A kind of hydroxyl radical ratiometric fluorescent probe and its preparation method and application
A technology of fluorescent probes and free radicals, applied in the direction of fluorescence/phosphorescence, chemical instruments and methods, luminescent materials, etc., can solve the problems of limited applications, achieve high selectivity and sensitivity, and excellent mitochondrial localization ability
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Embodiment 1
[0060] Example 1 Synthesis of Fluorescent Probes
[0061] The synthetic route of the fluorescent probe is as follows:
[0062]
[0063]
[0064] Wherein, the above-mentioned reaction conditions are: a.POBr 3 , DMF / DCM, 45℃; b.Pd(PPh 3 ) 4 , Na 2 CO 3 , toluene, 75℃, EtOH / NaOH reflux; c.4-dimethyl-3-ethylpyrrole, POCl 3 , DCM, 0°C, then 4-carboxyphenylboronic acid, DCM, reflux; d. EDC, HOBt, DMF, room temperature.
[0065] (1) Synthesis of compound 3 according to the reported method
[0066]
[0067] Compound 2: black solid (84%). 1 H NMR (400MHz, CDCl 3 )δ7.53–7.49(m,2H),7.26–7.22(m,1H),7.18–7.13(m,2H),3.62(s,3H),3.27(s,3H).ESI[M+H] + m / z calcd.for[C 11 H 12 BrN 2 ]251.01,found 251.00[M+H] + .compound 2 1 H NMR spectrum as figure 2 shown.
[0068] Compound 3: yellow solid (75%). 1 H NMR (400MHz, d 6 -DMSO)δ13.39(s,1H),10.24(s,1H),9.91(s,1H),8.18(s,1H),7.82(d,J=8.4Hz,1H),7.62–7.60(m ,1H),7.38–7.30(m,2H),7.21–7.19(s,1H),7.09(d,J=8.0Hz,1H),7.02–6.98(m...
Embodiment 2
[0080] Photophysical Properties of Example 2 Compound 4
[0081] The photophysical properties of compound 4 were tested, and the test results were as follows Figure 11 shown. where A is ACN / H 2 Fluorescence spectrum of compound 4 (20 μM) in O mixed solution; B is the fluorescence spectrum of compound 4 (20 μM) in ACN / PBS 2:1 solution before and after OH reaction, excited at 580 nm; C is before and after OH reaction, The corresponding UV-vis absorption spectrum of compound 4, OH was generated by the following conditions (H 2 O 2 50μM, EDTA-Fe 2+ 200 μM). Figure 11 The fluorescence spectrum in A shows that the fluorescence intensity of compound 4 is highly sensitive to changes in solvent hydrophobicity / hydrophilicity. Compound 4 shows weak fluorescence in pure water, but in acetonitrile (ACN) / H 2 The emission intensity of O mixed solvent varies with ACN and H 2 It increases with the increase of the O volume ratio. This property provides a potential possibility for the...
Embodiment 3
[0090] Example 3 Study on the reaction kinetics of compound 4 and OH
[0091] Coumarin-3-carboxylic acid (Coumarin-CA) is a commercial fluorescent probe for OH detection. The present invention selects Coumarin-CA to compare with compound 4. • The reaction between OH and Coumarin-CA yielded the fluorescent product 7-hydroxycoumarin-3-carboxylic acid with an emission peak at 454 nm upon excitation at 400 nm. Therefore, check the fluorescence intensity I 454 The reaction can then be monitored. Meanwhile, the reaction of OH with compound 4 can reduce its absorption value at 610 nm, thus providing a simple method to monitor the reaction. Coumarin-CA (100 μM) or compound 4 (40 μM) was mixed with Fenton’s reagent EDTA-Fe2 during the test + (100μM) / H 2 O 2 (10 mM) in sodium borate buffer (pH 9.0). In the competition experiment, Coumarin-CA and compound 4 were premixed, and then the OH reaction was carried out. The reaction was performed in a 96-well plate, and the emission int...
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