Pyrrole-containing triphenylamine conjugated schiff base compound, and preparation method and application thereof
A technology of pyrrolyltriphenylamine and Schiff base, applied in chemical instruments and methods, organic chemistry, color-changing fluorescent materials, etc., can solve the problems of high synthesis cost and complex synthesis method, and achieve the effect of high degree of conjugation
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specific Embodiment approach 1
[0042] Specific implementation mode 1: This implementation mode is a kind of pyrrolyltriphenylamine-containing conjugated Schiff base compound whose structural formula is as follows:
[0043] where the R 1 For H, R 2 for H; R 1 for when R 2 for H, -CH 3 or -OCH 2 CH 3 .
[0044] The beneficial effect of this implementation mode:
[0045]1. The Schiff base compound of the present embodiment changes the shortcomings of narrow application range and single function of Schiff base in the past, and provides a multifunctional Schiff base; a -C=N- double bond structure is formed in the molecule, and the double bond connects benzene Ring and pyrrole, forming a large conjugated structure, so that the electron cloud can be transported in a very long molecular chain, prone to light absorption, resulting in a color change after protonation in acid or oxidation with an applied voltage, and this change is reversible , accompanied by a reversible color change;
[0046] 2. In th...
specific Embodiment approach 2
[0047] Specific embodiment two: This embodiment is a preparation method of a conjugated Schiff base compound containing pyrrolyl triphenylamine, which is prepared according to the following method:
[0048] 1. Mix the triphenylamine derivative and absolute ethanol, and then magnetically stir for 10 minutes to 15 minutes at a temperature of 79°C to 80°C and a stirring speed of 200r / min to 300r / min to obtain an ethanol solution of the triphenylamine derivative;
[0049] The volume ratio of the mass of the triphenylamine derivative described in step 1 to absolute ethanol is 0.1g: (10mL~20mL);
[0050] 2. Under a nitrogen atmosphere, add pyrrole-2-carbaldehyde ethanol solution dropwise to triphenylamine derivative ethanol solution at a rate of 20 drops / min to 30 drops / min, and then react at a temperature of 79°C to 80°C 20h~24h, get the reactant;
[0051] The volume ratio of the mass of pyrrole-2-carbaldehyde in the pyrrole-2-carbaldehyde ethanol solution described in step 2 to a...
specific Embodiment approach 3
[0057] Specific embodiment three: the difference between this embodiment and specific embodiment two is: the triphenylamine derivative described in step one is Others are the same as in the second embodiment.
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