Check patentability & draft patents in minutes with Patsnap Eureka AI!

Triarylamine derivative and organic electroluminescence device thereof

A technology for electroluminescent devices and derivatives, which is applied in the fields of electro-solid devices, electrical components, luminescent materials, etc., can solve the problems of high cost, large power consumption, and small operating temperature range.

Inactive Publication Date: 2019-03-12
CHANGCHUN HYPERIONS TECH CO LTD
View PDF0 Cites 8 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0002] With the progress of the information industry, traditional displays can no longer meet people's requirements, such as: cathode ray tube (CRT) displays have large volume and high driving voltage; liquid crystal displays (liquid crystal display, LCD) have low brightness and narrow viewing angles. , The operating temperature range is small; plasma display panel (PDP) is expensive, the resolution is not high, and the power consumption is large

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
  • Triarylamine derivative and organic electroluminescence device thereof
  • Triarylamine derivative and organic electroluminescence device thereof
  • Triarylamine derivative and organic electroluminescence device thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Preparation of Compound 1

[0049]

[0050] Preparation of Compound 1

[0051] To 1-1 (43.52 g, 100 mmol) and a solution of 1-2 (32.10 g, 100 mmol) in degassed toluene (500 mL), and the mixture was heated at reflux for 2 hours. The reaction mixture was cooled to room temperature, diluted with toluene and filtered through celite. The filtrate was diluted with water and extracted with toluene, and the combined organic phases were evaporated under vacuum. The residue was filtered through silica gel (heptane / dichloromethane) and crystallized from isopropanol to give compound 1 (54.51 g, yield 81.32%). Mass Spectrum m / z: 676.29 (calculated: 676.31). Theoretical element content (%)C 51 h 36 N 2 : C, 90.50; H, 5.36; N, 4.14 Measured element content (%): C, 90.51; H, 5.35; N, 4.15. It was confirmed above that the obtained product was the target product 1.

Embodiment 2

[0053] Preparation of compound 16

[0054]

[0055] Preparation of compound 16

[0056] Compound 16 was obtained by replacing 1-1 in Example 1 with 16-1 shown above, and 1-2 with 16-2 shown above. Mass Spectrum m / z: 777.31 (calculated: 777.33). Theoretical element content (%)C 58 h 39 N 3 : C, 89.55; H, 5.05; N, 5.40 The measured element content (%): C, 89.53; H, 5.06; N, 5.41. It was confirmed above that the obtained product was the target product 16.

Embodiment 3

[0058] Preparation of compound 27

[0059]

[0060] Preparation of compound 27

[0061] Compound 27 is obtained by replacing 1-1 in Example 1 with 27-1 shown above, and 1-2 with 27-2 shown above. Mass Spectrum m / z: 776.32 (calculated: 776.35). Theoretical element content (%)C 59 h 40 N 2 : C, 91.21; H, 5.19; N, 3.61 The measured element content (%): C, 91.22; H, 5.18; N, 3.62. It was confirmed above that the obtained product was the target product 27.

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 a triarylamine derivative and an organic electroluminescence device thereof, and belongs to the technical field of organic photoelectric materials. The derivative has a structure as shown in a formula (I), a triarylamine structure is introduced to one end of the derivative, and the transmission property of a current carrier is increased. At a specific position, structurally,the obtained materials have high glass-transition temperature and melting points by introducing fluorenyl, joule heat is generated between an organic layer and a metal electrode, and the derivative has high heat resistance and high durability at high temperature and can prevent crystallization. A synthetic method is simple and easy to operate, and the organic electroluminescence device prepared from the triarylamine derivative has good electroluminescence efficiency and long service life.

Description

technical field [0001] The invention relates to the technical field of organic photoelectric materials, in particular to a triarylamine derivative and an organic electroluminescence device thereof. Background technique [0002] With the progress of the information industry, traditional displays can no longer meet people's requirements, such as: cathode ray tube (CRT) displays have large volume and high driving voltage; liquid crystal displays (liquid crystal display, LCD) have low brightness and narrow viewing angles. , The operating temperature range is small; the plasma display panel (PDP) is expensive, the resolution is not high, and the power consumption is large. [0003] Organic light-emitting diodes (organic light-emitting diodes, OLEDs) as a new display technology has unparalleled advantages in various performances of existing display technologies, such as full solid state, self-luminous, high brightness, high resolution , wide viewing angle (above 170 degrees), fas...

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): C07C211/61C07D209/80C07D209/86C07D209/88C07D307/77C07D307/91C07D333/50C07D333/76C07D401/04C09K11/06H01L51/54
CPCC09K11/06C07C211/61C07D209/80C07D209/86C07D209/88C07D307/77C07D307/91C07D333/50C07D333/76C07D401/04C07C2603/40C07C2603/18C09K2211/1011C09K2211/1029C09K2211/1088C09K2211/1092H10K85/622H10K85/624H10K85/636H10K85/626H10K85/633H10K85/615H10K85/6576H10K85/6574H10K85/6572
Inventor 张弘蔡辉
Owner CHANGCHUN HYPERIONS TECH CO LTD
Features
  • R&D
  • Intellectual Property
  • Life Sciences
  • Materials
  • Tech Scout
Why Patsnap Eureka
  • Unparalleled Data Quality
  • Higher Quality Content
  • 60% Fewer Hallucinations
Social media
Patsnap Eureka Blog
Learn More