Fluorescent polymeric materials containing lipid soluble rhodamine dyes
US-9034920-B2 · May 19, 2015 · US
US9455407B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9455407-B2 |
| Application number | US-201414303771-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 13, 2014 |
| Priority date | Mar 5, 2014 |
| Publication date | Sep 27, 2016 |
| Grant date | Sep 27, 2016 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
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:
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
Organic materials used in the body or electrodes of devices covered by this subclass · CPC title
comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom · CPC title
Electricity · mapped topic
Electricity · mapped topic
Electricity · mapped topic
Related publications grouped by family.
Answers are generated from the same data shown on this page.