SU499841A3 - Фотопровод щий слой - Google Patents
Фотопровод щий слойInfo
- Publication number
- SU499841A3 SU499841A3 SU1718917A SU1718917A SU499841A3 SU 499841 A3 SU499841 A3 SU 499841A3 SU 1718917 A SU1718917 A SU 1718917A SU 1718917 A SU1718917 A SU 1718917A SU 499841 A3 SU499841 A3 SU 499841A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- concentration
- mol per
- life
- electron
- mol
- Prior art date
Links
- 230000035945 sensitivity Effects 0.000 claims description 35
- 238000005286 illumination Methods 0.000 claims description 18
- -1 nitroso, carbonyl Chemical group 0.000 claims description 11
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 239000012190 activator Substances 0.000 claims description 5
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 4
- 229910052711 selenium Inorganic materials 0.000 claims description 4
- 239000011669 selenium Substances 0.000 claims description 4
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims description 4
- 229910052721 tungsten Inorganic materials 0.000 claims description 4
- 239000010937 tungsten Substances 0.000 claims description 4
- 239000011230 binding agent Substances 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 229920000642 polymer Polymers 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000005027 hydroxyaryl group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 239000004014 plasticizer Substances 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- KDDPNNXAZURUGP-UHFFFAOYSA-N 2-[2-(3,4-dichlorophenyl)-3-[2-(piperidin-3-ylamino)pyrimidin-4-yl]imidazol-4-yl]acetonitrile Chemical compound ClC=1C=C(C=CC=1Cl)C=1N(C(=CN=1)CC#N)C1=NC(=NC=C1)NC1CNCCC1 KDDPNNXAZURUGP-UHFFFAOYSA-N 0.000 claims 1
- RCABOJSOTWKUIB-UHFFFAOYSA-N 2-chloro-3-nitronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C([N+](=O)[O-])=C(Cl)C(=O)C2=C1 RCABOJSOTWKUIB-UHFFFAOYSA-N 0.000 claims 1
- 125000002252 acyl group Chemical group 0.000 claims 1
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 1
- 239000000178 monomer Substances 0.000 claims 1
- 239000000370 acceptor Substances 0.000 description 15
- 238000000034 method Methods 0.000 description 7
- 239000002253 acid Substances 0.000 description 5
- 239000011248 coating agent Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- BJCGIXCFEKJICC-UHFFFAOYSA-N 3,6-dinitronaphthalene-1-carboxylic acid Chemical compound [O-][N+](=O)C1=CC=C2C(C(=O)O)=CC([N+]([O-])=O)=CC2=C1 BJCGIXCFEKJICC-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 108010068370 Glutens Proteins 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 235000021312 gluten Nutrition 0.000 description 3
- 238000001429 visible spectrum Methods 0.000 description 3
- BFMBQYIQQLBGJA-UHFFFAOYSA-N 1,3,6,8-tetranitronaphthalene Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=CC2=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C21 BFMBQYIQQLBGJA-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- WJWGJSOWOZJYRP-UHFFFAOYSA-N 1-methoxy-2,4-dinitroanthracene-9,10-dione Chemical compound COC1=C(C=C(C=2C(C3=CC=CC=C3C(C12)=O)=O)[N+](=O)[O-])[N+](=O)[O-] WJWGJSOWOZJYRP-UHFFFAOYSA-N 0.000 description 2
- FKNIDKXOANSRCS-UHFFFAOYSA-N 2,3,4-trinitrofluoren-1-one Chemical compound C1=CC=C2C3=C([N+](=O)[O-])C([N+]([O-])=O)=C([N+]([O-])=O)C(=O)C3=CC2=C1 FKNIDKXOANSRCS-UHFFFAOYSA-N 0.000 description 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
- 206010034972 Photosensitivity reaction Diseases 0.000 description 2
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 230000008033 biological extinction Effects 0.000 description 2
- 239000002800 charge carrier Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical group [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 2
- 230000036211 photosensitivity Effects 0.000 description 2
- 150000005838 radical anions Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- JUSWGNJYSBSOFM-UHFFFAOYSA-N 1,3,6,8-tetranitro-9h-carbazole Chemical compound C1=C([N+]([O-])=O)C=C2C3=CC([N+](=O)[O-])=CC([N+]([O-])=O)=C3NC2=C1[N+]([O-])=O JUSWGNJYSBSOFM-UHFFFAOYSA-N 0.000 description 1
- OUKXOASCNUYYPS-UHFFFAOYSA-N 1,3,7-trinitroacridine Chemical compound [N+](=O)([O-])C1=CC(=CC2=NC3=CC=C(C=C3C=C12)[N+](=O)[O-])[N+](=O)[O-] OUKXOASCNUYYPS-UHFFFAOYSA-N 0.000 description 1
- MVHHMYJMIHKUFM-UHFFFAOYSA-N 1,3,7-trinitrophenazine Chemical compound [N+](=O)([O-])C1=CC2=NC3=CC(=CC=C3N=C2C(=C1)[N+](=O)[O-])[N+](=O)[O-] MVHHMYJMIHKUFM-UHFFFAOYSA-N 0.000 description 1
- PPJVBBJMDLANLB-UHFFFAOYSA-N 1,4,5-trinitronaphthalene Chemical compound C1=CC=C2C([N+](=O)[O-])=CC=C([N+]([O-])=O)C2=C1[N+]([O-])=O PPJVBBJMDLANLB-UHFFFAOYSA-N 0.000 description 1
- QPYHKSCVWSEXKZ-UHFFFAOYSA-N 1,4,6,7-tetranitro-1,2-dihydroacenaphthylene Chemical compound [N+](=O)([O-])C1CC=2C=C(C=C3C(=C(C=C1C23)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] QPYHKSCVWSEXKZ-UHFFFAOYSA-N 0.000 description 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- PXPBDJVBNWDUFM-UHFFFAOYSA-N 2,3,4,6-tetranitrophenol Chemical compound OC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C([N+]([O-])=O)=C1[N+]([O-])=O PXPBDJVBNWDUFM-UHFFFAOYSA-N 0.000 description 1
- VHQGURIJMFPBKS-UHFFFAOYSA-N 2,4,7-trinitrofluoren-9-one Chemical compound [O-][N+](=O)C1=CC([N+]([O-])=O)=C2C3=CC=C([N+](=O)[O-])C=C3C(=O)C2=C1 VHQGURIJMFPBKS-UHFFFAOYSA-N 0.000 description 1
- ICIBEJCLGQGRAK-UHFFFAOYSA-N 3,6,8-trinitroquinoline Chemical compound [N+](=O)([O-])C=1C=NC2=C(C=C(C=C2C1)[N+](=O)[O-])[N+](=O)[O-] ICIBEJCLGQGRAK-UHFFFAOYSA-N 0.000 description 1
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- KPYSYYIEGFHWSV-UHFFFAOYSA-N Baclofen Chemical compound OC(=O)CC(CN)C1=CC=C(Cl)C=C1 KPYSYYIEGFHWSV-UHFFFAOYSA-N 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- MCRWZBYTLVCCJJ-DKALBXGISA-N [(1s,3r)-3-[[(3s,4s)-3-methoxyoxan-4-yl]amino]-1-propan-2-ylcyclopentyl]-[(1s,4s)-5-[6-(trifluoromethyl)pyrimidin-4-yl]-2,5-diazabicyclo[2.2.1]heptan-2-yl]methanone Chemical compound C([C@]1(N(C[C@]2([H])C1)C(=O)[C@@]1(C[C@@H](CC1)N[C@@H]1[C@@H](COCC1)OC)C(C)C)[H])N2C1=CC(C(F)(F)F)=NC=N1 MCRWZBYTLVCCJJ-DKALBXGISA-N 0.000 description 1
- YELCXCFXSPPRTJ-UHFFFAOYSA-N [N+](=O)([O-])C1=CC(=CC2=C(C=CC(=C12)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] Chemical compound [N+](=O)([O-])C1=CC(=CC2=C(C=CC(=C12)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] YELCXCFXSPPRTJ-UHFFFAOYSA-N 0.000 description 1
- HXGDTGSAIMULJN-UHFFFAOYSA-N acetnaphthylene Natural products C1=CC(C=C2)=C3C2=CC=CC3=C1 HXGDTGSAIMULJN-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 229910052925 anhydrite Inorganic materials 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 239000002322 conducting polymer Substances 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 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 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 230000001235 sensitizing effect Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- AUHHYELHRWCWEZ-UHFFFAOYSA-N tetrachlorophthalic anhydride Chemical compound ClC1=C(Cl)C(Cl)=C2C(=O)OC(=O)C2=C1Cl AUHHYELHRWCWEZ-UHFFFAOYSA-N 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0644—Heterocyclic compounds containing two or more hetero rings
- G03G5/0646—Heterocyclic compounds containing two or more hetero rings in the same ring system
- G03G5/065—Heterocyclic compounds containing two or more hetero rings in the same ring system containing three relevant rings
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0618—Acyclic or carbocyclic compounds containing oxygen and nitrogen
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/062—Acyclic or carbocyclic compounds containing non-metal elements other than hydrogen, halogen, oxygen or nitrogen
-
- 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
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
- G03G5/0637—Heterocyclic compounds containing one hetero ring being six-membered containing one hetero atom
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0624—Heterocyclic compounds containing one hetero ring
- G03G5/0635—Heterocyclic compounds containing one hetero ring being six-membered
- G03G5/0638—Heterocyclic compounds containing one hetero ring being six-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
-
- 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
- G03G5/0672—Dyes containing a methine or polymethine group containing two or more methine or polymethine groups
-
- 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
- G03G5/0698—Compounds of unspecified structure characterised by a substituent only
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2059540A DE2059540C3 (de) | 1970-12-03 | 1970-12-03 | Elektrophotographisches Aufzeichnungsmaterial mit einer photoleitfähigen Schicht |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU499841A3 true SU499841A3 (ru) | 1976-01-15 |
Family
ID=5789902
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU1718917A SU499841A3 (ru) | 1970-12-03 | 1971-11-29 | Фотопровод щий слой |
Country Status (14)
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2841925A1 (de) * | 1978-09-27 | 1980-04-17 | Basf Ag | Fotoleitfaehige massen auf basis von kunststoffen |
| DE2951349A1 (de) * | 1979-12-20 | 1981-07-02 | Bayer Ag, 5090 Leverkusen | Naphthalintetracarbonsaeurediimide als elektrische halbleiter und photoleiter |
| JPS58152247A (ja) * | 1982-03-05 | 1983-09-09 | Mita Ind Co Ltd | 電子写真用有機感光体 |
| US4442193A (en) * | 1983-02-22 | 1984-04-10 | Eastman Kodak Company | Photoconductive compositions and elements containing naphthalene bis-dicarboximide compounds |
| DE3537979A1 (de) * | 1985-10-25 | 1987-04-30 | Hoechst Ag | Elektrophotographisches aufzeichnungsmaterial |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE606574A (enrdf_load_stackoverflow) * | 1959-05-29 | |||
| US3607258A (en) * | 1966-01-06 | 1971-09-21 | Xerox Corp | Electrophotographic plate and process |
| US3484237A (en) * | 1966-06-13 | 1969-12-16 | Ibm | Organic photoconductive compositions and their use in electrophotographic processes |
| DE1810757C3 (de) * | 1968-11-25 | 1979-02-22 | Hoechst Ag, 6000 Frankfurt | Verfahren zur Herstellung eines Ladungsbildes auf einer dielektrischen Schicht |
-
1970
- 1970-12-03 DE DE2059540A patent/DE2059540C3/de not_active Expired
-
1971
- 1971-11-23 NL NLAANVRAGE7116090,A patent/NL168632C/xx not_active IP Right Cessation
- 1971-11-29 SU SU1718917A patent/SU499841A3/ru active
- 1971-11-30 BE BE776060A patent/BE776060A/xx not_active IP Right Cessation
- 1971-11-30 AT AT1030671A patent/AT315638B/de not_active IP Right Cessation
- 1971-11-30 CA CA128,940,A patent/CA950734A/en not_active Expired
- 1971-11-30 CH CH1740871A patent/CH584918A5/xx not_active IP Right Cessation
- 1971-12-01 ES ES397550A patent/ES397550A1/es not_active Expired
- 1971-12-01 GB GB5575871A patent/GB1375719A/en not_active Expired
- 1971-12-01 IT IT54452/71A patent/IT945219B/it active
- 1971-12-02 ZA ZA718084A patent/ZA718084B/xx unknown
- 1971-12-02 SE SE7115431A patent/SE382123B/xx unknown
- 1971-12-02 AU AU36422/71A patent/AU473665B2/en not_active Expired
- 1971-12-03 FR FR7143421A patent/FR2117342A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| IT945219B (it) | 1973-05-10 |
| ZA718084B (en) | 1972-08-30 |
| FR2117342A5 (enrdf_load_stackoverflow) | 1972-07-21 |
| AU473665B2 (en) | 1976-07-01 |
| SE382123B (sv) | 1976-01-12 |
| NL168632B (nl) | 1981-11-16 |
| ES397550A1 (es) | 1975-04-01 |
| NL7116090A (enrdf_load_stackoverflow) | 1972-06-06 |
| AT315638B (de) | 1974-06-10 |
| CA950734A (en) | 1974-07-09 |
| GB1375719A (enrdf_load_stackoverflow) | 1974-11-27 |
| NL168632C (nl) | 1982-04-16 |
| CH584918A5 (enrdf_load_stackoverflow) | 1977-02-15 |
| DE2059540A1 (de) | 1972-06-08 |
| AU3642271A (en) | 1973-06-21 |
| DE2059540C3 (de) | 1985-05-15 |
| DE2059540B2 (de) | 1979-08-02 |
| BE776060A (fr) | 1972-05-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH0326384B2 (enrdf_load_stackoverflow) | ||
| JPH0516020B2 (enrdf_load_stackoverflow) | ||
| JPH0324664B2 (enrdf_load_stackoverflow) | ||
| JPS60122954A (ja) | 電子写真用記録材料及びその製法 | |
| EP0427890A1 (en) | Photoconductive recording element | |
| JPH0326383B2 (enrdf_load_stackoverflow) | ||
| SU499841A3 (ru) | Фотопровод щий слой | |
| US3624226A (en) | Electrographic organic photoconductor comprising of n,n,n{40 ,n{40 , tetrabenzyl 4,4{40 oxydianaline | |
| US3992203A (en) | Polyphenylenevinylene photoconductor composition sensitized with a 1,4-bis (styryl) benzene derivative | |
| US3935009A (en) | Electrophotographic reproduction element of an aniline compound electron acceptor | |
| US4315981A (en) | Organic double layer electrophotographic recording material | |
| US3867140A (en) | Organic photoconductor-(mononitro-2-aza-fluorenylidene)malononitrile charge transfer complex | |
| US3784376A (en) | Photoconductive element containing furans, indoles, or thiophenes | |
| EP0402979A1 (en) | Electrophotographic recording material | |
| EP0393787B1 (en) | Electrophotographic recording material | |
| US3796572A (en) | Electrophotographic light-sensitive material | |
| US3765882A (en) | Heterocyclic photoconductor containing o, s or se | |
| US3832172A (en) | Photosensitive material for electrophotography | |
| US4105446A (en) | Organic photoconductive coating compositions containing tricyanovinyl compounds for electrophotography | |
| US4224395A (en) | Electrophotographic recording material with cellulose acyl ester binder | |
| US3730712A (en) | Photoconductive material for electrography | |
| JPH0358105B2 (enrdf_load_stackoverflow) | ||
| US4055421A (en) | Sensitizer for photoconductive sensitive material | |
| US4209579A (en) | Electrophotographic photosensitive material with a quinocyanine pigment | |
| EP0062540B1 (en) | Photosensitive composition for electrophotography |