CN102627671A - 金属络合物 - Google Patents
金属络合物 Download PDFInfo
- Publication number
- CN102627671A CN102627671A CN2012100433282A CN201210043328A CN102627671A CN 102627671 A CN102627671 A CN 102627671A CN 2012100433282 A CN2012100433282 A CN 2012100433282A CN 201210043328 A CN201210043328 A CN 201210043328A CN 102627671 A CN102627671 A CN 102627671A
- Authority
- CN
- China
- Prior art keywords
- general formula
- compound
- situation
- under
- different
- 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
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 8
- 239000002184 metal Substances 0.000 title claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 79
- 229910052799 carbon Inorganic materials 0.000 claims description 21
- 150000001721 carbon Chemical group 0.000 claims description 17
- 239000003446 ligand Substances 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 16
- -1 polycyclic metal halide Chemical class 0.000 claims description 14
- 238000006243 chemical reaction Methods 0.000 claims description 9
- 239000000460 chlorine Substances 0.000 claims description 7
- 125000003118 aryl group Chemical group 0.000 claims description 6
- 229910052731 fluorine Inorganic materials 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 229910052794 bromium Inorganic materials 0.000 claims description 5
- 125000001072 heteroaryl group Chemical group 0.000 claims description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 239000002253 acid Substances 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 3
- 150000004703 alkoxides Chemical class 0.000 claims description 3
- 150000001450 anions Chemical class 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 230000005669 field effect Effects 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 230000010354 integration Effects 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 125000003107 substituted aryl group Chemical group 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- 239000011630 iodine Substances 0.000 claims description 2
- 229910001507 metal halide Inorganic materials 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 239000008204 material by function Substances 0.000 abstract description 2
- 239000000203 mixture Substances 0.000 description 36
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 32
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 24
- 238000005481 NMR spectroscopy Methods 0.000 description 17
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 14
- 230000008021 deposition Effects 0.000 description 14
- 229910052741 iridium Inorganic materials 0.000 description 14
- 229910052757 nitrogen Inorganic materials 0.000 description 14
- 239000007787 solid Substances 0.000 description 14
- 238000005406 washing Methods 0.000 description 14
- 239000000243 solution Substances 0.000 description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
- VHNILDKAFINLSQ-UHFFFAOYSA-N 1-[3-(aminomethyl)-4-(4-methylphenyl)-2-(2-methylpropyl)quinolin-6-yl]piperazine-2,5-dione Chemical compound NCC=1C(CC(C)C)=NC2=CC=C(N3C(CNC(=O)C3)=O)C=C2C=1C1=CC=C(C)C=C1 VHNILDKAFINLSQ-UHFFFAOYSA-N 0.000 description 12
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 11
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical compound [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 238000003756 stirring Methods 0.000 description 10
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 9
- 229910052698 phosphorus Inorganic materials 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 150000004696 coordination complex Chemical class 0.000 description 7
- 230000000875 corresponding effect Effects 0.000 description 7
- 229920000642 polymer Polymers 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 6
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 239000012074 organic phase Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 229920001609 Poly(3,4-ethylenedioxythiophene) Polymers 0.000 description 5
- 240000000203 Salix gracilistyla Species 0.000 description 5
- 150000002220 fluorenes Chemical class 0.000 description 5
- CECAIMUJVYQLKA-UHFFFAOYSA-N iridium 1-phenylisoquinoline Chemical compound [Ir].C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12.C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 CECAIMUJVYQLKA-UHFFFAOYSA-N 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N palladium Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 5
- 238000000967 suction filtration Methods 0.000 description 5
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 4
- VPKAHUMPZYVNIV-UHFFFAOYSA-N 1,4-dihydroisoquinoline Chemical compound C1=CC=C2CC=NCC2=C1 VPKAHUMPZYVNIV-UHFFFAOYSA-N 0.000 description 4
- ZPHQFGUXWQWWAA-UHFFFAOYSA-N 9-(2-phenylphenyl)carbazole Chemical compound C1=CC=CC=C1C1=CC=CC=C1N1C2=CC=CC=C2C2=CC=CC=C21 ZPHQFGUXWQWWAA-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 4
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical group NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000007872 degassing Methods 0.000 description 4
- CSJLBAMHHLJAAS-UHFFFAOYSA-N diethylaminosulfur trifluoride Chemical compound CCN(CC)S(F)(F)F CSJLBAMHHLJAAS-UHFFFAOYSA-N 0.000 description 4
- 238000004821 distillation Methods 0.000 description 4
- GNTDGMZSJNCJKK-UHFFFAOYSA-N divanadium pentaoxide Chemical compound O=[V](=O)O[V](=O)=O GNTDGMZSJNCJKK-UHFFFAOYSA-N 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- 150000002466 imines Chemical class 0.000 description 4
- 150000002576 ketones Chemical class 0.000 description 4
- 239000011777 magnesium Substances 0.000 description 4
- 229910052749 magnesium Inorganic materials 0.000 description 4
- CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 description 4
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 4
- 229910052697 platinum Inorganic materials 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 238000010992 reflux Methods 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 4
- NZCKTGCKFJDGFD-UHFFFAOYSA-N 2-bromobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Br NZCKTGCKFJDGFD-UHFFFAOYSA-N 0.000 description 3
- MTUBTKOZCCGPSU-UHFFFAOYSA-N 2-n-naphthalen-1-yl-1-n,1-n,2-n-triphenylbenzene-1,2-diamine Chemical compound C1=CC=CC=C1N(C=1C(=CC=CC=1)N(C=1C=CC=CC=1)C=1C2=CC=CC=C2C=CC=1)C1=CC=CC=C1 MTUBTKOZCCGPSU-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- REDXJYDRNCIFBQ-UHFFFAOYSA-N aluminium(3+) Chemical compound [Al+3] REDXJYDRNCIFBQ-UHFFFAOYSA-N 0.000 description 3
- 230000005540 biological transmission Effects 0.000 description 3
- 230000000903 blocking effect Effects 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 238000005401 electroluminescence Methods 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 125000005842 heteroatom Chemical group 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 238000004128 high performance liquid chromatography Methods 0.000 description 3
- 239000011159 matrix material Substances 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 229910052763 palladium Inorganic materials 0.000 description 3
- 239000002244 precipitate Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 230000027756 respiratory electron transport chain Effects 0.000 description 3
- 239000010948 rhodium Substances 0.000 description 3
- 150000003384 small molecules Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 239000000758 substrate Substances 0.000 description 3
- WPVBHUUZDFUIJA-UHFFFAOYSA-N (3-fluoro-4-methylphenyl)boronic acid Chemical compound CC1=CC=C(B(O)O)C=C1F WPVBHUUZDFUIJA-UHFFFAOYSA-N 0.000 description 2
- BLPWOMKYNJFENS-UHFFFAOYSA-N 1-(3-fluorophenyl)isoquinoline Chemical compound FC1=CC=CC(C=2C3=CC=CC=C3C=CN=2)=C1 BLPWOMKYNJFENS-UHFFFAOYSA-N 0.000 description 2
- LPCWDYWZIWDTCV-UHFFFAOYSA-N 1-phenylisoquinoline Chemical compound C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 LPCWDYWZIWDTCV-UHFFFAOYSA-N 0.000 description 2
- VDULMXJUOWIPGE-UHFFFAOYSA-N 1-phenylisoquinoline quinoline Chemical compound N1=CC=CC2=CC=CC=C12.C1(=CC=CC=C1)C1=NC=CC2=CC=CC=C12 VDULMXJUOWIPGE-UHFFFAOYSA-N 0.000 description 2
- AZFHXIBNMPIGOD-UHFFFAOYSA-N 4-hydroxypent-3-en-2-one iridium Chemical compound [Ir].CC(O)=CC(C)=O.CC(O)=CC(C)=O.CC(O)=CC(C)=O AZFHXIBNMPIGOD-UHFFFAOYSA-N 0.000 description 2
- HUKPVYBUJRAUAG-UHFFFAOYSA-N 7-benzo[a]phenalenone Chemical compound C1=CC(C(=O)C=2C3=CC=CC=2)=C2C3=CC=CC2=C1 HUKPVYBUJRAUAG-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 241000790917 Dioxys <bee> Species 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000005804 alkylation reaction Methods 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- YXVFYQXJAXKLAK-UHFFFAOYSA-N biphenyl-4-ol Chemical compound C1=CC(O)=CC=C1C1=CC=CC=C1 YXVFYQXJAXKLAK-UHFFFAOYSA-N 0.000 description 2
- 239000004327 boric acid Substances 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 210000004907 gland Anatomy 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 description 2
- 125000001979 organolithium group Chemical group 0.000 description 2
- 150000002902 organometallic compounds Chemical class 0.000 description 2
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N pentanoic acid group Chemical group C(CCCC)(=O)O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 2
- 125000004437 phosphorous atom Chemical group 0.000 description 2
- 229920000767 polyaniline Polymers 0.000 description 2
- 125000003367 polycyclic group Chemical group 0.000 description 2
- 229920001690 polydopamine Polymers 0.000 description 2
- 238000007639 printing Methods 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- 230000000171 quenching effect Effects 0.000 description 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 229910052703 rhodium Inorganic materials 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 2
- 125000005259 triarylamine group Chemical group 0.000 description 2
- 150000004818 1,2-dichlorobenzenes Chemical class 0.000 description 1
- SJBAPHJRDIIHMB-UHFFFAOYSA-N 1-(2-bromophenyl)isoquinoline Chemical compound BrC1=CC=CC=C1C1=NC=CC2=CC=CC=C12 SJBAPHJRDIIHMB-UHFFFAOYSA-N 0.000 description 1
- DJGXPFQIMLEVPA-UHFFFAOYSA-N 1-bromo-3-fluoro-2-methylbenzene Chemical compound CC1=C(F)C=CC=C1Br DJGXPFQIMLEVPA-UHFFFAOYSA-N 0.000 description 1
- QDFKKJYEIFBEFC-UHFFFAOYSA-N 1-bromo-3-fluorobenzene Chemical compound FC1=CC=CC(Br)=C1 QDFKKJYEIFBEFC-UHFFFAOYSA-N 0.000 description 1
- MSQCQINLJMEVNJ-UHFFFAOYSA-N 1-chloroisoquinoline Chemical compound C1=CC=C2C(Cl)=NC=CC2=C1 MSQCQINLJMEVNJ-UHFFFAOYSA-N 0.000 description 1
- CVBUKMMMRLOKQR-UHFFFAOYSA-N 1-phenylbutane-1,3-dione Chemical compound CC(=O)CC(=O)C1=CC=CC=C1 CVBUKMMMRLOKQR-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- NBYLBWHHTUWMER-UHFFFAOYSA-N 2-Methylquinolin-8-ol Chemical compound C1=CC=C(O)C2=NC(C)=CC=C21 NBYLBWHHTUWMER-UHFFFAOYSA-N 0.000 description 1
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- WPTCSQBWLUUYDV-UHFFFAOYSA-N 2-quinolin-2-ylquinoline Chemical compound C1=CC=CC2=NC(C3=NC4=CC=CC=C4C=C3)=CC=C21 WPTCSQBWLUUYDV-UHFFFAOYSA-N 0.000 description 1
- UEIZUEWXLJOVLD-UHFFFAOYSA-N 3-(1-methylpyrrolidin-3-yl)pyridine Chemical compound C1N(C)CCC1C1=CC=CN=C1 UEIZUEWXLJOVLD-UHFFFAOYSA-N 0.000 description 1
- MBPCKEZNJVJYTC-UHFFFAOYSA-N 4-[4-(n-phenylanilino)phenyl]aniline Chemical compound C1=CC(N)=CC=C1C1=CC=C(N(C=2C=CC=CC=2)C=2C=CC=CC=2)C=C1 MBPCKEZNJVJYTC-UHFFFAOYSA-N 0.000 description 1
- NMJQRWXNGBMMNH-UHFFFAOYSA-N 7,7-dimethyl-8-fluorodibenzo[de,h]quinoline Chemical compound C12=CC=CC(F)=C2C(C)(C)C2=CC=CC3=CC=NC1=C23 NMJQRWXNGBMMNH-UHFFFAOYSA-N 0.000 description 1
- XWWIRMYHZRWTON-UHFFFAOYSA-N 8,8-dimethyl-15-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1(17),2,4,6,9,11,13,15-octaene Chemical compound C1=CC(C(C)(C)C=2C3=CC=CC=2)=C2C3=CN=CC2=C1 XWWIRMYHZRWTON-UHFFFAOYSA-N 0.000 description 1
- QSPJLGPBPZWMCA-UHFFFAOYSA-N 8-bromo-1-(2-bromophenyl)isoquinoline Chemical compound BrC1=CC=CC=C1C1=NC=CC2=CC=CC(Br)=C12 QSPJLGPBPZWMCA-UHFFFAOYSA-N 0.000 description 1
- 229910016036 BaF 2 Inorganic materials 0.000 description 1
- LCOMFVDNVLHUEK-UHFFFAOYSA-N C(C)C(=O)C(=O)C.C1(=CC=CC=C1)C1=CC=CC=C1 Chemical compound C(C)C(=O)C(=O)C.C1(=CC=CC=C1)C1=CC=CC=C1 LCOMFVDNVLHUEK-UHFFFAOYSA-N 0.000 description 1
- JCVGDPVXTMFBHH-UHFFFAOYSA-N C1=CC(CC=2C3=CC=CC=2)=C2C3=NC=CC2=C1 Chemical class C1=CC(CC=2C3=CC=CC=2)=C2C3=NC=CC2=C1 JCVGDPVXTMFBHH-UHFFFAOYSA-N 0.000 description 1
- KXDHJXZQYSOELW-UHFFFAOYSA-N Carbamic acid Chemical compound NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 1
- UJOBWOGCFQCDNV-UHFFFAOYSA-N Carbazole Natural products C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- IPNFVCCZEUSVAK-UHFFFAOYSA-N FC1=NC=2C3=C(CC=4C2C(=C1)C=CC4)C=CC=C3 Chemical compound FC1=NC=2C3=C(CC=4C2C(=C1)C=CC4)C=CC=C3 IPNFVCCZEUSVAK-UHFFFAOYSA-N 0.000 description 1
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 1
- 235000001018 Hibiscus sabdariffa Nutrition 0.000 description 1
- 101000801643 Homo sapiens Retinal-specific phospholipid-transporting ATPase ABCA4 Proteins 0.000 description 1
- QNAYBMKLOCPYGJ-REOHCLBHSA-N L-alanine Chemical compound C[C@H](N)C(O)=O QNAYBMKLOCPYGJ-REOHCLBHSA-N 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 229920000265 Polyparaphenylene Polymers 0.000 description 1
- 102100033617 Retinal-specific phospholipid-transporting ATPase ABCA4 Human genes 0.000 description 1
- 235000005291 Rumex acetosa Nutrition 0.000 description 1
- 240000007001 Rumex acetosella Species 0.000 description 1
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical class [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
- NLESIEMIRNKQEI-UHFFFAOYSA-N [Ir]c1cccnc1-c1ccccc1 Chemical compound [Ir]c1cccnc1-c1ccccc1 NLESIEMIRNKQEI-UHFFFAOYSA-N 0.000 description 1
- CUJRVFIICFDLGR-UHFFFAOYSA-N acetylacetonate Chemical compound CC(=O)[CH-]C(C)=O CUJRVFIICFDLGR-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000029936 alkylation Effects 0.000 description 1
- FSEXLNMNADBYJU-UHFFFAOYSA-N alpha-Phenylquinoline Natural products C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 description 1
- 238000006254 arylation reaction Methods 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- UFVXQDWNSAGPHN-UHFFFAOYSA-K bis[(2-methylquinolin-8-yl)oxy]-(4-phenylphenoxy)alumane Chemical compound [Al+3].C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC=C([O-])C2=NC(C)=CC=C21.C1=CC([O-])=CC=C1C1=CC=CC=C1 UFVXQDWNSAGPHN-UHFFFAOYSA-K 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- 229910052792 caesium Inorganic materials 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 238000013375 chromatographic separation Methods 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000000536 complexating effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 229920001940 conductive polymer Polymers 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 230000002596 correlated effect Effects 0.000 description 1
- 150000003997 cyclic ketones Chemical class 0.000 description 1
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical group O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000003810 ethyl acetate extraction Methods 0.000 description 1
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- YLQWCDOCJODRMT-UHFFFAOYSA-N fluoren-9-one Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C2=C1 YLQWCDOCJODRMT-UHFFFAOYSA-N 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000013905 glycine and its sodium salt Nutrition 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 125000005553 heteroaryloxy group Chemical group 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 125000000468 ketone group Chemical group 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- IHLVCKWPAMTVTG-UHFFFAOYSA-N lithium;carbanide Chemical compound [Li+].[CH3-] IHLVCKWPAMTVTG-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000002905 metal composite material Substances 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- PYLWMHQQBFSUBP-UHFFFAOYSA-N monofluorobenzene Chemical compound FC1=CC=CC=C1 PYLWMHQQBFSUBP-UHFFFAOYSA-N 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 229910052762 osmium Inorganic materials 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TZMFJUDUGYTVRY-UHFFFAOYSA-N pentane-2,3-dione Chemical compound CCC(=O)C(C)=O TZMFJUDUGYTVRY-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920001088 polycarbazole Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920000123 polythiophene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- JUJWROOIHBZHMG-RALIUCGRSA-N pyridine-d5 Chemical compound [2H]C1=NC([2H])=C([2H])C([2H])=C1[2H] JUJWROOIHBZHMG-RALIUCGRSA-N 0.000 description 1
- 238000006862 quantum yield reaction Methods 0.000 description 1
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 235000003513 sheep sorrel Nutrition 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 238000001149 thermolysis Methods 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
Images
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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
-
- 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
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0033—Iridium compounds
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/09—Esters of phosphoric acids
- C07F9/10—Phosphatides, e.g. lecithin
-
- 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
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B57/00—Other synthetic dyes of known constitution
- C09B57/10—Metal complexes of organic compounds not being dyes in uncomplexed form
-
- 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
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
- H05B33/00—Electroluminescent light sources
- H05B33/12—Light sources with substantially two-dimensional radiating surfaces
- H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
-
- 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
-
- 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
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
-
- 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
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/346—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising platinum
-
- 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
- H10K85/361—Polynuclear complexes, i.e. complexes comprising two or more metal centers
-
- 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
- C09K2211/1018—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
- C09K2211/1088—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
- C09K2211/185—Metal complexes of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P70/00—Climate change mitigation technologies in the production process for final industrial or consumer products
- Y02P70/50—Manufacturing or production processes characterised by the final manufactured product
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Physics & Mathematics (AREA)
- High Energy & Nuclear Physics (AREA)
- Electroluminescent Light Sources (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
本发明描述新型的金属络合物。这样的化合物在最广义上分类为电子工业中的一系列不同类型的应用场合中能用作功能材料。所述有创造性的化合物由通式(1)和(4)描述。
Description
本申请是申请日为2004年9月28日,申请号为200480028250.0(国际申请号PCT/EP2004/010836),名称为“金属络合物”的中国国家申请的分案申请。
本发明涉及新颖的材料和材料混合物在有机电子器件比如电致发光元件中的用途,及它们在基于电致发光元件的显示器中的用途。
在一系列不同类型的在电子工业中在最宽广意义上分类的应用场合中,有机半导体用作活性组分(=功能材料)在最近或者在不久的将来可以预期成为现实。例如,光敏有机材料(例如酞菁)和有机电荷迁移材料(通常三芳胺基空穴输送器)好几年已经发现可用于复印机中。特定的半导体有机化合物,其中有一些同样能够在可见光谱区发射光,正开始要引入市场例如用于有机场致发光器件中。它们单独的元件,有机发光二极管(OLEDs),具有非常宽的光谱应用,作为:
1.用于单色的或者多色的显示元件(例如袖珍式计算器,移动电话及其他手提式的应用场合)的白色或者彩色背光,
2.大表面面积的显示器(例如交通标志、告示板等),
3.以所有的颜色和形式的照明元件,
4.用于手提式应用场合(例如移动电话、PDAs、录像摄像机等)的单色的或者全色彩无源矩阵显示器,
5.用于各式各样应用场合(例如移动电话、PDAs、膝上计算机、电视接收机等)的全色彩、大表面面积、高分辨率的活性基质显示器。
一些应用场合的开发已经非常先进。例如,包含简单的OLEDs的器件已经引入市场,如具有有机显示器的Pioneer汽车收音机或者Kodak的数字式摄象机所表明;然而仍然强烈需要技术改进。
最近几年中在这个方向进行的开发是使用有机金属络合物,其显示磷光代替荧光作用[M.A.Baldo,S.Lamansky,P.E.Burrows,M.E.Thompson,S.R.Forrest,Applied Physics Letters,1999,75,4-6]。由于量子力学的原因,利用有机金属化合物高到四倍量子效率、能量效率和功率效率是可能的。这种新发展能否形成本身首先强烈地取决于能否找到对应的同样利用这些OLEDs优点(与单线态发射=荧光作用相比三重态发射=磷光)的器件构造。本发明用于实际用途的主要条件特别是高的有效寿命、抗热应力的高稳定性、低耗费和工作电压,以能够用于可携带的应用场合。
有机电致发光器件的一般结构描述在例如US 4,539,507和US 5,151,629中。通常,一种有机电致发光器件由多个通过真空法或者各种各样的印刷方法施加到彼此上的层组成。这些层具体是:
1.载板=底物(通常为玻璃或者塑料薄膜)。
2.透明阳极(通常为氧化锡铟,ITO)。
3.空穴注入层(空穴注入层=HIL):例如基于铜酞菁(CuPc)或者导电聚合物比如聚苯胺(PANI)或者聚噻吩衍生物(比如PEDOT)。
4.一种或多种空穴传输层(空穴传输层=HTL):通常基于三芳胺衍生物例如4,4’,4”-三(N-1-萘基-N-苯基氨基)三苯胺(NaphDATA)作为第一层,N,N’-二(石脑油-1-基)-N,N’-二苯胺联苯(NPB)作为第二空穴传输层。
5.一种或多种发射层(发射层=EML):该层可以部分与层4-8一致,但是通常由基质组成,比如4,4’-双(咔唑-9-基)二苯基(CBP),掺杂有磷光染料,例如三(2-苯基吡啶基)铱(Ir(PPy)3)或者三(2-苯并噻吩甲基吡啶基)铱(Ir(BTP)3);然而,所述发射层同样可以由聚合物、聚合物混合物、聚合物和低分子量化合物的混合物或者不同低分子量化合物的混合物组成。
6.空穴阻挡层(空穴阻挡层=HBL):该层可以部分与层7和8一致。它通常由BCP(2,9-二甲基-4,7-联苯基-1,10-菲绕啉=深亚铜试剂)或者双(2-甲基-8-喹啉醇合)(4-苯基苯酚合)铝(III)(BAlq)组成。
7.电子传递层(电子传递层=ETL):通常基于三-8-羟基喹啉铝(AlQ3)。
8.电子注入层(电子注入层=EIL):薄层由具有高介电常数的材料例如LiF、Li2O、BaF2、MgO、NaF组成。
9.阴极:本发明,通常使用具有低功函数的金属、金属组合物或者金属合金,例如Ca、Ba、Cs、Mg、Al、In、Mg/Ag。
然而,仍然存在相当大的问题需要迫切改进显示三重态发射的OLEDs。这对于三重态发射体本身来说同样尤其是正确的。
在文献中,基于金属络合物的发射体最近描述于(例如US2003/0068526,WO2003/000661,EP1211257)中,其包含铱配位的1-苯基异喹啉配位体作为通式A和通式B的结构部分。所述显示的结构部分区别在于在苯基和异喹啉环之间存在桥(通式B)和不存在桥(通式A)。所述桥包含2-20个可以任选由杂原子取代的烷基桥接碳原子。
实际上,该类型化合物存在一些缺点,使得这些化合物的工业应用似乎不可能:
1.它们常常在有机溶剂中仅具有低溶解度,这显著妨碍乃至阻止高效的重结晶提纯或者色谱分离。这特别适合如在显示器制造中需要的相对大量的纯化情况。
2.特别是在溶液中,它们是非常氧化敏感的。有时,这些化合物必须在惰性气体下提纯、存储、运输和处理。
3.另外的关键缺点是上述描述化合物低的热稳定性。例如,所述均片段(homoleptic)络合物面式-三(1-苯基异喹啉-C2,N)铱(III),在有关的文献中通常熟知作为Ir(piq)3,不能在没分解的情况下就升华。甚至在典型的高真空条件(p<10-7毫巴)下,也观察到该化合物相当多的分解,除其他低分子量化合物之外,不仅可检测出占面式-三(1-苯基异喹啉-C2,N)铱(III)量30wt%的含铱灰分,而且可检测出1-苯基异喹啉的释放。这种热分解导致器件再现性低的特性,寿命受到特别不利的影响。
目前令人惊讶地发现,苯环与异喹啉环之间的键通过一个原子桥接的化合物作为OLEDs三重态发射体具有优异的性能。
1.所述有创造性的化合物特征在于有机溶剂中良好的溶解度,这大幅减轻了它们通过通常的方法比如重结晶或者色层分离法进行的纯化。这可以同样从溶液中通过涂敷或者印刷技术处理所述化合物。该性能在通过蒸发进行的通常的加工中同样是有利的,因为因此大幅减轻了使用的装置和障板的清洁。
2.所述有创造性的化合物特征在于改进的氧化稳定性,这对纯化和通常对这些化合物的操作产生正面影响。另外,这在用于相应有创造性的器件情况下导致操作寿命显著的增加。
3.所述有创造性的化合物同样特征在于高的热稳定性,从而它们通常可以在高真空下蒸发而没有分解。该性能是OLEDs可重复制备的一个基础先决条件,尤其是对操作寿命具有正面影响。而且,因此可以资源保护性地利用这些稀有金属化合物。
4.所述有创造性的化合物可以可靠的高纯度完全可重复地制备,而没有批量变化。因此生产所述有创造性的电致发光器件的生产过程显著地更加高效。
本发明提供通式(1)的化合物
M(L)n(L′)m(L″)o
通式(1)
包含结构部分M(L)n的通式(2)
通式(2)
其中使用的符号和标记是:
M在每一情况是过渡金属离子;
Y在每一情况下是相同或者不同的,是BR1,CR2,C=O,C=NR1,C=CR2,SiR1 2,NR1,PR1,AsR1,SbR1,BiR1,P(O)R1,P(S)R1,P(Se)R1,As(O)R1,As(S)R1,As(Se)R1,Sb(O)R1,Sb(S)R1,Sb(Se)R1,Bi(O)R1,Bi(S)R1,Bi(Se)R1,O,S,Se,Te,SO,SeO,TeO,SO2,SeO2,TeO2或者单键;
D在每一情况下是相同或者不同的,是碳原子或者具有与金属配位非键电子对的杂原子,条件是每个配位体中的一个D是碳原子,另一个是具有非键电子对的杂原子;
E在每一情况下是相同或者不同的,是C或者N,条件是至少一个符号E是C;
Cy1在每一情况下是相同或者不同的,是通过原子D结合到金属M的饱和的、不饱和或者芳香碳环或者杂环,同样有结合到环Cy2部分的单键和结合到Y基团的单键;
Cy2在每一情况下是相同或者不同的,是通过原子D结合到金属M的饱和的、不饱和或者芳香碳环或者杂环,同样有结合到环Cy1部分的单键和与Cy3环部分具有共用的边;
Cy3在每一情况下是相同或者不同的,是具有结合到所述Y基团的单键和与环Cy2部分共用边的饱和的、不饱和或者芳香的部分碳环或者杂环;
R1 R在每一个情况相同或者不同,是H或者具有1~20个碳原子的脂族或者芳烃基团,
n是1、2或者3;
所述通式(1)的配位体L’和L“是单阴离子、有双齿的螯合配位体,m和o在每一情况下是相同或者不同的是0,1或者2。
优选通式(1)化合物包含通式(2a)的结构部分M(L)n
通式(2a)
其中Y,R1,L’,L”和n每一个如上所述定义,所述另外的标记是:
M是Mo,W,Re,Ru,Os,Rh,Ir,Pd,Pt或者Au;
D在每一情况下是相同或者不同的,是碳原子、氮原子或者磷原子,条件是一个D是碳原子,另一个D是氮原子或者磷原子;
X在每一情况下是相同或者不同的,是CR,N或者P;或者一个或多个X-X单元(即两个相邻的X)是NR,S或者O;或者稠合环Cy2和Cy3部分中的一个X-X单元(即两个相邻的X)是CR,N或者P,条件是所述标记E之一是N;
E在每一情况下是相同或者不同的,是C或者N,条件是符号E至少之一是C,以及条件是如果符号E之一是N,则稠合环Cy2和Cy3部分中确切地一个X-X单元(即两个相邻的X)是CR,N或者P;
R在每一情况下相同或者不同,是H,F,Cl,Br,I,OH,NO2,CN,具有1-20个碳原子的直链、支链、环状的烷基或者烷氧基,其中一个或多个不相邻的CH2基团可以被-R1C=CR1-,-C≡C-,Si(R1)2,Ge(R1)2,Sn(R1)2,-O-,-S-,-NR1-,-(C=O)-,-(C=NR1)-,-P=O(R1)-或者-CONR1-取代,其中一个或多个氢原子可以被F,或者1-14个碳原子的可被一个或多个非芳香性的R基团取代的芳基、杂芳基、芳氧基或者杂芳氧基基团取代,其中在相同环和在不同环上的多个取代基R随后可以形成另外的单或者多环的、脂族或者芳香环体系。
本发明一个优选实施方案是通式(1A)化合物的那个,
M(L)n(L′)m(L″)o
通式(1a)
在每一情况下包含相同或者不同的至少一个通式(2b)M(L)n的结构部分,
通式(2b)
及任选在每一情况包含相同或者不同的通式(3)的M(L′)m的结构部分,
通式(3)
其中M,X,Y,R1,L′,L″和n每一个如上所述定义,所述另外的标记和符号每一个定义如下:
D在每一情况相同或者不同,是N或者P;
A在每一情况下是相同或者不同的,是-CR=CR-,-N=CR-,-P=CR-,-N=N-,-P=N-,NR,PR,O,S,Se。
有创造性的单阴离子、二齿配位体L″是1,3-二酮酸酯,选自1,3-二酮,例如乙酰丙酮、苯甲酰丙酮、1,5-二苯基乙酰丙酮、双(1,1,1-三氟乙酰基)甲烷,3-三酮,选自3-酮酸酯,例如乙酰醋酸乙酯,羧化物,选自氨基羧酸,例如吡啶-2-羧酸、喹啉-2-羧酸、甘氨酸、N,N-二甲基甘氨酸、丙氨酸、N,N-二甲基丙氨酸,水扬基亚胺盐类(salicyliminates),选自水扬基亚胺,例如甲基水扬基亚胺、乙基水扬基亚胺、苯基水扬基亚胺,含氮杂环化合物的硼酸酯,例如四(1-咪唑啉基)硼酸酯和四(1-吡唑基)硼酸酯。
所述有创造性的化合物优选具有通式(1)或者通式(1a),其中符号M=Rh,Ir,Pd或者Pt;更优选M=Ir或者Pt。
同样优选所述有创造性的化合物具有通式(1)或者通式(1a),其中所述符号n=2或者3。特别优选其中符号m=O=0的化合物。N=2和=O=0的钯和铂络合物,n=3和m=O=0的铑和铱络合物尤其是理想的。
优选所述有创造性的化合物具有通式(1)或者通式(1a),其中符号D=N。
优选所述有创造性的化合物具有通式(1)或者通式(1a),其中符号X=CR。
优选所述有创造性的化合物具有通式(1)或者(1a),其中符号Y=Y=CR2,C=O,C=CR2,NR1,PR1,P(O)R1,O,S,SO,SO2或者单键。符号Y更优选为CR2。
同样优选所述有创造性的化合物具有通式(1)或者通式(1a),其中符号R是:
R在每一情况下是相同或者不同的,是H,F,1-4个碳原子的直链、支链或者环烷基或者烷氧基,其中一个或多个氢原子可以被F,或者具有1-6个碳原子的芳基或者杂芳基取代,以及可被一个或多个非芳香性的R基团取代,其中在相同环和在不同环上的多个取代基R随后一起可以形成另外的脂族或者芳香的单或者多环体系。尽管从上述陈述中显而易见,但应该指出本发明再次明确,在Y=CR2情况下,所述两个取代基R可以形成另外的脂族或者芳香的单或者多环的环系。在这种情况下,所述桥接碳原子变成结合两个彼此垂直的环状体系的螺碳原子。
根据上述的说明,同样优选包含至少一个通式(2)M(L)n的结构部分的通式(1)的化合物,所述的通式(2)结构在每一情况下是相同或者不同的,特征在于Y是螺碳原子。
从上述描述的有创造性的通式(1)化合物的结构显而易见,通式(2)M(L)n的结构部分具有平面的结构,由于环1与两个环Cy2/Cy3的稠合部分(或者所述芳基与异喹啉环)刚性的结合,因此形成该平面性桥联基团Y是必要的。所述有创造性的化合物的性能与迄今为止在文献中描述的通式A和B体系的非可平面性相反。在该文献中,如在通式A化合物的苯环6位上的氢原子和异喹啉环8位上的氢原子,或者如通式B化合物中的包含2-20个烷基桥接碳原子的桥连基阻止结合的芳基部分环状体系变平。上述物质的基本结构与所述有创造性的化合物的区别对于发光量子效率具有广泛的影响。根据在稠合和稠合杂芳系光谱学中观察到的一般倾向(N.Turro,University Science Books,55D GateFive Road,Sausalito,CA 94965,ISBN 0 935702 71 7),与通式A和B中更加挠性的非平面的体系相比,本发明中刚性的平面的体系也具有更大的量子发光效率。正如所料,更大的量子发光效率在OLED中导致有创造性的通式(1)化合物显著的改进效率。
本发明进一步提供通式(4)的化合物
通式(4)
其中所述标记E,Cy1,Cy2和Cy3每一个如上所述定义,另外的标记是:
Y′在每一情况下是相同或者不同的,是BR1,CR2,C=NR1,C=CR2,SiR1 2,PR1,AsR1,SbR1,BiR1,P(O)R1,P(S)R1,P(Se)R1,As(O)R1,As(S)R1,As(Se)R1,Sb(O)R1,Sb(S)R1,Sb(Se)R1,Bi(O)R1,Bi(S)R1,Bi(Se)R1,Se,SO,SeO,TeO,SO2,SeO2,TeO2;
D‘在每一情况下是相同或者不同的,是C-H,N或者P,条件是一个符号D′是C-H,另一个符号D′是N或者P。
优选通式(4a)的化合物
通式(4a)
其中所述标记每一个如上所述通式(2a)和通式(4)的定义,
本发明一个优选实施方案是通式(4b)化合物的那个。
通式(4b)
其中D是N或者P,所述另外的标记每一个如上所述的通式(2b)和(4a)的定义。
通式(4)或者(4a)或者(4b)优选实施方式的化合物类似于上述的对于通式(2)或者(2a)或者(2b)结构部分的评论。
这些化合物构成上述的通式(1)化合物的配位体L,因此是有用的合成这些化合物的中间体。
所述有创造性的通式(4)或者(4a)或者(4b)的化合物可以通过通常的有机化学方法制备,举例来说如下所述:
1)7,7-二氟苯并[de,h]喹啉(见实施例1)
如果适当在路易斯酸存在下,偶氮苯蒽酮和类似的7H-二苯并[de,H]喹啉-7-酮与四氟化硫直接氟化作用,以良好的产率顺利地得到7,7-二氟类似物。
2)7,7-二甲基二苯并[de,h]异喹啉(也见实施例2)
通过上述示意的路径,可以良好的产率得到对称的7,7-二基取代的7H-二苯并[de,H]喹啉。类似地,通过其他酮在步骤4替换丙酮可以容易地得到另外的衍生物。例如,使用酮,戊-3-酮得到如实施例结构3所示的配位体体系,使用二苯甲酮得到如实施例结构7所示的配位体体系。使用环酮,例如环戊酮或者芴酮,得到如实施例结构6和8所示的配位体体系,即具有螺碳原子的配位体体系。做为选择,同样可以不使用酮,而使用氯甲酸甲酯,其在随后步骤中与有机锂试剂或者格利雅化合物反应。当不用2-溴苯甲酰氯化物,而利用其他官能化的2-溴苯甲酰氯化物,可以得到苯环上官能化的7,7-二烷基-7H-二苯并[de,H]异喹啉。例如,使用2-溴烟碱基氯化物、2-溴异烟碱基氯化物、2-溴代-4-氟代苯甲酰基氯化物、2-溴代-3,4-二甲苯酰氯化物、2-溴代-3-甲基-4-氟代苯甲酰基氯化物、2-溴代-3-氰基-4-氟代苯甲酰基氯化物得到如实施例结构13、14、16、17、18和19所示的配位体体系。
3)7-烷基-/7-芳基-7-烷氧基二苯并[de,h]喹啉
7-烷基-/7-芳基-7-氟代二苯并[de,h]喹啉
如上所述,通过借助于格里尼亚或者有机锂试剂或者其他有机金属化合物,进行连续的偶氮苯蒽酮羰基官能的C-烷基化或者C-芳基化,及随后进行羟基的烷基化或者氟化作用(例如与DAST=二乙基氨基三氟化硫),得到由烷基、芳基、烷氧基或者氟在位置7不对称取代的通式(4a)或者(4b)的化合物。该反应顺序导致包括在实施例结构9、10和12中示意的那些的配位体体系。
4)7,7-Y″二苯并[de,h]喹啉
当在上述合成顺序2〕中使用2-(3-溴苯基)乙胺代替2-苯基乙胺,完全类似地可以得到1-(2-溴苯基)-8-溴代异喹啉,在双锂化,与亲电子试剂Y“Cl2和Y”Cl随后反应以后得到如实施例结构25、26、30和32所示的配位体体系。
如果适当,如实施例结构30和32所示的情况,这些可以通过与空气或者过氧化氢进一步氧化进行官能化以得到如实施例结构31和33所示的配位体体系。
原则上有创造性的金属络合物可以通过各种各样的方法制备;然而如下所述的方法被认为是特别适当的。
因此本发明进一步提供通过通式(4)、(4a)或者(4b)的化合物与通式(5)的金属醇盐、与通式(6)的酮酮酸盐或者通式(7)、(8)或者(9)的单或者多环的金属卤化物反应,制备所述金属络合物的方法,
通式(5) 通式(6) 通式(7)
通式(8) 通式(9)
其中标记M和R1每一个定义如上,p=1或者2,Hal=氟、氯、溴或者碘。
如果适当,同样可以优选使用带有醇盐和/或卤化物和/或羟基和酮酮酸盐基团的铱化合物。这些化合物同样可以是带电荷的。特别适当作为反应物的相应铱化合物已经公开在DE10314102.2中。
所述络合物的合成优选按象描述在WO02/060910和DE10314102.2中那样的方法进行。值得注意的是在在其它方面相同反应条件下所述有创造性的金属络合物比现有技术的金属络合物显著更快地形成。因此,与上述现有技术方法不同的反应时间优选为1-60h,更优选为20-50h。
该方法可以高纯度提供通式(1)的有创造性的化合物,优选大于99%(通过1NMR和/或HPLC确定)。
用本发明中说明的合成法可以制备用于通式(1)化合物的包括以下示意的实施例结构1-95的化合物。
上述描述的有创造性的化合物例如实施例24、43、44、74和75的化合物,同样可以用作共聚单体和单元用于形成相应共轭的、部分共轭或者非共轭的聚合物或者树枝状聚合物。优选通过溴官能度将适当的聚合引入主链或者引入侧链。例如,它们可以特别是聚合为可溶的聚芴(例如根据EP842208或者WO00/22026),聚螺二芴(例如根据EP707020或者EP894107),聚对亚苯基(例如根据WO92/18552)),聚咔唑(例如根据DE10304819.7或者DE10328627.6)或聚噻吩(例如根据EP1028136),或为包含多个这些中不同单元的共聚物。
因此本发明进一步提供包含一个或多个通式(1)化合物的共轭、部分共轭或者非共轭聚合物或者树枝状聚合物,其中上述定义的R构成与所述聚合物或者树枝状聚合物的键合。上述的聚合物、共聚物和树枝状聚合物特征在于它们在有机溶剂中良好的溶解度。而且,通式(1)有创造性的化合物当然也可以通过通常的反应类型进一步官能化,因此转变为通式(1)扩展的化合物。本发明中提及的例子是根据SUZUKI用烯丙基硼酸进行官能化,或者用胺根据HARTWIG-BUCHWALD进行官能化。
通式(1)有创造性的化合物、聚合物、树枝状聚合物或者扩展的化合物可以用作电子元件的有效元件,例如有机发光二极管(OLEDs)、有机集成电路(O-ICs)、有机场效应晶体管(O-FETs)、有机薄膜晶体管(O-TFTs)、有机太阳能电池(O-SCs)或有机激光器二极管(O-激光器)。
因此本发明进一步提供通式(1)有创造性的化合物、通式(1)有创造性的聚合物和树枝状聚合物及相应的扩展化合物在电子元件中作为有效元件的用途。
本发明进一步提供电子元件,尤其是有机发光二极管(OLEDs)、有机集成电路(O-ICs)、有机场效应晶体管(O-FETs)、有机薄膜晶体管(O-TFTs)、有机太阳能电池(O-SCs)或有机激光器二极管(O-激光器),包括一种或多种通式(1)有创造性的化合物、通式(1)有创造性的聚合物和树枝状聚合物和相应的扩展化合物。
通过随后的实施例详细地说明本发明,没有任何意图将本发明限制于此。本领域普通技术人员根据本发明的描述不需要有创造性的工作可以制备另外的有创造性的化合物或者应用所述方法。
实施例:
所述随后的合成除非另有说明在保护气体气氛下干燥溶剂中进行。所述反应物从ALDRICH购买[2-溴苯甲酰氯化物、3-氟代-4-甲基苯硼酸、二氧化锰、镁]和从Fluka购买[四氟化硫]。1-氮杂苯并蒽酮(7H-二苯并[de,H]喹啉-7-酮)根据“Deutschen Reichs PatentschriftNr:614196”[German Empire patent no.614196]制备。
实施例1:面式-三[7,7-二氟-7H-二苯并[de,H]喹啉-C2,N]铱(III)(Ir1)的合成
A:7,7-二氟二苯并[de,h]喹啉
23.1g(100mmol)1-氮杂苯并蒽酮首先加入惰性化的弹管中。随后,22.7g(210mmol)的四氟化硫冷凝加入。该反应混合物加热到180℃保持10h。在弹管已经冷却以后,排出过量的四氟化硫,从二噁烷/乙醇(4∶1)中两次再结晶褐色残余物。
纯度为约99.0%的产率为18.3g(72.3mmol),理论值的72.3%。
1H NMR(CDCl3):[ppm]=8.86(m,1H),8.73(m,1H),8.62(m,1H),8.40(m,1H),8.09(m,1H),7.88(m,1H),7.76(m,1H),7.70(m,1H),7.60(m,1H).
B:面式-三[7,7-二氟二苯并[de,h]喹啉-C2,N]铱(III)(Ir1)
15.20g(60mmol)的7,7-二氟-7H-二苯并[de,H]喹啉和4.90g(10mmol)铱(III)乙酰丙酮化物的混合物悬浮在200ml乙二醇中,在165℃下搅拌140h。在冷却到室温以后,逐滴地加入160ml乙醇和40ml 1N HCl的混合物。在搅拌20分钟以后,用抽吸过滤掉深红细微的晶状沉淀,用50ml的乙醇/1N HCl(4∶1)混合物的洗涤四次,用50ml乙醇/水(4∶1)混合物洗涤四次,用乙醇洗涤四次,随后减压下干燥。在高真空升(p=10-5毫巴,T=385℃)华以后,纯度约为99.8%的产率是7.80g(8.2mmol),理论值的82.2%。
MS(FAB,m/z):M+=949.7.
实施例2:面式-三[7,7-二甲基二苯并[de,H]喹啉-C2,N]铱(III)(Ir2)的合成
A:N-苯乙基-2-溴苯甲酰胺
62.7ml(500mmol)苯基乙胺、70.4ml(506mmol)三乙胺和150ml二氯甲烷的混合物在0℃逐滴地与109.2g的2-溴苯甲酰的50ml二氯甲烷的溶液混合,保持良好的搅拌速率以使温度不超过30℃。随后,在室温下搅拌混合物另外的1h。用抽吸过滤掉因此得到的无色固体,用200ml二氯甲烷洗涤三次,减压干燥。纯度为约99.0%的产率为138.2g(453mmol),理论值的90.7%。
1H NMR(CDCl3):[ppm]=7.55(m,1H),7.44(m,1H),7.34-7.28(m,4H),7.28-7.21(m,3H),6.18(br.t,NH,1H),3.73(dt,NCH2CH2,2H),2.95(t,NCH2CH2,2H).
B:1-(2-溴苯基)-3,4-二氢异喹啉
在200ml二甲苯中50.0g(164mmol)的N-苯乙基-2-溴苯甲酰胺和27.9g的五氧化二磷的悬浮液加热到100℃,逐滴地与45.6g(492mmol)的三氯氧化磷混合。随后,所述反应混合物在回流下加热2小时。在冷却到80℃以后,所述反应混合物搅拌进入4000g冰中,用NaOH(固体)调节到pH=12。除去所述有机相,用300ml甲苯提取水相三次,合并的有机相用500ml水洗涤,随后用硫酸镁干燥。在干燥剂过滤去以及除去溶剂后,得到黄色油产品。纯度约为99.0%的产率为46.9g(164mmol),理论值的99.9%。
1H NMR(CDCl3):[ppm]=7.61(m,1H),7.41(m,2H),7.38-7.34(m,1H),7.30-7.24(m,2H),7.19-7.16(m,1H),6.89(m,1H),4.10(br.m,1H),3.73(br.m,1H),2.88(br.m,2H).
C:1-(2-溴苯基)异喹啉
28.6g(100mmol)的1-(2-溴苯基)-3,4-二氢异喹啉,86.9g(1mol)二氧化锰和200ml的1,2-二氯苯混合物在180℃下搅拌5小时。在冷却以后,用500ml甲苯稀释混合物,通过硅胶过滤。在除去溶剂以后,得到黄色油产品。纯度约为99.0%的产率是26.0g(91mmol),理论值的91.4%。
1H NMR(CDCl3):[ppm]=8.63(m,1H),7.86(m,1H),7.73-7.61(m,4H),7.51-7.42(m,3H),7.37-7.33(m,1H).
D:1-(2-(2-羟基-异丙基)苯基)异喹啉
由在200mlTHF中22.7g(80mmol)的1-(2-溴代苯基)异喹啉和2.1g(85mmol)镁制备的格利雅化合物在0℃逐滴地与8.8ml(120mmol)丙酮和100ml的THF混合物混合。在从温热冷却到室温以后,所述反应混合物在回流下加热3小时。在冷却以后,加入800ml的乙酸乙酯和500ml的水,除去有机相,并用200ml的乙酸乙酯提取水相两次。用饱和的氯化钠溶液洗涤合并的有机相,用硫酸镁干燥。所述溶剂除去之后,得到黄色油产品。纯度为约99.0%时的产率为19.2g(73mmol),理论值的91.2%。
1H NMR(CDCl3):[ppm]=8.66(m,1H),7.74(m,1H),7.70-759(m,4H),7.50-7.43(m,3H),7.34-7.30(m,1H),4.87(br.s,1H,OH),2.15(s,6H,CH3).
E:7,7-二甲基二苯并[de,h]喹啉
13.2g(50mmol)的1-(2-(2-羟基异丙基)苯基)异喹啉的250ml乙酸的溶液与50ml浓硫酸混合,加热回流16小时。冷却之后,所述反应混合物倒在1000g冰上,用5N氢氧化钠溶液调节pH=10,用300ml二氯甲烷提取三次。合并的有机相用水洗涤,用硫酸镁干燥。除去溶剂之后,从甲苯/乙醇(5∶1)进行重结晶。得到黄色固体产品。纯度为约99.0%的产率为8.4g(34mmol),理论值的68.4%。
1H NMR(CDCl3):[ppm]=8.41(m,1H),7.94(m,1H),7.77-769(m,3H),7.61(m,1H),7.45-7.40(m,3H),7.27-7.21(m,1H),2.65(s,6H,CH3).
F:面式-三[7,7-二甲基二苯并[de,h]喹啉-C2,N]铱(III)(Ir2)
14.72g(60mmol)的7,7-二甲基-7H-二苯并[de,H]喹啉和4.90g(10mmol)铱(III)乙酰丙酮化物的混合物悬浮在200ml乙二醇中,在165℃下搅拌140h。在冷却到室温以后,逐滴地加入160ml乙醇和40ml的1N的HCl的混合物。在搅拌20分钟以后,用抽吸过滤掉深红细微的晶状沉淀,用50ml的乙醇/1N HCl(4∶1)混合物的洗涤四次,用50ml乙醇/水(4∶1)混合物洗涤四次,用乙醇洗涤四次,随后减压下干燥。在高真空升(p=10-5毫巴,T=385℃)华以后,纯度约为99.8%的产率是7.97g(8.6mmol),理论值的86.1%。
MS(FAB,m/z):M+=925.9.
1H NMR(CD2Cl2):[ppm]=7.72(d,J=7.96Hz,1H),7.69(t,J=8.03Hz,1H),7.60(d,J=8.03Hz,1H),7.48(d,J=6.36Hz,1H),7.22(d,J=6.36Hz,1H),7.03(d,J=6.36Hz),7.03(d,J=7.70Hz,1H),6.88(t,J=7.7Hz,1H),6.72(d,J=7.37Hz,1H),1.69(s,3H,CH3),1.71(s,3H,CH3).
实施例3:实施例2:面式-三[7,7-二甲基二苯并-13-氟代[de,H]喹啉-C2,N]铱(III)(Ir3)的合成
A:N-苯乙基-3-氟苯甲酰胺
174.9ml(1.39mol)苯基乙胺溶解在600ml二氯甲烷中,与196.0ml(1.41mol,1.01当量)三乙胺混合。随后,在0℃逐滴地向所述溶液加入221.0g(1.39mmol)3-氟代苯甲酰基氯化物,以使温度不超过40℃。在RT下搅拌混合物18h,所述沉淀固体溶解在1000ml二氯甲烷中。用200ml稀释的NaOH、1NHCl和饱和的NaHCO3溶液洗涤混合物四次。除去有机相,用MgSO4干燥减压浓缩。用抽吸过滤掉固体,用少许二氯甲烷洗涤两次。得到纯度为>99%(通过HPLC确定)的289.52g白色固体,相当于理论值的85.4%。
1H NMR(CDCl3):[ppm]=7.42(dd,J=7.03Hz,1.67Hz,1H),7.3-7.39(m,3H),7.24(mc,3H),7.17(dt,J=9.03Hz,1.68Hz,1H),6.1(sbr,1H,NH),3.70(t,J=7.02Hz,2H,CH2),2.90(t,J=7.03Hz,2H,CH2).
B:1-(3-氟代苯基)-3,4-二氢异喹啉
289.0g(1.19mol)N-苯乙基-3-氟苯甲酰胺溶解在1000ml二甲苯中,在90℃以份包装与202.7g(1.43mol,1.2当量)的五氧化二磷混合。随后,逐滴地加入326.8ml(3.57mol,3.0当量)的三氯氧化磷。所述混合物回流加热4小时。所述反应溶液随后趁热倒在冰上,在用冰冷却下用固体NaOH小心调节pH=12。用500ml甲苯提取沉淀三次,用MgSO4干燥减压浓缩为高度粘性油并随后结晶。得到纯度约99%的267.41g产品,相当于理论值的99.8%。
1H NMR(CDCl3):[ppm]=7.37(mc,3H),7.33(dd,J=9.3,2.0Hz,1H),7.26(d,J=7.8Hz,1H),7.24(d,J=3.68Hz,2H),7.12(mc,1H),3.84(t,J=7.36Hz,2H,CH2),2.79(t,J=7.36Hz,2H,CH2).
C:1-(3-氟代苯基)异喹啉
266.41g(1.183mol)的1-(3-氟代苯基)-3,4-二氢异喹啉溶解在1500ml的o-二氯苯中,与901.2g(10.37mol,8.7当量)的锰混合。所述混合物在160-170℃下搅拌16小时。随后,通过硅藻土过滤反应溶液,用二氯甲烷/乙醇(25∶1)清洗。随后,在减压下蒸馏掉溶剂,得到纯度99%的264.74g结晶固体,相当于理论值的99%。
1H NMR(CDCl3):[ppm]=8.59(d,J=5.69Hz,1H),8.05(d,J=8.36Hz,1H),7.83(d,J=8.37Hz,1H),7.65(t,J=8.03Hz,1H),7.12(d,J=5.62Hz,1H),7.46(mc,2H),7.42(d,J=8.7Hz,1H),7.17(mc,1H).
D:1-[3-氟代-2-(羧甲基)苯基]异喹啉
50.0g(0.224mol)1-(3-氟代苯基)异喹啉溶解在1000ml的THF中,在-78℃下逐滴地与134.4ml(0.336mol,1.50当量)的正丁基锂(己烷中2.5M)混合。在添加结束以后,在-78℃搅拌混合物另外3h,随后在-78℃通过管将红褐色锂有机物转移到190.8ml(2.47mol,11.0当量)的氯甲酸甲酯的2000mlTHF溶液中。在-78℃到-20℃下搅拌混合物另外18小时。利用外部冰冷却用乙醇骤冷反应溶液,并浓缩到三分之一体积。随后,反应溶液与300ml二氯甲烷混合,洗涤三次,每一次用100mlNH4Cl溶液和NaHCO3溶液和水洗涤,用硫酸镁干燥减压浓缩。从庚烷中结晶得到的高度粘性油。得到纯度为98%的44.68g结晶固体,相当于理论值的70.4%。
1H NMR(CDCl3):[ppm]=8.56(d,J=5.69Hz,1H),7.89(d,J=8.36Hz,1H),7.86(d,J=8.37Hz,1H),7.69(t,J=8.03Hz,1H),7.66(d,J=5.69Hz,1H),7.55(mc,2H),7.37(d,J=7.7Hz,1H),7.27(t,J=9.37Hz,1H),3.46(s,3H,OMe).
E:1-[2-(1-甲基-1-羟乙基)-3-氟代苯基]异喹啉
45.27g(0.16lmol)的1-[3-氟代-2-(羧甲基)苯基]异喹啉溶解在950mlTHF中,在-78℃逐滴地与185.12ml(0.370mol,2.3当量)的甲基锂(在二乙醚中2M)混合。在添加以后,在-78℃~-20℃下搅拌混合物18小时。利用冰冷却用甲醇随后骤冷反应混合物,并与500ml二氯甲烷混合。随后用100mlNaHCO3溶液和水洗涤混合物三次,用硫酸镁干燥减压浓缩。从600ml庚烷中结晶得到的固体。得到纯度为97.5%的29.72g白色固体,相当于理论值的65.8%。
1H NMR(DMSO-d6):[ppm]=8.42(d,J=5.5Hz,1H),7.84(d,J=8.25Hz,1H),7.65(t,J=7.79Hz),7.62(d(overlapping),J=6.24Hz,1H),7.60(d(overlapping),J=9.62Hz,1H),7.48(t,J=7.33Hz,1H),7.27(mc,1H),7.17(dd,J=12.38Hz,7.79Hz),6.96(d,J=7.79Hz),1.90(sbr.,1H,OH),1.67(s,3H,CH3),1.48(s,3H,CH3).
F:7,7-二甲基-8-氟代二苯并[de,h]喹啉
26.1g(92.82mmol)1-[2-(1-甲基-1-羟乙基)-3-氟代苯基]异喹啉在150℃加入到260ml的邻二氯苯和104.2ml的硫酸混合物中,搅拌60分钟。将反应溶液随后倒在1000ml冰上,利用冰冷却用固体NaOH小心调节pH=12。随后,用500ml二氯甲烷提取混合物,用硫酸镁干燥减压浓缩。粗制品溶解在100ml甲苯中,在50℃引入空气4小时。随后,用二氯甲烷通过柱色谱法实现纯化。得到纯度99.6%的18.45g固体,相当于理论值的75.5%。
1H NMR(CDCl3):[ppm]=8.74(d,J=8.03Hz,1H),8.56(d,J=5.69Hz,1H),7.66-7.77(m,3H),7.57(d,J=5.69Hz,1H),7.4(mc,1H),7.16(dd,J=12.71Hz,8.03Hz),1.86(s,6H,CH3).
G:面式-三[7,7-二甲基-8-氟代二苯并[de,h]喹啉-C2,N]铱(III)(Ir3)
15.13g(57.48mmol,5.93当量)7,7-二甲基-13-氟代二苯并[de,h]喹啉和4.69g(9.68mmol)Na[Ir(acac)2Cl2]溶解在180ml脱气乙二醇(光谱纯)中,在198℃氩气氛下搅拌48小时。随后反应溶液冷却到50℃,加入到350ml 50℃的乙醇/1N HCl脱气混合物中,气封搅拌60分钟。气封下抽吸过滤掉固体,在每一情况下用乙醇/1N HCl(350ml)、乙醇/水(1∶1,350ml)和乙醇(350ml)脱气混合物洗涤,减压干燥。得到的8.45g红色固体从甲苯/乙醇(16∶1)中再结晶。得到纯度99.5%的5.29g红色粉末,相当于理论值的56.4%。
1H NMR(CDCl3):[ppm]=7.96(d,J=7.69Hz,1H),7.88(t,J=7.7Hz,1H),7.82(d,J=7.7Hz,1H),7.57(d,J=6.36Hz,1H),7.43(d,J=6.36Hz,1H),6.76(dd,J=14.05Hz,8.03Hz,1H),6.57(dd,J=8.04Hz,5.36Hz,1H),1.80(s,3H),1.77(s,3H).
实施例4:合成面式三[7,7-二甲基-8-氟代-4-甲基二苯并[de,h]喹啉-C2,N]铱(III)(Ir4)
以类似3A-3G生产方法合成所述化合物Ir4,得到可比的产率和纯度。
1H NMR(吡啶-d5):[ppm]=7.68(d,J=7.7Hz,1H),7.58(d,J=6.69Hz,1H),7.50(d,J=7.69Hz,1H),7.39(dd,J=8.37Hz,5.96Hz,1H),7.12(d,J=6.36Hz,1H),6.97(dd,J=13.72Hz,8.36Hz,1H),2.38(s,3H,CH3),1.95(s,3H,CH3),1.90(s,3H,CH3).
实施例5:面式三[7,7-二甲基-8-氟代-4-甲基二苯并[de,h]喹啉-C2,N]铱(III)(Ir5)
A:1-(3-氟代-4-甲基苯基)异喹啉
首先加入500ml脱气的二噁烷,与10.0g(61.14mmol)的1-氯代异喹啉、18.8g(122.0mmol,2.0当量)的3-氟代-4-甲基苯硼酸和24.0g(73.66mmol,1.2当量)的Cs2CO3混合。反应混合物脱气10分钟,与1.25ml(5.49mmol,9mol%)的t-Bu3P和0.412g(1.83mmol,3mol%)Pd(OAc)2混合。在105℃搅拌混合物18h,随后与400ml二氯甲烷混合,用200ml NaHCO3溶液和水洗涤三次。随后,通过硅藻土过滤混合物,用硫酸镁干燥减压浓缩。用乙酸乙酯/庚烷(1∶5)使粘性油通过硅胶柱子。得到10.47g纯度99.5%的产品,相当于理论值的72.2%。
1H NMR(CDCl3):[ppm]=8.60(d,J=5.69Hz,1H),8.12(d,J=8.70Hz,1H),7.89(d,J=8.37Hz,1H),7.70(t,J=8.03Hz,1H)7.65(d,J=5.69Hz,1H),7.55(t,J=8.36Hz,1H),7.39-7.35(m,2H),7.34(t,J=8.03Hz,1H),2.40(s,3H,CH3).
B:面式-三[7,7-二甲基-8-氟代-4-甲基二苯并[de,h]喹啉-C2,N]铱(III)(Ir5)
类似3D-3G方法另外合成Ir5。得到的产品具有可比的产率和纯度。
1H NMR(DMSO-d6):[ppm]=7.73(d,J=4.86Hz,2H),7.62(t,J=4.69Hz,1H),7.40(d,J=6.36Hz,1H),7.19(d,J=6.36Hz,1H),6.52(d,J=7.69Hz,1H),2.11(s,3H,CH3),1.89(s,3H,CH3),1.81(s,3H,CH3).
实施例6:与Ir(piq)3热稳定性的对比
根据US2003/0068526合成Ir(piq)3。在高真空(p=10-7毫巴,T=385℃)下升华此处描述的2g粗制品得到,除HPLC测定的纯度99.7%的相当于Ir(piq)3的1.38g升华物之外,还有607mg含铱灰分。这因此显示出在与有创造性的化合物相同温度下升华时,约三分之一所述产品分解,而有创造性的化合物可以毫无损失全部地升华,如实施例1和2所见。
实施例7:包括有创造性的化合物Ir1的有机电致发光器件的制造和表征
有创造性的电致发光器件如在专利申请DE10330761.3中描述的那样制备。本发明中比较了两种不同OLEDs的结果。为了更好的可比较性,基本结构、使用材料、掺杂度和它们的层厚度相同。仅改变发光层中的掺杂物。第一实施例描述根据现有技术的比较标准,其中发射器层由基质材料CBP和客体材料Ir(piq)3组成。另外,描述了一种具有由宿主材料CBP和客体材料面式-三[7,7-二氟二苯并[de,h]喹啉-C2,N]铱(III)(Ir1根据实施例1合成)组成的发射器层的OLED。类似上述通常的方法,得到具有以下结构的OLEDs:
PEDOT 60纳米(从水中旋转涂敷;PEDOT从H.C.Starck Goslar购买;聚-[3,4-亚乙基二氧基-2,5-噻吩]),(HIL)
NaphDATA20纳米(通过气相沉积施加;从SynTec购买NaphDATA;4,4′,4″-三(N-1-萘基-N-苯基氨基)三苯胺),(HTL)
S-TAD 20纳米(通过气相沉积施加;根据WO99/12888制备S-TAD;2,2′,7,7′-四(二苯胺)螺二芴),(HTL)
发射器层:(EML)
CPB 20纳米(通过气相沉积施加;CPB从ALDRICH购买并进一步提纯,最后升华两次;4,4′-双-(N-咔唑基)二苯基)
Ir1(20%掺杂,通过气相沉积施加;根据实施例1合成)
或者:
Ir(piq)3(20%掺杂,通过气相沉积施加;根据实施例6合成)
BCP 10纳米(通过气相沉积施加;BCP从ABCR购买,以得到形式使用;2,9-二甲基-4,7-联苯基-1,10-菲绕啉),(HBL)
AlQ3 10纳米(通过气相沉积施加:AlQ3从SynTec购买;三(喹啉醇合)铝(III)),(ETL)
Ba-Al其上3纳米的Ba,150纳米的Al。
以标准方式表征还有待于优化的这些OLEDs;为了该目的,确定电致发光光谱、由电流-电压-明亮度特征(IUL特征)计算的作为明亮度函数的效率(以cd/A测定)和寿命。
电致发光光谱:
具有Ir(piq)3比较例的OLEDs和具有Ir1作为掺杂物的OLEDs都显示出具有可比彩色座标的红色发光。
作为明亮度函数的效率:
在上面描述的条件下,用掺杂物Ir(piq)3生产的OLEDs通常的最高效率为约6.5cd/A,对于基准亮度100cd/m2要求6.2V。相反,用所述有创造性的掺杂物Ir1生产的OLEDs显示出最高效率为8.7cd/A,对于基准亮度100cd/m2的需要的电压甚至下降到5.4V。
寿命对比:
为了更好的可比较性,在同一图中示意两条寿命曲线(图1)。所述图显示出按cd/m2计的明亮度随时间的变化。在80℃温度及10mA/cm2的恒定电流密度下进行测量,这相应于加速测量。所述寿命指到达50%起始亮度之后的时间。在示意的明亮度下,对于掺杂物Ir(piq)3起始明亮度为约650cd/m2的寿命为约130h。对于掺杂物Ir1,起始明亮度为约900cd/m2,在80℃相同电流密度下寿命大于5000h,这相应于与具有Ir(piq)3用作掺杂物的OLEDs相比所述寿命增加到几乎是其40倍。
实施例8-11:具有有创造性掺杂物的另外的器件例子
所述另外的有创造性的掺杂物Ir2到Ir5同样在OLEDs中试验,并与现有技术(实施例8)的Ir(piq)3相比较。类似于实施例7中详述的方法,得到具有以下结构的OLEDs:
PEDOT 60纳米(从水中旋转涂敷;PEDOT从H.C.Starck Goslar购买;聚-[3,4-亚乙基二氧基-2,5-噻吩]),(HIL)
NaphDATA20纳米(通过汽相淀积施加;从SynTec购买NaphDATA;4,4′,4″-三(N-1-萘基-N-苯基氨基)三苯胺),(HTL)
S-TAD 20纳米(通过气相沉积施加;根据WO99/12888合成S-TAD;2,2′,7,7′-四(二苯胺)螺二芴),(HTL)
发射器层::(EML)
M1双(9,9’-螺二芴-2-基)酮(通过气相沉积施加,根据DE10317556.3合成)
Ir2到Ir5(通过气相沉积施加;根据实施例2-5合成)
或者:
Ir(piq)3(通过气相沉积施加;根据实施例6合成)
HBM12,7-双(4-二苯基-1-基)-2’,7’-二叔丁基-螺-9,9’-二芴(通过气相沉积施加,根据DE 10357317.8合成),(HBL);没有用于所有的例子
AlQ3(通过气相沉积施加;从SynTec购买AlQ3;三(喹啉醇合)铝(III)),(ETL);未在所有的实施例中使用
Ba-Al其上3纳米的Ba,150纳米的Al。
选择层厚度以使发光层、空穴阻挡层和电子传递层的总的层厚度通常加在一起高达一共60nm。用这些OLEDs得到的结果收集在表1中。为清楚起见以下描述基质材料M1,空穴阻挡材料HBM1和所述对比的掺杂物Ir(piq)3:
Claims (11)
1.一种通式(1)的化合物:
M(L)n(L′)m(L″)o
通式(1)
其包含如通式(2b)所示的结构部分M(L)n,
通式(2b)
其中使用的符号和标记是:
M是Ir;
Y在每一情况下是相同或者不同的,是CR2;
D是N;
X在每一情况下是相同或者不同的,是CR;
R在每一情况下相同或者不同,是H,F,具有1-20个碳原子的直链、支链或环状的烷基,其中一个或多个氢原子可以被F替代,或者是具有1-14个碳原子并可被一个或多个非芳香性的R基团取代的芳基或杂芳基;
n是1、2或者3;
在通式(1)中的配位体L′和L″是单阴离子、双齿螯合配位体,和m和o在每一情况下是相同或者不同的是0、1或者2。
3.如权利要求1或2所述的化合物,特征在于符号n=2或者3。
4.如权利要求1至3中任一项所述的化合物,特征在于R是:
R在每一情况下是相同或者不同的,是H,F,具有1-4个碳原子的直链、支链或者环状的烷基,其中一个或多个氢原子可以被F替代,或者是具有1-6个碳原子的并可以被一个或多个非芳香性的R基团取代的芳基或者杂芳基。
5.如权利要求1至4中任一项所述的化合物,特征在于Y是螺碳原子。
8.一种制备权利要求1至5中任一项所述的化合物的方法,其通过使如权利要求6所述的通式(4b)的化合物与带有卤根和酮酮酸盐基团二者的铱化合物反应而完成。
9.如权利要求1至5中任一项所述的化合物在电子元件中的用途。
10.一种电子元件,其包括至少一种如权利要求1至5中任一项所述的化合物。
11.如权利要求10所述的电子元件,特征在于该电子元件是有机发光二极管、有机集成电路、有机场效应晶体管、有机薄膜晶体管、有机太阳能电池或有机激光器二极管。
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10345572.8 | 2003-09-29 | ||
DE10345572A DE10345572A1 (de) | 2003-09-29 | 2003-09-29 | Metallkomplexe |
Related Parent Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2004800282500A Division CN1860202A (zh) | 2003-09-29 | 2004-09-28 | 金属络合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN102627671A true CN102627671A (zh) | 2012-08-08 |
CN102627671B CN102627671B (zh) | 2015-05-06 |
Family
ID=34399135
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201210043328.2A Expired - Fee Related CN102627671B (zh) | 2003-09-29 | 2004-09-28 | 金属络合物 |
CNA2004800282500A Pending CN1860202A (zh) | 2003-09-29 | 2004-09-28 | 金属络合物 |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNA2004800282500A Pending CN1860202A (zh) | 2003-09-29 | 2004-09-28 | 金属络合物 |
Country Status (8)
Country | Link |
---|---|
US (2) | US7820822B2 (zh) |
EP (1) | EP1675929B1 (zh) |
JP (1) | JP5329041B2 (zh) |
KR (1) | KR101172336B1 (zh) |
CN (2) | CN102627671B (zh) |
AT (1) | ATE513889T1 (zh) |
DE (1) | DE10345572A1 (zh) |
WO (1) | WO2005033244A1 (zh) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106795428A (zh) * | 2014-04-03 | 2017-05-31 | 港大科桥有限公司 | 用于oled应用的铂(ii)发射体 |
CN108570074A (zh) * | 2017-03-08 | 2018-09-25 | 环球展览公司 | 有机电致发光材料和装置 |
CN116178447A (zh) * | 2023-01-10 | 2023-05-30 | 广西师范大学 | 氧化异阿朴菲生物碱的多吡啶类金属有机钌配合物及其合成方法和应用 |
Families Citing this family (509)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE602004008104T2 (de) * | 2003-11-18 | 2008-04-24 | Philips Intellectual Property & Standards Gmbh | Lichtemittierende vorrichtung mit iridiumkomplex |
WO2005053051A1 (de) | 2003-11-25 | 2005-06-09 | Merck Patent Gmbh | Organisches elektrolumineszenzelement |
US7430222B2 (en) * | 2004-02-27 | 2008-09-30 | Microsoft Corporation | Media stream splicer |
DE102004032527A1 (de) * | 2004-07-06 | 2006-02-02 | Covion Organic Semiconductors Gmbh | Elektrolumineszierende Polymere |
DE102005022903A1 (de) * | 2005-05-18 | 2006-11-23 | Merck Patent Gmbh | Lösungen organischer Halbleiter |
DE102005043165A1 (de) * | 2005-09-12 | 2007-03-22 | Merck Patent Gmbh | Metallkomplexe |
DE102005057963A1 (de) * | 2005-12-05 | 2007-06-06 | Merck Patent Gmbh | Verfahren zur Herstellung ortho-metallierter Metallverbindungen |
DE102007002714A1 (de) | 2007-01-18 | 2008-07-31 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
US20130032785A1 (en) * | 2011-08-01 | 2013-02-07 | Universal Display Corporation | Materials for organic light emitting diode |
JP2008231042A (ja) * | 2007-03-22 | 2008-10-02 | Sumitomo Chemical Co Ltd | イソキノリン系化合物及びその製造方法 |
DE102007028858A1 (de) | 2007-06-22 | 2009-01-02 | Wincor Nixdorf International Gmbh | Wertscheinautomat |
DE102007053771A1 (de) | 2007-11-12 | 2009-05-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
JP5050813B2 (ja) * | 2007-11-29 | 2012-10-17 | ソニー株式会社 | メモリセル |
DE102008015526B4 (de) | 2008-03-25 | 2021-11-11 | Merck Patent Gmbh | Metallkomplexe |
DE102008017591A1 (de) | 2008-04-07 | 2009-10-08 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102008027005A1 (de) * | 2008-06-05 | 2009-12-10 | Merck Patent Gmbh | Organische elektronische Vorrichtung enthaltend Metallkomplexe |
JP5609022B2 (ja) * | 2008-06-23 | 2014-10-22 | 住友化学株式会社 | 金属錯体の残基を含む高分子化合物及びそれを用いた素子 |
DE102008033943A1 (de) | 2008-07-18 | 2010-01-21 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102008036982A1 (de) | 2008-08-08 | 2010-02-11 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102008050841B4 (de) | 2008-10-08 | 2019-08-01 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
DE102008056688A1 (de) | 2008-11-11 | 2010-05-12 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
KR20110097612A (ko) | 2008-11-11 | 2011-08-31 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자 |
DE102009022858A1 (de) | 2009-05-27 | 2011-12-15 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
DE102008063490B4 (de) | 2008-12-17 | 2023-06-15 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung und Verfahren zum Einstellen des Farbortes einer weiß emittierenden Elektrolumineszenzvorrichtung |
DE102008063470A1 (de) | 2008-12-17 | 2010-07-01 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102009005290A1 (de) | 2009-01-20 | 2010-07-22 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
DE102009009277B4 (de) | 2009-02-17 | 2023-12-07 | Merck Patent Gmbh | Organische elektronische Vorrichtung, Verfahren zu deren Herstellung und Verwendung von Verbindungen |
DE102009011223A1 (de) | 2009-03-02 | 2010-09-23 | Merck Patent Gmbh | Metallkomplexe |
DE102009012346B4 (de) | 2009-03-09 | 2024-02-15 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung und Verfahren zu deren Herstellung |
DE102009013041A1 (de) * | 2009-03-13 | 2010-09-16 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
US8709615B2 (en) * | 2011-07-28 | 2014-04-29 | Universal Display Corporation | Heteroleptic iridium complexes as dopants |
DE102009014513A1 (de) | 2009-03-23 | 2010-09-30 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102009017064A1 (de) | 2009-04-09 | 2010-10-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102009023154A1 (de) | 2009-05-29 | 2011-06-16 | Merck Patent Gmbh | Zusammensetzung, enthaltend mindestens eine Emitterverbindung und mindestens ein Polymer mit konjugationsunterbrechenden Einheiten |
DE102009023156A1 (de) | 2009-05-29 | 2010-12-02 | Merck Patent Gmbh | Polymere, die substituierte Indenofluorenderivate als Struktureinheit enthalten, Verfahren zu deren Herstellung sowie deren Verwendung |
WO2010149259A2 (en) | 2009-06-22 | 2010-12-29 | Merck Patent Gmbh | Conducting formulation |
DE102009031021A1 (de) | 2009-06-30 | 2011-01-05 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102009032922B4 (de) | 2009-07-14 | 2024-04-25 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen, Verfahren zu deren Herstellung, deren Verwendung sowie elektronische Vorrichtung |
US8581262B2 (en) | 2009-08-04 | 2013-11-12 | Merck Patent Gmbh | Electronic devices comprising multi cyclic hydrocarbons |
US8455602B2 (en) * | 2009-08-24 | 2013-06-04 | University Of The Witwatersrand, Johannesburg | Supramolecular functional materials |
US8993754B2 (en) | 2009-08-27 | 2015-03-31 | National Institute Of Advanced Industrial Science And Technology | Iridium complex and light emitting material formed from same |
WO2011024761A1 (ja) | 2009-08-27 | 2011-03-03 | 住友化学株式会社 | 金属錯体組成物及び錯体高分子 |
DE102009053644B4 (de) | 2009-11-17 | 2019-07-04 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102009053645A1 (de) | 2009-11-17 | 2011-05-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtung |
DE102009041289A1 (de) | 2009-09-16 | 2011-03-17 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
JP5784608B2 (ja) | 2009-09-16 | 2015-09-24 | メルク パテント ゲーエムベーハー | 電子素子製造のための調合物 |
DE102009048791A1 (de) | 2009-10-08 | 2011-04-14 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102009052428A1 (de) | 2009-11-10 | 2011-05-12 | Merck Patent Gmbh | Verbindung für elektronische Vorrichtungen |
DE102009053382A1 (de) | 2009-11-14 | 2011-05-19 | Merck Patent Gmbh | Materialien für elektronische Vorrichtungen |
DE102009053836A1 (de) | 2009-11-18 | 2011-05-26 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
JP5723292B2 (ja) * | 2009-11-30 | 2015-05-27 | 三星電子株式会社Samsung Electronics Co.,Ltd. | イリジウム錯体化合物、有機エレクトロルミネッセンス素子およびその用途 |
EP2517275B1 (en) | 2009-12-22 | 2018-11-07 | Merck Patent GmbH | Formulations comprising phase-separated functional materials |
WO2011076314A1 (en) | 2009-12-22 | 2011-06-30 | Merck Patent Gmbh | Electroluminescent formulations |
JP5897472B2 (ja) | 2009-12-22 | 2016-03-30 | メルク パテント ゲーエムベーハー | エレクトロルミネセンス機能性界面活性剤 |
KR20120115338A (ko) | 2009-12-23 | 2012-10-17 | 메르크 파텐트 게엠베하 | 중합체성 결합제를 포함하는 조성물 |
WO2011076324A1 (en) | 2009-12-23 | 2011-06-30 | Merck Patent Gmbh | Compositions comprising organic semiconducting compounds |
DE102010004803A1 (de) | 2010-01-16 | 2011-07-21 | Merck Patent GmbH, 64293 | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010005697A1 (de) | 2010-01-25 | 2011-07-28 | Merck Patent GmbH, 64293 | Verbindungen für elektronische Vorrichtungen |
DE102010006377A1 (de) | 2010-01-29 | 2011-08-04 | Merck Patent GmbH, 64293 | Styrolbasierte Copolymere, insbesondere für die Anwendung in optoelektronischen Bauteilen |
DE102010009193B4 (de) | 2010-02-24 | 2022-05-19 | MERCK Patent Gesellschaft mit beschränkter Haftung | Zusammensetzung enthaltend Fluor-Fluor Assoziate, Verfahren zu deren Herstellung, deren Verwendung sowie organische elektronische Vorrichtung diese enthaltend |
DE102010009903A1 (de) | 2010-03-02 | 2011-09-08 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
DE102010010481A1 (de) | 2010-03-06 | 2011-09-08 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
JP6246468B2 (ja) | 2010-03-11 | 2017-12-13 | メルク パテント ゲーエムベーハー | 治療および化粧品におけるファイバー |
JP2013522816A (ja) | 2010-03-11 | 2013-06-13 | メルク パテント ゲーエムベーハー | 発光ファイバー |
CN102812573B (zh) | 2010-03-23 | 2015-09-30 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
DE102010012738A1 (de) | 2010-03-25 | 2011-09-29 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010013068A1 (de) | 2010-03-26 | 2011-09-29 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
KR101896723B1 (ko) | 2010-04-12 | 2018-09-07 | 메르크 파텐트 게엠베하 | 유기 전자 소자 제조용 조성물 및 방법 |
EP2559078A1 (en) | 2010-04-12 | 2013-02-20 | Merck Patent GmbH | Composition having improved performance |
DE102010014933A1 (de) | 2010-04-14 | 2011-10-20 | Merck Patent Gmbh | Materialien für elektronische Vorrichtungen |
DE102010018321A1 (de) | 2010-04-27 | 2011-10-27 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
CN105949177B (zh) | 2010-05-03 | 2019-02-01 | 默克专利有限公司 | 制剂和电子器件 |
DE102010019306B4 (de) | 2010-05-04 | 2021-05-20 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
DE102010020044A1 (de) | 2010-05-11 | 2011-11-17 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
WO2011147521A1 (en) | 2010-05-27 | 2011-12-01 | Merck Patent Gmbh | Down conversion |
US10190043B2 (en) | 2010-05-27 | 2019-01-29 | Merck Patent Gmbh | Compositions comprising quantum dots |
SG185680A1 (en) | 2010-05-27 | 2012-12-28 | Merck Patent Gmbh | Formulation and method for preparation of organic electronic devices |
DE102010024335A1 (de) | 2010-06-18 | 2011-12-22 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
DE102010024542A1 (de) | 2010-06-22 | 2011-12-22 | Merck Patent Gmbh | Materialien für elektronische Vorrichtungen |
DE102010024897A1 (de) | 2010-06-24 | 2011-12-29 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
KR101201721B1 (ko) * | 2010-07-14 | 2012-11-15 | 삼성디스플레이 주식회사 | 금속 착체 화합물 및 이를 포함하는 유기 발광 장치 |
JP2013539584A (ja) | 2010-07-26 | 2013-10-24 | メルク パテント ゲーエムベーハー | 量子ドットおよびホスト |
US20130226268A1 (en) | 2010-07-26 | 2013-08-29 | Merck Patent Gmbh | Nanocrystals in devices |
KR101877582B1 (ko) | 2010-07-30 | 2018-07-12 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스 |
DE102010033080A1 (de) | 2010-08-02 | 2012-02-02 | Merck Patent Gmbh | Polymere mit Struktureinheiten, die Elektronen-Transport-Eigenschaften aufweisen |
DE102010033548A1 (de) | 2010-08-05 | 2012-02-09 | Merck Patent Gmbh | Materialien für elektronische Vorrichtungen |
DE102010045369A1 (de) | 2010-09-14 | 2012-03-15 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010045405A1 (de) | 2010-09-15 | 2012-03-15 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010046412B4 (de) * | 2010-09-23 | 2022-01-13 | Merck Patent Gmbh | Metall-Ligand Koordinationsverbindungen |
DE102010048074A1 (de) | 2010-10-09 | 2012-04-12 | Merck Patent Gmbh | Materialien für elektronische Vorrichtungen |
DE102010048497A1 (de) | 2010-10-14 | 2012-04-19 | Merck Patent Gmbh | Formulierungen für organische Elektrolumineszenzvorrichtungen |
DE102010048498A1 (de) | 2010-10-14 | 2012-04-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010048608A1 (de) | 2010-10-15 | 2012-04-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
DE102010048607A1 (de) | 2010-10-15 | 2012-04-19 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
WO2012069121A1 (de) | 2010-11-24 | 2012-05-31 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
DE102010054316A1 (de) | 2010-12-13 | 2012-06-14 | Merck Patent Gmbh | Substituierte Tetraarylbenzole |
DE102010054525A1 (de) | 2010-12-15 | 2012-04-26 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102010055901A1 (de) | 2010-12-23 | 2012-06-28 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102010055902A1 (de) | 2010-12-23 | 2012-06-28 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtung |
DE102010056151A1 (de) | 2010-12-28 | 2012-06-28 | Merck Patent Gmbh | Materiallen für organische Elektrolumineszenzvorrichtungen |
WO2012095143A1 (de) | 2011-01-13 | 2012-07-19 | Merck Patent Gmbh | Verbindungen für organische elektrolumineszenzvorrichtungen |
DE102012000064A1 (de) | 2011-01-21 | 2012-07-26 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
US8751777B2 (en) | 2011-01-28 | 2014-06-10 | Honeywell International Inc. | Methods and reconfigurable systems to optimize the performance of a condition based health maintenance system |
DE102011010841A1 (de) | 2011-02-10 | 2012-08-16 | Merck Patent Gmbh | (1,3)-Dioxan-5-on-Verbindungen |
DE102011011104A1 (de) | 2011-02-12 | 2012-08-16 | Merck Patent Gmbh | Substituierte Dibenzonaphtacene |
US9492681B2 (en) | 2011-02-14 | 2016-11-15 | Merck Patent Gmbh | Device and method for treatment of cells and cell tissue |
DE102011011539A1 (de) | 2011-02-17 | 2012-08-23 | Merck Patent Gmbh | Verbindungen für elektronische Vorrichtungen |
WO2012126566A1 (en) | 2011-03-24 | 2012-09-27 | Merck Patent Gmbh | Organic ionic functional materials |
EP2695213B1 (de) | 2011-04-05 | 2019-11-13 | Merck Patent GmbH | Organische elektrolumineszenzvorrichtung |
US9876171B2 (en) | 2011-04-13 | 2018-01-23 | Merck Patent Gmbh | Materials for electronic devices |
WO2012139693A1 (de) | 2011-04-13 | 2012-10-18 | Merck Patent Gmbh | Verbindungen für elektronische vorrichtungen |
US9735371B2 (en) | 2011-04-18 | 2017-08-15 | Merck Patent Gmbh | Compounds for electronic devices |
KR101979469B1 (ko) | 2011-04-18 | 2019-05-16 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
WO2012149992A1 (de) | 2011-05-04 | 2012-11-08 | Merck Patent Gmbh | Vorrichtung zur aufbewahrung von frischwaren |
EP2705552B1 (de) | 2011-05-05 | 2015-03-04 | Merck Patent GmbH | Verbindungen für elektronische vorrichtungen |
CN103503188B (zh) | 2011-05-05 | 2016-08-31 | 默克专利有限公司 | 用于电子器件的化合物 |
JP6223961B2 (ja) | 2011-05-12 | 2017-11-01 | メルク パテント ゲーエムベーハー | 有機イオン性機能材料、組成物および電子素子 |
DE102011102586A1 (de) | 2011-05-27 | 2012-11-29 | Merck Patent Gmbh | Organische elektronische Vorrichtung |
US9118022B2 (en) | 2011-06-03 | 2015-08-25 | Merck Patent Gmbh | Organic electroluminescent device |
DE102011104745A1 (de) | 2011-06-17 | 2012-12-20 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
EP2737553A1 (en) | 2011-07-25 | 2014-06-04 | Merck Patent GmbH | Copolymers with functionalized side chains |
US9780311B2 (en) | 2011-07-29 | 2017-10-03 | Merck Patent Gmbh | Compounds for electronic devices |
EP2740165B1 (de) | 2011-08-03 | 2018-11-07 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
DE102012016192A1 (de) | 2011-08-19 | 2013-02-21 | Merck Patent Gmbh | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
SG11201400709VA (en) | 2011-09-21 | 2014-06-27 | Merck Patent Gmbh | Carbazole derivatives for organic electroluminescence devices |
CN103858249B (zh) | 2011-10-06 | 2017-10-17 | 默克专利有限公司 | 有机电致发光器件 |
DE102011116165A1 (de) | 2011-10-14 | 2013-04-18 | Merck Patent Gmbh | Benzodioxepin-3-on-Verbindungen |
KR102059793B1 (ko) | 2011-10-20 | 2019-12-27 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
WO2013060418A1 (en) | 2011-10-27 | 2013-05-02 | Merck Patent Gmbh | Materials for electronic devices |
DE102011117422A1 (de) | 2011-10-28 | 2013-05-02 | Merck Patent Gmbh | Hyperverzweigte Polymere, Verfahren zu deren Herstellung sowie deren Verwendung in elektronischen Vorrichtungen |
EP2773721B1 (de) | 2011-11-01 | 2015-11-25 | Merck Patent GmbH | Organische elektrolumineszenzvorrichtung |
KR102115018B1 (ko) | 2011-11-17 | 2020-05-26 | 메르크 파텐트 게엠베하 | 스피로디히드로아크리딘 유도체 및 이의 유기 전계발광 소자용 재료로서의 용도 |
TWI606051B (zh) | 2011-11-22 | 2017-11-21 | Udc愛爾蘭有限公司 | 有機電場發光元件、有機電場發光元件用材料以及使用該元件之發光裝置、顯示裝置、照明裝置及用於該元件之化合物 |
KR101921896B1 (ko) | 2011-12-12 | 2018-11-26 | 메르크 파텐트 게엠베하 | 전자 소자용 화합물 |
DE102012022880A1 (de) | 2011-12-22 | 2013-06-27 | Merck Patent Gmbh | Elektronische Vorrichtungen enthaltend organische Schichten |
JP6271442B2 (ja) | 2012-01-30 | 2018-01-31 | メルク パテント ゲーエムベーハー | ファイバー上のナノ結晶 |
KR102015765B1 (ko) | 2012-02-14 | 2019-10-21 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 스피로비플루오렌 화합물 |
KR20210068605A (ko) | 2012-03-15 | 2021-06-09 | 메르크 파텐트 게엠베하 | 전자 소자 |
WO2013139431A1 (de) | 2012-03-23 | 2013-09-26 | Merck Patent Gmbh | 9,9'-spirobixanthenderivate für elektrolumineszenzvorrichtungen |
JP6324948B2 (ja) | 2012-05-24 | 2018-05-16 | メルク パテント ゲーエムベーハー | 縮合複素環式芳香族環を含む金属錯体 |
DE102012011335A1 (de) | 2012-06-06 | 2013-12-12 | Merck Patent Gmbh | Verbindungen für Organische Elekronische Vorrichtungen |
EP2872589B1 (de) | 2012-07-10 | 2017-07-26 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
KR102006621B1 (ko) | 2012-07-23 | 2019-08-02 | 메르크 파텐트 게엠베하 | 화합물 및 유기 전계 발광 디바이스 |
EP3424907A3 (de) | 2012-07-23 | 2019-02-13 | Merck Patent GmbH | Verbindungen und organische elektronische vorrichtungen |
KR102104855B1 (ko) | 2012-07-23 | 2020-04-27 | 메르크 파텐트 게엠베하 | 2-디아릴아미노플루오렌의 유도체 및 이를 함유하는 유기 전자 화합물 |
WO2014015931A1 (de) | 2012-07-23 | 2014-01-30 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
US20150243897A1 (en) | 2012-08-10 | 2015-08-27 | Merck Patent Gmbh | Materials for organic electroluminescence devices |
KR102184852B1 (ko) | 2012-09-18 | 2020-12-01 | 메르크 파텐트 게엠베하 | 전자 소자용 물질 |
WO2014056567A1 (de) | 2012-10-11 | 2014-04-17 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
EP3806176A1 (de) | 2012-10-31 | 2021-04-14 | Merck Patent GmbH | Elektronische vorrichtung |
WO2014072017A1 (de) | 2012-11-12 | 2014-05-15 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
WO2014079532A1 (de) | 2012-11-20 | 2014-05-30 | Merck Patent Gmbh | Formulierung in hochreinem l?sungsmittel zur herstellung elektronischer vorrichtungen |
WO2014082705A1 (de) | 2012-11-30 | 2014-06-05 | Merck Patent Gmbh | Elektronische vorrichtung |
WO2014086454A1 (de) | 2012-12-05 | 2014-06-12 | Merck Patent Gmbh | Elektronische vorrichtung mit sauerstoffionenpumpe |
JP2016513357A (ja) | 2012-12-28 | 2016-05-12 | メルク パテント ゲーエムベーハー | ポリマー有機半導体化合物を含む組成物 |
JP2016506414A (ja) | 2013-01-03 | 2016-03-03 | メルク パテント ゲーエムベーハー | 電子素子のための材料 |
JP6367230B2 (ja) | 2013-01-03 | 2018-08-01 | メルク パテント ゲーエムベーハー | 電子素子 |
EP2941472B1 (de) | 2013-01-03 | 2018-07-25 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
KR102238849B1 (ko) | 2013-07-29 | 2021-04-09 | 메르크 파텐트 게엠베하 | 전기광학 소자 및 이의 용도 |
WO2015014429A1 (de) | 2013-07-29 | 2015-02-05 | Merck Patent Gmbh | Elekrolumineszenzvorrichtung |
CN105408448B (zh) | 2013-07-30 | 2018-11-02 | 默克专利有限公司 | 用于电子器件的材料 |
KR102363484B1 (ko) | 2013-07-30 | 2022-02-15 | 메르크 파텐트 게엠베하 | 전자 소자용 물질 |
JP6509855B2 (ja) | 2013-08-13 | 2019-05-08 | メルク パテント ゲーエムベーハー | 真空精製方法 |
EP3052505B1 (de) | 2013-10-02 | 2021-06-23 | Merck Patent GmbH | Borenthaltende verbindungen |
KR20240005971A (ko) | 2013-12-06 | 2024-01-12 | 메르크 파텐트 게엠베하 | 화합물 및 유기 전자 소자 |
WO2015082037A1 (en) | 2013-12-06 | 2015-06-11 | Merck Patent Gmbh | Compositions containing a polymeric binder which comprises acrylic and/or methacrylic acid ester units |
CN105793246B (zh) | 2013-12-06 | 2019-07-05 | 默克专利有限公司 | 取代的氧杂环庚三烯 |
US10158083B2 (en) | 2013-12-12 | 2018-12-18 | Merck Patent Gmbh | Materials for electronic devices |
CN112898254A (zh) | 2013-12-19 | 2021-06-04 | 默克专利有限公司 | 杂环螺环化合物 |
US9859504B2 (en) | 2014-03-31 | 2018-01-02 | Commonwealth Scientific And Industrial Research Organisation | Diamine compounds for phosphorescent diazaborole metal complexes and electroluminescent devices |
US9768397B2 (en) * | 2014-03-31 | 2017-09-19 | Commonwealth Scientific And Industrial Research Organisation | Phenylenediamine compounds for phosphorescent diazaborole metal complexes |
WO2015165563A1 (de) | 2014-04-30 | 2015-11-05 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
CN106459018B (zh) | 2014-05-05 | 2022-01-25 | 默克专利有限公司 | 用于有机发光器件的材料 |
DE102014008722B4 (de) | 2014-06-18 | 2024-08-22 | Merck Patent Gmbh | Zusammensetzungen für elektronische Vorrichtungen, Formulierung diese enthaltend, Verwendung der Zusammensetzung, Verwendung der Formulierung sowie organische elektronische Vorrichtung enthaltend die Zusammensetzung |
WO2015197156A1 (de) | 2014-06-25 | 2015-12-30 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
KR102388865B1 (ko) | 2014-09-05 | 2022-04-20 | 메르크 파텐트 게엠베하 | 제형 및 전자 소자 |
CN107108500A (zh) | 2014-11-11 | 2017-08-29 | 默克专利有限公司 | 有机电致发光器件的材料 |
EP3229288B1 (en) | 2014-12-04 | 2019-05-01 | Guangzhou Chinaray Optoelectronic Materials Ltd. | Polymer, and mixture, formulation and organic electronic device containing the same, and monomer thereof |
WO2016086885A1 (zh) | 2014-12-04 | 2016-06-09 | 广州华睿光电材料有限公司 | 氘化的有机化合物、包含该化合物的混合物、组合物及有机电子器件 |
WO2016091219A1 (zh) | 2014-12-11 | 2016-06-16 | 广州华睿光电材料有限公司 | 有机化合物、包含其的混合物、组合物和有机电子器件 |
EP3241248A1 (de) | 2014-12-30 | 2017-11-08 | Merck Patent GmbH | Formulierungen und elektronische vorrichtungen |
CN107108862B (zh) | 2015-01-13 | 2019-08-02 | 广州华睿光电材料有限公司 | 含乙炔基交联基团的共轭聚合物、包含其的混合物、组合物、有机电子器件及其应用 |
US20180006237A1 (en) | 2015-01-30 | 2018-01-04 | Merck Patent Gmbh | Materials for electronic devices |
US10916705B2 (en) | 2015-01-30 | 2021-02-09 | Merck Patent Gmbh | Formulations with a low particle content |
US9929361B2 (en) | 2015-02-16 | 2018-03-27 | Universal Display Corporation | Organic electroluminescent materials and devices |
US11056657B2 (en) | 2015-02-27 | 2021-07-06 | University Display Corporation | Organic electroluminescent materials and devices |
WO2016155866A1 (en) | 2015-03-30 | 2016-10-06 | Merck Patent Gmbh | Formulation of an organic functional material comprising a siloxane solvent |
US9859510B2 (en) | 2015-05-15 | 2018-01-02 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR102610370B1 (ko) | 2015-05-18 | 2023-12-05 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 물질 |
US10418568B2 (en) | 2015-06-01 | 2019-09-17 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR102543777B1 (ko) | 2015-06-10 | 2023-06-14 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
KR102654992B1 (ko) | 2015-06-12 | 2024-04-04 | 메르크 파텐트 게엠베하 | Oled 제제에 대한 용매로서 비-방향족 사이클을 함유하는 에스테르 |
US10873036B2 (en) | 2015-07-07 | 2020-12-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2017008883A1 (en) | 2015-07-15 | 2017-01-19 | Merck Patent Gmbh | Composition comprising organic semiconducting compounds |
WO2017012687A1 (en) | 2015-07-22 | 2017-01-26 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
KR102461250B1 (ko) * | 2015-07-27 | 2022-10-31 | 삼성전자주식회사 | 유기금속 화합물 및 이를 포함한 유기 발광 소자 |
US11127905B2 (en) | 2015-07-29 | 2021-09-21 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2017016630A1 (en) | 2015-07-30 | 2017-02-02 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
KR102486382B1 (ko) * | 2015-08-03 | 2023-01-09 | 삼성전자주식회사 | 유기금속 화합물 및 이를 포함한 유기 발광 소자 |
WO2017025166A1 (en) | 2015-08-13 | 2017-02-16 | Merck Patent Gmbh | Hexamethylindanes |
EP3334731B1 (en) | 2015-08-14 | 2021-03-03 | Merck Patent GmbH | Phenoxazine derivatives for organic electroluminescent devices |
EP3341448B1 (en) | 2015-08-28 | 2020-02-12 | Merck Patent GmbH | Compounds for electronic devices |
WO2017036572A1 (en) | 2015-08-28 | 2017-03-09 | Merck Patent Gmbh | Formulation of an organic functional material comprising an epoxy group containing solvent |
US10672996B2 (en) | 2015-09-03 | 2020-06-02 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP3368520B1 (en) | 2015-10-27 | 2023-04-26 | Merck Patent GmbH | Materials for organic electroluminescent devices |
WO2017080326A1 (zh) | 2015-11-12 | 2017-05-18 | 广州华睿光电材料有限公司 | 印刷组合物、包含其的电子器件及功能材料薄膜的制备方法 |
WO2017092545A1 (zh) | 2015-12-04 | 2017-06-08 | 广州华睿光电材料有限公司 | 一种金属有机配合物及其在电子器件中的应用 |
CN108368361A (zh) | 2015-12-10 | 2018-08-03 | 默克专利有限公司 | 含有包含非芳族环的酮的制剂 |
KR20180095854A (ko) | 2015-12-15 | 2018-08-28 | 메르크 파텐트 게엠베하 | 유기 전자 제형을 위한 용매로서의 방향족기를 함유하는 에스테르 |
WO2017102052A1 (en) | 2015-12-16 | 2017-06-22 | Merck Patent Gmbh | Formulations containing a solid solvent |
EP3390550B1 (en) | 2015-12-16 | 2022-09-28 | Merck Patent GmbH | Formulations containing a mixture of at least two different solvents |
US20190040034A1 (en) | 2016-02-05 | 2019-02-07 | Merck Patent Gmbh | Materials for electronic devices |
US20170229663A1 (en) | 2016-02-09 | 2017-08-10 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2017140404A1 (en) | 2016-02-17 | 2017-08-24 | Merck Patent Gmbh | Formulation of an organic functional material |
US10961230B2 (en) | 2016-03-03 | 2021-03-30 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
CN105693749A (zh) * | 2016-03-09 | 2016-06-22 | 中节能万润股份有限公司 | 一种含有吩噻嗪结构的有机光电材料及其应用 |
DE102016003104A1 (de) | 2016-03-15 | 2017-09-21 | Merck Patent Gmbh | Behälter umfassend eine Formulierung enthaltend mindestens einen organischen Halbleiter |
TWI745361B (zh) | 2016-03-17 | 2021-11-11 | 德商麥克專利有限公司 | 具有螺聯茀結構之化合物 |
KR20230010818A (ko) | 2016-04-11 | 2023-01-19 | 메르크 파텐트 게엠베하 | 디벤조푸란 및/또는 디벤조티오펜 구조를 포함하는 헤테로시클릭 화합물 |
US10236456B2 (en) | 2016-04-11 | 2019-03-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR102385482B1 (ko) | 2016-04-29 | 2022-04-12 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
JP7486921B2 (ja) | 2016-06-03 | 2024-05-20 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネッセントデバイス材料 |
KR20190019138A (ko) | 2016-06-16 | 2019-02-26 | 메르크 파텐트 게엠베하 | 유기 기능성 재료의 제형 |
EP3472249B1 (en) | 2016-06-17 | 2022-02-02 | Merck Patent GmbH | Formulation of an organic functional material |
US10862054B2 (en) | 2016-06-20 | 2020-12-08 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10672997B2 (en) | 2016-06-20 | 2020-06-02 | Universal Display Corporation | Organic electroluminescent materials and devices |
US11482683B2 (en) | 2016-06-20 | 2022-10-25 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW201815998A (zh) | 2016-06-28 | 2018-05-01 | 德商麥克專利有限公司 | 有機功能材料之調配物 |
WO2018007421A1 (en) | 2016-07-08 | 2018-01-11 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
JP6980757B2 (ja) | 2016-08-04 | 2021-12-15 | メルク パテント ゲーエムベーハー | 有機機能材料の調合物 |
EP3512848B1 (de) | 2016-09-14 | 2020-11-18 | Merck Patent GmbH | Verbindungen mit carbazol-strukturen |
EP3512841B1 (de) | 2016-09-14 | 2023-04-26 | Merck Patent GmbH | Verbindungen mit spirobifluoren-strukturen |
US10608186B2 (en) | 2016-09-14 | 2020-03-31 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10680187B2 (en) | 2016-09-23 | 2020-06-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
TWI766884B (zh) | 2016-09-30 | 2022-06-11 | 德商麥克專利有限公司 | 具有二氮雜二苯并呋喃或二氮雜二苯并噻吩結構的化合物、其製法及其用途 |
US20200028091A1 (en) | 2016-09-30 | 2020-01-23 | Merck Patent Gmbh | Carbazoles with diazadibenzofurane or diazadibenzothiophene structures |
US11196010B2 (en) | 2016-10-03 | 2021-12-07 | Universal Display Corporation | Organic electroluminescent materials and devices |
US11011709B2 (en) | 2016-10-07 | 2021-05-18 | Universal Display Corporation | Organic electroluminescent materials and devices |
TWI764942B (zh) | 2016-10-10 | 2022-05-21 | 德商麥克專利有限公司 | 電子裝置 |
DE102017008794A1 (de) | 2016-10-17 | 2018-04-19 | Merck Patent Gmbh | Materialien zur Verwendung in elektronischen Vorrichtungen |
KR102436600B1 (ko) | 2016-10-31 | 2022-08-25 | 메르크 파텐트 게엠베하 | 유기 기능성 재료의 제형 |
KR102451842B1 (ko) | 2016-10-31 | 2022-10-07 | 메르크 파텐트 게엠베하 | 유기 기능성 재료의 제형 |
KR102683884B1 (ko) | 2016-11-02 | 2024-07-11 | 메르크 파텐트 게엠베하 | 전자 소자용 재료 |
EP3538535A1 (en) | 2016-11-08 | 2019-09-18 | Merck Patent GmbH | Compounds for electronic devices |
KR102474328B1 (ko) | 2016-11-09 | 2022-12-06 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
US20180130956A1 (en) | 2016-11-09 | 2018-05-10 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10680188B2 (en) | 2016-11-11 | 2020-06-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
TWI756292B (zh) | 2016-11-14 | 2022-03-01 | 德商麥克專利有限公司 | 具有受體基團與供體基團之化合物 |
US20190352318A1 (en) | 2016-11-17 | 2019-11-21 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
TW201833118A (zh) | 2016-11-22 | 2018-09-16 | 德商麥克專利有限公司 | 用於電子裝置之材料 |
WO2018095381A1 (zh) | 2016-11-23 | 2018-05-31 | 广州华睿光电材料有限公司 | 印刷油墨组合物及其制备方法和用途 |
WO2018095388A1 (zh) | 2016-11-23 | 2018-05-31 | 广州华睿光电材料有限公司 | 有机化合物 |
CN109843837B (zh) | 2016-11-23 | 2022-03-18 | 广州华睿光电材料有限公司 | 含氮稠杂环的化合物及其应用 |
US20190378991A1 (en) | 2016-11-23 | 2019-12-12 | Guangzhou Chinaray Optoelectronic Materials Ltd. | Organic mixture, composition, and organic electronic component |
CN109791992B (zh) | 2016-11-23 | 2021-07-23 | 广州华睿光电材料有限公司 | 高聚物、包含其的混合物、组合物和有机电子器件以及用于聚合的单体 |
WO2018095397A1 (zh) | 2016-11-23 | 2018-05-31 | 广州华睿光电材料有限公司 | 含硼有机化合物及应用、有机混合物、有机电子器件 |
WO2018095379A1 (zh) | 2016-11-23 | 2018-05-31 | 广州华睿光电材料有限公司 | 金属有机配合物、高聚物、组合物及有机电子器件 |
TWI781123B (zh) | 2016-11-25 | 2022-10-21 | 德商麥克專利有限公司 | 用於有機電激發光裝置之材料 |
CN109963857A (zh) | 2016-11-25 | 2019-07-02 | 默克专利有限公司 | 作为用于有机电致发光器件(oled)的材料的双苯并呋喃稠合的2,8-二氨基茚并[1,2-b]芴衍生物和相关化合物 |
JP7127026B2 (ja) | 2016-11-30 | 2022-08-29 | 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 | バレロラクタム構造を有する化合物 |
US11466021B2 (en) | 2016-12-05 | 2022-10-11 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
TW201831468A (zh) | 2016-12-05 | 2018-09-01 | 德商麥克專利有限公司 | 含氮的雜環化合物 |
KR20190086028A (ko) | 2016-12-05 | 2019-07-19 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
TWI769198B (zh) | 2016-12-06 | 2022-07-01 | 德商麥克專利有限公司 | 電子裝置之製備方法 |
WO2018103744A1 (zh) | 2016-12-08 | 2018-06-14 | 广州华睿光电材料有限公司 | 混合物、组合物及有机电子器件 |
WO2018108109A1 (zh) * | 2016-12-13 | 2018-06-21 | 广州华睿光电材料有限公司 | 过渡金属配合物及其应用、混合物、有机电子器件 |
WO2018108760A1 (en) | 2016-12-13 | 2018-06-21 | Merck Patent Gmbh | Formulation of an organic functional material |
CN109790118A (zh) | 2016-12-13 | 2019-05-21 | 广州华睿光电材料有限公司 | 共轭聚合物及其在有机电子器件的应用 |
WO2018114744A1 (en) | 2016-12-20 | 2018-06-28 | Merck Patent Gmbh | A white light emitting solid state light source |
US11261291B2 (en) | 2016-12-22 | 2022-03-01 | Merck Patent Gmbh | Materials for electronic devices |
US20200098996A1 (en) | 2016-12-22 | 2020-03-26 | Merck Patent Gmbh | Mixtures comprising at least two organofunctional compounds |
CN109792003B (zh) | 2016-12-22 | 2020-10-16 | 广州华睿光电材料有限公司 | 基于狄尔斯-阿尔德反应的可交联聚合物及其在有机电子器件中的应用 |
WO2018113785A1 (zh) | 2016-12-22 | 2018-06-28 | 广州华睿光电材料有限公司 | 含呋喃交联基团的聚合物及其应用 |
EP3565816B1 (de) | 2017-01-04 | 2022-03-16 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
US11780865B2 (en) | 2017-01-09 | 2023-10-10 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP3571264B1 (en) | 2017-01-23 | 2021-11-24 | Merck Patent GmbH | Materials for organic electroluminescent devices |
CN110198936B (zh) | 2017-01-25 | 2024-03-12 | 默克专利有限公司 | 咔唑衍生物 |
CN110167940A (zh) | 2017-01-30 | 2019-08-23 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
TWI791481B (zh) | 2017-01-30 | 2023-02-11 | 德商麥克專利有限公司 | 形成有機電致發光(el)元件之方法 |
TWI763772B (zh) | 2017-01-30 | 2022-05-11 | 德商麥克專利有限公司 | 電子裝置之有機元件的形成方法 |
US20200013960A1 (en) | 2017-02-02 | 2020-01-09 | Merck Patent Gmbh | Materials for electronic devices |
TW201835075A (zh) | 2017-02-14 | 2018-10-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
CN110268544A (zh) | 2017-03-01 | 2019-09-20 | 默克专利有限公司 | 有机电致发光器件 |
CN110325524A (zh) | 2017-03-02 | 2019-10-11 | 默克专利有限公司 | 用于有机电子器件的材料 |
TW201843143A (zh) | 2017-03-13 | 2018-12-16 | 德商麥克專利有限公司 | 含有芳基胺結構之化合物 |
EP3596066B1 (de) | 2017-03-15 | 2022-05-18 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
US10844085B2 (en) | 2017-03-29 | 2020-11-24 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2018178136A1 (en) | 2017-03-31 | 2018-10-04 | Merck Patent Gmbh | Printing method for an organic light emitting diode (oled) |
KR102632027B1 (ko) | 2017-04-10 | 2024-01-31 | 메르크 파텐트 게엠베하 | 유기 기능성 재료의 제형 |
JP2020522876A (ja) | 2017-04-13 | 2020-07-30 | メルク パテント ゲーエムベーハー | 有機電子デバイス用組成物 |
US11649249B2 (en) | 2017-04-25 | 2023-05-16 | Merck Patent Gmbh | Compounds for electronic devices |
WO2018202603A1 (en) | 2017-05-03 | 2018-11-08 | Merck Patent Gmbh | Formulation of an organic functional material |
KR102592390B1 (ko) | 2017-05-11 | 2023-10-20 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 카르바졸계 바디피스 |
KR102592391B1 (ko) | 2017-05-11 | 2023-10-20 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 유기붕소 착물 |
US10944060B2 (en) | 2017-05-11 | 2021-03-09 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2018215318A1 (de) | 2017-05-22 | 2018-11-29 | Merck Patent Gmbh | Hexazyklische heteroaromatische verbindungen für elektronische vorrichtungen |
TW201920343A (zh) | 2017-06-21 | 2019-06-01 | 德商麥克專利有限公司 | 電子裝置用材料 |
CN109111486A (zh) | 2017-06-23 | 2019-01-01 | 环球展览公司 | 有机电致发光材料和装置 |
KR20200020841A (ko) | 2017-06-23 | 2020-02-26 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
CN110770363A (zh) | 2017-06-26 | 2020-02-07 | 默克专利有限公司 | 均质混合物 |
JP7317725B2 (ja) | 2017-06-28 | 2023-07-31 | メルク パテント ゲーエムベーハー | 電子デバイスのための材料 |
TWI813576B (zh) | 2017-07-03 | 2023-09-01 | 德商麥克專利有限公司 | 具有低含量苯酚類雜質的調配物 |
WO2019007867A1 (de) | 2017-07-05 | 2019-01-10 | Merck Patent Gmbh | Zusammensetzung für organische elektronische vorrichtungen |
CN110785415A (zh) | 2017-07-05 | 2020-02-11 | 默克专利有限公司 | 用于有机电子器件的组合物 |
CN110892543B (zh) | 2017-07-18 | 2023-07-28 | 默克专利有限公司 | 有机功能材料的制剂 |
US11228010B2 (en) | 2017-07-26 | 2022-01-18 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2019020654A1 (en) | 2017-07-28 | 2019-01-31 | Merck Patent Gmbh | SPIROBIFLUORENE DERIVATIVES FOR USE IN ELECTRONIC DEVICES |
US11744142B2 (en) | 2017-08-10 | 2023-08-29 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW201923028A (zh) | 2017-09-08 | 2019-06-16 | 德商麥克專利有限公司 | 用於電子裝置之材料 |
US11370965B2 (en) | 2017-09-12 | 2022-06-28 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
CN111164086A (zh) | 2017-10-06 | 2020-05-15 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
CN108675975A (zh) | 2017-10-17 | 2018-10-19 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
WO2019081391A1 (de) | 2017-10-24 | 2019-05-02 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
TWI785142B (zh) | 2017-11-14 | 2022-12-01 | 德商麥克專利有限公司 | 用於有機電子裝置之組成物 |
JP2021504356A (ja) | 2017-11-23 | 2021-02-15 | メルク パテント ゲーエムベーハー | 電子デバイス用材料 |
TWI838352B (zh) | 2017-11-24 | 2024-04-11 | 德商麥克專利有限公司 | 用於有機電致發光裝置的材料 |
US20190161504A1 (en) | 2017-11-28 | 2019-05-30 | University Of Southern California | Carbene compounds and organic electroluminescent devices |
EP3492480B1 (en) | 2017-11-29 | 2021-10-20 | Universal Display Corporation | Organic electroluminescent materials and devices |
US11937503B2 (en) | 2017-11-30 | 2024-03-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2019114764A1 (zh) | 2017-12-14 | 2019-06-20 | 广州华睿光电材料有限公司 | 一种有机金属配合物,包含其的聚合物、混合物和组合物,及其在电子器件中的应用 |
WO2019114668A1 (zh) | 2017-12-14 | 2019-06-20 | 广州华睿光电材料有限公司 | 一种过渡金属配合物材料及其在电子器件的应用 |
WO2019114608A1 (zh) | 2017-12-14 | 2019-06-20 | 广州华睿光电材料有限公司 | 过渡金属配合物、聚合物、混合物、组合物及其应用 |
JP7293229B2 (ja) | 2017-12-15 | 2023-06-19 | メルク パテント ゲーエムベーハー | 有機機能材料の調合物 |
TWI806938B (zh) | 2017-12-15 | 2023-07-01 | 德商麥克專利有限公司 | 經取代之芳族胺 |
TW201938562A (zh) | 2017-12-19 | 2019-10-01 | 德商麥克專利有限公司 | 雜環化合物 |
CN111479815A (zh) | 2017-12-20 | 2020-07-31 | 默克专利有限公司 | 杂芳族化合物 |
CN111315721B (zh) | 2017-12-21 | 2023-06-06 | 广州华睿光电材料有限公司 | 有机混合物及其在有机电子器件中的应用 |
TWI811290B (zh) | 2018-01-25 | 2023-08-11 | 德商麥克專利有限公司 | 用於有機電致發光裝置的材料 |
US11542289B2 (en) | 2018-01-26 | 2023-01-03 | Universal Display Corporation | Organic electroluminescent materials and devices |
CN111712551A (zh) | 2018-02-26 | 2020-09-25 | 默克专利有限公司 | 有机功能材料的制剂 |
TWI802656B (zh) | 2018-03-06 | 2023-05-21 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
TW201938761A (zh) | 2018-03-06 | 2019-10-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置的材料 |
EP3765444A1 (en) | 2018-03-16 | 2021-01-20 | Merck Patent GmbH | Materials for organic electroluminescent devices |
KR20210016423A (ko) | 2018-05-30 | 2021-02-15 | 메르크 파텐트 게엠베하 | 유기 전자 디바이스용 조성물 |
WO2019233904A1 (de) | 2018-06-07 | 2019-12-12 | Merck Patent Gmbh | Organische elektrolumineszenzvorrichtungen |
CN112236488A (zh) | 2018-06-15 | 2021-01-15 | 默克专利有限公司 | 有机功能材料的制剂 |
CN112384595B (zh) | 2018-07-09 | 2024-05-28 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
WO2020016264A1 (en) | 2018-07-20 | 2020-01-23 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
US20200075870A1 (en) | 2018-08-22 | 2020-03-05 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP3844243B1 (en) | 2018-08-28 | 2022-06-22 | Merck Patent GmbH | Materials for organic electroluminescent devices |
TWI823993B (zh) | 2018-08-28 | 2023-12-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
TWI837167B (zh) | 2018-08-28 | 2024-04-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
US20200071346A1 (en) * | 2018-09-05 | 2020-03-05 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
TWI826522B (zh) | 2018-09-12 | 2023-12-21 | 德商麥克專利有限公司 | 電致發光裝置 |
TW202030902A (zh) | 2018-09-12 | 2020-08-16 | 德商麥克專利有限公司 | 電致發光裝置 |
KR20210057092A (ko) | 2018-09-12 | 2021-05-20 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
CN110903323A (zh) * | 2018-09-17 | 2020-03-24 | 上海和辉光电有限公司 | 一种有机电致磷光材料、其制备方法、用途及包含其的oled器件 |
KR20210056432A (ko) | 2018-09-24 | 2021-05-18 | 메르크 파텐트 게엠베하 | 과립형 재료의 제조 방법 |
CN112739795A (zh) | 2018-09-27 | 2021-04-30 | 默克专利有限公司 | 可用作有机电子器件中的活性化合物的化合物 |
JP2022501400A (ja) | 2018-09-27 | 2022-01-06 | 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Merck Patent Gesellschaft mit beschraenkter Haftung | 立体障害窒素含有ヘテロ芳香族化合物を製造する方法 |
US20220223801A1 (en) | 2018-10-31 | 2022-07-14 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
JP2022506382A (ja) | 2018-11-05 | 2022-01-17 | メルク パテント ゲーエムベーハー | 有機電子デバイスに使用できる化合物 |
EP3878022A1 (en) | 2018-11-06 | 2021-09-15 | Merck Patent GmbH | Method for forming an organic element of an electronic device |
US20220020934A1 (en) | 2018-11-06 | 2022-01-20 | Merck Patent Gmbh | 5,6-diphenyl-5,6-dihydro-dibenz[c,e][1,2]azaphosphorin and 6-phenyl-6h-dibenzo[c,e][1,2]thiazin-5,5-dioxide derivatives and similar compounds as organic electroluminescent materials for oleds |
EP3880657A1 (de) | 2018-11-14 | 2021-09-22 | Merck Patent GmbH | Zur herstellung einer organischen elektronischen vorrichtung einsetzbare verbindungen |
EP3880682B1 (de) | 2018-11-15 | 2023-06-14 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
US11737349B2 (en) | 2018-12-12 | 2023-08-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW202039493A (zh) | 2018-12-19 | 2020-11-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
KR20210116519A (ko) | 2019-01-16 | 2021-09-27 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
TW202035345A (zh) | 2019-01-17 | 2020-10-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
US11780829B2 (en) | 2019-01-30 | 2023-10-10 | The University Of Southern California | Organic electroluminescent materials and devices |
US20200251664A1 (en) | 2019-02-01 | 2020-08-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
CN113424332A (zh) | 2019-02-18 | 2021-09-21 | 默克专利有限公司 | 用于有机电子器件的组合物 |
US20220127286A1 (en) | 2019-03-04 | 2022-04-28 | Merck Patent Gmbh | Ligands for nano-sized materials |
KR20210137148A (ko) | 2019-03-12 | 2021-11-17 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
CN113508117A (zh) | 2019-03-20 | 2021-10-15 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
WO2020193447A1 (de) | 2019-03-25 | 2020-10-01 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
JP2020158491A (ja) | 2019-03-26 | 2020-10-01 | ユニバーサル ディスプレイ コーポレイション | 有機エレクトロルミネセンス材料及びデバイス |
TW202104238A (zh) | 2019-04-11 | 2021-02-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
EP3956338A1 (de) * | 2019-04-15 | 2022-02-23 | Merck Patent GmbH | Metallkomplexe |
US20220259238A1 (en) | 2019-07-22 | 2022-08-18 | Merck Patent Gmbh | Method for producing ortho-metallated metal compounds |
US20210032278A1 (en) | 2019-07-30 | 2021-02-04 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20210047354A1 (en) | 2019-08-16 | 2021-02-18 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2021037401A1 (de) | 2019-08-26 | 2021-03-04 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
KR20220056223A (ko) | 2019-09-02 | 2022-05-04 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
TW202122558A (zh) | 2019-09-03 | 2021-06-16 | 德商麥克專利有限公司 | 用於有機電致發光裝置之材料 |
EP4031546A1 (en) | 2019-09-16 | 2022-07-27 | Merck Patent GmbH | Materials for organic electroluminescent devices |
US20230006143A1 (en) | 2019-09-19 | 2023-01-05 | Merck Patent Gmbh | Mixture of two host materials, and organic electroluminescent device comprising same |
KR20220066324A (ko) | 2019-09-20 | 2022-05-24 | 메르크 파텐트 게엠베하 | 전자 디바이스용 재료 |
WO2021078710A1 (en) | 2019-10-22 | 2021-04-29 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
WO2021078831A1 (de) | 2019-10-25 | 2021-04-29 | Merck Patent Gmbh | In einer organischen elektronischen vorrichtung einsetzbare verbindungen |
EP4055642B1 (en) | 2019-11-04 | 2024-09-04 | Merck Patent GmbH | Materials for organic electroluminescent devices |
TW202130783A (zh) | 2019-11-04 | 2021-08-16 | 德商麥克專利有限公司 | 有機電致發光裝置 |
US20210135130A1 (en) | 2019-11-04 | 2021-05-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW202134252A (zh) | 2019-11-12 | 2021-09-16 | 德商麥克專利有限公司 | 有機電致發光裝置用材料 |
TW202136181A (zh) | 2019-12-04 | 2021-10-01 | 德商麥克專利有限公司 | 有機電致發光裝置用的材料 |
TW202136471A (zh) | 2019-12-17 | 2021-10-01 | 德商麥克專利有限公司 | 有機電致發光裝置用的材料 |
EP4077335A1 (de) | 2019-12-18 | 2022-10-26 | Merck Patent GmbH | Aromatische verbindungen für organische elektrolumineszenzvorrichtungen |
EP4077336A1 (de) | 2019-12-19 | 2022-10-26 | Merck Patent GmbH | Polycyclische verbindungen für organische elektrolumineszenzvorrichtungen |
US20210217969A1 (en) | 2020-01-06 | 2021-07-15 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20220336759A1 (en) | 2020-01-28 | 2022-10-20 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20230139809A1 (en) | 2020-01-29 | 2023-05-04 | Merck Patent Gmbh | Benzimidazole derivatives |
WO2021170522A1 (de) | 2020-02-25 | 2021-09-02 | Merck Patent Gmbh | Verwendung von heterocyclischen verbindungen in einer organischen elektronischen vorrichtung |
CN115244728A (zh) | 2020-03-02 | 2022-10-25 | 默克专利有限公司 | 砜化合物在有机电子器件中的用途 |
WO2021180614A1 (de) | 2020-03-11 | 2021-09-16 | Merck Patent Gmbh | Organische elektrolumineszierende vorrichtung |
TW202200753A (zh) | 2020-03-11 | 2022-01-01 | 德商麥克專利有限公司 | 有機電致發光裝置 |
US20230147279A1 (en) | 2020-03-17 | 2023-05-11 | Merck Patent Gmbh | Heterocyclic compounds for organic electroluminescent devices |
CN115298187A (zh) | 2020-03-17 | 2022-11-04 | 默克专利有限公司 | 用于有机电致发光器件的杂芳族化合物 |
KR20220157456A (ko) | 2020-03-23 | 2022-11-29 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
CN115210234A (zh) | 2020-03-24 | 2022-10-18 | 默克专利有限公司 | 用于电子器件的材料 |
CN115335383A (zh) | 2020-03-26 | 2022-11-11 | 默克专利有限公司 | 用于有机电致发光器件的环状化合物 |
WO2021198213A1 (de) | 2020-04-02 | 2021-10-07 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
JP2023520710A (ja) | 2020-04-06 | 2023-05-18 | 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 | 有機エレクトロルミネッセンス素子のための多環式化合物 |
TW202214791A (zh) | 2020-04-21 | 2022-04-16 | 德商麥克專利有限公司 | 有機功能性材料之調配物 |
KR20230002860A (ko) | 2020-04-21 | 2023-01-05 | 메르크 파텐트 게엠베하 | 유기 기능성 재료를 포함하는 에멀젼 |
US20230255106A1 (en) | 2020-05-29 | 2023-08-10 | Merck Patent Gmbh | Organic electroluminescent apparatus |
US20230234937A1 (en) | 2020-06-18 | 2023-07-27 | Merck Patent Gmbh | Indenoazanaphthalenes |
WO2021259824A1 (de) | 2020-06-23 | 2021-12-30 | Merck Patent Gmbh | Verfahren zur herstellung einer mischung |
JP2023530915A (ja) | 2020-06-29 | 2023-07-20 | 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 | 有機エレクトロルミネッセンス素子のためのヘテロ環式化合物 |
EP4172164A1 (de) | 2020-06-29 | 2023-05-03 | Merck Patent GmbH | Heteroaromatische verbindungen für organische elektrolumineszenzvorrichtungen |
EP3937268A1 (en) | 2020-07-10 | 2022-01-12 | Universal Display Corporation | Plasmonic oleds and vertical dipole emitters |
EP4185574A1 (en) | 2020-07-22 | 2023-05-31 | Merck Patent GmbH | Materials for organic electroluminescent devices |
EP4193399A2 (de) | 2020-08-06 | 2023-06-14 | Merck Patent GmbH | Elektronische vorrichtung |
WO2022029096A1 (de) | 2020-08-06 | 2022-02-10 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
EP4196486A1 (de) | 2020-08-13 | 2023-06-21 | Merck Patent GmbH | Metallkomplexe |
EP4200294A1 (de) | 2020-08-18 | 2023-06-28 | Merck Patent GmbH | Materialien für organische elektrolumineszenzvorrichtungen |
US20230295104A1 (en) | 2020-08-19 | 2023-09-21 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
KR20230077725A (ko) | 2020-09-18 | 2023-06-01 | 삼성디스플레이 주식회사 | 유기 전계 발광 소자 |
TW202229215A (zh) | 2020-09-30 | 2022-08-01 | 德商麥克專利有限公司 | 用於有機電致發光裝置功能層之結構化的化合物 |
TW202222748A (zh) | 2020-09-30 | 2022-06-16 | 德商麥克專利有限公司 | 用於結構化有機電致發光裝置的功能層之化合物 |
KR20230088748A (ko) | 2020-10-16 | 2023-06-20 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 헤테로원자를 포함하는 화합물 |
EP4229064A1 (de) | 2020-10-16 | 2023-08-23 | Merck Patent GmbH | Heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen |
KR102352929B1 (ko) * | 2020-10-23 | 2022-01-18 | 엘지디스플레이 주식회사 | 유기 금속 화합물, 이를 포함하는 유기발광다이오드 및 유기발광장치 |
US20230422610A1 (en) | 2020-11-10 | 2023-12-28 | Merck Patent Gmbh | Sulfurous compounds for organic electroluminescent devices |
US20220158096A1 (en) | 2020-11-16 | 2022-05-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20220162243A1 (en) | 2020-11-24 | 2022-05-26 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20220165967A1 (en) | 2020-11-24 | 2022-05-26 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20230116023A (ko) | 2020-12-02 | 2023-08-03 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 복소환 화합물 |
WO2022122607A1 (en) | 2020-12-08 | 2022-06-16 | Merck Patent Gmbh | An ink system and a method for inkjet printing |
KR20230118615A (ko) | 2020-12-10 | 2023-08-11 | 메르크 파텐트 게엠베하 | 유기 전계발광 디바이스용 재료 |
KR20230122093A (ko) | 2020-12-18 | 2023-08-22 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 질소 함유 화합물 |
US20240101560A1 (en) | 2020-12-18 | 2024-03-28 | Merck Patent Gmbh | Nitrogenous heteroaromatic compounds for organic electroluminescent devices |
WO2022129116A1 (de) | 2020-12-18 | 2022-06-23 | Merck Patent Gmbh | Indolo[3.2.1-jk]carbazole-6-carbonitril-derivate als blau fluoreszierende emitter zur verwendung in oleds |
JP2024502093A (ja) | 2021-01-05 | 2024-01-17 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネッセントデバイスのための材料 |
WO2022157343A1 (de) | 2021-01-25 | 2022-07-28 | Merck Patent Gmbh | Stickstoffhaltige verbindungen für organische elektrolumineszenzvorrichtungen |
US20220271241A1 (en) | 2021-02-03 | 2022-08-25 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP4060758A3 (en) | 2021-02-26 | 2023-03-29 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP4059915A3 (en) | 2021-02-26 | 2022-12-28 | Universal Display Corporation | Organic electroluminescent materials and devices |
CN116964054A (zh) | 2021-03-02 | 2023-10-27 | 默克专利有限公司 | 用于有机电致发光器件的化合物 |
US20220298192A1 (en) | 2021-03-05 | 2022-09-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20220298190A1 (en) | 2021-03-12 | 2022-09-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20220298193A1 (en) | 2021-03-15 | 2022-09-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2022194799A1 (de) | 2021-03-18 | 2022-09-22 | Merck Patent Gmbh | Heteroaromatische verbindungen für organische elektrolumineszenzvorrichtungen |
US20220340607A1 (en) | 2021-04-05 | 2022-10-27 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP4075531A1 (en) | 2021-04-13 | 2022-10-19 | Universal Display Corporation | Plasmonic oleds and vertical dipole emitters |
US20220352478A1 (en) | 2021-04-14 | 2022-11-03 | Universal Display Corporation | Organic eletroluminescent materials and devices |
US20230006149A1 (en) | 2021-04-23 | 2023-01-05 | Universal Display Corporation | Organic electroluminescent materials and devices |
EP4326826A1 (en) | 2021-04-23 | 2024-02-28 | Merck Patent GmbH | Formulation of an organic functional material |
US20220407020A1 (en) | 2021-04-23 | 2022-12-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20240005782A (ko) | 2021-04-29 | 2024-01-12 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
CN117279902A (zh) | 2021-04-29 | 2023-12-22 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
WO2022229234A1 (de) | 2021-04-30 | 2022-11-03 | Merck Patent Gmbh | Stickstoffhaltige, heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen |
WO2022243403A1 (de) | 2021-05-21 | 2022-11-24 | Merck Patent Gmbh | Verfahren zur kontinuierlichen aufreinigung von mindestens einem funktionalen material und vorrichtung zur kontinuierlichen aufreinigung von mindestens einem funktionalen material |
US20230133787A1 (en) | 2021-06-08 | 2023-05-04 | University Of Southern California | Molecular Alignment of Homoleptic Iridium Phosphors |
DE112022003409A5 (de) | 2021-07-06 | 2024-05-23 | MERCK Patent Gesellschaft mit beschränkter Haftung | Materialien für organische elektrolumineszenzvorrichtungen |
WO2023012084A1 (en) | 2021-08-02 | 2023-02-09 | Merck Patent Gmbh | A printing method by combining inks |
CN113788858B (zh) * | 2021-08-27 | 2023-08-11 | 万华化学集团股份有限公司 | 一种用于催化烯醇氢甲酰化反应制备线性二元醇的配体及其制备方法和用途 |
KR20240058919A (ko) | 2021-09-13 | 2024-05-03 | 메르크 파텐트 게엠베하 | 유기 전계 발광 디바이스용 재료 |
EP4402221A1 (de) | 2021-09-14 | 2024-07-24 | Merck Patent GmbH | Borhaltige, heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen |
EP4151699A1 (en) | 2021-09-17 | 2023-03-22 | Universal Display Corporation | Organic electroluminescent materials and devices |
CN118056486A (zh) | 2021-09-28 | 2024-05-17 | 默克专利有限公司 | 用于电子器件的材料 |
DE112022004658A5 (de) | 2021-09-28 | 2024-07-25 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
EP4410074A1 (de) | 2021-09-28 | 2024-08-07 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
WO2023052275A1 (de) | 2021-09-28 | 2023-04-06 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
TW202349760A (zh) | 2021-10-05 | 2023-12-16 | 德商麥克專利有限公司 | 電子裝置之有機元件的形成方法 |
EP4423209A1 (de) | 2021-10-27 | 2024-09-04 | Merck Patent GmbH | Bor- und stickstoffhaltige, heterocyclische verbindungen für organische elektrolumineszenzvorrichtungen |
CN116082407A (zh) * | 2021-11-02 | 2023-05-09 | 北京夏禾科技有限公司 | 一种电致发光材料及其器件 |
WO2023094412A1 (de) | 2021-11-25 | 2023-06-01 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
CN118303151A (zh) | 2021-11-30 | 2024-07-05 | 默克专利有限公司 | 具有芴结构的化合物 |
CN118401524A (zh) | 2021-12-13 | 2024-07-26 | 默克专利有限公司 | 用于有机电致发光器件的材料 |
EP4212539A1 (en) | 2021-12-16 | 2023-07-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20240128020A (ko) | 2021-12-21 | 2024-08-23 | 메르크 파텐트 게엠베하 | 중수소화 유기 화합물의 제조 방법 |
WO2023152063A1 (de) | 2022-02-09 | 2023-08-17 | Merck Patent Gmbh | Materialien für organische elektrolumineszenzvorrichtungen |
WO2023152346A1 (de) | 2022-02-14 | 2023-08-17 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
EP4231804A3 (en) | 2022-02-16 | 2023-09-20 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2023161167A1 (de) | 2022-02-23 | 2023-08-31 | Merck Patent Gmbh | Stickstoffhaltige heterocyclen für organische elektrolumineszenzvorrichtungen |
CN118647622A (zh) | 2022-02-23 | 2024-09-13 | 默克专利有限公司 | 用于有机电致发光器件的芳族杂环 |
US20230292592A1 (en) | 2022-03-09 | 2023-09-14 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20230337516A1 (en) | 2022-04-18 | 2023-10-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2023213837A1 (de) | 2022-05-06 | 2023-11-09 | Merck Patent Gmbh | Cyclische verbindungen für organische elektrolumineszenzvorrichtungen |
WO2023222559A1 (de) | 2022-05-18 | 2023-11-23 | Merck Patent Gmbh | Verfahren zur herstellung von deuterierten organischen verbindungen |
US20230389421A1 (en) | 2022-05-24 | 2023-11-30 | Universal Display Corporation | Organic electroluminescent materials and devices |
TW202411366A (zh) | 2022-06-07 | 2024-03-16 | 德商麥克專利有限公司 | 藉由組合油墨來印刷電子裝置功能層之方法 |
EP4293001A1 (en) | 2022-06-08 | 2023-12-20 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2023247663A1 (de) | 2022-06-24 | 2023-12-28 | Merck Patent Gmbh | Zusammensetzung für organische elektronische vorrichtungen |
WO2023247662A1 (de) | 2022-06-24 | 2023-12-28 | Merck Patent Gmbh | Zusammensetzung für organische elektronische vorrichtungen |
US20240016051A1 (en) | 2022-06-28 | 2024-01-11 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2024013004A1 (de) | 2022-07-11 | 2024-01-18 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
WO2024033282A1 (en) | 2022-08-09 | 2024-02-15 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
US20240107880A1 (en) | 2022-08-17 | 2024-03-28 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2024061948A1 (de) | 2022-09-22 | 2024-03-28 | Merck Patent Gmbh | Stickstoffenthaltende heterocyclen für organische elektrolumineszenzvorrichtungen |
WO2024061942A1 (de) | 2022-09-22 | 2024-03-28 | Merck Patent Gmbh | Stickstoffenthaltende verbindungen für organische elektrolumineszenzvorrichtungen |
US20240188316A1 (en) | 2022-10-27 | 2024-06-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20240196730A1 (en) | 2022-10-27 | 2024-06-13 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20240188319A1 (en) | 2022-10-27 | 2024-06-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20240180025A1 (en) | 2022-10-27 | 2024-05-30 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20240188419A1 (en) | 2022-10-27 | 2024-06-06 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2024094592A2 (de) | 2022-11-01 | 2024-05-10 | Merck Patent Gmbh | Stickstoffhaltige heterocyclen für organische elektrolumineszenzvorrichtungen |
WO2024105066A1 (en) | 2022-11-17 | 2024-05-23 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
US20240247017A1 (en) | 2022-12-14 | 2024-07-25 | Universal Display Corporation | Organic electroluminescent materials and devices |
WO2024126635A1 (en) | 2022-12-16 | 2024-06-20 | Merck Patent Gmbh | Formulation of an organic functional material |
WO2024132993A1 (de) | 2022-12-19 | 2024-06-27 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
WO2024132892A1 (en) | 2022-12-19 | 2024-06-27 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
WO2024133048A1 (en) | 2022-12-20 | 2024-06-27 | Merck Patent Gmbh | Method for preparing deuterated aromatic compounds |
WO2024149694A1 (de) | 2023-01-10 | 2024-07-18 | Merck Patent Gmbh | Stickstoffhaltige heterocyclen für organische elektrolumineszenzvorrichtungen |
CN115974935A (zh) * | 2023-01-17 | 2023-04-18 | 广西师范大学 | 氧化异阿朴菲生物碱与联吡啶衍生物的环金属有机铑配合物及其合成方法和应用 |
WO2024153568A1 (de) | 2023-01-17 | 2024-07-25 | Merck Patent Gmbh | Heterocyclen für organische elektrolumineszenzvorrichtungen |
WO2024170605A1 (en) | 2023-02-17 | 2024-08-22 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
WO2024184050A1 (de) | 2023-03-07 | 2024-09-12 | Merck Patent Gmbh | Cyclische stickstoffverbindungen für organische elektrolumineszenzvorrichtungen |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002044189A1 (fr) * | 2000-11-30 | 2002-06-06 | Canon Kabushiki Kaisha | Element luminescent et afficheur |
CN1374315A (zh) * | 2001-03-08 | 2002-10-16 | 佳能株式会社 | 金属配位化合物,发光器件和显示设备 |
WO2003000661A1 (fr) * | 2001-06-25 | 2003-01-03 | Canon Kabushiki Kaisha | Compose de coordination metallique et dispositif electroluminescent |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2351656A1 (fr) * | 1976-05-21 | 1977-12-16 | Rhone Poulenc Ind | Nouveaux derives de la dibenzo(de, h) quinoleine, leur preparation et les compositions qui les contiennent |
DE3118521A1 (de) * | 1981-05-09 | 1982-12-02 | Gödecke AG, 1000 Berlin | Dibenzo(de,g)chinolin-derivate, verfahren zu deren herstellung und deren verwendung bei der bekaempfung von erkaeltungskrankheiten und allergien |
JP3769118B2 (ja) * | 1998-03-23 | 2006-04-19 | 三菱化学株式会社 | ジベンゾキノリノン系色素及びその製造方法 |
DE10104426A1 (de) | 2001-02-01 | 2002-08-08 | Covion Organic Semiconductors | Verfahren zur Herstellung von hochreinen, tris-ortho-metallierten Organo-Iridium-Verbindungen |
DE10314102A1 (de) | 2003-03-27 | 2004-10-14 | Covion Organic Semiconductors Gmbh | Verfahren zur Herstellung von hochreinen Organo-Iridium-Verbindungen |
-
2003
- 2003-09-29 DE DE10345572A patent/DE10345572A1/de not_active Withdrawn
-
2004
- 2004-09-28 CN CN201210043328.2A patent/CN102627671B/zh not_active Expired - Fee Related
- 2004-09-28 US US10/573,931 patent/US7820822B2/en active Active
- 2004-09-28 CN CNA2004800282500A patent/CN1860202A/zh active Pending
- 2004-09-28 JP JP2006530031A patent/JP5329041B2/ja not_active Expired - Fee Related
- 2004-09-28 AT AT04765652T patent/ATE513889T1/de active
- 2004-09-28 KR KR1020067006034A patent/KR101172336B1/ko active IP Right Grant
- 2004-09-28 WO PCT/EP2004/010836 patent/WO2005033244A1/de active Application Filing
- 2004-09-28 EP EP04765652A patent/EP1675929B1/de not_active Expired - Lifetime
-
2010
- 2010-09-01 US US12/873,406 patent/US8846920B2/en active Active
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2002044189A1 (fr) * | 2000-11-30 | 2002-06-06 | Canon Kabushiki Kaisha | Element luminescent et afficheur |
CN1374315A (zh) * | 2001-03-08 | 2002-10-16 | 佳能株式会社 | 金属配位化合物,发光器件和显示设备 |
WO2003000661A1 (fr) * | 2001-06-25 | 2003-01-03 | Canon Kabushiki Kaisha | Compose de coordination metallique et dispositif electroluminescent |
Non-Patent Citations (1)
Title |
---|
JOHNSON STANSLAS等: "Antitumor Polycyclic Acridines. 7.1 Synthesis and Biological Properties of DNA Affinic Tetra- and Pentacyclic Acridines", 《JOURNAL OF MEDICINAL CHEMISTRY 》 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN106795428A (zh) * | 2014-04-03 | 2017-05-31 | 港大科桥有限公司 | 用于oled应用的铂(ii)发射体 |
CN106795428B (zh) * | 2014-04-03 | 2020-09-25 | 港大科桥有限公司 | 用于oled应用的铂(ii)发射体 |
CN108570074A (zh) * | 2017-03-08 | 2018-09-25 | 环球展览公司 | 有机电致发光材料和装置 |
CN116178447A (zh) * | 2023-01-10 | 2023-05-30 | 广西师范大学 | 氧化异阿朴菲生物碱的多吡啶类金属有机钌配合物及其合成方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
EP1675929A1 (de) | 2006-07-05 |
US8846920B2 (en) | 2014-09-30 |
ATE513889T1 (de) | 2011-07-15 |
US20070034863A1 (en) | 2007-02-15 |
JP2007507448A (ja) | 2007-03-29 |
CN102627671B (zh) | 2015-05-06 |
CN1860202A (zh) | 2006-11-08 |
US20100331506A1 (en) | 2010-12-30 |
WO2005033244A1 (de) | 2005-04-14 |
JP5329041B2 (ja) | 2013-10-30 |
KR101172336B1 (ko) | 2012-08-14 |
EP1675929B1 (de) | 2011-06-22 |
KR20060088889A (ko) | 2006-08-07 |
US7820822B2 (en) | 2010-10-26 |
DE10345572A1 (de) | 2005-05-19 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN102627671B (zh) | 金属络合物 | |
JP6886451B2 (ja) | 発光体及びデバイス | |
KR101292376B1 (ko) | 유기금속 화합물 및 그러한 화합물로 만들어진 장치 | |
EP2871222B1 (en) | Compound for organic optoelectric device, organic optoelectric device comprising same, and display apparatus comprising organic optoelectric device | |
KR102173629B1 (ko) | 시클로금속화 이미다조[1,2-f]페난트리딘 및 디이미다조[1,2-a:1',2'-c]퀴나졸린 리간드, 및 이의 등전자성 및 벤즈고리화된 유사체의 금속 착체 | |
CN101230264B (zh) | 可溶液加工的磷光材料 | |
Tang et al. | Novel yellow phosphorescent iridium complexes containing a carbazole–oxadiazole unit used in polymeric light-emitting diodes | |
JP5410657B2 (ja) | 高分子化合物およびそれを利用した有機電界発光素子 | |
Park et al. | Synthesis, characterization of the phenylquinoline-based on iridium (III) complexes for solution processable phosphorescent organic light-emitting diodes | |
Chen et al. | Novel white-light-emitting polyfluorenes with benzothiadiazole and Ir complex on the backbone | |
JP5294560B2 (ja) | 過アリール化ボランをベースとする、ポリマー燐光性有機半導体エミッター物質、その製法及びその使用 | |
CN112409276A (zh) | 一种化合物及其应用 | |
CN101998983A (zh) | 用于光电子器件的发射聚合物材料 | |
CN101663339B (zh) | 聚咔唑基(甲基)丙烯酸酯光发射组合物 | |
EP1484380A1 (en) | Polymeric phosphors, process for production thereof, phosphorescent compositions and articles made by using the same | |
KR20140074857A (ko) | 유기전계발광 화합물 및 이를 포함하는 유기전계발광소자 | |
CN112707908A (zh) | 一种有机电子材料及其应用 | |
CN114478601A (zh) | 含有硼原子、氮原子和硒原子或碲原子的稠环化合物及有机电致发光器件 | |
CN104650148A (zh) | 蓝光有机电致磷光材料铱金属配合物及其制备方法和有机电致发光器件 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20150506 Termination date: 20170928 |