CN114621274B - Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same - Google Patents
Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same Download PDFInfo
- Publication number
- CN114621274B CN114621274B CN202011457921.2A CN202011457921A CN114621274B CN 114621274 B CN114621274 B CN 114621274B CN 202011457921 A CN202011457921 A CN 202011457921A CN 114621274 B CN114621274 B CN 114621274B
- Authority
- CN
- China
- Prior art keywords
- organic electroluminescent
- boron
- substituted
- compounds
- present disclosure
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 71
- -1 Boron nitride compound Chemical class 0.000 title claims description 55
- 229910052582 BN Inorganic materials 0.000 title claims description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 72
- TZHYBRCGYCPGBQ-UHFFFAOYSA-N [B].[N] Chemical compound [B].[N] TZHYBRCGYCPGBQ-UHFFFAOYSA-N 0.000 claims abstract description 29
- 229910017464 nitrogen compound Inorganic materials 0.000 claims abstract description 16
- 239000000463 material Substances 0.000 claims description 78
- 125000003118 aryl group Chemical group 0.000 claims description 47
- 125000000217 alkyl group Chemical group 0.000 claims description 38
- 125000003545 alkoxy group Chemical group 0.000 claims description 30
- 229910052805 deuterium Inorganic materials 0.000 claims description 30
- 238000006243 chemical reaction Methods 0.000 claims description 25
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 24
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 claims description 23
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 23
- 238000004770 highest occupied molecular orbital Methods 0.000 claims description 20
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims description 16
- 102100039856 Histone H1.1 Human genes 0.000 claims description 16
- 101001035402 Homo sapiens Histone H1.1 Proteins 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 125000003363 1,3,5-triazinyl group Chemical class N1=C(N=CN=C1)* 0.000 claims description 12
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 12
- 125000004429 atom Chemical group 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 229910052796 boron Inorganic materials 0.000 claims description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 7
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 7
- 238000010438 heat treatment Methods 0.000 claims description 7
- 238000010992 reflux Methods 0.000 claims description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000005036 alkoxyphenyl group Chemical group 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 239000000376 reactant Substances 0.000 claims description 6
- 125000006413 ring segment Chemical group 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 238000005286 illumination Methods 0.000 claims description 5
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims description 4
- 238000006069 Suzuki reaction reaction Methods 0.000 claims description 4
- 239000003054 catalyst Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 4
- 150000001638 boron Chemical class 0.000 claims description 3
- 230000005281 excited state Effects 0.000 claims description 3
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 3
- 238000004776 molecular orbital Methods 0.000 claims description 3
- 239000003960 organic solvent Substances 0.000 claims description 3
- 125000006736 (C6-C20) aryl group Chemical group 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
- 238000004519 manufacturing process Methods 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 28
- 238000001228 spectrum Methods 0.000 abstract description 13
- 238000005401 electroluminescence Methods 0.000 abstract description 4
- 239000010410 layer Substances 0.000 description 87
- 125000001072 heteroaryl group Chemical group 0.000 description 32
- 238000002347 injection Methods 0.000 description 27
- 239000007924 injection Substances 0.000 description 27
- 125000000753 cycloalkyl group Chemical group 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 19
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 18
- 230000000694 effects Effects 0.000 description 18
- 238000000295 emission spectrum Methods 0.000 description 18
- 229910052731 fluorine Inorganic materials 0.000 description 17
- 239000000243 solution Substances 0.000 description 17
- 238000004020 luminiscence type Methods 0.000 description 16
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 15
- 239000011737 fluorine Substances 0.000 description 15
- 230000008901 benefit Effects 0.000 description 12
- 230000005525 hole transport Effects 0.000 description 12
- 229910052757 nitrogen Inorganic materials 0.000 description 11
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- 238000003786 synthesis reaction Methods 0.000 description 10
- 150000003230 pyrimidines Chemical class 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
- 238000004440 column chromatography Methods 0.000 description 8
- 238000013461 design Methods 0.000 description 8
- 239000010408 film Substances 0.000 description 8
- 230000007246 mechanism Effects 0.000 description 8
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 229910052751 metal Inorganic materials 0.000 description 7
- 239000002184 metal Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 6
- 230000000903 blocking effect Effects 0.000 description 6
- 230000003111 delayed effect Effects 0.000 description 6
- 150000002367 halogens Chemical class 0.000 description 6
- 230000008569 process Effects 0.000 description 6
- 125000000714 pyrimidinyl group Chemical group 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 238000006467 substitution reaction Methods 0.000 description 6
- 239000000758 substrate Substances 0.000 description 6
- 238000012546 transfer Methods 0.000 description 6
- 229920000144 PEDOT:PSS Polymers 0.000 description 5
- 238000000151 deposition Methods 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-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
- 125000005073 adamantyl group Chemical group C12(CC3CC(CC(C1)C3)C2)* 0.000 description 4
- ILAHWRKJUDSMFH-UHFFFAOYSA-N boron tribromide Chemical compound BrB(Br)Br ILAHWRKJUDSMFH-UHFFFAOYSA-N 0.000 description 4
- 150000001716 carbazoles Chemical class 0.000 description 4
- 239000000460 chlorine Substances 0.000 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 description 4
- 230000007547 defect Effects 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- 239000003480 eluent Substances 0.000 description 4
- 239000011521 glass Substances 0.000 description 4
- 239000002346 layers by function Substances 0.000 description 4
- 238000001748 luminescence spectrum Methods 0.000 description 4
- 125000001624 naphthyl group Chemical group 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
- 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
- 239000000126 substance Substances 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 4
- 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 3
- KTYAQHYBYRVCGD-UHFFFAOYSA-N [Ir].COC1=CC=CCCCC1 Chemical class [Ir].COC1=CC=CCCCC1 KTYAQHYBYRVCGD-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000001819 mass spectrum Methods 0.000 description 3
- 125000002950 monocyclic group Chemical group 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 125000000547 substituted alkyl group Chemical group 0.000 description 3
- 238000001308 synthesis method Methods 0.000 description 3
- 238000007738 vacuum evaporation Methods 0.000 description 3
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 2
- 125000004641 (C1-C12) haloalkyl group Chemical group 0.000 description 2
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 description 2
- FIDRAVVQGKNYQK-UHFFFAOYSA-N 1,2,3,4-tetrahydrotriazine Chemical class C1NNNC=C1 FIDRAVVQGKNYQK-UHFFFAOYSA-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
- 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 2
- CINYXYWQPZSTOT-UHFFFAOYSA-N 3-[3-[3,5-bis(3-pyridin-3-ylphenyl)phenyl]phenyl]pyridine Chemical compound C1=CN=CC(C=2C=C(C=CC=2)C=2C=C(C=C(C=2)C=2C=C(C=CC=2)C=2C=NC=CC=2)C=2C=C(C=CC=2)C=2C=NC=CC=2)=C1 CINYXYWQPZSTOT-UHFFFAOYSA-N 0.000 description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 description 2
- 235000009161 Espostoa lanata Nutrition 0.000 description 2
- 240000001624 Espostoa lanata Species 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 description 2
- 241000720974 Protium Species 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 150000005840 aryl radicals Chemical class 0.000 description 2
- 235000010290 biphenyl Nutrition 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 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
- 230000021615 conjugation Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000012467 final product Substances 0.000 description 2
- 125000001153 fluoro group Chemical group F* 0.000 description 2
- 125000002541 furyl group Chemical group 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 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 description 2
- 239000005457 ice water Substances 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
- 150000002894 organic compounds Chemical class 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 125000002971 oxazolyl group Chemical group 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 description 2
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000003226 pyrazolyl group Chemical group 0.000 description 2
- 125000004076 pyridyl group Chemical group 0.000 description 2
- 229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 description 2
- 125000000168 pyrrolyl group Chemical group 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 2
- 238000004528 spin coating Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
- 125000000335 thiazolyl group Chemical group 0.000 description 2
- 125000001544 thienyl group Chemical group 0.000 description 2
- 239000010409 thin film Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 description 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- YBYIRNPNPLQARY-UHFFFAOYSA-N 1H-indene Natural products C1=CC=C2CC=CC2=C1 YBYIRNPNPLQARY-UHFFFAOYSA-N 0.000 description 1
- GPGIIKKUKINTGW-UHFFFAOYSA-N 2-bromo-4,6-diphenylpyrimidine Chemical compound N=1C(Br)=NC(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 GPGIIKKUKINTGW-UHFFFAOYSA-N 0.000 description 1
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
- OYFFSPILVQLRQA-UHFFFAOYSA-N 3,6-ditert-butyl-9h-carbazole Chemical compound C1=C(C(C)(C)C)C=C2C3=CC(C(C)(C)C)=CC=C3NC2=C1 OYFFSPILVQLRQA-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 125000005915 C6-C14 aryl group Chemical group 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 241001125671 Eretmochelys imbricata Species 0.000 description 1
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-NJFSPNSNSA-N Tritium Chemical compound [3H] YZCKVEUIGOORGS-NJFSPNSNSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000000862 absorption spectrum Methods 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
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 125000003828 azulenyl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 150000001555 benzenes Chemical group 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
- 230000005540 biological transmission Effects 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 150000005829 chemical entities Chemical class 0.000 description 1
- 125000003636 chemical 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
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000004132 cross linking Methods 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
- 230000002950 deficient Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 238000003795 desorption Methods 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000002019 doping agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 238000002189 fluorescence spectrum Methods 0.000 description 1
- 239000007850 fluorescent dye Substances 0.000 description 1
- 125000003709 fluoroalkyl group Chemical group 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 125000003838 furazanyl group Chemical group 0.000 description 1
- 125000004612 furopyridinyl group Chemical group O1C(=CC2=C1C=CC=N2)* 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 230000005283 ground state Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 125000004970 halomethyl group Chemical group 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000005945 imidazopyridyl group Chemical group 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
- 125000001041 indolyl group Chemical group 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 238000005040 ion trap Methods 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
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
- 230000000155 isotopic effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 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
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000001715 oxadiazolyl group Chemical group 0.000 description 1
- 235000012736 patent blue V Nutrition 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
- 238000011056 performance test Methods 0.000 description 1
- 125000005561 phenanthryl group Chemical group 0.000 description 1
- 238000000103 photoluminescence spectrum Methods 0.000 description 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 description 1
- 229920001467 poly(styrenesulfonates) Polymers 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 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
- 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
- 230000002285 radioactive effect Effects 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
- 238000010561 standard procedure Methods 0.000 description 1
- 125000005415 substituted alkoxy group Chemical group 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
- 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
- 229910052722 tritium Inorganic materials 0.000 description 1
- 230000004382 visual function Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/027—Organoboranes and organoborohydrides
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
- H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/636—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
- C09K2211/1055—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms with other heteroatoms
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Organic Chemistry (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
The present disclosure provides a boron nitrogen compound of formula I or II, compositions comprising the same, and their use in the field of organic electroluminescence. The present disclosure also provides a method of preparing a boron nitrogen compound of formula I or II. The organic electroluminescent device prepared by adopting the compound or the composition provided by the invention can realize high-efficiency green light and red light electroluminescence with narrow spectrum emission.
Description
Technical Field
The invention belongs to the technical field of organic electroluminescence, and particularly relates to a boron-nitrogen compound and a synthesis method thereof, an organic electroluminescent composition and an organic electroluminescent device containing the compound or the composition.
Background
The organic electroluminescent technology has a huge application prospect in the fields of full-color display and solid-state white light illumination, and is widely researched and focused in the scientific research and industry. The organic micromolecular photoelectric material is used as a high-performance electroluminescent material in a large quantity due to the advantages of clear structure, easiness in modification, simplicity in purification and processing and the like. At present, traditional fluorescent dye molecules often have very high photo-induced fluorescence quantum yield, but electroluminescent devices based on the fluorescent materials are limited by 25% internal quantum efficiency, and the external quantum efficiency of the electroluminescent devices is generally lower than 5%, which is far from the efficiency of phosphorescent devices. The current fluorescent electroluminescent device capable of breaking through the limit of 25% of internal quantum efficiency mainly adopts a delayed fluorescence mechanism, and the triplet excited state energy in the device can be effectively utilized by utilizing the delayed fluorescence mechanism. Delayed fluorescence mechanisms mainly include two classes: (1) TTA (Triplet-Triplet annihilation) mechanism; (2) TADF (Thermally Activated Delayed Fluorescence), thermally activated delayed fluorescence) mechanism. The TTA mechanism is a mechanism for generating singlet excitons by utilizing the fusion of two triplet excitons and improving the generation rate of the singlet excitons, but the maximum internal quantum efficiency of the device is only 40% -62.5%. The TADF mechanism is based on the use of a light singlet-triplet energy level difference (Δe ST ) Is prepared from the organic small molecular material,the triplet excitons can be converted into singlet excitons by reverse intersystem crossing (RISC) process under ambient heat energy. In theory, the quantum efficiency in the device can reach 100%. But its device has a large roll-off efficiency at high brightness, limiting its application in full color displays and white light illumination. The doping of TADF molecules primarily as guest materials in a wide bandgap host material achieves high efficiency of thermally activated delayed fluorescence (see j.am. Chem. Soc.2012,134,14706; nature,2012,492,234; mate. Horiz.,2014,1,264).
Unlike traditional fluorescent molecular localized state (LE) luminescence, TADF emission results primarily from transitions in the intramolecular charge transfer (ICT: intramolecular charge transfer) state. Since most TADF luminescent molecular structures employ a form in which an electron donor (D: donor) group is linked to an electron acceptor (a; receptor) group by conjugation or nonconjugated, i.e., a so-called D-a structure (structure 1), the electron donor group and the electron acceptor group are spatially separated, this class of molecules is defined as: a separate D-A structure. This D-A structure facilitates the spatial separation of the highest occupied orbital (HOMO: the highest occupied molecular orbital) and the lowest unoccupied orbital (LUMO: the lowest unoccupied molecular orbital) of the molecule, and thus facilitates the acquisition of TADF luminescence. Furthermore, the regulation of emission spectrum peak position (wavelength), i.e., emission color, is easily realized based on the D-a type structure, because the structure of the electron donor and the electron acceptor and the relative electron gain and loss capability are easily optimized. However, the D-a structure shown in structure 1 easily causes configuration and conformational changes when the molecule is in the ground state and excited state, and generates rich molecular vibration modes, so that the half-peak width of the emission spectrum of most of such luminescent molecules exceeds 100nm based on the broad emission spectrum band of TADF molecules shown in structure 1. The broad spectrum, while advantageous for illumination applications, does not meet the high color purity requirements of the display field. The main purpose of OLED luminescence is to display, so that narrow spectral design (i.e. smaller half-width) of TADF material is necessary.
Structure 1.D-A molecular Structure
In recent years, it has been reported (see Angew.chem.2018,130,11486; J.Am.Chem.Soc.,2018,140,1195;Adv.Mater.2016,28,2777;CN109155368A;WO2016/152544A1; WO2017/188111A1; WO2018/150832A1; WO2018/186374A1; WO2018/216990A 1) that luminescent compounds based on three coordinated B (boron) are structurally characterized in that the luminescent compounds contain at least one chromophore core structure having a very rigid structure formed by coordination of a B atom with three benzene rings, and in that the three benzene rings coordinated with B are covalently linked with N, such molecules are called B-N complexes (structure 2), i.e. the compounds are luminescent compounds formed by coordination of aromatic amine organic molecules with B.
The front molecular orbital of such a tridentate B complex has the feature that the highest occupied orbital (HOMO: the highest occupied molecular orbital) and the lowest unoccupied orbital (LUMO: the lowest unoccupied molecular orbital) are distributed in the coordination system in an alternating manner (so-called resonance structure), respectively, with B being in the LUMO orbital and N being in the HOMO orbital. The B-N complex has excitation state charge transfer and TADF luminescence property (the molecules are defined as resonant D-A molecules) due to the unique electron structure (resonance structure) of the alternate arrangement of HOMO and LUMO, and the very important thing is that the emission spectrum band is very narrow, and the half-peak width of the emission spectrum can reach about 20 nm. The compound can be used for preparing high-performance blue light or sky blue light (the peak value of the luminescence light spectrum is between 450 and 490 nm) organic electroluminescent devices, and the electroluminescent spectrum is very narrow (the half-peak width is about 25 nm). However, no report has been made on the basis of such a resonance type B-N coordination structure for preparing a green light (emission peak position is between 520 and 535 nm) and red light (emission peak position is between 625 and 640 nm) material having a narrower emission spectrum. The main reason is that although molecules having luminescence peaks in the green and even red regions can be obtained by enlarging the degree of conjugation of aromatic amines, the electron structure of the alternating arrangement of HOMO and LUMO is destroyed after the conjugated system is enlarged, thus leading to a widening of the emission spectrum, and a narrow-spectrum emission material cannot be obtained.
Thus, there remains a need for novel green and red organic electroluminescent materials having narrow spectral emission characteristics.
Disclosure of Invention
In order to overcome the defect that the emission spectrum of the existing green and red organic electroluminescent materials is too wide, the present disclosure provides an organic compound, a composition and an organic electroluminescent device thereof which emit light in the green to red region and have narrow spectrum TADF luminescence characteristics.
The present disclosure provides a boron nitrogen compound having a structure represented by formula I or II,
R 1 each occurrence is independently H, D (deuterium), fluorine, CN, C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R a Substituted C 6 ~C 14 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;
e is a single bond or
R 11 And R is 22 Each occurrence is independently H, D (deuterium), C 1 ~C 6 Alkyl or C 1 ~C 6 An alkoxy group;
r is:
H、C 1 ~C 20 alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 Aryl, 5-to 18-membered heteroaryl or substituted with one or more R d Substituted 5-to 18-membered heteroaryl;
R 4 、R 5 and R is 6 Each occurrence is independently H, D (deuterium), fluorine, CN, C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 Aryl, 5-to 18-membered heteroaryl or substituted with one or more R d Substituted 5-to 18-membered heteroaryl;
R a each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R b Substituted C 6 ~C 14 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 each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R c Substituted C 6 ~C 14 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 each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 Aryl group,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 each occurrence is independently D (deuterium), fluorine, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl radicals being optionally substituted by one or more R e Substituted C 6 ~C 14 An aryl group;
R e each occurrence is independently D (deuterium), fluorine, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, or C 6 ~C 14 An aryl group;
the above alkyl, alkoxy, cycloalkyl, aryl, heteroaryl groups are optionally substituted with one or more substituents selected from the group consisting of: halogen, -CN, C 1 -C 12 Alkyl, C 1 -C 12 Alkoxy, C 1 -C 12 Haloalkyl, C 2 -C 6 Alkenyl, C 3 -C 10 Cycloalkyl, C 6 -C 14 Aryl, or 5-to 18-membered heteroaryl.
In yet another aspect, the present disclosure provides a method of preparing the boron nitrogen compound described above, comprising the steps of:
in the reaction formula (1), a boron-nitrogen parent nucleus compound containing a carbazole skeleton is taken as a reactant, the reactant is dissolved in an organic solvent, heating reflux is carried out in the presence of a catalyst, and b boron atoms of a benzene ring are activated at para-hydrogen atoms and replaced by boron esters;
introducing an electron withdrawing group onto the boron-nitrogen skeleton by utilizing a Suzuki reaction in the reaction formula (2), wherein the introduced electron withdrawing group is positioned at the para position of the B atom of the B benzene ring in the boron-nitrogen skeleton;
in the reaction formula (2), arX is any one of the following three molecules:
x is Br or Cl;
R 1 、R 4 、R 5 、R 6 、R 11 、R 22 r is defined as above.
In another aspect, the present disclosure provides an organic electroluminescent composition comprising the above boron nitrogen compound. Further, the present disclosure also provides an organic electroluminescent composition comprising the above boron nitrogen compound and a host material.
In yet another aspect, the present disclosure provides an organic electroluminescent device comprising the boron nitrogen compound or the organic electroluminescent composition described above.
Drawings
In order to more clearly illustrate the technical solutions of the embodiments of the present disclosure, the drawings of the embodiments will be briefly described below, and it is apparent that the drawings in the following description relate only to some embodiments of the present disclosure, not to limit the present disclosure.
Fig. 1 is a schematic view of a device structure used in effect example 2, in which 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.
FIG. 2 is a photoluminescence spectrum of a doped film of compound BN-66, wherein the composition of the doped film is H1-1 (97 wt%) BN-66 (3 wt%).
FIG. 3 is an electroluminescent spectrum of a doped film of the compound BN-66 in effect example 2, wherein the composition of the doped film is H1-1 (97 wt.%): BN-66 (3 wt.%).
FIG. 4 is a temperature-varying time resolved spectrum of a doped film of compound BN-66, wherein the composition of the doped film is H1-1 (97 wt.%): BN-66 (3 wt.%).
FIG. 5 is a graph of external quantum efficiency as a function of luminance for a compound BN-66 doped device, wherein the light emitting layer doping weight percent composition is H1-1 (97 wt%) BN-66 (3 wt%).
Detailed Description
For the purpose of making the objects, technical solutions and advantages of the embodiments of the present disclosure more apparent, the technical solutions of the embodiments of the present disclosure will be clearly and completely described below with reference to the accompanying drawings of the embodiments of the present disclosure. It will be apparent that the described embodiments are some, but not all, of the embodiments of the present disclosure. All other embodiments, which can be made by one of ordinary skill in the art without the benefit of the present disclosure, are intended to be within the scope of the present invention based on the described embodiments.
It is to be understood that any and all embodiments of the invention may be combined with any other embodiment or features of multiple other embodiments to yield yet further embodiments without conflict. The present invention includes such combinations resulting in additional embodiments.
All publications and patents mentioned in this disclosure are incorporated herein by reference in their entirety. The use or terminology used in any publications and patents incorporated by reference conflicts with the use or terminology used in the present disclosure, based upon the use and terminology of the present disclosure.
The section headings used herein are for purposes of organizing articles only and should not be construed as limiting the subject matter.
Unless otherwise specified, all technical and scientific terms used herein have the ordinary meaning in the art to which the claimed subject matter belongs. In case there are multiple definitions for a term, the definitions herein control.
When any type of range (e.g., wavelength, half-width, and number of substituents) is disclosed or claimed, it is intended that each possible number that the range can reasonably cover be disclosed or claimed alone, including any subranges subsumed therein, unless otherwise indicated. For example, numerical ranges such as 0 to 6, 1-4, 1 to 3, etc. as defined herein for substituents indicate integers within the range, wherein 0-6 is understood to include 0, 1, 2, 3, 4, 5, 6, as well as 1-4 and 1-3.
The use of the terms "comprising," "including," or "containing," and the like, in this disclosure, are intended to cover an element listed after that term and its equivalents, but do not exclude the presence of other elements. The terms "comprising" or "including" as used herein, can be open, semi-closed, and closed. In other words, the term also includes "consisting essentially of …," or "consisting of ….
The terms "moiety", "structural moiety", "chemical moiety", "group", "chemical group" as used herein refer to a particular fragment or functional group in a molecule. Chemical moieties are generally considered to be chemical entities that are embedded or attached to a molecule.
It is to be understood that as used in this disclosure, the singular forms (e.g., "a") can include plural referents unless otherwise specified.
The present disclosure employs standard nomenclature for analytical chemistry, organic synthetic chemistry, and optics, and standard laboratory procedures and techniques, unless otherwise indicated. In some cases, standard techniques are used for chemical synthesis, chemical analysis, and light emitting device performance detection. Unless otherwise indicated, the present disclosure employs conventional methods of mass spectrometry, elemental analysis, and the various steps and conditions can be referenced to procedures and conditions conventional in the art.
The compounds of the present disclosure may contain non-natural proportions of atomic isotopes on one or more of the atoms comprising the compounds. For example, compounds such as deuterium (D) may be isotopically labeled. All isotopic variations of the compounds of the present disclosure, whether radioactive or not, are intended to be encompassed within the scope of the present invention.
Reagents and materials used in the present disclosure are commercially available or may be prepared by conventional chemical synthesis methods.
The term "optional" is used herein to describe a situation, and it may or may not occur. For example, optionally fused to a ring means that it is fused to a ring or not fused to a ring. For example, the term "optionally substituted" as used herein refers to a non-hydrogen substituent that is unsubstituted or has at least one property that does not interfere with the luminescence properties possessed by the unsubstituted analog.
In the present disclosure, the number of "substitutions" may be one or more, unless otherwise specified; when plural, it 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 disclosure, the "substituted" position may be any position unless otherwise specified.
In the present disclosure, unless otherwise specified, the hydrogen or H is a hydrogen element in natural abundance, i.e., a mixture of isotopes protium, deuterium and tritium, wherein the abundance of protium is 99.98%.
In the present disclosure, the deuterium is D or 2 H, also known as deuterium, has an abundance of deuterium at deuterium substitution sites greater than 95%.
The definition of standard chemical terms can be found in references (including Carey and Sundberg "ADVANCED ORGANIC CHEMISTRY TH ED." vols. A (2000) and B (2001), plenum Press, new York).
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. For example-CH 2 O-is equivalent to-OCH 2 -。
The term "halogen" or "halo" as used herein refers to fluorine, chlorine, bromine or iodine. In one embodiment, the halogen or halo is preferably fluoro or fluoro.
In the present disclosure, as part of a group or other group (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 disclosure, theC 1 ~C 6 Alkyl is each independently methyl, ethyl, propyl, butyl, pentyl or hexyl; wherein propyl is C 3 Alkyl (including isomers such as n-propyl or isopropyl); butyl is C 4 Alkyl (including isomers such as n-butyl, sec-butyl, isobutyl, or tert-butyl); pentyl is C 5 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 C 6 Alkyl (including isomers such as n-hexyl or isohexyl).
"substituted alkyl" refers to an alkyl group substituted at any available point of attachment with one or more substituents, preferably 1 to 4 substituents. The term "haloalkyl" refers to an alkyl group having one or more halogen substituents, e.g., halomethyl groups including, but not limited to, e.g., -CH 2 Br、-CH 2 I、-CH 2 Cl、-CH 2 F、-CHF 2 -CF 3 Such groups.
The term "alkoxy" as used herein refers to an alkyl group as defined above, each attached via an oxygen bond (-O-). The term "substituted alkoxy" refers to a substituted alkyl group as defined above attached via an oxygen bond.
In the present disclosure, 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, biphenyl, naphthyl, indenyl, azulenyl, fluorenyl, phenanthryl, or anthracyl. In one embodiment, the aryl group is preferably C 6-14 Aryl groups such as phenyl, biphenyl, and naphthyl, more preferably phenyl.
In the present disclosure, the term "n-m membered heteroaryl" as part of a group or other group refers to 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, the 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, triazinyl, purinyl, pteridinyl, naphthyridinyl, quinazolinyl, phthalazinyl, imidazopyridyl, imidazothiazolyl, imidazooxazolyl, benzothiazolyl, benzoxazolyl, benzimidazolyl, isoindolyl, indazolyl, pyrrolopyridinyl, thienopyridinyl, furopyridinyl, 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 "fused" as used herein means that two or more carbocycles or heterocycles form a polycyclic ring in a shared cyclic manner.
The term C as used herein n -C m Cycloalkyl means a mono-or polycyclic alkyl group having n to m carbon atoms, e.g. C 3 -C 10 Cycloalkyl and C 3 -C 6 Cycloalkyl groups. Examples include adamantyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and bicycloheptyl. In one embodiment, C 3 -C 10 Cycloalkyl is preferably adamantyl or cyclohexyl.
The present disclosure provides a method for synthesizing organic luminescent molecules with narrow emission spectrum characteristics, wherein the luminescence peak position is 495-630nm, and the principle is different from the principle that an electron donor group and an electron acceptor group are spatially separated (shown as a structure 1) and an electron structure (a resonance structure, shown as a structure 2) is alternately arranged between HOMO and LUMO. The specific molecular design adopted by the present disclosure is as follows:
structure 3 gives a representative molecular design model structure provided by the present disclosure, ar groups are defined as previously, for pyrimidine derivatives having electron withdrawing ability, the general method and principle of molecular design provided are: an additional pyrimidine derivative electron acceptor group is introduced into a functional skeleton having the characteristic of alternately arranging electron structures (resonance structures) of HOMO and LUMO, a certain C (carbon) atom of the introduced pyrimidine derivative is connected with a C atom on the resonance structure group by a single bond, and the additional pyrimidine derivative is covalently connected with respect to a B atom in the resonance structure by para-substitution (as shown in structure 3). Since the additional pyrimidine derivative C atom is attached to the C of the LUMO orbital arrangement on the resonance structure group, the LUMO orbitals of the molecules provided by the present disclosure are formed by the combination of the LUMO orbitals of the resonance structure moiety and the LUMO orbitals of the additional pyrimidine derivative acceptor, whereas the HOMO orbitals of the molecules provided by the present disclosure are identical to the HOMO orbitals of the resonance structure moiety of the molecules. Thus, the organic luminescent molecules provided by the present disclosure are different from the existing D-a type structure in which the electron donor group and the electron acceptor group are spatially separated from each other from the molecular structure to the front-line orbital electron structure, and from the electron structure (resonance structure) in which HOMO and LUMO are alternately laid out.
The organic luminescent molecule design method provided by the disclosure has the advantages of combining the advantages of the separation type D-A structure and the resonance type D-A molecule, and overcoming the defects of the two types of molecules. Because the added pyrimidine derivative acceptor and the B atom adopt para-position substitution, and because the pyrimidine derivative acceptor has stronger electron withdrawing capability, the intramolecular charge transfer characteristic of the target molecule can be obviously improved, and the strong intramolecular charge transfer characteristic is beneficial to the realization of long-wavelength emission. By utilizing the molecular design method provided by the disclosure, the organic luminescent material with a narrower luminescence spectrum with the emission peak wavelength from 495nm to 630nm can be obtained, for example, the half-peak width of the luminescence spectrum is less than or equal to 65nm.
The technical method provided by the disclosure can be used for effectively designing and synthesizing organic molecules which emit light in a green-to-red light region and have the light-emitting characteristic of narrow spectrum TADF, the organic molecules and the composition of the organic molecules and some materials can be used as luminescent materials for preparing a luminescent layer of an organic electroluminescent device, and the prepared organic electroluminescent device has the advantages of narrow emission spectrum, high efficiency, high device color purity and the like.
The present disclosure provides a boron nitrogen compound having a structure represented by formula I or II,
R 1 Each occurrence is independently H, D (deuterium), fluorine, CN, C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R a Substituted C 6 ~C 14 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;
e is a single bond or
R 11 And R is 22 Each occurrence is independently H, D (deuterium), C 1 ~C 6 Alkyl or C 1 ~C 6 An alkoxy group;
r is:
H、C 1 ~C 20 alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 Aryl, 5-to 18-membered heteroaryl or substitutedOne or more R d Substituted 5-to 18-membered heteroaryl;
R 4 、R 5 and R is 6 Each occurrence is independently H, D (deuterium), fluorine, CN, C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 Aryl, 5-to 18-membered heteroaryl or substituted with one or more R d Substituted 5-to 18-membered heteroaryl;
R a each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R b Substituted C 6 ~C 14 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 Each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R c Substituted C 6 ~C 14 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 each occurrence is independently D (deuterium), fluorine, CN, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl, substituted by one or more R d Substituted C 6 ~C 14 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 each occurrence is independently D (deuterium), fluorine, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, C 6 ~C 14 Aryl radicals being optionally substituted by one or more R e Substituted C 6 ~C 14 An aryl group;
R e each occurrence is independently D (deuterium), fluorine, C 1 ~C 12 Alkyl, C 1 ~C 12 Alkoxy, C 3 -C 10 Cycloalkyl, or C 6 ~C 14 An aryl group;
the above alkyl, alkoxy, cycloalkyl, aryl, heteroaryl groups are optionally substituted with one or more substituents selected from the group consisting of: halogen, -CN, C 1 -C 12 Alkyl, C 1 -C 12 Alkoxy, C 1 -C 12 Haloalkyl, C 2 -C 6 Alkenyl, C 3 -C 10 Cycloalkyl, C 6 -C 14 Aryl, or 5-to 18-membered heteroaryl.
In one embodiment of the present disclosure, R 1 Each occurrence is independently H, F, CF 3 、C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, cyclohexyl, adamantyl, phenyl, naphthyl, substituted with one or more R a Substituted phenyl, carbazolyl, substituted by one or more R a Substituted carbazolyl, diphenylamino, or substituted with one or more R a Substituted diphenylamino group, said R a Selected from C 1 ~C 6 Alkyl, C 1 -C 6 Fluoroalkyl and C 1 ~C 6 An alkoxy group.
In one embodiment of the present disclosure, R 4 、R 5 And R is 6 Each occurrence is independently H, F, CF 3 、C 1 ~C 20 Alkyl, C 1 ~C 20 Alkoxy, cyclohexyl, adamantyl, phenyl, naphthyl, substituted with one or more R d Substituted phenyl, carbazolyl and substituted by one or more R d Substituted carbazolyl, said R d Selected from C 1 ~C 12 Alkyl, C 1 -C 12 Fluoroalkyl, C 1 ~C 12 Alkoxy, phenyl and substituted with one or more R e Substituted phenyl, said R e Selected from C 1 ~C 6 Alkyl, C 1 -C 6 Fluoroalkyl and C 1 ~C 6 An alkoxy group.
In one embodiment of the present disclosure, R 11 And R is 22 Each occurrence is independently H, methyl, methoxy or CF 3 。
In one embodiment of the present disclosure, the front molecular orbital of the boron nitrogen compounds of formulas I and II have the following characteristics:
HOMO and LUMO are distributed in an alternating manner over ring atoms of rings c11, c12, c13, c14, B1 of formula I and over one B and two N simultaneously connected to three of the rings, HOMO being distributed over two N in formula I, LUMO being distributed over B atoms, ring m1 and ring ph 1;
HOMO and LUMO are distributed in an alternating fashion over ring atoms c21, c22, c23, c24, and B2 of formula II and over one B and two N simultaneously attached to three of them, two N in formula II having HOMO distributed thereon, and B atoms, ring m2 and ring ph2 having LUMO distributed thereon.
In one embodiment of the present disclosure, the emission spectra of the compounds of formulas I and II have emission peaks at 490-630nm and an emission spectrum half-width of 60nm or less.
In one embodiment of the present disclosure, the emission spectra of the compounds of formulas I and II have emission peak positions of 500-600nm and emission spectrum half-peak widths of 60nm or less.
In a certain embodiment of the disclosure, E is a single bond or a benzene ring; r is R 1 Independently for each occurrence H, methyl, t-butyl, phenyl, 4-tolyl, 3, 5-xylyl, 4-t-butylphenyl, 3, 5-di-t-butylphenyl, diphenylamino, di (p-tolyl) amino, or di (p-t-butylphenyl) amino; r is R 11 And R is 22 Is H; r is H orR 4 And R is 6 The same is tert-butyl, phenyl, 4-tolyl, 3, 5-xylyl, 4-tert-butylphenyl, 3, 5-di-tert-butylphenyl, 4-C 1 ~C 10 Alkoxyphenyl, 3-C 1 ~C 10 Alkoxyphenyl, or 3, 5-di C 1 ~C 10 An alkoxyphenyl group; r is R 5 H.
In one embodiment of the present disclosure, the molecular structural composition of the compounds of formula I and II satisfies the following definition:
wherein E in formula I is a single bond orWherein>Is->Or (b)Wherein +.>Is any one of the following groups: />
/>
/>
/>
/>
Wherein in formulae I and IIIs any one of the following groups:
/>
/>
in one embodiment of the present disclosure, the compound of formula I and II is any one of the following:
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
the present disclosure also provides a method of preparing the above boron nitrogen compound, comprising the steps of the following reaction formulae (1) and (2):
in the reaction formula (1), a boron-nitrogen parent nucleus compound containing a carbazole skeleton is taken as a reactant, the reactant is dissolved in an organic solvent, heating reflux is carried out in the presence of a catalyst, and b boron atoms of a benzene ring are activated at para-hydrogen atoms and replaced by boron esters;
introducing an electron withdrawing group onto the boron-nitrogen skeleton by utilizing a Suzuki reaction in the reaction formula (2), wherein the introduced electron withdrawing group is positioned at the para position of the B atom of the B benzene ring in the boron-nitrogen skeleton;
in the reaction formula (2), arX is any one of the following three molecules:
x is Br or Cl;
R 1 、R 4 、R 5 、R 6 、R 11 、R 22 R is defined as above.
The compounds of formula I described in the present disclosure may be prepared according to chemical synthesis methods conventional in the art, and the procedures and conditions may be referred to in the art as analogous procedures and conditions. The present disclosure provides a method for preparing a compound of formula (I and II), which may include the following schemes:
wherein the method comprises the steps of
The present disclosure also provides an organic electroluminescent device comprising an anode, a light emitting layer, an optional hole injection layer, an optional hole transport layer, an optional electron injection layer, and a cathode, wherein at least one of the light emitting layer, the electron injection layer, the electron transport layer, the hole injection layer comprises a boron nitride compound as described above. The organic electroluminescent device of the present disclosure may further include 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 of the present disclosure, the boron nitride compound as shown in formula I or II is used to prepare a light emitting layer in an organic electroluminescent device.
In one embodiment of the present disclosure, the boron nitride compound shown in formula I or II is used for preparing a light emitting layer in an organic electroluminescent device, and the molecular structures of the compounds shown in formula I and II are defined as follows:
wherein E in formula I is a single bond orWherein>Is->Or (b)Wherein +.>Is any one of the formulae B-1 to B-100;
wherein in formulae I and IIIs any one of formulas M-1 to M-88.
In one embodiment of the present disclosure, the boron nitrogen compounds as shown in formulas BN-1 to BN-584 are used to prepare light emitting layers in organic electroluminescent devices.
In one embodiment of the present disclosure, the organic electroluminescent device further includes 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.
The present disclosure provides an organic electroluminescent composition comprising a boron nitride compound (as a doping material) as shown in formula I or II and a host material; the host material is one having electron and/or hole transport capability and having a triplet energy that is higher than or near the triplet energy of the dopant material.
In one embodiment of the present disclosure, the host material in the organic electroluminescent composition may be a carbazole derivative and/or a carboline derivative as shown in formulae (H-1) to (H-6). The organic electroluminescent composition preferably contains 0.3-30.0wt% (weight percentage) of any one compound shown in formula I or II as doping material, and the rest 99.7-70.0wt% is host material composed of 1-2 compounds in formulas (H-1) to (H-6). In one embodiment, the host material contains 2 compounds of formulae (H-1) to (H-6) in a weight ratio of 1:5 to 5:1.
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 which is N.
Wherein R is 1H And R is 2H Independently any of the following groups:
wherein X is 2 、Y 2 And Z 2 Is CH or N, and X 2 、Y 2 And Z 2 At most one of which 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 groups.
In one embodiment of the present disclosure, the host material in the organic electroluminescent composition is 1-2 of the compounds H1-1 to H1-427; the organic electroluminescent composition contains 0.3-30.0wt% (weight percentage) of any one compound shown in formula I or II, and the rest 99.7-70.0wt% is 1-2 compounds from compounds H1-1 to H1-427. In a preferred embodiment of the present disclosure, the organic electroluminescent composition contains 2 compounds of the formulae H1-1 to H1-427 as host materials in a weight ratio of the two compounds of 1:5 to 5:1.
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
In one embodiment of the present disclosure, the doping material in the organic electroluminescent composition is any one of the compounds represented by formula I or II (the content is 0.3 wt% to 30.0 wt%); the host material (content of 99.7 wt% to 70.0 wt%) is composed of any one of 1,3, 5-triazine derivatives represented by the formulas Trz1-A, trz2-A and Trz3-A and any one of compounds represented by the formulas H-1 to H-6. In a preferred embodiment, the weight ratio of Trz1-A, trz2-A or Trz 3-A1, 3, 5-triazine derivative to H-1, H-2, H-3, H-4, H-5 or H-6 is from 1:5 to 5:1.
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 groups Tz-n (n=1-61) shown in the following formula:
/>
/>
in one embodiment of the present disclosure, the doping material in the organic electroluminescent composition is any one of the compounds represented by formula I or II (the content is 0.3 wt% to 30.0 wt%); the main material (content of 99.7wt% -70.0wt%) is composed of any one of 1,3, 5-triazine derivatives shown in formulas TRZ-1 to TRZ-56 and any one of carbazole or carboline derivatives shown in formulas H1-1 to H1-427. In a preferred embodiment, the weight ratio between the 1,3, 5-triazine derivative and the carbazole or carboline derivative in the host material is from 1:5 to 5:1.
/>
/>
The present disclosure provides the use of an organic electroluminescent composition as described above as an organic electroluminescent material.
In one embodiment of the present disclosure, the organic electroluminescent composition is used to prepare a light-emitting layer in an organic electroluminescent device.
The present disclosure also provides an organic electroluminescent device comprising an anode, a light emitting layer, an optional hole injection layer, an optional hole transport layer, an optional electron injection layer, and a cathode, wherein at least one of the light emitting layer, the electron injection layer, the electron transport layer, the hole injection layer comprises the organic electroluminescent composition as described above. In a preferred embodiment, the light-emitting layer of the organic electroluminescent device comprises an organic electroluminescent composition as described above.
In one embodiment of the present disclosure, the organic electroluminescent composition is a light-emitting layer, and the light-emitting principle of the light-emitting layer is based on energy transfer of a host material to any one of the compounds represented by formula I or II or carrier capture of the light-emitting material itself.
In one embodiment of the present disclosure, 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 as shown in 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 of formula I or II, and the remaining 99.7 to 70.0wt% of the composition is a host composed of 1 to 2 compounds of formulae (H-1) to (H-6). For example, when the host contains 2 compounds 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 present disclosure, the organic electroluminescent composition is a light-emitting layer; the main materials in the composition are 1-2 of the compounds H1-1 to H1-427. In a preferred embodiment, the organic electroluminescent composition comprises 0.3-30.0wt% of any one of the compounds of formula I or II, 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 H1-427 are included in the composition, the weight ratio of the two compounds is 1:5 to 5:1.
In one embodiment of the present disclosure, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound shown in the formula I or II (the content is 0.3-30.0 wt%); the host material (content of 99.7 wt% to 70.0 wt%) is composed of any one of 1,3, 5-triazine derivatives represented by the formulas Trz1-A, trz2-A and Trz3-A and any one of compounds represented by the formulas H-1 to H-6. For example, in the host material, the weight ratio of Trz1-A, trz2-A or Trz 3-A1, 3, 5-triazine derivative to H-1, H-2, H-3, H-4, H-5 or H-6 compound is 1:5 to 5:1.
In one embodiment of the present disclosure, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound shown in the formula I or II (the content is 0.3-30.0 wt%); the main material (content of 99.7wt% -70.0wt%) is composed of any one of 1,3, 5-triazine derivatives shown in formulas TRZ-1 to TRZ-56 and any one of carbazole or carboline derivatives shown in formulas H1-1 to H1-427. For example, in the host material, the weight ratio between the 1,3, 5-triazine derivative and the carbazole or carboline derivative is 1:5 to 5:1.
In one embodiment of the present disclosure, the organic electroluminescent composition is a light-emitting layer; the doping material in the organic electroluminescent composition is any one compound (the content is 0.3-30.0 wt%) shown in the formulas BN-1 to BN-584; the main material (content of 99.7wt% -70.0wt%) is composed of any one of 1,3, 5-triazine derivatives shown in formulas TRZ-1 to TRZ-56 and any one of carbazole or carboline derivatives shown in formulas H1-1 to H1-427. For example, in the host material, the weight ratio between the 1,3, 5-triazine derivative and the carbazole or carboline derivative is 1:5 to 5:1.
In one embodiment of the present disclosure, the organic electroluminescent device further includes 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 more 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.
The disclosure provides an application of the organic electroluminescent device in an organic electroluminescent display or an organic electroluminescent illumination source.
The present disclosure provides a molecular structure design method for designing and synthesizing an organic light emitting material, which has the advantages that: the advantages of the isolated D-A structure and the resonance type D-A molecule are combined, and the defects of the two types of molecules are overcome. The method can effectively overcome the defect of the existing green light and red light organic electroluminescent materials that the emission spectrum is too wide, and provides a technical method for designing, synthesizing and preparing organic molecules with narrow spectrum luminescence characteristics in a green-red light region or even near infrared luminescence; and further provides an organic compound which emits light in the green to red light region and has narrow-spectrum light emitting characteristics as shown in formulas I and II, a composition and application thereof in the field of organic electroluminescence. The organic molecules and the composition of the organic molecules and some materials can be used as luminescent materials to prepare the luminescent layer of the organic electroluminescent device, and the prepared organic electroluminescent device has the advantages of narrow emission spectrum (electroluminescent spectrum relative to the luminescent material with a separated D-A structure), high efficiency and the like.
The present disclosure provides a synthesis method of coupling a tri-coordination B complex based on 1, 3-dicarbazole (or a derivative thereof) benzene with a pyrimidine derivative, which has an advantage in that a pyrimidine derivative group having an electron withdrawing property can be coupled with a C atom occupied by LUMO orbitals in a tri-coordination B resonance skeleton, and thus a pyrimidine derivative group having a conjugated structure and having a strong electron withdrawing property can be effectively introduced into the tri-coordination B resonance skeleton based on the synthesis method.
According to the conventional synthesis concept, a researcher in the art generally synthesizes a molecule containing a three-coordinate B resonance skeleton and a pyrimidine derivative group according to the following reaction scheme (3), in which in the following reaction test, ar is a pyrimidine derivative, and as proved by experimental research results, a three-coordinate B structure cannot be formed according to the following reaction scheme, i.e., the boron atom cannot realize coordination with 1, 3-dicarbazole (or its derivative) benzene under the condition, and the target product cannot be obtained according to the reaction mode. The main reason is that when pyrimidine derivatives with strong electron withdrawing groups exist, para carbon atoms are in electron-deficient state, namely, the electron cloud density is low, so that the carbon atoms cannot form covalent bonds with boron atoms.
R 1 And Ar is as defined above.
For the purpose of making the objects, technical solutions and advantages of the embodiments of the present disclosure more apparent, the technical solutions of the embodiments of the present disclosure will be clearly and completely described below with reference to the accompanying drawings. It will be apparent that the described embodiments are some, but not all, of the embodiments of the present disclosure. All other embodiments, which can be made by one of ordinary skill in the art without the benefit of the present disclosure, are intended to be within the scope of the present invention based on the described embodiments.
The present disclosure is further illustrated by way of examples below, but is not thereby limited to the scope of the examples described. The experimental methods, in which specific conditions are not noted in the following examples, were selected according to conventional methods and conditions, or according to the commercial specifications.
Molecular Mass spectrum data (Mass Spectra: MS) with a relative molecular weight below 1000 were measured by ITQ1100 ion trap gas chromatograph-Mass spectrometer (ITQ) from Thermo Fisher, and molecular Mass spectrum data with a relative molecular weight above 1000 were measured by Autoflex Speed matrix assisted laser desorption time-of-flight Mass spectrometer (Bruker). The elemental analysis of the final product was performed using a machine from company Elemental analysis, flash EA1112.
The UV-visible absorption spectrum of the sample film was measured by a LAMBDA model 35 UV-visible spectrophotometer from Perkinelmer. The fluorescence spectrum was measured by an RF-5301PC fluorescence photometer of Shimadzu corporation, japan, and the excitation wavelength selected at the time of the test was the maximum absorption wavelength.
The specifically adopted raw material-1 comprises the following molecules:
the specifically adopted raw material-2 comprises the following molecules:
the specifically adopted raw material-3 comprises the following molecules:
/>
/>
/>
/>
the basic process route of the compound synthesis related by the invention is as follows, and the reaction is divided into four steps. The first two steps of synthesis are BNCz mother nucleus synthesis; the final product synthesis is most core to the successful preparation of the precursor BN-Bpin. The boron-nitrogen mother nucleus containing carbazole skeleton is first synthesized and dissolved in tetrahydrofuran, and the reaction system is heated and refluxed under the condition of adding 1% equivalent of main catalyst methoxy (cyclooctadiene) iridium dimer and 2% equivalent of cocatalyst 4,4 '-di-tert-butyl-2, 2' -bipyridine, and the boron atom substituted benzene ring is activated to para-hydrogen atom and substituted by boron ester. In the following, various electron-withdrawing substituted compounds can be flexibly obtained by only one-step simple Suzuki reaction. The specific synthesis process comprises the following steps:
Wherein the method comprises the steps ofSynthetic examples
In the first step, 60ml of a solution of carbazole derivative in anhydrous DMF (N, N-dimethylformamide) was slowly dropped into a solution of carbazole derivative in anhydrous DMF containing 5.4g of potassium tert-butoxide (48.0 mmol), and after stirring at room temperature for 2 hours, 20ml of a solution of 2-bromo-1, 3-difluorobenzene (16.0 mmol) in anhydrous DMF was added dropwise thereto. The reaction system was stirred at 140 ℃ for 24 hours, then cooled to room temperature and poured into ice water. 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 BrNCz as a white solid.
In the second step, 19.4mL of a solution of tert-butyllithium in n-hexane (25.2 mmol) was slowly added to a solution of 100mL of tert-butylbenzene containing 12.6mmol of intermediate BrNCz (-30 ℃ C.) under nitrogen atmosphere. After slowly heating to 60℃and stirring for 2 hours, n-hexane was removed in vacuo, then cooled to-30℃and 2.4mL of boron tribromide (6.3 mmol) was added and the reaction mixture was stirred at room temperature for 1 hour. 15.6mL of N, N-diisopropylethylamine (91.1 mmol) was then added at 0deg.C, and the reaction mixture was allowed to cool to room temperature after stirring for an additional 5 hours at 130deg.C. To the reaction mixture was added 5ml of methanol to quench Residual BBr 3 . The reaction system was concentrated in vacuo and purified by column chromatography with a dichloromethane/petroleum ether mixture eluent to give a BNCz mother nucleus.
In the third step, a boron nitrogen starting material (6.5 mmol) containing carbazole skeleton, 1.7g of bisboronic acid pinacol ester (6.5 mmol) were added to tetrahydrofuran (60 mL) at room temperature, the mixture was bubbled with nitrogen for 10 minutes, and 34.9mg of 4,4 '-di-tert-butyl-2, 2' -bipyridine (0.13 mmol) and 43.1mg of methoxy (cyclooctadiene) iridium dimer (0.065 mmol) were added under high flow nitrogen. After stirring for 10 minutes, the mixture was heated to reflux and stirred for 24 hours. And after the reaction system is cooled to room temperature, directly concentrating under reduced pressure, and purifying by column chromatography to obtain a precursor BN-Bpin.
In the fourth step, ar-X (Ar is defined as before, X is bromine) (0.6 mmol), BN-Bpin (0.5 mmol), 0.14g potassium carbonate (1 mmol) and water (2 mL) were added to tetrahydrofuran (16 mL), the mixture was bubbled with nitrogen for 10 minutes, 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 objective product BN-n (n=1-584).
Experimental details of the synthetic examples are illustrated by the compound BN-66: in the first step, 60ml of a solution of anhydrous DMF (N, N-dimethylformamide) containing 9.8g of 3, 6-di-t-butylcarbazole (35.2 mmol) was slowly added dropwise to a solution of 50ml of anhydrous DMF containing 5.4g of potassium t-butoxide (48.0 mmol), and after stirring at room temperature for 2 hours, 20ml of a solution of anhydrous DMF containing 3.1g of 2-bromo-1, 3-difluorobenzene (16.0 mmol) was added dropwise thereto. The reaction system was stirred at 140 ℃ for 24 hours, then cooled to room temperature and poured into ice water. 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 10.5g of intermediate BrNCz as a white solid (92% yield).
Second step, 19.4mL of a solution of tert-butyllithium in n-hexane (25.2 mmol) was slowly added to 100mL of tert-butyl containing 9.0g (12.6 mmol) of intermediate BrNCz under nitrogen atmosphereIn the alkylbenzene solution (-30 ℃). After slowly heating to 60℃and stirring for 2 hours, n-hexane was removed in vacuo, then cooled to-30℃and 2.4mL of boron tribromide (6.3 mmol) was added and the reaction mixture was stirred at room temperature for 1 hour. 15.6mL of N, N-diisopropylethylamine (91.1 mmol) was then added at 0deg.C, and the reaction mixture was allowed to cool to room temperature after stirring for an additional 5 hours at 130deg.C. To the reaction mixture was added 5ml of methanol to quench the residual BBr 3 . The reaction system was concentrated in vacuo and purified by column chromatography with a dichloromethane/petroleum ether mixture eluent to give 2.9g of BNCz mother nucleus as a yellow solid (yield 35%) (the experiment was repeated multiple times to enrich the starting material).
In the third step, 4.2g BNCz (6.5 mmol), 1.7g of bisboronic acid pinacol ester (6.5 mmol) were added to tetrahydrofuran (60 mL) and the mixture was bubbled with nitrogen for 10 min and 34.9mg 4,4 '-di-tert-butyl-2, 2' -bipyridine (0.13 mmol) and 43.1mg methoxy (cyclooctadiene) iridium dimer (0.065 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 was cooled to room temperature, it was directly concentrated under reduced pressure and purified by column chromatography to give 4.5g of the precursor BN-Bpin (yield 90%).
In the fourth step, 187mg of 2-bromo-4, 6-diphenylpyrimidine (0.6 mmol), 383mg of BN-Bpin (0.5 mmol), 0.14g of potassium carbonate (1 mmol) and water (2 mL) were added to tetrahydrofuran (16 mL), the mixture was bubbled with nitrogen for 10 minutes, 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 dichloromethane and water, the organic phase was dried by heating under vacuum, and then purified by column chromatography to give 284mg of the objective product BN-66 as a yellow solid (yield 58%).
Table 1 elemental analysis (C, H and N percent in the compounds), mass spectrometry molecular weight and synthesis reaction yield data (total yield of four steps) for compounds BN-1 through BN-584.
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
Effect example 1
The luminescent molecular structure used in the comparative effect examples is as follows:
the compounds represented by the formulas BN-1 to BN-584 are molecular structures of materials provided by the disclosure (specific molecular structures are shown in the foregoing), and the compounds represented by the formulas BN-R-1 to BN-R-7 are molecular structures of comparison materials. Any one of the compounds represented by the formula BN-n (n=1-584) or BN-R-m (m=1-7) was used as a doped luminescent material and H-1 was used as a host material to prepare a doped thin film (thickness: 150±15 nm) having a doping concentration of 3wt% (weight percentage concentration), and then the doped thin film was subjected to emission spectrum test, respectively, and the test results are shown in table 2.
Comparison of the luminescence peak positions of the luminescent compounds provided by the present disclosure with the luminescence peak positions of the corresponding comparative compounds, as set forth in table 2, shows that the luminescence peak positions of the luminescent compounds provided by the present disclosure are red shifted by 7-62nm, i.e., shifted to long wavelengths by 7-62nm, than the luminescence peak positions of the corresponding comparative compounds. The above-described effect examples demonstrate that the luminescence peak of the boron nitrogen compound of the present disclosure is significantly red-shifted with respect to its isomer without significant degradation (still narrower) in the half-width of the luminescence spectrum, and thus the luminescent molecular design principle and method provided by the present disclosure are effective in providing a luminescent material having a narrow emission peak from the green region to the red region.
Table 2.Bn-n (n=1-584) emission spectrum test parameters.
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
Electroluminescent device embodiment
Some of the material molecular structures involved in the device effect embodiments are as follows:
the following examples of electroluminescent devices prepared using the materials of the present disclosure, the specific device preparation process is as follows:
(1) And (3) substrate processing: the transparent ITO glass is used as a substrate material for preparing devices, is subjected to ultrasonic treatment for 30min by using 5% ITO washing liquid, is sequentially subjected to ultrasonic washing by using distilled water (2 times), acetone (2 times) and isopropanol (2 times), and is finally stored in 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 preparation of the device is completed by combining spin coating and vacuum evaporation process.
(2) Hole injection layer and hole transport layer preparation: a layer of 20nm thick PEDOT PSS (Poly 3, 4-ethylenedioxythiophene) polystyrene sulfonate, which is commercially available from Heraeus Corp. Germany, was first spin-coated on the ITO surface as a hole injection layer, then a 50nm thick Poly-HTL was spin-coated on the hole injection layer as a hole transport layer, and then the ITO glass with the hole injection layer and the hole transport layer was annealed at 200℃for 30 minutes in a nitrogen-protected glove box (cross-linking the Poly-HTL).
(3) Preparing a light-emitting layer: the main material and the luminescent material are dissolved in dimethylbenzene according to the proportion of 97wt% (weight percent concentration) to prepare a solution with the concentration of 2wt%, and the prepared solution is used for preparing the luminescent layer with the thickness of 50nm by a spin coating method.
(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 And starting evaporation when Pa is lower, wherein the deposition rate is equal to or lower than that of the Sien film thickness meter, and sequentially depositing an organic electronic transmission layer, a LiF electron injection layer and a metal Al electrode on the light-emitting layer by utilizing a vacuum evaporation process (the specific device structure is shown in the following effect example). Wherein the deposition rate of the organic material isThe deposition rate of LiF is +.>Al deposition rate is +.>。
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.
Effect example 2
In the organic electroluminescent device (structure shown in FIG. 1) in effect example 2, PEDOT: PSS was used as a hole injection layer, poly-HTL was used as a hole transport layer, H1-48 was used as a host material in a light emitting layer, BN-1 to BN-584 were used as doped light emitting materials, respectively (doping concentration was 3 wt%), tmPyPB was used as an electron transport material, liF was used as an electron injection layer, and Al was used as a metal cathode. Effect example the organic electroluminescent device structure was [ ITO/PEDOT: PSS (20 nm)/Poly-HTL (50 nm)// H1-48+3wt% bn-n/TmPyPB (50 nm)/LiF (1 nm)/Al (100 nm) ]. Where n=1-584. Effect example the results are shown in table 3. The electroluminescent device effect implementation data listed in table 3 demonstrate that the luminescent materials provided by the present disclosure can be used to prepare high efficiency organic electroluminescent devices, and that the electroluminescent spectrum has narrow band characteristics with a half-width of less than 60nm.
Table 3.Bn-n (n=1-584) electroluminescent performance main parameters.
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
Effect example 3
In the organic electroluminescent device in effect example 3, in the organic electroluminescent device (structure shown in FIG. 1) in effect example 2, PEDOT: PSS was used as a hole injection layer, poly-HTL was used as a hole transport layer, a mixture of H1-33 and TRZ-1 in a light emitting layer was used as a host material (weight mixing ratio of H1-33 and TRZ-1 was 1:1), BN-1 to BN-584 were used as doped light emitting materials (doping concentration was 3 wt%), tmPyPB was used as an electron transport material, liF was used as an electron injection layer, and Al was used as a metal cathode, respectively. Effect example the organic electroluminescent device structure was [ ITO/PEDOT: PSS (20 nm)/Poly-HTL (50 nm)/H1-33: trz-1+3wt% bn-n/TmPyPB (50 nm)/LiF (1 nm)/Al (100 nm) ]. Where n=1-584. Effect example the results are shown in table 4. The electroluminescent device effect implementation data listed in table 4 demonstrate that the luminescent materials provided by the present disclosure can be used to prepare high efficiency organic electroluminescent devices, and that the electroluminescent spectrum has narrow band characteristics with a half-width of less than 60nm. Effect example the results are shown in table 4.
Table 4.Bn-n (n=1-584) electroluminescent performance main parameters.
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
The foregoing is merely exemplary embodiments of the present invention and is not intended to limit the scope of the invention, which is defined by the appended claims.
Claims (15)
1. A boron nitride compound having a structure represented by formula I or II,
e is a benzene ring;
R 1 independently for each occurrence H, methyl, t-butyl, phenyl, 4-tolyl, 3, 5-xylyl, 4-t-butylphenyl, 3, 5-di-t-butylphenyl, diphenylamino, di (p-tolyl) amino, or di (p-t-butylphenyl) amino;
R 11 and R is 22 Is H;
r is H or
R 4 And R is 6 The same is tert-butyl, phenyl, 4-tolyl, 3, 5-xylyl, 4-tert-butylphenyl, 3, 5-di-tert-butylphenyl, 4-C 1 ~C 10 Alkoxyphenyl, 3-C 1 ~C 10 Alkoxyphenyl, or 3, 5-di C 1 ~C 10 An alkoxyphenyl group;
R 5 h.
2. The boron nitride compound of claim 1, wherein the front molecular orbital has the following characteristics:
HOMO and LUMO are distributed in an alternating manner over ring atoms of rings c11, c12, c13, c14, B1 of formula I and over one B and two N simultaneously connected to three of the rings, HOMO being distributed over two N in formula I, LUMO being distributed over B atoms, ring m1 and ring ph 1;
HOMO and LUMO are distributed in an alternating fashion over ring atoms c21, c22, c23, c24, and B2 of formula II and over one B and two N simultaneously attached to three of them, two N in formula II having HOMO distributed thereon, and B atoms, ring m2 and ring ph2 having LUMO distributed thereon.
3. A boron nitride compound which is any one of the following compounds:
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
4. an organic electroluminescent composition comprising the boron nitride compound according to any one of claims 1 to 3.
5. The organic electroluminescent composition of claim 4, further comprising a host material having an electron and/or hole transporting capability, and the host material has a triplet excited state energy higher than that of the boron-nitrogen compound.
6. The organic electroluminescent composition according to claim 5, wherein the host material comprises 99.7 to 70.0wt% of the composition, and the boron nitrogen compound comprises 0.3 to 30.0wt% of the composition.
7. The organic electroluminescent composition according to claim 6, wherein the host material comprises one or more of the compounds represented by 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 2 、Y 2 And Z 2 Is CH or N, and X 2 、Y 2 And Z 2 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 groups.
8. The organic electroluminescent composition according to claim 7, wherein the host material comprises 2 compounds of formulae (H-1) to (H-6) and the weight ratio of the two compounds is 1:5 to 5:1.
9. The organic electroluminescent composition according to claim 7, wherein the host material is 1-2 of the compounds H1-1 to H1-427, and when the host material is two of the compounds H1-1 to H1-427, the weight ratio of the two compounds is 1:5 to 5:1,
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
/>
10. the organic electroluminescent composition according to claim 7, wherein the host material further comprises any one of 1,3, 5-triazine derivatives represented by formulae Trz1-A, trz2-a and Trz 3-a; and the weight ratio between the 1,3, 5-triazine derivative shown by Trz1-A, trz-A or Trz3-A and the compounds shown by H-1, H-2, H-3, H-4, H-5 and H-6 is 1:5 to 5:1,
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 An aryl group; r is R Tz Is any one of substituent groups shown in the following formula:
/>
/>
11. the organic electroluminescent composition according to claim 10, wherein the host material comprises any one of 1,3, 5-triazine derivatives represented by formulae TRZ-1 to TRZ-56 and any one of carbazole or carboline derivatives represented by formulae H1-1 to H1-427; in the host material, the weight ratio of the 1,3, 5-triazine derivative to the carbazole or carboline derivative is 1:5 to 5:1,
/>
/>
12. an organic electroluminescent device, at least one of which comprises the boron-nitrogen compound according to any one of claims 1 to 3 or the organic electroluminescent composition according to any one of claims 4 to 11.
13. The organic electroluminescent device of claim 12, wherein the light-emitting layer comprises the boron nitride compound or the organic electroluminescent composition.
14. The organic electroluminescent device of claim 12 or 13, for use in the preparation of an organic electroluminescent display or an illumination source.
15. A process for preparing the boron nitrogen compound of claim 1, comprising the steps of the following reaction formulae (1) and (2):
in the reaction formula (1), a boron-nitrogen parent nucleus compound containing a carbazole skeleton is taken as a reactant, the reactant is dissolved in an organic solvent, heating reflux is carried out in the presence of a catalyst, and b boron atoms of a benzene ring are activated at para-hydrogen atoms and replaced by boron esters;
Introducing an electron withdrawing group onto the boron-nitrogen skeleton by utilizing a Suzuki reaction in the reaction formula (2), wherein the introduced electron withdrawing group is positioned at the para position of the B atom of the B benzene ring in the boron-nitrogen skeleton;
in the reaction formula (2), arX is:
x is Br or Cl;
R 1 、R 4 、R 5 、R 6 、R 11 、R 22 r is as defined in claim 1.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011457921.2A CN114621274B (en) | 2020-12-10 | 2020-12-10 | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same |
PCT/CN2021/136306 WO2022121920A1 (en) | 2020-12-10 | 2021-12-08 | Boron-nitrogen compound, organic electroluminescent composition and organic electroluminescent device containing same |
TW110146178A TWI804097B (en) | 2020-12-10 | 2021-12-09 | Boron-nitrogen compound, organic electroluminescence composition, and organic electroluminescence device comprising the same |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202011457921.2A CN114621274B (en) | 2020-12-10 | 2020-12-10 | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same |
Publications (2)
Publication Number | Publication Date |
---|---|
CN114621274A CN114621274A (en) | 2022-06-14 |
CN114621274B true CN114621274B (en) | 2024-03-22 |
Family
ID=81896336
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202011457921.2A Active CN114621274B (en) | 2020-12-10 | 2020-12-10 | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same |
Country Status (3)
Country | Link |
---|---|
CN (1) | CN114621274B (en) |
TW (1) | TWI804097B (en) |
WO (1) | WO2022121920A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114524837B (en) * | 2022-02-28 | 2024-02-13 | 中国科学院长春应用化学研究所 | Condensed-cyclic compound containing boron nitrogen and dendritic structure, preparation method and application thereof, and organic electroluminescent device |
CN115557979A (en) * | 2022-10-27 | 2023-01-03 | 深圳大学 | Boron-nitrogen hybrid compound, preparation method thereof and organic electroluminescent device |
CN117642043A (en) * | 2023-02-21 | 2024-03-01 | 季华恒烨(佛山)电子材料有限公司 | Organic electroluminescent device and application thereof |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110407859A (en) * | 2019-07-18 | 2019-11-05 | 清华大学 | A kind of luminescent material and its organic electroluminescence device using and comprising it |
CN110627822A (en) * | 2019-10-08 | 2019-12-31 | 吉林大学 | Green light narrow spectrum three-coordination boron luminescent compound, luminescent composition and application thereof |
CN110799571A (en) * | 2017-06-30 | 2020-02-14 | 住友化学株式会社 | Polymer compound and light-emitting element using same |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN111278838B (en) * | 2017-12-27 | 2023-01-10 | 广州华睿光电材料有限公司 | Boron-containing heterocyclic compounds, polymers, mixtures, compositions and uses thereof |
CN111610871A (en) * | 2019-02-25 | 2020-09-01 | 英属维尔京群岛商天材创新材料科技股份有限公司 | Electrode structure and touch panel thereof |
CN111718364A (en) * | 2019-03-19 | 2020-09-29 | 赛诺拉有限公司 | Organic molecules for optoelectronic devices |
CN112028912B (en) * | 2019-06-03 | 2024-07-12 | 北京鼎材科技有限公司 | Novel boron-containing organic electroluminescent material and application thereof |
CN112898324A (en) * | 2019-12-03 | 2021-06-04 | 北京鼎材科技有限公司 | Compound, application thereof and organic electroluminescent device |
CN111029477B (en) * | 2019-12-10 | 2022-10-18 | 昆山国显光电有限公司 | Organic light-emitting device, display panel and display device |
CN112480154B (en) * | 2020-11-26 | 2023-01-24 | 深圳大学 | Chiral thermal activation delayed fluorescent material and circular polarization electroluminescent device thereof |
-
2020
- 2020-12-10 CN CN202011457921.2A patent/CN114621274B/en active Active
-
2021
- 2021-12-08 WO PCT/CN2021/136306 patent/WO2022121920A1/en active Application Filing
- 2021-12-09 TW TW110146178A patent/TWI804097B/en active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110799571A (en) * | 2017-06-30 | 2020-02-14 | 住友化学株式会社 | Polymer compound and light-emitting element using same |
CN110407859A (en) * | 2019-07-18 | 2019-11-05 | 清华大学 | A kind of luminescent material and its organic electroluminescence device using and comprising it |
CN110627822A (en) * | 2019-10-08 | 2019-12-31 | 吉林大学 | Green light narrow spectrum three-coordination boron luminescent compound, luminescent composition and application thereof |
Also Published As
Publication number | Publication date |
---|---|
TWI804097B (en) | 2023-06-01 |
WO2022121920A1 (en) | 2022-06-16 |
CN114621274A (en) | 2022-06-14 |
TW202222808A (en) | 2022-06-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN113666951B (en) | Boron-nitrogen compound, organic electroluminescent composition and organic electroluminescent device comprising same | |
CN114621274B (en) | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same | |
CN114773286B (en) | Nitrogen-containing heterocyclic organic compound and organic light-emitting device thereof | |
JP7236772B2 (en) | Substituted 1,3,5-triazine compounds, compositions and uses thereof | |
CN114621271B (en) | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same | |
CN114621272B (en) | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same | |
TW202223066A (en) | Materials for organic electroluminescent devices | |
CN116023402B (en) | Boron-nitrogen compound and preparation method and application thereof | |
CN114478588B (en) | Organic compound based on pyrene and indolocarbazole, organic electroluminescent composition and organic electroluminescent device | |
CN116903648A (en) | Boron nitride compound and application thereof | |
CN114621273B (en) | Boron nitride compound, organic electroluminescent composition and organic electroluminescent device comprising same | |
CN116120349B (en) | Boron-nitrogen compound and preparation method and application thereof | |
CN116120350B (en) | Boron-nitrogen compound and preparation method and application thereof | |
CN111205273A (en) | Bivalent platinum complex and preparation method and application thereof | |
CN114478416B (en) | Pyrene-triazine-based organic compound, organic electroluminescent composition and organic electroluminescent device | |
CN114507188B (en) | Organic compound based on pyrene and benzimidazole, organic electroluminescent composition and organic electroluminescent device | |
CN114736224A (en) | Boron-nitrogen compound, composition thereof and organic electroluminescent device | |
CN112679555B (en) | Broad-spectrum divalent platinum complex and preparation method and application thereof | |
CN116082374A (en) | Boron nitride compound, composition containing boron nitride compound and application of boron nitride compound | |
CN116082373A (en) | Boron nitride compound, composition containing boron nitride compound and application of boron nitride compound | |
CN116082375A (en) | Boron nitride compound and application thereof | |
CN116925113A (en) | Boron nitrogen heterocyclic compound, composition containing same and application thereof | |
CN116082372A (en) | Boron-nitrogen compound and preparation method and application thereof | |
CN116120351A (en) | Boron-nitrogen compound and preparation method and application thereof | |
CN116143759A (en) | Substituted 1,3, 5-triazines, compositions and uses thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant |