Composite nanomaterial of organic naphthalene and inorganic phosphate
A technology of composite nanomaterials and inorganic phosphates, applied in the field of composite materials, to achieve the effects of good biocompatibility, excellent cell membrane permeability, and low biological toxicity
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[0060] On the other hand, the present invention provides the preparation method of the above-mentioned composite nanomaterial of organic naphthalene and inorganic phosphate of the present invention, comprising the following steps:
[0061] 1) 4-bromo-1,8-naphthoside and 4-bromoacenaphthenequinone react with L-H in a molar ratio of 1:1-1:6 to prepare compound i and compound ii;
[0062]
[0063] In a specific embodiment, the reaction temperature of the step 1) is 0-200°C, preferably 25-180°C, more preferably 50-180°C, most preferably 60-150°C; the reaction time is 1-36 hours, Preferably 1-23 hours, more preferably 1-22 hours, most preferably 1-20 hours; the reaction solvent is selected from dichloromethane, ethanol, methanol, acetone, 1,4-dioxane, glycerol, Ethyl acetate, acetic acid or mixtures thereof, more preferably dichloromethane, ethanol, methanol, 1,4-dioxane, glycerol, ethyl acetate, acetic acid or mixtures thereof, most preferably ethanol, methanol, glycerol , eth...
Embodiment 1
[0083] Composite nanomaterial A of organic naphthalene and inorganic phosphate 1 (referred to as material A 1 ), the synthetic route is as follows:
[0084]
[0085] (1) Compound A 1 Synthesis of -1
[0086] Add 20mmol of 4-bromo-1,8-naphthoside and 70mmol of diethanolamine into a round bottom flask containing 10ml of ethanol solution under nitrogen protection. The reaction was heated to reflux for 16h and then stopped. The mixture was poured into ice water, precipitated out, and suction filtered to obtain the crude product of yellow solid powder, Compound A 1 -1, yield 90%.
[0087] (2) Compound A 1 Synthesis of -2
[0088] 20mmol compound A 1 -1 and 30mmol of aminovaleric acid were added to a round bottom flask of 20ml of acetic acid solution, under nitrogen protection. The reaction was heated to reflux at 125°C for 12 hours and then stopped. The solvent was distilled off under reduced pressure and separated by column chromatography to obtain compound A as a yel...
Embodiment 2
[0098] Example 2: Material A 1 water solubility detection test
[0099] Using the material A synthesized above 1 Added to water, measured at different concentrations (0.27, 0.65, 0.86, 1.1, 1.5, 2.0, 3.0mg / mL) A 1 Absorbance at the wavelength of maximum absorption of an aqueous solution. The test result is image 3 , shows: when material A 1When the concentration is 2.0mg / mL, the absorbance value does not shift, that is, material A 1 The solubility in water is 2.0mg / mL.
[0100] The instruments used in this example are Agilent 8453 UV spectrophotometers.
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