IP Library Granted Patent US 9,960,363
Granted Patent B2
US 9,960,363 · App. 15/538,781 · Granted May 1, 2018

Organic electroluminescent element

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Quick Facts
Patent No.
US 9,960,363
App. No.
15/538,781
Granted
May 1, 2018
Kind
B2
Abstract

The present invention provides an organic electroluminescent element which comprises: an anode; a cathode; and an organic layer interposed between the anode and the cathodes, wherein the organic layer comprises one or more types of layer from the group consisting of a hole-injection layer, hole-transport layer, light-emitting layer, lifetime enhancement layer, electron-transport layer, and electron-injection layer.

Claims (44)

1. An organic electroluminescent element, comprising: an anode; a cathode; and an organic layer interposed therebetween, wherein the organic layer comprises a compound of the following Formula 1:

wherein,

R a and R b are the same or different from each other and are each independently selected from the group consisting of a C 1 -C 40 alkyl group and a C 6 -C 60 aryl group, or combine with each other to form a fused ring,

R 1 to R 3 are the same or different from each other and are each independently selected from the group consisting of a hydrogen, a deuterium, a halogen, a cyano group, a nitro group, an amino group, a C 1 -C 40 alkyl group, a C 2 -C 40 alkenyl group, a C 2 -C 40 alkynyl group, a C 3 -C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 -C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 1 -C 40 alkyloxy group, a C 6 -C 60 aryloxy group, a C 1 -C 40 alkylsilyl group, a C 6 -C 60 arylsilyl group, a C 1 -C 40 alkylboron group, a C 6 -C 60 arylboron group, a C 1 -C 40 phosphine group, a C 1 -C 40 phosphine oxide group, and a C 6 -C 60 arylamine group, or each of R 1 to R 3 forms a fused ring when combined with an adjacent one,

L is selected from the group consisting of a single bond, a C 6 -C 18 arylene group, and a heteroarylene group having 5 to 18 nuclear atoms,

Z 1 to Z 5 are the same or different from each other and are each independently N or C(R 4 ), provided that at least one of Z 1 to Z 5 is N, and when C(R 4 ) is present in a plural number, they are the same or different from each other,

c and e are each an integer of 0 to 4,

d is an integer of 0 to 3,

m and n are each an integer of 1 to 3,

R 4 is selected from the group consisting of a hydrogen, a deuterium, a halogen, a cyano group, a nitro group, an amino group, a C 1 -C 40 alkyl group, a C 2 -C 40 alkenyl group, a C 2 -C 40 alkynyl group, a C 3 -C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 -C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 1 -C 40 alkyloxy group, a C 6 -C 60 aryloxy group, a C 1 -C 40 alkylsilyl group, a C 6 -C 60 arylsilyl group, a C 1 -C 40 alkylboron group, a C 6 -C 60 arylboron group, a C 1 -C 40 phosphine group, a C 1 -C 40 phosphine oxide group and a C 6 -C 60 arylamine group, or bonded to an adjacent substituent to form a fused ring,

the alkyl and aryl groups of R a and R b , the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, alkyloxy, aryloxy, alkylsilyl, arylsilyl, alkylboron, arylboron, phosphine, phosphine oxide, and arylamine groups of R 1 to R 4 , and the arylene and heteroarylene groups of L may be each independently unsubstituted or substituted with at least one substituent selected from the group consisting of a deuterium, a halogen, a cyano group, a nitro group, an amino group, a C 1 -C 40 alkyl group, a C 2 -C 40 alkenyl group, a C 2 -C 40 alkynyl group, a C 3 -C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 -C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 1 -C 40 alkyloxy group, a C 6 -C 60 aryloxy group, a C 1 -C 40 alkylsilyl group, a C 6 -C 60 arylsilyl group, a C 1 -C 40 alkylboron group, a C 6 -C 60 arylboron group, a C 1 -C 40 phosphine group, a C 1 -C 40 phosphine oxide group, and a C 6 -C 60 arylamine group, provided that when the substituent is present in a plural number, they are the same or different from each other.

2. The organic electroluminescent element of claim 1 , wherein the organic layer comprises at least one selected form the group consisting of a hole injection layer, a hole transport layer, a light-emitting layer, a lifetime enhancement layer, an electron transport layer, and an electron injection layer, and

at least one of the lifetime enhancement layer, the electron transport layer, and the electron injection layer contains the compound of Formula 1.

3. The organic electroluminescent element of claim 2 , wherein the lifetime enhancement layer contains the compound of Formula 1.

4. The organic electroluminescent element of claim 3 , wherein the light-emitting layer contains a green phosphorescent material and

the compound of Formula 1, contained in the lifetime enhancement layer has an ionization potential of 6.0 eV or higher and a triplet energy of 2.5 eV or higher.

5. The organic electroluminescent element of claim 3 , wherein the light-emitting layer contains a blue phosphorescent material and

the compound of Formula 1, contained in the lifetime enhancement layer has an ionization potential of 6.0 eV or higher and a triplet energy of 2.7 eV or higher.

6. The organic electroluminescent element of claim 2 , wherein the electron transport layer contains a compound of Formula 1,

the lifetime enhancement layer contains a compound of Formula 1, and

the respective compounds contained in the electron transport layer and the lifetime enhancement layer are identical.

7. The organic electroluminescent element of claim 2 , wherein the electron injection layer contains a compound of Formula 1,

the lifetime enhancement layer contains a compound of Formula 1, and

the respective compounds contained in the electron injection layer and the lifetime enhancement layer are identical.

8. The organic electroluminescent element of claim 1 , wherein the compound of Formula 1 has an ionization potential of 5.5 eV or higher, a gap between HOMO and LUMO of greater than 3.0 eV, a triplet energy of 2.3 eV or higher, and a gap between singlet energy and triplet energy of less than 0.7 eV.

9. The organic electroluminescent element of claim 1 , wherein the compound of Formula 1 has a hole motility of 1×10 −6 cm 2 /V·s or greater and an electron motility of 1×10 −6 cm 2 /V·s or greater at room temperature.

10. The organic electroluminescent element of claim 1 , wherein the compound of Formula 1 is selected from the group consisting of respective compounds of the following Formulas 2 to 4:

wherein,

R a , R b , R 1 to R 3 , Z 1 to Z 5 , c, d, and e are each the same as defined in claim 1 .

11. The organic electroluminescent element of claim 1 , wherein the substituent of

wherein * is a site where to bond with L, in Formula 1 is selected from the group consisting of the structures of the following C-1 to C-15:

wherein,

R 4 is the same as defined in claim 1 ,

R 5 is selected from the group consisting of a hydrogen, a deuterium, a halogen, a cyano group, a nitro group, a C 1 -C 40 alkyl group, a C 2 -C 40 alkenyl group, a C 2 -C 40 alkynyl group, a C 3 -C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 6 -C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 6 -C 60 aryloxy group, a C 1 -C 40 alkyloxy group, a C 6 -C 60 arylamine group, a C 1 -C 40 alkylsilyl group, a C 1 -C 40 alkylboron group, a C 6 -C 60 arylboron group, a C 6 -C 60 arylphosphine group, a C 6 -C 60 arylphosphine oxide group, and a C 6 -C 60 arylsilyl group, or bonded to an adjacent substituent to form a fused ring, and

p is an integer of 1 to 4,

the alkyl, alkenyl, alkynyl, cycloalkyl, heterocycloalkyl, aryl, heteroaryl, aryloxy, alkyloxy, arylamine, alkylsilyl, alkylboron, arylboron, arylphosphine, arylphosphine oxide and arylsilyl groups of R 5 may be each independently unsubstituted or substituted with at least one substituent selected from the group consisting of a deuterium, a halogen, a cyano group, a nitro group, a C 1 -C 40 alkyl group, a C 2 -C 40 alkenyl group, a C 2 -C 40 alkynyl group, a C 6 -C 60 aryl group, a heteroaryl group having 5 to 60 nuclear atoms, a C 6 -C 60 aryloxy group, a C 1 -C 40 alkyloxy group, a C 6 -C 60 aryl amine group, a C 3 -C 40 cycloalkyl group, a heterocycloalkyl group having 3 to 40 nuclear atoms, a C 1 -C 40 alkylsilyl group, a C 1 -C 40 alkylboron group, a C 6 -C 60 arylboron group, a C 6 -C 60 arylphosphine group, a C 6 -C 60 arylphosphine oxide group, and a C 6 -C 60 arylsilyl group, provided that when the substituent is present in a plural number, they are the same or different from each other.

12. The organic electroluminescent element of claim 11 , wherein the compound of Formula 1 is a compound of the following Formula 5:

wherein,

R a , R b , R 1 to R 4 , L, c, d, e, m, and n are each the same as defined in claim 1 .

13. The organic electroluminescent element of claim 12 , wherein R 4 's are identical.

14. The organic electroluminescent element of claim 1 , wherein R a and R b are the same or different from each other and are each independently a methyl group or a phenyl group or bond each other to form a fused ring of

wherein * is a site where to bond.

15. The organic electroluminescent element of claim 1 , wherein L is selected from the group consisting of the structures of the following L-1 to L-9, wherein * is a site where to bond:

16. The organic electroluminescent element of claim 1 , wherein the compound of Formula 1 is selected from the group consisting compounds of the following Formulas LE-01 to LE-12:

Assignments (3)
CHANGE OF NAME Recorded Jan 4, 2021
From: DOOSAN SOLUS CO., LTD.
To: SOLUS ADVANCED MATERIALS CO., LTD.
Reel/Frame 054887/0911 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 18, 2020
From: DOOSAN CORPORATION
To: DOOSAN SOLUS CO., LTD.
Reel/Frame 052970/0277 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 22, 2017
From: EUM, MIN-SIK; PARK, HO-CHEOL; LEE, CHANG JUN; KIM, TAE HYUNG; KIM, JIYI; BEAK, YOUNGMI
To: DOOSAN CORPORATION
Reel/Frame 042788/0929 →