Benzothiazole derivative containing triphenylethylene or tetraphenylethylene structure and having aggregation-induced emission property and preparation method and application thereof

A technology of aggregation-induced luminescence and tetraphenylethylene, which is applied in the direction of luminescent materials, chemical instruments and methods, semiconductor/solid-state device manufacturing, etc., can solve the problems of limited luminescent performance of benzothiazole derivatives, etc., and achieve low raw material cost and simple synthesis , the effect of obvious aggregation-induced luminescent properties

Active Publication Date: 2014-05-21
SUN YAT SEN UNIV
View PDF3 Cites 26 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, so far, the benzothiazole derivatives with luminescent properties developed are relatively limited. Many of these compounds are still slightly modified on the traditional structure, and there is a certain gap in luminous efficiency compared with AIE materials. Styrene and tetraphenylethylene structures not only have obvious aggregation-induced luminescent properties, but also have high thermal stability and luminous intensity, and are used in the preparation of organic electroluminescent devices and other luminescent materials (Chi Zhenguo, Xu Bingjia, Li Xiaofang, etc., Synthesis method and application of aggregation-induced luminescence materials containing both triphenylethylene and tetraphenylethylene structures, Chinese patent 201010219154.1)

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
  • Benzothiazole derivative containing triphenylethylene or tetraphenylethylene structure and having aggregation-induced emission property and preparation method and application thereof
  • Benzothiazole derivative containing triphenylethylene or tetraphenylethylene structure and having aggregation-induced emission property and preparation method and application thereof
  • Benzothiazole derivative containing triphenylethylene or tetraphenylethylene structure and having aggregation-induced emission property and preparation method and application thereof

Examples

Experimental program
Comparison scheme
Effect test

preparation example Construction

[0018] The synthetic method of above-mentioned benzothiazole derivative, comprises the following steps:

[0019] The first step: 2-amino-6-methoxybenzothiazole ring-opening to generate 2-amino-5-methoxythiophenol

[0020] 2-Amino-6-methoxybenzothiazole is heated and refluxed in water under alkaline conditions to generate 2-amino-5-methoxythiophenol. This step does not use organic solvents, which is economical and environmentally friendly.

[0021]

[0022] Step 2: Synthesis of aromatic aldehydes containing triphenylethylene or tetraphenylethylene

[0023] Using benzophenone derivatives or tristyrene bromide as raw materials, it is synthesized by conventional organic synthesis methods, such as Friedel-Crafts alkylation, amine alkylation, halogenation, Suzuki reaction, Heck reaction, Wittig reaction, etc. Aromatic aldehyde containing triphenylethylene or tetraphenylethylene, its structure is as shown in general formula (4):

[0024]

[0025] where R 2 is a direct single...

Embodiment 1

[0042] Synthesis of 6-methoxy-2-(4-(1,2,3-triphenylethylene)phenyl)benzothiazole:

[0043] (1) Synthetic intermediate 2-amino-5-methoxythiophenol

[0044] Add 2-amino-6-methoxybenzothiazole (9g, 50mmol) into a three-necked flask, and add 50% potassium hydroxide aqueous solution (100g potassium hydroxide, 100g water), heat to reflux, and react for 24h , stop heating, cool to room temperature, suction filter, and the filtrate is neutralized with 30% hydrochloric acid aqueous solution to obtain a tan precipitate, which is repeatedly washed with ultrapure water and dried to obtain 5.4 g of tan powder with a yield of 70%.

[0045]

[0046] (2) Synthesis of intermediate tetraphenyl vinyl aldehyde:

[0047] Add bromotriphenylethylene (6.70g, 20mmol) and p-aldehyde phenylboronic acid (4.50g, 30mmol) into a three-necked flask under Ar atmosphere, then add 80mL of toluene, 25mL of 2mol / L potassium carbonate aqueous solution, tetrabutyl bromide Tribasic ammonium (TBAB) (0.64g, 2.0mm...

Embodiment 2

[0053] Synthesis of 2-(4-(1,2,3-triphenylethylene)phenyl)benzothiazol-6-ol:

[0054] Under an Ar atmosphere, the target product 6-methoxy-2-(4-(1,2,3-triphenylethylene)phenyl)benzothiazole (2g, 4mmol) in Example 1 was added into a three-necked flask, Then add 15mL of dried dichloromethane, stir, cool to 0°C, add boron tribromide (1.00g, 4mmol), react for 12h, add water to quench the excess boron tribromide, and then extract three times with dichloromethane , the organic layer was dried with anhydrous sodium sulfate, the solvent was removed by rotary evaporation under reduced pressure, and purified by silica gel column chromatography, and the eluent was a mixed solvent of dichloromethane and n-hexane with a volume ratio of 1:1. 1.34 g of white product was obtained with a yield of 96%.

[0055]

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 benzothiazole derivative containing a triphenylethylene or tetraphenylethylene structure and having aggregation-induced emission property and a preparation method and application thereof. The preparation method comprises the following steps: with 2-amino-6-methoxybenzothiazole as a start raw material, performing a ring-opening reaction under an alkaline condition to generate 2-amino-5-methoxythiophenol; performing a ring-closing reaction with an aromatic aldehyde compound containing a triphenylethylene or tetraphenylethylene structure to obtain a methoxy-containing benzothiazole derivative, or performing demethylation to obtain a hydroxyl-containing benzothiazole derivative, wherein the compound also can be modified through a group substitution reaction to generate a benzothiazole derivative containing other functional groups. The benzothiazole derivative disclosed by the invention has relatively low luminous intensity in a solution, emits strong fluorescence in an aggregation state or solid state, and belongs to good aggregation-induced emission materials; the synthesis is relatively simple, and the cost of the raw materials is low, so that large-scale commercial production is easy to realize; the benzothiazole derivative plays an important role in the fields of electroluminescent devices, fluorescent probes, fluorescent switches, organism imaging and the like.

Description

technical field [0001] The invention belongs to the technical field of organic luminescent materials, and in particular relates to a class of benzothiazole derivatives with triphenylethylene or tetraphenylethylene structures and aggregation-induced luminescent materials, as well as their preparation methods and applications. Background technique [0002] Benzothiazole and its derivatives are widely found in nature. The luciferin extracted from fireflies contains a benzothiazole structure, and benzothiazole derivatives can be isolated and identified from corn coleoptiles, and the derivatives have plant growth inhibitory functions. Crude oils formed from lake swamps have a high content of benzothiazoles. Benzothiazole and its derivatives can be widely used in organic light-emitting diodes (OLED), biomedicine, metal ion detection and industrial production. [0003] However, when traditional benzothiazole derivatives are in a high concentration or in a solid state, the molecul...

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 Applications(China)
IPC IPC(8): C07D277/66C09K11/06H01L51/54G01N21/64
CPCC07D277/66C09K11/06C09K2211/1037
Inventor 马春平池振国周勰张艺刘四委许家瑞
Owner SUN YAT SEN UNIV
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