Nitrogen-containing compound, organic electroluminescent device and electronic apparatus

US11588115B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11588115-B2
Application numberUS-202017623484-A
CountryUS
Kind codeB2
Filing dateJul 23, 2020
Priority dateDec 31, 2019
Publication dateFeb 21, 2023
Grant dateFeb 21, 2023

How to read this patent

A practical reading order for non-experts. Skip the full description unless you need deep technical detail.

  1. Title

    What the patent document calls the invention.

  2. Abstract

    A short plain-language summary of the technical disclosure.

  3. Assignees and inventors

    Who owns or filed the patent and who is credited as inventor.

  4. Key dates

    Filing, priority, publication, and grant dates set the timeline.

  5. First independent claim

    The legal scope of protection — read this for what is actually claimed.

  6. CPC / IPC classifications

    Technology tags used to group this patent with similar filings.

  7. Citations and related patents

    Prior art links and similar publications in this corpus.

Abstract

Official abstract text for this publication.

The present disclosure provides a nitrogen-containing compound, an organic electroluminescent device and an electronic apparatus, belonging to the technical field of organic materials. The nitrogen-containing compound of the present disclosure has a carbazole structure and a fluorenyl group, two cooperating with each other and has a high first triplet energy level. Therefore, the nitrogen-containing compound of the present disclosure is suitable for use as a host material of a light-emitting in an organic electroluminescent device. The nitrogen-containing compound can improve the performance of the organic electroluminescent device.

First claim

Opening claim text (preview).

The invention claimed is: 1. A nitrogen-containing compound, wherein the nitrogen-containing compound has a structural formula as shown in a chemical formula 1: wherein, ring A is a benzene ring or naphthalene ring; R 1 and R 2 are the same or different from each other, and are each independently selected from deuterium, fluorine, chlorine, cyano, methyl, isopropyl, ethyl, cyclopropyl and tert-butyl; n 1 is 0, 1, 2, 3 or 4; when n 1 is greater than 1, any two of R 1 are the same or different; n 2 is 0, 1, 2, 3 or; when n 2 is greater than 1, any two of R 2 are the same or different; and W is wherein L is independently selected from a single bond, or an unsubstituted L 1 , or a substituted L 1 , wherein the unsubstituted L 1 is selected from the group consisting of the following groups: wherein, the substituted L 1 is a group formed by substituting the unsubstituted L 1 by one or more substituents selected from deuterium, F, Cl, cyano, methyl, ethyl, isopropyl, n-propyl, tert-butyl and phenyl; and when the substituted L 1 has a plurality of substituents, any two of the substituents are the same or different; the Ar is selected from an unsubstituted Ar 1 or a substituted Ar 1 , wherein the unsubstituted Ar 1 is selected from the group consisting of the following groups: the substituted Ar 1 is a group formed by substituting the unsubstituted Ar 1 by one or more of substituents selected from deuterium, F, Cl, Br, cyano, alkyl with 1 to 4 carbon atoms, phenyl, naphthyl, dibenzothienyl, dibenzofuranyl, carbazolyl, pyridinyl, halomethyl and trimethylsilyl; and when the substituted Ar 1 has a plurality of substituents, any two of the substituents are the same or different; or, the Ar is selected from the group consisting of the following substituents: wherein, Ar 2 is selected from hydrogen, deuterium, substituted or unsubstituted aryl with 6 to 15 carbon atoms, and substituted or unsubstituted heteroaryl with 3 to 12 carbon atoms: any two of Ar 2 are the same or different; and the heteroaryl comprises 1, 2 or 3 heteroatoms of any choice from O, S or N; substituents in Ar 2 are selected from deuterium, F, Cl and cyano; and when Ar 2 has a plurality of substituents, any two of the substituents are the same or different. 2. The nitrogen-containing compound according to claim 1 , wherein the nitrogen-containing compound has a structural formula as shown in any one of the chemical formulas (f-1) to (f-12): 3. The nitrogen-containing compound according to claim 1 , wherein the Ar 2 is selected from: hydrogen, substituted or unsubstituted phenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted anthracyl, substituted or unsubstituted phenanthryl, substituted or unsubstituted biphenyl, substituted or unsubstituted fluorenyl, substituted or unsubstituted dibenzothiophenyl, substituted or unsubstituted dibenzofuryl, substituted or unsubstituted pyridyl, substituted or unsubstituted pyrimidyl, substituted or unsubstituted pyrazinyl, substituted or unsubstituted quinolyl, substituted or unsubstituted isoquinolyl, and substituted or unsubstituted quinazolinyl; and substituents in Ar 2 are each independently selected from: F, deuterium, and cyano. 4. A nitrogen-containing compound, wherein the nitrogen-containing compound is selected from the group consisting of the following compounds:

Assignees

Inventors

Classifications

  • comprising only nitrogen as heteroatom (H10K85/652 takes precedence) · CPC title

  • containing three or more hetero rings · CPC title

  • C07D405/10Primary

    linked by a carbon chain containing aromatic rings · CPC title

  • linked by a carbon chain containing aromatic rings · CPC title

  • the oxygen-containing ring being five-membered · CPC title

Patent family

Related publications grouped by family.

External sources

Frequently asked questions

Answers are generated from the same data shown on this page.

What does patent US11588115B2 cover?
The present disclosure provides a nitrogen-containing compound, an organic electroluminescent device and an electronic apparatus, belonging to the technical field of organic materials. The nitrogen-containing compound of the present disclosure has a carbazole structure and a fluorenyl group, two cooperating with each other and has a high first triplet energy level. Therefore, the nitrogen-conta…
Who is the assignee on this patent?
Shaanxi Lighte Optoelectronics Mat Co Ltd
What technology area does this patent fall under?
Primary CPC classification C07D405/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Feb 21 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).