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Pyrroles oligomer and application thereof

A technology of oligomer and pyrrole oligo, which is applied in the direction of conductors, non-metallic conductors, organic material conductors, etc., can solve the problems of products with short reaction time, difficult to dissolve, and difficult to obtain, and achieve environmental friendliness, low cost, and reduced cost effect

Active Publication Date: 2018-08-31
东营曜康医药科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Both methods have their own advantages and disadvantages: the advantage of the former is that the monomer polymerization reaction time is short, it is easy to realize the controlled synthesis of particle morphology, and the conductivity of the product is better; the disadvantage is that the product is difficult to dissolve in conventional organic solvents, and it is not easy to obtain Conductive polymer film and solution post-treatment are cumbersome; the advantage of the latter is that there is no solvent in the polymerization process of the monomer, and a conductive polymer film can be deposited on the surface of any substrate without the need for conductive polymer dissolution. ; The disadvantage is that before coating the surface of the substrate, it is necessary to coat a layer of oxidant film. After the reaction, the oxidant needs to be removed by cleaning.
However, using oxygen or air as an oxidant to synthesize polypyrrole or pyrrole oligomers by chemical vapor deposition has not been reported in the literature so far.

Method used

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  • Pyrroles oligomer and application thereof
  • Pyrroles oligomer and application thereof
  • Pyrroles oligomer and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0059] A preparation method of pyrrole oligomer, the steps are as follows:

[0060] (1) Add 50 μL of pyrrole into a 50 mL container containing 1 g of activated carbon powder, seal the container, shake the container to mix the activated carbon powder and pyrrole evenly, and mature at room temperature for 30 days. During the aging period, the container was shaken twice a day, and the shaking time was not less than 1 min each time. After the aging period, the activated carbon / pyrrole oligomer complex was obtained.

[0061] (2) Disperse the activated carbon / pyrrole oligomer complex obtained in step (1) in 10 mL N,N-dimethylformamide solution, shake well, and let it stand at room temperature for 24 h; centrifuge, and collect the supernatant liquid.

[0062] (3) The supernatant obtained in step (2) was distilled off the solvent under reduced pressure to obtain a pyrrole oligomer sample.

[0063] Result analysis

[0064] The N,N-dimethylformamide solution of the pyrrole oligomer o...

Embodiment 2

[0072] A preparation method of pyrrole oligomer, the steps are as follows:

[0073] (1) Add 10 μL of pyrrole into a 50 mL container containing 1 g of carbon cloth, seal the container, and mature at room temperature for 7 days to obtain a carbon cloth / pyrrole oligomer complex.

[0074] (2) Soak the carbon cloth / pyrrole oligomer composite obtained in step (1) in 5 mL of methanol solution, and let it stand at room temperature for 24 h; take out the carbon cloth and keep the liquid.

[0075] (3) Distill the liquid obtained in step (2) to remove the solvent under reduced pressure to obtain a sample of pyrrole oligomer.

Embodiment 3

[0077] Others are the same as embodiment 1, the difference is:

[0078] 30 μL of pyrrole was added to a 50 mL container containing 1 g of granular carbon, and the container was stirred to mix the activated carbon powder and pyrrole evenly, and aged at room temperature for 10 days. During the aging period, the container was shaken 3 times a day, and the shaking time was not less than 15 min each time. The obtained complex was immersed in 5 mL tetrahydrofuran solution, and stood at room temperature for 28 h; centrifuged, and the supernatant was collected.

[0079] It was determined that the weight-average molecular weight of the prepared pyrrole oligomer was 522, corresponding to an oligomer containing 8 pyrrole rings. The molecular weight distribution coefficient is 1.1, and the prepared pyrrole oligomer is a p-type semiconductor with a charge carrier density of 1.1 × 10 20 cm ‒3 .

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Abstract

The invention relates to a conductive Polymer oligomer and applications thereof, and belongs to the conductive Polymer preparation technical field; the Pyrroles oligomer is featured in that the weightaverage molecular weight (Mw) is 522-912, the molecular weight distribution coefficient is 1.1-1.3, and 8-14 pyrroles ring oligomers are correspondingly contained. The invention also provides a carbon material / Pyrroles oligomer compound, wherein the Pyrroles oligomer is deposited on the surface of the carbon material; the Pyrroles oligomer can be applied to an electrochemistry energy storage material; the invention also provides the carbon material / Pyrroles oligomer compound applications, and the compound can serve as ion battery and super capacitor electrode materials. The prepared Pyrroles oligomer has a higher charge carrier density which facilitates applications thereof in the electrochemistry energy storage field.

Description

technical field [0001] The invention relates to a conductive polymer oligomer and its application, belonging to the technical field of conductive polymer preparation. Background technique [0002] Conductive polymers, also known as conductive polymers, are a class of polymer materials with large π-conjugated molecular skeletons that can be converted from insulators to conductors by chemical or electrochemical doping. Common conductive polymers are polypyrrole, polyaniline, polythiophene and polyacetylene. [0003] Polypyrrole, polyaniline and polythiophene obtained by chemical or electrochemical oxidation polymerization with five-membered aromatic heterocyclic molecules (pyrrole, aniline, thiophene) as monomers have the advantages of easy synthesis, high electrical conductivity, environmental friendliness and biological The advantages of compatibility (J. Phys. Chem. C, 2009, 113, 21586-21595.), in energy storage and conversion, microwave absorption, electrostatic protectio...

Claims

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Application Information

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IPC IPC(8): H01B1/12H01G11/48H01M4/60C08G73/06
CPCC08G73/0611H01B1/127H01G11/48H01M4/602Y02E60/10Y02E60/13
Inventor 班青盖利刚郭秀梅
Owner 东营曜康医药科技有限公司
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