DE1772830B2 - Elektrophotographisches aufzeichnungsmaterial - Google Patents
Elektrophotographisches aufzeichnungsmaterialInfo
- Publication number
- DE1772830B2 DE1772830B2 DE19681772830 DE1772830A DE1772830B2 DE 1772830 B2 DE1772830 B2 DE 1772830B2 DE 19681772830 DE19681772830 DE 19681772830 DE 1772830 A DE1772830 A DE 1772830A DE 1772830 B2 DE1772830 B2 DE 1772830B2
- Authority
- DE
- Germany
- Prior art keywords
- recording material
- photoconductor
- dicyanomethylene
- electron acceptor
- optionally
- 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 13
- 230000003287 optical effect Effects 0.000 claims description 7
- 239000000945 filler Substances 0.000 claims description 6
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 claims description 6
- -1 4-diethylaminophenyl Chemical group 0.000 claims description 5
- 239000011230 binding agent Substances 0.000 claims description 5
- PPBGQASTADVQQM-UHFFFAOYSA-N 2-fluoren-1-ylidenepropanedinitrile Chemical compound C1=CC=C2C=C3C(=C(C#N)C#N)C=CC=C3C2=C1 PPBGQASTADVQQM-UHFFFAOYSA-N 0.000 claims description 4
- 230000035945 sensitivity Effects 0.000 claims description 4
- 150000002220 fluorenes Chemical class 0.000 claims description 3
- VEUMBMHMMCOFAG-UHFFFAOYSA-N 2,3-dihydrooxadiazole Chemical compound N1NC=CO1 VEUMBMHMMCOFAG-UHFFFAOYSA-N 0.000 claims description 2
- DBOFUBZQRADHSA-UHFFFAOYSA-N 2-(2,7-dinitrofluoren-9-ylidene)propanedinitrile Chemical compound [O-][N+](=O)C1=CC=C2C3=CC=C([N+](=O)[O-])C=C3C(=C(C#N)C#N)C2=C1 DBOFUBZQRADHSA-UHFFFAOYSA-N 0.000 claims description 2
- 239000000126 substance Substances 0.000 claims description 2
- DIUMIVHQDHIHQY-UHFFFAOYSA-N N#CC=C(C=C1)C([N+]([O-])=O)=C2C1=C(C=CC=C1)C1=C2 Chemical class N#CC=C(C=C1)C([N+]([O-])=O)=C2C1=C(C=CC=C1)C1=C2 DIUMIVHQDHIHQY-UHFFFAOYSA-N 0.000 claims 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims 2
- UZGVMZRBRRYLIP-UHFFFAOYSA-N 4-[5-[4-(diethylamino)phenyl]-1,3,4-oxadiazol-2-yl]-n,n-diethylaniline Chemical compound C1=CC(N(CC)CC)=CC=C1C1=NN=C(C=2C=CC(=CC=2)N(CC)CC)O1 UZGVMZRBRRYLIP-UHFFFAOYSA-N 0.000 claims 1
- 238000002845 discoloration Methods 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- SBMXAWJSNIAHFR-UHFFFAOYSA-N n-naphthalen-2-ylnaphthalen-2-amine Chemical compound C1=CC=CC2=CC(NC=3C=C4C=CC=CC4=CC=3)=CC=C21 SBMXAWJSNIAHFR-UHFFFAOYSA-N 0.000 claims 1
- 238000007645 offset printing Methods 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 150000001875 compounds Chemical class 0.000 description 7
- 238000000576 coating method Methods 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 4
- 239000000370 acceptor Substances 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- ZXBSSAFKXWFUMF-UHFFFAOYSA-N 1,2,3-trinitrofluoren-9-one Chemical compound C12=CC=CC=C2C(=O)C2=C1C=C([N+](=O)[O-])C([N+]([O-])=O)=C2[N+]([O-])=O ZXBSSAFKXWFUMF-UHFFFAOYSA-N 0.000 description 2
- JWWQNDLIYXEFQL-UHFFFAOYSA-N 2,3-dinitrofluoren-1-one Chemical compound C1=CC=C2C3=CC([N+](=O)[O-])=C([N+]([O-])=O)C(=O)C3=CC2=C1 JWWQNDLIYXEFQL-UHFFFAOYSA-N 0.000 description 2
- CRGCBMJOFNGBRW-UHFFFAOYSA-N 2-(5,6,7,8-tetranitrofluoren-4-ylidene)propanedinitrile Chemical compound C(#N)C(C#N)=C1C2=C3C(=C(C(=C(C3=CC2=CC=C1)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] CRGCBMJOFNGBRW-UHFFFAOYSA-N 0.000 description 2
- POXIZPBFFUKMEQ-UHFFFAOYSA-N 2-cyanoethenylideneazanide Chemical group [N-]=C=[C+]C#N POXIZPBFFUKMEQ-UHFFFAOYSA-N 0.000 description 2
- DBJKIYVWFSACIT-UHFFFAOYSA-N 2-fluoren-9-ylidenepropanedinitrile Chemical compound C1=CC=C2C(=C(C#N)C#N)C3=CC=CC=C3C2=C1 DBJKIYVWFSACIT-UHFFFAOYSA-N 0.000 description 2
- FGFOZLCWAHRUAJ-UHFFFAOYSA-N 2-nitrofluoren-1-one Chemical class C1=CC=C2C3=CC=C([N+](=O)[O-])C(=O)C3=CC2=C1 FGFOZLCWAHRUAJ-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 230000009918 complex formation Effects 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000011787 zinc oxide Substances 0.000 description 2
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 description 1
- KPAPHODVWOVUJL-UHFFFAOYSA-N 1-benzofuran;1h-indene Chemical compound C1=CC=C2CC=CC2=C1.C1=CC=C2OC=CC2=C1 KPAPHODVWOVUJL-UHFFFAOYSA-N 0.000 description 1
- JOERSAVCLPYNIZ-UHFFFAOYSA-N 2,4,5,7-tetranitrofluoren-9-one Chemical compound O=C1C2=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C2C2=C1C=C([N+](=O)[O-])C=C2[N+]([O-])=O JOERSAVCLPYNIZ-UHFFFAOYSA-N 0.000 description 1
- GOJCEBIJPCJITE-UHFFFAOYSA-N 2-(1,2,3-trinitrofluoren-4-ylidene)propanedinitrile Chemical compound C(#N)C(C#N)=C1C(=C(C(=C2C=C3C=CC=CC3=C12)[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-] GOJCEBIJPCJITE-UHFFFAOYSA-N 0.000 description 1
- LGEFAQWZYGDRGD-UHFFFAOYSA-N 2-(1,2-dinitrofluoren-3-ylidene)propanedinitrile Chemical compound C1=CC=C2C=C3C([N+](=O)[O-])=C([N+]([O-])=O)C(=C(C#N)C#N)C=C3C2=C1 LGEFAQWZYGDRGD-UHFFFAOYSA-N 0.000 description 1
- KLFKNCQKWDDRNO-UHFFFAOYSA-N 9-(dicyanomethylidene)fluorene-2-carboxylic acid Chemical compound C1=CC=C2C(=C(C#N)C#N)C3=CC(C(=O)O)=CC=C3C2=C1 KLFKNCQKWDDRNO-UHFFFAOYSA-N 0.000 description 1
- 206010034960 Photophobia Diseases 0.000 description 1
- 206010034972 Photosensitivity reaction Diseases 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- HCWCAKKEBCNQJP-UHFFFAOYSA-N magnesium orthosilicate Chemical compound [Mg+2].[Mg+2].[O-][Si]([O-])([O-])[O-] HCWCAKKEBCNQJP-UHFFFAOYSA-N 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229910052919 magnesium silicate Inorganic materials 0.000 description 1
- 235000019792 magnesium silicate Nutrition 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000036211 photosensitivity Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 230000036515 potency Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 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
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing 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
- G03G5/05—Organic bonding materials; Methods for coating a substrate with a photoconductive layer; Inert supplements for use in photoconductive layers
- G03G5/0503—Inert supplements
- G03G5/051—Organic non-macromolecular compounds
- G03G5/0517—Organic non-macromolecular compounds comprising one or more cyclic groups consisting of carbon-atoms only
-
- 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
- G03G5/09—Sensitisors or activators, e.g. dyestuffs
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Photoreceptors In Electrophotography (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US65208367A | 1967-07-10 | 1967-07-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE1772830A1 DE1772830A1 (de) | 1970-11-12 |
| DE1772830B2 true DE1772830B2 (de) | 1972-02-10 |
Family
ID=24615448
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19681772830 Pending DE1772830B2 (de) | 1967-07-10 | 1968-07-09 | Elektrophotographisches aufzeichnungsmaterial |
Country Status (5)
| Country | Link |
|---|---|
| BE (1) | BE717490A (enExample) |
| DE (1) | DE1772830B2 (enExample) |
| FR (1) | FR1573528A (enExample) |
| GB (1) | GB1222252A (enExample) |
| NL (1) | NL6809655A (enExample) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3363782B1 (en) * | 2015-11-17 | 2020-03-18 | LG Chem, Ltd. | Compound and organic electronic element comprising same |
-
1968
- 1968-07-02 BE BE717490D patent/BE717490A/xx unknown
- 1968-07-08 GB GB3254968A patent/GB1222252A/en not_active Expired
- 1968-07-09 FR FR1573528D patent/FR1573528A/fr not_active Expired
- 1968-07-09 DE DE19681772830 patent/DE1772830B2/de active Pending
- 1968-07-09 NL NL6809655A patent/NL6809655A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB1222252A (en) | 1971-02-10 |
| BE717490A (enExample) | 1968-12-16 |
| DE1772830A1 (de) | 1970-11-12 |
| FR1573528A (enExample) | 1969-07-04 |
| NL6809655A (enExample) | 1969-01-14 |
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