Liquid crystal alignment agent, liquid crystal alignment film and liquid crystal display element
A technology of liquid crystal alignment agent and repeating unit, applied in liquid crystal materials, chemical instruments and methods, instruments, etc., can solve the problem of insufficient improvement of screen burn-in, and achieve excellent liquid crystal orientation control and excellent coating properties
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Synthetic example 1
[0225] Synthesis Example 1 (Synthesis (1) of Compound (1'))
[0226] Tocopheryl methacrylate is synthesized according to the following reaction scheme 1.
[0227]
[0228] Reaction scheme 1
[0229] Dissolve 89g of α-tocopherol in 800ml of dehydrated tetrahydrofuran (THF), add 27g of triethylamine, slowly add 36g of methacryloyl chloride dropwise, and stir at room temperature for 3 hours to carry out the reaction. After completion of the reaction, triethylamine hydrochloride was removed by filtration, THF was distilled off under reduced pressure, and then 400 ml of chloroform was added. This solution was washed with water, and the organic layer was dried over magnesium sulfate, and then chloroform was distilled off under reduced pressure to obtain 85 g of the target product α-tocopheryl methacrylate (yield: 83%).
Synthetic example 2
[0230] Synthesis Example 2 (Synthesis (2) of Compound (1'))
[0231] Tocopheryl acrylate is synthesized according to the following reaction scheme 2.
[0232]
[0233] Reaction Scheme 2
[0234] In the above Synthesis Example 1, except that 32 g of acryloyl chloride was used instead of methacryloyl chloride, 80 g of the target product α-tocopheryl acrylate was obtained in the same manner as in Synthesis Example 1 (yield: 80%).
Synthetic example 3
[0235] Synthesis Example 3 (Synthesis (1) of Polymer (1))
[0236] In a four-necked flask equipped with a stirring bar, a three-way valve and a thermometer, add 33 g (0.066 moles) of α-tocopheryl methacrylate prepared in the above-mentioned Synthesis Example 1, glycidyl methacrylate Esters 25g (0.18 moles), methacrylic acid 14g (0.16 moles), styrene 7.0g (0.067 moles), N-cyclohexylmaleimide 7.0g (0.039 moles) and 2-hydroxyethyl methacrylate 14g (0.11 moles), then add 200 g of diethylene glycol ethyl methyl ether as a solvent, 2,2'-azobis(2,4-dimethylvaleronitrile) 4.5 g as a polymerization initiator and molecular weight adjustment α-methylstyrene dimer 2.0g. 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 32% by weight of the polymer (1-1). The molecular weight of the polymer (1-1) was measured by GPC, Mw=24000, Mw / Mn=2.4, and...
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