Copper (ii) complex constructed by ibuprofen and quinoline-8-formaldehyde Schiff base and its synthesis method and application
A synthesis method and complex technology, which is applied in the field of medicine, can solve problems such as no synthesis method and achieve good proliferation inhibitory activity
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Embodiment 1
[0039] Take the ligand L2 and [Cu(L1) of the amount (1.0mmol) of equal substance 2] placed in a 50ml round bottom flask, then add 20ml of methanol, stir at room temperature for 24h, filter, collect the filtrate in a 50ml beaker, seal with plastic wrap, then pierce small holes on the plastic wrap, volatilize at room temperature, and obtain a block after one week Dark green crystals, yield 80%.
[0040] The obtained crystal of this embodiment carries out X-ray single crystal diffraction, infrared spectrum and high-resolution mass spectrometry analysis, and its collection of illustrative plates is respectively as follows figure 1 , figure 2 with image 3 As shown, therefore, it can be determined that the blocky dark green crystals obtained are [Cu(L1)(L2)] of the present invention, wherein L1 is ibuprofen with a negative charge of one unit; L2 is quinoline- 8-Formaldehyde salicylhydrazone Schiff base, with a negative charge of one unit.
Embodiment 2
[0046] Example 1 was repeated except that the solvent was changed to ethanol. After ten days, massive dark green crystals were obtained with a yield of 78%.
[0047] Carry out X-ray single crystal diffraction, infrared spectrum and high-resolution mass spectrometry analysis to the crystal obtained in this embodiment, can confirm that the block dark green crystal of gained is [Cu(L1)(L2)] described in the present invention, wherein, L1 is ibuprofen with one unit of negative charge; L2 is quinoline-8-formaldehyde salicylhydrazone Schiff base with one unit of negative charge.
Embodiment 3
[0049] Repeat Example 1, the difference is that the solvent is changed to a mixed solvent composed of methanol and methylene chloride (volume ratio is 4:1), and the total amount of solvent used remains unchanged. One week later, massive dark green crystals were obtained with a yield of 75%.
[0050] Carry out X-ray single crystal diffraction, infrared spectrum and high-resolution mass spectrometry analysis to the crystal obtained in this embodiment, can confirm that the block dark green crystal of gained is [Cu(L1)(L2)] described in the present invention, wherein, L1 is ibuprofen with one unit of negative charge; L2 is quinoline-8-formaldehyde salicylhydrazone Schiff base with one unit of negative charge.
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