Carbazole compound, material for organic electroluminescence device and organic electroluminescence device
US-9203036-B2 · Dec 1, 2015 · US
US9847496B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9847496-B2 |
| Application number | US-201414560010-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 4, 2014 |
| Priority date | Dec 23, 2013 |
| Publication date | Dec 19, 2017 |
| Grant date | Dec 19, 2017 |
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Novel iridium complexes containing a tetradentate or a hexadentate ligand, wherein a part of the ligand that is coordinated to iridium comprise an acetylacetonate structure. These complexes are useful as emitters for phosphorescent OLEDs.
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What is claimed is: 1. A compound having a structure selected from the group consisting of: wherein G 1 , G 2 , and G 3 are linkers that connect the ligands; wherein R A , R B , R C , and R D each independently represent mono, di, tri, or tetra-substitution, or no substitution; wherein R A , R B , R C , R D , R 1 , R 2 ,and R 3 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfonyl, sulfonyl, phosphino, and combinations thereof; wherein any adjacent substitution can be optionally jointed to form a ring. 2. The compound of claim 1 , wherein the phenylpyridine ligand substituted by R A and R B is the same as the phenylpyridine ligand substituted by R C and R D . 3. The compound of claim 1 , wherein the compound is selected from the group consisting of: 4. The compound of claim 1 , wherein the compound has the structure 5. The compound of claim 1 , wherein the compound has the structure 6. The compound of claim 1 , wherein the compound has the structure 7. The compound of claim 1 , wherein the compound has the structure 8. The compound of claim 1 , wherein the compound has the structure 9. A device comprising one or more organic light emitting devices, wherein at least one of the one or more organic light emitting devices comprising: an anode; a cathode; and an organic layer, disposed between the anode and the cathode, comprising a compound having a structure selected from the group consisting of: wherein G 1 , G 2 , and G 3 are linkers that connect the ligands; wherein R A , R B , R C , and R D each independently represent mono, di, tri, or tetra-substitution, or no substitution; wherein R A , R B , R C , R D , R 1 , R 2 , and R 3 are each independently selected from the group consisting of hydrogen, deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acids, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein any adjacent substitution can be optionally jointed to form a ring. 10. The device of claim 9 , wherein the device is selected from the group consisting of a consumer product, an electronic component module, an organic light-emitting device, and a lighting panel. 11. The device of claim 9 , wherein the organic layer is an emissive layer and the compound is an emissive dopant or a non-emissive dopant. 12. The device of claim 9 , wherein the organic layer further comprises a host, wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan; wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C n H 2n+1 , OC 2 H 2n+1 , OAr 1 , N(C n H 2n+1 ) 2 , N(Ar 1 )(Ar 2 ), CH═CH—C n H 2n+1 , C≡CC n H 2n+1 , Ar 1 , Ar 1 —Ar 2 , C n H 2n —Ar 1 , or no substitut
Electricity · mapped topic
Non-condensed systems · CPC title
containing organic luminescent materials · CPC title
of the platinum group, i.e. Os, Ir, Pt, Ru, Rh or Pd · CPC title
Iridium compounds · CPC title
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