DE1058836B - Material fuer elektrophotographische Reproduktion - Google Patents
Material fuer elektrophotographische ReproduktionInfo
- Publication number
- DE1058836B DE1058836B DEK29014A DEK0029014A DE1058836B DE 1058836 B DE1058836 B DE 1058836B DE K29014 A DEK29014 A DE K29014A DE K0029014 A DEK0029014 A DE K0029014A DE 1058836 B DE1058836 B DE 1058836B
- Authority
- DE
- Germany
- Prior art keywords
- formula
- oxdiazole
- paper
- solution
- acid
- 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.)
- Pending
Links
- 239000000463 material Substances 0.000 title claims description 10
- 229920005989 resin Polymers 0.000 claims description 44
- 239000011347 resin Substances 0.000 claims description 44
- 239000000243 solution Substances 0.000 claims description 40
- 150000001875 compounds Chemical class 0.000 claims description 39
- 238000000034 method Methods 0.000 claims description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 17
- FUSNOPLQVRUIIM-UHFFFAOYSA-N 4-amino-2-(4,4-dimethyl-2-oxoimidazolidin-1-yl)-n-[3-(trifluoromethyl)phenyl]pyrimidine-5-carboxamide Chemical compound O=C1NC(C)(C)CN1C(N=C1N)=NC=C1C(=O)NC1=CC=CC(C(F)(F)F)=C1 FUSNOPLQVRUIIM-UHFFFAOYSA-N 0.000 claims description 15
- 239000012493 hydrazine sulfate Substances 0.000 claims description 15
- 229910000377 hydrazine sulfate Inorganic materials 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 11
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 claims description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 9
- 239000000155 melt Substances 0.000 claims description 9
- 238000002844 melting Methods 0.000 claims description 9
- 230000008018 melting Effects 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 7
- 239000004033 plastic Substances 0.000 claims description 6
- 239000011541 reaction mixture Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 5
- 238000001953 recrystallisation Methods 0.000 claims description 5
- YDIYEOMDOWUDTJ-UHFFFAOYSA-N 4-(dimethylamino)benzoic acid Chemical compound CN(C)C1=CC=C(C(O)=O)C=C1 YDIYEOMDOWUDTJ-UHFFFAOYSA-N 0.000 claims description 4
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 claims description 4
- LNYTUARMNSFFBE-UHFFFAOYSA-N 4-(diethylazaniumyl)benzoate Chemical compound CCN(CC)C1=CC=C(C(O)=O)C=C1 LNYTUARMNSFFBE-UHFFFAOYSA-N 0.000 claims description 3
- 239000006229 carbon black Substances 0.000 claims description 3
- 239000000025 natural resin Substances 0.000 claims description 3
- 239000006104 solid solution Substances 0.000 claims description 3
- 238000003756 stirring Methods 0.000 claims description 3
- 239000004801 Chlorinated PVC Substances 0.000 claims description 2
- 229920000457 chlorinated polyvinyl chloride Polymers 0.000 claims description 2
- 239000011521 glass Substances 0.000 claims description 2
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 2
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 6
- 235000019441 ethanol Nutrition 0.000 claims 5
- 239000007795 chemical reaction product Substances 0.000 claims 3
- 239000002253 acid Substances 0.000 claims 2
- 239000000084 colloidal system Substances 0.000 claims 2
- SWXFMMWYVSYQGF-UHFFFAOYSA-N 4-(ethylamino)benzoic acid Chemical compound CCNC1=CC=C(C(O)=O)C=C1 SWXFMMWYVSYQGF-UHFFFAOYSA-N 0.000 claims 1
- MJZXFMSIHMJQBW-UHFFFAOYSA-N 4-[5-(4-aminophenyl)-1,3,4-oxadiazol-2-yl]aniline Chemical compound C1=CC(N)=CC=C1C1=NN=C(C=2C=CC(N)=CC=2)O1 MJZXFMSIHMJQBW-UHFFFAOYSA-N 0.000 claims 1
- YIYBPEDZAUFQLO-UHFFFAOYSA-N 4-amino-3-chlorobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1Cl YIYBPEDZAUFQLO-UHFFFAOYSA-N 0.000 claims 1
- 240000000972 Agathis dammara Species 0.000 claims 1
- 206010034972 Photosensitivity reaction Diseases 0.000 claims 1
- 239000011324 bead Substances 0.000 claims 1
- 238000005266 casting Methods 0.000 claims 1
- 238000005660 chlorination reaction Methods 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 claims 1
- 230000008025 crystallization Effects 0.000 claims 1
- JVICFMRAVNKDOE-UHFFFAOYSA-M ethyl violet Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 JVICFMRAVNKDOE-UHFFFAOYSA-M 0.000 claims 1
- 238000001640 fractional crystallisation Methods 0.000 claims 1
- 230000036211 photosensitivity Effects 0.000 claims 1
- 239000004800 polyvinyl chloride Substances 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- 239000011888 foil Substances 0.000 description 11
- 239000000843 powder Substances 0.000 description 9
- 229910052782 aluminium Inorganic materials 0.000 description 7
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 7
- 238000009833 condensation Methods 0.000 description 7
- 230000005494 condensation Effects 0.000 description 7
- 239000000975 dye Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- 229920003002 synthetic resin Polymers 0.000 description 7
- 239000000057 synthetic resin Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 238000010438 heat treatment Methods 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 238000001816 cooling Methods 0.000 description 5
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 5
- 239000004071 soot Substances 0.000 description 5
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 4
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 4
- NKHOUDMZYQDBQE-UHFFFAOYSA-N 4-(cyclopentylamino)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1NC1CCCC1 NKHOUDMZYQDBQE-UHFFFAOYSA-N 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 229920000137 polyphosphoric acid Polymers 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 description 3
- ALYNCZNDIQEVRV-UHFFFAOYSA-N 4-aminobenzoic acid Chemical compound NC1=CC=C(C(O)=O)C=C1 ALYNCZNDIQEVRV-UHFFFAOYSA-N 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 3
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 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
- 239000007859 condensation product Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 3
- 229910052753 mercury Inorganic materials 0.000 description 3
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 3
- 229960000907 methylthioninium chloride Drugs 0.000 description 3
- 230000035515 penetration Effects 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- 230000011514 reflex Effects 0.000 description 3
- 230000033458 reproduction Effects 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 150000002688 maleic acid derivatives Chemical class 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000004888 n-propyl amino group Chemical group [H]N(*)C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- 229920001568 phenolic resin Polymers 0.000 description 2
- 229920006255 plastic film Polymers 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- GUEIZVNYDFNHJU-UHFFFAOYSA-N quinizarin Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 2
- 229940043267 rhodamine b Drugs 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 230000035945 sensitivity Effects 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- MXODCLTZTIFYDV-UHFFFAOYSA-L zinc;1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Zn+2].C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O.C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C([O-])=O MXODCLTZTIFYDV-UHFFFAOYSA-L 0.000 description 2
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 description 1
- UIFVCPMLQXKEEU-UHFFFAOYSA-N 2,3-dimethylbenzaldehyde Chemical compound CC1=CC=CC(C=O)=C1C UIFVCPMLQXKEEU-UHFFFAOYSA-N 0.000 description 1
- MZTRWFKMSGCRBT-UHFFFAOYSA-N 2-[ethyl(propyl)amino]benzoic acid Chemical compound CCCN(CC)C1=CC=CC=C1C(O)=O MZTRWFKMSGCRBT-UHFFFAOYSA-N 0.000 description 1
- GSSBNCOGHHSWCJ-UHFFFAOYSA-N 2-chloro-4-(propylamino)benzoic acid Chemical compound CCCNC1=CC=C(C(O)=O)C(Cl)=C1 GSSBNCOGHHSWCJ-UHFFFAOYSA-N 0.000 description 1
- KKAJSJJFBSOMGS-UHFFFAOYSA-N 3,6-diamino-10-methylacridinium chloride Chemical compound [Cl-].C1=C(N)C=C2[N+](C)=C(C=C(N)C=C3)C3=CC2=C1 KKAJSJJFBSOMGS-UHFFFAOYSA-N 0.000 description 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 1
- POZIYEZBRDCICV-UHFFFAOYSA-N 4-(3-methylbutylamino)benzoic acid Chemical compound CC(C)CCNC1=CC=C(C(O)=O)C=C1 POZIYEZBRDCICV-UHFFFAOYSA-N 0.000 description 1
- QADQJGKSFQRUSS-UHFFFAOYSA-N 4-(cyclohexylamino)benzoic acid Chemical compound C1=CC(C(=O)O)=CC=C1NC1CCCCC1 QADQJGKSFQRUSS-UHFFFAOYSA-N 0.000 description 1
- BFPWLARXKLUGHY-UHFFFAOYSA-N 4-(propylamino)benzoic acid Chemical compound CCCNC1=CC=C(C(O)=O)C=C1 BFPWLARXKLUGHY-UHFFFAOYSA-N 0.000 description 1
- TZXJLFBEXYSTJG-UHFFFAOYSA-N 4-acetamido-2-chlorobenzoic acid Chemical compound CC(=O)NC1=CC=C(C(O)=O)C(Cl)=C1 TZXJLFBEXYSTJG-UHFFFAOYSA-N 0.000 description 1
- QCXJEYYXVJIFCE-UHFFFAOYSA-N 4-acetamidobenzoic acid Chemical compound CC(=O)NC1=CC=C(C(O)=O)C=C1 QCXJEYYXVJIFCE-UHFFFAOYSA-N 0.000 description 1
- VGVHNLRUAMRIEW-UHFFFAOYSA-N 4-methylcyclohexan-1-one Chemical compound CC1CCC(=O)CC1 VGVHNLRUAMRIEW-UHFFFAOYSA-N 0.000 description 1
- FJKUOCCQEBLPNX-UHFFFAOYSA-N 8-hydroxyquinoline N-oxide Chemical compound C1=C[N+]([O-])=C2C(O)=CC=CC2=C1 FJKUOCCQEBLPNX-UHFFFAOYSA-N 0.000 description 1
- 235000007173 Abies balsamea Nutrition 0.000 description 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 239000004857 Balsam Substances 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 244000018716 Impatiens biflora Species 0.000 description 1
- 101000913968 Ipomoea purpurea Chalcone synthase C Proteins 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 241001076195 Lampsilis ovata Species 0.000 description 1
- 244000203416 Melaleuca leucadendron Species 0.000 description 1
- 235000001136 Melaleuca leucadendron Nutrition 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- 101000907988 Petunia hybrida Chalcone-flavanone isomerase C Proteins 0.000 description 1
- 206010034960 Photophobia Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
- 229920001807 Urea-formaldehyde Polymers 0.000 description 1
- JSQFXMIMWAKJQJ-UHFFFAOYSA-N [9-(2-carboxyphenyl)-6-(ethylamino)xanthen-3-ylidene]-diethylazanium;chloride Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(NCC)=CC=C2C=1C1=CC=CC=C1C(O)=O JSQFXMIMWAKJQJ-UHFFFAOYSA-N 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 239000000999 acridine dye Substances 0.000 description 1
- BGLGAKMTYHWWKW-UHFFFAOYSA-N acridine yellow Chemical compound [H+].[Cl-].CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=CC2=C1 BGLGAKMTYHWWKW-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 229960004050 aminobenzoic acid Drugs 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- BRTFVKHPEHKBQF-UHFFFAOYSA-N bromocyclopentane Chemical compound BrC1CCCC1 BRTFVKHPEHKBQF-UHFFFAOYSA-N 0.000 description 1
- DBZJJPROPLPMSN-UHFFFAOYSA-N bromoeosin Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC(Br)=C(O)C(Br)=C1OC1=C(Br)C(O)=C(Br)C=C21 DBZJJPROPLPMSN-UHFFFAOYSA-N 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- VYXSBFYARXAAKO-WTKGSRSZSA-N chembl402140 Chemical compound Cl.C1=2C=C(C)C(NCC)=CC=2OC2=C\C(=N/CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-WTKGSRSZSA-N 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- CEJANLKHJMMNQB-UHFFFAOYSA-M cryptocyanin Chemical compound [I-].C12=CC=CC=C2N(CC)C=CC1=CC=CC1=CC=[N+](CC)C2=CC=CC=C12 CEJANLKHJMMNQB-UHFFFAOYSA-M 0.000 description 1
- ZXJXZNDDNMQXFV-UHFFFAOYSA-M crystal violet Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1[C+](C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 ZXJXZNDDNMQXFV-UHFFFAOYSA-M 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- JBBPTUVOZCXCSU-UHFFFAOYSA-L dipotassium;2',4',5',7'-tetrabromo-4,7-dichloro-3-oxospiro[2-benzofuran-1,9'-xanthene]-3',6'-diolate Chemical compound [K+].[K+].O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(Br)=C([O-])C(Br)=C1OC1=C(Br)C([O-])=C(Br)C=C21 JBBPTUVOZCXCSU-UHFFFAOYSA-L 0.000 description 1
- 238000005421 electrostatic potential Methods 0.000 description 1
- YQGOJNYOYNNSMM-UHFFFAOYSA-N eosin Chemical compound [Na+].OC(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C(O)=C(Br)C=C21 YQGOJNYOYNNSMM-UHFFFAOYSA-N 0.000 description 1
- SEACYXSIPDVVMV-UHFFFAOYSA-L eosin Y Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(Br)C(=O)C(Br)=C2OC2=C(Br)C([O-])=C(Br)C=C21 SEACYXSIPDVVMV-UHFFFAOYSA-L 0.000 description 1
- IINNWAYUJNWZRM-UHFFFAOYSA-L erythrosin B Chemical compound [Na+].[Na+].[O-]C(=O)C1=CC=CC=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 IINNWAYUJNWZRM-UHFFFAOYSA-L 0.000 description 1
- 229940011411 erythrosine Drugs 0.000 description 1
- 235000012732 erythrosine Nutrition 0.000 description 1
- 239000004174 erythrosine Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- GNBHRKFJIUUOQI-UHFFFAOYSA-N fluorescein Chemical compound O1C(=O)C2=CC=CC=C2C21C1=CC=C(O)C=C1OC1=CC(O)=CC=C21 GNBHRKFJIUUOQI-UHFFFAOYSA-N 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 150000002429 hydrazines Chemical class 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000011810 insulating material Substances 0.000 description 1
- 208000013469 light sensitivity Diseases 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 239000005445 natural material Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000005011 phenolic resin Substances 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
- QWYZFXLSWMXLDM-UHFFFAOYSA-M pinacyanol iodide Chemical compound [I-].C1=CC2=CC=CC=C2N(CC)C1=CC=CC1=CC=C(C=CC=C2)C2=[N+]1CC QWYZFXLSWMXLDM-UHFFFAOYSA-M 0.000 description 1
- 238000006068 polycondensation reaction Methods 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- AZJPTIGZZTZIDR-UHFFFAOYSA-L rose bengal Chemical compound [K+].[K+].[O-]C(=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1C1=C2C=C(I)C(=O)C(I)=C2OC2=C(I)C([O-])=C(I)C=C21 AZJPTIGZZTZIDR-UHFFFAOYSA-L 0.000 description 1
- 229940081623 rose bengal Drugs 0.000 description 1
- 229930187593 rose bengal Natural products 0.000 description 1
- STRXNPAVPKGJQR-UHFFFAOYSA-N rose bengal A Natural products O1C(=O)C(C(=CC=C2Cl)Cl)=C2C21C1=CC(I)=C(O)C(I)=C1OC1=C(I)C(O)=C(I)C=C21 STRXNPAVPKGJQR-UHFFFAOYSA-N 0.000 description 1
- AXMCIYLNKNGNOT-UHFFFAOYSA-M sodium;3-[[4-[(4-dimethylazaniumylidenecyclohexa-2,5-dien-1-ylidene)-[4-[ethyl-[(3-sulfonatophenyl)methyl]amino]phenyl]methyl]-n-ethylanilino]methyl]benzenesulfonate Chemical compound [Na+].C=1C=C(C(=C2C=CC(C=C2)=[N+](C)C)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=CC=1N(CC)CC1=CC=CC(S([O-])(=O)=O)=C1 AXMCIYLNKNGNOT-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- -1 sulfo- Chemical class 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000001016 thiazine dye Substances 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N urea group Chemical group NC(=O)N XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- JEVGKYBUANQAKG-UHFFFAOYSA-N victoria blue R Chemical compound [Cl-].C12=CC=CC=C2C(=[NH+]CC)C=CC1=C(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 JEVGKYBUANQAKG-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001018 xanthene dye Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
- C07D271/107—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with two aryl or substituted aryl radicals attached in positions 2 and 5
-
- 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
- G03G5/0605—Carbocyclic compounds
- G03G5/0607—Carbocyclic compounds containing at least one non-six-membered ring
-
- 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
- G03G5/0627—Heterocyclic compounds containing one hetero ring being five-membered
- G03G5/0631—Heterocyclic compounds containing one hetero ring being five-membered containing two hetero atoms
-
- 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
- G03G5/0664—Dyes
- G03G5/0666—Dyes containing a methine or polymethine group
- G03G5/0668—Dyes containing a methine or polymethine group containing only one methine or polymethine group
- G03G5/067—Dyes containing a methine or polymethine group containing only one methine or polymethine group containing hetero rings
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Photoreceptors In Electrophotography (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL217825D NL217825A (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | 1956-06-04 | ||
| LU35193D LU35193A1 (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | 1956-06-04 | ||
| NL99369D NL99369C (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | 1956-06-04 | ||
| BE558078D BE558078A (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | 1956-06-04 | ||
| DEK29014A DE1058836B (de) | 1956-06-04 | 1956-06-04 | Material fuer elektrophotographische Reproduktion |
| US662319A US3189447A (en) | 1956-06-04 | 1957-05-29 | Electrophotographic material and method |
| CH360899D CH360899A (de) | 1956-06-04 | 1957-06-03 | Material für elektrophotographische Reproduktion |
| FR1176457D FR1176457A (fr) | 1956-06-04 | 1957-06-03 | Matériel pour la reproduction électrophotographique |
| GB17519/57A GB851218A (en) | 1956-06-04 | 1957-06-03 | Improvements in or relating to photographic reproduction |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEK29014A DE1058836B (de) | 1956-06-04 | 1956-06-04 | Material fuer elektrophotographische Reproduktion |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE1058836B true DE1058836B (de) | 1959-06-04 |
Family
ID=7218378
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DEK29014A Pending DE1058836B (de) | 1956-06-04 | 1956-06-04 | Material fuer elektrophotographische Reproduktion |
Country Status (8)
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1193363B (de) * | 1961-01-28 | 1965-05-20 | Kalle Ag | Photoleitfaehige Schicht fuer elektro-photographische Zwecke |
| DE2336094A1 (de) * | 1973-07-16 | 1975-02-06 | Hoechst Ag | Elektrophotographisches aufzeichungsmaterial |
| DE2715714A1 (de) * | 1976-04-12 | 1977-10-13 | Ricoh Kk | 1,3,4-oxadiazolderivate sowie diese enthaltende elektrophotographische aufzeichnungsmaterialien |
| DE2659709A1 (de) * | 1976-12-31 | 1978-07-13 | Hoechst Ag | 1,3,4-oxadiazole, verfahren zu ihrer herstellung und ihre verwendung |
| DE3246250A1 (de) * | 1981-12-14 | 1983-06-16 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | Photoleitfaehige zusammensetzungen und elektrophotographische aufzeichnungsmaterialien |
| DE3414791A1 (de) * | 1983-04-18 | 1984-10-18 | Canon K.K., Tokio/Tokyo | Fotoleitfaehiges aufzeichnungselement und traeger fuer das fotoleitfaehige aufzeichnungselement |
| EP0125481A1 (de) * | 1983-04-15 | 1984-11-21 | Hoechst Aktiengesellschaft | Elektrophotographisches Aufzeichnungsmaterial |
| EP0127862A1 (de) * | 1983-05-31 | 1984-12-12 | Hoechst Aktiengesellschaft | Elektrophotographisches Aufzeichnungsmaterial |
| US4492747A (en) * | 1980-06-30 | 1985-01-08 | Hoechst Aktiengesellschaft | Flexible laminatable photosensitive layer |
| US4533612A (en) * | 1983-04-27 | 1985-08-06 | Basf Aktiengesellschaft | Electrophotographic recording materials containing special charge carrier-transporting compounds |
| US4556621A (en) * | 1983-07-05 | 1985-12-03 | Basf Aktiengesellschaft | Electrophotographic recording material containing a metal-1,3-diketone complex |
| US4559285A (en) * | 1983-07-05 | 1985-12-17 | Basf Aktiengesellschaft | Electrophotographic recording materials containing a metal acetylacetonate |
| US4739053A (en) * | 1983-02-09 | 1988-04-19 | Basf Aktiengesellschaft | 2H-v-triazolo[4-5-d]pyrimidines |
| US4906541A (en) * | 1987-11-28 | 1990-03-06 | Basf Aktiengesellschaft | Electrophotographic recording element containing a naphtholactam dye sensitizer |
| US5132189A (en) * | 1989-09-07 | 1992-07-21 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography |
| US5178981A (en) * | 1990-03-08 | 1993-01-12 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography with a charge generating substance comprising a polycyclic and azo compound |
| US5286590A (en) * | 1989-06-06 | 1994-02-15 | Fuji Electric Co., Ltd. | Bisazo photoconductor for electrophotography |
| US5316881A (en) * | 1991-12-27 | 1994-05-31 | Fuji Electric Co., Ltd. | Photoconductor for electrophotgraphy containing benzidine derivative |
| DE3890861C2 (de) * | 1987-10-07 | 1994-10-13 | Fuji Electric Co Ltd | Elektrophotographisches Auzeichnungsmaterial |
| US5368966A (en) * | 1992-05-14 | 1994-11-29 | Fuji Electric Co., Ltd. | Photosensitive member for electrophotography with indole derivative |
| US5393627A (en) * | 1992-02-12 | 1995-02-28 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography |
| EP1515191A2 (en) | 2003-09-05 | 2005-03-16 | Xerox Corporation | Dual charge transport layer and photoconductive imaging member including the same |
Families Citing this family (131)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU37913A1 (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) * | 1958-12-19 | |||
| NL129066C (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) * | 1959-01-07 | |||
| NL254565A (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) * | 1959-08-04 | |||
| US3287120A (en) * | 1961-07-24 | 1966-11-22 | Azoplate Corp | Process for the sensitization of photoconductors |
| DE1250736B (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) * | 1962-10-13 | |||
| DE1265582B (de) * | 1963-10-12 | 1968-04-04 | Kalle Ag | Elektrophotographisches Aufzeichnungsmaterial zur Herstellung von Bildern oder Flachdruckformen |
| DE2160812C2 (de) * | 1971-12-08 | 1982-04-15 | Hoechst Ag, 6000 Frankfurt | Elektrophotographisches Aufzeichnungsmaterial |
| US3873312A (en) * | 1973-05-04 | 1975-03-25 | Eastman Kodak Co | Photoconductive composition and elements containing a styryl amino group containing photoconductor |
| US3873311A (en) * | 1973-05-04 | 1975-03-25 | Eastman Kodak Co | Aggregate photoconductive compositions and elements containing a styryl amino group containing photoconductor |
| US4099970A (en) * | 1976-04-12 | 1978-07-11 | Ricoh Co., Ltd. | Derivatives of 1,3,4-oxadiazole and electrophotographic elements contaning same |
| US4192677A (en) * | 1976-05-18 | 1980-03-11 | Ricoh Co., Ltd. | 1,3,4-Oxadiazole derivatives and use thereof |
| US4141729A (en) * | 1976-05-18 | 1979-02-27 | Ricoh Company, Ltd. | 1,3,4-Oxadiazole derivatives and electrophotographic plates containing same |
| US4055420A (en) * | 1977-01-27 | 1977-10-25 | Xerox Corporation | Single phase organic photoconductive composition |
| US4399206A (en) | 1980-10-06 | 1983-08-16 | Canon Kabushiki Kaisha | Disazo electrophotographic photosensitive member |
| JPS57148750A (en) * | 1981-03-11 | 1982-09-14 | Konishiroku Photo Ind Co Ltd | Electrophotographic receptor |
| DE3210576A1 (de) * | 1982-03-23 | 1983-10-06 | Hoechst Ag | Elektrophotographisches aufzeichnungsmaterial |
| JPS5942352A (ja) | 1982-09-01 | 1984-03-08 | Fuji Photo Film Co Ltd | ジスアゾ化合物、それを含む光導電性組成物及び電子写真感光体 |
| DE3404365A1 (de) * | 1984-02-08 | 1985-08-08 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
| DE3409888A1 (de) * | 1984-03-17 | 1985-09-19 | Hoechst Ag, 6230 Frankfurt | Lichtempfindliches aufzeichnungsmaterial und dessen verwendung in einem verfahren zum herstellen einer druckform oder einer gedruckten schaltung |
| DE3417951A1 (de) * | 1984-05-15 | 1985-11-21 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
| NL8402705A (nl) * | 1984-09-05 | 1986-04-01 | Oce Nederland Bv | Ladingstransporterende verbindingen en fotogeleidende elementen voorzien van dergelijke ladingstransporterende verbindingen. |
| DE3506436A1 (de) * | 1985-02-23 | 1986-08-28 | Hoechst Ag, 6230 Frankfurt | Neue sulfonhaltige styrolderivate, verfahren zu deren herstellung und deren verwendung |
| DE3509147A1 (de) * | 1985-03-14 | 1986-09-18 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
| DE3513747A1 (de) * | 1985-04-17 | 1986-10-23 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
| EP0238095A1 (en) * | 1986-03-20 | 1987-09-23 | Minolta Camera Kabushiki Kaisha | Photosensitive member composed of charge transporting layer and charge generating layer |
| JPH0693124B2 (ja) * | 1986-05-12 | 1994-11-16 | ミノルタ株式会社 | 感光体 |
| DE3706880A1 (de) * | 1987-03-04 | 1988-09-15 | Hoechst Ag | 4-chloroxazol-derivate, verfahren zu ihrer herstellung und ihre verwendung |
| US5000831A (en) * | 1987-03-09 | 1991-03-19 | Minolta Camera Kabushiki Kaisha | Method of production of amorphous hydrogenated carbon layer |
| DE3813459A1 (de) * | 1987-04-24 | 1988-11-10 | Minolta Camera Kk | Funktionsmaessig geteiltes photoempfindliches element |
| JP2595531B2 (ja) * | 1987-04-27 | 1997-04-02 | ミノルタ株式会社 | 感光体 |
| DE3814105C2 (de) * | 1987-04-27 | 1999-02-04 | Minolta Camera Kk | Elektrophotographisches Aufzeichnungsmaterial |
| US4886720A (en) * | 1987-08-31 | 1989-12-12 | Minolta Camera Kabushiki Kaisha | Photosensitive medium having a styryl charge transport material |
| JP2717569B2 (ja) * | 1989-02-23 | 1998-02-18 | コニカ株式会社 | 感光体 |
| US5130603A (en) | 1989-03-20 | 1992-07-14 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| US5198318A (en) * | 1989-06-06 | 1993-03-30 | Fuji Electric Co., Ltd. | Bisazo photoconductor for electrophotography |
| JPH03255453A (ja) * | 1990-01-17 | 1991-11-14 | Fuji Electric Co Ltd | 電子写真用感光体 |
| US5294510A (en) * | 1990-06-14 | 1994-03-15 | Minolta Camera Kabushiki Kaisha | Photosensitive member containing specific coumarin fluorescent bleaching agent |
| JPH04119360A (ja) * | 1990-09-11 | 1992-04-20 | Fuji Electric Co Ltd | 電子写真用感光体 |
| US5382477A (en) * | 1991-02-27 | 1995-01-17 | Sanyo Electric Co., Ltd. | Organic electroluminescent element and process for producing the same |
| JP3134077B2 (ja) * | 1991-03-15 | 2001-02-13 | コニカ株式会社 | ビススチリル化合物及び電子写真感光体 |
| US5336546A (en) * | 1991-07-12 | 1994-08-09 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| US5443922A (en) * | 1991-11-07 | 1995-08-22 | Konica Corporation | Organic thin film electroluminescence element |
| JP3142331B2 (ja) * | 1991-11-28 | 2001-03-07 | 京セラミタ株式会社 | 電子写真感光体 |
| WO1994003032A1 (en) * | 1992-07-23 | 1994-02-03 | Idemitsu Kosan Co., Ltd. | Organic el device |
| US5585213A (en) | 1994-06-10 | 1996-12-17 | Toyo Ink Manufacturing Co., Ltd. | Hole-transporting material and its use |
| US5681664A (en) | 1994-08-04 | 1997-10-28 | Toyo Ink Manufacturing Co., Ltd. | Hole-transporting material and use thereof |
| DE19510526A1 (de) * | 1995-03-23 | 1996-09-26 | Hoechst Ag | Elektrophotographisches Aufzeichnungsmaterial für die Herstellung von Druckplatten |
| JPH09222741A (ja) | 1995-12-11 | 1997-08-26 | Toyo Ink Mfg Co Ltd | 正孔輸送材料およびその用途 |
| US6027840A (en) * | 1996-12-30 | 2000-02-22 | Orion Electric Co., Ltd. | Solution for making photoconductive layers in CRTS |
| US6617051B1 (en) | 1998-12-28 | 2003-09-09 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| US6277873B1 (en) * | 1999-03-25 | 2001-08-21 | Dingwei Tim Yu | Oxadiazole antifungal agents |
| TW463528B (en) | 1999-04-05 | 2001-11-11 | Idemitsu Kosan Co | Organic electroluminescence element and their preparation |
| US6376144B1 (en) | 2000-08-03 | 2002-04-23 | Kodak Polychrome Graphics, Llc | Organic photoconductive composition |
| MY151199A (en) * | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
| JP4506113B2 (ja) | 2002-09-20 | 2010-07-21 | 東ソー株式会社 | フルオレン骨格を有する新規アリールアミン誘導体、その合成中間体及びこれらの製造方法並びに有機ｅｌ素子 |
| EP1620412A2 (en) * | 2003-05-02 | 2006-02-01 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds and hydro isomers thereof |
| US7115642B2 (en) * | 2003-05-02 | 2006-10-03 | Rigel Pharmaceuticals, Inc. | Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating HCV infection |
| US7220745B2 (en) * | 2003-05-15 | 2007-05-22 | Rigel Pharmaceuticals | Heterocyclic compounds useful to treat HCV |
| KR101196558B1 (ko) | 2003-07-02 | 2012-11-01 | 이데미쓰 고산 가부시키가이샤 | 유기 전기발광 소자 및 이를 이용한 표시 장치 |
| WO2005049065A2 (en) * | 2003-11-19 | 2005-06-02 | Rigel Pharmaceuticals, Inc. | Synergistic combinations of dihaloacetamide with interferon or ribavirin for treatment hcv infections |
| EP1707550B1 (en) | 2003-12-01 | 2016-08-03 | Idemitsu Kosan Co., Ltd. | Asymmetric monoanthracene derivative, material for organic electroluminescent device and organic electroluminescent device utilizing the same |
| KR20100052573A (ko) | 2003-12-19 | 2010-05-19 | 이데미쓰 고산 가부시키가이샤 | 유기 전기 발광 소자용 발광 재료, 이를 이용한 유기 전기 발광 소자 및 유기 전기 발광 소자용 재료 |
| US7514434B2 (en) | 2004-02-23 | 2009-04-07 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds having an oxadiazole moiety and hydro isomers thereof |
| JP2007530582A (ja) * | 2004-03-26 | 2007-11-01 | ライジェル ファーマシューティカルズ， インコーポレイテッド | 代謝可能部分を含む複素環抗ウイルス化合物およびその使用 |
| CN1926926A (zh) * | 2004-04-06 | 2007-03-07 | 出光兴产株式会社 | 电极基板及其制造方法 |
| CN102643203A (zh) | 2005-01-05 | 2012-08-22 | 出光兴产株式会社 | 芳香族胺衍生物及使用了它的有机电致发光元件 |
| CN101203498A (zh) * | 2005-05-02 | 2008-06-18 | 里格尔药品股份有限公司 | 包括可代谢部分的杂环抗病毒化合物及其用途 |
| JP5032317B2 (ja) | 2005-07-14 | 2012-09-26 | 出光興産株式会社 | ビフェニル誘導体、有機エレクトロルミネッセンス素子用材料、及びそれを用いた有機エレクトロルミネッセンス素子 |
| JP4848152B2 (ja) | 2005-08-08 | 2011-12-28 | 出光興産株式会社 | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| KR20080052589A (ko) | 2005-09-15 | 2008-06-11 | 이데미쓰 고산 가부시키가이샤 | 비대칭 플루오렌 유도체 및 그것을 이용한 유기 전기발광소자 |
| WO2007032162A1 (ja) | 2005-09-16 | 2007-03-22 | Idemitsu Kosan Co., Ltd. | ピレン系誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
| US20070104977A1 (en) | 2005-11-07 | 2007-05-10 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent device |
| JP2007137784A (ja) | 2005-11-15 | 2007-06-07 | Idemitsu Kosan Co Ltd | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| WO2007058127A1 (ja) | 2005-11-16 | 2007-05-24 | Idemitsu Kosan Co., Ltd. | 芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
| KR20080069190A (ko) | 2005-11-17 | 2008-07-25 | 이데미쓰 고산 가부시키가이샤 | 유기 일렉트로루미네센스 소자 |
| CN101316826A (zh) | 2005-11-28 | 2008-12-03 | 出光兴产株式会社 | 胺系化合物以及利用其的有机电致发光元件 |
| JP2007149941A (ja) | 2005-11-28 | 2007-06-14 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP2007153778A (ja) | 2005-12-02 | 2007-06-21 | Idemitsu Kosan Co Ltd | 含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| WO2007077766A1 (ja) | 2005-12-27 | 2007-07-12 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子 |
| JP2007186461A (ja) | 2006-01-13 | 2007-07-26 | Idemitsu Kosan Co Ltd | 芳香族アミン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| US20090021160A1 (en) | 2006-02-23 | 2009-01-22 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescent device, method for producing same and organic electroluminescent device |
| US9214636B2 (en) | 2006-02-28 | 2015-12-15 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| TW200740290A (en) | 2006-02-28 | 2007-10-16 | Idemitsu Kosan Co | Organic electroluminescent device using fluoranthene derivative and indenoperylene derivative |
| JPWO2007105448A1 (ja) | 2006-02-28 | 2009-07-30 | 出光興産株式会社 | ナフタセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| JPWO2007102361A1 (ja) | 2006-03-07 | 2009-07-23 | 出光興産株式会社 | 芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
| WO2007111263A1 (ja) | 2006-03-27 | 2007-10-04 | Idemitsu Kosan Co., Ltd. | 含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| JPWO2007111262A1 (ja) | 2006-03-27 | 2009-08-13 | 出光興産株式会社 | 含窒素複素環誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
| JPWO2007116750A1 (ja) | 2006-03-30 | 2009-08-20 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料、及びこれを用いた有機エレクトロルミネッセンス素子 |
| CN101415662A (zh) | 2006-04-03 | 2009-04-22 | 出光兴产株式会社 | 联蒽衍生物及利用了它的有机电致发光元件 |
| JP4995475B2 (ja) | 2006-04-03 | 2012-08-08 | 出光興産株式会社 | ベンズアントラセン誘導体、及びそれを用いた有機エレクトロルミネッセンス素子 |
| US8993805B2 (en) * | 2006-04-13 | 2015-03-31 | Tosoh Corporation | Benzofluorene compound and use thereof |
| KR101453109B1 (ko) | 2006-04-26 | 2014-10-27 | 이데미쓰 고산 가부시키가이샤 | 방향족 아민 유도체 및 그들을 이용한 유기 전기 발광 소자 |
| CN101444141A (zh) | 2006-05-11 | 2009-05-27 | 出光兴产株式会社 | 有机电致发光元件 |
| US8076839B2 (en) | 2006-05-11 | 2011-12-13 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| WO2007138906A1 (ja) | 2006-05-25 | 2007-12-06 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子及びフルカラー発光装置 |
| TW200815446A (en) * | 2006-06-05 | 2008-04-01 | Idemitsu Kosan Co | Organic electroluminescent device and material for organic electroluminescent device |
| KR101422864B1 (ko) | 2006-06-22 | 2014-07-24 | 소니 주식회사 | 복소환 함유 아릴아민 유도체를 이용한 유기 전계발광 소자 |
| WO2008001551A1 (fr) | 2006-06-27 | 2008-01-03 | Idemitsu Kosan Co., Ltd. | Dérivé d'amine aromatique et dispositif a électroluminescence organique utilisant celui-ci |
| WO2008015949A1 (en) | 2006-08-04 | 2008-02-07 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| US20080049413A1 (en) | 2006-08-22 | 2008-02-28 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| WO2008023549A1 (en) | 2006-08-23 | 2008-02-28 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivatives and organic electroluminescent devices made by using the same |
| EP2081240A4 (en) | 2006-11-09 | 2010-08-18 | Idemitsu Kosan Co | SOLUTION WITH AN ORGANIC ELECTRICAL MATERIAL, METHOD FOR SYNTHESIS OF AN ORGANIC ELECTRICAL MATERIAL, SYNTHETIZED COMPOUND THROUGH THE SYNTHESIS METHOD, METHOD FOR FORMING A THIN FILM FROM ORGANIC ELECTRICAL MATERIAL, THIN FILM FROM ORGANIC ELECTRICAL MATERIAL AND ORGANIC ELECTRICAL DEVICE |
| JP2008124156A (ja) | 2006-11-09 | 2008-05-29 | Idemitsu Kosan Co Ltd | 有機ｅｌ材料含有溶液、有機ｅｌ材料の薄膜形成方法、有機ｅｌ材料の薄膜、有機ｅｌ素子 |
| JP2008124157A (ja) | 2006-11-09 | 2008-05-29 | Idemitsu Kosan Co Ltd | 有機ｅｌ材料含有溶液、有機ｅｌ材料の薄膜形成方法、有機ｅｌ材料の薄膜、有機ｅｌ素子 |
| CN101595080B (zh) | 2006-11-15 | 2013-12-18 | 出光兴产株式会社 | 荧蒽化合物和使用该荧蒽化合物的有机电致发光元件以及含有机电致发光材料的溶液 |
| WO2008062636A1 (en) | 2006-11-24 | 2008-05-29 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent element using the same |
| JP2008166629A (ja) | 2006-12-29 | 2008-07-17 | Idemitsu Kosan Co Ltd | 有機ｅｌ材料含有溶液、有機ｅｌ材料の合成法、この合成法による合成された化合物、有機ｅｌ材料の薄膜形成方法、有機ｅｌ材料の薄膜、有機ｅｌ素子 |
| WO2008102740A1 (ja) | 2007-02-19 | 2008-08-28 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子 |
| US8278819B2 (en) | 2007-03-09 | 2012-10-02 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and display |
| EP2133932A4 (en) | 2007-03-23 | 2011-06-22 | Idemitsu Kosan Co | ORGANIC EL-INSTALLATION |
| US8586199B2 (en) | 2007-04-06 | 2013-11-19 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
| JP5289979B2 (ja) | 2007-07-18 | 2013-09-11 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子 |
| KR20100038193A (ko) | 2007-08-06 | 2010-04-13 | 이데미쓰 고산 가부시키가이샤 | 방향족 아민 유도체 및 그것을 사용한 유기 전기 발광 소자 |
| EP2221897A4 (en) | 2007-11-22 | 2012-08-08 | Idemitsu Kosan Co | Organic el element and solution containing organic el material |
| ATE554073T1 (de) | 2007-11-30 | 2012-05-15 | Idemitsu Kosan Co | Azaindenofluorendionderivat, material für ein organisches elektrolumineszierendes gerät und organisches lumineszierendes gerät |
| CN101904028A (zh) | 2007-12-21 | 2010-12-01 | 出光兴产株式会社 | 有机电致发光元件 |
| JP5193295B2 (ja) | 2008-05-29 | 2013-05-08 | 出光興産株式会社 | 芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
| US20120007059A1 (en) | 2008-12-26 | 2012-01-12 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence element and compound |
| CN102265424A (zh) | 2008-12-26 | 2011-11-30 | 出光兴产株式会社 | 有机电致发光元件用材料和有机电致发光元件 |
| CN102272969A (zh) | 2009-01-05 | 2011-12-07 | 出光兴产株式会社 | 有机电致发光元件用材料及使用其的有机电致发光元件 |
| US8039127B2 (en) | 2009-04-06 | 2011-10-18 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
| WO2011015265A2 (en) | 2009-08-04 | 2011-02-10 | Merck Patent Gmbh | Electronic devices comprising multi cyclic hydrocarbons |
| JPWO2011046182A1 (ja) | 2009-10-16 | 2013-03-07 | 出光興産株式会社 | 含フルオレン芳香族化合物、有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
| DE102010006280A1 (de) | 2010-01-30 | 2011-08-04 | Merck Patent GmbH, 64293 | Farbkonvertierung |
| JP2012028634A (ja) | 2010-07-26 | 2012-02-09 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
| JP6047761B2 (ja) | 2011-05-13 | 2016-12-21 | ソニー株式会社 | 有機ｅｌ多色発光装置 |
| JP2014517524A (ja) | 2011-06-01 | 2014-07-17 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | ハイブリッド両極性ｔｆｔ |
| EP2737553A1 (en) | 2011-07-25 | 2014-06-04 | Merck Patent GmbH | Copolymers with functionalized side chains |
| WO2013035275A1 (ja) | 2011-09-09 | 2013-03-14 | 出光興産株式会社 | 含窒素へテロ芳香族環化合物 |
| US9991447B2 (en) | 2011-09-28 | 2018-06-05 | Idemitsu Korea Co., Ltd. | Material for organic electroluminescent element, and organic electroluminescent element produced using same |
| KR20140090133A (ko) | 2011-11-07 | 2014-07-16 | 이데미쓰 고산 가부시키가이샤 | 유기 전계 발광 소자용 재료 및 그것을 이용한 유기 전계 발광 소자 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1730505A (en) * | 1928-01-30 | 1929-10-08 | Hart Russell | Photo-electric cell |
| FR1008598A (fr) * | 1948-04-30 | 1952-05-19 | Onera (Off Nat Aerospatiale) | Procédé pour l'enregistrement graphique ou l'inscription dirccte en matériaux pour la mise en oeuvre de ce procédé |
| US2663636A (en) * | 1949-05-25 | 1953-12-22 | Haloid Co | Electrophotographic plate and method of producing same |
| US2765304A (en) * | 1952-05-21 | 1956-10-02 | Ciba Ltd | New ox-diazole compounds and process for their manufacture |
| US2825814A (en) * | 1953-07-16 | 1958-03-04 | Haloid Co | Xerographic image formation |
| US2800559A (en) * | 1953-07-23 | 1957-07-23 | Nat Res Dev | Electrical semi-conductors comprising organo metallic compounds and process of producing same |
-
0
- NL NL217825D patent/NL217825A/xx unknown
- LU LU35193D patent/LU35193A1/xx unknown
- NL NL99369D patent/NL99369C/xx active
- BE BE558078D patent/BE558078A/xx unknown
-
1956
- 1956-06-04 DE DEK29014A patent/DE1058836B/de active Pending
-
1957
- 1957-05-29 US US662319A patent/US3189447A/en not_active Expired - Lifetime
- 1957-06-03 FR FR1176457D patent/FR1176457A/fr not_active Expired
- 1957-06-03 CH CH360899D patent/CH360899A/de unknown
- 1957-06-03 GB GB17519/57A patent/GB851218A/en not_active Expired
Cited By (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1193363B (de) * | 1961-01-28 | 1965-05-20 | Kalle Ag | Photoleitfaehige Schicht fuer elektro-photographische Zwecke |
| DE2336094A1 (de) * | 1973-07-16 | 1975-02-06 | Hoechst Ag | Elektrophotographisches aufzeichungsmaterial |
| DE2715714A1 (de) * | 1976-04-12 | 1977-10-13 | Ricoh Kk | 1,3,4-oxadiazolderivate sowie diese enthaltende elektrophotographische aufzeichnungsmaterialien |
| DE2659709A1 (de) * | 1976-12-31 | 1978-07-13 | Hoechst Ag | 1,3,4-oxadiazole, verfahren zu ihrer herstellung und ihre verwendung |
| US4492747A (en) * | 1980-06-30 | 1985-01-08 | Hoechst Aktiengesellschaft | Flexible laminatable photosensitive layer |
| DE3246250A1 (de) * | 1981-12-14 | 1983-06-16 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | Photoleitfaehige zusammensetzungen und elektrophotographische aufzeichnungsmaterialien |
| US4739053A (en) * | 1983-02-09 | 1988-04-19 | Basf Aktiengesellschaft | 2H-v-triazolo[4-5-d]pyrimidines |
| EP0125481A1 (de) * | 1983-04-15 | 1984-11-21 | Hoechst Aktiengesellschaft | Elektrophotographisches Aufzeichnungsmaterial |
| US4528256A (en) * | 1983-04-15 | 1985-07-09 | Hoechst Aktiengesellschaft | Electrophotographic recording material with condensation product |
| DE3414791A1 (de) * | 1983-04-18 | 1984-10-18 | Canon K.K., Tokio/Tokyo | Fotoleitfaehiges aufzeichnungselement und traeger fuer das fotoleitfaehige aufzeichnungselement |
| US4533612A (en) * | 1983-04-27 | 1985-08-06 | Basf Aktiengesellschaft | Electrophotographic recording materials containing special charge carrier-transporting compounds |
| EP0127862A1 (de) * | 1983-05-31 | 1984-12-12 | Hoechst Aktiengesellschaft | Elektrophotographisches Aufzeichnungsmaterial |
| US4562134A (en) * | 1983-05-31 | 1985-12-31 | Hoechst Aktiengesellschaft | Electrophotographic material with cyanine sensitizer with betaine group |
| US4559285A (en) * | 1983-07-05 | 1985-12-17 | Basf Aktiengesellschaft | Electrophotographic recording materials containing a metal acetylacetonate |
| US4556621A (en) * | 1983-07-05 | 1985-12-03 | Basf Aktiengesellschaft | Electrophotographic recording material containing a metal-1,3-diketone complex |
| DE3890861C2 (de) * | 1987-10-07 | 1994-10-13 | Fuji Electric Co Ltd | Elektrophotographisches Auzeichnungsmaterial |
| US4906541A (en) * | 1987-11-28 | 1990-03-06 | Basf Aktiengesellschaft | Electrophotographic recording element containing a naphtholactam dye sensitizer |
| US5286590A (en) * | 1989-06-06 | 1994-02-15 | Fuji Electric Co., Ltd. | Bisazo photoconductor for electrophotography |
| US5292608A (en) * | 1989-06-06 | 1994-03-08 | Fugi Electric Co., Ltd. | Bisazo photoconductor for electrophotography |
| US5292602A (en) * | 1989-06-06 | 1994-03-08 | Fugi Electric Co., Ltd. | Bisazo photoconductor for electrophotography |
| US5132189A (en) * | 1989-09-07 | 1992-07-21 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography |
| US5178981A (en) * | 1990-03-08 | 1993-01-12 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography with a charge generating substance comprising a polycyclic and azo compound |
| US5316881A (en) * | 1991-12-27 | 1994-05-31 | Fuji Electric Co., Ltd. | Photoconductor for electrophotgraphy containing benzidine derivative |
| US5393627A (en) * | 1992-02-12 | 1995-02-28 | Fuji Electric Co., Ltd. | Photoconductor for electrophotography |
| US5368966A (en) * | 1992-05-14 | 1994-11-29 | Fuji Electric Co., Ltd. | Photosensitive member for electrophotography with indole derivative |
| EP1515191A2 (en) | 2003-09-05 | 2005-03-16 | Xerox Corporation | Dual charge transport layer and photoconductive imaging member including the same |
Also Published As
| Publication number | Publication date |
|---|---|
| NL99369C (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | |
| CH360899A (de) | 1962-03-15 |
| US3189447A (en) | 1965-06-15 |
| NL217825A (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | |
| LU35193A1 (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | |
| BE558078A (c_deeref_Disk_and_Scratch_Disk_Pools_and_Their_Defaults.html) | |
| GB851218A (en) | 1960-10-12 |
| FR1176457A (fr) | 1959-04-10 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE1058836B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1060260B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1060714B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1120875B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1101145B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1105713B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1908345A1 (de) | Elektrophotographisches Aufzeichnungsmaterial | |
| DE1137625B (de) | Material fuer die elektrophotographische Reproduktion | |
| DE3208455A1 (de) | Elektrophotographische lichtempfindliche druckmaterialien | |
| DE1105714B (de) | Material fuer elektrophotographische Reproduktion | |
| DE2917486A1 (de) | Verfahren zum herstellen einer lithographischen druckplatte | |
| DE1145184B (de) | Verfahren zur Herstellung von lithographischen Flachdruckformen | |
| DE1060713B (de) | Material fuer die elektrophotographische Reproduktion | |
| DE2322046B2 (de) | Verfahren zum Herstellen von Druckformen | |
| EP0125481B1 (de) | Elektrophotographisches Aufzeichnungsmaterial | |
| DE1447008C3 (de) | Verfahren zur Herstellung einer Druckform | |
| DE1116057B (de) | Material fuer elektrophotographische Reproduktion | |
| DE1099846B (de) | Material fuer elektrophotographische Reproduktion | |
| DE2726116C3 (de) | Elektrophotographische Druckform | |
| DE2109626C3 (de) | p- oder m-Xylolderivate und deren Verwendung als fotoleitendes Material für die Elektrofotografie | |
| AT216343B (de) | Material für elektrophotographische Reproduktion | |
| DE1060712B (de) | Material fuer elektrophotographische Reproduktion | |
| DE2526720C3 (de) | Material für elektrophotographische Reproduktion | |
| DE1254467B (de) | Photoleitfaehige Schichten | |
| AT207248B (de) | Material für elektrophotographische Reproduktion |