Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

A kind of organometallic chelate and its preparation method and application

An organometallic and chelate technology, applied in the fields of botanical equipment and methods, applications, organic chemistry, etc., can solve the problems of poor bactericidal effect, high toxicity and high preparation cost of existing compounds, and achieve good protection and therapeutic activity. , low cost and simple preparation method

Active Publication Date: 2015-09-09
江苏乐尔环境科技股份有限公司
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, the research on new heterocycles is very active. Pyrazole heterocycles have attracted much attention due to their wide range of biological activities. Many pyrazole fungicides, insecticides, herbicides, plant growth regulators and drugs have been found. However, the bactericidal effect of the existing compounds is not good, or the toxicity is relatively large, or the preparation cost is relatively high

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
  • A kind of organometallic chelate and its preparation method and application
  • A kind of organometallic chelate and its preparation method and application
  • A kind of organometallic chelate and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0045] Under stirring, add 50ml of water to 1-phenyl-5-(4-methoxyphenyl)-3-hydroxypyrazole (0.05mol), add dropwise an aqueous solution of sodium hydroxide, stir at high speed, and wait until the solution is clear Then add a saturated copper chloride solution, react at 80°C for 3 hours, a solid precipitates out, cool to room temperature, stand and filter, wash with water, wash with ethanol, and dry to obtain 1-phenyl-5-(4-methoxy Phenyl)-3-hydroxypyrazole copper (compound 1) 4.59g.

[0046] 1 H-NMRδ: 3.79 (s, 6H), 6.80 (d, 2H), 7.03-7.39 (m, 18H).

[0047] ESI-MS: [M+H]=594.

Embodiment 2

[0049] Under stirring, add 50ml of water to 1-phenyl-5-(3,4,5-trimethoxyphenyl)-3-hydroxypyrazole (0.05mol), add dropwise an aqueous solution of sodium hydroxide, and stir at a high speed , after the solution is clarified, add a saturated zinc chloride solution, react at 100°C for 1 hour, a solid precipitates, cool to room temperature, stand and filter, wash with water, wash with ethanol, and dry to obtain 1-phenyl-5-(3 , 4,5-trimethoxyphenyl)-3-hydroxypyrazole zinc (compound 2) 5.58g.

[0050] 1 H NMRδ: 2.98 (s, 18H), 6.56 (d, 2H), 6.86 (d, 4H), 7.14-7.40 (m, 10H).

[0051] ESI-MS: [M+H]=715.

Embodiment 3

[0053] Under stirring, add 70ml of water to 1-(4-fluorophenyl)-5-(4-bromophenyl)-3-hydroxypyrazole (0.05mol), add dropwise an aqueous solution of sodium hydroxide, stir at high speed, After the solution is clarified, add saturated magnesium chloride solution, react at 80°C for 2 hours, a solid precipitates, cool to room temperature, stand and filter, wash with water, wash with ethanol, and dry to obtain 1-(4-fluorophenyl)-5- Magnesium (4-bromophenyl)-3-hydroxypyrazole (compound 3) 3.98g.

[0054] 1 H NMRδ: 6.06 (d, 2H), 6.96 (d, 4H), 7.11 (d, 4H), 7.14-7.40 (m, 8H).

[0055] ESI-MS: [M+H]=687.

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 provides an organic metal chelate, which has a structural formula as the following. The invention also provides a preparation method of the organic metal chelate and its application in wastewater treatment, disinsection and sterilization. The preparation method of the organic metal chelate has the characteristics of simplicity, low cost, and mild reaction condition. Meanwhile, the organic metal chelate can achieve a good effect of removing heavy metal ions from wastewater and good antibacterial effects.

Description

technical field [0001] The invention belongs to the field of organic chemistry, and particularly relates to an organometallic chelate, and also relates to a preparation method and application of the organometallic chelate. Background technique [0002] Plant diseases caused by oomycetes, especially downy mildew, vegetable gray mold, wheat head blight, wheat sheath blight, and rice blast, have a short incubation period and many re-infection times. The disease can develop rapidly and cause epidemics, and it is difficult to control. [0003] Nitrogen-containing heterocycles are a class of compounds with important application value and good biological activity. Many heterocycles have been developed into new medicines and pesticides, which play an important role in human health and agricultural production. At present, the research on new heterocycles is very active. Pyrazole heterocycles have attracted much attention due to their wide range of biological activities. Many pyrazol...

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 Patents(China)
IPC IPC(8): C07D231/22A01N43/56A01P7/04A01P3/00C02F1/00C02F101/20
Inventor 贾红圣
Owner 江苏乐尔环境科技股份有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com