Sanduryl boron compound and its preparation method and use

A compound and nitrogen heterocyclic compound technology, applied in the field of fluorescent devices, can solve the problems of cumbersome data reading, low spatial resolution, unsuitable miniaturization, etc., achieve wide response temperature range, high sensitivity, and avoid uneven concentration distribution the effect of interference

Active Publication Date: 2017-05-03
INST OF CHEM CHINESE ACAD OF SCI
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, there are defects such as not suitable for miniaturization, cumbersome data reading, and low spatial resolution.

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
  • Sanduryl boron compound and its preparation method and use
  • Sanduryl boron compound and its preparation method and use
  • Sanduryl boron compound and its preparation method and use

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0048] Preparation of tris(2,3,5,6-tetramethyl-4-morpholinophenyl)borane (MPB)

[0049]

[0050] a) Dissolve 13.4 g of durene (compound 1) in 25 ml of chloroform, add 2 equivalents of bromine, react for 2 hours, and wash with water; obtain white solid compound 2 (26.0 g, 90%).

[0051] b) Dissolve 10g of p-dibromotetramethylbenzene (compound 2) in 300ml of degassed ether, protect with argon, cool down to -78°C, add 1.2 equivalents of n-butyllithium and stir, gradually raise the temperature to 0°C, then cool down again to -78°C. Add 0.3 equivalent of boron trifluoride diethyl ether, return to normal temperature and continue to react for 2 hours. After the reaction, it was washed with water, and purified by silica gel column using petroleum ether as developing solvent. Compound 3 (3.3 g, 45%) was obtained as a white solid.

[0052] c) 4.5 equivalents of sodium tert-butoxide (NaOtBu), 50 ml of toluene, 0.09 equivalents of 2,2'-bisdiphenylphosphino-1,1'-binaphthyl (BINAP) an...

Embodiment 2

[0054] Preparation of 4,4'-(((4-bromo-2,3,5,6-tetramethylphenyl)boron)bis(2,3,5,6-tetramethyl-4,1-benzene))bis Morpholine (BrMPB)

[0055]

[0056] a) Dissolve 13.4 g of durene (compound 1) in 25 ml of chloroform, add 2 equivalents of bromine, react for 2 hours, and wash with water; obtain white solid compound 2 (26.0 g, 90%).

[0057] b) Dissolve 10g of p-dibromotetramethylbenzene (compound 2) in 300ml of degassed ether, protect with argon, cool down to -78°C, add 1.2 equivalents of n-butyllithium and stir, gradually raise the temperature to 0°C, then cool down again to -78°C. Add 0.3 equivalent of boron trifluoride diethyl ether, return to normal temperature and continue to react for 2 hours. After the reaction, it was washed with water, and purified by silica gel column using petroleum ether as developing solvent. Compound 3 (3.3 g, 45%) was obtained as a white solid.

[0058] c) 3 equivalents of sodium tert-butoxide (NaOtBu) in 50 ml of toluene, 0.06 equivalents of ...

Embodiment 3

[0060] Fabrication of MPB's PEG-4000 solid-state polymer temperature-fluorescent device

[0061] Polymer solid-state polymer temperature-fluorescent device with an action range of -20°C to 40°C, the compound used is the tris(2,3,5,6-tetramethyl-4-morpholine benzene) boron (MPB ). The temperature-fluorescence device is obtained through the response of its two fluorescent excited states to the viscosity of the environment, and the viscosity of the PEG4000 polymer changes with the change of the environment temperature.

[0062] (1) The preparation concentration is 1×10 -3 mol / liter carbon dichloride solution of MPB compound;

[0063] (2) Take 1ml of the solution and drop it into 12.7g (room temperature 10cm 3 ) The melted PEG4000 macromolecule is mixed evenly, and the dichloromethane is removed in a vacuum oven, and the temperature is kept above the melting point of PEG4000;

[0064] (3) At this time, the concentration of MPB in PEG4000 polymer is 1×10 -4 mol / cubic decimeter...

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

Sanduryl boron compound and its preparation method and use. The invention provides a kind of Sanduryl boron fluorescent compound, which can be used as a liquid and solid self-referencing temperature fluorescent device in a liquid organic solvent and a solid polymer. Because such compounds are monodispersed in organic liquid solvents or specific solid polymers, the color and intensity of the luminescence of the system change with temperature, and the fluorescence quantum efficiency is always high. The fluorescent device of the invention has low cost, strong shape plasticity, high sensitivity and self-reference property. .

Description

technical field [0001] The invention belongs to fluorescent devices in the field of analytical chemistry, in particular to temperature-fluorescent devices in liquid phase and solid state. Background technique [0002] Temperature is one of the most important physical parameters. Due to the development of technology and science, irregular, high spatial resolution, and ultra-small thermometers are becoming more and more important. It is useful for studying biological processes in organisms, especially intracellular biological processes; various chemical reaction processes; or large-scale temperature distribution with high spatial resolution. and other studies can provide key data. Traditional temperature measurement is mainly through thermometers that expand with heat and contract with cold, thermocouples and infrared thermometers. But there are defects such as not suitable for miniaturization, cumbersome data reading, and low spatial resolution. Therefore, there is a great...

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): C07F5/02C09K9/02G01K11/32
Inventor 杨国强刘玄王双青李沙瑜
Owner INST OF CHEM CHINESE ACAD OF SCI
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap