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

A kind of red light material and its preparation method and application

A red light and reaction technology, applied in luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc., can solve problems such as the reduction of fluorescence quantum yield, and achieve reduced quenching effect, good fluorescence quantum efficiency, high efficiency and stability The effect of red light emission

Active Publication Date: 2016-03-23
NANJING UNIV OF POSTS & TELECOMM
View PDF4 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0003] Due to the strong π-π interaction and charge transfer characteristics in red light materials, it is easy to reduce the fluorescence quantum yield caused by concentration quenching

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 kind of red light material and its preparation method and application
  • A kind of red light material and its preparation method and application
  • A kind of red light material and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0033]

[0034] Target compound T1

[0035] 【Reaction route】

[0036]

[0037] According to the reaction scheme, compound 1 and 4-(4-hexylthiophen-2-yl)-7-(5-bromo-4-hexylthiophen-2-yl)benzothiadiazole were catalysts Compound 2 was prepared by Suzuki coupling reaction under the conditions of , and NBS dissolved in DMF was slowly added dropwise in ice bath and protected from light to obtain compound 3 . Finally, the target compound T1 was prepared by Suzuki coupling reaction between 3 and boronate of pyrene under the condition of tetrakistriphenylphosphopalladium as catalyst. The specific steps of the Suzuki coupling reaction are as follows: in a 50 mL two-necked round-bottomed flask with a magnetic stirrer, sequentially add compound 13 (0.40 g, 0.21 mmol), pyrene borate (0.32 g, 0.96 mmol) and Pd(pph 3 ) 4 (10mg), vacuum three times for nitrogen. Add deoxygenated toluene (20mL), and then add K 2 CO 3 aqueous solution (2M, 8 mL). Turn on the condensed water, heat ...

Embodiment 2

[0039]

[0040] Target compound T2

[0041] 【Reaction route】

[0042]

[0043] According to the reaction scheme, 3 and 2-naphthylboronic acid undergo Suzuki coupling reaction under the condition of tetrakistriphenylphosphopalladium as a catalyst to obtain the target compound T2. The specific steps are: under the condition of avoiding light, in a 50mL two-necked round bottom flask with a magnetic stirrer, sequentially add compound 13 (0.30g, 0.16mmol), 2-naphthylboronic acid (0.14g, 0.72mmol), Pd (pph 3 ) 4(10mg), vacuum three times for nitrogen. Add deoxygenated toluene (20mL), and then add K 2 CO 3 aqueous solution (2M, 8 mL). Turn on the condensed water, heat to reflux at 95°C, and react for 48h. Extract with dichloromethane and water, dry the organic phase with anhydrous magnesium sulfate, filter with suction, and spin dry the organic phase. The eluent of column chromatography was dichloromethane and petroleum ether (1:3 by volume), and 0.164 g of the target pr...

Embodiment 3

[0045]

[0046] Target compound T3

[0047] 【Reaction route】

[0048]

[0049] According to the reaction scheme, 3 and p-trifluoromethylphenylboronic acid were subjected to Suzuki coupling reaction under the condition of tetrakistriphenylphosphopalladium as a catalyst to obtain the target compound T3. The specific reaction steps are: under dark conditions, in a 50mL two-necked round-bottomed flask with a magnetic stirrer, sequentially add compound 13 (0.30g, 0.16mmol), p-trifluoromethylphenylboronic acid (0.14g, 0.72mmol), Pd(pph 3 ) 4 (10mg), vacuum three times for nitrogen. Add deoxygenated toluene (20mL), and then add K 2 CO 3 aqueous solution (2M, 8 mL). Turn on the condensed water, heat to reflux at 95°C, and react for 48h. Extract with dichloromethane and water, dry the organic phase with anhydrous magnesium sulfate, filter with suction, and spin dry the organic phase. The eluent of column chromatography was dichloromethane and petroleum ether (1:3 volume r...

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 relates to a red light material and a preparation method thereof. The material is a multi-arm structure compound which takes triphenylamine as a core, takes thiophene-benzothiazole derivatives as branch arms, and is end-capped by an electron withdrawing or neutral group; the material is shown in the general formula I, wherein X refers to an end-capping group and selected from one of the following groups shown in the specification: R refers to C1-C12 alkyls; N refers to a nitrogen atom, S refers to a sulfur atom, F refers to a fluorine atom, and -CN refers to cyan. The material can be purified easily, has amorphous characteristics, good solubility, reversible electrochemical oxidation-reduction properties, can obtain a high chemical purity through a simple column chromatography method; and the material can be used as an active material and widely applied to organic light-emitting devices, especially to stable and efficient red organic electroluminescent devices.

Description

Technical field: [0001] The invention belongs to the technical field of optoelectronic materials and applications, and specifically relates to an organic electroluminescent material, more specifically to a multi-arm structure material and its preparation method and application; the material uses triphenylamine as the core and thiophene-benzene The thiazole derivatives are multi-substitution compounds of branches, and can be widely used as light-emitting materials in organic light-emitting devices, especially stable and efficient red organic electroluminescent thin film devices. Background technique: [0002] Organic / Polymer Light-Emitting Device (OLED / PLED) is one of the current research hotspots in the scientific and industrial circles, and it shows broad application prospects in the fields of information display and solid-state lighting. Red light-emitting materials are one of the three primary colors (red, green, blue) materials that are essential to realize information d...

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): C07D417/14H01L51/54C09K11/06
Inventor 赖文勇黄维范晓春王芳李祥春赵玲玲
Owner NANJING UNIV OF POSTS & TELECOMM
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