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

Derivative containing triazine structure and preparation method thereof as well as organic electroluminescence device

A derivative, triazine technology, applied in the field of organic photoelectric materials, can solve the problems of poor thermal stability, short life of organic light-emitting devices, and reduce the use of materials, and achieve high thermal stability, simple preparation method, and low driving voltage. Effect

Inactive Publication Date: 2018-02-27
CHANGCHUN HYPERIONS TECH CO LTD
View PDF0 Cites 4 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the thermal stability of such materials is poor, resulting in a short lifetime of organic light-emitting devices using phosphorescent materials, thus reducing the use of such 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
  • Derivative containing triazine structure and preparation method thereof as well as organic electroluminescence device
  • Derivative containing triazine structure and preparation method thereof as well as organic electroluminescence device
  • Derivative containing triazine structure and preparation method thereof as well as organic electroluminescence device

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0051] Preparation of compound 1

[0052]

[0053] Preparation of Intermediates 1-3

[0054] Under the protection of nitrogen, 1-1 (16.01g, 100.08mmol), 1-2 (21.02g, 100.08mmol), potassium carbonate (1.24g, 9.00mmol), and toluene 200mL were added into a 2L reactor and stirred.

[0055] The temperature in the reactor was raised to 70°C, and Pd(PPh 3 ) 4 (1.04g, 0.90mmol), stirred with 100mL distilled water, stirred and refluxed for 11h, fully reacted.

[0056] After adding 70mL of distilled water to terminate the reaction, filter under reduced pressure, wash the solid with distilled water, and then use acetone, toluene, THF to recrystallize, after the solid is obtained, sublimate, and toluene recrystallize to obtain 23.23g of intermediate 1-3, with a yield of 80.44 %.

[0057] Preparation of Intermediate 1-3(1)

[0058] Under the condition of avoiding light, add 1-3 (24.53g, 100.00mmol), NBS (29.44g, 120.00mmol) and 200mL of carbon tetrachloride to the 2L reaction kettle ...

Embodiment 2

[0066] Preparation of compound 7

[0067]

[0068] R in Example 1 1 , R 2 , R 5 The group is replaced by R as indicated above 1 , R 2 , R 5 Group, other steps are the same as in Example 1 to obtain compound 7. Mass Spectrum m / z: 801.31 (calculated: 801.32). Theoretical element content (%)C 60 h 39 N 3 : C, 89.86; H, 4.90; N, 5.24. Measured element content (%): C, 89.87; H, 4.89; N, 5.23.

Embodiment 3

[0070] Preparation of compound TM12

[0071]

[0072] R in Example 1 1 , R 2 , R 3 , R 4 , R 5 The group is replaced by R as indicated above 1 , R 2 , R 3 , R 4 , R 5 Group, other steps are the same as in Example 1 to obtain compound 7. Mass Spectrum m / z: 953.38 (calculated: 953.36). Theoretical element content (%)C 72 h 47 N 3 : C, 90.63; H, 4.97; N, 4.40. Measured element content (%): C, 90.62; H, 4.96; N, 4.41.

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
Login to View More

Abstract

The invention provides a derivative containing a triazine structure and a preparation method thereof as well as an organic electroluminescence device, and belongs to the technical field of organic photoelectric materials. The compound has a structure as shown in formula (I). The derivative containing the triazine structure provided by the invention is high in thermal stability and is high in glasstransition temperature; the preparation method is simple, raw materials are easily available, and products are prepared through conventional coupling reaction, so that industrial development needs can be met; and the device manufactured from the derivative containing the triazine structure has the advantages of low drive voltage and high light emitting efficiency, and is an organic light emittingmaterial with excellent performances.

Description

technical field [0001] The invention relates to the technical field of organic photoelectric materials, in particular to a derivative containing a triazine structure, a preparation method thereof, and an organic electroluminescent device. 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 , wi...

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): C07D251/24C07D401/10C07D401/14C07D409/14C07D405/10C07D405/14C07D403/10C07D403/14C07D401/04C09K11/06H01L51/50H01L51/54
CPCC09K11/06C07D251/24C07D401/04C07D401/10C07D401/14C07D403/10C07D403/14C07D405/10C07D405/14C07D409/14C09K2211/1007C09K2211/1011C09K2211/1029C09K2211/1088C09K2211/1092C09K2211/1059H10K85/626H10K85/654H10K85/6572H10K85/6576H10K85/6574H10K50/12H10K2102/00H10K2102/301
Inventor 张弘蔡辉
Owner CHANGCHUN HYPERIONS 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