Patent classifications
C07D235/20
ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME
The present disclosure provides a compound represented by formula (I):
##STR00001##
and an organic electroluminescent device including the same.
ORGANIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING THE SAME
The present disclosure provides a compound represented by formula (I):
##STR00001##
and an organic electroluminescent device including the same.
ORGANIC EL DEVICE AND DISPLAY UNIT
An organic EL device of the disclosure includes: a first electrode and a second electrode; and an organic layer provided between the first electrode and the second electrode. The organic layer includes a light-emitting layer. The organic layer includes, between the first electrode and the light-emitting layer, a first layer that contains a polycyclic aromatic hydrocarbon compound having orientation, and a second layer that contains a larger amount of nitrogen element than the first layer.
2,2'-BIBENZO[D]IMIDAZOLIDENE COMPOUND HAVING CONDENSED RINGS AT THE 1-, 1'-, 3- AND 3'-POSITIONS, AND ORGANIC LIGHT-EMITTING ELEMENT, DISPLAY DEVICE, IMAGE INFORMATION PROCESSING APPARATUS, LIGHTING DEVICE, IMAGE FORMING APPARATUS AND EXPOSURE UNIT, EACH CONTAINING THE SAME
A stable 2,2′-bibenzo[d]imidazolidene compound is provided. The 2,2′-bibenzo[d]imidazolidene compound is expressed by the following General Formula (1). In General Formula (1), Ar.sub.1 to Ar.sub.8 each represent a substituted or unsubstituted condensed ring. R.sub.1 to R.sub.8 each represent a hydrogen atom or a substituent.
##STR00001##
2,2'-BIBENZO[D]IMIDAZOLIDENE COMPOUND HAVING CONDENSED RINGS AT THE 1-, 1'-, 3- AND 3'-POSITIONS, AND ORGANIC LIGHT-EMITTING ELEMENT, DISPLAY DEVICE, IMAGE INFORMATION PROCESSING APPARATUS, LIGHTING DEVICE, IMAGE FORMING APPARATUS AND EXPOSURE UNIT, EACH CONTAINING THE SAME
A stable 2,2′-bibenzo[d]imidazolidene compound is provided. The 2,2′-bibenzo[d]imidazolidene compound is expressed by the following General Formula (1). In General Formula (1), Ar.sub.1 to Ar.sub.8 each represent a substituted or unsubstituted condensed ring. R.sub.1 to R.sub.8 each represent a hydrogen atom or a substituent.
##STR00001##
A CONVERGENT APPROACH TO THE TOTAL SYNTHESIS OF TELMISARTAN VIA A SUZUKI CROSS-COUPLING REACTION
Methods of synthesizing the angiotensin II receptor antagonist telmisartan in high yield and purity are provided. The methods involve the coupling of two structurally distinct benzimidazole units via a Suzuki cross-coupling reaction. Methods of regioselectively synthesizing one of the benzimidazole units are also provided.
A CONVERGENT APPROACH TO THE TOTAL SYNTHESIS OF TELMISARTAN VIA A SUZUKI CROSS-COUPLING REACTION
Methods of synthesizing the angiotensin II receptor antagonist telmisartan in high yield and purity are provided. The methods involve the coupling of two structurally distinct benzimidazole units via a Suzuki cross-coupling reaction. Methods of regioselectively synthesizing one of the benzimidazole units are also provided.
Thermosetting polyimides derived from resveratrol
A method for making thermosetting polyimides from resveratrol including converting resveratrol to trisaniline, reacting trisaniline with one or more dianhydride and thermosetting endcap to form amic acid, thermally imidizing amic acid to form polyimide oligomer, and cross-linking polyimide oligomer with heat and pressure to generate polyimide thermoset.
Thermosetting polyimides derived from resveratrol
A method for making thermosetting polyimides from resveratrol including converting resveratrol to trisaniline, reacting trisaniline with one or more dianhydride and thermosetting endcap to form amic acid, thermally imidizing amic acid to form polyimide oligomer, and cross-linking polyimide oligomer with heat and pressure to generate polyimide thermoset.
HETEROCYCLIC COMPOUND AND ORGANIC ELECTROLUMINESCENT DEVICE COMPRISING SAME
Provided are a heterocyclic compound and an organic electroluminescent device comprising the same, which relate to the field of organic electroluminescent technologies. The heterocyclic compound has advantages of good film-forming property, good thermal stability, and relatively high glass-transition temperature, and the service life of the device can be prolonged when the heterocyclic compound is applied to an organic layer of the organic electroluminescent device; meanwhile, the structure has a deep HOMO energy level so that holes can be effectively prevented from diffusing from the emissive layer to the electron transport layer and the recombination probability of the holes and electrons in the emissive layer can be effectively improved; and when the heterocyclic compound is applied to the electron transport layer or hole blocking layer, the luminous efficiency of the device can be effectively improved.