JP2018528271A5 - - Google Patents
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- JP2018528271A5 JP2018528271A5 JP2018532833A JP2018532833A JP2018528271A5 JP 2018528271 A5 JP2018528271 A5 JP 2018528271A5 JP 2018532833 A JP2018532833 A JP 2018532833A JP 2018532833 A JP2018532833 A JP 2018532833A JP 2018528271 A5 JP2018528271 A5 JP 2018528271A5
- Authority
- JP
- Japan
- Prior art keywords
- complex
- optionally substituted
- formula
- light emitting
- group
- 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
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- -1 2,6-diisopropylphenyl Chemical group 0.000 claims 29
- 125000003118 aryl group Chemical group 0.000 claims 17
- 150000001875 compounds Chemical class 0.000 claims 16
- 239000010949 copper Substances 0.000 claims 16
- 125000004122 cyclic group Chemical group 0.000 claims 16
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- 239000003446 ligand Substances 0.000 claims 14
- 125000000962 organic group Chemical group 0.000 claims 13
- 125000001072 heteroaryl group Chemical group 0.000 claims 12
- 150000001879 copper Chemical class 0.000 claims 11
- 125000001424 substituent group Chemical group 0.000 claims 11
- 125000003107 substituted aryl group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 8
- 229910052739 hydrogen Inorganic materials 0.000 claims 8
- 239000001257 hydrogen Substances 0.000 claims 8
- 125000000217 alkyl group Chemical group 0.000 claims 7
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 7
- 150000001721 carbon Chemical group 0.000 claims 7
- 239000010931 gold Substances 0.000 claims 7
- 229910052757 nitrogen Inorganic materials 0.000 claims 7
- 125000000547 substituted alkyl group Chemical group 0.000 claims 7
- 125000003342 alkenyl group Chemical group 0.000 claims 6
- 125000004429 atom Chemical group 0.000 claims 6
- 229910052802 copper Inorganic materials 0.000 claims 6
- 229910052737 gold Inorganic materials 0.000 claims 6
- 239000002904 solvent Substances 0.000 claims 6
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims 5
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical group [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 claims 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 5
- 238000000034 method Methods 0.000 claims 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 5
- 125000005017 substituted alkenyl group Chemical group 0.000 claims 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 4
- 150000001408 amides Chemical class 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 4
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical group [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 3
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims 3
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 claims 3
- 150000002343 gold Chemical class 0.000 claims 3
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
- 125000001484 phenothiazinyl group Chemical group C1(=CC=CC=2SC3=CC=CC=C3NC12)* 0.000 claims 3
- 229910052709 silver Inorganic materials 0.000 claims 3
- 239000004332 silver Substances 0.000 claims 3
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 claims 2
- XOUQAVYLRNOXDO-UHFFFAOYSA-N 2-tert-butyl-5-methylphenol Chemical compound CC1=CC=C(C(C)(C)C)C(O)=C1 XOUQAVYLRNOXDO-UHFFFAOYSA-N 0.000 claims 2
- LCGTWRLJTMHIQZ-UHFFFAOYSA-N 5H-dibenzo[b,f]azepine Chemical class C1=CC2=CC=CC=C2NC2=CC=CC=C21 LCGTWRLJTMHIQZ-UHFFFAOYSA-N 0.000 claims 2
- GDALETGZDYOOGB-UHFFFAOYSA-N Acridone Natural products C1=C(O)C=C2N(C)C3=CC=CC=C3C(=O)C2=C1O GDALETGZDYOOGB-UHFFFAOYSA-N 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000005977 Ethylene Substances 0.000 claims 2
- ZRALSGWEFCBTJO-UHFFFAOYSA-N Guanidine Chemical compound NC(N)=N ZRALSGWEFCBTJO-UHFFFAOYSA-N 0.000 claims 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims 2
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 2
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 2
- FZEYVTFCMJSGMP-UHFFFAOYSA-N acridone Chemical class C1=CC=C2C(=O)C3=CC=CC=C3NC2=C1 FZEYVTFCMJSGMP-UHFFFAOYSA-N 0.000 claims 2
- 150000004703 alkoxides Chemical class 0.000 claims 2
- 150000001450 anions Chemical class 0.000 claims 2
- 150000007942 carboxylates Chemical class 0.000 claims 2
- 238000000151 deposition Methods 0.000 claims 2
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000005842 heteroatom Chemical group 0.000 claims 2
- 230000005525 hole transport Effects 0.000 claims 2
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 2
- 150000002540 isothiocyanates Chemical class 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 125000002524 organometallic group Chemical group 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 229950000688 phenothiazine Drugs 0.000 claims 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 150000007944 thiolates Chemical class 0.000 claims 2
- ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 1,2-dihydrophenazine Chemical class C1=CC=C2N=C(C=CCC3)C3=NC2=C1 ZIZMDHZLHJBNSQ-UHFFFAOYSA-N 0.000 claims 1
- LNETULKMXZVUST-UHFFFAOYSA-N 1-naphthoic acid Chemical compound C1=CC=C2C(C(=O)O)=CC=CC2=C1 LNETULKMXZVUST-UHFFFAOYSA-N 0.000 claims 1
- ILHYRNCXUBXJRW-UHFFFAOYSA-N 10,11-dihydro-9H-benzo[d][1]benzazepine Chemical class C1=CN=C2C=CC=CC2=C2CCCC=C21 ILHYRNCXUBXJRW-UHFFFAOYSA-N 0.000 claims 1
- XZPNVGKRRGOOMS-UHFFFAOYSA-N 10-methyl-5h-phenazine Chemical compound C1=CC=C2N(C)C3=CC=CC=C3NC2=C1 XZPNVGKRRGOOMS-UHFFFAOYSA-N 0.000 claims 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 claims 1
- ZAYUOSICZWFJSW-UHFFFAOYSA-N 10h-phenothiazine 5,5-dioxide Chemical class C1=CC=C2S(=O)(=O)C3=CC=CC=C3NC2=C1 ZAYUOSICZWFJSW-UHFFFAOYSA-N 0.000 claims 1
- HIYWOHBEPVGIQN-UHFFFAOYSA-N 1h-benzo[g]indole Chemical compound C1=CC=CC2=C(NC=C3)C3=CC=C21 HIYWOHBEPVGIQN-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- UQNBYLDISARGLS-UHFFFAOYSA-N 2,3-ditert-butyl-9H-carbazole-1-carboxylic acid Chemical compound CC(C)(C)c1cc2c3ccccc3[nH]c2c(C(O)=O)c1C(C)(C)C UQNBYLDISARGLS-UHFFFAOYSA-N 0.000 claims 1
- CKKOVFGIBXCEIJ-UHFFFAOYSA-N 2,6-difluorophenol Chemical class OC1=C(F)C=CC=C1F CKKOVFGIBXCEIJ-UHFFFAOYSA-N 0.000 claims 1
- NXXYKOUNUYWIHA-UHFFFAOYSA-M 2,6-dimethylphenolate Chemical compound CC1=CC=CC(C)=C1[O-] NXXYKOUNUYWIHA-UHFFFAOYSA-M 0.000 claims 1
- PWOBDMNCYMQTCE-UHFFFAOYSA-N 2-chlorobenzenethiol Chemical compound SC1=CC=CC=C1Cl PWOBDMNCYMQTCE-UHFFFAOYSA-N 0.000 claims 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-M 2-chlorophenolate Chemical compound [O-]C1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-M 0.000 claims 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-M 2-methylphenolate Chemical compound CC1=CC=CC=C1[O-] QWVGKYWNOKOFNN-UHFFFAOYSA-M 0.000 claims 1
- BCHZICNRHXRCHY-UHFFFAOYSA-N 2h-oxazine Chemical compound N1OC=CC=C1 BCHZICNRHXRCHY-UHFFFAOYSA-N 0.000 claims 1
- CDIDGWDGQGVCIB-UHFFFAOYSA-N 3,5-bis(trifluoromethyl)aniline Chemical class NC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 CDIDGWDGQGVCIB-UHFFFAOYSA-N 0.000 claims 1
- ODSXJQYJADZFJX-UHFFFAOYSA-N 3,5-bis(trifluoromethyl)phenol Chemical compound OC1=CC(C(F)(F)F)=CC(C(F)(F)F)=C1 ODSXJQYJADZFJX-UHFFFAOYSA-N 0.000 claims 1
- TUAMRELNJMMDMT-UHFFFAOYSA-M 3,5-dimethylphenolate Chemical compound CC1=CC(C)=CC([O-])=C1 TUAMRELNJMMDMT-UHFFFAOYSA-M 0.000 claims 1
- IVZUKFYFBUPLRZ-UHFFFAOYSA-N 3,5-ditert-butylbenzenethiol Chemical compound CC(C)(C)C1=CC(S)=CC(C(C)(C)C)=C1 IVZUKFYFBUPLRZ-UHFFFAOYSA-N 0.000 claims 1
- ZDWSNKPLZUXBPE-UHFFFAOYSA-N 3,5-ditert-butylphenol Chemical compound CC(C)(C)C1=CC(O)=CC(C(C)(C)C)=C1 ZDWSNKPLZUXBPE-UHFFFAOYSA-N 0.000 claims 1
- SVDIEPICPYSAJB-UHFFFAOYSA-N 3,6-ditert-butyl-9H-carbazole-1-carboxylic acid Chemical compound CC(C)(C)c1ccc2[nH]c3c(cc(cc3c2c1)C(C)(C)C)C(O)=O SVDIEPICPYSAJB-UHFFFAOYSA-N 0.000 claims 1
- KCSURCKZGJUTCH-UHFFFAOYSA-N 3,7-dinitro-10h-phenothiazine Chemical compound C1=C([N+]([O-])=O)C=C2SC3=CC([N+](=O)[O-])=CC=C3NC2=C1 KCSURCKZGJUTCH-UHFFFAOYSA-N 0.000 claims 1
- OKIHXNKYYGUVTE-UHFFFAOYSA-N 4-Fluorothiophenol Chemical compound FC1=CC=C(S)C=C1 OKIHXNKYYGUVTE-UHFFFAOYSA-N 0.000 claims 1
- BPMFPOGUJAAYHL-UHFFFAOYSA-N 9H-Pyrido[2,3-b]indole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=N1 BPMFPOGUJAAYHL-UHFFFAOYSA-N 0.000 claims 1
- DHHFGQADZVYGIE-UHFFFAOYSA-N 9h-carbazole-1-carboxylic acid Chemical compound C12=CC=CC=C2NC2=C1C=CC=C2C(=O)O DHHFGQADZVYGIE-UHFFFAOYSA-N 0.000 claims 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical group [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical group N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 claims 1
- CHJJGSNFBQVOTG-UHFFFAOYSA-N N-methyl-guanidine Natural products CNC(N)=N CHJJGSNFBQVOTG-UHFFFAOYSA-N 0.000 claims 1
- 101150034699 Nudt3 gene Proteins 0.000 claims 1
- 102000035195 Peptidases Human genes 0.000 claims 1
- 108091005804 Peptidases Proteins 0.000 claims 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical group [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 claims 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M Thiocyanate anion Chemical compound [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 claims 1
- WIUZHVZUGQDRHZ-UHFFFAOYSA-N [1]benzothiolo[3,2-b]pyridine Chemical group C1=CN=C2C3=CC=CC=C3SC2=C1 WIUZHVZUGQDRHZ-UHFFFAOYSA-N 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 150000001448 anilines Chemical class 0.000 claims 1
- 125000000129 anionic group Chemical group 0.000 claims 1
- 229910052787 antimony Inorganic materials 0.000 claims 1
- 229910052785 arsenic Inorganic materials 0.000 claims 1
- 150000001538 azepines Chemical class 0.000 claims 1
- RFRXIWQYSOIBDI-UHFFFAOYSA-N benzarone Chemical compound CCC=1OC2=CC=CC=C2C=1C(=O)C1=CC=C(O)C=C1 RFRXIWQYSOIBDI-UHFFFAOYSA-N 0.000 claims 1
- 150000001716 carbazoles Chemical class 0.000 claims 1
- 150000003857 carboxamides Chemical class 0.000 claims 1
- 150000001805 chlorine compounds Chemical group 0.000 claims 1
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- FNIATMYXUPOJRW-UHFFFAOYSA-N cyclohexylidene Chemical group [C]1CCCCC1 FNIATMYXUPOJRW-UHFFFAOYSA-N 0.000 claims 1
- 230000008021 deposition Effects 0.000 claims 1
- SWSQBOPZIKWTGO-UHFFFAOYSA-N dimethylaminoamidine Natural products CN(C)C(N)=N SWSQBOPZIKWTGO-UHFFFAOYSA-N 0.000 claims 1
- 150000004820 halides Chemical group 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims 1
- 150000004694 iodide salts Chemical class 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 239000012948 isocyanate Substances 0.000 claims 1
- 150000002513 isocyanates Chemical class 0.000 claims 1
- 125000001518 isoselenocyanato group Chemical group *N=C=[Se] 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 230000007935 neutral effect Effects 0.000 claims 1
- QWVGKYWNOKOFNN-UHFFFAOYSA-N o-cresol Chemical compound CC1=CC=CC=C1O QWVGKYWNOKOFNN-UHFFFAOYSA-N 0.000 claims 1
- 239000011368 organic material Substances 0.000 claims 1
- 150000004893 oxazines Chemical class 0.000 claims 1
- 150000002988 phenazines Chemical class 0.000 claims 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 claims 1
- 229940031826 phenolate Drugs 0.000 claims 1
- 150000002990 phenothiazines Chemical class 0.000 claims 1
- 125000001644 phenoxazinyl group Chemical class C1(=CC=CC=2OC3=CC=CC=C3NC12)* 0.000 claims 1
- 150000003003 phosphines Chemical class 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 229920001690 polydopamine Polymers 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 235000019833 protease Nutrition 0.000 claims 1
- 125000002577 pseudohalo group Chemical group 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000004426 substituted alkynyl group Chemical group 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 238000002207 thermal evaporation Methods 0.000 claims 1
- RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical class SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 0 CC(*1N*1)(C=C1)N=Cc2c1c(C=C*(*1N*1)C=C1)c1[n]2 Chemical compound CC(*1N*1)(C=C1)N=Cc2c1c(C=C*(*1N*1)C=C1)c1[n]2 0.000 description 3
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2021110974A JP7306615B2 (ja) | 2015-09-14 | 2021-07-02 | 金属錯体 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1516230.8A GB201516230D0 (en) | 2015-09-14 | 2015-09-14 | Complexes of copper and silver |
| GB1516230.8 | 2015-09-14 | ||
| GB1609707.3 | 2016-06-03 | ||
| GBGB1609707.3A GB201609707D0 (en) | 2016-06-03 | 2016-06-03 | Metal complexes |
| PCT/GB2016/052797 WO2017046572A1 (en) | 2015-09-14 | 2016-09-09 | Metal complexes |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021110974A Division JP7306615B2 (ja) | 2015-09-14 | 2021-07-02 | 金属錯体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2018528271A JP2018528271A (ja) | 2018-09-27 |
| JP2018528271A5 true JP2018528271A5 (cg-RX-API-DMAC7.html) | 2020-10-22 |
| JP6960633B2 JP6960633B2 (ja) | 2021-11-05 |
Family
ID=56926229
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2018532833A Active JP6960633B2 (ja) | 2015-09-14 | 2016-09-09 | 金属錯体 |
| JP2021110974A Active JP7306615B2 (ja) | 2015-09-14 | 2021-07-02 | 金属錯体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2021110974A Active JP7306615B2 (ja) | 2015-09-14 | 2021-07-02 | 金属錯体 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10700295B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP3350189B1 (cg-RX-API-DMAC7.html) |
| JP (2) | JP6960633B2 (cg-RX-API-DMAC7.html) |
| KR (1) | KR20180055853A (cg-RX-API-DMAC7.html) |
| CN (1) | CN108699086B (cg-RX-API-DMAC7.html) |
| AU (1) | AU2016322694B2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2017046572A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11038115B2 (en) | 2017-05-18 | 2021-06-15 | Universal Display Corporation | Organic electroluminescent materials and device |
| US12180230B2 (en) | 2017-11-28 | 2024-12-31 | University Of Southern California | Carbene compounds and organic electroluminescent devices |
| US11306681B2 (en) * | 2019-01-15 | 2022-04-19 | The Boeing Company | Sheared exhaust nozzle |
| KR102867203B1 (ko) | 2020-07-13 | 2025-10-16 | 삼성디스플레이 주식회사 | 발광 소자, 이를 포함한 전자 장치 및 유기금속 화합물 |
| US20230165135A1 (en) * | 2021-11-23 | 2023-05-25 | Versitech Limited | d10 METAL CARBENE COMPLEXES FOR OLED APPLICATIONS |
| CN117024450A (zh) * | 2023-07-18 | 2023-11-10 | 武汉大学 | 一种卡宾货币金属配合物及其制备与应用 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200946537A (en) * | 2008-03-13 | 2009-11-16 | Ube Industries | Substituted ethynyl golden-cyclic alkylaminocarbene complex and organic electroluminescent element |
| US8580990B2 (en) * | 2008-05-09 | 2013-11-12 | The Regents Of The University Of California | Gold catalyzed hydroamination of alkynes and allenes |
| US8580394B2 (en) * | 2009-11-19 | 2013-11-12 | Universal Display Corporation | 3-coordinate copper(I)-carbene complexes |
| US20130190510A1 (en) * | 2011-07-22 | 2013-07-25 | The Regents Of The University Of California | Neutral Tricoordinate Organoboron Derivatives Isoelectronic with Amines and Phosphines |
| JP6284336B2 (ja) | 2013-10-17 | 2018-02-28 | ルネサスエレクトロニクス株式会社 | 半導体装置 |
| US9853229B2 (en) * | 2013-10-23 | 2017-12-26 | University Of Southern California | Organic electroluminescent materials and devices |
-
2016
- 2016-09-09 AU AU2016322694A patent/AU2016322694B2/en active Active
- 2016-09-09 CN CN201680053084.2A patent/CN108699086B/zh active Active
- 2016-09-09 US US15/760,037 patent/US10700295B2/en active Active
- 2016-09-09 JP JP2018532833A patent/JP6960633B2/ja active Active
- 2016-09-09 KR KR1020187010540A patent/KR20180055853A/ko not_active Ceased
- 2016-09-09 WO PCT/GB2016/052797 patent/WO2017046572A1/en not_active Ceased
- 2016-09-09 EP EP16766064.6A patent/EP3350189B1/en active Active
-
2021
- 2021-07-02 JP JP2021110974A patent/JP7306615B2/ja active Active
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