CN1263542A - 含芴聚合物及由其制成的场致发光器件 - Google Patents
含芴聚合物及由其制成的场致发光器件 Download PDFInfo
- Publication number
- CN1263542A CN1263542A CN99800587A CN99800587A CN1263542A CN 1263542 A CN1263542 A CN 1263542A CN 99800587 A CN99800587 A CN 99800587A CN 99800587 A CN99800587 A CN 99800587A CN 1263542 A CN1263542 A CN 1263542A
- Authority
- CN
- China
- Prior art keywords
- multipolymer
- formula
- organic membrane
- group
- alkyl
- 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
Links
- 229920000642 polymer Polymers 0.000 title claims description 24
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 title description 5
- 239000000203 mixture Substances 0.000 claims abstract description 48
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 10
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 7
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 7
- 125000004429 atom Chemical group 0.000 claims abstract description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 3
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 3
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 3
- 239000000126 substance Substances 0.000 claims description 32
- 239000012528 membrane Substances 0.000 claims description 22
- 150000002220 fluorenes Chemical group 0.000 claims description 11
- 230000021615 conjugation Effects 0.000 claims description 9
- 239000010405 anode material Substances 0.000 claims description 8
- 239000010406 cathode material Substances 0.000 claims description 8
- 238000005401 electroluminescence Methods 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 239000000377 silicon dioxide Substances 0.000 claims description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 abstract description 15
- 125000003118 aryl group Chemical group 0.000 abstract description 9
- 229910052799 carbon Inorganic materials 0.000 abstract description 3
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 abstract description 2
- 125000006659 (C1-C20) hydrocarbyl group Chemical group 0.000 abstract 3
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 abstract 2
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000005389 trialkylsiloxy group Chemical group 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 34
- 238000000034 method Methods 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- 238000000576 coating method Methods 0.000 description 12
- 239000011248 coating agent Substances 0.000 description 11
- 239000000178 monomer Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- -1 boric acid ester Chemical class 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000006116 polymerization reaction Methods 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 230000005540 biological transmission Effects 0.000 description 5
- 239000004327 boric acid Substances 0.000 description 5
- SKOWZLGOFVSKLB-UHFFFAOYSA-N hypodiboric acid Chemical compound OB(O)B(O)O SKOWZLGOFVSKLB-UHFFFAOYSA-N 0.000 description 5
- 229910052738 indium Inorganic materials 0.000 description 5
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- 239000002356 single layer Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- YMMGRPLNZPTZBS-UHFFFAOYSA-N 2,3-dihydrothieno[2,3-b][1,4]dioxine Chemical compound O1CCOC2=C1C=CS2 YMMGRPLNZPTZBS-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthene Chemical compound C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 description 4
- 238000004020 luminiscence type Methods 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 239000003960 organic solvent Substances 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
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 4
- 241000894007 species Species 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229920005603 alternating copolymer Polymers 0.000 description 3
- 239000011575 calcium Substances 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 229920001940 conductive polymer Polymers 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- 239000011777 magnesium Substances 0.000 description 3
- 229910052749 magnesium Inorganic materials 0.000 description 3
- 229920000767 polyaniline Polymers 0.000 description 3
- 229920006254 polymer film Polymers 0.000 description 3
- 238000004528 spin coating Methods 0.000 description 3
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 2
- VEUMBMHMMCOFAG-UHFFFAOYSA-N 2,3-dihydrooxadiazole Chemical compound N1NC=CO1 VEUMBMHMMCOFAG-UHFFFAOYSA-N 0.000 description 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000006069 Suzuki reaction reaction Methods 0.000 description 2
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000004411 aluminium 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
- 125000003368 amide group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000003849 aromatic solvent Substances 0.000 description 2
- 150000001502 aryl halides Chemical class 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Chemical group 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000002322 conducting polymer Substances 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 229920006158 high molecular weight polymer Polymers 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 2
- 150000002641 lithium Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 2
- 229920005547 polycyclic aromatic hydrocarbon Polymers 0.000 description 2
- 229920005604 random copolymer Polymers 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 1
- GKWLILHTTGWKLQ-UHFFFAOYSA-N 2,3-dihydrothieno[3,4-b][1,4]dioxine Chemical compound O1CCOC2=CSC=C21 GKWLILHTTGWKLQ-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 241000208340 Araliaceae Species 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- KESRRRLHHXXBRW-UHFFFAOYSA-N C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 Chemical compound C1=CC=NC2=C3C(O)=CC=CC3=CC=C21 KESRRRLHHXXBRW-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
- 229910000861 Mg alloy Inorganic materials 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 1
- 235000005035 Panax pseudoginseng ssp. pseudoginseng Nutrition 0.000 description 1
- 235000003140 Panax quinquefolius Nutrition 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- 230000010748 Photoabsorption Effects 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000005864 Sulphur Substances 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- XOCUXOWLYLLJLV-UHFFFAOYSA-N [O].[S] Chemical compound [O].[S] XOCUXOWLYLLJLV-UHFFFAOYSA-N 0.000 description 1
- CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthene Chemical compound C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 125000005418 aryl aryl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 125000005605 benzo group Chemical group 0.000 description 1
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical compound C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000000259 cinnolinyl group Chemical class N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 210000001072 colon Anatomy 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 1
- OBISXEJSEGNNKL-UHFFFAOYSA-N dinitrogen-n-sulfide Chemical compound [N-]=[N+]=S OBISXEJSEGNNKL-UHFFFAOYSA-N 0.000 description 1
- 238000003618 dip coating Methods 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 229920000775 emeraldine polymer Polymers 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 150000002240 furans Chemical class 0.000 description 1
- 238000005227 gel permeation chromatography Methods 0.000 description 1
- 235000008434 ginseng 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
- 230000005283 ground state Effects 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 150000002367 halogens Chemical group 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000005525 hole transport Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 150000002460 imidazoles Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- ZLTPDFXIESTBQG-UHFFFAOYSA-N isothiazole Chemical compound C=1C=NSC=1 ZLTPDFXIESTBQG-UHFFFAOYSA-N 0.000 description 1
- CTAPFRYPJLPFDF-UHFFFAOYSA-N isoxazole Chemical compound C=1C=NOC=1 CTAPFRYPJLPFDF-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 150000005053 phenanthridines Chemical class 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000005424 photoluminescence Methods 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000003880 polar aprotic solvent Substances 0.000 description 1
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 1
- 229920000128 polypyrrole Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- YYMBJDOZVAITBP-UHFFFAOYSA-N rubrene Chemical compound C1=CC=CC=C1C(C1=C(C=2C=CC=CC=2)C2=CC=CC=C2C(C=2C=CC=CC=2)=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 YYMBJDOZVAITBP-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 238000000935 solvent evaporation Methods 0.000 description 1
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 description 1
- 235000021286 stilbenes Nutrition 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 150000004655 tetrazenes Chemical class 0.000 description 1
- 238000002207 thermal evaporation Methods 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- VWQVUPCCIRVNHF-UHFFFAOYSA-N yttrium atom Chemical compound [Y] VWQVUPCCIRVNHF-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
- C07C25/22—Polycyclic aromatic halogenated hydrocarbons with condensed rings
-
- 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
- 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
- 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
- C08G61/12—Macromolecular compounds containing atoms other than carbon 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
-
- 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
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/02—Polyamines
- C08G73/026—Wholly aromatic polyamines
-
- 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
- C08G83/00—Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- 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
- H10K85/151—Copolymers
-
- 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
- H10K85/115—Polyfluorene; Derivatives thereof
-
- 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
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
-
- 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
-
- 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
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31678—Of metal
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silicon Polymers (AREA)
Abstract
Description
器件 | 膜厚(nm) | 胺共聚物 | 比例* | V | J(mA/cm2) | 流明/瓦特 |
1a | 150 | 无 | 0∶1 | 16.8 | 39.1 | 0.48 |
1b | 100 | TFB | 1∶3 | 6.6 | 21.9 | 2.17 |
1c | 100 | PFB | 1∶3 | 5.6 | 63.4 | 0.88 |
1d | 150 | PFMO | 1∶3 | 9.3 | 41.6 | 0.81 |
1e | 150 | BFE | 1∶5 | 10.9 | 47.7 | 0.60 |
1f | 150 | BFE | 1∶3 | 5.6 | 21.1 | 2.66 |
1g | 150 | PFE | 1∶3 | 9.3 | 37.5 | 0.90 |
器件 | 层1(nm) | 层2(nm)* | V | J(mA/cm2) | 流明/瓦特 |
1a | 5BTF8(150) | 16.8 | 39.1 | 0.48 | |
2a | BFA(25) | 5BTF8(100) | 9.3 | 36.5 | 0.93 |
2b | PFA(25) | 3BTF8(100) | 8.4 | 31.8 | 1.17 |
2c | BFA(40) | F8(150) | 24伏下的最大亮度=120Cd/m2 | ||
2d | BFA(60) | 10wt.%TFMO/90WT.%F8(100) | 11 | 174 | 0.16 |
Claims (16)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/063,615 US6309763B1 (en) | 1997-05-21 | 1998-04-21 | Fluorene-containing polymers and electroluminescent devices therefrom |
US09/063,615 | 1998-04-21 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2007101091169A Division CN101058672B (zh) | 1998-04-21 | 1999-04-09 | 一种组合物及由其制成的场致发光器件 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1263542A true CN1263542A (zh) | 2000-08-16 |
CN100341922C CN100341922C (zh) | 2007-10-10 |
Family
ID=22050379
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2007101091169A Expired - Lifetime CN101058672B (zh) | 1998-04-21 | 1999-04-09 | 一种组合物及由其制成的场致发光器件 |
CNB998005878A Expired - Lifetime CN100341922C (zh) | 1998-04-21 | 1999-04-09 | 含芴聚合物及由其制成的场致发光器件 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2007101091169A Expired - Lifetime CN101058672B (zh) | 1998-04-21 | 1999-04-09 | 一种组合物及由其制成的场致发光器件 |
Country Status (9)
Country | Link |
---|---|
US (2) | US6309763B1 (zh) |
EP (1) | EP0988337B2 (zh) |
JP (2) | JP4375820B2 (zh) |
KR (1) | KR100575382B1 (zh) |
CN (2) | CN101058672B (zh) |
CA (1) | CA2294485C (zh) |
DE (1) | DE69908522T3 (zh) |
TW (1) | TWI243187B (zh) |
WO (1) | WO1999054385A1 (zh) |
Cited By (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100417703C (zh) * | 2001-05-11 | 2008-09-10 | 剑桥显示技术有限公司 | 取代的芴聚合物,其制备方法和在光学设备中的用途 |
CN100580002C (zh) * | 2003-03-20 | 2010-01-13 | 剑桥显示技术有限公司 | 聚合物及其制备和用途 |
CN100583486C (zh) * | 2002-09-03 | 2010-01-20 | 剑桥显示技术有限公司 | 光学器件 |
CN100583490C (zh) * | 2003-03-20 | 2010-01-20 | 剑桥显示技术有限公司 | 电致发光器件 |
US7893160B2 (en) | 2003-11-17 | 2011-02-22 | Sumitomo Chemical Company, Limited | Crosslinkable substituted fluorene compounds and conjugated oligomers or polymers based thereon |
CN1898292B (zh) * | 2003-12-12 | 2011-04-13 | 住友化学株式会社 | 聚合物化合物和使用该聚合物化合物的聚合物发光器件 |
CN1739204B (zh) * | 2002-12-20 | 2011-06-08 | 默克专利股份有限公司 | 改进有机半导体材料及与其有关的改进 |
CN101061089B (zh) * | 2004-12-03 | 2011-07-27 | 住友化学株式会社 | 水杨酸酯取代的共轭聚合物及器件 |
CN101184811B (zh) * | 2005-06-01 | 2011-08-17 | 住友化学株式会社 | 高分子组合物以及高分子发光元件 |
CN1749295B (zh) * | 2004-09-18 | 2011-09-14 | 三星移动显示器株式会社 | 蓝色发光聚合物及使用它的有机电致发光器件 |
CN101134814B (zh) * | 2006-08-24 | 2011-10-26 | E.I.内穆尔杜邦公司 | 空穴传输聚合物 |
CN101851190B (zh) * | 2005-03-04 | 2012-04-25 | 住友化学株式会社 | 二咔唑-9-基-取代的三芳基胺 |
CN101490862B (zh) * | 2006-07-25 | 2013-03-13 | 默克专利有限公司 | 聚合物共混物和它们在有机发光器件中的用途 |
CN103396533A (zh) * | 2013-08-14 | 2013-11-20 | 黑龙江大学 | 含甲氧基三苯胺-芴共聚物、制备方法及其应用 |
CN103814091A (zh) * | 2011-09-21 | 2014-05-21 | 日产化学工业株式会社 | 电荷传输性清漆 |
CN103980731A (zh) * | 2014-03-27 | 2014-08-13 | 中南大学 | 聚(三苯胺-芴)染料及其应用 |
CN101384639B (zh) * | 2005-12-22 | 2015-09-09 | 剑桥显示技术有限公司 | 芳胺聚合物 |
US9399702B2 (en) | 2003-11-17 | 2016-07-26 | Sumitomo Chemical Company, Limited | Crosslinkable arylamine compounds and conjugated oligomers or polymers based thereon |
CN107994131A (zh) * | 2017-11-28 | 2018-05-04 | 武汉华星光电半导体显示技术有限公司 | 用于封装oled器件的封装结构、显示装置 |
Families Citing this family (258)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE69608446T3 (de) * | 1995-07-28 | 2010-03-11 | Sumitomo Chemical Company, Ltd. | 2,7-aryl-9-substituierte fluorene und 9-substituierte fluorenoligomere und polymere |
US5708130A (en) | 1995-07-28 | 1998-01-13 | The Dow Chemical Company | 2,7-aryl-9-substituted fluorenes and 9-substituted fluorene oligomers and polymers |
US6309763B1 (en) * | 1997-05-21 | 2001-10-30 | The Dow Chemical Company | Fluorene-containing polymers and electroluminescent devices therefrom |
KR100697861B1 (ko) | 1998-03-13 | 2007-03-22 | 캠브리지 디스플레이 테크놀로지 리미티드 | 전장 발광 디바이스들 |
GB9805476D0 (en) * | 1998-03-13 | 1998-05-13 | Cambridge Display Tech Ltd | Electroluminescent devices |
DE19846768A1 (de) * | 1998-10-10 | 2000-04-20 | Aventis Res & Tech Gmbh & Co | Konjugierte Polymere enthaltend 2,7-Fluorenyleinheiten mit verbesserten Eigenschaften |
CN1167146C (zh) | 1999-01-15 | 2004-09-15 | 陶氏环球技术公司 | 高分子半导体场效应晶体管 |
EP1155096B1 (en) * | 1999-02-04 | 2005-03-09 | Dow Global Technologies Inc. | Fluorene copolymers and devices made therefrom |
EP2267814A1 (en) * | 1999-03-12 | 2010-12-29 | Sumitomo Chemical Company, Limited | Polymers, their preparation and uses |
CN1310930A (zh) * | 1999-03-29 | 2001-08-29 | 精工爱普生株式会社 | 组合物及膜的制造方法以及功能元件及其制造方法 |
JP2001035660A (ja) * | 1999-07-16 | 2001-02-09 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
GB9920543D0 (en) * | 1999-08-31 | 1999-11-03 | Cambridge Display Tech Ltd | A formulation for depositing a light-emitting polymer layer |
US6611096B1 (en) | 1999-09-03 | 2003-08-26 | 3M Innovative Properties Company | Organic electronic devices having conducting self-doped polymer buffer layers |
KR100331688B1 (ko) * | 1999-11-05 | 2002-04-09 | 오길록 | 백색 발광 고분자 블렌드 및 이를 이용한 백색 전기 발광소자 |
US6582504B1 (en) | 1999-11-24 | 2003-06-24 | Sharp Kabushiki Kaisha | Coating liquid for forming organic EL element |
GB0005842D0 (en) * | 2000-03-10 | 2000-05-03 | Cambridge Display Tech Ltd | Copoymer |
US6512082B2 (en) | 2000-01-05 | 2003-01-28 | Cambridge Display Technology Ltd. | Polymers, their preparation and uses |
DE60107380T2 (de) * | 2000-01-05 | 2005-12-01 | Cambridge Display Technology Ltd. | Lumineszente polymere |
CN1205247C (zh) * | 2000-01-05 | 2005-06-08 | 剑桥显示技术有限公司 | 聚合物,及其制备和应用 |
GB0004541D0 (en) | 2000-02-25 | 2000-04-19 | Cambridge Display Tech Ltd | Luminescent polymer |
US6858324B2 (en) | 2000-03-10 | 2005-02-22 | Cambridge Display Technology Limited | Copolymer |
DE60007080T2 (de) | 2000-04-26 | 2004-09-23 | Sony International (Europe) Gmbh | Polyfluore mit Endgruppen, Filme und darauf beruhende Anordnungen |
US6329086B1 (en) * | 2000-06-13 | 2001-12-11 | Eastman Kodak Company | Electroluminescent devices having arylamine polymers |
US7023012B2 (en) * | 2000-08-30 | 2006-04-04 | Cambridge Display Technology Limited | Formulation for depositing a conjugated polymer layer |
JP4643810B2 (ja) * | 2000-09-08 | 2011-03-02 | ケミプロ化成株式会社 | 新規フルオレン含有アリールアミン共重合体、その製造方法およびそれを用いた有機el素子 |
DE60121611T2 (de) * | 2000-09-26 | 2007-07-26 | Cambridge Display Technology Ltd. | Verdrehte Polymere, deren Verwendung und Verfahren zur Herstellung von Statistischen Copopymeren |
EP1326942B1 (en) | 2000-10-03 | 2007-03-28 | Cambridge Display Technology Limited | Light-emissive polymer blends and light-emissive devices made from the same |
GB0028317D0 (en) * | 2000-11-21 | 2001-01-03 | South Bank Univ Entpr Ltd | Electroluminescent device incorporating polyaniline |
GB0031634D0 (en) * | 2000-12-23 | 2001-02-07 | Johnson Matthey Plc | Organic materials |
EP1366046B1 (en) * | 2001-01-24 | 2006-10-18 | Cambridge Display Technology Limited | Monomer for use in preparation of a polymer to be used in optical devices |
JP2004532291A (ja) | 2001-02-21 | 2004-10-21 | ケンブリッジ ディスプレイ テクノロジー リミテッド | ポリマー |
CN100377380C (zh) | 2001-02-28 | 2008-03-26 | 剑桥显示技术有限公司 | 供沉积在基材上的材料配方和方法 |
US8232116B2 (en) | 2001-02-28 | 2012-07-31 | Cambridge Display Technology Limited | Method for fabricating a polymer L.E.D. |
SG92833A1 (en) | 2001-03-27 | 2002-11-19 | Sumitomo Chemical Co | Polymeric light emitting substance and polymer light emitting device using the same |
GB0109108D0 (en) | 2001-04-11 | 2001-05-30 | Cambridge Display Tech Ltd | Polymer, its preparation and uses |
TW541855B (en) * | 2001-04-27 | 2003-07-11 | Sumitomo Chemical Co | Polymeric fluorescent substance and polymer light-emitting device using the same |
US7074885B2 (en) * | 2001-05-03 | 2006-07-11 | E.I. Du Pont De Nemours And Company | Electroactive fluorene copolymers and devices made with such polymers |
US7074886B2 (en) * | 2001-05-07 | 2006-07-11 | E. I. Du Pont De Memours And Company | Electroactive fluorene polymers having perfluoroalkyl groups, process for preparing such polymers and devices made with such polymers |
KR100580026B1 (ko) * | 2001-05-11 | 2006-05-12 | 캠브리지 디스플레이 테크놀로지 리미티드 | 치환된 플루오렌 중합체, 이들의 제조방법 및광학장치에서의 이들의 용도 |
KR100424073B1 (ko) * | 2001-05-22 | 2004-03-22 | 한국과학기술연구원 | 관능기를 함유한 플로렌계 화합물, 그 중합체 및 이들을이용한 el 소자 |
JP2003007475A (ja) * | 2001-06-20 | 2003-01-10 | Honda Motor Co Ltd | 有機エレクトロルミネッセンス素子 |
JP2004532348A (ja) * | 2001-06-22 | 2004-10-21 | ケンブリッジ ディスプレイ テクノロジー リミテッド | 置換されたトリフェニルアミン繰返し単位を含有するポリマー |
ATE414330T1 (de) * | 2001-07-10 | 2008-11-15 | Dow Global Technologies Inc | Elektroaktive polymere und daraus hergestellte vorrichtungen |
AU2002316734A1 (en) * | 2001-07-20 | 2003-03-03 | University Of Rochester | Light-emitting organic oligomer compositions |
SG94878A1 (en) | 2001-07-30 | 2003-03-18 | Sumitomo Chemical Co | Polymeric fluorescent substance and polymer light-emitting device using the same |
KR100414394B1 (ko) * | 2001-08-16 | 2004-01-07 | 일진다이아몬드(주) | 신규한 플루오렌계 발광 고분자 및 이를 이용한 전기발광소자 |
TWI306721B (en) | 2001-08-25 | 2009-02-21 | Cambridge Display Tech Ltd | Display device |
DE60124702T2 (de) * | 2001-09-04 | 2007-12-06 | Sony Deutschland Gmbh | Justierte lichtemittierende Polymermischungen, Film und Vorrichung auf Basis dieser Mischungen |
US6670213B2 (en) * | 2001-10-10 | 2003-12-30 | Cambridge Display Technology Limited | Method of preparing photoresponsive devices, and devices made thereby |
GB0125621D0 (en) | 2001-10-25 | 2001-12-19 | Cambridge Display Technology | Polymer preparation |
GB0125620D0 (en) | 2001-10-25 | 2001-12-19 | Cambridge Display Tech Ltd | Monomers and low band gap polymers formed therefrom |
SG124249A1 (en) | 2001-12-07 | 2006-08-30 | Sumitomo Chemical Co | New polymer and polymer light-emitting device using the same |
US6686065B2 (en) | 2001-12-12 | 2004-02-03 | Canon Kabushiki Kaisha | [5]-helicene and dibenzofluorene materials for use in organic light emitting devices |
SG125077A1 (en) * | 2001-12-19 | 2006-09-29 | Sumitomo Chemical Co | Copolymer, polymer composition and polymer light-emitting device |
DE10211648A1 (de) * | 2002-03-15 | 2003-09-25 | Basf Ag | Polymere auf Basis von Fluoranthen und ihre Verwendung |
SG128438A1 (en) | 2002-03-15 | 2007-01-30 | Sumitomo Chemical Co | Polymer compound and polymer light emitting deviceusing the same |
US7241512B2 (en) * | 2002-04-19 | 2007-07-10 | 3M Innovative Properties Company | Electroluminescent materials and methods of manufacture and use |
EP1504075B1 (en) * | 2002-05-10 | 2013-08-07 | Cambridge Display Technology Limited | Polymers their preparation and uses |
US7135241B2 (en) * | 2002-05-24 | 2006-11-14 | Board Of Regents, The University Of Texas System | Light-emitting block copolymers composition, process and use |
EP1509959A2 (en) | 2002-05-31 | 2005-03-02 | E. I. du Pont de Nemours and Company | Copolymers having tunable energy levels and color of emission |
JP5073151B2 (ja) * | 2002-07-22 | 2012-11-14 | 住友化学株式会社 | 共重合体およびそれを用いた高分子発光素子 |
WO2004014985A1 (ja) * | 2002-08-09 | 2004-02-19 | Tosoh Corporation | 新規トリアリールアミンポリマー、その製造方法及びその用途 |
TWI280973B (en) * | 2002-08-28 | 2007-05-11 | Sumitomo Chemical Co | Polymer compound and polymer light-emitting device using the same |
AU2003263360A1 (en) | 2002-09-03 | 2004-03-29 | Cambridge Display Technology Limited | Optical device |
DE10241814A1 (de) | 2002-09-06 | 2004-03-25 | Covion Organic Semiconductors Gmbh | Prozeß zur Herstellung von Aryl-Aryl gekoppelten Verbindungen |
KR100490539B1 (ko) * | 2002-09-19 | 2005-05-17 | 삼성에스디아이 주식회사 | 유기 전계 발광소자 및 그 제조방법 |
US7094902B2 (en) * | 2002-09-25 | 2006-08-22 | 3M Innovative Properties Company | Electroactive polymers |
DE10249723A1 (de) | 2002-10-25 | 2004-05-06 | Covion Organic Semiconductors Gmbh | Arylamin-Einheiten enthaltende konjugierte Polymere, deren Darstellung und Verwendung |
EP2325224A1 (en) | 2002-10-30 | 2011-05-25 | Sumitomo Chemical Company, Limited | Aryl copolymer compounds and polymer light emitting devices made by using the same |
EP1416028A1 (en) | 2002-10-30 | 2004-05-06 | Covion Organic Semiconductors GmbH | New method for the production of monomers useful in the manufacture of semiconductive polymers |
GB0225869D0 (en) | 2002-11-06 | 2002-12-11 | Cambridge Display Tech Ltd | Polymer |
AU2003280260A1 (en) * | 2002-11-08 | 2004-06-07 | National Research Council Of Canada | Thermally crosslinkable materials and multi-layered devices therefrom |
GB0226010D0 (en) | 2002-11-08 | 2002-12-18 | Cambridge Display Tech Ltd | Polymers for use in organic electroluminescent devices |
EP1579518B1 (en) * | 2002-12-20 | 2016-03-23 | Merck Patent GmbH | Improvements in and relating to organic semiconducting materials |
GB0229659D0 (en) * | 2002-12-20 | 2003-01-22 | Avecia Ltd | Electronic devices |
US20040131881A1 (en) * | 2002-12-31 | 2004-07-08 | Eastman Kodak Company | Complex fluorene-containing compounds for use in OLED devices |
US6849348B2 (en) * | 2002-12-31 | 2005-02-01 | Eastman Kodak Company | Complex fluorene-containing compounds |
DE10304819A1 (de) | 2003-02-06 | 2004-08-19 | Covion Organic Semiconductors Gmbh | Carbazol-enthaltende konjugierte Polymere und Blends, deren Darstellung und Verwendung |
US7049392B2 (en) * | 2003-02-12 | 2006-05-23 | E. I. Du Pont De Nemour And Company | Electroluminescent copolymers with multi-functional monomers and methods for use thereof |
US20040185302A1 (en) * | 2003-02-12 | 2004-09-23 | Uckert Frank P. | Aromatic polymers with multiple side chains and methods for use thereof |
US7138483B2 (en) * | 2003-02-12 | 2006-11-21 | E.I. Du Pont De Nemours And Company | Monomers, conjugated polymers and electronic devices using such polymers |
KR20050121232A (ko) * | 2003-03-31 | 2005-12-26 | 스미또모 가가꾸 가부시키가이샤 | 중합체 및 그것을 사용한 고분자 발광 소자 |
US7014925B2 (en) | 2003-04-29 | 2006-03-21 | Canon Kabushiki Kaisha | Heterogeneous spiro compounds in organic light emitting device elements |
US8530269B2 (en) | 2003-05-12 | 2013-09-10 | Cambridge Enterprise Ltd | Manufacture of a polymer device |
US20040232385A1 (en) * | 2003-05-21 | 2004-11-25 | Kram Shari L. | Blend of viscosity modifier and luminescent compound |
EP1633801B1 (en) * | 2003-05-30 | 2008-04-09 | MERCK PATENT GmbH | Semiconducting polymer |
US20050019607A1 (en) * | 2003-06-30 | 2005-01-27 | Franky So | OLED device with mixed emissive layer |
DE10337077A1 (de) | 2003-08-12 | 2005-03-10 | Covion Organic Semiconductors | Konjugierte Copolymere, deren Darstellung und Verwendung |
JP4885717B2 (ja) * | 2003-08-19 | 2012-02-29 | メルク パテント ゲーエムベーハー | トリフェニルホスフィン単位を含むオリゴマーおよびポリマー |
DE10340711A1 (de) * | 2003-09-04 | 2005-04-07 | Covion Organic Semiconductors Gmbh | Elektronische Vorrichtung enthaltend organische Halbleiter |
US7652126B2 (en) * | 2003-10-07 | 2010-01-26 | General Electric Company | Monomers and polymers comprising conjugated groups and methods for making thereof |
DE112004002193B4 (de) * | 2003-11-14 | 2017-03-23 | Sumitomo Chemical Co., Ltd. | Polymere von halogenierten Bisdiarylamino-polycyclischen aromatischen Verbindungen |
CN100558791C (zh) * | 2003-12-13 | 2009-11-11 | 默克专利有限公司 | 低聚物和聚合物 |
GB0329364D0 (en) * | 2003-12-19 | 2004-01-21 | Cambridge Display Tech Ltd | Optical device |
KR100718793B1 (ko) | 2003-12-30 | 2007-05-16 | 에스케이 주식회사 | 9,9-디(3,3'-바이카바질)-2,7-플루오레닐 단위 함유 유기전기발광고분자 및 이를 이용한 전기발광소자 |
CA2554940C (en) * | 2004-01-30 | 2013-05-28 | Sk Corporation | Organic electroluminescent polymer having 9,9-di(fluorenyl)-2,7-fluorenyl unit and organic electroluminescent device manufactured using the same |
US20080274303A1 (en) * | 2004-02-26 | 2008-11-06 | Katsumi Agata | Polymer Compound and Polymer Light Emitting Device Using the Same |
JP4736471B2 (ja) * | 2004-02-26 | 2011-07-27 | 住友化学株式会社 | 高分子化合物およびそれを用いた高分子発光素子 |
DE102004020299A1 (de) * | 2004-04-26 | 2005-12-01 | Covion Organic Semiconductors Gmbh | Konjugierte Polymere, deren Darstellung und Verwendung |
JP4533015B2 (ja) | 2004-06-15 | 2010-08-25 | キヤノン株式会社 | 化合物及びそれを用いた有機エレクトロルミネッセンス素子 |
DE102004036496A1 (de) * | 2004-07-28 | 2006-03-23 | Siemens Ag | Organische Leuchtdiode mit erhöhter Radikalanionenstabilität, sowie Verwendungen davon |
EP1627891A1 (en) | 2004-08-11 | 2006-02-22 | Covion Organic Semiconductors GmbH | Polymers for use in organic electroluminescent devices |
TWI328604B (en) * | 2004-09-24 | 2010-08-11 | Lg Chemical Ltd | New compound and organic light emitting device using the same(4) |
TWI308142B (en) * | 2004-09-24 | 2009-04-01 | Lg Chemical Ltd | New compound and organic light emitting device using the same (9) |
GB0422391D0 (en) | 2004-10-08 | 2004-11-10 | Cambridge Display Tech Ltd | Light emitting device |
GB0423006D0 (en) * | 2004-10-15 | 2004-11-17 | Cambridge Display Tech Ltd | Organic transistor |
US20060094859A1 (en) * | 2004-11-03 | 2006-05-04 | Marrocco Matthew L Iii | Class of bridged biphenylene polymers |
US7960037B2 (en) | 2004-12-03 | 2011-06-14 | The Regents Of The University Of California | Carbon nanotube polymer composition and devices |
KR20070089145A (ko) * | 2004-12-03 | 2007-08-30 | 스미또모 가가꾸 가부시키가이샤 | 트리아릴아민 함유 중합체 및 전자 장치 |
US20060121314A1 (en) * | 2004-12-06 | 2006-06-08 | Sk Corporation | Electroluminescent polymer having 9-fluoren-2-yl-9-aryl-2,7-fluorenyl unit and electroluminescent device manufactured using the same |
GB0427965D0 (en) | 2004-12-22 | 2005-01-26 | Cambridge Display Technology O | Process for the synthesis of arylfluorenes and analogues thereof |
US7818401B2 (en) * | 2004-12-23 | 2010-10-19 | General Instrument Corporation | Method and apparatus for providing decentralized load distribution |
US7102156B1 (en) | 2004-12-23 | 2006-09-05 | Spansion Llc Advanced Micro Devices, Inc | Memory elements using organic active layer |
GB2460358B (en) | 2004-12-29 | 2010-01-13 | Cambridge Display Tech Ltd | Rigid amines |
GB0428445D0 (en) * | 2004-12-29 | 2005-02-02 | Cambridge Display Tech Ltd | Blue-shifted triarylamine polymer |
JP2006190759A (ja) * | 2005-01-05 | 2006-07-20 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
KR101146976B1 (ko) | 2005-01-06 | 2012-05-23 | 삼성모바일디스플레이주식회사 | 청색 발광 고분자 및 이를 채용한 유기 전계 발광 소자 |
US20060177690A1 (en) * | 2005-02-07 | 2006-08-10 | Osram Opto Semiconductors Gmbh & Co. Ohg | Tri-layer PLED devices with both room-temperature and high-temperature operational stability |
US9109081B2 (en) | 2005-02-16 | 2015-08-18 | Sumitomo Chemical Company, Limited | Method for producing aromatic polymer |
WO2006091799A2 (en) | 2005-02-22 | 2006-08-31 | Sumation Co. Ltd. | High bandgap arylene polymers |
JP2006245021A (ja) * | 2005-02-28 | 2006-09-14 | Sanyo Electric Co Ltd | 有機エレクトロルミネッセンス素子用正孔輸送材料及びそれを用いた有機エレクトロルミネッセンス素子 |
CN101495534A (zh) * | 2005-03-04 | 2009-07-29 | 住友化学株式会社 | 二咔唑芳族胺聚合物和电子器件 |
KR101179321B1 (ko) * | 2005-03-25 | 2012-09-05 | 에스케이이노베이션 주식회사 | 9-플루오렌-2-일-2,7-플루오레닐 단위 함유 전기발광 고분자 및 이를 이용한 전기발광 소자 |
GB0507684D0 (en) * | 2005-04-15 | 2005-05-25 | Cambridge Display Tech Ltd | Pulsed driven displays |
US8153276B2 (en) * | 2005-04-28 | 2012-04-10 | Sumitomo Chemical Company, Limited | Polymer compound and polymer light emitting device using the same |
US8802245B2 (en) * | 2005-06-01 | 2014-08-12 | Sumitomo Chemical Company, Limited | Polymer composition and polymer light emitting device |
JP5119611B2 (ja) * | 2005-06-01 | 2013-01-16 | 住友化学株式会社 | 高分子組成物および高分子発光素子 |
JP4956918B2 (ja) * | 2005-06-03 | 2012-06-20 | 住友化学株式会社 | 高分子化合物およびそれを用いた高分子発光素子 |
TW200708591A (en) * | 2005-06-10 | 2007-03-01 | Sumitomo Chemical Co | Aromatic graft polymer |
GB2442655B (en) | 2005-06-22 | 2010-05-05 | Sumitomo Chemical Co | Polymeric material and polymeric luminescent element |
US20070111027A1 (en) * | 2005-07-29 | 2007-05-17 | Chen Shaw H | Light-emitting organic materials |
US7576356B2 (en) * | 2005-08-08 | 2009-08-18 | Osram Opto Semiconductors Gmbh | Solution processed crosslinkable hole injection and hole transport polymers for OLEDs |
WO2007020954A1 (ja) | 2005-08-12 | 2007-02-22 | Sumitomo Chemical Company, Limited | 高分子化合物およびそれを用いた高分子発光素子 |
KR101193179B1 (ko) * | 2005-08-26 | 2012-10-19 | 삼성디스플레이 주식회사 | 오가노실록산 화합물 및 이를 구비한 유기 발광 소자 |
WO2007043495A1 (ja) | 2005-10-07 | 2007-04-19 | Sumitomo Chemical Company, Limited | 共重合体およびそれを用いた高分子発光素子 |
WO2007043439A1 (ja) | 2005-10-07 | 2007-04-19 | Sumitomo Chemical Company, Limited | 高分子化合物とそれを用いた高分子発光素子 |
WO2007043607A1 (ja) | 2005-10-13 | 2007-04-19 | Mitsui Chemicals, Inc. | スルホ基を含有する高分子化合物、および該化合物を含有する有機電界発光素子 |
WO2007055407A1 (ja) | 2005-11-11 | 2007-05-18 | Sumitomo Chemical Company, Limited | 共役高分子化合物およびそれを用いた高分子発光素子 |
KR101193180B1 (ko) * | 2005-11-14 | 2012-10-19 | 삼성디스플레이 주식회사 | 전도성 고분자 조성물 및 이로부터 얻은 막을 구비한 전자소자 |
CN101360773B (zh) | 2005-11-18 | 2012-01-04 | 住友化学株式会社 | 高分子化合物及用其形成的高分子发光元件 |
EP1961780A4 (en) | 2005-12-02 | 2010-06-30 | Sumitomo Chemical Co | POLYMERIC COMPOUND AND POLYMERIC ELECTROLUMINESCENT DEVICE USING THE SAME |
DE102005060473A1 (de) | 2005-12-17 | 2007-06-28 | Merck Patent Gmbh | Konjugierte Polymere, deren Darstellung und Verwendung |
KR101243917B1 (ko) * | 2005-12-19 | 2013-03-14 | 삼성디스플레이 주식회사 | 전도성 고분자 조성물 및 이로부터 얻은 막을 구비한 전자소자 |
JP4328801B2 (ja) | 2005-12-20 | 2009-09-09 | キヤノン株式会社 | フルオレン化合物及び有機エレクトロルミネッセンス素子 |
GB0526185D0 (en) | 2005-12-22 | 2006-02-01 | Cambridge Display Tech Ltd | Electronic device |
US8440324B2 (en) | 2005-12-27 | 2013-05-14 | E I Du Pont De Nemours And Company | Compositions comprising novel copolymers and electronic devices made with such compositions |
KR20080083021A (ko) | 2005-12-28 | 2008-09-12 | 스미또모 가가꾸 가부시키가이샤 | 블록 공중합체 |
EP1974401A1 (en) | 2006-01-21 | 2008-10-01 | Merck Patent GmbH | Electronic short channel device comprising an organic semiconductor formulation |
GB2434916A (en) * | 2006-02-03 | 2007-08-08 | Cdt Oxford Ltd | OLED for full colour display |
GB2434915A (en) * | 2006-02-03 | 2007-08-08 | Cdt Oxford Ltd | Phosphoescent OLED for full colour display |
JP2007220772A (ja) * | 2006-02-15 | 2007-08-30 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス用高分子化合物及びその製造方法 |
US20090043064A1 (en) | 2006-02-22 | 2009-02-12 | Sumitomo Chemical Company, Limited | Metal complex, polymer compound, and device containing it |
KR20070101984A (ko) * | 2006-04-13 | 2007-10-18 | 삼성에스디아이 주식회사 | 전하분리층을 구비한 유기 전기발광 소자 |
GB2440934B (en) * | 2006-04-28 | 2009-12-16 | Cdt Oxford Ltd | Opto-electrical polymers and devices |
WO2007131582A1 (en) | 2006-05-12 | 2007-11-22 | Merck Patent Gmbh | Indenofluorene polymer based organic semiconductor materials |
CN101495535B (zh) | 2006-07-21 | 2012-06-20 | 默克专利有限公司 | 茚并芴和噻吩的共聚物 |
KR20090034398A (ko) | 2006-08-01 | 2009-04-07 | 스미또모 가가꾸 가부시키가이샤 | 고분자 화합물 및 고분자 발광 소자 |
TW200818981A (en) | 2006-08-30 | 2008-04-16 | Sumitomo Chemical Co | Organic electroluminescence device |
WO2008033388A2 (en) * | 2006-09-12 | 2008-03-20 | Qd Vision, Inc. | A composite including nanoparticles, methods, and products including a composite |
KR101463271B1 (ko) | 2006-09-14 | 2014-11-18 | 스미또모 가가꾸 가부시키가이샤 | 유기 전계발광 소자 |
JP5233228B2 (ja) * | 2006-10-05 | 2013-07-10 | Jnc株式会社 | ベンゾフルオレン化合物、該化合物を用いた発光層用材料及び有機電界発光素子 |
US8277955B2 (en) * | 2006-10-17 | 2012-10-02 | Seiko Epson Corporation | Compound for organic EL device and organic EL device |
JP2010509775A (ja) * | 2006-11-13 | 2010-03-25 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 有機電子デバイス |
JP5262104B2 (ja) | 2006-12-27 | 2013-08-14 | 住友化学株式会社 | 金属錯体、高分子化合物及びこれらを含む素子 |
US8465848B2 (en) | 2006-12-29 | 2013-06-18 | E I Du Pont De Nemours And Company | Benzofluorenes for luminescent applications |
JP5144938B2 (ja) | 2007-02-02 | 2013-02-13 | 住友化学株式会社 | 高分子発光素子、高分子化合物、組成物、液状組成物及び導電性薄膜 |
JP4811314B2 (ja) * | 2007-03-27 | 2011-11-09 | セイコーエプソン株式会社 | 有機elデバイス |
JP5374908B2 (ja) | 2007-04-27 | 2013-12-25 | 住友化学株式会社 | ピレン系高分子化合物及びそれを用いてなる発光素子 |
JP5248910B2 (ja) | 2007-05-30 | 2013-07-31 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子および該素子を用いた表示装置 |
CN101689467B (zh) * | 2007-06-01 | 2012-10-03 | E.I.内穆尔杜邦公司 | 化合物和含该化合物的材料 |
JP2009021104A (ja) | 2007-07-12 | 2009-01-29 | Sumitomo Chemical Co Ltd | 有機発光素子の製造方法 |
WO2009017056A1 (ja) | 2007-07-31 | 2009-02-05 | Sumitomo Chemical Company, Limited | 化合物及びその製造方法、並びにそれを用いたインク組成物、薄膜、有機トランジスタ及び有機電界発光素子 |
JP5254347B2 (ja) | 2007-10-24 | 2013-08-07 | メルク パテント ゲーエムベーハー | 光電子デバイス |
EP2203944B1 (de) | 2007-10-24 | 2014-04-16 | Merck Patent GmbH | Optoelektronische vorrichtung |
DE102008045664A1 (de) | 2008-09-03 | 2010-03-04 | Merck Patent Gmbh | Optoelektronische Vorrichtung |
DE102008045662A1 (de) | 2008-09-03 | 2010-03-04 | Merck Patent Gmbh | Optoelektronische Vorrichtung |
US8063399B2 (en) | 2007-11-19 | 2011-11-22 | E. I. Du Pont De Nemours And Company | Electroactive materials |
JP5217931B2 (ja) | 2007-11-29 | 2013-06-19 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子及びその製造方法 |
EP2233508A4 (en) * | 2007-12-11 | 2012-01-04 | Idemitsu Kosan Co | POLYMER COMPOUND AND ORGANIC ELECTROLUMINESCENT ELEMENT THEREWITH |
KR20100106426A (ko) | 2007-12-28 | 2010-10-01 | 스미또모 가가꾸 가부시키가이샤 | 고분자 발광 소자, 제조 방법 및 고분자 발광 디스플레이 장치 |
GB0803950D0 (en) | 2008-03-03 | 2008-04-09 | Cambridge Display Technology O | Solvent for printing composition |
EP2249411A4 (en) | 2008-03-07 | 2014-03-26 | Sumitomo Chemical Co | LAYER STRUCTURE |
WO2009122445A2 (en) * | 2008-03-31 | 2009-10-08 | Council Of Scientific & Industrial Research | Novel donor-acceptor fluorene scaffolds : a process and uses thereof |
US8343381B1 (en) | 2008-05-16 | 2013-01-01 | E I Du Pont De Nemours And Company | Hole transport composition |
US8062768B2 (en) | 2008-05-22 | 2011-11-22 | General Electric Company | Compound comprising phenyl pyridine units |
US8039125B2 (en) * | 2008-05-22 | 2011-10-18 | General Electric Company | Compound comprising phenyl pyridine units |
JP5609022B2 (ja) | 2008-06-23 | 2014-10-22 | 住友化学株式会社 | 金属錯体の残基を含む高分子化合物及びそれを用いた素子 |
JP5556063B2 (ja) | 2008-06-23 | 2014-07-23 | 住友化学株式会社 | 組成物及び該組成物を用いてなる発光素子 |
KR20110055563A (ko) | 2008-07-30 | 2011-05-25 | 스미또모 가가꾸 가부시키가이샤 | 적층 구조체, 그의 제조 방법 및 그것을 포함하는 전자 소자 |
DE102008045663A1 (de) | 2008-09-03 | 2010-03-04 | Merck Patent Gmbh | Fluorverbrückte Assoziate für optoelektronische Anwendungen |
DE102008049037A1 (de) | 2008-09-25 | 2010-04-22 | Merck Patent Gmbh | Neue Polymere mit niedriger Polydispersität |
JP5515542B2 (ja) | 2008-10-06 | 2014-06-11 | 住友化学株式会社 | 含窒素複素環構造を含む高分子化合物 |
US7635792B1 (en) | 2008-10-14 | 2009-12-22 | General Electric Company | 2,5-linked polyfluorenes for optoelectronic devices |
EP2352801B1 (en) | 2008-12-01 | 2017-06-21 | E. I. du Pont de Nemours and Company | Electroactive materials |
EP2352802A4 (en) | 2008-12-01 | 2012-10-31 | Du Pont | ELECTROACTIVE MATERIALS |
EP2352803B1 (en) * | 2008-12-04 | 2020-02-05 | LG Chem, Ltd. | Electroactive materials |
JP5691177B2 (ja) | 2009-01-29 | 2015-04-01 | 住友化学株式会社 | 高分子化合物及びそれを用いる発光素子 |
US8759818B2 (en) | 2009-02-27 | 2014-06-24 | E I Du Pont De Nemours And Company | Deuterated compounds for electronic applications |
KR101582707B1 (ko) | 2009-04-03 | 2016-01-05 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전기활성 재료 |
GB2469500B (en) | 2009-04-16 | 2012-06-06 | Cambridge Display Tech Ltd | Method of forming a polymer |
WO2010149259A2 (en) | 2009-06-22 | 2010-12-29 | Merck Patent Gmbh | Conducting formulation |
EP2448033A4 (en) * | 2009-06-23 | 2014-07-23 | Sumitomo Chemical Co | ORGANIC ELECTROLUMINESCENT ELEMENT |
EP2459379A4 (en) * | 2009-07-27 | 2015-05-06 | Du Pont | PROCESS AND MATERIALS FOR MANUFACTURING DELIMITED LAYERS AND DEVICES MADE THEREBY |
KR20120052356A (ko) | 2009-07-31 | 2012-05-23 | 스미또모 가가꾸 가부시키가이샤 | 고분자 발광 소자 |
JP2011046699A (ja) | 2009-07-31 | 2011-03-10 | Sumitomo Chemical Co Ltd | 金属錯体、それを含む組成物及びそれを用いた発光素子 |
US20110077373A1 (en) * | 2009-09-29 | 2011-03-31 | General Electric Company | Polymer and optoelectronic device comprising the same |
KR101790854B1 (ko) | 2009-09-29 | 2017-10-26 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 발광 응용을 위한 중수소화된 화합물 |
KR101704090B1 (ko) | 2009-09-30 | 2017-02-07 | 스미또모 가가꾸 가부시키가이샤 | 적층 구조체, 중합체, 전계 발광 소자 및 광전 변환 소자 |
JP2013508380A (ja) | 2009-10-19 | 2013-03-07 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 電子用途用のトリアリールアミン化合物 |
KR20120086319A (ko) | 2009-10-19 | 2012-08-02 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 전자적 응용을 위한 트라이아릴아민 화합물 |
WO2011049241A1 (ja) | 2009-10-22 | 2011-04-28 | 住友化学株式会社 | 有機エレクトロルミネッセンス素子 |
CN102596950A (zh) | 2009-10-29 | 2012-07-18 | E.I.内穆尔杜邦公司 | 用于电子应用的氘代化合物 |
US8617720B2 (en) | 2009-12-21 | 2013-12-31 | E I Du Pont De Nemours And Company | Electroactive composition and electronic device made with the composition |
EP2517273B1 (en) | 2009-12-23 | 2019-04-03 | Merck Patent GmbH | Compositions comprising organic semiconducting compounds |
JP2011146307A (ja) | 2010-01-15 | 2011-07-28 | Sumitomo Chemical Co Ltd | 高分子発光素子 |
KR101769173B1 (ko) | 2010-01-28 | 2017-08-17 | 스미또모 가가꾸 가부시키가이샤 | 고분자 화합물 및 그것을 이용하여 이루어지는 발광 소자 |
KR101759367B1 (ko) | 2010-01-29 | 2017-07-18 | 스미또모 가가꾸 가부시키가이샤 | 발광 재료, 잉크 조성물, 박막, 발광 소자 및 발광 소자의 제조 방법 |
JP5734681B2 (ja) * | 2010-01-29 | 2015-06-17 | 住友化学株式会社 | 発光性組成物、及びそれを用いた発光素子 |
JP5501864B2 (ja) | 2010-03-10 | 2014-05-28 | 住友化学株式会社 | 薄膜及びこれに用いられる化合物 |
WO2011128035A1 (en) | 2010-04-12 | 2011-10-20 | Merck Patent Gmbh | Composition and method for preparation of organic electronic devices |
JP4832605B2 (ja) | 2010-04-20 | 2011-12-07 | 住友化学株式会社 | 有機発光素子 |
US8822634B2 (en) * | 2010-04-23 | 2014-09-02 | Ocean's King Lighting Science & Technology Co., Ltd. | Copolymer comprising anthracene and benzoselenadiazole, preparing method and uses thereof |
GB2484253B (en) | 2010-05-14 | 2013-09-11 | Cambridge Display Tech Ltd | Organic light-emitting composition and device |
CN102906216B (zh) | 2010-05-27 | 2016-03-09 | 默克专利股份有限公司 | 组合物以及生产有机电子器件的方法 |
US9184388B2 (en) | 2010-07-29 | 2015-11-10 | Sumitomo Chemical Company, Limited | Layered structure, electronic device using same, aromatic compound, and method for manufacturing said compound |
GB201021277D0 (en) * | 2010-12-15 | 2011-01-26 | Cambridge Display Tech Ltd | Semiconductor blend |
WO2012087955A1 (en) | 2010-12-20 | 2012-06-28 | E. I. Du Pont De Nemours And Company | Compositions for electronic applications |
WO2012086670A1 (ja) | 2010-12-21 | 2012-06-28 | 住友化学株式会社 | 組成物及びブロック型共重合体 |
GB2494096B (en) | 2011-01-31 | 2013-12-18 | Cambridge Display Tech Ltd | Polymer |
CN103339167B (zh) | 2011-01-31 | 2018-01-12 | 剑桥显示技术有限公司 | 聚合物 |
JP5914069B2 (ja) | 2011-03-17 | 2016-05-11 | 住友化学株式会社 | 金属複合体組成物及びその混合物 |
US8940411B2 (en) | 2011-04-25 | 2015-01-27 | General Electric Company | Materials for optoelectronic devices |
GB201108865D0 (en) * | 2011-05-26 | 2011-07-06 | Ct For Process Innovation The Ltd | Semiconductor compounds |
GB201108864D0 (en) | 2011-05-26 | 2011-07-06 | Ct For Process Innovation The Ltd | Transistors and methods of making them |
JP2014527550A (ja) | 2011-07-25 | 2014-10-16 | メルク パテント ゲーエムベーハー | 機能性側鎖基を有するポリマーおよびオリゴマー |
WO2013018951A1 (ko) * | 2011-08-03 | 2013-02-07 | 포항공과대학교 산학협력단 | 3,6-카바졸을 포함하는 전도성 고분자 및 이를 이용한 유기태양전지 |
GB201210131D0 (en) | 2011-11-02 | 2012-07-25 | Cambridge Display Tech Ltd | Light emitting composition and device |
TWI574987B (zh) * | 2012-01-31 | 2017-03-21 | 劍橋顯示科技有限公司 | 聚合物 |
JP5939423B2 (ja) * | 2012-03-01 | 2016-06-22 | 日立化成株式会社 | ポリマー又はオリゴマー、及びこれを用いた有機エレクトロニクス素子 |
EP2744004B1 (en) * | 2012-12-11 | 2019-02-27 | Nissan Chemical Corporation | Process for the manufacture of a multilayer structure |
US9312485B2 (en) | 2012-12-13 | 2016-04-12 | Ei Du Pont De Nemours And Company | Process and materials for making contained layers and devices made with same |
US9912127B2 (en) | 2013-12-05 | 2018-03-06 | Schneider Electric USA, Inc. | Retracting mechanism for sensing components in a switchgear cabinet |
CN103741259B (zh) * | 2014-01-16 | 2016-10-26 | 齐齐哈尔大学 | 壳核结构芴-三苯胺共聚物/石墨烯复合纳米纤维材料 |
GB2524747B (en) | 2014-03-31 | 2017-03-01 | Cambridge Display Tech Ltd | Amine/fluorene copolymers and organic electronic devices comprising said copolymers |
JP6724924B2 (ja) * | 2015-09-18 | 2020-07-15 | 住友化学株式会社 | 高分子化合物及びそれを用いた発光素子 |
CN108780845A (zh) * | 2016-04-27 | 2018-11-09 | 武汉新驱创柔光电科技有限公司 | 半导体组合物 |
CN110036051B (zh) | 2016-11-30 | 2023-02-28 | 保土谷化学工业株式会社 | 含有取代三芳基胺结构单元的高分子化合物 |
WO2018168667A1 (ja) | 2017-03-15 | 2018-09-20 | 保土谷化学工業株式会社 | 置換トリアリールアミン骨格を有する高分子量化合物 |
US11999818B2 (en) | 2018-07-03 | 2024-06-04 | Hodogaya Chemical Co., Ltd. | High molecular weight triarylamine compound comprising terphenyl structure in molecular main chain and organic electroluminescent element comprising said high molecular weight compound |
GB2581141A (en) | 2019-01-31 | 2020-08-12 | Sumitomo Chemical Co | Light-emitting composition |
KR20220016828A (ko) | 2019-06-05 | 2022-02-10 | 호도가야 가가쿠 고교 가부시키가이샤 | 치환 트리아릴아민 구조 단위를 포함하는 고분자량 화합물 및 유기 일렉트로 루미네선스 소자 |
KR20220079517A (ko) | 2019-10-09 | 2022-06-13 | 호도가야 가가쿠 고교 가부시키가이샤 | 고분자량 화합물로 이루어지는 유기층을 갖는 유기 일렉트로 루미네선스 소자 |
EP4108701A4 (en) | 2020-02-20 | 2024-03-06 | Hodogaya Chemical Co., Ltd. | HIGH MOLECULAR WEIGHT COMPOUND AND LIGHT EMITTING DIODE COMPRISING SAID HIGH MOLECULAR WEIGHT COMPOUND |
KR20210148546A (ko) * | 2020-05-29 | 2021-12-08 | 삼성디스플레이 주식회사 | 정공 수송성 잉크 조성물, 발광 소자 및 이의 제조 방법 |
US11910697B2 (en) | 2020-09-09 | 2024-02-20 | Samsung Electronics Co., Ltd. | Copolymer, electroluminescence device material including copolymer, and electroluminescence device |
EP4219586A4 (en) | 2020-09-23 | 2024-09-18 | Hodogaya Chemical Co Ltd | COMPOSITION CONTAINING A LOW MOLECULAR WEIGHT COMPOUND, HEAT-CROSSLINKABLE, FOR LIGHT-EMITTING DIODE |
KR20230156317A (ko) | 2021-03-12 | 2023-11-14 | 호도가야 가가쿠 고교 가부시키가이샤 | 인데노디벤조헤테롤 구조를 부분 구조로서 갖는 고분자량화합물, 및 이들 고분자량 화합물을 함유하는 유기 일렉트로루미네선스 소자 |
WO2022244822A1 (ja) | 2021-05-21 | 2022-11-24 | 保土谷化学工業株式会社 | トリアリールアミン高分子量化合物およびこれらの高分子量化合物を含む有機エレクトロルミネッセンス素子 |
Family Cites Families (31)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3641115A (en) | 1968-08-22 | 1972-02-08 | Union Carbide Corp | Method for producing esters of polycyclic compounds |
US4400499A (en) * | 1981-12-29 | 1983-08-23 | Union Carbide Corporation | Integrated process for the preparation of substantially linear high molecular weight thermoplastic polymers from aryl polyhalide monomers |
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
DE3821567A1 (de) * | 1988-06-25 | 1989-12-28 | Bayer Ag | Loesliche polyaromaten |
DE69027697T2 (de) * | 1989-03-31 | 1997-01-23 | Toshiba Kawasaki Kk | Organische elektrolumineszente Vorrichtung |
GB8909011D0 (en) | 1989-04-20 | 1989-06-07 | Friend Richard H | Electroluminescent devices |
US5679760A (en) | 1991-04-11 | 1997-10-21 | Hoechst Aktiengesellschaft | Ladder polymers containing conjugated double bonds |
FR2702870B1 (fr) | 1993-03-19 | 1995-04-21 | Thomson Csf | Ecran électroluminescent. |
WO1995001871A1 (en) | 1993-07-09 | 1995-01-19 | The Regents Of The University Of California | Electroluminescent diodes utilizing blends of polymers |
US5682043A (en) | 1994-06-28 | 1997-10-28 | Uniax Corporation | Electrochemical light-emitting devices |
DE4436773A1 (de) | 1994-10-14 | 1996-04-18 | Hoechst Ag | Konjugierte Polymere mit Spirozentren und ihre Verwendung als Elektrolumineszenzmaterialien |
JP3505257B2 (ja) | 1995-02-24 | 2004-03-08 | 三洋電機株式会社 | 有機エレクトロルミネッセンス素子 |
JP3640090B2 (ja) * | 1995-05-19 | 2005-04-20 | 東洋インキ製造株式会社 | 正孔輸送材料およびその用途 |
DE59607957D1 (de) | 1995-07-25 | 2001-11-22 | Clariant Gmbh | Katalysatoren zur durchführung von kreuzkupplungsreaktionen |
US5708130A (en) | 1995-07-28 | 1998-01-13 | The Dow Chemical Company | 2,7-aryl-9-substituted fluorenes and 9-substituted fluorene oligomers and polymers |
DE69608446T3 (de) * | 1995-07-28 | 2010-03-11 | Sumitomo Chemical Company, Ltd. | 2,7-aryl-9-substituierte fluorene und 9-substituierte fluorenoligomere und polymere |
JP2002515078A (ja) | 1995-09-04 | 2002-05-21 | ヘキスト・リサーチ・アンド・テクノロジー・ドイチュラント・ゲーエムベーハー・ウント・コンパニー・カーゲー | エレクトロルミネセンス物質としてトリアリールアミン単位を含むポリマー |
DE19614971A1 (de) | 1996-04-17 | 1997-10-23 | Hoechst Ag | Polymere mit Spiroatomen und ihre Verwendung als Elektrolumineszenzmaterialien |
US5929194A (en) * | 1996-02-23 | 1999-07-27 | The Dow Chemical Company | Crosslinkable or chain extendable polyarylpolyamines and films thereof |
WO1997033193A2 (en) | 1996-02-23 | 1997-09-12 | The Dow Chemical Company | Cross-linkable or chain extendable polyarylpolyamines and films thereof |
EP0885461B1 (en) * | 1996-03-04 | 2003-08-13 | DuPont Displays, Inc. | Polyfluorenes as materials for photoluminescence and electroluminescence |
KR0176331B1 (ko) * | 1996-05-16 | 1999-04-01 | 박원훈 | 전계 발광 소자용 플로렌계 교대 공중합체 및 이를 발광재료로 사용한 전계 발광 소자 |
WO1997046052A1 (en) | 1996-05-28 | 1997-12-04 | Philips Electronics N.V. | Organic electroluminescent device |
US5728801A (en) | 1996-08-13 | 1998-03-17 | The Dow Chemical Company | Poly (arylamines) and films thereof |
KR0176336B1 (ko) * | 1996-12-31 | 1999-04-01 | 박원훈 | 아세틸렌기를 함유한 플로렌계 교대 공중합체 및 이를 이용한 전계발광소자 |
US6309763B1 (en) * | 1997-05-21 | 2001-10-30 | The Dow Chemical Company | Fluorene-containing polymers and electroluminescent devices therefrom |
US5998045A (en) | 1997-07-03 | 1999-12-07 | International Business Machines Corporation | Polymeric light-emitting device |
US5777070A (en) * | 1997-10-23 | 1998-07-07 | The Dow Chemical Company | Process for preparing conjugated polymers |
US5879821A (en) | 1997-11-13 | 1999-03-09 | Xerox Corporation | Electroluminescent polymer compositions and processes thereof |
GB9805476D0 (en) * | 1998-03-13 | 1998-05-13 | Cambridge Display Tech Ltd | Electroluminescent devices |
CN1167146C (zh) * | 1999-01-15 | 2004-09-15 | 陶氏环球技术公司 | 高分子半导体场效应晶体管 |
-
1998
- 1998-04-21 US US09/063,615 patent/US6309763B1/en not_active Expired - Lifetime
-
1999
- 1999-04-09 EP EP99918475A patent/EP0988337B2/en not_active Expired - Lifetime
- 1999-04-09 KR KR1019997012097A patent/KR100575382B1/ko not_active IP Right Cessation
- 1999-04-09 CN CN2007101091169A patent/CN101058672B/zh not_active Expired - Lifetime
- 1999-04-09 DE DE69908522T patent/DE69908522T3/de not_active Expired - Lifetime
- 1999-04-09 CN CNB998005878A patent/CN100341922C/zh not_active Expired - Lifetime
- 1999-04-09 WO PCT/US1999/007768 patent/WO1999054385A1/en active IP Right Grant
- 1999-04-09 JP JP55304899A patent/JP4375820B2/ja not_active Expired - Fee Related
- 1999-04-09 CA CA002294485A patent/CA2294485C/en not_active Expired - Fee Related
- 1999-04-20 TW TW088106301A patent/TWI243187B/zh active
-
2001
- 2001-03-15 US US09/808,788 patent/US6605373B2/en not_active Expired - Fee Related
-
2009
- 2009-06-15 JP JP2009142786A patent/JP5300612B2/ja not_active Expired - Fee Related
Cited By (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101215370B (zh) * | 2001-05-11 | 2012-06-20 | 剑桥显示技术有限公司 | 取代的芴聚合物,其制备方法和在光学设备中的用途 |
CN100417703C (zh) * | 2001-05-11 | 2008-09-10 | 剑桥显示技术有限公司 | 取代的芴聚合物,其制备方法和在光学设备中的用途 |
CN100583486C (zh) * | 2002-09-03 | 2010-01-20 | 剑桥显示技术有限公司 | 光学器件 |
CN1739204B (zh) * | 2002-12-20 | 2011-06-08 | 默克专利股份有限公司 | 改进有机半导体材料及与其有关的改进 |
CN100580002C (zh) * | 2003-03-20 | 2010-01-13 | 剑桥显示技术有限公司 | 聚合物及其制备和用途 |
CN100583490C (zh) * | 2003-03-20 | 2010-01-20 | 剑桥显示技术有限公司 | 电致发光器件 |
US7893160B2 (en) | 2003-11-17 | 2011-02-22 | Sumitomo Chemical Company, Limited | Crosslinkable substituted fluorene compounds and conjugated oligomers or polymers based thereon |
US9399702B2 (en) | 2003-11-17 | 2016-07-26 | Sumitomo Chemical Company, Limited | Crosslinkable arylamine compounds and conjugated oligomers or polymers based thereon |
CN1882632B (zh) * | 2003-11-17 | 2012-04-04 | 住友化学株式会社 | 可交联的取代芴化合物和基于其的共轭低聚物或聚合物 |
CN1898292B (zh) * | 2003-12-12 | 2011-04-13 | 住友化学株式会社 | 聚合物化合物和使用该聚合物化合物的聚合物发光器件 |
CN1749295B (zh) * | 2004-09-18 | 2011-09-14 | 三星移动显示器株式会社 | 蓝色发光聚合物及使用它的有机电致发光器件 |
CN101061089B (zh) * | 2004-12-03 | 2011-07-27 | 住友化学株式会社 | 水杨酸酯取代的共轭聚合物及器件 |
CN101851190B (zh) * | 2005-03-04 | 2012-04-25 | 住友化学株式会社 | 二咔唑-9-基-取代的三芳基胺 |
CN101184811B (zh) * | 2005-06-01 | 2011-08-17 | 住友化学株式会社 | 高分子组合物以及高分子发光元件 |
CN101384639B (zh) * | 2005-12-22 | 2015-09-09 | 剑桥显示技术有限公司 | 芳胺聚合物 |
CN101490862B (zh) * | 2006-07-25 | 2013-03-13 | 默克专利有限公司 | 聚合物共混物和它们在有机发光器件中的用途 |
CN101134814B (zh) * | 2006-08-24 | 2011-10-26 | E.I.内穆尔杜邦公司 | 空穴传输聚合物 |
CN103814091A (zh) * | 2011-09-21 | 2014-05-21 | 日产化学工业株式会社 | 电荷传输性清漆 |
CN103814091B (zh) * | 2011-09-21 | 2016-09-28 | 日产化学工业株式会社 | 电荷传输性清漆 |
CN103396533A (zh) * | 2013-08-14 | 2013-11-20 | 黑龙江大学 | 含甲氧基三苯胺-芴共聚物、制备方法及其应用 |
CN103980731A (zh) * | 2014-03-27 | 2014-08-13 | 中南大学 | 聚(三苯胺-芴)染料及其应用 |
CN103980731B (zh) * | 2014-03-27 | 2016-06-08 | 中南大学 | 聚(三苯胺-芴)染料及其应用 |
CN107994131A (zh) * | 2017-11-28 | 2018-05-04 | 武汉华星光电半导体显示技术有限公司 | 用于封装oled器件的封装结构、显示装置 |
Also Published As
Publication number | Publication date |
---|---|
JP4375820B2 (ja) | 2009-12-02 |
US20010026878A1 (en) | 2001-10-04 |
JP2002506481A (ja) | 2002-02-26 |
CA2294485A1 (en) | 1999-10-28 |
KR100575382B1 (ko) | 2006-05-03 |
EP0988337B1 (en) | 2003-06-04 |
US6605373B2 (en) | 2003-08-12 |
WO1999054385A1 (en) | 1999-10-28 |
DE69908522T3 (de) | 2007-05-24 |
CN101058672A (zh) | 2007-10-24 |
DE69908522D1 (de) | 2003-07-10 |
CA2294485C (en) | 2008-02-19 |
EP0988337A1 (en) | 2000-03-29 |
KR20010014061A (ko) | 2001-02-26 |
US6309763B1 (en) | 2001-10-30 |
TWI243187B (en) | 2005-11-11 |
EP0988337B2 (en) | 2006-11-02 |
CN101058672B (zh) | 2012-07-04 |
JP5300612B2 (ja) | 2013-09-25 |
JP2009256679A (ja) | 2009-11-05 |
DE69908522T2 (de) | 2004-04-15 |
CN100341922C (zh) | 2007-10-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN100341922C (zh) | 含芴聚合物及由其制成的场致发光器件 | |
CN100471899C (zh) | 用于光电子器件的含有导电聚合物的分散体和膜 | |
CN1130956C (zh) | 具有电极保护的场致发光元件 | |
CN1231515C (zh) | 制备共轭聚合物的方法 | |
CN1337987A (zh) | 芴共聚物以及由该共聚物制成的器件 | |
JP2008517135A (ja) | 架橋ポリマー製造のためのモノマー | |
CN1768093B (zh) | 聚合物 | |
US7220820B2 (en) | Electroactive fluorene copolymers and devices made with such polymers | |
US20030082401A1 (en) | Electroluminescent devices having diarylanthracene ladder polymers in emissive layers | |
CN1784445B (zh) | 在光学器件中使用的含苯并三唑的新聚合物 | |
KR102466243B1 (ko) | 유기 발광 조성물, 소자 및 방법 | |
CN100415802C (zh) | 用于光学器件的聚合物 | |
US20050119491A1 (en) | 2, 7-Substituted carbazoles and oligomers, polymers and co-polymers thereof | |
CN101092560A (zh) | 电致发光聚合物及其制备方法 | |
KR20080103772A (ko) | 트리페닐 아민기를 포함하는 유기 전기발광고분자 및 이를이용한 유기 전기발광소자 | |
KR20080104821A (ko) | 신규 청색 도판트를 포함하는 유기 전기발광고분자 및 이를이용한 유기 전기발광소자 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
ASS | Succession or assignment of patent right |
Owner name: DOW GLOBAL TECHNICAL COMPANY Free format text: FORMER OWNER: THE DOW CHEMICAL CO. Effective date: 20021228 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20021228 Address after: Michigan Applicant after: Dow Global Technologies Inc. Address before: Michigan Applicant before: The Dow Chemical Co. |
|
ASS | Succession or assignment of patent right |
Owner name: SUMITOMO CHEMICAL CO. Free format text: FORMER OWNER: DOW GLOBAL TECHNICAL COMPANY Effective date: 20060714 |
|
C41 | Transfer of patent application or patent right or utility model | ||
TA01 | Transfer of patent application right |
Effective date of registration: 20060714 Address after: Tokyo, Japan Applicant after: SUMITOMO CHEMICAL Co.,Ltd. Address before: Michigan Applicant before: Dow Global Technologies Inc. |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CI01 | Publication of corrected invention patent application |
Correction item: Claim 5 Correct: Compositions described in claim 3 False: Copolymer of claim 3 Number: 41 Volume: 23 |
|
CI03 | Correction of invention patent |
Correction item: Claim 5 Correct: Compositions described in claim 3 False: Copolymer of claim 3 Number: 41 Page: Description Volume: 23 |
|
ERR | Gazette correction |
Free format text: CORRECT: CLAIM OF RIGHT 5; FROM: CLAIM OF RIGHT COPOLYMER ACCORDING TO 3 TO: CLAIM OF RIGHT COMPOSITION ACCORDING TO 3 |
|
CX01 | Expiry of patent term | ||
CX01 | Expiry of patent term |
Granted publication date: 20071010 |