Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Tetraazacyclo tetradecane derived ligand complex and its synthesis process

A technology of tetraaza heterocycle and synthesis method, which is applied in the field of macrocyclic ligand complexes and synthesis, can solve the problems of industrial application obstacles and high preparation cost, and achieves the effects of easy industrial production, low production cost and environmental improvement.

Inactive Publication Date: 2005-12-14
长春师范学院 +2
View PDF4 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] TAMLR catalysts are a class of macrocyclic ligand complexes, which have very good performance in activating peroxides, but the high cost of preparation of such complexes hinders industrial application

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
  • Tetraazacyclo tetradecane derived ligand complex and its synthesis process
  • Tetraazacyclo tetradecane derived ligand complex and its synthesis process

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0021] The implementation process of the present invention will be further elaborated below through specific examples.

[0022] 1. Synthesis of 5,5,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane

[0023] Synthesized according to the method of J.Chem..Soc.Perkin I, 591-593,1975.

[0024] 2. Synthesis of 1-acetyl-5,5,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane

[0025] Dissolve 28.5 grams (0.1 mol) of 5,5,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane in 500 milliliters of dichloromethane, add 20 grams (0.14 mol) anhydrous potassium carbonate, stirred and cooled to 0°C. A solution of 7.9 g of acetyl chloride dissolved in 100 ml of dichloromethane was added dropwise in one hour. After the addition, the temperature was gradually raised to room temperature, and stirring was continued for 3 hours, then heated to reflux for 3 hours, and the reaction was completed and cooled to room temperature. After filtration, the filtrate was concentrated by distil...

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 present invention is tetraazacyclo tetradecane derived ligand complexes and their synthesis process in fine chemical technology. Their macrocyclic ligand is 5, 5, 7, 12, 14, 14-hexamethyl-1, 4, 8, 11- tetraazacyclo tetradecane with 1-substituent; the metal ion in the complexes may be Fe, Cu or Mg ion. These complexes have the property of activating hydrogen peroxide and per-acids.

Description

Technical field: [0001] The invention belongs to the field of fine chemical industry, and relates to a class of macrocyclic ligand complexes and a synthesis method. Background technique: [0002] Peroxide bleaching has important applications in both industrial and household bleaching and washing processes. This application often requires a catalyst to activate peroxides. For example, in the paper industry, some catalysts are very effective in activating hydrogen peroxide, thereby It can greatly improve the efficiency of pulp hydrogen peroxide bleaching. [0003] Some transition metal complexes are mainly used as catalysts for activating peroxides, such as the iron, manganese, and copper complexes disclosed in the invention patent No. 99813089.3 filed by the Netherlands Unilever Co., Ltd. in China. In recent years, the application of catalyst-activated peroxide systems has been significantly expanded. For example, the research group led by Professor TerryCollins of Carnegie ...

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): C07F15/02
Inventor 李志宏刘启民孙凌晨王冲李晓莉高丽娟张永宏赵伦
Owner 长春师范学院
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
Eureka Blog
Learn More
PatSnap group products