IP Library › Granted Patent US 12,120,948
Granted Patent B2
US 12,120,948 · App. 17/284,760 · Granted Oct 15, 2024

Boron-containing compound and organic light-emitting element comprising same

Inventors: Sujeong Geum (Daejeon, KR); Kyunghee Kim (Daejeon, KR); Wanpyo Hong (Daejeon, KR); Jaegoo Lee (Daejeon, KR); Sang Duk Suh (Daejeon, KR)
Assignee: LG Chem, Ltd.
H10K85/40C07F7/0812C09K11/06C07B2200/05C09K2211/1018H10K50/11H10K50/15H10K50/16H10K50/17H10K50/171H10K50/18H10K2101/10
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Quick Facts
Patent No.
US 12,120,948
App. No.
17/284,760
Granted
Oct 15, 2024
Kind
B2
Abstract

A compound represented by Chemical Formula 1, and an organic light emitting device comprising the same, the compound used in an organic material layer of the organic light emitting device, and providing low driving voltage and high efficiency properties of the organic light emitting device.

Claims (41)

1. A compound of Chemical Formula 1:

wherein, in Chemical Formula 1:

A1, A2, A3, B1 and B2 are the same as or different from each other, and are each independently a hydrocarbon ring;

Ar1, Ar2, Ar4 and Ar5 are the same as or different from each other, and are each independently a substituted or unsubstituted aryl group;

Ar3 and Ar6 are the same as or different from each other, and are each independently a substituted or unsubstituted alkyl group or a substituted or unsubstituted aryl group;

R1 and R3 are the same as or different from each other, and are each independently deuterium, a halogen group, a cyano group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted amine group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, or a substituted or unsubstituted heterocyclic group;

R2 and R5 are the same as or different from each other, and are each independently hydrogen, deuterium, a halogen group, a cyano group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted amine group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, or a substituted or unsubstituted heterocyclic group;

R4 is deuterium, a halogen group, a cyano group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted alkynyl group, a substituted or unsubstituted alkoxy group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted amine group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aryloxy group, or a substituted or unsubstituted heterocyclic group;

n1 to n3 and n5 are each an integer of 0 to 10, n4 is an integer of 1 to 10, and when any of n1 to n5 is 2 or greater, the two or more substituents in the parentheses are the same as or different from each other;

n1+n3 is 1 or greater; and

m1 and m2 are each 0 or 1, and m1+m2 is 1.

2. The compound of claim 1 , wherein A1, A2, A3, B1 and B2 are the same as or different from each other, and are each independently an aromatic hydrocarbon ring having 6 to 30 carbon atoms.

3. The compound of claim 1 , wherein R4 is deuterium, a halogen group, a substituted or unsubstituted linear or branched alkyl group having 1 to 20 carbon atoms, a substituted or unsubstituted aryl group having 6 to 30 carbon atoms, or a substituted or unsubstituted heterocyclic group having 2 to 30 carbon atoms and comprising one or more heteroatoms selected from the group consisting of O, S, N and Si.

4. The compound of claim 1 , wherein the compound of Chemical Formula 1 is represented by the following Chemical Formula 2 or 3:

wherein, in Chemical Formulae 2 and 3,

A1, A2, A3, B1, B2, R1 to R5, n1 to n5 and Ar1 to Ar6 are the same as defined in Chemical Formula 1.

5. The compound of claim 1 , wherein the compound of Chemical Formula 1 is represented by—the following Chemical Formula 4:

wherein, in Chemical Formula 4,

A1, A3, B1, R1 to R5, n1 to n3, Ar1 to Ar6, m1 and m2 are the same as defined in Chemical Formula 1, and

n11 is an integer of 1 to 5, n12 is an integer of 0 to 4, and when n11 and n12 are 2 or greater, the two or more substituents in the parentheses are the same as or different from each other.

6. The compound of claim 1 , wherein the compound of Chemical Formula 1 is represented by the following Chemical Formula 5:

wherein, in Chemical Formula 5,

R1 to R5, Ar1 to Ar6, m1 and m2 are the same as defined in Chemical Formula 1, and

n11 is an integer of 1 to 5, n14 is an integer of 0 to 5, n12 and n13 are each an integer of 0 to 4, and n15 is an integer of 0 to 3, and when any of n11 to n15 are 2 or greater, the two or more substituents in the parentheses are the same as or different from each other, and n13+n15 is 1 or greater.

7. The compound of claim 1 , wherein the compound of Chemical Formula 1 is represented by the following Chemical Formula 6 or 7:

wherein, in Chemical Formulae 6 and 7,

R1 to R5 and Ar1 to Ar6 are the same as defined in Chemical Formula 1, and

n11 is an integer of 1 to 5, n14 is an integer of 0 to 5, n12 and n13 are each an integer of 0 to 4, n15 and n12′ are each an integer of 0 to 3, n11′ is an integer of 1 to 4, and when any of n11 to n15, n11′ or n12′ are 2 or greater, the two or more substituents in the parentheses are the same as or different from each other, and n13+n15 is 1 or greater.

8. The compound of claim 1 , wherein the compound of Chemical Formula 1 is any one compound selected from among the following compounds:

9. The compound of claim 1 , which is a fluorescence dopant for a thermally activated delayed fluorescence device.

10. An organic light emitting device comprising:

a first electrode;

a second electrode; and

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

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

11. The organic light emitting device of claim 10 , wherein the organic material layer comprises a hole injection layer or a hole transfer layer, and the hole injection layer or the hole transfer layer comprises the compound.

12. The organic light emitting device of claim 10 , wherein the organic material layer comprises an electron transfer layer or an electron injection layer, and the electron transfer layer or the electron injection layer comprises the compound.

13. The organic light emitting device of claim 10 , wherein the organic material layer comprises a light emitting layer, and the light emitting layer comprises the compound.

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

15. The organic light emitting device of claim 13 , wherein the light emitting layer comprises the compound as a thermally activated delayed fluorescence dopant.

16. The organic light emitting device of claim 10 , wherein the organic material layer comprises one or more of a hole transfer layer, a hole injection layer, an electron blocking layer, a layer carrying out hole transfer and hole injection at the same time, a light emitting layer, an electron transfer layer, an electron injection layer, a hole blocking layer, and a layer carrying out electron transfer and electron injection at the same time.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2021
From: GEUM, SUJEONG; KIM, KYUNGHEE; HONG, WANPYO; LEE, JAEGOO; SUH, SANG DUK
To: LG CHEM, LTD.
Reel/Frame 055896/0389 →
Priority Claims (1)
KR 10-2019-0016634 · Feb 13, 2019 · national
Continuity (1)
Related Publication 20210391547A1 · Dec 16, 2021