Separable nanosheet and production method therefor
A manufacturing method and separation technology, applied in the direction of nanotechnology, nanotechnology, nanomedicine, etc., can solve problems such as difficult reformation or modification, complex synthesis process and film formation process, sheet adhesion or aggregation, etc.
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[0224] Now, the present invention is described in more detail by way of examples, but the present invention is by no means limited to the following examples.
Synthetic example 1
[0225] [Synthesis Example 1: Synthesis of α,ω-dicarboxylated polyethylene glycol-block-polypropylene glycol-block-polyethylene glycol]
[0226] α,ω-Dihydroxypolyethylene glycol-block-polypropylene glycol-block-polyethylene glycol (Pluronic (trade mark) F68; PEO 76 PPOs 29 PEOs 76 ,M w =8,400g / mol; 2.50g, 0.30mmol), 2,2,6,6-tetramethylpiperidine 1-oxyl group (TEMPO; 203mg, 1.30mmol) and sodium bromide NaBr (202mg, 1.96mmol) in 28 mL of water. Thereafter, while stirring the solution, a 5 wt % sodium hypochlorite aqueous solution was slowly added dropwise until the pH value stopped changing. The resulting aqueous solution was stirred at room temperature for an additional 10 minutes. After that, 2.5 mL of ethanol was put into the solution to quench the reaction. Then, a 6M aqueous hydrochloric acid solution was put into the solution until the pH reached 2, and the target product was extracted with 40 mL of dichloromethane. Then, the obtained methylene chloride solution was ...
Synthetic example 2
[0227] [Synthesis Example 2: Synthesis of α,ω-bisaminopolyethylene glycol-block-polypropylene glycol-block-polyethylene glycol]
[0228] Preparation of α,ω-dihydroxypolyethylene glycol-block-polypropylene glycol-block-polyethylene glycol (Pluronic (trademark) F68; PEO 76 PPOs 29 PEOs 76 ,M w =8,400 g / mol; 1 g, 0.119 mmol) in 10 mL of tetrahydrofuran, and was added dropwise to a solution of 0.212 g (1.31 mmol) of 1,1′-carbonyldiimidazole in 6.3 mL of tetrahydrofuran obtained separately. The resulting solution was further stirred overnight at room temperature, and then added dropwise to ethylenediamine (794 μL, 11.9 mmol). After the reaction was completed, tetrahydrofuran was evaporated, the resulting white solid was dissolved in water, and then purified by dialysis. After purification, water was removed by lyophilization to obtain the target product (0.92 g, 92%).
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