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

Azobenzene polymer and its preparation method and application

A technology of azobenzene and polymers, applied in the field of supramolecular chiral immobilization, which can solve the problems of limited types of chiral polymers, high price, and constraints on the development of chiral polymers

Active Publication Date: 2022-02-25
SUZHOU UNIV
View PDF2 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, most of the chiral polymers obtained directly through organic synthesis use expensive chiral reagents, and the types of chiral polymers synthesized are also very limited, which greatly restricts the development of chiral polymers.

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
  • Azobenzene polymer and its preparation method and application
  • Azobenzene polymer and its preparation method and application
  • Azobenzene polymer and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0106] 1) Synthesis of achiral methoxyazobenzene monomer

[0107] The raw material methoxyaniline (12.32 g, 0.1 mol) and concentrated hydrochloric acid were added to deionized aqueous solution (80 mL), magnetically stirred in an ice-salt bath for 0.5 h, and then 30 mL NaNO 2 (7 g, 0.1 mol / L) aqueous solution, after the dropwise addition, the reaction was continued for 0.5 h in an ice-salt bath to obtain a diazonium salt solution, and the system was red.

[0108] Phenol (16 g, 0.15 mol), NaOH (8 g, 0.2 mol), NaHCO 3 (8.4 g, 0.1 mol) was dissolved in 50 mL of deionized water, under ice-salt bath conditions (control temperature 0-5 °C), mechanically stirred, and then the previously obtained diazonium salt solution of p-methoxyaniline was added dropwise to the above In the phenol solution, the ice-salt bath condition still needs to be maintained at this time, and the solution gradually changes from colorless to yellow, and finally turns into brownish yellow. After the dropwise a...

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 discloses an azobenzene polymer and its preparation method and application; the azobenzene polymer is prepared from monomers Az and AzOH, a RAFT reagent and an initiator; the azobenzene polymer is prepared into a film; and then passed through a chiral reagent Induction, the chiral azobenzene polymer film was obtained. The design of the present invention first synthesizes azobenzene random copolymers with hydroxyl groups at the end of the side chain through a series of organic synthesis reactions and RAFT polymerization, and uses NMR, GPC, DSC, POM and XRD to evaluate the molecular weight and liquid crystal properties of the polymer. A detailed investigation is carried out; the next step is to make a polymer film by spin coating. The polymer film prepared by the invention can be chiralally induced by chiral limonene vapor to obtain an optically active polymer film and can be further cross-linked to obtain a cross-linked film.

Description

technical field [0001] The invention belongs to the technical field of supramolecular chiral immobilization, and relates to an achiral side chain type azobenzene polymer, which can be induced and cross-linked by chirality to obtain a chiral azobenzene polymer cross-linked film. Background technique [0002] In the prior art, supramolecular chiral self-assembly is based on weak supramolecular forces such as hydrogen bonds, π-π stacking, acid-base interactions, metal-coordination interactions, and host-guest interactions. The element is a chiral small molecule or polymer, and its driving force is a reversible non-covalent weak interaction. This non-covalent weak interaction is less stable due to its weaker energy (generally less than 10 KJ / mol). , the chiral supramolecular ordered structure is easily affected by external stimuli (light, heat, pH, solvents, metal ions, etc.) and responds to a certain extent, and even dissociates irreversibly, thereby destroying the formed chira...

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): C08F220/36C08J5/18C08L33/14
CPCC08F220/36C08J5/18C08F2438/03C08J2333/14
Inventor 张伟钱伊琳缪腾飞程笑笑庄雅灵陆航朱筱妍熊联虎周年琛朱秀林
Owner SUZHOU UNIV
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