CA1065180A - Compose utilise en photographie contenant un absorbant d'uv de type 1-amino-4-cyano-1,3-butadiene - Google Patents

Compose utilise en photographie contenant un absorbant d'uv de type 1-amino-4-cyano-1,3-butadiene

Info

Publication number: CA1065180A
Authority: CA; Canada
Prior art keywords: group; photographic element; support; carbon atoms; hydrogen
Prior art date: 1974-09-17
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

CA234,657A

Other languages

English (en)

Other versions

CA234657S (en

Inventor

Wayne W. Weber (Ii)

Donald W. Heseltine

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.)

1974-09-17

Filing date

1975-09-03

Publication date

1979-10-30

1975-09-03 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1979-10-30 Application granted granted Critical

1979-10-30 Publication of CA1065180A publication Critical patent/CA1065180A/fr

Status Expired legal-status Critical Current

Links

GZRHRSDQICJXPV-UHFFFAOYSA-N 5-aminopenta-2,4-dienenitrile Chemical class NC=CC=CC#N GZRHRSDQICJXPV-UHFFFAOYSA-N 0.000 title abstract 2
150000001875 compounds Chemical class 0.000 claims abstract description 73
-1 piperidino, morpholino, pyrrolidino Chemical group 0.000 claims abstract description 42
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 16
239000001257 hydrogen Substances 0.000 claims abstract description 16
125000000217 alkyl group Chemical group 0.000 claims abstract description 15
125000006575 electron-withdrawing group Chemical group 0.000 claims abstract description 8
125000002947 alkylene group Chemical group 0.000 claims abstract description 7
125000006165 cyclic alkyl group Chemical group 0.000 claims abstract description 7
125000004435 hydrogen atom Chemical class [H]* 0.000 claims abstract description 6
125000003118 aryl group Chemical group 0.000 claims abstract description 5
125000000732 arylene group Chemical group 0.000 claims abstract description 5
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 4
239000000839 emulsion Substances 0.000 claims description 31
229910052709 silver Inorganic materials 0.000 claims description 24
239000004332 silver Substances 0.000 claims description 24
239000011230 binding agent Substances 0.000 claims description 22
125000004432 carbon atom Chemical group C* 0.000 claims description 16
UKRHKLHRSIUATR-UHFFFAOYSA-N 2-(4-tert-butylphenyl)sulfonylacetonitrile Chemical compound CC(C)(C)C1=CC=C(S(=O)(=O)CC#N)C=C1 UKRHKLHRSIUATR-UHFFFAOYSA-N 0.000 claims description 7
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 6
FOTRKCAZUSJCQD-UHFFFAOYSA-N (methylsulfonyl)acetonitrile Chemical compound CS(=O)(=O)CC#N FOTRKCAZUSJCQD-UHFFFAOYSA-N 0.000 claims description 3
239000000084 colloidal system Substances 0.000 claims description 3
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 5
125000004429 atom Chemical group 0.000 claims 5
150000002431 hydrogen Chemical class 0.000 claims 5
239000006096 absorbing agent Substances 0.000 abstract description 7
125000003277 amino group Chemical group 0.000 abstract description 2
125000004122 cyclic group Chemical group 0.000 abstract description 2
125000000547 substituted alkyl group Chemical group 0.000 abstract description 2
125000003107 substituted aryl group Chemical group 0.000 abstract description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 45
239000010410 layer Substances 0.000 description 32
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
238000000576 coating method Methods 0.000 description 16
239000011248 coating agent Substances 0.000 description 11
238000000034 method Methods 0.000 description 10
239000000047 product Substances 0.000 description 10
108010010803 Gelatin Proteins 0.000 description 9
239000008273 gelatin Substances 0.000 description 9
229920000159 gelatin Polymers 0.000 description 9
235000019322 gelatine Nutrition 0.000 description 9
235000011852 gelatine desserts Nutrition 0.000 description 9
239000002904 solvent Substances 0.000 description 9
239000006185 dispersion Substances 0.000 description 8
239000004816 latex Substances 0.000 description 8
229920000126 latex Polymers 0.000 description 8
239000000543 intermediate Substances 0.000 description 7
239000000463 material Substances 0.000 description 7
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
238000004821 distillation Methods 0.000 description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 5
230000003287 optical effect Effects 0.000 description 5
238000010992 reflux Methods 0.000 description 5
238000010521 absorption reaction Methods 0.000 description 4
239000000975 dye Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
230000005855 radiation Effects 0.000 description 4
239000011541 reaction mixture Substances 0.000 description 4
239000007787 solid Substances 0.000 description 4
GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
239000008199 coating composition Substances 0.000 description 3
239000013078 crystal Substances 0.000 description 3
SMFUSAKSENKDOJ-UHFFFAOYSA-N n-methyl-n-[(1-methylbenzimidazol-2-yl)methyl]butan-1-amine Chemical compound C1=CC=C2N(C)C(CN(C)CCCC)=NC2=C1 SMFUSAKSENKDOJ-UHFFFAOYSA-N 0.000 description 3
239000000123 paper Substances 0.000 description 3
229920000642 polymer Polymers 0.000 description 3
230000004224 protection Effects 0.000 description 3
238000012546 transfer Methods 0.000 description 3
PCNAYTOJVHTNKK-UHFFFAOYSA-N 2-sulfonylacetonitrile Chemical compound O=S(=O)=CC#N PCNAYTOJVHTNKK-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000011358 absorbing material Substances 0.000 description 2
238000009835 boiling Methods 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
239000007788 liquid Substances 0.000 description 2
CUONGYYJJVDODC-UHFFFAOYSA-N malononitrile Chemical compound N#CCC#N CUONGYYJJVDODC-UHFFFAOYSA-N 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
239000002245 particle Substances 0.000 description 2
XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000000126 substance Substances 0.000 description 2
NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 description 1
PUVGBKOHDJUFRZ-UHFFFAOYSA-N 2-(2-pyridin-3-ylpiperidin-1-yl)acetonitrile Chemical compound N#CCN1CCCCC1C1=CC=CN=C1 PUVGBKOHDJUFRZ-UHFFFAOYSA-N 0.000 description 1
SPMMZKAWNAKPJM-UHFFFAOYSA-N 2-(butylamino)acetonitrile Chemical compound CCCCNCC#N SPMMZKAWNAKPJM-UHFFFAOYSA-N 0.000 description 1
QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
HMHNXNLXWXZTQC-UHFFFAOYSA-N 2-methylsulfonylacetonitrile morpholine Chemical compound CS(=O)(=O)CC#N.N1CCOCC1 HMHNXNLXWXZTQC-UHFFFAOYSA-N 0.000 description 1
HWXOWLVWCZTSKY-UHFFFAOYSA-N 3,3,3-trimethoxyprop-1-ene Chemical compound COC(OC)(OC)C=C HWXOWLVWCZTSKY-UHFFFAOYSA-N 0.000 description 1
SBAJRGRUGUQKAF-UHFFFAOYSA-N 3-(2-cyanoethylamino)propanenitrile Chemical compound N#CCCNCCC#N SBAJRGRUGUQKAF-UHFFFAOYSA-N 0.000 description 1
ZUSHGEWXNIYOPH-UHFFFAOYSA-N C(C)#N.CN1C(CNCC1)S(=O)(=O)C1=CC=C(C=C1)C(C)(C)C Chemical compound C(C)#N.CN1C(CNCC1)S(=O)(=O)C1=CC=C(C=C1)C(C)(C)C ZUSHGEWXNIYOPH-UHFFFAOYSA-N 0.000 description 1
YMPJQKIWEAPFKJ-UHFFFAOYSA-N C(C)(C)(C)C1=CC=C(C=C1)S(=O)(=O)CC#N.N1CCNCC1 Chemical compound C(C)(C)(C)C1=CC=C(C=C1)S(=O)(=O)CC#N.N1CCNCC1 YMPJQKIWEAPFKJ-UHFFFAOYSA-N 0.000 description 1
OQHKLKKBLKUTCR-UHFFFAOYSA-N C(C)(C)(C)C1=CC=C(C=C1)S(=O)(=O)CC#N.N1CCOCC1 Chemical compound C(C)(C)(C)C1=CC=C(C=C1)S(=O)(=O)CC#N.N1CCOCC1 OQHKLKKBLKUTCR-UHFFFAOYSA-N 0.000 description 1
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
229920001747 Cellulose diacetate Polymers 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
102100035861 Cytosolic 5'-nucleotidase 1A Human genes 0.000 description 1
241000483002 Euproctis similis Species 0.000 description 1
101000802744 Homo sapiens Cytosolic 5'-nucleotidase 1A Proteins 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
230000006750 UV protection Effects 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
ZSIQJIWKELUFRJ-UHFFFAOYSA-N azepane Chemical compound C1CCCNCC1 ZSIQJIWKELUFRJ-UHFFFAOYSA-N 0.000 description 1
235000015241 bacon Nutrition 0.000 description 1
230000008033 biological extinction Effects 0.000 description 1
KVNRLNFWIYMESJ-UHFFFAOYSA-N butyronitrile Chemical compound CCCC#N KVNRLNFWIYMESJ-UHFFFAOYSA-N 0.000 description 1
235000011089 carbon dioxide Nutrition 0.000 description 1
238000005266 casting Methods 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
229920001429 chelating resin Polymers 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000006184 cosolvent Substances 0.000 description 1
229930003836 cresol Natural products 0.000 description 1
125000004093 cyano group Chemical group *C#N 0.000 description 1
125000004966 cyanoalkyl group Chemical group 0.000 description 1
238000011161 development Methods 0.000 description 1
238000009792 diffusion process Methods 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000010408 film Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000000499 gel Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000007970 homogeneous dispersion Substances 0.000 description 1
ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
238000005213 imbibition Methods 0.000 description 1
239000011229 interlayer Substances 0.000 description 1
239000003456 ion exchange resin Substances 0.000 description 1
229920003303 ion-exchange polymer Polymers 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000000155 melt Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
238000003801 milling 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
UAQHXLYLALUITG-UHFFFAOYSA-N n-(2,2-diethoxyethyl)-2,2-diethoxyethanamine Chemical compound CCOC(OCC)CNCC(OCC)OCC UAQHXLYLALUITG-UHFFFAOYSA-N 0.000 description 1
OBYVIBDTOCAXSN-UHFFFAOYSA-N n-butan-2-ylbutan-2-amine Chemical compound CCC(C)NC(C)CC OBYVIBDTOCAXSN-UHFFFAOYSA-N 0.000 description 1
PXSXRABJBXYMFT-UHFFFAOYSA-N n-hexylhexan-1-amine Chemical compound CCCCCCNCCCCCC PXSXRABJBXYMFT-UHFFFAOYSA-N 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
PBKBURVPAHHUIK-AVUWLFEKSA-N phenyl-[(e)-3-phenyliminoprop-1-enyl]azanium;chloride Chemical compound Cl.C=1C=CC=CC=1N\C=C\C=NC1=CC=CC=C1 PBKBURVPAHHUIK-AVUWLFEKSA-N 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-L phthalate(2-) Chemical compound [O-]C(=O)C1=CC=CC=C1C([O-])=O XNGIFLGASWRNHJ-UHFFFAOYSA-L 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000728 polyester Polymers 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
229920002223 polystyrene Polymers 0.000 description 1
235000020004 porter Nutrition 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
238000012545 processing Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
229920005989 resin Polymers 0.000 description 1
239000011347 resin Substances 0.000 description 1
150000003335 secondary amines Chemical class 0.000 description 1
230000035945 sensitivity Effects 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
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
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 description 1
238000003756 stirring Methods 0.000 description 1
239000000725 suspension Substances 0.000 description 1
YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
239000002023 wood Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/145—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- 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
- G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
- G03C1/8155—Organic compounds therefor

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Compositions Of Macromolecular Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Optical Filters (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

CA234,657A 1974-09-17 1975-09-03 Compose utilise en photographie contenant un absorbant d'uv de type 1-amino-4-cyano-1,3-butadiene Expired CA1065180A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US50691374A	1974-09-17	1974-09-17

Publications (1)

Publication Number	Publication Date
CA1065180A true CA1065180A (fr)	1979-10-30

Family

ID=24016452

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA234,657A Expired CA1065180A (fr)	1974-09-17	1975-09-03	Compose utilise en photographie contenant un absorbant d'uv de type 1-amino-4-cyano-1,3-butadiene

Country Status (7)

Country	Link
JP (1)	JPS5826016B2 (fr)
BE (1)	BE833511A (fr)
CA (1)	CA1065180A (fr)
CH (1)	CH611724A5 (fr)
DE (1)	DE2541267C3 (fr)
FR (1)	FR2285379A1 (fr)
GB (1)	GB1523472A (fr)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5699250A (en) *	1980-01-14	1981-08-10	Toyobo Co Ltd	Modified polyester composition
JPS59149350A (ja) *	1983-02-16	1984-08-27	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料
IT1181384B (it) *	1983-06-07	1987-09-23	Minnesota Mining & Mfg	Assorbitore di ultravioletto e materiale fotografico che lo comprende
IT1186757B (it) *	1985-07-11	1987-12-16	Minnesota Mining & Mfg	Composti assorbitori di uv 3-amminoallilidenmalononitrile ed elementi fotografici che li congengono
US5206372A (en) *	1990-06-05	1993-04-27	Shell Research Limited	Preparation of 2-chloropyridine derivatives
EP1974948A3 (fr)	2007-03-29	2012-02-08	FUJIFILM Corporation	Procédé de formation d'images utilisant un système de transfert thermosensible
US8119562B2 (en)	2007-03-29	2012-02-21	Fujifilm Corporation	Heat-sensitive transfer sheet and image-forming method using heat-sensitive transfer system
EP1980409A3 (fr)	2007-03-29	2010-09-29	FUJIFILM Corporation	Feuille de transfert thermosensible à utiliser dans un système de transfert thermosensible et procédé de formation d'image utilisant le système de transfert thermosensible
JP2008273641A (ja)	2007-04-25	2008-11-13	Fujifilm Corp	感熱転写受像シート用紙管、感熱転写受像シートのロール形態加工物、及び画像形成方法
JP5061066B2 (ja) *	2007-09-07	2012-10-31	富士フイルム株式会社	ポリマーフィルム、偏光板保護フィルム、偏光板及び液晶表示装置
WO2009038463A1 (fr) *	2007-09-18	2009-03-26	Fujifilm Manufacturing Europe B.V.	Composés absorbant les uv
JP5147499B2 (ja) *	2008-02-13	2013-02-20	富士フイルム株式会社	感光性着色組成物、並びにカラーフィルタ及びその製造方法
JP5250289B2 (ja)	2008-03-31	2013-07-31	富士フイルム株式会社	紫外線吸収剤組成物
JP2009270062A (ja)	2008-05-09	2009-11-19	Fujifilm Corp	紫外線吸収剤組成物
JP5192964B2 (ja) *	2008-09-25	2013-05-08	富士フイルム株式会社	透明膜形成用組成物、透明膜、カラーフィルタ用下地透明膜及び固体撮像素子
JP5544239B2 (ja)	2010-07-29	2014-07-09	富士フイルム株式会社	重合性組成物

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB786168A (en) *	1954-11-04	1957-11-13	Ici Ltd	Photographic emulsions
BE588539A (fr) *	1959-03-12

1975
- 1975-09-03 CA CA234,657A patent/CA1065180A/fr not_active Expired
- 1975-09-16 FR FR7528311A patent/FR2285379A1/fr active Granted
- 1975-09-16 DE DE19752541267 patent/DE2541267C3/de not_active Expired
- 1975-09-16 CH CH1197575A patent/CH611724A5/xx not_active IP Right Cessation
- 1975-09-17 GB GB3824075A patent/GB1523472A/en not_active Expired
- 1975-09-17 JP JP11247675A patent/JPS5826016B2/ja not_active Expired
- 1975-09-17 BE BE160120A patent/BE833511A/fr not_active IP Right Cessation

Also Published As

Publication number	Publication date
JPS5156620A (ja)	1976-05-18
DE2541267A1 (de)	1976-07-29
DE2541267B2 (de)	1981-06-19
GB1523472A (en)	1978-08-31
FR2285379A1 (fr)	1976-04-16
FR2285379B1 (fr)	1979-04-20
BE833511A (fr)	1976-03-17
CH611724A5 (en)	1979-06-15
DE2541267C3 (de)	1982-03-11
JPS5826016B2 (ja)	1983-05-31

Publication	Publication Date	Title
US4045229A (en)	1977-08-30	Novel UV absorbing compounds and photographic elements containing UV absorbing compounds
CA1065180A (fr)	1979-10-30	Compose utilise en photographie contenant un absorbant d'uv de type 1-amino-4-cyano-1,3-butadiene
CA1317148C (fr)	1993-05-04	Film de cinematographie en couleurs
US4050938A (en)	1977-09-27	Photographic elements incorporating chelated-metal quenching compounds
CA1286139C (fr)	1991-07-16	Colorant-filtre pour element photographique
EP0382225B1 (fr)	1994-11-02	Colorants filtrants pour éléments photographiques
JPS6256957A (ja)	1987-03-12	Ｕｖ吸収剤を含有する写真記録材料
EP0251282B1 (fr)	1991-04-17	Colorants absorbant l'infrarouge et éléments photographiques les contenant
US4871656A (en)	1989-10-03	Photographic silver halide elements containing infrared filter dyes
US4900653A (en)	1990-02-13	Photographic elements containing filter dye particle dispersions
EP0288076B1 (fr)	1991-09-04	Colorants filtrant les infrarouges pour éléments photographiques
US4042394A (en)	1977-08-16	Photographic dye image stabilization
US5098820A (en)	1992-03-24	Solid particle dispersions of filter dyes for photographic elements
JP3455326B2 (ja)	2003-10-14	アシル置換オキソノール色素含有写真要素
US4657846A (en)	1987-04-14	Silver halide photographic printing paper
US4876181A (en)	1989-10-24	Photographic elements containing infrared filter dyes
JPS6214149A (ja)	1987-01-22	３−アミノアリリデンマロノニトリル化合物よりなる紫外線吸収剤を含有する写真材料
USRE30303E (en)	1980-06-10	Novel (UV absorbing compounds and) photographic elements containing UV absorbing compounds
EP0523465B1 (fr)	1994-12-28	Eléments photographiques à l'halogénure d'argent
US2622980A (en)	1952-12-23	Photographic filter and antihalation layers containing 3-(benzylidene)-sulfo-oxindoles
CA1037761A (fr)	1978-09-05	Elements et emulsions a l'halogenure d'argent et a phosphine
GB2171215A (en)	1986-08-20	Silver halide color photographic material
US3250617A (en)	1966-05-10	Photographic elements protected against ultraviolet radiation
CA1063414A (fr)	1979-10-02	Materiau photosensible contenant des substances emulsifiees
EP0582000A1 (fr)	1994-02-09	Film photographique, negatif en couleurs ou intermédiaire