Multifunctional polyurethane derivative containing triarylamine structure and tetrastyrene group as well as preparation method and application thereof.

A technology of polyurethane derivatives and tetraphenylethylene, applied in the preparation of urea derivatives, preparation of organic compounds, chemical instruments and methods, etc., can solve the problem of few functional types, and achieve accelerated processing and application, high temperature resistance, and high heat The effect of stability

Active Publication Date: 2019-02-15
HEILONGJIANG UNIV
View PDF10 Cites 7 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The present invention aims to solve the problem that the existing multifunctional materials have few types of functions, and provides multifunctional polyurethane derivatives containing triarylamine structures and tetraphenylethylene groups, as well as their preparation methods and applications

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
  • Multifunctional polyurethane derivative containing triarylamine structure and tetrastyrene group as well as preparation method and application thereof.
  • Multifunctional polyurethane derivative containing triarylamine structure and tetrastyrene group as well as preparation method and application thereof.
  • Multifunctional polyurethane derivative containing triarylamine structure and tetrastyrene group as well as preparation method and application thereof.

Examples

Experimental program
Comparison scheme
Effect test

specific Embodiment approach 1

[0044] Specific embodiment 1: In this embodiment, the multifunctional polyurethane derivative containing triarylamine structure and tetraphenylethylene group is N, N'-bis(4-aminophenyl)-N, N'-diphenyl-1 , Multifunctional polyurethane derivatives of 4-phenylenediamine and tetraphenylethylene groups or N, N'-bis(4-aminophenyl)-N, N'-diphenyl-1,4-biphenyl Multifunctional polyurethane derivatives of amine groups and tetraphenylethylene groups;

[0045] The structural formula of the multifunctional polyurethane derivative containing N, N'-bis(4-aminophenyl)-N, N'-diphenyl-1,4-phenylenediamine and tetraphenylethylene group is as follows:

[0046] In the formula, n is an integer of 3 to 10;

[0047] The structural formula of the multifunctional polyurethane derivative containing N, N'-bis(4-aminophenyl)-N, N'-diphenyl-1,4-biphenylenediamine group and tetraphenylethylene group is as follows:

[0048] ,

[0049] In the formula, n is an integer of 3-10.

[0050] In this embodime...

specific Embodiment approach 2

[0053] Specific implementation mode two: the method of the multifunctional polyurethane derivative containing triarylamine structure and tetraphenylethylene group in this implementation mode is as follows: 1. 1,2-bis(4-hydroxyphenyl)-1,2-diphenyl Ethylene, 4,4'-diphenylmethane diisocyanate and solvent N,N-dimethylacetamide (DMAC) are mixed, stirred and refluxed at room temperature for 5-15 hours, and the stirring speed is 800r / min~900r / min, to obtain Precursor; 2. It will contain N, N'-bis(4-aminophenyl)-N,N'-diphenyl-1,4-phenylenediamine or N,N'-bis(4-aminophenyl) )-N,N'-diphenyl-1,4-biphenyldiamine diamine monomer is added to the precursor prepared in step 1, the temperature is raised to 70-120°C, stirred and refluxed for 5-15h, cooled and poured into in methanol, and then filtered, and the obtained solid phase is vacuum-dried to obtain a multifunctional polyurethane derivative containing a triarylamine structure and a tetraphenylethylene group;

[0054] Which contains N,N'...

specific Embodiment approach 3

[0056] Specific embodiment 3: The difference between this embodiment and specific embodiment 2 is that it contains N,N'-bis(4-aminophenyl)-N,N'-diphenyl-1,4-phenylenediamine or N , N'-bis(4-aminophenyl)-N,N'-diphenyl-1,4-biphenylenediamine diamine monomer, 1,2-bis(4-hydroxyphenyl)-1 , 2-diphenylethylene, 4,4'-diphenylmethane diisocyanate molar ratio: 2:1:2. Others are the same as in the second embodiment.

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 relates to a multifunctional polyurethane derivative containing a triarylamine structure and a tetrastyrene group as well as a preparation method and the application thereof. The invention aims to solve the problem that conventional multifunctional materials have few function types. The multifunctional polyurethane derivative provided by the invention is prepared by firstly synthesizing two monomers and 1,2-bis(4-hydroxyphenyl)-1,2-diphenylethylene containing a hydroxyl structure and simultaneously introducing 4,4'-diphenylmethane diisocyanate by means of copolymerization. The multifunctional polyurethane derivative has electrochromism and fluorescence sensing hole transport functions, can be used as an automotive rearview mirror material and a display material and can be used for preparing explosive detection and memory performance devices. The multifunctional polyurethane derivative provided by the invention is applied to the field of multifunctional materials.

Description

technical field [0001] The invention relates to a multifunctional polyurethane derivative containing a triarylamine structure and a tetraphenylethylene group, a preparation method and application thereof. Background technique [0002] Polyurethane (PU) has many desirable properties, such as better flexibility, greater tensile strength, higher hardness, more resistance to chemical solvents and temperature conditions, higher abrasion resistance, higher oil resistance and Longer fatigue life. Polyurethanes are also potential candidates for membrane preparation due to their good mechanical and chemical properties. Although polyurethane has excellent comprehensive properties, traditional PU has some disadvantages, such as high processing difficulty and poor solubility, which greatly limit the industrial application of polyurethane materials. Therefore, in recent years, more and more researchers have begun to pay attention to the research on the preparation and modification of p...

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): C07C275/40C07C273/18C09K11/06C09K9/02H01L51/54G01N21/64
CPCG01N21/6428G01N21/643C09K9/02C09K11/06C07C273/18C07C275/40C09K2211/1014C09K2211/1007G01N2021/6432H10K85/631
Inventor 牛海军张旭路庆义陈烨王岩
Owner HEILONGJIANG 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
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap