WO2008006454A1 - Elektrolumineszierende polymere und ihre verwendung - Google Patents
Elektrolumineszierende polymere und ihre verwendung Download PDFInfo
- Publication number
- WO2008006454A1 WO2008006454A1 PCT/EP2007/005500 EP2007005500W WO2008006454A1 WO 2008006454 A1 WO2008006454 A1 WO 2008006454A1 EP 2007005500 W EP2007005500 W EP 2007005500W WO 2008006454 A1 WO2008006454 A1 WO 2008006454A1
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- Prior art keywords
- atoms
- polymers
- formula
- alkyl chain
- derivatives
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 110
- 125000004432 carbon atom Chemical group C* 0.000 claims description 66
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 23
- 150000003254 radicals Chemical class 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 16
- 229910052794 bromium Inorganic materials 0.000 claims description 15
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- -1 aromatic radicals Chemical class 0.000 claims description 12
- 229910052757 nitrogen Inorganic materials 0.000 claims description 12
- 229910052717 sulfur Inorganic materials 0.000 claims description 12
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 11
- 238000002347 injection Methods 0.000 claims description 10
- 239000007924 injection Substances 0.000 claims description 10
- 229910052799 carbon Inorganic materials 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 9
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 8
- 125000002950 monocyclic group Chemical group 0.000 claims description 8
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 125000003367 polycyclic group Chemical group 0.000 claims description 7
- 125000004122 cyclic group Chemical group 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 5
- 230000001588 bifunctional effect Effects 0.000 claims description 5
- 229920000547 conjugated polymer Polymers 0.000 claims description 5
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 5
- 238000004770 highest occupied molecular orbital Methods 0.000 claims description 5
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 claims description 5
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 claims description 4
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 230000007704 transition Effects 0.000 claims description 4
- SNFCXVRWFNAHQX-UHFFFAOYSA-N 9,9'-spirobi[fluorene] Chemical class C12=CC=CC=C2C2=CC=CC=C2C21C1=CC=CC=C1C1=CC=CC=C21 SNFCXVRWFNAHQX-UHFFFAOYSA-N 0.000 claims description 3
- 238000006069 Suzuki reaction reaction Methods 0.000 claims description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- 230000008878 coupling Effects 0.000 claims description 3
- 238000010168 coupling process Methods 0.000 claims description 3
- 238000005859 coupling reaction Methods 0.000 claims description 3
- 125000003983 fluorenyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 3
- 125000005259 triarylamine group Chemical group 0.000 claims description 3
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical compound C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims description 2
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 claims description 2
- XDFUNRTWHPWCKO-UHFFFAOYSA-N 4,5,9,10-tetrahydropyrene Chemical class C1CC2=CC=CC3=C2C2=C1C=CC=C2CC3 XDFUNRTWHPWCKO-UHFFFAOYSA-N 0.000 claims description 2
- WPCIUCNVWJNRCD-UHFFFAOYSA-N 4,5-dihydropyrene Chemical class C1=CC=C2CCC3=CC=CC4=CC=C1C2=C34 WPCIUCNVWJNRCD-UHFFFAOYSA-N 0.000 claims description 2
- MZCJSUCRGWIKHH-UHFFFAOYSA-N 6,7-dihydrobenzo[d][1]benzoxepine Chemical class O1CCC2=CC=CC=C2C2=CC=CC=C21 MZCJSUCRGWIKHH-UHFFFAOYSA-N 0.000 claims description 2
- XXPBFNVKTVJZKF-UHFFFAOYSA-N 9,10-dihydrophenanthrene Chemical class C1=CC=C2CCC3=CC=CC=C3C2=C1 XXPBFNVKTVJZKF-UHFFFAOYSA-N 0.000 claims description 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 2
- 238000006619 Stille reaction Methods 0.000 claims description 2
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 claims description 2
- 230000008859 change Effects 0.000 claims description 2
- 230000005669 field effect Effects 0.000 claims description 2
- 238000009472 formulation Methods 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 150000002240 furans Chemical class 0.000 claims description 2
- PJULCNAVAGQLAT-UHFFFAOYSA-N indeno[2,1-a]fluorene Chemical class C1=CC=C2C=C3C4=CC5=CC=CC=C5C4=CC=C3C2=C1 PJULCNAVAGQLAT-UHFFFAOYSA-N 0.000 claims description 2
- 150000002576 ketones Chemical class 0.000 claims description 2
- WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 claims description 2
- NFBOHOGPQUYFRF-UHFFFAOYSA-N oxanthrene Chemical compound C1=CC=C2OC3=CC=CC=C3OC2=C1 NFBOHOGPQUYFRF-UHFFFAOYSA-N 0.000 claims description 2
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical class [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 claims description 2
- 125000001791 phenazinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 claims description 2
- 229950000688 phenothiazine Drugs 0.000 claims description 2
- GJSGGHOYGKMUPT-UHFFFAOYSA-N phenoxathiine Chemical compound C1=CC=C2OC3=CC=CC=C3SC2=C1 GJSGGHOYGKMUPT-UHFFFAOYSA-N 0.000 claims description 2
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002904 solvent Substances 0.000 claims description 2
- 150000003462 sulfoxides Chemical class 0.000 claims description 2
- GVIJJXMXTUZIOD-UHFFFAOYSA-N thianthrene Chemical compound C1=CC=C2SC3=CC=CC=C3SC2=C1 GVIJJXMXTUZIOD-UHFFFAOYSA-N 0.000 claims description 2
- 239000010409 thin film Substances 0.000 claims description 2
- 229930192474 thiophene Natural products 0.000 claims description 2
- 125000004958 1,4-naphthylene group Chemical group 0.000 claims 1
- 150000001716 carbazoles Chemical class 0.000 claims 1
- 150000004756 silanes Chemical class 0.000 claims 1
- 150000003457 sulfones Chemical class 0.000 claims 1
- 239000000178 monomer Substances 0.000 description 15
- 229920001577 copolymer Polymers 0.000 description 7
- 238000006116 polymerization reaction Methods 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000004020 conductor Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 125000001424 substituent group Chemical group 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- RICKKZXCGCSLIU-UHFFFAOYSA-N 2-[2-[carboxymethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]ethyl-[[3-hydroxy-5-(hydroxymethyl)-2-methylpyridin-4-yl]methyl]amino]acetic acid Chemical compound CC1=NC=C(CO)C(CN(CCN(CC(O)=O)CC=2C(=C(C)N=CC=2CO)O)CC(O)=O)=C1O RICKKZXCGCSLIU-UHFFFAOYSA-N 0.000 description 3
- BQOYJICDFRPTHI-UHFFFAOYSA-N 3,9-dibromo-7h-benzo[a]phenalene Chemical compound C1=CC(C2=CC=C(C=C2C2)Br)=C3C2=CC=CC3=C1Br BQOYJICDFRPTHI-UHFFFAOYSA-N 0.000 description 3
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000003086 colorant Substances 0.000 description 3
- 230000021615 conjugation Effects 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 230000037230 mobility Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- MNSNFBDVMQSWPA-UHFFFAOYSA-N 3,9-dibromo-7,7-dimethylbenzo[a]phenalene Chemical compound C1=CC(C(C)(C)C=2C3=CC=C(Br)C=2)=C2C3=CC=C(Br)C2=C1 MNSNFBDVMQSWPA-UHFFFAOYSA-N 0.000 description 2
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000005265 energy consumption Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 125000002524 organometallic group Chemical group 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- ICPSWZFVWAPUKF-UHFFFAOYSA-N 1,1'-spirobi[fluorene] Chemical compound C1=CC=C2C=C3C4(C=5C(C6=CC=CC=C6C=5)=CC=C4)C=CC=C3C2=C1 ICPSWZFVWAPUKF-UHFFFAOYSA-N 0.000 description 1
- XBZKJGBIPSQKAU-UHFFFAOYSA-N 3,9-dibromobenzo[b]phenalen-7-one Chemical compound C1=CC(C2=CC=C(C=C2C2=O)Br)=C3C2=CC=CC3=C1Br XBZKJGBIPSQKAU-UHFFFAOYSA-N 0.000 description 1
- DOJFBBMXBZGEAG-UHFFFAOYSA-N 5,6-dibromobenzo[a]phenalen-7-one Chemical compound Brc1cc2cccc3-c4ccccc4C(=O)c(c1Br)c23 DOJFBBMXBZGEAG-UHFFFAOYSA-N 0.000 description 1
- HUKPVYBUJRAUAG-UHFFFAOYSA-N 7-benzo[a]phenalenone Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC=CC2=C1 HUKPVYBUJRAUAG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229910010082 LiAlH Inorganic materials 0.000 description 1
- 229920000144 PEDOT:PSS Polymers 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
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 125000005264 aryl amine group Chemical group 0.000 description 1
- 229920005601 base polymer Polymers 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 239000002800 charge carrier Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 230000005525 hole transport Effects 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000007641 inkjet printing Methods 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 239000005267 main chain polymer Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 125000004430 oxygen atom Chemical group O* 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920001690 polydopamine Polymers 0.000 description 1
- 229920002098 polyfluorene Polymers 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000007790 solid phase Substances 0.000 description 1
- 238000004528 spin coating 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
- 239000000758 substrate Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- XTQHKBHJIVJGKJ-UHFFFAOYSA-N sulfur monoxide Chemical compound S=O XTQHKBHJIVJGKJ-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 230000001960 triggered effect Effects 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
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- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/687—Unsaturated compounds containing a keto groups being part of a ring containing halogen
- C07C49/697—Unsaturated compounds containing a keto groups being part of a ring containing halogen containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/269—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of only halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D221/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
- C07D221/02—Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
- C07D221/04—Ortho- or peri-condensed ring systems
- C07D221/18—Ring systems of four or more rings
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/78—Ring systems having three or more relevant rings
- C07D311/80—Dibenzopyrans; Hydrogenated dibenzopyrans
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
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- 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
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- 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
- C08G61/121—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from organic halides
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- 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
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- 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
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Definitions
- the present invention relates to electroluminescent polymers containing structural units of formula (1) and their use.
- the polymers according to the invention show improved efficiency and a longer service life, especially when used in polymeric organic light-emitting diodes.
- PLEDs polymeric (organic) light-emitting diodes
- full-color display elements full-color displays
- various classes of materials have already been proposed or developed.
- poly-fluorene derivatives and poly-spirobifluorene, poly-Dihydrophenanthren- and poly-Indenofluoren- derivatives come into consideration.
- Polymers which contain a combination of the mentioned structural elements have also been proposed.
- polymers containing poly-para-phenylene (PPP) as a structural element are used.
- the life of the green and especially the blue-emitting polymers is not sufficient for many applications.
- the invention relates to polymers containing units of the formula (1).
- RR 22 is the same or different at each instance and is H or an aliphatic or aromatic hydrocarbon radical having 1 to 20 C atoms;
- n is the same or different 0, 1, 2 or 3 at each occurrence;
- n is the same or different 0, 1 or 2 at each occurrence
- R 2 is the same or different at each occurrence and is H or an aliphatic or aromatic hydrocarbon radical having 1 to 20 C atoms;
- G is the same or different at each instance and is a bivalent moiety selected from the group 1, group 2, group 3, group 4, group 5, group 6, group 7 or a mixture of several of the groups 1 to 7;
- n is the same or different 0, 1, 2 or 3 at each occurrence;
- n is the same or different 0, 1 or 2 at each occurrence;
- p is the same or different 0 or 1 at each occurrence
- aromatic or heteroaromatic ring system in the context of the present invention is to be understood as meaning a system which does not necessarily contain only aromatic or heteroaromatic groups, but in which several aromatic or heteroaromatic groups are also present.
- aromatic groups may be interrupted by a short non-aromatic moiety ( ⁇ 10% of the atoms other than H, preferably ⁇ 5% of the atoms other than H), such as sp 3 -hybridized C, O, N, etc.
- systems such as 9,9'-spirobifluorene, 9,9-diaryl fluorene, triarylamine, etc. are to be understood as aromatic ring systems.
- the polymer according to the invention usually contains at least 5 mol%, preferably at least 10 mol%, particularly preferably at least 30 mol% and in particular at least 50 mol%, of units of the formula (1) or (1a). It has been found that when different units of the formula (1) or (1a) are present at the same time, the sum of all units of the formula (1) or (1a) is in the aforementioned range, so that the content of individual units of the Formula (1) or (1a) may also be less than 5 mol% in such cases.
- the polymers according to the invention are conjugated or partially conjugated polymers.
- conjugated polymers are polymers which have been mainly sp 2 -hybridized in the main chain
- Carbon atoms which may also be replaced by corresponding heteroatoms contain. In the simplest case this means alternating presence of double and single bonds in the main chain. Mainly, of course, suggests that naturally occurring defects that lead to conjugation disruptions do not invalidate the term "conjugated polymer". Furthermore, in this application text is also referred to as conjugated, if in the main chain, for example arylamine units and / or certain heterocycles (ie conjugation of N, O or S atoms) and / or organometallic complexes (ie, conjugation via the metal atom) ,
- units such as simple alkyl bridges, (thio) ether, ester, amide or imide linkages are clearly defined as non-conjugated segments.
- a partially conjugated polymer is meant a polymer in which longer conjugated portions in of the main chain are interrupted by non-conjugated portions, or containing longer conjugated portions in the side chains of a non-conjugated in the main chain polymer.
- the polymers according to the invention may contain, in addition to the units of the formula (1) or (1a), further structural elements. These are u.a. those as disclosed in WO 02/077060 A1 and DE 10337346 A1 and listed extensively. These are considered via quotation as part of the present application.
- the further structural units can come, for example, from the following classes:
- Group 1 units which increase the hole injection and / or transport properties of the polymers
- Group 2 units containing the electron injection and / or
- Group 3 units comprising combinations of Group 1 and Group 2 individual units
- Group 4 units which change the emission characteristics to the extent that electrophosphorescence can be obtained instead of electrofluorescence;
- Group 5 units which improve the transition from the so-called singlet to triplet state
- Group 6 Units which have the morphology and / or the
- Group 7 units which are typically used as backbone.
- Preferred polymers according to the invention are those in which at least one structural element has charge transport properties, ie contain the units from groups 1 and / or 2.
- these arylamines and heterocycles lead to a HOMO in the polymer of greater than -5.8 eV (at vacuum level), more preferably greater than -5.5 eV.
- these units in the polymer result in a LUMO of less than -2.7 eV (vs. vacuum level), more preferably less than -3.0 eV.
- the polymers according to the invention may contain units from group 3 in which structures which increase hole mobility and which increase electron mobility (that is to say units from groups 1 and 2) are bonded directly to one another. Some of these units can serve as emitters and shift the emission color to green, yellow or red. Their use is thus suitable, for example, for the production of other emission colors from originally blue-emitting polymers.
- Structural units according to group 4 are those which can emit light from the triplet state even at room temperature with high efficiency, ie show electrophosphorescence instead of electrofluorescence, which frequently causes an increase in energy efficiency. For this purpose, compounds which are heavy atoms with a first
- Group 5 structural elements are those which improve the singlet to triplet state transition and which, when used in support of the Group 4 structural elements, improve the phosphorescence properties of these structural elements.
- carbazole and bridged carbazole dimer units are suitable for this purpose, as described in DE 10304819 A1 and DE 10328627 A1.
- ketones, phosphine oxides, sulfoxides and similar compounds are suitable for this purpose.
- Group 6 structural elements which influence the morphology and / or the emission color of the polymers are, besides those mentioned above, those which have at least one further aromatic or another conjugated structure which does not fall under the abovementioned groups, ie which has little charge carrier mobilities which are not organometallic complexes or have no effect on the singlet-triplet transition.
- Such structural elements can the Morphology and / or the emission color of the resulting polymers influence. Depending on the unit, they can therefore also be used as emitters.
- Particularly preferred is the incorporation of 1, 4 phenylene, 1, 4-naphthlenylene, 1, 4 or 9,10-anthrylene, 1, 6, 2,7 or 4,9-pyrenylene , 3,9- or 3,10-perylenylene, 4,4'-biphenylylene, 4,4'-terphenylylene, 4,4'-bi-I 1 I 1 -naphthylylene, 4,4'-tolanylene, 4,4'-stilbenylene or 4,4 "bisstyrylarylene derivatives.
- Group 7 structural elements are units containing aromatic structures of 6 to 40 carbon atoms, which are typically used as a backbone. These are, for example, 4,5 dihydropyrene derivatives, 4,5,9,10-tetrahydropyrene derivatives, fluorene derivatives, 9,9'-spirobifluorene derivatives, 9,10-dihydrophenanthrene derivatives, 5,7-dihydrodibenzooxepine derivatives and cis and trans indenofluorene derivatives. However, since the proportion of units according to formula (1) or (1a) is at least 50 mol%, these structural elements from group 7 are not used here preferably as the main polymer backbone, but at most as a backbone that is present in minor proportion ,
- polymers according to the invention which, in addition to structural units of the formula (1) or (1a), additionally contain one or more units selected from groups 1 to 7. It may also be preferred if more than one structural unit from a group is present at the same time.
- the proportion of units of the formula (1) or (1a) is preferably at least 10 mol%, particularly preferably at least 30 mol% and in particular at least 50 mol%. This preference applies above all if the units of the formula (1) or (1a) are the polymer backbone. In other functions, other proportions may be preferred, for example, in the order of 5 to 20 mol%, if the hole conductor or emitter is in an electroluminescent polymer. For other applications, for example, for organic transistors, the preferred proportion may again be different, for example, up to 100 mol%, when it comes to hole- or electron-conducting units.
- polymers according to the invention which, in addition to structural units of the formula (1) or (1a), also contain at least one structural unit from the abovementioned groups. Particularly preferred are at least two structural units from different of the above classes. If present, the proportion of these
- Structural elements preferably in each case at least 5 mol%, particularly preferably in each case at least 10 mol%.
- one of these structural units is selected from the group of hole-conducting units and the other group is an emitting unit, whereby these two functions (hole conduction and emission) can also be assumed by the same unit.
- a smaller proportion of the emitting units in particular green and red emitting units, may also be preferred, for example for the synthesis of white-emitting copolymers. How white, emitting copolymers can be synthesized is described in detail in DE 10343606 A1.
- the polymers according to the invention preferably have from 10 to 10,000, more preferably from 50 to 5000 and in particular from 50 to 2000 repeat units.
- the necessary solubility of the polymers is ensured, inter alia, by the substituents R or R 1 on the units of the formula (1) or (1a) and optionally on further units present. If further substituents are present, these too may contribute to the solubility.
- At least 2 non-aromatic C atoms be present in the substituents.
- Some of these C atoms can also be replaced by O or S. However, this may well mean that a certain proportion of repeating units carries no further non-aromatic substituents.
- Non-aromatic C atoms are, as described for example in the description for R and R 1 in formula (1) or (1a), in corresponding straight-chain, branched or cyclic alkyl or alkoxy chains.
- R for each occurrence, identically or differently, a straight-chain alkyl chain having 1 to 25 C atoms, a branched alkyl chain having 3 to
- the two radicals R together can also form a further mono- or polycyclic, aromatic or aliphatic 5 ring system;
- R 1 for each occurrence identical or different H 1 is a straight-chain alkyl chain having 1 to 22 carbon atoms, a branched alkyl chain with 3 to
- R 15 is an aryl, heteroaryl, aryloxy or heteroaryloxy group having 5 to 40 carbon atoms, which may also be substituted by one or more non-aromatic radicals R 1 ; two or more of the radicals R 1 with one another and / or with R here can also form a mono- or polycyclic, aliphatic or aromatic ring system; or F, Cl 1 Br, I 1 CN, N (R 2 ) 2 , Si (R 2 ) 3 or B (R 2 ) 2 ; and
- X is C at each occurrence
- p stands for the number zero.
- the units of the formula (1) or (1a) are suitable in particular for various functions in the polymer.
- these units can preferably be used as (electron-conducting) polymer backbone, as a hole conductor or as an emitter.
- 7,7 ' positions are symmetrically substituted. This preference is due to the better synthetic accessibility of the monomers.
- R are the same and most preferably also the same.
- Examples of preferred units of the formula (1) or (1a) are the following structures wherein the linkage in the polymer in each case via the 3,9-positions, as indicated by the dashed bonds. Possible substituents are generally not listed or not everywhere because of the clarity.
- alkyl is generally an aliphatic alkyl group
- aryl is an aromatic or heteroaromatic system as described for R.
- the polymers of the invention are either homopolymers or copolymers.
- copolymers according to the invention can potentially have one or more further structures, for example from the abovementioned groups 1 to 7.
- the copolymers according to the invention may have random, alternating or block-like structures or alternatively have several of these structures in turn. How copolymers with block-like structures can be obtained is described in detail, for example, in DE 10337077 A1. This publication is incorporated by reference in the present application.
- properties such as solubility, solid phase morphology, color, charge injection and transport properties, temperature stability, electro-optical characteristics, etc. can be adjusted.
- the polymers according to the invention are generally prepared by polymerization of one or more types of monomer, of which at least one monomer in the polymer leads to units of the formula (1) or (1a). Corresponding polymerization reactions are in principle many. However, some types have proved particularly useful here, leading to C-C or C-N linkages:
- Monomers which lead to structural units of the formula (1) in the polymers according to the invention are derivatives which have suitable functionalities at the 3,9-position which allow this monomer unit to be incorporated in the To incorporate polymer. Insofar as a different link is desired, the functionality must be changed accordingly.
- Monomers which lead to units of the formula (1) or (1a) in the polymer are novel and therefore also the subject of the present invention.
- the invention furthermore relates to bifunctional monomeric compounds of the formula (2) or (2a)
- A is selected from Cl, Br, I, O-tosylate, O-triflate, O-SO 2 R 2 , B (OR 2 ) 2 and Sn (R 2 ) 3 , more preferably from Br, I and B (OR 2 ) 2 , wherein R 2 has the same meaning as described above, and wherein two or more R 2 can also form a ring system with each other.
- the C-C linkages are preferably selected from the groups of SUZUKI coupling, YAMAMOTO coupling and STILLE coupling; the C-N linkage is preferably a coupling according to
- the polymer according to the invention may be preferred not to use as a pure substance, but as a mixture (blend) together with further optional polymeric, oligomeric, dendritic or low molecular weight substances. These can, for example, improve the electronic properties, influence the transfer from the singlet to the triplet state or even emit light from the singlet or from the triplet state. But also electronically inert substances may be useful, for example, the morphology of the formed
- Polymer film or the viscosity of polymer solutions Such blends are therefore also the subject of the present invention.
- the invention furthermore relates to solutions and formulations 30 of one or more polymers or blends according to the invention in one or more solvents.
- polymer solutions can be prepared is described, for example, in WO 02/072714 A1, in WO 03/019694 A2 and in the literature cited therein.
- These solutions can be used to thin polymer layers For example, by surface coating method (eg spin-coating) or printing method (eg ink jet printing).
- the polymers of the invention can be used in PLEDs.
- cathode anode
- emission layer optionally further layers, such as e.g. preferably a hole injection layer and optionally an intermediate layer between the hole injection and the emission layer.
- PLEDs can be produced is described in detail as a general method in DE 10304819 A1, which is to be adapted accordingly for the individual case.
- the polymers according to the invention are very particularly suitable as electroluminescent materials in the PLEDs or displays produced in this way.
- Electroluminescent materials in the context of the invention apply materials that can be used as an active layer in a PLED use.
- Active layer means that the layer is able to emit light upon application of an electric field (light-emitting layer) and / or that it improves the injection and / or transport of the positive and / or negative charges (charge injection or charge transport layer). It may also be an intermediate layer between a hole injection layer and an emission layer.
- the invention therefore also relates to the use of a polymer according to the invention in a PLED, in particular as an electroluminescent material.
- the invention thus likewise provides a PLED having one or more active layers, wherein at least one of these is active
- the active layer may be, for example, a light-emitting layer and / or a transport layer and / or a charge injection layer and / or an intermediate layer.
- the polymers according to the invention have the following surprising advantages over the poly-spirobifluorenes and polyfluorenes described in WO 03/020790 A2 and WO 02/077060 A1, which are hereby named as the closest prior art:
- the polymers according to the invention have higher operative lifetimes, in particular in the case of green and blue-emitting PLEDs.
- the polymers according to the invention are good electron conductors, even without the use of electron-conducting comonomers. Electron conductive properties in polymers have hitherto been difficult to realize because many prior art electron conductors are not sufficiently stable for high value applications.
- the use of polymers or blends according to the invention with respect to PLEDs and the corresponding displays is aimed at. Despite this limitation of the description, it is possible for the person skilled in the art without further inventive step, the polymers according to the invention also for other uses in other electronic devices
- O-ICs organic integrated circuits
- OFETs organic field effect transistors
- OTFTs organic thin film transistors
- O-SCs organic solar cells
- O-lasers organic laser diodes
- the polymers according to the invention and the comparative polymers are synthesized by SUZUKI coupling according to WO 03/048225.
- the composition of the polymers P1 and P2 of the invention and the comparative polymers V1 and V2 synthesized is shown in Table 1.
- the polymers are being investigated for use in PLEDs.
- the PLEDs are each two-layer systems, ie substrate // ITO // PEDOT // polymer // cathode.
- PEDOT is a polythiophene derivative (Baytron P, from HC Starck, Goslar).
- the cathode used is Ba / Ag (Aldrich) in all cases. How PLEDs are represented is described in detail in WO 04/037887 and in the literature cited therein. Examples 5 to 8: Device examples
- the efficiency of the polymers according to the invention is better than that of the comparative polymers.
- the emission color is comparable and the lifetimes are significantly improved considering this. This shows that the polymers according to the invention are more suitable for use in displays than polymers according to the prior art.
- CIE coordinates color coordinates of the Commision Internationale de l'Eclairage 1931 Lifetime: Time to decrease brightness to 50% of initial brightness, initial brightness 400 cd / m 2
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Abstract
Description
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Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US12/373,004 US7790057B2 (en) | 2006-07-11 | 2007-06-22 | Electroluminescent polymers and use thereof |
KR1020097002413A KR101412923B1 (ko) | 2006-07-11 | 2007-06-22 | 전계발광 중합체 및 이의 용도 |
JP2009518738A JP5657250B2 (ja) | 2006-07-11 | 2007-06-22 | エレクトロルミネセンスポリマー及びその使用 |
EP07764773A EP2038241B1 (de) | 2006-07-11 | 2007-06-22 | Elektrolumineszierende polymere und ihre verwendung |
DE502007005425T DE502007005425D1 (de) | 2006-07-11 | 2007-06-22 | Elektrolumineszierende polymere und ihre verwendung |
CN200780026014.9A CN101489961B (zh) | 2006-07-11 | 2007-06-22 | 电致发光聚合物及其用途 |
AT07764773T ATE485254T1 (de) | 2006-07-11 | 2007-06-22 | Elektrolumineszierende polymere und ihre verwendung |
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DE102006031991.5 | 2006-07-11 | ||
DE102006031991A DE102006031991A1 (de) | 2006-07-11 | 2006-07-11 | Elektrolumineszierende Polymere und ihre Verwendung |
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US (1) | US7790057B2 (de) |
EP (1) | EP2038241B1 (de) |
JP (1) | JP5657250B2 (de) |
KR (1) | KR101412923B1 (de) |
CN (1) | CN101489961B (de) |
AT (1) | ATE485254T1 (de) |
DE (2) | DE102006031991A1 (de) |
TW (1) | TW200819474A (de) |
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Cited By (2)
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JP2013528927A (ja) * | 2010-03-17 | 2013-07-11 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 新規有機電界発光化合物およびこれを使用する有機電界発光素子 |
US9543528B2 (en) | 2013-09-05 | 2017-01-10 | Cheil Industries, Inc. | Compound for an organic optoelectric device, organic optoelectric device including the same, and display device including the optoelectric device |
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JP5617150B2 (ja) * | 2005-11-11 | 2014-11-05 | 住友化学株式会社 | 共役高分子化合物およびそれを用いた高分子発光素子 |
US20120116050A1 (en) * | 2009-06-15 | 2012-05-10 | Technische Universitaet Graz | Pyrene-based polymers for organic light emitting diodes (oleds) |
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CN104017586B (zh) * | 2014-05-29 | 2015-07-15 | 京东方科技集团股份有限公司 | 液晶化合物、液晶组合物及其制备方法、液晶显示面板 |
KR20180013958A (ko) * | 2015-05-29 | 2018-02-07 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 발광 소자, 발광 장치, 표시 장치, 전자 기기, 및 조명 장치 |
KR102032023B1 (ko) * | 2016-09-09 | 2019-10-14 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 전자 소자 |
CN106519733B (zh) * | 2016-09-18 | 2018-01-09 | 大连理工大学 | 一类含3位取代基的苯绕蒽酮液晶染料,其制备方法及应用 |
CN108484656B (zh) * | 2018-06-01 | 2020-05-05 | 华侨大学 | 一种四配位三芳基硼化合物的制备方法 |
CN111808125B (zh) * | 2020-07-07 | 2023-03-03 | 武汉天马微电子有限公司 | 一种有机化合物、有机电致发光材料及其应用 |
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- 2007-06-22 JP JP2009518738A patent/JP5657250B2/ja active Active
- 2007-06-22 US US12/373,004 patent/US7790057B2/en not_active Expired - Fee Related
- 2007-06-22 EP EP07764773A patent/EP2038241B1/de active Active
- 2007-06-22 DE DE502007005425T patent/DE502007005425D1/de active Active
- 2007-06-22 KR KR1020097002413A patent/KR101412923B1/ko active IP Right Grant
- 2007-06-22 CN CN200780026014.9A patent/CN101489961B/zh active Active
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013528927A (ja) * | 2010-03-17 | 2013-07-11 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 新規有機電界発光化合物およびこれを使用する有機電界発光素子 |
US9543528B2 (en) | 2013-09-05 | 2017-01-10 | Cheil Industries, Inc. | Compound for an organic optoelectric device, organic optoelectric device including the same, and display device including the optoelectric device |
Also Published As
Publication number | Publication date |
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JP5657250B2 (ja) | 2015-01-21 |
US20090318625A1 (en) | 2009-12-24 |
TW200819474A (en) | 2008-05-01 |
US7790057B2 (en) | 2010-09-07 |
CN101489961A (zh) | 2009-07-22 |
JP2009542868A (ja) | 2009-12-03 |
ATE485254T1 (de) | 2010-11-15 |
EP2038241B1 (de) | 2010-10-20 |
CN101489961B (zh) | 2014-05-14 |
DE102006031991A1 (de) | 2008-01-17 |
DE502007005425D1 (de) | 2010-12-02 |
KR20090028812A (ko) | 2009-03-19 |
KR101412923B1 (ko) | 2014-06-26 |
EP2038241A1 (de) | 2009-03-25 |
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