Aromatic amine derivative, and preparation method, use and organic electroluminescent device thereof

A technology of aromatic amine derivatives and triarylamine, which is applied in the field of organic electroluminescence, can solve the problems of low lifetime of organic electroluminescent devices, unfavorable preparation of organic electroluminescent devices, and insufficient stability of redox repeatability, etc., and achieves good results. Film-forming properties, large molecular weight, and good service life

Active Publication Date: 2014-08-20
BOE TECH GRP CO LTD
View PDF1 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

For example, the triaryl amine substances invented during the development of photocopying technology in the early days have high carrier mobility, but the glass transition temperature is low and the film-forming properties are not good, which is not conducive to the preparation of organic electroluminescent devices.
Another example is the pentacene compound, which shows high carrier mobility, but this kind of substance has a high HOMO energy level, and its redox repeatability is not stable enough, that is, the life of the organic electroluminescent device is not high.

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
  • Aromatic amine derivative, and preparation method, use and organic electroluminescent device thereof
  • Aromatic amine derivative, and preparation method, use and organic electroluminescent device thereof
  • Aromatic amine derivative, and preparation method, use and organic electroluminescent device thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0058] Corresponding to the above-mentioned aromatic amine derivatives, the present invention also provides its preparation method, such as figure 1 shown, including:

[0059] 101. Add 5,11-disubstituted thiophene[3',2':5,6]indole[3,2-b]thiophene[3,2-f]indole with structural formula II into the reaction vessel , a triarylamine with a structural formula III, a triarylamine with a structural formula IV, a catalyst, a base, a phase transfer catalyst and a solvent and mix them.

[0060]

[0061] X and Y in the triarylamines III and IV each independently represent a halogen, such as F, Cl, Br, I and the like.

[0062] The 5,11-disubstituted thiophene[3',2':5,6]indole[3,2-b]thiophene[3,2-f]indole in this example can be obtained through literature Chem.Commun ., 2012, 48, 12225-12227 records the method to prepare, and will not repeat them here.

[0063] The triarylamines with the structural formula III and the triarylamines with the structural formula IV can be obtained through...

Embodiment 1

[0181] ITO / I-1(40nm) / CBP:6%(Firpic30nm) / Bphen(25nm) / LiF(0.5nm) / Al(100nm)

Embodiment 2

[0183] ITO / I-9(40nm) / CBP:6%Firpic(30nm) / Bphen(25nm) / LiF(0.5nm) / Al(100nm)

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 embodiment of the invention provides an aromatic amine derivative, and a preparation method, a use and an organic electroluminescent device thereof, and relates to the technical field of organic electroluminescence. The aromatic amine derivative is invented to improve the film forming ability and the redox repetition stability. The structural general formula I of the aromatic amine derivative is shown in the specification; and in the formula I, R1, R2, R3 and R4 respectively independently represent hydrogen, substituted or unsubstituted C1-C40 alkyl groups, substituted or unsubstituted C1-C40 alkyloxy groups, substituted or unsubstituted C3-C40 cycloalkyl groups, substituted or unsubstituted C6-C50 aryl groups, substituted or unsubstituted C3-C50 heteroaryl groups containing one or two selected from hetero atoms of N, O or S, or substituted or unsubstituted C10-C40 fused aryl groups, m, n, p and q respectively independently represent 0, 1, 2, 3, 4 or 5, and substituent can be one or more groups selected from halogens, C1-C10 alkyl groups, C1-C10 alkyloxy groups, C3-C20 cycloalkyl groups, C6-C20 aryl groups or C4-C20 heteroaryl groups. The aromatic amine derivative can be used in the organic electroluminescent device.

Description

technical field [0001] The invention relates to the technical field of organic electroluminescence, in particular to an aromatic amine derivative, its preparation method, application, and an organic electroluminescence device. Background technique [0002] Organic light emitting diode (OrganiC Light Emitting Diode, OLED) refers to the technology that organic semiconductor materials emit light under the action of electric field, because of its active light emission, all solid state, low driving voltage, high efficiency, fast response speed, wide viewing angle and simple manufacturing process And it can realize many advantages such as large area and flexible display, and has broad application prospects in flat panel display and lighting. [0003] Generally known OLED device structures include a hole transport layer, a light emitting layer, an electron transport layer and an electron injection layer. In order to improve the luminous efficiency and service life of OLED devices,...

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): C07D495/22H01L51/54
CPCC07D495/22H10K85/657H05B33/22C07D519/00H10K85/655H10K85/636H10K85/626H10K85/633H10K85/654H10K85/342H10K50/15H10K85/622H10K85/6572C09K11/06H05B33/14
Inventor 刘飞徐晓光高雪
Owner BOE TECH GRP CO LTD
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products