IP Library › Granted Patent US 12,660,500
Granted Patent B2
US 12,660,500 · App. 18/509,471 · Granted Jun 16, 2026

Composition for organic light emitting device and organic light emitting device comprising same

Inventors: Young-Jin Lee (Yongin-City, KR); Jun-Tae Mo (Yongin-City, KR); Yu-Jin Heo (Yongin-City, KR); Yong-Hui Lee (Yongin-City, KR); Seung-Woo Lee (Yongin-City, KR); Dong-Jun Kim (Yongin-City, KR); Dae-Hyuk Choi (Yongin-City, KR)
Assignee: LT MATERIALS CO., LTD.
H10K85/636C07D405/04C07D405/14C09K11/06H10K85/615H10K85/626H10K85/654H10K85/6574C07B2200/05C09K2211/1018H10K50/12H10K2101/90
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Quick Facts
Patent No.
US 12,660,500
App. No.
18/509,471
Granted
Jun 16, 2026
Kind
B2
Abstract

The present specification provides a composition for an organic light emitting device and an organic light emitting device including the same.

Claims (48)

1 . A composition for an organic light emitting device, comprising a heterocyclic compound represented by the following Chemical Formula A, a heterocyclic compound represented by the following Chemical Formula B, and a heterocyclic compound represented by the following Chemical Formula C:

wherein, in Chemical Formulae A, B and C,

X1 to X3 are the same as or different from each other, and are each independently O; or S,

Cy1 is a substituted or unsubstituted benzene ring; or a substituted or unsubstituted naphthalene ring,

R1, R3, and R4 are the same as or different from each other, and are each independently selected from the group consisting of hydrogen; deuterium; a halogen; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C1 to C60 alkoxy group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; —SiRR′R″; and —P(═O)RR′,

any one of R5 to R14 is -(L5)m5-(Ar4)n4, the other one is -(L6)m6-(N-Het3)l3, and the others are the same as or different from each other, and are each independently selected from the group consisting of hydrogen; deuterium; a halogen; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C1 to C60 alkoxy group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; —SiRR′R″; and —P(═O)RR′,

R, R′, and R″ are the same as or different from each other, and are each independently hydrogen; deuterium; —CN; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 cycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group,

L1 to L6 are the same as or different from each other, and are each independently a direct bond; a substituted or unsubstituted C6 to C60 arylene group; or a substituted or unsubstituted C2 to C60 heteroarylene group,

Ar1 to Ar4 are the same as or different from each other, and are each independently a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; or a combination thereof,

N-Het1, N-Het2, and N-Het3 are the same as or different from each other, and are each independently represented by the following Structural Formula D,

in Structural Formula D,

means a moiety linked to another structure,

Y1 to Y5 are the same as or different from each other, and are each independently CRa or N, and at least one is N,

Ra is a substituted or unsubstituted C6 to C60 aryl group; or a substituted or unsubstituted C2 to C60 heteroaryl group, or two or more adjacent Ra groups are bonded to each other to form a ring,

a is an integer from 0 to 4,

c is an integer from 0 to 2,

d is an integer from 0 to 6,

l1 to l3, m1 to m6, n3, and n4 are the same as or different from each other, and are each independently an integer from 0 to 4, and

when each of a, c, d, l1 to l3, m1 to m6, n3, and n4 is 2 or higher, substituents in the parenthesis are the same as or different from each other.

2 . The composition of claim 1 , wherein Chemical Formula A is represented by any one of the following Chemical Formulae A-1 to A-4:

in Chemical Formulae A-1 to A-4,

the definitions of X1, Cy1, R1, L1, L2, N-Het1, Ar1, Ar2, a, 11 , m1, and m2 are the same as those described in Chemical Formula A.

3 . The composition of claim 1 , wherein Chemical Formula A is represented by any one of the following Chemical Formulae Aa to Ad:

in Chemical Formulae Aa, Ab, Ac, and Ad,

the definitions of X1, R1, L1, L2, N-Het1, Ar1, Ar2, a, 11 , m1, and m2 are the same as those described in Chemical Formula A,

R21 and R22 are the same as or different from each other, and are each independently selected from the group consisting of hydrogen; deuterium; a halogen; a substituted or unsubstituted C1 to C60 alkyl group; a substituted or unsubstituted C2 to C60 alkenyl group; a substituted or unsubstituted C2 to C60 alkynyl group; a substituted or unsubstituted C1 to C60 alkoxy group; a substituted or unsubstituted C3 to C60 cycloalkyl group; a substituted or unsubstituted C2 to C60 heterocycloalkyl group; a substituted or unsubstituted C6 to C60 aryl group; a substituted or unsubstituted C2 to C60 heteroaryl group; —SiRR′R″; and —P(═O)RR′,

b21 is an integer from 0 to 4,

b22 is an integer from 0 to 6, and

when each of b21 and b22 is 2 or higher, substituents in the parenthesis are the same as or different from each other.

4 . The composition of claim 1 , wherein Chemical Formula B is represented by any one of the following Chemical Formulae B-1 to B-6:

in Chemical Formulae B-1 to B-6,

the definitions of X2, R3, R4, L3, L4, N-Het2, Ar3, c, d, l2, m3, m4, and n3 are the same as those described in Chemical Formula B.

5 . The composition of claim 1 , wherein Chemical Formula C is represented by the following Chemical Formula Ca or Cb:

in Chemical Formulae Ca and Cb,

the definitions of X3 and R5 to R14 are the same as those described in Chemical Formula C.

6 . The composition of claim 1 , wherein any one of R5 to R14 is -(L5)m5-(Ar4)n4, the other one is -(L6)m6-(N-Het3)l3, and the others are the same as or different from each other, and are each independently hydrogen; or deuterium.

7 . The composition of claim 1 , wherein any one of R5 to R8 is -(L5)m5-(Ar4)n4, any one of R9 to R14 is -(L6)m6-(N-Het3)l3, and the others are the same as or different from each other, and are each independently hydrogen; or deuterium; or

any one of R9 to R14 is -(L5)m5-(Ar4)n4, any one of R5 to R8 is -(L6)m6-(N-Het3)l3, and the others are the same as or different from each other, and are each independently hydrogen, or deuterium.

8 . The composition of claim 1 , wherein Chemical Formula A comprises any one of the following compounds:

9 . The composition of claim 1 , wherein Chemical Formula B comprises any one of the following compounds:

10 . The composition of claim 1 , wherein Chemical Formula C comprises any one of the following compounds:

11 . The composition of claim 1 , wherein a molar ratio of the heterocyclic compound represented by Chemical Formula A, the heterocyclic compound represented by Chemical Formula B, and the heterocyclic compound represented by Chemical Formula C is 0.1 to 3:0.1 to 2.5:0.1 to 2.

12 . An organic light emitting device comprising:

a first electrode;

a second electrode provided to face the first electrode; and

an organic material layer having one or more layers provided between the first electrode and the second electrode,

wherein one or more layers of the organic material layer comprise the composition according to claim 1 .

13 . The organic light emitting device of claim 12 , wherein the organic material layer further comprises a light emitting layer (emission layer), and the light emitting layer comprises the composition for an organic light emitting device.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 15, 2023
From: LEE, YOUNG-JIN; MO, JUN-TAE; HEO, YU-JIN; LEE, YONG-HUI; LEE, SEUNG-WOO; KIM, DONG-JUN; CHOI, DAE-HYUK
To: LT MATERIALS CO., LTD.
Reel/Frame 065569/0710 →
Priority Claims (1)
KR 10-2022-0163046 · Nov 29, 2022 · national
Continuity (1)
Related Publication 20240237515A1 · Jul 11, 2024
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