Heterocyclic compound and organic light-emitting element using same

US10103336B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10103336-B2
Application numberUS-201415025046-A
CountryUS
Kind codeB2
Filing dateSep 29, 2014
Priority dateSep 30, 2013
Publication dateOct 16, 2018
Grant dateOct 16, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

The present specification provides a heterocyclic compound and an organic light emitting device using the same.

First claim

Opening claim text (preview).

The invention claimed is: 1. A heterocyclic compound represented by the following Chemical Formula 1: wherein, in Chemical Formula 1, X is a direct bond; or CRR′, when X is the direct bond, R1 is deuterium; a halogen group; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted alkylamine group; a substituted or unsubstituted aralkylamine group; a substituted or unsubstituted arylamine group; a substituted or unsubstituted heteroarylamine group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted heteroring group including one or more of N, O and S atoms, when X is the CRR′, R1 is deuterium; a halogen group; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted alkylamine group; a substituted or unsubstituted aralkylamine group; a substituted or unsubstituted arylamine group; a substituted or unsubstituted heteroarylamine group; a substituted or unsubstituted arylphosphine group; or a substituted or unsubstituted phosphine oxide group, and R, R′ and R2 to R8 are the same as or different from each other, and each independently hydrogen; deuterium; a halogen group; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted alkylamine group; a substituted or unsubstituted aralkylamine group; a substituted or unsubstituted arylamine group; a substituted or unsubstituted heteroarylamine group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted heteroring group including one or more of N, O and S atoms, or adjacent groups among R, R′ and R2 to R8 bond to each other to form an aliphatic ring, an aromatic ring, an aliphatic heteroring or an aromatic heteroring, or form a spiro bond. 2. The heterocyclic compound of claim 1 , wherein when X is the direct bond, R1 is deuterium; a substituted or unsubstituted aryl group; or a substituted or unsubstituted alkyl group, and wherein when X is the CRR′, R1 is deuterium; or a substituted or unsubstituted alkyl group. 3. The heterocyclic compound of claim 1 , wherein R, R′ and R2 to R8 are the same as or different from each other, and each independently hydrogen; a substituted or unsubstituted alkyl group; a substituted or unsubstituted aryl group; or a substituted or unsubstituted phosphine oxide group. 4. The heterocyclic compound of claim 1 , wherein R2 to R8 are the same as or different from each other, and each independently hydrogen; a substituted or unsubstituted phenyl group; a substituted or unsubstituted anthracene group; a substituted or unsubstituted fluorene group; or a substituted or unsubstituted phosphine oxide group. 5. The heterocyclic compound of claim 1 , wherein R2 to R8 are the same as or different from each other, and each independently hydrogen; or any one of the following structures: wherein, the structures may be unsubstituted or further substituted with one, two or more substituents selected from the group consisting of deuterium; a halogen group; a nitrile group; a nitro group; a hydroxyl group; a carbonyl group; an ester group; an imide group; an amide group; a substituted or unsubstituted alkyl group; a substituted or unsubstituted cycloalkyl group; a substituted or unsubstituted alkoxy group; a substituted or unsubstituted aryloxy group; a substituted or unsubstituted alkylthioxy group; a substituted or unsubstituted arylthioxy group; a substituted or unsubstituted alkylsulfoxy group; a substituted or unsubstituted arylsulfoxy group; a substituted or unsubstituted alkenyl group; a substituted or unsubstituted silyl group; a substituted or unsubstituted boron group; a substituted or unsubstituted alkylamine group; a substituted or unsubstituted aralkylamine group; a substituted or unsubstituted arylamine group; a substituted or unsubstituted heteroarylamine group; a substituted or unsubstituted arylphosphine group; a substituted or unsubstituted phosphine oxide group; a substituted or unsubstituted aryl group; and a substituted or unsubstituted heteroring group including one or more of N, O and S atoms. 6. The heterocyclic compound of claim 1 , wherein the heterocyclic compound represented by Chemical Formula 1 is represented by any one of the following Chemical Formulae: 7. The heterocyclic compound of claim 1 , wherein the heterocyclic compound represented by Chemical Formula 1 is represented by any one of the following Chemical Formulae 2-1 to 2-25: 8. An organic light emitting device comprising: a first electrode; a second electrode provided opp

Assignees

Inventors

Classifications

  • H05B33/20Primary

    characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded · CPC title

  • Electricity · mapped topic

  • Electricity · mapped topic

  • of other metals not provided for in one of the previous groups · CPC title

  • Electricity · mapped topic

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Frequently asked questions

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What does patent US10103336B2 cover?
The present specification provides a heterocyclic compound and an organic light emitting device using the same.
Who is the assignee on this patent?
Lg Chemical Ltd
What technology area does this patent fall under?
Primary CPC classification H05B33/20. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Oct 16 2018 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 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).