JP2001166516A5 - - Google Patents
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- Publication number
- JP2001166516A5 JP2001166516A5 JP1999353227A JP35322799A JP2001166516A5 JP 2001166516 A5 JP2001166516 A5 JP 2001166516A5 JP 1999353227 A JP1999353227 A JP 1999353227A JP 35322799 A JP35322799 A JP 35322799A JP 2001166516 A5 JP2001166516 A5 JP 2001166516A5
- Authority
- JP
- Japan
- Prior art keywords
- substituent
- group
- general formula
- photosensitive member
- electrophotographic photosensitive
- 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.)
- Granted
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- 125000001424 substituent group Chemical group 0.000 description 78
- 125000003118 aryl group Chemical group 0.000 description 32
- 125000000217 alkyl group Chemical group 0.000 description 18
- 150000001875 compounds Chemical class 0.000 description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 16
- 239000010410 layer Substances 0.000 description 13
- 125000003710 aryl alkyl group Chemical group 0.000 description 12
- 125000000524 functional group Chemical group 0.000 description 11
- 239000000126 substance Substances 0.000 description 10
- 125000000732 arylene group Chemical group 0.000 description 8
- 238000010894 electron beam technology Methods 0.000 description 8
- 230000015654 memory Effects 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 125000002947 alkylene group Chemical group 0.000 description 5
- 238000000113 differential scanning calorimetry Methods 0.000 description 5
- 125000004430 oxygen atom Chemical group O* 0.000 description 5
- 229910052717 sulfur Inorganic materials 0.000 description 5
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 4
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- 230000001133 acceleration Effects 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- WZJYKHNJTSNBHV-UHFFFAOYSA-N benzo[h]quinoline Chemical compound C1=CN=C2C3=CC=CC=C3C=CC2=C1 WZJYKHNJTSNBHV-UHFFFAOYSA-N 0.000 description 4
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 4
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 4
- 125000005843 halogen group Chemical group 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- 239000002344 surface layer Substances 0.000 description 4
- 230000001678 irradiating effect Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical group O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 2
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 2
- 230000020169 heat generation Effects 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000000962 organic group Chemical group 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 229950000688 phenothiazine Drugs 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 230000000379 polymerizing effect Effects 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 125000004434 sulfur atom Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 229930192474 thiophene Natural products 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LVDRREOUMKACNJ-BKMJKUGQSA-N N-[(2R,3S)-2-(4-chlorophenyl)-1-(1,4-dimethyl-2-oxoquinolin-7-yl)-6-oxopiperidin-3-yl]-2-methylpropane-1-sulfonamide Chemical group CC(C)CS(=O)(=O)N[C@H]1CCC(=O)N([C@@H]1c1ccc(Cl)cc1)c1ccc2c(C)cc(=O)n(C)c2c1 LVDRREOUMKACNJ-BKMJKUGQSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 150000004292 cyclic ethers Chemical group 0.000 description 1
- 238000004455 differential thermal analysis Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35322799A JP4136238B2 (ja) | 1999-12-13 | 1999-12-13 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP35322799A JP4136238B2 (ja) | 1999-12-13 | 1999-12-13 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001166516A JP2001166516A (ja) | 2001-06-22 |
| JP2001166516A5 true JP2001166516A5 (enExample) | 2007-01-25 |
| JP4136238B2 JP4136238B2 (ja) | 2008-08-20 |
Family
ID=18429422
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP35322799A Expired - Lifetime JP4136238B2 (ja) | 1999-12-13 | 1999-12-13 | 電子写真感光体、プロセスカートリッジ及び電子写真装置 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JP4136238B2 (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4657900B2 (ja) * | 2004-12-21 | 2011-03-23 | 株式会社リコー | 電子写真感光体、それを用いた画像形成方法、画像形成装置及び画像形成装置用プロセスカートリッジ |
| JP4796348B2 (ja) * | 2005-07-27 | 2011-10-19 | 株式会社リコー | 静電潜像担持体、並びに画像形成装置、画像形成方法及びプロセスカートリッジ |
| JP4813092B2 (ja) * | 2005-05-19 | 2011-11-09 | 株式会社リコー | 電子写真感光体、それを用いた画像形成方法、画像形成装置及び画像形成装置用プロセスカートリッジ |
| JP4699804B2 (ja) * | 2005-05-11 | 2011-06-15 | 株式会社リコー | アクリル酸エステル化合物とその製造方法及び製造中間体 |
| KR100914018B1 (ko) | 2005-05-10 | 2009-08-28 | 가부시키가이샤 리코 | 아크릴 에스테르 화합물 및 이의 제조 중간체, 아크릴에스테르 화합물의 제조 방법, 및 정전 잠상 담지체, 화상형성 방법, 화상 형성 장치 및 프로세스 카트리지 |
| JP4699803B2 (ja) * | 2005-05-10 | 2011-06-15 | 株式会社リコー | アクリル酸エステル化合物とその製造方法及び製造中間体 |
| JP5262014B2 (ja) * | 2006-08-07 | 2013-08-14 | 三菱化学株式会社 | 架橋基を有する有機化合物、有機電界発光素子用組成物および有機電界発光素子 |
| JP5049109B2 (ja) * | 2006-12-11 | 2012-10-17 | 株式会社リコー | 電子写真感光体、それを用いた画像形成方法、画像形成装置及び画像形成装置用プロセスカートリッジ |
| JP5046678B2 (ja) * | 2007-02-22 | 2012-10-10 | 株式会社リコー | 電子写真装置及びプロセスカートリッジ |
| US8846280B2 (en) | 2011-08-22 | 2014-09-30 | Fuji Xerox Co., Ltd. | Compound, charge transporting film, photoelectric conversion device, electrophotographic photoreceptor, process cartridge, and image forming apparatus |
| CN102952030B (zh) | 2011-08-22 | 2016-02-24 | 富士施乐株式会社 | 化合物、电荷输送膜、光电转换装置和电子照相感光体 |
| JP6015264B2 (ja) * | 2012-09-12 | 2016-10-26 | 富士ゼロックス株式会社 | 電子写真感光体、プロセスカートリッジ、及び画像形成装置 |
| JP5892013B2 (ja) | 2012-09-12 | 2016-03-23 | 富士ゼロックス株式会社 | 電荷輸送性膜、光電変換装置、電子写真感光体、プロセスカートリッジ、及び画像形成装置 |
| CN110709780B (zh) * | 2017-06-12 | 2023-05-05 | 京瓷办公信息系统株式会社 | 电子照相感光体、处理盒和图像形成装置 |
| JP7052890B2 (ja) * | 2019-07-17 | 2022-04-12 | 富士電機株式会社 | 電子写真用感光体、その製造方法および電子写真装置 |
-
1999
- 1999-12-13 JP JP35322799A patent/JP4136238B2/ja not_active Expired - Lifetime
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