A kind of supercapacitor of manganese porphyrin compound, preparation method and application thereof
A technology of supercapacitor and manganese porphyrin, applied in the field of supercapacitor, can solve the problems of high cost, cumbersome process, easy sublimation and loss of ferrocene, etc., and achieve the effect of improving performance, good cycle stability and excellent redox characteristics
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[0034] The reagents used in the following preparation methods include:
[0035] 5,10,15,20-tetrakis(4-hydroxyphenyl)porphine [meso-Tetra(p-hydroxyphenyl)porphine, THPP] was purchased from Bailingwei Technology Co., Ltd. and used directly.
[0036] 11-Bromo-n-undecyl ferrocene, self-made in the laboratory.
[0037] Anhydrous potassium carbonate (purity 99%) and 18-crown-6 (18-Crown-6, purity 99%) were purchased from MACKLIN Company and used directly.
[0038]Manganese acetate hydrate, N,N-dimethylformamide (DMF), dichloromethane, methanol, petroleum ether, hydrochloric acid, analytically pure, were purchased from Guangzhou Chemical Reagent Factory and used directly.
[0039] Nickel foam, polytetrafluoroethylene emulsion, and acetylene carbon black were purchased from Lizhiyuan Battery Sales Department, Yingze District, Taiyuan.
[0040] All experimental water was deionized water.
[0041] The invention provides a specific preparation method of four-p-ferrocenyl undecyloxyphe...
Embodiment 1
[0048] In the first aspect, this embodiment provides a tetrakis-p-ferrocenyl undecyloxyphenyl manganese porphyrin compound, the chemical structural formula of which is as follows:
[0049]
[0050] In a second aspect, this embodiment provides a method for preparing four-p-ferrocenyl undecyloxyphenyl manganese porphyrin compound (such as figure 1 ), including:
[0051] Step 1, synthesis of four-p-ferrocenyl undecyloxyphenyl porphyrin: 40.5 mg of four-p-hydroxyphenyl porphyrin of 0.06 mmol, 11-bromo-n-undecyl ferrocene of 0.24 mmol Add 100.0mg, 2.40mmol of anhydrous potassium carbonate 330.0mg, 0.048mmol of 18-crown-6 to 12.7mg, and 20mL of anhydrous N,N-dimethylformamide into a 100mL three-necked flask, Stir mechanically under protection for 30 minutes, heat up to 85°C and react for 6 hours, and distill off the solvent under reduced pressure to obtain a crude product of tetrakis-p-ferrocenylundecyloxyphenylporphyrin; further purify by column chromatography, Obtain 90 mg of...
Embodiment 2
[0056] Compared with Example 1, the reagent consumption and experimental conditions used in the preparation method of four-p-ferrocenyl undecyloxyphenyl manganese porphyrin compound are different, specifically including:
[0057] Step 1. Synthesis of tetra-p-ferrocenyl undecyloxyphenyl porphyrin: 0.12 mmol of tetra-p-hydroxyphenyl porphyrin 81 mg, 0.72 mmol of 11-bromo-n-undecyl ferrocene 300.0 mg, 7.20mmol of anhydrous potassium carbonate 990.0mg, 0.096mmol of 18-crown-6, 25.4mg, and 50mL of anhydrous N,N-dimethylformamide were added to a 100mL three-necked flask, under argon protection Under mechanical stirring for 240 minutes, the temperature was raised to 85 ° C and reacted for 24 hours, and the solvent was distilled off under reduced pressure to obtain a crude product of four-p-ferrocenyl undecyloxyphenylporphyrin; further purified by column chromatography to obtain 180 Four-p-ferrocenyl undecyloxyphenylporphyrin;
[0058] Step 2, synthesis of tetra-p-ferrocenyl undecylo...
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