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

A kind of polyarylsulfone polymer containing reduced phenazine structure and preparation method thereof

A polyarylsulfone and polymer technology is applied in the field of polyarylsulfone polymers containing a reduced phenolazine structure and the preparation thereof, and can solve the problems of difficult photoelectric activity, electrochemical stability, thermal stability, solubility and the like, Achieve the effect of easy processing into film, improved solubility, and broad development prospects

Active Publication Date: 2021-11-16
JILIN UNIV
View PDF0 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At the same time, reduced phenazine is a common compound with excellent photoelectric function. Because of its good photoelectric activity, the polymer photoelectric functional material constructed by this has been widely used in hole transport, electrochromism, electroluminescence, etc. , information storage, solar cells and other optoelectronic fields, but it is difficult for polymer optoelectronic functional materials constructed with reduced phenazine compounds to simultaneously take into account good optoelectronic activity, electrochemical stability, thermal stability and solubility

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
  • A kind of polyarylsulfone polymer containing reduced phenazine structure and preparation method thereof
  • A kind of polyarylsulfone polymer containing reduced phenazine structure and preparation method thereof
  • A kind of polyarylsulfone polymer containing reduced phenazine structure and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0044] The preparation method of the polyarylsulfone polymer containing the reduced phenazine structure of the present invention comprises the following steps:

[0045]Put the difluoro monomer containing sulfone group, bisphenol A, reduced phenazine, catalyst potassium carbonate, solvent sulfolane or N-methylpyrrolidone, and water-carrying agent toluene into a three-stage tank equipped with nitrogen port, oil-water separator, and mechanical stirring. In a nitrogen atmosphere, stir and heat to 140-150°C to reflux the toluene for 3 hours, then use an oil-water separator to release toluene and water after fully carrying water, then raise the temperature to 200-220°C and stir for 3-8 hours to obtain To reduce the phenazine polyarylsulfone polymer, the reaction formula is (i):

[0046]

[0047] In the formula, n is the degree of polymerization, 0<m≤1 represents the copolymerization ratio, and Ar is one of the formulas (a) to (d):

[0048]

[0049] In formula (c), X is select...

Embodiment 1

[0056] Embodiment 1: the preparation of polymer P1

[0057] Put reduced phenazine (3.685g, 20mmol), 4,4'-difluorodiphenyl sulfone (5.334g, 20mmol), catalyst potassium carbonate (5.521g, 40mmol), 26mL NMP, 20mL water-carrying agent toluene into a nitrogen ventilator In a 100mL three-necked flask with an oil-water separator and a mechanical stirrer, stir and heat in a nitrogen atmosphere until the toluene refluxes for 3 hours. After fully carrying water, release toluene and water with an oil-water separator. Then raise the temperature to 200°C and stir the reaction for 8h. After the reaction was completed, the solution was poured into 800 mL of cold water with stirring. Use a tissue pulverizer to grind it into powder, filter under reduced pressure, collect the solid precipitate, and then boil and wash with hot water (5 times, 800 mL each) and ethanol (3 times, 300 mL each), filter and collect, and put it in an oven Dry at 80°C for 10 hours. An orange-yellow polymer powder (7....

Embodiment 2

[0061] Embodiment 2: the preparation of polymer P1-50%

[0062] Reduced phenazine (1.842g, 10mmol), 4,4'-difluorodiphenylsulfone (5.334g, 20mmol), bisphenol A (2.284g, 10mmol), catalyst potassium carbonate (5.521g, 40mmol), 34mL sulfolane Put 20mL of toluene with water agent into a 100mL three-necked flask equipped with a nitrogen port, an oil-water separator, and a mechanical stirrer, stir and heat in a nitrogen atmosphere until the toluene refluxes for 3 hours, and release toluene and water with an oil-water separator after fully carrying water . Then raise the temperature to 220°C and stir the reaction for 4h. After the reaction was completed, the solution was poured into 800 mL of cold water with stirring. Use a tissue pulverizer to grind it into powder, filter under reduced pressure, collect the solid precipitate, and then boil and wash with hot water (5 times, 800 mL each) and ethanol (3 times, 300 mL each), filter and collect, and put it in an oven Dry at 80°C for 10...

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
glass transition temperatureaaaaaaaaaa
Login to View More

Abstract

The invention relates to a polyarylsulfone polymer containing a reduced phenazine structure and a preparation method thereof. The polymer comprises a structural segment of the following formula (I): in the formula (I), n is the degree of polymerization; m is the degree of copolymerization Ratio, 0<m≤1; Ar is one of the following formulas (a) to (d): in formula (c), X is an integer 1, 2 or 3, and in formula (d), R is 1 , 4-position disubstituted naphthalene, 1,5-position di-substituted naphthalene, 2,6-position di-substituted naphthalene or 2,7-position di-substituted naphthalene. The polymer not only has good photoelectric activity, but also has good thermal stability. It is foreseeable that this kind of material will have great potential in the field of optoelectronics, especially electrochromism, information storage, carbon nanotube coating, thermal response delayed fluorescence, etc. Broad development prospects and huge application potential.

Description

technical field [0001] The invention belongs to the field of polymer materials, in particular to a polyarylsulfone polymer containing a reduced phenazine structure and a preparation method thereof. Background technique [0002] The widespread application of information system transmission and display technology marks that mankind has opened the door to the "information age" in the early 21st century. Since then, human life has undergone revolutionary changes and has benefited a lot from it. The rapid development of information industry technology requires the continuous improvement of technology and the development and innovation of theoretical knowledge. The development of new materials can not only provide a basis for theoretical research, but also better meet the requirements of production technology and promote the improvement of production technology. Therefore, The development of new functional materials has become the key to the development of this field, and the deve...

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 Patents(China)
IPC IPC(8): C08G75/20C08G75/23
CPCC08G75/20C08G75/23
Inventor 陈峥韩韫韬邢真罗浩李苏
Owner JILIN UNIV
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