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A method for protein-induced preparation of chiral polyaniline

A chiral polyaniline and protein technology, which is applied in the fields of chemistry and biochemistry, can solve the problems of complex biological extraction steps, cumbersome operation, high price, etc., and achieves the effects of simple, mild and environmentally friendly experimental conditions, wide sources and low price.

Inactive Publication Date: 2016-07-06
SHANGHAI NORMAL UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

However, DNA requires complex biological extraction steps, which are cumbersome and expensive, thus limiting its application in large-scale production due to high cost.

Method used

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  • A method for protein-induced preparation of chiral polyaniline
  • A method for protein-induced preparation of chiral polyaniline
  • A method for protein-induced preparation of chiral polyaniline

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0028] Weigh 0.0204 g of DBSA and dissolve it in 9.7 mL of pH 2.0 buffer solution; add 0.125 mmol of aniline monomer after stirring evenly; weigh 10 mg of bovine hemoglobin and dissolve it in 200 μl of distilled water and add it to the system; then add the concentration to 9.823 mol 100 μL / L of hydrogen peroxide solution was added to the reaction system in four times within one hour. After stirring the reaction for 8 hours, 10 ml of methanol was added for demulsification to terminate the reaction. The product was collected by centrifugation after precipitation, and dried to obtain a dark green powder with an apparent yield of 138.8%. Characterized by circular dichroism, a positive circular dichroism peak is generated at about 475 nm, which proves that the product is chiral polyaniline, and its molar ellipticity value is 1100 degree cm. 2 ·decimole -1 . Circular dichroism spectrum as attached figure 1 shown.

Embodiment 2

[0030] Weigh 0.0408 g of DBSA and dissolve it in 9.5 mL of pH 2.0 buffer solution; add 0.250 mmol of aniline monomer after stirring evenly; weigh 2 mg of bovine hemoglobin and 8 mg of bovine serum albumin with 200 μl of distilled water to dissolve and add to the system ; Then, 100 μL of hydrogen peroxide solution with a concentration of 9.823 mol / L was added to the reaction system 8 times within one hour. After stirring the reaction for 12 hours, 10 ml of methanol was added for demulsification to terminate the reaction. The product was collected by centrifugation after precipitation, and dried to obtain a dark green powder with an apparent yield of 124.3%. Characterized by circular dichroism, a positive circular dichroism peak is generated at about 475 nm, which proves that the product is chiral polyaniline, and its molar ellipticity value is 910 degree·cm 2 ·decimole -1 . Circular dichroism spectrum as attached figure 2 shown.

Embodiment 3

[0032] Weigh 0.0216 g of SDS and dissolve it in 9.7 mL of pH 1.0 buffer solution; add 0.1875 mmol of aniline monomer after stirring evenly; weigh 10 mg of bovine hemoglobin and dissolve it in 200 μl of distilled water and add it to the system; then add the concentration to 12.5 mmol 100 μL / L of ammonium persulfate solution was added to the reaction system in 5 times within one hour. After stirring the reaction for 18 hours, 10 ml of methanol was added to break the demulsification, and the reaction was terminated. The product was collected by centrifugation after precipitation, and dried to obtain a dark green powder with an apparent yield of 121.2%. Characterized by circular dichroism, a positive circular dichroism peak is generated at about 475nm, which proves that the product is chiral polyaniline, and its molar ellipticity value is 860degree·cm 2 ·decimole -1 . Circular dichroism spectrum as attached image 3 shown

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Abstract

The invention discloses a method for preparing chiral polyaniline through protein induction in acidic aqueous solution containing anionic surfactant. In the citric acid-disodium hydrogen phosphate buffer solution with pH 1~3, add anionic surfactant and aniline monomer respectively, mix and stir; then add the aqueous protein solution into the system; stir well and then add hydrogen peroxide or persulfuric acid ammonium solution, stirring and reacting at room temperature for a period of time to prepare chiral polyaniline. The present invention uses protein as a chiral inducer to prepare chiral polyaniline. The chiral inducer in the method has a wide range of sources and is low in price; the required experimental conditions are simple, mild and environmentally friendly; the obtained chiral product has good stereospecificity and high yield , has potential application value for large-scale use.

Description

technical field [0001] The invention relates to the fields of chemistry and biochemistry, in particular to a method for preparing chiral polyaniline by protein induction in an anionic surfactant solution. Background technique [0002] Among many conductive polymers, polyaniline is one of the most promising conductive polymers at present due to its easy availability of raw materials, controllable structure and properties, simple synthesis and good environmental stability, which expands the application scope of polymers. The generation of chiral polymers has opened up a new field for functional materials. In recent years, chiral polymers have shown promising applications in chemical and biosensors, surface-repaired electrodes, chiral separation, and chiral recognition. [0003] Generally speaking, the synthesis of chiral polymers mostly adopts enantioselective polymerization of chiral substituted monomers, while the preparation process of chiral monomers is complicated and ex...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C08G73/02
Inventor 陈建波郭红冲徐毅
Owner SHANGHAI NORMAL UNIVERSITY