Electrode for active oxygen species and sensor using the electrode
A technology for reactive oxygen species and sensors, which is applied in the field of electrodes for reactive oxygen species and sensors using the electrodes, and can solve problems such as enzyme inactivation
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[0091] The present invention will be described in more detail in the following reference examples, examples and test examples, but these examples should not be regarded as limiting the present invention.
reference example 1
[0093] 5,10,15,20-tetrakis(3-thienyl)porphyrin (H 2 Synthesis of T3ThP)
[0094] A 100ml round bottom flask was charged with 50ml propionic acid, 2.0ml 3-thiopheneacetaldehyde and 1.4ml pyrrole. While stirring the mixture, it was refluxed at 160° C. for one hour. After reflux, the reaction product was cooled to room temperature, cooled with ice cubes, and 200 ml of cold methanol was added. The mixture was filtered with suction. The filtrate was washed with methanol and purified by silica gel chromatography (developing solvent: chloroform). The solvent was evaporated to dryness and the solid was recrystallized, and then dried under reduced pressure to obtain H in the form of black powder crystals. 2 T3ThP (yield: 0.63 g, 19%). The product was measured using an ultraviolet-visible spectrophotometer (UV-2100, manufactured by Shimadzu Corporation) and 1 H-NMR identification. The results are shown in Table 1 and Table 2.
reference example 2
[0096] 5,10,15,20-tetrakis(2-aminophenyl)porphyrin (H 2 Synthesis of T2AmP)
[0097] Charge 500 ml of propionic acid into a 2L four-necked flask with a reflux condenser. After adding 25 g of 2-nitrobenzaldehyde, the mixture was heated while being stirred and refluxed at 110°C. 12 ml of pyrrole were added, and the mixture was refluxed at the boiling point for 30 minutes. After adding 50 ml of chloroform, the mixture was cooled with ice and filtered off with suction. The filtrate was washed with 400ml of chloroform, and dried under reduced pressure (100°C, 6 hours, 0.1kPa), thereby obtaining the precursor 5,10,15,20-tetrakis(2-nitrophenyl ) porphyrin (H 2 T2NO 2 P) (Yield: 5.0 g, 14%).
[0098] Charge 300ml of 12N HCL into a 2L four-necked flask. After adding the above-mentioned synthetic 5,10,15,20-tetrakis(2-nitrophenyl)porphyrin (H 2 T2NO 2 P) and 20.0 g of tin(II) chloride dihydrate, the mixture was heated at 65°C-70°C for 30 minutes. Aqueous ammonia was gradually ...
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