Preparation method for constructing two-dimensional ultra-long room-temperature phosphorescent material based on cation-pi action driving
A room temperature phosphorescence, two-dimensional material technology, used in luminescent materials, chemical instruments and methods, sustainable architecture, etc., can solve the problems of poor controllability and poor stability, and achieve the effects of good stability, high strength and great application prospects.
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0034] A preparation method for constructing two-dimensional ultra-long room temperature phosphorescent materials driven by cation-π interaction. The room temperature phosphorescent materials are composed of 2,4,6-tris(9hydrogen-carbazol-9-yl)-1,3,5- The solid powder formed by the assembly of triazine and fluorescent pink B under the force of cation-π supramolecule, the phosphorescent color of the phosphorescent two-dimensional material can be changed by changing the different equivalents of the two components (between 1:0 and 0:1 ) ratio is adjusted, it is characterized in that the steps are as follows:
[0035] Step 1: Prepare the Schlenk tube, reflux the condenser, put it into a magnetic stirrer, weigh carbazole and place it in a bottle, add anhydrous tetrahydrofuran, seal it, remove oxygen from the solution through Schlenk technology, and place the reaction bottle under the protection of nitrogen atmosphere In a low-temperature reactor at -70 to -78°C, after the temperatur...
Embodiment 1
[0045] Step 1: Prepare a 100mL Schlenk tube, reflux the condenser, put it into a magnetic stirrer, weigh 0.84g of carbazole and place it in a bottle, add 10mL of anhydrous tetrahydrofuran, seal it, and remove oxygen from the solution by Schlenk technology, under the protection of nitrogen atmosphere Place the reaction bottle in a low-temperature reactor at -78°C. After the temperature of the reaction solution drops to -78°C, add 6mL of 2.5M n-butyllithium solution and react at -78°C for two hours; then add 306mg of trimeric chloride The anhydrous tetrahydrofuran solution of cyanide was slowly added dropwise to the reaction solution, and after the dropwise addition was complete, the reaction bottle was placed in an oil bath for reflux reaction for 12 hours.
[0046] Cool down to room temperature after the reaction, add 20mL of distilled water to the reaction bottle, and then stir for 2 hours. During this process, a large amount of yellow solid precipitates. Suction filtration, w...
Embodiment 2
[0054] Step 1: Prepare a 100mL Schlenk tube, reflux the condenser, put it into a magnetic stirrer, weigh 1.67g of carbazole and place it in a bottle, add 20mL of anhydrous tetrahydrofuran, seal it, and remove oxygen from the solution by Schlenk technology, under the protection of nitrogen atmosphere Place the reaction bottle in a low-temperature reactor at -78°C. After the temperature of the reaction solution drops to -78°C, add 12mL of n-butyllithium solution (2.5M n-hexane solution) and react at -78°C for two hours; Anhydrous tetrahydrofuran solution of cyanuric chloride (612 mg cyanuric chloride dissolved in 10 mL anhydrous tetrahydrofuran) was slowly added dropwise to the reaction solution, and after the addition was complete, the reaction bottle was placed in an oil bath for reflux reaction for 12 hours. Cool down to room temperature after the reaction, add 30mL of distilled water to the reaction bottle, and then stir for 2 hours. During this process, a large amount of yel...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
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