Organic electroluminescent materials and devices
US-2024166670-A1 · May 23, 2024 · US
US9978963B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9978963-B2 |
| Application number | US-201415023797-A |
| Country | US |
| Kind code | B2 |
| Filing date | Aug 28, 2014 |
| Priority date | Sep 30, 2013 |
| Publication date | May 22, 2018 |
| Grant date | May 22, 2018 |
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.
Provided are an organic electroluminescent device (organic EL device) that is improved in luminous efficacy, sufficiently secures driving stability, and has a simple construction, and a material for organic EL devices to be used in the organic EL device. The material for organic EL devices is a material for organic EL devices formed of an ortho-carborane compound having a structure in which a silyl group (—SiR 3 ) is bonded to a divalent ortho-carborane group represented by C 2 B 10 H 10 through an aromatic group. In addition, the organic electroluminescent device is an organic electroluminescent device having a structure in which an anode, an organic layer, and a cathode are laminated on a substrate, the device having an organic layer containing the ortho-carborane compound, and the organic layer being a light-emitting layer, an electron-transporting layer, a hole-blocking layer, or an exciton-blocking layer.
Opening claim text (preview).
The invention claimed is: 1. A material for organic electroluminescent devices, comprising an ortho-carborane compound represented by the general formula (1): where ring A represents a divalent ortho-carborane group C 2 B 10 H 10 represented by the formula (1a), L 1 and L 2 each independently represent a substituted or unsubstituted aromatic hydrocarbon group having 6 to 30 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 30 carbon atoms, or a linked aromatic group formed by linking 2 to 6 aromatic rings selected from the aromatic hydrocarbon group and the aromatic heterocyclic group, when L 1 or L 2 represents the linked aromatic group, the group may be linear or branched, and the aromatic rings to be linked may be identical to or different from each other, and L 1 represents a p+1-valent group and L 2 represents a q+1-valent group, R 1 , R 2 , R 3 , R 4 , R 5 , and R 6 each independently represent an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, R 7 and R 8 each independently represent hydrogen, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, or a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, p represents an integer of from 1 to 5, q represents an integer of from 0 to 5, and r represents an integer of from 1 to 4. 2. A material for organic electroluminescent devices according to claim 1 , wherein the ortho-carborane compound represented by the general formula (1) comprises an ortho-carborane compound represented by the general formula (2): where L 1 , L 2 , R 1 to R 8 , p, q, and r are identical in meaning to those in the general formula (1). 3. A material for organic electroluminescent devices according to claim 2 , wherein in the general formula (2), L 1 and L 2 each independently represent a substituted or unsubstituted aromatic hydrocarbon group having 6 to 18 carbon atoms, a substituted or unsubstituted aromatic heterocyclic group having 3 to 17 carbon atoms, or a linked aromatic group formed by linking 2 to 6 aromatic rings selected from the aromatic hydrocarbon group and the aromatic heterocyclic group. 4. A material for organic electroluminescent devices according to claim 3 , wherein in the general formula (2), R 1 to R 6 each independently represent an aliphatic hydrocarbon group having 1 to 10 carbon atoms, or an aromatic hydrocarbon group having 6 to 12 carbon atoms. 5. An organic electroluminescent device having a structure in which an anode, an organic layer, and a cathode are laminated on a substrate, wherein the organic layer comprises an organic layer containing the material for organic electroluminescent devices of claim 1 . 6. An organic electroluminescent device according to claim 5 , wherein the organic layer containing the material for organic electroluminescent devices comprises at least one layer selected from the group consisting of a light-emitting layer, an electron-transporting layer, a hole-blocking layer, and an exciton-blocking layer. 7. An organic electroluminescent device according to claim 5 , wherein the organic layer containing the material for organic electroluminescent devices comprises an electron-transporting layer, a hole-blocking layer, or an exciton-blocking layer.
said ring is substituted at a C ring atom by Si · CPC title
containing other heteroatoms · CPC title
Compounds with Si-C or Si-Si linkages · CPC title
containing organic luminescent materials · CPC title
Electricity · mapped topic
Related publications grouped by family.
Answers are generated from the same data shown on this page.