A kind of fluorene-containing liquid crystal polymer and its preparation method
A technology of liquid crystal polymer and bisether fluorene, which is applied in the field of polymer chemistry, can solve the problems of fluidity that needs to be improved, and achieve the effects of good appearance and dimensional stability, mild reaction conditions, and low content of small molecules
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[0022] The method for preparing the above-mentioned fluorene-containing liquid crystal polymer comprises the following steps: prepolymerizing a catalyst derived from an aromatic hydroxycarboxylic acid, derived from an aromatic dicarboxylic acid, diether fluorene and acetic anhydride, and performing a prepolymerization reaction on the catalyst; Further termination is carried out to finally obtain the reaction product.
[0023] For the preparation method of the fluorene-containing liquid crystal polymer, the prepolymerization reaction conditions are: refluxing at 130-160° C. for 3-8 hours, then heating up to 280-350° C. for 2-5 hours, and the final polymerization reaction temperature is 230-300° C. , the reaction time is 3-7h.
[0024] In the preparation method of the fluorene-containing liquid crystal polymer, the dosage of acetic anhydride is 1.1 times of the total amount of hydroxyl groups in the monomer.
[0025] In the preparation method of the fluorene-containing liquid c...
Embodiment 1
[0036] 20 moles of p-hydroxybenzoic acid, 40 moles of 2-hydroxy-6-naphthoic acid, 5 moles of terephthalic acid, 15 moles of isophthalic acid, 20 moles of diether fluorene, sulfamic acid and zinc acetate, acetic anhydride at 150°C Under reflux for 6 hours, then heated to 300°C, and reacted for 4 hours to obtain a prepolymer; the prepolymer was further reacted at 260°C for 5 hours to obtain a final polymer.
Embodiment 2
[0038] 14 moles of p-hydroxybenzoic acid, 56 moles of 2-hydroxy-6-naphthoic acid, 3 moles of 1,1'-biphenyl-3,4'-dicarboxylic acid, 12 moles of 1,6-naphthalenedicarboxylic acid, diether fluorene 15 moles, sulfamic acid, zinc acetate, and acetic anhydride were refluxed at 140°C for 7 hours, then heated to 320°C, and reacted for 3 hours to obtain a prepolymer; the prepolymer was further reacted at 250°C for 6 hours to obtain a final polymer.
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