Preparation method of ferrocene-based conjugated microporous polymer
A conjugated microporous and ferrocene-based technology, which is applied in the field of preparing ferrocenyl-based conjugated microporous polymer polymer materials, can solve the problems of ferrocenyl-based conjugated microporous materials and achieve good results. Effects of chemical and thermal stability, high BET surface area, and high pore volume
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Embodiment 1
[0018] In a 100mL three-necked flask equipped with an argon gas line, magnetic stirring and condenser, add 0.298g 1,3,6,8-tetraacetylene pyrene, 0.488g 1,1'-dibromoferrocene, 25mg tetrakis(tri phenylphosphine) palladium(0), 25 mg cuprous iodide, 1.5 ml N,N-dimethylformamide and 1.5 ml triethylamine. After ultrasonic dispersion for 30 minutes, fill with nitrogen, freeze with liquid nitrogen for 10 minutes, pump air for 30 minutes with a vacuum pump, and thaw for 2 hours, and cycle three times. Slowly raise the temperature to 65°C within 2h and keep the temperature constant for 72h. After the reaction, it was cooled to room temperature, filtered, and washed three times with chloroform, distilled water, methanol, and acetone. Soxhlet extraction with methanol for 48h. The product was dried in a vacuum oven at 70°C for 24 h. The specific surface area of the product is 585m 2 / g, the pore volume is 1.2cm 3 / g.
Embodiment 2
[0020] In a 100mL three-necked flask with an argon line, magnetic stirring and condenser, add 0.57g 2,2′-bipyridine , 1g bis(1,5-cyclooctadiene)nickel(0), 0.45ml1,5-cyclooctadiene, 0.488g1,1'-dibromoferrocene, 0.517g1,3,6,8- Tetrabromopyrene, 36ml tetrahydrofuran and 24ml N,N-dimethylformamide. After ultrasonic dispersion for 30 minutes, fill with nitrogen, freeze with liquid nitrogen for 10 minutes, pump air for 30 minutes with a vacuum pump, and thaw for 2 hours, and cycle three times. Slowly raise the temperature to 65°C within 2h and keep the temperature constant for 72h. After the reaction, it was cooled to room temperature, filtered, and washed three times with chloroform, distilled water, methanol, and acetone. Soxhlet extraction with methanol for 48h. The product was dried in a vacuum oven at 70°C for 24 h. The specific surface area of the product is 625m 2 / g, the pore volume is 1.35cm 3 / g.
Embodiment 3
[0022] In a 100mL three-necked flask with an argon line, magnetic stirring and condenser, add 0.57g 2,2′-bipyridine , 1g bis(1,5-cyclooctadiene)nickel(0), 0.45ml 1,5-cyclooctadiene, 0.488g 1,1'-dibromoferrocene, 0.636g tetrakis(4-bromophenyl ) methane, 10ml mesitylene, 26ml dioxane and 24ml N,N-dimethylformamide. After ultrasonic dispersion for 30 minutes, fill with nitrogen, freeze with liquid nitrogen for 10 minutes, pump air for 30 minutes with a vacuum pump, and thaw for 2 hours, and cycle three times. Slowly raise the temperature to 65°C within 2h and keep the temperature constant for 72h. After the reaction, it was cooled to room temperature, filtered, and washed three times with chloroform, distilled water, methanol, and acetone. Soxhlet extraction with methanol for 48h. The product was dried in a vacuum oven at 70°C for 24 h. The specific surface area of the product is 515m 2 / g, the pore volume is 1.05cm 3 / g.
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