Multifunctional triarylamine-containing oxazine polymer and preparation method and application thereof
A triarylamine-based, polymer technology, applied in chemical instruments and methods, through chemical reaction of materials for analysis, fluorescence/phosphorescence, etc., can solve the problems of poor film adhesion and poor heat resistance, etc. Effects of solubility, good heat resistance, excellent electrochromic properties and memory properties
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specific Embodiment approach 1
[0032] Specific embodiment 1: The structural formula of a kind of multifunctional triarylamino-containing oxazine polymer in this embodiment is as follows: In the formula, n is an integer of 3 to 10.
[0033] In this embodiment, the triphenylamine-based monomer is prepared first, and this embodiment uses N 4 ,N 4 -Di-naphthalene-2-yl-biphenyl-4,4-diamine is used as raw material and then reacted with p-fluoronitrobenzene to realize nitration, and then the nitro group is reduced to amino, with bisphenol A, paraformaldehyde , the prepared triphenylamine-based monomers are used as raw materials and synthesized through Mannich condensation reaction under certain conditions to synthesize a series of polymers with relatively small molecular weights. Such polymers can be ring-opened and polymerized under the action of heating or catalysts.
[0034] This implementation mode has the following special effects:
[0035] 1. In this embodiment, the benzoxazine structure is introduced into...
specific Embodiment approach 2
[0040] Specific embodiment two: the preparation method of a kind of multifunctional triarylamino-containing oxazine polymer of this embodiment is:
[0041] 1. N,N'-bis(4-aminophenyl)-N,N'-di-2-naphthyl-1,4-biphenyldiamine
[0042] in N 2 Atmosphere, set N 4 ,N 4 - Di-naphthalene-2-yl-biphenyl-4,4-diamine monomer, sodium hydride and anhydrous N, N-dimethylformamide are placed in a three-necked flask, and stirred at 1 to 2 drops per second Add p-fluoronitrobenzene at the dropping speed, heat up to 114-115°C, carry out constant temperature reaction, and then cool down; put the reaction product in water at 24-25°C until the crude product precipitates, then filter out the crude product, and use 99-100°C The crude product was washed with water for 2 to 3 times, the obtained crude product was dried in a vacuum drying oven, and then recrystallized with ethanol, and the crystallized product was filtered out after recrystallized, and the crystallized product was vacuum-dried to obtai...
specific Embodiment approach 3
[0047] Specific embodiment three: the difference between this embodiment and specific embodiment two is that the powder M2 in step one ① is N, N'-bis(4-nitrophenyl)-N, N'-two-2-naphthyl -1,4-Benphenyldiamine. Others are the same as in the second embodiment.
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