US20220356193A1 - Plurality of host materials and organic electroluminescent device comprising the same - Google Patents
Plurality of host materials and organic electroluminescent device comprising the same Download PDFInfo
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- US20220356193A1 US20220356193A1 US17/214,253 US202117214253A US2022356193A1 US 20220356193 A1 US20220356193 A1 US 20220356193A1 US 202117214253 A US202117214253 A US 202117214253A US 2022356193 A1 US2022356193 A1 US 2022356193A1
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- 239000000463 material Substances 0.000 title claims abstract description 98
- 150000001875 compounds Chemical class 0.000 claims abstract description 138
- -1 benzoquinazolinyl Chemical group 0.000 claims description 350
- 125000003118 aryl group Chemical group 0.000 claims description 73
- 125000001072 heteroaryl group Chemical group 0.000 claims description 72
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 claims description 54
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 43
- 229910052805 deuterium Inorganic materials 0.000 claims description 43
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 41
- 229910052739 hydrogen Inorganic materials 0.000 claims description 34
- 239000001257 hydrogen Substances 0.000 claims description 34
- 125000001424 substituent group Chemical group 0.000 claims description 31
- 150000002431 hydrogen Chemical class 0.000 claims description 30
- 125000005104 aryl silyl group Chemical group 0.000 claims description 29
- 229910052736 halogen Inorganic materials 0.000 claims description 23
- 150000002367 halogens Chemical class 0.000 claims description 23
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 22
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 20
- 125000005549 heteroarylene group Chemical group 0.000 claims description 18
- 125000001769 aryl amino group Chemical group 0.000 claims description 17
- 125000000732 arylene group Chemical group 0.000 claims description 17
- 125000004432 carbon atom Chemical group C* 0.000 claims description 14
- 125000001624 naphthyl group Chemical group 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 229910052760 oxygen Inorganic materials 0.000 claims description 13
- 229910052717 sulfur Chemical group 0.000 claims description 13
- 125000003545 alkoxy group Chemical group 0.000 claims description 11
- 125000000739 C2-C30 alkenyl group Chemical group 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 10
- 125000006822 tri(C1-C30) alkylsilyl group Chemical group 0.000 claims description 9
- 125000005241 heteroarylamino group Chemical group 0.000 claims description 8
- 125000004306 triazinyl group Chemical group 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 7
- 125000004076 pyridyl group Chemical group 0.000 claims description 7
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims description 7
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 claims description 7
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 6
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical group C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000000304 alkynyl group Chemical group 0.000 claims description 5
- 125000002993 cycloalkylene group Chemical group 0.000 claims description 5
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical group C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 5
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 5
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 claims description 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 4
- 125000006323 alkenyl amino group Chemical group 0.000 claims description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 239000001301 oxygen Chemical group 0.000 claims description 4
- 239000011593 sulfur Chemical group 0.000 claims description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000003282 alkyl amino group Chemical group 0.000 claims description 3
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical group C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 claims description 3
- 125000005956 isoquinolyl group Chemical group 0.000 claims description 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 3
- 125000005493 quinolyl group Chemical group 0.000 claims description 3
- 125000001425 triazolyl group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 2
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 125000005107 alkyl diaryl silyl group Chemical group 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 2
- 125000005110 aryl thio group Chemical group 0.000 claims description 2
- 125000004104 aryloxy group Chemical group 0.000 claims description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 2
- 125000005105 dialkylarylsilyl group Chemical group 0.000 claims description 2
- 125000005843 halogen group Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 2
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 2
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 2
- 125000005717 substituted cycloalkylene group Chemical group 0.000 claims description 2
- 125000004665 trialkylsilyl group Chemical group 0.000 claims description 2
- 125000005106 triarylsilyl group Chemical group 0.000 claims description 2
- 150000003233 pyrroles Chemical group 0.000 claims 1
- 239000010410 layer Substances 0.000 description 93
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 36
- 238000006243 chemical reaction Methods 0.000 description 34
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 238000002347 injection Methods 0.000 description 25
- 239000007924 injection Substances 0.000 description 25
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 22
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 17
- 238000004440 column chromatography Methods 0.000 description 16
- 239000012044 organic layer Substances 0.000 description 16
- 239000002019 doping agent Substances 0.000 description 15
- 230000000903 blocking effect Effects 0.000 description 14
- 230000005525 hole transport Effects 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical group C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 12
- 235000010290 biphenyl Nutrition 0.000 description 11
- 239000004305 biphenyl Substances 0.000 description 11
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 10
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 10
- 235000019341 magnesium sulphate Nutrition 0.000 description 10
- 238000000034 method Methods 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- 239000011541 reaction mixture Substances 0.000 description 10
- 125000005509 dibenzothiophenyl group Chemical group 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- 238000010992 reflux Methods 0.000 description 9
- 238000007740 vapor deposition Methods 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000012153 distilled water Substances 0.000 description 8
- 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 8
- 239000002904 solvent Substances 0.000 description 8
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 7
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 7
- 0 C.C1=NC=NCC1.CCC(C)(C)C.CCC(C)(C)C.[20*]C.[21*]C.c1ccc2c(c1)Cc1cncnc1-2 Chemical compound C.C1=NC=NCC1.CCC(C)(C)C.CCC(C)(C)C.[20*]C.[21*]C.c1ccc2c(c1)Cc1cncnc1-2 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- SAHIZENKTPRYSN-UHFFFAOYSA-N [2-[3-(phenoxymethyl)phenoxy]-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound O(C1=CC=CC=C1)CC=1C=C(OC2=NC(=CC(=C2)CN)C(F)(F)F)C=CC=1 SAHIZENKTPRYSN-UHFFFAOYSA-N 0.000 description 6
- 125000004429 atom Chemical group 0.000 description 6
- 239000000872 buffer Substances 0.000 description 6
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 6
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 6
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 6
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 description 5
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 5
- 229940126062 Compound A Drugs 0.000 description 5
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 125000002950 monocyclic group Chemical group 0.000 description 5
- 229940078552 o-xylene Drugs 0.000 description 5
- 230000002829 reductive effect Effects 0.000 description 5
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 5
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
- 150000001555 benzenes Chemical class 0.000 description 4
- 229910052796 boron Inorganic materials 0.000 description 4
- 229910000024 caesium carbonate Inorganic materials 0.000 description 4
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- VNFWTIYUKDMAOP-UHFFFAOYSA-N sphos Chemical compound COC1=CC=CC(OC)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 VNFWTIYUKDMAOP-UHFFFAOYSA-N 0.000 description 4
- 239000000758 substrate Substances 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 3
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- ZEEBGORNQSEQBE-UHFFFAOYSA-N [2-(3-phenylphenoxy)-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound C1(=CC(=CC=C1)OC1=NC(=CC(=C1)CN)C(F)(F)F)C1=CC=CC=C1 ZEEBGORNQSEQBE-UHFFFAOYSA-N 0.000 description 3
- ABRVLXLNVJHDRQ-UHFFFAOYSA-N [2-pyridin-3-yl-6-(trifluoromethyl)pyridin-4-yl]methanamine Chemical compound FC(C1=CC(=CC(=N1)C=1C=NC=CC=1)CN)(F)F ABRVLXLNVJHDRQ-UHFFFAOYSA-N 0.000 description 3
- 229940117389 dichlorobenzene Drugs 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 229910052741 iridium Inorganic materials 0.000 description 3
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 3
- 229910000027 potassium carbonate Inorganic materials 0.000 description 3
- 125000000168 pyrrolyl group Chemical group 0.000 description 3
- 125000003003 spiro group Chemical group 0.000 description 3
- 238000006467 substitution reaction Methods 0.000 description 3
- 125000001935 tetracenyl group Chemical group C1(=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C12)* 0.000 description 3
- 125000003960 triphenylenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C3=CC=CC=C3C12)* 0.000 description 3
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 3
- 125000006736 (C6-C20) aryl group Chemical group 0.000 description 2
- IANQTJSKSUMEQM-UHFFFAOYSA-N 1-benzofuran Chemical group C1=CC=C2OC=CC2=C1 IANQTJSKSUMEQM-UHFFFAOYSA-N 0.000 description 2
- KPGPIQKEKAEAHM-UHFFFAOYSA-N 2-chloro-3-phenylquinoxaline Chemical compound ClC1=NC2=CC=CC=C2N=C1C1=CC=CC=C1 KPGPIQKEKAEAHM-UHFFFAOYSA-N 0.000 description 2
- AYJJTPLDSZAGGA-UHFFFAOYSA-N 2-ethyl-7-methyl-5-(4-methylphenyl)-1,3,4,4a,5,9b-hexahydroindeno[1,2-c]pyridine Chemical compound C1N(CC)CCC2C1C1=CC=C(C)C=C1C2C1=CC=C(C)C=C1 AYJJTPLDSZAGGA-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- WNHQHXQXDBZKIB-UHFFFAOYSA-N B.BB.BB(B)B.BB(B)B(B)B.BBB.BBB(B)B.BBB(B)B(B)B.C1CCCC2C[Y]CC2CC1 Chemical compound B.BB.BB(B)B.BB(B)B(B)B.BBB.BBB(B)B.BBB(B)B(B)B.C1CCCC2C[Y]CC2CC1 WNHQHXQXDBZKIB-UHFFFAOYSA-N 0.000 description 2
- RZTRONOPJZFEAD-UHFFFAOYSA-N CC(C)(C)c1cc(-c2ccccc2)cc(-c2ccccc2)c1.CC(C)(C)c1cc2ccccc2cc1-c1ccccc1.CC(C)(C)c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1ccc(-c2ccccc2)cc1.CC(C)(C)c1ccc(-c2ccccc2)cc1-c1ccccc1.CC(C)(C)c1ccc(-c2ccccc2-c2ccccc2)cc1.CC(C)(C)c1ccc2c(ccc3ccccc32)c1.CC(C)(C)c1cccc(-c2ccccc2)c1.CC(C)(C)c1cccc(-c2ccccc2-c2ccccc2)c1.CC(C)(C)c1ccccc1.CC(C)(C)c1ccccc1-c1ccccc1 Chemical compound CC(C)(C)c1cc(-c2ccccc2)cc(-c2ccccc2)c1.CC(C)(C)c1cc2ccccc2cc1-c1ccccc1.CC(C)(C)c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1ccc(-c2ccccc2)cc1.CC(C)(C)c1ccc(-c2ccccc2)cc1-c1ccccc1.CC(C)(C)c1ccc(-c2ccccc2-c2ccccc2)cc1.CC(C)(C)c1ccc2c(ccc3ccccc32)c1.CC(C)(C)c1cccc(-c2ccccc2)c1.CC(C)(C)c1cccc(-c2ccccc2-c2ccccc2)c1.CC(C)(C)c1ccccc1.CC(C)(C)c1ccccc1-c1ccccc1 RZTRONOPJZFEAD-UHFFFAOYSA-N 0.000 description 2
- QHWAGVJWBVKIQP-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccccc2)c2ccccc2n1.CC(C)(C)c1nc2c(ccc3ccccc32)nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2c(ccc3ccccc32)nc1-c1ccccc1.CC(C)(C)c1nc2c3ccccc3c3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1cccc(-c2ccccc2)c1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccccc2)c2ccccc2n1.CC(C)(C)c1nc2c(ccc3ccccc32)nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2c(ccc3ccccc32)nc1-c1ccccc1.CC(C)(C)c1nc2c3ccccc3c3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1cccc(-c2ccccc2)c1 QHWAGVJWBVKIQP-UHFFFAOYSA-N 0.000 description 2
- FZCAWKWASMJENI-LXCONJKVSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1ccc(N(c2ccccc2)c2ccccc2)cc1.c1ccc(N(c2ccccc2)c2ccc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)cc2)cc1.c1ccc(N(c2ccccc2)c2ccc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)cc2)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1ccc(N(c2ccccc2)c2ccccc2)cc1.c1ccc(N(c2ccccc2)c2ccc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)cc2)cc1.c1ccc(N(c2ccccc2)c2ccc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)cc2)cc1 FZCAWKWASMJENI-LXCONJKVSA-N 0.000 description 2
- JHNPWASLUSITNB-FAQUWRFOSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1nc(-c4ccccc4)nc(-c4ccccc4)n1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1nc(-c4ccccc4)nc(-c4ccccc4)n1)c23 JHNPWASLUSITNB-FAQUWRFOSA-N 0.000 description 2
- BWKJAOVWJZPNJJ-BPBSCXAYSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc(N(c4ccccc4)c4ccccc4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccccc4)n1)c23.[2H]c1c([2H])c([2H])c(-c2nc(-c3c([2H])c([2H])c([2H])c([2H])c3[2H])nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(ccc3c6c54)C7(C)C)n2)c([2H])c1[2H] Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc(N(c4ccccc4)c4ccccc4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccccc4)n1)c23.[2H]c1c([2H])c([2H])c(-c2nc(-c3c([2H])c([2H])c([2H])c([2H])c3[2H])nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(ccc3c6c54)C7(C)C)n2)c([2H])c1[2H] BWKJAOVWJZPNJJ-BPBSCXAYSA-N 0.000 description 2
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- COFKIXILDQTVKK-UBUOTJTFSA-L CC(C)(C)c1ccc2-c3ccccc3[Ir]3(c4ccc(-c5ccccc5)cc4-c4ccc(C(C)(C)C)cn->34)<-n2c1.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(C)ccc3n->21.Cc1cc(C)cc(-c2ccn3->[Ir]4(O/C(=C\C(CC(C)C)=O->4)CC(C)C)c4ccccc4-c3c2)c1.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c3c2)c2ccccc2-c2ccc(C)cn->42)cc1.Cc1ccc2-c3ccccc3[Ir]3(c4cc5oc6ccccc6c5cc4-c4ccccn->34)<-n2c1 Chemical compound CC(C)(C)c1ccc2-c3ccccc3[Ir]3(c4ccc(-c5ccccc5)cc4-c4ccc(C(C)(C)C)cn->34)<-n2c1.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(C)ccc3n->21.Cc1cc(C)cc(-c2ccn3->[Ir]4(O/C(=C\C(CC(C)C)=O->4)CC(C)C)c4ccccc4-c3c2)c1.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c3c2)c2ccccc2-c2ccc(C)cn->42)cc1.Cc1ccc2-c3ccccc3[Ir]3(c4cc5oc6ccccc6c5cc4-c4ccccn->34)<-n2c1 COFKIXILDQTVKK-UBUOTJTFSA-L 0.000 description 1
- FQKGXPLZPBCCQE-PVAXDIORSA-M CC(C)(C)c1ccc2-c3ccccc3[Ir]3(c4ccc5c(oc6ccccc65)c4-c4ccccn->34)<-n2c1.CC(C)(C)c1ccn2->[Ir]3(c4ccccc4-c2c1)c1ccc2c(oc4ccccc42)c1-c1ccccn->31.CC(C)Cc1cccc2c1oc1c3-c4ccccn4->[Ir]4(c5ccccc5-c5ccc(C(C)(C)C)cn->45)c3ccc12.CC(C)Cc1cccc2c1oc1c3-c4ccccn4->[Ir]4(c5ccccc5-c5ccccn->45)c3ccc12.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cc(C)cc(C)c3)ccn->21 Chemical compound CC(C)(C)c1ccc2-c3ccccc3[Ir]3(c4ccc5c(oc6ccccc65)c4-c4ccccn->34)<-n2c1.CC(C)(C)c1ccn2->[Ir]3(c4ccccc4-c2c1)c1ccc2c(oc4ccccc42)c1-c1ccccn->31.CC(C)Cc1cccc2c1oc1c3-c4ccccn4->[Ir]4(c5ccccc5-c5ccc(C(C)(C)C)cn->45)c3ccc12.CC(C)Cc1cccc2c1oc1c3-c4ccccn4->[Ir]4(c5ccccc5-c5ccccn->45)c3ccc12.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cc(C)cc(C)c3)ccn->21 FQKGXPLZPBCCQE-PVAXDIORSA-M 0.000 description 1
- HGLHUHROGVOFEH-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1ccc2c(c1)-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1ccc2c(c1)oc1c3ccccc3ccc21.CC(C)(C)c1cccc2c1-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1cccc2c1-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1cccc2c1oc1c3ccccc3ccc21 Chemical compound CC(C)(C)c1ccc2c(c1)-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1ccc2c(c1)-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1ccc2c(c1)oc1c3ccccc3ccc21.CC(C)(C)c1cccc2c1-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1cccc2c1-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1cccc2c1oc1c3ccccc3ccc21 HGLHUHROGVOFEH-UHFFFAOYSA-N 0.000 description 1
- YORQRLFNIUPNQT-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1ccc2c(c1)sc1ccccc12.CC(C)(C)c1ccc2sc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1cccc2c1sc1ccccc12.CC(C)(C)c1cccc2sc3ccccc3c12.Cn1c2ccccc2c2c(C(C)(C)C)cccc21.Cn1c2ccccc2c2cc(C(C)(C)C)ccc21.Cn1c2ccccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccccc2c2cccc(C(C)(C)C)c21 Chemical compound CC(C)(C)c1ccc2c(c1)-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1ccc2c(c1)sc1ccccc12.CC(C)(C)c1ccc2sc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1c(ccc3ccccc13)C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1cccc2c1sc1ccccc12.CC(C)(C)c1cccc2sc3ccccc3c12.Cn1c2ccccc2c2c(C(C)(C)C)cccc21.Cn1c2ccccc2c2cc(C(C)(C)C)ccc21.Cn1c2ccccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccccc2c2cccc(C(C)(C)C)c21 YORQRLFNIUPNQT-UHFFFAOYSA-N 0.000 description 1
- KABHBLMJIFFYGR-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1ccc2c(c1)oc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3c4ccccc4ccc3c2c1.CC(C)(C)c1cccc2c1-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1cccc2c1oc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3c4ccccc4ccc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1ccc2c(c1)oc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3c4ccccc4ccc3c2c1.CC(C)(C)c1cccc2c1-c1cc3ccccc3cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc3ccccc3cc1-2.CC(C)(C)c1cccc2c1oc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3c4ccccc4ccc3c12 KABHBLMJIFFYGR-UHFFFAOYSA-N 0.000 description 1
- MJJKUWMYVRRBAP-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1ccc(-c3ccccc3)cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc(-c3ccccc3)ccc1-2.CC(C)(C)c1cccc2c1-c1ccc(-c3ccccc3)cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc(-c3ccccc3)ccc1-2 Chemical compound CC(C)(C)c1ccc2c(c1)-c1ccc(-c3ccccc3)cc1C2(C)C.CC(C)(C)c1ccc2c(c1)C(C)(C)c1cc(-c3ccccc3)ccc1-2.CC(C)(C)c1cccc2c1-c1ccc(-c3ccccc3)cc1C2(C)C.CC(C)(C)c1cccc2c1C(C)(C)c1cc(-c3ccccc3)ccc1-2 MJJKUWMYVRRBAP-UHFFFAOYSA-N 0.000 description 1
- VKCMKSNEBCPARF-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1ccccc1C2(C)C.CC(C)(C)c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)oc1ccccc12.CC(C)(C)c1ccc2oc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1ccccc1C2(C)C.CC(C)(C)c1cccc2c1-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1cccc2c1C(C)(C)c1ccccc1-2.CC(C)(C)c1cccc2c1C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1cccc2c1oc1ccccc12 Chemical compound CC(C)(C)c1ccc2c(c1)-c1ccccc1C2(C)C.CC(C)(C)c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)oc1ccccc12.CC(C)(C)c1ccc2oc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1ccccc1C2(C)C.CC(C)(C)c1cccc2c1-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1cccc2c1C(C)(C)c1ccccc1-2.CC(C)(C)c1cccc2c1C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1cccc2c1oc1ccccc12 VKCMKSNEBCPARF-UHFFFAOYSA-N 0.000 description 1
- GYGADMMBTUNCJT-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)-c1ccccc1C2(C)C.CC(C)(C)c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)oc1ccccc12.CC(C)(C)c1ccc2oc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1ccccc1C2(C)C.CC(C)(C)c1cccc2c1-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1cccc2c1C(C)(C)c1ccccc1-2.CC(C)(C)c1cccc2c1C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1cccc2c1oc1ccccc12.CC(C)(C)c1cccc2oc3ccccc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)-c1ccccc1C2(C)C.CC(C)(C)c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1ccc2c(c1)oc1ccccc12.CC(C)(C)c1ccc2oc3ccccc3c2c1.CC(C)(C)c1cccc2c1-c1ccccc1C2(C)C.CC(C)(C)c1cccc2c1-c1ccccc1C21c2ccccc2-c2ccccc21.CC(C)(C)c1cccc2c1C(C)(C)c1ccccc1-2.CC(C)(C)c1cccc2c1C1(c3ccccc3-c3ccccc31)c1ccccc1-2.CC(C)(C)c1cccc2c1oc1ccccc12.CC(C)(C)c1cccc2oc3ccccc3c12 GYGADMMBTUNCJT-UHFFFAOYSA-N 0.000 description 1
- UJTDSDXQUHWAHW-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1ccc2c(c1)sc1ccccc12.CC(C)(C)c1ccc2sc3ccccc3c2c1.CC(C)(C)c1cccc2c1C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1cccc2c1sc1ccccc12.CC(C)(C)c1cccc2oc3ccccc3c12.CC(C)(C)c1cccc2sc3ccccc3c12.Cn1c2ccccc2c2c(C(C)(C)C)cccc21.Cn1c2ccccc2c2cc(C(C)(C)C)ccc21.Cn1c2ccccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccccc2c2cccc(C(C)(C)C)c21 Chemical compound CC(C)(C)c1ccc2c(c1)C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1ccc2c(c1)sc1ccccc12.CC(C)(C)c1ccc2sc3ccccc3c2c1.CC(C)(C)c1cccc2c1C(C)(C)c1ccc3ccccc3c1-2.CC(C)(C)c1cccc2c1sc1ccccc12.CC(C)(C)c1cccc2oc3ccccc3c12.CC(C)(C)c1cccc2sc3ccccc3c12.Cn1c2ccccc2c2c(C(C)(C)C)cccc21.Cn1c2ccccc2c2cc(C(C)(C)C)ccc21.Cn1c2ccccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccccc2c2cccc(C(C)(C)C)c21 UJTDSDXQUHWAHW-UHFFFAOYSA-N 0.000 description 1
- SNQFIZQPAZLHGU-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)oc1cc3ccccc3cc12.CC(C)(C)c1ccc2c(c1)oc1ccc3ccccc3c12.CC(C)(C)c1ccc2c(c1)sc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3cc4ccccc4cc3c2c1.CC(C)(C)c1ccc2oc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2c1oc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1oc1ccc3ccccc3c12.CC(C)(C)c1cccc2c1sc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3cc4ccccc4cc3c12.CC(C)(C)c1cccc2oc3ccc4ccccc4c3c12 Chemical compound CC(C)(C)c1ccc2c(c1)oc1cc3ccccc3cc12.CC(C)(C)c1ccc2c(c1)oc1ccc3ccccc3c12.CC(C)(C)c1ccc2c(c1)sc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3cc4ccccc4cc3c2c1.CC(C)(C)c1ccc2oc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2c1oc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1oc1ccc3ccccc3c12.CC(C)(C)c1cccc2c1sc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3cc4ccccc4cc3c12.CC(C)(C)c1cccc2oc3ccc4ccccc4c3c12 SNQFIZQPAZLHGU-UHFFFAOYSA-N 0.000 description 1
- QXPNVHXWNSRDCM-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)oc1cc3ccccc3cc12.CC(C)(C)c1ccc2oc3c4ccccc4ccc3c2c1.CC(C)(C)c1ccc2oc3cc4ccccc4cc3c2c1.CC(C)(C)c1cccc2c1oc1cc3ccccc3cc12.CC(C)(C)c1cccc2oc3c4ccccc4ccc3c12.CC(C)(C)c1cccc2oc3cc4ccccc4cc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)oc1cc3ccccc3cc12.CC(C)(C)c1ccc2oc3c4ccccc4ccc3c2c1.CC(C)(C)c1ccc2oc3cc4ccccc4cc3c2c1.CC(C)(C)c1cccc2c1oc1cc3ccccc3cc12.CC(C)(C)c1cccc2oc3c4ccccc4ccc3c12.CC(C)(C)c1cccc2oc3cc4ccccc4cc3c12 QXPNVHXWNSRDCM-UHFFFAOYSA-N 0.000 description 1
- CTXNUGMXFMYHDW-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)oc1ccc(-c3ccccc3)cc12.CC(C)(C)c1ccc2oc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1oc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2oc3ccc(-c4ccccc4)cc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)oc1ccc(-c3ccccc3)cc12.CC(C)(C)c1ccc2oc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1oc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2oc3ccc(-c4ccccc4)cc3c12 CTXNUGMXFMYHDW-UHFFFAOYSA-N 0.000 description 1
- JCIPWPFXZIRTBM-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)oc1ccc3ccccc3c12.CC(C)(C)c1ccc2c(c1)sc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3ccc4ccccc4c3c2c1.CC(C)(C)c1ccc2sc3c4ccccc4ccc3c2c1.CC(C)(C)c1cccc2c1oc1ccc3ccccc3c12.CC(C)(C)c1cccc2c1sc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3ccc4ccccc4c3c12.CC(C)(C)c1cccc2sc3c4ccccc4ccc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)oc1ccc3ccccc3c12.CC(C)(C)c1ccc2c(c1)sc1c3ccccc3ccc21.CC(C)(C)c1ccc2oc3ccc4ccccc4c3c2c1.CC(C)(C)c1ccc2sc3c4ccccc4ccc3c2c1.CC(C)(C)c1cccc2c1oc1ccc3ccccc3c12.CC(C)(C)c1cccc2c1sc1c3ccccc3ccc21.CC(C)(C)c1cccc2oc3ccc4ccccc4c3c12.CC(C)(C)c1cccc2sc3c4ccccc4ccc3c12 JCIPWPFXZIRTBM-UHFFFAOYSA-N 0.000 description 1
- KPCAXYHJKIQPSV-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)sc1cc(-c3ccccc3)ccc12.CC(C)(C)c1ccc2sc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1sc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2oc3ccc(-c4ccccc4)cc3c12.CC(C)(C)c1cccc2sc3cc(-c4ccccc4)ccc3c12.Cn1c2cc(-c3ccccc3)ccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccc(-c3ccccc3)cc2c2cccc(C(C)(C)C)c21 Chemical compound CC(C)(C)c1ccc2c(c1)sc1cc(-c3ccccc3)ccc12.CC(C)(C)c1ccc2sc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1sc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2oc3ccc(-c4ccccc4)cc3c12.CC(C)(C)c1cccc2sc3cc(-c4ccccc4)ccc3c12.Cn1c2cc(-c3ccccc3)ccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccc(-c3ccccc3)cc2c2cccc(C(C)(C)C)c21 KPCAXYHJKIQPSV-UHFFFAOYSA-N 0.000 description 1
- NEHVMAQUWDMLFX-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)sc1cc(-c3ccccc3)ccc12.CC(C)(C)c1ccc2sc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1sc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2sc3cc(-c4ccccc4)ccc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)sc1cc(-c3ccccc3)ccc12.CC(C)(C)c1ccc2sc3cc(-c4ccccc4)ccc3c2c1.CC(C)(C)c1cccc2c1sc1ccc(-c3ccccc3)cc12.CC(C)(C)c1cccc2sc3cc(-c4ccccc4)ccc3c12 NEHVMAQUWDMLFX-UHFFFAOYSA-N 0.000 description 1
- FYNPLYVGIQGLGL-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)sc1cc3ccccc3cc12.CC(C)(C)c1ccc2c(c1)sc1ccc3ccccc3c12.CC(C)(C)c1ccc2sc3cc4ccccc4cc3c2c1.CC(C)(C)c1ccc2sc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2c1sc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1sc1ccc3ccccc3c12.CC(C)(C)c1cccc2sc3cc4ccccc4cc3c12.CC(C)(C)c1cccc2sc3ccc4ccccc4c3c12 Chemical compound CC(C)(C)c1ccc2c(c1)sc1cc3ccccc3cc12.CC(C)(C)c1ccc2c(c1)sc1ccc3ccccc3c12.CC(C)(C)c1ccc2sc3cc4ccccc4cc3c2c1.CC(C)(C)c1ccc2sc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2c1sc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1sc1ccc3ccccc3c12.CC(C)(C)c1cccc2sc3cc4ccccc4cc3c12.CC(C)(C)c1cccc2sc3ccc4ccccc4c3c12 FYNPLYVGIQGLGL-UHFFFAOYSA-N 0.000 description 1
- FOYJKQBJSZWQMX-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)sc1cc3ccccc3cc12.CC(C)(C)c1ccc2sc3c4ccccc4ccc3c2c1.CC(C)(C)c1ccc2sc3cc4ccccc4cc3c2c1.CC(C)(C)c1cccc2c1sc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1sc1ccc3ccccc3c12.CC(C)(C)c1cccc2sc3c4ccccc4ccc3c12.CC(C)(C)c1cccc2sc3cc4ccccc4cc3c12 Chemical compound CC(C)(C)c1ccc2c(c1)sc1cc3ccccc3cc12.CC(C)(C)c1ccc2sc3c4ccccc4ccc3c2c1.CC(C)(C)c1ccc2sc3cc4ccccc4cc3c2c1.CC(C)(C)c1cccc2c1sc1cc3ccccc3cc12.CC(C)(C)c1cccc2c1sc1ccc3ccccc3c12.CC(C)(C)c1cccc2sc3c4ccccc4ccc3c12.CC(C)(C)c1cccc2sc3cc4ccccc4cc3c12 FOYJKQBJSZWQMX-UHFFFAOYSA-N 0.000 description 1
- ZOGKERUYOYIJHZ-UHFFFAOYSA-N CC(C)(C)c1ccc2c(c1)sc1ccc3ccccc3c12.CC(C)(C)c1ccc2sc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2sc3ccc4ccccc4c3c12.Cn1c2c(C(C)(C)C)cccc2c2ccc3ccccc3c21.Cn1c2cc(C(C)(C)C)ccc2c2ccc3ccccc3c21.Cn1c2cc3ccccc3cc2c2cccc(C(C)(C)C)c21.Cn1c2ccc(C(C)(C)C)cc2c2ccc3ccccc3c21.Cn1c2cccc(C(C)(C)C)c2c2ccc3ccccc3c21 Chemical compound CC(C)(C)c1ccc2c(c1)sc1ccc3ccccc3c12.CC(C)(C)c1ccc2sc3ccc4ccccc4c3c2c1.CC(C)(C)c1cccc2sc3ccc4ccccc4c3c12.Cn1c2c(C(C)(C)C)cccc2c2ccc3ccccc3c21.Cn1c2cc(C(C)(C)C)ccc2c2ccc3ccccc3c21.Cn1c2cc3ccccc3cc2c2cccc(C(C)(C)C)c21.Cn1c2ccc(C(C)(C)C)cc2c2ccc3ccccc3c21.Cn1c2cccc(C(C)(C)C)c2c2ccc3ccccc3c21 ZOGKERUYOYIJHZ-UHFFFAOYSA-N 0.000 description 1
- ZIGFJSPXMWEIME-UHFFFAOYSA-N CC(C)(C)c1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.CC(C)Cc1ccn2->[Ir]3(c4ccccc4-c4ccccn->34)c3ccc(-c4ccccc4)cc3-c2c1.CC(C)Cc1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.CC(C)c1ccc2-c3cc(-c4ccccc4)ccc3[Ir]<-n2c1.Cc1ccc2-c3cc(-c4ccccc4)ccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2c1 Chemical compound CC(C)(C)c1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.CC(C)Cc1ccn2->[Ir]3(c4ccccc4-c4ccccn->34)c3ccc(-c4ccccc4)cc3-c2c1.CC(C)Cc1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.CC(C)c1ccc2-c3cc(-c4ccccc4)ccc3[Ir]<-n2c1.Cc1ccc2-c3cc(-c4ccccc4)ccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2c1 ZIGFJSPXMWEIME-UHFFFAOYSA-N 0.000 description 1
- VGAXVOFYBRAEQJ-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2oc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2oc3ccccc3c2n1 VGAXVOFYBRAEQJ-UHFFFAOYSA-N 0.000 description 1
- RHMWAJQEKMHAJM-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2ccc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)oc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2ccc3ccccc3c2n1 RHMWAJQEKMHAJM-UHFFFAOYSA-N 0.000 description 1
- HWMXVDGDDFGMTN-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2oc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2c(n1)sc1ccccc12.CC(C)(C)c1nc(-c2ccccc2)c2oc3ccccc3c2n1 HWMXVDGDDFGMTN-UHFFFAOYSA-N 0.000 description 1
- AKVCWDDKXAPYDV-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2sc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2sc3ccccc3c2n1 AKVCWDDKXAPYDV-UHFFFAOYSA-N 0.000 description 1
- MCNADDXJBSCIBU-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2sc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccccc2)c2sc3ccccc3c2n1 MCNADDXJBSCIBU-UHFFFAOYSA-N 0.000 description 1
- ALIPTLZVCNZMLB-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccccc2)n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccccc2)n1 ALIPTLZVCNZMLB-UHFFFAOYSA-N 0.000 description 1
- LYPDCTXNUSTCTO-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3c2oc2ccccc23)n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3c2oc2ccccc23)n1 LYPDCTXNUSTCTO-UHFFFAOYSA-N 0.000 description 1
- SIARQQQWGOQQJW-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccccc2)n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccccc2)n1 SIARQQQWGOQQJW-UHFFFAOYSA-N 0.000 description 1
- WEPWERZFWUIMNL-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccccc2)n1 Chemical compound CC(C)(C)c1nc(-c2ccc(-c3ccccc3)cc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc(-c3ccccc3)cc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccccc2)n1 WEPWERZFWUIMNL-UHFFFAOYSA-N 0.000 description 1
- NKMWWPTXPSOPNX-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2oc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2sc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2oc3ccccc3c2n1 NKMWWPTXPSOPNX-UHFFFAOYSA-N 0.000 description 1
- RKHWCLLBIRWLHF-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2oc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc3c(c2)-c2ccccc2C3(C)C)c2oc3ccccc3c2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2oc3ccccc3c2n1 RKHWCLLBIRWLHF-UHFFFAOYSA-N 0.000 description 1
- AKEAEBBAZAFVQU-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc3c(c2)oc2ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3c4ccccc4n(-c4ccccc4)c3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc3ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccccc2)c2ccc3ccccc3c2n1 Chemical compound CC(C)(C)c1nc(-c2ccc3c(c2)oc2ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3c4ccccc4n(-c4ccccc4)c3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccc3ccccc3c2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc3ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccccc2)c2ccc3ccccc3c2n1 AKEAEBBAZAFVQU-UHFFFAOYSA-N 0.000 description 1
- OXUHVQBEGLSFHQ-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccc3c(c2)oc2ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3c4ccccc4n(-c4ccccc4)c3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc3ccccc23)c2ccccc2n1 Chemical compound CC(C)(C)c1nc(-c2ccc3c(c2)oc2ccccc23)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3c4ccccc4n(-c4ccccc4)c3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2ccc3ccccc3c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc(-c3ccccc3)c2)c2ccccc2n1.CC(C)(C)c1nc(-c2cccc3ccccc23)c2ccccc2n1 OXUHVQBEGLSFHQ-UHFFFAOYSA-N 0.000 description 1
- ONQBBUNJZVTVCI-UHFFFAOYSA-N CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)cc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3oc4ccccc4c23)n1 Chemical compound CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)cc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3oc4ccccc4c23)n1 ONQBBUNJZVTVCI-UHFFFAOYSA-N 0.000 description 1
- QIPUFBZIKKNWEM-UHFFFAOYSA-N CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)nc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccccc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc(-c3ccccc3)c2)n1 Chemical compound CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)nc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccc3ccccc3c2)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc3ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)cc(-c2ccccc2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc(-c3ccccc3)c2)n1 QIPUFBZIKKNWEM-UHFFFAOYSA-N 0.000 description 1
- NMWSZXFMPSYWLV-UHFFFAOYSA-N CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)nc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc(-c3ccccc3)c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3oc4ccccc4c23)n1 Chemical compound CC(C)(C)c1nc(-c2cccc3oc4ccccc4c23)nc(-c2cccc3oc4ccccc4c23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)sc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc(-c3ccccc3)c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3oc4ccccc4c23)n1 NMWSZXFMPSYWLV-UHFFFAOYSA-N 0.000 description 1
- QMSMSLGTOQBMQI-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc(-c3ccccc3)c2)n1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2ccccc2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2oc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2c1oc1ccccc12.CC(C)(C)c1nc2ccccc2nc1-c1ccccc1 Chemical compound CC(C)(C)c1nc(-c2ccccc2)cc(-c2cccc(-c3ccccc3)c2)n1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2ccccc2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2oc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2c1oc1ccccc12.CC(C)(C)c1nc2ccccc2nc1-c1ccccc1 QMSMSLGTOQBMQI-UHFFFAOYSA-N 0.000 description 1
- LXFKZQNHIVDYEC-UHFFFAOYSA-N CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3oc4ccccc4c23)n1 Chemical compound CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3c(c2)oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2ccc3oc4ccccc4c3c2)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3c2oc2ccccc23)n1.CC(C)(C)c1nc(-c2ccccc2)nc(-c2cccc3oc4ccccc4c23)n1 LXFKZQNHIVDYEC-UHFFFAOYSA-N 0.000 description 1
- LMHURZNWRWYWQG-UHFFFAOYSA-N CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccccc2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2c3ccccc3n(-c3ccccc3)c2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2sc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2nc(-c3ccccc3)oc12 Chemical compound CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccccc2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2c3ccccc3n(-c3ccccc3)c2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2sc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2nc(-c3ccccc3)oc12 LMHURZNWRWYWQG-UHFFFAOYSA-N 0.000 description 1
- GPHUISQAQGQGHK-UHFFFAOYSA-N CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccccc2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2c3ccccc3n(-c3ccccc3)c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2nc(-c3ccccc3)oc12 Chemical compound CC(C)(C)c1nc2ccc3ccccc3c2nc1-c1ccccc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccc3ccccc3c2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc(-c2ccccc2)cc1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2c3ccccc3n(-c3ccccc3)c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2nc(-c3ccccc3)oc12 GPHUISQAQGQGHK-UHFFFAOYSA-N 0.000 description 1
- HFCCKRANUHWWLZ-UHFFFAOYSA-N CC(C)(C)c1nc2ccccc2nc1-c1ccc2ccccc2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2oc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2sc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2c1oc1ccccc12.CC(C)(C)c1nc2ccccc2nc1-c1ccccc1 Chemical compound CC(C)(C)c1nc2ccccc2nc1-c1ccc2ccccc2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2oc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1ccc2sc3ccccc3c2c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc(-c2ccccc2)c1.CC(C)(C)c1nc2ccccc2nc1-c1cccc2c1oc1ccccc12.CC(C)(C)c1nc2ccccc2nc1-c1ccccc1 HFCCKRANUHWWLZ-UHFFFAOYSA-N 0.000 description 1
- CVBFIXMIRFDYTI-UHFFFAOYSA-N CC(C)C.Cn1c2cc(-c3ccccc3)ccc2c2c(C(C)(C)C)cccc21.Cn1c2cc(-c3ccccc3)ccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccc(-c3ccccc3)cc2c2cc(C(C)(C)C)ccc21.Cn1c2ccc(-c3ccccc3)cc2c2cccc(C(C)(C)C)c21.c1ccc(-n2c3ccccc3c3ccccc32)cc1 Chemical compound CC(C)C.Cn1c2cc(-c3ccccc3)ccc2c2c(C(C)(C)C)cccc21.Cn1c2cc(-c3ccccc3)ccc2c2ccc(C(C)(C)C)cc21.Cn1c2ccc(-c3ccccc3)cc2c2cc(C(C)(C)C)ccc21.Cn1c2ccc(-c3ccccc3)cc2c2cccc(C(C)(C)C)c21.c1ccc(-n2c3ccccc3c3ccccc32)cc1 CVBFIXMIRFDYTI-UHFFFAOYSA-N 0.000 description 1
- AMMTVMYOGMPBOC-UHFFFAOYSA-N CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(c1ccccc1)c1c(-c2ccccc2)ccc2ccccc12.CC(C)N(c1ccccc1)c1cc2ccccc2cc1-c1ccccc1.CC1(C)c2ccccc2-c2ccccc21.c1ccc(-n2c3ccccc3c3ccccc32)cc1.c1ccc(C2(c3ccccc3)c3ccccc3-c3ccccc32)cc1.c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.c1ccc2c(c1)oc1ccccc12.c1ccc2c(c1)sc1ccccc12 Chemical compound CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(C)c1ccccc1.CC(C)N(c1ccccc1)c1c(-c2ccccc2)ccc2ccccc12.CC(C)N(c1ccccc1)c1cc2ccccc2cc1-c1ccccc1.CC1(C)c2ccccc2-c2ccccc21.c1ccc(-n2c3ccccc3c3ccccc32)cc1.c1ccc(C2(c3ccccc3)c3ccccc3-c3ccccc32)cc1.c1ccc2c(c1)-c1ccccc1C21c2ccccc2-c2ccccc21.c1ccc2c(c1)oc1ccccc12.c1ccc2c(c1)sc1ccccc12 AMMTVMYOGMPBOC-UHFFFAOYSA-N 0.000 description 1
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- SRWAAYDOHJJGRO-DCROFEAVSA-N CC1(C)OB(c2cccc3c2-c2ccccc2[Y]3[Y])OC1(C)C.Cc1cccc(C)c1-c1cccc2c1-c1ccccc1[Y]2[Y].Cc1cccc(C)c1C.Cc1cccc2c1-c1c(ccc3c1-c1ccccc1[Y]3[Y])[Y]2.Cc1ccccc1-c1cccc2c1-c1c(ccc3c1-c1ccccc1[Y]3[Y])[Y]2.Cc1ccccc1B1OC(C)(C)C(C)(C)O1.Cc1ccccc1OBO.OB(O)c1cccc2c1-c1ccccc1[Y]2[Y].[Y][Y]1c2cccc3c2-c2c1ccc1c2-c2c(cccc2-c2ccccc2-3)[Y]1 Chemical compound CC1(C)OB(c2cccc3c2-c2ccccc2[Y]3[Y])OC1(C)C.Cc1cccc(C)c1-c1cccc2c1-c1ccccc1[Y]2[Y].Cc1cccc(C)c1C.Cc1cccc2c1-c1c(ccc3c1-c1ccccc1[Y]3[Y])[Y]2.Cc1ccccc1-c1cccc2c1-c1c(ccc3c1-c1ccccc1[Y]3[Y])[Y]2.Cc1ccccc1B1OC(C)(C)C(C)(C)O1.Cc1ccccc1OBO.OB(O)c1cccc2c1-c1ccccc1[Y]2[Y].[Y][Y]1c2cccc3c2-c2c1ccc1c2-c2c(cccc2-c2ccccc2-3)[Y]1 SRWAAYDOHJJGRO-DCROFEAVSA-N 0.000 description 1
- DNYCIGVCURKYLF-WHWALVEXSA-N CC1(C)OB(c2cccc3c2-c2ccccc2[Y]3[Y])OC1(C)C.Cc1cccc2c1-c1c(ccc([Y])c1-c1cccc3c1-c1ccccc1[Y]3[Y])[Y]2[Y][Y].Cc1cccc2c1-c1c(ccc([Y])c1C)[Y]2[Y][Y].Cc1cccc2c1-c1c(ccc3c1-c1c(ccc4c1-c1ccccc1[Y]4[Y])[Y]3)[Y]2[Y][Y].OB(O)c1cccc2c1-c1ccccc1[Y]2[Y].[Y][Y][Y]1c2cccc3c2-c2c1ccc1c2-c2c(ccc4c2-c2c-3cccc2[Y]4[Y])[Y]1 Chemical compound CC1(C)OB(c2cccc3c2-c2ccccc2[Y]3[Y])OC1(C)C.Cc1cccc2c1-c1c(ccc([Y])c1-c1cccc3c1-c1ccccc1[Y]3[Y])[Y]2[Y][Y].Cc1cccc2c1-c1c(ccc([Y])c1C)[Y]2[Y][Y].Cc1cccc2c1-c1c(ccc3c1-c1c(ccc4c1-c1ccccc1[Y]4[Y])[Y]3)[Y]2[Y][Y].OB(O)c1cccc2c1-c1ccccc1[Y]2[Y].[Y][Y][Y]1c2cccc3c2-c2c1ccc1c2-c2c(ccc4c2-c2c-3cccc2[Y]4[Y])[Y]1 DNYCIGVCURKYLF-WHWALVEXSA-N 0.000 description 1
- BKPPJPLINLMFQV-UHFFFAOYSA-N CC1(C)c2cc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4c(c5c3ccc3sc(-c6ccccc6)nc35)CCCC4)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-8)c8ccccc8-c8cc9ccccc9cc87)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2cc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4c(c5c3ccc3sc(-c6ccccc6)nc35)CCCC4)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-8)c8ccccc8-c8cc9ccccc9cc87)nc6c54)c3)n2)cc1 BKPPJPLINLMFQV-UHFFFAOYSA-N 0.000 description 1
- VMSSHIPVVPTKJV-UHFFFAOYSA-N CC1(C)c2cc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccccc4c4c3ccc3sc(-c5ccccc5)nc34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-8)c8ccccc8-c8cc9ccccc9cc87)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2cc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccccc4c4c3ccc3sc(-c5ccccc5)nc34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-8)c8ccccc8-c8cc9ccccc9cc87)nc6c54)c3)n2)cc1 VMSSHIPVVPTKJV-UHFFFAOYSA-N 0.000 description 1
- HYUBDPVQBGQTGO-UHFFFAOYSA-N CC1(C)c2cc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccc5ccccc5c4c4nc(-c5ccccc5)sc34)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-c9ccccc97)c7ccccc7-8)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2cc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccc5ccccc5c4c4nc(-c5ccccc5)sc34)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c(c7)C7(c9ccccc9-c9ccccc97)c7ccccc7-8)nc6c54)c3)n2)cc1 HYUBDPVQBGQTGO-UHFFFAOYSA-N 0.000 description 1
- KUBUIXLLTMAOGN-UHFFFAOYSA-N CC1(C)c2cc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccc5ccccc5c4c4nc(-c5ccccc5)sc34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccc8c9ccccc9n(-c9ccccc9)c8c7)oc6c54)c3)n2)cc1 Chemical compound CC1(C)c2cc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)ccc2-c2cc3ccccc3cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3cc4ccc5ccccc5c4c4nc(-c5ccccc5)sc34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccc8c9ccccc9n(-c9ccccc9)c8c7)oc6c54)c3)n2)cc1 KUBUIXLLTMAOGN-UHFFFAOYSA-N 0.000 description 1
- TWCBYQCOOGHSOD-UHFFFAOYSA-N CC1(C)c2cc(-c3nc4ccccc4nc3-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)ccc2C2C=CC=CC21.c1ccc(-c2nc3ccc4ccc5cc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)ccc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6ccc7nc(-c8ccccc8)c(-c8ccccc8)nc7c6)cc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)cc5c4c3o2)cc1 Chemical compound CC1(C)c2cc(-c3nc4ccccc4nc3-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)ccc2C2C=CC=CC21.c1ccc(-c2nc3ccc4ccc5cc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)ccc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6ccc7nc(-c8ccccc8)c(-c8ccccc8)nc7c6)cc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)cc5c4c3o2)cc1 TWCBYQCOOGHSOD-UHFFFAOYSA-N 0.000 description 1
- KKFLXPKZVPCRNZ-POESQYPKSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)c2ccccc2n1.c1ccc(-c2nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7oc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)c2ccccc2n1.c1ccc(-c2nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7oc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1 KKFLXPKZVPCRNZ-POESQYPKSA-N 0.000 description 1
- HSCYSVLVUJNCEA-DWGJSPTRSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)c2ccccc2n1.c1ccc(-c2nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)c2ccccc2n1.c1ccc(-c2nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)nc3ccccc23)cc1.c1ccc(-c2nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)nc3ccccc23)cc1 HSCYSVLVUJNCEA-DWGJSPTRSA-N 0.000 description 1
- PZHLMBUMIKIIHT-PJVDWYGSSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cc7c(cc6c6cccc8oc9ccc3c(c9c86)c54)oc3ccccc37)n2)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cc7c(cc6c6cccc8oc9ccc3c(c9c86)c54)oc3ccccc37)n2)cc1 PZHLMBUMIKIIHT-PJVDWYGSSA-N 0.000 description 1
- MULPRIGXKBJSBZ-BLCGKKTLSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)n2)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6ccc7oc8ccc9oc%10ccc3c3c%10c9c8c7c6c5c34)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cccc7sc8ccc9oc%10ccc3c(c%10c9c8c76)c54)n2)cc1 MULPRIGXKBJSBZ-BLCGKKTLSA-N 0.000 description 1
- JDTKGEMCRJJSGU-DWGJSPTRSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5ccc6oc7ccc8oc9ccc2c2c9c8c7c6c5c4c23)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cccc6sc7ccc8oc9ccc2c(c9c8c7c65)c43)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5ccc6oc7ccc8oc9ccc2c2c9c8c7c6c5c4c23)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cccc6sc7ccc8oc9ccc2c(c9c8c7c65)c43)cc1 JDTKGEMCRJJSGU-DWGJSPTRSA-N 0.000 description 1
- MWDUTPRQSYEMEH-DLWALQRHSA-N CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6c(cc5c5cccc7oc8ccc2c(c8c75)c43)oc2ccccc26)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cc6oc7ccccc7c6c6oc7ccc2c(c7c56)c43)cc1 Chemical compound CC1(C)c2ccc3oc4ccc5c6c4c3c2c2c1ccc1oc3ccc(c6c3c12)n5-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6c(cc5c5cccc7oc8ccc2c(c8c75)c43)oc2ccccc26)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cc6oc7ccccc7c6c6oc7ccc2c(c7c56)c43)cc1 MWDUTPRQSYEMEH-DLWALQRHSA-N 0.000 description 1
- CWVLMWFKXZFPNW-APKSRLAYSA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc(-c8ccccc8)c7)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc8oc9ccccc9c78)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc(-c7ccccc7)c7ccccc7n1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccc8ccccc8c7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1cccc7oc8ccccc8c17)c6ccc4n5-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc(-c8ccccc8)c7)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc8oc9ccccc9c78)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc(-c7ccccc7)c7ccccc7n1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccc8ccccc8c7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1cccc7oc8ccccc8c17)c6ccc4n5-c1ccccc1)c23 CWVLMWFKXZFPNW-APKSRLAYSA-N 0.000 description 1
- JQERIXOKOMYNIN-KYHIHFSFSA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc(-c7ccccc7)c7ccccc7n1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1cccc7oc8ccccc8c17)c6ccc4n5-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc(-c7ccccc7)c7ccccc7n1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1cccc7oc8ccccc8c17)c6ccc4n5-c1ccccc1)c23 JQERIXOKOMYNIN-KYHIHFSFSA-N 0.000 description 1
- JWCRHSCVTJZIIT-DTTHWBISSA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(N(c7ccccc7)c7ccccc7)cc1)c6ccc4n5-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(N(c7ccccc7)c7ccccc7)cc1)c6ccc4n5-c1ccccc1)c23 JWCRHSCVTJZIIT-DTTHWBISSA-N 0.000 description 1
- HBVDQHZRDARTFI-UHXBYCORSA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(N(c7ccccc7)c7ccccc7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc(-c8ccccc8)c7)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc8oc9ccccc9c78)c1)c6ccc4n5-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1ccc(N(c7ccccc7)c7ccccc7)cc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc(-c8ccccc8)c7)c1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1cccc(-c7cccc8oc9ccccc9c78)c1)c6ccc4n5-c1ccccc1)c23 HBVDQHZRDARTFI-UHXBYCORSA-N 0.000 description 1
- QRAYPAJJZFKWKI-MZYUIKKSSA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccc8ccccc8c7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.[2H]c1c([2H])c([2H])c(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc3ccccc3nc2-c2ccccc2)c([2H])c1[2H] Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccc8ccccc8c7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.[2H]c1c([2H])c([2H])c(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc3ccccc3nc2-c2ccccc2)c([2H])c1[2H] QRAYPAJJZFKWKI-MZYUIKKSSA-N 0.000 description 1
- KEQWSZRYZKECBR-JKGXEUHISA-N CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.[2H]c1c([2H])c([2H])c(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc3ccccc3nc2-c2ccccc2)c([2H])c1[2H].c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)cc3)c2)cc1.c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3nc4ccc5ccccc5c4nc3-c3ccccc3)c2)cc1.c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3nc4ccccc4nc3-c3ccccc3)c2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccccc3-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccn3)n2)cc1 Chemical compound CC1(C)c2cccc3c4cccc5c4c4c6c7c(c1ccc7n(-c1nc7ccccc7nc1-c1ccccc1)c6ccc4n5-c1ccccc1)c23.[2H]c1c([2H])c([2H])c(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc3ccccc3nc2-c2ccccc2)c([2H])c1[2H].c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)cc3)c2)cc1.c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3nc4ccc5ccccc5c4nc3-c3ccccc3)c2)cc1.c1ccc(-c2cccc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3nc4ccccc4nc3-c3ccccc3)c2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccccc3-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccn3)n2)cc1 KEQWSZRYZKECBR-JKGXEUHISA-N 0.000 description 1
- AHPIFFMBIHPXDA-SYXWKGAPSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc(-c4ccccc4)cc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4c(c1)oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4ccc(-c5ccccc5)cc4)c1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc(-c4ccccc4)cc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4c(c1)oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4ccc(-c5ccccc5)cc4)c1)c23 AHPIFFMBIHPXDA-SYXWKGAPSA-N 0.000 description 1
- OVBXNMVNTOIJFH-XJQAVZMPSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc(-c4ccccc4)cc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4c(c1)oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4ccc(-c5ccccc5)cc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1cccc(-c4ccccc4)c1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc(-c4ccccc4)cc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4c(c1)oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cccc(-c4ccc(-c5ccccc5)cc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1cccc(-c4ccccc4)c1)c23 OVBXNMVNTOIJFH-XJQAVZMPSA-N 0.000 description 1
- DMPUBTXNEQGQMD-XFBOBTHCSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc4ccc5ccccc5c4cc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4cc(-c5ccccc5)c(-c5ccccc5)cc4c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccc(-c4ccccc4)cc1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1cc4ccc5ccccc5c4cc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4cc(-c5ccccc5)c(-c5ccccc5)cc4c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccc(-c4ccccc4)cc1)c23 DMPUBTXNEQGQMD-XFBOBTHCSA-N 0.000 description 1
- ZNSBVYSVRRQDAY-HZLNDJGCSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4nc(-c5ccccc5)c(-c5ccccc5)nc4c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4c(ccc5ccccc54)nc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccc5ccccc5c4nc1-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccc4nc(-c5ccccc5)c(-c5ccccc5)nc4c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4c(ccc5ccccc54)nc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccc5ccccc5c4nc1-c1ccccc1)c23 ZNSBVYSVRRQDAY-HZLNDJGCSA-N 0.000 description 1
- VZMJRUBGOMQLSN-DYKBIEDZSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4cccc5c4sc4ccccc45)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4oc5ccccc5c4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4sc5ccccc5c4n1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1ccccc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4cccc5c4sc4ccccc45)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4oc5ccccc5c4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4sc5ccccc5c4n1)c23 VZMJRUBGOMQLSN-DYKBIEDZSA-N 0.000 description 1
- MGYYKELGVVMZRY-SMDQBHQQSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc(-c5ccccc5)cc4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc5ccccc5c4)nc(-c4ccc5ccccc5c4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccc(-c5ccccc5)cn4)n1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc(-c5ccccc5)cc4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc5ccccc5c4)nc(-c4ccc5ccccc5c4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccc(-c5ccccc5)cn4)n1)c23 MGYYKELGVVMZRY-SMDQBHQQSA-N 0.000 description 1
- FIPJNKFAOQXRRF-SMDQBHQQSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc(-c5ccccc5)cc4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc5ccccc5c4)nc(-c4ccc5ccccc5c4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccc(-c5ccccc5)nc4)n1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc(-c5ccccc5)cc4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccc5ccccc5c4)nc(-c4ccc5ccccc5c4)n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)nc(-c4ccc(-c5ccccc5)nc4)n1)c23 FIPJNKFAOQXRRF-SMDQBHQQSA-N 0.000 description 1
- FLVJNOISEBJRBZ-GPWXOHAHSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4cccc5c4sc4ccccc45)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4oc5ccccc5c4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4sc5ccccc5c4n1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4cccc5c4sc4ccccc45)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4oc5ccccc5c4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4sc5ccccc5c4n1)c23 FLVJNOISEBJRBZ-GPWXOHAHSA-N 0.000 description 1
- PUGLORXBNDAXLR-APFIPORISA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4c(ccc5ccccc54)nc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1sc1ccccc14)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4c(ccc5ccccc54)nc1-c1ccccc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1sc1ccccc14)c23 PUGLORXBNDAXLR-APFIPORISA-N 0.000 description 1
- NCZQVTSORBEZOP-LKWIEEJDSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1sc1ccccc14)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc(-c4ccccc4)c4ccccc4n1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1oc1ccccc14)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc4c1sc1ccccc14)c23 NCZQVTSORBEZOP-LKWIEEJDSA-N 0.000 description 1
- PWSZAZSFHLRUCO-JISIZVBFSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccc(-c4ccccc4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccccc1)c23 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccc(-c4ccccc4)cc1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccccc1)c23 PWSZAZSFHLRUCO-JISIZVBFSA-N 0.000 description 1
- KDTCBGHVYDMYHG-JISIZVBFSA-N CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccccc1)c23.c1ccc(-c2nc(-c3ccccc3)nc(-c3cccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)c3)n2)cc1 Chemical compound CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1cccc(-c4ccccc4)c1)c23.CC1(C)c2cccc3c4ccccc4c4cccc5c4c4c(c1ccc4n5-c1nc4ccccc4nc1-c1ccccc1)c23.c1ccc(-c2nc(-c3ccccc3)nc(-c3cccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)c3)n2)cc1 KDTCBGHVYDMYHG-JISIZVBFSA-N 0.000 description 1
- IWOFNJFXAGYMHF-CXJMBLCQSA-N CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cccc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cn2)cc1.c1ccc(-c2nc(-c3ccc4ccccc4c3)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc(-c3ccc4ccccc4c3)nc(-c3ccc4ccccc4c3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cccc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cn2)cc1.c1ccc(-c2nc(-c3ccc4ccccc4c3)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc(-c3ccc4ccccc4c3)nc(-c3ccc4ccccc4c3)n2)cc1 IWOFNJFXAGYMHF-CXJMBLCQSA-N 0.000 description 1
- SKSMEAZSOVTZTM-KRODPZDDSA-N CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cccc21.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccccc3-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cccc21.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccccc3-n3c4cccc5c6ccccc6c6cccc7c6c6c(c54)c3ccc6n7-c3ccccc3)n2)cc1 SKSMEAZSOVTZTM-KRODPZDDSA-N 0.000 description 1
- LEJLXEGOMZOAFG-ZTOSQSGCSA-N CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cccc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cn2)cc1 Chemical compound CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cccc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cn2)cc1 LEJLXEGOMZOAFG-ZTOSQSGCSA-N 0.000 description 1
- XZSJWDOZQNXMNO-XZRPNDLQSA-N CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cccc21.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1.c1ccc(-c2nc(-c3cccc4sc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2c(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)n3)cccc21.c1ccc(-c2nc(-c3cccc4oc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1.c1ccc(-c2nc(-c3cccc4sc5ccccc5c34)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1 XZSJWDOZQNXMNO-XZRPNDLQSA-N 0.000 description 1
- BZQIVAGCDGHJMK-PCGYHOPRSA-N CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6cccc7c8ccccc8c8cc9ccccc9c3c8c4c5c67)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cc7ccccc7cc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc(-c2ccccc2)nc(-c2ccccc2)n1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4ccc5oc6cccc7c8ccccc8c8cc9ccccc9c3c8c4c5c67)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6cc7ccccc7cc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1 BZQIVAGCDGHJMK-PCGYHOPRSA-N 0.000 description 1
- KWQMXUGPGIKKRU-WSKFBCKASA-N CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5cccc6c7ccccc7c7cc8c9ccccc9oc8c2c7c3c4c56)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6ccccc6cc5c5cccc6oc7ccc2c(c7c65)c43)cc1 Chemical compound CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5cccc6c7ccccc7c7cc8c9ccccc9oc8c2c7c3c4c56)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6ccccc6cc5c5cccc6oc7ccc2c(c7c65)c43)cc1 KWQMXUGPGIKKRU-WSKFBCKASA-N 0.000 description 1
- CKURGOJNCNXLHT-RMDLRXDXSA-N CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5cccc6c7ccccc7c7cc8ccccc8c2c7c3c4c56)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6ccccc6cc5c5cccc6oc7ccc2c(c7c65)c43)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cc6ccccc6c6oc7ccc2c(c7c56)c43)cc1 Chemical compound CC1(C)c2ccccc2-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c21)n7-c1nc2ccccc2nc1-c1ccccc1.c1ccc(-c2nc3ccccc3nc2-n2c3ccc4oc5cccc6c7ccccc7c7cc8ccccc8c2c7c3c4c56)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5cc6ccccc6cc5c5cccc6oc7ccc2c(c7c65)c43)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cc6ccccc6c6oc7ccc2c(c7c56)c43)cc1 CKURGOJNCNXLHT-RMDLRXDXSA-N 0.000 description 1
- RYWJTKDOFBMDSQ-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5ccccc5c4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5ccccc5c4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21 RYWJTKDOFBMDSQ-UHFFFAOYSA-N 0.000 description 1
- RTMNRXUDSXMUPS-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.c1ccc(-c2cc(-c3ccc4c5ccccc5n(-c5ccccc5)c4c3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3cccc4c3sc3ccccc34)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3ccccc3-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.c1ccc(-c2cc(-c3ccc4c5ccccc5n(-c5ccccc5)c4c3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3cccc4c3sc3ccccc34)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3ccccc3-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccccc7)nc6c54)c3)n2)cc1 RTMNRXUDSXMUPS-UHFFFAOYSA-N 0.000 description 1
- DMRQHTYFXKLMOW-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5ccccc5c4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7c(nc(-c8ccccc8)n7-c7ccccc7)c65)c4)n3)cc2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccc5ccccc5c4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7sc(-c8ccccc8)nc7c65)c4)n3)cc21.c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7c(nc(-c8ccccc8)n7-c7ccccc7)c65)c4)n3)cc2)cc1 DMRQHTYFXKLMOW-UHFFFAOYSA-N 0.000 description 1
- XYQBKNYGQYRNGS-IZWQJFLZSA-N CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)cc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)c3)cc21.c1ccc(-c2cc(-c3ccccc3)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1.c1ccc(-c2ccc(-c3ccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)nc3)cc2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3cc(-c4ccccc4)cc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)c3)cc21.c1ccc(-c2cc(-c3ccccc3)nc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)n2)cc1.c1ccc(-c2ccc(-c3ccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)nc3)cc2)cc1 XYQBKNYGQYRNGS-IZWQJFLZSA-N 0.000 description 1
- OQGNVMAEZQSJPG-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)nc(-c3cccc4oc5ccccc5c34)n2)cc1.c1ccc(-c2nc(-c3ccc4oc5ccccc5c4c3)nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)nc(-c3cccc4oc5ccccc5c34)n2)cc1.c1ccc(-c2nc(-c3ccc4oc5ccccc5c4c3)nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)n2)cc1 OQGNVMAEZQSJPG-UHFFFAOYSA-N 0.000 description 1
- WTRRYOHSWPNZNX-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)nc(-c3cccc4oc5ccccc5c34)n2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(C6=NC(c7ccc8oc9ccccc9c8c7)=NC(c7ccccc7)N6)cc5c4c3o2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc21.c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-c4ccc5ccc6ccc7nc(-c8ccccc8)oc7c6c5c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)nc(-c3cccc4oc5ccccc5c34)n2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(C6=NC(c7ccc8oc9ccccc9c8c7)=NC(c7ccccc7)N6)cc5c4c3o2)cc1 WTRRYOHSWPNZNX-UHFFFAOYSA-N 0.000 description 1
- OMDTUSYJJFBYMG-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5ccccc5c4)n3)cc21 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc(-c4ccc5c(c4)C(C)(C)c4ccccc4-5)nc(-c4ccc5ccccc5c4)n3)cc21 OMDTUSYJJFBYMG-UHFFFAOYSA-N 0.000 description 1
- ABRGUXNPDVFHRW-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)cc21.CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8ccccc8c7)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)cc21.CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8ccccc8c7)nc6c54)c3)n2)cc1 ABRGUXNPDVFHRW-UHFFFAOYSA-N 0.000 description 1
- LIGXXINUIHIJCZ-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2cc(-c3ccc4ccccc4c3)nc(-c3ccc4c(ccc5ccc6oc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8ccccc8c7)nc6c54)c3)n2)cc1.c1ccc(-c2nc3c(ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)cc(-c7ccc8ccccc8c7)n6)ccc5c43)o2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)cc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2cc(-c3ccc4ccccc4c3)nc(-c3ccc4c(ccc5ccc6oc(-c7ccccc7)nc6c54)c3)n2)cc1.c1ccc(-c2cc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8ccccc8c7)nc6c54)c3)n2)cc1.c1ccc(-c2nc3c(ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)cc(-c7ccc8ccccc8c7)n6)ccc5c43)o2)cc1 LIGXXINUIHIJCZ-UHFFFAOYSA-N 0.000 description 1
- QKAXBWCVOUMTMP-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2ccc3ccc(-c4nc5c(ccc6ccc7cc(-c8nc(-c9ccccc9)nc(-c9ccccc9)n8)ccc7c65)s4)cc3c2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c9ccccc9n(-c9ccccc9)c8c7)nc6c54)c3)n2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc4c(ccc5ccc6cc(-c7nc(-c8ccccc8)nc(-c8ccccc8)n7)ccc6c54)s3)cc21.c1ccc(-c2ccc3ccc(-c4nc5c(ccc6ccc7cc(-c8nc(-c9ccccc9)nc(-c9ccccc9)n8)ccc7c65)s4)cc3c2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6sc(-c7ccc8c9ccccc9n(-c9ccccc9)c8c7)nc6c54)c3)n2)cc1 QKAXBWCVOUMTMP-UHFFFAOYSA-N 0.000 description 1
- FXGDEACORZJWPB-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(-c3nc4ccccc4nc3-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)cc21.c1ccc(-c2nc3ccc4ccc5cc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)ccc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)cc5c4c3o2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(-c3nc4ccccc4nc3-c3ccc4ccc5ccc6nc(-c7ccccc7)oc6c5c4c3)cc21.c1ccc(-c2nc3ccc4ccc5cc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)ccc5c4c3o2)cc1.c1ccc(-c2nc3ccc4ccc5ccc(-c6cccc7nc(-c8ccccc8)c(-c8ccccc8)nc67)cc5c4c3o2)cc1 FXGDEACORZJWPB-UHFFFAOYSA-N 0.000 description 1
- CICUYZNJLBICAG-UHFFFAOYSA-N CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccccc4)cc3)c3ccc(-c4ccc5c(c4)c4ccccc4n5-c4ccccc4)cc3)cc21.[H-] Chemical compound CC1(C)c2ccccc2-c2ccc(N(c3ccc(-c4ccccc4)cc3)c3ccc(-c4ccc5c(c4)c4ccccc4n5-c4ccccc4)cc3)cc21.[H-] CICUYZNJLBICAG-UHFFFAOYSA-N 0.000 description 1
- NNUSABLHOYACDJ-FIBIDPDLSA-N CC1(C)c2ccccc2-c2ccc(N(c3ccccc3)c3ccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)cc3)cc21.c1ccc(-c2ccccc2-c2ccc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)cc2)cc1.c1ccc(N(c2ccccc2)c2cccc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)c2)cc1 Chemical compound CC1(C)c2ccccc2-c2ccc(N(c3ccccc3)c3ccc(-n4c5cccc6c7ccccc7c7cccc8oc9ccc4c(c9c87)c65)cc3)cc21.c1ccc(-c2ccccc2-c2ccc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)cc2)cc1.c1ccc(N(c2ccccc2)c2cccc(-n3c4cccc5c6ccccc6c6cccc7oc8ccc3c(c8c76)c54)c2)cc1 NNUSABLHOYACDJ-FIBIDPDLSA-N 0.000 description 1
- TWIKYCJGUJJWTE-WONUTKFHSA-I CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(-c3ccccc3)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)oc1ccccc14.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)sc1ccccc14.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3c(-c2c1)cc(CC(C)C)c1cc2c(cc13)oc1ccccc12 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(-c3ccccc3)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)oc1ccccc14.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)sc1ccccc14.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3c(-c2c1)cc(CC(C)C)c1cc2c(cc13)oc1ccccc12 TWIKYCJGUJJWTE-WONUTKFHSA-I 0.000 description 1
- SUPNKEKJORSHIL-KBHDBPIGSA-J CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccc(C)cc4)ccc3n->21.Cc1cc(C)c2[Ir]3(O/C(=C\C(=O->3)C(C)(C)C)C(C)(C)C)<-n3c(-c2c1)cc(CC(C)C)c1cc(-c2ccccc2)ccc13.Cc1ccc(-c2ccc3c(c2)c(CC(C)C)cc2-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(C)C)C(C)(C)C)<-n23)cc1.Cc1ccc(-c2ccc3c(c2)c(CC(C)C)cc2-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(CC(C)C)=O->4)CC(C)C)<-n23)cc1.[2H]C([2H])([2H])c1ccc2-c3ccccc3[Ir]3(c4ccc(-c5ccccc5)cc4-c4ccc(C([2H])([2H])[2H])cn->34)<-n2c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccc(C)cc4)ccc3n->21.Cc1cc(C)c2[Ir]3(O/C(=C\C(=O->3)C(C)(C)C)C(C)(C)C)<-n3c(-c2c1)cc(CC(C)C)c1cc(-c2ccccc2)ccc13.Cc1ccc(-c2ccc3c(c2)c(CC(C)C)cc2-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(C)C)C(C)(C)C)<-n23)cc1.Cc1ccc(-c2ccc3c(c2)c(CC(C)C)cc2-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(CC(C)C)=O->4)CC(C)C)<-n23)cc1.[2H]C([2H])([2H])c1ccc2-c3ccccc3[Ir]3(c4ccc(-c5ccccc5)cc4-c4ccc(C([2H])([2H])[2H])cn->34)<-n2c1 SUPNKEKJORSHIL-KBHDBPIGSA-J 0.000 description 1
- SDNVJZHTBCGMQL-PVAXDIORSA-M CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21.Cc1ccc2-c3cc(-c4ccccc4)ccc3[Ir]3(c4ccccc4-c4ccc(C(C)(C)C)cn->34)<-n2c1.Cc1ccc2-c3ccccc3[Ir]3(c4cc5sc6ccccc6c5cc4-c4ccccn->34)<-n2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3cc4oc5ccccc5c4cc3-c2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3cc4sc5ccccc5c4cc3-c2c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21.Cc1ccc2-c3cc(-c4ccccc4)ccc3[Ir]3(c4ccccc4-c4ccc(C(C)(C)C)cn->34)<-n2c1.Cc1ccc2-c3ccccc3[Ir]3(c4cc5sc6ccccc6c5cc4-c4ccccn->34)<-n2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3cc4oc5ccccc5c4cc3-c2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3cc4sc5ccccc5c4cc3-c2c1 SDNVJZHTBCGMQL-PVAXDIORSA-M 0.000 description 1
- ZIIAMGMQCOIMIC-IILIYOGMSA-L CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc(-c3ccccc3)cn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1cc(C)cc(C)c1-c1ccc(-c3ccccc3)cn->21.Cc1cc(C)c2[Ir]<-n3cc(-c4ccccc4)ccc3-c2c1.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c3c2)<-n2ccccc2-c2ccccn->42)cc1.c1ccc(-c2ccn3->[Ir]c4ccccc4-c3c2)cc1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc(-c3ccccc3)cn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1cc(C)cc(C)c1-c1ccc(-c3ccccc3)cn->21.Cc1cc(C)c2[Ir]<-n3cc(-c4ccccc4)ccc3-c2c1.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c3c2)<-n2ccccc2-c2ccccn->42)cc1.c1ccc(-c2ccn3->[Ir]c4ccccc4-c3c2)cc1 ZIIAMGMQCOIMIC-IILIYOGMSA-L 0.000 description 1
- OTMVBALPYFEGSY-DJZACKBQSA-J CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3c(CC(C)C)cccc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3ccc(CC(C)C)cc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3ccc(C)cc3C)ccn->21.CCCc1ccc2ccc3-c4cc(C)cc(C)c4[Ir]4(O/C(C)=C\C(C)=O->4)<-n3c2c1.Cc1cc(C)cc(-c2ccn3->[Ir]4(c5ccccc5-c5ccccn->45)c4ccccc4-c3c2)c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3c(CC(C)C)cccc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3ccc(CC(C)C)cc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3ccc(C)cc3C)ccn->21.CCCc1ccc2ccc3-c4cc(C)cc(C)c4[Ir]4(O/C(C)=C\C(C)=O->4)<-n3c2c1.Cc1cc(C)cc(-c2ccn3->[Ir]4(c5ccccc5-c5ccccn->45)c4ccccc4-c3c2)c1 OTMVBALPYFEGSY-DJZACKBQSA-J 0.000 description 1
- ISCJTCNDVAGVPK-XCXAHRAVSA-K CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3ccccc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3ccc(C)cc3)ccn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cccc(C)c3)ccn->21.CCc1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.c1ccc2-c3ccccn3->[Ir]c2c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3ccccc3n->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3ccc(C)cc3)ccn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cccc(C)c3)ccn->21.CCc1ccn2->[Ir]c3ccc(-c4ccccc4)cc3-c2c1.c1ccc2-c3ccccn3->[Ir]c2c1 ISCJTCNDVAGVPK-XCXAHRAVSA-K 0.000 description 1
- PFEXPZIVOIHTRK-PVAXDIORSA-M CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4c(C)cccc43)c1-c1cc(-c3ccccc3)ccn->21.Cc1ccc2-c3ccccc3[Ir]3(c4ccccc4-c4cc(C)c(-c5ccccc5)cn->34)<-n2c1.Cc1ccc2-c3ccccc3[Ir]3(c4ccccc4-c4cc(C)c(-c5ccccc5)cn->34)<-n2c1.Cc1cccc2c1oc1c3-c4cc(-c5ccccc5)ccn4->[Ir]4(c5ccccc5-c5ccccn->45)c3ccc12.Cc1ccn2->[Ir]3(c4ccccc4-c4ccccn->34)c3ccc(-c4ccccc4)cc3-c2c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4c(C)cccc43)c1-c1cc(-c3ccccc3)ccn->21.Cc1ccc2-c3ccccc3[Ir]3(c4ccccc4-c4cc(C)c(-c5ccccc5)cn->34)<-n2c1.Cc1ccc2-c3ccccc3[Ir]3(c4ccccc4-c4cc(C)c(-c5ccccc5)cn->34)<-n2c1.Cc1cccc2c1oc1c3-c4cc(-c5ccccc5)ccn4->[Ir]4(c5ccccc5-c5ccccn->45)c3ccc12.Cc1ccn2->[Ir]3(c4ccccc4-c4ccccn->34)c3ccc(-c4ccccc4)cc3-c2c1 PFEXPZIVOIHTRK-PVAXDIORSA-M 0.000 description 1
- IVROEOBEXNGVGF-DPDCUOCVSA-L CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4ccccc43)c1-c1cc(-c3ccc(C)cc3)ccn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4ccccc43)c1-c1cc(-c3ccccc3)ccn->21.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c5ccccn->45)c4ccc5c(oc6ccccc65)c4-c3c2)cc1.Cc1ccc2-c3ccccc3[Ir]3(c4ccc5c(oc6ccccc65)c4-c4cc(C)c(C)cn->34)<-n2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3ccc4c(oc5ccccc54)c3-c2c1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4ccccc43)c1-c1cc(-c3ccc(C)cc3)ccn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccc3c(oc4ccccc43)c1-c1cc(-c3ccccc3)ccn->21.Cc1ccc(-c2ccn3->[Ir]4(c5ccccc5-c5ccccn->45)c4ccc5c(oc6ccccc65)c4-c3c2)cc1.Cc1ccc2-c3ccccc3[Ir]3(c4ccc5c(oc6ccccc65)c4-c4cc(C)c(C)cn->34)<-n2c1.Cc1ccn2->[Ir]3(c4ccccc4-c4ccc(C)cn->34)c3ccc4c(oc5ccccc54)c3-c2c1 IVROEOBEXNGVGF-DPDCUOCVSA-L 0.000 description 1
- MXPXWXQYNQCXAD-HEAUDDNOSA-M CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cc(C)cc(C)c3)ccn->21.CCc1cc2-c3ccccc3[Ir]<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]<-n2cc1-c1ccccc1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1cc(-c3cc(C)cc(C)c3)ccn->21.CCc1cc2-c3ccccc3[Ir]<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]3(c4ccccc4-c4ccccn->34)<-n2cc1-c1ccccc1.Cc1cc2-c3ccccc3[Ir]<-n2cc1-c1ccccc1 MXPXWXQYNQCXAD-HEAUDDNOSA-M 0.000 description 1
- JHCKJWWJKHAHQA-PMSWNOEESA-L CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1ccc(-c3cc(C)cc(C)c3)cn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1ccc(-c3ccccc3)cn->21.Cc1cc(C)c2-c3ccc(-c4ccccc4)cn3->[Ir]c2c1.Cc1cc(C)cc(-c2ccc3-c4ccccc4[Ir]<-n3c2)c1.c1ccc(-c2ccc3-c4ccccc4[Ir]<-n3c2)cc1 Chemical compound CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1ccc(-c3cc(C)cc(C)c3)cn->21.CC1/C=C(/C)O[Ir]2(<-O=1)c1ccccc1-c1ccc(-c3ccccc3)cn->21.Cc1cc(C)c2-c3ccc(-c4ccccc4)cn3->[Ir]c2c1.Cc1cc(C)cc(-c2ccc3-c4ccccc4[Ir]<-n3c2)c1.c1ccc(-c2ccc3-c4ccccc4[Ir]<-n3c2)cc1 JHCKJWWJKHAHQA-PMSWNOEESA-L 0.000 description 1
- PMVUUMAIJASOAY-GRGVBPCRSA-J CCC(C)(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(C(C)C)cc3ccn->21)C(C)(C)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(C(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)c1ccc2c3-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)<-n3ccc2c1.Cc1cc(C)c2[Ir]3(O/C(=C\C(=O->3)C(C)(C)C)C(C)(C)C)<-n3ccc4cc(C(C)C)ccc4c3-c2c1 Chemical compound CCC(C)(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(C(C)C)cc3ccn->21)C(C)(C)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(C(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)c1ccc2c3-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)<-n3ccc2c1.Cc1cc(C)c2[Ir]3(O/C(=C\C(=O->3)C(C)(C)C)C(C)(C)C)<-n3ccc4cc(C(C)C)ccc4c3-c2c1 PMVUUMAIJASOAY-GRGVBPCRSA-J 0.000 description 1
- QWDGJZLUCOXZIH-GSLZBRRESA-K CCC(C)(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21)C(C)(C)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4)C(C)(CC)CC Chemical compound CCC(C)(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21)C(C)(C)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc(-c4ccccc4)ccc3n->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1cc(CC(C)C)c3cc4c(cc3n->21)C(C)(C)c1ccccc1-4)C(C)(CC)CC QWDGJZLUCOXZIH-GSLZBRRESA-K 0.000 description 1
- VSDBYCVIZAEBEP-JZMAWXABSA-J CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(CC(C)(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(CC(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)c1ccc2ccn3->[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)c4c(C)cc(C)cc4-c3c2c1 Chemical compound CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(CC(C)(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(CC(C)C)ccc3ccn->21)C(C)(CC)CC.CCC(C)c1ccc2ccn3->[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)c4c(C)cc(C)cc4-c3c2c1 VSDBYCVIZAEBEP-JZMAWXABSA-J 0.000 description 1
- NKVOYMUKRGEXGR-JZMAWXABSA-J CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(CC(C)(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(CC(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3c(CC(C)C)cccc3n->21)C(C)(CC)CC.CCC(CC)c1ccc2c3-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)<-n3ccc2c1 Chemical compound CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(CC(C)(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3ccc(CC(C)C)cc3ccn->21)C(C)(CC)CC.CCC(C)(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1ccc3c(CC(C)C)cccc3n->21)C(C)(CC)CC.CCC(CC)c1ccc2c3-c4cc(C)cc(C)c4[Ir]4(O/C(=C\C(=O->4)C(C)(CC)CC)C(C)(CC)CC)<-n3ccc2c1 NKVOYMUKRGEXGR-JZMAWXABSA-J 0.000 description 1
- IYCXXABNDGYNPE-NWVJVCIQSA-J CCC(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(C)CC.CCC(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(CC)CC.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3ccc4cc(CC(C)C)ccc4c3-c2c1.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3ccc4ccc(CC(C)C)cc4c3-c2c1 Chemical compound CCC(C)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(C)CC.CCC(CC)C1/C=C(\O[Ir]2(<-O=1)c1c(C)cc(C)cc1-c1c3cc(C(C)C)ccc3ccn->21)C(CC)CC.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3ccc4cc(CC(C)C)ccc4c3-c2c1.Cc1cc(C)c2[Ir]3(O/C(=C\C(CC(C)C)=O->3)CC(C)C)<-n3ccc4ccc(CC(C)C)cc4c3-c2c1 IYCXXABNDGYNPE-NWVJVCIQSA-J 0.000 description 1
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- 238000006069 Suzuki reaction reaction Methods 0.000 description 1
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- VOUTWXOTABTBGZ-XETTWKNYSA-N c1ccc(-c2cc3c4c5c(cccc5n3-c3ccccc3)c3ccccc3c3cccc5c3c4c2n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4c5c(cccc5n3-c3ccccc3)c3ccccc3c3cccc5c3c4c2n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc(-c3ccccc3)c3ccccc3n2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccc4ccccc4c3nc2-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2cccc3oc4ccccc4c23)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2ccccc2)cc1 Chemical compound c1ccc(-c2cc3c4c5c(cccc5n3-c3ccccc3)c3ccccc3c3cccc5c3c4c2n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4c5c(cccc5n3-c3ccccc3)c3ccccc3c3cccc5c3c4c2n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc(-c3ccccc3)c3ccccc3n2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccc4ccccc4c3nc2-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2cccc3oc4ccccc4c23)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2ccccc2)cc1 VOUTWXOTABTBGZ-XETTWKNYSA-N 0.000 description 1
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- BEJGRIOUYVGWBC-VOAXVMKNSA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(-c3nc(-c7ccccc7)nc(-c7ccccc7)n3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cc(-c6ccccc6)cc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(-c3nc(-c7ccccc7)nc(-c7ccccc7)n3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cc(-c6ccccc6)cc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 BEJGRIOUYVGWBC-VOAXVMKNSA-N 0.000 description 1
- FVROLLKKVYHTQG-BRRSZFLUSA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2cccc(-c3cccc7oc8ccccc8c37)c2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cc(-c6ccccc6)cc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1.c1ccc(-c2nc3c(ccc4ccccc43)nc2-n2c3cc(-c4cccc5ccccc45)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cc(-c4ccc5ccccc5c4)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccn2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2cccc(-c3cccc7oc8ccccc8c37)c2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cc(-c6ccccc6)cc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1.c1ccc(-c2nc3c(ccc4ccccc43)nc2-n2c3cc(-c4cccc5ccccc45)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cc(-c4ccc5ccccc5c4)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccn2)cc1 FVROLLKKVYHTQG-BRRSZFLUSA-N 0.000 description 1
- AGZZNPHXSZYSJA-RULOURRISA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2cccc(-c3cccc7oc8ccccc8c37)c2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cc(-c4ccc5ccccc5c4)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccc(N(c3ccccc3)c3ccccc3)cc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2cccc(-c3cccc7oc8ccccc8c37)c2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2nc3ccccc3nc2-n2c3cc(-c4ccc5ccccc5c4)cc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2ccccc2)cc1 AGZZNPHXSZYSJA-RULOURRISA-N 0.000 description 1
- NJTXAUJDOXWOFC-ZRVJXXBRSA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cccc6c7ccccc7c7cc(-c8ccccc8)cc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cccc6c7ccccc7c7cc(-c8ccccc8)cc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 NJTXAUJDOXWOFC-ZRVJXXBRSA-N 0.000 description 1
- XECVCIPLJSYLKO-IJIMOUFISA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cccc6c7ccccc7c7cc(-c8ccccc8)cc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccccc4)n3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2cccc(-c3cccc(-n4c5cccc6c7ccccc7c7cc(-c8ccccc8)cc8c7c7c(c65)c4ccc7n8-c4ccccc4)c3)c2)cc1 XECVCIPLJSYLKO-IJIMOUFISA-N 0.000 description 1
- BYXOZESJFMUXLN-KWHFSLDESA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccccc3nc2-c2ccccc2)c6ccc4n5-c2ccccc2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2ccc(N(c3ccccc3)c3ccccc3)cc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2cccc(-c3cccc4oc5ccccc5c34)c2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccccc3nc2-c2ccccc2)c6ccc4n5-c2ccccc2)cc1 BYXOZESJFMUXLN-KWHFSLDESA-N 0.000 description 1
- ACFRHZVKKMZUDB-BKKWFREZSA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc(-c3ccccc3)c3ccccc3n2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccc4ccccc4c3nc2-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2cccc3oc4ccccc4c23)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc(-c3ccccc3)c3ccccc3n2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccc4ccccc4c3nc2-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2ccccc2)c6ccc4n5-c2nc3ccccc3nc2-c2cccc3oc4ccccc4c23)cc1 ACFRHZVKKMZUDB-BKKWFREZSA-N 0.000 description 1
- UGUFUNMMSQLYBT-BKKWFREZSA-N c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc(-c3ccccc3)c3ccccc3n2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccc7ccccc7c3nc2-c2ccccc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccccc3nc2-c2cccc3oc7ccccc7c23)c6ccc4n5-c2ccccc2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc(-c3ccccc3)c3ccccc3n2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccc7ccccc7c3nc2-c2ccccc2)c6ccc4n5-c2ccccc2)cc1.c1ccc(-c2cc3c4ccccc4c4cccc5c4c4c6c3c(c2)n(-c2nc3ccccc3nc2-c2cccc3oc7ccccc7c23)c6ccc4n5-c2ccccc2)cc1 UGUFUNMMSQLYBT-BKKWFREZSA-N 0.000 description 1
- VWTGGDFSAMDRAK-UQJBJZBGSA-N c1ccc(-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c2)n7-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(c3)c3cccc5oc6ccc7c(c6c53)c3c4cccc3n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6ccccc6c6cccc7oc8c(-c9ccccc9)cc3c(c8c76)c54)n2)cc1 Chemical compound c1ccc(-c2cc3c4ccccc4c4cccc5oc6ccc7c(c6c54)c3c(c2)n7-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(c3)c3cccc5oc6ccc7c(c6c53)c3c4cccc3n7-c3ccccc3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-n3c4cccc5c6ccccc6c6cccc7oc8c(-c9ccccc9)cc3c(c8c76)c54)n2)cc1 VWTGGDFSAMDRAK-UQJBJZBGSA-N 0.000 description 1
- ZZIUPOHBRIGRLM-UHFFFAOYSA-N c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7c(nc(-c8ccccc8)n7-c7ccccc7)c65)c4)n3)cc2)cc1.c1ccc(-c2cccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)c2)cc1.c1ccc(-c2nc3ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)cc(-c7ccc8ccccc8c7)n6)ccc5c4c3o2)cc1 Chemical compound c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7c(nc(-c8ccccc8)n7-c7ccccc7)c65)c4)n3)cc2)cc1.c1ccc(-c2cccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)c2)cc1.c1ccc(-c2nc3ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)cc(-c7ccc8ccccc8c7)n6)ccc5c4c3o2)cc1 ZZIUPOHBRIGRLM-UHFFFAOYSA-N 0.000 description 1
- NMAGZESUQNWSPK-UHFFFAOYSA-N c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)oc6c54)c3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)sc6c54)c3)n2)cc1 Chemical compound c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)oc6c54)c3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)sc6c54)c3)n2)cc1 NMAGZESUQNWSPK-UHFFFAOYSA-N 0.000 description 1
- YDXXVRJNUFPGJA-UHFFFAOYSA-N c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)oc6c54)c3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)sc6c54)c3)n2)cc1.c1ccc(-c2nc3ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)nc(-c7cccc8ccccc78)n6)ccc5c4c3s2)cc1 Chemical compound c1ccc(-c2ccc(-c3cc(-c4ccccc4)nc(-c4ccc5c(ccc6ccc7oc(-c8ccccc8)nc7c65)c4)n3)cc2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)oc6c54)c3)n2)cc1.c1ccc(-c2nc(-c3ccccc3)nc(-c3ccc4c(ccc5ccc6nc(-c7ccccc7)sc6c54)c3)n2)cc1.c1ccc(-c2nc3ccc4ccc5cc(-c6nc(-c7ccc8ccccc8c7)nc(-c7cccc8ccccc78)n6)ccc5c4c3s2)cc1 YDXXVRJNUFPGJA-UHFFFAOYSA-N 0.000 description 1
- CQODIOFPNHYLRC-ZURMSOFHSA-N c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cn2)cc1.c1ccc(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc(-c3ccc4ccccc4c3)nc(-c3ccc4ccccc4c3)n2)cc1 Chemical compound c1ccc(-c2ccc(-c3nc(-c4ccc(-c5ccccc5)cc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cc2)cc1.c1ccc(-c2ccc(-c3nc(-c4ccccc4)nc(-n4c5cccc6c7ccccc7c7cccc8c7c7c(c65)c4ccc7n8-c4ccccc4)n3)cn2)cc1.c1ccc(-n2c3cccc4c5ccccc5c5cccc6c5c5c(c43)c2ccc5n6-c2nc(-c3ccc4ccccc4c3)nc(-c3ccc4ccccc4c3)n2)cc1 CQODIOFPNHYLRC-ZURMSOFHSA-N 0.000 description 1
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- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000005558 triazinylene group Chemical group 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- 238000007738 vacuum evaporation Methods 0.000 description 1
- 238000002061 vacuum sublimation Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
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Definitions
- the present disclosure relates to a plurality of host materials and an organic electroluminescent device comprising the same.
- OLED organic electroluminescent device
- Korean Patent Application Laying-Open No. 2020-0000329 discloses a plurality of host materials comprising a compound having a heteroaryl bonded to a phenanthrene moiety and a compound having a heteroaryl bonded to a carbazole moiety.
- said reference does not specifically disclose a specific combination of host materials claimed in the present disclosure.
- development of a light-emitting material having improved performances, for example, improved driving voltage, luminous efficiency, power efficiency and/or lifetime property as compared with combinations of specific compounds conventionally disclosed is still required.
- the objective of the present disclosure is to provide an organic electroluminescent device having low driving voltage, high luminous efficiency, high power efficiency and/or excellent lifetime property by comprising a plurality of host materials including a specific combination of compounds.
- the present inventors found that the above objective can be achieved by a plurality of host materials comprising at least one first host compound and at least second host compound, wherein the first host compound is represented by the following formula 1, and the second host compound is represented by the following formula 2:
- B 1 to B 7 each independently, are not present, or represent a substituted or unsubstituted (C5-C20) ring, in which carbon atoms of the ring may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur, with the proviso that at least five of B 1 to B 7 are present, and adjacent rings of B 1 to B 7 are fused with each other;
- Y represents —N(L 1 -(Ar 1 ) n )—, —O—, —S—, or —C(R 1 )(R 2 )—;
- L 1 represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene;
- Ar 1 represents a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or —N(R 3 )(R 4 );
- R 1 to R 4 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or may be linked to an adjacent substituent to form a ring(s); and
- n an integer of 1 or 2, where if n is 2, each of Ar 1 may be the same or different;
- X represents —N ⁇ , —NR 35 —, —O— or —S—;
- Z represents —N ⁇ , —NR 36 —, —O— or —S—, where if X represents —N ⁇ , Z represents —NR 36 —, —O— or —S—, and if X represents —NR 35 —, Z represents —N ⁇ , —O— or —S—;
- HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl
- R 31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl;
- R 32 to R 34 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6
- R 35 and R 36 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6
- L 2 and L 3 each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
- Ar 2 and Ar 3 each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted fused ring group of a (C3-C30) aliphatic ring(s) and a (C6-C30) aromatic ring(s), a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl; and
- a′ represents 1, b′ and c′, each independently, represent an integer of 1 or 2
- d′ represents an integer of 1 to 4, where if each of b′, c′ and d′ is an integer of 2 or more, each of R 32 to each of R 34 may be the same or different.
- an organic electroluminescent device having lower driving voltage, higher luminous efficiency, higher power efficiency and/or better lifetime property compared to conventional organic electroluminescent devices can be provided, and it is possible to produce a display system or a lighting system using the same.
- organic electroluminescent material in the present disclosure means a material that may be used in an organic electroluminescent device, and may comprise at least one compound.
- the organic electroluminescent material may be comprised in any layer constituting an organic electroluminescent device as necessary.
- the organic electroluminescent material may be a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting auxiliary material, an electron blocking material, a light-emitting material (including a host material and a dopant material), an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc.
- a plurality of organic electroluminescent materials in the present disclosure means an organic electroluminescent material comprising a combination of at least two compounds, which may be comprised in any layer constituting an organic electroluminescent device. It may mean both a material before being comprised in an organic electroluminescent device (for example, before vapor deposition) and a material after being comprised in an organic electroluminescent device (for example, after vapor deposition).
- a plurality of organic electroluminescent materials of the present disclosure may be a combination of at least two compounds, which may be comprised in at least one layer of a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer, an electron blocking layer, a light-emitting layer, an electron buffer layer, a hole blocking layer, an electron transport layer, and an electron injection layer.
- the at least two compounds may be comprised in the same layer or different layers, and may be mixture-evaporated or co-evaporated, or may be individually evaporated.
- a plurality of host materials in the present disclosure means an organic electroluminescent material comprising a combination of at least two host materials. It may mean both a material before being comprised in an organic electroluminescent device (for example, before vapor deposition) and a material after being comprised in an organic electroluminescent device (for example, after vapor deposition).
- the plurality of host materials of the present disclosure may be comprised in any light-emitting layer constituting an organic electroluminescent device.
- At least two compounds comprised in the plurality of host materials of the present disclosure may be comprised together in one light-emitting layer or may respectively be comprised in different light-emitting layers.
- at least two host materials are comprised in one layer, for example, they may be mixture-evaporated to form a layer or may be separately co-evaporated at the same time to form a layer.
- (C1-C30)alkyl is meant to be a linear or branched alkyl having 1 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 1 to 20, and more preferably 1 to 10.
- the above alkyl may include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, etc.
- (C2-C30)alkenyl is meant to be a linear or branched alkenyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, and more preferably 2 to 10.
- the above alkenyl may include vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylbut-2-enyl, etc.
- (C2-C30)alkynyl is meant to be a linear or branched alkynyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, and more preferably 2 to 10.
- the above alkynyl may include ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methylpent-2-ynyl, etc.
- (C3-C30)cycloalkyl is meant to be a mono- or polycyclic hydrocarbon having 3 to 30 ring backbone carbon atoms, in which the number of carbon atoms is preferably 3 to 20, and more preferably 3 to 7.
- the above cycloalkyl may include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
- (3- to 7-membered)heterocycloalkyl is meant to be a cycloalkyl having 3 to 7, preferably 5 to 7, ring backbone atoms, and including at least one heteroatom selected from the group consisting of B, N, O, S, Si, and P, and preferably the group consisting of O, S, and N.
- the above heterocycloalkyl may include tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc.
- (C6-C30)aryl(ene) is meant to be a monocyclic or fused ring radical derived from an aromatic hydrocarbon having 6 to 30 ring backbone carbon atoms, in which the number of the ring backbone carbon atoms is preferably 6 to 25, and more preferably 6 to 18.
- the above aryl(ene) may be partially saturated, and may comprise a spiro structure.
- the above aryl may include phenyl, biphenyl, terphenyl, naphthyl, binaphthyl, phenylnaphthyl, naphthylphenyl, phenylterphenyl, fluorenyl, phenylfluorenyl, benzofluorenyl, dibenzofluorenyl, phenanthrenyl, phenylphenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, spirobifluorenyl, azulenyl, etc.
- the above aryl may include phenyl, 1-naphthyl, 2-naphthyl, 1-anthryl, 2-anthryl, 9-anthryl, benzanthryl, 1-phenanthryl, 2-phenanthryl, 3-phenanthryl, 4-phenanthryl, 9-phenanthryl, naphthacenyl, pyrenyl, 1-chrysenyl, 2-chrysenyl, 3-chrysenyl, 4-chrysenyl, 5-chrysenyl, 6-chrysenyl, benzo[c]phenanthryl, benzo[g]chrysenyl, 1-triphenylenyl, 2-triphenylenyl, 3-triphenylenyl, 4-triphenylenyl, 1-fluorenyl, 2-fluorenyl, 3-fluorenyl, 4-fluorenyl, 9-fluorenyl, benzo[a]fluorenyl, benzo[a
- (3- to 30-membered)heteroaryl” or “(3- to 50-membered)heteroaryl” is meant to be an aryl having 3 to 30 ring backbone atoms or 3 to 50 ring backbone atoms, and including at least one, preferably 1 to 4 heteroatoms selected from the group consisting of B, N, O, S, Si, and P.
- the above heteroaryl may be a monocyclic ring, or a fused ring condensed with at least one benzene ring; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and may comprise a spiro structure.
- the above heteroaryl may include a monocyclic ring-type heteroaryl such as furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, and pyridazinyl, and a fused ring-type heteroaryl such as benzofuranyl, benzothiophenyl, isobenzofuranyl, dibenzofuranyl, dibenzothiophenyl, naphthobenzofuranyl, naphthobenzothiophenyl, benzimidazolyl, benzothiazolyl, benzoisothiazolyl, be
- the above heteroaryl may include 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, pyrazinyl, 2-pyridinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 6-pyrimidinyl, 1,2,3-triazin-4-yl, 1,2,4-triazin-3-yl, 1,3,5-triazin-2-yl, 1-imidazolyl, 2-imidazolyl, 1-pyrazolyl, 1-indolidinyl, 2-indolidinyl, 3-indolidinyl, 5-indolidinyl, 6-indolidinyl, 7-indolidinyl, 8-indolidinyl, 2-imidazopyridinyl, 3-imidazopyridinyl, 5-imidazopyridinyl, 6-imidazopyridinyl, 7-imidazopyridinyl, 8-imidazopyridinyl, 3-pyridinyl, 5-imidazo
- ortho indicates that two substituents are adjacent to each other, and for example, when two substituents in a benzene derivative occupy positions 1 and 2, it is called an ortho position.
- Meta indicates that two substituents are at positions 1 and 3, and for example, when two substituents in a benzene derivative occupy positions 1 and 3, it is called a meta position.
- Para indicates that two substituents are at positions 1 and 4, and for example, when two substituents in a benzene derivative occupy positions 1 and 4, it is called a para position.
- substituted in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or another functional group, i.e., a substituent.
- the substituents are at least one selected from the group consisting of deuterium; a (C1-C20)alkyl; a (3- to 30-membered)heteroaryl unsubstituted or substituted with at least one of a (C1-C20)alkyl(s) and a (C6-C25)aryl(s); a (C6-C25)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C20)alkyl(s), a (3- to 30-membered)heteroaryl(s), and a di(C6-C25)arylamino(s); and a mono- or di-(C6-C25)arylamino.
- the substituents are at least one selected from the group consisting of deuterium; a (C1-C10)alkyl; a (5- to 26-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s); a (C6-C20)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C10)alkyl(s), a (5- to 26-membered)heteroaryl(s), and a di(C6-C18)arylamino(s); and a di(C6-C18)arylamino.
- the substituents may be at least one selected from the group consisting of deuterium; a methyl; a phenyl unsubstituted or substituted with at least one of deuterium, a 26-membered heteroaryl(s), and a diphenylamino(s); a naphthyl; a biphenyl; a naphthylphenyl; a phenylnaphthyl; a phenanthrenyl; a dimethylfluorenyl; a dimethylbenzofluorenyl; a terphenyl; a triphenylenyl; a pyridyl unsubstituted or substituted with a phenyl(s); a triazinyl substituted with a phenyl(s); a dibenzofuranyl; a dibenzothiophenyl; a benzonaphthothiophenyl; a carb
- the ring may be a substituted or unsubstituted, mono- or polycyclic, (3- to 30-membered) alicyclic or aromatic ring, or the combination thereof, which two or more adjacent substituents are linked to form.
- the formed ring may contain at least one heteroatom selected from B, N, O, S, Si, and P, preferably at least one heteroatom selected from N, O, and S.
- the number of the ring backbone atoms is 5 to 20.
- the number of the ring backbone atoms is 5 to 15.
- heteroaryl and heteroarylene may, each independently, contain at least one heteroatom selected from B, N, O, S, Si, and P.
- the heteroatom may be bonded to at least one selected from the group consisting of hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubsti
- the plurality of host materials according to one embodiment of the present disclosure comprises a first host material comprising the compound represented by formula 1 and a second host material comprising the compound represented by formula 2, and may be comprised in a light-emitting layer of an organic electroluminescent device according to one embodiment of the present disclosure.
- B 1 to B 7 each independently, are not present, or represent a substituted or unsubstituted (C5-C20) ring, preferably a substituted or unsubstituted (C5-C13) ring, in which carbon atoms of the ring may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur, with the proviso that at least five of B 1 to B 7 are present, and adjacent rings of B 1 to B 7 are fused with each other.
- an adjacent ring may not be present, or may be a C5 ring, carbon atoms of which may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur.
- B 1 to B 7 each independently, are not present, or represent a substituted or unsubstituted benzene ring, a substituted or unsubstituted naphthalene ring, a substituted or unsubstituted pyrrole ring, a substituted or unsubstituted furan ring, a substituted or unsubstituted thiophene ring, a substituted or unsubstituted cyclopentadiene ring, a substituted or unsubstituted fluorene ring, a substituted or unsubstituted pyridine ring, or a substituted or unsubstituted dibenzofuran ring.
- B 1 to B 7 each independently, may not be present, or may represent a benzene ring unsubstituted or substituted with a phenyl(s), a naphthyl(s) and/or a diphenyltriazinyl(s); a naphthalene ring; a cyclopentadiene ring unsubstituted or substituted with a methyl(s); a fluorene ring substituted with a methyl(s); a pyrrole ring substituted with an unsubstituted phenyl(s), a phenyl(s) substituted with at least one deuterium, a biphenyl(s) and/or a pyridiyl(s); a furan ring; a thiophene ring; a pyridine ring; or a dibenzofuran ring unsubstituted or substituted with a diphenyltriaziny
- Y represents —N(L 1 -(Ar 1 ) n )—, —O—, —S—, or —C(R 1 )(R 2 )—. According to one embodiment of the present disclosure, Y represents —N(L 1 -(Ar 1 ) n )—.
- L 1 represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene.
- L 1 represents a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene.
- L 1 represents a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 25-membered)heteroarylene.
- L 1 may be a single bond, a phenylene, a naphthylene, a biphenylene, a pyridylene, a pyrimidinylene, a triazinylene, a quinoxalinylene, a quinazolinylene, a dibenzofuranylene, a benzofuropyrimidinylene, a benzothienopyrimidinylene, an indolopyrimidinylene, or a benzoquinoxalinylene.
- Ar 1 represents a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or —N(R 3 )(R 4 ). According to one embodiment of the present disclosure, Ar 1 represents a substituted or unsubstituted (C6-C25)aryl, a substituted or unsubstituted (5- to 25-membered)heteroaryl, or —N(R 3 )(R 4 ).
- Ar 1 represents a (C6-C25)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C6)alkyl(s), and a (3- to 30-membered)heteroaryl(s); a (5- to 25-membered)heteroaryl unsubstituted or substituted with at least one of deuterium, a (C6-C18)aryl(s), and a (3- to 30-membered)heteroaryl(s); or —N(R 3 )(R 4 ).
- Ar 1 may be an unsubstituted phenyl, a phenyl substituted with at least one deuterium, a phenyl substituted with a 26-membered heteroaryl(s), a naphthyl, a biphenyl, a fluorenyl substituted with a methyl(s), a spirobifluorenyl, a terphenyl, a triphenylenyl, a pyridyl unsubstituted and substituted with a phenyl(s), a pyrmidinyl substituted with a phenyl(s), a substituted triazinyl, a substituted quinoxalinyl, a substituted quinazolinyl, a benzoquinoxalinyl substituted with a phenyl(s), a carbazolyl, a dibenzofuranyl, a dibenzothiophenyl, a benzofuropyr
- the substituents of the substituted triazinyl, the substituted quinoxalinyl, and the substituted quinazolinyl may be at least one selected from the group consisting of a phenyl unsubstituted or substituted with at least one of deuterium and a 26-membered heteroaryl(s), a naphthyl, a biphenyl, a terphenyl, a dibenzofuranyl, a pyridyl substituted with a phenyl(s), a dimethylfluorenyl, and a dibenzothiophenyl.
- R 1 to R 4 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or may be linked to an adjacent substituent to form a ring(s).
- R 1 to R 4 each independently, represent hydrogen, deuterium, a substituted or unsubstituted (C1-C20)alkyl, or a substituted or unsubstituted (C6-C25)aryl.
- R 1 and R 2 each independently, represent an unsubstituted (C1-C10)alkyl
- R 3 and R 4 each independently, represent an unsubstituted (C6-C18)aryl.
- R 1 and R 2 may be a methyl
- R 3 and R 4 may be a phenyl.
- n an integer of 1 or 2, where if n is 2, each of Ar 1 may be the same or different
- Formula 1 may be represented by at least one of the following formulas 1-1 to 1-4.
- Y 1 , Y 2 , Y 3 , and Y 4 are the same as the definition of Y in formula 1, where if a plurality of Ar 1 's are present, each of Ar 1 may be the same or different;
- X 1 to X 12 each independently, represent —N ⁇ or —C(R a ) ⁇ ;
- R a each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or adjacent R a 's may be linked to each other to form a ring(s), where if a plurality of R a
- R a represents hydrogen, deuterium, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl; or adjacent R a 's may be linked to each other to form a ring(s).
- R a represents hydrogen, an unsubstituted (C6-C18)aryl, or a (5- to 25-membered)heteroaryl substituted with a (C6-C18)aryl(s); or adjacent R a 's may be linked to each other to form a benzene ring(s), an indene ring(s) substituted with a methyl(s), or a benzofuran ring(s) unsubstituted or substituted with a diphenyltriazinyl(s).
- At least one of Ar 1 (s) and R a (s), each independently, may be at least one selected from those listed in the following group 1.
- D1 and D2 each independently, represent a benzene ring or a naphthalene ring;
- X 21 represents O, S, NR 5 , or C(R 6 )(R 7 );
- X 22 each independently, represents CR or N, with the proviso that at least one of X 22 represents N;
- X 23 each independently, represents CR 9 or N;
- L 11 to L 18 each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
- R 11 to R 21 and R 5 to R 9 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3
- D1 may be a benzene ring
- X 21 may be O, S, or C(R 6 )(R 7 );
- L 11 to L 18 each independently, may be a single bond;
- R 11 to R 21 and R 5 to R 9 each independently, may be hydrogen, deuterium, a substituted or unsubstituted (C1-C20)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl, or may be linked to an adjacent substituent to form a ring(s);
- aa, bb, ff, and gg each independently, may be an integer of 1 to 5
- cc, dd, and ee each independently, may be an integer of 1 to 4.
- R 11 may be hydrogen, deuterium, a phenyl, a biphenyl, or a 26-membered heteroaryl
- R 12 may be hydrogen, or adjacent R 12 's may be linked to each other to form a benzene ring(s)
- R 13 , R 18 , and R 17 may be hydrogen
- R 18 and R 19 may be hydrogen or a phenyl
- R 21 may be phenyl
- R 6 and R 7 may be a methyl
- R 8 may be hydrogen, a phenyl, a biphenyl, a dibenzofuranyl, or a dibenzothiophenyl, or adjacent R 8 's may be linked to each other to form a benzene ring(s)
- R 9 may be hydrogen, an unsubstituted phenyl, a phenyl substituted with at least one deuterium, a phenyl substituted with a 26-membered heteroaryl(s), a
- At least one of Ar 1 (s) and R a (s), each independently, may be at least one selected from those listed in the following group 2.
- L represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene; and A 1 to A 3 , each independently, represent a substituted or unsubstituted (C1-C30)alkyl, or a substituted or unsubstituted (C6-C30)aryl.
- L represents a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (3- to 25-membered)heteroarylene; and A 1 to A 3 , each independently, represent a substituted or unsubstituted (C1-C20)alkyl, or a substituted or unsubstituted (C6-C25)aryl.
- a 1 and A 2 may be the same or different.
- a 1 and A 2 each independently, may be a methyl or a phenyl.
- At least one of Ar 1 (s) and R a (s), each independently, may be at least one selected from those listed in the following group 3.
- formula 2 may be represented by at least one selected from the following formulas 2-1 to 2-8.
- X, Z, HAr, R 31 to R 36 , L 2 and a′ to d′ are as defined in formula 2;
- Z 1 to Z 5 and Z 11 to Z 17 each independently, represent N or CR 37 ;
- R 37 each independently, is the same as the definition of R 32 of formula 2.
- R 37 each independently, represents hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl.
- R 37 each independently, represents hydrogen; deuterium; a (C6-C18)aryl unsubstituted or substituted with at least one of a (C1-C10)alkyl(s) and a di(C6-C18)arylamino(s); or a (5- to 20-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s).
- R 37 may be hydrogen, a phenyl unsubstituted or substituted with a diphenylamino(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a dibenzothiophenyl, a dibenzofuranyl, a benzonaphthothiophenyl, a phenylcarbazolyl, or a phenylbenzocarbazolyl.
- X represents —N ⁇ , —NR 35 —, —O— or —S—
- Z represents —N ⁇ , —NR 36 —, —O— or —S—
- X represents —N ⁇ , —NR 35 —, —O— or —S—
- Z represents —N ⁇ , —NR 36 —, —O— or —S—
- R 35 and R 36 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6
- R 35 and R 36 each independently, represent a substituted or unsubstituted (C1-C20)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl.
- R 35 and R 36 each independently, represent an unsubstituted (C6-C18)aryl.
- R 35 and R 36 may be a phenyl.
- HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl. According to one embodiment of the present disclosure, HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl containing a nitrogen atom(s). According to another embodiment of the present disclosure, HAr represents a substituted or unsubstituted (5- to 25-membered)heteroaryl containing a nitrogen atom(s).
- HAr represents a (5- to 20-membered)heteroaryl containing a nitrogen atom(s), substituted with a (5- to 25-membered)heteroaryl(s) and/or a (C6-C25)aryl(s).
- HAr may be a substituted or unsubstituted triazinyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted benzoquinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted benzoquinoxalinyl, a substituted or unsubstituted quinolyl, a substituted or unsubstituted benzoquinolyl, a substituted or unsubstituted isoquinolyl, a substituted or unsubstituted benzoisoquinolyl, a substituted or unsubstituted triazolyl, a substituted or unsubstituted pyrazolyl, a substituted or unsubstituted naphth
- HAr may be a substituted triazinyl, a substituted pyrimidinyl, a substituted quinoxalinyl, a substituted quinazolinyl, or a substituted naphthyridinyl.
- the substituents of the substituted triazinyl, the substituted pyrimidinyl, the substituted quinoxalinyl, the substituted quinazolinyl, and the substituted naphthyridinyl may be at least one of a phenyl unsubstituted or substituted with a diphenylamino(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a dibenzothiophenyl, a dibenzofuranyl, a benzonaphthothiophenyl, a phenylcarbazolyl, and a phenylbenzocarbazolyl.
- R 31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl. According to one embodiment of the present disclosure, R 31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl.
- R 31 represents a (C6-C29)aryl unsubstituted or substituted with at least one of a (C1-C10)alkyl(s) and a (C6-C18)aryl(s); or a (5- to 25-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s).
- R 31 may be a phenyl, a naphthyl, a phenylnaphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a spirobifluorenyl, a spiro[fluoren-benzofluoren]yl, a phenylcarbazolyl, a phenylbenzocarbazolyl, a dibenzofuranyl, or a dibenzothiophenyl.
- R 32 to R 34 each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri
- L 2 and L 3 each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene.
- L 2 and L 3 each independently, represent a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (5- to 25-membered)heteroarylene.
- L 2 and L 3 each independently, represent a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 20-membered)heteroarylene.
- L 2 and L 3 each independently, may be a single bond, a phenylene, or a pyridylene.
- Ar 2 and Ar 3 each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted fused ring group of a (C3-C30) aliphatic ring(s) and a (C6-C30) aromatic ring(s), a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl.
- a′ represents 1, b′ and c′, each independently, represent an integer of 1 or 2
- d′ represents an integer of 1 to 4, where if each of b′, c′ and d′ is an integer of 2 or more, each of R 32 to each of R 34 may be the same or different.
- the compound represented by formula 1 may be at least one selected from the following compounds, but is not limited thereto.
- the compound represented by formula 2 may be at least one selected from the following compounds, but is not limited thereto.
- the combination of at least one of compounds C-1 to C-300 and at least one of compounds C2-1 to C2-125 may be used in an organic electroluminescent device.
- the compound represented by formula 1 of the present disclosure may be produced by a synthetic method known to one skilled in the art, and for example, according to the following reaction schemes 1 to 4, but is not limited thereto:
- the compound represented by formula 2 of the present disclosure may be produced by a synthetic method known to one skilled in the art, and for example, according to the methods disclosed in Korean Patent Application Laying-Open No. 2020-0000329 (published on Jan. 2, 2020), etc.
- non-deuterated analogues of the compound represented by formula 2 can be prepared by known coupling and substitution reactions.
- the non-deuterated analogues may be prepared in a similar manner by using deuterated precursor materials, or more generally may be prepared by treating the non-deuterated compound with a deuterated solvent or D6-benzene in the presence of an H/D exchange catalyst such as a Lewis acid, e.g., aluminum trichloride or ethyl aluminum chloride, a trifluoromethanesulfonic acid, or a trifluoromethanesulfonic acid-D.
- an H/D exchange catalyst such as a Lewis acid, e.g., aluminum trichloride or ethyl aluminum chloride, a trifluoromethanesulfonic acid, or a trifluoromethanesulfonic acid-D.
- the degree of deuteration can be controlled by changing the reaction conditions such as the reaction temperature.
- the organic electroluminescent device may comprise an anode, a cathode, and at least one organic layer between the anode and cathode in which the organic layer may comprise a plurality of organic electroluminescent materials, including the compound represented by formula 1 as the first organic electroluminescent material, and the compound represented by formula 2 as the second organic electroluminescent material.
- the organic electroluminescent device according to the present disclosure may comprise an anode, a cathode, and at least one light-emitting layer between the anode and cathode in which the light-emitting layer may comprise the compound represented by formula 1 and the compound represented by formula 2.
- the light-emitting layer includes a host and a dopant, in which the host includes a plurality of host materials and the compound represented by formula 1 may be included as the first host compound of the plurality of host materials, and the compound represented by formula 2 may be included as the second host compound of the plurality of host materials.
- the weight ratio of the first host compound and the second host compound is about 1:99 to about 99:1, preferably about 10:90 to about 90:10, more preferably about 30:70 to about 70:30, even more preferably about 40:60 to about 60:40, and most preferably about 50:50.
- the light-emitting layer is a layer from which light is emitted, and may be a single layer or a multi-layer of which two or more layers are stacked. All of the first host material and the second host material may be included in one layer, or the first host material and the second host material may be included in respective different light-emitting layers. According to one embodiment of the present disclosure, the doping concentration of the dopant compound with respect to the host compound in the light-emitting layer may be less than 20 wt %.
- the organic electroluminescent device of the present disclosure may further comprise at least one layer selected from a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer, an electron transport layer, an electron injection layer, an interlayer, an electron buffer layer, a hole blocking layer, and an electron blocking layer.
- the organic electroluminescent device of the present disclosure may further comprise an amine-based compound besides the plurality of host materials of the present disclosure as at least one of a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting material, a light-emitting auxiliary material, and an electron blocking material.
- the organic electroluminescent device of the present disclosure may further comprise an azine-based compound besides the plurality of host materials of the present disclosure as at least one of an electron transport material, an electron injection material, an electron buffer material, and a hole blocking material.
- the plurality of host materials according to the present disclosure may be used as light-emitting materials for a white organic light-emitting device.
- the white organic light-emitting device has been suggested to have various structures such as a parallel arrangement (side-by-side) method, a stacking method, or color conversion material (CCM) method, etc., according to the arrangement of R (red), G (green) or YG (yellowish green), B (blue) light-emitting units.
- the plurality of host materials according to one embodiment of the present disclosure may also be used in an organic electroluminescent device comprising a quantum dot (QD).
- QD quantum dot
- a hole injection layer, a hole transport layer, an electron blocking layer, or a combination thereof can be used between the anode and the light-emitting layer.
- the hole injection layer may be multilayers in order to lower the hole injection barrier (or hole injection voltage) from the anode to the hole transport layer or the electron blocking layer, wherein each of the multilayers may use two compounds simultaneously. Further, the hole injection layer may be doped with a p-dopant.
- the electron blocking layer may be placed between the hole transport layer (or hole injection layer) and the light-emitting layer, and may block overflowing electrons from the light-emitting layer and confine the excitons in the light-emitting layer to prevent light leakage.
- the hole transport layer or the electron blocking layer may also be multilayers, wherein each of the multilayers may use a plurality of compounds.
- An electron buffer layer, a hole blocking layer, an electron transport layer, an electron injection layer, or a combination thereof can be used between the light-emitting layer and the cathode.
- the electron buffer layer may be multilayers in order to control the electron injection and improve the interfacial properties between the light-emitting layer and the electron injection layer, wherein each of the multilayers may use two compounds simultaneously.
- the hole blocking layer or the electron transport layer may also be multilayers, wherein each of the multilayers may use a plurality of compounds.
- the electron injection layer may be doped with an n-dopant.
- the dopant comprised in the organic electroluminescent device of the present disclosure may be at least one phosphorescent or fluorescent dopant, and is preferably phosphorescent dopant.
- the phosphorescent dopant material applied to the organic electroluminescent device of the present disclosure is not particularly limited, but may be preferably selected from the metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), more preferably selected from ortho-metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), and even more preferably ortho-metallated iridium complex compounds.
- the dopant comprised in the organic electroluminescent device of the present disclosure may comprise a compound represented by the following formula 101, but is not limited thereto.
- L′ is selected from the following structures 1 to 3:
- R 100 to R 103 each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a cyano, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C1-C30)alkoxy; or may be linked to an adjacent substituent to form a ring(s), e.g., a substituted or unsubstituted, quinoline, isoquinoline, benzofuropyridine, benzothienopyridine, indenopyridine, benzofuroquinoline, benzothienoquinoline, or indenoquinoline, together with pyridine;
- R 104 to R 107 each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a cyano, or a substituted or unsubstituted (C1-C30)alkoxy; or may be linked to an adjacent substituent to form a ring(s), e.g., a substituted or unsubstituted, naphthalene, fluorene, dibenzothiophene, dibenzofuran, indenopyridine, benzofuropyridine, or benzothienopyridine, together with benzene;
- R 201 to R 220 each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, or a substituted or unsubstituted (C6-C30)aryl; or may be linked to an adjacent substituent to form a ring(s); and
- s represents an integer of 1 to 3.
- dopant compound is as follows, but are not limited thereto.
- dry film-forming methods such as vacuum evaporation, sputtering, plasma, ion plating methods, etc.
- wet film-forming methods such as ink jet printing, nozzle printing, slot coating, spin coating, dip coating, flow coating methods, etc.
- a thin film can be formed by dissolving or diffusing materials forming each layer into any suitable solvent such as ethanol, chloroform, tetrahydrofuran, dioxane, etc.
- the solvent can be any solvent where the materials forming each layer can be dissolved or diffused, and where there are no problems in film-formation capability.
- the first and the second host compounds of the present disclosure may be film-formed by the above-listed methods, commonly by a co-evaporation process or a mixture-evaporation process.
- the co-evaporation is a mixed deposition method in which two or more materials are placed in a respective individual crucible source and a current is applied to both cells at the same time to evaporate the materials.
- the mixture-evaporation is a mixed deposition method in which two or more materials are mixed in one crucible source before evaporating them, and a current is applied to the cell to evaporate the materials.
- the two host compounds may individually form films.
- the second host compound may be deposited after depositing the first host compound.
- the present disclosure may provide a display device by using the plurality of host materials including the compound represented by formula 1 and the compound represented by formula 2. That is, by using the plurality of host materials of the present disclosure, it is possible to manufacture a display system or a lighting system. Specifically, by using the plurality of host materials of the present disclosure, a display system, for example, for white organic light emitting devices, smart phones, tablets, notebooks, PCs, TVs, or cars; or a lighting system, for example an outdoor or indoor lighting system, can be produced.
- reaction mixture was cooled to room temperature, filtered by cellite with methylene chloride (MC), distilled under reduced pressure, and then separated by column chromatography with methylene chloride/hexane (MC/Hex) to obtain compound C2-86 (2.7 g, yield: 57%).
- MC methylene chloride
- OLEDs according to the present disclosure were produced.
- a transparent electrode indium tin oxide (ITO) thin film (10 ⁇ /sq) on a glass substrate for an OLED (GEOMATEC CO., LTD., Japan) was subjected to an ultrasonic washing with acetone and isopropyl alcohol, sequentially, and then was stored in isopropyl alcohol.
- the ITO substrate was then mounted on a substrate holder of a vacuum vapor deposition apparatus.
- Compound HI-1 shown in Table 2 as a first hole injection compound was introduced into a cell of the vacuum vapor deposition apparatus, and compound HT-1 shown in Table 2 was introduced into another cell of the vacuum vapor deposition apparatus.
- compound HI-1 was deposited in a doping amount of 3 wt % based on the total amount of compound HI-1 and compound HT-1 to form a hole injection layer having a thickness of 10 nm on the ITO substrate.
- compound HT-1 was deposited on the hole injection layer to form a first hole transport layer having a thickness of 80 nm.
- Compound HT-2 was then introduced into another cell of the vacuum vapor deposition apparatus and was evaporated by applying an electric current to the cell, thereby forming a second hole transport layer having a thickness of 60 nm on the first hole transport layer.
- a light-emitting layer was formed thereon as follows:
- the first host compound and the second host compound shown in Table 1 below were introduced into two cells of the vacuum vapor depositing apparatus as hosts, and compound D-71 was introduced into another cell as a dopant.
- the two host materials were evaporated at a rate of 1:1 and the dopant material was simultaneously evaporated at a different rate, and the dopant was deposited in a doping amount of 3 wt % based on the total amount of the hosts and the dopant to form a light-emitting layer having a thickness of 40 nm on the second hole transport layer.
- Compound ETL-1 and compound EIL-1 were evaporated in a weight ratio of 50:50 to form an electron transport layer having a thickness of 35 nm on the light-emitting layer.
- an Al cathode having a thickness of 80 nm was deposited on the electron injection layer by another vacuum vapor deposition apparatus.
- an OLED was produced. All the materials used for producing the OLED were purified by vacuum sublimation at 10 ⁇ 8 torr.
- Comparative Examples 1 to 3 Producing an OLED Comprising a Comparative Compound as a Host
- OLEDs were produced in the same manner as in Device Example 1, except that the compound shown in Table 1 below was used alone as a first host or a second host.
- the driving voltage, luminous efficiency, and light-emitting color at a luminance of 1,000 nit, and the time taken for luminance to decrease from 100% to 95% at a luminance of 5,000 nit (lifetime; T95) of the OLEDs produced in Device Examples 1 to 3, and Comparative Examples 1 to 3 are provided in Table 1 below.
- the OLEDs comprising the plurality of host materials according to the present disclosure as host materials have improved driving voltage, luminous efficiency, and/or lifespan property, compared to the conventional OLED.
- the HOMO highest occupied molecular orbital
- the hole injection from a hole transport layer becomes easier, and the balance between hole and electron and the formation of exciton may be improved, thereby improving the driving voltage, luminous efficiency and/or lifetime property of an OLED.
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Abstract
The present disclosure relates to a plurality of host materials comprising at least one first host compound and at least one second host compound, and an organic electroluminescent device comprising the same. By comprising a specific combination of the compounds wherein the first host compound is represented by formula 1 and the second host compound is represented by formula 2, it is possible to provide an organic electroluminescent device having improved driving voltage, luminous efficiency, power efficiency and/or lifetime property.
Description
- The present disclosure relates to a plurality of host materials and an organic electroluminescent device comprising the same.
- A small molecular green organic electroluminescent device (OLED) was first developed by Tang, et al., of Eastman Kodak in 1987 by using TPD/ALq3 bi-layer consisting of a light-emitting layer and a charge transport layer. Thereafter, the development of OLEDs was rapidly effected and OLEDs have been commercialized. At present, OLEDs primarily use phosphorescent materials having excellent luminous efficiency in panel implementation. An OLED having high luminous efficiency and/or long lifetime characteristics is required for long time use and high resolution of a display.
- In order to enhance luminous efficiency, driving voltage and/or lifetime, various materials or concepts for an organic layer of an organic electroluminescent device have been proposed. However, they were not satisfactory in practical use.
- Korean Patent Application Laying-Open No. 2020-0000329 discloses a plurality of host materials comprising a compound having a heteroaryl bonded to a phenanthrene moiety and a compound having a heteroaryl bonded to a carbazole moiety. However, said reference does not specifically disclose a specific combination of host materials claimed in the present disclosure. In addition, development of a light-emitting material having improved performances, for example, improved driving voltage, luminous efficiency, power efficiency and/or lifetime property as compared with combinations of specific compounds conventionally disclosed is still required.
- The objective of the present disclosure is to provide an organic electroluminescent device having low driving voltage, high luminous efficiency, high power efficiency and/or excellent lifetime property by comprising a plurality of host materials including a specific combination of compounds.
- The present inventors found that the above objective can be achieved by a plurality of host materials comprising at least one first host compound and at least second host compound, wherein the first host compound is represented by the following formula 1, and the second host compound is represented by the following formula 2:
- wherein
- B1 to B7, each independently, are not present, or represent a substituted or unsubstituted (C5-C20) ring, in which carbon atoms of the ring may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur, with the proviso that at least five of B1 to B7 are present, and adjacent rings of B1 to B7 are fused with each other;
- Y represents —N(L1-(Ar1)n)—, —O—, —S—, or —C(R1)(R2)—;
- L1 represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene;
- Ar1 represents a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or —N(R3)(R4);
- R1 to R4, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or may be linked to an adjacent substituent to form a ring(s); and
- n represents an integer of 1 or 2, where if n is 2, each of Ar1 may be the same or different;
- wherein
- X represents —N═, —NR35—, —O— or —S—;
- Z represents —N═, —NR36—, —O— or —S—, where if X represents —N═, Z represents —NR36—, —O— or —S—, and if X represents —NR35—, Z represents —N═, —O— or —S—;
- HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl;
- R31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl;
- R32 to R34, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3); or may be linked to an adjacent substituent to form a ring(s);
- R35 and R36, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3);
- L2 and L3, each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
- Ar2 and Ar3, each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted fused ring group of a (C3-C30) aliphatic ring(s) and a (C6-C30) aromatic ring(s), a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl; and
- a′ represents 1, b′ and c′, each independently, represent an integer of 1 or 2, and d′ represents an integer of 1 to 4, where if each of b′, c′ and d′ is an integer of 2 or more, each of R32 to each of R34 may be the same or different.
- By comprising a plurality of host materials according to the present disclosure, an organic electroluminescent device having lower driving voltage, higher luminous efficiency, higher power efficiency and/or better lifetime property compared to conventional organic electroluminescent devices can be provided, and it is possible to produce a display system or a lighting system using the same.
- Hereinafter, the present disclosure will be described in detail. However, the following description is intended to explain the invention and is not meant in any way to restrict the scope of the present disclosure.
- The term “organic electroluminescent material” in the present disclosure means a material that may be used in an organic electroluminescent device, and may comprise at least one compound. The organic electroluminescent material may be comprised in any layer constituting an organic electroluminescent device as necessary. For example, the organic electroluminescent material may be a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting auxiliary material, an electron blocking material, a light-emitting material (including a host material and a dopant material), an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc.
- The term “a plurality of organic electroluminescent materials” in the present disclosure means an organic electroluminescent material comprising a combination of at least two compounds, which may be comprised in any layer constituting an organic electroluminescent device. It may mean both a material before being comprised in an organic electroluminescent device (for example, before vapor deposition) and a material after being comprised in an organic electroluminescent device (for example, after vapor deposition). For example, a plurality of organic electroluminescent materials of the present disclosure may be a combination of at least two compounds, which may be comprised in at least one layer of a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer, an electron blocking layer, a light-emitting layer, an electron buffer layer, a hole blocking layer, an electron transport layer, and an electron injection layer. The at least two compounds may be comprised in the same layer or different layers, and may be mixture-evaporated or co-evaporated, or may be individually evaporated.
- The term “a plurality of host materials” in the present disclosure means an organic electroluminescent material comprising a combination of at least two host materials. It may mean both a material before being comprised in an organic electroluminescent device (for example, before vapor deposition) and a material after being comprised in an organic electroluminescent device (for example, after vapor deposition). The plurality of host materials of the present disclosure may be comprised in any light-emitting layer constituting an organic electroluminescent device. At least two compounds comprised in the plurality of host materials of the present disclosure may be comprised together in one light-emitting layer or may respectively be comprised in different light-emitting layers. When at least two host materials are comprised in one layer, for example, they may be mixture-evaporated to form a layer or may be separately co-evaporated at the same time to form a layer.
- Herein, the term “(C1-C30)alkyl” is meant to be a linear or branched alkyl having 1 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 1 to 20, and more preferably 1 to 10. The above alkyl may include methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, tert-butyl, etc. The term “(C2-C30)alkenyl” is meant to be a linear or branched alkenyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, and more preferably 2 to 10. The above alkenyl may include vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methylbut-2-enyl, etc. The term “(C2-C30)alkynyl” is meant to be a linear or branched alkynyl having 2 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 2 to 20, and more preferably 2 to 10. The above alkynyl may include ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-methylpent-2-ynyl, etc. The term “(C3-C30)cycloalkyl” is meant to be a mono- or polycyclic hydrocarbon having 3 to 30 ring backbone carbon atoms, in which the number of carbon atoms is preferably 3 to 20, and more preferably 3 to 7. The above cycloalkyl may include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc. The term “(3- to 7-membered)heterocycloalkyl” is meant to be a cycloalkyl having 3 to 7, preferably 5 to 7, ring backbone atoms, and including at least one heteroatom selected from the group consisting of B, N, O, S, Si, and P, and preferably the group consisting of O, S, and N. The above heterocycloalkyl may include tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc. The term “(C6-C30)aryl(ene)” is meant to be a monocyclic or fused ring radical derived from an aromatic hydrocarbon having 6 to 30 ring backbone carbon atoms, in which the number of the ring backbone carbon atoms is preferably 6 to 25, and more preferably 6 to 18. The above aryl(ene) may be partially saturated, and may comprise a spiro structure. The above aryl may include phenyl, biphenyl, terphenyl, naphthyl, binaphthyl, phenylnaphthyl, naphthylphenyl, phenylterphenyl, fluorenyl, phenylfluorenyl, benzofluorenyl, dibenzofluorenyl, phenanthrenyl, phenylphenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, spirobifluorenyl, azulenyl, etc. More specifically, the above aryl may include phenyl, 1-naphthyl, 2-naphthyl, 1-anthryl, 2-anthryl, 9-anthryl, benzanthryl, 1-phenanthryl, 2-phenanthryl, 3-phenanthryl, 4-phenanthryl, 9-phenanthryl, naphthacenyl, pyrenyl, 1-chrysenyl, 2-chrysenyl, 3-chrysenyl, 4-chrysenyl, 5-chrysenyl, 6-chrysenyl, benzo[c]phenanthryl, benzo[g]chrysenyl, 1-triphenylenyl, 2-triphenylenyl, 3-triphenylenyl, 4-triphenylenyl, 1-fluorenyl, 2-fluorenyl, 3-fluorenyl, 4-fluorenyl, 9-fluorenyl, benzo[a]fluorenyl, benzo[b]fluorenyl, benzo[c]fluorenyl, dibenzofluorenyl, 2-biphenyl, 3-biphenylyl, 4-biphenylyl, o-terphenyl, m-terphenyl-4-yl, m-terphenyl-3-yl, m-terphenyl-2-yl, p-terphenyl-4-yl, p-terphenyl-3-yl, p-terphenyl-2-yl, m-quaterphenyl, 3-fluoranthenyl, 4-fluoranthenyl, 8-fluoranthenyl, 9-fluoranthenyl, benzofluoranthenyl, o-tolyl, m-tolyl, p-tolyl, 2,3-xylyl, 3,4-xylyl, 2,5-xylyl, mesityl, o-cumenyl, m-cumenyl, p-cumenyl, p-t-butylphenyl, p-(2-phenylpropyl)phenyl, 4′-methylbiphenylyl, 4″-t-butyl-p-terphenyl-4-yl, 9,9-dimethyl-1-fluorenyl, 9,9-dimethyl-2-fluorenyl, 9,9-dimethyl-3-fluorenyl, 9,9-dimethyl-4-fluorenyl, 9,9-diphenyl-1-fluorenyl, 9,9-diphenyl-2-fluorenyl, 9,9-diphenyl-3-fluorenyl, 9,9-diphenyl-4-fluorenyl, 11,11-dimethyl-1-benzo[a] fluorenyl, 11,11-dimethyl-2-benzo[a] fluorenyl, 11,11-dimethyl-3-benzo[a]fluorenyl, 11,11-dimethyl-4-benzo[a] fluorenyl, 11,11-dimethyl-5-benzo[a] fluorenyl, 11,11-dimethyl-6-benzo[a] fluorenyl, 11,11-dimethyl-7-benzo[a] fluorenyl, 11,11-dimethyl-8-benzo[a]fluorenyl, 11,11-dimethyl-9-benzo[a] fluorenyl, 11,11-dimethyl-10-benzo[a] fluorenyl, 11,11-dimethyl-1-benzo[b] fluorenyl, 11,11-dimethyl-2-benzo[b] fluorenyl, 11,11-dimethyl-3-benzo[b]fluorenyl, 11,11-dimethyl-4-benzo[b] fluorenyl, 11,11-dimethyl-5-benzo[b] fluorenyl, 11,11-dimethyl-6-benzo[b] fluorenyl, 11,11-dimethyl-7-benzo[b] fluorenyl, 11,11-dimethyl-8-benzo[b]fluorenyl, 11,11-dimethyl-9-benzo[b] fluorenyl, 11,11-dimethyl-10-benzo[b] fluorenyl, 11,11-dimethyl-1-benzo[c] fluorenyl, 11,11-dimethyl-2-benzo[c] fluorenyl, 11,11-dimethyl-3-benzo[c]fluorenyl, 11,11-dimethyl-4-benzo[c] fluorenyl, 11,11-dimethyl-5-benzo[c] fluorenyl, 11,11-dimethyl-6-benzo[c] fluorenyl, 11,11-dimethyl-7-benzo[c] fluorenyl, 11,11-dimethyl-8-benzo[c]fluorenyl, 11,11-dimethyl-9-benzo[c] fluorenyl, 11,11-dimethyl-10-benzo[c] fluorenyl, 11,11-diphenyl-1-benzo[a] fluorenyl, 11,11-diphenyl-2-benzo[a] fluorenyl, 11,11-diphenyl-3-benzo[a]fluorenyl, 11,11-diphenyl-4-benzo[a] fluorenyl, 11,11-diphenyl-5-benzo[a] fluorenyl, 11,11-diphenyl-6-benzo[a] fluorenyl, 11,11-diphenyl-7-benzo[a] fluorenyl, 11,11-diphenyl-8-benzo[a]fluorenyl, 11,11-diphenyl-9-benzo[a] fluorenyl, 11,11-diphenyl-10-benzo[a] fluorenyl, 11,11-diphenyl-1-benzo[b] fluorenyl, 11,11-diphenyl-2-benzo[b] fluorenyl, 11,11-diphenyl-3-benzo[b]fluorenyl, 11,11-diphenyl-4-benzo[b] fluorenyl, 11,11-diphenyl-5-benzo[b] fluorenyl, 11,11-diphenyl-6-benzo[b] fluorenyl, 11,11-diphenyl-7-benzo[b] fluorenyl, 11,11-diphenyl-8-benzo[b]fluorenyl, 11,11-diphenyl-9-benzo[b] fluorenyl, 11,11-diphenyl-10-benzo[b] fluorenyl, 11,11-diphenyl-1-benzo[c] fluorenyl, 11,11-diphenyl-2-benzo[c] fluorenyl, 11,11-diphenyl-3-benzo[c]fluorenyl, 11,11-diphenyl-4-benzo[c] fluorenyl, 11,11-diphenyl-5-benzo[c] fluorenyl, 11,11-diphenyl-6-benzo[c] fluorenyl, 11,11-diphenyl-7-benzo[c] fluorenyl, 11,11-diphenyl-8-benzo[c]fluorenyl, 11,11-diphenyl-9-benzo[c] fluorenyl, 11,11-diphenyl-10-benzo[c] fluorenyl, etc.
- The term “(3- to 30-membered)heteroaryl” or “(3- to 50-membered)heteroaryl” is meant to be an aryl having 3 to 30 ring backbone atoms or 3 to 50 ring backbone atoms, and including at least one, preferably 1 to 4 heteroatoms selected from the group consisting of B, N, O, S, Si, and P. The above heteroaryl may be a monocyclic ring, or a fused ring condensed with at least one benzene ring; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and may comprise a spiro structure. The above heteroaryl may include a monocyclic ring-type heteroaryl such as furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl, tetrazinyl, triazolyl, tetrazolyl, furazanyl, pyridyl, pyrazinyl, pyrimidinyl, and pyridazinyl, and a fused ring-type heteroaryl such as benzofuranyl, benzothiophenyl, isobenzofuranyl, dibenzofuranyl, dibenzothiophenyl, naphthobenzofuranyl, naphthobenzothiophenyl, benzimidazolyl, benzothiazolyl, benzoisothiazolyl, benzoisoxazolyl, benzoxazolyl, isoindolyl, indolyl, benzoindolyl, indazolyl, benzothiadiazolyl, quinolyl, isoquinolyl, cinnolinyl, quinazolinyl, benzoquinazolinyl, quinoxalinyl, benzoquinoxalinyl, naphthyridinyl, carbazolyl, benzocarbazolyl, dibenzocarbazolyl, phenoxazinyl, phenothiazinyl, phenanthridinyl, benzodioxolyl, and dihydroacridinyl. More specifically, the above heteroaryl may include 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, pyrazinyl, 2-pyridinyl, 2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 6-pyrimidinyl, 1,2,3-triazin-4-yl, 1,2,4-triazin-3-yl, 1,3,5-triazin-2-yl, 1-imidazolyl, 2-imidazolyl, 1-pyrazolyl, 1-indolidinyl, 2-indolidinyl, 3-indolidinyl, 5-indolidinyl, 6-indolidinyl, 7-indolidinyl, 8-indolidinyl, 2-imidazopyridinyl, 3-imidazopyridinyl, 5-imidazopyridinyl, 6-imidazopyridinyl, 7-imidazopyridinyl, 8-imidazopyridinyl, 3-pyridinyl, 4-pyridinyl, 1-indolyl, 2-indolyl, 3-indolyl, 4-indolyl, 5-indolyl, 6-indolyl, 7-indolyl, 1-isoindolyl, 2-isoindolyl, 3-isoindolyl, 4-isoindolyl, 5-isoindolyl, 6-isoindolyl, 7-isoindolyl, 2-furyl, 3-furyl, 2-benzofuranyl, 3-benzofuranyl, 4-benzofuranyl, 5-benzofuranyl, 6-benzofuranyl, 7-benzofuranyl, 1-isobenzofuranyl, 3-isobenzofuranyl, 4-isobenzofuranyl, 5-isobenzofuranyl, 6-isobenzofuranyl, 7-isobenzofuranyl, 2-quinolyl, 3-quinolyl, 4-quinolyl, 5-quinolyl, 6-quinolyl, 7-quinolyl, 8-quinolyl, 1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 5-isoquinolyl, 6-isoquinolyl, 7-isoquinolyl, 8-isoquinolyl, 2-quinoxalinyl, 5-quinoxalinyl, 6-quinoxalinyl, 1-carbazolyl, 2-carbazolyl, 3-carbazolyl, 4-carbazolyl, 9-carbazolyl, azacarbazolyl-1-yl, azacarbazolyl-2-yl, azacarbazolyl-3-yl, azacarbazolyl-4-yl, azacarbazolyl-5-yl, azacarbazolyl-6-yl, azacarbazolyl-7-yl, azacarbazolyl-8-yl, azacarbazolyl-9-yl, 1-phenanthridinyl, 2-phenanthridinyl, 3-phenanthridinyl, 4-phenanthridinyl, 6-phenanthridinyl, 7-phenanthridinyl, 8-phenanthridinyl, 9-phenanthridinyl, 10-phenanthridinyl, 1-acridinyl, 2-acridinyl, 3-acridinyl, 4-acridinyl, 9-acridinyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-oxadiazolyl, 5-oxadiazolyl, 3-furazanyl, 2-thienyl, 3-thienyl, 2-methylpyrrol-1-yl, 2-methylpyrrol-3-yl, 2-methylpyrrol-4-yl, 2-methylpyrrol-5-yl, 3-methylpyrrol-1-yl, 3-methylpyrrol-2-yl, 3-methylpyrrol-4-yl, 3-methylpyrrol-5-yl, 2-t-butylpyrrol-4-yl, 3-(2-phenylpropyl)pyrrol-1-yl, 2-methyl-1-indolyl, 4-methyl-1-indolyl, 2-methyl-3-indolyl, 4-methyl-3-indolyl, 2-t-butyl-1-indolyl, 4-t-butyl-1-indolyl, 2-t-butyl-3-indolyl, 4-t-butyl-3-indolyl, 1-dibenzofuranyl, 2-dibenzofuranyl, 3-dibenzofuranyl, 4-dibenzofuranyl, 1-dibenzothiophenyl, 2-dibenzothiophenyl, 3-dibenzothiophenyl, 4-dibenzothiophenyl, 1-naphtho-[1,2-b]-benzofuranyl, 2-naphtho-[1,2-b]-benzofuranyl, 3-naphtho-[1,2-b]-benzofuranyl, 4-naphtho-[1,2-b]-benzofuranyl, 5-naphtho-[1,2-b]-benzofuranyl, 6-naphtho-[1,2-b]-benzofuranyl, 7-naphtho-[1,2-b]-benzofuranyl, 8-naphtho-[1,2-b]-benzofuranyl, 9-naphtho-[1,2-b]-benzofuranyl, 10-naphtho-[1,2-b]-benzofuranyl, 1-naphtho-[2,3-b]-benzofuranyl, 2-naphtho-[2,3-b]-benzofuranyl, 3-naphtho-[2,3-b]-benzofuranyl, 4-naphtho-[2,3-b]-benzofuranyl, 5-naphtho-[2,3-b]-benzofuranyl, 6-naphtho-[2,3-b]-benzofuranyl, 7-naphtho-[2,3-b]-benzofuranyl, 8-naphtho-[2,3-b]-benzofuranyl, 9-naphtho-[2,3-b]-benzofuranyl, 10-naphtho-[2,3-b]-benzofuranyl, 1-naphtho-[2,1-b]-benzofuranyl, 2-naphtho-[2,1-b]-benzofuranyl, 3-naphtho-[2,1-b]-benzofuranyl, 4-naphtho-[2,1-b]-benzofuranyl, 5-naphtho-[2,1-b]-benzofuranyl, 6-naphtho-[2,1-b]-benzofuranyl, 7-naphtho-[2,1-b]-benzofuranyl, 8-naphtho-[2,1-b]-benzofuranyl, 9-naphtho-[2,1-b]-benzofuranyl, 10-naphtho-[2,1-b]-benzofuranyl, 1-naphtho-[1,2-b]-benzothiophenyl, 2-naphtho-[1,2-b]-benzothiophenyl, 3-naphtho-[1,2-b]-benzothiophenyl, 4-naphtho-[1,2-b]-benzothiophenyl, 5-naphtho-[1,2-b]-benzothiophenyl, 6-naphtho-[1,2-b]-benzothiophenyl, 7-naphtho-[1,2-b]-benzothiophenyl, 8-naphtho-[1,2-b]-benzothiophenyl, 9-naphtho-[1,2-b]-benzothiophenyl, 10-naphtho-[1,2-b]-benzothiophenyl, 1-naphtho-[2,3-b]-benzothiophenyl, 2-naphtho-[2,3-b]-benzothiophenyl, 3-naphtho-[2,3-b]-benzothiophenyl, 4-naphtho-[2,3-b]-benzothiophenyl, 5-naphtho-[2,3-b]-benzothiophenyl, 1-naphtho-[2,1-b]-benzothiophenyl, 2-naphtho-[2,1-b]-benzothiophenyl, 3-naphtho-[2,1-b]-benzothiophenyl, 4-naphtho-[2,1-b]-benzothiophenyl, 5-naphtho-[2,1-b]-benzothiophenyl, 6-naphtho-[2,1-b]-benzothiophenyl, 7-naphtho-[2,1-b]-benzothiophenyl, 8-naphtho-[2,1-b]-benzothiophenyl, 9-naphtho-[2,1-b]-benzothiophenyl, 10-naphtho-[2,1-b]-benzothiophenyl, 1-silafluorenyl, 2-silafluorenyl, 3-silafluorenyl, 4-silafluorenyl, 1-germafluorenyl, 2-germafluorenyl, 3-germafluorenyl, 4-germafluorenyl, etc. Furthermore, “halogen” includes F, Cl, Br, and I.
- In addition, “ortho (o-),” “meta (m-),” and “para (p-)” are prefixes, which represent the relative positions of substituents respectively. Ortho indicates that two substituents are adjacent to each other, and for example, when two substituents in a benzene derivative occupy positions 1 and 2, it is called an ortho position. Meta indicates that two substituents are at positions 1 and 3, and for example, when two substituents in a benzene derivative occupy positions 1 and 3, it is called a meta position. Para indicates that two substituents are at positions 1 and 4, and for example, when two substituents in a benzene derivative occupy positions 1 and 4, it is called a para position.
- Herein, “substituted” in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or another functional group, i.e., a substituent. The substituents of the substituted alkyl, the substituted alkylene, the substituted alkenyl, the substituted aryl, the substituted arylene, the substituted heteroaryl, the substituted heteroarylene, the substituted cycloalkyl, the substituted cycloalkylene, the substituted alkoxy, the substituted trialkylsilyl, the substituted dialkylarylsilyl, the substituted alkyldiarylsilyl, the substituted triarylsilyl, the substituted fused ring of an aliphatic ring(s) and an aromatic ring(s), and the substituted ring in the formulas of the present disclosure, each independently, are at least one selected from the group consisting of deuterium; a halogen; a cyano; a carboxyl; a nitro; a hydroxyl; a (C1-C30)alkyl; a halo(C1-C30)alkyl; a (C2-C30)alkenyl; a (C2-C30)alkynyl; a (C1-C30)alkoxy; a (C1-C30)alkylthio; a (C3-C30)cycloalkyl; a (C3-C30)cycloalkenyl; a (3- to 7-membered)heterocycloalkyl; a (C6-C30)aryloxy; a (C6-C30)arylthio; a (3- to 50-membered)heteroaryl unsubstituted or substituted with at least one of a (C1-C30)alkyl(s), a (C6-C30)aryl(s), and a di(C6-C30)arylamino(s); a (C6-C30)aryl unsubstituted or substituted with at least one of deuterium, a cyano(s), a (C1-C30)alkyl(s), a (3- to 50-membered)heteroaryl(s), a mono- or di-(C6-C30)arylamino(s), and a tri(C6-C30)arylsilyl(s); a tri(C1-C30)alkylsilyl; a tri(C6-C30)arylsilyl; a di(C1-C30)alkyl(C6-C30)arylsilyl; a (C1-C30)alkyldi(C6-C30)arylsilyl; an amino; a mono- or di-(C1-C30)alkylamino; a mono- or di-(C2-C30)alkenylamino; a mono- or di-(C6-C30)arylamino; a mono- or di-(3- to 30-membered)heteroarylamino; a (C1-C30)alkyl(C2-C30)alkenylamino; a (C1-C30)alkyl(C6-C30)arylamino; a (C1-C30)alkyl(3- to 30-membered)heteroarylamino; a (C2-C30)alkenyl(C6-C30)arylamino; a (C2-C30)alkenyl(3- to 30-membered)heteroarylamino; a (C6-C30)aryl(3- to 30-membered)heteroarylamino; a (C1-C30)alkylcarbonyl; a (C1-C30)alkoxycarbonyl; a (C6-C30)arylcarbonyl; a di(C6-C30)arylboronyl; a di(C1-C30)alkylboronyl; a (C1-C30)alkyl(C6-C30)arylboronyl; a (C6-C30)aryl(C1-C30)alkyl; and a (C1-C30)alkyl(C6-C30)aryl. According to one embodiment of the present disclosure, the substituents, each independently, are at least one selected from the group consisting of deuterium; a (C1-C20)alkyl; a (3- to 30-membered)heteroaryl unsubstituted or substituted with at least one of a (C1-C20)alkyl(s) and a (C6-C25)aryl(s); a (C6-C25)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C20)alkyl(s), a (3- to 30-membered)heteroaryl(s), and a di(C6-C25)arylamino(s); and a mono- or di-(C6-C25)arylamino. According to another embodiment of the present disclosure, the substituents, each independently, are at least one selected from the group consisting of deuterium; a (C1-C10)alkyl; a (5- to 26-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s); a (C6-C20)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C10)alkyl(s), a (5- to 26-membered)heteroaryl(s), and a di(C6-C18)arylamino(s); and a di(C6-C18)arylamino. Specifically, the substituents, each independently, may be at least one selected from the group consisting of deuterium; a methyl; a phenyl unsubstituted or substituted with at least one of deuterium, a 26-membered heteroaryl(s), and a diphenylamino(s); a naphthyl; a biphenyl; a naphthylphenyl; a phenylnaphthyl; a phenanthrenyl; a dimethylfluorenyl; a dimethylbenzofluorenyl; a terphenyl; a triphenylenyl; a pyridyl unsubstituted or substituted with a phenyl(s); a triazinyl substituted with a phenyl(s); a dibenzofuranyl; a dibenzothiophenyl; a benzonaphthothiophenyl; a carbazolyl unsubstituted or substituted with a phenyl(s); a benzocarbazolyl unsubstituted or substituted with a phenyl(s); a dibenzocarbazolyl; a 26-membered heteroaryl; and a diphenylamino.
- In the formulas of the present disclosure, if a substituent is linked to an adjacent substituent to form a ring, the ring may be a substituted or unsubstituted, mono- or polycyclic, (3- to 30-membered) alicyclic or aromatic ring, or the combination thereof, which two or more adjacent substituents are linked to form. In addition, the formed ring may contain at least one heteroatom selected from B, N, O, S, Si, and P, preferably at least one heteroatom selected from N, O, and S. According to one embodiment of the present disclosure, the number of the ring backbone atoms is 5 to 20. According to another embodiment of the present disclosure, the number of the ring backbone atoms is 5 to 15.
- In the formulas of the present disclosure, heteroaryl and heteroarylene may, each independently, contain at least one heteroatom selected from B, N, O, S, Si, and P. In addition, the heteroatom may be bonded to at least one selected from the group consisting of hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, a substituted or unsubstituted mono- or di-(C1-C30)alkylamino, a substituted or unsubstituted mono- or di-(C6-C30)arylamino, and a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino.
- The plurality of host materials according to one embodiment of the present disclosure comprises a first host material comprising the compound represented by formula 1 and a second host material comprising the compound represented by formula 2, and may be comprised in a light-emitting layer of an organic electroluminescent device according to one embodiment of the present disclosure.
- Hereinafter, the compound represented by formula 1 will be described in more detail.
- In formula 1, B1 to B7, each independently, are not present, or represent a substituted or unsubstituted (C5-C20) ring, preferably a substituted or unsubstituted (C5-C13) ring, in which carbon atoms of the ring may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur, with the proviso that at least five of B1 to B7 are present, and adjacent rings of B1 to B7 are fused with each other. Herein, “adjacent rings of B1 to B7 are fused with each other” means that ring B1 and ring B2, ring B2 and ring B3, ring B3 and ring B4, ring B4 and ring B5, ring B5 and ring B6, or ring B6 and ring B7 are fused with each other. According to one embodiment of the present disclosure, if any one of B1 to B7, represents a (C6-C20)aryl, an adjacent ring may not be present, or may be a C5 ring, carbon atoms of which may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur. According to another embodiment of the present disclosure, B1 to B7 each independently, are not present, or represent a substituted or unsubstituted benzene ring, a substituted or unsubstituted naphthalene ring, a substituted or unsubstituted pyrrole ring, a substituted or unsubstituted furan ring, a substituted or unsubstituted thiophene ring, a substituted or unsubstituted cyclopentadiene ring, a substituted or unsubstituted fluorene ring, a substituted or unsubstituted pyridine ring, or a substituted or unsubstituted dibenzofuran ring. For example, B1 to B7, each independently, may not be present, or may represent a benzene ring unsubstituted or substituted with a phenyl(s), a naphthyl(s) and/or a diphenyltriazinyl(s); a naphthalene ring; a cyclopentadiene ring unsubstituted or substituted with a methyl(s); a fluorene ring substituted with a methyl(s); a pyrrole ring substituted with an unsubstituted phenyl(s), a phenyl(s) substituted with at least one deuterium, a biphenyl(s) and/or a pyridiyl(s); a furan ring; a thiophene ring; a pyridine ring; or a dibenzofuran ring unsubstituted or substituted with a diphenyltriazinyl(s).
- In formula 1, Y represents —N(L1-(Ar1)n)—, —O—, —S—, or —C(R1)(R2)—. According to one embodiment of the present disclosure, Y represents —N(L1-(Ar1)n)—.
- L1 represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene. According to one embodiment of the present disclosure, L1 represents a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene. According to another embodiment of the present disclosure, L1 represents a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 25-membered)heteroarylene. For example, L1 may be a single bond, a phenylene, a naphthylene, a biphenylene, a pyridylene, a pyrimidinylene, a triazinylene, a quinoxalinylene, a quinazolinylene, a dibenzofuranylene, a benzofuropyrimidinylene, a benzothienopyrimidinylene, an indolopyrimidinylene, or a benzoquinoxalinylene.
- Ar1 represents a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or —N(R3)(R4). According to one embodiment of the present disclosure, Ar1 represents a substituted or unsubstituted (C6-C25)aryl, a substituted or unsubstituted (5- to 25-membered)heteroaryl, or —N(R3)(R4). According to another embodiment of the present disclosure, Ar1 represents a (C6-C25)aryl unsubstituted or substituted with at least one of deuterium, a (C1-C6)alkyl(s), and a (3- to 30-membered)heteroaryl(s); a (5- to 25-membered)heteroaryl unsubstituted or substituted with at least one of deuterium, a (C6-C18)aryl(s), and a (3- to 30-membered)heteroaryl(s); or —N(R3)(R4). For example, Ar1 may be an unsubstituted phenyl, a phenyl substituted with at least one deuterium, a phenyl substituted with a 26-membered heteroaryl(s), a naphthyl, a biphenyl, a fluorenyl substituted with a methyl(s), a spirobifluorenyl, a terphenyl, a triphenylenyl, a pyridyl unsubstituted and substituted with a phenyl(s), a pyrmidinyl substituted with a phenyl(s), a substituted triazinyl, a substituted quinoxalinyl, a substituted quinazolinyl, a benzoquinoxalinyl substituted with a phenyl(s), a carbazolyl, a dibenzofuranyl, a dibenzothiophenyl, a benzofuropyrimidinyl substituted with a phenyl(s), a benzothienopyrimidinyl substituted with a phenyl(s), an indolopyrimidinyl substituted with a phenyl(s), or —N(R3)(R4). The substituents of the substituted triazinyl, the substituted quinoxalinyl, and the substituted quinazolinyl, each independently, may be at least one selected from the group consisting of a phenyl unsubstituted or substituted with at least one of deuterium and a 26-membered heteroaryl(s), a naphthyl, a biphenyl, a terphenyl, a dibenzofuranyl, a pyridyl substituted with a phenyl(s), a dimethylfluorenyl, and a dibenzothiophenyl.
- R1 to R4, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or may be linked to an adjacent substituent to form a ring(s). According to one embodiment of the present disclosure, R1 to R4, each independently, represent hydrogen, deuterium, a substituted or unsubstituted (C1-C20)alkyl, or a substituted or unsubstituted (C6-C25)aryl. According to another embodiment of the present disclosure, R1 and R2, each independently, represent an unsubstituted (C1-C10)alkyl, and R3 and R4, each independently, represent an unsubstituted (C6-C18)aryl. For example, R1 and R2 may be a methyl, and R3 and R4 may be a phenyl.
- n represents an integer of 1 or 2, where if n is 2, each of Ar1 may be the same or different
- Formula 1 may be represented by at least one of the following formulas 1-1 to 1-4.
- In formulas 1-1 to 1-4, Y1, Y2, Y3, and Y4, each independently, are the same as the definition of Y in formula 1, where if a plurality of Ar1's are present, each of Ar1 may be the same or different; X1 to X12, each independently, represent —N═ or —C(Ra)═; Ra, each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or adjacent Ra's may be linked to each other to form a ring(s), where if a plurality of Ra's are present, each of Ra may be the same or different.
- According to one embodiment of the present disclosure, Ra represents hydrogen, deuterium, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl; or adjacent Ra's may be linked to each other to form a ring(s). According to another embodiment of the present disclosure, Ra represents hydrogen, an unsubstituted (C6-C18)aryl, or a (5- to 25-membered)heteroaryl substituted with a (C6-C18)aryl(s); or adjacent Ra's may be linked to each other to form a benzene ring(s), an indene ring(s) substituted with a methyl(s), or a benzofuran ring(s) unsubstituted or substituted with a diphenyltriazinyl(s).
- In any one of formulas 1-1 to 1-4, at least one of Ar1(s) and Ra(s), each independently, may be at least one selected from those listed in the following group 1.
- In group 1, D1 and D2, each independently, represent a benzene ring or a naphthalene ring; X21 represents O, S, NR5, or C(R6)(R7); X22, each independently, represents CR or N, with the proviso that at least one of X22 represents N; X23, each independently, represents CR9 or N; L11 to L18, each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene; R11 to R21 and R5 to R9, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl, or may be linked to an adjacent substituent to form a ring(s); and aa, ff, and gg, each independently, represent an integer of 1 to 5, bb represents an integer of 1 to 7, and cc, dd, and ee, each independently, represent an integer of 1 to 4.
- According to one embodiment of the present disclosure, D1 may be a benzene ring; X21 may be O, S, or C(R6)(R7); L11 to L18, each independently, may be a single bond; R11 to R21 and R5 to R9, each independently, may be hydrogen, deuterium, a substituted or unsubstituted (C1-C20)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl, or may be linked to an adjacent substituent to form a ring(s); and aa, bb, ff, and gg, each independently, may be an integer of 1 to 5, and cc, dd, and ee, each independently, may be an integer of 1 to 4. For example, R11 may be hydrogen, deuterium, a phenyl, a biphenyl, or a 26-membered heteroaryl; R12 may be hydrogen, or adjacent R12's may be linked to each other to form a benzene ring(s); R13, R18, and R17 may be hydrogen; R18 and R19 may be hydrogen or a phenyl; R21 may be phenyl; R6 and R7 may be a methyl; R8 may be hydrogen, a phenyl, a biphenyl, a dibenzofuranyl, or a dibenzothiophenyl, or adjacent R8's may be linked to each other to form a benzene ring(s); R9 may be hydrogen, an unsubstituted phenyl, a phenyl substituted with at least one deuterium, a phenyl substituted with a 26-membered heteroaryl(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a terphenyl, a pyridyl substituted with a phenyl(s), a dibenzofuranyl, or a dibenzothiophenyl; and aa may be an integer of 1 or 5, bb may be an integer of 1 or 4, and cc may be 1.
- In any one of formulas 1-1 to 1-4, at least one of Ar1(s) and Ra(s), each independently, may be at least one selected from those listed in the following group 2.
- In group 2, L represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene; and A1 to A3, each independently, represent a substituted or unsubstituted (C1-C30)alkyl, or a substituted or unsubstituted (C6-C30)aryl. According to one embodiment of the present disclosure, L represents a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (3- to 25-membered)heteroarylene; and A1 to A3, each independently, represent a substituted or unsubstituted (C1-C20)alkyl, or a substituted or unsubstituted (C6-C25)aryl. A1 and A2 may be the same or different. For example, A1 and A2, each independently, may be a methyl or a phenyl.
- In any one of formulas 1-1 to 1-4, at least one of Ar1(s) and Ra(s), each independently, may be at least one selected from those listed in the following group 3.
- Hereinafter, the compound represented by formula 2 will be described in more detail.
- According to one embodiment of the present disclosure, formula 2 may be represented by at least one selected from the following formulas 2-1 to 2-8.
- In formulas 2-1 to 2-8, X, Z, HAr, R31 to R36, L2 and a′ to d′ are as defined in formula 2; Z1 to Z5 and Z11 to Z17, each independently, represent N or CR37; and R37, each independently, is the same as the definition of R32 of formula 2.
- According to one embodiment of the present disclosure, R37, each independently, represents hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl. According to another embodiment of the present disclosure, R37, each independently, represents hydrogen; deuterium; a (C6-C18)aryl unsubstituted or substituted with at least one of a (C1-C10)alkyl(s) and a di(C6-C18)arylamino(s); or a (5- to 20-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s). For example, R37, each independently, may be hydrogen, a phenyl unsubstituted or substituted with a diphenylamino(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a dibenzothiophenyl, a dibenzofuranyl, a benzonaphthothiophenyl, a phenylcarbazolyl, or a phenylbenzocarbazolyl.
- In formula 2, X represents —N═, —NR35—, —O— or —S—, and Z represents —N═, —NR36—, —O— or —S—, where if X represents —N═, Z represents —NR36—, —O— or —S—, and if X represents —NR35—, Z represents —N═, —O— or —S—. According to an embodiment of the present disclosure, X represents —N═, —NR35—, —O— or —S—, and Z represents —N═, —NR36—, —O— or —S—, with the proviso that at least one of X and Z represents —N═.
- R35 and R36, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3). According to one embodiment of the present disclosure, R35 and R36, each independently, represent a substituted or unsubstituted (C1-C20)alkyl, a substituted or unsubstituted (C6-C25)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl. According to another embodiment of the present disclosure, R35 and R36, each independently, represent an unsubstituted (C6-C18)aryl. For example, R35 and R36 may be a phenyl.
- In formula 2, HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl. According to one embodiment of the present disclosure, HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl containing a nitrogen atom(s). According to another embodiment of the present disclosure, HAr represents a substituted or unsubstituted (5- to 25-membered)heteroaryl containing a nitrogen atom(s). According to further embodiment of the present disclosure, HAr represents a (5- to 20-membered)heteroaryl containing a nitrogen atom(s), substituted with a (5- to 25-membered)heteroaryl(s) and/or a (C6-C25)aryl(s). Specifically, HAr may be a substituted or unsubstituted triazinyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted benzoquinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted benzoquinoxalinyl, a substituted or unsubstituted quinolyl, a substituted or unsubstituted benzoquinolyl, a substituted or unsubstituted isoquinolyl, a substituted or unsubstituted benzoisoquinolyl, a substituted or unsubstituted triazolyl, a substituted or unsubstituted pyrazolyl, a substituted or unsubstituted naphthyridinyl, a substituted or unsubstituted benzothienopyrimidinyl. For example, HAr may be a substituted triazinyl, a substituted pyrimidinyl, a substituted quinoxalinyl, a substituted quinazolinyl, or a substituted naphthyridinyl. The substituents of the substituted triazinyl, the substituted pyrimidinyl, the substituted quinoxalinyl, the substituted quinazolinyl, and the substituted naphthyridinyl may be at least one of a phenyl unsubstituted or substituted with a diphenylamino(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a dibenzothiophenyl, a dibenzofuranyl, a benzonaphthothiophenyl, a phenylcarbazolyl, and a phenylbenzocarbazolyl.
- In formula 2, R31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl. According to one embodiment of the present disclosure, R31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 25-membered)heteroaryl. According to another embodiment of the present disclosure, R31 represents a (C6-C29)aryl unsubstituted or substituted with at least one of a (C1-C10)alkyl(s) and a (C6-C18)aryl(s); or a (5- to 25-membered)heteroaryl unsubstituted or substituted with a (C6-C18)aryl(s). For example, R31 may be a phenyl, a naphthyl, a phenylnaphthyl, a biphenyl, a dimethylfluorenyl, a dimethylbenzofluorenyl, a spirobifluorenyl, a spiro[fluoren-benzofluoren]yl, a phenylcarbazolyl, a phenylbenzocarbazolyl, a dibenzofuranyl, or a dibenzothiophenyl.
- In formula 2, R32 to R34, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3); or may be linked to an adjacent substituent to form a ring(s). For example, R32 to R34 may represent hydrogen.
- In formula 2, L2 and L3, each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene. According to one embodiment of the present disclosure, L2 and L3, each independently, represent a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (5- to 25-membered)heteroarylene. According to another embodiment of the present disclosure, L2 and L3, each independently, represent a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 20-membered)heteroarylene. For example, L2 and L3, each independently, may be a single bond, a phenylene, or a pyridylene.
- In formula 2, Ar2 and Ar3, each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted fused ring group of a (C3-C30) aliphatic ring(s) and a (C6-C30) aromatic ring(s), a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl.
- In formula 2, a′ represents 1, b′ and c′, each independently, represent an integer of 1 or 2, and d′ represents an integer of 1 to 4, where if each of b′, c′ and d′ is an integer of 2 or more, each of R32 to each of R34 may be the same or different.
- The compound represented by formula 1 may be at least one selected from the following compounds, but is not limited thereto.
- The compound represented by formula 2 may be at least one selected from the following compounds, but is not limited thereto.
- The combination of at least one of compounds C-1 to C-300 and at least one of compounds C2-1 to C2-125 may be used in an organic electroluminescent device.
- The compound represented by formula 1 of the present disclosure may be produced by a synthetic method known to one skilled in the art, and for example, according to the following reaction schemes 1 to 4, but is not limited thereto:
- In reaction schemes 1 to 4, Y1 to Y4, and X1 to X12 are as defined in formulas 1-1 to 1-4.
- Although illustrative synthesis examples of the compound represented by formula 1 of the present disclosure are described above, one skilled in the art will be able to readily understand that all of them are based on a Buchwald-Hartwig cross-coupling reaction, an N-arylation reaction, an H-mont-mediated etherification reaction, a Miyaura borylation reaction, a Suzuki cross-coupling reaction, an Intramolecular acid-induced cyclization reaction, a Pd(II)-catalyzed oxidative cyclization reaction, a Grignard reaction, a Heck reaction, a Cyclic Dehydration reaction, an SN1 substitution reaction, an SN2 substitution reaction, a Phosphine-mediated reductive cyclization reaction, etc., and the reactions above proceed even when substituents which are defined in formula 1, but are not specified in the specific synthesis examples, are bonded.
- The compound represented by formula 2 of the present disclosure may be produced by a synthetic method known to one skilled in the art, and for example, according to the methods disclosed in Korean Patent Application Laying-Open No. 2020-0000329 (published on Jan. 2, 2020), etc.
- In addition, the non-deuterated analogues of the compound represented by formula 2 can be prepared by known coupling and substitution reactions. Also, the non-deuterated analogues may be prepared in a similar manner by using deuterated precursor materials, or more generally may be prepared by treating the non-deuterated compound with a deuterated solvent or D6-benzene in the presence of an H/D exchange catalyst such as a Lewis acid, e.g., aluminum trichloride or ethyl aluminum chloride, a trifluoromethanesulfonic acid, or a trifluoromethanesulfonic acid-D. In addition, the degree of deuteration can be controlled by changing the reaction conditions such as the reaction temperature. For example, the number of deuterium in formula 2 can be controlled by adjusting the reaction temperature and time, the equivalent of the acid, etc.
- The organic electroluminescent device according to the present disclosure may comprise an anode, a cathode, and at least one organic layer between the anode and cathode in which the organic layer may comprise a plurality of organic electroluminescent materials, including the compound represented by formula 1 as the first organic electroluminescent material, and the compound represented by formula 2 as the second organic electroluminescent material. According to one embodiment of the present disclosure, the organic electroluminescent device according to the present disclosure may comprise an anode, a cathode, and at least one light-emitting layer between the anode and cathode in which the light-emitting layer may comprise the compound represented by formula 1 and the compound represented by formula 2.
- The light-emitting layer includes a host and a dopant, in which the host includes a plurality of host materials and the compound represented by formula 1 may be included as the first host compound of the plurality of host materials, and the compound represented by formula 2 may be included as the second host compound of the plurality of host materials. The weight ratio of the first host compound and the second host compound is about 1:99 to about 99:1, preferably about 10:90 to about 90:10, more preferably about 30:70 to about 70:30, even more preferably about 40:60 to about 60:40, and most preferably about 50:50.
- Herein, the light-emitting layer is a layer from which light is emitted, and may be a single layer or a multi-layer of which two or more layers are stacked. All of the first host material and the second host material may be included in one layer, or the first host material and the second host material may be included in respective different light-emitting layers. According to one embodiment of the present disclosure, the doping concentration of the dopant compound with respect to the host compound in the light-emitting layer may be less than 20 wt %.
- The organic electroluminescent device of the present disclosure may further comprise at least one layer selected from a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer, an electron transport layer, an electron injection layer, an interlayer, an electron buffer layer, a hole blocking layer, and an electron blocking layer. According to one embodiment of the present disclosure, the organic electroluminescent device of the present disclosure may further comprise an amine-based compound besides the plurality of host materials of the present disclosure as at least one of a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting material, a light-emitting auxiliary material, and an electron blocking material. Further, according to one embodiment of the present disclosure, the organic electroluminescent device of the present disclosure may further comprise an azine-based compound besides the plurality of host materials of the present disclosure as at least one of an electron transport material, an electron injection material, an electron buffer material, and a hole blocking material.
- The plurality of host materials according to the present disclosure may be used as light-emitting materials for a white organic light-emitting device. The white organic light-emitting device has been suggested to have various structures such as a parallel arrangement (side-by-side) method, a stacking method, or color conversion material (CCM) method, etc., according to the arrangement of R (red), G (green) or YG (yellowish green), B (blue) light-emitting units. In addition, the plurality of host materials according to one embodiment of the present disclosure may also be used in an organic electroluminescent device comprising a quantum dot (QD).
- A hole injection layer, a hole transport layer, an electron blocking layer, or a combination thereof can be used between the anode and the light-emitting layer. The hole injection layer may be multilayers in order to lower the hole injection barrier (or hole injection voltage) from the anode to the hole transport layer or the electron blocking layer, wherein each of the multilayers may use two compounds simultaneously. Further, the hole injection layer may be doped with a p-dopant. The electron blocking layer may be placed between the hole transport layer (or hole injection layer) and the light-emitting layer, and may block overflowing electrons from the light-emitting layer and confine the excitons in the light-emitting layer to prevent light leakage. The hole transport layer or the electron blocking layer may also be multilayers, wherein each of the multilayers may use a plurality of compounds.
- An electron buffer layer, a hole blocking layer, an electron transport layer, an electron injection layer, or a combination thereof can be used between the light-emitting layer and the cathode. The electron buffer layer may be multilayers in order to control the electron injection and improve the interfacial properties between the light-emitting layer and the electron injection layer, wherein each of the multilayers may use two compounds simultaneously. The hole blocking layer or the electron transport layer may also be multilayers, wherein each of the multilayers may use a plurality of compounds. In addition, the electron injection layer may be doped with an n-dopant.
- The dopant comprised in the organic electroluminescent device of the present disclosure may be at least one phosphorescent or fluorescent dopant, and is preferably phosphorescent dopant. The phosphorescent dopant material applied to the organic electroluminescent device of the present disclosure is not particularly limited, but may be preferably selected from the metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), more preferably selected from ortho-metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), and even more preferably ortho-metallated iridium complex compounds.
- The dopant comprised in the organic electroluminescent device of the present disclosure may comprise a compound represented by the following formula 101, but is not limited thereto.
- In formula 101, L′ is selected from the following structures 1 to 3:
- R100 to R103, each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a cyano, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C1-C30)alkoxy; or may be linked to an adjacent substituent to form a ring(s), e.g., a substituted or unsubstituted, quinoline, isoquinoline, benzofuropyridine, benzothienopyridine, indenopyridine, benzofuroquinoline, benzothienoquinoline, or indenoquinoline, together with pyridine;
- R104 to R107, each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a cyano, or a substituted or unsubstituted (C1-C30)alkoxy; or may be linked to an adjacent substituent to form a ring(s), e.g., a substituted or unsubstituted, naphthalene, fluorene, dibenzothiophene, dibenzofuran, indenopyridine, benzofuropyridine, or benzothienopyridine, together with benzene;
- R201 to R220, each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium and/or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, or a substituted or unsubstituted (C6-C30)aryl; or may be linked to an adjacent substituent to form a ring(s); and
- s represents an integer of 1 to 3.
- The specific examples of the dopant compound are as follows, but are not limited thereto.
- In order to form each layer of the organic electroluminescent device of the present disclosure, dry film-forming methods such as vacuum evaporation, sputtering, plasma, ion plating methods, etc., or wet film-forming methods such as ink jet printing, nozzle printing, slot coating, spin coating, dip coating, flow coating methods, etc., can be used.
- When using a wet film-forming method, a thin film can be formed by dissolving or diffusing materials forming each layer into any suitable solvent such as ethanol, chloroform, tetrahydrofuran, dioxane, etc. The solvent can be any solvent where the materials forming each layer can be dissolved or diffused, and where there are no problems in film-formation capability.
- The first and the second host compounds of the present disclosure may be film-formed by the above-listed methods, commonly by a co-evaporation process or a mixture-evaporation process. The co-evaporation is a mixed deposition method in which two or more materials are placed in a respective individual crucible source and a current is applied to both cells at the same time to evaporate the materials. The mixture-evaporation is a mixed deposition method in which two or more materials are mixed in one crucible source before evaporating them, and a current is applied to the cell to evaporate the materials. Further, if the first and the second host compounds are present in the same layer or different layers in an organic electroluminescent device, the two host compounds may individually form films. For example, the second host compound may be deposited after depositing the first host compound.
- The present disclosure may provide a display device by using the plurality of host materials including the compound represented by formula 1 and the compound represented by formula 2. That is, by using the plurality of host materials of the present disclosure, it is possible to manufacture a display system or a lighting system. Specifically, by using the plurality of host materials of the present disclosure, a display system, for example, for white organic light emitting devices, smart phones, tablets, notebooks, PCs, TVs, or cars; or a lighting system, for example an outdoor or indoor lighting system, can be produced.
- Hereinafter, the preparation method of the compounds according to the present disclosure and the properties thereof, and the properties of an organic electroluminescent device comprising the plurality of host materials of the present disclosure will be explained in detail with reference to the representative compounds of the present disclosure. However, the present disclosure is not limited by the following examples.
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- (9-phenyl-9H-carbazol-4-yl)boronic acid (96 g, 334.3 mmol), 2-bromo-1-chloro-3-nitrobenzene (71.8 g, 304 mmol), Pd2(dba)3 (15 g, 16.71 mmol), S-Phos (10.9 g, 26.76 mmol), and K3PO4 (315 g, 1.64 mol) were dissolved in 1500 mL of toluene in a flask, and the mixture was stirred at 130° C. for 4 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and the residual moisture was removed using magnesium sulfate. The residue was dried, and separated by column chromatography to obtain compound 1-1 (67 g, yield: 56.6%).
- Compound 1-1 (23.5 g, 58.9 mmol), (2-chlorophenyl)boronic acid (18.4 g, 117.8 mmol), Pd2(dba)3 (2.7 g, 2.95 mmol), S-Phos (2.4 g, 5.89 mmol), and K3PO4 (63 g, 294.5 mmol) were dissolved in 300 mL of toluene in a flask, and the mixture was stirred at 130° C. for 12 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and the residual moisture was removed using magnesium sulfate. The residue was dried, and separated by column chromatography to obtain compound 1-2 (14 g, yield: 50%).
- Compound 1-2 (13 g, 27.4 mmol), and triphenylphosphine (21.5 g, 82.1 mmol) were dissolved in 140 mL of o-DCB in a flask, and the mixture was stirred at 220° C. for 7 hours. After completion of the reaction, the reaction mixture was removed by distillation, and separated by column chromatography to obtain compound 1-3 (4 g, yield: 32%).
- Compound 1-3 (10 g, 22.5 mmol), Pd(OAc)2 (505 mg, 2.25 mmol), Pcy3-HBF4 (1.63 g, 4.5 mmol), and Cs2CO3 (22 g, 67.5 mmol) were dissolved in 113 mL of o-xylene in a flask, and the mixture was stirred at 160° C. for 4 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and the residual moisture was removed using magnesium sulfate. The residue was dried, and separated by column chromatography to obtain compound 1-4 (1 g, yield: 11%).
- Compound 1-4 (4.5 g, 11.06 mmol), 2-chloro-3-phenylquinoxaline (4 g, 16.6 mmol), 4-dimethylaminopyridine (DMAP) (67 mg, 0.553 mmol), and Cs2CO3 (10.8 g, 331.8 mmol) were dissolved in 60 mL of dimethylsulfoxide (DMSO) in a flask, and the mixture was refluxed at 140° C. for 4 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and the residual moisture was removed using magnesium sulfate. The residue was dried, and separated by column chromatography to obtain compound C-1 (2.5 g, yield: 37%).
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Compound MW M.P. C-1 610.22 246° C. -
- Compound 1-4 (4 g, 9.84 mmol), 3-bromo-1,1′:2′,1″-terphenyl (3.65 g, 11.8 mmol), Pd2(dba)3 (448 mg, 0.492 mmol), S-Phos (448 mg, 0.984 mmol), and NaOtBu (2.84 g, 29.52 mmol) were dissolved in 50 mL of o-xylene in a flask, and the mixture was stirred at 170° C. for 4 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and the residual moisture was removed using magnesium sulfate. The residue was dried, and separated by column chromatography to obtain compound C-29 (1.5 g, yield: 24%).
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Compound MW M.P. C-29 643.78 282° C. -
- Compound A (60 g, 283 mmol), Compound B (100 g, 424 mmol), tetrakis(triphenylphosphine)palladium (16.3 g, 14.1 mmol), cesium carbonate (276 g, 849 mmol), 1400 mL of toluene, 350 mL of ethanol and 350 mL of distilled water were added into a reaction vessel, and the mixture was stirred at 130° C. for 12 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and extracted with ethyl acetate. The extracted organic layer was dried with magnesium sulfate, and the solvent was removed by rotary evaporator. Then, the residue was separated by column chromatography to obtain compound 3-1 (38 g, yield: 41%).
- Compound 3-1 (38 g, 117 mmol), phenylboronic acid (35 g, 234 mmol), tris(dibenzylindeneacetone)dipalladium (5.3 g, 5.86 mmol). S-Phos (4.8 g, 11.7 mmol), tripotassium phosphate (62 g, 293 mmol), and 600 mL of toluene were added into a reaction vessel, and the mixture was stirred under reflux for 2 hours. After completion of the reaction, the reaction mixture was washed with distilled water, and extracted with ethyl acetate. The extracted organic layer was dried with magnesium sulfate, and the solvent was removed by rotary evaporator. Then, the residue was separated by column chromatography to obtain compound 3-2 (31 g, yield: 67%).
- Compound 3-2 (21 g, 53.7 mmol), triphenylphosphite (70 mL, 268 mmol), and 180 mL of dichlorobenzene (DCB) were added into a reaction vessel, and the mixture was stirred at 200° C. for 12 hours. After completion of the reaction, the reaction mixture was distilled under reduced pressure to remove DCB, and washed with distilled water and extracted with ethyl acetate. The extracted organic layer was dried with magnesium sulfate, and the solvent was removed by rotary evaporator. Then, the residue was separated by column chromatography to obtain compound 3-3 (10 g, yield: 55%).
- Compound 3-3 (6.6 g, 17.9 mmol), palladium (II) acetate (0.2 g, 0.89 mmol), PCy3-BF4 (1.3 g, 3.58 mmol), cesium carbonate (17 g, 53.7 mmol), and 90 mL of o-xylene were added into a reaction vessel, and the mixture was stirred under reflux at 160° C. for 4 hours. After completion of the reaction, the reaction mixture was washed with distilled water, and extracted with ethyl acetate. The extracted organic layer was dried with magnesium sulfate, and the solvent was removed by rotary evaporator. Then, the residue was separated by column chromatography to obtain compound 3-4 (1.8 g, yield: 32%).
- Compound 3-4 (1.8 g, 5.43 mmol), 2-(3-bromophenyl)-4,6-diphenyl-1,3,5-triazine (2.3 g, 5.97 mmol), tris(dibenzylindeneacetone)dipalladium (0.2 g, 0.27 mmol), tri-tert-butylphosphine (0.3 mL, 0.54 mmol), sodium tert-butoxide (1.3 g, 13.5 mmol), and 30 mL of toluene were added into a reaction vessel, and the mixture was stirred under reflux for 3 hours. After completion of the reaction, the reaction mixture was washed with distilled water, and extracted with ethyl acetate. The extracted organic layer was dried with magnesium sulfate, and the solvent was removed by rotary evaporator. Then, the residue was separated by column chromatography to obtain compound C-196 (3.3 g, yield: 95%).
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Compound MW UV PL M.P. C-196 638.21 410 nm 522 nm 240° C. -
- Compound 1-4 (4.0 g, 9.84 mmol), 4-bromo-N,N-diphenylaniline (3.2 g, 9.84 mmol), Pd2(dba)3 (0.45 g, 0.5 mmol), s-phos (0.4 g, 0.98 mmol), and NaOtBu (1.9 g, 19.7 mmol) were dissolved in 50 mL of o-xylene in a flask, and the mixture was stirred under reflux for 5 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and separated by column chromatography to obtain compound C-36 (2.67 g, yield: 42%).
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Compound MW M.P. C-36 649.78 312° C. -
- Compound 1-4 (4.0 g, 9.84 mmol), 2-bromodibenzo[b,d]furan (1.7 g, 9.84 mmol), Pd2(dba)3 (0.45 g, 0.5 mmol), s-phos (0.4 g, 0.98 mmol), and NaOtBu (1.9 g, 19.7 mmol) were dissolved in 50 mL of o-xylene in a flask, and the mixture was stirred under reflux for 5 hours. After completion of the reaction, an organic layer was extracted with ethyl acetate, and separated by column chromatography to obtain compound C-32 (1.68 g, yield: 30%).
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Compound MW M.P. C-32 572.65 291° C. -
- Compound A (CAS: 2085325-18-2, 4.0 g, 9.5 mmol), 2-chloro-3-phenylquinoxaline (2.8 g, 11.4 mmol), tetrakis(triphenylphosphine)palladium (Pd(PPh3)4) (0.5 g, 0.5 mmol), potassium carbonate (K2CO3) (2.0 g, 19 mmol), 30 mL of toluene, 7 mL of EtOH, and 10 mL of water were added into a reaction vessel, and the mixture was stirred under reflux for one day. After completion of the reaction, the reaction mixture was cooled to room temperature, filtered by cellite with methylene chloride (MC), distilled under reduced pressure, and then separated by column chromatography with methylene chloride/hexane (MC/Hex) to obtain compound C2-86 (2.7 g, yield: 57%).
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Compound MW M.P. C2-86 499.6 266° C. -
- Compound A (23.8 g, 56.6 mmol), 2-chloro-4-(naphthalen-1-yl)-6-phenyl-1,3,5-triazine (15.0 g, 47.2 mmol), Pd(PPh3)4 (2.72 g, 2.36 mmol), K2CO3 (16.3 g, 118 mmol), 240 mL of toluene, 60 mL of EtOH, and 60 mL of distilled water were added into a reaction vessel, and the mixture was stirred under reflux for 2 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and filtered by silica gel. Then, an organic layer was distilled under reduced pressure, and recrystallized with toluene to obtain compound C2-125 (13.8 g, yield: 51%).
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Compound MW M.P. C2-125 576.6 231° C. -
- Compound A (4.0 g, 9.5 mmol), 2-([1,1′-biphenyl]-3-yl)-4-chloro-6-phenyl-1,3,5-triazine (3.9 g, 11.4 mmol), Pd(PPh3)4 (0.5 g, 0.5 mmol), K2CO3 (2.6 g, 19 mmol), 30 mL of toluene, 7 mL of EtOH, and 10 mL of distilled water were added into a reaction vessel, and the mixture was stirred under reflux for 6 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and stirred at room temperature. The solid obtained by adding MeOH was filtered under reduced pressure, and separated by column chromatography with MC to obtain compound C2-116 (4.6 yield: 80%).
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Compound MW M.P. C2-116 602.7 227° C. -
- Compound A (3.0 g, 7.1 mmol), 2-chloro-4-(dibenzo[b,d]furan-1-yl)-6-phenyl-1,3,5-triazine (3.4 g, 9.26 mmol), Pd(PPh3)4 (0.4 g, 0.36 mmol), K2CO3 (2.0 g, 14 mmol). 36 mL of toluene, 8 mL of EtOH, and 12 mL of distilled water were added into a reaction vessel, and the mixture was stirred under reflux for 6 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and stirred at room temperature. The solid obtained by adding MeOH was filtered under reduced pressure, and separated by column chromatography with MC to obtain compound C2-120 (3.3 g, yield: 75%).
-
Compound MW M.P. C2-120 616.7 282° C. - OLEDs according to the present disclosure were produced. A transparent electrode indium tin oxide (ITO) thin film (10 Ω/sq) on a glass substrate for an OLED (GEOMATEC CO., LTD., Japan) was subjected to an ultrasonic washing with acetone and isopropyl alcohol, sequentially, and then was stored in isopropyl alcohol. The ITO substrate was then mounted on a substrate holder of a vacuum vapor deposition apparatus. Compound HI-1 shown in Table 2 as a first hole injection compound was introduced into a cell of the vacuum vapor deposition apparatus, and compound HT-1 shown in Table 2 was introduced into another cell of the vacuum vapor deposition apparatus. The two materials were evaporated at different rates, and compound HI-1 was deposited in a doping amount of 3 wt % based on the total amount of compound HI-1 and compound HT-1 to form a hole injection layer having a thickness of 10 nm on the ITO substrate. Next, compound HT-1 was deposited on the hole injection layer to form a first hole transport layer having a thickness of 80 nm. Compound HT-2 was then introduced into another cell of the vacuum vapor deposition apparatus and was evaporated by applying an electric current to the cell, thereby forming a second hole transport layer having a thickness of 60 nm on the first hole transport layer. After forming the hole injection layer and the hole transport layers, a light-emitting layer was formed thereon as follows: The first host compound and the second host compound shown in Table 1 below were introduced into two cells of the vacuum vapor depositing apparatus as hosts, and compound D-71 was introduced into another cell as a dopant. The two host materials were evaporated at a rate of 1:1 and the dopant material was simultaneously evaporated at a different rate, and the dopant was deposited in a doping amount of 3 wt % based on the total amount of the hosts and the dopant to form a light-emitting layer having a thickness of 40 nm on the second hole transport layer. Compound ETL-1 and compound EIL-1 were evaporated in a weight ratio of 50:50 to form an electron transport layer having a thickness of 35 nm on the light-emitting layer. After depositing compound EIL-1 as an electron injection layer having a thickness of 2 nm on the electron transport layer, an Al cathode having a thickness of 80 nm was deposited on the electron injection layer by another vacuum vapor deposition apparatus. Thus, an OLED was produced. All the materials used for producing the OLED were purified by vacuum sublimation at 10−8 torr.
- OLEDs were produced in the same manner as in Device Example 1, except that the compound shown in Table 1 below was used alone as a first host or a second host.
- The driving voltage, luminous efficiency, and light-emitting color at a luminance of 1,000 nit, and the time taken for luminance to decrease from 100% to 95% at a luminance of 5,000 nit (lifetime; T95) of the OLEDs produced in Device Examples 1 to 3, and Comparative Examples 1 to 3 are provided in Table 1 below.
-
TABLE 1 Life- Driving Luminous Light- time Fist Second Voltage Efficiency Emitting (T95, Host Host (V) (cd/A) Color hr) Comparative C-29 — 4.7 5.8 Red 9.3 Example 1 Comparative — C2-120 3.5 30.8 Red 55 Example 2 Comparative — C2-116 3.2 28.0 Red 33.9 Example 3 Device C-29 C2-120 3.0 35.3 Red 551 Example 1 Device C-32 C2-120 3.1 35.4 Red 563 Example 2 Device C-32 C2-116 3.0 35.1 Red 322 Example 3 - From Table 1 above, it can be confirmed that the OLEDs comprising the plurality of host materials according to the present disclosure as host materials have improved driving voltage, luminous efficiency, and/or lifespan property, compared to the conventional OLED. Without wishing to be bound by theory, it is considered that by using the compound represented by formula 1 of the present disclosure in combination with the compound represented by formula 2 of the present disclosure, the HOMO (highest occupied molecular orbital) energy level increases compared to the case when using the conventional compound, which is a carbazole derivative, resulting in increase of the hole mobility. Thus, the hole injection from a hole transport layer becomes easier, and the balance between hole and electron and the formation of exciton may be improved, thereby improving the driving voltage, luminous efficiency and/or lifetime property of an OLED.
- The compounds used in the Device Examples and the Comparative Examples are shown in Table 2 below.
Claims (11)
1. A plurality of host materials comprising at least one first host compound and at least second host compound, wherein the first host compound is represented by the following formula 1, and the second host compound is represented by the following formula 2:
wherein
B1 to B7, each independently, are not present, or represent a substituted or unsubstituted (C5-C20) ring, in which carbon atoms of the ring may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur, with the proviso that at least five of B1 to B7 are present, and adjacent rings of B1 to B7 are fused with each other;
Y represents —N(L1-(Ar1)n)—, —O—, —S—, or —C(R1)(R2)—;
L1 represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene;
Ar1 represents a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or —N(R3)(R4);
R1 to R4, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or may be linked to an adjacent substituent to form a ring(s); and
n represents an integer of 1 or 2, where if n is 2, each of Ar1 may be the same or different;
wherein
X represents —N═, —NR35—, —O— or —S—;
Z represents —N═, —NR36—, —O— or —S—, where if X represents —N═, Z represents —NR36—, —O— or —S—, and if X represents —NR35—, Z represents —N═, —O— or —S—;
HAr represents a substituted or unsubstituted (3- to 30-membered)heteroaryl;
R31 represents a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl;
R32 to R34, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3); or may be linked to an adjacent substituent to form a ring(s);
R35 and R36, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)arylsilyl, or -L3-N(Ar2)(Ar3);
L2 and L3, each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
Ar2 and Ar3, each independently, represent hydrogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C2-C30)alkenyl, a substituted or unsubstituted fused ring group of a (C3-C30) aliphatic ring(s) and a (C6-C30) aromatic ring(s), a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (3- to 30-membered)heteroaryl; and
a′ represents 1, b′ and c′, each independently, represent an integer of 1 or 2, and d′ represents an integer of 1 to 4, where if each of b′, c′ and d′ is an integer of 2 or more, each of R32 to each of R34 may be the same or different.
2. The plurality of host materials according to claim 1 , wherein the substituents of the substituted alkyl, the substituted alkylene, the substituted alkenyl, the substituted aryl, the substituted arylene, the substituted heteroaryl, the substituted heteroarylene, the substituted cycloalkyl, the substituted cycloalkylene, the substituted alkoxy, the substituted trialkylsilyl, the substituted dialkylarylsilyl, the substituted alkyldiarylsilyl, the substituted triarylsilyl, the substituted fused ring of an aliphatic ring(s) and an aromatic ring(s), and the substituted ring, each independently, are at least one selected from the group consisting of deuterium; a halogen; a cyano; a carboxyl; a nitro; a hydroxyl; a (C1-C30)alkyl; a halo(C1-C30)alkyl; a (C2-C30)alkenyl; a (C2-C30)alkynyl; a (C1-C30)alkoxy; a (C1-C30)alkylthio; a (C3-C30)cycloalkyl; a (C3-C30)cycloalkenyl; a (3- to 7-membered)heterocycloalkyl; a (C6-C30)aryloxy; a (C6-C30)arylthio; a (3- to 50-membered)heteroaryl unsubstituted or substituted with at least one of a (C1-C30)alkyl(s), a (C6-C30)aryl(s), and a di(C6-C30)arylamino(s); a (C6-C30)aryl unsubstituted or substituted with at least one of deuterium, a cyano(s), a (C1-C30)alkyl(s), a (3- to 50-membered)heteroaryl(s), a mono- or di-(C6-C30)arylamino(s), and a tri(C6-C30)arylsilyl(s); a tri(C1-C30)alkylsilyl; a tri(C6-C30)arylsilyl; a di(C1-C30)alkyl(C6-C30)arylsilyl; a (C1-C30)alkyldi(C6-C30)arylsilyl; an amino; a mono- or di-(C1-C30)alkylamino; a mono- or di-(C2-C30)alkenylamino; a mono- or di-(C6-C30)arylamino; a mono- or di-(3- to 30-membered)heteroarylamino; a (C1-C30)alkyl(C2-C30)alkenylamino; a (C1-C30)alkyl(C6-C30)arylamino; a (C1-C30)alkyl(3- to 30-membered)heteroarylamino; a (C2-C30)alkenyl(C6-C30)arylamino; a (C2-C30)alkenyl(3- to 30-membered)heteroarylamino; a (C6-C30)aryl(3- to 30-membered)heteroarylamino; a (C1-C30)alkylcarbonyl; a (C1-C30)alkoxycarbonyl; a (C6-C30)arylcarbonyl; a di(C6-C30)arylboronyl; a di(C1-C30)alkylboronyl; a (C1-C30)alkyl(C6-C30)arylboronyl; a (C6-C30)aryl(C1-C30)alkyl; and a (C1-C30)alkyl(C6-C30)aryl.
3. The plurality of host materials according to claim 1 , wherein formula 1 is represented by at least one of the following formulas 1-1 to 1-4:
wherein
Y1, Y2, Y3, and Y4, each independently, are the same as the definition of Y in claim 1 , where if a plurality of Ar1's are present, each of Ar1 may be the same or different;
X1 to X12, each independently, represent —N═ or —C(Ra)═; and
Ra, each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl; or adjacent Ra's may be linked to each other to form a ring(s), where if a plurality of Ra's are present, each of Ra may be the same or different.
4. The plurality of host materials according to claim 3 , wherein at least one of Ar1(s) and Ra(s), each independently, is at least one selected from those listed in the following group 1:
wherein
D1 and D2, each independently, represent a benzene ring or a naphthalene ring;
X21 represents O, S, NR5, or C(R6)(R7);
X22, each independently, represents CR8 or N, with the proviso that at least one of X22 represents N;
X23, each independently, represents CR9 or N;
L11 to L18, each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
R11 to R21 and R5 to R9, each independently, represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C3-C30)cycloalkyl, or may be linked to an adjacent substituent to form a ring(s); and
aa, ff, and gg, each independently, represent an integer of 1 to 5, bb represents an integer of 1 to 7, and cc, dd, and ee, each independently, represent an integer of 1 to 4, where if each of aa to gg is an integer of 2 or more, each of R11 to each of R17 may be the same or different.
5. The plurality of host materials according to claim 3 , wherein at least one of Ar1(s) and Ra(s), each independently, is at least one selected from those listed in the following groups 2 and 3:
in group 2,
L represents a single bond, a substituted or unsubstituted (C1-C30)alkylene, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene; and
A1 to A3, each independently, represent a substituted or unsubstituted (C1-C30)alkyl, or a substituted or unsubstituted (C6-C30)aryl.
6. The plurality of host materials according to claim 1 , wherein in formula 1, B1 to B7, each independently, are not present, or represent a substituted or unsubstituted benzene ring, a substituted or unsubstituted naphthalene ring, a substituted or unsubstituted pyrrole ring, a substituted or unsubstituted furan ring, a substituted or unsubstituted thiophene ring, a substituted or unsubstituted cyclopentadiene ring, a substituted or unsubstituted fluorene ring, a substituted or unsubstituted pyridine ring, or a substituted or unsubstituted dibenzofuran ring, with the proviso that at least five of B1 to B7 are present, and adjacent rings of B1 to B7 are fused with each other.
7. The plurality of host materials according to claim 1 , wherein formula 2 is represented by at least one selected from the following formulas 2-1 to 2-8:
8. The plurality of host materials according to claim 1 , wherein in formula 2, HAr represents a substituted or unsubstituted triazinyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted benzoquinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted benzoquinoxalinyl, a substituted or unsubstituted quinolyl, a substituted or unsubstituted benzoquinolyl, a substituted or unsubstituted isoquinolyl, a substituted or unsubstituted benzoisoquinolyl, a substituted or unsubstituted triazolyl, a substituted or unsubstituted pyrazolyl, a substituted or unsubstituted naphthyridinyl, a substituted or unsubstituted triazanaphthyl, or a substituted or unsubstituted benzothienopyrimidinyl.
11. An organic electroluminescent device comprising an anode, a cathode, and at least one light-emitting layer between the anode and the cathode, wherein at least one of the light-emitting layers comprises the plurality of host materials according to claim 1 .
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