Electrochemical sensor based on CoCuCdTCPP coordination polymer modification and preparation method and application thereof
A coordination polymer and electrochemical technology, applied in the direction of material electrochemical variables, etc., can solve the problems of limiting the use range of sensors and poor stability, and achieve the effect of widening the use range, low cost and good stability
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[0054] An electrochemical sensor modified based on CoCuCdTCPP coordination polymer and its preparation method and application, comprising the following steps:
[0055] The first step: Synthesis of metal TCPP coordination polymers, including Cu1Cd3TCPP, Cu2Cd2TCPP, Cu3Cd1TCPP, Co1Cd3TCPP1, Co2Cd2TCPP, Co3Cd1TCPP, CuCoCdTCPP;
[0056] The second step: modify the synthesized coordination polymer electrode: dissolve the synthesized metal TCPP coordination polymer in twice distilled water, and ultrasonically disperse to obtain a suspension; apply the suspension dropwise and polish it through a polishing cloth to The mirror surface was ultrasonically cleaned in double-distilled water and ethanol, and the surface of the glassy carbon electrode after drying was dried, and placed to dry at room temperature, and then fixed by dropping naphthol solution on the surface of the polymer, and air-dried at room temperature for later use to obtain a polymer matter / glassy carbon electrode; if ca...
Embodiment 1
[0061] Ligand H 2 TCPP synthesis:
[0062] Heat 160mL of propionic acid to boiling, then rapidly add pyrrole (1.38mL, 20mmol) and methyl p-formylbenzoate (3.28g, 20mmol) to the solvent in sequence, and the reaction is refluxed for 2h. After cooling down to room temperature, let stand to cool overnight. The reaction mixture was suction-filtered, washed with absolute ethanol until the filtrate was colorless, and dried to obtain a dark purple solid as H 2 TCPP-OMe crude product. Recrystallization method (CHCl 3 :methanol=1:3) to obtain pure H 2 TCPP-OMe.
[0063] Will and H 2 TCPP-OMe or (904mg, 0.1mmol) was dissolved in 30mL tetrahydrofuran solution, then 30mL NaOH aqueous solution (0.1M) was added to the reaction system, and reacted at 50°C for 48 hours. After cooling, tetrahydrofuran was removed by rotary evaporation, and the pH value of the solution was adjusted to about 2 with 0.1M HCl(aq) at room temperature. Buchner funnel suction filtration to obtain a purple soli...
Embodiment 2
[0081] Coordination polymer modified GCE and MWCNTs / GCE
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