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

Preparation method of nucleotide rare earth coordination polymer light-emitting material

A technology of coordination polymers and luminescent materials, which is applied in the direction of luminescent materials, chemical instruments and methods, and compounds containing elements of group 3/13 of the periodic table, can solve the problems of poor hydrophilicity and biocompatibility, and achieve Good hydrophilicity and biocompatibility, easy to operate and master, avoiding the effect of complex synthesis

Active Publication Date: 2016-06-29
SOUTHEAST UNIV
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Deficiencies in the prior art: The reported preparation of rare earth coordination polymers is mainly through hydrothermal reaction, the reaction temperature is above 100°C, the reaction time is as long as ten hours to several days, and some require further high-temperature burning; The prepared rare earth coordination polymer is mainly composed of organic ligands. The hydrophilicity and biocompatibility of the rare earth coordination polymer are poor, and most of them are used in organic solvents

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
  • Preparation method of nucleotide rare earth coordination polymer light-emitting material
  • Preparation method of nucleotide rare earth coordination polymer light-emitting material
  • Preparation method of nucleotide rare earth coordination polymer light-emitting material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Example 1: Preparation of adenosine monophosphate-terbium-pyridinedicarboxylic acid (AMP-Tb-DPA) coordination polymer

[0025] In 0.5 mL of N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES) buffer (100 mM, pH 7.4) containing 10 mM adenosine monophosphate (AMP), add 0.5 mL of 10 mM Tb(NO 3 ) 3 Aqueous solution and 0.5mL dipicolinic acid (DPA) aqueous solution with a concentration of 10mM produced a white precipitate. The solution continued to react for 3 hours under stirring, and the precipitate was collected by centrifugation (6000rpm×10min). The obtained precipitate was washed with deionized water and centrifuged. Separation, washing with deionized water was repeated three times, and finally, the precipitate was dried in an oven at 70°C, and stored in a desiccator after drying.

[0026] figure 1 It is the transmission electron microscope image of the prepared adenosine monophosphate-terbium-pyridinedicarboxylic acid (AMP-Tb-DPA) coordination polymer, and t...

Embodiment 2

[0027] Example 2: Preparation of adenosine monophosphate-europium-tetracycline (AMP-Eu-Tc) coordination polymer

[0028] In 2 mL of N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES) buffer (100 mM, pH 7.4) containing 10 mM adenosine monophosphate (AMP), add 1.5 mL of 10 mM Eu(NO 3 ) 3 Aqueous solution and 0.5mL tetracycline (Tc) aqueous solution with a concentration of 10mM produced a white precipitate, the solution continued to react for 3 hours under stirring, centrifuged (14000rpm×10min) to collect the precipitate, the obtained precipitate was washed with deionized water, centrifuged, repeated Wash with deionized water three times, and finally, dry the precipitate in an oven at 70°C, and store it in a desiccator after drying.

[0029] image 3 It is a transmission electron micrograph of the prepared adenosine monophosphate-europium-tetracycline (AMP-Eu-Tc) coordination polymer, and the coordination polymer shows a network nanostructure. Figure 4 It is the flu...

Embodiment 3

[0030] Example 3: Preparation of adenosine diphosphate-terbium-phenanthroline (ADP-Tb-Phen) coordination polymer

[0031] In 1 mL of N-2-hydroxyethylpiperazine-N'-2-ethanesulfonic acid (HEPES) buffer (100 mM, pH 7.4) containing 3 mM adenosine diphosphate (ADP), add 1 mL of Tb at a concentration of 3 mM (NO 3 ) 3 Aqueous solution, then add 2mL of 1.5mM o-phenanthroline (Phen) aqueous solution, stir the mixed solution at room temperature for 3h, centrifuge at 10000rpm for 20min to collect the precipitate, wash the resulting precipitate with deionized water to remove unreacted reagents, centrifuge, Washing with deionized water was repeated three times, and finally, the precipitate was dried in an oven at 70°C, and stored in a desiccator after drying.

[0032] Figure 5 It is the transmission electron micrograph of the prepared adenosine diphosphate-terbium-phenanthroline (ADP-Tb-Phen) coordination polymer, and the coordination polymer shows a network nanostructure. Figure 6 It...

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 method for preparing a luminescent material of a nucleotide rare earth coordination polymer. The method uses biomolecular nucleotides, rare earth ions and small molecule ligands to obtain a hydrophilic luminescent rare earth coordination polymer through molecular self-assembly Material. Due to the use of biomolecules in the present invention, the prepared nucleotide rare earth coordination polymer luminescent material not only has high luminous intensity, but also has good biocompatibility and hydrophilicity; through the preparation of molecular self-assembly , the reaction is carried out at room temperature without the high temperature and long reaction time required for the usual preparation, the method is simple and easy to operate. The prepared luminescent materials have good application prospects in molecular sensing, tracer imaging, drug delivery and so on.

Description

technical field [0001] The invention relates to a preparation method of a nucleotide rare earth coordination polymer luminescent material. The prepared nucleotide rare earth coordination polymer luminescent material can be used for sensing, marking and imaging of molecules / ions, and belongs to the preparation of rare earth luminescent nanomaterials field. Background technique [0002] Fluorescence technology has a wide range of applications in life sciences, medicine, food safety, environmental protection and other fields. Traditional fluorescence analysis mainly uses various organic dye molecules. Since the excitation wavelength of organic dye molecules is close to the emission wavelength, the Stokes shift is small (20-30nm), and the detection is easily interfered by excitation light; organic dye molecules are also prone to photobleaching. and quenching effect, leading to a decrease in fluorescence intensity. In addition, in fluorescence analysis, especially the fluoresce...

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): C07F5/00C09K11/06
Inventor 陈扬尤其刘保霞
Owner SOUTHEAST UNIV
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