A kind of preparation method and application of Schiff base cyclic compound applied to iodine adsorption
A technology for cyclic compounds and Schiff bases is applied in the field of preparation of Schiff base cyclic compounds to achieve the effects of excellent adsorption cycle performance, simple and efficient method, and excellent iodine adsorption and storage performance.
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Embodiment 1
[0040] Add 1,8-diaminoanthracene (41.6mg, 0.2mmol), terephthalaldehyde (26.8mg, 0.2mmol), mesitylene (19mL), dioxane (1mL) and 6M aqueous acetic acid into a reaction tube (2 mL). The above-mentioned reaction tube was subjected to three freezing-vacuumizing-thawing-nitrogen gas removal operations to remove oxygen. After the reaction tube was sealed, the reaction tube was allowed to stand at 120°C for 3 days. After the reaction, it was cooled to room temperature, and the product was vacuum filtered and washed thoroughly with acetone and tetrahydrofuran. The fully washed product was vacuum-dried at 120°C for 10 hours to obtain a brick-red solid powder (53 mg, yield 86%), which was named Compound 1.
Embodiment 2
[0042] Add 1,8-diaminoanthracene (62.4mg, 0.3mmol), isophthalaldehyde (40.2mg, 0.3mmol), mesitylene (19mL), dioxane (1mL) and 6M aqueous acetic acid into a reaction tube (2 mL). The above-mentioned reaction tube was subjected to three freezing-vacuumizing-thawing-nitrogen gas removal operations to remove oxygen. After the reaction tube was sealed, the reaction tube was allowed to stand at 120°C for 3 days. After the reaction, it was cooled to room temperature, and the product was vacuum filtered and washed thoroughly with acetone and tetrahydrofuran. The fully washed product was vacuum-dried at 120°C for 10 hours to obtain a yellow solid powder (92 mg, yield 83%), which was named Compound 2.
Embodiment 3
[0044] Add 1,8-diaminoanthracene (41.6mg, 0.2mmol), 4,4'-biphenyldicarbaldehyde (42mg, 0.2mmol), mesitylene (19mL), dioxane (1mL) into the reaction tube and 6M aqueous acetic acid (2 mL). The above-mentioned reaction tube was subjected to three freezing-vacuumizing-thawing-nitrogen gas removal operations to remove oxygen. After the reaction tube was sealed, the reaction tube was allowed to stand at 120°C for 3 days. After the reaction, it was cooled to room temperature, and the product was vacuum filtered and washed thoroughly with acetone and tetrahydrofuran. The fully washed product was vacuum-dried at 120° C. for 10 hours to obtain a brick-red solid powder (58 mg, yield 75%), named compound 3.
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