Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Method for synthesizing pyrazoline derivatives capable of irradiating yellow green light

A synthesis method and pyrazoline technology are applied in the field of synthesis of pyrazoline derivatives, and can solve the problems of limiting the development and expansibility of pyrazoline compounds, low product purity, low yield and the like

Inactive Publication Date: 2008-08-13
TAIYUAN UNIV OF TECH
View PDF0 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] The thermal stability of pyrazoline compounds is relatively poor, which also limits its scope of application in organic electroluminescent devices. In the prior art, the synthesis and preparation methods of pyrazoline compounds also have many disadvantages and deficiencies. For example, crystallinity problems, thermal stability problems, low product purity and low yield also limit the further development and extended application of pyrazoline compounds

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
  • Method for synthesizing pyrazoline derivatives capable of irradiating yellow green light
  • Method for synthesizing pyrazoline derivatives capable of irradiating yellow green light
  • Method for synthesizing pyrazoline derivatives capable of irradiating yellow green light

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0158] The present invention will be further described below in conjunction with accompanying drawing:

[0159] As shown in Figure 1, it is a flow chart of the preparation process, which must be carried out in strict accordance with the process parameters and operated in sequence.

[0160] The raw materials of chemical substances required in the preparation of synthetic products are determined within pre-set value ranges in grams, milliliters, centimeters 3 , minute is the unit of measurement, when it is produced industrially, it is measured in kilograms, liters, meters 3 , minute is the unit of measurement.

[0161] The chemical raw materials and auxiliary materials required for the preparation must be strictly selected and their purity controlled. Impurities must not intervene to prevent the formation of by-products and affect the purity and luminescence performance of the product.

[0162] Four-necked flasks, three-necked flasks, beakers, suction filtration flasks, chroma...

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

Disclosed is a synthesis method of pyrazoline derivatives emitting olivine light, in which the pyrazoline derivative, 1-phenyl-3-[4-(N-phenyl-1-naphthylamine)ethylene]-5-[4-(N-phenyl-1-naphthylamine)phenyl]-2-pyrazoline brown-green crystals are finally prepared through three-times intermediates, by selecting material, preparing sollution, chemical combination reaction, heating, mixing, water-circulation condensation, ice water washing, argon protection, column chromatography purification, recrystallization purification, vacuum filtering, evaporation and drying, the products are grain diamond-shaped, the color coordinate is that x=0.3257, y=0.5452, the maximal emission wavelength of photoluminescence spectrum is 523 nm and the full width at half maximum is 96 nm. The products have high purity, pure color, excellent irradiance performance, high irradiance intensity and high lighteness, the products are also capable of improving the stability, reliability and life time of organic electroluminescent devices, being used in the fields of advance electronic display and irradiance illumination technology, the method of the invention is strictness and reasonable.

Description

technical field [0001] The invention relates to a synthesis method of pyrazoline derivatives emitting yellow-green light, and belongs to the technical field of application, synthesis and preparation methods of organic electroluminescent materials. Background technique [0002] Organic electroluminescent materials - pyrazoline compounds have good hole transport function and high fluorescence quantum efficiency. Pyrazoline compounds have been used as blue light emitting materials and hole transport materials in organic electroluminescent devices It has been applied and is often used in technical fields such as organic light guides and electrostatic printing. [0003] The thermal stability of pyrazoline compounds is relatively poor, which also limits its scope of application in organic electroluminescent devices. In the prior art, the synthesis and preparation methods of pyrazoline compounds also have many disadvantages and deficiencies. For example, crystallinity problems, th...

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): C07D231/06C09K11/06
Inventor 许并社陈简王华周禾丰郝玉英陈柳青许慧侠贾虎生
Owner TAIYUAN UNIV OF TECH
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
Eureka Blog
Learn More
PatSnap group products