IP Library Granted Patent US 12,540,124
Granted Patent B2
US 12,540,124 · App. 17/465,705 · Granted Feb 3, 2026

Compound, material for an organic electroluminescent device and application thereof

Inventors: Wenpeng Dai (Shanghai, CN); Wei Gao (Shanghai, CN); Lei Zhang (Shanghai, CN); Lu Zhai (Shanghai, CN); Xia Li (Shanghai, CN)
Assignees: Wuhan Tianma Micro-Electronics Co., Ltd.; Wuhan Tianma Micro-Electronics Co., Ltd. Shanghai Branch
C07D277/84C07D263/57H10K85/633H10K85/636H10K59/879H10K85/615H10K85/626H10K85/657
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,540,124
App. No.
17/465,705
Granted
Feb 3, 2026
Kind
B2
Abstract

The present disclosure relates to a compound, a material for an organic electroluminescent device and an application thereof. The compound has a structure represented by Formula (1). The compound has a relatively high refractive index in the region of visible light (400-750 nm), which is conducive to improving the light-emitting efficiency.

Claims (29)

1 . A compound having a structure represented by Formula (1):

wherein, X 1 to X 10 are each independently selected from the group consisting of N, CH and CRa, wherein Ra is selected from the group consisting of a deuterium atom, CD 3 , CD 2 CH 3 , CD 2 CD 3 , cyano, substituted or unsubstituted C 6 -C 60 aryl, and a combination of at least two selected therefrom;

wherein, n is an integer from 0 to 4, and L is selected from the group consisting of substituted or unsubstituted C 6 -C 60 arylene and substituted or unsubstituted C 3 -C 60 heteroarylene;

wherein, m1 and m2 are each independently an integer from 0 to 4, and Ar 1 and Ar 2 are each independently selected from the following substituted or unsubstituted groups: phenylene, biphenylene, terphenylene, tetraphenylene, naphthylene, phenanthrylene, carbazolylene, dibenzofurylene, dibenzothienylene, pyrimidinylene, triazinylene, indolocarbazolylene, indolobenzofurylene, indolobenzothienylene, benzofuropyrimidinylene, benzothienopyrimidinylene, anthrylene and pyrenylene;

wherein, X and Y are each independently selected from substituted or unsubstituted C3-C60 electron withdrawing heteroaryl;

wherein the C3-C60 electron withdrawing heteroaryl is any one selected from the group consisting of the following groups:

wherein, if the group only has one #, the # represents a linkage site of the group, and wherein if the group has at least two #, a linkage site of the group is selected from any one of the #;

wherein Q is selected from the group consisting of an O atom, a S atom and NR 8 ;

wherein each of R 6 to R 7 is independently selected from the group consisting of hydrogen, protium, deuterium, tritium, halogen, cyano, C1-C10 alkyl, C1-C10 alkoxy, C6-C60 aryl and C3-C60 heteroaryl; and

wherein the ring A is fused at any position of a benzene ring where the ring A is able to be fused and the ring A is selected from the group consisting of substituted or unsubstituted C6-C30 aromatic rings and substituted or unsubstituted C3-C30 heteroaromatic rings;

and

wherein substituted groups in Ra, L, Ar 1 , Ar 2 , X and Y are each independently selected from the group consisting of protium, deuterium, tritium, cyano, halogen, C1-C10 alkyl, C1-C10 haloalkyl, C1-C10 alkoxy, C6-C60 aryl, C3-C60 heteroaryl, and a combination of at least two selected therefrom.

2 . The compound according to claim 1 , wherein the compound has a structure represented by Formula (2);

wherein in Formula (2), X 1 to X 10 , n, m1, m2, X and Y each have the same ranges as defined in claim 1 .

3 . The compound according to claim 1 , wherein X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 and X 10 are each CH.

4 . The compound according to claim 1 , wherein at least one of X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 and X 10 is selected from N.

5 . The compound according to claim 1 , wherein at least one of X 1 , X 2 , X 3 , X 4 , X 5 , X 6 , X 7 , X 8 , X 9 and X 10 is selected from CD.

6 . The compound according to claim 1 , wherein X 2 and X 7 are each selected from CD.

7 . The compound according to claim 1 , wherein L is any one selected from the group consisting of the following substituted or unsubstituted groups: phenylene, biphenylene, terphenylene, tetraphenylene, naphthylene, phenanthrylene, fluorenylidene, carbazolylene, dibenzofurylene, dibenzothienylene, pyrimidinylene, triazinylene, indolocarbazolylene, indolobenzofurylene, indolobenzothienylene, benzofuropyrimidinylene, benzothienopyrimidinylene, anthrylene and pyrenylene.

8 . The compound according to claim 1 , wherein the difference between the refractive index of the compound at a wavelength of 460 nm and the refractive index of the compound at a wavelength of 530 nm is 0.10-0.17, the difference between the refractive index of the compound at a wavelength of 530 nm and the refractive index of the compound at a wavelength of 620 nm is 0.03-0.10, and the difference between the refractive index of the compound at a wavelength of 460 nm and the refractive index of the compound at a wavelength of 620 nm is 0.15-0.40.

9 . The compound according to claim 1 , wherein the compound has any one of structures represented by P91 to P103 and P118 to P123:

10 . A material for an organic electroluminescent device, comprising any one or a combination of at least two of the compound according to claim 1 .

11 . An organic electroluminescent element, comprising a first electrode layer, an organic function layer and a second electrode layer which are stacked in sequence;

wherein the organic function layer comprises the material according to claim 10 .

12 . An organic electroluminescent element, comprising a first capping layer, a first electrode layer, an organic function layer and a second electrode layer which are stacked in sequence;

wherein the first capping layer comprises the material according to claim 10 .

13 . The organic electroluminescent element according to claim 12 , further comprising a second capping layer disposed on a side of the first capping layer facing away from the first electrode layer, wherein the second capping layer comprises lithium fluoride and/or a material containing small organic molecules with a refractive index of 1.40-1.65.

14 . A display panel, comprising the organic electroluminescent element according to claim 11 , wherein the display panel is optionally used in a display device.

15 . A display panel, comprising the organic electroluminescent element according to claim 12 , wherein the display panel is optionally used in a display device.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2022
From: SHANGHAI TIANMA AM-OLED CO.,LTD.
To: WUHAN TIANMA MICRO-ELECTRONICS CO., LTD.; WUHAN TIANMA MICROELECTRONICS CO., LTD. SHANGHAI BRANCH
Reel/Frame 059498/0307 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 3, 2021
From: DAI, WENPENG; GAO, WEI; ZHANG, LEI; ZHAI, LU; LI, XIA
To: SHANGHAI TIANMA AM-OLED CO., LTD.
Reel/Frame 057418/0911 →
Priority Claims (1)
CN 202110227698.0 · Mar 1, 2021 · national
Continuity (1)
Related Publication 20220293861A1 · Sep 15, 2022
References Cited (8)
US 20200258946A1 · Kim · 2020 [cited by examiner]
US 20210210684A1 · Lee · 2021 [cited by examiner]
US 20220119360A1 · Mochizuki · 2022 [cited by examiner]
US 20220281870A1 · Dai · 2022 [cited by examiner]
CN 108774175A · 2018 [cited by examiner]
CN 109824659A · 2019 [cited by applicant]
CN 110964002A · 2019 [cited by applicant]
Machine Translation of CN108774175A (Year: 2018). [cited by examiner]