ES251855A1 - Un procedimiento de fabricacion de un material para reproduccion electrofotografica - Google Patents
Un procedimiento de fabricacion de un material para reproduccion electrofotograficaInfo
- Publication number
- ES251855A1 ES251855A1 ES0251855A ES251855A ES251855A1 ES 251855 A1 ES251855 A1 ES 251855A1 ES 0251855 A ES0251855 A ES 0251855A ES 251855 A ES251855 A ES 251855A ES 251855 A1 ES251855 A1 ES 251855A1
- Authority
- ES
- Spain
- Prior art keywords
- phenyl
- resins
- alkyl
- amino
- substituted
- 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
- -1 aminophenyl Chemical group 0.000 abstract 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 12
- 229920005989 resin Polymers 0.000 abstract 12
- 239000011347 resin Substances 0.000 abstract 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 5
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 abstract 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 3
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical compound C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 abstract 2
- WKHQADGJXFRQJD-UHFFFAOYSA-N 2,4,5-triphenyl-1,3-oxazole Chemical class C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)O1 WKHQADGJXFRQJD-UHFFFAOYSA-N 0.000 abstract 2
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 abstract 2
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000000068 chlorophenyl group Chemical group 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 239000000975 dye Substances 0.000 abstract 2
- 230000008018 melting Effects 0.000 abstract 2
- 238000002844 melting Methods 0.000 abstract 2
- 239000000025 natural resin Substances 0.000 abstract 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 229920002554 vinyl polymer Chemical group 0.000 abstract 2
- VIAMIUDTTIDZCA-ODZAUARKSA-N (z)-but-2-enedioic acid;propane-1,2,3-triol Chemical class OCC(O)CO.OC(=O)\C=C/C(O)=O VIAMIUDTTIDZCA-ODZAUARKSA-N 0.000 abstract 1
- YJWZHHLRVPCSGP-UHFFFAOYSA-N 1-(2-amino-4-chlorophenyl)ethanone Chemical compound CC(=O)C1=CC=C(Cl)C=C1N YJWZHHLRVPCSGP-UHFFFAOYSA-N 0.000 abstract 1
- MBUPVGIGAMCMBT-UHFFFAOYSA-N 2-bromo-1-(4-nitrophenyl)ethanone Chemical compound [O-][N+](=O)C1=CC=C(C(=O)CBr)C=C1 MBUPVGIGAMCMBT-UHFFFAOYSA-N 0.000 abstract 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 abstract 1
- NHRHTQRGWGFACW-UHFFFAOYSA-N 2-phenyl-1h-pyrrol-3-amine Chemical class C1=CNC(C=2C=CC=CC=2)=C1N NHRHTQRGWGFACW-UHFFFAOYSA-N 0.000 abstract 1
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 abstract 1
- OAPKOHYAIHCLSG-UHFFFAOYSA-N 4-(4-nitrophenyl)-2-phenyl-1,3-oxazole Chemical compound C1=CC([N+](=O)[O-])=CC=C1C1=COC(C=2C=CC=CC=2)=N1 OAPKOHYAIHCLSG-UHFFFAOYSA-N 0.000 abstract 1
- UGJDXRVQCYBXAJ-UHFFFAOYSA-N 4-(dimethylamino)benzoyl chloride Chemical compound CN(C)C1=CC=C(C(Cl)=O)C=C1 UGJDXRVQCYBXAJ-UHFFFAOYSA-N 0.000 abstract 1
- 235000007173 Abies balsamea Nutrition 0.000 abstract 1
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 abstract 1
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004857 Balsam Substances 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- 244000018716 Impatiens biflora Species 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- 229920000877 Melamine resin Polymers 0.000 abstract 1
- 239000004952 Polyamide Substances 0.000 abstract 1
- 244000028419 Styrax benzoin Species 0.000 abstract 1
- 235000000126 Styrax benzoin Nutrition 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 abstract 1
- 235000008411 Sumatra benzointree Nutrition 0.000 abstract 1
- 229920001807 Urea-formaldehyde Polymers 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 239000004411 aluminium Substances 0.000 abstract 1
- 229910052782 aluminium Inorganic materials 0.000 abstract 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract 1
- 150000003935 benzaldehydes Chemical class 0.000 abstract 1
- 229920003086 cellulose ether Polymers 0.000 abstract 1
- 229930002875 chlorophyll Natural products 0.000 abstract 1
- 235000019804 chlorophyll Nutrition 0.000 abstract 1
- ATNHDLDRLWWWCB-AENOIHSZSA-M chlorophyll a Chemical compound C1([C@@H](C(=O)OC)C(=O)C2=C3C)=C2N2C3=CC(C(CC)=C3C)=[N+]4C3=CC3=C(C=C)C(C)=C5N3[Mg-2]42[N+]2=C1[C@@H](CCC(=O)OC\C=C(/C)CCC[C@H](C)CCC[C@H](C)CCCC(C)C)[C@H](C)C2=C5 ATNHDLDRLWWWCB-AENOIHSZSA-M 0.000 abstract 1
- 239000008199 coating composition Substances 0.000 abstract 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 abstract 1
- ZJXZSIYSNXKHEA-UHFFFAOYSA-N ethyl dihydrogen phosphate Chemical compound CCOP(O)(O)=O ZJXZSIYSNXKHEA-UHFFFAOYSA-N 0.000 abstract 1
- 239000011521 glass Substances 0.000 abstract 1
- 235000019382 gum benzoic Nutrition 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- QDKCNONIHRLWDD-UHFFFAOYSA-N n,n-diethyl-4-(2-phenyl-1,3-oxazol-4-yl)aniline Chemical compound C1=CC(N(CC)CC)=CC=C1C1=COC(C=2C=CC=CC=2)=N1 QDKCNONIHRLWDD-UHFFFAOYSA-N 0.000 abstract 1
- GTDQGKWDWVUKTI-UHFFFAOYSA-N o-aminoacetophenone Chemical compound CC(=O)C1=CC=CC=C1N GTDQGKWDWVUKTI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002916 oxazoles Chemical class 0.000 abstract 1
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 abstract 1
- 229920001568 phenolic resin Polymers 0.000 abstract 1
- 239000005011 phenolic resin Substances 0.000 abstract 1
- 229920002647 polyamide Polymers 0.000 abstract 1
- 229920000728 polyester Polymers 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 229920000137 polyphosphoric acid Polymers 0.000 abstract 1
- 229920005990 polystyrene resin Polymers 0.000 abstract 1
- 239000004814 polyurethane Substances 0.000 abstract 1
- 229920002635 polyurethane Polymers 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 238000007761 roller coating Methods 0.000 abstract 1
- 230000001235 sensitizing effect Effects 0.000 abstract 1
- 238000005507 spraying Methods 0.000 abstract 1
- 235000011149 sulphuric acid Nutrition 0.000 abstract 1
- 239000001117 sulphuric acid Substances 0.000 abstract 1
- 229920003002 synthetic resin Polymers 0.000 abstract 1
- 239000000057 synthetic resin Substances 0.000 abstract 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
- 239000011701 zinc Substances 0.000 abstract 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
- G03G5/0624—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/32—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon 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
- G03G5/0644—Heterocyclic compounds containing two or more hetero rings
- G03G5/0661—Heterocyclic compounds containing two or more hetero rings in different ring systems, each system containing at least one hetero ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEK35572A DE1120875B (de) | 1958-08-20 | 1958-08-20 | Material fuer elektrophotographische Reproduktion |
Publications (1)
Publication Number | Publication Date |
---|---|
ES251855A1 true ES251855A1 (es) | 1960-03-16 |
Family
ID=7220394
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES0251855A Expired ES251855A1 (es) | 1958-08-20 | 1959-08-20 | Un procedimiento de fabricacion de un material para reproduccion electrofotografica |
Country Status (8)
Country | Link |
---|---|
US (1) | US3257203A (es) |
BE (1) | BE581861A (es) |
CH (1) | CH379280A (es) |
DE (1) | DE1120875B (es) |
ES (1) | ES251855A1 (es) |
FR (1) | FR1232805A (es) |
GB (1) | GB874634A (es) |
NL (2) | NL126440C (es) |
Families Citing this family (133)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE585507A (es) * | 1960-03-31 | |||
NL301475A (es) * | 1962-12-18 | |||
DE1597784C3 (de) * | 1967-08-31 | 1976-01-02 | Hoechst Ag, 6000 Frankfurt | Sensibilisierte Druckplatte |
US3944417A (en) * | 1968-11-27 | 1976-03-16 | Hoechst Aktiengesellschaft | Process for the electrophotographic production of printing plates |
DE2336094C2 (de) * | 1973-07-16 | 1983-03-03 | Hoechst Ag, 6000 Frankfurt | Elektrophotographisches Aufzeichungsmaterial |
US4123541A (en) * | 1976-02-12 | 1978-10-31 | Mitsubishi Chemical Industries Limited | 2-Aminomethyl-5-phenyloxazoles and the pharmaceutically acceptable salts thereof |
DE3005695A1 (de) * | 1980-02-15 | 1981-08-20 | Hoechst Ag, 6000 Frankfurt | Verfahren zur herstellung einer flachdruckform auf elektrophotographischem wege |
US4340657A (en) * | 1980-02-19 | 1982-07-20 | Polychrome Corporation | Novel radiation-sensitive articles |
DE3024772A1 (de) * | 1980-06-30 | 1982-01-28 | Hoechst Ag, 6000 Frankfurt | Elastische, laminierbare lichtempfindliche schicht |
DE3210576A1 (de) * | 1982-03-23 | 1983-10-06 | Hoechst Ag | Elektrophotographisches aufzeichnungsmaterial |
JPS5942352A (ja) | 1982-09-01 | 1984-03-08 | Fuji Photo Film Co Ltd | ジスアゾ化合物、それを含む光導電性組成物及び電子写真感光体 |
DE3304330A1 (de) * | 1983-02-09 | 1984-08-09 | Basf Ag, 6700 Ludwigshafen | Neue 2h-v-triazolyl(4,5-d)-pyrimidine und deren verwendung |
DE3313798A1 (de) * | 1983-04-15 | 1984-10-18 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
US4533612A (en) * | 1983-04-27 | 1985-08-06 | Basf Aktiengesellschaft | Electrophotographic recording materials containing special charge carrier-transporting compounds |
DE3324090A1 (de) * | 1983-07-05 | 1985-01-17 | Basf Ag, 6700 Ludwigshafen | Elektrophotographische aufzeichnungsmaterialien mit verbesserter photoempfindlichkeit |
DE3324089A1 (de) * | 1983-07-05 | 1985-01-17 | Basf Ag, 6700 Ludwigshafen | Elektrophotographische aufzeichnungsmaterialien mit verbesserter photoempfindlichkeit |
DE3409888A1 (de) * | 1984-03-17 | 1985-09-19 | Hoechst Ag, 6230 Frankfurt | Lichtempfindliches aufzeichnungsmaterial und dessen verwendung in einem verfahren zum herstellen einer druckform oder einer gedruckten schaltung |
JPS60237454A (ja) * | 1984-05-09 | 1985-11-26 | Hitachi Chem Co Ltd | 電子写真感光体 |
DE3417951A1 (de) * | 1984-05-15 | 1985-11-21 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
DE3506436A1 (de) * | 1985-02-23 | 1986-08-28 | Hoechst Ag, 6230 Frankfurt | Neue sulfonhaltige styrolderivate, verfahren zu deren herstellung und deren verwendung |
DE3509147A1 (de) * | 1985-03-14 | 1986-09-18 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
DE3513747A1 (de) * | 1985-04-17 | 1986-10-23 | Hoechst Ag, 6230 Frankfurt | Elektrophotographisches aufzeichnungsmaterial |
DE3523180A1 (de) * | 1985-06-28 | 1987-01-08 | Hoechst Ag | Neue 1,3,4-tri-(het-)aryl-isochinoline, verfahren zu ihrer herstellung und ihre verwendung als photoleitfaehige verbindungen |
US4663121A (en) * | 1985-10-15 | 1987-05-05 | The Dow Chemical Company | Use of phenyloxazoles as corrosion inhibitors |
DE3706880A1 (de) * | 1987-03-04 | 1988-09-15 | Hoechst Ag | 4-chloroxazol-derivate, verfahren zu ihrer herstellung und ihre verwendung |
DE3740421A1 (de) * | 1987-11-28 | 1989-06-08 | Basf Ag | Mehrschichtiges, elektrophotographisches aufzeichnungsmaterial |
DE3740420A1 (de) * | 1987-11-28 | 1989-06-08 | Basf Ag | Mehrschichtiges elektrophotographisches aufzeichnungsmaterial |
US5121029A (en) * | 1987-12-11 | 1992-06-09 | Idemitsu Kosan Co., Ltd. | Electroluminescence device having an organic electroluminescent element |
DE68921437T2 (de) * | 1988-12-14 | 1995-06-29 | Idemitsu Kosan Co | Elektrolumineszierende Vorrichtung. |
US5130603A (en) | 1989-03-20 | 1992-07-14 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
DE3932160A1 (de) * | 1989-09-27 | 1991-04-11 | Hoechst Ag | Elektrophotographisches aufzeichnungsmaterial |
US5443922A (en) * | 1991-11-07 | 1995-08-22 | Konica Corporation | Organic thin film electroluminescence element |
EP0605739A4 (en) * | 1992-07-23 | 1994-11-30 | Idemitsu Kosan Co | ORGANIC ELECTROLUMINESCENT DEVICE. |
US5585213A (en) | 1994-06-10 | 1996-12-17 | Toyo Ink Manufacturing Co., Ltd. | Hole-transporting material and its use |
US5681664A (en) | 1994-08-04 | 1997-10-28 | Toyo Ink Manufacturing Co., Ltd. | Hole-transporting material and use thereof |
DE19510526A1 (de) * | 1995-03-23 | 1996-09-26 | Hoechst Ag | Elektrophotographisches Aufzeichnungsmaterial für die Herstellung von Druckplatten |
JPH09222741A (ja) | 1995-12-11 | 1997-08-26 | Toyo Ink Mfg Co Ltd | 正孔輸送材料およびその用途 |
CN1962583A (zh) | 1998-12-28 | 2007-05-16 | 出光兴产株式会社 | 有机场致发光装置 |
TW463528B (en) | 1999-04-05 | 2001-11-11 | Idemitsu Kosan Co | Organic electroluminescence element and their preparation |
US6376144B1 (en) | 2000-08-03 | 2002-04-23 | Kodak Polychrome Graphics, Llc | Organic photoconductive composition |
MY151199A (en) | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
RS20050175A (en) * | 2002-08-23 | 2007-09-21 | Rigel Pharmaceuticals Inc., | Pyridyl substituted heterocycles useful for treating or preventing hcv infection |
JP4506113B2 (ja) | 2002-09-20 | 2010-07-21 | 東ソー株式会社 | フルオレン骨格を有する新規アリールアミン誘導体、その合成中間体及びこれらの製造方法並びに有機el素子 |
US7115642B2 (en) | 2003-05-02 | 2006-10-03 | Rigel Pharmaceuticals, Inc. | Substituted diphenyl isoxazoles, pyrazoles and oxadiazoles useful for treating HCV infection |
EP1620412A2 (en) * | 2003-05-02 | 2006-02-01 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds and hydro isomers thereof |
US7220745B2 (en) * | 2003-05-15 | 2007-05-22 | Rigel Pharmaceuticals | Heterocyclic compounds useful to treat HCV |
KR101164687B1 (ko) | 2003-07-02 | 2012-07-11 | 이데미쓰 고산 가부시키가이샤 | 유기 전기발광 소자 및 이를 이용한 표시 장치 |
WO2005006945A2 (en) * | 2003-07-03 | 2005-01-27 | The Salk Institute For Biological Studies | Methods for treating neural disorders and compounds useful therefor |
US7018756B2 (en) | 2003-09-05 | 2006-03-28 | Xerox Corporation | Dual charge transport layer and photoconductive imaging member including the same |
US7410979B2 (en) * | 2003-11-19 | 2008-08-12 | Rigel Pharmaceuticals, Inc. | Synergistically effective combinations of dihaloacetamide compounds and interferon or ribavirin against HCV infections |
US8568902B2 (en) | 2003-12-01 | 2013-10-29 | Idemitsu Kosan Co., Ltd. | Asymmetric monoanthracene derivative, material for organic electroluminescent device and organic electroluminescent device utilizing the same |
CN1914293B (zh) | 2003-12-19 | 2010-12-01 | 出光兴产株式会社 | 有机电致发光器件用发光材料、使用该材料的有机电致发光器件以及有机电致发光器件用材料 |
US7514434B2 (en) | 2004-02-23 | 2009-04-07 | Rigel Pharmaceuticals, Inc. | Heterocyclic compounds having an oxadiazole moiety and hydro isomers thereof |
JP2007530582A (ja) * | 2004-03-26 | 2007-11-01 | ライジェル ファーマシューティカルズ, インコーポレイテッド | 代謝可能部分を含む複素環抗ウイルス化合物およびその使用 |
EP1734794A1 (en) * | 2004-04-06 | 2006-12-20 | Idemitsu Kosan Company Limited | Electrode substrate and its manufacturing method |
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Publication number | Priority date | Publication date | Assignee | Title |
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US2620282A (en) * | 1952-12-02 | Fibrous synthetic material of | ||
US2069807A (en) * | 1934-09-28 | 1937-02-09 | Du Pont | Cellulosic substances and method for preparing same |
US2341009A (en) * | 1936-03-19 | 1944-02-08 | Richards Chemical Works | Method of improving brightness of fibrous materials |
US2176516A (en) * | 1936-06-12 | 1939-10-17 | Agfa Ansco Corp | Polarizing layer |
FR1008598A (fr) * | 1948-04-30 | 1952-05-19 | Onera (Off Nat Aerospatiale) | Procédé pour l'enregistrement graphique ou l'inscription dirccte en matériaux pour la mise en oeuvre de ce procédé |
US2663636A (en) * | 1949-05-25 | 1953-12-22 | Haloid Co | Electrophotographic plate and method of producing same |
GB669590A (en) * | 1949-06-03 | 1952-04-02 | Ilford Ltd | Improvements in or relating to a process for improving the whiteness of colour materials |
US2726246A (en) * | 1951-05-02 | 1955-12-06 | Cassella Farbwerke Mainkur Ag | Fluorescent heterocyclic compounds and process for their manufacture |
US2709702A (en) * | 1951-10-12 | 1955-05-31 | Gen Aniline & Film Corp | Fluorescent agents |
US2704286A (en) * | 1954-05-07 | 1955-03-15 | Du Pont | Fluorescent whitening agents |
BE553516A (es) * | 1955-12-19 |
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0
- NL NL242505D patent/NL242505A/xx unknown
- BE BE581861D patent/BE581861A/xx unknown
- NL NL126440D patent/NL126440C/xx active
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1959
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- 1959-08-13 CH CH7694459A patent/CH379280A/de unknown
- 1959-08-18 FR FR803023A patent/FR1232805A/fr not_active Expired
- 1959-08-18 US US834417A patent/US3257203A/en not_active Expired - Lifetime
- 1959-08-20 ES ES0251855A patent/ES251855A1/es not_active Expired
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DE1120875B (de) | 1961-12-28 |
NL242505A (es) | |
GB874634A (en) | 1961-08-10 |
FR1232805A (fr) | 1960-10-12 |
CH379280A (de) | 1964-06-30 |
NL126440C (es) | |
US3257203A (en) | 1966-06-21 |
BE581861A (es) |
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