Novel ratio type sulfite fluorescent probe as well as preparation method and biological application thereof
A fluorescent probe and sulfite technology, applied in the direction of fluorescence/phosphorescence, chemical instruments and methods, luminescent materials, etc., can solve the problems of long reaction time and limited application, and achieve high detection sensitivity, high selectivity, and easy identification Effect
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Embodiment 1
[0036] Preparation of Compound 1
[0037] React m-N-diethylaminophenol (0.50g, 3.03mmol) with phthalic anhydride (0.49g, 3.33mmol) in 180mL of toluene at 110°C for 24 hours to obtain a white solid, then add the white solid to 20mL containing 6ml of propane in 98wt% concentrated sulfuric acid was reacted at 50°C for 3 hours, and the solid was recrystallized from ethanol to obtain compound 1 (0.22g, 0.45mmol).
[0038] The synthetic route is as follows:
[0039]
Embodiment 2
[0041] Preparation of a New Fluorescent Probe for Detecting Sulfite
[0042] The reaction scheme is as follows:
[0043]
[0044] The preparation process comprises steps as follows:
[0045] Compound 1 (0.377g, 1.0mmol) prepared in Example 1 was reacted with 4-dimethylaminobenzaldehyde (0.178g, 1.2mmol) in 20ml of acetic acid at 110°C for 5h to obtain a dark solution, which was removed by rotary distillation. Solvent, the solid was dissolved in dichloromethane, and separated by column chromatography with a mixed solvent of dichloromethane and methanol to obtain the target compound CS-NMe; yield: 50%. 1 HNMR(400MHz,MeOD)δ8.05(d,J=15.5Hz,2H),8.00–7.91(m,2H),7.63(d,J=8.9Hz,5H),7.60–7.54(m,4H), 7.39(d,J=9.4Hz,2H),7.37–7.31(m,2H),7.08(d,J=2.9Hz,3H),7.05(d,J=2.4Hz,1H),7.01(d,J =2.3Hz, 2H), 6.94(d, J=15.5Hz, 2H), 6.74(d, J=9.0Hz, 4H), 3.62(q, J=7.2Hz, 9H), 3.07(s, 12H), 1.27(d,J=7.1Hz,14H). 13 C NMR(101MHz,MeOD)δ166.57,162.66,158.37,154.69,153.53,146.02,134.19,131.86,129.81,1...
Embodiment 3
[0047] The preparation method of sulfite fluorescent probe as described in embodiment 2, difference is:
[0048] The amount of 4-dimethylaminobenzaldehyde was 3 mmol, acetic acid was replaced by acetic anhydride, the amount of acid was 20 mL, the reaction temperature was 60° C., and the reaction time was 12 h.
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