IP Library Granted Patent US 11,316,114
Granted Patent B2
US 11,316,114 · App. 16/077,765 · Granted Apr 26, 2022

Organic electroluminescent compound and organic electroluminescent device comprising the same

Inventors: Sang Hee Cho (Hwaseong-si, KR); Hong Yeop Na (Hwaseong-si, KR); Zhengming Tang (Shanghai, CN); Shaoguang Feng (Shanghai, CN); Doo-Hyeon Moon (Hwaseong-si, KR)
Assignee: DOW GLOBAL TECHNOLOGIES LLC
H01L51/0067C07D403/10C07D417/10H01L51/0071H01L51/0072H01L51/5012H01L51/5096C07D413/04H01L51/5004H01L51/508H01L51/5056H01L51/5092
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Quick Facts
Patent No.
US 11,316,114
App. No.
16/077,765
Granted
Apr 26, 2022
Kind
B2
Abstract

The present invention relates to an organic EL device comprising an electron buffer material, and a first electrode, a second electrode opposing the first electrode, a light-emitting layer disposed between the two electrodes, and an electron transport zone and an electron buffer layer disposed between the light-emitting layer and the second electrode. By using an electron buffer material according to the present invention, the organic EL device having low driving voltage, high luminous efficiency, and excellent lifespan can be provided.

Claims (23)

1. An electron buffer material selected from the group consisting of the following compounds:

2. An organic electroluminescent device comprising a first electrode, a second electrode opposing the first electrode, a light-emitting layer disposed between the two electrodes, and an electron transport zone and an electron buffer layer disposed between the light-emitting layer and the second electrode,

wherein the electron transport zone comprises an electron injection layer and an electron transport layer,

wherein the electron buffer layer comprises the compound represented by the following formula 2 or 5:

wherein

X 2 represents N or CR 8 ;

X 3 represents N or CR 9 ;

with the proviso that when X 2 represents N, X 3 represents CR 9 , and if X 2 represents CR 8 , X 3 represents N;

R 8 and R 9 each independently represent hydrogen or deuterium;

L 1 represents a single bond, an unsubstituted (C6-C30)arylene group, or an unsubstituted 3- to 30-membered heteroarylene group;

X represents O, S, or NR 2 ;

R 1 , R 2 and R 14 each independently represent hydrogen, deuterium, a halogen, a cyano group, a carboxyl group, a nitro group, a hydroxyl group, a substituted or unsubstituted (C1-C30)alkyl group, a substituted or unsubstituted (C3-C30)cycloalkyl group, a substituted or unsubstituted (C3-C30)cycloalkenyl group, a substituted or unsubstituted 3- to 7-membered heterocycloalkyl group, a substituted or unsubstituted (C6-C30)aryl group, a substituted or unsubstituted 3- to 30-membered heteroaryl group, —NR 3 R 4 , or —SiR 5 R 6 R 7 ; or are linked to an adjacent substituent(s) to form a substituted or unsubstituted mono- or polycyclic (C3-C30) alicyclic or aromatic ring whose carbon atom(s) may be replaced with at least one hetero atom selected from nitrogen, oxygen, and sulfur;

R 3 to R 7 , R 10 and R 11 each independently represent hydrogen, deuterium, a halogen, a cyano group, a carboxyl group, a nitro group, a hydroxyl group, a substituted or unsubstituted (C1-C30)alkyl group, a substituted or unsubstituted (C3-C30)cycloalkyl group, a substituted or unsubstituted (C3-C30)cycloalkenyl group, a substituted or unsubstituted 3- to 7-membered heterocycloalkyl group, a substituted or unsubstituted (C6-C30)aryl group, or a substituted or unsubstituted 3- to 30-membered heteroaryl group;

a and c each independently represents an integer of 1 to 4; where a is an integer of 2 or more, each R 1 is the same or different; where c is an integer of 2 or more, each R 14 is the same or different; and

the heteroaryl(ene) and heterocycloalkyl groups each independently contain at least one hetero atom selected from B, N, O, S, P(═O), Si, and P.

3. The organic electroluminescent device according to claim 2 , wherein the light-emitting layer comprises a host compound and a dopant compound, and LUMO (lowest unoccupied molecular orbital) energy value of the electron buffer layer is higher than that of the host compound.

4. The organic electroluminescent device according to claim 2 , wherein the electron transport zone comprises an electron transport compound, a reducing dopant, or the combination thereof.

5. The organic electroluminescent device according to claim 4 , wherein the electron transport compound is at least one selected from the group consisting of oxazole-based compounds, isoxazole-based compounds, triazole-based compounds, isothiazole-based compounds, oxadiazole-based compounds, thiadiazole-based compounds, perylene-based compounds, anthracene-based compounds, aluminum complexes, and gallium complexes, and the reducing dopant is at least one selected from the group consisting of an alkaline metal, an alkaline metal compound, an alkaline earth metal, a rare-earth metal, halides thereof, oxides thereof, and complexes thereof.

6. The organic electroluminescent device according to claim 2 , wherein a hole injection layer, a hole transport layer, or both of them are further included between the first electrode and the light-emitting layer.

7. The compound according to claim 2 , wherein X represents NR 2 .

8. The compound according to claim 2 , wherein X represents O or S.

9. The compound according to claim 2 , wherein the substituents of the substituted alkyl group, the substituted aryl(ene) group, the substituted heteroaryl(ene) group, the substituted cycloalkyl group, the substituted cycloalkenyl group, the substituted heterocycloalkyl group, or the substituted mono- or polycyclic (C3-C30) alicyclic or aromatic ring in formula 2 or 5 are each independently at least one selected from the group consisting of deuterium; a halogen; a cyano group; a carboxyl group; a nitro group; a hydroxyl group; a (C1-C30)alkyl group; a halo(C1-C30)alkyl group; a (C2-C30)alkenyl group; a (C2-C30)alkynyl group; a (C1-C30)alkoxy group; a (C1-C30)alkylthio group; a (C3-C30)cycloalkyl group; a (C3-C30)cycloalkenyl group; a 3- to 7-membered heterocycloalkyl group; a (C6-C30)aryloxy group; a (C6-C30)arylthio group; a 5- to 30-membered heteroaryl group which is unsubstituted or substituted with a (C6-C30)aryl group; a (C6-C30)aryl group which is unsubstituted or substituted with a 5- to 30-membered heteroaryl group; a tri(C1-C30)alkylsilyl group; a tri(C6-C30)arylsilyl group; a di(C1-C30)alkyl(C6-C30)arylsilyl group; a (C1-C30)alkyldi(C6-C30)arylsilyl group; an amino group; a mono- or di(C1-C30)alkylamino group; a mono- or di(C6-C30)arylamino group; a (C1-C30)alkyl(C6-C30)arylamino group; a (C1-C30)alkylcarbonyl group; a (C1-C30)alkoxycarbonyl group; a (C6-C30)arylcarbonyl group; a di(C6-C30)arylboronyl group; a di(C1-C30)alkylboronyl group; a (C1-C30)alkyl(C6-C30)arylboronyl group; a (C6-C30)aryl(C1-C30)alkyl group; and a (C1-C30)alkyl(C6-C30)aryl group.

10. The compound according to claim 2 , wherein the compound represented by formula 2 or 5: is selected from the group consisting of the following compounds:

Assignments (9)
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: U.S. BANK TRUST COMPANY, NATIONAL ASSOCIATION, AS NOTES COLLATERAL AGENT
Reel/Frame 073517/0298 →
SECURITY INTEREST Recorded Nov 3, 2025
From: QNITY ELECTRONICS, INC.
To: JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT
Reel/Frame 073515/0243 →
CHANGE OF LEGAL ENTITY Recorded Sep 17, 2024
From: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
To: DDP SPECIALTY ELECTRONIC MATERIALS US, LLC
Reel/Frame 068972/0210 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2024
From: DOW GLOBAL TECHNOLOGIES LLC
To: THE DOW CHEMICAL COMPANY
Reel/Frame 068971/0226 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 17, 2024
From: THE DOW CHEMICAL COMPANY
To: DDP SPECIALTY ELECTRONIC MATERIALS US, INC
Reel/Frame 068971/0362 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2022
From: DOW CHEMICAL (CHINA) INVESTMENT COMPANY LIMITED
To: THE DOW CHEMICAL COMPANY
Reel/Frame 059226/0013 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2022
From: THE DOW CHEMICAL COMPANY
To: DOW GLOBAL TECHNOLOGIES LLC
Reel/Frame 059359/0810 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2022
From: TANG, ZHENGMING; FENG, SHAOGUANG
To: DOW CHEMICAL (CHINA) INVESTMENT COMPANY LIMITED
Reel/Frame 059225/0941 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2022
From: CHO, SANG HEE; NA, HONG YEOP; MOON, DOO-HYEON
To: ROHM AND HAAS ELECTRONIC MATERIALS KOREA LTD.
Reel/Frame 059682/0592 →