Novel high-selectivity fluorescence probe for bivalent copper ions as well as preparation method and biological application of novel high-selectivity fluorescence probe
A divalent copper ion, high-selectivity technology, applied in fluorescence/phosphorescence, chemical instruments and methods, luminescent materials, etc., can solve the problem of lack of near-infrared luminescent fluorescent probes, low biological application value, and insufficient sensitivity of detection signals, etc. problems, to achieve the effect of simple preparation method, easy identification and obvious phenomenon
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Embodiment 1
[0042] A novel highly selective divalent copper ion fluorescent probe has a structure shown in formula (I):
[0043]
[0044] The reaction scheme is as follows:
[0045]
[0046] The preparation process comprises steps as follows:
[0047] (1) Compound 1 (0.377g, 1.0mmol) and p-cyanobenzaldehyde (0.157g, 1.2mmol) were reacted in 20ml of acetic acid at 50°C for 12h to obtain a dark solution, and the solvent was removed by rotary distillation. Dissolved in methyl chloride, separated by column chromatography with a mixed solvent of dichloromethane and methanol to obtain compound 2; yield: 50%. 1 H NMR (400MHz, CDCl3) δ7.96(d, J=7.2,1H),7.65(m,3H),7.56(t,J=7.2,1H),7.48(d,J=8.4,1H),7.37 (s,1H),7.23(d,J=7.6,1H),6.50(d,J=8.8,1H),6.38(m,2H),3.36(q,J=6.4,4H),2.65(m, 2H), 2.07(m, 1H), 1.63(m, 4H), 1.17(t, J=6.8, 2H). 13 C NMR(101MHz,CDCl3)δ169.94,152.38,152.09,149.39,146.29,142.08,134.56,133.47,131.95,129.98,129.38,128.59,127.52,125.04,123.45,119.00,110.20,109.77,108.93,104.61...
Embodiment 2
[0050] The preparation method of novel highly selective divalent copper ion fluorescent probe as described in Example 1, the difference is:
[0051] The amount of cyanobenzaldehyde described in step (1) 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.
[0052] The consumption of hydrazine hydrate in step (2) is 3mL.
Embodiment 3
[0054] The preparation method of novel highly selective divalent copper ion fluorescent probe as described in Example 1, the difference is:
[0055] The amount of cyanobenzaldehyde described in step (1) was 1 mmol, acetic acid was replaced by methanesulfonic acid, the amount of acid was 10 mL, the reaction temperature was 50° C., and the reaction time was 10 h.
[0056] The consumption of hydrazine hydrate in step (2) is 2mL.
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