US20030077480A1 - Organic electroluminescence device - Google Patents
Organic electroluminescence device Download PDFInfo
- Publication number
- US20030077480A1 US20030077480A1 US10/141,982 US14198202A US2003077480A1 US 20030077480 A1 US20030077480 A1 US 20030077480A1 US 14198202 A US14198202 A US 14198202A US 2003077480 A1 US2003077480 A1 US 2003077480A1
- Authority
- US
- United States
- Prior art keywords
- group
- substituted
- unsubstituted
- carbon atoms
- phenanthrolin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 238000005401 electroluminescence Methods 0.000 title claims abstract description 36
- 239000000463 material Substances 0.000 claims abstract description 51
- 150000004696 coordination complex Chemical class 0.000 claims abstract description 45
- 239000010409 thin film Substances 0.000 claims abstract description 25
- -1 amine compound Chemical class 0.000 claims description 1331
- 125000004432 carbon atom Chemical group C* 0.000 claims description 153
- 150000001875 compounds Chemical class 0.000 claims description 42
- 125000003118 aryl group Chemical group 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 239000003446 ligand Substances 0.000 claims description 24
- 125000005843 halogen group Chemical group 0.000 claims description 21
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 18
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 17
- 230000001603 reducing effect Effects 0.000 claims description 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 14
- 125000003277 amino group Chemical group 0.000 claims description 13
- 239000002019 doping agent Substances 0.000 claims description 13
- 125000002947 alkylene group Chemical group 0.000 claims description 12
- 125000004104 aryloxy group Chemical group 0.000 claims description 12
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 8
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 125000005504 styryl group Chemical group 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 7
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 125000001624 naphthyl group Chemical group 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 125000002529 biphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C12)* 0.000 claims description 6
- 125000002950 monocyclic group Chemical group 0.000 claims description 6
- 125000003367 polycyclic group Chemical group 0.000 claims description 6
- 150000002430 hydrocarbons Chemical group 0.000 claims description 5
- 239000000203 mixture Substances 0.000 claims description 5
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 4
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 4
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims description 4
- UGUHFDPGDQDVGX-UHFFFAOYSA-N 1,2,3-thiadiazole Chemical group C1=CSN=N1 UGUHFDPGDQDVGX-UHFFFAOYSA-N 0.000 claims description 3
- FCNCGHJSNVOIKE-UHFFFAOYSA-N 9,10-diphenylanthracene Chemical group C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C1=CC=CC=C1 FCNCGHJSNVOIKE-UHFFFAOYSA-N 0.000 claims description 3
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000004062 acenaphthenyl group Chemical group C1(CC2=CC=CC3=CC=CC1=C23)* 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000005577 anthracene group Chemical group 0.000 claims description 3
- 125000005110 aryl thio group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 113
- 239000010408 film Substances 0.000 description 31
- 238000000034 method Methods 0.000 description 25
- 0 [1*]C/C(=C/c1ccc(Cc2ccc(/C=C(/C[4*])C[5*])cc2)cc1)C[2*] Chemical compound [1*]C/C(=C/c1ccc(Cc2ccc(/C=C(/C[4*])C[5*])cc2)cc1)C[2*] 0.000 description 19
- 230000000052 comparative effect Effects 0.000 description 17
- 229910052783 alkali metal Inorganic materials 0.000 description 13
- 238000002347 injection Methods 0.000 description 13
- 239000007924 injection Substances 0.000 description 13
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- 150000001340 alkali metals Chemical class 0.000 description 9
- 230000015572 biosynthetic process Effects 0.000 description 8
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 8
- 125000006083 1-bromoethyl group Chemical group 0.000 description 7
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 description 7
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 7
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 7
- 125000005999 2-bromoethyl group Chemical group 0.000 description 7
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 description 7
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 description 7
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 7
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 7
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 7
- 125000005997 bromomethyl group Chemical group 0.000 description 7
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 7
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 7
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 7
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 7
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- BRSRUYVJULRMRQ-UHFFFAOYSA-N 1-phenylanthracene Chemical class C1=CC=CC=C1C1=CC=CC2=CC3=CC=CC=C3C=C12 BRSRUYVJULRMRQ-UHFFFAOYSA-N 0.000 description 6
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 6
- 125000000389 2-pyrrolyl group Chemical group [H]N1C([*])=C([H])C([H])=C1[H] 0.000 description 6
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 description 6
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 description 6
- 125000001397 3-pyrrolyl group Chemical group [H]N1C([H])=C([*])C([H])=C1[H] 0.000 description 6
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical group C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 6
- 229910052792 caesium Inorganic materials 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 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 5
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 description 5
- 150000001342 alkaline earth metals Chemical class 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 125000002078 anthracen-1-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([*])=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 5
- 125000000748 anthracen-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C([H])=C([*])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 5
- 230000003247 decreasing effect Effects 0.000 description 5
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 5
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 5
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- 238000010521 absorption reaction Methods 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 125000004429 atom Chemical group 0.000 description 4
- 239000013522 chelant Substances 0.000 description 4
- 229910052733 gallium Inorganic materials 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 150000004820 halides Chemical class 0.000 description 4
- 230000031700 light absorption Effects 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 125000005561 phenanthryl group Chemical group 0.000 description 4
- 229910052761 rare earth metal Inorganic materials 0.000 description 4
- 150000002910 rare earth metals Chemical class 0.000 description 4
- 238000005215 recombination Methods 0.000 description 4
- 230000006798 recombination Effects 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 238000007740 vapor deposition Methods 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 229910001508 alkali metal halide Inorganic materials 0.000 description 3
- 150000008045 alkali metal halides Chemical class 0.000 description 3
- 229910001615 alkaline earth metal halide Inorganic materials 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 3
- 230000006866 deterioration Effects 0.000 description 3
- 229910052744 lithium Inorganic materials 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 125000001725 pyrenyl group Chemical group 0.000 description 3
- 229910052701 rubidium Inorganic materials 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 125000006836 terphenylene group Chemical group 0.000 description 3
- 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 3
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 2
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 description 2
- AQAZUWSITJUIEW-UHFFFAOYSA-N C.CNC(C)COC Chemical compound C.CNC(C)COC AQAZUWSITJUIEW-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N CN(C)C Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000005427 anthranyl group Chemical group 0.000 description 2
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 2
- 125000000732 arylene group Chemical group 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 150000004770 chalcogenides Chemical class 0.000 description 2
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical class C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 125000004185 ester group Chemical group 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 150000002222 fluorine compounds Chemical class 0.000 description 2
- 229910052738 indium Inorganic materials 0.000 description 2
- 150000002484 inorganic compounds Chemical class 0.000 description 2
- 229910010272 inorganic material Inorganic materials 0.000 description 2
- 239000011810 insulating material Substances 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000001989 lithium alloy Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 238000001451 molecular beam epitaxy Methods 0.000 description 2
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 2
- 150000004767 nitrides Chemical class 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000001275 scanning Auger electron spectroscopy Methods 0.000 description 2
- 239000004065 semiconductor Substances 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- KLCLIOISYBHYDZ-UHFFFAOYSA-N 1,4,4-triphenylbuta-1,3-dienylbenzene Chemical class C=1C=CC=CC=1C(C=1C=CC=CC=1)=CC=C(C=1C=CC=CC=1)C1=CC=CC=C1 KLCLIOISYBHYDZ-UHFFFAOYSA-N 0.000 description 1
- 125000004973 1-butenyl group Chemical group C(=CCC)* 0.000 description 1
- XOYZGLGJSAZOAG-UHFFFAOYSA-N 1-n,1-n,4-n-triphenyl-4-n-[4-[4-(n-[4-(n-phenylanilino)phenyl]anilino)phenyl]phenyl]benzene-1,4-diamine Chemical group C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 XOYZGLGJSAZOAG-UHFFFAOYSA-N 0.000 description 1
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000006280 2-bromobenzyl group Chemical group [H]C1=C([H])C(Br)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006290 2-hydroxybenzyl group Chemical group [H]OC1=C(C([H])=C([H])C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000006481 2-iodobenzyl group Chemical group [H]C1=C([H])C(I)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 125000006279 3-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Br)=C1[H])C([H])([H])* 0.000 description 1
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 1
- 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 description 1
- 125000006291 3-hydroxybenzyl group Chemical group [H]OC1=C([H])C([H])=C([H])C(=C1[H])C([H])([H])* 0.000 description 1
- 125000006482 3-iodobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(I)=C1[H])C([H])([H])* 0.000 description 1
- CMSGUKVDXXTJDQ-UHFFFAOYSA-N 4-(2-naphthalen-1-ylethylamino)-4-oxobutanoic acid Chemical compound C1=CC=C2C(CCNC(=O)CCC(=O)O)=CC=CC2=C1 CMSGUKVDXXTJDQ-UHFFFAOYSA-N 0.000 description 1
- 125000006281 4-bromobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Br)C([H])([H])* 0.000 description 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
- CVNOWLNNPYYEOH-UHFFFAOYSA-N 4-cyanophenol Chemical compound OC1=CC=C(C#N)C=C1 CVNOWLNNPYYEOH-UHFFFAOYSA-N 0.000 description 1
- 125000003143 4-hydroxybenzyl group Chemical group [H]C([*])([H])C1=C([H])C([H])=C(O[H])C([H])=C1[H] 0.000 description 1
- 125000006483 4-iodobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1I)C([H])([H])* 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
- 229910001316 Ag alloy Inorganic materials 0.000 description 1
- 229910000838 Al alloy Inorganic materials 0.000 description 1
- 229910001148 Al-Li alloy Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 1
- SJYMZIBVCWGJEQ-UHFFFAOYSA-N C(=C(c1ccccc1)c1ccccc1)c1c2ccccc2c(-c2ccc(-c3c4ccccc4c(C=C(c4ccccc4)c4ccccc4)c4ccccc34)cc2)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2c3ccccc3c(-c3ccc(C=C(c4ccccc4)c4ccccc4)cc3)c3ccccc23)cc1.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)c4ccccc34)c3ccccc23)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)c4ccccc34)cc2)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)cc3)c3ccccc23)cc1 Chemical compound C(=C(c1ccccc1)c1ccccc1)c1c2ccccc2c(-c2ccc(-c3c4ccccc4c(C=C(c4ccccc4)c4ccccc4)c4ccccc34)cc2)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2c3ccccc3c(-c3ccc(C=C(c4ccccc4)c4ccccc4)cc3)c3ccccc23)cc1.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)c4ccccc34)c3ccccc23)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)c4ccccc34)cc2)c2ccccc12.C(=C(c1ccccc1)c1ccccc1)c1ccc(-c2ccc(-c3ccc(C=C(c4ccccc4)c4ccccc4)cc3)c3ccccc23)cc1 SJYMZIBVCWGJEQ-UHFFFAOYSA-N 0.000 description 1
- IDSFVJWYTBCVLG-IKIIQHDXSA-N C(=C/c1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)cc1)\c1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)cc1.C(=C/c1ccc(N(c2ccccc2)c2ccc(/C=C/c3ccc(N(c4ccccc4)c4ccc(/C=C/c5ccccc5)cc4)cc3)cc2)cc1)\c1ccccc1.C(=C/c1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccc(/C=C/c4ccccc4)cc3)c3ccccc23)cc1)\c1ccccc1 Chemical compound C(=C/c1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)cc1)\c1ccc(N(c2ccc(-c3ccccc3)cc2)c2ccc(-c3ccccc3)cc2)cc1.C(=C/c1ccc(N(c2ccccc2)c2ccc(/C=C/c3ccc(N(c4ccccc4)c4ccc(/C=C/c5ccccc5)cc4)cc3)cc2)cc1)\c1ccccc1.C(=C/c1ccc(N(c2ccccc2)c2ccc(N(c3ccccc3)c3ccc(/C=C/c4ccccc4)cc3)c3ccccc23)cc1)\c1ccccc1 IDSFVJWYTBCVLG-IKIIQHDXSA-N 0.000 description 1
- BIJHOXVSOJUIPD-UHFFFAOYSA-N CNC(C)COC Chemical compound CNC(C)COC BIJHOXVSOJUIPD-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229910000846 In alloy Inorganic materials 0.000 description 1
- 229910000733 Li alloy Inorganic materials 0.000 description 1
- FUJCRWPEOMXPAD-UHFFFAOYSA-N Li2O Inorganic materials [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 229910052769 Ytterbium Inorganic materials 0.000 description 1
- JFBZPFYRPYOZCQ-UHFFFAOYSA-N [Li].[Al] Chemical compound [Li].[Al] JFBZPFYRPYOZCQ-UHFFFAOYSA-N 0.000 description 1
- JHYLKGDXMUDNEO-UHFFFAOYSA-N [Mg].[In] Chemical compound [Mg].[In] JHYLKGDXMUDNEO-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910000272 alkali metal oxide Inorganic materials 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 229910001632 barium fluoride Inorganic materials 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- JZKFIPKXQBZXMW-UHFFFAOYSA-L beryllium difluoride Chemical compound F[Be]F JZKFIPKXQBZXMW-UHFFFAOYSA-L 0.000 description 1
- 229910001633 beryllium fluoride Inorganic materials 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- 125000005566 carbazolylene group Chemical group 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- VDQVEACBQKUUSU-UHFFFAOYSA-M disodium;sulfanide Chemical compound [Na+].[Na+].[SH-] VDQVEACBQKUUSU-UHFFFAOYSA-M 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000003914 fluoranthenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC=C4C1=C23)* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000005524 hole trap Effects 0.000 description 1
- APFVFJFRJDLVQX-UHFFFAOYSA-N indium atom Chemical compound [In] APFVFJFRJDLVQX-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000003564 m-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(C#N)=C1[H])C([H])([H])* 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- SJCKRGFTWFGHGZ-UHFFFAOYSA-N magnesium silver Chemical compound [Mg].[Ag] SJCKRGFTWFGHGZ-UHFFFAOYSA-N 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 125000005394 methallyl group Chemical group 0.000 description 1
- DCZNSJVFOQPSRV-UHFFFAOYSA-N n,n-diphenyl-4-[4-(n-phenylanilino)phenyl]aniline Chemical class C1=CC=CC=C1N(C=1C=CC(=CC=1)C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=CC=CC=1)C1=CC=CC=C1 DCZNSJVFOQPSRV-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004957 naphthylene group Chemical group 0.000 description 1
- 125000006504 o-cyanobenzyl group Chemical group [H]C1=C([H])C(C#N)=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000004866 oxadiazoles Chemical class 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 125000006505 p-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C#N)C([H])([H])* 0.000 description 1
- 125000006503 p-nitrobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1[N+]([O-])=O)C([H])([H])* 0.000 description 1
- 125000004817 pentamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000005562 phenanthrylene group Chemical group 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 125000005548 pyrenylene group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000005551 pyridylene group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- ZXZKYYHTWHJHFT-UHFFFAOYSA-N quinoline-2,8-diol Chemical compound C1=CC(=O)NC2=C1C=CC=C2O ZXZKYYHTWHJHFT-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- VPQBLCVGUWPDHV-UHFFFAOYSA-N sodium selenide Chemical compound [Na+].[Na+].[Se-2] VPQBLCVGUWPDHV-UHFFFAOYSA-N 0.000 description 1
- 229910052979 sodium sulfide Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 229910001637 strontium fluoride Inorganic materials 0.000 description 1
- FVRNDBHWWSPNOM-UHFFFAOYSA-L strontium fluoride Chemical compound [F-].[F-].[Sr+2] FVRNDBHWWSPNOM-UHFFFAOYSA-L 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005730 thiophenylene group Chemical group 0.000 description 1
- 229910001887 tin oxide Inorganic materials 0.000 description 1
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical class [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 1
- 238000005019 vapor deposition process Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B9/00—Layered products comprising a layer of a particular substance not covered by groups B32B11/00 - B32B29/00
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/80—Constructional details
- H10K50/805—Electrodes
- H10K50/82—Cathodes
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/18—Metal complexes
- C09K2211/188—Metal complexes of other metals not provided for in one of the previous groups
-
- 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]
- H10K50/14—Carrier transporting 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]
- H10K50/17—Carrier injection layers
- H10K50/171—Electron injection layers
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
-
- 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
-
- 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/326—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising gallium
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24942—Structurally defined web or sheet [e.g., overall dimension, etc.] including components having same physical characteristic in differing degree
Definitions
- the present invention relates to an organic electroluminescence device and, more particularly, to an organic electroluminescence device emitting light of a high luminance at a high efficiency and having a long life.
- An organic electroluminescence device (hereinafter, referred to as an organic EL device) is a spontaneous light emitting device which utilizes the principle that a fluorescent substance emits light by recombination of holes injected from an anode and electrons injected from a cathode when an electric field is applied.
- the efficiency of hole injection into the light emitting layer can be increased, that the efficiency of forming excited particles which are formed by blocking and recombining electrons injected from the cathode can be increased and that excited particles formed within the light emitting layer can be enclosed.
- a two-layered structure having a hole transporting (injecting) layer and an electron transporting and light emitting layer and a three-layered structure having a hole transporting (injecting) layer, a light emitting layer and an electron transporting (injecting) layer are well known.
- the structure of the device and the process for forming the device have been studied.
- chelate complexes such as tris(8-quinolinolato)aluminum, coumarine derivatives, tetraphenylbutadiene derivatives, bisstyrylarylene derivatives and oxadiazole derivatives are known. It is reported that light in the visible region ranging from blue light to red light can be obtained by using these light emitting materials and development of a device exhibiting color images is expected (For example, Japanese Patent Application Laid-Open Nos. Heisei 8(1996)-239655, Heisei 7(1995)-138561 and Heisei 3(1991)-200289).
- a device using a phenylanthracene derivative as the light emitting material is disclosed in Japanese Patent Application Laid-Open No. Heisei 8(1996)-12600.
- the phenylanthracene derivative is used as the light emitting material emitting blue light.
- this compound is used as the layer emitting blue light as a laminate in combination with a layer of tris(8-quinolinolato)aluminum (Alq).
- Alq tris(8-quinolinolato)aluminum
- the present invention has been made to overcome the above problems and has an object of providing an organic EL device emitting light of a higher luminance at a higher efficiency and having a longer life than those of conventional devices.
- the present inventors used a layer of a metal complex having an energy gap of 2.8 eV or greater in place of the layer of Alq having an energy gap of 2.7 eV to overcome the above problems (1) and (2) and an organic EL device emitting light of a higher luminance at a higher efficiency and having a longer life than those of conventional devices has been completed.
- the present invention provides an organic electroluminescence device comprising a cathode, an anode and a layer of an organic thin film comprising one or a plurality of layers and disposed between the cathode and the anode, wherein at least one of the layers in the layer of an organic thin film comprises a laminate of a layer comprising a metal complex having an energy gap of 2.8 eV or greater and a layer of a host material; and an organic electroluminescence device comprising a cathode, an anode and a layer of an organic thin film comprising one or a plurality of layers and disposed between the cathode and the anode, wherein at least one of the layers in the layer of an organic thin film comprises a mixture of a metal complex having an energy gap of 2.8 eV or greater and a host material.
- the layer of the host material or the layer of the mixture comprises light emitting guest molecules which have an electron affinity smaller than the electron affinity of the host material and an ionization energy the same as or smaller than the ionization energy of the host material.
- the amounts of electrons and holes are kept in good balance since the electron affinity and the ionization potential satisfy the above conditions and injection of holes into the electron injecting layer can be suppressed. Therefore, the device exhibiting a higher efficiency and having a longer life than those of conventional devices can be obtained.
- the host material is a material constituting the layer of a host material.
- the host material has an energy gap greater than that of the light emitting guest molecules.
- One of the following cases (1) and (2) is more preferable.
- the host material has an energy gap of 2.8 eV or greater. The reason is that, when the energy gap is great, the ionization energy of the host material is increased and the host material can work more effectively as the hole trap even when the same light emitting guest molecules are used. In particular, this case is preferable for obtaining emission of blue light.
- the layer of the host material has the hole transporting property.
- the hole transporting property is defined as the charge transporting property when the mobility of holes is greater than the mobility of electrons and can be measured in accordance with a conventional method such as the method of time of flight.
- the host material is at least one compound selected from distyrylarylene derivatives, diarylanthracene derivatives and diarylbisanthracene derivatives.
- Ar 1 , Ar 2 , Ar 3 , Ar 4 and Ar 5 each independently represent a substituted or unsubstituted phenylene group, a substituted or unsubstituted naphthalene group, a substituted or unsubstituted anthracene group, a substituted or unsubstituted diphenylanthracene group, a substituted or unsubstituted phenanthrene group, a substituted or unsubstituted acenaphthene group, a substituted or unsubstituted biphenylene group, a substituted or unsubstituted fluorene group, a substituted or unsubstituted carbazole group, a substituted or unsubstituted thiophene group, a substituted or unsubstituted triazole group or a substituted or unsubstituted thiadiazole group.
- R 1 , R 2 , R 3 and R 4 each independently represent hydrogen atom, an alkyl group having 1 to 30 carbon atoms, an alkoxyl group having 1 to 30 carbon atoms, an aryl group having 1 to 30 carbon atoms, a trialkylsilyl group having 1 to 30 carbon atoms or cyano group.
- diarylanthracene derivative arylbisanthracene derivatives represented by the following general formula (2) are preferable.
- R 10 to R 13 , R 15 to R 18 , R 20 to R 23 and R 25 to R 28 each independently represent hydrogen atom, a halogen atom, hydroxyl group, a substituted or unsubstituted amino group, nitro group, cyano group, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 5 to 30 carbon atoms, a substituted or unsubstituted alkoxyl group having 1 to 30 carbon atoms, a substituted or unsubstituted a romatic hydrocarbon group having 6 to 40 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 2 to 40 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 40 carbon
- arylanthracene derivatives expressed by formulae (1′) to (5′) and distyrylarylene derivatives expressed by formulae (6′) to (9′) are more preferable as the host material.
- the amino group is represented by —NX 1 X 2 .
- X 1 and X 2 each independently represent hydrogen atom, methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxyisopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-
- alkyl group examples include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxyisopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichloroisopropyl group, 2,3-dichloro-t-but
- alkenyl group examples include vinyl group, allyl group, 1-butenyl group, 2-butenyl group, 3-butenyl group, 1,3-butadienyl group, 1-methylvinyl group, styryl group, 2,2-diphenylvinyl group, 1,2-diphenylvinyl group, 1-methylallyl group, 1,1-dimethylallyl group, 2-methylallyl group, 1-phenylallyl group, 2-phenylallyl group, 3-phenylallyl group, 3,3-diphenylallyl group, 1,2-dimethylallyl group, 1-phenyl-1-butenyl group and 3-phenyl-1-butenyl group.
- Examples of the cycloalkyl group include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group and 4-methylcyclohexyl group.
- the alkoxyl group is represented by —OY.
- Examples of the group represented by Y include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxy-isopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichloroiso
- aromatic hydrocarbon group examples include phenyl group, 1-naphthyl group, 2-naphthyl group, 1-anthryl group, 2-anthryl group, 9-anthryl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl group, m-terphenyl-2-yl group, m-ter
- aromatic heterocyclic group examples include 1-pyrrolyl group, 2-pyrrolyl group, 3-pyrrolyl group, pyradinyl group, 2-pyridinyl group, 3-pyridinyl group, 4-pyridinyl group, 1-indolyl group, 2-indolyl group, 3-indolyl group, 4-indolyl group, 5-indolyl group, 6-indolyl group, 7-indolyl group, 1-isoindolyl group, 2-isoindolyl group, 3-isoindolyl group, 4-isoindolyl group, 5-isoindolyl group, 6-isoindolyl group, 7-isoindolyl group, 2-furyl group, 3-furyl group, 2-benzofuranyl group, 3-benzofuranyl group, 4-benzofuranyl group, 5-benzofuranyl group, 6-benzofuranyl group, 7-benzofuranyl group,
- Examples of the aralkyl group include benzyl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, 2-phenylisopropyl group, phenyl-t-butyl group, ⁇ -naphthylmethyl group, 1- ⁇ -naphthylethyl group, 2- ⁇ -naphthylethyl group, 1- ⁇ -naphthylisopropyl group, 2- ⁇ -naphthylisopropyl group, ⁇ -naphthylmethyl group, 1- ⁇ -naphthylethyl group, 2- ⁇ -naphthylethyl group, 1- ⁇ -naphthylisopropyl group, 2- ⁇ -naphthylisopropyl group, 1-pyrrolylmethyl group, 2-(1-pyrrolyl)ethyl group, p-methylbenzy
- the aryloxyl group is represented by —OZ.
- Examples of the group represented by Z include phenyl group, 1-naphthyl group, 2-naphthyl group, 1-anthryl group, 2-anthryl group, 9-anthryl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl
- the alkoxycarbonyl group is represented by —COOY.
- Examples of the group represented by Y include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxy-isopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichlor
- Examples of the divalent group forming the ring include tetramethylene group, pentamethylene group, hexamethylene group, diphenylmethane-2,2′-diyl group, diphenylethane-3,3′-diyl group and diphenylpropane-4,4′-diyl group.
- Examples of the aryl group include phenyl group, naphthyl group, anthryl group, phenanthryl group, naphthaceyl group and pyrenyl group.
- Examples of the substituent to the aryl group include halogen atoms, hydroxyl group, substituted or unsubstituted amino groups described above, nitro group, cyano group, substituted or unsubstituted alkyl groups described above, substituted or unsubstituted alkenyl groups described above, substituted or unsubstituted cycloalkyl groups described above, substituted or unsubstituted alkoxyl groups described above, substituted or unsubstituted aromatic hydrocarbon groups described above, substituted or unsubstituted aromatic heterocyclic groups described above, substituted or unsubstituted aralkyl groups described above, substituted or unsubstituted aryloxyl groups described above, substituted or unsubstituted alkoxycarbonyl groups described above
- the light emitting guest molecule has an electron affinity smaller than that of the host material and an ionization potential the same as or smaller than that of the host material.
- amine compounds having styryl group and condensed aromatic amine compounds are preferable and the amine compounds having styryl group are more preferable.
- the amine compounds having styryl group include compounds represented by the following general formulae (8) and (9):
- Ar 5 ′ represents a divalent group selected from phenylene group, biphenylene group, terphenylene group and stylbene group
- Ar 6 ′ and Ar 7 ′ each independently represent hydrogen atom or an aromatic group having 6 to 20 carbon atoms
- the groups represented by Ar 5 ′, Ar 6 ′ and Ar 7 ′ may be substituted and
- m′ represents a number of condensation which is an integer of 1 to 4.
- At least one of the groups represented by Ar 6 ′ and Ar 7 ′ is substituted with styryl group.
- the aromatic group having 6 to 20 carbon atoms include phenyl group, naphthyl group, anthranyl group, phenanthryl group and terphenyl group.
- Ar 8 ′ represents an aromatic group having 6 to 40 carbon atoms
- Ar 9 ′ and Ar 10 ′ represents hydrogen atom or an aromatic group having 6 to 20 carbon atoms
- the groups represented by Ar 8 ′, Ar 9 ′ and Ar 10 ′ may be substituted with proviso that at least one of the groups represented by Ar 8 ′, Ar 9 ′ and Ar 10 ′ is substituted with an alkylamino group and n′ represents an integer of 1 to 4.
- Examples of the aromatic group having 6 to 40 carbon atoms in general formula (9) include aryl groups such as phenyl group, naphthyl group, anthranyl group, phenanthryl group, pyrenyl group, coronyl group, biphenyl group, terphenyl group, pyrrolyl group, furanyl group, thiophenyl group, benzothiophenyl group, oxadiazolyl group, diphenylanthranyl group, indolyl group, carbazolyl group, pyridyl group, benzoquinolyl group, fluoranthenyl group and acenaphthofluoranthenyl group; and arylene groups such as phenylene group, naphthylene group, anthranylene group, phenanthrylene group, pyrenylene group, coronylene group, biphenylene group, terphenylene group, pyrrolylene group, furanylene group,
- the aromatic group having 6 to 40 carbon atoms may further be substituted with a substituent.
- substituents include alkyl groups having 1 to 6 carbon atoms such as ethyl group, methyl group, isopropyl group, n-propyl group, s-butyl group, t-butyl group, pentyl group, hexyl group, cyclopentyl group and cyclohexyl group; alkoxyl groups having 1 to 6 carbon atoms such as ethoxyl group, methoxyl group, isopropoxyl group, n-propoxyl group, s-butoxyl group, t-butoxyl group, pentoxyl group, hexyloxyl group, cyclopentoxyl group and cyclohexyloxyl group; aryl groups having 5 to 40 carbon atoms in the nucleus; amino group substituted with the aryl group having 5 to 40 carbon atoms in the nucleus; ester groups having the
- the metal complex comprised in the layer of an organic thin film has an energy gap of 2.8 eV or greater and is preferably a metal complex having a ring having nitrogen as the ligand.
- the metal complex is a complex represented by general formula (3) or general formula (5).
- Q 1 and Q 2 each independently represent a ligand represented by general formula (4)
- L represents a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 5 to 30 carbon atoms, a substituted or unsubstituted aryl group having 6 to 40 carbon atoms, a substituted or unsubstituted heterocyclic group having 2 to 40 carbon atoms or a ligand represented by —OR, —OAr, —ORAr, —OC(O)R, —OC(O)Ar, —OP(O)R 2 , —SeAr, —TeAr, —SAr, —X, —OP(O)Ar 2 , —OS(O 2 )R, —OS(O 2 )Ar, —OSiR 3 , —OB(OR) 2 , —
- a 1 and A 2 each independently represents a substituted or unsubstituted six-membered aryl cyclic structure and the structures represented by A 1 and A 2 are condensed with each other.
- Q 5 to Q 8 each independently represent a ligand represented by general formula (4);
- a 3 and A 4 represent a substituted or unsubstituted alkylene group having 1 to 30 carbon atoms, a substituted or unsubstituted divalent monocyclic group having 5 to 30 carbon atoms or a substituted or unsubstituted divalent condensed polycyclic group having 6 to 40 carbon atoms;
- X represents a substituted or unsubstituted alkylene group having 1 to 30 carbon atoms, O, S, SO 2 , >C ⁇ O, >SiR 40 R 41 or >NR 42 ; when A 3 and A 4 represent a substituted or unsubstituted alkylene group, X does not represent an alkylene group;
- n represents an integer of 0 to 2;
- R 40 to R 42 each independently represent hydrogen atom, a halogen atom, cyano group, nitro group, a substituted or unsubstituted
- At least one of Q 1 and Q 2 represents a ligand represented by the following general formula (6):
- R 30 to R 35 each independently represent hydrogen atom, a halogen atom, cyano group, nitro group, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 5 to 40 carbon atoms, a substituted or unsubstituted aryl group having 6 to 40 carbon atoms or a substituted or unsubstituted heterocyclic group having 2 to 40 carbon atoms.
- halogen atom examples include fluorine atom, chlorine atom, bromine atom and iodine atom.
- the amino group is represented by —NX 1 X 2 .
- X 1 and X 2 each independently represent methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxyisopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichloro
- alkyl group examples include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1, 2-dihydroxyethyl group, 1,3-dihydroxy-isopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichloroisopropyl group, 2,3-dichloro-t-
- Examples of the cycloalkyl group include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group and 4-methylcyclohexyl group.
- the alkoxyl group is represented by —OY.
- Examples of the group represented by Y include methyl group, ethyl group, propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, hydroxymethyl group, 1-hydroxyethyl group, 2-hydroxyethyl group, 2-hydroxyisobutyl group, 1,2-dihydroxyethyl group, 1,3-dihydroxy-isopropyl group, 2,3-dihydroxy-t-butyl group, 1,2,3-trihydroxypropyl group, chloromethyl group, 1-chloroethyl group, 2-chloroethyl group, 2-chloroisobutyl group, 1,2-dichloroethyl group, 1,3-dichloroiso
- heterocyclic group examples include 1-pyrrolyl group, 2-pyrrolyl group, 3-pyrrolyl group, pyradinyl group, 2-pyridinyl group, 3-pyridinyl group, 4-pyridinyl group, 1-indolyl group, 2-indolyl group, 3-indolyl group, 4-indolyl group, 5-indolyl group, 6-indolyl group, 7-indolyl group, 1-isoindolyl group, 2-isoindolyl group, 3-isoindolyl group, 4-isoindolyl group, 5-isoindolyl group, 6-isoindolyl group, 7-isoindolyl group, 2-furyl group, 3-furyl group, 2-benzofuranyl group, 3-benzofuranyl group, 4-benzofuranyl group, 5-benzofuranyl group, 6-benzofuranyl group, 7-benzofuranyl group, 1-
- the aryloxyl group is represented by —OZ.
- Examples of the group represented by Z include phenyl group, 1-naphthyl group, 2-naphthyl group, 1-anthryl group, 2-anthryl group, 9-anthryl group, 1-phenanthryl group, 2-phenanthryl group, 3-phenanthryl group, 4-phenanthryl group, 9-phenanthryl group, 1-naphthacenyl group, 2-naphthacenyl group, 9-naphthacenyl group, 1-pyrenyl group, 2-pyrenyl group, 4-pyrenyl group, 2-biphenylyl group, 3-biphenylyl group, 4-biphenylyl group, p-terphenyl-4-yl group, p-terphenyl-3-yl group, p-terphenyl-2-yl group, m-terphenyl-4-yl group, m-terphenyl-3-yl
- Examples of the aryl group include phenyl group, naphthyl group, anthryl group, phenanthryl group, naphthaceyl group and pyrenyl group.
- Examples of the substituent to the aryl group include halogen atoms, hydroxyl group, substituted or unsubstituted amino groups described above, nitro group, cyano group, substituted or unsubstituted alkyl groups described above, substituted or unsubstituted alkenyl groups described above, substituted or unsubstituted cycloalkyl groups described above, substituted or unsubstituted alkoxyl groups described above, substituted or unsubstituted aromatic hydrocarbon groups described above, substituted or unsubstituted aromatic heterocyclic groups described above, substituted or unsubstituted aralkyl groups described above, substituted or unsubstituted aryloxyl groups described above, substituted or unsubstituted alkoxycarbonyl groups described above
- the complex represented by the following general formula (7) is also preferable.
- L′ represents a group represented by —R′, —Ar′, —OR′, —OAr′, —OR′Ar′, —OC(O)R′, —OC(O)Ar′, —OP(O)R′ 2 , —SeAr′, —TeAr′, —SAr′, —X′, —OP(O)Ar′ 2 , —OS(O 2 )R′, —OS(O 2 )Ar′, —OSiR′ 3 , —OB(OR′) 2 , —OSiAr′ 3 , —OAr′O— or —OC(O)Ar′C(O)O—, wherein R′ represents a hydrocarbon group having 1 to 6 carbon atoms, X′ represents a halogen atom
- examples of the hydrocarbon group, the halogen and the aryl group include the atoms and the groups described as the examples of the corresponding atoms and groups in the above.
- metal complex examples include compounds expressed by the following formulae (1) to (32):
- the layer of an organic thin film comprises a light emitting layer comprising a diarylanthracene derivative or a diarylbisanthracene derivative and the hole transporting layer adjacent to the light emitting layer comprises an N,N,N′,N′-tetra(biphenyl)diaminoarylene derivative.
- the organic EL device By laminating the layer comprising a specific N,N,N′,N′-tetra(biphenyl)diaminoarylene derivative to the light emitting layer, the balance between the amounts of electrons and holes is improved. Therefore, injection of holes into the electron injecting layer is suppressed and deterioration of the electron injecting layer is prevented. As the result, the organic EL device can exhibit a higher efficiency and have a longer life.
- N,N,N′,N′-tetra(biphenyl)diaminoarylene derivative compounds represented by the following general formulae (10) and (11) are preferable.
- R 1 ′ to R 9 ′ each independently represent hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxyl group having 1 to 6 carbon atoms or a substituted or unsubstituted phenyl group
- R 10 ′ to R 17 ′ each independently represent hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxyl group having 1 to 6 carbon atoms or a substituted or unsubstituted phenyl group
- N,N,N′,N′-tetra(biphenyl)diaminoarylene derivative include N,N,N′,N′-tetra(4-biphenyl)diaminoarylenes.
- arylene include biphenylene, fluorenyl, terphenylene and quaterphenylene which may be substituted or unsubstituted.
- the organic EL device of the present invention has a laminate structure having one or more organic layers laminated between the electrodes.
- Examples of the structure include structures of an anode/a light emitting layer/a cathode, an anode/a hole transporting layer/a light emitting layer/an electron transporting layer/a cathode, an anode/a hole transporting layer/a light emitting layer/a cathode and an anode/a light emitting layer/an electron transporting layer/a cathode.
- the compound described in the present invention may be used in any of the above layers of an organic thin film and may also be used by doping into other hole transporting materials, light emitting materials and electron transporting materials.
- a region transporting electrons or an interface region between the cathode and a layer of an organic thin film comprises a reducing dopant.
- the reducing dopant is defined as a substance which reduces an electron transporting compound. Therefore, various types of substances can be used as long as the substance has the specific reducing property.
- Examples of the reducing dopant include at least one alkali metal selected from the group consisting of Na (the work function: 2.36 eV), K (the work function: 2.28 eV), Rb (the work function: 2.16 eV) and Cs (the work function: 1.95 eV) and at least one alkaline earth metal selected from the group consisting of Ca (the work function: 2.9 eV), Sr (the work function: 2.0 to 2.5 eV) and Ba (the work function: 2.52 eV).
- reducing dopants having a work function of 2.9 eV or smaller are preferable.
- More preferable reducing dopants are at least one alkali metal selected from the group consisting of K, Rb and Cs. Still more preferable reducing dopants are Rb and Cs and the most preferable reducing dopant is Cs. These alkali metals have high reducing ability and the luminance of emitted light and the life of the organic EL device are improved by adding these alkali metals in a relatively small amount into the region of electron injection.
- the reducing dopant having a work function of 2.9 eV or smaller combinations of two or more alkali metals are preferable and combinations including Cs such as combinations of Cs and Na, Cs and K, Cs and Rb, and Cs, Na and K are more preferable.
- Cs is include in the combination, the reducing ability can be efficiently exhibited and the luminance of emitted light and the life of the organic EL device can be improved by adding the combination into the region of electron injection.
- an electron injecting layer constituted with an insulating material or a semiconductor may be disposed between the cathode and the layer of an organic thin film.
- the electron injecting layer By disposing the electron injecting layer, leak of electric current can be effectively prevented and the electron injecting property can be improved.
- at least one metal compound selected from the group consisting of alkali metal chalcogenides, alkaline earth metal chalcogenides, alkali metal halides and alkaline earth metal halides is used as the insulating material.
- the electron injecting layer is constituted with the alkali metal chalcogenide or the like since the electron injecting property can be further improved.
- Preferable examples of the alkali metal chalcogenide include Li 2 O, LiO, Na 2 S, Na 2 Se and NaO.
- Preferable examples of the alkaline earth chalcogenide include CaO, BaO, SrO, BeO, BaS and CaSe.
- Preferable examples of the alkali metal halide include LiF, NaF, KF, LiCl, KCl and NaCl.
- Preferable examples of the alkaline earth metal halide include fluorides such as CaF 2 , BaF 2 , SrF 2 , MgF 2 and BeF 2 and halides other than the fluorides.
- Examples of the semiconductor constituting the electron transporting layer include oxides, nitrides and oxide nitrides containing at least one element selected from Ba, Ca, Sr, Yb, Al, Ga, In, Li, Na, Cd, Mg, Si, Ta, Sb and Zn used singly or as a combination of two or more. It is preferable that the inorganic compound constituting the electron transporting layer is in the form of a fine crystalline or amorphous insulating thin film. When the electron transporting layer is constituted with the above insulating thin film, a more uniform thin film can be formed and defects of pixels such as dark spots can be decreased.
- Examples of the inorganic compound include the alkali metal chalcogenides, the alkaline earth metal chalcogenides, the alkali metal halides and the alkaline earth metal halides which are described above.
- the anode of the organic EL device plays the role of injecting holes into the hole transporting layer or the light emitting layer. It is effective that the anode has a work function of 4.5 eV or greater.
- the material of the anode used in the present invention include indium tin oxide alloys (ITO), tin oxides (NESA), gold, silver, platinum and copper.
- ITO indium tin oxide alloys
- NESA tin oxides
- gold silver
- platinum platinum
- copper copper
- a material having a small work function is preferable so that electrons can be injected into the electron transporting layer or the light emitting layer.
- the material of the cathode is not particularly limited.
- Examples of the material of the cathode include indium, aluminum, magnesium, magnesium-indium alloys, magnesium-aluminum alloys, aluminum-lithium alloys, aluminum-scandium-lithium alloys and magnesium-silver alloys.
- the process for forming the layers in the organic EL device of the present invention is not particularly limited.
- a conventional process such as the vacuum vapor deposition and the spin coating can be used.
- the layer of an organic thin film containing the light emitting compound represented by the above general formula (1) which is used in the present invention can be formed in accordance with the vacuum vapor deposition process or the molecular beam epitaxy process (the MBE process).
- the layer of an organic thin film can be formed also from a solution prepared by dissolving the material into a solvent in accordance with a conventional coating process such as the dipping process, the spin coating process, the casting process, the bar coating process and the roll coating process.
- each layer in the layer of an organic thin film in the organic EL device of the present invention is not particularly limited.
- an excessively thin layer tends to have defects such as pin holes and an excessively thick layer requires a high applied voltage to decrease the efficiency. Therefore, a thickness in the range of several nm to 1 ⁇ m is preferable.
- the ionization energy (Ip) was measured by using an atmospheric photoelectronic spectrophotometer AC1 manufactured by RIKEN KEIKI Co., Ltd.
- a glass substrate manufactured by GEOMATEC Company of 25 mm ⁇ 75 mm ⁇ 1.1 mm thickness having an ITO transparent electrode was cleaned by application of ultrasonic wave in isopropyl alcohol for 5 minutes and then by exposure to ozone generated by ultraviolet light for 30 minutes.
- the glass substrate having the transparent electrode lines which had been cleaned was attached to a substrate holder of a vacuum vapor deposition apparatus.
- a film of N,N′-bis(N,N′-diphenyl-4-aminophenyl)-N,N′-diphenyl-4,4′-diamino-1,1′-biphenyl (TPD232) having a thickness of 60 nm was formed in a manner such that the formed film covered the transparent electrode.
- the formed film of TPD232 worked as the hole injecting layer.
- a film of 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPD) having a thickness of 20 nm was formed on the formed film of TPD232.
- the formed film of NPD worked as the hole transporting layer.
- a film of the above compound (E1) as the host material having a thickness of 40 nm was formed on the formed film of NPD by vapor deposition.
- the above amine compound having styryl group (D1) as the light emitting molecule was vapor deposited in an amount such that the ratio of the amounts by weight of compound (D1) to compound (E1) was 3:40.
- the formed film worked as the light emitting layer.
- a film of the above metal complex (16) having a thickness of 20 nm was formed.
- the film of metal complex (16) worked as the electron injecting layer.
- the laminate of compound (E1): amine compound (D1)/metal complex (16) worked as the light emitting medium emitting blue light.
- Li the source of lithium: manufactured by SAES GETTERS Company
- Alq the electron injecting layer
- metallic aluminum was vapor deposited to form a metal cathode and an organic EL device was prepared.
- blue light was emitted at a luminance of 200 cd/m 2 and an efficiency of the light emission of 8.5 cd/A.
- the device was driven by continuously passing a current constantly at an initial luminance of 500 cd/m 2 and the time before the luminance decreased to the half of the original value (the half-life) was found to be 3,200 hours.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D2) was used in place of amine compound (D1).
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D3) was used in place of amine compound (D1).
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D4) was used in place of amine compound (D1).
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D5) was used in place of amine compound (D1).
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D3) was used in place of amine compound (D1) and compound (C1) was used in place of compound (E1) in the light emitting layer.
- amine compound (D3) was used in place of amine compound (D1)
- compound (C1) was used in place of compound (E1) in the light emitting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D3) was used in place of amine compound (D1) and compound (C2) was used in place of compound (E1) in the light emitting layer.
- amine compound (D3) was used in place of amine compound (D1)
- compound (C2) was used in place of compound (E1) in the light emitting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that amine compound (D3) was used in place of amine compound (D1) and compound (C3) was used in place of compound (E1) in the light emitting layer.
- amine compound (D3) was used in place of amine compound (D1)
- compound (C3) was used in place of compound (E1) in the light emitting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that aluminum complex of 8-hydroxyquinoline was used in place of metal complex (16).
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 2.
- the organic EL devices of Examples 1 to 5 exhibited higher efficiencies of the light emission and had longer lives than those of the organic EL devices of Comparative Examples 1 to 4.
- the organic EL devices of Examples 2 to 4 emitted blue light having excellent purity at higher efficiency than conventional devices.
- Comparative Example 4 and Example 1 it was found that the efficiency of the light emission and the life could be improved by using the laminate of the layer of the host material containing the light emitting molecules and the layer of the metal complex using the metal complex having an energy gap of 2.8 eV or greater.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that compound (E2) was used in place of compound (E1) in the light emitting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 3.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that compound (E3) was used in place of compound (E1) in the light emitting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 3.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 1 except that 4,4′-bis[N-(1-naphthyl)-N-phenylamino]biphenyl (NPD) was used in place of compound (E1) in the light emitting layer.
- NPD had an ionization energy of 5.40 eV and an electron affinity of 2.40 eV.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 3.
- a glass substrate (manufactured by GEOMATEC Company) of 25 mm ⁇ 75 mm ⁇ 1.1 mm thickness having an ITO transparent electrode was cleaned by application of ultrasonic wave in isopropyl alcohol for 5 minutes and then by exposure to ozone generated by ultraviolet light for 30 minutes.
- the glass substrate having the transparent electrode lines which had been cleaned was attached to a substrate holder of a vacuum vapor deposition apparatus.
- a film TPD232 having a thickness of 60 nm was formed in a manner such that the formed film covered the transparent electrode.
- the formed film of TPD232 worked as the hole injecting layer.
- a film of N,N,N′,N′-tetra(4-biphenyl)diaminobiphenylene (TBDB) having a thickness of 20 nm was formed on the formed film of TPD232.
- the formed film of TBDB worked as the hole transporting layer.
- a film of compound (E1) having a thickness of 40 nm was formed on the film of TBDB formed above.
- the formed film worked as the light emitting layer.
- a film of the above metal complex (27) having a thickness of 20 nm was formed.
- the film of metal complex (27) worked as the electron injecting layer.
- the laminate of compound (E1) and metal complex (27) worked as the light emitting medium emitting blue light.
- Li the source of lithium: manufactured by SAES GETTERS Company
- metal complex (27):Li film the ratio of the amounts by mole: 1:1
- metallic aluminum was vapor deposited to form a metal cathode and an organic EL device was prepared.
- blue light was emitted at a luminance of 200 cd/m 2 and an efficiency of the light emission of 7.5 cd/A.
- the device was driven by continuously passing a current constantly at an initial luminance of 500 cd/m 2 and the time before the luminance decreased to the half of the original value (the half-life) was found to be 2,000 hours.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 8 except that Cs metal was used in place of Li in the electron injecting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 4.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 8 except that an alkali fluoride CsF was used in place of Li in the electron injecting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 4.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 8 except that an alkali chalcogenide CsTe was used in place of Li in the electron injecting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 4.
- An organic EL device was prepared in accordance with the same procedures as those conducted in Example 8 except that NPD was used in place of TBDB in the hole transporting layer.
- the luminance of the emitted light, the efficiency of the light emission and the color of the emitted light under application of a direct current voltage of 6 V and the half-life of the light emission at the initial luminance of 500 cd/m 2 of this device are shown in Table 4.
- the organic EL device of the present invention exhibits a higher efficiency of light emission and has a longer life than conventional devices while the emitted light has a high luminance.
- the organic EL device of the present invention is very useful as the light source for various electronic instruments.
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Optics & Photonics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US10/935,102 US7087322B2 (en) | 2001-06-06 | 2004-09-08 | Organic electroluminescence device |
| US11/480,469 US20060257687A1 (en) | 2001-06-06 | 2006-07-05 | Organic electroluminescence device |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001-170960 | 2001-06-06 | ||
| JP2001170960 | 2001-06-06 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/935,102 Continuation US7087322B2 (en) | 2001-06-06 | 2004-09-08 | Organic electroluminescence device |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20030077480A1 true US20030077480A1 (en) | 2003-04-24 |
Family
ID=19012804
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/141,982 Abandoned US20030077480A1 (en) | 2001-06-06 | 2002-05-10 | Organic electroluminescence device |
| US10/935,102 Expired - Lifetime US7087322B2 (en) | 2001-06-06 | 2004-09-08 | Organic electroluminescence device |
| US11/480,469 Abandoned US20060257687A1 (en) | 2001-06-06 | 2006-07-05 | Organic electroluminescence device |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/935,102 Expired - Lifetime US7087322B2 (en) | 2001-06-06 | 2004-09-08 | Organic electroluminescence device |
| US11/480,469 Abandoned US20060257687A1 (en) | 2001-06-06 | 2006-07-05 | Organic electroluminescence device |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US20030077480A1 (ja) |
| EP (1) | EP1404160A4 (ja) |
| JP (1) | JP4029071B2 (ja) |
| KR (1) | KR100900375B1 (ja) |
| CN (1) | CN100431193C (ja) |
| TW (2) | TWI286911B (ja) |
| WO (1) | WO2002102118A1 (ja) |
Cited By (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20040207312A1 (en) * | 2003-01-23 | 2004-10-21 | Seiko Epson Corporation | Manufacturing method for organic electroluminescence device, and electronic device therewith |
| US20040258957A1 (en) * | 2003-06-18 | 2004-12-23 | Pei-Chuan Yeh | Organic electroluminescent device and manufacturing method thereof |
| US20050048317A1 (en) * | 2003-08-29 | 2005-03-03 | Semiconductor Energy Laboratory Co., Ltd. | Electroluminescent device and light-emitting device including the same |
| US20050064235A1 (en) * | 2003-09-24 | 2005-03-24 | Eastman Kodak Company | Blue organic electroluminescent devices having a non-hole-blocking layer |
| US20050064233A1 (en) * | 2002-07-19 | 2005-03-24 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20050104511A1 (en) * | 2003-11-14 | 2005-05-19 | Eastman Kodak Company | Organic electroluminescent devices having a stability-enhancing layer |
| US20050173700A1 (en) * | 2004-02-06 | 2005-08-11 | Eastman Kodak Company | Full-color organic display having improved blue emission |
| US20050233166A1 (en) * | 2004-04-14 | 2005-10-20 | Eastman Kodak Company | OLED device using reduced drive voltage |
| US20070092756A1 (en) * | 2005-10-26 | 2007-04-26 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
| EP1790631A1 (en) * | 2004-09-17 | 2007-05-30 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent device using same |
| US20070120115A1 (en) * | 2005-10-21 | 2007-05-31 | Seiko Epson Corporation | Organic light-emitting element, method of manufacturing organic light-emitting element, light-emitting device, and electronic apparatus |
| US20080157657A1 (en) * | 2006-12-22 | 2008-07-03 | Sony Corporation | Organic electroluminescent device and display |
| US20120025181A1 (en) * | 2009-03-25 | 2012-02-02 | Panasonic Electric Works Co., Ltd. | Organic el element |
| US20120286653A1 (en) * | 2009-12-11 | 2012-11-15 | Mitsubishi Chemical Corporation | Organic electroluminescent element, organic el display device, and organic el illuminator |
| US9331285B2 (en) | 2009-12-16 | 2016-05-03 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent element using same |
| US9902687B2 (en) | 2014-09-19 | 2018-02-27 | Idemitsu Kosan Co., Ltd. | Compound |
| US10263191B2 (en) | 2009-04-24 | 2019-04-16 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescent element comprising the same |
| US10297765B2 (en) | 2007-12-28 | 2019-05-21 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent device using the same |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4860849B2 (ja) * | 2001-09-14 | 2012-01-25 | 一般財団法人石油エネルギー技術センター | アミノ基を有する新規芳香族化合物及びそれを利用した有機エレクトロルミネッセンス素子 |
| JP4152173B2 (ja) * | 2002-11-18 | 2008-09-17 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| EP1437395B2 (en) | 2002-12-24 | 2015-08-26 | LG Display Co., Ltd. | Organic electroluminescent device |
| EP1604974A4 (en) * | 2003-03-20 | 2007-11-14 | Idemitsu Kosan Co | AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT PRODUCED WITH THIS DERIVATIVE |
| US7898168B2 (en) * | 2003-10-27 | 2011-03-01 | Semiconductor Energy Laboratory Co., Ltd. | Organic electroluminescent device having light-emitting layer with guest dopant |
| KR100581918B1 (ko) * | 2004-06-03 | 2006-05-23 | 삼성에스디아이 주식회사 | 유기 전계 발광 소자 |
| US7670506B1 (en) * | 2004-12-30 | 2010-03-02 | E. I. Du Pont De Nemours And Company | Photoactive compositions for liquid deposition |
| KR100796032B1 (ko) * | 2006-01-26 | 2008-01-16 | 순천대학교 산학협력단 | 청색 전계발광 고분자 및 이를 이용한 유기 전계발광 소자 |
| US7768195B2 (en) * | 2006-05-25 | 2010-08-03 | Idemitsu Kosan Co., Ltd. | Organic electroluminescent device with improved luminous efficiency |
| KR101315379B1 (ko) * | 2006-11-23 | 2013-10-10 | 삼성디스플레이 주식회사 | 디스플레이장치의 제조방법 |
| CN103456897B (zh) * | 2012-05-30 | 2016-03-09 | 京东方科技集团股份有限公司 | 有机电致发光器件 |
| CN103450883B (zh) * | 2012-05-30 | 2016-03-02 | 京东方科技集团股份有限公司 | 有机电子材料 |
| US11036295B2 (en) * | 2016-11-23 | 2021-06-15 | Microsoft Technology Licensing, Llc | Electrostatic slide clutch |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5536949A (en) * | 1992-08-28 | 1996-07-16 | Idemistu Kosan Co., Ltd. | Charge injection auxiliary material and organic electroluminescence device containing the same |
| JP3332491B2 (ja) * | 1993-08-27 | 2002-10-07 | 三洋電機株式会社 | 有機ｅｌ素子 |
| WO1995009147A1 (fr) * | 1993-09-29 | 1995-04-06 | Idemitsu Kosan Co., Ltd. | Element electroluminescent organique et derive d'arylenediamine |
| DE69511755T2 (de) * | 1994-04-26 | 2000-01-13 | Tdk Corp | Phenylanthracenderivat und organisches EL-Element |
| JPH08102360A (ja) * | 1994-09-29 | 1996-04-16 | Toyota Central Res & Dev Lab Inc | 有機無機複合薄膜型電界発光素子 |
| JP2931229B2 (ja) * | 1995-02-13 | 1999-08-09 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子 |
| JP2982699B2 (ja) * | 1995-08-04 | 1999-11-29 | 東洋インキ製造株式会社 | 多層型有機エレクトロルミネッセンス素子の電子注入層形成用材料 |
| US6001284A (en) * | 1995-08-04 | 1999-12-14 | Toyo Ink Manufacturing Co., Ltd. | Organoelectroluminescence device material and organoelectroluminescence device for which the material is adapted |
| EP0765106B1 (en) * | 1995-09-25 | 2002-11-27 | Toyo Ink Manufacturing Co., Ltd. | Light-emitting material for organic electroluminescence device, and organic electroluminescence device for which the light-emitting material is adapted |
| US5811834A (en) * | 1996-01-29 | 1998-09-22 | Toyo Ink Manufacturing Co., Ltd. | Light-emitting material for organo-electroluminescence device and organo-electroluminescence device for which the light-emitting material is adapted |
| JPH10270171A (ja) * | 1997-01-27 | 1998-10-09 | Junji Kido | 有機エレクトロルミネッセント素子 |
| US5972247A (en) * | 1998-03-20 | 1999-10-26 | Eastman Kodak Company | Organic electroluminescent elements for stable blue electroluminescent devices |
| US6140763A (en) * | 1998-07-28 | 2000-10-31 | Eastman Kodak Company | Interfacial electron-injecting layer formed from a doped cathode for organic light-emitting structure |
| JP3287344B2 (ja) * | 1998-10-09 | 2002-06-04 | 株式会社デンソー | 有機ｅｌ素子 |
| JP2000315581A (ja) * | 1999-04-30 | 2000-11-14 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子およびその製造方法 |
| JP3650552B2 (ja) * | 1999-09-14 | 2005-05-18 | 三星エスディアイ株式会社 | 有機エレクトロルミネッセンス素子およびこれを用いたパネル |
| JP2001097897A (ja) * | 1999-09-30 | 2001-04-10 | Idemitsu Kosan Co Ltd | 有機化合物及びそれを用いた有機エレクトロルミネッセンス素子 |
| EP1143773A4 (en) * | 1999-10-05 | 2007-02-21 | Matsushita Electric Ind Co Ltd | ELECTROLUMINESCENT DEVICE AND CORRESPONDING MANUFACTURING METHOD, AND DISPLAY AND LIGHTING DEVICE COMPRISING SAID DEVICE |
-
2002
- 2002-05-07 CN CNB028113322A patent/CN100431193C/zh not_active Expired - Lifetime
- 2002-05-07 WO PCT/JP2002/004427 patent/WO2002102118A1/ja active Application Filing
- 2002-05-07 EP EP02724697A patent/EP1404160A4/en not_active Withdrawn
- 2002-05-07 JP JP2003504716A patent/JP4029071B2/ja not_active Expired - Lifetime
- 2002-05-07 KR KR1020037015965A patent/KR100900375B1/ko active IP Right Grant
- 2002-05-10 US US10/141,982 patent/US20030077480A1/en not_active Abandoned
- 2002-05-13 TW TW091109908A patent/TWI286911B/zh not_active IP Right Cessation
- 2002-05-13 TW TW095148537A patent/TWI299749B/zh not_active IP Right Cessation
-
2004
- 2004-09-08 US US10/935,102 patent/US7087322B2/en not_active Expired - Lifetime
-
2006
- 2006-07-05 US US11/480,469 patent/US20060257687A1/en not_active Abandoned
Cited By (51)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10243145B2 (en) | 2002-07-19 | 2019-03-26 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US8334648B2 (en) | 2002-07-19 | 2012-12-18 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US9343682B2 (en) | 2002-07-19 | 2016-05-17 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US7927716B2 (en) | 2002-07-19 | 2011-04-19 | Idemitsu Kosan, Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20050064233A1 (en) * | 2002-07-19 | 2005-03-24 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20100277061A1 (en) * | 2002-07-19 | 2010-11-04 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20100270913A1 (en) * | 2002-07-19 | 2010-10-28 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US9728727B2 (en) | 2002-07-19 | 2017-08-08 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US7732063B2 (en) | 2002-07-19 | 2010-06-08 | Idemitsu Kosan, Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US7651786B2 (en) | 2002-07-19 | 2010-01-26 | Idemitsu Kosan, Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US8324802B2 (en) | 2002-07-19 | 2012-12-04 | Idemitsu Kosan, Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20060033421A1 (en) * | 2002-07-19 | 2006-02-16 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US9960358B2 (en) | 2002-07-19 | 2018-05-01 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20070237984A1 (en) * | 2002-07-19 | 2007-10-11 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and organic light emitting medium |
| US20040207312A1 (en) * | 2003-01-23 | 2004-10-21 | Seiko Epson Corporation | Manufacturing method for organic electroluminescence device, and electronic device therewith |
| US7252570B2 (en) * | 2003-01-23 | 2007-08-07 | Seiko Epson Corporation | Manufacturing method for organic electroluminescence device, and electronic device therewith |
| US20040258957A1 (en) * | 2003-06-18 | 2004-12-23 | Pei-Chuan Yeh | Organic electroluminescent device and manufacturing method thereof |
| US20050048317A1 (en) * | 2003-08-29 | 2005-03-03 | Semiconductor Energy Laboratory Co., Ltd. | Electroluminescent device and light-emitting device including the same |
| US20050064235A1 (en) * | 2003-09-24 | 2005-03-24 | Eastman Kodak Company | Blue organic electroluminescent devices having a non-hole-blocking layer |
| US6881502B2 (en) | 2003-09-24 | 2005-04-19 | Eastman Kodak Company | Blue organic electroluminescent devices having a non-hole-blocking layer |
| US20050104511A1 (en) * | 2003-11-14 | 2005-05-19 | Eastman Kodak Company | Organic electroluminescent devices having a stability-enhancing layer |
| US7138763B2 (en) | 2003-11-14 | 2006-11-21 | Eastman Kodak Company | Organic electroluminescent devices having a stability-enhancing layer |
| US7030554B2 (en) | 2004-02-06 | 2006-04-18 | Eastman Kodak Company | Full-color organic display having improved blue emission |
| US7528545B2 (en) | 2004-02-06 | 2009-05-05 | Eastman Kodak Company | Color organic OLED device |
| US20050173700A1 (en) * | 2004-02-06 | 2005-08-11 | Eastman Kodak Company | Full-color organic display having improved blue emission |
| US20060181202A1 (en) * | 2004-02-06 | 2006-08-17 | Liang-Sheng Liao | Color organic OLED device |
| US7192659B2 (en) | 2004-04-14 | 2007-03-20 | Eastman Kodak Company | OLED device using reduced drive voltage |
| WO2005109543A3 (en) * | 2004-04-14 | 2006-01-05 | Eastman Kodak Co | Oled device using reduced drive voltage |
| WO2005109543A2 (en) * | 2004-04-14 | 2005-11-17 | Eastman Kodak Company | Oled device using reduced drive voltage |
| US20050233166A1 (en) * | 2004-04-14 | 2005-10-20 | Eastman Kodak Company | OLED device using reduced drive voltage |
| US20070292714A1 (en) * | 2004-09-17 | 2007-12-20 | Idemitsu Kosan Co., Ltd. | Aromatic Amine Derivative and Organic Electroluminescent Device Using Same |
| EP1790631A4 (en) * | 2004-09-17 | 2007-10-31 | Idemitsu Kosan Co | AROMATIC AMINE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT DEVICE USING THE DERIVATIVE |
| EP1790631A1 (en) * | 2004-09-17 | 2007-05-30 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent device using same |
| US20070120115A1 (en) * | 2005-10-21 | 2007-05-31 | Seiko Epson Corporation | Organic light-emitting element, method of manufacturing organic light-emitting element, light-emitting device, and electronic apparatus |
| WO2007050301A3 (en) * | 2005-10-26 | 2008-09-12 | Eastman Kodak Co | Organic element for low voltage electroluminescent devices |
| US20070092756A1 (en) * | 2005-10-26 | 2007-04-26 | Eastman Kodak Company | Organic element for low voltage electroluminescent devices |
| US7767317B2 (en) | 2005-10-26 | 2010-08-03 | Global Oled Technology Llc | Organic element for low voltage electroluminescent devices |
| US20080157657A1 (en) * | 2006-12-22 | 2008-07-03 | Sony Corporation | Organic electroluminescent device and display |
| US11133478B2 (en) | 2007-12-28 | 2021-09-28 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent device using the same |
| US10297765B2 (en) | 2007-12-28 | 2019-05-21 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent device using the same |
| US20120025181A1 (en) * | 2009-03-25 | 2012-02-02 | Panasonic Electric Works Co., Ltd. | Organic el element |
| US20130228764A1 (en) * | 2009-03-25 | 2013-09-05 | Panasonic Corporation | Organic el element |
| US10686137B2 (en) | 2009-04-24 | 2020-06-16 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescent element comprising the same |
| US10263191B2 (en) | 2009-04-24 | 2019-04-16 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescent element comprising the same |
| US11024806B2 (en) | 2009-04-24 | 2021-06-01 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescent element comprising the same |
| US20120286653A1 (en) * | 2009-12-11 | 2012-11-15 | Mitsubishi Chemical Corporation | Organic electroluminescent element, organic el display device, and organic el illuminator |
| US9923146B2 (en) | 2009-12-16 | 2018-03-20 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent element using same |
| US9331285B2 (en) | 2009-12-16 | 2016-05-03 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent element using same |
| US10118889B2 (en) | 2014-09-19 | 2018-11-06 | Idemitsu Kosan Co., Ltd. | Compound |
| US10435350B2 (en) | 2014-09-19 | 2019-10-08 | Idemitsu Kosan Co., Ltd. | Organic electroluminecence device |
| US9902687B2 (en) | 2014-09-19 | 2018-02-27 | Idemitsu Kosan Co., Ltd. | Compound |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2002102118A1 (fr) | 2002-12-19 |
| US7087322B2 (en) | 2006-08-08 |
| US20060257687A1 (en) | 2006-11-16 |
| CN100431193C (zh) | 2008-11-05 |
| CN1513283A (zh) | 2004-07-14 |
| TWI286911B (en) | 2007-09-11 |
| US20050227111A1 (en) | 2005-10-13 |
| TW200722501A (en) | 2007-06-16 |
| JPWO2002102118A1 (ja) | 2004-09-30 |
| EP1404160A1 (en) | 2004-03-31 |
| KR100900375B1 (ko) | 2009-06-02 |
| JP4029071B2 (ja) | 2008-01-09 |
| KR20040010686A (ko) | 2004-01-31 |
| EP1404160A4 (en) | 2008-09-24 |
| TWI299749B (en) | 2008-08-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US7087322B2 (en) | Organic electroluminescence device | |
| US10217943B2 (en) | Organic electroluminescence device and anthracene derivative | |
| US7790892B2 (en) | Aromatic compound and organic electroluminescent element containing the same | |
| US6582837B1 (en) | Organic electroluminescence device | |
| US7745016B2 (en) | White organic electroluminescence device | |
| US20080160344A1 (en) | Novel soluble compound and organic electroluminescent devices | |
| JP3424812B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| US7125614B2 (en) | Organic electroluminescent device | |
| US20060134458A1 (en) | Aromatic amine derivative and organic electroluminescence element | |
| JP2956691B1 (ja) | 有機エレクトロルミネッセンス素子 | |
| JP2002124385A (ja) | 有機エレクトロルミネッセンス素子 | |
| JP3389905B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| JPH11228951A (ja) | 有機エレクトロルミネッセンス素子 | |
| US6682831B2 (en) | Organic electroluminescent device | |
| JP3961200B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| JP3008917B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| JP3139622B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| JP2882403B1 (ja) | 有機エレクトロルミネッセンス素子用材料及びこれを用いた有機エレクトロルミネッセンス素子 | |
| US20020168543A1 (en) | Organic electroluminscent device | |
| JP4139055B2 (ja) | 有機エレクトロルミネッセンス素子 | |
| JP3156679B2 (ja) | 有機エレクトロルミネッセンス素子 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: IDEMITSU KOSAN CO., LTD., JAPAN Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:HOSOKAWA, CHISHIO;FUNAHASHI, MASAKAZU;SAKAI, TOSHIO;AND OTHERS;REEL/FRAME:012888/0548 Effective date: 20011017 |
|
| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |