IP Library › Granted Patent US 12,495,717
Granted Patent B2
US 12,495,717 · App. 17/042,696 · Granted Dec 9, 2025

Amine compound and organic light emitting diode comprising same

Inventors: Minjun Kim (Daejeon, KR); Kongkyeom Kim (Daejeon, KR); Hyoung Seok Kim (Daejeon, KR); Min Woo Lee (Daejeon, KR)
Assignee: LG CHEM, LTD.
H10K85/636C07D209/80C07D405/14C07D409/14C07D487/06C09K11/06C09K2211/1007C09K2211/1018H10K50/11H10K85/6572H10K85/6574H10K85/6576
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Quick Facts
Patent No.
US 12,495,717
App. No.
17/042,696
Granted
Dec 9, 2025
Kind
B2
Abstract

Provided is a compound of Chemical Formula 1: wherein: Ar11 to Ar15 are each independently a substituted or unsubstituted aryl or heteroaryl group, or are bonded to an adjacent substituent to form a substituted or unsubstituted ring, L and L2 to L5 are each independently a direct bond or a substituted or unsubstituted arylene group, R1 is hydrogen, deuterium, a halogen group, a nitrile group, or a substituted or unsubstituted aryl or heteroaryl group, and is bonded to an adjacent substituent to form a substituted or unsubstituted ring, r1 is 0 to 8, and when r1 is 2 or more, the R1s are the same as or different from each other, and n is an integer from 1 to 3, and when n is 2 or 3, the Ls are the same as or different from each other, and an organic light emitting diode comprising the same.

Claims (46)

1 . A compound of Chemical Formula 2:

Chemical Formula 2

wherein in Chemical Formula 2:

-(L) n -Ar15 is a phenyl group substituted with deuterium, a halogen group, a nitrile group, an alkoxy group, a silyl group, or an alkyl group which is unsubstituted or substituted with deuterium; or a biphenyl group which is unsubstituted or substituted with deuterium, a halogen group, a nitrile group, an alkoxy group, a silyl group, or an alkyl group which is unsubstituted or substituted with deuterium;

Ar11 to Ar14 are the same as or different from each other, and each independently is a phenyl group, a naphthyl group, a biphenyl group, a fluorenyl group, or a benzofluorenyl group, wherein the phenyl group, the naphthyl group, the biphenyl group, the fluorenyl group, or the benzofluorenyl group is unsubstituted or substituted with a substituent that is deuterium; a halogen group; a nitrile group; an alkyl group having 1 to 5 carbon atoms, which is unsubstituted or substituted with deuterium; a haloalkyl group having 1 to 5 carbon atoms; an alkoxy group having 1 to 5 carbon atoms; a haloalkoxy group having 1 to 5 carbon atoms; a silyl group having 3 to 20 carbon atoms; or a cycloalkyl group having 3 to 20 carbon atoms; or a substituted or unsubstituted heteroaryl group; or are bonded to an adjacent substituent to form a substituted or unsubstituted ring;

L2 to L5 are the same as or different from each other, and each independently is a direct bond or a substituted or unsubstituted arylene group;

R1 is hydrogen, deuterium, a halogen group, a nitrile group, or a substituted or unsubstituted aryl group; and

r1 is an integer from 0 to 8, and when r1 is 2 or more, the R1s are the same as or different from each other.

2 . The compound of claim 1 , wherein the compound of Chemical Formula 2 is any one of the following compounds:

3 . 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 two or more layers provided between the first electrode and the second electrode,

wherein one or more layers of the organic material layer comprise the compound of claim 1 .

4 . The organic light emitting device of claim 3 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound.

5 . The organic light emitting device of claim 3 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound as a dopant of the light emitting layer.

6 . The organic light emitting device of claim 3 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound and a compound of Chemical Formula H:

wherein in Chemical Formula H:

L21 and L22 are the same as or different from each other, and are each independently a direct bond, a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group;

R31 to R38 are the same as or different from each other, and are each independently hydrogen, deuterium, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted phosphine oxide group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; and

Ar101 and Ar102 are the same as or different from each other, and each independently is a substituted or unsubstituted aryl group or a substituted or unsubstituted heteroaryl group.

7 . The compound of claim 1 , wherein when any of Ar11 to Ar14 is a substituted heteroaryl group, the substituent of the heteroaryl group is deuterium; a halogen group; a nitrile group; an alkyl group having 1 to 5 carbon atoms, which is unsubstituted or substituted with deuterium; a haloalkyl group having 1 to 5 carbon atoms; an alkoxy group having 1 to 5 carbon atoms; a haloalkoxy group having 1 to 5 carbon atoms; a silyl group having 3 to 20 carbon atoms; a cycloalkyl group having 3 to 20 carbon atoms; or an aryl group having 6 to 20 carbon atoms, which is unsubstituted or substituted with deuterium.

8 . A compound of the following Chemical Formula 402 or 403:

Chemical Formula 402

wherein in Chemical Formulae 402 and 403:

R21 and R22 are the same as or different from each other, and are each independently hydrogen, deuterium, a halogen group, a nitrile group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted haloalkyl group, a substituted or unsubstituted silyl group, substituted or unsubstituted alkoxy group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group;

k1 and k2 are 1;

r21 and r22 are an integer from 0 to 6, wherein:

when r21 is 2 or more, the R21s are the same as or different from each other, and

when r22 is 2 or more, the R22s are the same as or different from each other;

Ar11 to Ar14 are the same as or different from each other, and each independently is a substituted or unsubstituted aryl group or a substituted or unsubstituted heteroaryl group, or are bonded to an adjacent substituent to form a substituted or unsubstituted ring; and

L2 to L5 are the same as or different from each other, and each independently is a direct bond or a substituted or unsubstituted arylene group.

9 . The compound of claim 8 , wherein Ar11 to Ar14 are the same as or different from each other, and each independently is an aryl group which is unsubstituted or substituted with one substituent selected from the group consisting of deuterium, a halogen group, a nitrile group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, a silyl group, and a cycloalkyl group, or a substituent in which two or more of the recited substituents in the group of substituents of the aryl group are linked; or a heteroaryl group which is unsubstituted or substituted with one substituent selected from the group consisting of deuterium, a halogen group, a nitrile group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, a silyl group, and a cycloalkyl group, or a substituent in which two or more of the recited substituents in the group of substituents of the heteroaryl group are linked.

10 . The compound of claim 8 , wherein the compound of Chemical Formula 402 or 403 is any one of the following compounds:

11 . 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 two or more layers provided between the first electrode and the second electrode,

wherein one or more layers of the organic material layer comprise the compound of claim 3 .

12 . The organic light emitting device of claim 11 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound.

13 . The organic light emitting device of claim 11 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound as a dopant of the light emitting layer.

14 . The organic light emitting device of claim 11 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound and a compound of Chemical Formula H:

wherein in Chemical Formula H:

L21 and L22 are the same as or different from each other, and are each independently a direct bond, a substituted or unsubstituted arylene group, or a substituted or unsubstituted heteroarylene group;

R31 to R38 are the same as or different from each other, and are each independently hydrogen, deuterium, a substituted or unsubstituted alkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted phosphine oxide group, a substituted or unsubstituted aryl group, or a substituted or unsubstituted heteroaryl group; and

Ar101 and Ar102 are the same as or different from each other, and are each independently is a substituted or unsubstituted aryl group or a substituted or unsubstituted heteroaryl group.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 28, 2020
From: KIM, MINJUN; KIM, KONGKYEOM; KIM, HYOUNG SEOK; LEE, MIN WOO
To: LG CHEM, LTD.
Reel/Frame 053906/0626 →
Priority Claims (1)
KR 10-2018-0039620 · Apr 5, 2018 · national
Continuity (1)
Related Publication 20210057650A1 · Feb 25, 2021
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