IP Library Granted Patent US 12,590,076
Granted Patent B2
US 12,590,076 · App. 17/053,630 · Granted Mar 31, 2026

Compound, material for organic electroluminescent element, organic electroluminescent element, and electronic device

Inventors: Hirokatsu Ito (Sodegaura, JP); Tasuku Haketa (Sodegaura, JP); Yu Kudo (Sodegaura, JP)
Assignee: IDEMITSU KOSAN CO., LTD.
C07D307/91H10K85/615H10K85/636H10K85/6574H10K50/156H10K50/157
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Quick Facts
Patent No.
US 12,590,076
App. No.
17/053,630
Granted
Mar 31, 2026
Kind
B2
Abstract

Provided is an organic electroluminescent element including a compound that is represented by formula (1) and having a more improved lifetime. In the formula, X, R 1 -R 8 , R 11 -R 17 , R 21 -R 30 , L 1 , L 2 , n, and Ar 1 -Ar 3 are as defined in the description:

Claims (59)

1 . A compound selected from the group consisting of Compound 1, Compound 3, Compound 5, Compound 6, Compound 7, Compound 8, Compound 9, Compound 10, Compound 11, Compound 12, Compound 13, Compound 14, Compound 15, Compound 16, Compound 17, and Compound 18:

2 . An organic electroluminescence device comprising:

an anode;

a cathode; and

an organic layer between the anode and the cathode,

wherein the organic layer comprises a light emitting layer and at least one layer of the organic layer comprises the compound according to claim 1 .

3 . The organic electroluminescence device according to claim 2 , wherein the organic layer comprises a hole transporting region between the anode and the light emitting layer and the hole transporting region comprises the compound.

4 . The organic electroluminescence device according to claim 3 , wherein the hole transporting region comprises a first hole transporting layer at anode side and a second hole transporting layer at cathode side and the first hole transporting layer, the second hole transporting, or both comprise the compound.

5 . The organic electroluminescence device according to claim 4 , wherein the first hole transporting layer comprises the compound.

6 . The organic electroluminescence device according to claim 4 , wherein the second hole transporting layer comprises the compound.

7 . The organic electroluminescence device according to claim 6 , wherein the second hole transporting layer is in contact with the light emitting layer.

8 . The organic electroluminescence device according to claim 2 , wherein the light emitting layer comprises a fluorescent dopant material.

9 . The organic electroluminescence device according to claim 2 , wherein the light emitting layer comprises a phosphorescent dopant material.

10 . An electronic device comprising:

the organic electroluminescence device according to claim 2 .

11 . The compound according to claim 1 , wherein the compound is Compound 1.

12 . A compound represented by one selected from the group consisting of formula (3a-1), formula (3a-2) and formula (3a-3)

where X is an oxygen atom;

one selected from R 1 to R 4 is a single bond bonded to *f;

R 5 to R 8 and R 1 to R 4 not the single bond bonded to *f are hydrogen atoms;

R 11 to R 17 and R 21 to R 30 are hydrogen atoms;

L 1 and L 2 are each independently an unsubstituted phenylene group;

n is 0 or 1, when n is 0, -(L 2 ) 0 - is a single bond; and

R 32 , R 33 , R 35 , R 36 , R 42 to R 46 , and R 52 to R 56 are hydrogen atoms.

13 . The compound according to claim 12 , wherein the compound is represented by formula (3a-1).

14 . The compound according to claim 13 , wherein n is 1.

15 . The compound according to claim 14 , wherein R 4 is a single bond bonded to *f.

16 . The compound according to claim 12 , wherein n is 0.

17 . The compound according to claim 16 , wherein R 1 is a single bond bonded to *f.

18 . The compound according to claim 16 , wherein R 3 is a single bond bonded to *f.

19 . The compound according to claim 16 , wherein R 4 is a single bond bonded to *f.

20 . The compound according to claim 12 , wherein the compound is represented by formula (3a-2) or (3a-3), and n is 0.

21 . A compound represented by formula (4a-1) or (4a-2)

where X is an oxygen atom;

one selected from R 1 to R 4 is a single bond bonded to *f;

R 5 to R 8 and R 1 to R 4 not the single bond bonded to *f are hydrogen atoms;

R 11 to R 17 and R 21 to R 30 are hydrogen atoms;

L 1 and L 2 are each independently an unsubstituted phenylene group;

n is 0 or 1, when n is 0, -(L 2 ) 0 - is a single bond; and

R 31 to R 38 , R 42 , R 43 , R 45 , R 46 , and R 52 to R 56 are hydrogen atoms.

22 . The compound according to claim 21 , wherein n is 0, and R 4 is a single bond bonded to *f.

23 . A compound represented by formula (5a-1) or (5a-2)

where X is an oxygen atom;

one selected from R 1 to R 4 is a single bond bonded to *f;

R 5 to R 8 and R 1 to R 4 not the single bond bonded to *f are hydrogen atoms;

R 11 to R 17 and R 21 to R 30 are hydrogen atoms;

L 1 and L 2 are each independently an unsubstituted phenylene group;

n is 0 or 1, when n is 0, -(L 2 ) 0 - is a single bond; and

R 32 , R 33 , R 35 , R 36 , R 41 to R 48 , and R 52 to R 56 are hydrogen atoms.

24 . The compound according to claim 23 , wherein n is 0, and R 4 is a single bond bonded to *f.

25 . A compound represented by formula (6a-1) or (6a-2)

where X is an oxygen atom;

one selected from R 1 to R 4 is a single bond bonded to *f;

R 5 to R 8 and R 1 to R 4 not the single bond bonded to *f are hydrogen atoms;

R 11 to R 17 and R 21 to R 30 are hydrogen atoms;

L 1 and L 2 are each independently an unsubstituted phenylene group;

n is 0 or 1, when n is 0, -(L 2 ) 0 - is a single bond; and

R 32 , R 33 , R 35 , R 36 , R 42 , R 43 , R 45 , R 46 , and R 51 to R 58 are hydrogen atoms.

26 . The compound according to claim 25 , wherein n is 0, and R 4 is a single bond bonded to *f.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2020
From: ITO, HIROKATSU; HAKETA, TASUKU; KUDO, YU
To: IDEMITSU KOSAN CO.,LTD.
Reel/Frame 054302/0848 →
Priority Claims (1)
JP 2018-091763 · May 10, 2018 · national
Continuity (1)
Related Publication 20210253546A1 · Aug 19, 2021
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