A kind of schiff base polymer and its synthetic method and application
A synthesis method and polymer technology, applied in electrical components, electrochemical generators, battery electrodes, etc., can solve the problems of unsatisfactory voltage of positive and negative materials, low working voltage, low energy density, etc., and achieve excellent redox reversibility. performance and electrochemical stability, low equilibrium electrode potential, high working voltage effect
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Embodiment 1
[0035] Embodiment 1, the present embodiment synthesizes Schiff base polymer, and the steps are as follows:
[0036] (1) Synthesize 4,4',4"-trialdehyde substituted triphenylamine according to the prior art, the synthetic route is as follows:
[0037]
[0038] Specifically include the following steps:
[0039] (1.1) Preparation of 4,4'-dialdehyde-substituted triphenylamine
[0040] Weigh 10.001g of triphenylamine into a 250mL two-necked flask, then add 41.0mL of DMF, and stir. The flask was placed in an ice-water bath (guaranteed at 0°C), protected by argon. Add 37.5 mL of POCl into the constant pressure separatory funnel with a syringe 3 , open the constant pressure funnel, control the flow rate, POCl 3 Slowly added dropwise to a two-necked flask, and stirred for 1 hour.
[0041] The oil change pan was heated to 105°C and stirred for 4 hours. After cooling to room temperature, it was slowly added to ice water with stirring, the system was black, and a brown solid was p...
Embodiment 2
[0071] Example 2: In this example, the Schiff base polymer prepared in Example 1 is used as the negative electrode material of the battery, and polytriphenylamine is used as the positive electrode material to prepare a high-voltage organic polymer full battery with a voltage of 3V. The steps are as follows:
[0072] (1) According to the existing technology, polytriphenylamine is synthesized.
[0073] To match the negative electrode, polytriphenylamine was used as the positive electrode. Polytriphenylamine was synthesized with reference to the method in the literature. The specific process was: 0.025mol (~6.1g) triphenylamine was dissolved in 100mL of anhydrous chloroform; under the protection of argon, the total amount of 0.1mol (~16.22 g) anhydrous ferric chloride, add once every hour; and continue to react for 2 hours. The reaction mixture was poured into methanol and the product precipitated out. The crude product was dissolved in chloroform, filtered, the filtrate was co...
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