H10K85/322

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

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

##STR00001##

is disclosed. In Formula I, ring A′ is a 7-, 8-, or 9-membered ring structure; X is of NR.sup.2, O, CR, CRR′, S, or SiRR′; each of R.sup.A′, R.sup.1, and R.sup.2 is independently hydrogen or a substituent; R.sup.1′ is independently absent or a hydrogen or a substituent; any two adjacent R.sup.A′, R.sup.1, R.sup.1′, and R.sup.2 can be joined or fused to form a ring; the ligand L.sub.A is coordinated to a metal, which is selected from Os, Ir, Pd, Pt, Cu, Ag, or Au; and (1) at least one of R.sup.1 and R.sup.2 is coordinated to the metal M, or (2) at least one R.sup.A′ comprises a 5- or 6-membered carbocyclic or heterocyclic ring that is not directly fused to Ring A′ and is coordinated to the metal M, or both (1) and (2) are true. Formulations, devices, and consumer products including the compound are also disclosed.

LIGHT EMITTING DEVICE

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.

##STR00001##

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Provided are boron substituted organometallic compounds of Formula I:

##STR00001##

Also provided are formulations including these organometallic compounds. Further provided are OLEDs and related consumer products that utilize these organometallic compounds.

ORGANIC ELECTROLUMINESCENT MATERIALS AND DEVICES

Provided is a new composition of matter for boron containing organic molecules which can be used as hosts or emitters in OLED devices. The compound can have a structure of Formula I

##STR00001##

Organic compound based on triazine and benzoxazole and application thereof in organic electroluminescent device

Disclosed are an organic compound based on triazine and benzoxazole and an application thereof in an OLED device. The compound of the present application has a relatively high glass transition temperature and molecular thermal stability, is low in absorption and high in refractive index in the field of visible light, and is capable of effectively improving the light extraction efficiency of an OLED device when applied to a capping layer of the OLED device; with a deep HOMO energy level and high electronic mobility, the compound of the present application can be used as the hole blocking layer or the electron transport layer material, so that the recombination degree of the hole and the electron in the light-emitting layer can be improved, and thus the light-emitting efficiency of the OLED device can be enhanced and the service life of the OLED device can be prolonged.

Organic electroluminescent materials and devices

A compound of Formula I: ##STR00001##
wherein: X.sup.1-X.sup.8 are each independently C or N, wherein two adjacent X.sup.1-X.sup.8 are carbon-fused to a structure of Formula II: ##STR00002## X.sup.9-X.sup.12 are each independently C or N; A.sup.1, A.sup.2, and A.sup.3 are each independently selected from the group consisting of O, S, Se, N, NR, CR, CRR′, SiR, SiRR′, GeR, and GeRR′, with at least one of A.sup.1 and A.sup.2 being N or NR; each occurrence of custom character is independently a single bond or a double bond, wherein one occurrence of custom character is a single bond and one occurrence of custom character is a double bond; each of R.sup.A, R.sup.B, and R.sup.c independently represents zero, mono, or up to a maximum allowed substitution to its associated ring; each of occurrence R, R′, R.sup.A, R.sup.B, and R.sup.C is independently a hydrogen or a substituent selected from the group consisting of Formula III, Formula IV, Formula V, Formula VI, Formula VII, Formula VIII, Formula IX, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, with at least one of R, R′, R.sup.A, R.sup.B, and R.sup.C comprising a group of Formula III, Formula IV, Formula V, Formula VI, Formula VII, Formula VIII, or Formula IX: ##STR00003## ##STR00004## each occurrence of Y.sup.1, Y.sup.2, and Y.sup.3 is independently absent, O, S, Se, NR, CRR′, SiRR′, or GeRR′; each occurrence of Ar.sup.1, and Ar.sup.2 is independently an optionally substituted aryl group or an optionally substituted heteroaryl group, wherein Ar.sup.1 and Ar.sup.2 are optionally joined or fused together to form a ring; each occurrence of X.sup.13-X.sup.20 is independently C or N, with the proviso that at least one of X.sup.13-X.sup.20 is N; each occurrence of A.sup.4 is selected from the group consisting of O, S, Se, NR, CRR′, SiRR′, and GeRR′; each occurrence of R.sup.X independently represents zero, mono, or up to a maximum allowed substitution to its associated ring; each occurrence of R.sup.X is in

LIGHT EMITTING ELEMENT AND POLYCYCLIC COMPOUND FOR LIGHT EMITTING ELEMENT
20230225183 · 2023-07-13 ·

A light emitting element includes a polycyclic compound having a B-N-B structure and including a specific substituent in an emission layer, thereby showing high efficiency and long-life characteristics.

LIGHT EMITTING ELEMENT AND POLYCYCLIC COMPOUND FOR THE SAME

Embodiments provide a polycyclic compound and a light emitting element that includes the polycyclic compound. The light emitting element 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, wherein the at least one functional layer includes the polycyclic compound, which is represented by Formula 1. Formula 1 is defined in the specification. The light emitting element exhibits a long service life.

##STR00001##

Photoelectric conversion element and solid-state imaging device

A photoelectric conversion element according to an embodiment of the present disclosure includes: a first electrode and a second electrode facing each other; and a photoelectric conversion layer provided between the first electrode and the second electrode, and including a first organic semiconductor material, a second organic semiconductor material, and a third organic semiconductor material that have mother skeletons different from one another. The first organic semiconductor material is one of fullerenes and fullerene derivatives. The second organic semiconductor material in a form of a single-layer film has a higher linear absorption coefficient of a maximal light absorption wavelength in a visible light region than a single-layer film of the first organic semiconductor material and a single-layer film of the third organic semiconductor material. The third organic semiconductor material has a value equal to or higher than a HOMO level of the second organic semiconductor material.

Light-emitting device and apparatus including the same

A light-emitting device includes: a first electrode; a second electrode facing the first electrode; light-emitting units in the number of n between the first electrode and the second electrode; and a charge-generation unit(s) in the number of n−1 between the adjacent light-emitting units. The light-emitting units each include an emission layer, and at least one of the charge-generation unit(s) includes an n-type charge-generation layer, a p-type charge-generation layer, and an interlayer between the n-type charge-generation layer and the p-type charge-generation layer. The p-type charge-generation layer includes a first material and a second material, the first material includes a hole-transporting organic compound, an inorganic insulation compound, or any combination thereof, the second material includes at least one inorganic semiconductor compound, the interlayer comprises a third material, and the third material is selected from an organic compound, an inorganic semiconductor compound, and an inorganic insulation compound.