Hyperbranched polyimide containing benzothiazole structure and preparation method and application thereof
A polyimide, benzothiazole technology, applied in the field of material science, can solve the problems of limited wide application, large inter-chain distance, decreased heat resistance, etc., to achieve good application prospects, improve heat resistance, and increase freedom volume effect
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Embodiment 1
[0037] Add 0.4362g (2mmol) of pyromellitic dianhydride (PMDA) and 36ml of N,N-dimethylformamide into a three-necked flask, blow in argon, raise the temperature to 30°C, and add the triamine monomer N 1 -(4-aminophenyl)-N 1 -(6-(4-aminophenyl)benzo[d]thiazol-2-yl)benzene-1,4-diamine 0.4235g (1mmol) was dissolved in 40ml N,N-dimethylformamide with constant pressure dropping funnel 1~2h, evenly drop into the three-necked flask, then continue to react for 14h, then add 6ml of acetic anhydride and 2ml of triethylamine, heat up to 45°C and continue to react for 12h, after the reaction is completed, cool to room temperature and discharge in ethanol, filter, wash, Repeat 2 to 3 times, and finally place it in a vacuum drying oven at 80°C for 24 hours to obtain a brown hyperbranched polyimide polymer, whose structural formula is as follows:
[0038]
Embodiment 2
[0040] Add 0.4515g (2.07mmol) of pyromellitic dianhydride (PMDA) and 15ml of N,N-dimethylacetamide into a three-necked flask, blow in argon, raise the temperature to 30°C, and add the triamine monomer N 2 -(5-(4-aminophenyl)benzo[d]thiazol-2-yl)-N 2 -(5-aminothiophen-2-yl)thiophene-2,5-diamine 0.4356g (1mmol) was dissolved in 16ml of N,N-dimethylacetamide and added dropwise into the three-necked flask with a constant pressure dropping funnel in 1~2h, Then continue to react for 16h, then add 6.2ml of acetic anhydride and 2.1ml of triethylamine, heat up to 45°C and continue to react for 16h, after the reaction is completed, cool to room temperature and discharge the material in ethanol, filter, wash, repeat 2 to 3 times, and finally place Dried in a vacuum oven at 80°C for 24 hours to obtain a reddish-brown hyperbranched polyimide polymer, whose structural formula is as follows:
[0041]
Embodiment 3
[0043] Add 0.4413g (1.5mmol) of 3,3',4,4'--biphenyltetracarboxylic dianhydride (BPDA) and 20ml of N-methylpyrrolidone into a three-necked flask, pass in argon, raise the temperature to 30°C, and Triamine Monomer N 2 -(6-aminonaphthalen-2-yl)-N 2 -(7-(4-aminophenyl)benzo[d]thiazol-2-yl)naphthalene-2,6-diamine 0.5237g (1mmol) dissolved in 26.5ml N-methylpyrrolidone using a constant pressure dropping funnel at 1~ Evenly drop into the three-necked flask for 2 hours, then continue to react for 20 hours, then add 12ml of acetic anhydride and 3ml of triethylamine, heat up to 45°C and continue to react for 14 hours, after the reaction is completed, cool to room temperature and discharge in methanol, filter, wash, repeat 2 ~3 times, and finally placed in a vacuum drying oven at 80°C for 24 hours to obtain a light yellow hyperbranched polyimide polymer, whose structural formula is as follows:
[0044]
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