Binol-diform-o-aminophenol type Schiff base, and synthesis method and application thereof
A technology of o-aminophenol and synthesis method, which is applied in the preparation of imino compounds, chemical instruments and methods, fluorescence/phosphorescence, etc., can solve the problem that Schiff base has no ability to recognize metals, and achieve enhanced fluorescence recognition ability and excellent fluorescence performance effect
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specific Embodiment approach 1
[0036] Specific embodiment 1: In this embodiment, the structural formula of the Binol-diform condensed o-aminophenol Schiff base fluorescent probe compound is as follows:
[0037]
[0038] where R is -H or -NO 2 .
specific Embodiment approach 2
[0039] Specific embodiment two: the synthesis method of Binol-diform adeno-aminophenol Schiff base of this embodiment, the steps are as follows:
[0040] 1. Dissolve o-aminophenols in an organic solvent, then add Binol-diform, and heat for 1 to 2 hours to obtain a red liquid, namely 2,2'-dihydroxy-1,1'-binaphthyl-3,3 Crude product of '-diformaldehyde-condensed o-aminophenol Schiff base;
[0041] 2. Concentrate the crude product of 2,2'-dihydroxy-1,1'-binaphthalene-3,3'-dicarbaldehyde adeno-aminophenol Schiff base, dissolve it in methanol, filter it with suction, and wash it to obtain a red solid. Vacuum drying, the obtained pure product is 2,2'-dihydroxy-1,1'-binaphthyl-3,3'-dimethylaldehyde adeno-aminophenol Schiff base; wherein in step 1, Binol-diform and o-amino The molar ratio of phenol is 1:2~3.
[0042] The Binol-diform described in Step 1 is 2,2'-dihydroxy-1,1'-bi-3,3'-dinaphthaldehyde.
specific Embodiment approach 3
[0043] Embodiment 3: This embodiment is different from Embodiment 2 in that: in the preparation step 1, the o-aminophenol is o-aminophenol or 2-amino-5-nitrophenol. Others are the same as in the second embodiment.
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