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

Organic electroluminescent material, preparation method of organic electroluminescent material and organic electroluminescent device

An electroluminescence and electromechanical technology, applied in the field of phosphorescent materials, can solve the problems of the luminous color purity of blue phosphorescent materials, the bottleneck of luminous efficiency device efficiency attenuation, etc.

Inactive Publication Date: 2015-04-29
OCEANS KING LIGHTING SCI&TECH CO LTD +2
View PDF0 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0011] People's research on iridium metal complexes of organic electroluminescent materials has been in-depth, but there are bottlenecks in the luminous color purity, luminous efficiency and device efficiency attenuation of blue phosphorescent materials.

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 electroluminescent material, preparation method of organic electroluminescent material and organic electroluminescent device
  • Organic electroluminescent material, preparation method of organic electroluminescent material and organic electroluminescent device
  • Organic electroluminescent material, preparation method of organic electroluminescent material and organic electroluminescent device

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0047] The preparation process of the organic electroluminescent material (P) of the present invention is roughly divided into the following steps:

[0048] (1) Synthesize compound C through Suzuki coupling reaction of compound E and compound F; wherein, compound F is 2,4-difluoro-3-cyanophenylboronic acid, and the structural formulas of compound E and compound C are as follows:

[0049] Compound E is Compound C is Among them, R is a hydrogen atom, C 1～20 straight chain alkyl, C 1～20 Branched chain alkyl, C 1～20 Linear alkoxy or C 1～20 branched chain alkoxy.

[0050] (2) Reaction of compound C prepared in step (1) with compound D to generate a chlorine-bridged dimer, namely compound A. Wherein, compound D is trihydrate iridium trichloride IrCl 3 ·3H 2 O. The structural formula of compound A is as follows:

[0051]

[0052] (3) Compound A prepared in step (2) is used as a ring metal ligand, and compound B is used as an auxiliary ligand source to react compound A ...

Embodiment 1

[0057] The organic electroluminescent material (P) disclosed in this example is the complex bis(2-(4′,6′-difluoro-5′-cyanophenyl)pyrimidine-N,C 2 ') (acetylacetonate) iridium, its structural formula is as follows:

[0058]

[0059] It is prepared by the following steps:

[0060] (1) Synthesis of 2-(2′,4′-difluoro-3′-cyanophenyl)pyrimidine

[0061] The synthetic reaction formula of 2-(2',4'-difluoro-3'-cyanophenyl)pyrimidine is as follows:

[0062]

[0063] The specific steps are: under nitrogen atmosphere, 1.59g (10mmol) 2-bromopyrimidine, 2.20g (12mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.58g (0.5mmol) tetrakis (triphenylphosphine) Palladium was dissolved in 40ml of toluene, and then 20ml of potassium carbonate solution containing 2.76g (20mmol) was added dropwise to the reaction system. Heated and stirred at 100°C for 6h. After the reaction solution was cooled to room temperature, it was extracted with dichloromethane, separated, washed with water until ne...

Embodiment 2

[0077] The organic electroluminescent material disclosed in this example is the complex bis(2-(4′,6′-difluoro-5′-cyanophenyl)-5-methylpyrimidine-N,C 2 ') (acetylacetonate) iridium, its structural formula is as follows:

[0078]

[0079] It is prepared by the following steps:

[0080] (1) Synthesis of 2-(2′,4′-difluoro-3′-cyanophenyl)-5-methylpyrimidine

[0081] The reaction formula for the synthesis of 2-(2′,4′-difluoro-3′-cyanophenyl)-5-methylpyrimidine is as follows:

[0082]

[0083] The specific steps are: under nitrogen atmosphere, 1.73g (10mmol) 2-bromo-5-methylpyrimidine, 1.83g (10mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.28g (0.4mmol) Chlorobis(triphenylphosphine)palladium was dissolved in 50ml of DMF, and then 25ml of sodium carbonate solution containing 3.18g (30mmol) was added dropwise to the reaction system. Stir the reaction under heating to 90°C for 8 hours. After the reaction solution was cooled to room temperature, it was extracted with dichlor...

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

PropertyMeasurementUnit
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
thicknessaaaaaaaaaa
Login to View More

Abstract

The invention provides an organic electroluminescent material, a preparation method of the organic electroluminescent material and an organic electroluminescent device. The organic electroluminescent material has a general formula (P) as shown in the specification, wherein R1 is hydrogen atom, C1-20 linear alkyl, C1-20 branched alkyl, C1-20 linear alkoxy or C1-20 branched alkoxy. According to the organic electroluminescent material, 2-(2',4'-difluoro-3'-cyanophenyl) pyrimidine serving as a cyclometalated ligand and acetylacetone serving as an auxiliary ligand are adopted to synthesize a blue-light organic electroluminescent material iridium complex, and the illuminating color of the material is adjusted through chemical modification performed by introducing alkyl chain on the pyrimidine ring of the cyclometalated ligand, so that phosphorescence emission having blue emission wavelength and high luminescence efficiency can be obtained.

Description

technical field [0001] The invention relates to the field of phosphorescent materials, in particular to an organic electroluminescent material. The invention also relates to the preparation method of the organic electroluminescent material and its application in organic electroluminescent devices. Background technique [0002] Organic electroluminescence refers to a luminescence phenomenon in which organic materials directly convert electrical energy into light energy under the action of an electric field. In the early days, the research on organic electroluminescence was stagnant because of the high driving voltage and low luminous efficiency of organic electroluminescent devices. Until 1987, people such as Tang of American Kodak Company invented 8-hydroxyquinoline aluminum (Alq 3 ) is a light-emitting material, and a uniform and dense high-quality thin film is made with aromatic diamines, and an organic electroluminescent device with low operating voltage, high brightnes...

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 Applications(China)
IPC IPC(8): C09K11/06C07F15/00H01L51/54
Inventor 周明杰王平张娟娟冯小明
Owner OCEANS KING LIGHTING SCI&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