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

Nopinic alkyl beta-dione boron difluoride complexes and preparation method and application thereof

A technology of diketone boron difluoride and nopinyl group, which is applied in the field of nopinyl β-diketone boron difluoride complex and its preparation, achieving the effects of high yield, simple synthesis operation and low price

Inactive Publication Date: 2018-08-17
NANJING FORESTRY UNIV
View PDF2 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] In recent years, compounds such as tetraphenylethylenes, siloles, tetraphenyl-1,4-butadiene, 6,13-pentabenzoquinone, and boron fluoride dipyrrole have been widely used in electroluminescent materials. However, there is no report on the synthesis of electroluminescent materials using natural products as raw materials

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
  • Nopinic alkyl beta-dione boron difluoride complexes and preparation method and application thereof
  • Nopinic alkyl beta-dione boron difluoride complexes and preparation method and application thereof
  • Nopinic alkyl beta-dione boron difluoride complexes and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0042] 1) Preparation of norpinyl β-diketone

[0043] Add 0.06mol sodium hydride into the reaction vessel, slowly inject 8mL of ethylene glycol dimethyl ether under the protection of nitrogen, dissolve 0.02mol of nopinone in 9mL of ethylene glycol dimethyl ether, slowly inject into the reaction vessel under the protection of nitrogen, and control the reaction by raising the temperature The temperature was 82°C, heated to reflux for 0.5h, 0.024mol of aromatic esters 1a and 1b were dissolved in 9mL of ethylene glycol dimethyl ether, and then slowly injected into the reaction vessel under the protection of nitrogen. The reaction progress was tracked by thin-layer chromatography, and the reaction was carried out for 7-8h. The reactant was extracted three times with 100 mL of ethyl acetate, and the organic phase was concentrated to recover the solvent to obtain the crude product of nopinone β-diketone compound. Recrystallize with methanol, get nopinyl β-diketone 2a and 2b, the stru...

Embodiment 2

[0054] The norpinyl β-diketone boron difluoride complex is used as a light-emitting material in electroluminescent devices.

[0055] 1) Use a 0.001g electronic scale to weigh the conductive adhesive A glue and the curing agent B glue, and the weight ratio is 1:4.

[0056] 2) Conductive adhesive A needs to be stirred for more than 2 minutes before use. Then mix the conductive adhesive A glue with the fluorescent powder and stir well before adding the curing agent B glue. After adding the curing agent B glue, the stirring time generally takes 5 minutes. Make the fluorescent powder and the glue fully mix evenly, then defoam and set aside.

[0057] 3) The debubbled fluorescent glue must be properly stirred before dispensing. It is best to dispensing glue when the bracket is full and the cup is slightly convex, but not overflowing. After drying, the glue can be a flat cup.

[0058] 4) Baking conditions: 60°C / 40min+135°C / 90min. After dispensing, enter the oven for baking immedi...

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 nopinic alkyl beta-dione boron difluoride complexes and a preparation method and application thereof. The natural reusable resource beta-pinene oxidation product, namely nopinone, is used as a raw material to prepare novel nopinic alkyl beta-dione boron difluoride complexes 3a and 3b; nopinone is subjected to Claisen condensation with methyl p-methoxybenzoate 1a and methyl4-bromobenzoate 1b to separately obtain nopinic alkyl beta-dione compounds 2a and 2b; the compounds 2a and 2 b are subjected to complexing with boron trifluoride etherate to separately obtain nopinicalkyl beta-dione boron difluoride complexes 3a and 3b. The nopinic alkyl beta-dione boron difluoride complexes 3a and 3b have good fluorescent performance and high fluorescent quantum yield; an electroluminescent device made with the nopinic alkyl beta-dione boron difluoride complexes can emit blue-green light. It is shown that the nopinic alkyl beta-dione boron difluoride complexes as light-emitting materials have good application value in the preparation of electroluminescent devices.

Description

technical field [0001] The invention belongs to the technical field of fine organic synthesis and the technical field of novel electroluminescent material synthesis, and relates to a nopinyl β-diketone boron difluoride complex and its preparation method and application. Background technique [0002] As an important class of fluorescent dyes, β-diketone fluoroboron compounds have many optical and structural advantages, such as high fluorescence quantum yield, high electron mobility, and large molar absorptivity, so they are widely used in molecular probes. , optical imaging, solar cells, laser dyes, gels and other fields, and the synthesis of this type of compound has the advantages of simple process, high yield, easy purification, etc., so it has attracted the attention of the majority of scientific researchers. Numerous studies have shown that complete BF 2 It is the basic unit of this type of β-diketone fluoroboron compound, and changing the structure of the aldehyde este...

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): C07F5/02C09K11/06H01L51/54
CPCC09K11/06C07F5/022C09K2211/1096C09K2211/1007H10K85/657
Inventor 杨益琴姜倩王石发徐海军王忠龙谷文徐徐李明新匡洪波杨丽娟张燕
Owner NANJING FORESTRY 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