Novel quinone compound and preparation method thereof

A compound and quinone technology, applied in the field of new organic compounds and their preparation, can solve the problems of low theoretical specific capacity, limited raw material reserves, environmental pollution by heavy metal elements, etc.

Inactive Publication Date: 2012-01-11
NO 63971 TROOPS PLA
View PDF0 Cites 12 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

From the perspective of sustainable development, this type of positive electrode material has the following disadvantages when used in future power sources: first, the

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
  • Novel quinone compound and preparation method thereof
  • Novel quinone compound and preparation method thereof
  • Novel quinone compound and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

[0018] Dissolve 0.6 g of 1,4,5,8-tetrahydroxy-9,10-anthraquinone (THAQ) in 160 mL of acetonitrile, then add 6.0 g (NH 4 ) 2 S 2 o 8 , The stirring reaction was continued at room temperature for 16h. Afterwards, the product was filtered, washed with deionized water, and finally washed with acetone until the filtrate was colorless. The obtained dimer product (THHQ) was vacuum-dried at room temperature for 16 h to obtain a black solid powder with a yield of about 80%.

example 2

[0020] Add 0.6g of 1,4,5,8-tetrahydroxy-9,10-anthraquinone (THAQ) into 160mL of ethyl acetate, heat to boiling and add 10.0g of FeCl 3 , Continuous reflux reaction for 20h. The product was then filtered and washed with deionized water to be free of Cl - (with AgNO 3 test), and finally washed with acetone until the filtrate was colorless. The obtained product was vacuum-dried at room temperature for 16 hours to obtain a black solid powder with a yield of about 70%.

example 3

[0022] Add 1.0g of 1,4,5,8-tetrahydroxy-9,10-anthraquinone (THAQ) into 160mL of N,N-dimethylformamide, heat to boil and dissolve it, add 5.0g of KClO 3 , Continuous reflux reaction for 5h. After cooling to room temperature, the product was filtered, washed with deionized water, and finally washed with acetone until the filtrate was colorless. The obtained product was vacuum-dried at room temperature for 16 hours to obtain a black solid powder with a yield of about 75%.

[0023] figure 1 It is the FT-IR spectrum of dimer THHQ (a) and THAQ (b): both are at 3424cm -1 The strong absorption peak of represents the -OH stretching vibration. 1589cm -1 、1598cm -1 They are respectively the stretching vibration peaks of C=O on the aromatic rings of THHQ and THAQ. Due to the enhancement of the conjugation effect, the infrared absorption peak of the group can be blue-shifted, which proves that THHQ has a larger conjugated system than THAQ molecules. For the same reason, the stretchin...

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 novel quinone compound and a preparation method thereof. The compound has a structural formula which is shown in the specification, wherein n is equal to 4-28; and 1,4,5,8-tetrahydroxy-9,10-anthraquinone is used as a raw material and is subjected to one-step reaction in a solvent in the presence of a catalyst to prepare polyquinone oligomer. The oligomer can be used for a positive material of a high-specific-energy battery and can also be used for a photoelectric device material. The preparation method is simple and practical; a pure product can be obtained without purification; and the yield reaches over 80 percent.

Description

technical field [0001] The present invention relates to a novel organic compound and its preparation method. The compound can be used in the positive electrode material of high specific energy batteries, and can also be used in photoelectric device materials. Background technique [0002] In recent years, lithium-ion batteries have been widely used due to their high specific energy and good cycle performance, and the research on inorganic transition metal compounds for cathode materials has also become a hot spot. From the perspective of sustainable development, this type of cathode material has the following disadvantages when used in future power sources: first, the theoretical specific capacity is low, second, the reserves of raw materials in nature are limited, and third, some of them pollute the environment with heavy metal elements. Compared with inorganic materials, organic cathode materials whose raw materials are drawn from nature can have the advantages of high th...

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
IPC IPC(8): C08G61/10C07C50/36C07C46/00H01M4/137
CPCY02E60/122Y02E60/10
Inventor 王安邦王维坤苑克国余仲宝杨裕生
Owner NO 63971 TROOPS PLA
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