JP5700771B2 - 化合物 - Google Patents
化合物 Download PDFInfo
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- JP5700771B2 JP5700771B2 JP2010236325A JP2010236325A JP5700771B2 JP 5700771 B2 JP5700771 B2 JP 5700771B2 JP 2010236325 A JP2010236325 A JP 2010236325A JP 2010236325 A JP2010236325 A JP 2010236325A JP 5700771 B2 JP5700771 B2 JP 5700771B2
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- emitting element
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- 150000001875 compounds Chemical class 0.000 title claims description 78
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 78
- 125000004432 carbon atom Chemical group C* 0.000 claims description 67
- 125000000217 alkyl group Chemical group 0.000 claims description 52
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 30
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 21
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 15
- 125000006267 biphenyl group Chemical group 0.000 claims description 13
- 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 claims description 3
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 claims description 3
- 125000003933 pentacenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC5=CC=CC=C5C=C4C=C3C=C12)* 0.000 claims description 3
- 125000005561 phenanthryl group Chemical group 0.000 claims description 3
- 125000001725 pyrenyl group Chemical group 0.000 claims description 3
- 125000001935 tetracenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C12)* 0.000 claims description 3
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000003205 fragrance Substances 0.000 claims 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 468
- 239000010410 layer Substances 0.000 description 288
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 204
- 229910052757 nitrogen Inorganic materials 0.000 description 191
- 239000000243 solution Substances 0.000 description 136
- 239000000203 mixture Substances 0.000 description 132
- 239000007787 solid Substances 0.000 description 130
- 238000000862 absorption spectrum Methods 0.000 description 122
- 239000000126 substance Substances 0.000 description 110
- 239000010409 thin film Substances 0.000 description 102
- 230000000052 comparative effect Effects 0.000 description 95
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 89
- 230000015572 biosynthetic process Effects 0.000 description 88
- 238000005481 NMR spectroscopy Methods 0.000 description 83
- 238000003786 synthesis reaction Methods 0.000 description 82
- 238000000295 emission spectrum Methods 0.000 description 79
- 150000002220 fluorenes Chemical class 0.000 description 79
- 239000000706 filtrate Substances 0.000 description 74
- 238000005259 measurement Methods 0.000 description 73
- 239000000463 material Substances 0.000 description 71
- -1 amine compound Chemical class 0.000 description 67
- 239000000758 substrate Substances 0.000 description 67
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 66
- 238000004770 highest occupied molecular orbital Methods 0.000 description 62
- 239000010453 quartz Substances 0.000 description 58
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 54
- 238000000859 sublimation Methods 0.000 description 52
- 230000008022 sublimation Effects 0.000 description 52
- 238000010521 absorption reaction Methods 0.000 description 48
- 238000003756 stirring Methods 0.000 description 47
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 45
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 45
- 239000012298 atmosphere Substances 0.000 description 44
- 238000005401 electroluminescence Methods 0.000 description 44
- 239000010408 film Substances 0.000 description 44
- 239000002904 solvent Substances 0.000 description 43
- 238000000034 method Methods 0.000 description 42
- 238000000746 purification Methods 0.000 description 41
- 238000001228 spectrum Methods 0.000 description 40
- 238000002347 injection Methods 0.000 description 36
- 239000007924 injection Substances 0.000 description 36
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 34
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 34
- 230000005525 hole transport Effects 0.000 description 32
- 230000005284 excitation Effects 0.000 description 31
- 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 29
- 150000002894 organic compounds Chemical class 0.000 description 28
- 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 28
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 27
- FKHIFSZMMVMEQY-UHFFFAOYSA-N talc Chemical compound [Mg+2].[O-][Si]([O-])=O FKHIFSZMMVMEQY-UHFFFAOYSA-N 0.000 description 27
- 150000001412 amines Chemical class 0.000 description 24
- 238000010438 heat treatment Methods 0.000 description 24
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 24
- 238000010898 silica gel chromatography Methods 0.000 description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 20
- 238000000151 deposition Methods 0.000 description 20
- 239000012044 organic layer Substances 0.000 description 20
- 229910052751 metal Inorganic materials 0.000 description 19
- 239000002184 metal Substances 0.000 description 19
- 239000000047 product Substances 0.000 description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 18
- 230000008021 deposition Effects 0.000 description 18
- 229910052786 argon Inorganic materials 0.000 description 17
- 238000004455 differential thermal analysis Methods 0.000 description 17
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 17
- 235000019341 magnesium sulphate Nutrition 0.000 description 17
- 239000012046 mixed solvent Substances 0.000 description 17
- UQVFZEYHQJJGPD-UHFFFAOYSA-N 9-[4-(10-phenylanthracen-9-yl)phenyl]carbazole Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C1=CC=C(N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 UQVFZEYHQJJGPD-UHFFFAOYSA-N 0.000 description 16
- 230000006870 function Effects 0.000 description 16
- 238000002411 thermogravimetry Methods 0.000 description 16
- 230000004580 weight loss Effects 0.000 description 16
- 229910045601 alloy Inorganic materials 0.000 description 15
- 239000000956 alloy Substances 0.000 description 15
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 15
- 238000004519 manufacturing process Methods 0.000 description 15
- 239000003960 organic solvent Substances 0.000 description 15
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000007789 gas Substances 0.000 description 14
- 238000001420 photoelectron spectroscopy Methods 0.000 description 14
- 238000005092 sublimation method Methods 0.000 description 14
- 238000001308 synthesis method Methods 0.000 description 14
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 14
- JRCJYPMNBNNCFE-UHFFFAOYSA-N 1,6-dibromopyrene Chemical compound C1=C2C(Br)=CC=C(C=C3)C2=C2C3=C(Br)C=CC2=C1 JRCJYPMNBNNCFE-UHFFFAOYSA-N 0.000 description 13
- 239000002131 composite material Substances 0.000 description 13
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical class C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 13
- 239000011159 matrix material Substances 0.000 description 13
- 230000007704 transition Effects 0.000 description 13
- 238000002484 cyclic voltammetry Methods 0.000 description 12
- 238000001704 evaporation Methods 0.000 description 12
- 239000011777 magnesium Substances 0.000 description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 11
- 239000004305 biphenyl Substances 0.000 description 11
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 11
- 230000003647 oxidation Effects 0.000 description 11
- 238000007254 oxidation reaction Methods 0.000 description 11
- JJYPMNFTHPTTDI-UHFFFAOYSA-N 3-methylaniline Chemical compound CC1=CC=CC(N)=C1 JJYPMNFTHPTTDI-UHFFFAOYSA-N 0.000 description 10
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 10
- 238000002330 electrospray ionisation mass spectrometry Methods 0.000 description 10
- 239000012299 nitrogen atmosphere Substances 0.000 description 10
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 10
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
- 239000003054 catalyst Substances 0.000 description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 8
- 229910052783 alkali metal Inorganic materials 0.000 description 8
- 150000001340 alkali metals Chemical class 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 239000011575 calcium Substances 0.000 description 8
- 239000012212 insulator Substances 0.000 description 8
- 230000003287 optical effect Effects 0.000 description 8
- 238000005381 potential energy Methods 0.000 description 8
- 238000000967 suction filtration Methods 0.000 description 8
- 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 7
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 7
- 229910052749 magnesium Inorganic materials 0.000 description 7
- 238000002156 mixing Methods 0.000 description 7
- 238000010791 quenching Methods 0.000 description 7
- 230000000171 quenching effect Effects 0.000 description 7
- 238000004544 sputter deposition Methods 0.000 description 7
- 238000001771 vacuum deposition Methods 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- OOKRYIPMHLUQHU-UHFFFAOYSA-N 9-(4-bromophenyl)-9-phenylfluorene Chemical compound C1=CC(Br)=CC=C1C1(C=2C=CC=CC=2)C2=CC=CC=C2C2=CC=CC=C21 OOKRYIPMHLUQHU-UHFFFAOYSA-N 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 150000001342 alkaline earth metals Chemical class 0.000 description 6
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 6
- 235000010290 biphenyl Nutrition 0.000 description 6
- 230000005281 excited state Effects 0.000 description 6
- 229910052744 lithium Inorganic materials 0.000 description 6
- 230000007935 neutral effect Effects 0.000 description 6
- 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 6
- 230000000737 periodic effect Effects 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
- 229910001930 tungsten oxide Inorganic materials 0.000 description 6
- IYZMXHQDXZKNCY-UHFFFAOYSA-N 1-n,1-n-diphenyl-4-n,4-n-bis[4-(n-phenylanilino)phenyl]benzene-1,4-diamine Chemical compound C1=CC=CC=C1N(C=1C=CC(=CC=1)N(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)C1=CC=CC=C1 IYZMXHQDXZKNCY-UHFFFAOYSA-N 0.000 description 5
- IDVFGKSPIBIJGL-UHFFFAOYSA-N 2-(3-methylphenyl)pyrene-1,6-diamine Chemical compound CC1=CC=CC(C=2C(=C3C=CC4=CC=C(N)C5=CC=C(C3=C54)C=2)N)=C1 IDVFGKSPIBIJGL-UHFFFAOYSA-N 0.000 description 5
- 238000010549 co-Evaporation Methods 0.000 description 5
- 238000002425 crystallisation Methods 0.000 description 5
- 230000008025 crystallization Effects 0.000 description 5
- 239000002019 doping agent Substances 0.000 description 5
- 230000002349 favourable effect Effects 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N o-biphenylenemethane Natural products C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 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
- 229910052763 palladium Inorganic materials 0.000 description 5
- 238000005192 partition Methods 0.000 description 5
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 5
- 238000007789 sealing Methods 0.000 description 5
- 239000004065 semiconductor Substances 0.000 description 5
- 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 5
- KTADSLDAUJLZGL-UHFFFAOYSA-N 1-bromo-2-phenylbenzene Chemical group BrC1=CC=CC=C1C1=CC=CC=C1 KTADSLDAUJLZGL-UHFFFAOYSA-N 0.000 description 4
- XQYGCWSZCDHROU-UHFFFAOYSA-N 9-(3-bromophenyl)-9-(3-methylphenyl)fluorene Chemical compound CC1=CC=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(Br)C=CC=2)=C1 XQYGCWSZCDHROU-UHFFFAOYSA-N 0.000 description 4
- LWBYEDXZPBXTFL-UHFFFAOYSA-N 9-(3-bromophenyl)-9-phenylfluorene Chemical compound BrC1=CC=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=CC=CC=2)=C1 LWBYEDXZPBXTFL-UHFFFAOYSA-N 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 4
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical class CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 4
- 235000002597 Solanum melongena Nutrition 0.000 description 4
- XHCLAFWTIXFWPH-UHFFFAOYSA-N [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[V+5].[V+5] XHCLAFWTIXFWPH-UHFFFAOYSA-N 0.000 description 4
- AZWHFTKIBIQKCA-UHFFFAOYSA-N [Sn+2]=O.[O-2].[In+3] Chemical compound [Sn+2]=O.[O-2].[In+3] AZWHFTKIBIQKCA-UHFFFAOYSA-N 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 4
- 229910052792 caesium Inorganic materials 0.000 description 4
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 description 4
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 4
- 229910052791 calcium Inorganic materials 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 239000000412 dendrimer Substances 0.000 description 4
- 229920000736 dendritic polymer Polymers 0.000 description 4
- GUVUOGQBMYCBQP-UHFFFAOYSA-N dmpu Chemical compound CN1CCCN(C)C1=O GUVUOGQBMYCBQP-UHFFFAOYSA-N 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 239000012362 glacial acetic acid Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 description 4
- 229910003437 indium oxide Inorganic materials 0.000 description 4
- PJXISJQVUVHSOJ-UHFFFAOYSA-N indium(iii) oxide Chemical compound [O-2].[O-2].[O-2].[In+3].[In+3] PJXISJQVUVHSOJ-UHFFFAOYSA-N 0.000 description 4
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 239000000565 sealant Substances 0.000 description 4
- 229910052814 silicon oxide Inorganic materials 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 238000004528 spin coating Methods 0.000 description 4
- 229910001935 vanadium oxide Inorganic materials 0.000 description 4
- 239000011787 zinc oxide Substances 0.000 description 4
- DIOAPUWBVWDIEW-UHFFFAOYSA-N 1-N,6-N-bis(3-methylphenyl)-1-N,6-N-bis[3-[9-(3-methylphenyl)fluoren-9-yl]phenyl]pyrene-1,6-diamine Chemical compound CC1=CC=CC(N(C=2C=C(C=CC=2)C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C=CC=2)C=2C3=CC=C4C=CC(=C5C=CC(C3=C54)=CC=2)N(C=2C=C(C)C=CC=2)C=2C=C(C=CC=2)C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C=CC=2)=C1 DIOAPUWBVWDIEW-UHFFFAOYSA-N 0.000 description 3
- 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 3
- IXPKKPNQRSWPNV-UHFFFAOYSA-N 2,3-diphenylpyrene-1,6-diamine Chemical compound C=1C=CC=CC=1C=1C(C2=C34)=CC=C4C(N)=CC=C3C=CC2=C(N)C=1C1=CC=CC=C1 IXPKKPNQRSWPNV-UHFFFAOYSA-N 0.000 description 3
- FQJQNLKWTRGIEB-UHFFFAOYSA-N 2-(4-tert-butylphenyl)-5-[3-[5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl]phenyl]-1,3,4-oxadiazole Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=C(C=CC=2)C=2OC(=NN=2)C=2C=CC(=CC=2)C(C)(C)C)O1 FQJQNLKWTRGIEB-UHFFFAOYSA-N 0.000 description 3
- GEQBRULPNIVQPP-UHFFFAOYSA-N 2-[3,5-bis(1-phenylbenzimidazol-2-yl)phenyl]-1-phenylbenzimidazole Chemical compound C1=CC=CC=C1N1C2=CC=CC=C2N=C1C1=CC(C=2N(C3=CC=CC=C3N=2)C=2C=CC=CC=2)=CC(C=2N(C3=CC=CC=C3N=2)C=2C=CC=CC=2)=C1 GEQBRULPNIVQPP-UHFFFAOYSA-N 0.000 description 3
- BWXANYMTRAGZOW-UHFFFAOYSA-N 2-[4-(9-phenylfluoren-9-yl)phenyl]pyrene-1,6-diamine Chemical compound C1(=CC=CC=C1)C1(C2=CC=CC=C2C=2C=CC=CC1=2)C1=CC=C(C=C1)C1=C(C=2C=CC3=CC=C(C=4C=CC(=C1)C=2C=43)N)N BWXANYMTRAGZOW-UHFFFAOYSA-N 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 3
- ZJQCOVBALALRCC-UHFFFAOYSA-N 9-phenyl-9h-fluorene Chemical compound C1=CC=CC=C1C1C2=CC=CC=C2C2=CC=CC=C21 ZJQCOVBALALRCC-UHFFFAOYSA-N 0.000 description 3
- 229910017073 AlLi Inorganic materials 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
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- 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
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- 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
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- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 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
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- 229910000449 hafnium oxide Inorganic materials 0.000 description 1
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- 239000007788 liquid Substances 0.000 description 1
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- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 1
- 150000002680 magnesium Chemical class 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- DVSDBMFJEQPWNO-UHFFFAOYSA-N methyllithium Chemical compound C[Li] DVSDBMFJEQPWNO-UHFFFAOYSA-N 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- RVNSDHLVRKJPJZ-UHFFFAOYSA-N n-(4-tert-butylphenyl)-4-(9-phenylfluoren-9-yl)aniline Chemical compound C1=CC(C(C)(C)C)=CC=C1NC1=CC=C(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=CC=CC=2)C=C1 RVNSDHLVRKJPJZ-UHFFFAOYSA-N 0.000 description 1
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- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910000484 niobium oxide Inorganic materials 0.000 description 1
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
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- 230000033116 oxidation-reduction process Effects 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
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- RVTZCBVAJQQJTK-UHFFFAOYSA-N oxygen(2-);zirconium(4+) Chemical compound [O-2].[O-2].[Zr+4] RVTZCBVAJQQJTK-UHFFFAOYSA-N 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
- 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
- 150000002989 phenols Chemical class 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 229920000767 polyaniline Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000005581 pyrene group Chemical group 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 229910001923 silver oxide Inorganic materials 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000003115 supporting electrolyte Substances 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 description 1
- JIIYLLUYRFRKMG-UHFFFAOYSA-N tetrathianaphthacene Chemical compound C1=CC=CC2=C3SSC(C4=CC=CC=C44)=C3C3=C4SSC3=C21 JIIYLLUYRFRKMG-UHFFFAOYSA-N 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- WLPUWLXVBWGYMZ-UHFFFAOYSA-N tricyclohexylphosphine Chemical compound C1CCCCC1P(C1CCCCC1)C1CCCCC1 WLPUWLXVBWGYMZ-UHFFFAOYSA-N 0.000 description 1
- FPZZZGJWXOHLDJ-UHFFFAOYSA-N trihexylphosphane Chemical compound CCCCCCP(CCCCCC)CCCCCC FPZZZGJWXOHLDJ-UHFFFAOYSA-N 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- COIOYMYWGDAQPM-UHFFFAOYSA-N tris(2-methylphenyl)phosphane Chemical compound CC1=CC=CC=C1P(C=1C(=CC=CC=1)C)C1=CC=CC=C1C COIOYMYWGDAQPM-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- 229910001928 zirconium oxide Inorganic materials 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/54—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to two or three six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
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- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/43—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
- C07C211/57—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton
- C07C211/61—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton having amino groups bound to carbon atoms of six-membered aromatic rings being part of condensed ring systems of the carbon skeleton with at least one of the condensed ring systems formed by three or more rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
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- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
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- 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
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- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
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- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
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- 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
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- 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
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- C07C2601/14—The ring being saturated
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- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/06—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members
- C07C2603/10—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings
- C07C2603/12—Ortho- or ortho- and peri-condensed systems containing three rings containing at least one ring with less than six ring members containing five-membered rings only one five-membered ring
- C07C2603/18—Fluorenes; Hydrogenated fluorenes
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- C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
- C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
- C07C2603/24—Anthracenes; Hydrogenated anthracenes
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- C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
- C07C2603/42—Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
- C07C2603/50—Pyrenes; Hydrogenated pyrenes
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
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- 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
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- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/917—Electroluminescent
Description
本実施の形態では、本発明の一態様のフルオレン誘導体について説明する。
合成スキーム(A−1)に示すように、1−ハロゲン化ビフェニル誘導体(a1)をリチオ化またはグリニア試薬化としたのち、ベンゾイル誘導体(a2)と反応させ、これを脱水させることで、ハロゲン化アリールフルオレン誘導体(a3)が得られる。
本実施の形態では、本発明の一態様のフルオレン誘導体について説明する。
本実施の形態では、実施の形態1または実施の形態2で説明したフルオレン誘導体を用いて形成した発光素子について説明する。
本実施の形態は、複数の発光ユニット(EL層とも記す)を積層した構成の発光素子(以下、積層型素子という)の態様について、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3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3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、画素部に実施の形態3または4の発光素子を有する発光装置について図4を用いて説明する。なお、図4(A)は、発光装置を示す上面図、図4(B)は図4(A)をA−A’およびB−B’で切断した断面図である。
本実施の形態では、実施の形態5に示す発光装置をその一部に含む電子機器及び照明装置について説明する。電子機器としては、ビデオカメラ、デジタルカメラ等のカメラ、ゴーグル型ディスプレイ、ナビゲーションシステム、音響再生装置(カーオーディオ、オーディオコンポ等)、コンピュータ、ゲーム機器、携帯情報端末(モバイルコンピュータ、携帯電話、携帯型ゲーム機または電子書籍等)、記録媒体を備えた画像再生装置(具体的には、Digital Versatile Disc(DVD)等の記録媒体を再生し、その画像を表示しうる表示装置を備えた装置)などが挙げられる。これらの電子機器の具体例を図6に示す。
1H NMR(CDCl3,300MHz):δ=7.03−7.40(m、26H)、7.46−7.49(m、4H)、7.54−7.63(m、3H)、7.66−7.70(m、2H)、7.77−7.81(m、4H)
MS(ESI−MS):m/z=738(M+H)+;C57H39N2(737.31)
まず、本実施例で用いる参照電極(Ag/Ag+電極)の真空準位に対するポテンシャルエネルギー(eV)を算出した。つまり、Ag/Ag+電極のフェルミ準位を算出した。メタノール中におけるフェロセンの酸化還元電位は、標準水素電極に対して+0.610[V vs. SHE]であることが知られている(参考文献;Christian R.Goldsmith et al., J.Am.Chem.Soc., Vol.124, No.1,83−96, 2002)。一方、本実施例で用いる参照電極を用いて、メタノール中におけるフェロセンの酸化還元電位を求めたところ、+0.11V[vs.Ag/Ag+]であった。したがって、この参照電極のポテンシャルエネルギーは、標準水素電極に対して0.50[eV]低くなっていることがわかった。
CV測定における溶液は、溶媒として脱水ジメチルホルムアミド(DMF)((株)アルドリッチ製、99.8%、カタログ番号;22705−6)を用い、支持電解質である過塩素酸テトラ−n−ブチルアンモニウム(n−Bu4NClO4)((株)東京化成製カタログ番号;T0836)を100mmol/Lの濃度となるように溶解させ、さらに測定対象を2mmol/Lの濃度となるように溶解させて調製した。また、作用電極としては白金電極(ビー・エー・エス(株)製、PTE白金電極)を、補助電極としては白金電極(ビー・エー・エス(株)製、VC−3用Ptカウンター電極(5cm))を、参照電極としてはAg/Ag+電極(ビー・エー・エス(株)製、RE7非水溶媒系参照電極)をそれぞれ用いた。なお、測定は室温(20〜25℃)で行った。また、CV測定時のスキャン速度は、0.1V/secに統一した。
まず、合成例1を示す。
次に、合成例2では、合成例1とは異なる合成法による1,6FLPAPrnの合成方法を示す。
1H NMR(CDCl3,300MHz):δ=6.88−6.91(m、6H)、7.00−7.03(m、8H)、7.13−7.40(m、26H)、7.73−7.80(m、6H)、7.87(d、J=9.0Hz、2H)、8.06−8.09(m、4H)
MS(ESI−MS):m/z=1017(M+H)+;C78H52N2(1016.41)
1H NMR(CDCl3,300MHz):δ=1.25(s、18H)、6.84−6.87(m、4H)、6.95−7.00(m、8H)、7.15−7.36(m、22H)、7.39(d、J=7.2Hz、4H)、7.74(d、J=7.2Hz、4H)、7.79(d、J=8.4Hz、2H)、7.87(d、J=9.3Hz、2H)、8.06(d、J=8.4Hz、2H)、8.09(d、J=9.3Hz、2H)
MS(ESI−MS):m/z=1130(M+H)+;C86H68N2(1128.54)
まず、ガラス基板である基板2101上に、酸化珪素を含む酸化インジウム−酸化スズをスパッタリング法にて成膜し、陽極2102を形成した。なお、その膜厚は110nmとし、電極面積は2mm×2mmとした。
比較発光素子1は、発光層2105及び電子輸送層2106以外は、発光素子1と同様に形成した。比較発光素子1においては、発光層2105として、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)と4−(10−フェニル−9−アントリル)トリフェニルアミン(略称:DPhPA)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAとDPhPAとの重量比は、1:0.1(=CzPA:DPhPA)となるように蒸着レートを調節した。
発光素子2において、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N’−ビス〔4−(9−フェニル−9H−フルオレン−9−イル)フェニル〕−N,N’−ジフェニル−ピレン−1,6−ジアミン(略称:1,6FLPAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6FLPAPrnとの重量比は、1:0.05(=CzPA:1,6FLPAPrn)となるように蒸着レートを調節した。
比較発光素子2Aにおいて、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)N,N,N’,N’−テトラフェニルピレン−1,6−ジアミン(略称:1,6DPhAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6DPhAPrnとの重量比は、1:0.05(=CzPA:1,6DPhAPrn)となるように蒸着レートを調節した。
比較発光素子2Bにおいて、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N,N’,N’−テトラ(3−メチルフェニル)ピレン−1,6−ジアミン(略称:1,6mMeDPhAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mMeDPhAPrnとの重量比は、1:0.05(=CzPA:1,6mMeDPhAPrn)となるように蒸着レートを調節した。
発光素子3において、第1の発光層2105aは、4−(10−フェニル−9−アントリル)−4’−(9−フェニル−9H−カルバゾール−3−イル)トリフェニルアミン(略称:PCBAPA)を蒸着することにより、25nmの膜厚で形成した。
比較発光素子3Aにおいて、第1の発光層2105aは、発光素子3と同様に形成した。また、第2の発光層2105bは、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N,N’,N’−テトラフェニルピレン−1,6ジアミン(略称:1,6DPhAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6DPhAPrnとの重量比は、1:0.05(=CzPA:1,6DPhAPrn)となるように蒸着レートを調節した。
比較発光素子3Bにおいて、第1の発光層2105aは、発光素子3と同様に形成した。また、第2の発光層2105bは、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N,N’,N’−テトラ(3−メチルフェニル)ピレン−1,6ジアミン(略称:1,6mMeDPhAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mMeDPhAPrnとの重量比は、1:0.05(=CzPA:1,6mMeDPhAPrn)となるように蒸着レートを調節した。
1H NMR(CDCl3,300MHz):δ=1.31−1.51(m、10H)、1.78−1.87(m、10H)、3.44−3.53(m、2H)、6.85−7.41(m、40H)、7.73−7.76(m、6H)、8.07−8.16(m、4H)
MS(ESI−MS):m/z=1181(M+H)+;C90H72N2(1180.57)
(略称:1,6mMeFLPAPrn)の合成法]
1H NMR(CDCl3,300MHz):δ=2.17(s、6H)、6.73(d、J=7.2Hz、2H)、6.83−6.91(m、8H)、6.98−7.08(m、6H)、7.12−7.41(m、22H)、7.73−7.79(m、6H)、7.88(d、J=9.3Hz、2H)、8.05−8.10(m、4H)
1H NMR(CDCl3,300MHz):δ=2.14(s、12H)、6.57(s、2H)、6.67(s、4H)、6.84(d、J=8.7Hz、4H)、6.99(d、J=8.7Hz、4H)、7.19−7.41(m、22H)、7.73−7.79(m、6H)、7.89(d、J=9.3Hz、2H)、8.06−8.11(m、4H)
(略称:mFLPA)の合成法]
1H NMR(CDCl3,300MHz):δ=6.68(d、J=7.8Hz、2H)、6.87−7.23(m、38H)、7.61(d、J=7.2Hz、4H)、7.74(d、J=7.8Hz、2H)、7.85(d、J=8.7Hz、2H)、8.03(d、J=8.7Hz、4H)
MS(ESI−MS):m/z=1017(M+H)+;C78H52N2(1016.41)
1H NMR(CDCl3,300MHz):δ=2.14(s、6H)、6.68(d、J=8.1Hz、2H)、6.86−7.23(m、36H)、7.61(d、J=7.8Hz、4H)、7.73(d、J=7.8Hz、2H)、7.85(d、J=9.3Hz、2H)、8.02−8.05(m、4H)
1H NMR(CDCl3,300MHz):δ=2.14(s、6H)、6.68(d、J=7.5Hz、2H)、6.81−7.21(m、36H)、7.60(d、J=7.2Hz、4H)、7.73(d、J=8.4Hz、2H)、7.85(d、J=9.3Hz、2H)、8.04(d、J=9.0Hz、4H)
1H NMR(CDCl3,300MHz):δ=2.21(s、6H)、6.67(d、J=7.2Hz、2H)、6.74(d、J=7.2Hz、2H)、7.17−7.23(m、34H)、7.62(d、J=7.8Hz、4H)、7.74(d、J=7.8Hz、2H)、7.86(d、J=9.0Hz、2H)、8.04(d、J=8.7Hz、4H)
MS(ESI−MS):m/z=1045(M+H)+;C80H56N2(1044.44)
1H NMR(CDCl3,300MHz):δ=2.14(s、6H)、2.20(s、6H)、6.66−7.25(m、36H)、7.61(d、J=7.2Hz、4H)、7.73(d、J=7.8Hz、2H)、7.86(d、J=9.3Hz、2H)、8.03−8.06(m、4H)
MS(ESI−MS):m/z=1073(M+H)+;C82H60N2(1072.48)
1H NMR(CDCl3,300MHz):δ=2.15(s、6H)、2.21(s、6H)、6.66−7.25(m、36H)、7.61(d、J=7.5Hz、4H)、7.73(d、J=7.8Hz、2H)、7.86(d、J=9.0Hz、2H)、8.04(d、J=8.7Hz、4H)
MS(ESI−MS):m/z=1073(M+H)+;C82H60N2(1072.48)
本実施例の発光素子4は、正孔注入層2103、正孔輸送層2104および発光層2105以外は、実施例4の発光素子1と同様に作製した。
本実施例の発光素子5は、発光層2105以外は、発光素子4と同様に作製した。
本実施例の発光素子6は、発光層2105以外は、発光素子4と同様に作製した。
発光素子7において、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N’−ビス〔3−(9−フェニル−9H−フルオレン−9−イル)フェニル〕−N,N’−ジフェニル−ピレン−1,6−ジアミン(略称:1,6mFLPAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mFLPAPrnとの重量比は、1:0.05(=CzPA:1,6mFLPAPrn)となるように蒸着レートを調節した。
発光素子8において、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N’−ビス(3−メチルフェニル)−N,N’−ビス〔3−(9−フェニル−9H−フルオレン−9−イル)フェニル〕−ピレン−1,6−ジアミン(略称:1,6mMemFLPAPrn)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mMemFLPAPrnとの重量比は、1:0.05(=CzPA:1,6mMemFLPAPrn)となるように蒸着レートを調節した。
発光素子9において、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N’−ビス{3−〔9−(3−メチルフェニル)−9H−フルオレン−9−イル〕フェニル}−N,N’−ビス(3−メチルフェニル)−ピレン−1,6−ジアミン(略称:1,6mMemFLPAPrn−II)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mMemFLPAPrn−IIとの重量比は、1:0.05(=CzPA:1,6mMemFLPAPrn−II)となるように蒸着レートを調節した。
発光素子10において、発光層2105は、9−[4−(10−フェニル−9−アントリル)フェニル]−9H−カルバゾール(略称:CzPA)とN,N’−ビス{3−〔9−(4−メチルフェニル)−9H−フルオレン−9−イル〕フェニル}−N,N’−ビス(3−メチルフェニル)−ピレン−1,6−ジアミン(略称:1,6mMemFLPAPrn−III)とを共蒸着することにより、30nmの膜厚で形成した。ここで、CzPAと1,6mMemFLPAPrn−IIIとの重量比は、1:0.05(=CzPA:1,6mMemFLPAPrn−III)となるように蒸着レートを調節した。
1H NMR((DMSO−d6,300MHz,50℃):δ=2.10(s、6H)、6.80−7.30(m、46H)、7.70(d、J=7.2Hz、4H)、7.86(d、J=8.1Hz、2H)、8.11(s、4H)、8.28(d、J=7.8Hz、2H)
MS(ESI−MS):m/z=1198(M+H)+;C92H64N2(1196.51)
1H NMR(CDCl3,300MHz):δ=6.59(d、J=8.4Hz、4H)、6.95(d、J=8.7Hz、4H)、7.11−7.23(m、15H)、7.28−7.48(m、15H)、7.64−7.74(m、8H)、7.79(d、J=9.3Hz、2H)、7.85(d、J=7.8Hz、2H)、7.93(d、J=8.1Hz、2H)、8.09−8.16(m、4H)
MS(ESI−MS):m/z=1117(M+H)+;C86H56N2(1116.44)
102 電極
103 EL層
104 電極
111 第1の層(正孔注入層)
112 第2の層(正孔輸送層)
113 第3の層(発光層)
114 第4の層(電子輸送層)
115 第5の層(電子注入層)
401 ソース側駆動回路
402 画素部
403 ゲート側駆動回路
404 封止基板
405 シール材
407 空間
408 配線
409 FPC(フレキシブルプリントサーキット)
410 素子基板
411 スイッチング用TFT
412 電流制御用TFT
413 電極
414 絶縁物
416 EL層
417 電極
418 発光素子
423 Nチャネル型TFT
424 Pチャネル型TFT
501 基板
502 電極
503 電極
504 EL層
505 絶縁層
506 隔壁層
511 発光ユニット
512 発光ユニット
513 電荷発生層
521 電極
522 電極
611 筐体
612 支持台
613 表示部
614 スピーカー部
615 ビデオ入力端子
621 本体
622 筐体
623 表示部
624 キーボード
625 外部接続ポート
626 ポインティングデバイス
631 本体
632 筐体
633 表示部
634 音声入力部
635 音声出力部
636 操作キー
637 外部接続ポート
638 アンテナ
641 本体
642 表示部
643 筐体
644 外部接続ポート
645 リモコン受信部
646 受像部
647 バッテリー
648 音声入力部
649 操作キー
650 接眼部
2101 基板
2102 陽極
2103 正孔注入層
2104 正孔輸送層
2105 発光層
2105a 発光層
2105b 発光層
2106 電子輸送層
2107 電子注入層
2108 陰極
3000 卓上照明器具
3001 照明装置
Claims (10)
- 式(G1)で表される化合物(ただし、式(G2)で表される化合物を除く)。
(式(G1)中、R1〜R8は、それぞれ独立に、水素原子、炭素数1〜6のアルキル基、置換若しくは無置換のフェニル基、または、置換若しくは無置換のビフェニル基のいずれかを表す。また、α1〜α4は、それぞれ独立に、置換または無置換のフェニレン基を表す。また、Ar1は、環を形成する炭素数14〜18の、置換または無置換の縮合芳香族炭化水素を表す。また、Ar2は、環を形成する炭素数6〜13の、置換または無置換のアリール基(ただし、フルオレニル基を除く)を表す。また、Ar3は、炭素数1〜6のアルキル基、または、アルキル基を置換基として有する若しくは無置換の炭素数6〜12のアリール基のいずれかを表す。j、m、nは、それぞれ独立に0または1であり、pは、1または2である。)
(式(G2)中、R1〜R8は、それぞれ独立に、水素原子、炭素数1〜6のアルキル基、置換若しくは無置換のフェニル基、または、置換若しくは無置換のビフェニル基のいずれかを表す。また、R21、R23はそれぞれ独立に、水素原子または炭素数1〜6のアルキル基のいずれかを表す。また、α2〜α4は、それぞれ独立に、置換または無置換のフェニレン基を表す。また、Ar2は、環を形成する炭素数6〜13の、置換または無置換のアリール基を表す。また、Ar3は、炭素数1〜6のアルキル基、または、置換若しくは無置換の炭素数6〜12のアリール基のいずれかを表す。また、j、nは、それぞれ独立に0または1である。) - 請求項1において、
前記式(G1)中のAr1は、置換または無置換のフェナントリル基、置換または無置換のピレニル基、置換または無置換のトリフェニレニル基、置換または無置換のクリセニル基、置換または無置換のアントリル基、置換または無置換のペンタセニル基、置換または無置換のテトラセニル基のいずれか一である化合物。 - 請求項1において、
前記式(G1)中のAr1は、下記式(Ar1−1)〜(Ar1−4)で表されるいずれか一である化合物。
(式(Ar1−1)〜(Ar1−4)中、R11〜R17、及びR21〜R23はそれぞれ独立に、水素原子または炭素数1〜6のアルキル基のいずれかを表す。ただし、(Ar1−1)および(Ar1−3)の場合、前記式(G1)中のpは1であり、(Ar1−2)および(Ar1−4)の場合、前記pは2である。) - 請求項1乃至請求項3のいずれか一において、
前記α1〜α4は、それぞれ独立に、下記構造式(α−1)〜(α−3)で表されるいずれか一である化合物。
- 式(G3)で表される化合物。
(式中、R1〜R8およびR31〜R34は、それぞれ独立に、水素原子、炭素数1〜6のアルキル基、置換若しくは無置換のフェニル基、または、置換若しくは無置換のビフェニル基のいずれかを表す。また、α1〜α3は、それぞれ独立に、置換または無置換のフェニレン基を表す。また、Ar1は、環を形成する炭素数14〜18の、置換または無置換の縮合芳香族炭化水素を表す。また、Ar2は、環を形成する炭素数6〜13の、置換または無置換のアリール基(ただし、フルオレニル基を除く)を表す。また、Ar3は、炭素数1〜6のアルキル基、または、アルキル基を置換基として有する若しくは無置換の炭素数6〜12のアリール基のいずれかを表す。j、m、nは、それぞれ独立に0または1であり、pは、1または2である。) - 式(G4)で表される化合物。
(式中、R1〜R8、R31〜R34およびR41〜R45は、それぞれ独立に、水素原子、炭素数1〜6のアルキル基、置換若しくは無置換のフェニル基、または、置換若しくは無置換のビフェニル基のいずれかを表す。また、α1〜α3は、それぞれ独立に、置換または無置換のフェニレン基を表す。また、Ar1は、環を形成する炭素数14〜18の、置換または無置換の縮合芳香族炭化水素を表す。また、Ar2は、環を形成する炭素数6〜13の、置換または無置換のアリール基(ただし、フルオレニル基を除く)を表す。j、m、nは、それぞれ独立に0または1であり、pは、1または2である。) - 請求項1乃至請求項6のいずれか一において、
前記Ar2は、下記式(Ar2−1)〜(Ar2−3)で表されるいずれか一である化合物。
- 請求項1乃至請求項7のいずれか一において、
前記Ar3は、下記式(Ar3−1)〜(Ar3−8)で表されるいずれか一である化合物。
- 請求項1乃至請求項8のいずれか一において、
前記R1〜R8は、それぞれ独立に、下記式(R−1)〜(R−9)で表されるいずれか一である化合物。
- 式(124)で表される化合物。
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JP2015167232A (ja) * | 2009-10-22 | 2015-09-24 | 株式会社半導体エネルギー研究所 | 発光装置、電子機器および照明装置 |
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