Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Organic Small Molecule Luminescent Materials and Organic Electroluminescent Devices

A technology of light-emitting materials and small molecules, applied in the fields of light-emitting materials, electro-solid devices, organic chemistry, etc., can solve the problems of limited organic small-molecule optoelectronic materials, and achieve the effect of improving external quantum efficiency, excellent device performance, and high decomposition temperature.

Active Publication Date: 2020-08-04
TCL CHINA STAR OPTOELECTRONICS TECH CO LTD
View PDF3 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But so far, organic small molecule optoelectronic materials with simple structure, good performance and meeting commercial needs are still very limited, and the development of new organic optoelectronic materials is still of great significance

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Organic Small Molecule Luminescent Materials and Organic Electroluminescent Devices
  • Organic Small Molecule Luminescent Materials and Organic Electroluminescent Devices
  • Organic Small Molecule Luminescent Materials and Organic Electroluminescent Devices

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0058] The synthetic method 1 of 2-bromo-N-phenylaniline, chemical reaction formula is as follows:

[0059]

[0060] In a 250mL three-necked flask, add aniline (0.2mol, 18.6g), o-bromoiodobenzene (0.2mol, 56.58g), palladium acetate (0.6mmol, 134.4mg), sodium tert-butoxide (0.4 mol) into the flask in turn, then add 150mL of toluene, pass N 2 20 minutes, then add tert-butylphosphine (1.2mmol, 1.2ml), continue to pass through N 2 20 minutes, heat to reflux and stir for 12 hours. The temperature was lowered to room temperature, sodium tert-butoxide was removed by suction filtration, the solvent was distilled off under pressure, and the solvent was separated and purified by silica gel chromatography to obtain a colorless oily liquid (27.8 g, yield 56%).

Embodiment 2

[0062] The synthetic method 2 of 2-bromo-N-phenylaniline, chemical reaction formula is as follows:

[0063]

[0064] In a 250mL three-necked flask, add aniline (0.2mol, 18.6g), o-bromoiodobenzene (0.2mol, 56.58g), palladium acetate (0.6mmol, 134.4mg), sodium tert-butoxide (0.4 mol) was added in the flask successively, o-bis(2-phenyl)bis(diphenylphosphine) (0.6mmol, 340mg), then added the toluene of 150mL, logical N 2 20 minutes, heat to reflux and stir for 12 hours. The temperature was lowered to room temperature, sodium tert-butoxide was removed by suction filtration, the solvent was distilled off under pressure, and the solvent was separated and purified by silica gel chromatography to obtain a colorless oily liquid (44.2 g, yield 89%).

[0065] After comparing the above Example 1 and Example 2, it can be found that by changing the catalyst ligand from t-butylphosphine to o-bis(2-phenyl)bis(diphenylphosphine), 2-bromo-N-benzene Aniline yield increased from 56% to 89%. ...

Embodiment 3

[0067] The preparation method 1 of (4-bromophenyl)-phenyl-carbamic acid tert-butyl ester, chemical reaction formula is as follows:

[0068]

[0069] In a 500 ml one-necked flask, di-tert-butyl dicarbonate (BOC) (0.2mol, 43.6g) was added to 400 ml of tetrahydrofuran at room temperature, and then p-N-(dibromophenyl)aniline (0.1mol , 24.8g), heated to reflux and stirred for 24 hours. The mixture was then poured into 1 L of water, and the product was extracted with dichloromethane. Dry the organic phase with anhydrous magnesium sulfate, remove the solvent after separation, and separate and purify with silica gel chromatography to obtain a colorless oily liquid (32.0 g, yield 92%).

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention provides an organic small molecule luminescent material and an organic electroluminescent device. The organic small molecule luminescent material of the present invention is obtained by coupling a novel acridine donor unit 10H-spiro[acridine-9,2'-adamantane] with an acceptor unit, and has a single structure, a definite molecular weight, and is easy to purify , multiple synthesis reproducibility, low sublimation temperature and high decomposition temperature, stable film morphology, and due to the non-aromatic rigid structure of adamantane as the donor part of the structure, the organic small molecule light-emitting material in the film state It has a very high photoluminescence quantum yield, and when it is applied to organic electroluminescent devices, it can effectively solve the problem of low device efficiency due to severe non-radiative attenuation of excited state molecules due to configuration relaxation.

Description

technical field [0001] The invention relates to the field of organic electroluminescence, in particular to an organic small molecule luminescent material and an organic electroluminescent device using the organic small molecule luminescent material. Background technique [0002] Organic electroluminescence (OLED) device is a self-luminous device, which has the advantages of low voltage, wide viewing angle, fast response speed, and good temperature adaptability. It is a new generation of display technology. At present, a few manufacturers have mass-produced OLED panels, and more companies have also entered the stage of R&D and mass production. [0003] The principle of an organic electroluminescent device is that, under the action of an electric field, holes and electrons are injected from the anode and cathode respectively, pass through the hole injection layer, the hole transport layer, the electron injection layer, and the electron transport layer respectively, and then re...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C07D221/20C07D401/10C09K11/06H01L51/50H01L51/54
CPCC09K11/06C07D221/20C07D401/10C09K2211/1007C09K2211/1059H10K85/654H10K50/12
Inventor 吴元均矫士博史婷苏仕健李伟李彬彬
Owner TCL CHINA STAR OPTOELECTRONICS TECH CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com