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

Organic electro-phosphorescent material and preparation method thereof, and organic electroluminescent device

A phosphorescent material, electromechanical technology, applied in the field of phosphorescent materials, can solve the problems of the luminous color purity of blue phosphorescent materials, the efficiency attenuation bottleneck of luminous efficiency devices, etc.

Inactive Publication Date: 2015-02-11
OCEANS KING LIGHTING SCI&TECH CO LTD +2
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] People's research on iridium metal complexes of organic electrophosphorescent materials has been in-depth, but there are bottlenecks in the luminous color purity, luminous efficiency and device efficiency decay 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 electro-phosphorescent material and preparation method thereof, and organic electroluminescent device
  • Organic electro-phosphorescent material and preparation method thereof, and organic electroluminescent device
  • Organic electro-phosphorescent material and preparation method thereof, and organic electroluminescent device

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0038] The preparation process of the organic electrophosphorescent material (P) of the present invention is roughly divided into the following steps:

[0039] (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:

[0040] Compound E is Compound C is Among them, R is C 1 ~C 20 straight-chain or branched-chain alkoxy groups.

[0041] (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:

[0042]

[0043] (3) Compound A prepared in step (2) is used as the main structure of the ring metal ligand, and 3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole (ie Compound B) is used as an auxiliary ligand source to react com...

Embodiment 1

[0049] The organic electrophosphorescent material (P) disclosed in this example is the complex bis(2-(4',6'-difluoro-5'-cyanophenyl)-5-methoxypyrimidine-N,C 2' )(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium, its structural formula is as follows:

[0050]

[0051] It is prepared by the following steps:

[0052] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-5-methoxypyrimidine

[0053] The synthetic reaction formula of 2-(2',4'-difluoro-3'-cyanophenyl)-5-methoxypyrimidine is as follows:

[0054]

[0055] The specific steps are: under nitrogen protection, mix 1.89g (10mmol) 2-bromo-5-methoxypyrimidine, 2.20g (12mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.58g (0.5mmol ) Tetrakis(triphenylphosphine)palladium was dissolved in 35mL of toluene solution, and then 15mL of potassium carbonate solution containing 2.76g (20mmol) was added dropwise to the reaction system. Heat to 100°C and stir the reaction for 6h. After the reaction solution was cooled to ...

Embodiment 2

[0070] The organic electrophosphorescent material disclosed in this example is the complex bis(2-(4',6'-difluoro-5'-cyanophenyl)-4-hexyloxypyrimidine-N,C 2 ')(3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole) iridium, its structural formula is as follows:

[0071]

[0072] It is prepared by the following steps:

[0073] (1) Synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-4-hexyloxypyrimidine

[0074] The reaction formula for the synthesis of 2-(2',4'-difluoro-3'-cyanophenyl)-4-hexyloxypyrimidine is as follows:

[0075]

[0076] The specific steps are: under the protection of nitrogen, mix 2.59g (10mmol) 2-bromo-4-hexyloxypyrimidine, 1.83g (10mmol) 2,4-difluoro-3-cyanophenylboronic acid and 0.21g (0.3mmol ) dichlorobis(triphenylphosphine)palladium was dissolved in 40mL of N,N-dimethylformamide solution (ie DMF), and then 20mL of sodium carbonate solution containing 1.06g (10mmol) was added dropwise to the reaction system. Stir the reaction under heating to 80°C for 10h. ...

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
Sheet resistanceaaaaaaaaaa
Thicknessaaaaaaaaaa
Thicknessaaaaaaaaaa
Login to View More

Abstract

The invention provides an organic electro-phosphorescent material and a preparation method thereof, and an organic electroluminescent device. The invention provides the organic electro-phosphorescent material with the general formula (P), wherein R is C1-C20 straight-chain or branched-chain alkoxy. The organic electro-phosphorescent material (P) is an iridium metal complex synthesized with 2-(2',4'-difluoro-3'-cyanophenyl)pyrimidine as a cyclo-metal ligand and with 3-trifluoromethyl-5-(2'-pyridyl)-1,2,4-triazole as a subsidiary ligand. According to the organic electro-phosphorescent material, the adjustment upon material luminescent colors is realized through introducing alkoxy chain chemical modifications to the pyrimidine ring of the cyclo-metal ligand, such that high-luminous-efficiency blue phosphorescent emission is obtained.

Description

technical field [0001] The invention relates to the field of phosphorescent materials, in particular to an organic electrophosphorescent 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 phosphorescent material, and a uniform and dense high-quality thin film is made with aromatic diamine, and an organic electroluminescent device with low operating voltage, high brightn...

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
IPC IPC(8): C09K11/06C07F15/00H01L51/54
Inventor 周明杰王平张娟娟黄辉
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