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

Substituted pyridine complex and preparation method thereof, and application of substituted pyridine complex as near ultraviolet photoluminescence material

A complex and pyridine technology, which is applied in the direction of luminescent materials, cadmium organic compounds, chemical instruments and methods, etc., can solve the problems of large damage and burn skin, etc., and achieve the effects of high yield, easy operation and low production cost

Inactive Publication Date: 2014-05-07
HUAINAN NORMAL UNIV
View PDF3 Cites 3 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Short-wave ultraviolet rays are very harmful to the human body. Short-term exposure can burn the skin, and long-term or high-intensity exposure can also cause skin cancer.

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
  • Substituted pyridine complex and preparation method thereof, and application of substituted pyridine complex as near ultraviolet photoluminescence material
  • Substituted pyridine complex and preparation method thereof, and application of substituted pyridine complex as near ultraviolet photoluminescence material
  • Substituted pyridine complex and preparation method thereof, and application of substituted pyridine complex as near ultraviolet photoluminescence material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0031] In conjunction with the accompanying drawings, a substituted pyridine complex of this embodiment, the chemical formula of the complex is Cd 3 (SO 4 ) 2 (C 6 h 5 N 2 o 2 ) 2 (H 2 O) 4 , the complex belongs to the monoclinic crystal system, the space group is P2(1) / c(No.14), and the unit cell parameters are a=16.934(7), b=10.365(4), c=7.251(3) α=γ=90°, β=92.875(9)°, Z=2. The schematic diagram of the molecular structure of the substituted pyridine complex is as follows: figure 1 Shown (the symmetric code indicates the symmetric relationship between the atoms). The substituted pyridine complex of this embodiment is to adopt 3CdSO 4 .8H 2 O, 6-aminopyridine-3-carboxylic acid (molecular formula is C 6 h 6 N 2 o 2 , after dehydrogenation is C 6 h 5 N 2 o 2 ) as a reactant, prepared by solvothermal method, 3CdSO 4 .8H 2 The molar ratio of O and 6-aminopyridine-3-carboxylic acid was 1:1. The maximum excitation wavelength of the substituted pyridine comple...

Embodiment 2

[0039] A substituted pyridine complex and its application as a near-ultraviolet photoluminescent material in this embodiment are basically the same as in Example 1, except that the preparation method of a substituted pyridine complex in this embodiment is as follows: 0.308g , 0.4mmol of 3CdSO 4 .8H 2 O, 0.110g, 0.8mmol of 6-aminopyridine-3-carboxylic acid, 4mL of water and 4mL of ethanol were successively loaded into a polytetrafluoroethylene reactor and heated. Under sealed conditions, the temperature was raised to 160°C at 12°C / h, and the temperature was constant. After 89 hours, the temperature was lowered to 30° C. at a rate of 4° C. / h to obtain the colorless flaky crystals, that is, the substituted pyridine complex.

Embodiment 3

[0041] A substituted pyridine complex and its application as a near-ultraviolet photoluminescent material in this embodiment are basically the same as in Example 1, except that the preparation method of a substituted pyridine complex in this embodiment is as follows: 0.308g , 0.4mmol of 3CdSO 4 .8H 2 O, 0.165g, 1.2mmol of 6-aminopyridine-3-carboxylic acid, 6mL of water and 3mL of ethanol were successively loaded into a polytetrafluoroethylene reactor and heated. Under sealed conditions, the temperature was raised to 180°C at 15°C / h, and the temperature was constant. After 96 hours, the temperature was lowered to 30° C. at a rate of 5° C. / h to obtain the colorless flaky crystals, that is, the substituted pyridine complex.

[0042] A substituted pyridine complex described in Examples 1 to 3, its preparation method and its application as a near-ultraviolet photoluminescence material, the fluorescence emitted by the substituted pyridine complex is near-ultraviolet light, which ca...

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 discloses a substituted pyridine complex and a preparation method thereof, and an application of the substituted pyridine complex as a near ultraviolet photoluminescence material, and belongs to the technical field of chemical new material synthesis. The chemical formula of the complex is Cd3(SO4)2(C6H5N2O2)2(H2O)4; the substituted pyridine complex is a monoclinic system, the space group of the monoclinic system is P2(1) / c(No.14), and the unit cell parameters of the monoclinic system are as follows: a=16.934 (7), b=10.365 (4), c=7.251 (3) as shown in specification, alpha=gamma=90 degrees, beta=92.875 (9) degrees, and Z=2. The substituted pyridine complex is prepared by a solvothermal method. The substituted pyridine complex is simple in synthesis process and abundant in raw material source, and can be applied as the near ultraviolet photoluminescence material to numerous fields such as scientific experiments, and medicine production and research, and thus is wide in use.

Description

technical field [0001] The invention relates to the technical field of synthesis of new chemical materials, in particular to a substituted pyridine complex, a preparation method thereof and an application as a near-ultraviolet photoluminescent material. Background technique [0002] Luminescent materials, also known as luminous bodies, are functional materials that can convert various forms of energy absorbed from the outside into non-equilibrium light radiation. There are two types of light radiation, equilibrium radiation and non-equilibrium radiation, namely thermal radiation and luminescence. As long as any object has a certain temperature, the object must have radiation (red light, infrared radiation) that is in thermal equilibrium with this temperature. Non-equilibrium radiation means that under the excitation of some external action, the system deviates from the original equilibrium state. If the object returns to the equilibrium state, its excess energy is released ...

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): C07F3/08C09K11/06
Inventor 周薇薇赵旺王凤武赵星秦楠楠陈莹吴玉洁
Owner HUAINAN NORMAL 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