A novel organic compound having high stability is provided. The organic compound is represented by Formula (1) described in claim 1: In Formula (1), R.sub.1 and R.sub.2 each independently selected from a hydrogen atom, Substituent group A, and Substituent group B shown in claim 1, wherein at least one of R.sub.1 and R.sub.2 is selected from Substituent group A or Substituent group B; and R.sub.11 and R.sub.12 of a substituent belonging to Substituent group A are each independently selected from Substituent group B.

Disclosed is a cross-coupling reaction method which forms a chemical bond selected from C—N, C—B, C—C, C—O and C—S bonds, the method comprising: preparing an aromatic compound (1) having a leaving group; preparing a compound (2) capable of undergoing a cross-coupling reaction selected from an aromatic amino compound (2-1), a diboronic acid ester or the like (2-2), an aromatic boronic acid or the like (2-3), an aromatic compound (2-4) having a hydroxyl group and an aromatic compound (2-5) having a thiol group; and performing a cross-coupling reaction of the compound (1) with the compound (2) in the presence of a palladium catalyst, a base and a compound (4) having a carbon-carbon double bond or a carbon-carbon triple bond, in the absence of a solvent.

The invention relates to compounds that can be used in an organic electronic device as an active compound, in particular for use in electronic devices. The invention further relates to a method for producing the compounds according to the invention, and to electronic devices comprising same.

Disclosed are amine-substituted naphthalene derivatives and organic light emitting diodes including the same. In the organic light emitting diodes, at least one of the amine-substituted naphthalene derivatives is employed in a hole auxiliary layer interposed between a hole transport layer and a light emitting layer to enable efficient hole transport to the light emitting layer, achieving high luminous efficiency and long lifetime.

Provided are a heterocyclic derivative and an organic electroluminescent device thereof, which relates to the field of organic photoelectric materials. The heterocyclic derivative of Formula I has high electron mobility and great hole blocking performance, and thus the organic electroluminescent device prepared by using the heterocyclic derivative as the electron transport region material, especially the hole blocking material, has low drive voltage and high luminous efficiency. The organic electroluminescent device can also include a hole transport region, and the hole transport region, especially the emissive auxiliary layer, contains the triarylamine compound of Formula II. Since the electron transport region and the hole transport region of the device can effectively balance carriers, which reduces the quenching of excitons and improves the recombination probability of carriers, the device shows low drive voltage and high luminous efficiency.

Provided is a method for producing a deuterated aromatic compound and a deuterated reaction composition. The method includes performing a deuterated reaction of an aromatic compound including one or more hydrocarbon aromatic rings using a solution comprising heavy water, an organic compound which can be hydrolyzed by the heavy water, the aromatic compound, and an organic solvent. The method has an advantage in that impurities due to hydrogen gas are not generated, the deuterium substitution rate is high, and the deuterated reaction can be performed under a lower pressure and a lower temperature.

A compound represented by the following formula (1), provided that at least one of R.sub.1 to R.sub.8 is a deuterium atom; and at least one of Ar.sub.1 and Ar.sub.2 is a substituted or unsubstituted fused aryl group in which only four or more benzene rings are fused.

##STR00001##

A compound represented by formula (1) provides a high performance organic electroluminescence device and a novel material for realizing such an organic electroluminescence device:

##STR00001##

wherein R.sup.1 to R.sup.6, a to f, L.sup.1 to L.sup.3, and Ar are as defined in the description.

Provided is an organic light-emitting element comprising: a first electrode; a second electrode provided to face the first electrode; and an organic material layer provided between the first electrode and the second electrode, in which the organic material layer comprises a layer comprising a compound of Formula 1:

##STR00001## wherein: L1 is a direct bond, or a substituted or unsubstituted arylene or heteroarylene group; Ar1 is a substituted or unsubstituted aryl or heteroaryl group; R1 to R12 are each independently hydrogen, a nitrile group, a halogen, or a substituted or unsubstituted alkyl, silyl, aryl or heteroaryl group, or adjacent groups bond together to form a ring; and any two adjacent R1 to R4 bond together to form a substituted or unsubstituted aromatic ring,
and a layer comprising a compound of Formula 2:

##STR00002## wherein: Ar2 to Ar4 are each independently a substituted or unsubstituted aryl group having 6 to 20 carbon atoms, or -L2-Z.

The present specification relates to an organic light emitting element comprising: an anode; a cathode disposed opposite to the anode; and a light emitting layer disposed between the anode and the cathode, wherein the light emitting layer comprises: a host including a P-type host and an N-type host for generating an exciplex; and a phosphorescent dopant, and the host including the P-type host and the N-type host for generating an exciplex emits photoluminescence light having a longer wavelength than that emitted from each of the P-type host and the N-type host.