CN1219805C - 聚合物、其制备方法和电子器件 - Google Patents
聚合物、其制备方法和电子器件 Download PDFInfo
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- CN1219805C CN1219805C CNB028018966A CN02801896A CN1219805C CN 1219805 C CN1219805 C CN 1219805C CN B028018966 A CNB028018966 A CN B028018966A CN 02801896 A CN02801896 A CN 02801896A CN 1219805 C CN1219805 C CN 1219805C
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- polymkeric substance
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- alkyl
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- Expired - Fee Related
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 17
- 238000000034 method Methods 0.000 title claims description 20
- 239000000203 mixture Substances 0.000 claims abstract description 29
- 238000007641 inkjet printing Methods 0.000 claims abstract description 18
- -1 polyphenylene-vinylene Polymers 0.000 claims abstract description 8
- 238000004519 manufacturing process Methods 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 53
- 239000000463 material Substances 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 229910052740 iodine Inorganic materials 0.000 claims description 5
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 3
- 239000005864 Sulphur Substances 0.000 claims description 3
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 150000008051 alkyl sulfates Chemical class 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000005842 heteroatom Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 3
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 229920000553 poly(phenylenevinylene) Polymers 0.000 abstract description 24
- 239000000758 substrate Substances 0.000 abstract 1
- 239000002585 base Substances 0.000 description 32
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 25
- 238000007639 printing Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 description 11
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 10
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Divinylene sulfide Natural products C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 7
- 229920002120 photoresistant polymer Polymers 0.000 description 6
- 229930192474 thiophene Natural products 0.000 description 5
- 238000005401 electroluminescence Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 238000011161 development Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000002243 precursor Substances 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- KUFFULVDNCHOFZ-UHFFFAOYSA-N 2,4-xylenol Chemical compound CC1=CC=C(O)C(C)=C1 KUFFULVDNCHOFZ-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Natural products CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- 241000790917 Dioxys <bee> Species 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000004416 alkarylalkyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 229920006335 epoxy glue Polymers 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 210000003746 feather Anatomy 0.000 description 1
- 244000144992 flock Species 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000011221 initial treatment Methods 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 231100000989 no adverse effect Toxicity 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- SGDMQXAOPGGMAH-UHFFFAOYSA-N phenol;thiophene Chemical compound C=1C=CSC=1.OC1=CC=CC=C1 SGDMQXAOPGGMAH-UHFFFAOYSA-N 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/02—Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/26—Removing halogen atoms or halogen-containing groups from the molecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G2261/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G2261/30—Monomer units or repeat units incorporating structural elements in the main chain
- C08G2261/31—Monomer units or repeat units incorporating structural elements in the main chain incorporating aromatic structural elements in the main chain
- C08G2261/312—Non-condensed aromatic systems, e.g. benzene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K71/00—Manufacture or treatment specially adapted for the organic devices covered by this subclass
- H10K71/10—Deposition of organic active material
- H10K71/12—Deposition of organic active material using liquid deposition, e.g. spin coating
- H10K71/13—Deposition of organic active material using liquid deposition, e.g. spin coating using printing techniques, e.g. ink-jet printing or screen printing
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/114—Poly-phenylenevinylene; Derivatives thereof
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Electroluminescent Light Sources (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Abstract
Description
No. | 溶剂 | 浓度[g/l] | 粘度40s-1 | 粘度500s-1 | 柔性US[h] | 刚性US[h] | Mw/103 | Mn/103 | 印刷质量 |
1 | 四氢萘 | 8,81 | 11,6 | 11,0 | 21 | 10 | 170 | 90 | 良好 |
2 | 苯*** | 9,92 | 7,5 | 7,1 | 22 | 20 | 190 | 110 | 良好 |
3 | 4-甲基-苯甲醚 | 9,24 | 10,9 | 8,5 | 14,5 | 12 | 250 | 130 | 良好 |
4 | 苯甲醚 | 7,56 | 8,4 | 6,8 | 23 | 0 | 370 | 150 | 良好 |
5 | 苯甲醚 | 11,47 | 12,4 | 9,3 | 29 | 7,5 | 265 | 150 | 良好 |
6 | 苯甲醚 | 8,86 | 8,5 | 7,7 | 7 | 13 | 310 | 170 | 良好 |
7 | 4-甲基苯甲醚/邻二甲苯3∶1 | 8,40 | 8,7 | 8,2 | 16 | 12 | 350 | 170 | 良好 |
8 | 苯甲醚 | 8,80 | 11,3 | 9,6 | 32 | 0 | 400 | 180 | 良好 |
9 | 邻二甲苯 | 7,93 | 9,5 | 8,3 | 22 | 13 | 390 | 180 | 良好 |
10 | 苯甲醚/邻二甲苯1∶1 | 11,7 | 13 | 12,5 | 23 | 24,5 | 380 | 190 | 良好 |
11 | 苯甲醚/邻二甲苯1∶1 | 8,1 | 8,8 | 8,6 | 9,5 | 12 | 400 | 190 | 良好 |
12 | 邻二甲苯 | 7,81 | 9,4 | 9,6 | 16,5 | 20 | 400 | 200 | 良好 |
13 | 苯甲醚/邻二甲苯 | 8,89 | 9,3 | 9,3 | 15 | 10 | 450 | 210 | 良好 |
14 | 邻二甲苯/苯甲醚 | 8,98 | 11,9 | 11,4 | 13,5 | 30 | 440 | 215 | 良好 |
15 | 甲苯 | 7,81 | 8,7 | 8,1 | 21 | 0 | 490 | 220 | 适宜 |
16 | 甲苯 | 5,99 | 6,5 | 6,1 | 4 | 0 | 600 | 230 | 适宜 |
17 | 邻二甲苯 | 9,00 | 17,3 | 16,3 | 52 | 0 | 520 | 240 | 中等 |
18 | 苯甲醚/邻二甲苯3∶1 | 8,29 | 13,3 | 12,0 | 20 | 0 | 500 | 250 | 不可印刷 |
19 | 苯甲醚/邻二甲苯1∶1 | 8,89 | 23,4 | 19,1 | 9,5 | 0 | 690 | 290 | 不可印刷 |
20 | 甲苯 | 6.72 | 14.7 | 4 | 0 | 880 | 310 | 不可印刷 | |
21 | 甲苯 | 6.75 | 18.1 | 3 | 0 | 980 | 320 | 不可印刷 | |
22 | 甲苯 | 5,99 | 7,60 | 7,12 | 2 | 0 | 890 | 390 | 中等 |
23 | 甲苯 | 6.85 | 16.1 | 2 | 0 | 840 | 400 | 不可印刷 | |
24 | 甲苯 | 6.52 | 25.2 | 1 | 0 | 1100 | 420 | 不可印刷 | |
25 | 苯甲醚 | 4,3 | 11.0 | 11.7 | 0 | 0 | 530 | 450 | 不可印刷 |
Claims (11)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01202029 | 2001-05-29 | ||
EP012020293 | 2001-05-29 | ||
EP01202029.3 | 2001-05-29 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1463278A CN1463278A (zh) | 2003-12-24 |
CN1219805C true CN1219805C (zh) | 2005-09-21 |
Family
ID=8180385
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB028018966A Expired - Fee Related CN1219805C (zh) | 2001-05-29 | 2002-05-27 | 聚合物、其制备方法和电子器件 |
Country Status (6)
Country | Link |
---|---|
US (1) | US7084236B2 (zh) |
EP (1) | EP1397411A1 (zh) |
JP (1) | JP2004520477A (zh) |
KR (1) | KR100921361B1 (zh) |
CN (1) | CN1219805C (zh) |
WO (1) | WO2002096970A1 (zh) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE10318096A1 (de) | 2003-04-17 | 2004-11-11 | Covion Organic Semiconductors Gmbh | Verfahren zur Molekulargewichtskontrolle bei der Synthese von Poly(arylenvinylenen) |
US7417111B2 (en) * | 2004-03-31 | 2008-08-26 | Intel Corporation | Liquid crystalline epoxy resins |
US7910025B2 (en) | 2004-10-15 | 2011-03-22 | Sumitomo Chemical Co., Ltd. | Solution composition and polymer light-emitting device |
EP1894976B1 (en) | 2005-05-20 | 2015-09-30 | Sumitomo Chemical Company, Limited | Polymer composition and polymer light-emitting device using same |
JP4762630B2 (ja) * | 2005-08-03 | 2011-08-31 | 東京応化工業株式会社 | レジスト組成物およびレジストパターン形成方法 |
DE102005061628A1 (de) * | 2005-12-21 | 2007-06-28 | Lanxess Deutschland Gmbh | Hydrierter Nitrilkautschuk mit enger Molekulargewichtsverteilung, ein Verfahren zu seiner Herstellung und seine Verwendung |
DE102005061627A1 (de) * | 2005-12-21 | 2007-06-28 | Lanxess Deutschland Gmbh | Synthetischer Kautschuk mit enger Molekulargewichtsverteilung, ein Verfahren zu seiner Herstellung und seine Verwendung |
EP2227512A1 (en) * | 2007-12-18 | 2010-09-15 | Lumimove, Inc., Dba Crosslink | Flexible electroluminescent devices and systems |
KR101259865B1 (ko) | 2011-11-21 | 2013-05-02 | 광주과학기술원 | 저밴드갭의 공중합체 및 이의 제조방법 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4576688A (en) * | 1982-11-04 | 1986-03-18 | Celanese Corporation | Production of poly(p-phenylene) from 4,4'-dihalobiphenyl and lithium using ultrasonic waves |
DD254389A1 (de) * | 1986-12-06 | 1988-02-24 | Univ Schiller Jena | Verfahren zur herstellung von arylsubstituierten poly(arylenvinylenen) |
DE3816560A1 (de) * | 1987-06-22 | 1989-01-05 | Robotron Veb K | Photoleitendes, schichtbildendes material, insbesondere fuer elektrophotographische zwecke, aus substituierten poly(phenylenvinylenen) und verfahren zu ihrer herstellung |
WO1995031831A1 (en) * | 1994-05-18 | 1995-11-23 | Philips Electronics N.V. | Method of providing a film of conjugated, substituted or unsubstituted poly(p-phenylene vinylene) on a substrate by chemical vapour deposition (cvd), as well as a method of manufacturing an electroluminescent (el) device |
JPH09501022A (ja) * | 1994-05-19 | 1997-01-28 | フィリップス エレクトロニクス ネムローゼ フェンノートシャップ | 2,5−置換ポリ(p−フェニレンビニレン)の活性層を含む発光ダイオード |
JPH08143821A (ja) * | 1994-11-18 | 1996-06-04 | Meiji Seika Kaisha Ltd | ゼラチンの加工法 |
WO1998004611A1 (en) * | 1996-07-25 | 1998-02-05 | International Business Machines Corporation | Control of polymerization kinetics and rate of polymer precipitation as a means of controlling the aggregation and morphology in conductive polymers and precursors thereof |
DE19652261A1 (de) * | 1996-12-16 | 1998-06-18 | Hoechst Ag | Arylsubstituierte Poly(p-arylenvinylene), Verfahren zur Herstellung und deren Verwendung in Elektroluminszenzbauelementen |
US6843937B1 (en) | 1997-07-16 | 2005-01-18 | Seiko Epson Corporation | Composition for an organic EL element and method of manufacturing the organic EL element |
US20020001732A1 (en) | 1997-10-23 | 2002-01-03 | Hermannus F.M. Schoo | Polymer electroluminescent device |
DE19748814A1 (de) * | 1997-11-05 | 1999-05-06 | Hoechst Ag | Substituierte Poly(arylenvinylene), Verfahren zur Herstellung und deren Verwendung in Elektrolumineszenz |
DE19857661A1 (de) * | 1998-12-15 | 2000-06-21 | Aventis Res & Tech Gmbh & Co | Verfahren zur Herstellung von Derivaten des Polyarylenvinylenen |
TW484341B (en) * | 1999-08-03 | 2002-04-21 | Sumitomo Chemical Co | Polymeric fluorescent substance and polymer light emitting device |
WO2001018090A1 (en) * | 1999-09-02 | 2001-03-15 | Koninklijke Philips Electronics N.V. | Polymers containing heterocyclic groups, method of preparing, use thereof as a layer and heterocyclic compounds |
JP4477726B2 (ja) * | 1999-12-09 | 2010-06-09 | シャープ株式会社 | 有機led素子の製造方法 |
JP2003535199A (ja) * | 2000-05-30 | 2003-11-25 | コーニンクレッカ フィリップス エレクトロニクス エヌ ヴィ | ポリマーの製造方法、化合物の製造方法、化合物、ポリマー、及び電子装置の製造方法 |
-
2002
- 2002-05-27 CN CNB028018966A patent/CN1219805C/zh not_active Expired - Fee Related
- 2002-05-27 KR KR1020037001088A patent/KR100921361B1/ko active IP Right Grant
- 2002-05-27 JP JP2003500149A patent/JP2004520477A/ja active Pending
- 2002-05-27 EP EP02774053A patent/EP1397411A1/en not_active Withdrawn
- 2002-05-27 WO PCT/IB2002/001880 patent/WO2002096970A1/en not_active Application Discontinuation
- 2002-05-27 US US10/478,894 patent/US7084236B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JP2004520477A (ja) | 2004-07-08 |
US20040176566A1 (en) | 2004-09-09 |
KR20030022313A (ko) | 2003-03-15 |
CN1463278A (zh) | 2003-12-24 |
WO2002096970A1 (en) | 2002-12-05 |
KR100921361B1 (ko) | 2009-10-13 |
EP1397411A1 (en) | 2004-03-17 |
US7084236B2 (en) | 2006-08-01 |
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