CN116903648A - Boron nitride compound and application thereof - Google Patents
Boron nitride compound and application thereof Download PDFInfo
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- CN116903648A CN116903648A CN202310878816.3A CN202310878816A CN116903648A CN 116903648 A CN116903648 A CN 116903648A CN 202310878816 A CN202310878816 A CN 202310878816A CN 116903648 A CN116903648 A CN 116903648A
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- alkyl
- aryl
- alkoxy
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- -1 Boron nitride compound Chemical class 0.000 title claims abstract description 77
- 229910052582 BN Inorganic materials 0.000 title claims abstract description 13
- 239000000463 material Substances 0.000 claims abstract description 100
- TZHYBRCGYCPGBQ-UHFFFAOYSA-N [B].[N] Chemical compound [B].[N] TZHYBRCGYCPGBQ-UHFFFAOYSA-N 0.000 claims abstract description 23
- 229910017464 nitrogen compound Inorganic materials 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims description 71
- 239000000203 mixture Substances 0.000 claims description 62
- 125000000217 alkyl group Chemical group 0.000 claims description 45
- 229910052805 deuterium Inorganic materials 0.000 claims description 41
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 40
- 125000001072 heteroaryl group Chemical group 0.000 claims description 40
- 125000003118 aryl group Chemical group 0.000 claims description 37
- 238000002347 injection Methods 0.000 claims description 36
- 239000007924 injection Substances 0.000 claims description 36
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 35
- 125000005915 C6-C14 aryl group Chemical group 0.000 claims description 31
- 230000005525 hole transport Effects 0.000 claims description 30
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 28
- 229910052731 fluorine Inorganic materials 0.000 claims description 28
- 239000011737 fluorine Substances 0.000 claims description 28
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 25
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims description 22
- 229910052757 nitrogen Inorganic materials 0.000 claims description 22
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims description 21
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 18
- 102100039856 Histone H1.1 Human genes 0.000 claims description 16
- 101001035402 Homo sapiens Histone H1.1 Proteins 0.000 claims description 16
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 12
- 239000010409 thin film Substances 0.000 claims description 9
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims description 8
- 230000000903 blocking effect Effects 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 150000001716 carbazoles Chemical class 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 238000005286 illumination Methods 0.000 claims description 3
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 3
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 claims description 2
- 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 239000002019 doping agent Substances 0.000 claims description 2
- 230000005281 excited state Effects 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- GBXQPDCOMJJCMJ-UHFFFAOYSA-M trimethyl-[6-(trimethylazaniumyl)hexyl]azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCCCCC[N+](C)(C)C GBXQPDCOMJJCMJ-UHFFFAOYSA-M 0.000 claims description 2
- 238000001228 spectrum Methods 0.000 abstract description 14
- 238000004020 luminiscence type Methods 0.000 abstract description 6
- 230000021615 conjugation Effects 0.000 abstract description 2
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-UHFFFAOYSA-N 0.000 abstract description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 126
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 42
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 37
- 238000004440 column chromatography Methods 0.000 description 16
- 239000011541 reaction mixture Substances 0.000 description 16
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 14
- 238000006243 chemical reaction Methods 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 238000010438 heat treatment Methods 0.000 description 12
- 238000000151 deposition Methods 0.000 description 11
- 229910052751 metal Inorganic materials 0.000 description 11
- 239000002184 metal Substances 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- 238000000034 method Methods 0.000 description 10
- 239000012074 organic phase Substances 0.000 description 10
- 239000007787 solid Substances 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 9
- 239000002994 raw material Substances 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 8
- 230000008021 deposition Effects 0.000 description 8
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- 230000003595 spectral effect Effects 0.000 description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 238000001748 luminescence spectrum Methods 0.000 description 6
- 239000002243 precursor Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 238000003786 synthesis reaction Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 230000003111 delayed effect Effects 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 239000012298 atmosphere Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000005457 ice water Substances 0.000 description 4
- 239000002346 layers by function Substances 0.000 description 4
- 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 4
- 238000011056 performance test Methods 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 238000006467 substitution reaction Methods 0.000 description 4
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 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
- 238000007738 vacuum evaporation Methods 0.000 description 4
- 238000007740 vapor deposition Methods 0.000 description 4
- 230000004382 visual function Effects 0.000 description 4
- 238000005401 electroluminescence Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000012544 monitoring process Methods 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 125000004076 pyridyl group Chemical group 0.000 description 3
- 125000000714 pyrimidinyl group Chemical group 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 238000005019 vapor deposition process Methods 0.000 description 3
- 125000003363 1,3,5-triazinyl group Chemical class N1=C(N=CN=C1)* 0.000 description 2
- IUVCFHHAEHNCFT-INIZCTEOSA-N 2-[(1s)-1-[4-amino-3-(3-fluoro-4-propan-2-yloxyphenyl)pyrazolo[3,4-d]pyrimidin-1-yl]ethyl]-6-fluoro-3-(3-fluorophenyl)chromen-4-one Chemical compound C1=C(F)C(OC(C)C)=CC=C1C(C1=C(N)N=CN=C11)=NN1[C@@H](C)C1=C(C=2C=C(F)C=CC=2)C(=O)C2=CC(F)=CC=C2O1 IUVCFHHAEHNCFT-INIZCTEOSA-N 0.000 description 2
- HRZTZLCMURHWFY-UHFFFAOYSA-N 2-bromo-1,3-difluorobenzene Chemical compound FC1=CC=CC(F)=C1Br HRZTZLCMURHWFY-UHFFFAOYSA-N 0.000 description 2
- TXNLQUKVUJITMX-UHFFFAOYSA-N 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine Chemical compound CC(C)(C)C1=CC=NC(C=2N=CC=C(C=2)C(C)(C)C)=C1 TXNLQUKVUJITMX-UHFFFAOYSA-N 0.000 description 2
- 235000009161 Espostoa lanata Nutrition 0.000 description 2
- 240000001624 Espostoa lanata Species 0.000 description 2
- 238000006069 Suzuki reaction reaction Methods 0.000 description 2
- KTYAQHYBYRVCGD-UHFFFAOYSA-N [Ir].COC1=CC=CCCCC1 Chemical class [Ir].COC1=CC=CCCCC1 KTYAQHYBYRVCGD-UHFFFAOYSA-N 0.000 description 2
- 230000004913 activation Effects 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 230000005540 biological transmission Effects 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 2
- 229910000024 caesium carbonate Inorganic materials 0.000 description 2
- 230000008878 coupling Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 238000000921 elemental analysis Methods 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000002883 imidazolyl group Chemical group 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001786 isothiazolyl group Chemical group 0.000 description 2
- 125000000842 isoxazolyl group Chemical group 0.000 description 2
- UBJFKNSINUCEAL-UHFFFAOYSA-N lithium;2-methylpropane Chemical compound [Li+].C[C-](C)C UBJFKNSINUCEAL-UHFFFAOYSA-N 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 125000002950 monocyclic group Chemical group 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- IVDFJHOHABJVEH-UHFFFAOYSA-N pinacol Chemical compound CC(C)(O)C(C)(C)O IVDFJHOHABJVEH-UHFFFAOYSA-N 0.000 description 2
- 238000007747 plating Methods 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 235000011009 potassium phosphates Nutrition 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000003373 pyrazinyl group Chemical group 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000002098 pyridazinyl group Chemical group 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 125000006413 ring segment Chemical group 0.000 description 2
- VNFWTIYUKDMAOP-UHFFFAOYSA-N sphos Chemical compound COC1=CC=CC(OC)=C1C1=CC=CC=C1P(C1CCCCC1)C1CCCCC1 VNFWTIYUKDMAOP-UHFFFAOYSA-N 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- ORPVVAKYSXQCJI-UHFFFAOYSA-N 1-bromo-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1Br ORPVVAKYSXQCJI-UHFFFAOYSA-N 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- BMIBJCFFZPYJHF-UHFFFAOYSA-N 2-methoxy-5-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine Chemical compound COC1=NC=C(C)C=C1B1OC(C)(C)C(C)(C)O1 BMIBJCFFZPYJHF-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- 239000005725 8-Hydroxyquinoline Substances 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- PZNSFCLAULLKQX-UHFFFAOYSA-N Boron nitride Chemical class N#B PZNSFCLAULLKQX-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000641 acridinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 150000004982 aromatic amines Chemical class 0.000 description 1
- 150000001543 aryl boronic acids Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 125000003828 azulenyl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 description 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 description 1
- 125000005874 benzothiadiazolyl group Chemical group 0.000 description 1
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 description 1
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 1
- 239000012964 benzotriazole Substances 0.000 description 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 description 1
- 125000002619 bicyclic group Chemical group 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- WYEMLYFITZORAB-UHFFFAOYSA-N boscalid Chemical compound C1=CC(Cl)=CC=C1C1=CC=CC=C1NC(=O)C1=CC=CN=C1Cl WYEMLYFITZORAB-UHFFFAOYSA-N 0.000 description 1
- 238000005893 bromination reaction Methods 0.000 description 1
- KMGBZBJJOKUPIA-UHFFFAOYSA-N butyl iodide Chemical compound CCCCI KMGBZBJJOKUPIA-UHFFFAOYSA-N 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 239000003153 chemical reaction reagent Substances 0.000 description 1
- 125000000259 cinnolinyl group Chemical group N1=NC(=CC2=CC=CC=C12)* 0.000 description 1
- 229920000547 conjugated polymer Polymers 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- ARUKYTASOALXFG-UHFFFAOYSA-N cycloheptylcycloheptane Chemical group C1CCCCCC1C1CCCCCC1 ARUKYTASOALXFG-UHFFFAOYSA-N 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 125000003838 furazanyl group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 description 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 description 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
- 230000000155 isotopic effect Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000004593 naphthyridinyl group Chemical group N1=C(C=CC2=CC=CN=C12)* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229910000510 noble metal Inorganic materials 0.000 description 1
- 230000005693 optoelectronics Effects 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 238000013086 organic photovoltaic Methods 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- HWLDNSXPUQTBOD-UHFFFAOYSA-N platinum-iridium alloy Chemical compound [Ir].[Pt] HWLDNSXPUQTBOD-UHFFFAOYSA-N 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000001567 quinoxalinyl group Chemical group N1=C(C=NC2=CC=CC=C12)* 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000002285 radioactive effect Effects 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000011593 sulfur Chemical group 0.000 description 1
- 229910052717 sulfur Chemical group 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000000147 tetrahydroquinolinyl group Chemical group N1(CCCC2=CC=CC=C12)* 0.000 description 1
- 125000003831 tetrazolyl group Chemical group 0.000 description 1
- 238000009210 therapy by ultrasound Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000004306 triazinyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- 238000001195 ultra high performance liquid chromatography Methods 0.000 description 1
Classifications
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Abstract
The boron-nitrogen compound introduces nitrogen atoms through extended conjugation, so that not only is the fine adjustment of spectrum realized, but also the luminous efficiency is further improved. The boron nitride compound has a narrow spectrum, is used as a narrow spectrum luminescent material for preparing a luminescent layer of an organic electroluminescent device, and the prepared organic electroluminescent device realizes narrow spectrum yellow light-red light TADF emission, has a luminescence peak position between 540 and 640nm, has a half-peak width smaller than 50nm, and ensures that the electroluminescent external quantum efficiency of the device is more than 30 percent.
Description
Technical Field
The invention belongs to the technical field of organic electroluminescence, and relates to a boron-nitrogen compound and a preparation method and application thereof.
Background
The organic photoelectric material (Organic Optoelectronic Materials) is an organic material having the characteristics of generation, conversion, transmission and the like of photons and electrons. Currently, controllable photoelectric properties of Organic photoelectric materials have been applied to Organic Light-Emitting diodes (OLEDs), organic solar cells (Organic Photovoltage, OPVs), organic field effect transistors (Organic Field Effect Transistor, OFETs), and even Organic lasers. In recent years, OLEDs have become a very popular new flat display product at home and abroad. The OLED display has the characteristics of self-luminescence, wide viewing angle, short reaction time, high luminous efficiency, wide color gamut, low working voltage, thin panel, capability of manufacturing a large-size flexible panel and low cost, and is known as a star flat display product in the 21 st century.
As regards the history of organic electroluminescence, it can be traced back to the report by Bernanose et al in 1953 (Holst G A, kster T, voges E, et al FLOX-an oxygen-flux-measuring system using a phase-modulation method to evaluate the oxygen-dependent fluorescence lifetime, science directors and operators B: chemical,1995,29,213.), about 10 years later, the fluorescent emission of anthracene was observed by applying a voltage to crystals of anthracene with Pope et al in 1963, new York university (M.Pope, H.Kallmann and P. Magnante, electroluminescence in Organic Crystals, J. Chem. Phys.,1963,38,2042). In 1987, C.W.Tang et al, kodak, U.S. used an ultrathin film technique to prepare a light-emitting device with an aromatic amine having a good hole transport effect as a hole transport layer, an aluminum complex of 8-hydroxyquinoline as a light-emitting layer, and an Indium Tin Oxide (ITO) film and a metal alloy as an anode and a cathode, respectively. The device obtains brightness of up to 1000cd/m under 10V driving voltage 2 The efficiency of the device was 1.5lm/W (c.w. tang and s.a. vanslyke, organic electroluminescent diodes, appl. Phys. Lett.,1987, 51, 913), a breakthrough development has led to rapid and intensive development of organic electroluminescent research worldwide. In 1990, burroughes et al, university of Cambridge, proposed the first polymer (PPV) based light emitting diode. It has been shown that PPV can be used as an emissive material with high fluorescence in single layer devices, which has a high luminous efficiency (Burroughe s.J.H.et al., light-emitting diodes based on conjugated polymers, nature,1990,347,539.). Baldo and Forrest et al, university of Pranceton, 1998 reported that the first electroluminescent-based phosphorescent device, which in principle can have an internal quantum yield of 100% (M.A.Baldo, D.F.O' Briiental., highly efficient phosphorescent emission from organic electroluminescent devices, nature,1998, 395, 151), but on the one hand the phosphorescent material generally uses noble metals such as iridium platinum, which are expensive, and on the other hand the deep blue phosphorescent material still has chemical instability, and the device has a large efficiency roll-off problem at high current density, so it is very important to develop an OLED device using inexpensive and stable organic small molecular materials while achieving high-efficiency luminescence.
In 2012, adachi' S group reports that highly efficient fully fluorescent OLED devices based on the Thermally Activated Delayed Fluorescence (TADF) mechanism (Uoyama H, goushi K, shizu K, et al Highly efficient organic light-emitting diodes from delayed fluorescence, nature,2012,492 (7428):234-238.) can absorb thermal energy when the S1 and T1 energy levels of the molecule are sufficiently small, return to singlet state through RISC process, and thus fluoresce, and their Internal Quantum Efficiency (IQE) can theoretically reach 100%, and External Quantum Efficiency (EQE) even up to 30%, as compared to the level of shoulder phosphorescence devices. As a next-generation light-emitting material, a TADF material is being studied.
The TADF molecules are primarily doped as guest materials in a wide bandgap host material to achieve high efficiency thermally activated delayed fluorescence (Q.Zhang, J.Li, K.Shizu, et al design of Efficient Thermally Activated Delayed Fluorescence Materials for Pure Blue Organic Light Emitting Diodes, J.Am.chem.Soc.2012,134,14706; H.Uoyama, K.Goushi, K.Shizu, H.Nomura, C.Adachi, highly efficient organic light-emitting diodes from delayed fluorescence, nature,2012,492,234;T.Nishimoto,T.Yasuda,et al., asix-carbazole-decorated cyclophosphazene as a host with high triplet energy to realize efficient delayed-fluorescence OLEDs, mater.Horiz.,2014,1,264). Unlike traditional fluorescent molecular Localized (LE) state luminescence, TADF emission is mainly derived from transitions in ICT state, and is therefore susceptible to interdonor-acceptor vibration and rotational movement, resulting in a broader spectrum. The broad spectrum, while advantageous for illumination applications, does not meet the high color purity requirements of the display field. While the most important use of OLEDs is in display, narrow spectral designs (i.e., smaller full width at half maximum, FWHM) of TADF materials are necessary.
Disclosure of Invention
Aiming at the defects of the prior art, the invention aims to provide a boron-nitrogen compound, and a preparation method and application thereof. The compound provided by the invention aims to overcome the defect of TADF luminescent molecules, provides a narrow spectrum luminescent material for preparing a luminescent layer of an organic electroluminescent device, enables the organic electroluminescent device to realize narrow spectrum TADF emission, and enables the device to have high electroluminescent highest external quantum efficiency and longer service life.
In order to achieve the aim of the invention, the invention adopts the following technical scheme:
the invention provides a boron-nitrogen compound which is a narrow-spectrum yellow-red light organic luminescent material (the luminescence peak position is in the range of 540-640 nm), and the molecular structure of the boron-nitrogen compound is shown as the following formula I or formula II:
wherein R is 1 、R 2 、R 4 And R is 5 Independently selected from H, deuterium, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C18 aryl, substituted with one or more R a Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R a Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R a Substituted diphenylamino groups;
R a independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl, C6-C14 aryl, substituted with one or more R b Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R b Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R b Substituted diphenylamino groups;
R b independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R c Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R c Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R c Substituted diphenylamino groups;
R c independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R d Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R d Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R d Substituted diphenylamino groups;
R d independently at each occurrence deuterium, fluorine, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl or by one or more R e Substituted C6-C14 aryl;
R e independently for each occurrence deuterium, fluorine, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, or C6-C14 aryl;
the alkyl, alkoxy, cycloalkyl, aryl, heteroaryl groups are optionally substituted with one or more substituents selected from the group consisting of: halogen, -CN, C1-C12 alkyl, C1-C12 alkoxy, C1-C12 haloalkyl, C3-C10 cycloalkyl, C6-C14 aryl and 5-to 18-membered heteroaryl;
R 3 and R is 6＊ -L-R s Represents a bonding site, L is C1-C12 alkyl, C1-C12 alkoxy, R s Is hydrogen, C3-C10 cycloalkyl, C6-C24 aryl or 5-to 24-membered heteroaryl;
Y 1 、Y 2 、Y 3 And Y 4 Independently selected from N or C-R y1 、C-R y2 、C-R y3 、C-R y4 And Y is 1 、Y 2 、Y 3 And Y 4 At least one is N;
R y1 、R y2 、R y3 or R is y4 Independently selected from H, deuterium, fluorine, CN, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R y Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R y Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R y Substituted diphenylamino groups;
R y independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R y1 、R y2 、R y3 、R y4 independently or R y1 、R y2 、R y3 、R y4 Any adjacent two groups are condensed into an aromatic ring;
R 01 and R is 02 Selected from H, deuterium, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C18 aryl, 5-to 18-membered heteroaryl substituted with one or more R f Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R f Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R f Substituted diphenylamino groups;
R f independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R 7 、R 8 、R 9 and R is 10 Independently selected from H, deuterium, fluorine, CN, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R g Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R g Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R g Substituted diphenylamino groups;
R g independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R 7 、R 8 、R 9 and R is 10 Independently or R 7 、R 8 、R 9 And R is 10 Any adjacent two groups are condensed into an aromatic ring.
In one embodiment, the R 1 、R 2 、R 4 And R is 5 Is independently H, D (deuterium), C1-C12 alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, phenyl, substituted with at least one C 1 -C 12 Aryl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted aryl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
Preferably, said R a Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
Preferably, said R b Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
Preferably, said R c Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
Preferably, said R d Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Phenyl substituted by alkoxy, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
Preferably, said R 1 、R 2 、R 4 And R is 5 Independently H, deuterium, methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, hexyl, octyl, decyl,Methoxy, ethoxy, butoxy, hexyloxy, < > >Cyclohexyl, adamantyl, phenyl, 4-methyl-phenyl, 4-ethyl-phenyl, 4-propyl-phenyl, 4-isopropyl-phenyl, 4-n-butyl-phenyl, -/-, and->
Wherein the wavy line represents the attachment site of the group.
Preferably, said R 1 、R 2 、R 4 And R is 5 Independently H, methyl,Phenyl group,/->
Wherein the wavy line represents the attachment site of the group.
Preferably, said R 1 And R is 2 Identical, R 4 And R is 5 The same is selected from H, methyl,Phenyl group, Any one of them;
wherein R is h Is H, methyl, isopropyl, tert-butyl,
Preferably, said R 01 And R is 02 Selected from hydrogen, phenyl or
Preferably, said R 3 And R6 is selected from n-butyl, n-pentyl, n-hexyl or
Preferably, said R 7 、R 8 、R 9 And R is 10 Independently selected from hydrogen.
In some embodiments of the invention, the compound is any one of the following compounds:
the first molecular structural formula:
the second molecular structural formula:
in another aspect, the present invention provides an organic electroluminescent material comprising a boron nitrogen compound as described above.
In another aspect, the present invention provides an organic electroluminescent device comprising an anode and a cathode, and an organic thin film layer interposed between the anode and the cathode, the organic thin film layer comprising the boron-nitrogen compound as described above.
Preferably, the organic thin film layer comprises a light emitting layer, an optional hole injection layer, an optional hole transport layer, an optional electron transport layer, and an optional electron injection layer, wherein at least one of the light emitting layer, the electron injection layer, the electron transport layer, the hole transport layer, and the hole injection layer comprises a boron nitride compound as described above.
In the invention, the boron nitride compound with the structure shown in the formulas I and II can be used as a functional material in at least one layer of a light-emitting layer, an electron injection layer, an electron transport layer, a hole transport layer and a hole injection layer of an organic electroluminescent device.
In one embodiment, the organic electroluminescent device of the present invention may further comprise an optional hole blocking layer, an optional electron blocking layer, an optional capping layer, and the like.
In one embodiment, the organic electroluminescent device has a structure as shown in fig. 1, wherein 1 is an ITO anode, 2 is a hole injection layer, 3 is a hole transport layer, 4 is a light emitting layer, 5 is an electron transport layer, 6 is an electron injection layer, and 7 is a metal cathode.
In one embodiment, the boron nitrogen compound with the structures shown in the formulas I and II is used for preparing a light-emitting layer in an organic electroluminescent device.
In one embodiment, the organic electroluminescent device further comprises a substrate, and an anode layer, an organic light-emitting functional layer and a cathode layer sequentially formed on the substrate; the organic light-emitting functional layer comprises a light-emitting layer containing the boron-nitrogen compound, and can further comprise any one or a combination of a plurality of hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer and an electron injection layer.
In another aspect, the present invention provides an organic electroluminescent composition comprising a boron nitride compound as described above as a doping material and a host material;
preferably, the host material is a material having an electron transport ability and/or a hole transport ability and having a triplet excited state energy equal to or higher than that of the dopant material.
In one embodiment of the present invention, the host material in the organic electroluminescent composition is a carbazole derivative and/or carboline derivative having a structure represented by any one of the formulae (H-1) to (H-6):
wherein X is 1 、Y 1 And Z 1 Is CH or N, and X 1 、Y 1 And Z 1 At most one of them is N;
wherein R is 1H And R is 2H Independently any of the following groups:
Wherein X is 1 、Y 1 And Z 1 Is CH or N, and X 1 、Y 1 And Z 1 At most one of them is N;
wherein R is aH And R is bH H, C independently 1 -C 20 Alkyl, C 1 -C 20 Alkoxy, C 6 -C 20 Aryl, C 1 -C 20 Alkyl substituted C 6 -C 20 Aryl or C 1 -C 20 Alkoxy substituted C 6 -C 20 Aryl, number represents the attachment site of the group.
In one embodiment of the present invention, the organic electroluminescent composition preferably contains 0.3 to 30.0wt% of the boron-nitrogen compound having the structure shown in formula I as described above as a doping material, and the remaining 99.7 to 70.0wt% of the boron-nitrogen compound is a host material composed of 1 to 2 compounds having the structures of formulae (H-1) to (H-6).
In one embodiment of the invention, the host material contains 2 compounds having the structures of formula (H-1) to formula (H-6) in a weight ratio of 1:5 to 5:1, such as 1:5, 1:4, 1:3, 1:2, 1:1, 2:1, 3:1, 4:1, 5:1, etc.
In one embodiment of the present invention, the host material in the organic electroluminescent composition is one or two of the compounds H1-1 to H1-429.
In one embodiment of the present invention, the organic electroluminescent composition comprises 0.3 to 30.0wt% of boron nitrogen compound having the structure shown in the formulas I and II as described above, and the remaining 99.7 to 70.0wt% of the composition is 1 or 2 of the compounds H1-1 to H1-429.
In a preferred embodiment of the present invention, the organic electroluminescent composition comprises 2 of the compounds H1-1 to H1-429 as host material in a weight ratio of 1:5 to 5:1, such as 1:5, 1:4, 1:3, 1:2, 1:1, 2:1, 3:1, 4:1, 5:1, etc.
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In one embodiment of the invention, the doping material in the organic electroluminescent composition is any one of boron-nitrogen compounds with structures shown in formulas I and II (the content is 0.3 wt% to 30.0 wt%); the main body material (content of 99.7wt% -70.0wt%) is composed of any one of compounds shown as formula Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A and any one of compounds with structures shown as formulas H-1 to H-6.
In a preferred embodiment, the weight ratio between the compound indicated by Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A and the compound indicated by H-1, H-2, H-3, H-4, H-5 or H-6 in the host material is from 1:5 to 5:1, such as 1:5, 1:4, 1:3, 1:2, 1:1, 2:1, 3:1, 4:1, 5:1, etc.
Wherein R is 1a 、R 1b 、R 2a 、R 2b 、R 3a And R is 3b Wherein 1 or 2 are independently R Tz The remainder being the same or different and independently hydrogen, deuterium, C 1 -C 8 Alkyl, C 1 -C 8 Alkoxy, C 6 -C 18 Aryl, C 1 -C 8 Alkyl substituted C 6 -C 18 Aryl or C 1 -C 8 Alkoxy substituted C 6 -C 18 Aryl of (a); r is R Tz Is any one of substituent groups shown in the following formula:
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wherein asterisks represent the attachment site of the group;
in one embodiment of the present invention, the doping material in the organic electroluminescent composition is any one of boron-nitrogen compounds (the content is 0.3 wt% to 30.0 wt%) having the structures shown in formulas I and II as described above; the main material (the content is 99.7wt% -70.0wt%) is composed of any one of compounds shown as formulas TRZ-1 to TRZ-80 and any one of carbazole or carboline derivatives shown as formulas H1-1 to H1-429.
In a preferred embodiment, the weight ratio between the compound of formulae TRZ-1 to TRZ-81 and the carbazole or carboline derivative of formulae H1-1 to H1-429 in the host material is from 1:20 to 20:1, for example: 1:20, 1: 10. 1:5, 1:4, 1:3, 1:2, 1:1, 2:1, 3:1, 4:1, 5:1, 10:1, 20:1, etc.
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In another aspect, the present invention provides an organic electroluminescent device comprising an anode and a cathode and an organic thin film layer interposed between the anode and the cathode, the organic thin film layer comprising the organic electroluminescent composition as described above.
Preferably, the organic thin film layer comprises a light emitting layer, an optional hole injection layer, an optional hole transport layer, an optional electron injection layer, wherein at least one of the light emitting layer, the electron injection layer, the electron transport layer, the hole injection layer comprises an organic electroluminescent composition as described above.
In the present invention, the organic electroluminescent composition may be used as a functional material in at least one of a light emitting layer, an electron injection layer, an electron transport layer, a hole transport layer, and a hole injection layer of an organic electroluminescent device.
In a certain embodiment of the invention, the material of the light emitting layer in the organic electroluminescent device comprises an organic electroluminescent composition as described above.
In one embodiment of the present invention, the organic electroluminescent composition is a light-emitting layer, and the light-emitting principle of the light-emitting layer is based on energy transfer from a host material to either of the compounds represented by formulas I and II or carrier capture of the light-emitting material itself.
In one embodiment of the invention, the organic electroluminescent composition is a light-emitting layer; the host material in the organic electroluminescent composition may be a carbazole derivative and/or a carboline derivative represented by the formulae (H-1) to (H-6). In a preferred embodiment, the organic electroluminescent composition comprises 0.3 to 30.0wt% of any one of the compounds represented by the formulas I and II, and the remaining 99.7 to 70.0wt% of the composition is a host composed of 1 to 2 compounds having the structures of the formulas (H-1) to (H-6). For example, when the host contains 2 compounds having the structures of formulas (H-1) to (H-6), the weight ratio of the two compounds is 1:5 to 5:1.
In one embodiment of the invention, the organic electroluminescent composition is a light-emitting layer; the main material in the composition is 1-2 of the compounds H1-1 to H1-429. In a preferred embodiment, the organic electroluminescent composition comprises 0.3-30.0wt% of any one of the compounds of formulae I, II and III, and the remaining 99.7-70.0wt% of the composition is 1-2 of the compounds H1-1 to H1-427. For example, when 2 compounds of formulas H1-1 to H1-429 are included in the composition, the weight ratio of the two compounds is 1:5 to 5:1.
In one embodiment of the invention, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound shown in the formulas I and II (the content is 0.3-30.0 wt%); the main body material (content of 99.7wt% -70.0wt%) is composed of any one of the compounds shown as the formula Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A and any one of the compounds shown as the formulas H-1 to H-6. For example, in the host material, the weight ratio of Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A compound to the compound indicated as H-1, H-2, H-3, H-4, H-5 or H-6 is 1:20 to 20:1.
In one embodiment of the invention, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound shown in the formulas I and II (the content is 0.3-30.0 wt%); the main material (content of 99.7-70.0wt%) is composed of any one of 1,3, 5-triazine derivatives shown in formulas TRZ-1 to TRZ-81 and any one of carbazole or carboline derivatives shown in formulas H1-1 to H1-429. For example, in the host material, the weight ratio between the 1,3, 5-triazine derivative and the carbazole or carboline derivative is from 1:20 to 20:1.
In one embodiment of the invention, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound shown in the formulas BN-11 to BN-112 (the content is 0.3wt percent to 30.0wt percent); the main body material (the content is 99.7wt% -70.0wt%) is composed of any one of the compounds shown as the formula Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A and Trz6-A and any one of carbazole or carboline derivatives shown as the formulas H1-1 to H1-427. For example, in the host materials, the weight ratio between the compounds of formulae Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A, and Trz6-A, and carbazole or carboline derivatives of formulae H1-1 to H1-429 is 1:20 to 20:1.
In one embodiment of the present invention, the organic electroluminescent device further comprises a substrate, and an anode layer, an organic light-emitting functional layer and a cathode layer sequentially formed on the substrate; the organic light-emitting functional layer comprises a light-emitting layer containing the organic electroluminescent composition, and can also comprise any one or a combination of at least two of a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer and an electron injection layer.
In another aspect, the invention provides an application of the organic electroluminescent device in an organic electroluminescent display or an organic electroluminescent illumination source.
Description of the terms
Unless defined otherwise, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
As used herein, the term "comprising" or "including" can be open, semi-closed, and closed. In other words, the term also includes "consisting essentially of …," or "consisting of ….
Definition of groups
In this specification, groups and substituents thereof can be selected by one skilled in the art to provide stable moieties and compounds. When substituents are described by conventional formulas written from left to right, the substituents also include chemically equivalent substituents obtained when writing formulas from right to left.
The section headings used in this specification are for organizational purposes only and are not to be construed as limiting the subject matter described. All documents or portions of documents cited in this disclosure, including but not limited to patents, patent applications, articles, books, operating manuals, and treatises, are hereby incorporated by reference in their entirety.
Unless otherwise specified, all technical and scientific terms used herein have the standard meaning of the art to which the claimed subject matter belongs. In case there are multiple definitions for a term, the definitions herein control.
As used herein, the singular forms "a", "an", and "the" are understood to include plural referents unless the context clearly dictates otherwise. Furthermore, the term "comprising" is an open-ended limitation and does not exclude other aspects, i.e. it includes the content indicated by the invention.
Unless otherwise indicated, the present invention employs conventional methods of mass spectrometry, elemental analysis, and the various steps and conditions are referred to in the art by conventional procedures and conditions.
The present invention employs, unless otherwise indicated, standard nomenclature for analytical chemistry, organic synthetic chemistry and optics, and standard laboratory procedures and techniques. In some cases, standard techniques are used for chemical synthesis, chemical analysis, and light emitting device performance detection.
The compounds of the present invention may contain non-natural proportions of atomic isotopes on one or more of the atoms comprising the compounds. For example, compounds such as deuterium (2H) may be labeled with a radioisotope. All isotopic variations of the compounds of the present invention, whether radioactive or not, are intended to be encompassed within the scope of the present invention.
In the present invention, the number of "substitutions" may be one or more unless otherwise specified; when plural, it means two or more, for example, may be 2, 3 or 4. In addition, when the number of "substitutions" is plural, the "substitutions" may be the same or different. In the present invention, the "substituted" position may be any position unless otherwise specified.
In the present invention, as part of a group or other groups (e.g., as used in halogen-substituted alkyl groups and the like), the term "alkyl" is meant to include both branched and straight-chain saturated aliphatic hydrocarbon groups having the indicated number of carbon atoms. For example, C 1 ～C 20 Alkyl groups include straight or branched chain alkyl groups having 1 to 20 carbon atoms. As in "C 1 ～C 6 Alkyl "is defined to include groups having 1, 2, 3, 4, 5, or 6 carbon atoms in a straight or branched chain structure. For example, in the present invention, the C1-C6 alkyl groups are each independently methyl, ethyl, propyl, butyl, pentyl or hexyl; wherein propyl is C3 alkyl (including isomers such as n-propyl or isopropyl); butyl is C4 alkyl (including isomers such as n-butyl, sec-butyl, isobutyl, or tert-butyl); pentyl is C5 alkyl (including isomers such as n-pentyl, 1-methyl-butyl, 1-ethyl-propyl, 2-methyl-1-butyl, 3-methyl-1-butyl, isopentyl, t-pentyl or neopentyl); hexyl is C6 alkyl (including isomers such as n-hexyl or isohexyl).
The term "alkoxy" as used herein refers to an alkyl group as defined above, each attached via an oxygen bond (-O-).
In the present invention, the term "Cn-m aryl" as part of a group or other group refers to a monocyclic or polycyclic aromatic group having n to m ring carbon atoms (the ring atoms being carbon atoms only) having at least one carbocyclic ring with a conjugated pi-electron system. Examples of the above aryl unit include phenyl, naphthyl, indenyl, azulenyl, fluorenyl, phenanthryl, or anthracyl. In one embodiment, the aryl group is preferably a C6-14 aryl group, such as phenyl and naphthyl, more preferably phenyl.
In the present invention, the term "n-m membered heteroaryl" as part of a group or other group means an aromatic group having one or more (e.g., 1, 2, 3 and 4) heteroatoms selected from nitrogen, oxygen and sulfur, having from n to m ring atoms, said heteroaryl being a monocyclic, bicyclic, tricyclic or tetracyclic ring system, wherein at least one ring is an aromatic ring. Heteroaryl groups within the scope of this definition include, but are not limited to: acridinyl, carbazolyl, cinnolinyl, quinoxalinyl, pyrazolyl, indolyl, benzotriazole, furanyl, thienyl, benzothienyl, benzofuranyl, quinolinyl, isoquinolinyl, oxazolyl, isoxazolyl, pyrazinyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, tetrahydroquinolinyl, imidazolyl, triazolyl, tetrazolyl, thiazolyl, isothiazolyl, furazanyl, thiadiazolyl, oxadiazolyl, pyridyl, pyrazinyl, pyridazinyl, pyrimidinyl, triazinyl, purinyl, pteridinyl, naphthyridinyl, quinazolinyl, phthalazinyl, imidazopyridinyl, imidazothiazolyl, imidazooxazolyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, isoindolyl, indazolyl, pyrrolopyridinyl, thienopyridinyl, benzothiadiazolyl, benzoxadiazolyl, pyrrolopyrimidinyl, thienofuranyl. In one embodiment, as preferable examples of the "5-to 18-membered heteroaryl group", furyl, thienyl, pyrrolyl, imidazolyl, thiazolyl, pyrazolyl, oxazolyl, isoxazolyl, isothiazolyl, pyridyl, pyrimidinyl and carbazolyl groups are cited, and carbazolyl groups are more preferable.
The term Cn-Cm cycloalkyl as used herein refers to mono-or multicyclic alkyls having from n to m carbon atoms, such as 3-C10 cycloalkyl and C3-C6 cycloalkyl. Examples include adamantyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and bicycloheptyl. In one embodiment, the C3-C10 cycloalkyl is preferably adamantyl or cyclohexyl.
The definition of a carbon number range for a group as described in the present invention means that any integer included in the definition, such as C, of carbon atoms 1 ～C 20 It is meant that the number of carbon atoms of the radical may be 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19 or 20, C 3 -C 10 It is meant that the number of carbon atoms of the group may be 3, 4, 5, 6, 7, 8, 9 or 10, and so on for the other groups.
The weight percentage of the substances involved in the organic electroluminescent composition or the organic electroluminescent device of the present invention may be any value within the range, for example, 0.3 to 30.0wt%, 0.3wt%, 1wt%, 3wt%, 5wt%, 8.5wt%, 8.8wt%, 9wt%, 10wt%, 13wt%, 15wt%, 18wt%, 20wt%, 25wt% or 30wt%, etc., 99.7 to 70.0wt% may be 99.7wt%, 98wt%, 95wt%, 90wt%, 88wt%, 85wt%, 80wt%, 78wt%, 75wt%, 70wt%, etc., and so on.
The above preferred conditions can be arbitrarily combined on the basis of not deviating from the common knowledge in the art, and thus, each preferred embodiment of the present invention can be obtained.
The reagents and materials used in the present invention are commercially available.
Compared with the prior art, the invention has the following beneficial effects:
the boron nitrogen compound introduces nitrogen atoms through extended conjugation, so that not only is fine adjustment of spectrum realized, but also the luminous efficiency is further improved. The boron nitride compound has a narrow spectrum, is used as a narrow spectrum luminescent material for preparing a luminescent layer of an organic electroluminescent device, and the prepared organic electroluminescent device realizes narrow spectrum yellow light-red light TADF emission, has a luminescence peak position between 540 and 640nm, has a half-peak width smaller than 50nm, and ensures that the electroluminescent external quantum efficiency of the device is more than 30 percent.
Drawings
Fig. 1 is a schematic structural diagram of a vacuum evaporation type organic electroluminescent device provided by the invention, wherein 1 is an ITO anode, 2 is a first hole transport layer, 3 is a second hole transport layer, 4 is a light emitting layer, 5 is an electron transport layer, 6 is an electron injection layer, and 7 is a metal cathode.
FIG. 2 is a luminescence spectrum of a toluene solution using the compound BN-11.
FIG. 3 is an electroluminescent spectrum of the device of example A1 using compound BN-11.
Detailed Description
The technical scheme of the invention is further described by the following specific embodiments. It will be apparent to those skilled in the art that the examples are merely to aid in understanding the invention and are not to be construed as a specific limitation thereof.
In the examples of the present invention, the starting materials used for the synthesis of the indicated compounds were as follows:
specifically employed raw materials Mn (n=3-8) include the following molecules:
the raw materials BN-M-n (n=3-8)) specifically employed include the following molecules:
specifically employed raw materials An (n=1-5) include the following molecules:
specifically employed raw material Bn (n=1-2) includes the following molecules:
synthetic route and specific operation:
synthesis of a first class of compounds:
firstly, carbazole raw material Mn (n=3-8) is taken as a substrate, and an intermediate BN-M-n (n=3-8) is synthesized. And (3) taking BN-M-n (n=3-8) as a substrate, performing boron esterification reaction to obtain an intermediate BN-M-n-Bpin, performing one-step simple Suzuki reaction and coupling with a nitro-substituted aryl halogenated compound to obtain a precursor BN-M-Ai, performing cyclization reaction to obtain an intermediate H-BN-M-Ai, and performing alkyl chain protection to obtain a final product BN-n (n=11-40).
In the first step, 50.0mmol of raw material Mn (n=3-8), 4.73g of raw material 1-bromo-2, 6-difluorobenzene (24.5 mmol), 21.2g of cesium carbonate (65.0 mmol) were added to 150mL of anhydrous DMF (N, N-dimethylformamide), and the reaction system was stirred at 160℃for 18 hours, then cooled to room temperature and poured into ice water (2L). The white solid was filtered off with suction, dried in vacuo and then further purified by column chromatography using a mixed eluent of dichloromethane/petroleum ether to give intermediate Br-M-n (n=3-8).
In the second step, 19.4mL of a solution of t-butyllithium in n-hexane (25.2 mmol) was slowly added to 100mL of a solution of t-butylbenzene (-30 ℃ C.) containing 12.6mmol of intermediate Br-M-n under nitrogen atmosphere. After slowly heating to 60℃and stirring for 2 hours, n-hexane was removed in vacuo, then cooled to-30℃and 2.38mL of boron tribromide (25.2 mmol) was added and the reaction mixture was stirred at room temperature for 1 hour. 4.13mL of N, N-diisopropylethylamine (25.2 mmol) was then added at 0deg.C, and the reaction mixture was cooled to room temperature after stirring continued for 5 hours at 130deg.C. To the reaction mixture was added 5ml of methanol to quench the residual boron tribromide. The reaction system was concentrated in vacuo and purified by column chromatography with a dichloromethane/petroleum ether mixture eluent to give the target intermediate BN-M-n (n=3-8).
In a third step, intermediate BN-M-n (0.65 mmol), 170mg of pinacol diboronate (1.3 mmol) were added to tetrahydrofuran (10 mL), the mixture was bubbled with nitrogen for 10 min, and 3.49mg of 4,4 '-di-tert-butyl-2, 2' -bipyridine (0.013 mmol) and 4.31mg of methoxy (cyclooctadiene) iridium dimer (0.0065 mmol) were added at high flow of nitrogen. After stirring for 10 minutes, the mixture was heated to reflux and stirred for 24 hours. After the reaction system is cooled to room temperature, the reaction system is directly concentrated under reduced pressure and purified by column chromatography to obtain an intermediate BN-M-n-Bpin (n=3-8).
In the fourth step, nitro-substituted aryl halide Ai (A1-A5) (0.6 mmol), 383mg BN-M-n-Bpin (0.5 mmol), 140mg potassium carbonate (1 mmol) and water (2 mL) were added to tetrahydrofuran (16 mL), the mixture was bubbled with nitrogen for 10 min, and 28.9mg tetrakis (triphenylphosphine) palladium (0.025 mmol) was added under high flow of nitrogen. The mixture was heated to reflux and stirred for 12 hours. After the reaction system was cooled to room temperature, the reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give the precursor BN-M-Ai (i=11-40).
In a fifth step, 0.3mmol of BN-M-Ai (i=11-40), 470mg of triphenylphosphine (1.8 mmol) was dissolved in 20mL o-dichlorobenzene and the mixture was bubbled with nitrogen for 10 minutes. After which it was heated to 180℃and refluxed for 24 hours. The reaction mixture was extracted with dichloromethane and water, and the organic phase was dried by heating under vacuum and then purified by column chromatography to give the desired product H-BN-M-Ai (i=11-40).
In a sixth step, 0.24mmol of H-BN-M-Ai (i=11-40), 81mg of potassium hydroxide (1.44 mmol) are added to dry DMF and the mixture is bubbled with nitrogen for 10 minutes and heated for activation at 60℃for 2 hours. At this time, the system was dark black, and then iodoalkane (R) 3 /R 6 -I) the system quickly became deep orange and reacted for 10 hours at 50 ℃. The reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then passed throughPurifying by column chromatography to obtain target product BN-n (n=11-40). The data obtained for the target compounds are shown in Table 1.
Experimental details of the synthetic examples are illustrated by the compound BN-11:
in the first step, L4 g of starting material M3 (50.0 mmol), 4.73g of starting material 1-bromo-2, 6-difluorobenzene (24.5 mmol), 21.2g of cesium carbonate (65.0 mmol) were added to 150mL of anhydrous DMF (N, N-dimethylformamide), and the reaction system was stirred at 160℃for 18 hours, then cooled to room temperature and poured into ice water (2L). The white solid was filtered off with suction, dried in vacuo and then further purified by column chromatography using a mixed eluent of dichloromethane/petroleum ether to give intermediate Br-M-3 as a white solid, yield: 90 percent of
In a second step, 19.4mL of a solution of t-butyllithium in n-hexane (25.2 mmol) was slowly added to a solution of 40mL of t-butylbenzene (-30 ℃ C.) containing 8.81g of intermediate Br-M-3 (12.6 mmol) under nitrogen atmosphere. After slowly heating to 60℃and stirring for 2 hours, n-hexane was removed in vacuo, then cooled to-30℃and 2.38mL of boron tribromide (25.2 mmol) was added and the reaction mixture was stirred at room temperature for 1 hour. 4.13mL of N, N-diisopropylethylamine (25.2 mmol) was then added at 0deg.C, and the reaction mixture was cooled to room temperature after stirring continued for 5 hours at 130deg.C. To the reaction mixture was added 5ml of methanol to quench the residual boron tribromide. The reaction was concentrated in vacuo and purified by column chromatography with dichloromethane/petroleum ether mixture eluent to give the target intermediate BN-M-3 as a yellow solid yield: 40 percent of
In a third step, 420mg of intermediate BN-M-3 (0.65 mmol), 170mg of bisboronic acid pinacol ester (1.3 mmol) are added to tetrahydrofuran (10 mL), the mixture is bubbled with nitrogen for 10 min, and 3.49mg of 4,4 '-di-tert-butyl-2, 2' -bipyridine (0.013 mmol) and 4.31mg of methoxy (cyclooctadiene) iridium dimer (0.0065 mmol) are added at high flow of nitrogen. After stirring for 10 minutes, the mixture was heated to reflux and stirred for 24 hours. After the reaction system was cooled to room temperature, it was concentrated directly under reduced pressure and purified by column chromatography to give intermediate 430mg BN-M-3-Bpin as a yellow solid in 87% yield.
In the fourth step, 121mg of o-bromonitrobenzene A1 (0.6 mmol), 383mg of BN-M-3-Bpin (0.5 mmol), 140mg of potassium carbonate (1 mmol) and water (2 mL) were added to tetrahydrofuran (16 mL), the mixture was bubbled with nitrogen for 10 min, and 28.9mg of tetrakis (triphenylphosphine) palladium (0.025 mmol) was added under high flow of nitrogen. The mixture was heated to reflux and stirred for 12 hours. After the reaction system was cooled to room temperature, the reaction mixture was extracted with methylene chloride and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give 304mg of BN-M-A11 as a yellow-orange solid (yield: 80%)
In the fifth step, 228mg of BN-M-A11 (0.3 mmol), 470mg of triphenylphosphine (1.8 mmol) were dissolved in 20mL of o-dichlorobenzene, and the mixture was bubbled with nitrogen for 10 minutes. After which it was heated to 180℃and refluxed for 24 hours. The reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give 175mg of the desired product H-BN-M-A11 as an orange solid (yield 81%)
In the sixth step, 175mg of H-BN-M-A11 (0.24 mmol), 81mg of potassium hydroxide (1.44 mmol) were added to the dried DMF, and the mixture was bubbled with nitrogen for 10 minutes and heated at 60℃for 2 hours for activation. At this time, the system was dark black, then 441mg of n-butyl iodide (2.4 mmol) was added, and the system rapidly became dark orange-red, and reacted at 50℃for 10 hours. The reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give 141mg of the desired product BN-11 as a reddish brown solid (58% yield)
Synthesis of Compounds of the second class
The second class of compounds can be prepared on the basis of the first class of compounds, the second class of compounds are taken as raw materials, a precursor Br-BN-n is formed through bromination reaction, and then the second class of compounds BN-i (i=61-120) is finally obtained through sukuzi coupling.
In the first step, 3mmol of the above first compound BN-n (n=11-40) was dissolved in 20mL of dry chloroform, and 640mg NBS (3.6 mmol) was slowly added to the above system under ice water bath. Liquid nitrogen is degassed and displaced for 30min. After that, the reaction was slowly warmed to room temperature and continued for 4 hours. The reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum and then purified by column chromatography to give the precursor Br-BN-n (n=11-40).
Second step, arylboronic acid/ester Bi (B1-B2) (2 mmol), br-BN-n (1 mmol) as a precursor, 850mg of potassium phosphate (4 mmol) were added to dry toluene (20 mL), the mixture was bubbled with nitrogen for 10 minutes, and 220mg of Pd was added under a high flow of nitrogen 2 (dba) 3 (0.05 mmol) and 400mg S-Phos (0.1 mmol). The mixture was heated to 90 ℃ and stirred for 16 hours. After the reaction system was cooled to room temperature, the reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give the objective product BN-i (i=61-120). The data obtained for the target compounds are shown in Table 2.
Experimental details of the synthetic examples are illustrated by the compound BN-61:
in the first step, 2.35g BN-11 (3 mmol) was dissolved in 20mL of dry chloroform and 640mg of NBS (3.6 mmol) was slowly added to the above system under ice water bath. Liquid nitrogen is degassed and displaced for 30min. Then slowly warmed to room temperature and the reaction was continued for an hour. The reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum and then purified by column chromatography to give 2.0g of the precursor Br-BN-11 as a reddish brown solid. (yield 80%);
Second step, 244mg of B1 (2 mmol), 860mg of Br-BN-11 (1 mmol), 850mg of potassium phosphate (4 mmol) are added to dry toluene (20 mL), the mixture is bubbled with nitrogen for 10 minutes, and 224mg of Pd is added under high flow of nitrogen 2 (dba) 3 (0.05 mmol) and 410mg S-Phos (0.1 mmol). The mixture was heated to 90 ℃ and stirred for 16 hours. After the reaction system was cooled to room temperature, the reaction mixture was extracted with dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give 517mg of the objective product BN-61 as a reddish brown solid. (yield 60%).
The product was characterized in that the elemental analysis used a test instrument of Vario Micro Cube from Agilent, U.S.A., test element type C, H, N. The instrument used for mass spectrometry is a triple quadrupole mass spectrometer in tandem by using ultra-high performance liquid chromatography (UHF-HPLC) in the United states Thermo Fisher TSQ Endura
TABLE 1 summary of the data for the products of the synthesis examples (first class of compounds)
TABLE 2 summary of the data for the products of the synthesis examples (second class of compounds)
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The specific luminescent material molecular structure included in the device examples is shown below:
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the following are some representative organic electroluminescent device embodiments, and some of the material molecular structures involved in the device embodiments are as follows:
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The molecules involved in the comparative device examples are shown below:
the preparation process of the organic electroluminescent device in the device embodiment is as follows:
(1) And (3) substrate processing: the transparent ITO glass is used as a substrate material for preparing devices, firstly, 5% ITO washing liquid is used for ultrasonic treatment for 30min, then distilled water (2 times), acetone (2 times) and isopropanol (2 times) are used for ultrasonic washing in sequence, and finally, the ITO glass is stored in the isopropanol. Before each use, the surface of the ITO glass is carefully wiped by acetone cotton balls and isopropanol cotton balls, and after the isopropanol is washed, the ITO glass is dried, and then is treated by plasma for 5min for standby. The subsequent preparation of the device is completed by combining spin coating and vacuum evaporation process.
(2) Hole injection layer or hole transport layer preparation: adopting vapor deposition process to prepare hole transport layer or hole injection layer, when vacuum degree of vacuum vapor deposition system reaches 5×10 -4 Starting vapor deposition when Pa is lower, monitoring the deposition rate by a Saint film thickness instrument, and sequentially depositing a hole transport layer or a hole injection layer on the surface of the ITO electrode by utilizing a vacuum vapor deposition process, wherein the deposition rate of a hole transport layer material or a hole injection layer material is as follows
(3) Preparing a light-emitting layer: the luminous layer is prepared by adopting the vapor plating process, when the vacuum degree of the vacuum vapor plating system reaches 5 multiplied by 10 - 4 Starting vapor deposition when Pa is lower, monitoring the deposition rate by a Saint film thickness instrument, and depositing a luminescent layer on the hole transport layer by using a vacuum vapor deposition process, wherein the deposition rate of the luminescent layer material is as follows
(4) Preparation of an electron transport layer, an electron injection layer and a metal electrode: an electron transport layer, an electron injection layer and a metal electrode are prepared by adopting an evaporation process, and when the vacuum degree of a vacuum evaporation system reaches 5 multiplied by 10 -4 Starting vapor deposition when Pa is less than or equal to Pa, wherein the deposition rate is equal to the thickness of the Saint filmAnd monitoring by using a meter, and sequentially depositing an electron transmission layer, an electron injection layer and a metal electrode on the light-emitting layer by using a vacuum evaporation process. Wherein the deposition rate of the electron transport layer material isThe deposition rate of the electron injection layer isThe deposition rate of the metal electrode is +.>
The structure of the organic electroluminescent device is shown in fig. 1, and the structure sequentially comprises an ITO anode 1, a first hole transport layer 2, a second hole transport layer 3, a light emitting layer 4, an electron transport layer 5, an electron injection layer 6 and a metal cathode 7 from bottom to top.
Device examples A1 to a32:
the organic electroluminescent devices in device examples A1 to a32 were structured as shown in fig. 1, HTL-1 was used as the material of the first hole transport layer 2, HTL-2 was used as the material of the second hole transport layer 3, H1-172 (content 99 wt%) was used as the host material in the light emitting layer 4, BN-n was used as the doped light emitting material (content 1 wt%) (BN-n represents any of the light emitting materials involved in the device examples), ETL was used as the material of the electron transport layer 5, liF was used as the electron injection layer 6, and Al was used as the metal cathode 7. The organic electroluminescent device structure of the device example was [ ITO/HTL-1 (50 nm)/HTL-2 (5 nm)/99 wt% H1-172+1wt% BN-n (30 nm)/ETL (30 nm)/LiF (1 nm)/Al (100 nm) ].
The current, voltage, brightness, luminescence spectrum and other characteristics of the device were synchronously tested using a Photo Research PR 655 spectral scanning luminance meter and a Keithley K2400 digital source meter system. The performance test of the device was performed at room temperature under ambient atmosphere. The External Quantum Efficiency (EQE) of the device is calculated from the current density, brightness and electro-spectral combined with the visual function in the case of the light emission as a langerhans distribution.
The performance data for device examples A1 through A32 are shown in Table 2, table 2Device lifetime (T95, hours) refers to an initial luminance of 1000cd/m 2 When the brightness of the device drops to 95% of the initial brightness (i.e., the device brightness drops to 950 cd/m) 2 Time) is required.
TABLE 2
FIG. 2 is a luminescence spectrum of a toluene solution using compound BN-11 (measured using a Shimadzu RF-6000 fluorescence spectrometer), which has an intrinsic narrow spectral emission characteristic, as can be seen from FIG. 2.
FIG. 3 is an electroluminescent spectrum of the device of example A1 using the compound BN-11, as can be seen from FIG. 3, the device of which exhibits yellow light and narrow spectral emission.
Comparative device examples D1-1 to D1-8
The organic electroluminescent devices in comparative device examples D1-1 to D1-8 were structured as shown in fig. 1, HTL-1 was used as the material of the first hole transport layer 2, HTL-2 was used as the material of the second hole transport layer 3, H1-172 (content 99 wt%) was used as the host material, R-m was used as the doped luminescent material (content 1 wt%) (m=1-8), ETL was used as the material of the electron transport layer 5, liF was used as the electron injection layer 6, and Al was used as the metal cathode 7 in the luminescent layer 4. The organic electroluminescent device structure of the comparative device example was [ ITO/HTL-1 (50 nm)/HTL-2 (5 nm)/99 wt% H1-172+1wt% R-m (30 nm)/ETL (30 nm)/LiF (1 nm)/Al (100 nm) ].
The current, voltage, brightness, luminescence spectrum and other characteristics of the device were synchronously tested using a Photo Research PR 655 spectral scanning luminance meter and a Keithley K2400 digital source meter system. The performance test of the device was performed at room temperature under ambient atmosphere. The External Quantum Efficiency (EQE) of the device is calculated from the current density, brightness and electro-spectral combined with the visual function in the case of the light emission as a langerhans distribution.
The performance data for comparative device examples D1-1 to D1-8 are shown in Table 3, and the device lifetime (T95, hours) in Table 3 refers to an initial luminance of 1000cd/m for the device 2 When the brightness of the device drops to 95% of the initial brightness (i.e., the device brightness drops to 950 cd/m) 2 Time) is required.
TABLE 3 Table 3
Device examples B1 to B32:
the organic electroluminescent devices in device examples B1 to B32 were structured as shown in fig. 1, HTL-1 was used as the material of the first hole transport layer 2, HTL-2 was used as the material of the second hole transport layer 3, H1-172 (content of 75 wt%) + TRZ-79 (content of 24 wt%) was used as the host material in the light emitting layer 4, BN-n was used as the doped light emitting material (content of 1 wt%) (BN-n represents any of the light emitting materials involved in the device examples), ETL was used as the material of the electron transport layer 5, liF was used as the electron injection layer 6, and Al was used as the metal cathode 7. The organic electroluminescent device structure of the device example was [ ITO/HTL-1 (50 nm)/HTL-2 (5 nm)/75 wt% H1-172+24wt% TRZ-79+1wt% BN-n (30 nm)/ETL (30 nm)/LiF (1 nm)/Al (100 nm) ].
The current, voltage, brightness, luminescence spectrum and other characteristics of the device were synchronously tested using a Photo Research PR 655 spectral scanning luminance meter and a Keithley K2400 digital source meter system. The performance test of the device was performed at room temperature under ambient atmosphere. The External Quantum Efficiency (EQE) of the device is calculated from the current density, brightness and electro-spectral combined with the visual function in the case of the light emission as a langerhans distribution.
The performance data for device examples B1 through B32 are shown in Table 4, and the device lifetime (T95, hours) in Table 4 refers to an initial luminance of 1000cd/m 2 When the brightness of the device drops to 95% of the initial brightness (i.e., the device brightness drops to 950 cd/m) 2 Time) is required.
TABLE 4 Table 4
Comparative device examples D2-1 to D2-8
The organic electroluminescent devices in comparative device examples D2-1 to D2-8 were structured as shown in fig. 1, HTL-1 was used as the material of the first hole transport layer 2, HTL-2 was used as the material of the second hole transport layer 3, H1-172 (content 75 wt%) + TRZ-79 (content 24 wt%) was used as the host material, R-m was used as the doped luminescent material (content 1 wt%) (m=1-8), ETL was used as the material of the electron transport layer 5, liF was used as the electron injection layer 6, and Al was used as the metal cathode 7 in the luminescent layer 4. The organic electroluminescent device structure of the comparative device example was [ ITO/HTL-1 (50 nm)/HTL-2 (5 nm)/75 wt% H1-172+24wt% TRZ-79+1wt% R-m (30 nm)/ETL (30 nm)/LiF (1 nm)/Al (100 nm) ].
The current, voltage, brightness, luminescence spectrum and other characteristics of the device were synchronously tested using a Photo Research PR 655 spectral scanning luminance meter and a Keithley K2400 digital source meter system. The performance test of the device was performed at room temperature under ambient atmosphere. The External Quantum Efficiency (EQE) of the device is calculated from the current density, brightness and electro-spectral combined with the visual function in the case of the light emission as a langerhans distribution.
The performance data for comparative device examples D2-1 to D2-8 are shown in Table 5, and the device lifetime (T95, hours) in Table 5 refers to an initial luminance of 1000cd/m for the device 2 When the brightness of the device drops to 95% of the initial brightness (i.e., the device brightness drops to 950 cd/m) 2 Time) is required.
TABLE 5
By comparing the performance data of the organic electroluminescent devices listed in tables 2, 3, 4 and 5, it can be seen that the organic electroluminescent device provided by the invention has high efficiency under high brightness and good device stability, and the highest external quantum efficiency of the electroluminescent device can reach more than 30%, and the service life of the device can reach more than 350h, which indicates that the organic electroluminescent device provided by the invention has the advantages of high external quantum efficiency and good stability.
The applicant states that the present invention is illustrated by the above examples of boron nitride compounds of the present invention and their use, but the present invention is not limited to the above examples, i.e. it is not meant that the present invention must be practiced in dependence upon the above examples. It should be apparent to those skilled in the art that any modification of the present invention, equivalent substitution of selected raw materials, addition of auxiliary components, selection of specific modes, etc. fall within the scope of the present invention and the scope of disclosure.
Claims (10)
1. A boron nitride compound, characterized in that the boron nitride compound has a structure represented by formula I or formula II:
wherein R is 1 、R 2 、R 4 And R is 5 Independently selected from H, deuterium, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C18 aryl, substituted with one or more R a Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R a Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R a Substituted diphenylamino groups;
R a independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl, C6-C14 aryl, substituted with one or more R b Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R b Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R b Substituted diphenylamino groups;
R b independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R c Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R c Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R c Substituted diphenylamino groups;
R c independently at each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R d Substituted C6-C14 aryl, 5-to 18-membered heteroaryl, substituted with one or more R d Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R d Substituted diphenylamino groups;
R d independently at each occurrence deuterium, fluorine, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl or by one or more R e Substituted C6-C14 aryl;
R e independently for each occurrence deuterium, fluorine, C1-C12 alkyl, C1-C12 alkoxy, C3-C10 cycloalkyl, or C6-C14 aryl;
the alkyl, alkoxy, cycloalkyl, aryl, heteroaryl groups are optionally substituted with one or more substituents selected from the group consisting of: halogen, -CN, C1-C12 alkyl, C1-C12 alkoxy, C1-C12 haloalkyl, C3-C10 cycloalkyl, C6-C14 aryl and 5-to 18-membered heteroaryl;
R 3 and R is 6 Is that ＊ -L-R s Represents a bonding site, L is C1-C12 alkyl, C1-C12 alkoxy, R s Is hydrogen, C3-C10 cycloalkyl, C6-C24 aryl or 5-to 24-membered heteroaryl;
Y 1 、Y 2 、Y 3 and Y 4 Independently selected from N or C-R y1 、C-R y2 、C-R y3 、C-R y4 And Y is 1 、Y 2 、Y 3 And Y 4 At least one of which is N;
R y1 、R y2 、R y3 or R is y4 Independently selected from H, deuterium, fluorine, CN, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R y Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted by one or moreMultiple R' s y Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R y Substituted diphenylamino groups;
R y independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R y1 、R y2 、R y3 、R y4 independently or R y1 、R y2 、R y3 、R y4 Any adjacent two groups are condensed into an aromatic ring;
R 01 and R is 02 Selected from H, deuterium, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C18 aryl, 5-to 18-membered heteroaryl substituted with one or more R f Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R f Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R f Substituted diphenylamino groups;
R f independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R 7 、R 8 、R 9 and R is 10 Independently selected from H, deuterium, fluorine, CN, C1-C20 alkyl, C1-C20 alkoxy, C3-C10 cycloalkyl, C6-C14 aryl, substituted with one or more R g Substituted C6-C18 aryl, 5-to 18-membered heteroaryl, substituted with one or more R g Substituted 5-to 18-membered heteroaryl, diphenylamino, or substituted with one or more R g Substituted diphenylamino groups;
R g independently for each occurrence deuterium, fluorine, CN, C1-C12 alkyl, C1-C12 alkoxy, C3-C12 cycloalkyl or C6-C14 aryl;
R 7 、R 8 、R 9 and R is 10 Independently or R 7 、R 8 、R 9 And R is 10 Any adjacent two groups are condensed into an aromatic ring.
2. The boron nitride compound according to claim 1, wherein theR 1 、R 2 、R 4 And R is 5 Is independently H, D (deuterium), C1-C12 alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, phenyl, substituted with at least one C 1 -C 12 Aryl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted aryl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl;
preferably, said R a Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl;
preferably, said R b Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy-substituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl;
preferably, said R c Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Alkoxy is takenSubstituted phenyl, phenyl-C 1 ～C 12 Alkyl, diphenylamino, and at least one C 1 -C 12 Alkyl-substituted diphenylamino, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl;
preferably, said R d Each occurrence is independently deuterium, fluorine, C 1 ～C 12 Alkyl, C 1 ～C 12 Alkoxy, C 3 -C 10 Cycloalkyl, at least one C 1 -C 12 Phenyl substituted by alkyl, substituted by at least one C 1 -C 12 Phenyl substituted by alkoxy, carbazolyl, substituted by at least one C 1 -C 12 Alkyl-substituted carbazolyl.
3. The boron nitride compound according to claim 1 or 2, wherein R 1 、R 2 、R 4 And R is 5 Independently H, deuterium, methyl, ethyl, n-propyl, isopropyl, n-butyl, t-butyl, hexyl, octyl, decyl,Methoxy, ethoxy, butoxy, hexyloxy, < >>Cyclohexyl, adamantyl, phenyl, 4-methyl-phenyl, 4-ethyl-phenyl, 4-propyl-phenyl, 4-isopropyl-phenyl, 4-n-butyl-phenyl, -/-, and- >
Wherein the wavy line represents the attachment site of the group;
preferably, said R 1 、R 2 、R 4 And R is 5 Independently H, methyl,Phenyl group,/-> Wherein the wavy line represents the attachment site of the group;
preferably, said R 1 And R is 2 Identical, R 4 And R is 5 The same is selected from H, methyl,Phenyl group,/-> Any one of them;
wherein R is h Is H, methyl, isopropyl, tert-butyl,
Preferably, said R 01 And R is 02 Selected from hydrogen, phenyl or
Preferably, said R 3 And R is 6 Selected from n-butyl, n-pentyl, n-hexyl or
Preferably, said R 7 、R 8 、R 9 And R is 10 Selected from hydrogen.
4. A boron nitride compound according to any one of claims 1 to 3, wherein said compound is any one of the following compounds:
the first molecular structural formula:
the second molecular structural formula:
5. an organic electroluminescent composition, characterized in that it comprises the boron nitride compound according to any one of claims 1 to 4 and a host material as doping materials;
preferably, the host material is a material having an electron transport ability and/or a hole transport ability and having a triplet excited state energy higher than or equal to that of the dopant material.
6. The organic electroluminescent composition according to claim 5, wherein the host material is a carbazole derivative and/or carboline derivative having a structure represented by any one of formulae (H-1) to (H-6):
Wherein X is 1 、Y 1 And Z 1 Is CH or N, and X 1 、Y 1 And Z 1 At most one of them is N;
wherein R is 1H And R is 2H Independently any of the following groups:
wherein X is 1 、Y 1 And Z 1 Is CH or N, and X 1 、Y 1 And Z 1 At most one of them is N;
wherein R is aH And R is bH H, C independently 1 -C 20 Alkyl, C 1 -C 20 Alkoxy, C 6 -C 20 Aryl, C 1 -C 20 Alkyl substituted C 6 -C 20 Aryl or C 1 -C 20 Alkoxy substituted C 6 -C 20 Aryl, number represents the attachment site of the group;
preferably, the organic electroluminescent composition preferably contains 0.3 to 30.0wt% of the boron-nitrogen compound as defined in any one of claims 1 to 3 as a doping material, and the remaining 99.7 to 70.0wt% of the composition is a host material composed of 1 to 2 compounds having the structures of formulae (H-1) to (H-6);
preferably, the host material contains 2 compounds having the structures of formulae (H-1) to (H-6) in a weight ratio of 1:5 to 5:1;
preferably, the host material in the organic electroluminescent composition is one or two of the compounds H1-1 to H1-429;
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preferably, the organic electroluminescent composition comprises 0.3-30.0wt% of boron-nitrogen compound of the structure shown in formula I or II as defined in any one of claims 1-3, and the rest 99.7-70.0wt% is 1 or 2 of the compounds H1-1 to H1-429:
Preferably, the organic electroluminescent composition contains 2 compounds from the group consisting of compounds H1-1 to H1-429 as a host material, wherein the weight ratio of the two compounds is 1:5 to 5:1;
preferably, the doping material in the organic electroluminescent composition is any one of the boron-nitrogen compounds according to any one of claims 1 to 3; the main material is composed of any one of compounds shown as the formulas Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A and any one of compounds with structures shown as the formulas H-1 to H-6;
wherein R is 1a 、R 1b 、R 2a 、R 2b 、R 3a And R is 3b Wherein 1 or 2 are independently R Tz The remainder being the same or different and independently hydrogen, deuterium, C 1 -C 8 Alkyl, C 1 -C 8 Alkoxy, C 6 -C 18 Aryl, C 1 -C 8 Alkyl substituted C 6 -C 18 Aryl or C 1 -C 8 Alkoxy substituted C 6 -C 18 Aryl of (a); r is R Tz Is any one of substituent groups shown in the following formula:
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wherein asterisks represent the attachment site of the group;
preferably, the weight ratio of the Trz1-A, trz2-A, trz3-A, trz4-A, trz5-A or Trz6-A compound to the H-1, H-2, H-3, H-4, H-5 or H-6 compound in the main material is 1:20-20:1;
preferably, the doping material in the organic electroluminescent composition is any one of boron-nitrogen compounds with a structure shown in formula I or II; the main material is composed of any one of compounds shown as formulas TRZ-1 to TRZ-81 and any one of carbazole or carboline derivatives shown as formulas H1-1 to H1-429;
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Preferably, the weight ratio between the compound represented by the formulas TRZ-1 to TRZ-81 and the carbazole or carboline derivative of the formulas H1-1 to H1-429 in the host material is 1:20 to 20:1.
7. An organic electroluminescent material, characterized in that it comprises the boron-nitrogen compound according to any one of claims 1 to 4 or the organic electroluminescent composition according to claim 5 or 6.
8. An organic electroluminescent device comprising an anode and a cathode and an organic thin film layer interposed between the anode and the cathode, the organic thin film layer comprising the boron-nitrogen compound of any one of claims 1 to 4 or the organic electroluminescent composition of claim 5 or 6.
Preferably, the organic thin film layer comprises a light emitting layer, an optional hole injection layer, an optional hole transport layer, an optional electron injection layer, wherein at least one of the light emitting layer, the electron injection layer, the electron transport layer, the hole injection layer comprises the boron nitrogen compound of any of claims 1-4 or the organic electroluminescent composition of claim 5 or 6.
9. The organic electroluminescent material according to claim 8, wherein the light-emitting layer comprises the boron-nitrogen compound according to any one of claims 1 to 4 or the organic electroluminescent composition according to claim 5 or 6;
preferably, the organic electroluminescent device further comprises an optional hole blocking layer, an optional electron blocking layer and an optional capping layer.
10. Use of an organic electroluminescent device according to claim 8 or 9 in an organic electroluminescent display or an organic electroluminescent illumination source.
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| CN202310878816.3A CN116903648A (en) | 2023-07-18 | 2023-07-18 | Boron nitride compound and application thereof |
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| CN202310878816.3A CN116903648A (en) | 2023-07-18 | 2023-07-18 | Boron nitride compound and application thereof |
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