Compound and organic light emitting element comprising same
AssigneeLG Chem, Ltd.
InventorsHongsik Yoon, Yujin Kang, Wanpyo Hong, Sang Duk Suh
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AssigneeLG Chem, Ltd.
InventorsHongsik Yoon, Yujin Kang, Wanpyo Hong, Sang Duk Suh
Estimating the term…
Provided are boron-containing polycyclic compounds of Chemical Formula 1: wherein X1 to X4 are identical to or different from one another and are each independently O, S, NR2 or CR3R4, and a to d are each 0 or 1, with the proviso that 1≤a+b+c+d, and the other substituents are as described in the specification. The compounds have a high electron accepting ability and excellent heat resistance, and can be highly purified by sublimation purification due to their high sublimation temperature. The compounds can form a stable interface with an electrode or an adjacent organic material layer of an organic light emitting device. Also provided is an organic light emitting device including the compound of Chemical Formula 1. The compound can lower driving voltage and lengthen lifetime of the organic light emitting device.
A compound of Chemical Formula 1:
Dependencies are inferred from the claim text.
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Boron compounds: organoboranes and organoborohydrides
Compounds containing elements of Groups 3 or 13 of the Periodic Table: boron compounds
Luminescent materials, e.g. electroluminescent or chemiluminescent: containing organic luminescent materials
Polycyclic condensed heteroaromatic hydrocarbons: comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or…
About 13 years 5 months of term left · ends 27 Mar 2040 (estimated)
This application is a National Stage Application of International Application No. PCT/KR2018/016650 filed on Dec. 26, 2018, which claims priority to and the benefit of Korean Patent Application No. 10-2017-0179561, filed with the Korean Intellectual Property Office on Dec. 26, 2017, the entire contents of which are incorporated herein by reference.
The present specification relates to a compound and an organic light emitting device including the same.
An organic light emitting device has a configuration in which an organic thin film is disposed between two electrodes. Upon application of a voltage to such an organic light emitting device with a configuration, holes and electrons injected from two electrodes are combined and paired in an organic thin film. When such electron-pair pairs are decayed, light is emitted. The organic thin film can have a single or multiple layer structure, if necessary.
FIG. 1 illustrates an example of an organic light emitting device in which a substrate 1, an anode 2, a light emitting layer 3 and a cathode 4 are sequentially laminated;
FIG. 2 illustrates an organic light emitting device in which a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, a light emitting layer 3, an electron transport layer 7 and a cathode 4 are sequentially laminated; and
FIG. 3 illustrates an organic light emitting device in which a substrate 1, an anode 2, a hole injection layer 5, a hole transport layer 6, an electron blocking layer 8, a light emitting layer 3, an electron injection and transport layer 9 and a cathode 4 are sequentially laminated. 1: Substrate 2: Anode 3: Light emitting layer 4: Cathode 5: Hole injection layer 6: Hole transport layer 7: Electron transport layer 8: Electronic blocking layer 9: Electron injection and transport layer
Hereinafter, the present specification will be described in more detail.
An embodiment of the present specification provides the compound of Chemical Formula 1 above.
In the present specification, compounds having various energy bandgaps can be synthesized by introducing various substituents into the core structure as described above. Typically, it is easy to control the energy band gap by introducing a substituent into a core structure having a large energy band gap. On the other hand, when a core structure has a small energy band gap, it is difficult to control the energy band gap by introduction of a substituent. In addition, in the present specification, the HOMO and LUMO energy levels of the compound can be controlled by introducing various substituents into the core structure as described above.