Electrochemiluminescent reagent prepared from a macrocyclic compound and its application
A macrocyclic compound, electrochemical technology, applied in the field of electrochemiluminescence, can solve the problems of long time consumption, high analysis cost, difficult sample preparation, etc., and achieve the effect of short time consumption and simple operation.
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Embodiment 1
[0031] A macrocyclic compound, the chemical formula of the macrocyclic compound is C 60 h 60 N 12 o 6 , whose structural formula is:
[0032]
[0033] The synthetic method of described macrocyclic compound is synthesized according to the following steps:
[0034] (1) 2-hydroxybenzimidazole (2g, 0.015mol), tetrabutylammonium bromide (0.24g, 0.75mmol), toluene 50mL, 40% sodium hydroxide solution 20mL and iodomethane (2mL, 0.032mol) , heated at 60-80°C for 19 hours to obtain product A;
[0035] (2) Mix product A, hydrochloric acid solution and formic acid to obtain product B;
[0036] (3) adding concentration to product B is 40% formaldehyde solution, stir evenly, obtain product C;
[0037] (4) Product C was stirred at room temperature for 5 hours, a white precipitate appeared, and product D was obtained;
[0038] (5) Product D was filtered by suction, washed with methanol and dichloromethane successively, and dried to obtain a white solid.
[0039] Described hydrochlo...
Embodiment 2
[0045] (1) Prepare 1.0×10 with acetonitrile -5 mol / l, 1.0×10 -6 mol / l…1.0×10 -14 mol / l, 1.0×10 - 15 mol / l equal concentration of the above-mentioned various condensed ring aromatic hydrocarbon solutions;
[0046] (2) Stir the glassy carbon electrode modified with the macrocyclic compound with the condensed ring aromatic hydrocarbons in the above step (1) for 25 minutes at room temperature, dry and set aside;
[0047] (3) Measure the electrode to be used in the above step (2) in an electrochemiluminescence tester;
[0048] (4) Graphing the data completed by the measurement, the results are shown in figure 2 ,in figure 2 (b), it was found that the electrochemiluminescence of the macrocyclic compound was not completely quenched by the 9.10-triphenylene triphenylene guest, and all other guests were completely quenched.
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