A stimulus-responsive helical polyyne infrared radiation material and its preparation method
An infrared radiation and responsive technology, which is applied in the preparation of organic functional polymer materials and the field of infrared stealth materials, can solve the problems of large thickness, low emission colored pigment molecular design difficulty, high infrared emissivity, etc., and achieve mild reaction conditions , good thermal stability and controllability of infrared radiation performance, and the effect of simple preparation process
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
example 1
[0025] a) Under ice bath, 1.73g (S)-2-(6-hydroxyl-2-naphthalene)propionic acid, 1.51g isobutyl chloroformate, 1.01g N-methylmorpholine were added to a tank containing 50mL tetrahydrofuran In the reaction kettle, after 15 minutes of reaction, add 10 mL of propargylamine tetrahydrofuran solution with a concentration of 0.8 mol / L dropwise into the mixed solution. After 15 minutes of dropwise addition, continue the reaction at 30°C for 12 hours, filter, and distill off the tetrahydrofuran under reduced pressure at 60°C. Then extract with 30mL ethyl acetate each time, combine the extracts 3 times to get the extraction mixture, and successively use 25mL of hydrochloric acid aqueous solution with a mass fraction of 2wt%, 25mL of saturated NaHCO 3 aqueous solution and 25mL saturated NaCl aqueous solution to wash the extract, and the obtained extract was washed with 2.2g of anhydrous MgSO 4Dry for 12 hours, filter, and distill the filtrate to remove ethyl acetate under reduced pressure...
example 2
[0032] a) Under ice bath, 2g (S)-2-(6-hydroxyl-2-naphthalene)propionic acid, 1.8g isobutyl chloroformate, 1.4g N-methylmorpholine were added to the tank containing 100mL tetrahydrofuran solution React in the reaction kettle for 20min, then add 30mL propargylamine tetrahydrofuran solution with a concentration of 1.2mol / L dropwise to the mixed solution, after 20min dropwise, react the reaction mixture at 30°C for 20h, filter, and depressurize at 50°C THF was distilled off, and then extracted with 30 mL of ethyl acetate each time, and the extracts were combined three times to obtain an extraction mixture, which was successively washed with 30 mL of aqueous hydrochloric acid solution with a mass fraction of 3 wt%, and 30 mL of saturated NaHCO 3 aqueous solution and 30mL saturated NaCl aqueous solution to wash the extract, and the obtained extraction mixture was washed with 2g of anhydrous MgSO 4 Dry for 12 hours, filter, distill the filtrate under reduced pressure at 40°C to remov...
example 3
[0039] a) Under ice bath, 1.50g (S)-2-(6-hydroxy-2-naphthalene)propionic acid, 1.37g isobutyl chloroformate, 0.81g N-methylmorpholine were added to a tank containing 40mL tetrahydrofuran In the reaction kettle, after 25 minutes of reaction, add 10 mL of propargylamine tetrahydrofuran solution with a concentration of 1.00 mol / L dropwise into the mixed solution. After 25 minutes of dropwise addition, continue the reaction at 30°C for 18 hours, filter, and distill off the tetrahydrofuran under reduced pressure at 55°C. Then extract with 20mL ethyl acetate each time, combine the extracts 3 times to obtain the extraction mixture, and successively use 20mL of hydrochloric acid aqueous solution with a mass fraction of 2wt%, 20mL of saturated NaHCO 3 aqueous solution and 20mL saturated NaCl aqueous solution to wash the extract, and the washed extract mixture was washed with 3.6g of anhydrous MgSO 4 Dry at 25°C for 12h, filter, evaporate the filtrate to remove ethyl acetate under redu...
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