Amphiprotic lanthanum carboxylate metal organic framework and synthesis method thereof, and application of amphiprotic lanthanum carboxylate metal organic framework
A metal-organic framework, amphoteric carboxylic acid technology, applied in biochemical equipment and methods, microbial determination/inspection, etc., can solve problems such as application research limitations, MOFs framework collapse, etc.
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Embodiment 1
[0027] A kind of amphoteric lanthanum carboxylate metal organic framework, its chemical formula is {[La 4 (Cmdcp) 6 (H 2 O) 9 ]} n (1) (n represents the degree of aggregation, which is a natural number).
Embodiment 2
[0029] The preparation reaction formula of complex of the present invention is as follows:
[0030]
[0031] Specific steps are as follows:
[0032] a. Weigh the solid H according to the amount of the substance 3 CmdcpBr (91.5 mg, 0.3 mmol) was suspended in MeOH (5 mL) solution, and the pH was adjusted to 7.0 with 0.1 mM NaOH solution to obtain a clear solution.
[0033] b. Weigh the solid La(NO 3 ) 3 ·6H 2 O (86.6 mg, 0.2 mmol) was dissolved in MeOH solution (5 mL) to give a clear solution of the lanthanum salt.
[0034] c, the molar ratio of 2:3 La(NO 3 ) 3 ·6H 2 O solution was added dropwise to H 3 In the clear solution of CmdcpBr, the reaction was stirred at room temperature for 0.5h, and a large amount of white precipitates appeared in the reaction.
[0035] d, the precipitate is filtered, and the precipitate is washed with MeOH (5mL), and the white precipitate is washed with H 2 O (100 mL) was dissolved at 100 °C and filtered to obtain a clear solution.
[...
Embodiment 3
[0052] Compound {[La 4 (Cmdcp) 6 (H 2 O) 9 ]} n (1) Detect HIVds-DNA and SUDVRNA experiment (obtain compound in embodiment 1)
[0053] (1) Preparation of compound 1 solution
[0054] Compound 1 was dissolved in distilled water to prepare a solution with a concentration of 0.1mM, sealed and stored at room temperature; 2 ) to dissolve DNA and RNA to a concentration of 0.1 mM, seal and store in a refrigerator.
[0055] (2) Detection of HIVds-DNA and SUDVRNA experiments
[0056] Dilute the probe DNA solution with a buffer solution to a concentration of 50nM, take 2mL of the solution and put it into a cuvette with a capacity of 4mL. After adjusting the parameters of the fluorometer, test the initial fluorescence intensity of the solution. A certain amount of compound solution was added to the solution, and after stirring for a period of time, the fluorescence intensity of the mixed solution was tested. The compound was continuously added and tested until the fluorescence in...
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