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

Triphenylamine two-photon fluorescence probe compound and preparation method and application thereof

A two-photon fluorescence and triphenylamine technology, applied in chemical instruments and methods, fluorescence/phosphorescence, luminescent materials, etc., can solve problems such as harming human health, increasing environmental pollution, and calmness, and achieves non-destructive detection, high reactivity, and The effect of improving water solubility

Inactive Publication Date: 2013-11-20
SHANGHAI NORMAL UNIVERSITY
View PDF1 Cites 15 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, because of such a wide range of applications, it increases its pollution to the environment
Although metallic silver is considered a safe metal, silver ions or silver salts will deposit on the skin, eyes and mucous membranes after being absorbed by the human body, causing lesions and endangering human health

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
  • Triphenylamine two-photon fluorescence probe compound and preparation method and application thereof
  • Triphenylamine two-photon fluorescence probe compound and preparation method and application thereof
  • Triphenylamine two-photon fluorescence probe compound and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0043] 1. Synthesis of dimethyl chloride-4-methylenetriphenylphosphino-pyridine-2,6-dicarboxylate

[0044] (1) Synthesis of pyridine-2,6-dicarboxylic acid

[0045]Put 500mL of distilled water and 12mL (92mmol) of 2,6-lutidine in a 1000mL round-bottomed flask, slowly add 80g (506mmol) of potassium permanganate under magnetic stirring, and insert a reflux condenser. Reflux at 110°C-115°C for 3.5h. The reaction was stopped, cooled to room temperature, and the black solid was removed by suction filtration. The colorless filtrate was collected, and four fifths of the filtrate was removed under reduced pressure. With continuous stirring, slowly pour about 20 mL of sulfuric acid with a volume concentration of 70%, and a large amount of white crude product is precipitated. After cooling, filter with suction to obtain pyridine-2,6-dicarboxylic acid.

[0046] (2) Synthesis of dimethyl pyridine-2,6-dicarboxylate

[0047] Put 33.5g (200mmol) of pyridine-2,6-dicarboxylic acid, 120mL (1...

Embodiment 2

[0061] The selectivity of compound I to silver ion

[0062] Using the probe compound I synthesized in Example 1, the selectivity to silver ions was evaluated by absorption spectroscopy. Dissolve compound I in a mixed solvent of dimethyl sulfoxide: distilled water = 5:95 (volume ratio), and prepare compound I with a concentration of 1×10 -5 mol / L mixed solution, add different metal ions respectively, so that the concentration of metal ions is 1×10 -5 mol / L, test its single-photon absorption spectrum, the specific results are as follows image 3 shown, from image 3 It can be seen that compound I has high selectivity to silver ions (the metal ion is Ag + 、Na + , Ca 2+ 、Cd 2+ , Fe 2+ , Zn 2+ , Hg 2+ , Mg 2+ , Pb 2+ , Mn 2+ ), when silver ions were added to the solution of compound I, the absorbance of the solution around 305nm increased significantly; while other metal ions were added to the solution of compound I, the absorbance hardly changed.

[0063] It is 1×10 t...

Embodiment 3

[0065] Absorption responses of compound I to different concentrations of silver ions

[0066] Using the probe compound I synthesized in Example 1, dissolve compound I in a mixed solvent of dimethyl sulfoxide:distilled water=5:95 (volume ratio), and prepare the compound I with a concentration of 1×10 -5 mol / L mixed solution, adding different concentrations of silver ions, the concentration of silver ions changes from small to large in order of 0, 1×10 -7 mol / L, 5×10 -7 mol / L, 1×10 -6 mol / L, 2×10 -6 mol / L, 4×10 -6 mol / L, 6×10 -6 mol / L, 8×10 -6 mol / L, 1×10 -5 mol / L, 2×10 -5 mol / L, 4×10 -5 mol / L, 6×10 -5 mol / L, 8×10 -5 mol / L and 1×10 -4 mol / L, specifically as Figure 5 As can be seen from the figure, the single-photon absorbance of Compound I of the present invention is positively related to the concentration of silver ions.

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 belongs to the field of organic nonlinear optical materials, and particularly relates to a triphenylamine two-photon fluorescence probe compound and a preparation method and an application thereof. The preparation method of the triphenylamine two-photon fluorescence probe compound comprises the following steps of: injecting anhydrous benzene into 4-nitrapyrin-2, 6-dimethyl isophthalate and triphenylphosphine under the protection of nitrogen; increasing temperature, refluxing, and cooling; filtering and washing to obtain chlorination-4-methylene triphenylphosphine group-pyridine-2,6-dimethyl isophthalate, and dissolving into methanol; mixing and stirring tri(4-formylphenyl)amine and absolute methanol; adding the methanol solution of the chlorination-4-methylene triphenylphosphine group-pyridine-2,6-dimethyl isophthalate and the methanol solution of sodium methylate; stirring at 0-5 DEG C for 1-2 hours, stirring at normal temperature for 3-4 hours; separating through column chromatography. The triphenylamine two-photon fluorescence probe compound disclosed by the invention has the advantages of outstandingly enhanced two-photon absorption section, good water solubility, higher reaction activity and very high coordination capacity and can be applied to silver ion detection and pH detection.

Description

technical field [0001] The invention belongs to the field of organic nonlinear optical materials, in particular to a triphenylamine two-photon fluorescent probe compound and its preparation method and application. Background technique [0002] In 1990, Denk of Cornell University in the United States proposed to apply the two-photon excitation phenomenon to the confocal laser scanning microscope, which opened up a new field of two-photon fluorescence microscopy and imaging. Two-photon fluorescence microscopy has features such as near-infrared excitation, dark-field imaging, avoidance of fluorescence bleaching and phototoxicity, targeted excitation, high horizontal and vertical resolution, reduced biological tissue absorption coefficient, and reduced tissue autofluorescence interference. It is significantly better than single-photon fluorescence microscopy imaging, providing a sharper tool for life sciences. In order to achieve the maximum range of applications of two-photon ...

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): C09K11/06C07D213/79G01N21/64G01N21/31
Inventor 肖海波张晓瑛
Owner SHANGHAI 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