Cathodic electrochromic compound, and relevant medium and device thereof
An electrochromic and electrochromic device technology, applied in color-changing fluorescent materials, chemical instruments and methods, organic chemistry, etc., can solve the problem of single color change of viologen compounds
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Embodiment 1
[0059] (1) synthesize the cathodic electroactive compound of following structural formula:
[0060]
[0061] The synthetic route and operation steps are as follows:
[0062]
[0063] Step 1: Disperse NaOH (20mmol) in polyethylene glycol (200mL) with an average molecular weight of 300g / mol, then add 4-acetylpyridine (20mmol) and 3,4-dimethoxy in sequence at 0°C Base benzaldehyde (10mmol), and react 2h at 0 ℃;
[0064] The second step: add ammonium acetate (0.5mol) to the reaction system obtained in the first step, and then incubate at 100° C. for 2 hours, during which precipitation gradually occurs;
[0065] Step 3: Add 500 mL of deionized water to the reaction system in the second step, and filter to obtain a precipitate. The obtained precipitate was washed with water and a small amount of ethanol in sequence, and dried under vacuum at 50°C for 12 hours to obtain the intermediate product 4;
[0066] Step 4: Take 4 mmol of the intermediate product 4 and dissolve it in ...
Embodiment 2
[0073] (1) synthesize the cathodic electroactive compound of following structural formula:
[0074]
[0075] The synthetic route and operation steps are as follows:
[0076]
[0077] Step 1: Disperse NaOH (20mmol) in polyethylene glycol (200mL) with an average molecular weight of 300g / mol, then add 4-acetylpyridine (20mmol) and 4-pyridinecarbaldehyde (10mmol) in sequence at 0°C , and react at 0°C for 2h;
[0078] The second step: add ammonium acetate (0.5mol) to the reaction system obtained in the first step, and then incubate at 100° C. for 2 hours, during which precipitation gradually occurs;
[0079] Step 3: Add 500 mL of deionized water to the reaction system in the second step, and filter to obtain a precipitate. The obtained precipitate was washed with water and a small amount of ethanol in sequence, and dried under vacuum at 50° C. for 12 hours to obtain the intermediate product 9;
[0080]Step 4: Dissolve 4 mmol of intermediate product 9 in 20 mL of acetonitri...
Embodiment 3
[0087] (1) synthesize the cathodic electroactive compound of following structural formula:
[0088]
[0089] The synthetic route and operation steps are as follows:
[0090]
[0091] The intermediate product 9 was obtained according to the first three steps of Example 2; 4 mmol of the intermediate product 10 was dissolved in 20 mL of acetonitrile solvent, and 20 mmol of bromoheptane was added, and the reaction was refluxed for 8 h. After the reaction, the solid was obtained by filtration, that is, the intermediate product 12; the intermediate product 12 was dissolved in deionized water, and then sodium tetrafluoroborate (20 mmol) was added to precipitate a precipitate, which was washed with water and dried to obtain the target product 13.
[0092] (2) Preparation of electrochromic device:
[0093] Dissolve the target product 13 in dimethylformamide according to the concentration of 50mmol / L and 2-tert-butyl-5,10-dihydro-5,10-dimethylphenazine according to the concentrat...
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