Hexafluoroaluminate of organic onium, and preparation method and application thereof
A technology of hexafluoroaluminate and organic onium, which is applied in the fields of organic chemistry, chemical instruments and methods, and compounds of Group 5/15 elements of the periodic table, etc., which can solve the problems of demanding equipment and materials, high equipment requirements, and operating procedures. Complicated issues
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Embodiment 1 4
[0063] Synthesis of the hexafluoroaluminate of embodiment 1 tetramethylammonium
[0064] Weigh 17.30g ammonium fluoroaluminate (purchased from Guangzhou Weber Chemical Company, chemically pure) in a three-necked polytetrafluoroethylene flask, feed nitrogen from the mouth of the flask while adding 240.12g of 10% analytically pure tetramethyl hydroxide Ammonium (purchased from Sinopharm Group Beijing Skiing Reagent Co., Ltd.), condensed and refluxed at 90°C, and mechanically stirred for 48 hours. After the reacted solid component was filtered off, the solvent was removed by vacuum rotary evaporation, and vacuum-dried at 80° C. for 24 hours to obtain the product tetramethylammonium hexafluoroaluminate. First, carry out Raman spectrum analysis on the obtained product, the instrument used is laser Raman spectrometer (produced in France HORIBAJOBIN YNON), Raman laser wavelength: 514nm, 785nm, Raman shift range 100-4000cm -1 , microscopic size range ≤ 1μm, spectral range: 200-1050...
Embodiment 2
[0067] Example 2 Synthesis of hexafluoroaluminate of 1,3 dimethylimidazole
[0068] Weigh 15.62g of ammonium fluoroaluminate (purchased from Guangzhou Weber Chemical Company, chemically pure) in a polytetrafluoroethylene three-necked flask, feed nitrogen from the mouth of the flask while adding 271.23g of 10% analytically pure 1,3 dimethyl The hydroxide salt of imidazole was refluxed at 90°C and mechanically stirred for 48 hours. After the reacted solid component was filtered off, the solvent was removed by rotary evaporation in vacuo, and vacuum-dried at 80° C. for 24 hours to obtain the title product.
Embodiment 3 6
[0069] Synthesis of the hexafluoroaluminate of embodiment 3 hexamethylguanidine
[0070] Weigh 11.14g ammonium fluoroaluminate (purchased from Guangzhou Weber Chemical Company, chemically pure) in a polytetrafluoroethylene three-necked flask, feed nitrogen from the flask mouth while adding 273.02g of 10% analytically pure hexamethylguanidine The hydroxide salt was refluxed at 90°C and mechanically stirred for 48 hours. After the reacted solid component was filtered off, the solvent was removed by rotary evaporation in vacuo, and vacuum-dried at 80° C. for 24 hours to obtain the title product.
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