JPS6319867B2 - - Google Patents
Info
- Publication number
- JPS6319867B2 JPS6319867B2 JP56148346A JP14834681A JPS6319867B2 JP S6319867 B2 JPS6319867 B2 JP S6319867B2 JP 56148346 A JP56148346 A JP 56148346A JP 14834681 A JP14834681 A JP 14834681A JP S6319867 B2 JPS6319867 B2 JP S6319867B2
- Authority
- JP
- Japan
- Prior art keywords
- carrier
- group
- photoreceptor
- layer
- substance
- 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
- 108091008695 photoreceptors Proteins 0.000 claims description 59
- 239000000126 substance Substances 0.000 claims description 28
- 125000005259 triarylamine group Chemical group 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000732 arylene group Chemical group 0.000 claims description 3
- 125000004104 aryloxy group Chemical group 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 60
- 239000011230 binding agent Substances 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 14
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 13
- 239000000463 material Substances 0.000 description 10
- 238000000034 method Methods 0.000 description 9
- 230000035945 sensitivity Effects 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- 239000000049 pigment Substances 0.000 description 7
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 6
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 6
- 239000004417 polycarbonate Substances 0.000 description 6
- 229920000515 polycarbonate Polymers 0.000 description 6
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 5
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 229910052711 selenium Inorganic materials 0.000 description 5
- 239000011669 selenium Substances 0.000 description 5
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 4
- 229920000728 polyester Polymers 0.000 description 4
- 229920006267 polyester film Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- 238000012360 testing method Methods 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 239000004419 Panlite Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 230000014759 maintenance of location Effects 0.000 description 3
- 239000000203 mixture Substances 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
- LVGLBCQZYRCDFB-UHFFFAOYSA-N 10,10-dibromoanthracen-9-one Chemical compound C1=CC=C2C(Br)(Br)C3=CC=CC=C3C(=O)C2=C1 LVGLBCQZYRCDFB-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 239000012790 adhesive layer Substances 0.000 description 2
- 230000004888 barrier function Effects 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000010419 fine particle Substances 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 239000005457 ice water Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000003252 repetitive effect Effects 0.000 description 2
- -1 sodium alkoxide Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- NKARVHNAACNYGE-UHFFFAOYSA-N 1-(diethoxyphosphorylmethyl)-4-methoxybenzene Chemical compound CCOP(=O)(OCC)CC1=CC=C(OC)C=C1 NKARVHNAACNYGE-UHFFFAOYSA-N 0.000 description 1
- MEKOFIRRDATTAG-UHFFFAOYSA-N 2,2,5,8-tetramethyl-3,4-dihydrochromen-6-ol Chemical compound C1CC(C)(C)OC2=C1C(C)=C(O)C=C2C MEKOFIRRDATTAG-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
- KXGFMDJXCMQABM-UHFFFAOYSA-N 2-methoxy-6-methylphenol Chemical compound [CH]OC1=CC=CC([CH])=C1O KXGFMDJXCMQABM-UHFFFAOYSA-N 0.000 description 1
- WUPHOULIZUERAE-UHFFFAOYSA-N 3-(oxolan-2-yl)propanoic acid Chemical compound OC(=O)CCC1CCCO1 WUPHOULIZUERAE-UHFFFAOYSA-N 0.000 description 1
- 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 description 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004420 Iupilon Substances 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 229910001370 Se alloy Inorganic materials 0.000 description 1
- 206010070834 Sensitisation Diseases 0.000 description 1
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 150000003934 aromatic aldehydes Chemical class 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 229910052980 cadmium sulfide Inorganic materials 0.000 description 1
- 150000001716 carbazoles Chemical class 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- QKGBKPZAXXBLJE-UHFFFAOYSA-N diethyl 4-methylbenzylphosphonate Chemical compound CCOP(=O)(OCC)CC1=CC=C(C)C=C1 QKGBKPZAXXBLJE-UHFFFAOYSA-N 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- HTENFZMEHKCNMD-UHFFFAOYSA-N helio brilliant orange rk Chemical compound C1=CC=C2C(=O)C(C=C3Br)=C4C5=C2C1=C(Br)C=C5C(=O)C1=CC=CC3=C14 HTENFZMEHKCNMD-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 229910003437 indium oxide Inorganic materials 0.000 description 1
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical group C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 238000010030 laminating Methods 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- NYGZLYXAPMMJTE-UHFFFAOYSA-M metanil yellow Chemical group [Na+].[O-]S(=O)(=O)C1=CC=CC(N=NC=2C=CC(NC=3C=CC=CC=3)=CC=2)=C1 NYGZLYXAPMMJTE-UHFFFAOYSA-M 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- 238000006053 organic reaction Methods 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 125000003367 polycyclic group Chemical group 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000008313 sensitization Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 239000011787 zinc oxide Substances 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
- G03G5/0616—Hydrazines; Hydrazones
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14834681A JPS5865440A (ja) | 1981-09-18 | 1981-09-18 | 電子写真感光体 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14834681A JPS5865440A (ja) | 1981-09-18 | 1981-09-18 | 電子写真感光体 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5865440A JPS5865440A (ja) | 1983-04-19 |
| JPS6319867B2 true JPS6319867B2 (de) | 1988-04-25 |
Family
ID=15450702
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14834681A Granted JPS5865440A (ja) | 1981-09-18 | 1981-09-18 | 電子写真感光体 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5865440A (de) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0709364A1 (de) | 1994-10-31 | 1996-05-01 | Hodogaya Chemical Co Ltd | Tetrahydronaphthylaminostyrolverbindungen und ihre Verwendung in electrophotographischen Photorezeptoren |
| JP2005289842A (ja) * | 2004-03-31 | 2005-10-20 | Hodogaya Chem Co Ltd | 電子製品材料の精製方法 |
| WO2007086439A1 (ja) | 2006-01-25 | 2007-08-02 | Hodogaya Chemical Co., Ltd. | ｐ－ターフェニル化合物混合物及び該化合物混合物を用いた電子写真用感光体 |
| EP2518046A1 (de) | 2004-05-25 | 2012-10-31 | Hodogaya Chemical Co., Ltd. | p-Terphenyl-Verbindung und elektrophotographischer Photoleiter damit |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58190953A (ja) * | 1982-04-30 | 1983-11-08 | Ricoh Co Ltd | 電子写真用感光体 |
| US4515883A (en) * | 1983-04-14 | 1985-05-07 | Ricoh Company, Ltd. | Stilbene derivatives, distyryl derivatives and electrophotographic photoconductor comprising at least one of the derivatives |
| JPS59195658A (ja) * | 1983-04-21 | 1984-11-06 | Ricoh Co Ltd | 電子写真用感光体 |
| JPS6093444A (ja) * | 1983-10-28 | 1985-05-25 | Ricoh Co Ltd | 電子写真用感光体 |
| JPS6098437A (ja) * | 1983-11-04 | 1985-06-01 | Ricoh Co Ltd | 電子写真用感光体 |
| JPS6114642A (ja) * | 1984-06-29 | 1986-01-22 | Konishiroku Photo Ind Co Ltd | 電子写真感光体 |
| JPS62103651A (ja) * | 1985-10-31 | 1987-05-14 | Konishiroku Photo Ind Co Ltd | 電子写真感光体 |
| WO1988002880A1 (en) * | 1986-10-20 | 1988-04-21 | Konica Corporation | Photosensitive member |
| JPS63149652A (ja) * | 1986-12-15 | 1988-06-22 | Konica Corp | 感光体 |
| US5000831A (en) * | 1987-03-09 | 1991-03-19 | Minolta Camera Kabushiki Kaisha | Method of production of amorphous hydrogenated carbon layer |
| DE3814105C2 (de) * | 1987-04-27 | 1999-02-04 | Minolta Camera Kk | Elektrophotographisches Aufzeichnungsmaterial |
| JPH0675204B2 (ja) * | 1987-08-13 | 1994-09-21 | コニカ株式会社 | 電子写真感光体 |
| 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 |
| EP0437310B1 (de) * | 1990-01-08 | 1997-03-26 | Hitachi, Ltd. | Lichtempfindliches Element für Elektrophotographie |
| JPH0751540B2 (ja) * | 1990-02-20 | 1995-06-05 | 株式会社リコー | スチルベン誘導体 |
| JPH02243657A (ja) * | 1990-02-23 | 1990-09-27 | Ricoh Co Ltd | スチルベン誘導体 |
| US5278014A (en) * | 1991-06-21 | 1994-01-11 | Konica Corporation | Electrophotographic photoreceptor |
| JP3196568B2 (ja) * | 1995-05-12 | 2001-08-06 | 日本電気株式会社 | 電子写真感光体 |
| JP2940502B2 (ja) * | 1996-02-28 | 1999-08-25 | 日本電気株式会社 | 電子写真感光体 |
| JP3235661B2 (ja) * | 1998-03-30 | 2001-12-04 | 日本電気株式会社 | 三ハロゲン化窒素を用いたトリフェニルアミン化合物の製造方法 |
| US6225015B1 (en) | 1998-06-04 | 2001-05-01 | Mitsubishi Paper Mills Ltd. | Oxytitanium phthalocyanine process for the production thereof and electrophotographic photoreceptor to which the oxytitanium phthalocyanine is applied |
| EP2309584A4 (de) | 2008-08-06 | 2012-08-15 | Mitsubishi Paper Mills Ltd | Farbstoff für eine farbstoffsensibilisierte solarzelle, halbleiterelektrode und farbstoffsensibilisierte solarzelle |
| JP5636728B2 (ja) * | 2009-11-05 | 2014-12-10 | 三菱化学株式会社 | 電子写真感光体、電子写真感光体カートリッジ、及び画像形成装置 |
| JP2011118177A (ja) * | 2009-12-03 | 2011-06-16 | Mitsubishi Chemicals Corp | フタロシアニン顔料及びスチルベン系化合物を含有する電子写真感光体、電子写真感光体カートリッジ及び画像形成装置 |
| JP5346326B2 (ja) * | 2010-07-21 | 2013-11-20 | 高砂香料工業株式会社 | 電子写真感光体 |
| JP5762932B2 (ja) | 2010-11-30 | 2015-08-12 | 信越化学工業株式会社 | シラノール基を有するトリアリールアミン誘導体 |
| JP5894945B2 (ja) | 2013-02-18 | 2016-03-30 | 信越化学工業株式会社 | 蛍光性化合物、その製造方法、及び蛍光性樹脂組成物 |
| JP6337561B2 (ja) | 2014-03-27 | 2018-06-06 | 株式会社リコー | ペロブスカイト型太陽電池 |
| EP3975278A1 (de) | 2014-04-16 | 2022-03-30 | Ricoh Company, Ltd. | Element zur photoelektrischen umwandlung |
| EP3410506B1 (de) | 2016-01-25 | 2022-03-30 | Ricoh Company, Ltd. | Element zur photoelektrischen umwandlung |
| US10651390B2 (en) | 2016-06-08 | 2020-05-12 | Ricoh Company, Ltd. | Tertiary amine compound, photoelectric conversion element, and solar cell |
| CN117812920A (zh) | 2016-12-07 | 2024-04-02 | 株式会社理光 | 光电转换元件 |
| US20220302399A1 (en) | 2019-06-10 | 2022-09-22 | Ricoh Company, Ltd. | Photoelectric conversion element, photoelectric conversion element module, electronic device, and power supply module |
| EP4000098A1 (de) | 2019-07-16 | 2022-05-25 | Ricoh Company, Ltd. | Solarzellenmodul, elektronisches gerät und stromversorgungsmodul |
| US20210167287A1 (en) | 2019-11-28 | 2021-06-03 | Tamotsu Horiuchi | Photoelectric conversion element, photoelectric conversion module, electronic device, and power supply module |
| JP7413833B2 (ja) | 2020-02-27 | 2024-01-16 | 株式会社リコー | 光電変換素子及び光電変換モジュール |
| EP3872861B1 (de) | 2020-02-27 | 2023-06-28 | Ricoh Company, Ltd. | Fotoelektrisches umwandlungselement und fotoelektrisches umwandlungsmodul |
| EP4064355A1 (de) | 2021-03-23 | 2022-09-28 | Ricoh Company, Ltd. | Solarzellenmodul |
| EP4377978A1 (de) | 2021-07-29 | 2024-06-05 | Ricoh Company, Ltd. | Photoelektrisches umwandlungselement und solarzellenmodul |
| JP2023137773A (ja) | 2022-03-18 | 2023-09-29 | 株式会社リコー | 光電変換素子、光電変換モジュール、電子機器、及び太陽電池モジュール |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3567450A (en) * | 1968-02-20 | 1971-03-02 | Eastman Kodak Co | Photoconductive elements containing substituted triarylamine photoconductors |
| JPS4829063A (de) * | 1971-08-16 | 1973-04-17 | ||
| JPS5188226A (de) * | 1974-12-20 | 1976-08-02 | ||
| JPS5387227A (en) * | 1976-12-22 | 1978-08-01 | Eastman Kodak Co | Photoconductive element |
| JPS5461936A (en) * | 1977-10-26 | 1979-05-18 | Ricoh Co Ltd | Photoreceptor for electrophotography |
-
1981
- 1981-09-18 JP JP14834681A patent/JPS5865440A/ja active Granted
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3567450A (en) * | 1968-02-20 | 1971-03-02 | Eastman Kodak Co | Photoconductive elements containing substituted triarylamine photoconductors |
| JPS4829063A (de) * | 1971-08-16 | 1973-04-17 | ||
| JPS5188226A (de) * | 1974-12-20 | 1976-08-02 | ||
| JPS5387227A (en) * | 1976-12-22 | 1978-08-01 | Eastman Kodak Co | Photoconductive element |
| JPS5461936A (en) * | 1977-10-26 | 1979-05-18 | Ricoh Co Ltd | Photoreceptor for electrophotography |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0709364A1 (de) | 1994-10-31 | 1996-05-01 | Hodogaya Chemical Co Ltd | Tetrahydronaphthylaminostyrolverbindungen und ihre Verwendung in electrophotographischen Photorezeptoren |
| JP2005289842A (ja) * | 2004-03-31 | 2005-10-20 | Hodogaya Chem Co Ltd | 電子製品材料の精製方法 |
| EP2518046A1 (de) | 2004-05-25 | 2012-10-31 | Hodogaya Chemical Co., Ltd. | p-Terphenyl-Verbindung und elektrophotographischer Photoleiter damit |
| EP2759531A1 (de) | 2004-05-25 | 2014-07-30 | Hodogaya Chemical Co., Ltd. | p-Terphenyl-Verbindung und elektrofotografischer Photoleiter damit |
| WO2007086439A1 (ja) | 2006-01-25 | 2007-08-02 | Hodogaya Chemical Co., Ltd. | ｐ－ターフェニル化合物混合物及び該化合物混合物を用いた電子写真用感光体 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5865440A (ja) | 1983-04-19 |