Nano-layered compound with regular arrays of amino acid and preparation method thereof
A technology for layered compounds and amino acids, which is applied in the fields of compounds of Group 4/14 elements of the periodic table, chemical instruments and methods, organic chemistry, etc. problems such as the layered nanospace environment
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Embodiment 1
[0090] Preparation of natural (L-type) and racemic (DL-type)-p-amino acid succinamide phenyl silica layered compound (A);
[0091] (1) Prepare p-aminophenyl silicon oxide-dodecylsulfate layered compound in advance; its preparation method is: first dissolve 2.88mmol of sodium laurylsulfate into 250ml of deionized water, then add 2.74mmol of p-aminophenyltrimethoxysilane, then slowly drop 0.5mol / L hydrochloric acid to adjust the pH value of the mixed solution to 2.07, and magnetically stir at room temperature for 12 days to carry out the sol-gel process; Washing with deionized water and acetylene, and drying in vacuum to obtain p-aminophenyl silicon oxide-dodecylsulfuric acid layered structure compound;
[0092] In order to prove the chemical and three-dimensional structure of p-aminophenyl silica-dodecylsulfuric acid nanocomposite layered structure, a series of analytical experiments were carried out. Firstly, octaalkyl sulfate anion is used, and chloride anion carries out anion...
Embodiment 2
[0110] Preparation of natural (L-type) and racemic (DL-type)-p-amino acid butenediamide phenyl silica layered compound (C);
[0111] (1) Prepare p-aminophenyl silicon oxide-dodecylsulfuric acid layered compound in advance; its preparation method is the same as (1) step in the above-mentioned embodiment 1;
[0112] (2) Disperse 0.1mol of p-aminophenyl silica-dodecyl sulfuric acid in 50ml of THF, then add 0.5mol of butenedioic anhydride, heat to 50°C, and stir magnetically for 1 day; Washing with ethanol, drying in vacuo, the final product p-carboxyacrylamide phenyl silicon oxide layered compound;
[0113] Carry out infrared spectroscopic analysis to the product, the alkyl group of dodecylsulfuric acid is in 2700 to 3000cm -1 The peak disappears in the infrared spectrum of p-carboxyacrylamide phenyl silicon oxide compound. It can be seen that there is no dodecylsulfuric acid present in the p-carboxypropionamidophenyl silicon oxide compound. In addition, two new peaks at 1700 ...
Embodiment 3
[0120] Preparation of natural (L-type) and racemic (DL-type)-p-amino acid glutaramide phenyl silica layered compound (D);
[0121] (1) Prepare p-aminophenyl silicon oxide-dodecylsulfuric acid layered compound in advance; its preparation method is the same as (1) step in the above-mentioned embodiment 1;
[0122] (2) Disperse 0.1mol of p-aminophenyl silica-dodecylsulfuric acid in 50ml of THF, then add 0.5mol of glutaric anhydride, heat to 50°C, and stir magnetically for 1 day; finally filter with ethanol Washing, drying in vacuo, the final product p-carboxybutyramide phenyl silicon oxide layered compound;
[0123] Infrared and 13 C CP / MAS NMR analysis, obtained similar to Figure 5 and 6 the infrared and 13 The CCP / MAS NMR spectrum proves that one carbonyl group in glutaric anhydride reacts with the amino group in p-aminophenyl silica-dodecylsulfuric acid to form an amide, while the other carbonyl group in glutaric anhydride is transformed into a carboxylic acid group, thu...
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