Abstract: A nitrogen-containing compound and an organic electroluminescence device including the same, the nitrogen-containing compound being represented by the following Formula 1:

Abstract: An organic electroluminescence device and a polycyclic compound, the device including a first electrode; a hole transport region on the first electrode; an emission layer on the hole transport region; an electron transport region on the emission layer; and a second electrode on the electron transport region, wherein the emission layer includes a polycyclic compound represented by the following Formula 1:

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: An organic electroluminescence device includes a first electrode, a hole transport region on the first electrode, an emission layer on the hole transport region, an electron transport region on the emission layer, and a second electrode on the electron transport region, wherein the emission layer includes a polycyclic compound represented by Formula 1. In Formula 1, X1 may be C, Si or Ge; and AC may be an electron acceptor.

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: Provided are a polycyclic compound and an organic electroluminescence device including the same. The polycyclic compound according to an exemplary embodiment of the present disclosure is represented by the following formula 1. In Formula 1, X is O, SiR?R?, S, or BAr1. At least one of R1 to R8 is an aryl amine-containing electron donor. When X is O, SiR?R?, or S, the aryl amine-containing electron donor further includes a Si.

Abstract: A nitrogen-containing compound represented by Formula 1 below may be included in a light emitting layer of an organic electroluminescence device.

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: A polycyclic compound may be represented by Formula 1 below. The polycyclic compound may improve the light emitting efficiency of a blue light emitting region, and an organic electroluminescence device including the polycyclic compound may have improved blue light emission, high external quantum efficiency, and long life. The polycyclic compound may be used as a thermally activated delayed fluorescence material, which emits blue light, to improve the blue light emitting efficiency of the organic electroluminescence device.

Abstract: Provided are a compound for thermally activated delayed fluorescence having a molecular aspect ratio of 1.5 or more, represented by the following Formula 1 and an organic electroluminescence device including the same in an emission layer. The organic electroluminescence 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.

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: An organic electroluminescent (EL) material and an organic EL device, the material being represented by the following Formula 1:

Abstract: A heterocyclic compound is represented by Formula 1 and has an absolute value of a difference between a singlet energy level and a triplet energy level of about 0.2 eV or less: wherein in Formula 1, at least one of R1 to R11 is represented by Formula 2.

Abstract: A phosphorus-containing compound and an organic electroluminescence device including the same, the phosphorus-containing compound being represented by the following Formula 1:

Abstract: An organic electroluminescence device including a first electrode, a hole transport region on the first electrode, an emission layer on the hole transport region, an electron transport region on the emission layer, and a second electrode on the electron transport region, wherein the hole transport region includes a first heterocyclic compound including 1 to 3 structures derived from a compound represented by Formula 1 below, and the emission layer includes a second heterocyclic compound including 1 or 2 structures derived from a compound represented by Formula 1.

Abstract: Provided are an aromatic compound enhancing emission efficiency of blue light emitting region and an organic electroluminescence device including the same. The aromatic compound according to an embodiment of the inventive concept is represented by Formula 1, and more details about the constituents are provided in the disclosure.

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: An organic electroluminescent device of which emission life may be improved. The organic electroluminescent device includes an anode, an emission layer, and an anode-side hole transport layer provided between the anode and the emission layer and including an anode-side hole transport material. An electron accepting material is doped in the anode-side hole transport layer. An intermediate hole transport material layer is provided between the anode-side hole transport layer and the emission layer and includes an intermediate hole transport material, and an emission layer-side hole transport layer is provided between the intermediate hole transport material layer and the emission layer and adjacent to the emission layer. The emission layer-side hole transport layer includes an emission layer-side hole transport material represented by the following Formula 1.

Abstract: Provided are a polycyclic compound and an organic electroluminescence device including the same. The polycyclic compound according to an exemplary embodiment of the present disclosure is represented by the following formula 1. In Formula 1, X is O, SiR?R?, S, or BAr1. At least one of R1 to R8 is an aryl amine-containing electron donor. When X is O, SiR?R?, or S, the aryl amine-containing electron donor further includes a Si.

Abstract: A polycyclic compound and an organic electroluminescence device including the same. The polycyclic compound according to an example embodiment is represented by the following Formula 1. wherein in Formula 1, Cy1 is carbonyl-containing five- or six-membered and substituted or unsubstituted cyclic hydrocarbon or substituted or unsubstituted heterocycle, and R1 to R4 are each independently a hydrogen atom or a group represented by the following Formula 2 or 3.