Liquid crystal alignment agent, liquid crystal alignment film and liquid crystal display element
A technology of liquid crystal alignment agent and compound, which is applied in the field of liquid crystal alignment film and liquid crystal display elements, liquid crystal display elements, and liquid crystal alignment agents, and can solve problems such as impact, liquid crystal layer impurity pollution, and restriction
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preparation example Construction
[0185] The preparation method of polysiloxane (B)
[0186] step (i)
[0187] The polycondensation reaction of the polysiloxane compound can use a general method, for example, adding an organic solvent, water, or optionally a catalyst to the above-mentioned silane compound or a mixture thereof, and then using an oil bath or the like to perform condensation at 50°C to 150°C. Heating, the preferred heating time is 0.5 hours to 120 hours. During heating, the mixture can be stirred or placed under reflux conditions.
[0188] The above-mentioned organic solvent is not particularly limited, and may be the same as or different from the solvent (D) contained in the liquid crystal alignment agent of the present invention.
[0189] Specific examples of the organic solvent include hydrocarbon compounds such as toluene and xylene; ketones such as methyl ethyl ketone, methyl isobutyl ketone, methyl n-amyl ketone, diethyl ketone, cyclohexanone, etc. Compounds; ester compounds of ethyl ace...
Synthetic example
[0281] Synthesis Example A-1-1 to Synthesis Example A-1-6 of the polymer (A) are described below:
Synthetic example A-1-1
[0283] A nitrogen inlet, a stirrer, a condenser, and a thermometer were arranged on a four-necked flask with a capacity of 500 milliliters, and nitrogen was introduced. Then, in the four-necked flask, add 1.16 grams (0.0025 moles) of the diamine compound (abbreviated as a2-1-1) represented by formula (II-10), 4.86 grams (0.045 moles) of p-diaminobenzene (referred to as a2-2-1), 0.49 grams (0.0025 moles) of 4,4'-diaminodicyclohexylmethane (referred to as a2-2-4) and 80 grams of N-methyl-2-pyrrolidone ( Abbreviated as NMP), and stirred at room temperature until dissolved. Next, 9.80 g (0.05 mol) of 1,2,3,4-cyclobutanetetracarboxylic dianhydride (abbreviated as a1-1) and 20 g of NMP were added and reacted at room temperature for 2 hours. After the reaction was finished, the reaction solution was poured into 1500 milliliters of water, so that the polymer was precipitated. Then, the obtained polymer was filtered, washed with methanol and filtered three times, placed in a vacuum o...
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