Zinc and cobalt metal complex taking nantenine oxide as ligand as well as synthetic method and application thereof
A technology of Nandina and a synthesis method, applied in the fields of cobalt metal complexes and their synthesis, and zinc, can solve problems such as unseen and blank research reports, and achieve the effects of good medicinal value and strong anti-tumor activity.
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Embodiment 1
[0037] Embodiment 1: Synthesis of ONT-Zn (Ⅱ) complexes with normal pressure solution method
[0038] 1mmol Zn(NO 3 ) 2 .6H 2 O and 2mmol of ONT were dissolved in 20mL of methanol solution, and reacted at 65°C (reflux) for 10h, the solution gradually changed from yellow to reddish brown, and a large amount of complex solids were formed; after cooling and filtering the solution, followed by water , washing and filtering the obtained solid with ethanol, and drying to finally obtain a red solid product, yield: 67%. The product is subjected to infrared spectroscopy (the spectrogram is as figure 1 shown), electrospray mass spectrometry (spectrum as shown in figure 2 shown) and X-ray single crystal diffraction analysis (spectrum as image 3 Shown) for structure determination, identified as the target complex [Zn(ONT) 2 (CH 3 OH)(NO 3 )] NO 3 .
Embodiment 2
[0039] Example 2: Synthesis of ONT-Co(II) complexes by normal pressure solution method
[0040] 1mmol Co(ClO 4 ) 2 .6H2 O and 2 mmol of ONT were dissolved in 40 mL of a mixed solution of ethanol and dimethyl sulfoxide (volume ratio 4:5), and reacted at 80°C (reflux for condensation) for 24 hours. After the reaction, a red suspension was obtained with a large amount of The complex solid was formed; the solution was filtered, the filtered solid was washed with water and ethanol in turn, and dried to finally obtain a red solid product with a yield of 71%. The product is subjected to infrared spectroscopy (the spectrogram is as Figure 4 shown), electrospray mass spectrometry (spectrum as shown in Figure 5 shown) and X-ray single crystal diffraction analysis (spectrum as Image 6 Shown) for structure determination, identified as the target complex [Co(ONT) 2 (H 2 O) 2 ](ClO 4 ) 2 .
Embodiment 3
[0041] Embodiment 3: Synthesis of ONT-Zn (Ⅱ) complex with solvothermal method
[0042] Weigh 0.1mmol Zn(NO 3 ) 2 .6H 2 O and 0.2 mmol ONT were placed in a thick-walled borosilicate glass tube with an open end, and then 1.5 mL of a mixed solvent of ethanol and water (volume ratio 1:2) was added. Melting and sealing, and then fully reacting at 110°C for 12 hours, a red crystalline solid product can be obtained, with a yield of 53%. The product was determined to be the target complex [Zn(ONT) 2 (CH 3 OH)(NO 3 )] NO 3 .
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