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

A boron-containing organic free radical compound and its preparation method and application

A technology of free radicals and compounds, applied in the field of boron-containing organic free radical compounds and its preparation, can solve the problems of difficult synthesis, limited means of free radical characteristics, and small number of organic free radical compounds, and achieve reasonable and effective yields. Conducive to a large number of synthesis, increase the effect of stability

Active Publication Date: 2022-05-13
JILIN UNIV
View PDF6 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] In view of this, in order to solve the technical problems such as the small number of stable organic free radical compounds in the prior art, the difficulty of synthesis, and the limited means for adjusting the characteristics of free radicals, the present invention provides a boron-containing organic free radical compound and its preparation method and application

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
  • A boron-containing organic free radical compound and its preparation method and application
  • A boron-containing organic free radical compound and its preparation method and application
  • A boron-containing organic free radical compound and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0037] In the preparation method of boron-containing organic free radical compounds of the present invention, under the protection of inert gas (generally adopting argon), the precursor to be oxidized is dissolved in toluene or xylene, and then 2,3-dichloro-5,6- Dicyano-1,4-benzoquinone in toluene or xylene, the precursor to be oxidized, 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in a molar ratio of 1 : (1~2), carry out the oxidation reaction under the heating condition of 50-100 ℃, the duration is 0.5~1.5h, after the reaction finishes, cool down, purify through column chromatography, recrystallization, obtain formula (I) or formula (II ) the boron-containing organic free radical compound shown.

[0038] Be that a boron-containing organic free radical compound of formula (I) is example with structural formula, general reaction formula is as follows:

[0039]

[0040] In the above technical scheme, the chemical structural formula of the precursor to be oxidized is shown in f...

Embodiment 1

[0047] Boron-containing organic radical compound, the structural formula is as follows:

[0048]

[0049] The preparation of above-mentioned boron-containing organic radical compound:

[0050] Step 1, put 2,5-dibromo-1,3-difluorobenzene (1g, 36.8mmol), 4-ethylphenol (13.46g, 110.4mmol) and potassium carbonate (15.26g, 110.4mmol) into a dry In the reaction flask with a condenser tube, after more than three vacuum pumping and argon gas pumping operations, inject dry N,N-dimethylformamide solvent (45mL) to fully dissolve, and then heat up to 170°C for reaction 12h. The resulting reaction mixture was diluted with toluene and poured into water. The aqueous layer was extracted three times with toluene (30 mL). The toluene layer was collected and dried over anhydrous sodium sulfate. After toluene was removed under reduced pressure, it was purified by silica gel column chromatography (eluent: petroleum ether: dichloromethane = 12:1) to obtain a colorless powder, which was designate...

Embodiment 2

[0068] Boron-containing organic radical compound, the structural formula is as follows:

[0069]

[0070] The preparation of above-mentioned boron-containing organic radical compound:

[0071] Step 1, put 2,5-dibromo-1,3-difluorobenzene (1g, 36.8mmol), 4-tert-butylphenol (16.58g, 110.4mmol) and potassium carbonate (15.26g, 110.4mmol) into dry In the reaction flask with a condenser tube, after more than three times of vacuuming and argon gas pumping operations, inject dry N,N-dimethylformamide solvent (45mL) to fully dissolve, and then heat up to 170°C Under reaction 12h. The resulting reaction mixture was diluted with toluene and poured into water. The aqueous layer was extracted three times with toluene (30 mL). The toluene layer was collected and dried over anhydrous sodium sulfate. After rotary evaporation to remove toluene, the crude product was purified by silica gel column chromatography (eluent: petroleum ether: dichloromethane = 12:1) to obtain a colorless powder,...

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

PropertyMeasurementUnit
band gapaaaaaaaaaa
Login to View More

Abstract

The invention relates to a boron-containing organic free radical compound and its preparation method and application, belonging to the technical field of organic free radical compounds. The invention solves the technical problems in the prior art, such as less number of stable organic free radical compounds, high synthesis difficulty, limited means for adjusting free radical characteristics, and the like. The boron-containing organic radical compound of the present invention has a chemical structural formula as shown in formula (I) or formula (II). In formula (I) and formula (II), n is independently an integer of 1-6. The boron-containing organic radical compound has near-infrared light absorption properties and has the potential to prepare near-infrared dyes; it has narrow band gap characteristics, and the energy level distribution can provide bipolar transport properties, and is useful for preparing bipolar organic field effect transistor devices. Potential; the boron-containing organic free radical compound shows obvious paramagnetic properties, and has the potential to prepare organic electronic spin devices.

Description

technical field [0001] The invention belongs to the technical field of organic free radical compounds, and in particular relates to a boron-containing organic free radical compound and its preparation method and application. Background technique [0002] Organic free radical compounds are molecules or ions that have one or more unpaired electrons. Due to the existence of unpaired electrons, such compounds often exhibit unique electronic structures and physicochemical properties. On the one hand, the unpaired electrons in molecular orbitals endow them with infrared / near-infrared light-absorbing properties, spin magnetism, and charge transport capabilities, which endow them with great potential as optical, electrical, and magnetic functional materials; on the other hand, unpaired electrons The high reactivity brought by it makes free radicals easy to decompose or react with water and oxygen in the environment, reducing its chemical stability. Therefore, the stabilization str...

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): C07F5/02C09B57/00H01L51/00
CPCC07F5/02C09B57/00H10K85/657
Inventor 窦传冬郭家祥
Owner JILIN 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