Liquid crystal aligning agent and liquid crystal display element
A liquid crystal aligning agent and all technologies, applied in the directions of liquid crystal materials, chemical instruments and methods, instruments, etc., can solve the problem of not being able to improve the charge leakage of liquid crystal panels, and achieve the effect of excellent charge leakage
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Synthetic example 1
[0144] Synthesis Example 1 (Synthesis Example 1 of Imidized Polymer)
[0145] 224g (1.0 mol) of 2,3,5-tricarboxycyclopentyl acetic dianhydride as tetracarboxylic dianhydride, 96.1g (0.89 mol) of p-phenylenediamine as diamine, 3,6-bis(4 -aminobenzoyloxy)cholestane 2.6g (0.010 mole) and N,N'-bis(4-aminophenyl)piperazine 27g (0.10 mole) were dissolved in 3100g N-methyl-2-pyrrolidone , and reacted at room temperature for 6 hours to obtain a solution containing 10% by weight of polyamic acid. The solution viscosity of this polyamic acid solution was 90 mPa·s.
[0146] Then, 600 g of N-methyl-2-pyrrolidone was added to the obtained polyamic acid solution, 136 g of pyridine and 105 g of acetic anhydride were added, and a dehydration ring-closure reaction was performed at 110° C. for 4 hours. After the dehydration ring-closing reaction, the solvent in the system is replaced by new γ-butyrolactone (through this solvent replacement, the pyridine and acetic anhydride used in the dehydrat...
Synthetic example 2
[0147] Synthesis Example 2 (Synthesis Example 2 of Imidized Polymer)
[0148] 112g (0.50 mol) of 2,3,5-tricarboxycyclopentyl acetic dianhydride as tetracarboxylic dianhydride, 38.0g (0.35 mol) of p-phenylenediamine as diamine, 3-(3,5- Diaminobenzoyloxy) cholestane 53.0g (0.10 mol) and N, N'-bis (4-aminophenyl) piperazine 13.4g (0.050 mol) dissolved in 1900g N-methyl-2-pyrrolidone , reacted at room temperature for 6 hours to obtain a solution containing 10% by weight of polyamic acid. The solution viscosity of this polyamic acid solution was 58 mPa·s.
[0149] Then, 600 g of N-methyl-2-pyrrolidone was added to the obtained polyamic acid solution, 116 g of pyridine and 90 g of acetic anhydride were added, and a dehydration ring-closure reaction was performed at 110° C. for 4 hours. After the dehydration ring-closing reaction, the solvent in the system was replaced with a new N-methyl-2-pyrrolidone, and then concentrated to obtain about 1430 g of imidization compound containing...
Synthetic example 3
[0150] Synthesis Example 3 (Synthesis Example 3 of Imidized Polymer)
[0151] 110 g (0.50 mol) of 2,3,5-tricarboxycyclopentyl acetic dianhydride as tetracarboxylic dianhydride, 49 g (0.45 mol) of p-phenylenediamine as diamine, N, N'-bis(4 -Aminophenyl) piperazine 13.4g (0.050 moles) and 3-(3,5-diaminobenzoyloxy) cholestane 26g (0.050 moles) were dissolved in 1800g N-methyl-2-pyrrolidone, It reacted at 60 degreeC for 6 hours, and obtained the solution containing 10 weight% of polyamic acids. The solution viscosity of this polyamic acid solution was 60 mPa·s.
[0152] Then, 1800 g of NMP was added to the obtained polyamic acid solution, and 40 g of pyridine and 51 g of acetic anhydride were added, and a dehydration ring-closure reaction was performed at 110° C. for 4 hours. After the dehydration ring-closing reaction, the solvent in the system is replaced with new N-methyl-2-pyrrolidone to obtain about 1200g of imidized polymer containing 15% by weight of imidization rate of a...
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