Liquid crystal aligning agent and lateral field style liquid crystal display element
A technology of liquid crystal display element and liquid crystal aligning agent, which is applied in the direction of liquid crystal materials, chemical instruments and methods, optics, etc., can solve the problems of unresolved, insufficient afterimage and afterimage countermeasures, etc., and achieve high display quality and afterimage mitigation performance excellent effect
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[0022] At least 50 mole % of the tetracarboxylic dianhydride used in the preparation of the polyamic acid polymer is pyromellitic dianhydride. Other tetracarboxylic dianhydrides that may be contained at 50% by mole or less include, for example, butane tetracarboxylic dianhydride, 1,2,3,4-cyclobutane tetracarboxylic dianhydride, 1,2-dimethyl -1,2,3,4-cyclobutanetetracarboxylic dianhydride, 1,3-dimethyl-1,2,3,4-cyclobutanetetracarboxylic dianhydride, 1,3-dichloro- 1,2,3,4-cyclobutanetetracarboxylic dianhydride, 1,2,3,4-tetramethyl-1,2,3,4-cyclobutanetetracarboxylic dianhydride, 1,2, 3,4-cyclopentane tetracarboxylic dianhydride, 1,2,4,5-cyclohexane tetracarboxylic dianhydride, 3,3',4,4'-dicyclohexyl tetracarboxylic dianhydride, 2 , 3,5-tricarboxycyclopentyl acetic dianhydride, 3,5,6-tricarboxynorbornane-2-acetic dianhydride, 2,3,4,5-tetrahydrofuran tetracarboxylic dianhydride, 1,3 , 3a, 4, 5, 9b-hexahydro-5-(tetrahydro-2,5-dioxo-3-furyl)-naphthalene[1,2-c]-furan-1,3-dione, 1,3...
Synthetic example 1
[0096] Synthesis example 1 (synthesis of imidized polymer)
[0097] 22.1 g (0.1 mol) of 2,3,5-tricarboxycyclopentyl acetic acid dianhydride as tetracarboxylic dianhydride, 9.7 g (0.09 mol) of p-phenylenediamine as diamine compound, and 4,4' -Diamino-2,2'-bis(trifluoromethyl)biphenyl 3.2g (0.01mol) was dissolved in 315g of N-methyl-2-pyrrolidone and reacted at 60°C for 4 hours to obtain 350g of a solution A polyamic acid solution with a viscosity of 35mPa·s. Next, 350 g of N-methyl-2-pyrrolidone, 39.5 g of pyridine and 30.6 g of acetic anhydride were added to the obtained polyamic acid solution, and dehydration and ring closure were performed at 110° C. for 4 hours. After the imidization reaction, perform solvent replacement with N-methyl-2-pyrrolidone that does not use a solvent in the system (in this operation, pyridine and acetic anhydride used in the imidization reaction are removed from the system) 340 g of an imidized polymer (A-1) solution having a solid content concen...
Synthetic example 2
[0098] Synthesis example 2 (synthesis of imidized polymer)
[0099] In Synthesis Example 1, in addition to using 8.7 g (0.08 moles) of p-phenylenediamine, 2.0 g (0.01 moles) of 4,4'-diaminodiphenylmethane and 4,4'-diamino-2,2' - 3.2 g (0.01 mol) of bis(trifluoromethyl)biphenyl was used as a diamine compound, and a polyamic acid was obtained in the same manner as in Synthesis Example 1, which was further used for imidization reaction in the same manner as in Synthesis Example 1, 24.9 g of imidized polymers (A-2) whose solid content concentration was 10 wt%, solution viscosity 30 mPa·s, and imidization rate 93% were obtained.
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