CN106467553A - 一种含硼有机电致发光化合物及其在oled器件上的应用 - Google Patents
一种含硼有机电致发光化合物及其在oled器件上的应用 Download PDFInfo
- Publication number
- CN106467553A CN106467553A CN201610614309.9A CN201610614309A CN106467553A CN 106467553 A CN106467553 A CN 106467553A CN 201610614309 A CN201610614309 A CN 201610614309A CN 106467553 A CN106467553 A CN 106467553A
- Authority
- CN
- China
- Prior art keywords
- formula
- independently
- aryl
- compound
- expressed
- 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.)
- Granted
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 50
- 239000000463 material Substances 0.000 claims abstract description 78
- 125000003118 aryl group Chemical group 0.000 claims abstract description 19
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- -1 formula (1) Chemical class 0.000 claims abstract description 13
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 13
- 239000001257 hydrogen Substances 0.000 claims abstract description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 10
- 150000004982 aromatic amines Chemical class 0.000 claims abstract description 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 5
- 238000005401 electroluminescence Methods 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000002019 doping agent Substances 0.000 claims description 8
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 150000002431 hydrogen Chemical class 0.000 claims description 6
- MYKQKWIPLZEVOW-UHFFFAOYSA-N 11h-benzo[a]carbazole Chemical compound C1=CC2=CC=CC=C2C2=C1C1=CC=CC=C1N2 MYKQKWIPLZEVOW-UHFFFAOYSA-N 0.000 claims description 4
- 125000001118 alkylidene group Chemical group 0.000 claims description 4
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 claims description 4
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical group C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims description 4
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical class C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 claims description 4
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical compound C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 claims description 4
- 229960005544 indolocarbazole Drugs 0.000 claims description 4
- 125000005561 phenanthryl group Chemical group 0.000 claims description 4
- 125000001791 phenazinyl group Chemical group C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 claims description 4
- 125000003386 piperidinyl group Chemical group 0.000 claims description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- 125000005493 quinolyl group Chemical group 0.000 claims description 4
- 125000004305 thiazinyl group Chemical group S1NC(=CC=C1)* 0.000 claims description 4
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical group [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 150000001721 carbon Chemical group 0.000 claims description 2
- 125000005266 diarylamine group Chemical group 0.000 claims description 2
- 125000000623 heterocyclic group Chemical group 0.000 claims description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229910052711 selenium Inorganic materials 0.000 claims description 2
- 229910052717 sulfur Inorganic materials 0.000 claims description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 125000001302 tertiary amino group Chemical group 0.000 claims 1
- 229910052796 boron Inorganic materials 0.000 abstract description 3
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract description 2
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 abstract 2
- 239000011203 carbon fibre reinforced carbon Substances 0.000 abstract 2
- CKUAXEQHGKSLHN-UHFFFAOYSA-N [C].[N] Chemical compound [C].[N] CKUAXEQHGKSLHN-UHFFFAOYSA-N 0.000 abstract 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 1
- CSJDCSCTVDEHRN-UHFFFAOYSA-N methane;molecular oxygen Chemical compound C.O=O CSJDCSCTVDEHRN-UHFFFAOYSA-N 0.000 abstract 1
- 239000010409 thin film Substances 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 72
- 239000010410 layer Substances 0.000 description 59
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 34
- 238000012360 testing method Methods 0.000 description 30
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 20
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 17
- 239000007787 solid Substances 0.000 description 14
- 238000004458 analytical method Methods 0.000 description 13
- 238000006243 chemical reaction Methods 0.000 description 13
- 229910052757 nitrogen Inorganic materials 0.000 description 13
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- 238000001816 cooling Methods 0.000 description 12
- 239000000706 filtrate Substances 0.000 description 12
- 238000004128 high performance liquid chromatography Methods 0.000 description 12
- 229910002027 silica gel Inorganic materials 0.000 description 12
- 239000000741 silica gel Substances 0.000 description 12
- 229960001866 silicon dioxide Drugs 0.000 description 12
- 239000012046 mixed solvent Substances 0.000 description 11
- 238000010992 reflux Methods 0.000 description 11
- 239000000126 substance Substances 0.000 description 11
- 238000001953 recrystallisation Methods 0.000 description 8
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 7
- 230000005540 biological transmission Effects 0.000 description 6
- 238000002347 injection Methods 0.000 description 6
- 239000007924 injection Substances 0.000 description 6
- MFRIHAYPQRLWNB-UHFFFAOYSA-N sodium tert-butoxide Chemical compound [Na+].CC(C)(C)[O-] MFRIHAYPQRLWNB-UHFFFAOYSA-N 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229910052763 palladium Inorganic materials 0.000 description 5
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 4
- 230000008025 crystallization Effects 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- SYXYWTXQFUUWLP-UHFFFAOYSA-N sodium;butan-1-olate Chemical compound [Na+].CCCC[O-] SYXYWTXQFUUWLP-UHFFFAOYSA-N 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 0 C*C1*C(C2)C2C(CC2CC2)C1 Chemical compound C*C1*C(C2)C2C(CC2CC2)C1 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 150000003851 azoles Chemical class 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 239000007772 electrode material Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 238000001704 evaporation Methods 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000001771 vacuum deposition Methods 0.000 description 3
- GLGNXYJARSMNGJ-VKTIVEEGSA-N (1s,2s,3r,4r)-3-[[5-chloro-2-[(1-ethyl-6-methoxy-2-oxo-4,5-dihydro-3h-1-benzazepin-7-yl)amino]pyrimidin-4-yl]amino]bicyclo[2.2.1]hept-5-ene-2-carboxamide Chemical compound CCN1C(=O)CCCC2=C(OC)C(NC=3N=C(C(=CN=3)Cl)N[C@H]3[C@H]([C@@]4([H])C[C@@]3(C=C4)[H])C(N)=O)=CC=C21 GLGNXYJARSMNGJ-VKTIVEEGSA-N 0.000 description 2
- BKQXUNGELBDWLS-UHFFFAOYSA-N 9,9-diphenylfluorene Chemical compound C1=CC=CC=C1C1(C=2C=CC=CC=2)C2=CC=CC=C2C2=CC=CC=C21 BKQXUNGELBDWLS-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 229940125758 compound 15 Drugs 0.000 description 2
- 229940125782 compound 2 Drugs 0.000 description 2
- 125000004122 cyclic group Chemical group 0.000 description 2
- 230000003111 delayed effect Effects 0.000 description 2
- 230000005611 electricity Effects 0.000 description 2
- 230000005284 excitation Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical compound OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 230000027756 respiratory electron transport chain Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- TVIVIEFSHFOWTE-UHFFFAOYSA-K tri(quinolin-8-yloxy)alumane Chemical compound [Al+3].C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1.C1=CN=C2C([O-])=CC=CC2=C1 TVIVIEFSHFOWTE-UHFFFAOYSA-K 0.000 description 2
- 238000007738 vacuum evaporation Methods 0.000 description 2
- STBLNCCBQMHSRC-BATDWUPUSA-N (2s)-n-[(3s,4s)-5-acetyl-7-cyano-4-methyl-1-[(2-methylnaphthalen-1-yl)methyl]-2-oxo-3,4-dihydro-1,5-benzodiazepin-3-yl]-2-(methylamino)propanamide Chemical compound O=C1[C@@H](NC(=O)[C@H](C)NC)[C@H](C)N(C(C)=O)C2=CC(C#N)=CC=C2N1CC1=C(C)C=CC2=CC=CC=C12 STBLNCCBQMHSRC-BATDWUPUSA-N 0.000 description 1
- OOKAZRDERJMRCJ-KOUAFAAESA-N (3r)-7-[(1s,2s,4ar,6s,8s)-2,6-dimethyl-8-[(2s)-2-methylbutanoyl]oxy-1,2,4a,5,6,7,8,8a-octahydronaphthalen-1-yl]-3-hydroxy-5-oxoheptanoic acid Chemical compound C1=C[C@H](C)[C@H](CCC(=O)C[C@@H](O)CC(O)=O)C2[C@@H](OC(=O)[C@@H](C)CC)C[C@@H](C)C[C@@H]21 OOKAZRDERJMRCJ-KOUAFAAESA-N 0.000 description 1
- KQZLRWGGWXJPOS-NLFPWZOASA-N 1-[(1R)-1-(2,4-dichlorophenyl)ethyl]-6-[(4S,5R)-4-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-5-methylcyclohexen-1-yl]pyrazolo[3,4-b]pyrazine-3-carbonitrile Chemical compound ClC1=C(C=CC(=C1)Cl)[C@@H](C)N1N=C(C=2C1=NC(=CN=2)C1=CC[C@@H]([C@@H](C1)C)N1[C@@H](CCC1)CO)C#N KQZLRWGGWXJPOS-NLFPWZOASA-N 0.000 description 1
- PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 description 1
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 1
- QGHDLJAZIIFENW-UHFFFAOYSA-N 4-[1,1,1,3,3,3-hexafluoro-2-(4-hydroxy-3-prop-2-enylphenyl)propan-2-yl]-2-prop-2-enylphenol Chemical group C1=C(CC=C)C(O)=CC=C1C(C(F)(F)F)(C(F)(F)F)C1=CC=C(O)C(CC=C)=C1 QGHDLJAZIIFENW-UHFFFAOYSA-N 0.000 description 1
- WYFCZWSWFGJODV-MIANJLSGSA-N 4-[[(1s)-2-[(e)-3-[3-chloro-2-fluoro-6-(tetrazol-1-yl)phenyl]prop-2-enoyl]-5-(4-methyl-2-oxopiperazin-1-yl)-3,4-dihydro-1h-isoquinoline-1-carbonyl]amino]benzoic acid Chemical compound O=C1CN(C)CCN1C1=CC=CC2=C1CCN(C(=O)\C=C\C=1C(=CC=C(Cl)C=1F)N1N=NN=C1)[C@@H]2C(=O)NC1=CC=C(C(O)=O)C=C1 WYFCZWSWFGJODV-MIANJLSGSA-N 0.000 description 1
- AWXGSYPUMWKTBR-UHFFFAOYSA-N 4-carbazol-9-yl-n,n-bis(4-carbazol-9-ylphenyl)aniline Chemical compound C12=CC=CC=C2C2=CC=CC=C2N1C1=CC=C(N(C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=2C=CC(=CC=2)N2C3=CC=CC=C3C3=CC=CC=C32)C=C1 AWXGSYPUMWKTBR-UHFFFAOYSA-N 0.000 description 1
- UIRBZUWMKAUCQT-UHFFFAOYSA-N C1C=CC=C2Oc(cccc3)c3NC12 Chemical compound C1C=CC=C2Oc(cccc3)c3NC12 UIRBZUWMKAUCQT-UHFFFAOYSA-N 0.000 description 1
- ZNKKYYNWFKHNHZ-UHFFFAOYSA-N CC1C=CC=CC1 Chemical compound CC1C=CC=CC1 ZNKKYYNWFKHNHZ-UHFFFAOYSA-N 0.000 description 1
- 101000837344 Homo sapiens T-cell leukemia translocation-altered gene protein Proteins 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 102100028692 T-cell leukemia translocation-altered gene protein Human genes 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- SPXSEZMVRJLHQG-XMMPIXPASA-N [(2R)-1-[[4-[(3-phenylmethoxyphenoxy)methyl]phenyl]methyl]pyrrolidin-2-yl]methanol Chemical compound C(C1=CC=CC=C1)OC=1C=C(OCC2=CC=C(CN3[C@H](CCC3)CO)C=C2)C=CC=1 SPXSEZMVRJLHQG-XMMPIXPASA-N 0.000 description 1
- IOSLINNLJFQMFF-XMMPIXPASA-N [(2R)-1-[[4-[[3-[(4-fluorophenyl)methylsulfanyl]phenoxy]methyl]phenyl]methyl]pyrrolidin-2-yl]methanol Chemical compound FC1=CC=C(CSC=2C=C(OCC3=CC=C(CN4[C@H](CCC4)CO)C=C3)C=CC=2)C=C1 IOSLINNLJFQMFF-XMMPIXPASA-N 0.000 description 1
- LNUFLCYMSVYYNW-ZPJMAFJPSA-N [(2r,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[(2r,3r,4s,5r,6r)-6-[[(3s,5s,8r,9s,10s,13r,14s,17r)-10,13-dimethyl-17-[(2r)-6-methylheptan-2-yl]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1h-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-disulfo Chemical compound O([C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1[C@@H](COS(O)(=O)=O)O[C@H]([C@@H]([C@H]1OS(O)(=O)=O)OS(O)(=O)=O)O[C@@H]1C[C@@H]2CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)[C@H]1O[C@H](COS(O)(=O)=O)[C@@H](OS(O)(=O)=O)[C@H](OS(O)(=O)=O)[C@H]1OS(O)(=O)=O LNUFLCYMSVYYNW-ZPJMAFJPSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000004913 activation Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N c1ccccc1 Chemical compound c1ccccc1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 1
- 229940125773 compound 10 Drugs 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 229940125877 compound 31 Drugs 0.000 description 1
- 229940125878 compound 36 Drugs 0.000 description 1
- 229940127271 compound 49 Drugs 0.000 description 1
- 229940125900 compound 59 Drugs 0.000 description 1
- 238000002484 cyclic voltammetry Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000011982 device technology Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 150000004826 dibenzofurans Chemical class 0.000 description 1
- DKHNGUNXLDCATP-UHFFFAOYSA-N dipyrazino[2,3-f:2',3'-h]quinoxaline-2,3,6,7,10,11-hexacarbonitrile Chemical compound C12=NC(C#N)=C(C#N)N=C2C2=NC(C#N)=C(C#N)N=C2C2=C1N=C(C#N)C(C#N)=N2 DKHNGUNXLDCATP-UHFFFAOYSA-N 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000004770 highest occupied molecular orbital Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- ZLVXBBHTMQJRSX-VMGNSXQWSA-N jdtic Chemical compound C1([C@]2(C)CCN(C[C@@H]2C)C[C@H](C(C)C)NC(=O)[C@@H]2NCC3=CC(O)=CC=C3C2)=CC=CC(O)=C1 ZLVXBBHTMQJRSX-VMGNSXQWSA-N 0.000 description 1
- 239000004973 liquid crystal related substance Substances 0.000 description 1
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 1
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010970 precious metal Substances 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 150000003512 tertiary amines Chemical group 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000012780 transparent material Substances 0.000 description 1
- ODHXBMXNKOYIBV-UHFFFAOYSA-N triphenylamine Chemical compound C1=CC=CC=C1N(C=1C=CC=CC=1)C1=CC=CC=C1 ODHXBMXNKOYIBV-UHFFFAOYSA-N 0.000 description 1
- 238000004017 vitrification Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 230000004580 weight loss 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
-
- 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
-
- 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/322—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising boron
-
- 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
-
- 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
-
- 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
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the nitrogen atom
-
- 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
-
- 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
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
-
- 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
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
-
- 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
- C09K2211/1011—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
- C09K2211/1022—Heterocyclic 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
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
- C09K2211/1033—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with oxygen
-
- 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
- C09K2211/1037—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with sulfur
-
- 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
- C09K2211/104—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom with other 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
-
- 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
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only 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
- C09K2211/1092—Heterocyclic compounds characterised by ligands containing sulfur as the only 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
- C09K2211/1096—Heterocyclic compounds characterised by ligands containing other 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
- C09K2211/18—Metal complexes
- C09K2211/188—Metal complexes of other metals not provided for in one of the previous groups
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
Description
Claims (8)
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201810513455.1A CN108530475A (zh) | 2016-07-29 | 2016-07-29 | 一种高色纯度含硼有机电致发光化合物及其应用 |
CN201610614309.9A CN106467553B (zh) | 2016-07-29 | 2016-07-29 | 一种含硼有机电致发光化合物及其在oled器件上的应用 |
CN201810513502.2A CN108640940A (zh) | 2016-07-29 | 2016-07-29 | 一种稳定型含硼有机电致发光化合物及其应用 |
CN201810513476.3A CN108409769A (zh) | 2016-07-29 | 2016-07-29 | 一种发光效率高的含硼有机电致发光化合物及其应用 |
CN201810560525.9A CN108610357A (zh) | 2016-07-29 | 2016-07-29 | 一种高效率含硼有机电致发光化合物及其应用 |
CN201810513454.7A CN108586507B (zh) | 2016-07-29 | 2016-07-29 | 一种长寿命含硼有机电致发光化合物及其应用 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201610614309.9A CN106467553B (zh) | 2016-07-29 | 2016-07-29 | 一种含硼有机电致发光化合物及其在oled器件上的应用 |
Related Child Applications (5)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810513502.2A Division CN108640940A (zh) | 2016-07-29 | 2016-07-29 | 一种稳定型含硼有机电致发光化合物及其应用 |
CN201810560525.9A Division CN108610357A (zh) | 2016-07-29 | 2016-07-29 | 一种高效率含硼有机电致发光化合物及其应用 |
CN201810513455.1A Division CN108530475A (zh) | 2016-07-29 | 2016-07-29 | 一种高色纯度含硼有机电致发光化合物及其应用 |
CN201810513476.3A Division CN108409769A (zh) | 2016-07-29 | 2016-07-29 | 一种发光效率高的含硼有机电致发光化合物及其应用 |
CN201810513454.7A Division CN108586507B (zh) | 2016-07-29 | 2016-07-29 | 一种长寿命含硼有机电致发光化合物及其应用 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN106467553A true CN106467553A (zh) | 2017-03-01 |
CN106467553B CN106467553B (zh) | 2019-08-23 |
Family
ID=58229899
Family Applications (6)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810560525.9A Pending CN108610357A (zh) | 2016-07-29 | 2016-07-29 | 一种高效率含硼有机电致发光化合物及其应用 |
CN201810513502.2A Pending CN108640940A (zh) | 2016-07-29 | 2016-07-29 | 一种稳定型含硼有机电致发光化合物及其应用 |
CN201810513476.3A Pending CN108409769A (zh) | 2016-07-29 | 2016-07-29 | 一种发光效率高的含硼有机电致发光化合物及其应用 |
CN201610614309.9A Active CN106467553B (zh) | 2016-07-29 | 2016-07-29 | 一种含硼有机电致发光化合物及其在oled器件上的应用 |
CN201810513454.7A Active CN108586507B (zh) | 2016-07-29 | 2016-07-29 | 一种长寿命含硼有机电致发光化合物及其应用 |
CN201810513455.1A Withdrawn CN108530475A (zh) | 2016-07-29 | 2016-07-29 | 一种高色纯度含硼有机电致发光化合物及其应用 |
Family Applications Before (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810560525.9A Pending CN108610357A (zh) | 2016-07-29 | 2016-07-29 | 一种高效率含硼有机电致发光化合物及其应用 |
CN201810513502.2A Pending CN108640940A (zh) | 2016-07-29 | 2016-07-29 | 一种稳定型含硼有机电致发光化合物及其应用 |
CN201810513476.3A Pending CN108409769A (zh) | 2016-07-29 | 2016-07-29 | 一种发光效率高的含硼有机电致发光化合物及其应用 |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201810513454.7A Active CN108586507B (zh) | 2016-07-29 | 2016-07-29 | 一种长寿命含硼有机电致发光化合物及其应用 |
CN201810513455.1A Withdrawn CN108530475A (zh) | 2016-07-29 | 2016-07-29 | 一种高色纯度含硼有机电致发光化合物及其应用 |
Country Status (1)
Country | Link |
---|---|
CN (6) | CN108610357A (zh) |
Cited By (52)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN107417715A (zh) * | 2017-07-14 | 2017-12-01 | 瑞声科技(南京)有限公司 | 一种有机电致发光材料及其发光器件 |
CN107507921A (zh) * | 2017-09-29 | 2017-12-22 | 江苏三月光电科技有限公司 | 一种含硼有机电致发光器件及其制备方法 |
CN107602601A (zh) * | 2017-09-29 | 2018-01-19 | 江苏三月光电科技有限公司 | 一种含硼多元杂环有机化合物及其在有机电致发光器件中的应用 |
CN107793441A (zh) * | 2016-09-07 | 2018-03-13 | 学校法人关西学院 | 多环芳香族化合物 |
KR20180112721A (ko) * | 2017-04-03 | 2018-10-12 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR20180112722A (ko) * | 2017-04-03 | 2018-10-12 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR20180120619A (ko) * | 2017-04-27 | 2018-11-06 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
WO2018212169A1 (ja) * | 2017-05-16 | 2018-11-22 | 学校法人関西学院 | 多環芳香族化合物 |
WO2019009687A1 (ko) * | 2017-07-07 | 2019-01-10 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기 발광 소자 |
KR20190037174A (ko) * | 2017-09-28 | 2019-04-05 | 주식회사 엘지화학 | 다환 화합물 및 이를 포함하는 유기 발광 소자 |
CN110511223A (zh) * | 2019-08-13 | 2019-11-29 | 武汉华星光电半导体显示技术有限公司 | 空穴传输材料及其制备方法、有机电致发光器件 |
CN110600634A (zh) * | 2018-06-12 | 2019-12-20 | 三星显示有限公司 | 缩合环化合物和包括其的有机发光器件 |
CN110590790A (zh) * | 2019-08-29 | 2019-12-20 | 武汉华星光电半导体显示技术有限公司 | 一种基于螺并三苯胺的空穴传输材料及其制备方法及有机电致发光器件 |
CN110669059A (zh) * | 2019-09-04 | 2020-01-10 | 武汉华星光电半导体显示技术有限公司 | 空穴传输材料及其制备方法、有机发光器件 |
WO2020017931A1 (ko) * | 2018-07-19 | 2020-01-23 | 주식회사 엘지화학 | 다환 화합물 및 이를 포함하는 유기 발광 소자 |
JP6641069B1 (ja) * | 2019-03-29 | 2020-02-05 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
CN110799571A (zh) * | 2017-06-30 | 2020-02-14 | 住友化学株式会社 | 高分子化合物及使用其的发光元件 |
CN110838549A (zh) * | 2018-08-15 | 2020-02-25 | 江苏三月光电科技有限公司 | 一种基于激基复合物和激基缔合物体系的有机电致发光器件 |
KR20200020637A (ko) * | 2018-08-16 | 2020-02-26 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR20200032658A (ko) * | 2018-09-18 | 2020-03-26 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
WO2020101001A1 (ja) * | 2018-11-15 | 2020-05-22 | 学校法人関西学院 | 有機電界発光素子、表示装置、および照明装置 |
WO2020135687A1 (zh) * | 2018-12-29 | 2020-07-02 | 江苏三月光电科技有限公司 | 一种含硼化合物及其制备方法和其应用 |
WO2020149716A1 (ko) * | 2019-01-18 | 2020-07-23 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR20200100008A (ko) * | 2019-02-15 | 2020-08-25 | 주식회사 엘지화학 | 유기 발광 소자 |
JP2020167377A (ja) * | 2019-12-26 | 2020-10-08 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
JP2020167389A (ja) * | 2019-03-29 | 2020-10-08 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
CN112010883A (zh) * | 2019-05-29 | 2020-12-01 | 学校法人关西学院 | 多环芳香族化合物、有机器件用材料、有机电场发光元件、显示装置及照明装置 |
CN112110943A (zh) * | 2019-06-21 | 2020-12-22 | 南京高光半导体材料有限公司 | 一种长寿命深蓝色荧光掺杂材料及oled有机电致发光器件 |
US20200411771A1 (en) * | 2018-06-11 | 2020-12-31 | Lg Chem, Ltd. | Organic light-emitting device |
CN112585145A (zh) * | 2018-09-04 | 2021-03-30 | 株式会社Lg化学 | 多环化合物和包含其的有机发光器件 |
JP2021073192A (ja) * | 2016-03-23 | 2021-05-13 | コニカミノルタ株式会社 | π共役系ホウ素化合物及び電子デバイス |
WO2021107681A1 (ko) * | 2019-11-29 | 2021-06-03 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
WO2021107680A1 (ko) * | 2019-11-29 | 2021-06-03 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
CN112920211A (zh) * | 2021-02-02 | 2021-06-08 | 吉林奥来德光电材料股份有限公司 | 含硼多环芳族化合物、其制备方法及有机电致发光器件 |
CN113072925A (zh) * | 2020-01-03 | 2021-07-06 | 罗门哈斯电子材料韩国有限公司 | 多种有机电致发光材料和包含其的有机电致发光装置 |
WO2021135750A1 (zh) * | 2019-12-31 | 2021-07-08 | 陕西莱特光电材料股份有限公司 | 一种有机化合物、其应用以及有机电致发光器件 |
CN113292584A (zh) * | 2021-05-31 | 2021-08-24 | 上海天马有机发光显示技术有限公司 | 一种含硼和氮的有机化合物及其电致发光的应用 |
CN113348171A (zh) * | 2019-11-29 | 2021-09-03 | 株式会社Lg化学 | 化合物和包含其的有机发光元件 |
US20210292342A1 (en) * | 2016-10-18 | 2021-09-23 | Konica Minolta, Inc. | Organic borane complex, composition containing organic borane, and organic electroluminescent element |
JP2021163871A (ja) * | 2020-03-31 | 2021-10-11 | 住友化学株式会社 | 発光素子及び組成物 |
KR20220000832A (ko) * | 2020-06-26 | 2022-01-04 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
US11239430B2 (en) | 2018-01-05 | 2022-02-01 | Beijing Summer Sprout Technology Co., Ltd. | Boron and nitrogen containing heterocyclic compounds |
CN114075228A (zh) * | 2020-08-20 | 2022-02-22 | 江苏三月科技股份有限公司 | 一种含硼有机化合物及其应用 |
EP4023652A1 (en) * | 2020-12-29 | 2022-07-06 | LG Display Co., Ltd. | Organic light emitting diode and organic light emitting device including the same |
US11393985B2 (en) | 2018-07-11 | 2022-07-19 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
CN115093417A (zh) * | 2022-06-16 | 2022-09-23 | 京东方科技集团股份有限公司 | 发光分子、发光器件及其制备方法、显示装置 |
US11502259B2 (en) | 2019-03-05 | 2022-11-15 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
CN115417888A (zh) * | 2022-05-17 | 2022-12-02 | 苏州大学 | 一种含硼氮的红色热激活延迟荧光材料及其合成方法 |
US11825733B2 (en) | 2019-01-11 | 2023-11-21 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
US11919914B2 (en) | 2019-10-25 | 2024-03-05 | Universal Display Corporation | Organic electroluminescent materials and devices |
JP7456757B2 (ja) | 2018-12-05 | 2024-03-27 | 三星ディスプレイ株式會社 | 有機電界発光素子及び有機電界発光素子用多環化合物 |
US11950492B2 (en) | 2019-01-29 | 2024-04-02 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN108774258B (zh) * | 2018-09-10 | 2021-04-09 | 陕西蒲城海泰新材料产业有限责任公司 | 一种含硼杂环化合物及其在有机光电器件中的应用 |
JP2022509303A (ja) * | 2018-11-29 | 2022-01-20 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 電子素子 |
TW202200529A (zh) | 2020-03-13 | 2022-01-01 | 德商麥克專利有限公司 | 有機電致發光裝置 |
CN113594375B (zh) * | 2020-04-30 | 2023-12-01 | 江苏三月科技股份有限公司 | 一种绿光有机电致发光器件 |
KR20230043106A (ko) | 2020-07-22 | 2023-03-30 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
WO2022017998A1 (en) | 2020-07-22 | 2022-01-27 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
TW202237797A (zh) | 2020-11-30 | 2022-10-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
CN117084000A (zh) | 2021-04-09 | 2023-11-17 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
EP4320649A1 (en) | 2021-04-09 | 2024-02-14 | Merck Patent GmbH | Materials for organic electroluminescent devices |
TW202309243A (zh) | 2021-04-09 | 2023-03-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
EP4079742A1 (de) | 2021-04-14 | 2022-10-26 | Merck Patent GmbH | Metallkomplexe |
CN113336782B (zh) * | 2021-06-22 | 2022-10-14 | 吉林大学 | 含咔唑骨架的绿光窄光谱三配位硼发光化合物、制备方法及其应用 |
DE112022003409A5 (de) | 2021-07-06 | 2024-05-23 | MERCK Patent Gesellschaft mit beschränkter Haftung | Materialien für organische elektrolumineszenzvorrichtungen |
CN117917983A (zh) | 2021-09-13 | 2024-04-23 | 默克专利有限公司 | 有机电致发光器件的材料 |
WO2023208899A1 (en) | 2022-04-28 | 2023-11-02 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
WO2024033282A1 (en) | 2022-08-09 | 2024-02-15 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090295275A1 (en) * | 2005-09-12 | 2009-12-03 | Merck Patent Gmbh | Compounds for organic electronic devices |
CN103502252A (zh) * | 2011-03-03 | 2014-01-08 | 国立大学法人九州大学 | 新型化合物、电荷输送材料和有机器件 |
CN105431439A (zh) * | 2014-02-18 | 2016-03-23 | 学校法人关西学院 | 多环芳香族化合物 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5959171B2 (ja) * | 2011-09-08 | 2016-08-02 | 国立大学法人名古屋大学 | π共役有機ホウ素化合物及びその製造方法 |
JP6729589B2 (ja) * | 2015-07-24 | 2020-07-22 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
KR102237305B1 (ko) * | 2016-05-13 | 2021-04-06 | 코니카 미놀타 가부시키가이샤 | 유기 일렉트로루미네센스 소자용 재료, 유기 일렉트로루미네센스 소자, 표시 장치 및 조명 장치 |
-
2016
- 2016-07-29 CN CN201810560525.9A patent/CN108610357A/zh active Pending
- 2016-07-29 CN CN201810513502.2A patent/CN108640940A/zh active Pending
- 2016-07-29 CN CN201810513476.3A patent/CN108409769A/zh active Pending
- 2016-07-29 CN CN201610614309.9A patent/CN106467553B/zh active Active
- 2016-07-29 CN CN201810513454.7A patent/CN108586507B/zh active Active
- 2016-07-29 CN CN201810513455.1A patent/CN108530475A/zh not_active Withdrawn
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090295275A1 (en) * | 2005-09-12 | 2009-12-03 | Merck Patent Gmbh | Compounds for organic electronic devices |
CN103502252A (zh) * | 2011-03-03 | 2014-01-08 | 国立大学法人九州大学 | 新型化合物、电荷输送材料和有机器件 |
CN105431439A (zh) * | 2014-02-18 | 2016-03-23 | 学校法人关西学院 | 多环芳香族化合物 |
Non-Patent Citations (2)
Title |
---|
KINOSHITA K ET AL.: "Synthesis and physical properties of BN-embedded Triangulene", 《5TH JACI/GSC SYMPOSIUM JAPAN ASSOCIATION FOR CHMICAL INNOVATION》 * |
TOMOKATSU KUSHIDA ET AL.: "A Planarized Triphenylborane Mesogen: Discotic Liquid Crystals with Ambipolar Charge-Carrier Transport Properties", 《ANGEW. CHEM. INT. ED.》 * |
Cited By (104)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2021073192A (ja) * | 2016-03-23 | 2021-05-13 | コニカミノルタ株式会社 | π共役系ホウ素化合物及び電子デバイス |
US11476427B2 (en) * | 2016-03-23 | 2022-10-18 | Konica Minolta, Inc. | π-conjugated boron compound, electronic device, and methods respectively for producing triarylborane and intermediate thereof |
JP2018043984A (ja) * | 2016-09-07 | 2018-03-22 | 学校法人関西学院 | 多環芳香族化合物 |
US11653565B2 (en) | 2016-09-07 | 2023-05-16 | Kwansei Gakuin Educational Foundation | Polycyclic aromatic compound |
CN107793441A (zh) * | 2016-09-07 | 2018-03-13 | 学校法人关西学院 | 多环芳香族化合物 |
JP7190720B2 (ja) | 2016-09-07 | 2022-12-16 | 学校法人関西学院 | 多環芳香族化合物 |
JP7038371B2 (ja) | 2016-09-07 | 2022-03-18 | 学校法人関西学院 | 多環芳香族化合物 |
JP2022033287A (ja) * | 2016-09-07 | 2022-02-28 | 学校法人関西学院 | 多環芳香族化合物 |
US20210292342A1 (en) * | 2016-10-18 | 2021-09-23 | Konica Minolta, Inc. | Organic borane complex, composition containing organic borane, and organic electroluminescent element |
US11708383B2 (en) * | 2016-10-18 | 2023-07-25 | Konica Minolta, Inc. | Organic borane complex, composition containing organic borane, and organic electroluminescent element |
KR20180112722A (ko) * | 2017-04-03 | 2018-10-12 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR20180112721A (ko) * | 2017-04-03 | 2018-10-12 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR102099002B1 (ko) * | 2017-04-03 | 2020-04-08 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR102097862B1 (ko) * | 2017-04-03 | 2020-04-07 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR20180120619A (ko) * | 2017-04-27 | 2018-11-06 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR102088096B1 (ko) * | 2017-04-27 | 2020-03-11 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
JPWO2018212169A1 (ja) * | 2017-05-16 | 2020-03-19 | 学校法人関西学院 | 多環芳香族化合物 |
JP7202572B2 (ja) | 2017-05-16 | 2023-01-12 | 学校法人関西学院 | 多環芳香族化合物 |
WO2018212169A1 (ja) * | 2017-05-16 | 2018-11-22 | 学校法人関西学院 | 多環芳香族化合物 |
US11021568B2 (en) | 2017-06-30 | 2021-06-01 | Sumitomo Chemical Company, Limited | Polymer compound and light emitting device using the same |
CN110799571A (zh) * | 2017-06-30 | 2020-02-14 | 住友化学株式会社 | 高分子化合物及使用其的发光元件 |
EP3647338A4 (en) * | 2017-06-30 | 2021-03-24 | Sumitomo Chemical Company Limited | MACROMOLECULAR COMPOUND AND LIGHT EMITTING ELEMENT WITH USE THEREOF |
CN110799571B (zh) * | 2017-06-30 | 2022-09-20 | 住友化学株式会社 | 高分子化合物及使用其的发光元件 |
CN110573516B (zh) * | 2017-07-07 | 2023-07-28 | 株式会社Lg化学 | 化合物及包含其的有机发光器件 |
CN115850310A (zh) * | 2017-07-07 | 2023-03-28 | 株式会社Lg化学 | 新型化合物及包含其的有机发光器件 |
WO2019009687A1 (ko) * | 2017-07-07 | 2019-01-10 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기 발광 소자 |
CN110573516A (zh) * | 2017-07-07 | 2019-12-13 | 株式会社Lg化学 | 新型化合物及包含其的有机发光器件 |
CN107417715A (zh) * | 2017-07-14 | 2017-12-01 | 瑞声科技(南京)有限公司 | 一种有机电致发光材料及其发光器件 |
KR20190037174A (ko) * | 2017-09-28 | 2019-04-05 | 주식회사 엘지화학 | 다환 화합물 및 이를 포함하는 유기 발광 소자 |
KR102117765B1 (ko) | 2017-09-28 | 2020-06-02 | 주식회사 엘지화학 | 다환 화합물 및 이를 포함하는 유기 발광 소자 |
WO2019062685A1 (zh) * | 2017-09-29 | 2019-04-04 | 江苏三月光电科技有限公司 | 一种含硼有机电致发光器件及其制备方法 |
CN107507921B (zh) * | 2017-09-29 | 2019-05-14 | 江苏三月光电科技有限公司 | 一种含硼有机电致发光器件及其制备方法 |
US11778894B2 (en) | 2017-09-29 | 2023-10-03 | Jiangsu Sunera Technology Co., Ltd. | Boron-containing organic light-emitting diode device and preparation method thereof |
CN107507921A (zh) * | 2017-09-29 | 2017-12-22 | 江苏三月光电科技有限公司 | 一种含硼有机电致发光器件及其制备方法 |
CN107602601A (zh) * | 2017-09-29 | 2018-01-19 | 江苏三月光电科技有限公司 | 一种含硼多元杂环有机化合物及其在有机电致发光器件中的应用 |
US11329237B2 (en) | 2018-01-05 | 2022-05-10 | Beijing Summer Sprout Technology Co., Ltd. | Boron and nitrogen containing heterocyclic compounds |
US11239430B2 (en) | 2018-01-05 | 2022-02-01 | Beijing Summer Sprout Technology Co., Ltd. | Boron and nitrogen containing heterocyclic compounds |
US20200411771A1 (en) * | 2018-06-11 | 2020-12-31 | Lg Chem, Ltd. | Organic light-emitting device |
CN110600634A (zh) * | 2018-06-12 | 2019-12-20 | 三星显示有限公司 | 缩合环化合物和包括其的有机发光器件 |
US11299502B2 (en) * | 2018-06-12 | 2022-04-12 | Samsung Display Co., Ltd. | Condensed cyclic compound and organic light-emitting device including condensed cyclic compound |
US11393985B2 (en) | 2018-07-11 | 2022-07-19 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
CN111372938A (zh) * | 2018-07-19 | 2020-07-03 | 株式会社Lg化学 | 多环化合物及包含其的有机发光器件 |
CN111372938B (zh) * | 2018-07-19 | 2023-08-08 | 株式会社Lg化学 | 多环化合物及包含其的有机发光器件 |
WO2020017931A1 (ko) * | 2018-07-19 | 2020-01-23 | 주식회사 엘지화학 | 다환 화합물 및 이를 포함하는 유기 발광 소자 |
CN110838549A (zh) * | 2018-08-15 | 2020-02-25 | 江苏三月光电科技有限公司 | 一种基于激基复合物和激基缔合物体系的有机电致发光器件 |
CN110838549B (zh) * | 2018-08-15 | 2020-09-18 | 江苏三月科技股份有限公司 | 一种基于激基复合物和激基缔合物体系的有机电致发光器件 |
KR20200020637A (ko) * | 2018-08-16 | 2020-02-26 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR102262698B1 (ko) | 2018-08-16 | 2021-06-09 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
CN112585145A (zh) * | 2018-09-04 | 2021-03-30 | 株式会社Lg化学 | 多环化合物和包含其的有机发光器件 |
US11845768B2 (en) | 2018-09-04 | 2023-12-19 | Lg Chem, Ltd. | Polycyclic compound and organic light-emitting device including same |
CN112585145B (zh) * | 2018-09-04 | 2023-09-29 | 株式会社Lg化学 | 多环化合物和包含其的有机发光器件 |
KR102268235B1 (ko) | 2018-09-18 | 2021-06-23 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
KR20200032658A (ko) * | 2018-09-18 | 2020-03-26 | 주식회사 엘지화학 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
WO2020101001A1 (ja) * | 2018-11-15 | 2020-05-22 | 学校法人関西学院 | 有機電界発光素子、表示装置、および照明装置 |
JP7456757B2 (ja) | 2018-12-05 | 2024-03-27 | 三星ディスプレイ株式會社 | 有機電界発光素子及び有機電界発光素子用多環化合物 |
WO2020135687A1 (zh) * | 2018-12-29 | 2020-07-02 | 江苏三月光电科技有限公司 | 一种含硼化合物及其制备方法和其应用 |
US11825733B2 (en) | 2019-01-11 | 2023-11-21 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
CN112888695B (zh) * | 2019-01-18 | 2023-12-22 | 株式会社Lg化学 | 化合物及包含其的有机发光二极管 |
CN112888695A (zh) * | 2019-01-18 | 2021-06-01 | 株式会社Lg化学 | 化合物及包含其的有机发光二极管 |
WO2020149716A1 (ko) * | 2019-01-18 | 2020-07-23 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
US11950492B2 (en) | 2019-01-29 | 2024-04-02 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
KR102324962B1 (ko) * | 2019-02-15 | 2021-11-11 | 주식회사 엘지화학 | 유기 발광 소자 |
KR20200100008A (ko) * | 2019-02-15 | 2020-08-25 | 주식회사 엘지화학 | 유기 발광 소자 |
US11502259B2 (en) | 2019-03-05 | 2022-11-15 | Samsung Display Co., Ltd. | Organic electroluminescence device and polycyclic compound for organic electroluminescence device |
JP6641069B1 (ja) * | 2019-03-29 | 2020-02-05 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
KR20210146961A (ko) * | 2019-03-29 | 2021-12-06 | 스미또모 가가꾸 가부시키가이샤 | 발광 소자 및 그의 제조 방법 그리고 발광 소자용 조성물 및 그의 제조 방법 |
CN113646914A (zh) * | 2019-03-29 | 2021-11-12 | 住友化学株式会社 | 发光元件及其制造方法以及发光元件用组合物及其制造方法 |
WO2020202279A1 (ja) * | 2019-03-29 | 2020-10-08 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
KR102407971B1 (ko) | 2019-03-29 | 2022-06-13 | 스미또모 가가꾸 가부시키가이샤 | 발광 소자 및 그의 제조 방법 그리고 발광 소자용 조성물 및 그의 제조 방법 |
CN113646914B (zh) * | 2019-03-29 | 2022-12-02 | 住友化学株式会社 | 发光元件及其制造方法以及发光元件用组合物及其制造方法 |
JP2020167389A (ja) * | 2019-03-29 | 2020-10-08 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
CN112010883A (zh) * | 2019-05-29 | 2020-12-01 | 学校法人关西学院 | 多环芳香族化合物、有机器件用材料、有机电场发光元件、显示装置及照明装置 |
WO2020252867A1 (zh) * | 2019-06-21 | 2020-12-24 | 南京高光半导体材料有限公司 | 一种长寿命深蓝色荧光掺杂材料及oled有机电致发光器件 |
CN112110943A (zh) * | 2019-06-21 | 2020-12-22 | 南京高光半导体材料有限公司 | 一种长寿命深蓝色荧光掺杂材料及oled有机电致发光器件 |
CN110511223A (zh) * | 2019-08-13 | 2019-11-29 | 武汉华星光电半导体显示技术有限公司 | 空穴传输材料及其制备方法、有机电致发光器件 |
CN110511223B (zh) * | 2019-08-13 | 2020-10-13 | 武汉华星光电半导体显示技术有限公司 | 空穴传输材料及其制备方法、有机电致发光器件 |
CN110590790A (zh) * | 2019-08-29 | 2019-12-20 | 武汉华星光电半导体显示技术有限公司 | 一种基于螺并三苯胺的空穴传输材料及其制备方法及有机电致发光器件 |
CN110669059A (zh) * | 2019-09-04 | 2020-01-10 | 武汉华星光电半导体显示技术有限公司 | 空穴传输材料及其制备方法、有机发光器件 |
US11919914B2 (en) | 2019-10-25 | 2024-03-05 | Universal Display Corporation | Organic electroluminescent materials and devices |
JP2022514108A (ja) * | 2019-11-29 | 2022-02-09 | エルジー・ケム・リミテッド | 化合物およびこれを含む有機発光素子 |
WO2021107681A1 (ko) * | 2019-11-29 | 2021-06-03 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
JP7184242B2 (ja) | 2019-11-29 | 2022-12-06 | エルジー・ケム・リミテッド | 化合物およびこれを含む有機発光素子 |
WO2021107680A1 (ko) * | 2019-11-29 | 2021-06-03 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
US11780856B2 (en) | 2019-11-29 | 2023-10-10 | Lg Chem, Ltd. | Compound and organic light-emitting device comprising same |
JP7095212B2 (ja) | 2019-11-29 | 2022-07-05 | エルジー・ケム・リミテッド | 化合物およびこれを含む有機発光素子 |
CN113348171A (zh) * | 2019-11-29 | 2021-09-03 | 株式会社Lg化学 | 化合物和包含其的有机发光元件 |
JP2022512453A (ja) * | 2019-11-29 | 2022-02-03 | エルジー・ケム・リミテッド | 化合物およびこれを含む有機発光素子 |
US11685751B2 (en) | 2019-11-29 | 2023-06-27 | Lg Chem, Ltd. | Compound and organic light-emitting element comprising same |
JP7245770B2 (ja) | 2019-12-26 | 2023-03-24 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
JP2020167377A (ja) * | 2019-12-26 | 2020-10-08 | 住友化学株式会社 | 発光素子及びその製造方法並びに発光素子用組成物及びその製造方法 |
WO2021135750A1 (zh) * | 2019-12-31 | 2021-07-08 | 陕西莱特光电材料股份有限公司 | 一种有机化合物、其应用以及有机电致发光器件 |
CN113072925A (zh) * | 2020-01-03 | 2021-07-06 | 罗门哈斯电子材料韩国有限公司 | 多种有机电致发光材料和包含其的有机电致发光装置 |
JP2021163871A (ja) * | 2020-03-31 | 2021-10-11 | 住友化学株式会社 | 発光素子及び組成物 |
JP7405676B2 (ja) | 2020-03-31 | 2023-12-26 | 住友化学株式会社 | 発光素子及び組成物 |
KR20220000832A (ko) * | 2020-06-26 | 2022-01-04 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
KR102648148B1 (ko) | 2020-06-26 | 2024-03-15 | 주식회사 엘지화학 | 화합물 및 이를 포함하는 유기 발광 소자 |
CN114075228A (zh) * | 2020-08-20 | 2022-02-22 | 江苏三月科技股份有限公司 | 一种含硼有机化合物及其应用 |
EP4023652A1 (en) * | 2020-12-29 | 2022-07-06 | LG Display Co., Ltd. | Organic light emitting diode and organic light emitting device including the same |
CN112920211A (zh) * | 2021-02-02 | 2021-06-08 | 吉林奥来德光电材料股份有限公司 | 含硼多环芳族化合物、其制备方法及有机电致发光器件 |
CN113292584A (zh) * | 2021-05-31 | 2021-08-24 | 上海天马有机发光显示技术有限公司 | 一种含硼和氮的有机化合物及其电致发光的应用 |
WO2023221317A1 (zh) * | 2022-05-17 | 2023-11-23 | 苏州大学 | 一种含硼氮的红色热激活延迟荧光材料及其合成方法 |
CN115417888A (zh) * | 2022-05-17 | 2022-12-02 | 苏州大学 | 一种含硼氮的红色热激活延迟荧光材料及其合成方法 |
CN115093417B (zh) * | 2022-06-16 | 2024-02-27 | 京东方科技集团股份有限公司 | 发光分子、发光器件及其制备方法、显示装置 |
CN115093417A (zh) * | 2022-06-16 | 2022-09-23 | 京东方科技集团股份有限公司 | 发光分子、发光器件及其制备方法、显示装置 |
Also Published As
Publication number | Publication date |
---|---|
CN108586507B (zh) | 2020-11-17 |
CN108640940A (zh) | 2018-10-12 |
CN108586507A (zh) | 2018-09-28 |
CN108610357A (zh) | 2018-10-02 |
CN108530475A (zh) | 2018-09-14 |
CN108409769A (zh) | 2018-08-17 |
CN106467553B (zh) | 2019-08-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106467553B (zh) | 一种含硼有机电致发光化合物及其在oled器件上的应用 | |
CN106467554A (zh) | 一种含硼有机电致发光化合物及其应用 | |
CN106467469A (zh) | 一种有机电致发光化合物及其应用 | |
CN106543205B (zh) | 一种含有苯并咪唑的化合物及其在oled上的应用 | |
CN106467523A (zh) | 一种有机芳香化合物及其应用 | |
CN106279203A (zh) | 一种含酮和氮杂环的化合物及其在有机电致发光器件上的应用 | |
CN106467740B (zh) | 一种有机电致荧光化合物及其在电致发光器件中的应用 | |
CN106220649A (zh) | 一种基于二芳基酮的化合物及其在有机电致发光器件上的应用 | |
CN106467482A (zh) | 一种基于二芳基酮的化合物及其应用 | |
CN106467468A (zh) | 一种具有二苯并庚烯结构的有机化合物及其应用 | |
CN106467544A (zh) | 一种有机荧光化合物及其应用 | |
CN106478611A (zh) | 一种以氧杂蒽为核心的有机化合物及其应用 | |
CN107652272A (zh) | 一种以酮类结构为母核的有机化合物及其在oled器件中的应用 | |
CN106432158A (zh) | 一种有机发光化合物材料及其应用 | |
CN106749050B (zh) | 一种以环状二酮为核心的热激活延迟荧光oled材料及其应用 | |
CN109354588A (zh) | 一种以含氮五元杂环为核心的有机电致发光化合物及其应用 | |
CN109384726A (zh) | 一种有机发光化合物及其制备方法和有机电致发光器件 | |
CN106543071A (zh) | 一种以二苯并庚烯酮为核心的化合物及其在oled上的应用 | |
CN106467510A (zh) | 一种有机电致发光材料及其应用 | |
CN106467524A (zh) | 一种有机芳香化合物及其在有机电致发光器件上的应用 | |
CN106941133B (zh) | 一种有机发光器件及其制备方法 | |
CN109575057A (zh) | 一种含硼六元杂环化合物及其在有机电致发光器件中的应用 | |
CN109575054A (zh) | 一种含硼六元杂环衍生物及其在有机电致发光器件中的应用 | |
CN106467511A (zh) | 一种以吖啶酮为核心的化合物及其在有机电致发光器件上的应用 | |
CN104672244B (zh) | 一种基于咔唑衍生物的化合物 |
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 | ||
TR01 | Transfer of patent right |
Effective date of registration: 20200327 Address after: 264006 No. 11 Wuzhishan Road, Yantai economic and Technological Development Zone, Shandong Patentee after: VALIANT Co.,Ltd. Address before: 214112 No. 210, Xinzhou Road, New District, Jiangsu, Wuxi Patentee before: JIANGSU SUNERA TECHNOLOGY Co.,Ltd. |
|
TR01 | Transfer of patent right | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right | ||
PE01 | Entry into force of the registration of the contract for pledge of patent right |
Denomination of invention: A boron containing organic electroluminescent compound and its application in OLED devices Effective date of registration: 20211202 Granted publication date: 20190823 Pledgee: Yantai Branch of China Merchants Bank Co.,Ltd. Pledgor: VALIANT Co.,Ltd. Registration number: Y2021980013807 |
|
PC01 | Cancellation of the registration of the contract for pledge of patent right | ||
PC01 | Cancellation of the registration of the contract for pledge of patent right |
Date of cancellation: 20220823 Granted publication date: 20190823 Pledgee: Yantai Branch of China Merchants Bank Co.,Ltd. Pledgor: VALIANT Co.,Ltd. Registration number: Y2021980013807 |
|
TR01 | Transfer of patent right | ||
TR01 | Transfer of patent right |
Effective date of registration: 20221101 Address after: 214112 No.210 Xinzhou Road, Wuxi City, Jiangsu Province Patentee after: Jiangsu March Technology Co.,Ltd. Address before: 264006 No. 11 Wuzhishan Road, Yantai economic and Technological Development Zone, Shandong Patentee before: VALIANT Co.,Ltd. |