JP5127289B2 - アントラセン誘導体および発光素子 - Google Patents
アントラセン誘導体および発光素子 Download PDFInfo
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- JP5127289B2 JP5127289B2 JP2007115318A JP2007115318A JP5127289B2 JP 5127289 B2 JP5127289 B2 JP 5127289B2 JP 2007115318 A JP2007115318 A JP 2007115318A JP 2007115318 A JP2007115318 A JP 2007115318A JP 5127289 B2 JP5127289 B2 JP 5127289B2
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- carbon atoms
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- emitting element
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- 150000001454 anthracenes Chemical class 0.000 title claims description 131
- 125000004432 carbon atom Chemical group C* 0.000 claims description 258
- 125000003118 aryl group Chemical group 0.000 claims description 160
- 125000000217 alkyl group Chemical group 0.000 claims description 89
- 239000001257 hydrogen Substances 0.000 claims description 75
- 229910052739 hydrogen Inorganic materials 0.000 claims description 75
- 150000001875 compounds Chemical class 0.000 claims description 74
- 150000002431 hydrogen Chemical class 0.000 claims description 51
- 125000001424 substituent group Chemical group 0.000 claims description 34
- 229910052799 carbon Inorganic materials 0.000 claims description 26
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 24
- 238000006467 substitution reaction Methods 0.000 claims description 21
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- 125000000732 arylene group Chemical group 0.000 claims description 15
- 150000001721 carbon Chemical group 0.000 claims description 10
- 125000001188 haloalkyl group Chemical group 0.000 claims description 5
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 360
- 239000010410 layer Substances 0.000 description 179
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 168
- 239000000243 solution Substances 0.000 description 153
- 238000005481 NMR spectroscopy Methods 0.000 description 90
- 230000015572 biosynthetic process Effects 0.000 description 82
- 238000003786 synthesis reaction Methods 0.000 description 82
- 238000000862 absorption spectrum Methods 0.000 description 71
- 239000000126 substance Substances 0.000 description 70
- 238000000295 emission spectrum Methods 0.000 description 68
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 66
- 239000010409 thin film Substances 0.000 description 66
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 60
- 238000005259 measurement Methods 0.000 description 59
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 54
- 239000000758 substrate Substances 0.000 description 53
- 239000007787 solid Substances 0.000 description 52
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 50
- 239000000203 mixture Substances 0.000 description 49
- 239000010408 film Substances 0.000 description 43
- 238000006243 chemical reaction Methods 0.000 description 42
- 230000005284 excitation Effects 0.000 description 40
- 238000010521 absorption reaction Methods 0.000 description 39
- 239000000706 filtrate Substances 0.000 description 39
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 38
- 238000000034 method Methods 0.000 description 35
- 229910052757 nitrogen Inorganic materials 0.000 description 34
- 239000002131 composite material Substances 0.000 description 32
- 238000002484 cyclic voltammetry Methods 0.000 description 32
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 32
- 239000010453 quartz Substances 0.000 description 32
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 32
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 31
- 239000000463 material Substances 0.000 description 30
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical class CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 28
- 239000012044 organic layer Substances 0.000 description 28
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
- 150000002894 organic compounds Chemical class 0.000 description 26
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 25
- 235000019341 magnesium sulphate Nutrition 0.000 description 25
- 239000011541 reaction mixture Substances 0.000 description 25
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 25
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- -1 or Chemical group 0.000 description 23
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 22
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 22
- NLKNQRATVPKPDG-UHFFFAOYSA-M potassium iodide Chemical compound [K+].[I-] NLKNQRATVPKPDG-UHFFFAOYSA-M 0.000 description 22
- 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 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- 230000008859 change Effects 0.000 description 21
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- 238000001228 spectrum Methods 0.000 description 19
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- UKSZBOKPHAQOMP-SVLSSHOZSA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 UKSZBOKPHAQOMP-SVLSSHOZSA-N 0.000 description 16
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 16
- 238000007254 oxidation reaction Methods 0.000 description 16
- 239000002904 solvent Substances 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 15
- 238000010438 heat treatment Methods 0.000 description 15
- 230000005525 hole transport Effects 0.000 description 15
- 239000000843 powder Substances 0.000 description 15
- 0 *[Al]c(c1ccccc11)c(cccc2)c2c1[Al]I Chemical compound *[Al]c(c1ccccc11)c(cccc2)c2c1[Al]I 0.000 description 14
- 239000012298 atmosphere Substances 0.000 description 14
- 229910010272 inorganic material Inorganic materials 0.000 description 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 14
- BWHDROKFUHTORW-UHFFFAOYSA-N tritert-butylphosphane Chemical compound CC(C)(C)P(C(C)(C)C)C(C)(C)C BWHDROKFUHTORW-UHFFFAOYSA-N 0.000 description 14
- 238000007740 vapor deposition Methods 0.000 description 14
- 150000002484 inorganic compounds Chemical class 0.000 description 13
- 229910052751 metal Inorganic materials 0.000 description 13
- 239000002184 metal Substances 0.000 description 13
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 13
- 229910052697 platinum Inorganic materials 0.000 description 13
- 238000010898 silica gel chromatography Methods 0.000 description 13
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 13
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 12
- 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 12
- 230000003647 oxidation Effects 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 238000000967 suction filtration Methods 0.000 description 12
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 12
- OZNXPZBQVNNJCS-UHFFFAOYSA-N 2-bromo-9,10-diphenylanthracene Chemical compound C=12C=CC=CC2=C(C=2C=CC=CC=2)C2=CC(Br)=CC=C2C=1C1=CC=CC=C1 OZNXPZBQVNNJCS-UHFFFAOYSA-N 0.000 description 11
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 description 11
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 11
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 11
- 229910052782 aluminium Inorganic materials 0.000 description 11
- 238000000151 deposition Methods 0.000 description 11
- 239000011521 glass Substances 0.000 description 11
- 230000009467 reduction Effects 0.000 description 11
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 10
- 238000003756 stirring Methods 0.000 description 10
- 230000002194 synthesizing effect Effects 0.000 description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 9
- 125000005577 anthracene group Chemical group 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- 239000012046 mixed solvent Substances 0.000 description 9
- JOYGIIGTQLWSCZ-UHFFFAOYSA-N n-(9,10-diphenylanthracen-2-yl)-n-naphthalen-1-yl-9-phenylcarbazol-3-amine Chemical compound C1=CC=CC=C1C(C1=CC=C(C=C11)N(C=2C=C3C4=CC=CC=C4N(C=4C=CC=CC=4)C3=CC=2)C=2C3=CC=CC=C3C=CC=2)=C(C=CC=C2)C2=C1C1=CC=CC=C1 JOYGIIGTQLWSCZ-UHFFFAOYSA-N 0.000 description 9
- 230000003287 optical effect Effects 0.000 description 9
- 239000000523 sample Substances 0.000 description 9
- 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 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- 238000004770 highest occupied molecular orbital Methods 0.000 description 8
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 8
- 239000004973 liquid crystal related substance Substances 0.000 description 8
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 8
- 229910044991 metal oxide Inorganic materials 0.000 description 8
- 150000004706 metal oxides Chemical class 0.000 description 8
- DZRDATNLTUIPAY-UHFFFAOYSA-N n,9-diphenylcarbazol-3-amine Chemical compound C=1C=C2N(C=3C=CC=CC=3)C3=CC=CC=C3C2=CC=1NC1=CC=CC=C1 DZRDATNLTUIPAY-UHFFFAOYSA-N 0.000 description 8
- AJNJGJDDJIBTBP-UHFFFAOYSA-N n-(9,10-diphenylanthracen-2-yl)-n,9-diphenylcarbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C(C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C=CC=CC=3)C2=CC=1)C1=CC=C(N(C=2C=CC=CC=2)C=2C3=CC=CC=2)C3=C1 AJNJGJDDJIBTBP-UHFFFAOYSA-N 0.000 description 8
- 238000001420 photoelectron spectroscopy Methods 0.000 description 8
- 229910052814 silicon oxide Inorganic materials 0.000 description 8
- 238000004544 sputter deposition Methods 0.000 description 8
- 238000001308 synthesis method Methods 0.000 description 8
- KBLZDCFTQSIIOH-UHFFFAOYSA-M tetrabutylazanium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC KBLZDCFTQSIIOH-UHFFFAOYSA-M 0.000 description 8
- 238000001771 vacuum deposition Methods 0.000 description 8
- RUFPHBVGCFYCNW-UHFFFAOYSA-N 1-naphthylamine Chemical compound C1=CC=C2C(N)=CC=CC2=C1 RUFPHBVGCFYCNW-UHFFFAOYSA-N 0.000 description 7
- HGHBHXZNXIDZIZ-UHFFFAOYSA-N 4-n-(9,10-diphenylanthracen-2-yl)-1-n,1-n,4-n-triphenylbenzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=C2C(C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C=CC=CC=3)C2=CC=1)C1=CC=CC=C1 HGHBHXZNXIDZIZ-UHFFFAOYSA-N 0.000 description 7
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- 229960000583 acetic acid Drugs 0.000 description 7
- 230000006866 deterioration Effects 0.000 description 7
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 7
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- ZAYWSHLQYXBFMJ-UHFFFAOYSA-N n-(9,10-diphenylanthracen-2-yl)-n,9-dinaphthalen-1-ylcarbazol-3-amine Chemical compound C1=CC=CC=C1C(C1=CC=C(C=C11)N(C=2C=C3C4=CC=CC=C4N(C=4C5=CC=CC=C5C=CC=4)C3=CC=2)C=2C3=CC=CC=C3C=CC=2)=C(C=CC=C2)C2=C1C1=CC=CC=C1 ZAYWSHLQYXBFMJ-UHFFFAOYSA-N 0.000 description 7
- KUGSVDXBPQUXKX-UHFFFAOYSA-N n-[9,10-bis(2-phenylphenyl)anthracen-2-yl]-n,9-diphenylcarbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C(C=3C(=CC=CC=3)C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C(=CC=CC=3)C=3C=CC=CC=3)C2=CC=1)C1=CC=C(N(C=2C=CC=CC=2)C=2C3=CC=CC=2)C3=C1 KUGSVDXBPQUXKX-UHFFFAOYSA-N 0.000 description 7
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 description 7
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- 229910001930 tungsten oxide Inorganic materials 0.000 description 7
- LFPVTSQDPXUEEE-UHFFFAOYSA-N 2-bromo-9,10-bis(2-phenylphenyl)anthracene Chemical compound C=12C=CC=CC2=C(C=2C(=CC=CC=2)C=2C=CC=CC=2)C2=CC(Br)=CC=C2C=1C1=CC=CC=C1C1=CC=CC=C1 LFPVTSQDPXUEEE-UHFFFAOYSA-N 0.000 description 6
- VTSDGYDTWADUJQ-UHFFFAOYSA-N 2-bromoanthracene-9,10-dione Chemical compound C1=CC=C2C(=O)C3=CC(Br)=CC=C3C(=O)C2=C1 VTSDGYDTWADUJQ-UHFFFAOYSA-N 0.000 description 6
- QTWVKYHIDBPQIL-UHFFFAOYSA-N 3-bromo-9-naphthalen-1-ylcarbazole Chemical compound C12=CC=CC=C2C2=CC(Br)=CC=C2N1C1=CC=CC2=CC=CC=C12 QTWVKYHIDBPQIL-UHFFFAOYSA-N 0.000 description 6
- KUBSCXXKQGDPPD-UHFFFAOYSA-N 3-bromo-9-phenylcarbazole Chemical compound C12=CC=CC=C2C2=CC(Br)=CC=C2N1C1=CC=CC=C1 KUBSCXXKQGDPPD-UHFFFAOYSA-N 0.000 description 6
- KLNDKWAYVMOOFU-UHFFFAOYSA-N 4-n-[9,10-bis(2-phenylphenyl)anthracen-2-yl]-1-n,1-n,4-n-triphenylbenzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(C=1C=CC=CC=1)C=1C=C2C(C=3C(=CC=CC=3)C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C(=CC=CC=3)C=3C=CC=CC=3)C2=CC=1)C1=CC=CC=C1 KLNDKWAYVMOOFU-UHFFFAOYSA-N 0.000 description 6
- QSOAYCUFEQGHDN-UHFFFAOYSA-N 9-naphthalen-1-ylcarbazole Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=CC2=CC=CC=C12 QSOAYCUFEQGHDN-UHFFFAOYSA-N 0.000 description 6
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- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 6
- 239000012362 glacial acetic acid Substances 0.000 description 6
- 229910003437 indium oxide Inorganic materials 0.000 description 6
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 6
- 239000012212 insulator Substances 0.000 description 6
- DKQKUOFOSZLDGL-UHFFFAOYSA-N n-(4-carbazol-9-ylphenyl)-n-phenyl-9,10-bis(2-phenylphenyl)anthracen-2-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C(C=3C(=CC=CC=3)C=3C=CC=CC=3)=C3C=CC=CC3=C(C=3C(=CC=CC=3)C=3C=CC=CC=3)C2=CC=1)C1=CC=C(N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 DKQKUOFOSZLDGL-UHFFFAOYSA-N 0.000 description 6
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- IEWZUAMHBCEFLR-UHFFFAOYSA-N 1-bromo-9,10-diphenylanthracene Chemical compound C12=CC=CC=C2C(C=2C=CC=CC=2)=C2C(Br)=CC=CC2=C1C1=CC=CC=C1 IEWZUAMHBCEFLR-UHFFFAOYSA-N 0.000 description 5
- XSDKKRKTDZMKCH-UHFFFAOYSA-N 9-(4-bromophenyl)carbazole Chemical compound C1=CC(Br)=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 XSDKKRKTDZMKCH-UHFFFAOYSA-N 0.000 description 5
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 5
- NRTOMJZYCJJWKI-UHFFFAOYSA-N Titanium nitride Chemical compound [Ti]#N NRTOMJZYCJJWKI-UHFFFAOYSA-N 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
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- 150000001716 carbazoles Chemical class 0.000 description 5
- 238000005859 coupling reaction Methods 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 239000011159 matrix material Substances 0.000 description 5
- MPPYRRTZYRAKJD-UHFFFAOYSA-N n,9-dinaphthalen-1-ylcarbazol-3-amine Chemical compound C1=CC=C2C(NC=3C=C4C5=CC=CC=C5N(C=5C6=CC=CC=C6C=CC=5)C4=CC=3)=CC=CC2=C1 MPPYRRTZYRAKJD-UHFFFAOYSA-N 0.000 description 5
- 229910052763 palladium Inorganic materials 0.000 description 5
- 238000005192 partition Methods 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 238000006479 redox reaction Methods 0.000 description 5
- 239000012488 sample solution Substances 0.000 description 5
- 238000007789 sealing Methods 0.000 description 5
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 5
- 235000017557 sodium bicarbonate Nutrition 0.000 description 5
- 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 5
- 229910001935 vanadium oxide Inorganic materials 0.000 description 5
- 239000011787 zinc oxide Substances 0.000 description 5
- CXTPIHZYOGDSLV-UHFFFAOYSA-N 1-bromoanthracene-9,10-dione Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C=CC=C2Br CXTPIHZYOGDSLV-UHFFFAOYSA-N 0.000 description 4
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- 238000013459 approach Methods 0.000 description 1
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- WZJYKHNJTSNBHV-UHFFFAOYSA-N benzo[h]quinoline Chemical group C1=CN=C2C3=CC=CC=C3C=CC2=C1 WZJYKHNJTSNBHV-UHFFFAOYSA-N 0.000 description 1
- GQVWHWAWLPCBHB-UHFFFAOYSA-L beryllium;benzo[h]quinolin-10-olate Chemical compound [Be+2].C1=CC=NC2=C3C([O-])=CC=CC3=CC=C21.C1=CC=NC2=C3C([O-])=CC=CC3=CC=C21 GQVWHWAWLPCBHB-UHFFFAOYSA-L 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 description 1
- UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XZCJVWCMJYNSQO-UHFFFAOYSA-N butyl pbd Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)O1 XZCJVWCMJYNSQO-UHFFFAOYSA-N 0.000 description 1
- IAFBVVRUEATLCO-UHFFFAOYSA-N c(cc1)ccc1-c1c(cccc2)c2c(-c(cc2)ccc2-[n]2c(nccc3)c3c3c2cccc3)c2c1cccc2 Chemical compound c(cc1)ccc1-c1c(cccc2)c2c(-c(cc2)ccc2-[n]2c(nccc3)c3c3c2cccc3)c2c1cccc2 IAFBVVRUEATLCO-UHFFFAOYSA-N 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000010406 cathode material Substances 0.000 description 1
- 238000010549 co-Evaporation Methods 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- JNGZXGGOCLZBFB-IVCQMTBJSA-N compound E Chemical compound N([C@@H](C)C(=O)N[C@@H]1C(N(C)C2=CC=CC=C2C(C=2C=CC=CC=2)=N1)=O)C(=O)CC1=CC(F)=CC(F)=C1 JNGZXGGOCLZBFB-IVCQMTBJSA-N 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- BHQBDOOJEZXHPS-UHFFFAOYSA-N ctk3i0272 Chemical group C1=CC=CC=C1C(C(=C(C=1C=CC=CC=1)C(=C1C=2C=CC=CC=2)C=2C3=CC=CC=C3C(C=3C4=CC=CC=C4C(C=4C(=C(C=5C=CC=CC=5)C(C=5C=CC=CC=5)=C(C=5C=CC=CC=5)C=4C=4C=CC=CC=4)C=4C=CC=CC=4)=C4C=CC=CC4=3)=C3C=CC=CC3=2)C=2C=CC=CC=2)=C1C1=CC=CC=C1 BHQBDOOJEZXHPS-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- SPWVRYZQLGQKGK-UHFFFAOYSA-N dichloromethane;hexane Chemical compound ClCCl.CCCCCC SPWVRYZQLGQKGK-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical group 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- OGPBJKLSAFTDLK-UHFFFAOYSA-N europium atom Chemical compound [Eu] OGPBJKLSAFTDLK-UHFFFAOYSA-N 0.000 description 1
- 239000000945 filler Substances 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
- 230000005283 ground state Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical compound [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 1
- DZFWNZJKBJOGFQ-UHFFFAOYSA-N julolidine Chemical compound C1CCC2=CC=CC3=C2N1CCC3 DZFWNZJKBJOGFQ-UHFFFAOYSA-N 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- WOYDRSOIBHFMGB-UHFFFAOYSA-N n,9-diphenyl-n-(9-phenylcarbazol-3-yl)carbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C=C2C3=CC=CC=C3N(C=3C=CC=CC=3)C2=CC=1)C1=CC=C(N(C=2C=CC=CC=2)C=2C3=CC=CC=2)C3=C1 WOYDRSOIBHFMGB-UHFFFAOYSA-N 0.000 description 1
- UMFJAHHVKNCGLG-UHFFFAOYSA-N n-Nitrosodimethylamine Chemical compound CN(C)N=O UMFJAHHVKNCGLG-UHFFFAOYSA-N 0.000 description 1
- COVCYOMDZRYBNM-UHFFFAOYSA-N n-naphthalen-1-yl-9-phenyl-n-(9-phenylcarbazol-3-yl)carbazol-3-amine Chemical compound C1=CC=CC=C1N1C2=CC=C(N(C=3C=C4C5=CC=CC=C5N(C=5C=CC=CC=5)C4=CC=3)C=3C4=CC=CC=C4C=CC=3)C=C2C2=CC=CC=C21 COVCYOMDZRYBNM-UHFFFAOYSA-N 0.000 description 1
- QCOIZKZASBFCJG-UHFFFAOYSA-N n-phenylanthracen-1-amine Chemical compound C=1C=CC2=CC3=CC=CC=C3C=C2C=1NC1=CC=CC=C1 QCOIZKZASBFCJG-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- SLIUAWYAILUBJU-UHFFFAOYSA-N pentacene Chemical compound C1=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C21 SLIUAWYAILUBJU-UHFFFAOYSA-N 0.000 description 1
- JZRYQZJSTWVBBD-UHFFFAOYSA-N pentaporphyrin i Chemical compound N1C(C=C2NC(=CC3=NC(=C4)C=C3)C=C2)=CC=C1C=C1C=CC4=N1 JZRYQZJSTWVBBD-UHFFFAOYSA-N 0.000 description 1
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 description 1
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 description 1
- NHKJPPKXDNZFBJ-UHFFFAOYSA-N phenyllithium Chemical compound [Li]C1=CC=CC=C1 NHKJPPKXDNZFBJ-UHFFFAOYSA-N 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 238000000103 photoluminescence spectrum Methods 0.000 description 1
- HRGDZIGMBDGFTC-UHFFFAOYSA-N platinum(2+) Chemical compound [Pt+2] HRGDZIGMBDGFTC-UHFFFAOYSA-N 0.000 description 1
- 229920000078 poly(4-vinyltriphenylamine) Polymers 0.000 description 1
- 229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 229910052761 rare earth metal Inorganic materials 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000027756 respiratory electron transport chain Effects 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- SIGUVTURIMRFDD-UHFFFAOYSA-M sodium dioxidophosphanium Chemical compound [Na+].[O-][PH2]=O SIGUVTURIMRFDD-UHFFFAOYSA-M 0.000 description 1
- 229910001379 sodium hypophosphite Inorganic materials 0.000 description 1
- 238000003980 solgel method Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 238000005092 sublimation method Methods 0.000 description 1
- ZGNPLWZYVAFUNZ-UHFFFAOYSA-N tert-butylphosphane Chemical compound CC(C)(C)P ZGNPLWZYVAFUNZ-UHFFFAOYSA-N 0.000 description 1
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- NAWDYIZEMPQZHO-UHFFFAOYSA-N ytterbium Chemical compound [Yb] NAWDYIZEMPQZHO-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- OYQCBJZGELKKPM-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O-2].[Zn+2].[O-2].[In+3] OYQCBJZGELKKPM-UHFFFAOYSA-N 0.000 description 1
- YVTHLONGBIQYBO-UHFFFAOYSA-N zinc indium(3+) oxygen(2-) Chemical compound [O--].[Zn++].[In+3] YVTHLONGBIQYBO-UHFFFAOYSA-N 0.000 description 1
- GWDUZCIBPDVBJM-UHFFFAOYSA-L zinc;2-(2-hydroxyphenyl)-3h-1,3-benzothiazole-2-carboxylate Chemical compound [Zn+2].OC1=CC=CC=C1C1(C([O-])=O)SC2=CC=CC=C2N1.OC1=CC=CC=C1C1(C([O-])=O)SC2=CC=CC=C2N1 GWDUZCIBPDVBJM-UHFFFAOYSA-L 0.000 description 1
- QEPMORHSGFRDLW-UHFFFAOYSA-L zinc;2-(2-hydroxyphenyl)-3h-1,3-benzoxazole-2-carboxylate Chemical compound [Zn+2].OC1=CC=CC=C1C1(C([O-])=O)OC2=CC=CC=C2N1.OC1=CC=CC=C1C1(C([O-])=O)OC2=CC=CC=C2N1 QEPMORHSGFRDLW-UHFFFAOYSA-L 0.000 description 1
Images
Description
本実施の形態では、本発明のアントラセン誘導体について説明する。
本発明のアントラセン誘導体を用いた発光素子の一態様について図1(A)を用いて以下に説明する。
本実施の形態では、実施の形態2で示した構成と異なる構成の発光素子について説明する。
本実施の形態では、実施の形態2および実施の形態3で示した構成と異なる構成の発光素子について説明する。
本実施の形態では、実施の形態2〜実施の形態3で示した構成と異なる構成の発光素子について説明する。
本実施の形態では、本発明に係る発光ユニットを複数積層した構成の発光素子(以下、積層型素子という)について、図3を参照して説明する。この発光素子は、第1の電極と第2の電極との間に、複数の発光ユニットを有する積層型発光素子である。各発光ユニットの構成としては、実施の形態2〜実施の形態5で示した構成と同様な構成を用いることができる。つまり、実施の形態2で示した発光素子は、1つの発光ユニットを有する発光素子である。本実施の形態では、複数の発光ユニットを有する発光素子について説明する。
本実施の形態では、本発明のアントラセン誘導体を用いて作製された発光装置について説明する。
本実施の形態では、実施の形態7に示す発光装置を含む本発明の電子機器について説明する。本発明の電子機器は、実施の形態1に示したアントラセン誘導体を含み、長寿命の表示部を有する。また、消費電力の低減された表示部を有する。
2−ブロモ−9,10−アントラキノンの合成スキームを(C−1)に示す。
2−ブロモ−9,10−ジフェニル−9,10−ジヒドロアントラセン−9,10−ジオールの合成スキームを(C−2)に示す。
2−ブロモ−9,10−ジフェニルアントラセンの合成スキームを(C−3)に示す。
2DPAPAの合成スキームを(C−4)に示す。
3−ブロモ−9−フェニルカルバゾールの合成スキームを(C−5)に示す。
N−フェニル−(9−フェニル−9H−カルバゾール−3−イル)アミン(略称:PCA)の合成スキームを(C−6)に示す。
2PCAPAの合成スキームを(C−7)に示す。
9,10−ジ(2−ビフェニリル)−2−ブロモアントラセンの合成スキームを(C−8)〜(C−10)に示す。
2DPABPhAの合成スキームを(C−11)に示す。
2PCABPhAの合成スキームを(C−12)に示す。
N−(4−ブロモフェニル)カルバゾールの合成スキームを(C−13)に示す。
4−(カルバゾール−9−イル)ジフェニルアミン(略称:YGA)の合成スキームを(C−14)に示す。
2YGABPhAの合成スキームを(C−15)に示す。
N−(1−ナフチル)−N−(9−フェニルカルバゾール−3−イル)アミン(略称:PCN)の合成スキームを(C−16)に示す。
2PCNPAの合成スキームを(C−17)に示す。
9−(1−ナフチル)カルバゾールの合成スキームを(C−18)に示す。
3−ブロモ−9−(1−ナフチル)カルバゾールの合成スキームを(C−19)に示す。
N,9−ジ(1−ナフチル)−9H−カルバゾール−3−アミン(略称:NCN)の合成スキームを(C−20)に示す。
2NCNPAの合成スキームを(C−21)に示す。
2YGAPAの合成スキームを(C−22)に示す。
1−ブロモ−9,10−アントラキノンの合成スキームを(C−23)に示す。
1−ブロモ−9,10−ジフェニル−9,10−ジヒドロアントラセン−9,10−ジオールの合成スキームを(C−24)に示す。
1−ブロモ−9,10−ジフェニルアントラセンの合成スキームを(C−25)に示す。
1PCAPAの合成スキームを(C−26)に示す。
2−ブロモ−9,9−ジメチルフルオレンの合成スキームを(C−27)に示す。
9,10−ビス(9,9−ジメチルフルオレン−2−イル)−2−ブロモ−9,10−ジヒドロアントラセン−9,10−ジオールの合成スキームを(C−28)および(C−29)に示す。
9,10−ビス(9,9−ジメチルフルオレン−2−イル)−2−ブロモアントラセンの合成スキームを(C−30)に示す。
2PCADFAの合成スキームを(C−31)に示す。
トリフェニルアミン−4−ボロン酸の合成スキームを(C−32)に示す。
N,N’,N’−トリフェニルベンジジン(略称:DPBA)の合成スキームを(C−33)に示す。
2DPBAPAの合成スキームを(C−34)に示す。
9−フェニルカルバゾール−3−イルボロン酸の合成スキームを(C−35)に示す。
4−[4−(9H−カルバゾール−9−イル)フェニル]ジフェニルアミン(略称:YGBA)の合成スキームを(C−36)に示す。
2YGBAPAの合成スキームを(C−37)に示す。
102 第1の電極
103 第1の層
104 第2の層
105 第3の層
106 第4の層
107 第2の電極
301 基板
302 第1の電極
303 第1の層
304 第2の層
305 第3の層
306 第4の層
307 第2の電極
501 第1の電極
502 第2の電極
511 第1の発光ユニット
512 第2の発光ユニット
513 電荷発生層
601 ソース側駆動回路
602 画素部
603 ゲート側駆動回路
604 封止基板
605 シール材
607 空間
608 配線
609 FPC(フレキシブルプリントサーキット)
610 素子基板
611 スイッチング用TFT
612 電流制御用TFT
613 第1の電極
614 絶縁物
616 発光物質を含む層
617 第2の電極
618 発光素子
623 nチャネル型TFT
624 pチャネル型TFT
901 筐体
902 液晶層
903 バックライト
904 筐体
905 ドライバIC
906 端子
951 基板
952 電極
953 絶縁層
954 隔壁層
955 発光物質を含む層
956 電極
2001 筐体
2002 光源
2101 ガラス基板
2102 第1の電極
2103 複合材料を含む層
2104 正孔輸送層
2105 発光層
2106 電子輸送層
2107 電子注入層
2108 第2の電極
3001 照明装置
3002 テレビ装置
9101 筐体
9102 支持台
9103 表示部
9104 スピーカー部
9105 ビデオ入力端子
9201 本体
9202 筐体
9203 表示部
9204 キーボード
9205 外部接続ポート
9206 ポインティングデバイス
9401 本体
9402 筐体
9403 表示部
9404 音声入力部
9405 音声出力部
9406 操作キー
9407 外部接続ポート
9408 アンテナ
9501 本体
9502 表示部
9503 筐体
9504 外部接続ポート
9505 リモコン受信部
9506 受像部
9507 バッテリー
9508 音声入力部
9509 操作キー
9510 接眼部
Claims (9)
- 一般式(1)で表されるアントラセン誘導体。
(式中、Ar1〜Ar2は、それぞれ、炭素数6〜25のアリール基を表し、Aは、一般式(1−1)〜一般式(1−3)で表されるいずれかの置換基を表す。一般式(1−1)〜一般式(1−3)において、Ar11〜Ar13は、それぞれ、炭素数6〜25のアリール基を表し、αは、炭素数6〜25のアリーレン基を表し、Ar21は、炭素数6〜25のアリール基を表し、R31は、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R32は、炭素数6〜25のアリール基を表し、Ar31は、炭素数6〜25のアリール基を表し、βは、炭素数6〜25のアリーレン基を表し、R41〜R42は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表す。ただし、式(A−1)〜(A−9)で表される化合物を除く。)
- 一般式(2)で表されるアントラセン誘導体。
(式中、Ar1〜Ar2は、それぞれ、炭素数6〜25のアリール基を表し、Aは、一般式(2−1)〜一般式(2−3)で表されるいずれかの置換基を表す。一般式(2−1)〜一般式(2−3)において、Ar11は、炭素数6〜25のアリール基を表し、R11〜R24は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表し、Ar21は、炭素数6〜25のアリール基を表し、R31は、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R33〜R37は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表し、Ar31は、炭素数6〜25のアリール基を表し、R41〜R42は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R43〜R46は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表す。ただし、式(A−1)〜(A−9)で表される化合物を除く。)
- 一般式(5)で表されるアントラセン誘導体。
(式中、Ar1〜Ar2は、それぞれ、炭素数6〜25のアリール基を表し、Aは、一般式(5−1)〜一般式(5−3)で表されるいずれかの置換基を表す。一般式(5−1)〜一般式(5−3)において、Ar11〜Ar13は、それぞれ、炭素数6〜25のアリール基を表し、αは、炭素数6〜25のアリーレン基を表し、Ar21は、炭素数6〜25のアリール基を表し、R31は、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R32は、炭素数6〜25のアリール基を表し、Ar31は、炭素数6〜25のアリール基を表し、βは、炭素数6〜25のアリーレン基を表し、R41〜R42は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表す。ただし、式(A−1)〜(A−9)で表される化合物を除く。)
- 一般式(6)で表されるアントラセン誘導体。
(式中、Ar1〜Ar2は、それぞれ、炭素数6〜25のアリール基を表し、Aは、一般式(6−1)〜一般式(6−3)で表されるいずれかの置換基を表す。一般式(6−1)〜一般式(6−3)において、Ar11は、炭素数6〜25のアリール基を表し、R11〜R24は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表し、Ar21は、炭素数6〜25のアリール基を表し、R31は、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R33〜R37は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表し、Ar31は、炭素数6〜25のアリール基を表し、R41〜R42は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜25のアリール基のいずれかを表し、R43〜R46は、それぞれ、水素、炭素数1〜4のアルキル基、炭素数6〜15のアリール基のいずれかを表す。ただし、式(A−1)〜(A−9)で表される化合物を除く。)
- 請求項1乃至請求項5のいずれか一項において、
Ar1とAr2は、同一の構造を有する置換基であるアントラセン誘導体。 - 一対の電極間に、請求項1乃至請求項6のいずれか一項に記載のアントラセン誘導体を有することを特徴とする発光素子。
- 一対の電極間に発光層を有し、前記発光層は請求項1乃至請求項6のいずれか一項に記載のアントラセン誘導体を有することを特徴とする発光素子。
- 一対の電極間に発光層を有し、前記発光層は請求項1乃至請求項6のいずれか一項に記載のアントラセン誘導体を有し、前記アントラセン誘導体が発光することを特徴とする発光素子。
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