Compound and organic light-emitting device including the same

US9455407B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9455407-B2
Application numberUS-201414303771-A
CountryUS
Kind codeB2
Filing dateJun 13, 2014
Priority dateMar 5, 2014
Publication dateSep 27, 2016
Grant dateSep 27, 2016

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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.

A compound, an organic light-emitting device, and a flat panel display device, the compound being represented by Formula 1, below:

First claim

Opening claim text (preview).

What is claimed is: 1. A compound represented by Formula 1, below: wherein R 1 to R 4 are each independently a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, or a substituted or unsubstituted C 6 -C 60 condensed polycyclic group, A and B are each independently a substituted or unsubstituted C 6 -C 60 arylene group or a substituted or unsubstituted C 1 -C 60 heteroarylene group, and m and n are each independently an integer of 0 or 1. 2. The compound as claimed in claim 1 , wherein R 1 to R 4 are each independently selected from the group of moieties represented by Formulae 2a to 2d below: wherein Q 1 is —C(R 31 )(R 32 )—, —S—, or —O—; Z 1 , R 31 , and R 32 are each independently, a hydrogen atom, a deuterium atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a C 1 -C 20 alkylsilyl group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 1 -C 20 heteroaryl group, a substituted or unsubstituted C 6 -C 20 condensed polycyclic group, a halogen-containing group, a cyano group, a nitro group, a hydroxyl group, or a carboxyl group; P is an integer of 1 to 9; and * is a binding site. 3. The compound as claimed in claim 1 , wherein A and B are each independently a moiety represented by Formula 3a below: wherein Z 1 is a hydrogen atom, a deuterium atom, a substituted or unsubstituted C 1 -C 20 alkyl group, a substituted or unsubstituted C 6 -C 20 aryl group, a substituted or unsubstituted C 1 -C 20 heteroaryl group, a substituted or unsubstituted C 6 -C 20 condensed polycyclic group, a halogen-containing group, a cyano group, a nitro group, a hydroxyl group, or a carboxyl group; P is an integer of 1 to 4; and * is a binding site. 4. The compound as claimed in claim 1 , wherein the compound represented by Formula 1 is represented by Formula 2 below: wherein R 1 to R 4 are each independently a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, or a substituted or unsubstituted C 6 -C 60 condensed polycyclic group. 5. The compound as claimed in claim 1 , wherein the compound represented by Formula 1 is represented by Formula 3 below: wherein: R 1 to R 4 are each independently a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, or a substituted or unsubstituted C 6 -C 60 condensed polycyclic group, and A is a substituted or unsubstituted C 6 -C 60 arylene group or a substituted or unsubstituted C 1 -C 60 heteroarylene group. 6. The compound as claimed in claim 1 , wherein the compound represented by Formula 1 is represented by Formula 4 below: wherein: R 1 to R 4 are each independently a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, or a substituted or unsubstituted C 6 -C 60 condensed polycyclic group, and B is a substituted or unsubstituted C 6 -C 60 arylene group or a substituted or unsubstituted C 1 -C 60 heteroarylene group. 7. The compound as claimed in claim 1 , wherein the compound represented by Formula 1 is represented by Formula 5 below: wherein: R 1 to R 4 are each independently a substituted or unsubstituted C 6 -C 60 aryl group, a substituted or unsubstituted C 1 -C 60 heteroaryl group, or a substituted or unsubstituted C 6 -C 60 condensed polycyclic group, and A and B are each independently a substituted or unsubstituted C 6 -C 60 arylene group or a substituted or unsubstituted C 1 -C 60 heteroarylene group. 8. The compound as claimed in claim 1 , wherein the compound represented by Formula 1 is one of the following Compounds 1-102: 9. The compound as claimed in claim 1 , wherein the compound is represented by Formula 1-a below, wherein, a first aryl group includes the moiety -(A) m NR 1 R 2 and a second aryl group includes the moiety -(B) n NR 3 R 4 , the first aryl group is bonded to ring a or ring b, when the first aryl group is bonded to ring a, the second aryl group is bonded to ring c, and when the first aryl group is bonded to ring b, the second aryl group is bonded to ring d. 10. An organic light-emitting device, comprising: a first electrode; a second electrode; and an organic layer between the first electrode and second electrode, wherein the organic layer includes the compound as claimed in claim 1 . 11. The organic light-emitting device as claimed in claim 10 , wherein the organic layer includes an emission layer. 12. The organic light-emitting device as claimed in claim 10 , wherein the organic layer includes an emission layer, and the compound is a dopant. 13. The organic light-emitting device as claimed in claim 10 , wherein the organic layer includes an emission layer, and the compound is a blue fluorescent dopant. 14. The organic light-emitting device as claimed in claim 10 , wherein: the organic layer includes an emission layer, and further includes at least one of an electron injection layer, an electron transport layer, a functional layer having both electron injecting and electron transporting capabilities, a hole injection layer, a hole transport layer, or a functional layer having both hole injecting and hole transporting capabilities, and the emission layer includes an anthracene-based compound, arylamine-based compound, or a styryl-based compound. 15. The organic light-emitting device as claimed in claim 10 , wherein: the organic layer includes an emission layer, and fur

Assignees

Inventors

Classifications

  • Organic materials used in the body or electrodes of devices covered by this subclass · CPC title

  • H10K85/636Primary

    comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom · CPC title

  • Electricity · mapped topic

  • Electricity · mapped topic

  • Electricity · mapped topic

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Frequently asked questions

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What does patent US9455407B2 cover?
A compound, an organic light-emitting device, and a flat panel display device, the compound being represented by Formula 1, below:
Who is the assignee on this patent?
Samsung Display Co Ltd
What technology area does this patent fall under?
Primary CPC classification H10K85/636. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Sep 27 2016 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 2 related publications on this page (citations in our corpus or others sharing the same primary CPC).