JP2019112390A - 有機電界発光素子及び有機電界発光素子用含窒素化合物 - Google Patents
有機電界発光素子及び有機電界発光素子用含窒素化合物 Download PDFInfo
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- -1 nitrogen-containing compound Chemical class 0.000 title claims abstract description 135
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- 239000000126 substance Substances 0.000 claims abstract description 127
- 125000003118 aryl group Chemical group 0.000 claims abstract description 45
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 40
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 33
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- 229910052805 deuterium Inorganic materials 0.000 claims abstract description 22
- 125000004431 deuterium atom Chemical group 0.000 claims abstract description 22
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 12
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 84
- 230000005525 hole transport Effects 0.000 claims description 33
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 239000002019 doping agent Substances 0.000 claims description 18
- 125000001424 substituent group Chemical group 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 8
- 125000003277 amino group Chemical group 0.000 claims description 7
- 125000005843 halogen group Chemical group 0.000 claims description 7
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 7
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 6
- 238000007363 ring formation reaction Methods 0.000 claims description 6
- WSANLGASBHUYGD-UHFFFAOYSA-N sulfidophosphanium Chemical group S=[PH3] WSANLGASBHUYGD-UHFFFAOYSA-N 0.000 claims description 6
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 5
- 125000000707 boryl group Chemical group B* 0.000 claims description 5
- 125000005110 aryl thio group Chemical group 0.000 claims description 4
- 125000004104 aryloxy group Chemical group 0.000 claims description 4
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 4
- 150000001721 carbon Chemical class 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 102
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- 229910052757 nitrogen Inorganic materials 0.000 description 28
- 238000002347 injection Methods 0.000 description 23
- 239000007924 injection Substances 0.000 description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 19
- 230000000903 blocking effect Effects 0.000 description 14
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- 230000000052 comparative effect Effects 0.000 description 12
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- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 5
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- ZOKIJILZFXPFTO-UHFFFAOYSA-N 4-methyl-n-[4-[1-[4-(4-methyl-n-(4-methylphenyl)anilino)phenyl]cyclohexyl]phenyl]-n-(4-methylphenyl)aniline Chemical compound C1=CC(C)=CC=C1N(C=1C=CC(=CC=1)C1(CCCCC1)C=1C=CC(=CC=1)N(C=1C=CC(C)=CC=1)C=1C=CC(C)=CC=1)C1=CC=C(C)C=C1 ZOKIJILZFXPFTO-UHFFFAOYSA-N 0.000 description 4
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- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 101000837344 Homo sapiens T-cell leukemia translocation-altered gene protein Proteins 0.000 description 3
- 102100028692 T-cell leukemia translocation-altered gene protein Human genes 0.000 description 3
- 125000003342 alkenyl group Chemical group 0.000 description 3
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- VSIKJPJINIDELZ-UHFFFAOYSA-N 2,2,4,4,6,6,8,8-octakis-phenyl-1,3,5,7,2,4,6,8-tetraoxatetrasilocane Chemical compound O1[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si](C=2C=CC=CC=2)(C=2C=CC=CC=2)O[Si]1(C=1C=CC=CC=1)C1=CC=CC=C1 VSIKJPJINIDELZ-UHFFFAOYSA-N 0.000 description 1
- FUGJJMVGGAWCAU-UHFFFAOYSA-N 2,2,4,4,6,6-hexakis-phenyl-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound C1=CC=CC=C1P1(C=2C=CC=CC=2)=NP(C=2C=CC=CC=2)(C=2C=CC=CC=2)=NP(C=2C=CC=CC=2)(C=2C=CC=CC=2)=N1 FUGJJMVGGAWCAU-UHFFFAOYSA-N 0.000 description 1
- RKVIAZWOECXCCM-UHFFFAOYSA-N 2-carbazol-9-yl-n,n-diphenylaniline Chemical compound C1=CC=CC=C1N(C=1C(=CC=CC=1)N1C2=CC=CC=C2C2=CC=CC=C21)C1=CC=CC=C1 RKVIAZWOECXCCM-UHFFFAOYSA-N 0.000 description 1
- 125000006176 2-ethylbutyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(C([H])([H])*)C([H])([H])C([H])([H])[H] 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical compound CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- HNWFFTUWRIGBNM-UHFFFAOYSA-N 2-methyl-9,10-dinaphthalen-2-ylanthracene Chemical compound C1=CC=CC2=CC(C3=C4C=CC=CC4=C(C=4C=C5C=CC=CC5=CC=4)C4=CC=C(C=C43)C)=CC=C21 HNWFFTUWRIGBNM-UHFFFAOYSA-N 0.000 description 1
- XSUNFLLNZQIJJG-UHFFFAOYSA-N 2-n-naphthalen-2-yl-1-n,1-n,2-n-triphenylbenzene-1,2-diamine Chemical compound C1=CC=CC=C1N(C=1C(=CC=CC=1)N(C=1C=CC=CC=1)C=1C=C2C=CC=CC2=CC=1)C1=CC=CC=C1 XSUNFLLNZQIJJG-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DWYHDSLIWMUSOO-UHFFFAOYSA-N 2-phenyl-1h-benzimidazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2N1 DWYHDSLIWMUSOO-UHFFFAOYSA-N 0.000 description 1
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- CINYXYWQPZSTOT-UHFFFAOYSA-N 3-[3-[3,5-bis(3-pyridin-3-ylphenyl)phenyl]phenyl]pyridine Chemical compound C1=CN=CC(C=2C=C(C=CC=2)C=2C=C(C=C(C=2)C=2C=C(C=CC=2)C=2C=NC=CC=2)C=2C=C(C=CC=2)C=2C=NC=CC=2)=C1 CINYXYWQPZSTOT-UHFFFAOYSA-N 0.000 description 1
- 125000005917 3-methylpentyl group Chemical group 0.000 description 1
- 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 1
- 125000004920 4-methyl-2-pentyl group Chemical group CC(CC(C)*)C 0.000 description 1
- DIVZFUBWFAOMCW-UHFFFAOYSA-N 4-n-(3-methylphenyl)-1-n,1-n-bis[4-(n-(3-methylphenyl)anilino)phenyl]-4-n-phenylbenzene-1,4-diamine Chemical compound CC1=CC=CC(N(C=2C=CC=CC=2)C=2C=CC(=CC=2)N(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C=C(C)C=CC=2)=C1 DIVZFUBWFAOMCW-UHFFFAOYSA-N 0.000 description 1
- AOQKGYRILLEVJV-UHFFFAOYSA-N 4-naphthalen-1-yl-3,5-diphenyl-1,2,4-triazole Chemical compound C1=CC=CC=C1C(N1C=2C3=CC=CC=C3C=CC=2)=NN=C1C1=CC=CC=C1 AOQKGYRILLEVJV-UHFFFAOYSA-N 0.000 description 1
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- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- YDCSZPYCVCHNNH-UHFFFAOYSA-N ClC1=C(C=CC=C1)C1=NN=C(S1)C1=CC=CC=C1 Chemical compound ClC1=C(C=CC=C1)C1=NN=C(S1)C1=CC=CC=C1 YDCSZPYCVCHNNH-UHFFFAOYSA-N 0.000 description 1
- 229910052693 Europium Inorganic materials 0.000 description 1
- 229910018068 Li 2 O Inorganic materials 0.000 description 1
- NUGPIZCTELGDOS-QHCPKHFHSA-N N-[(1S)-3-[4-(3-methyl-5-propan-2-yl-1,2,4-triazol-4-yl)piperidin-1-yl]-1-pyridin-3-ylpropyl]cyclopentanecarboxamide Chemical compound C(C)(C)C1=NN=C(N1C1CCN(CC1)CC[C@@H](C=1C=NC=CC=1)NC(=O)C1CCCC1)C NUGPIZCTELGDOS-QHCPKHFHSA-N 0.000 description 1
- YXLXNENXOJSQEI-UHFFFAOYSA-L Oxine-copper Chemical compound [Cu+2].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 YXLXNENXOJSQEI-UHFFFAOYSA-L 0.000 description 1
- 239000004696 Poly ether ether ketone Substances 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910052771 Terbium Inorganic materials 0.000 description 1
- 229910052775 Thulium Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- WGCXSIWGFOQDEG-UHFFFAOYSA-N [Zn].[Sn].[In] Chemical compound [Zn].[Sn].[In] WGCXSIWGFOQDEG-UHFFFAOYSA-N 0.000 description 1
- WDJHALXBUFZDSR-UHFFFAOYSA-M acetoacetate Chemical compound CC(=O)CC([O-])=O WDJHALXBUFZDSR-UHFFFAOYSA-M 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
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- 150000001338 aliphatic hydrocarbons Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
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- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
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- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 125000002676 chrysenyl group Chemical group C1(=CC=CC=2C3=CC=C4C=CC=CC4=C3C=CC12)* 0.000 description 1
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- 125000004122 cyclic group Chemical group 0.000 description 1
- 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 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
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- CXPOFJRHCFPDRI-UHFFFAOYSA-N dodecylbenzene;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1 CXPOFJRHCFPDRI-UHFFFAOYSA-N 0.000 description 1
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- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
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- 125000002883 imidazolyl group Chemical group 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
- AOZVYCYMTUWJHJ-UHFFFAOYSA-K iridium(3+) pyridine-2-carboxylate Chemical compound [Ir+3].[O-]C(=O)C1=CC=CC=N1.[O-]C(=O)C1=CC=CC=N1.[O-]C(=O)C1=CC=CC=N1 AOZVYCYMTUWJHJ-UHFFFAOYSA-K 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
- 125000000842 isoxazolyl group Chemical group 0.000 description 1
- FZLIPJUXYLNCLC-UHFFFAOYSA-N lanthanum atom Chemical group [La] FZLIPJUXYLNCLC-UHFFFAOYSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 description 1
- 229910000476 molybdenum oxide Inorganic materials 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 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 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 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 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000005184 naphthylamino group Chemical group C1(=CC=CC2=CC=CC=C12)N* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 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 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 125000000962 organic group Chemical group 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 description 1
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 1
- 125000004625 phenanthrolinyl group Chemical group N1=C(C=CC2=CC=C3C=CC=NC3=C12)* 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 description 1
- XPPWLXNXHSNMKC-UHFFFAOYSA-N phenylboron Chemical group [B]C1=CC=CC=C1 XPPWLXNXHSNMKC-UHFFFAOYSA-N 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229920001088 polycarbazole Chemical class 0.000 description 1
- 229920002530 polyetherether ketone Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 125000001725 pyrenyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- VSZWPYCFIRKVQL-UHFFFAOYSA-N selanylidenegallium;selenium Chemical compound [Se].[Se]=[Ga].[Se]=[Ga] VSZWPYCFIRKVQL-UHFFFAOYSA-N 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 125000003107 substituted aryl group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- GZCRRIHWUXGPOV-UHFFFAOYSA-N terbium atom Chemical compound [Tb] GZCRRIHWUXGPOV-UHFFFAOYSA-N 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
- JLBRGNFGBDNNSF-UHFFFAOYSA-N tert-butyl(dimethyl)borane Chemical group CB(C)C(C)(C)C JLBRGNFGBDNNSF-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000001931 thermography Methods 0.000 description 1
- 150000004867 thiadiazoles Chemical group 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- FRNOGLGSGLTDKL-UHFFFAOYSA-N thulium atom Chemical compound [Tm] FRNOGLGSGLTDKL-UHFFFAOYSA-N 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- LALRXNPLTWZJIJ-UHFFFAOYSA-N triethylborane Chemical group CCB(CC)CC LALRXNPLTWZJIJ-UHFFFAOYSA-N 0.000 description 1
- WXRGABKACDFXMG-UHFFFAOYSA-N trimethylborane Chemical group CB(C)C WXRGABKACDFXMG-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- MXSVLWZRHLXFKH-UHFFFAOYSA-N triphenylborane Chemical group C1=CC=CC=C1B(C=1C=CC=CC=1)C1=CC=CC=C1 MXSVLWZRHLXFKH-UHFFFAOYSA-N 0.000 description 1
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 description 1
- ZQTYRTSKQFQYPQ-UHFFFAOYSA-N trisiloxane Chemical compound [SiH3]O[SiH2]O[SiH3] ZQTYRTSKQFQYPQ-UHFFFAOYSA-N 0.000 description 1
- 229910001930 tungsten oxide Inorganic materials 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
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
-
- 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
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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Abstract
Description
化学式1において、Q1は、NAr1、OまたはSであり、Ar1は水素原子、重水素原子、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、R1及びR2は、それぞれ独立して水素原子、重水素原子、ハロゲン原子、置換若しくは無置換のアミノ基、置換若しくは無置換のシリル基、置換若しくは無置換のボリル基、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の炭素数6以上30以下のアラルキル基、置換若しくは無置換の炭素数1以上10以下のハロアルキル基、置換若しくは無置換の炭素数6以上30以下のアリールオキシ基、置換若しくは無置換の炭素数6以上30以下のアリールチオ基、置換若しくは無置換のホスフィンオキシ基、置換若しくは無置換のホスフィンスルフィド基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と互いに結合して環を形成してもよい。a及びbはそれぞれ独立して0以上4以下の整数であり、nは0または1であり、M1及びM2はそれぞれ独立して下記化学式2または化学式3で表される。
化学式2及び化学式3において、X1〜X6は、それぞれ独立してCR3またはNであり、X1〜X4のうち少なくとも一つはNである。R3は、水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と互いに結合して環を形成してもよい。Wは、O、NAr3、またはCAr4Ar5である。Ar2〜Ar5はそれぞれ独立して水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の炭素数6以上30以下のアラルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と結合して環を形成してもよい。
化学式2−1〜化学式2−3において、X1及びX2は、それぞれ独立してCR3またはNであり、X1及びX2のうち少なくとも一つはNであり、X7〜X10は、それぞれ独立してCR6またはNであり、X7〜X10のうち少なくとも一つはNであり、R3〜R6は、それぞれ独立して水素原子、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。
化学式3−1、化学式3−3及び化学式3−4において、Ar2及びAr5は、それぞれ独立して置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。
化学式1−1及び化学式1−2において、Q1、R1、R2、M1、M2、n、a、及びbは上述したとおりである。aは0であってもよい。
化学式1−3において、Q1、R1、R2、a、及びbは上記のとおりであり、Q2はNAr1、OまたはSであり、Q2及びQ1は互いに同じであってもよく、或は異なっていてもよく、R7は水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、cは0以上5以下の整数であり、M3は下記化学式4で表される。
化学式4において、X11はC=O、またはCR8であり、R8は水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。bは0または1であってもよいが、bが1であれば、R2はM1と同じであってもよい。
本発明の一実施形態に係る含窒素化合物は、例えば、下記のように合成してもよい。但し、本発明の一実施形態に係る含窒素化合物の合成方法はこれらに限らない。
本発明の一実施形態に係る含窒素化合物である化合物1は、例えば、下記反応によって合成されてもよい。
本発明の一実施形態に係る含窒素化合物である化合物7は、例えば、下記反応によって合成されてもよい。
本発明の一実施形態に係る含窒素化合物である化合物9は、例えば、下記反応によって合成されてもよい。
本発明の一実施形態に係る含窒素化合物である化合物12は、例えば、下記反応によって合成されてもよい。
本発明の一実施形態に係る含窒素化合物である化合物21は、例えば、下記反応によって合成されてもよい。
上述した化合物1、7、9、12及び21を発光層のホスト材料として使用し、実施例1〜5の有機電界発光素子を製作した。
[実施例化合物]
[比較例化合物]
Claims (10)
- 下記化学式1で表される含窒素環化合物。
Q1はNAr1、OまたはSであり、
Ar1は水素原子、重水素原子、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、
R1及びR2はそれぞれ独立して水素原子、重水素原子、ハロゲン原子、置換若しくは無置換のアミノ基、置換若しくは無置換のシリル基、置換若しくは無置換のボリル基、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の炭素数6以上30以下のアラルキル基、置換若しくは無置換の炭素数1以上10以下のハロアルキル基、置換若しくは無置換の炭素数6以上30以下のアリールオキシ基、置換若しくは無置換の炭素数6以上30以下のアリールチオ基、置換若しくは無置換のホスフィンオキシ基、置換若しくは無置換のホスフィンスルフィド基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と互いに結合して環を形成するか、または形成せず、
a及びbはそれぞれ独立して0以上4以下の整数であり、
nは0または1であり、
M1及びM2はそれぞれ独立して下記化学式2または3で表され、
前記化学式2及び3において、
X1〜X6はそれぞれ独立してCR3またはNであり、
X1〜X4のうち少なくとも一つはNであり、
R3は水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と互いに結合して環を形成するか、または形成せず、
WはO、NAr3、またはCAr4Ar5であり、
Ar2〜Ar5はそれぞれ独立して水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の炭素数6以上30以下のアラルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、隣接する基と結合して環を形成するか、または形成しない。) - 前記化学式2は、下記化学式2−1〜化学式2−3のうちいずれか一つで表される、請求項1に記載の含窒素化合物。
X1及びX2はそれぞれ独立してCR3またはNであり、
X1及びX2のうち少なくとも一つはNであり、
X7〜X10はそれぞれ独立してCR6またはNであり、
X7〜X10のうち少なくとも一つはNであり、
R3〜R6はそれぞれ独立して水素原子、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。) - 前記化学式3は、下記化学式3−1〜化学式3−4のうちいずれか一つで表される、請求項1に記載の含窒素化合物。
Ar2〜Ar5はそれぞれ独立して置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。) - 前記化学式1は、下記化学式1−1及び化学式1−2のうちいずれか一つで表される、請求項1に記載の含窒素化合物。
- 前記化学式1は、下記化学式1−3で表される、請求項1に記載の含窒素化合物。
Q2は、NAr1、OまたはSであり、
Q2及びQ1は互いに同じであるか、異なっており、
R7は水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基であり、
cは0以上5以下の整数であり、
M3は下記化学式4で表され、
前記化学式4において、
X11はC=O、またはCR8であり、
R8は水素原子、重水素原子、置換若しくは無置換の炭素数1以上10以下のアルキル基、置換若しくは無置換の環形成炭素数6以上30以下のアリール基、または置換若しくは無置換の環形成炭素数2以上30以下のヘテロアリール基である。) - 最低三重項エネルギー準位が3.0eV以上である、請求項1に記載の含窒素化合物。
- 前記化学式1で表される含窒素化合物は、下記第1化合物群に示した化合物のうちから選択されるいずれか一つである請求項1に記載の含窒素環化合物。
- 第1電極と、
前記第1電極の上に設けられた正孔輸送領域と、
前記正孔輸送領域の上に設けられ、請求項1乃至請求項7のうちいずれか一項に記載の含窒素化合物を含む発光層と、
前記発光層の上に設けられた電子輸送領域と、
前記電子輸送領域の上に設けられた第2電極と、を含む有機電界発光素子。 - 前記発光層は、ホスト及びドーパントを含み、
前記ホストは、前記含窒素化合物を含む、請求項8に記載の有機電界発光素子。 - 前記ドーパントは、りん光ドーパントである、請求項9に記載の有機電界発光素子。
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005000903A1 (de) * | 2005-01-05 | 2006-07-20 | Sensient Imaging Technologies Gmbh | Neue 3,4,5-substituierte 1,2,4-Triazolderivate und sie enthaltende organische elektrolumineszente Vorrichtungen |
KR20150037133A (ko) * | 2013-09-30 | 2015-04-08 | (주)피엔에이치테크 | 새로운 유기전계발광소자용 화합물 및 그를 포함하는 유기전계발광소자 |
US20150243902A1 (en) * | 2014-02-25 | 2015-08-27 | Industrial Technology Research Institute | Carbazole derivative and organic electroluminescent device |
US20170162794A1 (en) * | 2015-12-04 | 2017-06-08 | Yuan Ze University | Organic electroluminescent materials containing n-phenylcarboline and organic electroluminescent device by using the same |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0548680T3 (da) | 1991-12-26 | 1998-09-23 | Mitsubishi Chem Corp | Beta-oxo-beta-benzenpropanthioamidderivater |
JPH08176148A (ja) | 1994-12-27 | 1996-07-09 | Chisso Corp | ヘテロ環を有するオキサジアゾール誘導体 |
PT1070708E (pt) | 1999-07-21 | 2004-05-31 | Hoffmann La Roche | Derivados de triazol |
FR2812633A1 (fr) | 2000-08-04 | 2002-02-08 | Aventis Cropscience Sa | Derives de phenyl(thio)urees et phenyl(thio)carbamates fongicides |
TWI239333B (en) | 2000-11-16 | 2005-09-11 | Hoffmann La Roche | Benzodiazepine derivatives as GABA A receptor modulators |
MY151199A (en) | 2001-11-02 | 2014-04-30 | Rigel Pharmaceuticals Inc | Substituted diphenyl heterocycles useful for treating hcv infection |
AR044503A1 (es) | 2003-03-18 | 2005-09-14 | Merck & Co Inc | Triazoles sustituidos con biarilo como bloqueantes del canal de sodio |
US7220745B2 (en) | 2003-05-15 | 2007-05-22 | Rigel Pharmaceuticals | Heterocyclic compounds useful to treat HCV |
JP2005225819A (ja) | 2004-02-13 | 2005-08-25 | Orient Chem Ind Ltd | ピロール環を有するアゾール化合物およびその製造方法 |
US7714099B2 (en) | 2004-10-15 | 2010-05-11 | Hitachi Chemical Co., Ltd. | Luminescent compositions and their uses |
CN101208088A (zh) | 2005-06-02 | 2008-06-25 | 拜尔农作物科学股份公司 | 苯基烷基取代的杂芳基衍生物 |
CN101333438B (zh) | 2008-07-15 | 2011-11-30 | 武汉大学 | 一种具有双极载流子传输性能的材料及其应用 |
US7994171B2 (en) | 2008-09-11 | 2011-08-09 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
US8048887B2 (en) | 2008-09-11 | 2011-11-01 | Bristol-Myers Squibb Company | Compounds for the treatment of hepatitis C |
JP2012051807A (ja) | 2009-02-26 | 2012-03-15 | Eisai R & D Management Co Ltd | アリールイミダゾール化合物 |
CA2763589A1 (en) | 2009-05-28 | 2010-12-02 | President And Fellows Of Harvard College | N,n'-diarylurea compounds and n,n'-diarylthiourea compounds as inhibitors of translation initiation |
US9359389B2 (en) | 2009-10-26 | 2016-06-07 | Research Foundation Of The City University Of New York | Caged ceramide-1-phosphate derivatives |
JP2013522192A (ja) | 2010-03-11 | 2013-06-13 | ブリストル−マイヤーズ スクイブ カンパニー | C型肝炎の処置のための化合物 |
KR101256205B1 (ko) | 2010-09-30 | 2013-04-19 | (주)씨에스엘쏠라 | 유기발광화합물 및 이를 구비한 유기발광소자 |
CN102709483A (zh) | 2012-06-26 | 2012-10-03 | 吉林大学 | 一种单层白光有机电致发光器件 |
KR20140125117A (ko) | 2013-04-18 | 2014-10-28 | 한국화학연구원 | 카르바닐리드 유도체를 유효성분으로 포함하는 이상증식혈관 질환의 예방 또는 치료용 조성물 |
WO2015038778A1 (en) | 2013-09-11 | 2015-03-19 | The Brigham And Women's Hospital, Inc. | SUBSTITUTED UREA EIF2α KINASE ACTIVATORS |
CA2956417C (en) | 2014-07-31 | 2022-09-13 | Inserm (Institut National De La Sante Et De La Recherche Medicale) | Flt3 receptor antagonists |
KR20160034528A (ko) * | 2014-09-19 | 2016-03-30 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
WO2016116485A1 (de) | 2015-01-20 | 2016-07-28 | Cynora Gmbh | Azole zur verwendung in optoelektronischen bauelementen |
EP3256461B1 (en) | 2015-02-13 | 2023-09-13 | Azienda Ospedaliera Universitaria Senese | Urea and sulfonamide derivatives as human helicase ddx3 inhibitors useful in the treatment of viral diseases |
GB201507340D0 (en) | 2015-04-29 | 2015-06-10 | Univ St Andrews | Light emitting devices and compounds |
-
2017
- 2017-12-22 KR KR1020170178632A patent/KR102512548B1/ko active IP Right Grant
-
2018
- 2018-09-12 US US16/129,666 patent/US10818850B2/en active Active
- 2018-12-07 EP EP18211134.4A patent/EP3502104B1/en active Active
- 2018-12-10 JP JP2018231111A patent/JP7267722B2/ja active Active
- 2018-12-20 CN CN201811561616.0A patent/CN109956910A/zh active Pending
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102005000903A1 (de) * | 2005-01-05 | 2006-07-20 | Sensient Imaging Technologies Gmbh | Neue 3,4,5-substituierte 1,2,4-Triazolderivate und sie enthaltende organische elektrolumineszente Vorrichtungen |
KR20150037133A (ko) * | 2013-09-30 | 2015-04-08 | (주)피엔에이치테크 | 새로운 유기전계발광소자용 화합물 및 그를 포함하는 유기전계발광소자 |
US20150243902A1 (en) * | 2014-02-25 | 2015-08-27 | Industrial Technology Research Institute | Carbazole derivative and organic electroluminescent device |
US20170162794A1 (en) * | 2015-12-04 | 2017-06-08 | Yuan Ze University | Organic electroluminescent materials containing n-phenylcarboline and organic electroluminescent device by using the same |
Non-Patent Citations (2)
Title |
---|
DATABASE REGISTRY, JPN7022004443, 2008, ISSN: 0004876537 * |
DATABASE REGISTRY, JPN7022004444, 2002, ISSN: 0004876538 * |
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