The present specification relates to a double spiro structure compound, and an organic light emitting device comprising the same.

The present invention relates to a compound of the formula (I), (II) or (III), to the use of the compound in an electronic device, and to an electronic device comprising a compound of the formula (I), (II) or (III). The present invention furthermore relates to a process for the preparation of a compound of the formula (I), (II) or (III) and to a formulation comprising one or more compounds of the formula (I), (II) or (III).

The present invention relates to a compound for organic light-emitting diodes that can operate organic light-emitting diodes at a low driving voltage and an organic light-emitting diode comprising the same and, more particularly, to a compound for use as a fluorescent host in organic light-emitting diodes, which can bring about excellent diode properties by operating organic light-emitting diodes at a low driving voltage, and an organic light-emitting diode comprising the same.

The present invention provides an organic electroluminescent element which comprises: an anode; a cathode; and an organic layer interposed between the anode and the cathodes, wherein the organic layer comprises one or more types of layer from the group consisting of a hole-injection layer, hole-transport layer, light-emitting layer, lifetime enhancement layer, electron-transport layer, and electron-injection layer.

A thermally activated, sensitized phosphorescence organic electroluminescence device includes a luminescent layer formed of a host material consisting of two materials, one being a hole transport material, and the other an electron transport material, at least one which is a thermally activated delayed fluorescence material. The host material is doped by a phosphorescent dye. The triplet state energy level of the CT excited state of the fluorescence material is higher than the triplet state energy level of the n-π excited state by 0 to 0.3 or the triplet state energy level of the CT excited state of the fluorescence material is higher than the triplet state energy level of the n-π excited state, wherein the difference is above 1.0 eV, and, a difference between the second triplet state energy level of its n-π excited state and the first singlet state energy level of its CT excited state is −0.1 to 0.1 eV.

The present disclosure relates to an organic light-emitting diode having a low driving voltage and long lifespan and more particularly, to an organic light-emitting diode, comprising a first electrode, a second electrode facing the first electrode, and a light-emitting layer interposed therebetween, wherein the light-emitting layer contains at least one of the amine compounds represented by the following Chemical Formula A or Chemical Formula B, plus the compound represented by Chemical Formula D. The structures of Chemical Formulas A, B, and D are the same as in the specification.

A novel compound is disclosed which includes a ligand L.sub.A of Formula II, ##STR00001##
wherein: ring B is independently a 5-membered or 6-membered carbocyclic or heterocyclic ring; X.sup.1 to X.sup.4 are each independently selected from the group consisting of C, N, and CR; at least one pair of adjacent X.sup.1 to X.sup.4 are each C and fused to Formula V ##STR00002##
where indicated by “”; X.sup.5 to X.sup.12 are each independently C or N; the maximum number of N within a ring is two; Z and Y are each independently selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, and GeR′R″; R.sup.B and R.sup.C each independently represents zero, mono, or up to a maximum allowed substitutions to its associated ring; each of R.sup.B, R.sup.C, R, R′, and R″ is independently hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, boryl, and combinations thereof; and two substituents can be joined or fused to form a ring; the ligand L.sub.A is complexed to a metal M through the two indicated dash lines of each Formula; and the ligand L.sub.A can be joined with other ligands to form a tridentate, tetradentate, pentadentate, or hexadentate ligand.

To provide an organic electroluminescent device in which energy efficiency is improved. An organic electroluminescent device includes a pair of electrode layers formed of an anode layer and a cathode layer, and a luminescent layer arranged between the pair of electrode layers, in which the luminescent layer includes a host material and a dopant material, and the dopant material is an anthracene-based compound represented by formula (1), and the luminescent layer further includes a polycyclic aromatic compound represented by formula (2) or a multimer of a polycyclic aromatic compound having a plurality of structures represented by formula (2). ##STR00001##

The present invention relates to an organic electroluminescent device containing a mixture which comprises an electron-transporting host material and a hole-transporting host material, to a formulation comprising a mixture of the host materials and to a mixture comprising the host materials. The electron-transporting host material corresponds to a compound of the formula (1) from the class of compounds containing two triazine units. The hole-transporting host material corresponds to a compound of the formula (2) from the class of the biscarbazoles or derivatives thereof.

A composition for manufacturing an organic electronic device includes at least three organic functional materials H1, H2, and H3, and at least one organic solvent. The organic functional materials H1 and H2 can form a type II semiconductor heterojunction structure. A LUMO value of the organic functional material H3 is greater than or equal to that of the organic functional materials H1 and H2, and a HOMO value thereof is less than or equal to that of the organic functional materials H1 and H2.