DE10037391A1 - Strukturierbare Materialien, Verfahren zu deren Herstellung und deren Verwendung - Google Patents
Strukturierbare Materialien, Verfahren zu deren Herstellung und deren VerwendungInfo
- Publication number
- DE10037391A1 DE10037391A1 DE10037391A DE10037391A DE10037391A1 DE 10037391 A1 DE10037391 A1 DE 10037391A1 DE 10037391 A DE10037391 A DE 10037391A DE 10037391 A DE10037391 A DE 10037391A DE 10037391 A1 DE10037391 A1 DE 10037391A1
- Authority
- DE
- Germany
- Prior art keywords
- replaced
- atoms
- aryl
- group
- organic
- 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.)
- Withdrawn
Links
- 239000000463 material Substances 0.000 title claims description 24
- 238000004519 manufacturing process Methods 0.000 title claims description 13
- 238000000034 method Methods 0.000 title claims description 7
- 125000003118 aryl group Chemical group 0.000 claims abstract description 56
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 49
- -1 Cl and F Chemical class 0.000 claims abstract description 48
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 47
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 26
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 23
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 19
- 125000006165 cyclic alkyl group Chemical group 0.000 claims abstract description 16
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 125000006374 C2-C10 alkenyl group Chemical group 0.000 claims abstract description 9
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 9
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 9
- 150000002367 halogens Chemical class 0.000 claims abstract description 9
- 125000005309 thioalkoxy group Chemical group 0.000 claims abstract description 9
- 239000011368 organic material Substances 0.000 claims abstract description 5
- 150000003384 small molecules Chemical class 0.000 claims description 13
- 125000003566 oxetanyl group Chemical group 0.000 claims description 10
- 238000004132 cross linking Methods 0.000 claims description 8
- 239000004020 conductor Substances 0.000 claims description 7
- 229920001577 copolymer Polymers 0.000 claims description 7
- 125000005580 triphenylene group Chemical group 0.000 claims description 6
- 150000004866 oxadiazoles Chemical class 0.000 claims description 5
- 125000003003 spiro group Chemical group 0.000 claims description 5
- ICPSWZFVWAPUKF-UHFFFAOYSA-N 1,1'-spirobi[fluorene] Chemical group C1=CC=C2C=C3C4(C=5C(C6=CC=CC=C6C=5)=CC=C4)C=CC=C3C2=C1 ICPSWZFVWAPUKF-UHFFFAOYSA-N 0.000 claims description 4
- NGDCLPXRKSWRPY-UHFFFAOYSA-N Triptycene Chemical group C12=CC=CC=C2C2C3=CC=CC=C3C1C1=CC=CC=C12 NGDCLPXRKSWRPY-UHFFFAOYSA-N 0.000 claims description 4
- DXDRCSFTBJNXCI-UHFFFAOYSA-K aluminum;quinoxaline-2-carboxylate Chemical class [Al+3].C1=CC=CC2=NC(C(=O)[O-])=CN=C21.C1=CC=CC2=NC(C(=O)[O-])=CN=C21.C1=CC=CC2=NC(C(=O)[O-])=CN=C21 DXDRCSFTBJNXCI-UHFFFAOYSA-K 0.000 claims description 4
- RPQOZSKWYNULKS-UHFFFAOYSA-N 1,2-dicarbamoylperylene-3,4-dicarboxylic acid Chemical class C1=C(C(O)=O)C2=C(C(O)=O)C(C(=N)O)=C(C(O)=N)C(C=3C4=C5C=CC=C4C=CC=3)=C2C5=C1 RPQOZSKWYNULKS-UHFFFAOYSA-N 0.000 claims description 3
- 239000004952 Polyamide Substances 0.000 claims description 3
- 239000004793 Polystyrene Substances 0.000 claims description 3
- 239000011149 active material Substances 0.000 claims description 3
- 229910052747 lanthanoid Inorganic materials 0.000 claims description 3
- 150000002602 lanthanoids Chemical class 0.000 claims description 3
- 230000006855 networking Effects 0.000 claims description 3
- 229920000058 polyacrylate Polymers 0.000 claims description 3
- 229920002647 polyamide Polymers 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920002223 polystyrene Polymers 0.000 claims description 3
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 22
- 125000001424 substituent group Chemical group 0.000 description 43
- 229920000642 polymer Polymers 0.000 description 26
- 239000000460 chlorine Substances 0.000 description 20
- 125000001072 heteroaryl group Chemical group 0.000 description 16
- 125000000217 alkyl group Chemical group 0.000 description 14
- 229910052799 carbon Inorganic materials 0.000 description 14
- 229910052760 oxygen Inorganic materials 0.000 description 11
- 229910052717 sulfur Inorganic materials 0.000 description 11
- AHHWIHXENZJRFG-UHFFFAOYSA-N oxetane Chemical compound C1COC1 AHHWIHXENZJRFG-UHFFFAOYSA-N 0.000 description 10
- 125000000753 cycloalkyl group Chemical group 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 8
- 125000005605 benzo group Chemical group 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 229920000553 poly(phenylenevinylene) Polymers 0.000 description 5
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 4
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 4
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- 150000001450 anions Chemical class 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 3
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000001397 3-pyrrolyl group Chemical group [H]N1C([H])=C([*])C([H])=C1[H] 0.000 description 3
- 125000004429 atom Chemical group 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229920000547 conjugated polymer Polymers 0.000 description 3
- 125000004122 cyclic group Chemical group 0.000 description 3
- 239000003446 ligand Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- 229920002098 polyfluorene Polymers 0.000 description 3
- 125000004307 pyrazin-2-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 description 3
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 description 3
- 125000004940 pyridazin-4-yl group Chemical group N1=NC=C(C=C1)* 0.000 description 3
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 3
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 description 3
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 229910052693 Europium Inorganic materials 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 150000002390 heteroarenes Chemical class 0.000 description 2
- 239000003999 initiator Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- FKASFBLJDCHBNZ-UHFFFAOYSA-N 1,3,4-oxadiazole Chemical compound C1=NN=CO1 FKASFBLJDCHBNZ-UHFFFAOYSA-N 0.000 description 1
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 1
- SNFCXVRWFNAHQX-UHFFFAOYSA-N 9,9'-spirobi[fluorene] Chemical group C12=CC=CC=C2C2=CC=CC=C2C21C1=CC=CC=C1C1=CC=CC=C21 SNFCXVRWFNAHQX-UHFFFAOYSA-N 0.000 description 1
- 229920001342 Bakelite® Polymers 0.000 description 1
- 101100377706 Escherichia phage T5 A2.2 gene Proteins 0.000 description 1
- 229910052688 Gadolinium Inorganic materials 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- 241000702619 Porcine parvovirus Species 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000003491 array Methods 0.000 description 1
- 239000004637 bakelite Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000011243 crosslinked material Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000012776 electronic material Substances 0.000 description 1
- 150000002220 fluorenes Chemical class 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- UIWYJDYFSGRHKR-UHFFFAOYSA-N gadolinium atom Chemical compound [Gd] UIWYJDYFSGRHKR-UHFFFAOYSA-N 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 150000002605 large molecules Chemical class 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- DCZNSJVFOQPSRV-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline Chemical class C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 DCZNSJVFOQPSRV-UHFFFAOYSA-N 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 238000004803 parallel plate viscometry Methods 0.000 description 1
- 229950000688 phenothiazine Drugs 0.000 description 1
- 125000001644 phenoxazinyl group Chemical class C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- UPUZGXILYFKSGE-UHFFFAOYSA-N quinoxaline-2-carboxylic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CN=C21 UPUZGXILYFKSGE-UHFFFAOYSA-N 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 238000007151 ring opening polymerisation reaction Methods 0.000 description 1
- 125000006413 ring segment Chemical group 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229920001187 thermosetting polymer Polymers 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/06—Cyclic ethers having no atoms other than carbon and hydrogen outside the ring
- C08G65/16—Cyclic ethers having four or more ring atoms
- C08G65/18—Oxetanes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D305/00—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms
- C07D305/02—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings
- C07D305/04—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
- C07D305/06—Heterocyclic compounds containing four-membered rings having one oxygen atom as the only ring hetero atoms not condensed with other rings having no 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 the ring atoms
-
- 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
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/04—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers only
- C08G65/22—Cyclic ethers having at least one atom other than carbon and hydrogen outside the ring
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
-
- 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)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Electroluminescent Light Sources (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Orthopedics, Nursing, And Contraception (AREA)
Priority Applications (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10037391A DE10037391A1 (de) | 2000-08-01 | 2000-08-01 | Strukturierbare Materialien, Verfahren zu deren Herstellung und deren Verwendung |
| AU57677/01A AU5767701A (en) | 2000-07-29 | 2001-07-26 | Wrist bandage |
| CNB018129056A CN1244607C (zh) | 2000-08-01 | 2001-08-01 | 可结构化的材料、其制备方法及其应用 |
| US10/343,465 US7592414B2 (en) | 2000-08-01 | 2001-08-01 | Materials that can be structured, method for producing the same and their use |
| EP01982205A EP1307498B1 (de) | 2000-08-01 | 2001-08-01 | Strukturierbare materialien, verfahren zu deren herstellung und deren verwendung |
| DE50108918T DE50108918D1 (de) | 2000-08-01 | 2001-08-01 | Strukturierbare materialien, verfahren zu deren herstellung und deren verwendung |
| KR1020037001500A KR100734198B1 (ko) | 2000-08-01 | 2001-08-01 | 구조화 가능 물질, 이의 제조방법 및 이의 용도 |
| JP2002516261A JP5274745B2 (ja) | 2000-08-01 | 2001-08-01 | 構造化できる材料、それを製造する方法およびその利用 |
| PCT/EP2001/009176 WO2002010129A2 (de) | 2000-08-01 | 2001-08-01 | Strukturierbare materialien, verfahren zu deren herstellung und deren verwendung |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10037391A DE10037391A1 (de) | 2000-08-01 | 2000-08-01 | Strukturierbare Materialien, Verfahren zu deren Herstellung und deren Verwendung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10037391A1 true DE10037391A1 (de) | 2002-02-14 |
Family
ID=7650910
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10037391A Withdrawn DE10037391A1 (de) | 2000-07-29 | 2000-08-01 | Strukturierbare Materialien, Verfahren zu deren Herstellung und deren Verwendung |
| DE50108918T Expired - Lifetime DE50108918D1 (de) | 2000-08-01 | 2001-08-01 | Strukturierbare materialien, verfahren zu deren herstellung und deren verwendung |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE50108918T Expired - Lifetime DE50108918D1 (de) | 2000-08-01 | 2001-08-01 | Strukturierbare materialien, verfahren zu deren herstellung und deren verwendung |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7592414B2 (enExample) |
| EP (1) | EP1307498B1 (enExample) |
| JP (1) | JP5274745B2 (enExample) |
| KR (1) | KR100734198B1 (enExample) |
| CN (1) | CN1244607C (enExample) |
| AU (1) | AU5767701A (enExample) |
| DE (2) | DE10037391A1 (enExample) |
| WO (1) | WO2002010129A2 (enExample) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102008054435A1 (de) | 2008-12-09 | 2010-06-10 | Universität Zu Köln | Organische Leuchtdiode mit optischem Resonator nebst Herstellungsverfahren |
| DE102013103156A1 (de) * | 2013-03-27 | 2014-10-16 | Osram Opto Semiconductors Gmbh | Strahlungsemittierende organisch-elektronische Vorrichtung und Verfahren zur Herstellung einer strahlungsemittierenden organisch-elektronischen Vorrichtung |
| EP1410448B1 (de) | 2000-09-11 | 2015-03-25 | OSRAM Opto Semiconductors GmbH | Photostrukturierbare neue organische halbleitermaterialien |
Families Citing this family (39)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1483354B1 (en) * | 2002-03-09 | 2009-12-02 | CDT Oxford Limited | Polymerisable compositions and organic light-emitting devices containing them |
| KR100478524B1 (ko) * | 2002-06-28 | 2005-03-28 | 삼성에스디아이 주식회사 | 고분자 및 저분자 발광 재료의 혼합물을 발광 재료로사용하는 유기 전계 발광 소자 |
| DE10238903A1 (de) | 2002-08-24 | 2004-03-04 | Covion Organic Semiconductors Gmbh | Rhodium- und Iridium-Komplexe |
| DE10340711A1 (de) | 2003-09-04 | 2005-04-07 | Covion Organic Semiconductors Gmbh | Elektronische Vorrichtung enthaltend organische Halbleiter |
| GB0325324D0 (en) * | 2003-10-30 | 2003-12-03 | Avecia Ltd | Process for producing semiconducting layers and devices containing the same |
| GB2424896B (en) * | 2003-11-17 | 2008-02-27 | Sumitomo Chemical Co | Crosslinkable substituted fluorene compounds and conjugated oligomers or polymers based thereon |
| TWI365218B (en) | 2003-11-17 | 2012-06-01 | Sumitomo Chemical Co | Conjugated oligomers or polymers based on crosslinkable arylamine compounds |
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- 2000-08-01 DE DE10037391A patent/DE10037391A1/de not_active Withdrawn
-
2001
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- 2001-08-01 JP JP2002516261A patent/JP5274745B2/ja not_active Expired - Fee Related
- 2001-08-01 US US10/343,465 patent/US7592414B2/en not_active Expired - Fee Related
- 2001-08-01 EP EP01982205A patent/EP1307498B1/de not_active Expired - Lifetime
- 2001-08-01 CN CNB018129056A patent/CN1244607C/zh not_active Expired - Lifetime
- 2001-08-01 DE DE50108918T patent/DE50108918D1/de not_active Expired - Lifetime
- 2001-08-01 KR KR1020037001500A patent/KR100734198B1/ko not_active Expired - Fee Related
- 2001-08-01 WO PCT/EP2001/009176 patent/WO2002010129A2/de not_active Ceased
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
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| EP1410448B1 (de) | 2000-09-11 | 2015-03-25 | OSRAM Opto Semiconductors GmbH | Photostrukturierbare neue organische halbleitermaterialien |
| DE102008054435A1 (de) | 2008-12-09 | 2010-06-10 | Universität Zu Köln | Organische Leuchtdiode mit optischem Resonator nebst Herstellungsverfahren |
| DE102013103156A1 (de) * | 2013-03-27 | 2014-10-16 | Osram Opto Semiconductors Gmbh | Strahlungsemittierende organisch-elektronische Vorrichtung und Verfahren zur Herstellung einer strahlungsemittierenden organisch-elektronischen Vorrichtung |
| DE102013103156B4 (de) * | 2013-03-27 | 2017-09-14 | Osram Oled Gmbh | Strahlungsemittierende organisch-elektronische Vorrichtung und Verfahren zur Herstellung einer strahlungsemittierenden organisch-elektronischen Vorrichtung |
| US10615346B2 (en) | 2013-03-27 | 2020-04-07 | Osram Oled Gmbh | Radiation-emitting organic-electronic device and method for producing a radiation-emitting organic-electronic device |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1443209A (zh) | 2003-09-17 |
| JP2004505169A (ja) | 2004-02-19 |
| EP1307498A2 (de) | 2003-05-07 |
| KR100734198B1 (ko) | 2007-07-02 |
| JP5274745B2 (ja) | 2013-08-28 |
| AU5767701A (en) | 2002-01-31 |
| DE50108918D1 (de) | 2006-04-20 |
| WO2002010129A3 (de) | 2002-06-20 |
| US20040054152A1 (en) | 2004-03-18 |
| WO2002010129A2 (de) | 2002-02-07 |
| KR20030057525A (ko) | 2003-07-04 |
| US7592414B2 (en) | 2009-09-22 |
| EP1307498B1 (de) | 2006-02-08 |
| CN1244607C (zh) | 2006-03-08 |
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