H10K85/60

P-TYPE ORGANIC SEMICONDUCTOR MATERIAL, MANUFACTURING METHOD OF SAME, AND DISPLAY PANEL
20230131274 · 2023-04-27 ·

A p-type organic semiconductor material, a manufacturing method of the same, and a display panel are provided by the present application. Substitutes are configured to replace hydrogens on ring in a molecular structure of the p-type organic semiconductor material of the present application, therefore a LUMO energy level of the p-type organic semiconductor material obtained is reduced.

ORGANIC ELECTROLUMINESCENCE DEVICE AND POLYCYCLIC COMPOUND FOR ORGANIC ELECTROLUMINESCENCE DEVICE
20230127951 · 2023-04-27 ·

An 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, wherein the hole transport region includes a polycyclic compound represented by Formula 5 or Formula 6, thereby showing high emission efficiency.

PLURALITY OF HOST MATERIALS AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME

The present disclosure relates to a plurality of host materials comprising a first host material having a compound represented by formula 1, and a second host material having a compound represented by formula 2, and an organic electroluminescent device comprising the same. By comprising a specific combination of compounds of the present disclosure as host materials, it is possible to provide an organic electroluminescent device having long lifetime properties while having an equivalent or improved level of power efficiency compared to conventional organic electroluminescent devices.

ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

An organic electroluminescence device (1) includes an anode (3), a cathode (4), and an emitting layer disposed between the anode (3) and the cathode (4). The emitting layer includes a first emitting layer (51) and a second emitting layer (52). The first emitting layer (51) contains, as a first host material, a first compound that has at least one group represented by a formula (11) below and that is represented by a formula (1) below, where at least one of R.sub.101 to R.sub.112 is a group represented by the formula (11). The second emitting layer (52) contains a second compound represented by a formula (2) below as a second host material,

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POLYCYCLIC AROMATIC DERIVATIVE COMPOUND AND ORGANIC LIGHT-EMITTING DEVICE USING SAME

The present invention relates to a polycyclic aromatic derivative compound and an organic light-emitting device having high efficiency and long lifespan, the device applying the compound in various organic layers so as to remarkably improve luminous efficiency. According to the invention, an organic light-emitting device having high efficiency and long lifespan and having remarkably improved luminous efficiency can be implemented, and thus can be industrially useful in various display devices and lighting devices.

ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

An organic electroluminescent device includes a cathode, an anode, and organic layers intervening between the cathode and the anode, where the organic layers include a light emitting layer and an electron transporting layer, where the electron transporting layer contains a compound A represented by formula (1), and the light emitting layer contains a host material B represented by formula (10):

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Organic Compound, Light-Emitting Device, Electronic Device, Electronic Apparatus, Light-Emitting Apparatus, and Lighting Apparatus

An organic compound that easily exhibits thermally activated delayed fluorescence (TADF) is provided. An organic compound represented by General Formula (G1) is provided. In General Formula (G1), R.sup.1 to R.sup.8 are each independently any one of hydrogen, an alkyl group having 1 to 6 carbon atoms, a cycloalkyl group having 3 to 7 carbon atoms, and a substituted or unsubstituted diarylamino group; at least one of R.sup.1 to R.sup.8 is a substituted or unsubstituted diarylamino group; a is a substituted or unsubstituted phenylene group; n is an integer of 0 to 4; and A represents a substituted or unsubstituted benzofuropyrimidine skeleton or benzothienopyrimidine skeleton.

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NOVEL COMPOUND AND APPLICATION THEREOF

Provided is a compound that is excellent in chemical stability, has a high solubility in a solvent, and exhibits an excellent carrier mobility.

A compound represented by Formula (1):

##STR00001## where in Formula (1), X.sup.1, X.sup.2, X.sup.3, and R.sup.1 to R.sup.10 are as defined in the specification.

ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC DEVICE

An organic electroluminescence device includes: an emitting layer between an anode and a cathode; and a first layer between the cathode and the emitting layer, in which the first layer has a thickness of 50 nm or more, the first layer contains a compound represented by a formula (1) below, and the first layer contains no metal doping material. In the formula (100), A is a substituted or unsubstituted fused aryl group having 13 to 50 ring carbon atoms, or a substituted or unsubstituted fused heterocyclic group having 14 to 50 ring atoms.

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ORGANIC ELECTROLUMINESCENT ELEMENT

To provide a practically useful organic electroluminescent device which is improved in luminous efficiency and at the same time, sufficiently secures the stability during driving. An organic electroluminescent device, wherein a light-emitting layer includes two host materials different from each other, and a dopant material, one of the host materials is a compound represented by general formula (1) and the other of the host materials is a compound represented by general formula (2). A ring A is a heterocycle represented by formula (1a), X represents N or C—Ar′, Y represents O, S, N—Ar.sup.3, or C—Ar.sup.4Ar.sup.5, and any one of Z.sup.1 to Z.sup.4 represents a carbon atom binding to a 6-membered ring containing X and the others and Z.sup.5 to Z.sup.8 each represent C—Ar′ or N. Ar, Ar′ and Ar.sup.1 to Ar.sup.5 each represent, for example, hydrogen, or an alkyl group having 1 to 20 carbon atoms. A ring B is a heterocycle represented by formula (2a), and Ar.sup.6 and Ar.sup.7 each represent, for example, hydrogen, or an alkyl group having 1 to 20 carbon atoms.