNY-UHFFFAOYSA-N 10-diazonioanthracen-9-olate Chemical class C1=CC=C2C([O-])=C(C=CC=C3)C3=C([N+]#N)C2=C1 ZAMUDYFFFFHBNY-UHFFFAOYSA-N 0.000 description 1
YPJUNDFVDDCYIH-UHFFFAOYSA-M 2,2,3,3,4,4,4-heptafluorobutanoate Chemical compound [O-]C(=O)C(F)(F)C(F)(F)C(F)(F)F YPJUNDFVDDCYIH-UHFFFAOYSA-M 0.000 description 1
LVKKFNORSNCNPP-UHFFFAOYSA-N 2,2-bis(prop-2-enoylamino)acetic acid Chemical group C=CC(=O)NC(C(=O)O)NC(=O)C=C LVKKFNORSNCNPP-UHFFFAOYSA-N 0.000 description 1
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
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
BNCADMBVWNPPIZ-UHFFFAOYSA-N 2-n,2-n,4-n,4-n,6-n,6-n-hexakis(methoxymethyl)-1,3,5-triazine-2,4,6-triamine Chemical compound COCN(COC)C1=NC(N(COC)COC)=NC(N(COC)COC)=N1 BNCADMBVWNPPIZ-UHFFFAOYSA-N 0.000 description 1
FLGUVXZLKJMWCN-UHFFFAOYSA-N 2-propan-2-yloxyanthracene-1,4-dione Chemical compound C1=CC=C2C=C(C(C(OC(C)C)=CC3=O)=O)C3=CC2=C1 FLGUVXZLKJMWCN-UHFFFAOYSA-N 0.000 description 1
MSTDXOZUKAQDRL-UHFFFAOYSA-N 4-Chromanone Chemical compound C1=CC=C2C(=O)CCOC2=C1 MSTDXOZUKAQDRL-UHFFFAOYSA-N 0.000 description 1
USQCUKQZXOWUDF-YWZLYKJASA-N 6-chloro-n-[(3s)-1-[(2s)-1-(4-methyl-5-oxo-1,4-diazepan-1-yl)-1-oxopropan-2-yl]-2-oxopyrrolidin-3-yl]naphthalene-2-sulfonamide Chemical compound O=C([C@@H](N1C([C@@H](NS(=O)(=O)C=2C=C3C=CC(Cl)=CC3=CC=2)CC1)=O)C)N1CCN(C)C(=O)CC1 USQCUKQZXOWUDF-YWZLYKJASA-N 0.000 description 1
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical group C=CC#N NLHHRLWOUZZQLW-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
101100400378 Mus musculus Marveld2 gene Proteins 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
239000007983 Tris buffer Substances 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
125000005041 acyloxyalkyl group Chemical group 0.000 description 1
238000012644 addition polymerization Methods 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000004448 alkyl carbonyl group Chemical group 0.000 description 1
125000000304 alkynyl group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000004103 aminoalkyl group Chemical group 0.000 description 1
229910021529 ammonia Inorganic materials 0.000 description 1
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
150000004056 anthraquinones Chemical class 0.000 description 1
125000005160 aryl oxy alkyl group Chemical group 0.000 description 1
125000004104 aryloxy group Chemical group 0.000 description 1
229940125717 barbiturate Drugs 0.000 description 1
URAPFRVSOJQECJ-UHFFFAOYSA-N benzene chromium Chemical compound [Cr].C1=CC=CC=C1 URAPFRVSOJQECJ-UHFFFAOYSA-N 0.000 description 1
UKXSKSHDVLQNKG-UHFFFAOYSA-N benzilic acid Chemical class C=1C=CC=CC=1C(O)(C(=O)O)C1=CC=CC=C1 UKXSKSHDVLQNKG-UHFFFAOYSA-N 0.000 description 1
230000005587 bubbling Effects 0.000 description 1
235000013877 carbamide Nutrition 0.000 description 1
YYZSIYPCFQYVFV-UHFFFAOYSA-N carbon monoxide;chromium;n,n-dimethylaniline Chemical group [Cr].[O+]#[C-].[O+]#[C-].[O+]#[C-].CN(C)C1=CC=CC=C1 YYZSIYPCFQYVFV-UHFFFAOYSA-N 0.000 description 1
125000005587 carbonate group Chemical group 0.000 description 1
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
239000013522 chelant Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
AIBMNIPKVUEGPW-UHFFFAOYSA-K cobalt(3+) methanamine triperchlorate Chemical compound CN.CN.Cl(=O)(=O)(=O)[O-].[Co+3].Cl(=O)(=O)(=O)[O-].Cl(=O)(=O)(=O)[O-] AIBMNIPKVUEGPW-UHFFFAOYSA-K 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
238000005336 cracking Methods 0.000 description 1
239000003431 cross linking reagent Substances 0.000 description 1
229940075894 denatured ethanol Drugs 0.000 description 1
238000000502 dialysis Methods 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
URQUNWYOBNUYJQ-UHFFFAOYSA-N diazonaphthoquinone Chemical class C1=CC=C2C(=O)C(=[N]=[N])C=CC2=C1 URQUNWYOBNUYJQ-UHFFFAOYSA-N 0.000 description 1
125000005594 diketone group Chemical group 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000012153 distilled water Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
229960004279 formaldehyde Drugs 0.000 description 1
235000019256 formaldehyde Nutrition 0.000 description 1
239000011521 glass Substances 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
229920001519 homopolymer Polymers 0.000 description 1
WJRBRSLFGCUECM-UHFFFAOYSA-N hydantoin Chemical compound O=C1CNC(=O)N1 WJRBRSLFGCUECM-UHFFFAOYSA-N 0.000 description 1
229940091173 hydantoin Drugs 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 1
150000002466 imines Chemical class 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
230000000977 initiatory effect Effects 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
LRDFRRGEGBBSRN-UHFFFAOYSA-N isobutyronitrile Chemical compound CC(C)C#N LRDFRRGEGBBSRN-UHFFFAOYSA-N 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
239000003446 ligand Substances 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
ZIPLKLQPLOWLTM-UHFFFAOYSA-N naphthalene-2,3-dicarbaldehyde Chemical compound C1=CC=C2C=C(C=O)C(C=O)=CC2=C1 ZIPLKLQPLOWLTM-UHFFFAOYSA-N 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
239000011368 organic material Substances 0.000 description 1
125000002524 organometallic group Chemical group 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
SCOAVUHOIJMIBW-UHFFFAOYSA-N phenanthrene-1,2-dione Chemical class C1=CC=C2C(C=CC(C3=O)=O)=C3C=CC2=C1 SCOAVUHOIJMIBW-UHFFFAOYSA-N 0.000 description 1
125000001791 phenazinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
229920002239 polyacrylonitrile Polymers 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
238000006116 polymerization reaction Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000008569 process Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
239000011253 protective coating Substances 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012966 redox initiator Substances 0.000 description 1
238000006479 redox reaction Methods 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000007789 sealing Methods 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
229960002317 succinimide Drugs 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
229920001897 terpolymer Polymers 0.000 description 1
238000012360 testing method Methods 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/67—Compositions containing cobalt salts or cobalt compounds as photosensitive substances
- 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
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/7614—Cover layers; Backing layers; Base or auxiliary layers characterised by means for lubricating, for rendering anti-abrasive or for preventing adhesion

Landscapes

Chemical & Material Sciences (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Compositions Of Macromolecular Compounds (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Heat Sensitive Colour Forming Recording (AREA)

CA000323824A 1978-12-20 1979-03-20 Element qui renferme une couche de colorant a base de o-dialdehyde aromatique, une composition de visualisation photosensible, et une couche surimposee de polymere Expired CA1144412A (fr)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US97130078A	1978-12-20	1978-12-20
US971,300		1978-12-20

Publications (1)

Publication Number	Publication Date
CA1144412A true CA1144412A (fr)	1983-04-12

Family

ID=25518180

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000323824A Expired CA1144412A (fr)	1978-12-20	1979-03-20	Element qui renferme une couche de colorant a base de o-dialdehyde aromatique, une composition de visualisation photosensible, et une couche surimposee de polymere

Country Status (4)

Country	Link
EP (1)	EP0012855B1 (fr)
JP (1)	JPS5588046A (fr)
CA (1)	CA1144412A (fr)
DE (1)	DE2964678D1 (fr)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4752547A (en) *	1986-06-04	1988-06-21	Eastman Kodak Company	Dye-forming electrothermographic material and process
US4727008A (en) *	1986-06-04	1988-02-23	Eastman Kodak Company	Dye-forming electrically activatable recording element and process
MX2021000531A (es) *	2018-07-17	2021-03-25	Evonik Operations Gmbh	Esteres metacrilicos acidos de ch para la preparacion de dispersiones polimericas acuosas.

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3102811A (en) *	1960-04-07	1963-09-03	Du Pont	Process for producing images, using light sensitive aromatic 1,2-dialdehydes and elements therefor
US3756814A (en) *	1970-07-27	1973-09-04	Polaroid Corp	Olymer wherein the grafted moiety has mordant capability color diffusion transfer image receiving layer comprising a graft cop
BE790872A (nl) *	1971-11-08	1973-05-03	Agfa Gevaert Nv	Ontwikkelbehandeling van fotografische zilverhalogenidematerialen bij hoge temperaturen
JPS5411694B2 (fr) *	1972-05-09	1979-05-17
US3893860A (en) *	1974-07-16	1975-07-08	Eastman Kodak Co	Photothermographic element and process
US4021246A (en) *	1975-12-15	1977-05-03	Horizons Incorporated, A Division Of Horizons Research Incorporated	Free radical photosensitive compositions containing bis-sulfides or sulfinyl esters as antifoggants
CA1116915A (fr) *	1977-12-28	1982-01-26	Anthony Adin	Inhibition de la formation d'images au moyen de complexes de cobalt (iii)

1979
- 1979-03-20 CA CA000323824A patent/CA1144412A/fr not_active Expired
- 1979-11-23 DE DE7979104668T patent/DE2964678D1/de not_active Expired
- 1979-11-23 EP EP79104668A patent/EP0012855B1/fr not_active Expired
- 1979-12-20 JP JP16496179A patent/JPS5588046A/ja active Pending

Also Published As

Publication number	Publication date
DE2964678D1 (en)	1983-03-10
JPS5588046A (en)	1980-07-03
EP0012855A1 (fr)	1980-07-09
EP0012855B1 (fr)	1983-02-02

Legal Events

Date	Code	Title	Description
2000-04-12	MKEX	Expiry

Publication	Publication Date	Title
EP0022813B1 (fr)	1984-03-14	Composition de formation d'images caracterisee par des liants a retention de dialdehyde aromatique
US4196002A (en)	1980-04-01	Photothermographic element containing heat sensitive dye materials
US4245031A (en)	1981-01-13	Photopolymerizable compositions based on salt-forming polymers and polyhydroxy polyethers
EP0019219B1 (fr)	1983-06-22	Systèmes photosensibles avec des hydrazides cycliques
US3871887A (en)	1975-03-18	Photothermographic composition, element and process
US4201590A (en)	1980-05-06	Heat sensitive reactive products of hexaarylbiimidazole and antihalation dyes
CA1093300A (fr)	1981-01-13	Pellicules thermosensibles
CA1144412A (fr)	1983-04-12	Element qui renferme une couche de colorant a base de o-dialdehyde aromatique, une composition de visualisation photosensible, et une couche surimposee de polymere
US4288531A (en)	1981-09-08	Imaging elements
US3954468A (en)	1976-05-04	Radiation process for producing colored photopolymer systems
US4291115A (en)	1981-09-22	Elements and method which use photopolymerizable compositions based on salt-forming polymers and polyhydroxy polyethers
EP0044729B1 (fr)	1984-09-26	Compositions formant des images contenant des complexes de cobalt-(III)
US4308341A (en)	1981-12-29	Non-silver imaging compositions having improved speeds and processing temperatures
US4968586A (en)	1990-11-06	Photoresist compositions containing cobalt (III) compound and redox transfer ligand
CA1146002A (fr)	1983-05-10	Materiau et procede photothermographiques
US4033773A (en)	1977-07-05	Radiation produced colored photopolymer systems
JPS6332177B2 (fr)	1988-06-28
US4318977A (en)	1982-03-09	Cobalt (III) complex imaging compositions having improved photographic properties
US4410623A (en)	1983-10-18	Phthalaldehyde adduct and imaging compositions, elements and methods incorporating same
CA1139148A (fr)	1983-01-11	Composes de visualisation a complexe de cobalt (iii) comprenant un precurseur d'agent reducteur et un antivoile organique
US4308342A (en)	1981-12-29	Dimensionally stabilized imaging element and method
US3877946A (en)	1975-04-15	Photographic element
US4347307A (en)	1982-08-31	Dimensionally stabilized imaging element and method
CA1125083A (fr)	1982-06-08	Compositions de visualisation a base de complexe de cobalt(iii) contenant un dialdehyde aromatique, comme agent precurseur reducteur, et de la triazine s, comme agent oxydant
CA1123147A (fr)	1982-05-04	Element forme d'une substance polymerique, photoreticulable contenant des groupements carbonyles