Pyrroles oligomer and application thereof
A technology of oligomer and pyrrole oligo, which is applied in the direction of conductors, non-metallic conductors, organic material conductors, etc., can solve the problems of products with short reaction time, difficult to dissolve, and difficult to obtain, and achieve environmental friendliness, low cost, and reduced cost effect
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Embodiment 1
[0059] A preparation method of pyrrole oligomer, the steps are as follows:
[0060] (1) Add 50 μL of pyrrole into a 50 mL container containing 1 g of activated carbon powder, seal the container, shake the container to mix the activated carbon powder and pyrrole evenly, and mature at room temperature for 30 days. During the aging period, the container was shaken twice a day, and the shaking time was not less than 1 min each time. After the aging period, the activated carbon / pyrrole oligomer complex was obtained.
[0061] (2) Disperse the activated carbon / pyrrole oligomer complex obtained in step (1) in 10 mL N,N-dimethylformamide solution, shake well, and let it stand at room temperature for 24 h; centrifuge, and collect the supernatant liquid.
[0062] (3) The supernatant obtained in step (2) was distilled off the solvent under reduced pressure to obtain a pyrrole oligomer sample.
[0063] Result analysis
[0064] The N,N-dimethylformamide solution of the pyrrole oligomer o...
Embodiment 2
[0072] A preparation method of pyrrole oligomer, the steps are as follows:
[0073] (1) Add 10 μL of pyrrole into a 50 mL container containing 1 g of carbon cloth, seal the container, and mature at room temperature for 7 days to obtain a carbon cloth / pyrrole oligomer complex.
[0074] (2) Soak the carbon cloth / pyrrole oligomer composite obtained in step (1) in 5 mL of methanol solution, and let it stand at room temperature for 24 h; take out the carbon cloth and keep the liquid.
[0075] (3) Distill the liquid obtained in step (2) to remove the solvent under reduced pressure to obtain a sample of pyrrole oligomer.
Embodiment 3
[0077] Others are the same as embodiment 1, the difference is:
[0078] 30 μL of pyrrole was added to a 50 mL container containing 1 g of granular carbon, and the container was stirred to mix the activated carbon powder and pyrrole evenly, and aged at room temperature for 10 days. During the aging period, the container was shaken 3 times a day, and the shaking time was not less than 15 min each time. The obtained complex was immersed in 5 mL tetrahydrofuran solution, and stood at room temperature for 28 h; centrifuged, and the supernatant was collected.
[0079] It was determined that the weight-average molecular weight of the prepared pyrrole oligomer was 522, corresponding to an oligomer containing 8 pyrrole rings. The molecular weight distribution coefficient is 1.1, and the prepared pyrrole oligomer is a p-type semiconductor with a charge carrier density of 1.1 × 10 20 cm ‒3 .
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