WO2005073340A1 - Organic materials with tunable electric and electroluminescent properties - Google Patents
Organic materials with tunable electric and electroluminescent properties Download PDFInfo
- Publication number
- WO2005073340A1 WO2005073340A1 PCT/US2005/001779 US2005001779W WO2005073340A1 WO 2005073340 A1 WO2005073340 A1 WO 2005073340A1 US 2005001779 W US2005001779 W US 2005001779W WO 2005073340 A1 WO2005073340 A1 WO 2005073340A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- phosphine oxide
- groups
- materials
- emitting device
- light emitting
- Prior art date
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- 239000011368 organic material Substances 0.000 title description 8
- 239000000463 material Substances 0.000 claims abstract description 94
- MPQXHAGKBWFSNV-UHFFFAOYSA-N oxidophosphanium Chemical group [PH3]=O MPQXHAGKBWFSNV-UHFFFAOYSA-N 0.000 claims abstract description 34
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 37
- 239000010410 layer Substances 0.000 claims description 21
- 235000010290 biphenyl Nutrition 0.000 claims description 19
- 239000004305 biphenyl Substances 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 17
- XYFCBTPGUUZFHI-UHFFFAOYSA-N phosphine group Chemical group P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 16
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 125000001072 heteroaryl group Chemical group 0.000 claims description 11
- 239000002019 doping agent Substances 0.000 claims description 10
- -1 phenylene vinylene Chemical group 0.000 claims description 8
- 239000010409 thin film Substances 0.000 claims description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 230000000903 blocking effect Effects 0.000 claims description 6
- 230000004044 response Effects 0.000 claims description 6
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 239000012044 organic layer Substances 0.000 claims description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-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
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000001475 halogen functional group Chemical group 0.000 claims description 3
- OHZAHWOAMVVGEL-UHFFFAOYSA-N 2,2'-bithiophene Chemical compound C1=CSC(C=2SC=CC=2)=C1 OHZAHWOAMVVGEL-UHFFFAOYSA-N 0.000 claims description 2
- ROFVEXUMMXZLPA-UHFFFAOYSA-N Bipyridyl Chemical compound N1=CC=CC=C1C1=CC=CC=N1 ROFVEXUMMXZLPA-UHFFFAOYSA-N 0.000 claims description 2
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 claims description 2
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical compound C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 claims description 2
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical compound C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims description 2
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-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
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims description 2
- 235000021286 stilbenes Nutrition 0.000 claims description 2
- 229930192474 thiophene Natural products 0.000 claims description 2
- 238000004770 highest occupied molecular orbital Methods 0.000 abstract description 9
- 230000021615 conjugation Effects 0.000 abstract description 6
- 238000000034 method Methods 0.000 description 13
- 238000000859 sublimation Methods 0.000 description 12
- 230000008022 sublimation Effects 0.000 description 12
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 description 10
- VURFVHCLMJOLKN-UHFFFAOYSA-N diphosphane Chemical compound PP VURFVHCLMJOLKN-UHFFFAOYSA-N 0.000 description 8
- 230000003287 optical effect Effects 0.000 description 8
- 125000002524 organometallic group Chemical group 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- YFPJFKYCVYXDJK-UHFFFAOYSA-N Diphenylphosphine oxide Chemical compound C=1C=CC=CC=1[P+](=O)C1=CC=CC=C1 YFPJFKYCVYXDJK-UHFFFAOYSA-N 0.000 description 7
- 238000010521 absorption reaction Methods 0.000 description 7
- 238000011161 development Methods 0.000 description 7
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 7
- 230000032258 transport Effects 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 6
- 238000013459 approach Methods 0.000 description 6
- 239000010408 film Substances 0.000 description 6
- 239000012535 impurity Substances 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- LERDAFCBKALCKT-UHFFFAOYSA-N 1,2,3,4,5-pentafluoro-6-(2,3,4-trifluorophenyl)benzene Chemical group FC1=C(F)C(F)=CC=C1C1=C(F)C(F)=C(F)C(F)=C1F LERDAFCBKALCKT-UHFFFAOYSA-N 0.000 description 5
- 238000000295 emission spectrum Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 5
- 238000012546 transfer Methods 0.000 description 5
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004440 column chromatography Methods 0.000 description 4
- 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 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 4
- 230000000704 physical effect Effects 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- JWUJQDFVADABEY-UHFFFAOYSA-N 2-methyltetrahydrofuran Chemical compound CC1CCCO1 JWUJQDFVADABEY-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 238000000113 differential scanning calorimetry Methods 0.000 description 3
- 238000001194 electroluminescence spectrum Methods 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 230000000670 limiting effect Effects 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000008188 pellet Substances 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000010453 quartz Substances 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- 230000009467 reduction Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- HQJQYILBCQPYBI-UHFFFAOYSA-N 1-bromo-4-(4-bromophenyl)benzene Chemical group C1=CC(Br)=CC=C1C1=CC=C(Br)C=C1 HQJQYILBCQPYBI-UHFFFAOYSA-N 0.000 description 2
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 2
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 description 2
- 238000004679 31P NMR spectroscopy Methods 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 239000007983 Tris buffer Substances 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 150000004985 diamines Chemical class 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- GPAYUJZHTULNBE-UHFFFAOYSA-N diphenylphosphine Chemical compound C=1C=CC=CC=1PC1=CC=CC=C1 GPAYUJZHTULNBE-UHFFFAOYSA-N 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- 230000002427 irreversible effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Chemical group 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- AKYHKWQPZHDOBW-UHFFFAOYSA-N (5-ethenyl-1-azabicyclo[2.2.2]octan-7-yl)-(6-methoxyquinolin-4-yl)methanol Chemical compound OS(O)(=O)=O.C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 AKYHKWQPZHDOBW-UHFFFAOYSA-N 0.000 description 1
- 238000004009 13C{1H}-NMR spectroscopy Methods 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 238000004057 DFT-B3LYP calculation Methods 0.000 description 1
- 239000001576 FEMA 2977 Substances 0.000 description 1
- 206010034962 Photopsia Diseases 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 150000001334 alicyclic compounds Chemical class 0.000 description 1
- 150000007824 aliphatic compounds Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- XGRJZXREYAXTGV-UHFFFAOYSA-N chlorodiphenylphosphine Chemical compound C=1C=CC=CC=1P(Cl)C1=CC=CC=C1 XGRJZXREYAXTGV-UHFFFAOYSA-N 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- LOUPRKONTZGTKE-UHFFFAOYSA-N cinchonine Natural products C1C(C(C2)C=C)CCN2C1C(O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000002860 competitive effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002484 cyclic voltammetry Methods 0.000 description 1
- BOXSCYUXSBYGRD-UHFFFAOYSA-N cyclopenta-1,3-diene;iron(3+) Chemical compound [Fe+3].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 BOXSCYUXSBYGRD-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000000840 electrochemical analysis Methods 0.000 description 1
- 238000000572 ellipsometry Methods 0.000 description 1
- 238000011066 ex-situ storage Methods 0.000 description 1
- 230000005281 excited state Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 150000002390 heteroarenes Chemical class 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 239000011229 interlayer Substances 0.000 description 1
- 229910052741 iridium Inorganic materials 0.000 description 1
- 238000004020 luminiscence type Methods 0.000 description 1
- 238000004776 molecular orbital Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- QZRXRMPNCPCMSW-UHFFFAOYSA-N phosphanyl(phosphanylidene)phosphane Chemical compound PP=P QZRXRMPNCPCMSW-UHFFFAOYSA-N 0.000 description 1
- 229910000065 phosphene Inorganic materials 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 238000001296 phosphorescence spectrum Methods 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 238000011002 quantification Methods 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 229960003110 quinine sulfate Drugs 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000001685 time-resolved fluorescence spectroscopy Methods 0.000 description 1
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 1
- 125000005259 triarylamine group Chemical group 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- FIQMHBFVRAXMOP-UHFFFAOYSA-N triphenylphosphane oxide Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)(=O)C1=CC=CC=C1 FIQMHBFVRAXMOP-UHFFFAOYSA-N 0.000 description 1
- ITHPEWAHFNDNIO-UHFFFAOYSA-N triphosphane Chemical compound PPP ITHPEWAHFNDNIO-UHFFFAOYSA-N 0.000 description 1
- 238000002061 vacuum sublimation Methods 0.000 description 1
- 239000003039 volatile agent Substances 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
- H10K2102/10—Transparent electrodes, e.g. using graphene
- H10K2102/101—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO]
- H10K2102/103—Transparent electrodes, e.g. using graphene comprising transparent conductive oxides [TCO] comprising indium oxides, e.g. ITO
-
- 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
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/18—Carrier blocking layers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Definitions
- organic materials In addition to providing unique chemical or physical properties which may be useful in electric and electroluminescent applications, organic materials often lend themselves to manufacturing processes that are readily adapted to large scales with little or no loss in precision, they may be engineered into an infinite variety of forms, and they often may be manufactured using inexpensive and abundant precursors. For all of these reasons, the development of novel and useful forms of organic materials for use in electrical and electroluminescent applications continues to attract investigation from governmental, educational and industrial researchers across the world. One example of such research is a result of the desire for solid state white lights that provide high power conversion efficiency. This goal has led to the investigation of organic light emitting devices (OLEDs) designed to simultaneously provide high quantum efficiency and low operating voltage.
- OLEDs organic light emitting devices
- Competing systems based on spin-coated or printed polymeric light emitters generally have lower quantum efficiency than small molecule organometallic phosphors, but operate at lower voltages and are therefore competitive on the basis of power efficiency.
- Combining the advantages of polymer and small molecule devices into an extremely high power efficiency package requires new materials development.
- the prior art white light devices described above are all limited by the efficiency of the generation of blue light.
- the lack of efficient long-lived blue OLEDs also limits the overall efficiency of R-G-B displays.
- organometallic phosphor doped OLEDs have demonstrated high quantum efficiencies (-90 % internal) for green devices, operating voltages are still high ( ⁇ 10 V at high brightness) for all colors compared to polymer based OLEDs, and stable, saturated blue light, critical for good white light with high color rendering index, has not yet been optimized.
- Blue phosphorescent OLEDs are currently limited by the lack of efficient charge transport layers into which to dope the phosphorescent emitter; to accomplish this, the triplet excited state of those materials must be engineered to be higher than those of the dopants.
- Currently available materials do not presently operate at optimum efficiency due to inefficient charge transport which leads to higher operating voltage.
- organometallic phosphors are doped into a conductive host matrix and emission results from energy transfer from the host to the triplet state of the phosphor.
- Development of efficient blue OLEDs based on this technology has been particularly challenging because the host material must exhibit triplet level emission ⁇ 450 nm to achieve efficient energy transfer without sacrificing charge transporting properties.
- outer groups may be linked or bonded to one and another, thereby approximating a single group or a ring, however for purposes of this disclosure they are still referred to as two outer groups, since they are bonded to the phosphine oxide via two single bonds.
- Outer groups as the term is used herein, are bound to a single phosphine oxide moiety.
- Bridging groups as the term is used herein, are bound to two or more phosphine oxide moieties.
- phosphine oxide The entire molecule; the one or more phosphine oxide moieties, the bridging group, and the two outer groups (whether bonded together or not bonded), is hereinafter referred to as a "phosphine oxide.”
- Examples of the general structure of the present invention are shown in Figures 1 and 2.
- a single phosphine oxide moiety is shown in Figure 1, and examples of a di-bonded and a tri-bonded phosphine oxide moiety are shown in Figure 2.
- the phosphine oxide structures of the present invention can generally be used in oligomer and polymer structures as indicated by the subscript "n" in Figure 2.
- this definition would therefore include diphosphine oxide, triphosphine oxide, and other polyphosphine oxides.
- the bridging groups themselves may contain phosphine oxides.
- the phosphine oxides of the present invention are further purified and configured as part of a circuit.
- the phrase "configured as part of a circuit” means that the phosphine oxides are configured to be exposed to an external stimulus, including but not limited to an electrical current, a voltage, a light source, or a temperature gradient. When the materials are exposed to an external stimulus, a predictable response is elicited.
- the present invention is a new class of materials, which, in part, are defined by their electrical and electroluminescent properties, and these properties are thus a fundamental aspect of the invention.
- Preferred embodiments of the present invention include circuits utilizing the materials of the present invention as an OLED, a photodetector, a solar cell, a thin film transistor, a bipolar transistor, and wherein the circuit is incorporated in an array to form an information display.
- the novel materials could potentially function in an electron transporting layer, a hole blocking layer, an exciton blocking layer, a host layer which either emits light or transfers energy to a light emitting dopant, or a combination of any of the four.
- the material In a transistor, either bipolar or thin film, the material would function as the charge transporting active semiconductor layer in a similar manner to doped silicon in a conventional field effect transistor. In a solar cell, the material would function as a charge transporting or exciton blocking layer.
- the materials be purified. Only phosphine oxides that are substantially purified will exhibit the electrical and electroluminescent properties which define the materials of the present invention. While not meant to be limiting, some stages of the purification process are generally performed when the materials are synthesized. A variety of techniques are known that produce phosphines which are typically used as precursors of the present invention.
- phosphine groups formed by these methods will eventually be oxidized, thereby producing a mixture of the phosphine oxide, partially oxidized phosphine oxide, and phosphine (i.e., no phosphine moieties oxidized) species.
- any technique that effectively separates the three species such as chromatographic separation or successive sublimation of each of the species, is in theory acceptable. However, in practice, successive sublimation is preferred.
- “Successive sublimation” simply means sublimating the various species one at a time under vacuum, taking advantage of the fact that typically the phosphine oxide species will have much different sublimation temperatures than the phosphine mono oxide and phosphine species, even though the bridging groups and outer groups may be the same.
- the sublimed species also have different physical appearances, further simplifying the process. Accordingly, the reasons successive sublimation is preferred are fairly straightforward. It is effective at producing the required degree of purification, it generally requires no additional solvents or other materials be introduced into the process, and it generally generates a minimum amount of waste.
- any method that produces substantially the same result; a substantially purified phosphine oxide should be understood as being encompassed by the present invention.
- the successive sublimation that produces the diphosphine oxide species of the present invention must be performed much more carefully and slowly than is typical. Rapid heating and/or poor vacuum in the sublimation process will not produce the purity required for the present invention, even though the substance may appear to be pure using standard chemical characterization techniques, such as thin layer chromatography, high pressure liquid chromatography, NMR, and elemental analysis.
- a phosphine oxide has been "substantially purified” when it will no longer produce any phosphine structures that are not fully oxidized at the phosphine moiety that are detectable by NMR when the mixture has been heated to a temperature above the sublimation temperature of the non-oxidized phosphine structures, but below the sublimation temperature of the phosphine oxide at a vacuum of at least 10 "6 Torr and for a period of at least 24 hours.
- the process of producing the "substantially pure" phosphine oxides of the present invention will typically remove many other undesirable impurities, and other chemical techniques can and should be used to remove such impurities. However, for purposes of defining "substantially pure,” these other impurities should not be viewed as limiting the scope of the present invention. Further, while successive sublimation is typically required to produce the requisite purity, it may not be used at all, or it may be used in conjunction with other standard chemical separation procedures such as column chromatography. The inventors have determined that column chromatography followed by successive sublimation is an efficient and effective separation regime to produce materials of the requisite purity.
- polymeric and large oligomeric molecules are not amenable to vacuum sublimation but are still useful as a thin film circuit element when applied by solution-based coating techniques such as spin-coating or printing.
- the purification requirements for such materials is generally similar to those described above, with the exception that purification is performed on the precursor monomer or oligomer before assembly of the final phosphine oxide.
- One of the principle advantages of the present invention is that by selecting appropriate bridging and outer groups, the new class of materials of the present invention enables designers to "tune" the electrical and electroluminescent characteristics of the materials.
- aromatic, heteroaromatic, alicyclic and aliphatic compounds may be used for the bridging group and for the outer groups.
- the bridging group can also include one or more phosphine oxide moieties, each bonded to an organic molecule.
- the particular selection of each will determine the electrical and luminescent properties of a specific material. Accordingly, the materials may be viewed as "tunable" meaning that a material with particular photophysical properties (such as triplet exciton energy) may be synthesized for use in a particular application which requires that property.
- a material with particular photophysical properties such as triplet exciton energy
- the lowest energy component (bridging group or outer group) will define the triplet state and highest occupied molecular orbital energies for the entire molecule. Accordingly, a specific requirement for a material may be met by choosing the appropriate bridging and outer groups, without having to consider the electrical interaction between the two.
- the present invention is therefore this entire class of materials, as the discovery of this isolating property of the phosphine oxide moiety has enabled a broad range of materials to be tuned to a wide variety of specific applications.
- materials such as naphthalene or biphenyl whose wide bandgap and high triplet state energies are desirable, but whose physical properties are unsuitable for practical device applications, can be combined and incorporated into the materials of the present invention, preserving their desirable photophysical properties (wide bandgap and high triplet state energies) while making them physically amenable to practical device applications, including but not limited to, thin film formation.
- the use of the materials of the present invention as charge transporting host materials in organometallic phosphor-doped electroluminescent devices provides an excellent example of how the phosphine oxide materials may be "tuned" for a specific application.
- a material suitable as a charge transporting host for a blue phosphorescent OLED is achieved by selecting the bridging group as octafluorobiphenyl and all outer groups as phenyl to give 4,4'- bis(diphenylphosphine oxide) octafluorobiphenyl (shown as PO5 in Figure 3).
- the melting point of the overall molecule is much higher than the octafluorobiphenyl, while the triplet energy of the octafluorobiphenyl is preserved.
- Materials suitable as charge transporting hosts for green phosphorescent OLEDs can be achieved, for example, by selecting the bridging group as biphenyl and all outer groups as phenyl to give 4,4'-bis(diphenylphosphine oxide) biphenyl (shown as POl in Figure 3).
- a green phosphorescent OLED is engineered when the bridging group is selected as biphenyl and the outer groups are selected as phenyl and 1- naphthyl to give 4,4'-bis(l-naphthylphenylphosphine oxide) biphenyl (shown as PO8 in Figure 3).
- tuning the materials in this manner achieves a material exhibiting similar photophysical properties to naphthalene, but with a much higher melting point (naphthalene 80°C, PO8
- Suitable outer groups include, but are not limited to, aryl, heteroaryl, cycloalkyl, or alkyl groups, as well as, R-substituted derivatives of these groups, where the substituted derivative is an alkyl, aryl, heteroaryl, halo, amino, hydroxyl, alkoxy, cyano, halogenated alkyl, aryl or heteroaryl.
- Preferred outer groups are shown in Figure 4 wherein x denotes a repeating unit, and can be an integer between 1 and 6. These outer groups can be used alone or in combinations to form the phosphine oxide structures shown Figures 1 and 2.
- Suitable bridging groups therefore include, but are not limited to, aryl, heteroaryl, cycloalkyl, or alkyl groups.
- Preferred bridging groups include, but are not limited to, difunctional or multifunctional groups (i.e., substituted at two or more positions) and selected from benzene, naphthalene, pyrene, stilbene, diphenylethyne, pyridine, quinoline, thiophene, phenylene vinylene, thienylene vinylene, biphenyl, diphenylmethane, bithiophene, bipyridine and substituted versions with R as defined above.
- FIG. 1 is a schematic drawing of a general structure of the mono phosphine oxide embodiment of the present invention.
- FIG. 2 is a schematic drawing of the general structure of the di phosphene oxide and tri phosphene oxide embodiment of the present invention.
- FIG. 3 shows examples of structures tuned to be used as the conductive host in blue and green organometallic phosphor doped OLED in accordance with the present invention.
- FIG. 4 shows the structures of preferred outer groups utilized in the present invention.
- FIG. 5 shows the structures of preferred bridging groups utilized in the present invention.
- FIG. 6 is a series of graphs showing the normalized absorption, phosphorescence and emission intensities as a function of wavelength for a preferred embodiment of the present invention (4,4'-bis(diphenylphosphine oxide) biphenyl) in a variety of differing configurations, (a) is the absorption spectrum in CH 2 C1 2 ; (b) is the emission spectrum in CH 2 CI 2 ; (c) is the emission spectrum in 2-MeTHF at 77K; (d) is the phosphorescence spectrum in 2-MeTHF at 77K; (e) is the absorption spectrum of 4,4'- bis(diphenylphosphine oxide) biphenyl film on quartz; (f) is the emission spectrum of 4,4'-bis(diphenylphosphine oxide) biphenyl film on quartz; and (g) is the EL spectrum of a device with the structure - ITO/200 A CuPc/400 A 4,4'-bis(diphenylphosphine oxide) biphen
- FIG. 7 is a graph of current density verses voltage from a preferred embodiment of the present invention composed of: ITO/200 A CuPc/400 A POl/10 A LiF/1000 A Al.
- FIG. 8 is a comparison of (a) computed structures for POl and DDB and orbital amplitude plots of their (b) LUMO and (c) HOMO.
- FIG. 9 is a schematic representation of one embodiment wherein the materials of the present invention are configured as an OLED, showing the anode layer, cathode layer, and organic layer.
- n-Butyl lithium [0.02 moles] was added dropwise using a syringe. Once the addition was completed, stirring was continued another hour at -66°C after which the reaction mixture was allowed to warm up and stabilize at 0°C for a 3 -hour period. The reaction flask was cooled again to -66°C prior to addition of 3.58 ml chlorodiphenylphosphine [0.02 moles] by syringe. As the addition was completed the color of the reaction mixture became pale yellow. The mixture was allowed to stir for 3 hours at -66°C before gradual warming to room temperature overnight. The reaction was then quenched with 2 mL of degassed methanol and all volatiles removed under reduced pressure.
- the crude white solid obtained was dissolved in degassed CH 2 CI 2 and immediately filtered through a short column of Celite (under nitrogen atmosphere). The CH 2 CI 2 was removed and the white solid was digested in degassed ethanol and gravity filtered affording 4.70 g of crude PI. A silica column was used with CH 2 C1 2 as the solvent to separate the PI (Rf- 0.99) from its monoxide (Rf- 0.03). Removal of volatile solvents under vacuum resulted in 4.16 g of chemically pure PI (80%). The resultant material was characterized as follows.
- NMR spectra were obtained using a Bruker AMX400 spectrometer at the following frequencies: 400.1 MHz (1H), 161.9 MHz ( 31 P) 100.6 MHz ( 13 C). Signals observed in the 1H and 13 C spectra were referenced to internal TMS and CDCI 3 and the P signals were externally referenced to 85% H 3 PO .
- IR spectra of samples prepared as KBr pellets were obtained using a Nicolette: Magna IR 860 Spectrometer. Melting points of chemically pure materials were determined by differential scanning calorimetry (DSC) using a Netzsch simultaneous thermal analyzer (STA400) with a heating rate of 20°C/min under N2 gas. Indium metal was used as the temperature standard.
- a simple bilayer electroluminescent device was grown by vacuum evaporation consisting of, in sequence, a 200 A thick layer of copper phthalocyanine (CuPc), a 400 A thick layer of POl and a cathode consisting of a 10 A LiF layer followed by a 1000 A Al layer.
- the cathode was deposited through a stencil mask to yield circular devices 1 mm in diameter.
- a quartz crystal oscillator placed near the substrate was used to measure the thickness of the films, which were calibrated ex situ using ellipsometry. Devices were tested in air with an electrical pressure contact
- the singlet lifetime in CH 2 CI2 was determined using the output of a frequency- doubled picosecond dye laser pumped by the second harmonic (280 nm) of a mode- locked ⁇ dNanadate laser (76 MHz) directed onto the sample where light emission was collected at right angles and focused into a 1/8 meter subtractive double monochromator equipped with a microchannel plate PMT operating in pulse-counting mode.
- the time resolution of the apparatus was measured to be 50 psec FWHM using a standard scattering material.
- Low temperature (77K) emission spectra and triplet lifetime were obtained in 2-methyltetrahydrofuran on a PTI QuantaMaster model C-60SE spectrofluorometer, equipped with a 928 PMT detector and corrected for detector response.
- triaryl amines are preferentially hole transporting with higher reduction potentials.
- the computed structures for POl and DDB are shown in Figure 8a.
- the N centers are trigonal planar allowing interaction of the nitrogen electron lone pairs with the bridging and outer aryl rings.
- the distorted tetrahedral geometry and absence of available lone pair electrons on the phosphorus site prevents electron delocalization between the two aryl domains.
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Cited By (6)
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WO2006130353A2 (en) * | 2005-05-31 | 2006-12-07 | Eastman Kodak Company | Light-emitting device containing bis-phosphineoxide compound |
WO2008005609A1 (en) * | 2006-04-17 | 2008-01-10 | Battelle Memorial Institute | Organic materials with phosphine sulfide moieties having tunable electric and electroluminescent properties |
JP2012082209A (en) * | 2004-04-20 | 2012-04-26 | Kyushu Electric Power Co Inc | Phosphorus-containing organic semiconductor compound and method for producing the same |
EP2452946A1 (en) * | 2010-11-16 | 2012-05-16 | Novaled AG | Pyridylphosphinoxides for organic electronic device and organic electronic device |
US9857705B2 (en) | 2015-10-23 | 2018-01-02 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus |
WO2018125512A1 (en) | 2016-12-27 | 2018-07-05 | Dow Global Technologies Llc | High triplet energy phosphine oxide compounds for oled application |
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KR102396300B1 (en) | 2014-12-30 | 2022-05-11 | 삼성디스플레이 주식회사 | An organic light emitting device employing a layer for improving a light efficiency |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01256584A (en) * | 1988-04-07 | 1989-10-13 | Idemitsu Kosan Co Ltd | Thin-film el element |
JP2002063989A (en) * | 2000-06-08 | 2002-02-28 | Toray Ind Inc | Light emitting element |
WO2003069961A1 (en) * | 2002-02-14 | 2003-08-21 | E.I. Du Pont De Nemours And Company | Electroluminescent iridium compounds with phosphinoalkoxides and phenylpyridines or phenylpyrimidines and devices made with such compounds |
JP2004095221A (en) * | 2002-08-29 | 2004-03-25 | Toray Ind Inc | Light-emitting device |
-
2005
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH01256584A (en) * | 1988-04-07 | 1989-10-13 | Idemitsu Kosan Co Ltd | Thin-film el element |
JP2002063989A (en) * | 2000-06-08 | 2002-02-28 | Toray Ind Inc | Light emitting element |
WO2003069961A1 (en) * | 2002-02-14 | 2003-08-21 | E.I. Du Pont De Nemours And Company | Electroluminescent iridium compounds with phosphinoalkoxides and phenylpyridines or phenylpyrimidines and devices made with such compounds |
JP2004095221A (en) * | 2002-08-29 | 2004-03-25 | Toray Ind Inc | Light-emitting device |
Non-Patent Citations (3)
Title |
---|
PATENT ABSTRACTS OF JAPAN vol. 014, no. 014 (C - 674) 12 January 1990 (1990-01-12) * |
PATENT ABSTRACTS OF JAPAN vol. 2002, no. 06 4 June 2002 (2002-06-04) * |
PATENT ABSTRACTS OF JAPAN vol. 2003, no. 12 5 December 2003 (2003-12-05) * |
Cited By (10)
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JP2012082209A (en) * | 2004-04-20 | 2012-04-26 | Kyushu Electric Power Co Inc | Phosphorus-containing organic semiconductor compound and method for producing the same |
EP1744598B1 (en) * | 2004-04-20 | 2017-05-31 | Kyushu Electric Power Co., Inc. | Organic electroluminescent element and manufacturing method thereof, organic compound containing phosphorus and manufacturing method thereof |
WO2006130353A2 (en) * | 2005-05-31 | 2006-12-07 | Eastman Kodak Company | Light-emitting device containing bis-phosphineoxide compound |
WO2006130353A3 (en) * | 2005-05-31 | 2007-01-25 | Eastman Kodak Co | Light-emitting device containing bis-phosphineoxide compound |
US7419728B2 (en) | 2005-05-31 | 2008-09-02 | Eastman Kodak Company | Light-emitting device containing bis-phosphineoxide compound |
WO2008005609A1 (en) * | 2006-04-17 | 2008-01-10 | Battelle Memorial Institute | Organic materials with phosphine sulfide moieties having tunable electric and electroluminescent properties |
EP2452946A1 (en) * | 2010-11-16 | 2012-05-16 | Novaled AG | Pyridylphosphinoxides for organic electronic device and organic electronic device |
US8778512B2 (en) | 2010-11-16 | 2014-07-15 | Novaled Ag | Chemical compound for organic electronic device and organic electronic device |
US9857705B2 (en) | 2015-10-23 | 2018-01-02 | Canon Kabushiki Kaisha | Electrophotographic photosensitive member, process cartridge, and electrophotographic apparatus |
WO2018125512A1 (en) | 2016-12-27 | 2018-07-05 | Dow Global Technologies Llc | High triplet energy phosphine oxide compounds for oled application |
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JP2007524672A (en) | 2007-08-30 |
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