3D-crosslinked supramolecular polymer based on column [n] arene conjugated polymer as well as preparation method and application of 3D-crosslinked supramolecular polymer

A supramolecular polymer, conjugated polymer technology, applied in chemical instruments and methods, information-carrying cards, printing, etc., to achieve the effects of being conducive to energy transfer, good fatigue resistance, and good luminous performance

Active Publication Date: 2019-07-05
SOUTH CHINA UNIV OF TECH
View PDF5 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, there is no report on the realization of rewritable and encrypted writing by supramolecular host-guest complexation

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
  • 3D-crosslinked supramolecular polymer based on column [n] arene conjugated polymer as well as preparation method and application of 3D-crosslinked supramolecular polymer
  • 3D-crosslinked supramolecular polymer based on column [n] arene conjugated polymer as well as preparation method and application of 3D-crosslinked supramolecular polymer
  • 3D-crosslinked supramolecular polymer based on column [n] arene conjugated polymer as well as preparation method and application of 3D-crosslinked supramolecular polymer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] A linear conjugated polymer host H(R 1 is methoxy; n=5; A 1 For the synthesis of triazole), the synthetic route is as follows:

[0046]

[0047] Concrete synthetic steps are as follows:

[0048] (1) Synthesis of Compound 2:

[0049]

[0050] Compound 1 (1737.8mg, 2mmol), 4-aminophenylboronic acid pinacol ester (525.8mg, 2.4mmol), potassium carbonate (2764.2mg, 20mmol), Pd (pph 3 ) 4 (115,6mg, 0.1mmol) and H 2 O (10ml) was dispersed in 40ml THF. The mixture was degassed with nitrogen and stirred at 90 °C for 12 hours (stirrer rate range 500 rpm). The mixture was dried under reduced pressure (the pressure of reduced pressure was 0.09Map), and then purified by column chromatography (petroleum ether / dichloromethane / ethyl acetate: 10 / 2 / 1) to obtain compound 2 white powder (1310.1mg , 1.5mmol), yield 75%.

[0051] Compound 2 melting point data: M.p.152.2–153.0°C.

[0052] Compound 2 H NMR spectrum data: 1 H NMR (400MHz, CDCl 3 ,298K),δ(ppm):6.96(s,2H),6.82(d,...

Embodiment 2

[0065] The conjugated guest molecule G(R 2 Branched isooctyl; A 2 For the synthesis of thiophene ring), the synthetic route is as follows:

[0066]

[0067] Concrete synthetic steps are as follows:

[0068] Synthesis of conjugated guest molecule G:

[0069]

[0070] Compound 4 (1153.2mg, 1.5mmol), 5-azidovaleronitrile (744.6mg, 6mmol) and CuBr (21.5mg, 0.15mmol) were added to 20mL degassed THF, nitrogen protection. The mixture was stirred at room temperature (please stir at 500 rpm) for 12 hours, poured into brine (100 mL), and extracted with dichloromethane. The organic layer was dried under vacuum with a rotary evaporator (vacuum degree 0.09Mpa), and recrystallized in ethanol to obtain product G (1050.1mg, 1.28mmol) with a yield of 85% as a dark purple powder.

Embodiment 3

[0072]The conjugated polymer host molecule H and the conjugated guest molecule G prepared in Examples 1 and 2 were respectively subjected to UV-visible absorption light test and fluorescence emission spectrum test (10 μM chloroform solution, room temperature), and the measured UV-visible absorption Spectral and fluorescence emission spectral overlay plots, such as figure 1 shown.

[0073] From figure 1 It can be seen that the fluorescence emission of the conjugated polymer host molecule H overlaps well with the ultraviolet absorption spectrum of the conjugated guest molecule G, indicating that the conjugated polymer host molecule H and the conjugated guest molecule G have good FRET conditions, and the energy can be From the host molecule H to the guest molecule G.

[0074] Mix the conjugated polymer host molecule H prepared in Examples 1 and 2 with the conjugated guest molecule G according to the molar ratio H:G=100:1 to prepare a column [5] aromatic hydrocarbon conjugated p...

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 a 3D-crosslinked supramolecular polymer based on a column [n] arene conjugated polymer as well as a preparation method and application of the 3D-crosslinked supramolecular polymer. The preparation method comprises the following step: mixing a conjugated polymer host molecule with a conjugated guest molecule according to a certain proportion to form the 3D-crosslinked supramolecular polymer based on the column [n] arene conjugated polymer. The polymer provided by the invention has good film forming property, the host molecule and the guest molecule are respectively an energy donor and an energy acceptor, and energy can be transferred from a host to a guest according to an antenna effect and a fluorescence resonance energy transfer mechanism so that the color of the guest is embodied; and a film and a spraying load of the 3D-crosslinked supramolecular polymer show multi-stimulus discoloration property according to different properties embodied by the 3D-crosslinked supramolecular polymer based on the column [n] arene conjugated polymer in a liquid environment and a solid state, and therefore, the 3D-crosslinked supramolecular polymer can be used as an erasableencrypted writing material.

Description

technical field [0001] The present invention relates to the technical field of supramolecular self-assembly materials and organic luminescent materials, in particular to a 3D cross-linked supramolecular polymer based on pillar [n] arene conjugated polymer and its preparation method and its application in rewritable materials and encrypted writing in the application. Background technique [0002] Rewritable optical materials have attracted widespread attention due to their potential applications in data storage, information encryption, and signal switching. Existing rewritable optical materials are mainly based on light-to-color switch molecules, such as diarylethene, spiropyran, azobenzene, etc. The light-to-color-changing molecule itself has strong photosensitivity, and it is prone to cis-trans conversion or switching rings under light, which makes the stored information invalid; its fatigue resistance also needs to be improved. It is necessary to develop a new type of du...

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): C08G83/00C08J3/24C09K11/06B42D25/36B42D25/415
CPCB42D25/36B42D25/415C08G83/008C08J3/24C08J2387/00C09K11/06C09K2211/1425C09K2211/1458C09K2211/1466
Inventor 曹德榕许林贤唐浩汪凌云
Owner SOUTH CHINA 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
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