GB946107A - Photoconductive coatings for electrophotography - Google Patents
Photoconductive coatings for electrophotographyInfo
- Publication number
- GB946107A GB946107A GB18436/60A GB1843660A GB946107A GB 946107 A GB946107 A GB 946107A GB 18436/60 A GB18436/60 A GB 18436/60A GB 1843660 A GB1843660 A GB 1843660A GB 946107 A GB946107 A GB 946107A
- Authority
- GB
- United Kingdom
- Prior art keywords
- naphthylamine
- carbazole
- alkyl
- amino
- benzene
- 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.)
- Expired
Links
- 238000000576 coating method Methods 0.000 title 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 9
- YZVWKHVRBDQPMQ-UHFFFAOYSA-N 1-aminopyrene Chemical compound C1=C2C(N)=CC=C(C=C3)C2=C2C3=CC=CC2=C1 YZVWKHVRBDQPMQ-UHFFFAOYSA-N 0.000 abstract 4
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 abstract 4
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Chemical compound C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 abstract 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 abstract 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 4
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 abstract 4
- -1 heterocyclic radicals Chemical class 0.000 abstract 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 abstract 4
- 238000000034 method Methods 0.000 abstract 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 abstract 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 abstract 2
- MYKQKWIPLZEVOW-UHFFFAOYSA-N 11h-benzo[a]carbazole Chemical compound C1=CC2=CC=CC=C2C2=C1C1=CC=CC=C1N2 MYKQKWIPLZEVOW-UHFFFAOYSA-N 0.000 abstract 2
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 2
- SJODITPGMMSNRF-UHFFFAOYSA-N 2-aminofluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC(N)=CC=C3C2=C1 SJODITPGMMSNRF-UHFFFAOYSA-N 0.000 abstract 2
- LTDYEGRQUIEUPD-UHFFFAOYSA-N 3-(2-phenylquinazolin-4-yl)aniline Chemical compound NC1=CC=CC(C=2C3=CC=CC=C3N=C(N=2)C=2C=CC=CC=2)=C1 LTDYEGRQUIEUPD-UHFFFAOYSA-N 0.000 abstract 2
- OXEUETBFKVCRNP-UHFFFAOYSA-N 9-ethyl-3-carbazolamine Chemical compound NC1=CC=C2N(CC)C3=CC=CC=C3C2=C1 OXEUETBFKVCRNP-UHFFFAOYSA-N 0.000 abstract 2
- LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 abstract 2
- CFRFHWQYWJMEJN-UHFFFAOYSA-N 9h-fluoren-2-amine Chemical compound C1=CC=C2C3=CC=C(N)C=C3CC2=C1 CFRFHWQYWJMEJN-UHFFFAOYSA-N 0.000 abstract 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 2
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003545 alkoxy group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001408 amides Chemical class 0.000 abstract 2
- LHNICELDCMPPDE-UHFFFAOYSA-N anthracen-9-amine Chemical compound C1=CC=C2C(N)=C(C=CC=C3)C3=CC2=C1 LHNICELDCMPPDE-UHFFFAOYSA-N 0.000 abstract 2
- VEQOALNAAJBPNY-UHFFFAOYSA-N antipyrine Chemical compound CN1C(C)=CC(=O)N1C1=CC=CC=C1 VEQOALNAAJBPNY-UHFFFAOYSA-N 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 abstract 2
- DMVOXQPQNTYEKQ-UHFFFAOYSA-N biphenyl-4-amine Chemical group C1=CC(N)=CC=C1C1=CC=CC=C1 DMVOXQPQNTYEKQ-UHFFFAOYSA-N 0.000 abstract 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 2
- 239000000178 monomer Substances 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 abstract 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 abstract 2
- 229960005222 phenazone Drugs 0.000 abstract 2
- 229920000642 polymer Polymers 0.000 abstract 2
- 229920005989 resin Polymers 0.000 abstract 2
- 239000011347 resin Substances 0.000 abstract 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract 1
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 abstract 1
- LDZYRENCLPUXAX-UHFFFAOYSA-N 2-methyl-1h-benzimidazole Chemical compound C1=CC=C2NC(C)=NC2=C1 LDZYRENCLPUXAX-UHFFFAOYSA-N 0.000 abstract 1
- KLLLJCACIRKBDT-UHFFFAOYSA-N 2-phenyl-1H-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=C1 KLLLJCACIRKBDT-UHFFFAOYSA-N 0.000 abstract 1
- MKASXAGBWHIGCF-UHFFFAOYSA-N 3-methoxy-n-phenylaniline Chemical compound COC1=CC=CC(NC=2C=CC=CC=2)=C1 MKASXAGBWHIGCF-UHFFFAOYSA-N 0.000 abstract 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- HFBMWMNUJJDEQZ-UHFFFAOYSA-N acryloyl chloride Chemical compound ClC(=O)C=C HFBMWMNUJJDEQZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000012190 activator Substances 0.000 abstract 1
- 238000010640 amide synthesis reaction Methods 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 150000001805 chlorine compounds Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229920001577 copolymer Polymers 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 239000000155 melt Substances 0.000 abstract 1
- WVFCDEWIOQYSID-UHFFFAOYSA-N n,n-dimethyl-9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N(C)C)=CC=C3NC2=C1 WVFCDEWIOQYSID-UHFFFAOYSA-N 0.000 abstract 1
- FHTSZHFGMOBHLN-UHFFFAOYSA-N n-quinolin-2-ylquinolin-2-amine Chemical compound C1=CC=CC2=NC(NC=3N=C4C=CC=CC4=CC=3)=CC=C21 FHTSZHFGMOBHLN-UHFFFAOYSA-N 0.000 abstract 1
- 239000000049 pigment Substances 0.000 abstract 1
- 239000004014 plasticizer Substances 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 150000004053 quinones Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000010561 standard procedure Methods 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 150000003852 triazoles Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
- C08F20/52—Amides or imides
- C08F20/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
- C08F20/62—Monocarboxylic acids having ten or more carbon atoms; Derivatives thereof
-
- 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
- G03G5/0609—Acyclic or carbocyclic compounds containing oxygen
-
- 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
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine 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
- G03G5/07—Polymeric photoconductive materials
- G03G5/071—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G5/072—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups
- G03G5/073—Polymeric photoconductive materials obtained by reactions only involving carbon-to-carbon unsaturated bonds comprising pending monoamine groups comprising pending carbazole 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
- G03G5/09—Sensitisors or activators, e.g. dyestuffs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Emergency Medicine (AREA)
- Photoreceptors In Electrophotography (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEK37869A DE1131988B (de) | 1959-05-30 | 1959-05-30 | Photoleiterschichten fuer Elektrophotographie |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB946107A true GB946107A (en) | 1964-01-08 |
Family
ID=7221173
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB18436/60A Expired GB946107A (en) | 1959-05-30 | 1960-05-25 | Photoconductive coatings for electrophotography |
Country Status (8)
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190041507A (ko) * | 2016-10-14 | 2019-04-22 | 닛뽕소다 가부시키가이샤 | 접착성 조성물 |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3421891A (en) * | 1964-06-18 | 1969-01-14 | Matsushita Electric Industrial Co Ltd | Electrophotographic materials comprising brominated poly-n-vinyl carbazoles |
| US3485625A (en) * | 1966-06-09 | 1969-12-23 | Eastman Kodak Co | Photoconductive elements containing 2,3,4,5-tetraaryl pyrrole |
| US3546085A (en) * | 1967-01-30 | 1970-12-08 | Xerox Corp | Photoelectrophoretic imaging process and suspension |
| GB1379387A (en) * | 1970-12-11 | 1975-01-02 | Agfa Gevaert | Photoconductive recording materials |
| GB1400993A (en) * | 1971-11-10 | 1975-07-16 | Agfa Gevaert | Electrophotographic material |
| JPS4949506B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1972-01-24 | 1974-12-27 | ||
| US3933492A (en) * | 1972-02-23 | 1976-01-20 | Kabushiki Kaisha Ricoh | Novel photoconductive substances and their application |
| US3871883A (en) * | 1972-12-28 | 1975-03-18 | Ricoh Kk | Electrophotographic photoconductive layer comprising an organic photoconductor and a dicyanomethylene-indenothiophene sensitizer |
| US3912506A (en) * | 1973-05-21 | 1975-10-14 | Eastman Kodak Co | Photoconductive elements containing polymeric binders |
| US3884689A (en) * | 1973-08-30 | 1975-05-20 | Xerox Corp | Polycyclic aromatic polymer as a photoconductor or overlayer |
| JPS5328097B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1973-09-14 | 1978-08-12 | ||
| US4117072A (en) * | 1974-10-16 | 1978-09-26 | Xerox Corporation | Process for enhancement of mechanical properties of photoconductive polymers |
| US4050934A (en) * | 1975-09-22 | 1977-09-27 | Xerox Corporation | Electron acceptor monomers and polymers |
| US4225692A (en) * | 1975-09-22 | 1980-09-30 | Xerox Corporation | Electron acceptor monomers and polymers |
| US4063947A (en) * | 1975-10-29 | 1977-12-20 | Xerox Corporation | Photoconductive insulating films comprising fluorenone-substituted oligomers |
| JPS56143438A (en) * | 1980-04-10 | 1981-11-09 | Mita Ind Co Ltd | Improvement of electrophotographic sensitive layer |
| DE3032773A1 (de) * | 1980-08-30 | 1982-05-06 | Hoechst Ag, 6000 Frankfurt | Elektrophotographisches aufzeichnungsmaterial und verfahren zu seiner herstellung |
| US4853308A (en) * | 1987-11-09 | 1989-08-01 | Xerox Corporation | Photoresponsive imaging members with fluorene hole transporting layers |
| US5356742A (en) * | 1991-03-01 | 1994-10-18 | Ricoh Company, Ltd. | Dipyrenylamine derivatives and electrophotographic photoconductor comprising the same |
| KR102383692B1 (ko) * | 2017-06-30 | 2022-04-05 | 동우 화인켐 주식회사 | 하드마스크용 조성물 |
| EP4549430A1 (en) * | 2022-06-30 | 2025-05-07 | Mitsubishi Chemical Corporation | Compound, polymerizable composition, polymer, holographic recording medium, optical material and optical component |
| CN117343059B (zh) * | 2023-12-04 | 2024-02-06 | 烟台九目化学股份有限公司 | 一种萘并咪唑并咔唑类化合物及其应用 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2146209A (en) * | 1936-07-31 | 1939-02-07 | Du Pont | Preparation of resinous imides of substituted acrylic acids |
| US2288197A (en) * | 1939-08-31 | 1942-06-30 | Kranzlein Georg | Acrylic acid amides |
| US2409126A (en) * | 1943-03-20 | 1946-10-08 | Eastman Kodak Co | Synthetic nitrogenous resins and intermediates therefor |
| US2643958A (en) * | 1949-08-03 | 1953-06-30 | Bayer Ag | Textile printing paste and method of coating therewith |
| US2566162A (en) * | 1950-08-18 | 1951-08-28 | Eastman Kodak Co | Acrylyl sulfanilamides and polymers thereof |
| US2886558A (en) * | 1953-08-17 | 1959-05-12 | American Cyanamid Co | Preparation of polymers containing carboxy groups from polymers of acrylamide |
| US2820777A (en) * | 1954-04-29 | 1958-01-21 | American Cyanamid Co | Process of preparing polyacrylamide |
| US2954291A (en) * | 1957-01-04 | 1960-09-27 | Haloid Xerox Inc | Method for preparing a spirit duplicating master |
| US2962376A (en) * | 1958-05-14 | 1960-11-29 | Haloid Xerox Inc | Xerographic member |
| US3070442A (en) * | 1958-07-18 | 1962-12-25 | Du Pont | Process for producing colored polymeric relief images and elements therefor |
| DE1248946B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1959-01-26 | |||
| BE588780A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1959-03-17 |
-
0
- NL NL252125D patent/NL252125A/xx unknown
- LU LU38672D patent/LU38672A1/xx unknown
- NL NL131776D patent/NL131776C/xx active
-
1959
- 1959-05-30 DE DEK37869A patent/DE1131988B/de active Pending
-
1960
- 1960-05-23 US US30747A patent/US3307940A/en not_active Expired - Lifetime
- 1960-05-23 CH CH588060A patent/CH406849A/de unknown
- 1960-05-25 GB GB18436/60A patent/GB946107A/en not_active Expired
- 1960-05-27 AU AU60917/60A patent/AU249377B2/en not_active Expired
- 1960-05-28 DK DK209060AA patent/DK104038C/da active
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20190041507A (ko) * | 2016-10-14 | 2019-04-22 | 닛뽕소다 가부시키가이샤 | 접착성 조성물 |
| CN109804033A (zh) * | 2016-10-14 | 2019-05-24 | 日本曹达株式会社 | 粘接性组合物 |
| JPWO2018070079A1 (ja) * | 2016-10-14 | 2019-06-24 | 日本曹達株式会社 | 接着性組成物 |
| JP2021091719A (ja) * | 2016-10-14 | 2021-06-17 | 日本曹達株式会社 | 接着性組成物 |
| KR20210097841A (ko) * | 2016-10-14 | 2021-08-09 | 닛뽕소다 가부시키가이샤 | 접착성 조성물 |
| EP4155361A1 (en) * | 2016-10-14 | 2023-03-29 | Nippon Soda Co., Ltd. | Adhesive composition |
| US11795353B2 (en) | 2016-10-14 | 2023-10-24 | Nippon Soda Co., Ltd. | Adhesive composition |
| US12104092B2 (en) | 2016-10-14 | 2024-10-01 | Nippon Soda Co., Ltd. | Adhesive composition |
Also Published As
| Publication number | Publication date |
|---|---|
| NL131776C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| AU6091760A (en) | 1960-12-01 |
| DE1131988B (de) | 1962-06-20 |
| US3307940A (en) | 1967-03-07 |
| CH406849A (de) | 1966-01-31 |
| AU249377B2 (en) | 1960-12-01 |
| NL252125A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| LU38672A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | |
| DK104038C (da) | 1966-03-21 |
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