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

Method for synthesis of novel pyrimidine fluorescent opening type optical probe materials and for applying materials in mercury ion detection

An optical probe and pyrimidine-based technology, which is applied in the synthesis field of new pyrimidine-based fluorescent open-type optical probe materials, can solve the problems of poor detection selectivity and anti-interference, fluorescence quenching of probe molecules, etc., and achieve simple detection methods , short time and cheap equipment

Inactive Publication Date: 2016-02-24
XINJIANG UNIVERSITY
View PDF2 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, from the current related reports, it can be seen that most of these probe molecules are in the optical signal "turn-off" mode, that is, Hg 2+ The presence of will cause the fluorescence quenching of the probe molecule
The detection selectivity and anti-interference of turn-off type probes are poor, and the current turn-on type Hg based on CPs 2+ There are few reports on optical probes, so it is necessary to prepare turn-on Hg based on CPs with relatively simple structure and high detection sensitivity. 2+ Optical Probe Materials

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
  • Method for synthesis of novel pyrimidine fluorescent opening type optical probe materials and for applying materials in mercury ion detection
  • Method for synthesis of novel pyrimidine fluorescent opening type optical probe materials and for applying materials in mercury ion detection
  • Method for synthesis of novel pyrimidine fluorescent opening type optical probe materials and for applying materials in mercury ion detection

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0026] (1) Synthetic polymer: 0.165mmol1,4-diethynyl-2,5-dialkoxybenzene, 0.165mmol2-amino-4,6-dichloropyrimidine, 0.008mmolPd4(PPh3), 0.008mmolCuI under nitrogen protection At the same time, 3 ml of diisopropylamine and 7 ml of toluene were added to the reactor, and the mixture was heated at 80° C. for 24 hours to form a polymer. The polymer first emitted green light and finally turned yellowish brown. After the reaction mixture had cooled to room temperature, it was added dropwise to rapidly stirring acetone and a precipitate formed, filtered, the filter cake was collected and washed repeatedly with acetone, hot ethanol and hot methanol, and it was recrystallized twice in EtOH / CHCl3 , dried at 40°C for 48h, and the yield was 92%. The structure of the polymer was confirmed by NMR.

[0027] (2) At room temperature, I was prepared from potassium salts - , Br - , F - , CI - , Ac - and SCN - Solution, CO prepared from sodium salt 3 2- , H 2 PO 4 - , HCO 3 - , NO 3 ...

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

When I<-> is added in a blue light emitting conjugated polymers with a main chain containing pyrimidine, along with increase of the I<-> (a KI aqueous solution), I<-> shows a heavy atom effect and makes fluorescence of a polymer solution (THF) quenched gradually, and the appearance color of the solution is changed from colorless to yellow. Contrast experiments under same conditions show that introduction of other anions does not make optical properties of the polymers produce similar change. With utilization of high binding constant and complexing ratio of Hg<2+> and I<->, addition of Hg<2+> makes the fluorescence of the polymer complex restored gradually, and the appearance color is restored to colorless from yellow; through analysis of fluorescence emission properties of the polymers in the presence of Hg<2+> with gradually increased concentration, the detection limit on Hg<2+> is indicated to reach about 0.89*10<-4> mol / L, and through the contrast experiments, the presence of background metal cations is indicated to have no obvious interference on Hg<2+> optical response. Experimental results show that the polymers are turn-on type Hg<2+> optical probe materials having relatively high sensitivity and interference resistance. Abstract attached drawings are ultraviolet-visible absorption (UV-Vis) and fluorescence emission spectra charts of the polymer solution (the concentration of THF is about 1.86*10<-5> mol / L).

Description

technical field [0001] The invention relates to the synthesis of a novel pyrimidine fluorescent open optical probe material and its application to mercury ion detection, and it is used as a selective optical probe for mercury ion sensing. Background technique [0002] With the continuous development of science and technology, selective optical probes for mercury ion sensing are widely used in various fields, and the requirements for their performance are getting higher and higher. On the basis of traditional detection methods such as atomic absorption spectroscopy, cold atomic fluorescence spectroscopy and gas chromatography, the probe material is properly modified to improve its measurement sensitivity, shorten the test consumption time, simplify the sample preparation process and the required equipment, and develop new Hg 2+ Detection related materials and methods have become one of the main research hotspots at home and abroad. [0003] Hg 2+ It is one of the transitio...

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): G01N21/64
Inventor 希尔艾力·买买提依明萨拉麦提·拜科日艾帕尔·玉苏普阿卜来提·艾则孜曼孜兰·阿不都西提祖丽非亚·阿西木
Owner XINJIANG 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