A D-A type organic light-emitting material includes a donor moiety and an acceptor moiety. The donor moiety is represented as follows:

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L is selected from any of aryl, heteroaryl, fused aryl and fused heteroaryl. When L is selected from any of aryl and heteroaryl, aryl and heteroaryl each have one or more substituents each selected from any of deuterium, tert-butyl, phenyl, cyano and methylimino, and at least one substituent is selected from cyano and methylimino. When L is selected from any of fused aryl and fused heteroaryl, fused aryl and fused to heteroaryl each have or do not have a substituent. When fused aryl and fused heteroaryl each have a substituent, the substituent is selected from any of deuterium, tert-butyl, phenyl, cyano and methylimino. The acceptor moiety is selected from any of a substituted or unsubstituted fused aromatic rings and a substituted or unsubstituted fused heterocyclic ring.

A light emitting device includes a first electrode, a hole transport region disposed on the first electrode, an emission layer disposed on the hole transport region, an electron transport region disposed on the emission layer, and a second electrode disposed on the electron transport region. The emission layer includes a fused polycyclic compound represented by Formula 1.

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A light emitting device includes a first electrode, a second electrode disposed on the first electrode, and at least one functional layer disposed between the first electrode and the second electrode. The at least one functional layer includes an amine compound represented by Formula 1. A light emitting device including the amine compound may show improved efficiency and life characteristics.

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An organic light-emitting device having low-driving voltage, improved efficiency, and long lifespan includes: a first electrode; a second electrode facing the first electrode; a first layer between the first electrode and the second electrode, the first layer including a first compound; a second layer between the first layer and the second electrode, the second layer including a second compound; and a third layer between the second layer and the second electrode, the third layer including a third compound; wherein the first compound does not include a nitrogen-containing heterocyclic group comprising *═N—*′ as a ring forming moiety, and wherein the first compound, the second compound, and the third compound each independently include at least one group selected from groups represented by Formulae A to C:

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Provided is a light-emitting element including a fluorescence-emitting material with high emission efficiency. The light-emitting element includes a pair of electrodes and an EL layer between the pair of electrodes. The EL layer includes a first organic compound, a second organic compound, and a guest material. The first organic compound has a function of emitting a thermally activated delayed fluorescence at room temperature. The guest material has a function of emitting fluorescence. A HOMO level of the first organic compound higher than or equal to a HOMO level of the second organic compound. A LUMO level of the first organic compound is lower than or equal to a LUMO level of the second organic compound.

Provided are an organic electronic element and an electronic device thereof, the organic electronic element being capable of achieving high light-emitting efficiency and a low driving voltage, and can also greatly improve the lifespan of the element by using a compound of the present invention as a phosphorescent host material.

An organic compound has a benzonaphthofuran skeleton and is represented by General Formula (G1). In General Formula (G1), A represents a pyrene skeleton. In the case where the pyrene skeleton has a substituent, the substituent is a diarylamino group including two substituted or unsubstituted aryl groups each having 6 to 13 carbon atoms, a substituted or unsubstituted aryl group having 6 to 13 carbon atoms, an alkyl group having 1 to 7 carbon atoms, a substituted or unsubstituted monocyclic saturated hydrocarbon group having 3 to 20 carbon atoms, or a substituted or unsubstituted polycyclic saturated hydrocarbon group having 7 to 10 carbon atoms. The two aryl groups of the diarylamino group may be the same or different. In X1 represented by General Formula (G1-1), one of R6 and R7 is bonded to N in General Formula (G1), and the other of R6 and R7 represents an alkyl group having 1 to 7 carbon atoms, a substituted or unsubstituted monocyclic saturated hydrocarbon group having 3 to 20 carbon atoms, or a substituted or unsubstituted polycyclic saturated hydrocarbon group having 7 to 10 carbon atoms.

An organic light-emitting device includes a first electrode, a second electrode facing the first electrode, an emission layer between the first electrode and the second electrode, and a hole transport region between the first electrode and the emission layer. The emission layer includes a first compound represented by Formula 1, and the hole transport region includes a second compound represented by Formula 2: ##STR00001##

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. The organic electroluminescent device with improved driving voltage and/or power efficiency can be provided by using the organic electroluminescent compound according to the present disclosure.

The present specification relates to a compound of Formula 1, a coating composition including the compound, an organic light emitting device formed by using the coating composition, and a manufacturing method thereof.