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

Metallic silver coordination polymer with two-dimensional lamellar structure, and preparation and application thereof

A coordination polymer, two-dimensional layered technology, applied in the field of preparation of coordination polymer materials

Inactive Publication Date: 2012-06-27
TIANJIN NORMAL UNIVERSITY
View PDF1 Cites 14 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, currently known coordination polymers with anion exchange function often show certain limitations

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
  • Metallic silver coordination polymer with two-dimensional lamellar structure, and preparation and application thereof
  • Metallic silver coordination polymer with two-dimensional lamellar structure, and preparation and application thereof
  • Metallic silver coordination polymer with two-dimensional lamellar structure, and preparation and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0061] Preparation and Discussion of Polypyridine-Bridged Organic Ligand L Containing 1,2,4-Triazole

[0062] 1. Synthesis experiment and post-processing:

[0063] Dissolve N-(4-pyridyl)-2-pyridine-thioamide (21.5 g, 0.1 mol) and 2-pyridinecarbohydrazide (13.7 g, 0.1 mol) in 200 mL of n-butanol, and heat to reflux for 36 hours After that, the heating was stopped, cooled to room temperature, filtered under reduced pressure, and washed with ethanol three times to obtain a light yellow solid. Recrystallized with ethanol to obtain a white powder product. Accurately weighed with an analytical balance, the calculated yield was 66%.

[0064] 2. Results and Discussion:

[0065] Analytical testing equipment:

[0066] Elemental analysis, C, H, N content determination using CE-440 (Leemanlabs) elemental analyzer

[0067] Infrared Spectroscopy, AVATAR-370 (Nicolet) Fourier Transform Infrared Spectrometer

[0068] Elemental Analysis: Theoretical Values ​​(C 17 h 12 N 6 , Mr = 30...

Embodiment 2

[0071] Preparation and Discussion of Polypyridine-Bridged Organic Ligand L Containing 1,2,4-Triazole

[0072] 1. Synthesis experiment and post-processing:

[0073] Dissolve N-(4-pyridyl)-2-pyridine-thioamide (21.5 g, 0.1 mol) and 2-pyridinecarbohydrazide (17.8 g, 0.13 mol) in 200 mL of n-butanol, and heat to reflux for 40 hours After that, the heating was stopped, cooled to room temperature, filtered under reduced pressure, and washed with ethanol three times to obtain a light yellow solid. Recrystallized with ethanol to obtain a white powder product. Accurately weighed with an analytical balance, the calculated yield was 70%.

[0074] 2. Results and Discussion:

[0075] Analytical testing equipment:

[0076] Elemental analysis, C, H, N content determination using CE-440 (Leemanlabs) elemental analyzer

[0077] Infrared Spectroscopy, AVATAR-370 (Nicolet) Fourier Transform Infrared Spectrometer

[0078] Elemental Analysis: Theoretical Values ​​(C 17 h 12 N 6 , Mr = 3...

Embodiment 3

[0081] Preparation and Discussion of Polypyridine-Bridged Organic Ligand L Containing 1,2,4-Triazole

[0082] 1. Synthesis experiment and post-processing:

[0083]Dissolve N-(4-pyridyl)-2-pyridine-thioamide (21.5 g, 0.1 mol) and 2-pyridinecarbohydrazide (20.5 g, 0.15 mol) in 200 mL of n-butanol, and heat to reflux for 38 hours After that, the heating was stopped, cooled to room temperature, filtered under reduced pressure, and washed with ethanol three times to obtain a light yellow solid. Recrystallized with ethanol to obtain a white powder product. Accurately weighed with an analytical balance, the calculated yield was 73%.

[0084] 2. Results and Discussion:

[0085] Analytical testing equipment:

[0086] Elemental analysis, C, H, N content determination using CE-440 (Leemanlabs) elemental analyzer

[0087] Infrared Spectroscopy, AVATAR-370 (Nicolet) Fourier Transform Infrared Spectrometer

[0088] Elemental Analysis: Theoretical Values ​​(C 17 h 12 N 6 , Mr = 30...

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 3,5-di(2-pyridyl)-4-(4-pyridyl)-1,2,4-triazolyl-silver (I) coordination polymer, and a preparation and application thereof. The compound is synthesized by the following steps: under normal temperature and pressure, mixing AgNO2 acetonitrile solution and ligand L chloroform solution, and keeping stirring for half an hour, and standing in a dark place to volatilize for about one week, thereby obtaining the colorless lumpy monocrystal product. The invention has the advantages of simple preparation technique, short reaction time, easy after-treatment and high yield. The experiment proves that nitrite ions in the material can selectively react with tetrafluoroborate ions, hexafluorosilicate ions, nitrate ions and perchlorate in an anion exchange mode, and benzoate ions and acetate ions can not perform similar anion exchange reaction. The material overcomes the limitation to the existing anion exchange material, the exchange process is simple and easy to implement, and thus, the invention is hopeful to practical application in the field of ion exchange materials.

Description

technical field [0001] The invention belongs to the technical field of synthesis, structure and performance of novel inorganic-organic hybrid materials, and in particular relates to the preparation of a coordination polymer material with a two-dimensional layered structure, more specifically 3,5-bis( 2-pyridyl)-4-(4-pyridyl)-1,2,4-triazole-silver coordination polymer and its preparation and application in selective anion exchange. Background technique [0002] With the development of coordination chemistry, the introduction of the concept of crystal engineering into the design of coordination supramolecular structures has extended an important branch of the discipline—coordination polymer (Coordination Polymer). It is defined as a class of crystalline materials with a highly regular infinite network structure and special physical and chemical properties formed by the assembly of ligand molecules or ions and metal ions through coordination bonds. The research on coordination...

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): C07F1/10B01J41/12B01J41/09
Inventor 杜淼阎艳陈静李承鹏
Owner TIANJIN NORMAL UNIVERSITY
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