The present disclosure provides an organic light emitting diode comprising a first electrode; a second electrode facing the first electrode; and an emitting material layer. The emitting material layer includes a p-type host, a n-type host and a phosphorescent dopant and positioned between the first electrode and the second electrode, wherein a first energy level of a HOMO of the p-type host is equal to or lower than a second energy level of a HOMO of the n-type host, and a difference between an energy level of a singlet state of the n-type host and an energy level of a triplet state of the n-type host is greater than 0.3 eV and smaller than 0.5 eV.

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. The organic electroluminescent device having improved driving voltage and/or current efficiency characteristics can be provided by comprising the organic electroluminescent compound according to the present disclosure.

The present disclosure relates to an organic electroluminescent compound and an organic electroluminescent device comprising the same. The organic electroluminescent device having improved driving voltage and/or current efficiency characteristics can be provided by comprising the organic electroluminescent compound according to the present disclosure.

A compound is represented by a formula (1). n is 2 to 4, m is 1 to 4, q is 0 to 3, and m+n+q=6; CN is a cyano group; D.sub.1 is a group represented by a formula (2), (3) or (3X), the plurality of D.sub.1 are the same; and Rx is a hydrogen atom or substituent. R.sub.1 to R.sub.8 are each independently a hydrogen atom or substituent. R.sub.31 to R.sub.38 and R.sub.41 to R.sub.48 are each independently a hydrogen atom or substituent; p, px and py are each independently 1 to 4; A to C are each independently a cyclic structure represented by a formula (131) or (132). R.sub.19 and R.sub.20 are each independently a hydrogen atom or substituent. X.sub.1 is a sulfur atom or the like, and * represents a bonding position with a carbon atom of a benzene ring in the formula (1).

##STR00001##

A compound is represented by a formula (1). n is 2 to 4, m is 1 to 4, q is 0 to 3, and m+n+q=6; CN is a cyano group; D.sub.1 is a group represented by a formula (2), (3) or (3X), the plurality of D.sub.1 are the same; and Rx is a hydrogen atom or substituent. R.sub.1 to R.sub.8 are each independently a hydrogen atom or substituent. R.sub.31 to R.sub.38 and R.sub.41 to R.sub.48 are each independently a hydrogen atom or substituent; p, px and py are each independently 1 to 4; A to C are each independently a cyclic structure represented by a formula (131) or (132). R.sub.19 and R.sub.20 are each independently a hydrogen atom or substituent. X.sub.1 is a sulfur atom or the like, and * represents a bonding position with a carbon atom of a benzene ring in the formula (1).

##STR00001##

There is provided a polycyclic aromatic compound having a single boron-nitrogen bond and including a core structure of Core A, Core B, or Core C

##STR00001##

In the formulas: Q.sup.1 and Q.sup.2 are the same or different and are a single bond, O, S, NR.sup.12, BR.sup.12, CR.sup.13R.sup.14, or SiR.sup.13R.sup.14; and R.sup.12-R.sup.14 are the same or different and are alkyl, carbocyclic aryl, heteroaryl, or substituted derivatives thereof.

The present invention relates to a novel polycyclic compound employed in an organic layer of an organoelectro luminescent device, wherein the organoelectro luminescent device employing the compound according to the present invention has remarkably improved luminous efficiency. According to the present invention, it is possible to implement a highly efficient organoelectro luminescent device that can be effectively applied to various display devices.

The present disclosure provides a nitrogen-containing compound, and an electronic component and an electronic device including the same, and belongs to the technical field of organic electroluminescence. The nitrogen-containing compound provided by the present disclosure has polycyclic conjugation properties, the compound has a core structure of fused indolocarbazole. The bond energy between the atoms is high, thus the compound has a good thermal stability, and facilitates solid state accumulation between the molecules. The electroluminescence device with the compound as a luminescent layer material has a long service life. According to the nitrogen-containing compound provided by the present disclosure with an indolocarbazole structure connecting with a nitrogen-containing group (triazine, pyridine and pyrimidine) and a benzoxazole or benzothiazole group respectively has a high dipole moment, thereby improving the polarity of the material. Using the nitrogen-containing compound of the present disclosure as the luminescent layer material of the organic electroluminescence device, the electron transport performance of the device can be improved, and the luminous efficiency and service life of the device can be improved.

An organic electroluminescence device includes an anode, a cathode, an emitting layer between the anode and the cathode, a first electron transporting layer between the cathode and the emitting layer, and a second electron transporting layer between the cathode and the first electron transporting layer. The first electron transporting layer is directly adjacent to the emitting layer, the second electron transporting layer is directly adjacent to the first electron transporting layer, the emitting layer contains a first compound represented by Formula (1) below, the first compound has at least one group represented by Formula (11) below, the first electron transporting layer contains a second compound represented by Formula (2) below, and the second electron transporting layer contains a third compound represented by Formula (3) below.

##STR00001##

The present disclosure relates to compounds of Formula (I), (II), or (III) ##STR00001## as compounds capable of emitting delayed fluorescence, and uses of these compounds in organic light-emitting diodes.