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.

Provided are a compound of 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-based bisoxazoline ligand, an intermediate, a preparation method and uses thereof. The compound of bisoxazoline ligand is a compound having a structure represented by formula I, or an enantiomer, a raceme, or diastereomer thereof. The bisoxazoline ligand can be prepared via a preparation scheme in which the cheap and easily available 6,6′-dihydroxyl-3,3,3′,3′-tetramethyl-1,1′-spirobiindane is used as a starting raw material and the compound represented by formula II serves as the key intermediate through a series of reactions. The new bisoxazoline ligand developed by the present application can be used in catalytic organic reaction, in particular as a chiral bisoxazoline ligand that is widely used in many asymmetric catalytic reactions of metal catalysis, and thus it has economic practicability and industrial application prospect.

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Provided are a compound of 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-based bisoxazoline ligand, an intermediate, a preparation method and uses thereof. The compound of bisoxazoline ligand is a compound having a structure represented by formula I, or an enantiomer, a raceme, or diastereomer thereof. The bisoxazoline ligand can be prepared via a preparation scheme in which the cheap and easily available 6,6′-dihydroxyl-3,3,3′,3′-tetramethyl-1,1′-spirobiindane is used as a starting raw material and the compound represented by formula II serves as the key intermediate through a series of reactions. The new bisoxazoline ligand developed by the present application can be used in catalytic organic reaction, in particular as a chiral bisoxazoline ligand that is widely used in many asymmetric catalytic reactions of metal catalysis, and thus it has economic practicability and industrial application prospect. ##STR00001##

A compound, a material for an organic electroluminescent device and an application thereof are disclosed herein. The compound has a structure represented by Formula (1). The compound has a relatively high refractive index and can effectively improve the light extraction efficiency. The external quantum efficiency of the compound makes it suitable for use as a capping layer when used in an organic electroluminescent device. The compound has a relatively high refractive index in the region of visible light (400-750 nm), which is advantageous for improving the light-emitting efficiency. The compound has a relatively large extinction coefficient in the ultraviolet region (less than 400 nm), which is advantageous for absorbing harmful light and protecting eyesight. Meanwhile, a deuterium atom may be introduced into the compound to significantly improve the device lifetime.

Disclosed are a central chirality induced spiro chiral tetradentate cyclometalated platinum (II) and palladium (II) complex-based circularly polarized luminescence material and an application thereof. Spiro chiral metal complex molecules can be autonomously induced by a whole tetradentate ligand to coordinate with metal ions in a less sterically hindered manner by means of a central chiral fragment L.sup.a in the tetradentate ligand, to form an optically pure spiro chiral metal complex-based circularly polarized luminescence material, without need for chiral resolution. Moreover, the material has high chemical stability and thermal stability, and has important applications in circularly polarized luminescence devices.

The present application discloses an arylamine organic compound and the use thereof. The arylamine organic compound has a structure as shown in general formula (1).

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The arylamine organic compound has a relatively high glass transition temperature, a relatively high thermal stability, a relatively small visible light extinction coefficient, and a relatively high refractive index; and when the arylamine organic compound is used as a capping layer material for an organic electronic device, the visible luminous efficiency of the organic electronic device can be effectively improved.

The present application discloses an arylamine organic compound and the use thereof. The arylamine organic compound has a structure as shown in general formula (1).

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The arylamine organic compound has a relatively high glass transition temperature, a relatively high thermal stability, a relatively small visible light extinction coefficient, and a relatively high refractive index; and when the arylamine organic compound is used as a capping layer material for an organic electronic device, the visible luminous efficiency of the organic electronic device can be effectively improved.

The present invention is a synthesis method for benzoxazole based optical brighteners characterized by comprising the steps of; placing in a reactor vessel at least one acid selected from thiophene-2,5-dicarboxylic acid or stilbene-4,4-dicarboxylic acid, at least one catalyst and at least one compound selected from liquid paraffin and/or xylene; obtaining a mixture by adding 2-amino-4-tert-butylphenol in the reactor vessel if the said at least one acid is selected as thiophene-2,5-dicarboxylic acid or adding 2-aminophenol in the reactor vessel if the said at least one acid is selected as stilbene-4,4-dicarboxylic acid; mixing the obtained mixture for a first time period under nitrogen atmosphere to carry out the synthesis reaction of benzoxazole based optical brighteners; during mixing the obtained mixture, increasing the temperature of the said mixture gradually to a first temperature; after mixing obtained mixture for the first time period, filtering the mixture; after filtering the mixture, obtaining a first benzoxazole based optical brightener or a second benzoxazole based optical brightener.

The present invention is a synthesis method for benzoxazole based optical brighteners characterized by comprising the steps of; placing in a reactor vessel at least one acid selected from thiophene-2,5-dicarboxylic acid or stilbene-4,4-dicarboxylic acid, at least one catalyst and at least one compound selected from liquid paraffin and/or xylene; obtaining a mixture by adding 2-amino-4-tert-butylphenol in the reactor vessel if the said at least one acid is selected as thiophene-2,5-dicarboxylic acid or adding 2-aminophenol in the reactor vessel if the said at least one acid is selected as stilbene-4,4-dicarboxylic acid; mixing the obtained mixture for a first time period under nitrogen atmosphere to carry out the synthesis reaction of benzoxazole based optical brighteners; during mixing the obtained mixture, increasing the temperature of the said mixture gradually to a first temperature; after mixing obtained mixture for the first time period, filtering the mixture; after filtering the mixture, obtaining a first benzoxazole based optical brightener or a second benzoxazole based optical brightener.

An arylamine compound and use thereof, an electroluminescent device and a display apparatus are provided, the arylamine compound has a general structural formula of Formula I; wherein each group and substituent have the same meaning as that in the description.

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