Preparation and application of a benzimidazolium salt and its supramolecular hydrogel
A benzimidazole and hydrogel technology, applied in benzimidazolium salt compounds and their preparation, in the field of supramolecular hydrogels, can solve the problems of ion/molecular detection limitations and the like, and achieve the effect of realizing sensitive detection
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Embodiment 1
[0030] Embodiment 1, the preparation of benzimidazolium salt BI
[0031]Weigh 1.03 g (3.0 mmol) 2-undecyl-1-H-benzimidazole-3-acetic acid methyl ester, 1.27 g (9.0 mmol) methyl iodide, add to 1ml acetonitrile, and store at 85~90°C React for 30~32 h; after the reaction, cool to room temperature, remove the solvent by suction filtration, and use DMF / EtOH / H 2 O was recrystallized to obtain a white solid product, namely benzimidazolium salt BI, with a yield of 53.9%.
Embodiment 2
[0032] Embodiment 2, preparation of supramolecular organic hydrogel BI-G
[0033] Take 0.001 g of benzimidazolium salt BI prepared in Example 1, add 1.00 mL of ethylene glycol / water (v / v=1:9), heat to fully dissolve, let stand, and cool to room temperature to form a mass volume Supramolecular organohydrogel BI-G with a ratio of 1 mg / mL. The gel BI-G is white and has a transition temperature of 46°C.
Embodiment 3
[0034] Example 3. Supramolecular organic hydrogel BI-G colorimetric-fluorescent recognition of nitrite ions
[0035] Pipette supramolecular organic hydrogel BI-G into a series of drip plates, add 15 μL NaCl, NaCl 2 SO 4 , NaClO 4 , NaNO 2 , NaNO 3 , Na 3 PO 4 , NaH 2 PO 4 , NaHSO 3 , Na 2 S 2 o 3 , Na 2 HPO 4 sodium salt solution (concentration is 0.1M), if the fluorescence of the supramolecular organic hydrogel BI-G is quenched, it means that the dropwise addition is NaNO 2 , if the fluorescence of the supramolecular organic hydrogel is not quenched, it means that NaNO is not added 2 .
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