IP Library › Granted Patent US 12,232,420
Granted Patent B2
US 12,232,420 · App. 17/981,689 · Granted Feb 18, 2025

Organic compound, light-emitting element, light-emitting device, electronic device, and lighting device

Inventors: Miki Kurihara (Kanagawa, JP); Hideko Yoshizumi (Kanagawa, JP); Satomi Watabe (Kanagawa, JP); Hiromitsu Kido (Kanagawa, JP); Satoshi Seo (Kanagawa, JP)
Assignee: Semiconductor Energy Laboratory Co., Ltd.
H10K85/6576C07D491/048H10K85/657H10K50/11H10K59/12H10K71/164
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Quick Facts
Patent No.
US 12,232,420
App. No.
17/981,689
Granted
Feb 18, 2025
Kind
B2
Abstract

A novel organic compound is provided. That is, a novel organic compound that is effective in improving reliability of a light-emitting element is provided. The organic compound includes a condensed ring including a pyrimidine ring and is represented by General Formula (G1). In General Formula (G1), A represents a group having 6 to 100 carbon atoms and includes at least one of an aromatic ring and a heteroaromatic ring. The aromatic ring and the heteroaromatic ring may each include a substituent. Furthermore, Q represents oxygen or sulfur. A ring X represents a substituted or unsubstituted naphthalene ring or a substituted or unsubstituted phenanthrene ring.

Claims (42)

1. A light-emitting device comprising:

a pair of electrodes; and

a light-emitting layer between the pair of electrodes,

wherein the light-emitting layer comprises a first organic compound, a second organic compound, and a light-emitting substance,

wherein the first organic compound and the second organic compound form an exciplex,

wherein the first organic compound is represented by General Formula (G2):

wherein α represents a substituted or unsubstituted phenylene group,

wherein n represents an integer of 0 to 4,

wherein Ht uni comprises a pyrrole ring structure, a furan ring structure, or a thiophene ring structure,

wherein Q represents oxygen or sulfur, and

wherein the ring X represents a substituted or unsubstituted naphthalene ring or a substituted or unsubstituted phenanthrene ring.

2. The light-emitting device according to claim 1 , wherein General Formula (G2) is represented by General Formula (G5):

3. The light-emitting device according to claim 1 , wherein Ht uni is represented by any one of General Formulae (Ht-1) to (Ht-7),

wherein R 2 to R 15 each represent 1 to 4 substituents and independently represent any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group, and

wherein Ar 1 represents a substituted or unsubstituted aryl group having 6 to 13 carbon atoms.

4. The light-emitting device according to claim 1 ,

wherein the ring X is represented by any one of General Formulae (X-1) to (X-4) and is condensed with an adjacent ring at a position represented by a, and

wherein R 16 to R 23 each represent 1 to 4 substituents and independently represent any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

5. The light-emitting device according to claim 1 , wherein the first organic compound is represented by Structural Formula (100) or Structural Formula (101):

6. The light-emitting device according to claim 1 , wherein the light-emitting substance is a phosphorescent material.

7. The light-emitting device according to claim 1 , wherein the light-emitting substance is a thermally activated delayed fluorescence material.

8. A light-emitting device comprising:

a pair of electrodes; and

a light-emitting layer between the pair of electrodes,

wherein the light-emitting layer comprises a first organic compound, a second organic compound, and a light-emitting substance,

wherein the first organic compound and the second organic compound form an exciplex,

wherein the first organic compound is represented by General Formula (G3):

wherein α represents a substituted or unsubstituted phenylene group,

wherein n represents an integer of 1 to 4,

wherein Ht uni comprises a pyrrole ring structure, a furan ring structure, or a thiophene ring structure,

wherein R 1 represents hydrogen, an alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted monocyclic saturated hydrocarbon having 5 to 7 carbon atoms, a substituted or unsubstituted polycyclic saturated hydrocarbon having 7 to 10 carbon atoms, or a substituted or unsubstituted aryl group having 6 to 13 carbon atoms,

wherein Q represents oxygen or sulfur, and

wherein a ring X represents a substituted or unsubstituted naphthalene ring or a substituted or unsubstituted phenanthrene ring.

9. The light-emitting device according to claim 8 , wherein General Formula (G3) is represented by General Formula (G4):

10. The light-emitting device according to claim 8 , wherein Ht uni is represented by any one of General Formulae (Ht-1) to (Ht-7),

wherein R 2 to R 15 each represent 1 to 4 substituents and independently represent any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group, and

wherein Ar 1 represents a substituted or unsubstituted aryl group having 6 to 13 carbon atoms.

11. The light-emitting device according to claim 8 ,

wherein the ring X is represented by any one of General Formulae (X-1) to (X-4) and is condensed with an adjacent ring at a position represented by a, and

wherein R 16 to R 23 each represent 1 to 4 substituents and independently represent any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, and a substituted or unsubstituted phenyl group.

12. The light-emitting device according to claim 8 , wherein the light-emitting substance is a phosphorescent material.

13. The light-emitting device according to claim 8 , wherein the light-emitting substance is a thermally activated delayed fluorescence material.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2022
From: KURIHARA, MIKI; YOSHIZUMI, HIDEKO; WATABE, SATOMI; KIDO, HIROMITSU; SEO, SATOSHI
To: SEMICONDUCTOR ENERGY LABORATORY CO., LTD.
Reel/Frame 061674/0713 →
Priority Claims (1)
JP 2017-051536 · Mar 16, 2017 · national
Continuity (2)
Continuation 16493842
Related Publication 20230112454A1 · Apr 13, 2023
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