C09K2211/1007

LIGHT EMITTING ELEMENT AND POLYCYCLIC COMPOUND FOR THE SAME

A light emitting element that includes a first electrode, a second electrode on the first electrode, and at least one functional layer between the first electrode and the second electrode is provided. The at least one functional layer includes a polycyclic compound represented by a specific chemical structure, and has a high efficiency and low driving voltage properties.

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

A compound comprising a ligand L.sub.A, having a structure of Formula I,

##STR00001##

is provided. In Formula I, A.sup.1 to A.sup.8 are each independently CR or N; at least two adjacent ones of A.sup.1 to A.sup.8 are CR and the Rs are joined together to form a six-membered ring fused to ring A or ring C; X is O, S, or Se; each R and R.sup.B is independently hydrogen or a substituent; any adjacent substituents are optionally joined or fused into a ring; the ligand L.sub.A is coordinated to a metal M; the metal M is bonded to ring A through a M-C bond; the metal M can be coordinated to other ligands; and the ligand L.sub.A is optionally linked with other ligands. Formulations, OLEDs, and consumer products containing such compounds are also disclosed.

Organic Electroluminescent Element And Novel Iridium Complex
20230217666 · 2023-07-06 ·

An iridium complex which has a phenylpyridine bidentate ligand containing a group represented by the following general formula (A):

##STR00001##

(In the general formula (A), X represents a cyano group or a halogenated alkyl group. L represents a single bond or a divalent linking group. R represents a substituent. n represents an integer of 0 to 4. * represents a binding site to a phenylpyridine bidentate ligand.)

COMPOUNDS AND ORGANIC ELECTRONIC DEVICES

The present invention relates to certain fluorenes, to the use of the compounds in an electronic device, and to an electronic device comprising at least one of these compounds. The present invention furthermore relates to a process for the preparation of the compounds and to a formulation and composition comprising one or more of the compounds.

Condensed cyclic compound and organic light-emitting device including the same

Provided are a condensed cyclic compound having the following structure: ##STR00001##
wherein ring D.sub.1 and ring D.sub.2 are each independently a C.sub.6-C.sub.20 aromatic ring, and an organic light-emitting device including the same.

Light Emitting Device and Light Emitting Display Device Including the Same

A light emitting device and a light emitting display device that are capable of improving efficiency, driving voltage, and lifespan by varying the configuration of a layer adjacent to a blue light emitting layer in a blue fluorescent stack contacting a cathode are disclosed. The light emitting device includes stacks between an anode and a cathode, wherein an n.sup.th stack contacting the cathode is a first blue stack that includes a first hole transport layer, a first electron-blocking layer, a first blue light emitting layer containing a boron-based dopant having an emission peak of 430 nm to 480 nm, a first electron transport layer contacting the first blue light emitting layer, and an electron injection layer having two sides contacting the first electron transport layer and the cathode, respectively, wherein the first electron transport layer contains a mixture of a first material and a second material.

ORGANIC ELECTRONIC ELEMENT, DISPLAY PANEL COMPRISING THE SAME AND DISPLAY DEVICE COMPRISING THE SAME

An organic electronic element, a display panel and a display device can each include a charge generating layer and a hole injection layer including a p-type dopant with low absorption rate for a blue wavelength band so that they can have excellent light extraction efficiency or luminous efficiency.

Thermally activated delayed fluorescent molecular material, a synthesizing method therefor, and an electroluminescent device

A thermally activated delayed fluorescent molecular material, a synthesizing method therefor, and an electroluminescent device are provided. The thermally activated delayed fluorescent molecular containing an indenobenzoselenoheteroaromatic ring donor is synthesized, so that an electron donating ability of the donor is increased, and an non-radiative transition rate is effectively inhibited, thereby increasing photo-luminescence quantum yield (PLQY) of the molecule; and increasing the twist angle between the electron donor and the electron acceptor. Meanwhile, electron cloud overlapping between highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) is reduced, thereby obtaining a smaller ΔE.sub.ST value. The organic electroluminescent device adopts the thermally activated delayed fluorescent molecular material prepared according to the synthesizing method, and thus has high luminous efficiency and long service life.

Heteroleptic transition metal-carbene complexes and their use in organic light-emitting diodes

The present invention relates to heteroleptic carbene complexes comprising at least two different carbene ligands, to a process for preparing the heteroleptic carbene complexes, to the use of the heteroleptic carbene complexes in organic light-emitting diodes, to organic light-emitting diodes comprising at least one inventive heteroleptic carbene complex, to a light-emitting layer comprising at least one inventive heteroleptic carbene complex, to organic light-emitting diodes comprising at least one inventive light-emitting layer, and to devices which comprise at least one inventive organic light-emitting diode.

Organic light-emitting device

An organic light-emitting device including a first electrode; a second electrode facing the first electrode; an emission layer between the first electrode and the second electrode; a hole transport region between the first electrode and the emission layer; and an electron transport region between the emission layer and the second electrode, wherein: the emission layer includes a first compound, at least one of the hole transport region and the electron transport region includes a second compound, the first compound is represented by Formula 1A or 1B, and the second compound is represented by Formula 2A or 2B: ##STR00001##