A kind of ionic microporous polymer catalyst and its preparation method and application
A microporous polymer and catalyst technology, which is applied in physical/chemical process catalysts, organic compound/hydride/coordination complex catalysts, separation methods, etc. and other problems to achieve the effect of high dispersion density
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Embodiment 1
[0045] Embodiment 1: the preparation of catalyst cat-Al-Zn
[0046] Preparation of tetraimidazole-based aluminum monomer: imidazole (4.2mmol, 0.29g), aluminum trichloride (1mmol, 133.4mg) were dissolved in 30ml of methanol, stirred at 30°C for 12 hours, methanol was removed, suction filtered, rinsed with THF, and dried , to obtain the monomer 1-Al.
[0047] Preparation of tetraimidazole-based zinc monomer: imidazole (4.2mmol, 0.29g), zinc chloride (1mmol, 136.3mg) were dissolved in methanol, stirred at 30°C for 12 hours, methanol was removed, suction filtered, rinsed with THF, dried to obtain Monomer 1-Zn.
[0048] 1-Al (1mmol, 0.41g), 1-Zn (1mmol, 0.41g) was dissolved in 25ml of NMP, and 1,4-p-dichlorobenzyl (5mmol, 0.9g) or 1,4-p-dibromobenzyl was added, Stir at 80°C for 30h, stop the reaction, cool to room temperature, filter with suction, and wash with CH 2 Cl 2 and CH 3 OH washing solid, Soxhlet extraction for 30h (extraction solution is CH 2 Cl 2 with CH 3 OH vol...
Embodiment 2
[0051] Preparation of tetraimidazole-based cobalt monomer: imidazole (4.2mmol, 0.29g), cobalt acetate (1mmol, 177.0mg) were dissolved in methanol 30ml, stirred at 30°C for 12 hours, methanol was removed, suction filtered, rinsed with THF, dried to obtain Monomer 1-Co.
[0052] Preparation of tetraimidazole-based zinc monomer: imidazole (4.2mmol, 0.29g), zinc chloride (1mmol, 136.3mg) were dissolved in methanol, stirred at 30°C for 12 hours, methanol was removed, suction filtered, rinsed with THF, dried to obtain Monomer 1-Zn.
[0053]1-Co (1mmol, 0.45g), 1-Zn (1mmol, 0.41g) was dissolved in 25ml of NMP, and 1,4-p-dichlorobenzyl (5mmol, 0.9g) or 1,4-p-dibromobenzyl was added, Stir at 80°C for 30h, stop the reaction, cool to room temperature, filter with suction, and wash with CH 2 Cl 2 and CH 3 OH washing solid, Soxhlet extraction for 30h (extraction solution is CH 2 Cl 2 with CH 3 OH volume ratio of 1.5:1 mixture), and finally vacuum-dried at 70°C for 12 hours to obtain...
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