JP2020164536A - 有機金属錯体のための補助配位子 - Google Patents
有機金属錯体のための補助配位子 Download PDFInfo
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- JP2020164536A JP2020164536A JP2020101997A JP2020101997A JP2020164536A JP 2020164536 A JP2020164536 A JP 2020164536A JP 2020101997 A JP2020101997 A JP 2020101997A JP 2020101997 A JP2020101997 A JP 2020101997A JP 2020164536 A JP2020164536 A JP 2020164536A
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- 239000003446 ligand Substances 0.000 title claims abstract description 56
- 125000002524 organometallic group Chemical group 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 83
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 22
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 19
- -1 metal complex compound Chemical class 0.000 claims description 40
- 229910052751 metal Inorganic materials 0.000 claims description 26
- 239000002184 metal Substances 0.000 claims description 26
- 125000003118 aryl group Chemical group 0.000 claims description 19
- 239000012044 organic layer Substances 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 17
- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 150000002431 hydrogen Chemical class 0.000 claims description 11
- 125000003342 alkenyl group Chemical group 0.000 claims description 10
- 125000000304 alkynyl group Chemical group 0.000 claims description 10
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 10
- 150000004696 coordination complex Chemical class 0.000 claims description 10
- 125000002252 acyl group Chemical group 0.000 claims description 9
- 125000003545 alkoxy group Chemical group 0.000 claims description 9
- 125000004104 aryloxy group Chemical group 0.000 claims description 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 9
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 9
- 150000002148 esters Chemical class 0.000 claims description 9
- 150000004820 halides Chemical class 0.000 claims description 9
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 9
- 150000002527 isonitriles Chemical class 0.000 claims description 9
- 150000002825 nitriles Chemical class 0.000 claims description 9
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 9
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 9
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 9
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 6
- 229910052805 deuterium Inorganic materials 0.000 claims description 6
- 238000000295 emission spectrum Methods 0.000 claims description 6
- 230000008021 deposition Effects 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 150000001735 carboxylic acids Chemical class 0.000 claims description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 3
- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 claims description 2
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 123
- 239000010410 layer Substances 0.000 description 90
- 239000000463 material Substances 0.000 description 72
- 239000000203 mixture Substances 0.000 description 65
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 57
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 44
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 42
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 42
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 36
- 239000007787 solid Substances 0.000 description 36
- 230000015572 biosynthetic process Effects 0.000 description 34
- 238000003786 synthesis reaction Methods 0.000 description 34
- 229910052757 nitrogen Inorganic materials 0.000 description 29
- 239000000243 solution Substances 0.000 description 26
- 239000011541 reaction mixture Substances 0.000 description 22
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 20
- 239000000047 product Substances 0.000 description 19
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 18
- MILUBEOXRNEUHS-UHFFFAOYSA-N iridium(3+) Chemical class [Ir+3] MILUBEOXRNEUHS-UHFFFAOYSA-N 0.000 description 18
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 14
- 239000007924 injection Substances 0.000 description 14
- 238000002347 injection Methods 0.000 description 14
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 14
- 230000032258 transport Effects 0.000 description 14
- 230000000052 comparative effect Effects 0.000 description 13
- 239000012043 crude product Substances 0.000 description 13
- 230000000903 blocking effect Effects 0.000 description 12
- 150000003384 small molecules Chemical class 0.000 description 12
- 239000002904 solvent Substances 0.000 description 12
- MFELLNQJMHCAKI-UHFFFAOYSA-N 3,7-diethylnonane-4,6-dione Chemical compound CCC(CC)C(=O)CC(=O)C(CC)CC MFELLNQJMHCAKI-UHFFFAOYSA-N 0.000 description 11
- 239000002019 doping agent Substances 0.000 description 11
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 230000004888 barrier function Effects 0.000 description 10
- 230000005525 hole transport Effects 0.000 description 10
- 239000000758 substrate Substances 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 230000005587 bubbling Effects 0.000 description 9
- 239000000706 filtrate Substances 0.000 description 9
- 229910052760 oxygen Inorganic materials 0.000 description 9
- 229940093475 2-ethoxyethanol Drugs 0.000 description 8
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 8
- 238000004440 column chromatography Methods 0.000 description 8
- 238000000151 deposition Methods 0.000 description 8
- 238000004770 highest occupied molecular orbital Methods 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 238000010898 silica gel chromatography Methods 0.000 description 8
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 7
- 229910052741 iridium Inorganic materials 0.000 description 7
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 7
- 229910000027 potassium carbonate Inorganic materials 0.000 description 7
- 239000000741 silica gel Substances 0.000 description 7
- 229910002027 silica gel Inorganic materials 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 6
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 6
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- 239000011368 organic material Substances 0.000 description 6
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 5
- 239000000412 dendrimer Substances 0.000 description 5
- 229920000736 dendritic polymer Polymers 0.000 description 5
- 239000000539 dimer Substances 0.000 description 5
- 239000003480 eluent Substances 0.000 description 5
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 description 5
- FVZVCSNXTFCBQU-UHFFFAOYSA-N phosphanyl Chemical group [PH2] FVZVCSNXTFCBQU-UHFFFAOYSA-N 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 238000000746 purification Methods 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 4
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- SLGBZMMZGDRARJ-UHFFFAOYSA-N Triphenylene Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 4
- WIUZHVZUGQDRHZ-UHFFFAOYSA-N [1]benzothiolo[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3SC2=C1 WIUZHVZUGQDRHZ-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 4
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 229940125797 compound 12 Drugs 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- 230000005693 optoelectronics Effects 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- 229910052938 sodium sulfate Inorganic materials 0.000 description 4
- 235000011152 sodium sulphate Nutrition 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 125000005580 triphenylene group Chemical group 0.000 description 4
- LFOIDLOIBZFWDO-UHFFFAOYSA-N 2-methoxy-6-[6-methoxy-4-[(3-phenylmethoxyphenyl)methoxy]-1-benzofuran-2-yl]imidazo[2,1-b][1,3,4]thiadiazole Chemical compound N1=C2SC(OC)=NN2C=C1C(OC1=CC(OC)=C2)=CC1=C2OCC(C=1)=CC=CC=1OCC1=CC=CC=C1 LFOIDLOIBZFWDO-UHFFFAOYSA-N 0.000 description 3
- MBDSEJRHICEFRU-UHFFFAOYSA-N CCC(CC)C(=O)CC(=O)C(C)C Chemical compound CCC(CC)C(=O)CC(=O)C(C)C MBDSEJRHICEFRU-UHFFFAOYSA-N 0.000 description 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 3
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- QBYJBZPUGVGKQQ-SJJAEHHWSA-N aldrin Chemical compound C1[C@H]2C=C[C@@H]1[C@H]1[C@@](C3(Cl)Cl)(Cl)C(Cl)=C(Cl)[C@@]3(Cl)[C@H]12 QBYJBZPUGVGKQQ-SJJAEHHWSA-N 0.000 description 3
- 239000004305 biphenyl Substances 0.000 description 3
- 235000010290 biphenyl Nutrition 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- DHFABSXGNHDNCO-UHFFFAOYSA-N dibenzoselenophene Chemical compound C1=CC=C2C3=CC=CC=C3[se]C2=C1 DHFABSXGNHDNCO-UHFFFAOYSA-N 0.000 description 3
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical class C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 3
- 239000000377 silicon dioxide Substances 0.000 description 3
- 229910000029 sodium carbonate Inorganic materials 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- 238000002207 thermal evaporation Methods 0.000 description 3
- 238000004809 thin layer chromatography Methods 0.000 description 3
- 229930192474 thiophene Natural products 0.000 description 3
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 2
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-bis(diphenylphosphino)propane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 2
- KKHFRAFPESRGGD-UHFFFAOYSA-N 1,3-dimethyl-7-[3-(n-methylanilino)propyl]purine-2,6-dione Chemical compound C1=NC=2N(C)C(=O)N(C)C(=O)C=2N1CCCN(C)C1=CC=CC=C1 KKHFRAFPESRGGD-UHFFFAOYSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- TZMSYXZUNZXBOL-UHFFFAOYSA-N 10H-phenoxazine Chemical compound C1=CC=C2NC3=CC=CC=C3OC2=C1 TZMSYXZUNZXBOL-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 2
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 2
- NPRYCHLHHVWLQZ-TURQNECASA-N 2-amino-9-[(2R,3S,4S,5R)-4-fluoro-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-7-prop-2-ynylpurin-8-one Chemical compound NC1=NC=C2N(C(N(C2=N1)[C@@H]1O[C@@H]([C@H]([C@H]1O)F)CO)=O)CC#C NPRYCHLHHVWLQZ-TURQNECASA-N 0.000 description 2
- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 2
- OLGGLCIDAMICTA-UHFFFAOYSA-N 2-pyridin-2-yl-1h-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=N1 OLGGLCIDAMICTA-UHFFFAOYSA-N 0.000 description 2
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- 239000010703 silicon Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012265 solid product Substances 0.000 description 1
- 230000007928 solubilization Effects 0.000 description 1
- 238000005063 solubilization Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- DANYXEHCMQHDNX-UHFFFAOYSA-K trichloroiridium Chemical compound Cl[Ir](Cl)Cl DANYXEHCMQHDNX-UHFFFAOYSA-K 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
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Abstract
Description
2つの隣接する置換基が結合して環を形成してもよい。
2つの隣接する置換基が結合して環を形成してもよい。式I中の破線は、金属との結合点を示す。
他の材料との組合せ
HIL/HTL:
kは1から20までの整数であり;X101からX108はC(CHを含む)又はNであり;Z101はNAr1、O、又はSであり;Ar1は、上記で定義したものと同じ基を有する。
Metは、40より大きい原子量を有し得る金属であり;(Y101−Y102)は二座配位子であり、Y101及びY102は、C、N、O、P及びSから独立に選択され;L101は補助配位子であり;k’は、1から金属に付着し得る配位子の最大数までの整数値であり;且つ、k’+k’’は、金属に付着し得る配位子の最大数である。
ホスト:
HBL:
ETL:
使用された比較化合物:
デバイス実施例の有機体層は、ITO表面から順に、ホール注入層(HIL)として100ÅのHAT−CN、ホール輸送層(HTL)として400ÅのNPD、式1の化合物、化合物SD、ホスト(BAIQ)を含む400Å発光層(EML)、BAIQの40Åブロッキング層(BL)、AlQ3の450Å電子輸送層(ETL)、及び電子注入層(EIL)として10ÅのLiFからなる。比較化合物1−4をEMLで発光体として使用する以外は、比較化合物をデバイス実施例と同じように作製した。
1表4の値はいずれも、CIE座標以外は相対的な数値(任意単位−a.u.)である。
材料合成:
110 基板
115 アノード
120 正孔注入層
125 正孔輸送層
130 電子ブロッキング層
135 発光層
140 正孔ブロッキング層
145 電子輸送層
150 電子注入層
155 保護層
160 カソード
162 第一の導電層
164 第二の導電層
200 反転させたOLED、デバイス
210 基板
215 カソード
220 発光層
225 正孔輸送層
230 アノード
Claims (15)
- リン光発光金属錯体化合物における補助配位子としての第1の配位子L1の使用であって、
前記第1の配位子L1が次の式Iを有し、
前記第1の配位子L1は、40超の原子番号を有する金属Mに配位していることを特徴とする第1の配位子L1の使用。
R1、R2、R3、及びR4の少なくとも1つは、少なくとも2つのCを有し;
R5は、水素、重水素、ハライド、アルキル、シクロアルキル、ヘテロアルキル、アリールアルキル、アルコキシ、アリールオキシ、アミノ、シリル、アルケニル、シクロアルケニル、ヘテロアルケニル、アルキニル、アリール、ヘテロアリール、アシル、カルボニル、カルボン酸、エステル、ニトリル、イソニトリル、スルファニル、スルフィニル、スルフォニル、ホスフィノ及びこれらの組み合わせからなる群から選択され;
2つの隣接する置換基は、結合して環を形成してもよい。) - 前記金属錯体の発光スペクトルを狭める及び/又は蒸着温度を低下させるため、及び/又は有機発光デバイスのデバイス効率を改善するための請求項1に記載の使用。
- 前記金属Mが、Irである請求項1又は2に記載の使用。
- 前記R5が水素、重水素、アルキル、シクロアルキル、及びこれらの組み合わせからなる群から選択される請求項1から3のいずれかに記載の使用。
- 前記R5が水素である請求項4に記載の使用。
- 前記R1、R2、R3、及びR4が、アルキル又はシクロアルキルである請求項1から3のいずれかに記載の使用。
- 前記R1、R2、R3、及びR4がメチル、エチル、プロピル、1−メチルエチル、ブチル、1−メチルプロピル、2−メチルプロピル、ペンチル、1−メチルブチル、2−メチルブチル、3−メチルブチル、1,1−ジメチルプロピル、1,2−ジメチルプロピル、2,2−ジメチルプロピル、シクロペンチル、シクロヘキシル、部分的又は完全に重水素化されたこれらのバリアント、及びこれらの組合せからなる群から選択される請求項6に記載の使用。
- 前記化合物は、M(L1)x(L2)y(L3)zの式を有する;
式中、L2は、第2の配位子であり、L3は、第3の配位子であり、L2及びL3は、同一であっても異なっていてもよく;
xは、1、2、又は3であり;
yは、0、1、又は2であり;
zは、0、1、又は2であり;
x+y+zは、金属Mの酸化状態であり;
前記第2の配位子L2及び前記第3の配位子L3は、独立して、下記からなる群から選択される請求項1から7のいずれかに記載の使用。
- 前記化合物は、M(L1)(L2)2の式を有する請求項8に記載の使用。
- 前記L1は、下記からなる群から選択される請求項8又は9に記載の使用。
- 前記L2は、下記からなる群から選択される請求項10に記載の使用。
- M(L1)(L2)2の式を有する化合物が、下記の表に記載の化合物1〜化合物1729からなる群から選択される請求項11に記載の使用。
- 化合物が、下記からなる群から選択される請求項1又は2に記載の使用。
- 前記化合物が第1の有機発光デバイスを含む第1のデバイスに組み込まれ、前記第1の有機発光デバイスが、
アノードと;
カソードと;
前記アノードと前記カソードとの間に配置され、前記化合物を含む有機層とを含む、請求項1から13のいずれかに記載の使用。 - 前記第1のデバイスが、消費者製品及び/又は照明パネルであり、好ましくは、フラットパネルディスプレイ、コンピュータモニター、メディカルモニター、テレビ、掲示板、屋内若しくは屋外照明及び/又は信号送信用のライト、ヘッドアップディスプレイ、完全透明ディスプレイ、フレキシブルディスプレイ、レーザープリンター、電話、携帯電話、パーソナルデジタルアシスタント(PDA)、ラップトップコンピュータ、デジタルカメラ、カムコーダー、ビューファインダー、マイクロディスプレイ、3−Dディスプレイ、車、大面積壁、劇場又はスタジアムのスクリーン、或いは看板からなる群から選択される消費者製品である請求項14に記載の使用。
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US11081658B2 (en) * | 2016-10-03 | 2021-08-03 | Universal Display Corporation | Organic electroluminescent materials and devices |
KR20180065353A (ko) | 2016-12-07 | 2018-06-18 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 재료 및 이를 포함하는 유기 전계 발광 소자 |
KR102359412B1 (ko) * | 2016-12-27 | 2022-02-09 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
US10686146B2 (en) | 2017-02-13 | 2020-06-16 | Feng-wen Yen | Paracyclophane-based iridium complexes for organic electroluminescence device |
EP3418285B1 (en) | 2017-06-20 | 2020-05-06 | Idemitsu Kosan Co., Ltd. | Composition comprising a substituted ir complex and a phenylquinazoline bridged with a heteroatom |
US11462697B2 (en) * | 2017-08-22 | 2022-10-04 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20190077818A1 (en) * | 2017-09-08 | 2019-03-14 | Chuanjun Xia | Organic luminescent materials containing fluorine ancillary ligands |
CN109575083A (zh) | 2017-09-29 | 2019-04-05 | 北京夏禾科技有限公司 | 含环烷基辅助配体的有机发光材料 |
US10400002B2 (en) * | 2017-10-02 | 2019-09-03 | Feng-wen Yen | Iridium complex and organic electroluminescence device using the same |
EP3466954A1 (en) | 2017-10-04 | 2019-04-10 | Idemitsu Kosan Co., Ltd. | Fused phenylquinazolines bridged with a heteroatom |
US11404651B2 (en) | 2017-12-14 | 2022-08-02 | Guangzhou Chinaray Optoelectronic Materials Ltd. | Transition metal complex material and application thereof in electronic devices |
CN111247658B (zh) * | 2017-12-14 | 2023-04-04 | 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 |
KR102625860B1 (ko) | 2018-02-23 | 2024-02-08 | 삼성디스플레이 주식회사 | 유기금속 화합물, 이를 포함한 유기 발광 소자 및 상기 유기 발광 소자를 포함한 유기 발광 장치 |
EP3549944B1 (en) | 2018-04-02 | 2021-12-29 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
US11459348B2 (en) | 2018-04-02 | 2022-10-04 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
EP3604477A1 (en) | 2018-07-30 | 2020-02-05 | Idemitsu Kosan Co., Ltd. | Polycyclic compound, organic electroluminescence device, and electronic device |
EP3604321B1 (en) | 2018-07-31 | 2022-02-09 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
CN108997437B (zh) * | 2018-08-01 | 2023-10-20 | 浙江华显光电科技有限公司 | 红色磷光化合物以及使用该化合物的有机发光二极管器件 |
CN108997438B (zh) * | 2018-08-06 | 2023-10-27 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机发光二极管器件 |
EP3608319A1 (en) | 2018-08-07 | 2020-02-12 | Idemitsu Kosan Co., Ltd. | Condensed aza cycles as organic light emitting device and materials for use in same |
EP3617216B1 (en) * | 2018-08-31 | 2021-12-01 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and diagnostic composition including the organometallic compound |
CN110922429B (zh) * | 2018-09-20 | 2023-11-03 | 北京夏禾科技有限公司 | 含有辅助配体的有机发光材料 |
CN109988192A (zh) * | 2019-01-16 | 2019-07-09 | 浙江华显光电科技有限公司 | 绿色磷光化合物和使用该化合物的有机电致发光器件 |
KR20200089799A (ko) | 2019-01-17 | 2020-07-28 | 삼성디스플레이 주식회사 | 근적외선광-발광 소자 및 이를 포함한 장치 |
EP3715355B1 (en) * | 2019-03-29 | 2022-12-14 | Samsung Electronics Co., Ltd. | Organometallic compound, organic light-emitting device including the same, and electronic apparatus including the organic light-emitting device |
CN111909212B (zh) | 2019-05-09 | 2023-12-26 | 北京夏禾科技有限公司 | 一种含有6-硅基取代异喹啉配体的有机发光材料 |
CN111909214B (zh) * | 2019-05-09 | 2024-03-29 | 北京夏禾科技有限公司 | 一种含有3-氘取代异喹啉配体的有机发光材料 |
CN111909213B (zh) * | 2019-05-09 | 2024-02-27 | 北京夏禾科技有限公司 | 一种含有三个不同配体的金属配合物 |
CN111943986B (zh) * | 2019-05-17 | 2023-08-15 | 夏禾科技(江苏)有限公司 | 一种含有多个稠合杂环结构配体的金属配合物 |
CN110452271A (zh) * | 2019-07-26 | 2019-11-15 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机电致发光器件 |
CN110467642A (zh) * | 2019-07-26 | 2019-11-19 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机电致发光器件 |
CN110922430A (zh) * | 2019-08-12 | 2020-03-27 | 宇瑞(上海)化学有限公司 | 一种绿色磷光化合物及使用绿色磷光化合物的有机电致发光器 |
CN110590851A (zh) * | 2019-08-29 | 2019-12-20 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机电致发光器件 |
CN110627836A (zh) * | 2019-08-29 | 2019-12-31 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机电致发光器件 |
CN110746464A (zh) * | 2019-09-09 | 2020-02-04 | 浙江华显光电科技有限公司 | 红色磷光化合物和使用该化合物的有机电致发光器件 |
US20210094978A1 (en) * | 2019-09-26 | 2021-04-01 | Universal Display Corporation | Organic electroluminescent materials and devices |
US20210101921A1 (en) * | 2019-10-02 | 2021-04-08 | Universal Display Corporation | Organic electroluminescent materials and devices |
CN112679548B (zh) | 2019-10-18 | 2023-07-28 | 北京夏禾科技有限公司 | 具有部分氟取代的取代基的辅助配体的有机发光材料 |
TW202132322A (zh) | 2020-01-10 | 2021-09-01 | 日商半導體能源研究所股份有限公司 | 有機金屬錯合物、頂部發射用發光材料、發光器件、發光裝置、電子裝置以及照明設備 |
CN113121609B (zh) * | 2020-01-16 | 2024-03-29 | 北京夏禾科技有限公司 | 一种金属配合物、包含其的电致发光器件及其用途 |
CN113321685A (zh) * | 2020-02-28 | 2021-08-31 | 北京夏禾科技有限公司 | 一种金属配合物、有机电致发光材料及其应用 |
CN113493482A (zh) * | 2020-04-01 | 2021-10-12 | 北京夏禾科技有限公司 | 含氰基取代的辅助配体的有机发光材料 |
CN112608342A (zh) * | 2020-12-27 | 2021-04-06 | 浙江华显光电科技有限公司 | 一种铱金属配合物和使用该化合物的有机光电元件 |
CN112679553A (zh) * | 2020-12-27 | 2021-04-20 | 浙江华显光电科技有限公司 | 一种铱金属配合物和使用该化合物的有机光电元件 |
CN112608737A (zh) * | 2020-12-27 | 2021-04-06 | 浙江华显光电科技有限公司 | 一种组合物及包含其的有机电致发光元件 |
CN112645988A (zh) * | 2020-12-27 | 2021-04-13 | 浙江华显光电科技有限公司 | 一种铱金属配合物和使用该化合物的有机光电元件 |
CN112680218A (zh) * | 2020-12-27 | 2021-04-20 | 浙江华显光电科技有限公司 | 一种组合物及包含其的有机电致发光元件 |
Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3950135A (en) * | 1974-07-24 | 1976-04-13 | Massachusetts Institute Of Technology | Method of sepctral analysis using nmr shift reagents |
JPH02145536A (ja) * | 1988-11-28 | 1990-06-05 | Mitsui Petrochem Ind Ltd | β‐ジカルボニル化合物のコバルト錯体 |
JPH0941144A (ja) * | 1995-07-27 | 1997-02-10 | Dowa Mining Co Ltd | 希土類元素のcvd用原料物質およびこれを用いた成膜法 |
JP2000212744A (ja) * | 1999-01-25 | 2000-08-02 | Asahi Denka Kogyo Kk | ルテニウム系薄膜 |
JP2002309373A (ja) * | 2001-04-13 | 2002-10-23 | Asahi Denka Kogyo Kk | 化学気相成長用原料及び金属化合物 |
JP2008504371A (ja) * | 2004-06-09 | 2008-02-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 有機金属化合物およびかかる化合物で形成された素子 |
US20080074033A1 (en) * | 2006-06-14 | 2008-03-27 | Alex Sergey Ionkin | Electroluminescent iridium compounds with silylated, germanylated, and stannylated ligands, and devices made with such compounds |
JP2009001546A (ja) * | 2007-05-18 | 2009-01-08 | Semiconductor Energy Lab Co Ltd | 有機金属錯体および有機金属錯体を含む組成物、発光素子、発光装置、電子機器、発光素子の作製方法 |
JP2009539768A (ja) * | 2006-06-02 | 2009-11-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Ir(iii)の赤色発光錯体およびそのような化合物を使用して製造したデバイス |
JP2012056949A (ja) * | 2010-08-10 | 2012-03-22 | Ube Industries Ltd | イットリウム化合物およびそれを用いた共役ジエン重合触媒 |
US20130137866A1 (en) * | 2011-11-30 | 2013-05-30 | Semiconductor Energy Laboratory Co., Ltd. | Organometallic Complex, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device |
JP2013121957A (ja) * | 2011-12-09 | 2013-06-20 | Universal Display Corp | 新規有機発光材料 |
WO2014148511A1 (ja) * | 2013-03-18 | 2014-09-25 | 独立行政法人産業技術総合研究所 | 光パワー監視装置、光パワー監視方法および光パワー監視装置を用いたレーザ発生装置 |
JP2014193856A (ja) * | 2013-03-01 | 2014-10-09 | Semiconductor Energy Lab Co Ltd | 有機金属錯体、発光素子、発光装置、電子機器、および照明装置 |
Family Cites Families (152)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4769292A (en) | 1987-03-02 | 1988-09-06 | Eastman Kodak Company | Electroluminescent device with modified thin film luminescent zone |
GB8909011D0 (en) | 1989-04-20 | 1989-06-07 | Friend Richard H | Electroluminescent devices |
US5061569A (en) | 1990-07-26 | 1991-10-29 | Eastman Kodak Company | Electroluminescent device with organic electroluminescent medium |
EP0650955B1 (en) | 1993-11-01 | 1998-08-19 | Hodogaya Chemical Co., Ltd. | Amine compound and electro-luminescence device comprising same |
US5703436A (en) | 1994-12-13 | 1997-12-30 | The Trustees Of Princeton University | Transparent contacts for organic devices |
US5707745A (en) | 1994-12-13 | 1998-01-13 | The Trustees Of Princeton University | Multicolor organic light emitting devices |
US6939625B2 (en) | 1996-06-25 | 2005-09-06 | Nôrthwestern University | Organic light-emitting diodes and methods for assembly and enhanced charge injection |
US5844363A (en) | 1997-01-23 | 1998-12-01 | The Trustees Of Princeton Univ. | Vacuum deposited, non-polymeric flexible organic light emitting devices |
US6091195A (en) | 1997-02-03 | 2000-07-18 | The Trustees Of Princeton University | Displays having mesa pixel configuration |
US6013982A (en) | 1996-12-23 | 2000-01-11 | The Trustees Of Princeton University | Multicolor display devices |
US5834893A (en) | 1996-12-23 | 1998-11-10 | The Trustees Of Princeton University | High efficiency organic light emitting devices with light directing structures |
US6303238B1 (en) | 1997-12-01 | 2001-10-16 | The Trustees Of Princeton University | OLEDs doped with phosphorescent compounds |
US6337102B1 (en) | 1997-11-17 | 2002-01-08 | The Trustees Of Princeton University | Low pressure vapor phase deposition of organic thin films |
US6087196A (en) | 1998-01-30 | 2000-07-11 | The Trustees Of Princeton University | Fabrication of organic semiconductor devices using ink jet printing |
US6528187B1 (en) | 1998-09-08 | 2003-03-04 | Fuji Photo Film Co., Ltd. | Material for luminescence element and luminescence element using the same |
US6097147A (en) | 1998-09-14 | 2000-08-01 | The Trustees Of Princeton University | Structure for high efficiency electroluminescent device |
US6830828B2 (en) | 1998-09-14 | 2004-12-14 | The Trustees Of Princeton University | Organometallic complexes as phosphorescent emitters in organic LEDs |
US6294398B1 (en) | 1999-11-23 | 2001-09-25 | The Trustees Of Princeton University | Method for patterning devices |
US6458475B1 (en) | 1999-11-24 | 2002-10-01 | The Trustee Of Princeton University | Organic light emitting diode having a blue phosphorescent molecule as an emitter |
KR100377321B1 (ko) | 1999-12-31 | 2003-03-26 | 주식회사 엘지화학 | 피-형 반도체 성질을 갖는 유기 화합물을 포함하는 전기소자 |
US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
JP2002050860A (ja) | 2000-08-04 | 2002-02-15 | Toray Eng Co Ltd | 実装方法および実装装置 |
EP1325671B1 (en) | 2000-08-11 | 2012-10-24 | The Trustees Of Princeton University | Organometallic compounds and emission-shifting organic electrophosphorescence |
US6579630B2 (en) | 2000-12-07 | 2003-06-17 | Canon Kabushiki Kaisha | Deuterated semiconducting organic compounds used for opto-electronic devices |
JP3812730B2 (ja) | 2001-02-01 | 2006-08-23 | 富士写真フイルム株式会社 | 遷移金属錯体及び発光素子 |
JP4307000B2 (ja) | 2001-03-08 | 2009-08-05 | キヤノン株式会社 | 金属配位化合物、電界発光素子及び表示装置 |
JP4310077B2 (ja) | 2001-06-19 | 2009-08-05 | キヤノン株式会社 | 金属配位化合物及び有機発光素子 |
WO2003001616A2 (en) | 2001-06-20 | 2003-01-03 | Showa Denko K.K. | Light emitting material and organic light-emitting device |
US7071615B2 (en) | 2001-08-20 | 2006-07-04 | Universal Display Corporation | Transparent electrodes |
US7250226B2 (en) | 2001-08-31 | 2007-07-31 | Nippon Hoso Kyokai | Phosphorescent compound, a phosphorescent composition and an organic light-emitting device |
US7431968B1 (en) | 2001-09-04 | 2008-10-07 | The Trustees Of Princeton University | Process and apparatus for organic vapor jet deposition |
US6835469B2 (en) * | 2001-10-17 | 2004-12-28 | The University Of Southern California | Phosphorescent compounds and devices comprising the same |
US7166368B2 (en) | 2001-11-07 | 2007-01-23 | E. I. Du Pont De Nemours And Company | Electroluminescent platinum compounds and devices made with such compounds |
US6863997B2 (en) | 2001-12-28 | 2005-03-08 | The Trustees Of Princeton University | White light emitting OLEDs from combined monomer and aggregate emission |
KR100691543B1 (ko) | 2002-01-18 | 2007-03-09 | 주식회사 엘지화학 | 새로운 전자 수송용 물질 및 이를 이용한 유기 발광 소자 |
US6878975B2 (en) | 2002-02-08 | 2005-04-12 | Agilent Technologies, Inc. | Polarization field enhanced tunnel structures |
US20030230980A1 (en) | 2002-06-18 | 2003-12-18 | Forrest Stephen R | Very low voltage, high efficiency phosphorescent oled in a p-i-n structure |
US7189989B2 (en) | 2002-08-22 | 2007-03-13 | Fuji Photo Film Co., Ltd. | Light emitting element |
EP2261301A1 (en) | 2002-08-27 | 2010-12-15 | Fujifilm Corporation | Organometallic complexes, organic electroluminescent devices and organic electroluminescent displays |
US6687266B1 (en) | 2002-11-08 | 2004-02-03 | Universal Display Corporation | Organic light emitting materials and devices |
JP4365199B2 (ja) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | 有機電界発光素子 |
JP4365196B2 (ja) | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | 有機電界発光素子 |
US7338722B2 (en) | 2003-03-24 | 2008-03-04 | The University Of Southern California | Phenyl and fluorenyl substituted phenyl-pyrazole complexes of Ir |
US7090928B2 (en) | 2003-04-01 | 2006-08-15 | The University Of Southern California | Binuclear compounds |
US7345301B2 (en) | 2003-04-15 | 2008-03-18 | Merck Patent Gmbh | Mixtures of matrix materials and organic semiconductors capable of emission, use of the same and electronic components containing said mixtures |
US7029765B2 (en) | 2003-04-22 | 2006-04-18 | Universal Display Corporation | Organic light emitting devices having reduced pixel shrinkage |
US20060186791A1 (en) | 2003-05-29 | 2006-08-24 | Osamu Yoshitake | Organic electroluminescent element |
JP2005011610A (ja) | 2003-06-18 | 2005-01-13 | Nippon Steel Chem Co Ltd | 有機電界発光素子 |
US20050025993A1 (en) | 2003-07-25 | 2005-02-03 | Thompson Mark E. | Materials and structures for enhancing the performance of organic light emitting devices |
TWI390006B (zh) | 2003-08-07 | 2013-03-21 | Nippon Steel Chemical Co | Organic EL materials with aluminum clamps |
DE10338550A1 (de) | 2003-08-19 | 2005-03-31 | Basf Ag | Übergangsmetallkomplexe mit Carbenliganden als Emitter für organische Licht-emittierende Dioden (OLEDs) |
US20060269780A1 (en) | 2003-09-25 | 2006-11-30 | Takayuki Fukumatsu | Organic electroluminescent device |
JP4822687B2 (ja) | 2003-11-21 | 2011-11-24 | 富士フイルム株式会社 | 有機電界発光素子 |
US7332232B2 (en) | 2004-02-03 | 2008-02-19 | Universal Display Corporation | OLEDs utilizing multidentate ligand systems |
EP2325191A1 (en) | 2004-03-11 | 2011-05-25 | Mitsubishi Chemical Corporation | Composition for charge-transporting film and ion compound, charge-transporting film and organic electroluminescent device using same |
TW200531592A (en) | 2004-03-15 | 2005-09-16 | Nippon Steel Chemical Co | Organic electroluminescent device |
JP4869565B2 (ja) | 2004-04-23 | 2012-02-08 | 富士フイルム株式会社 | 有機電界発光素子 |
US7393599B2 (en) | 2004-05-18 | 2008-07-01 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7534505B2 (en) | 2004-05-18 | 2009-05-19 | The University Of Southern California | Organometallic compounds for use in electroluminescent devices |
US7491823B2 (en) | 2004-05-18 | 2009-02-17 | The University Of Southern California | Luminescent compounds with carbene ligands |
US7445855B2 (en) | 2004-05-18 | 2008-11-04 | The University Of Southern California | Cationic metal-carbene complexes |
US7279704B2 (en) | 2004-05-18 | 2007-10-09 | The University Of Southern California | Complexes with tridentate ligands |
US7154114B2 (en) | 2004-05-18 | 2006-12-26 | Universal Display Corporation | Cyclometallated iridium carbene complexes for use as hosts |
WO2005123873A1 (ja) | 2004-06-17 | 2005-12-29 | Konica Minolta Holdings, Inc. | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
WO2006000544A2 (en) | 2004-06-28 | 2006-01-05 | Ciba Specialty Chemicals Holding Inc. | Electroluminescent metal complexes with triazoles and benzotriazoles |
US20060008670A1 (en) | 2004-07-06 | 2006-01-12 | Chun Lin | Organic light emitting materials and devices |
EP2271183B1 (en) | 2004-07-23 | 2015-03-18 | Konica Minolta Holdings, Inc. | Organic electroluminescent element, display and illuminator |
DE102004057072A1 (de) | 2004-11-25 | 2006-06-01 | Basf Ag | Verwendung von Übergangsmetall-Carbenkomplexen in organischen Licht-emittierenden Dioden (OLEDs) |
KR101272435B1 (ko) | 2004-12-30 | 2013-06-07 | 이 아이 듀폰 디 네모아 앤드 캄파니 | 유기금속 착체 |
US8377571B2 (en) | 2005-02-04 | 2013-02-19 | Konica Minolta Holdings, Inc. | Material for organic electroluminescence element, organic electroluminescence element, display device and lighting device |
KR100797469B1 (ko) | 2005-03-08 | 2008-01-24 | 엘지전자 주식회사 | 적색 인광 화합물 및 이를 사용한 유기전계발광소자 |
KR100803125B1 (ko) | 2005-03-08 | 2008-02-14 | 엘지전자 주식회사 | 적색 인광 화합물 및 이를 사용한 유기전계발광소자 |
JP5125502B2 (ja) | 2005-03-16 | 2013-01-23 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子 |
DE102005014284A1 (de) | 2005-03-24 | 2006-09-28 | Basf Ag | Verwendung von Verbindungen, welche aromatische oder heteroaromatische über Carbonyl-Gruppen enthaltende Gruppen verbundene Ringe enthalten, als Matrixmaterialien in organischen Leuchtdioden |
JPWO2006103874A1 (ja) | 2005-03-29 | 2008-09-04 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
JP5157442B2 (ja) | 2005-04-18 | 2013-03-06 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
US7807275B2 (en) | 2005-04-21 | 2010-10-05 | Universal Display Corporation | Non-blocked phosphorescent OLEDs |
US9051344B2 (en) | 2005-05-06 | 2015-06-09 | Universal Display Corporation | Stability OLED materials and devices |
JP4533796B2 (ja) | 2005-05-06 | 2010-09-01 | 富士フイルム株式会社 | 有機電界発光素子 |
US8007927B2 (en) | 2007-12-28 | 2011-08-30 | Universal Display Corporation | Dibenzothiophene-containing materials in phosphorescent light emitting diodes |
EP2277978B1 (en) | 2005-05-31 | 2016-03-30 | Universal Display Corporation | Triphenylene hosts in phosphorescent light emitting diodes |
JP4976288B2 (ja) | 2005-06-07 | 2012-07-18 | 新日鐵化学株式会社 | 有機金属錯体及びこれを用いた有機電界発光素子 |
US7638072B2 (en) | 2005-06-27 | 2009-12-29 | E. I. Du Pont De Nemours And Company | Electrically conductive polymer compositions |
WO2007004380A1 (ja) | 2005-07-01 | 2007-01-11 | Konica Minolta Holdings, Inc. | 有機エレクトロルミネッセンス素子材料、有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
WO2007028417A1 (en) | 2005-09-07 | 2007-03-15 | Technische Universität Braunschweig | Triplett emitter having condensed five-membered rings |
JP4887731B2 (ja) | 2005-10-26 | 2012-02-29 | コニカミノルタホールディングス株式会社 | 有機エレクトロルミネッセンス素子、表示装置及び照明装置 |
US9023489B2 (en) | 2005-11-07 | 2015-05-05 | Lg Display Co., Ltd. | Red phosphorescent compounds and organic electroluminescent devices using the same |
KR100662378B1 (ko) | 2005-11-07 | 2007-01-02 | 엘지전자 주식회사 | 적색 인광 화합물 및 이를 사용한 유기전계발광소자 |
US20090295276A1 (en) | 2005-12-01 | 2009-12-03 | Tohru Asari | Organic Electroluminescent Device |
CN102633820B (zh) | 2005-12-01 | 2015-01-21 | 新日铁住金化学株式会社 | 有机电致发光元件用化合物及有机电致发光元件 |
ATE553111T1 (de) | 2006-02-10 | 2012-04-15 | Universal Display Corp | Metallkomplexe aus imidazoä1,2-füphenanthridin- liganden und deren verwendung in oled vorrichtungen |
JP4823730B2 (ja) | 2006-03-20 | 2011-11-24 | 新日鐵化学株式会社 | 発光層化合物及び有機電界発光素子 |
KR20070097139A (ko) | 2006-03-23 | 2007-10-04 | 엘지전자 주식회사 | 적색 인광 화합물 및 이를 사용한 유기전계발광소자 |
US20070247061A1 (en) * | 2006-04-20 | 2007-10-25 | Vadim Adamovich | Multiple dopant emissive layer OLEDs |
EP2639231B1 (en) | 2006-04-26 | 2019-02-06 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, and organic electroluminescence element using the same |
WO2007132678A1 (ja) | 2006-05-11 | 2007-11-22 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子 |
EP2034538B1 (en) | 2006-06-02 | 2013-10-09 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescence element, and organic electroluminescence element using the material |
JP5139297B2 (ja) | 2006-08-23 | 2013-02-06 | 出光興産株式会社 | 芳香族アミン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
JP5589251B2 (ja) | 2006-09-21 | 2014-09-17 | コニカミノルタ株式会社 | 有機エレクトロルミネッセンス素子材料 |
US7968146B2 (en) | 2006-11-01 | 2011-06-28 | The Trustees Of Princeton University | Hybrid layers for use in coatings on electronic devices or other articles |
WO2008056746A1 (fr) | 2006-11-09 | 2008-05-15 | Nippon Steel Chemical Co., Ltd. | Composé pour un dispositif électroluminescent organique et dispositif électroluminescent organique |
EP2518045A1 (en) | 2006-11-24 | 2012-10-31 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative and organic electroluminescent element using the same |
US8778508B2 (en) | 2006-12-08 | 2014-07-15 | Universal Display Corporation | Light-emitting organometallic complexes |
US8119255B2 (en) | 2006-12-08 | 2012-02-21 | Universal Display Corporation | Cross-linkable iridium complexes and organic light-emitting devices using the same |
DE602008004738D1 (de) | 2007-02-23 | 2011-03-10 | Basf Se | Elektrolumineszente metallkomplexe mit benzotriazolen |
US9130177B2 (en) * | 2011-01-13 | 2015-09-08 | Universal Display Corporation | 5-substituted 2 phenylquinoline complexes materials for light emitting diode |
KR102312855B1 (ko) * | 2007-03-08 | 2021-10-14 | 유니버셜 디스플레이 코포레이션 | 인광성 물질 |
CN101687893B (zh) | 2007-04-26 | 2014-01-22 | 巴斯夫欧洲公司 | 含有吩噻嗪s-氧化物或吩噻嗪s,s-二氧化物基团的硅烷及其在oled中的用途 |
WO2008156879A1 (en) | 2007-06-20 | 2008-12-24 | Universal Display Corporation | Blue phosphorescent imidazophenanthridine materials |
EP2170911B1 (en) | 2007-06-22 | 2018-11-28 | UDC Ireland Limited | Light emitting cu(i) complexes |
WO2009003898A1 (de) | 2007-07-05 | 2009-01-08 | Basf Se | Organische leuchtdioden enthaltend carben-übergangsmetall-komplex-emitter und mindestens eine verbindung ausgewählt aus disilylcarbazolen; disilyldibenzofuranen, disilyldibenzothiophenen, disilyldibenzophospholen, disilyldibenzothiophen-s-oxiden und disilyldibenzothiophen-s,s-dioxiden |
JP5473600B2 (ja) | 2007-07-07 | 2014-04-16 | 出光興産株式会社 | クリセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子 |
US8779655B2 (en) | 2007-07-07 | 2014-07-15 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
US20090045731A1 (en) | 2007-07-07 | 2009-02-19 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device and material for organic electroluminescence device |
TW200911730A (en) | 2007-07-07 | 2009-03-16 | Idemitsu Kosan Co | Naphthalene derivative, material for organic electroluminescence device, and organic electroluminescence device using the same |
WO2009008205A1 (ja) | 2007-07-07 | 2009-01-15 | Idemitsu Kosan Co., Ltd. | 有機エレクトロルミネッセンス素子および有機エレクトロルミネッセンス素子用材料 |
JPWO2009008099A1 (ja) | 2007-07-10 | 2010-09-02 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
US8080658B2 (en) | 2007-07-10 | 2011-12-20 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescent element and organic electroluminescent element employing the same |
WO2009018009A1 (en) | 2007-07-27 | 2009-02-05 | E. I. Du Pont De Nemours And Company | Aqueous dispersions of electrically conducting polymers containing inorganic nanoparticles |
EP3159333B1 (en) | 2007-08-08 | 2020-04-22 | Universal Display Corporation | Benzo-fused thiophene or furan compounds comprising a triphenylene group |
JP2009040728A (ja) | 2007-08-09 | 2009-02-26 | Canon Inc | 有機金属錯体及びこれを用いた有機発光素子 |
US8956737B2 (en) | 2007-09-27 | 2015-02-17 | Lg Display Co., Ltd. | Red phosphorescent compound and organic electroluminescent device using the same |
EP2203461B1 (de) | 2007-10-17 | 2011-08-10 | Basf Se | Übergangsmetallkomplexe mit verbrückten carbenliganden und deren verwendung in oleds |
US20090101870A1 (en) | 2007-10-22 | 2009-04-23 | E. I. Du Pont De Nemours And Company | Electron transport bi-layers and devices made with such bi-layers |
US7914908B2 (en) | 2007-11-02 | 2011-03-29 | Global Oled Technology Llc | Organic electroluminescent device having an azatriphenylene derivative |
DE102007053771A1 (de) | 2007-11-12 | 2009-05-14 | Merck Patent Gmbh | Organische Elektrolumineszenzvorrichtungen |
KR101353635B1 (ko) | 2007-11-15 | 2014-01-20 | 이데미쓰 고산 가부시키가이샤 | 벤조크리센 유도체 및 이것을 사용한 유기 전계 발광 소자 |
KR101583097B1 (ko) | 2007-11-22 | 2016-01-07 | 이데미쓰 고산 가부시키가이샤 | 유기 el 소자 및 유기 el 재료 함유 용액 |
KR20100106414A (ko) | 2007-11-22 | 2010-10-01 | 이데미쓰 고산 가부시키가이샤 | 유기 el 소자 |
US8221905B2 (en) | 2007-12-28 | 2012-07-17 | Universal Display Corporation | Carbazole-containing materials in phosphorescent light emitting diodes |
CN105859792A (zh) | 2008-02-12 | 2016-08-17 | 巴斯夫欧洲公司 | 具有二苯并[f,h]喹噁啉的电致发光金属络合物 |
TWI482756B (zh) | 2008-09-16 | 2015-05-01 | Universal Display Corp | 磷光物質 |
US8770306B2 (en) * | 2010-05-25 | 2014-07-08 | The Board Of Trustees Of The Leland Stanford Junior University | Inert gas injection to help control or extinguish coal fires |
US8269317B2 (en) | 2010-11-11 | 2012-09-18 | Universal Display Corporation | Phosphorescent materials |
US10008677B2 (en) * | 2011-01-13 | 2018-06-26 | Universal Display Corporation | Materials for organic light emitting diode |
US8492006B2 (en) | 2011-02-24 | 2013-07-23 | Universal Display Corporation | Germanium-containing red emitter materials for organic light emitting diode |
US9163174B2 (en) * | 2012-01-04 | 2015-10-20 | Universal Display Corporation | Highly efficient phosphorescent materials |
US10199581B2 (en) * | 2013-07-01 | 2019-02-05 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10074806B2 (en) * | 2013-08-20 | 2018-09-11 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9847496B2 (en) * | 2013-12-23 | 2017-12-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9935277B2 (en) * | 2014-01-30 | 2018-04-03 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9590194B2 (en) * | 2014-02-14 | 2017-03-07 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9847497B2 (en) * | 2014-02-18 | 2017-12-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10003033B2 (en) * | 2014-02-18 | 2018-06-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9929353B2 (en) * | 2014-04-02 | 2018-03-27 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9691993B2 (en) * | 2014-04-09 | 2017-06-27 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10457699B2 (en) * | 2014-05-02 | 2019-10-29 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9929357B2 (en) * | 2014-07-22 | 2018-03-27 | Universal Display Corporation | Organic electroluminescent materials and devices |
US9397302B2 (en) * | 2014-10-08 | 2016-07-19 | Universal Display Corporation | Organic electroluminescent materials and devices |
ES1158665Y (es) * | 2016-02-29 | 2016-09-09 | Saez César Juan Munoz | Volante de inercia. |
US10608186B2 (en) * | 2016-09-14 | 2020-03-31 | Universal Display Corporation | Organic electroluminescent materials and devices |
US10862046B2 (en) * | 2017-03-30 | 2020-12-08 | Universal Display Corporation | Organic electroluminescent materials and devices |
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Patent Citations (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3950135A (en) * | 1974-07-24 | 1976-04-13 | Massachusetts Institute Of Technology | Method of sepctral analysis using nmr shift reagents |
JPH02145536A (ja) * | 1988-11-28 | 1990-06-05 | Mitsui Petrochem Ind Ltd | β‐ジカルボニル化合物のコバルト錯体 |
JPH0941144A (ja) * | 1995-07-27 | 1997-02-10 | Dowa Mining Co Ltd | 希土類元素のcvd用原料物質およびこれを用いた成膜法 |
JP2000212744A (ja) * | 1999-01-25 | 2000-08-02 | Asahi Denka Kogyo Kk | ルテニウム系薄膜 |
JP2002309373A (ja) * | 2001-04-13 | 2002-10-23 | Asahi Denka Kogyo Kk | 化学気相成長用原料及び金属化合物 |
JP2008504371A (ja) * | 2004-06-09 | 2008-02-14 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 有機金属化合物およびかかる化合物で形成された素子 |
JP2009539768A (ja) * | 2006-06-02 | 2009-11-19 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Ir(iii)の赤色発光錯体およびそのような化合物を使用して製造したデバイス |
US20080074033A1 (en) * | 2006-06-14 | 2008-03-27 | Alex Sergey Ionkin | Electroluminescent iridium compounds with silylated, germanylated, and stannylated ligands, and devices made with such compounds |
JP2009001546A (ja) * | 2007-05-18 | 2009-01-08 | Semiconductor Energy Lab Co Ltd | 有機金属錯体および有機金属錯体を含む組成物、発光素子、発光装置、電子機器、発光素子の作製方法 |
JP2012056949A (ja) * | 2010-08-10 | 2012-03-22 | Ube Industries Ltd | イットリウム化合物およびそれを用いた共役ジエン重合触媒 |
US20130137866A1 (en) * | 2011-11-30 | 2013-05-30 | Semiconductor Energy Laboratory Co., Ltd. | Organometallic Complex, Light-Emitting Element, Light-Emitting Device, Electronic Device, and Lighting Device |
JP2013121957A (ja) * | 2011-12-09 | 2013-06-20 | Universal Display Corp | 新規有機発光材料 |
JP2014193856A (ja) * | 2013-03-01 | 2014-10-09 | Semiconductor Energy Lab Co Ltd | 有機金属錯体、発光素子、発光装置、電子機器、および照明装置 |
WO2014148511A1 (ja) * | 2013-03-18 | 2014-09-25 | 独立行政法人産業技術総合研究所 | 光パワー監視装置、光パワー監視方法および光パワー監視装置を用いたレーザ発生装置 |
Non-Patent Citations (2)
Title |
---|
SEEBACH, D ET AL.: "Synthesis of the Lithium Enolate of (S)-(+)-sec-Butyl Methyl Ketone and Formation of Chiral 1,3-Dike", ANGEWANDTE CHEMIE INTERNATIONAL EDITION IN ENGLISH, vol. 11, JPN6017041122, 1972, pages 127 - 128, ISSN: 0004680020 * |
YOSHIDA, I ET AL.: "Thermal Properties of Copper(II) Chelates of some 1,5-Alkyl-pentane-2,4-diones", BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, vol. 45, JPN7017003425, 1972, pages 174 - 178, ISSN: 0004520725 * |
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