WO2018159970A1 - Dispositif électroluminescent organique - Google Patents
Dispositif électroluminescent organique Download PDFInfo
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- WO2018159970A1 WO2018159970A1 PCT/KR2018/002357 KR2018002357W WO2018159970A1 WO 2018159970 A1 WO2018159970 A1 WO 2018159970A1 KR 2018002357 W KR2018002357 W KR 2018002357W WO 2018159970 A1 WO2018159970 A1 WO 2018159970A1
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- 0 C*(*)*C1C(C)(*)C(*)C(C)C([*-])C2(C)C1***2 Chemical compound C*(*)*C1C(C)(*)C(*)C(C)C([*-])C2(C)C1***2 0.000 description 19
- VBMSQUHXMZWOPC-UHFFFAOYSA-N CC1(C=CC=CC1c1cccc2ccc3[n](C4c5ccccc5C(c5nc(-c6ccccc6)nc(-c6ccccc6)n5)=CC4)c(cc4C5)c6c3c12)c6c4-c1ccccc1C5c1ccccc1 Chemical compound CC1(C=CC=CC1c1cccc2ccc3[n](C4c5ccccc5C(c5nc(-c6ccccc6)nc(-c6ccccc6)n5)=CC4)c(cc4C5)c6c3c12)c6c4-c1ccccc1C5c1ccccc1 VBMSQUHXMZWOPC-UHFFFAOYSA-N 0.000 description 2
- XFSYQOIWGVERAL-YFKPBYRVSA-N C=C=C[C@@H](N=C)O Chemical compound C=C=C[C@@H](N=C)O XFSYQOIWGVERAL-YFKPBYRVSA-N 0.000 description 1
- AWRYOPFOFAPLIM-UHFFFAOYSA-N CC(C)(C1C2)c3ccccc3C1C=CC2N(c(cc1)cc2c1-c1cc(cccc3)c3cc1C21C(C=CCC2)=C2c2ccccc12)C(C=C1)=CCC1c1ccccc1 Chemical compound CC(C)(C1C2)c3ccccc3C1C=CC2N(c(cc1)cc2c1-c1cc(cccc3)c3cc1C21C(C=CCC2)=C2c2ccccc12)C(C=C1)=CCC1c1ccccc1 AWRYOPFOFAPLIM-UHFFFAOYSA-N 0.000 description 1
- RYBRKTJTPOHENK-UHFFFAOYSA-N CC(C)(c1ccccc1-1)c2cccc3c2c-1nc(-[n](c1ccc2)c4ccc5c6c4c1c2-c(cccc1)c1-c6ccc5)n3 Chemical compound CC(C)(c1ccccc1-1)c2cccc3c2c-1nc(-[n](c1ccc2)c4ccc5c6c4c1c2-c(cccc1)c1-c6ccc5)n3 RYBRKTJTPOHENK-UHFFFAOYSA-N 0.000 description 1
- FWXJLLHALRZVHE-UHFFFAOYSA-N CC(C1)C(c2nc(-c3ccccc3)nc(-c3ccccc3)n2)=CC=C1[n](cc1C(C)(CC=CC2)C2(C)C2=C3c4ccccc4C4C=CC=CC24)c2c1C3=CCC2 Chemical compound CC(C1)C(c2nc(-c3ccccc3)nc(-c3ccccc3)n2)=CC=C1[n](cc1C(C)(CC=CC2)C2(C)C2=C3c4ccccc4C4C=CC=CC24)c2c1C3=CCC2 FWXJLLHALRZVHE-UHFFFAOYSA-N 0.000 description 1
- GGTWWCSYBMCBME-UHFFFAOYSA-N CC(C1)C=Cc(c2ccc34)c1cc(C1C=CC=CC1c1ccc5)c2c3c1c5[n]4-c1ccccn1 Chemical compound CC(C1)C=Cc(c2ccc34)c1cc(C1C=CC=CC1c1ccc5)c2c3c1c5[n]4-c1ccccn1 GGTWWCSYBMCBME-UHFFFAOYSA-N 0.000 description 1
- KSUXKEAUEVMTKO-UHFFFAOYSA-N CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(c1c2cccc1)ccc2-c1nc(-c2ccccc2)nc(-c2ccccc2)n1 Chemical compound CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(c1c2cccc1)ccc2-c1nc(-c2ccccc2)nc(-c2ccccc2)n1 KSUXKEAUEVMTKO-UHFFFAOYSA-N 0.000 description 1
- WYMZASPWANWXMI-UHFFFAOYSA-N CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(cc1)ccc1-c1nc(-c2cc(cccc3)c3cc2)nc(-c2ccccc2)n1 Chemical compound CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(cc1)ccc1-c1nc(-c2cc(cccc3)c3cc2)nc(-c2ccccc2)n1 WYMZASPWANWXMI-UHFFFAOYSA-N 0.000 description 1
- IHWKZWURGMLBAZ-UHFFFAOYSA-N CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(cc1)ccc1-c1nc(-c2ccccc2)nc(-c2ccccc2)n1 Chemical compound CC(C1c2ccccc2-c2ccccc2-c2cccc3c12)N3c(cc1)ccc1-c1nc(-c2ccccc2)nc(-c2ccccc2)n1 IHWKZWURGMLBAZ-UHFFFAOYSA-N 0.000 description 1
- MSRJNLDVXWMERW-UHFFFAOYSA-N CC(Cc1c(cccc2)c2c2)c([n]3C4=CC=CC(c5ccccc5)N4)c4-c1c2-c1ccccc1-c1cccc3c41 Chemical compound CC(Cc1c(cccc2)c2c2)c([n]3C4=CC=CC(c5ccccc5)N4)c4-c1c2-c1ccccc1-c1cccc3c41 MSRJNLDVXWMERW-UHFFFAOYSA-N 0.000 description 1
- AQFUSGKNACRMCE-UHFFFAOYSA-N CC1(C)c(cc(cc2)N(c(cc3)ccc3-c3ccccc3)c(cc3)ccc3-c(cc3)cc(c4c(cccc5)c5ccc44)c3[n]4-c3ccccc3)c2-c2ccccc12 Chemical compound CC1(C)c(cc(cc2)N(c(cc3)ccc3-c3ccccc3)c(cc3)ccc3-c(cc3)cc(c4c(cccc5)c5ccc44)c3[n]4-c3ccccc3)c2-c2ccccc12 AQFUSGKNACRMCE-UHFFFAOYSA-N 0.000 description 1
- BAKZEVASKYKKPP-QHSFNAQHSA-N CC[C@@H]1C([n]2c3c(cccc4)c4cc(-c4c-5cccc4)c3c3c4c-5cccc4ccc23)=NC(c2ccccc2)=C2C=CC=CC12 Chemical compound CC[C@@H]1C([n]2c3c(cccc4)c4cc(-c4c-5cccc4)c3c3c4c-5cccc4ccc23)=NC(c2ccccc2)=C2C=CC=CC12 BAKZEVASKYKKPP-QHSFNAQHSA-N 0.000 description 1
- MJTFAUQSXDUUKZ-UHFFFAOYSA-N CN1C=CC=NC1[n]1c2cccc(-c3c(-c4ccccc4-4)cccc3)c2c-4c1 Chemical compound CN1C=CC=NC1[n]1c2cccc(-c3c(-c4ccccc4-4)cccc3)c2c-4c1 MJTFAUQSXDUUKZ-UHFFFAOYSA-N 0.000 description 1
- IDGPMECYKMTEPY-UHFFFAOYSA-N CS1c(c(c2c3cccc2)c(cc2)[n]3-c(cc3)ccc3-c(cc3)ccc3N(c3ccccc3)c3cc(cccc4)c4cc3)c2-c2ccccc12 Chemical compound CS1c(c(c2c3cccc2)c(cc2)[n]3-c(cc3)ccc3-c(cc3)ccc3N(c3ccccc3)c3cc(cccc4)c4cc3)c2-c2ccccc12 IDGPMECYKMTEPY-UHFFFAOYSA-N 0.000 description 1
- QKCKMUYSPUUMJI-SFPAEFIJSA-N C[C@@H]1C([n]2c3c(cccc4)c4cc(-c4c-5cccc4)c3c3c4c-5cccc4ccc23)=NC(c2ccccc2)=NC1c1ccccc1 Chemical compound C[C@@H]1C([n]2c3c(cccc4)c4cc(-c4c-5cccc4)c3c3c4c-5cccc4ccc23)=NC(c2ccccc2)=NC1c1ccccc1 QKCKMUYSPUUMJI-SFPAEFIJSA-N 0.000 description 1
- DBECAZZCFPIVMX-DXQDCMHZSA-N C[C@@H]1C(c(c2c3cccc2)ccc3-[n](c2c3C(C4(C)C=CC=CC4c4ccc5)=CC6C=CC=CC26)c2c3c4c5cc2)=[N+](Cc2ccccc2)[N-]C1C1=CC=CCC1 Chemical compound C[C@@H]1C(c(c2c3cccc2)ccc3-[n](c2c3C(C4(C)C=CC=CC4c4ccc5)=CC6C=CC=CC26)c2c3c4c5cc2)=[N+](Cc2ccccc2)[N-]C1C1=CC=CCC1 DBECAZZCFPIVMX-DXQDCMHZSA-N 0.000 description 1
- YIABHBWOZDLDFN-YFGLDMBDSA-N C[C@H](C1c2ccccc2)c(cccc2)c2-c2c1ccc(N(c1ccccc1)c(cc1)ccc1-c1c3[s]c(cccc4)c4c3ccc1)c2 Chemical compound C[C@H](C1c2ccccc2)c(cccc2)c2-c2c1ccc(N(c1ccccc1)c(cc1)ccc1-c1c3[s]c(cccc4)c4c3ccc1)c2 YIABHBWOZDLDFN-YFGLDMBDSA-N 0.000 description 1
- IXHWGNYCZPISET-UHFFFAOYSA-N N#CC(C#N)=C(C(F)=C(C1=C(C#N)C#N)F)C(F)=C1F Chemical compound N#CC(C#N)=C(C(F)=C(C1=C(C#N)C#N)F)C(F)=C1F IXHWGNYCZPISET-UHFFFAOYSA-N 0.000 description 1
- LQXFOLBBQWZYNH-UHFFFAOYSA-N N#CC(C#N)=C(C(F)=C(C1=C(C2=C(C#N)C#N)F)C(F)=C2F)C(F)=C1F Chemical compound N#CC(C#N)=C(C(F)=C(C1=C(C2=C(C#N)C#N)F)C(F)=C2F)C(F)=C1F LQXFOLBBQWZYNH-UHFFFAOYSA-N 0.000 description 1
- PCCVSPMFGIFTHU-UHFFFAOYSA-N N#CC(C#N)=C(C=C1)C=CC1=C(C#N)C#N Chemical compound N#CC(C#N)=C(C=C1)C=CC1=C(C#N)C#N PCCVSPMFGIFTHU-UHFFFAOYSA-N 0.000 description 1
- ZZWCCDDTBOOLNR-UHFFFAOYSA-N N#CC(C#N)=C(C=C1)C=CC1=C(C=C1)C=CC1=C(C#N)C#N Chemical compound N#CC(C#N)=C(C=C1)C=CC1=C(C=C1)C=CC1=C(C#N)C#N ZZWCCDDTBOOLNR-UHFFFAOYSA-N 0.000 description 1
- AVBBXEPXBKMMGT-UHFFFAOYSA-N N#CC(C1c(cc(-c2ccccc2C2=C(C#N)C#N)c2c2)c2-c2c1cccc2)C#N Chemical compound N#CC(C1c(cc(-c2ccccc2C2=C(C#N)C#N)c2c2)c2-c2c1cccc2)C#N AVBBXEPXBKMMGT-UHFFFAOYSA-N 0.000 description 1
- YAKFZVRTYZEDJB-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c(cc2)ccc2-[n](c2c3c(-c4ccccc4-c4ccc5)ccc2)c2c3c4c5cc2)nc2c1c1ccccc1c1ccccc21 Chemical compound c(cc1)ccc1-[n]1c(-c(cc2)ccc2-[n](c2c3c(-c4ccccc4-c4ccc5)ccc2)c2c3c4c5cc2)nc2c1c1ccccc1c1ccccc21 YAKFZVRTYZEDJB-UHFFFAOYSA-N 0.000 description 1
- WFNMMEUPABAHAX-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1)ccc1-[n]1c(cc(c(c2c3cccc2)c2)[n]3-c3ccccc3)c2c2ccccc12 Chemical compound c(cc1)ccc1-c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1)ccc1-[n]1c(cc(c(c2c3cccc2)c2)[n]3-c3ccccc3)c2c2ccccc12 WFNMMEUPABAHAX-UHFFFAOYSA-N 0.000 description 1
- NNEQFUIUGSDBIA-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-[n](c2ccc3)c4ccc5c6c4c2c3-c(cccc2)c2-c6ccc5)nc2c1cccn2 Chemical compound c(cc1)ccc1-c1cc(-[n](c2ccc3)c4ccc5c6c4c2c3-c(cccc2)c2-c6ccc5)nc2c1cccn2 NNEQFUIUGSDBIA-UHFFFAOYSA-N 0.000 description 1
- DOPVDBDFAAPOPO-UHFFFAOYSA-N c(cc1-c2cccc3c2c2c45)ccc1-c4cccc5ccc2[n]3-c1ccc2c3nccnc3c(cccc3)c3c2c1 Chemical compound c(cc1-c2cccc3c2c2c45)ccc1-c4cccc5ccc2[n]3-c1ccc2c3nccnc3c(cccc3)c3c2c1 DOPVDBDFAAPOPO-UHFFFAOYSA-N 0.000 description 1
- UISXQVLFENUEJY-UHFFFAOYSA-N c(cc12)ccc1[o]c1c2c(cccc2)c2c2c1c1ccccc1c(-[n](c1cccc(-c(cccc3)c3-c3ccc4)c11)c5c1c3c4cc5)n2 Chemical compound c(cc12)ccc1[o]c1c2c(cccc2)c2c2c1c1ccccc1c(-[n](c1cccc(-c(cccc3)c3-c3ccc4)c11)c5c1c3c4cc5)n2 UISXQVLFENUEJY-UHFFFAOYSA-N 0.000 description 1
- IYAZZUXGUPXGCT-UHFFFAOYSA-N c(cc1c2c3)ccc1[o]c2cc(-c1cccc2c1c1c45)c3-c4cccc5ccc1[n]2-c1ccccn1 Chemical compound c(cc1c2c3)ccc1[o]c2cc(-c1cccc2c1c1c45)c3-c4cccc5ccc1[n]2-c1ccccn1 IYAZZUXGUPXGCT-UHFFFAOYSA-N 0.000 description 1
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/94—[b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
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- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/78—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/10—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic rings
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/06—Peri-condensed systems
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- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/06—Peri-condensed systems
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/06—Peri-condensed systems
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- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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Definitions
- the present disclosure relates to an organic electroluminescent device comprising a light-emitting layer and a hole transport zone.
- OLED organic electroluminescent device
- TPD/Alq3 bilayer consisting of a light-emitting layer and a charge transport layer. Since then, the research on an OLED has been rapidly carried out, and it has been commercialized. At present, an OLED mainly uses phosphorescent materials having excellent luminous efficiency in panel implementation. Low driving voltage and high luminous efficiency are required for long lifespan and high resolution of display.
- U.S. Patent No. 6,902,831 discloses an azulene derivative as an organic electroluminescent compound, but it does not specifically disclose an organic electroluminescent compound of a fused azulene derivative. In addition, the document does not specifically disclose that the performance of an OLED can be improved by combining a host compound containing a fused azulene derivative and a specific material contained in a hole transport zone.
- the objective of the present disclosure is to provide an organic electroluminescent device having low driving voltage, high luminous efficiency and/or long lifespan properties by a combination of a light-emitting layer comprising a compound according to the present disclosure, and a hole transport zone comprising a compound having a specific HOMO (Highest Occupied Molecular Orbital) energy level.
- a specific HOMO Highest Occupied Molecular Orbital
- a light-emitting layer comprising a phosphorescent dopant is preferable to have a light-emitting material having excellent hole and electron current properties for low driving voltage, high efficiency, and long lifespan, and the material having the thermal stability for improvement of lifespan.
- using a light-emitting material having a narrow energy band gap can contribute to improve driving voltage and luminous efficiency by minimizing the charge trap.
- the azulene derivative comprised in the device of the present disclosure has a slow transition constant of the internal conversion of S 2 ⁇ S 1 , i.e. 7*10 -8 s, the transition constant of the internal conversion of S 1 ⁇ S 0 is fast, i.e.
- the fluorescence quantum yield of S 2 ⁇ S 0 increases, and so the azulene derivative is one of the representative materials which violates Kasha's rule.
- the levels of S 2 and S 1 of azulene are 3.565 eV and 1.771 eV, respectively, while the level difference of T 1 and S 0 is very small, i.e. the T 1 -S 0 transition is 1.711 eV.
- the conventional hole transport zone has limitations in increasing the efficiency of the light-emitting layer comprising the fused azulene derivative compound.
- a hole transport zone requires a compound having a high HOMO energy level in order to have a high hole mobility. If the HOMO energy level is high, the driving voltage decreases, but the efficiency of the light-emitting layer also decreases. On the contrary, if the HOMO energy level is low, the efficiency of the light-emitting layer increases, but the driving voltage also increases, and thus it is difficult to realize high luminous efficiency of the device.
- the present inventors found that the above-mentioned problems can be solved by comprising a fused azulene derivative of the present disclosure in a light-emitting layer, and an arylamine derivative having a specific HOMO energy level of the present disclosure in a hole transport zone.
- the present inventors found that the above objective can be achieved by an organic electroluminescent device comprising a first electrode, a second electrode facing the first electrode, a light-emitting layer between the first electrode and the second electrode, and a hole transport zone between the first electrode and the light-emitting layer, wherein the light-emitting layer comprises a compound represented by the following formula 1:
- X 1 represents N-L-(Ar) a , S, or O,
- L represents a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene,
- Ar represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, a substituted or unsubstituted mono- or di- (C6-C30)arylamino, or a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino,
- Y 1 to Y 12 each independently, represent N or CR 1 ,
- R 1 each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30
- a represents an integer of 1 to 4, where if a is an integer of 2 or more, each of Ar may be the same or different;
- the hole transport zone comprises an arylamine derivative
- the HOMO energy level of the arylamine derivative satisfies the following equation 11:
- an organic electroluminescent device having low driving voltage, high luminous efficiency and/or long lifespan properties can be provided. Also, it is possible to produce a display device or a lighting device by using the organic electroluminescent device of the present disclosure.
- the organic electroluminescent device of the present disclosure comprises a first electrode, a second electrode facing the first electrode, a light-emitting layer between the first electrode and the second electrode, a hole transport zone between the first electrode and the light-emitting layer, and an electron transport zone between the light-emitting layer and the second electrode.
- One of the first and second electrodes may be an anode, and the other may be a cathode.
- the hole transport zone means a zone wherein holes are transported between the first electrode and the light-emitting layer.
- the hole transport zone may comprise at least one of a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer and an electron blocking layer.
- the hole injection layer, the hole transport layer, the hole auxiliary layer, the light-emitting auxiliary layer and the electron blocking layer, respectively, may be a single layer, or a plurality of layers in which two or more layers are stacked.
- the hole transport zone may comprise a first hole transport layer and a second hole transport layer, wherein the second hole transport layer may be at least one layer of a plurality of hole transport layers, and it may comprise at least one of a hole auxiliary layer, a light-emitting auxiliary layer and a electron blocking layer.
- the hole transport zone may comprise a first hole transport layer and a second hole transport layer, wherein the first hole transport layer may be placed between the first electrode and the light-emitting layer, the second hole transport layer may be placed between the first hole transport layer and the light-emitting layer, and the second hole transport layer may serve as a hole transport layer, a light-emitting auxiliary layer, a hole auxiliary layer and/or an electron blocking layer.
- the hole transport zone may comprise a p-doped hole injection layer, a hole transport layer, and a light-emitting auxiliary layer.
- the p-doped hole injection layer means a hole injection layer doped with a p-dopant.
- the p-dopant is a material capable of imparting p-type semiconductor properties.
- the p-type semiconductor properties mean the properties of injecting or transporting holes at the HOMO energy level, i.e., the properties of materials having a high hole conductivity.
- the hole transport layer may be placed between the anode (or the hole injection layer) and the light-emitting layer.
- the hole transport layer may function to smoothly move the holes transferred from the anode to the light-emitting layer, and to block the electrons transferred from the cathode to remain in the light-emitting layer.
- the light-emitting auxiliary layer may be placed between the anode and the light-emitting layer, or between the cathode and the light-emitting layer. When the light-emitting auxiliary layer is placed between the anode and the light-emitting layer, it can be used for promoting the hole injection and/or the hole transport, or for preventing the overflow of electrons.
- the light-emitting auxiliary layer When the light-emitting auxiliary layer is placed between the cathode and the light-emitting layer, it can be used for promoting the electron injection and/or the electron transport, or for preventing the overflow of holes.
- the hole auxiliary layer may be placed between the hole transport layer (or hole injection layer) and the light-emitting layer, and may be effective to promote or block the hole transport rate (or the hole injection rate), thereby enabling the charge balance to be controlled.
- the electron blocking layer may be placed between the hole transport layer (or hole injection layer) and the light-emitting layer, and can confine the excitions within the light-emitting layer by blocking the overflow of electrons from the light-emitting layer to prevent a light-emitting leakage.
- the further included hole transport layer may be used as a hole auxiliary layer or an electron blocking layer.
- the light-emitting auxiliary layer, the hole auxiliary layer and/or the electron blocking layer may have an effect of improving the efficiency and/or the lifespan of the organic electroluminescent device.
- the electron transport zone may comprise at least one of an electron buffer layer, a hole blocking layer, an electron transport layer and an electron injection layer, and preferably, at least one of an electron transport layer and an electron injection layer.
- the electron buffer layer is a layer capable of improving the problem that light-emitting luminance deteriorates due to the change of current properties in the device when the device is exposed to a high temperature during a process of producing panels, and it can control the charge flow properties.
- the light-emitting layer in which light is emitted, may be a single layer, or a plurality of layers in which two or more layers are stacked.
- the doping concentration of the dopant compound with respect to the host compound of the light-emitting layer is preferably less than 20% by weight.
- (C1-C30)alkyl is meant to be a linear or branched alkyl having 1 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 1 to 10, more preferably 1 to 6, and includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert -butyl, etc.
- (C3-C30)cycloalkyl is a mono- or polycyclic hydrocarbon having 3 to 30 ring backbone carbon atoms, in which the number of carbon atoms is preferably 3 to 20, more preferably 3 to 7, and includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
- (3- to 7-membered)heterocycloalkyl is a cycloalkyl having at least one heteroatom selected from the group consisting of B, N, O, S, Si, and P, preferably O, S, and N, and 3 to 7 ring backbone atoms, and includes tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc.
- (C6-C30)aryl(ene) is a monocyclic or fused ring-type radical derived from an aromatic hydrocarbon having 6 to 30 ring backbone carbon atoms, in which the number of ring backbone carbon atoms is preferably 6 to 20, more preferably 6 to 15, may be partially saturated, and includes phenyl, biphenyl, terphenyl, naphthyl, binaphthyl, phenylnaphthyl, naphthylphenyl, fluorenyl, phenylfluorenyl, benzofluorenyl, dibenzofluorenyl, phenanthrenyl, phenylphenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc.
- (3- to 30-membered)heteroaryl(ene) is an aryl group having at least one, preferably 1 to 4 heteroatoms selected from the group consisting of B, N, O, S, Si, and P, and 3 to 30 ring backbone atoms, in which the number of ring backbone atoms is preferably 3 to 20, more preferably 5 to 15; is a monocyclic ring, or a fused ring condensed with at least one benzene ring; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and includes a monocyclic ring-type heteroaryl including furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl,
- substituted in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or functional group, i.e., a substituent.
- the above substituents may be at least one selected from the group consisting of a methyl, a tert -butyl, a phenyl unsubstituted or substituted with a pyridinyl(s), a naphthyl, a biphenyl, a dimethylfluorenyl, a phenylfluorenyl, a diphenylfluorenyl, a phenanthrenyl, a triphenylenyl, a pyridinyl, a triazinyl substituted with a phenyl(s) and/or a naphthyl(s), an indolyl substituted with a diphenyl(s), a benzoimidazolyl substituted with a phenyl(s), a quinolyl, a quinazolinyl substituted with a phenyl(s), a carbazolyl, a dibenzofuranyl,
- X 1 represents N-L-(Ar) a , S, or O.
- L represents a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene; preferably, a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (5- to 25-membered)heteroarylene; and more preferably, a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 18-membered)heteroarylene, wherein the heteroarylene may comprise at least one of nitrogen, oxygen, and/or sulfur.
- L may represent a single bond, a substituted or unsubstituted phenylene, a substituted or unsubstituted naphthylene, a substituted or unsubstituted biphenylene, a substituted or unsubstituted pyridylene, a substituted or unsubstituted pyrimidinylene, a substituted or unsubstituted triazinylene, a substituted or unsubstituted quinazolinylene, a substituted or unsubstituted quinoxalinylene, a substituted or unsubstituted naphthyridinylene, a substituted or unsubstituted benzoquinazolinylene, a substituted or unsubstituted benzothienopyrimidinylene, a substituted or unsubstituted acenaphthopyrimidinylene, a substituted or unsubstituted
- Ar represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, a substituted or unsubstituted mono- or di- (C6-C30)arylamino, or a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino; preferably, hydrogen, a substituted or unsubstituted (C6-C25)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, or a substituted or unsubstituted di(C6-C25)aryla
- Ar may represent a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted terphenyl, a substituted or unsubstituted triazinyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted benzoquinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted benzoquinoxalinyl, a substituted or unsubstituted quinolyl, a substituted or unsubstituted benzoquinolyl, a substituted or unsubstituted iso
- a represents an integer of 1 to 4, preferably, 1 or 2, where if a is an integer of 2 or more, each of Ar may be the same or different.
- Y 1 to Y 12 each independently, represent N or CR 1 . According to one embodiment of the present disclosure, all of Y 1 to Y 12 may represent CR 1 , and according to another embodiment of the present disclosure, at least one of Y 1 to Y 12 may represent N. Where there are a plurality of R 1 ’s, each of R 1 may be the same or different.
- R 1 each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30
- R 1 may each independently represent hydrogen, a substituted or unsubstituted methyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted triazinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted phenylbiphenylamino, etc.
- At least one adjacent pair of Y 1 to Y 12 in formula 1 are CR 1 , and the adjacent two R 1 ’s of CR 1 are fused together to each independently form a ring represented by any one of the following formulas 2 to 6, but is not limited thereto.
- the formed ring may be a substituted or unsubstituted benzene ring, a naphthalene ring, a furan ring, a thiophene ring, a substituted or unsubstituted pyrrole ring, a pyridine ring, a benzofuran ring, a benzothiophene ring, a substituted or unsubstituted indole ring, a dibenzofuran ring, a dibenzothiophene ring, a substituted or unsubstituted carbazole ring, a phenanthrene ring, etc., including the ring of formulas 2 to 6.
- A represents N or CR 2 . According to one embodiment of the present disclosure, A may all represent CR 2 , and according to another embodiment of the present disclosure, at least one of A may represent N. Where there are a plurality of R 2 ’s, each of R 2 may be the same or different.
- R 2 each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30
- R 3 represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)ary
- the OLED according to the present disclosure comprises a hole transport zone between the first electrode and the light-emitting layer, wherein the hole transport zone comprises an arylamine derivative, and the HOMO energy level of the arylamine derivative satisfies the following equation 11.
- the HOMO energy level of the arylamine derivative satisfies the following equation 12.
- the OLED according to the present disclosure comprises a first hole transport layer between the first electrode and the light-emitting layer, and a second hole transport layer between the first hole transport layer and the light-emitting layer, wherein the second hole transport layer comprises an arylamine derivative containing a fluorene or a fused flourene, and the HOMO energy level of the arylamine derivative satisfies the equation 11.
- the second hole transport layer may be a single layer or a plurality of layers, and the second hole transport layer may serve as a hole transport layer, a light-emitting auxiliary layer, a hole auxiliary layer and/or an electron blocking layer.
- the hole transport zone includes a compound having a HOMO energy level of less than -5.0, e.g., -5.1 or less, it has a value lower than the HOMO energy level of the compound represented by the formula 1 comprised in the light-emitting layer.
- the injection of holes is hindered, and the driving voltage is increased. That is, even if the luminous efficiency of the device increases, since the driving voltage increases as the luminous efficiency increases, there is no gain in terms of power efficiency (lm/W), and rather low power efficiency can be exhibited.
- the hole transport zone comprises a compound having a HOMO energy level exceeding -4.65
- the energy barrier between the layer containing it, e.g., the second hole transport layer, and the light-emitting layer becomes too large, and the injection of holes is hindered.
- the difference between the upper limit value and the lower limit value of the HOMO energy level of the compound comprised in the hole transport zone may be more appropriate about 0.3 eV or less.
- the arylamine derivative comprised in the hole transport zone, preferably the second hole transport layer, for example, at least one of the light-emitting auxiliary layer and the hole auxiliary layer may comprise a compound represented by the following formula 11.
- L a to L c each independently, represent a single bond, a substituted or unsubstituted (C6-C30)arylene, a substituted or unsubstituted (3- to 30-membered)heteroarylene, or a substituted or unsubstituted (C3-C30)cycloalkylene; preferably, a single bond, a substituted or unsubstituted (C6-C25)arylene, a substituted or unsubstituted (5- to 25-membered)heteroarylene, or a substituted or unsubstituted (C3-C25)cycloalkylene; more preferably, a single bond, a (C6-C18)arylene unsubstituted or substituted with a di(C6-C18)arylamino(s), an unsubstituted (5- to 18-membered)heteroarylene, or an unsubstituted (C3-C18
- L a to L c each independently, may represent a single bond, a phenylene unsubstituted or substituted with a diphenylamino(s), or an unsubstituted biphenylene.
- Ar 1 to Ar 3 each independently, represent a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 30-membered)heteroaryl, with the proviso that at least one of Ar 1 to Ar 3 is selected from the following formulas.
- * represents a bonding site with L a , L b , or L c .
- X each independently, represents O, S, NR 8 , or CR 9 R 10
- Z and V each independently, represent O or S.
- B ring represents a substituted or unsubstituted C10 aryl; preferably, an unsubstituted C10 aryl. According to one embodiment of the present disclosure, B ring may represent a naphthalene ring.
- L d represents a single bond, or a substituted or unsubstituted (C6-C30)arylene.
- R 11 to R 35 each independently, represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C6-C30)aryl(C1-C30)alkyl, -NR 36 R 37 , -SiR 38 R 39 R 40 , -SR 41 , -OR 42 , a cyano, a nitro, or a hydroxyl, or may be linked to an adjacent substituent(s) to form a substituted or unsubstitute
- R 11 to R 35 may represent hydrogen; R 11 , R 12 , R 14 to R 17 , R 22 to R 28 , and R 30 to R 35 , each independently, may be fused with the other adjacent R 11 , R 12 , R 14 to R 17 , R 22 to R 28 , and R 30 to R 35 to form a substituted or unsubstituted benzene ring.
- R 13 and R 17 each independently, may represent a biphenyl; R 17 may represent a phenyl substituted with a diphenylamino; two adjacent R 16 ’s may be fused with each other to form an unsubstituted benzene ring; R 18 and R 19 , each independently, may represent a methyl, a phenyl, or a triphenylenyl, and may be the same or different from each other; R 21 and R 22 , each independently, may represent a methyl; R 28 and R 29 , each independently, may represent a methyl or a phenyl, and may be the same or different from each other; and R 18 and R 19 , or R 20 and R 21 may be linked to each other to form a spiro structure, e.g., spiro[fluorene-fluorene] or spiro[fluorene-benzofluorene].
- a spiro structure e.g., spir
- R 8 to R 10 and R 36 to R 42 each independently, represent hydrogen, deuterium, a cyano, a halogen, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C
- a 1 to A 12 each independently, represent N or CR 43 .
- each R 43 may be the same or different from each other.
- R 43 each independently, represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted or unsubstituted
- b, c, e, g, h, j, k, m, n, o, q, r, and s each independently, represent an integer of 1 to 4; d, f, p, and t, each independently, represent an integer of 1 to 3; i represents an integer of 1 to 6; l represents 1 or 2; where each of b to t is an integer of 2 or more, each of R 11 , R 12 , R 14 to R 17 , R 22 to R 28 , and R 30 to R 35 may be the same or different.
- the heteroaryl(ene) or the heterocycloalkyl contains at least one heteroatom selected from B, N, O, S, Si, and P, and preferably, at least one heteroatom selected from N, O, and S.
- the compound represented by formula 1 may be specifically exemplified by the following compounds, but is not limited thereto.
- the arylamine derivative satisfying the equation 11 may be specifically exemplified by the following compounds, but is not limited thereto.
- the compound of formula 1 according to the present disclosure may be produced by a synthetic method known to one skilled in the art.
- the compound of formula 1 may be produced by referring to the following reaction schemes, but are not limited thereto.
- the compound represented by formula 11 may be produced by a synthetic method known to one skilled in the art, and for example, by using or modifying the synthetic methods disclosed in Korean Patent Application Laid-Open Nos. 2014-0104895 A, 2015-0012488 A, 2015-0066202 A, and Korean Patent No. 1476231 B.
- the organic electroluminescent device of the present disclosure may comprise a p-doped hole injection layer.
- the p-doped hole injection layer is doped with a p-dopant, and the p-dopant may preferably be distributed substantially uniformly in the p-doped layer, which may be achieved by co-deposition of a p-dopant and a hole injection material.
- the p-dopant may be contained in an amount of 0.01 to 50 wt%, preferably 0.1 to 20 wt%, more preferably 1 to 10 wt%, based on the hole injection material.
- the p-dopant according to one embodiment of the present disclosure may include at least one of the following compounds P-1 to P-7.
- T 1 to T 38 each independently, represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C50)alkyl fluoride, a cyano, a substituted or unsubstituted (C1-C50)alkoxy, a substituted or unsubstituted (C1-C50)alkyl, a substituted or unsubstituted (C6-C50)aryl, or substituted or unsubstituted (3-30 membered)heteroaryl.
- U 1 and U 2 each independently, represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C50)alkyl fluoride, a cyano, a substituted or unsubstituted (C1-C50)alkoxy, a substituted or unsubstituted (C1-C50)alkyl, a substituted or unsubstituted (C6-C50)aryl, or substituted or unsubstituted (3-30 membered)heteroaryl.
- U 3 to U 8 each independently, represent a substituted or unsubstituted (C1-C50)alkylene fluoride, a substituted or unsubstituted (C1-C50)alkylene, a substituted or unsubstituted (C6-C50)arylene, or substituted or unsubstituted (3-30 membered)heteroarylene.
- the p-dopant may be specifically exemplified by the following compounds, but is not limited thereto.
- the dopant comprised in the light-emitting layer of the organic electroluminescent device of the present disclosure may be at least one phosphorescent or fluorescent dopont, and is preferably at least one phosphorescent dopant.
- the phosphorescent dopant material applied to the organic electroluminescent device of the present disclosure is not particulary limited, but may be preferably selected from the metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), more preferably selected from ortho-metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), and even more preferably ortho-metallated iridium complex compounds.
- the dopant comprised in the light-emitting layer of the organic electroluminescent device of the present disclosure may comprise the compound represented by the following formula 101, but is not limited thereto.
- L is selected from the following structures 1 and 2:
- R 100 to R 103 , and R 104 to R 107 each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with a halogen and/or deuterium, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a cyano, a substituted or unsubstituted (3- to 30-membered)heteroaryl, or a substituted or unsubstituted (C1-C30)alkoxy; or R 100 to R 103 may be linked to adjacent R 100 to R 103 , to form a substituted or unsubstituted fused ring, e.g., a substituted or unsubstituted, quinoline, benzofuropyridine, benzothienopyridine, indenopyridine, benzofuro
- R 201 to R 211 each independently, represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with a halogen and/or deuterium, a substituted or unsubstituted (C3-C30)cycloalkyl, or a substituted or unsubstituted (C6-C30)aryl; or may be linked to adjacent R 201 to R 211 to form a substituted or unsubstituted fused ring; and
- n an integer of 1 to 3.
- dopant compound is as follows, but are not limited thereto.
- a display system e.g., a display system for smart phones, tablets, notebooks, PCs, TVs, or cars; or a lighting system, e.g., an outdoor or indoor lighting system, can be produced.
- the organic electroluminescent device of the present disclosure is intended to explain one embodiment of the present disclosure, and is not meant in any way to restrict the scope of the disclosure.
- the present disclosure may be embodied in other forms.
- the present disclosure may be embodied in other forms.
- the HOMO energy levels of the present disclosure were measured by using a density functional theory (DFT) in a Gaussian 03 program of Gaussian, Inc. Specifically, the HOMO and LUMO energy levels in the Device Examples and Comparative Examples of the present disclosure were extracted from the structure with the lowest energy by comparing the calculated energies of isomers after structurally optimizing all possible isomer structures at the level of B3LYP/6-31g*.
- DFT density functional theory
- the efficiency of the OLED device can be improved by comprising the compound of formula 1 in the light-emitting layer and the arylamine derivative having a specific HOMO energy level in the hole transport zone.
- the following examples merely explain the properties of the OLED device according to the present disclosure for a detailed understanding thereof, but the present disclosure is not limited by the following examples.
- OLED devices according to the present disclosure were produced.
- a transparent electrode indium tin oxide (ITO) thin film (10 ⁇ /sq) on a glass substrate for an OLED device (GEOMATEC CO., LTD., Japan) was subjected to an ultrasonic washing with acetone and isopropyl alcohol, sequentially, and then was stored in isopropyl alcohol.
- the ITO substrate was then mounted on a substrate holder of a vacuum vapor deposition apparatus.
- Compound HI-1 was introduced into a cell of the vacuum vapor deposition apparatus, and then the pressure in the chamber of the apparatus was controlled to 10 -6 torr.
- compound HI-2 was introduced into another cell of the vacuum vapor deposition apparatus and was evaporated by applying an electric current to the cell, thereby forming a second hole injection layer having a thickness of 5 nm on the first hole injection layer.
- Compound HT-2-46 was then introduced into a cell of the vacuum vapor deposition apparatus and was evaporated by applying an electric current to the cell, thereby forming a first hole transport layer having a thickness of 10 nm on the second hole injection layer.
- the compound of the second hole transport layer shown in Table 1 was then introduced into another cell of the vacuum vapor deposition apparatus and was evaporated by applying an electric current to the cell, thereby forming a second hole transport layer (auxiliary layer) having a thickness of 60 nm on the first hole transport layer.
- a light-emitting layer was formed thereon as follows:
- the host material shown in Table 1 was introduced into one cell of the vacuum vapor depositing apparatus as a host, and compound D-39 was introduced into another cell as a dopant.
- the two materials were evaporated and the dopant was deposited in a doping amount of 2 wt% based on the amount of the host and dopant to form a light-emitting layer having a thickness of 40 nm on the hole transport layer.
- Compound ET-1 and compound EI-1 were then introduced into the other two cells and evaporated at a rate of 1:1 to form an electron transport layer having a thickness of 35 nm on the light-emitting layer.
- an Al cathode having a thickness of 80 nm was deposited on the electron injection layer by another vacuum vapor deposition apparatus.
- an OLED device was produced.
- OLED devices were produced in the same manner as in Device Example 1, except that the compound shown in the following Table 1 was used in the second hole transport layer, and the compound CBP was used in the host.
- An OLED device was produced in the same manner as in Device Example 1, except that the compound shown in the following Table 1 was used in the second hole transport layer.
- OLED devices were produced in the same manner as in Device Example 1, except that compound HT-1 and compound HI-2 were deposited at a ratio of 1:0.03 instead of the first and second hole injection layers to form a hole injection layer having a thickness of 5 nm, and compound HT-1 was then evaporated to form a first hole transport layer having a thickness of 100 nm, and the compound shown in Table 1 was used in the second hole transport layer.
- the driving voltage, the luminous efficiency, and the CIE color coordinates at luminance of 1,000 nits, and the lifespan (measured as the percentage to which the luminance decreased from 100% after 16.6 hours at a constant current and at a luminance of 5,000 nits) of the OLED devices produced in Device Examples 1 to 33 and Comparative Examples 1 to 20 are provided in Table 1 below.
- the HOMO energy levels of the compounds comprised in the second hole transport layer of Device Examples 1 to 33 and Comparative Examples 1 to 20 are shown in Table 2 below.
- Device Examples 1 to 33 exhibit lower driving voltage, higher luminous efficiency and/or longer lifespan than the Comparative Examples, by comprising the fused azulene derivative compound of the present disclosure in the light-emitting layer and the compound having the specific HOMO energy level of the present disclosure between the first hole transport layer and the light-emitting layer.
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Abstract
La présente invention concerne un dispositif électroluminescent organique comprenant une couche électroluminescente et une zone de transport de trous. Par inclusion d'une combinaison spécifique d'une couche électroluminescente et d'une zone de transport de trous, il est possible d'obtenir un dispositif électroluminescent organique présentant une faible tension d'attaque, une efficacité lumineuse élevée et/ou des propriétés de longue durée de vie.
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US16/483,062 US11387417B2 (en) | 2017-02-28 | 2018-02-27 | Organic electroluminescent device |
CN201880011305.9A CN110268542B (zh) | 2017-02-28 | 2018-02-27 | 有机电致发光装置 |
JP2019544041A JP7109460B2 (ja) | 2017-02-28 | 2018-02-27 | 有機エレクトロルミネッセンスデバイス |
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KR1020180022906A KR102690159B1 (ko) | 2017-02-28 | 2018-02-26 | 유기 전계 발광 소자 |
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Cited By (4)
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---|---|---|---|---|
CN111004201A (zh) * | 2019-12-27 | 2020-04-14 | 吉林奥来德光电材料股份有限公司 | 有机电致发光化合物、其制备方法及有机电致发光器件 |
US20210028369A1 (en) * | 2018-03-27 | 2021-01-28 | Rohm And Haas Electronic Materials Korea Ltd. | Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same |
US11053437B2 (en) | 2019-06-28 | 2021-07-06 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescent devices, organic electroluminescent device and electronic device |
US11479544B2 (en) | 2017-03-08 | 2022-10-25 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element, and electronic device |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20150121337A (ko) * | 2014-04-18 | 2015-10-29 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
-
2018
- 2018-02-27 WO PCT/KR2018/002357 patent/WO2018159970A1/fr active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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Non-Patent Citations (4)
Title |
---|
CALUS, S. ET AL.: "Optical Absorption And Fluorescence Spectra of Novel Annulated Analogues of Azafluoranthene and Azulene Dyes", MATERIALS CHEMISTRY AND PHYSICS, vol. 121, no. 3, 2010, pages 477 - 483, XP055538261 * |
GASIORSKI, P. ET AL.: "From Pirazoloquinolines to Annulated Azulene Dyes: UV-VIS Spectroscopy and Quantum Chemical Study", JOURNAL OF LUMINESCENCE, vol. 130, no. 12, 2010, pages 2460 - 2468, XP055538257 * |
GASIORSKI, P. ET AL.: "Synthesis And Spectroscopic Study Of Several Novel Annulated Azulene And Azafluoranthene Based Derivatives", JOURNAL OF FLUORESCENCE, vol. 21, no. 1, 2011, pages 443 - 451, XP019879047 * |
SZLACHCIC, P. ET AL.: "Organic Light Emitting Diodes (OLED) Based On Helical Structures Containing 7-Membered Fused Rings", DYES AND PIGMENTS, vol. 114, 2015, pages 184 - 195, XP055538255 * |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US11479544B2 (en) | 2017-03-08 | 2022-10-25 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescence element, organic electroluminescence element, and electronic device |
US20210028369A1 (en) * | 2018-03-27 | 2021-01-28 | Rohm And Haas Electronic Materials Korea Ltd. | Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same |
US11053437B2 (en) | 2019-06-28 | 2021-07-06 | Idemitsu Kosan Co., Ltd. | Compound, material for organic electroluminescent devices, organic electroluminescent device and electronic device |
CN111004201A (zh) * | 2019-12-27 | 2020-04-14 | 吉林奥来德光电材料股份有限公司 | 有机电致发光化合物、其制备方法及有机电致发光器件 |
CN111004201B (zh) * | 2019-12-27 | 2023-04-07 | 吉林奥来德光电材料股份有限公司 | 有机电致发光化合物、其制备方法及有机电致发光器件 |
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