Polymer composition and liquid crystal alignment film for transverse electric field driving liquid crystal display element
A composition and polymer technology, applied in optics, instruments, nonlinear optics, etc., can solve the problems of inability to achieve liquid crystal alignment, inability to uniformly rub the liquid crystal alignment film, and dust generation.
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[0236] [Preparation of polymer composition]
[0237] The polymer composition used in the present invention is preferably prepared in the form of a coating liquid so as to be suitable for forming a liquid crystal aligning film. That is, the polymer composition used in the present invention is preferably prepared in the form of a solution in which a resin component for forming a resin coating is dissolved in an organic solvent. Here, the resin component refers to a resin component containing the above-mentioned photosensitive side chain type polymer capable of expressing liquid crystallinity. In this case, the content of the resin component is preferably 1% by mass to 20% by mass, more preferably 3% by mass to 15% by mass, particularly preferably 3% by mass to 10% by mass.
[0238] In the polymer composition of the present embodiment, all of the above-mentioned resin components may be the above-mentioned photosensitive side chain polymers capable of exhibiting liquid crystallin...
Embodiment
[0350] Methacrylic monomers MA1 and MA2 used in Examples; GMA, HBAGE, G1 and additive T1 which are monomers having an epoxy side chain are shown below.
[0351] In addition, MA1 and MA2 were respectively synthesize|combined as follows. That is, MA1 was synthesized by the synthesis method described in the patent document (WO2011-084546). MA2 was synthesized by the synthesis method described in the patent document (Japanese Patent Laid-Open No. 9-118717).
[0352] G1 was synthesized by the synthesis method described in Synthesis Example 1 below.
[0353] GMA (glycidyl methacrylate), HBAGE (hydroxybutyl acrylate glycidyl ether), and additive T1 (3-aminomethylpyridine) used commercially available ones.
[0354]
Synthetic example 1
[0356] Synthesis of Specific Glycidyl Compounds (C1)
[0357]
[0358] Add (COCl) to THF (tetrahydrofuran) solution (184 g) of carboxylic acid derivative (MA2) (18.4 g, 60 mmol) 2 (Oxalyl chloride) (11.4 g, 90 mmol) and 2 drops of DMF (dimethylformamide) were reacted at room temperature for 2 hours. The solid obtained by concentrating this solution was dissolved in THF (350 g). This solution was added dropwise to a THF solution (88 g) of glycidol (8.89 g, 120 mmol) and triethylamine (13.4 g, 132 mmol) over 1 hour, and reacted for 18 hours. Then, ethyl acetate (500g) was added, the organic phase was wash|cleaned 3 times with water (300g), and it dried with magnesium sulfate. After removing magnesium sulfate by filtration, it concentrated and obtained the crude product. The resulting crude product was chromatographed on silica gel using ethyl acetate and hexanes to afford C1 as a white solid. (yield: 14.9 g, yield: 69%).
[0359] Glycidyl derivatives (C1):
[0360] 1 H...
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