Copper complex, preparation method and application thereof
A technology of complexes and copper salts, applied in the field of copper complexes and their preparation, achieving the effects of low cost, high yield, and high purity
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Embodiment 1
[0023] Embodiment 1, the preparation of complex
[0024] 0.2g Cu(NO 3 ) 2 ·3H 2 O and 0.15g Phen were added in 30ml DMF in turn, stirring constantly. After reacting for 8 hours, filter, diethyl ether diffuse, and stand at room temperature. After a few days, blue blocky crystals can be obtained with a purity of 99%.
[0025] Elemental analysis: Calculated (exp.): C 40.77 (40.76); H 3.51 (3.50); N 15.86 (15.88). Infrared spectrum and X-ray diffraction single crystal structure diagram are shown in Fig. 1 and Fig. 2 respectively.
Embodiment 2
[0026] Embodiment 2, the preparation of complex
[0027] 0.2g Cu(CH 3 COO) 2 ·H 2 O, 0.2gNaNO 3 0.15g of Phen was sequentially added into a mixed solvent of 30ml of DMF and 10ml of methanol, and kept stirring. After reacting for 8 hours, filter, diethyl ether diffuse, and stand at room temperature. After a few days, blue blocky crystals can be obtained with a purity of 99%.
[0028] Elemental analysis: Calculated value (experimental value): C 40.77 (40.76); H 3.51 (3.50); N 15.86 (15.88), its infrared spectrum and X-diffraction single crystal structure diagram are shown in Figure 1 and Figure 2 respectively.
[0029] Similar blue block crystals can be obtained by using other copper salts (such as copper sulfate, copper chloride, copper acetate, etc.), nitrates (such as nitrate, dilute nitric acid), DMF and solvents (methanol, acetonitrile, DMSO, etc.) —that is, the copper complex of the present invention.
Embodiment 3
[0030] Embodiment 3, cell experiment
[0031] (1) Experimental group:
[0032] Adherent tumor cells (A-549 (lung cancer) cells, Bel-7402 (liver cancer) cells, HCT (colon adenocarcinoma) cells) in the logarithmic growth phase were selected, digested with trypsin, and RPM11640 with 10% calf serum The culture solution was made into a cell suspension of 5000 cells / mL, inoculated in a 96-well culture plate, and inoculated 100 μL in each well, at 37°C, 5% CO 2 Cultivate for 24h.
[0033] Add 10 μL of the sample solution obtained in Example 1 (dissolve the complex crystal obtained in Example 1 with DMSO, and then dilute with saline to a final concentration of 5 μg / mL), the final volume of each well is 200 μL, and make up with 1640 culture medium. 37°C, 5% CO 2 Culture 3d.
[0034] After culturing for 3 days, discard the supernatant, add 100 μL of freshly prepared 0.5 mg / mL MTT (thiazolium blue) serum-free culture solution to each well, continue culturing at 37°C for 4 h, discard ...
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