Side chain type electroactive polyarylether polymer and preparation method thereof
An electroactive, polyarylene ether technology, used in polyether coatings, chemical instruments and methods, other chemical processes, etc., can solve problems such as poor workability, and achieve the effect of improving solubility and workability
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Embodiment 1
[0044] Dissolve 11.35g (0.031mol) of aniline tetramer and 12mL of triethylamine in 60mL of dichloromethane; add 60mL of dichloromethane (containing 0.02mol of 2,6-difluorobenzoyl chloride) dropwise within 1.5h In the above solution, 0.01 mol of 2,6-difluorobenzoyl chloride was dissolved in 60 mL of dichloromethane, and added dropwise to the above solution within 3 h. The reaction was continued for 3 hours under nitrogen protection, filtered, and washed with dichloromethane and ethanol for 3 times. The product M was vacuum-dried at 45°C for 24 hours to obtain 12.9 g of a dark gray solid with a yield of 85%.
Embodiment 2
[0046] We synthesized five copolymers C with the molar ratios of difluoromonomer M and 4,4'-dichlorodiphenylsulfone of 100:0, 80:20, 60:40, 40:60 and 20:80, respectively. 1 (PAE-S-AT-X, X represents the percentage of the ratio of difluoromonomer to bisphenol monomer).
[0047] Difluoro monomer and 4,4'-dichlorodiphenyl sulfone (0.01mol), 2.2829g (0.01mol) of bisphenol A were added to a 100mL three-necked flask equipped with electromagnetic stirring, nitrogen inlet and outlet and oil-water separator, Add 30mL N,N'-dimethylacetamide (DMAc), 10mL toluene, 1.4236g (0.0103mol) anhydrous potassium carbonate, N 2 protection, heated to 140 ℃ and refluxed toluene with water for 2 h, increased the heating temperature to 160 ℃, and distilled the toluene out. After continuing the reaction for 8 h, the heating was stopped and cooled to room temperature. The material was discharged in 500 mL of distilled water, and the precipitate was obtained after filtration. Wash three times with dist...
Embodiment 3
[0049] We synthesized four copolymers C with the molar ratios of difluoromonomer M and 4,4'-difluorobenzophenone of 20:80, 15:85, 10:90 and 5:95, respectively. 2 (PEK-S-AT-X, X represents the percentage of the ratio of difluoro monomer to bisphenol monomer), and the bisphenol monomer adopts hydroquinone.
[0050] Add 4,4'-difluorobenzophenone and difluoromonomer (0.01mol), hydroquinone 2.2829g (0.01mol) into a 50mL three-neck flask equipped with electromagnetic stirring, nitrogen inlet and outlet and oil-water separator , add 20mL N-methylpyrrolidone (NMP), 10mL toluene, 1.4236g (0.0103mol) anhydrous potassium carbonate, N 2 protection, heated to 160 ℃ and refluxed toluene with water for 2 h, raised the heating temperature to 190 ℃, and distilled the toluene out. After continuing the reaction for 8 h, the heating was stopped and cooled to room temperature. The material was discharged in 250 mL of distilled water, and the precipitate was obtained after filtration. Wash three...
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