Liquid crystal aligning agent, liquid crystal aligning film and liquid crystal display device
A technology of liquid crystal alignment agent and repeating unit, which is applied in liquid crystal materials, chemical instruments and methods, optics, etc., can solve problems such as improvement, no envisioned burn-in performance, and no consideration of long-term durability, so as to improve burn-in performance and durability Excellent burn-in performance and high reliability
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Synthetic example 1
[0244] Synthesis Example 1 (Synthesis of Compound (4'))
[0245] Dissolve 800g of β-cholesterol in 8000ml of dehydrated tetrahydrofuran (THF), add 270g of triethylamine, slowly add 360g of methacryloyl chloride dropwise, and stir at room temperature for 3 hours to react. After completion of the reaction, triethylamine hydrochloride was removed by filtration, THF was distilled off under reduced pressure, and then 4000 ml of chloroform was added. The obtained solution was washed with water, and the organic layer was dried over magnesium sulfate, and then chloroform was removed by distillation under reduced pressure. Then, recrystallization was performed with ethanol to obtain 540 g of cholestanyl methacrylate as a white solid (yield: 57.4%).
Synthetic example 2
[0246] Synthesis Example 2 (Synthesis (1) of Polymer (1))
[0247] In a four-necked flask equipped with a stirring bar, a three-way valve and a thermometer, add 10.0 g (0.0595 moles) of 2,2,2-trifluoroethyl methacrylate as a monomer, the compound obtained in the above Synthesis Example 1 Cholesteryl methacrylate 30.0g (0.0657 mol), glycidyl methacrylate 25.0g (0.176 mol), methacrylic acid 10.0g (0.116 mol), styrene 2.50g (0.0240 mol), N-ring Hexylmaleimide 2.50g (0.0139 mole) and 2-hydroxyethyl methacrylate 20.0g (0.154 mole), add the diethylene glycol ethyl methyl ether 200g as solvent again, as polymerization initiator 2 , 4.50 g of 2'-azobis(2,4-dimethylvaleronitrile) and 2.00 g of α-methylstyrene dimer as a molecular weight modifier. This was bubbled with a nitrogen stream for about 10 minutes to ventilate the system with nitrogen, and then reacted at 70° C. for 5 hours under a nitrogen atmosphere to obtain a solution containing 33.2% by weight of the polymer (1-1). The ...
Synthetic example 3
[0248] Synthesis Example 3 (Synthesis (2) of Polymer (1))
[0249] In a four-necked flask equipped with a stirring bar, a three-way valve and a thermometer, add 5.00 g (0.00940 moles) of 2-(perfluorooctyl) ethyl methacrylate as a monomer, the methacrylic acid prepared in Synthesis Example 1 above. Cholesteryl methacrylate 30.0g (0.0657 mol), glycidyl methacrylate 25.0g (0.176 mol), methacrylic acid 10.0g (0.116 mol), styrene 2.50g (0.0240 mol), N-ring Hexylmaleimide 2.50g (0.0139 mole) and 2-hydroxyethyl methacrylate 25.0g (0.192 mole), add the diethylene glycol ethyl methyl ether 200g as solvent again, as polymerization initiator 2 , 4.50 g of 2'-azobis(2,4-dimethylvaleronitrile) and 2.00 g of α-methylstyrene dimer as a molecular weight modifier. This was bubbled with a nitrogen stream for about 10 minutes to ventilate the system with nitrogen, and then reacted at 70° C. for 5 hours under a nitrogen atmosphere to obtain a solution containing 33.5% by weight of the polymer (1...
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