The present application relates to a compound of Chemical Formula 1 and an organic light emitting device including the same.

The present disclosure relates to an organic electroluminescent compound represented by formula 1 and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound of the present disclosure, an organic electroluminescent device having improved driving voltage, luminous efficiency, and/or lifespan characteristics can be provided.

The present application relates to technical field of organic semiconductors and provides an arylamine compound and use thereof in photoelectric devices. The compound is composed of a N,N-dialkyl-dicarbazole amine functional group modified unit with larger conjugated system. The semiconductor material provided by the present application has high glass transition temperature, high solubility, good film forming property and high thermal stability of film morphology, and can be used as a hole transport material in photoelectric devices to realize excellent thermal stability. The compound has simple preparation process, easily available raw materials and low price, and is suitable for industrial production. High glass transition temperature and good thermal stability are beneficial to prolong the working life of optoelectronic devices. High solubility, can form amorphous film with excellent quality, and is beneficial to application in photoelectric devices; The device has high photoelectric conversion efficiency and is a hole transport material with excellent performance.

The present application relates to technical field of organic semiconductors and provides an arylamine compound and use thereof in photoelectric devices. The compound is composed of a N,N-dialkyl-dicarbazole amine functional group modified unit with larger conjugated system. The semiconductor material provided by the present application has high glass transition temperature, high solubility, good film forming property and high thermal stability of film morphology, and can be used as a hole transport material in photoelectric devices to realize excellent thermal stability. The compound has simple preparation process, easily available raw materials and low price, and is suitable for industrial production. High glass transition temperature and good thermal stability are beneficial to prolong the working life of optoelectronic devices. High solubility, can form amorphous film with excellent quality, and is beneficial to application in photoelectric devices; The device has high photoelectric conversion efficiency and is a hole transport material with excellent performance.

The present disclosure relates to an organic electroluminescent compound represented by formula 2′, a plurality of host materials comprising at least one first host compound and at least one second host compound, and an organic electroluminescent device comprising the same. By comprising the organic electroluminescent compound or a specific combination of compounds of the present disclosure, it is possible to provide an organic electroluminescent device having improved driving voltage, luminous efficiency, power efficiency, and/or lifespan characteristics.

Disclosed herein are novel rigid cannabidiol (CBD) analogues and their formulations that modulate cannabinoid receptors, method(s) of preparation, methods of modulating cannabinoid receptors, and methods of treating various conditions related to the modulation of cannabinoid receptors, such as, pain and inflammation, cancer, glaucoma, neurodegenerative disorders, multiple sclerosis, renal fibrosis, fibrotic disorders, addiction, anxiety, insomnia, motor function disorders and gastrointestinal and metabolic disorders.

Disclosed herein are novel rigid cannabidiol (CBD) analogues and their formulations that modulate cannabinoid receptors, method(s) of preparation, methods of modulating cannabinoid receptors, and methods of treating various conditions related to the modulation of cannabinoid receptors, such as, pain and inflammation, cancer, glaucoma, neurodegenerative disorders, multiple sclerosis, renal fibrosis, fibrotic disorders, addiction, anxiety, insomnia, motor function disorders and gastrointestinal and metabolic disorders.

Disclosed is a fluorination method comprising providing an aryl fluorosulfonate and a fluorinating reagent to a reaction mixture; and reacting the aryl fluorosulfonate and the fluorinating reagent to provide a fluorinated aryl species. Also disclosed is a fluorination method comprising providing, a salt comprising a cation and an aryloxylate, and SO.sub.2F.sub.2 to a reaction mixture; reacting the SO.sub.2F.sub.2 and the ammonium salt to provide a fluorinated aryl species. Further disclosed a fluorination method comprising providing a compound having the structure Ar—OH to a reaction mixture; where Ar is an aryl or heteroaryl; providing SO.sub.2F.sub.2 to the reaction mixture; providing a fluorinating reagent to the reaction mixture; reacting the SO.sub.2F.sub.2, the fluorinating reagent and the compound having the structure Ar—OH to provide a fluorinated aryl species having the structure Ar—F.

Disclosed is a fluorination method comprising providing an aryl fluorosulfonate and a fluorinating reagent to a reaction mixture; and reacting the aryl fluorosulfonate and the fluorinating reagent to provide a fluorinated aryl species. Also disclosed is a fluorination method comprising providing, a salt comprising a cation and an aryloxylate, and SO.sub.2F.sub.2 to a reaction mixture; reacting the SO.sub.2F.sub.2 and the ammonium salt to provide a fluorinated aryl species. Further disclosed a fluorination method comprising providing a compound having the structure Ar—OH to a reaction mixture; where Ar is an aryl or heteroaryl; providing SO.sub.2F.sub.2 to the reaction mixture; providing a fluorinating reagent to the reaction mixture; reacting the SO.sub.2F.sub.2, the fluorinating reagent and the compound having the structure Ar—OH to provide a fluorinated aryl species having the structure Ar—F.

Provided are a heterocyclic compound represented by Formula 1 and an organic light-emitting device including the same. The organic light-emitting device includes: a first electrode; a second electrode facing the first electrode; and an organic layer between the first electrode and the second electrode and including an emission layer, wherein the organic light-emitting device includes at least one heterocyclic compound represented by Formula 1.