Binuclear cobalt complex as well as preparation method and application thereof
A technology of cobalt complexes and chemical formulas, applied in the field of binuclear cobalt complexes and their preparation, to achieve significant catalytic effects, high catalytic activity and selectivity
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Embodiment 1
[0028] Take 2,6-bis((bis(pyridin-2-ylmethyl)amino)methyl)-4-methoxyphenol (0.055g, 0.01mmol) and Co(OAc) 2 4H 2 O (0.0498g, 0.02mmol) was placed in a 10mL round bottom flask, and 5mL of a mixed solvent composed of methanol and ethanol (the volume ratio of methanol and ethanol was 1:1) was added, and the pH of the system was adjusted to 8.5 with triethylamine, Afterwards, the reaction was refluxed in a water bath at 70°C for 8 hours. After the reaction was stopped, the temperature was slowly lowered to room temperature. Diethyl ether equivalent to twice the volume of the reaction solution was added to the reaction solution, and a dark brown powder was precipitated. The powder was collected and dried. Yield is 75% (0.064g, based on Co 2+ ).
[0029] The product obtained in this embodiment is characterized:
[0030] (1) Mass spectrum, its spectrum is as follows figure 1 shown.
[0031] Anion peaks showed a strong peak at 781 according to high resolution electrospray ionizati...
Embodiment 2
[0043] Repeat Example 1, except that the mixed solvent is replaced by ethanol, the pH of the system is adjusted to 7.5 with triethylamine, and the reaction is carried out in a water bath at 50°C.
[0044] The result was a dark brown powdery solid. Yield is 69% (0.059g, based on Co 2+ ).
[0045] The product obtained in this embodiment is characterized by the same method as in Example 1, and it is determined that the powdery solid obtained is the target product [(C 33 h 33 N 6 o 2 )Co 2 (CH 3 COO) 2 ](CH 3 COO)·H 2 O.
Embodiment 3
[0047] Example 1 was repeated, except that the mixed solvent was replaced with methanol, the pH of the system was adjusted to 9.5 with triethylamine, and the reaction was carried out in a water bath at 80°C.
[0048] The result was a dark brown powdery solid. Yield is 79% (0.067g, based on Co 2+ ).
[0049] The product obtained in this embodiment is characterized by the same method as in Example 1, and it is determined that the powdery solid obtained is the target product [(C 33 h 33 N 6 o 2 )Co 2 (CH 3 COO) 2 ](CH 3 COO)·H 2 O.
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