Liquid crystal aligning agent, method for forming liquid crystal aligning film, and liquid crystal display element
A technology of liquid crystal alignment agent and coating film, which is applied in the direction of liquid crystal materials, chemical instruments and methods, instruments, etc., can solve the problems of insufficient control of liquid crystal molecular orientation, and achieve the effect of excellent balance and low price
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[0253] Hereinafter, although an Example demonstrates this invention concretely, this invention is not limited to these Examples.
[0254] The weight-average molecular weights Mw in the following synthesis examples are polystyrene-equivalent values measured by gel permeation chromatography under the following conditions, respectively.
[0255] Column: manufactured by Tosoh Corporation, TSKgel GRCXLII
[0256] Solvent: THF
[0257] Temperature: 40°C
[0258] Pressure: 68kgf / cm 2
[0259]
Synthetic example ES-1
[0261] In a reaction vessel with a stirrer, a thermometer, a dropping funnel, and a reflux condenser, add 100.0 g of 2-(3,4-epoxycyclohexyl) ethyltrimethoxysilane as a raw material silane compound, 500 g of methyl isobutyl ketone and 10.0 g of triethylamine as a catalyst were mixed at room temperature.
[0262] Next, 100 g of deionized water was dropped from the dropping funnel over 30 minutes, mixed under reflux, and reacted at 80° C. for 6 hours. After the reaction is over, take out the organic layer, use 0.2% by weight of ammonium nitrate aqueous solution to wash it until the water after washing is neutral, then distill off the solvent and water under reduced pressure to obtain a viscous transparent liquid having epoxy groups polyorganosiloxane (ES-1).
[0263] The polyorganosiloxane with epoxy group is carried out 1 As a result of H-NMR analysis, an epoxy group-based peak with the same theoretical intensity was obtained around chemical shift (δ) = 3.2 ppm, thereby confir...
Synthetic example ES-2
[0265] Synthesis Example ES-2 and ES-3
[0266] Except that the added raw materials were as shown in Table 1, polyorganosiloxanes (ES-2) and (ES-3) having epoxy groups were obtained as viscous transparent liquids in the same manner as in Synthesis Example ES-1. .
[0267] Table 1 shows the Mw and epoxy equivalent of these epoxy group-containing polyorganosiloxanes.
[0268] In addition, in Table 1, the abbreviations of the raw material silane compounds have the following meanings, respectively.
[0269] ECETS: 2-(3,4-Epoxycyclohexyl)ethyltrimethoxysilane
[0270] MTMS: Methyltrimethoxysilane
[0271] PTMS: Phenyltrimethoxysilane
[0272] Table 1. Synthesis of polyorganosiloxanes with epoxy groups
[0273]
[0274]
[0275] According to the following synthetic route 1, the compound represented by the above-mentioned formula (A-1) (hereinafter referred to as "compound (A-1)") and the compound represented by the above-mentioned formula (A-2) (hereinafter referred to as ...
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