Cobalt-naphthalene ring nitrogen-oxygen free radical molecular magnet material with 6.3T coercive force and preparation method of molecular magnet material
A nitroxide radical, molecular magnet technology, applied in the fields of organic material/organic magnetic material magnetism, chemical instruments and methods, organic chemistry, etc., can solve the problems of poor sample stability, complicated operation, difficult characterization, etc. Stability, simple preparation method, and the effect of reducing information loss
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Embodiment 1
[0020] The preparation method of described cobalt-naphthalene ring nitroxide free radical molecular magnet material comprises the following steps:
[0021] 1) Synthesis of EtONapNIT:
[0022] Add 0.74g (5mmol) of 2,3-dimethyl-2,3-dihydroxyaminobutane into a 25mL round bottom flask, then add a mixed solvent of 10mL methanol and 10mL dichloromethane to dissolve, stir for 10 minutes and then add 1.00g (5mmol) of 2-ethoxy-1-naphthaldehyde was stirred for two days at 45°C under the protection of argon to obtain a light yellow oily liquid, which was evaporated under reduced pressure and dissolved in 80mL of chloroform, and placed in an ice bath Stir vigorously at low temperature for 10 minutes, add 30mL aqueous solution containing 1.1g sodium periodate to it, continue to stir in an ice bath for about 30 minutes, then carry out liquid separation, wash the water phase, dry the organic phase, and distill under reduced pressure to finally obtain deep purple Oily matter; select sherwood...
Embodiment 2
[0027] The preparation method of described cobalt-naphthalene ring nitroxide free radical molecular magnet material comprises the following steps:
[0028] 1) Synthesis of EtONapNIT:
[0029] Add 0.45g (3mmol) of 2,3-dimethyl-2,3-dihydroxyaminobutane into a 25mL round bottom flask, then add a mixed solvent of 8mL methanol and 5mL dichloromethane to dissolve, stir for 5 minutes and then add 0.65g (3.2mmol) of 2-ethoxy-1-naphthaldehyde was stirred at 30°C for 36 hours under the protection of argon to obtain a light yellow oily liquid, which was dissolved in 50mL of dichloromethane and stirred for 5 minutes under ice bath , add 30mL containing the aqueous solution of 0.65g sodium periodate wherein, continue ice-bath reaction 25 minutes, carry out liquid separation, wash water phase, dry organic phase, vacuum distillation subsequently, finally obtain dark purple oily substance; Use sherwood oil and A solvent with a volume ratio of ethyl acetate of 3:1 was used as an eluent, and t...
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