Hydrogen sulfide recognition and detection fluorescent probe, preparation method and applications thereof
A fluorescent probe and hydrogen sulfide technology, applied in the field of chemical analysis, can solve the problems of inability to detect hydrogen sulfide, and achieve the effect of fast response and good water solubility
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Embodiment 1
[0031] Preparation of compounds of general formula (1):
[0032]
[0033] Follow the steps below:
[0034] 1) Preparation of compound L2-1:
[0035]
[0036] Dissolve DMF (2.1mL, 27.3mmol) in 5mL of dichloromethane, and slowly add phosphorus oxychloride (2.3mL, 25mmol) in dichloromethane solution dropwise at 0°C, compound A (1.65g, 12.4mmol) Dichloromethane solution was added dropwise to the above solution, and refluxed at 45°C for 6h. The reaction was cooled to room temperature, 5M NaOH solution was added under an ice-water bath to adjust the pH to 8, the layers were separated, the organic layer was washed 3 times with saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and passed through a neutral alumina column (PE:EA= 8:1), to obtain 1.35 g of bright yellow solid L2-1 with a yield of 53%. LC-MS (ESI) m / z: 207.1 [M] + ;
[0037] 2) Preparation of compound L2-2:
[0038]
[0039] Compound L2-1 (898mg, 5mmol) was dissolved in NaOH in eth...
Embodiment 2
[0056] Example 2 Changes in the ultraviolet absorption spectrum of the probe (1) in response to hydrogen sulfide
[0057] Add 3 mL of PBS (10 mM, pH 7.4) to the quartz cuvette for zero baseline adjustment, then add 10 μL of L2-B acetonitrile stock solution to make the final concentration 10 μM, and then add 5 times the equivalent of NaSH solution to test the difference Changes in UV absorption of time probe L2-B reacting with hydrogen sulfide. Depend on image 3 It can be seen that with the prolongation of time, the absorption peak of the probe at 555nm gradually decreases, while the ultraviolet absorption at 470nm gradually increases, reaching the peak at 15min.
Embodiment 3
[0058] Example 3 Fluorescence Spectrum Change of Probe (1) Responding to Hydrogen Sulfide
[0059] Add 3mL of PBS (10mM, pH7.4) to the quartz cuvette, then add 10μL of L2-B acetonitrile stock solution to make the final concentration of 10μM, then add 2.5 times the equivalent of NaSH solution, detect probe L2-B and Fluorescence-time variation of the hydrogen sulfide response. Depend on Figure 4 It can be seen that as the reaction time prolongs, the fluorescence of the probe at 576nm is gradually quenched, and a new peak appears at 542nm, and the reaction reaches equilibrium in 15min.
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