IP Library › Granted Patent US 12,745,560
Granted Patent B2
US 12,745,560 · App. 17/926,721 · Granted Sep 22, 2026

Organic light emitting device

Inventors: Su Jin Han (Daejeon, KR); Dong Hoon Lee (Daejeon, KR); Sang Duk Suh (Daejeon, KR); Min Woo Jung (Daejeon, KR); Jungha Lee (Daejeon, KR); Seulchan Park (Daejeon, KR); Sunghyun Hwang (Daejeon, KR)
Assignee: LG CHEM, LTD.
H10K85/654H10K85/6572H10K85/6574H10K50/11
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Quick Facts
Patent No.
US 12,745,560
App. No.
17/926,721
Granted
Sep 22, 2026
Kind
B2
Abstract

Provided is an organic light emitting device comprising: an anode; a cathode; and a light-emitting layer disposed between the anode and the cathode, wherein the light-emitting layer comprises a compound of the following Chemical Formula 1, a compound of the following Chemical Formula 2, and a compound of the following Chemical Formula 3; as defined in the specification.

Claims (65)

1 . An organic light emitting device, comprising:

an anode, a cathode, and a light emitting layer between the anode and the cathode,

wherein the light emitting layer comprises a compound of the following Chemical Formula 1, a compound of the following Chemical Formula 2, and a compound of the following Chemical Formula 3:

wherein in Chemical Formula 1:

A is a benzene ring;

Ar 1 and Ar 2 are each independently a substituted or unsubstituted C 6-60 aryl or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S;

R 1 is hydrogen, deuterium, a substituted or unsubstituted C 1-60 alkyl, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S; and

a is an integer of 0 to 10;

wherein in Chemical Formula 2:

Ar 3 and Ar 4 are each independently a substituted or unsubstituted C 6-60 aryl or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S;

R 2 and R 3 are each independently hydrogen, deuterium, a substituted or unsubstituted C 1-60 alkyl, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S; and

b and c are each independently an integer of 0 to 7;

wherein in Chemical Formula 3:

B is a substituted or unsubstituted C 6-60 aromatic ring or a substituted or unsubstituted C 2-60 heteroaromatic ring containing any one or more heteroatoms selected from the group consisting of N, O and S;

X 1 to X 3 are each independently N or CH, provided that at least one of X 1 to X 3 is N;

Ar 5 and Ar 6 are each independently a substituted or unsubstituted C 6-60 aryl or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S;

L 1 is a single bond, a substituted or unsubstituted C 6-60 arylene, or a substituted or unsubstituted C 2-60 heteroarylene containing any one or more heteroatoms selected from the group consisting of N, O and S;

R 4 and R 5 are each independently hydrogen, deuterium, a substituted or unsubstituted C 1-60 alkyl, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S;

d is an integer of 0 to 10;

e is an integer of 0 to 3; and

Ar 7 is dibenzothiophenyl, or any one substituent selected from the group consisting of the following substituents:

wherein in the above group of substituents:

Y 1 to Y 3 are each independently N or CH, provided that at least one of Y 1 to Y 3 is N;

Ar′ 1 and Ar′ 2 are each independently a substituted or unsubstituted C 6-60 aryl or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S; and

R′ 1 to R′ 7 are each independently hydrogen, deuterium, a substituted or unsubstituted C 6-60 aryl, or a substituted or unsubstituted C 2-60 heteroaryl containing any one or more heteroatoms selected from the group consisting of N, O and S.

2 . The organic light emitting device according to claim 1 , wherein:

the Chemical Formula 1 is any one of the following Chemical Formula 1-1 to Chemical Formula 1-5:

wherein in Chemical Formulas 1-1 to 1-5:

Ar 1 , Ar 2 , R 1 and a are as defined in claim 1 .

3 . The organic light emitting device according to claim 1 , wherein:

Ar 1 and Ar 2 are each independently phenyl, biphenylyl, phenyl biphenylyl, terphenylyl, dimethylfluorenyl, dimethylfluorenyl phenyl, dibenzofuranyl phenyl, dibenzothiophenyl phenyl, dibenzofuranyl, dibenzothiophenyl, phenyl substituted with 5 deuteriums, biphenylyl substituted with 5 deuteriums, or terphenylyl substituted with 5 deuteriums.

4 . The organic light emitting device according to claim 1 , wherein:

at least one of Ar 1 and Ar 2 is a substituted or unsubstituted C 6-20 aryl.

5 . The organic light emitting device according to claim 1 , wherein:

the compound of Chemical Formula 1 is any one compound selected from the group consisting of the following compounds:

6 . The organic light emitting device according to claim 1 , wherein:

the Chemical Formula 2 is the following Chemical Formula 2-1:

wherein in Chemical Formula 2-1:

Ar 3 , Ar 4 , R 2 , R 3 , b and c are as defined in claim 1 .

7 . The organic light emitting device according to claim 1 , wherein:

Ar 3 and Ar 4 are each independently phenyl, biphenylyl, phenyl biphenylyl, terphenylyl, naphthyl, dimethylfluorenyl, dibenzofuranyl, dibenzothiophenyl, phenyl substituted with 5 deuteriums, or biphenylyl substituted with 1 to 5 deuteriums.

8 . The organic light emitting device according to claim 1 , wherein:

R 2 and R 3 are each independently hydrogen, deuterium or phenyl.

9 . The organic light emitting device according to claim 1 , wherein:

b and c are each independently 0, 1 or 5.

10 . The organic light emitting device according to claim 1 , wherein:

the compound of Chemical Formula 2 is any one compound selected from the group consisting of the following compounds:

11 . The organic light emitting device according to claim 1 , wherein:

B is a benzene ring, a naphthalene ring, a phenanthrene ring, a triphenylene ring, a phenyl carbazole ring, a dimethylfluorene ring, a dibenzofuran ring, or a dibenzothiophene ring.

12 . The organic light emitting device according to claim 1 , wherein:

the Chemical Formula 3 is any one of the following Chemical Formula 3-1 to Chemical Formula 3-10:

wherein in Chemical Formulas 3-1 to 3-10:

X 1 to X 3 , Ar 5 , Ar 6 , Ar 7 , L 1 , R 4 , R 5 , d and e are as defined in claim 1 .

13 . The organic light emitting device according to claim 1 , wherein:

Ar 5 and Ar 6 are each independently phenyl, phenyl substituted with 5 deuteriums, naphthyl, phenanthrenyl, triphenylenyl, dimethylfluorenyl, carbazolyl, carbazolyl substituted with 8 deuteriums, dibenzofuranyl, dibenzothiophenyl, or

14 . The organic light emitting device according to claim 1 , wherein:

Ar′ 1 and Ar′ 2 are each independently phenyl, biphenylyl, naphthyl, phenanthrenyl, triphenylenyl, phenyl substituted with 5 deuteriums, phenyl substituted with one cyano, phenyl substituted with one trifluoromethyl, benzothiophenyl, dibenzofuranyl, or dibenzothiophenyl.

15 . The organic light emitting device according to claim 1 , wherein:

R′ 1 to R′ 7 are each independently hydrogen, deuterium, or phenyl.

16 . The organic light emitting device according to claim 1 , wherein:

L 1 is a single bond, phenylene, naphthyldiyl, dibenzofuranyldiyl, or dibenzothiophenyldiyl.

17 . The organic light emitting device according to claim 1 , wherein:

R 4 and R 5 are each independently hydrogen, deuterium, phenyl, naphthyl, carbazolyl, benzothiophenyl, dibenzofuranyl, dibenzothiophenyl, phenyl substituted with 4 deuteriums, or phenyl substituted with 5 deuteriums.

18 . The organic light emitting device according to claim 1 , wherein:

the compound of Chemical Formula 3 is any one compound selected from the group consisting of the following compounds:

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2022
From: HAN, SU JIN; LEE, DONG HOON; SUH, SANG DUK; JUNG, MIN WOO; LEE, JUNGHA; PARK, SEULCHAN; HWANG, SUNGHYUN
To: LG CHEM, LTD.
Reel/Frame 061839/0405 →
Priority Claims (2)
KR 10-2020-0097618 · Aug 4, 2020 · national
KR 10-2021-0102171 · Aug 3, 2021 · national
Continuity (1)
Related Publication 20230240140A1 · Jul 27, 2023
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