Cobalt complexes constructed based on 8-methoxyquinoline as well as preparation methods of two complexes and application of one complex
A technology of methoxyquinoline and cobalt complexes, which is applied to cobalt organic compounds, compounds containing elements of group 8/9/10/18 of the periodic table, organic chemical methods, etc., achieving good repeatability and simple synthesis methods easy to control effect
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Embodiment 1
[0024] 1.1 Reagents used in the experiment
[0025] All reagents used in this experiment were of AR grade and were used directly without further purification. The reagents used are 8-methoxyquinoline (analytical pure), acetonitrile (analytical pure), anhydrous methanol (analytical pure), sodium thiocyanate (analytical pure).
[0026] 1.2 Test equipment
[0027] Elemental analysis for C, H and N was performed on a Vario Micro Cube. Thermogravimetric analysis (TGA) was performed using a NETZSCH TG 209F3 at a heating rate of 10°C / min in a nitrogen flow. By using PE Spectrum FT-IR spectrometer (400-4000cm -1 ) to test the infrared spectrum of the complex containing 0.5% of KBr particles. Magnetic susceptibility measurements were performed over the temperature range 2-300K using a QuantumDesign MPMS SQUID-XL-5 magnetometer equipped with a 5T magnet; the diamagnetic correction of these complexes was estimated using Pascal's constant and corrected for the diamagnetic contribution...
Embodiment 2
[0067] The preparation method of the complex Co1 in Example 1 was repeated, except that the reaction temperature was changed to 50°C. As a result, purple crystals were obtained. Yield 58% (based on Co(OAc) 2 4H 2 O). The obtained product was analyzed by single crystal diffraction, and the obtained purple crystal was determined to be the target product complex Co1.
[0068] The preparation method of the complex Co2 in Example 1 was repeated, except that the reaction temperature was changed to 50°C. As a result, red crystals were obtained. Yield 45% (based on Co(OAc) 2 4H 2 O). The obtained product was analyzed by single crystal diffraction, and the obtained red crystal was determined to be the target product complex Co2.
Embodiment 3
[0070] The preparation method of complex Co1 in Example 1 was repeated, except that potassium thiocyanate was used instead of sodium thiocyanate, and the reaction temperature was changed to 80°C. As a result, purple crystals were obtained. Yield 53% (based on Co(OAc) 2 4H 2 O). The obtained product was analyzed by single crystal diffraction, and the obtained purple crystal was determined to be the target product complex Co1.
[0071] The preparation method of the complex Co2 in Example 1 was repeated, except that sodium thiocyanate was replaced with potassium thiocyanate, and the reaction temperature was changed to 80°C. As a result, red crystals were obtained. Yield 41% (based on Co(OAc) 2 4H 2 O). The obtained product was analyzed by single crystal diffraction, and the obtained red crystal was determined to be the target product complex Co2.
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