Polymer composition, and liquid crystal alignment film for horizontal electric field drive-mode liquid crystal display element

A composition and polymer technology, applied in optics, instruments, nonlinear optics, etc., can solve problems such as inability to rub liquid crystal alignment film uniformly, failure to achieve liquid crystal alignment, and static electricity

Active Publication Date: 2016-05-18
NISSAN CHEM IND LTD +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, the brushing method of rubbing the surface of a liquid crystal alignment film made of polyimide or the like has problems of generating dust and static electricity.
In addition, due to the high-definition of liquid crystal display elements in recent years, the unevenness

Method used

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  • Polymer composition, and liquid crystal alignment film for horizontal electric field drive-mode liquid crystal display element
  • Polymer composition, and liquid crystal alignment film for horizontal electric field drive-mode liquid crystal display element
  • Polymer composition, and liquid crystal alignment film for horizontal electric field drive-mode liquid crystal display element

Examples

Experimental program
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Example Embodiment

[0243] [Preparation of polymer composition]

[0244] The polymer composition used in the present invention is preferably prepared in the form of a coating liquid, and is suitable for forming a liquid crystal alignment 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 film is dissolved in an organic solvent. Here, the resin component refers to a resin component containing the photosensitive side chain type polymer capable of expressing liquid crystallinity described above. At this time, the content of the resin component is preferably 1% by mass to 20% by mass, more preferably 3% by mass to 15% by mass, and particularly preferably 3% by mass to 10% by mass.

[0245] In the polymer composition of this embodiment, the aforementioned resin components may all be the above-mentioned photosensitive side chain type polymer capable of expressing liquid crystallinity, a...

Example Embodiment

[0313] Example

[0314] The abbreviations used in the examples are as follows.

[0315] (Methacrylic monomer)

[0316]

[0317]

[0318] MA1 was synthesized by the synthesis method described in the patent document (WO2011-084546).

[0319] MA2 was synthesized by the synthesis method described in the patent document (Japanese Patent Application Laid-Open No. 9-118717).

[0320] MA3 is a new compound that has not been disclosed in the literature, and its synthesis method is described in detail in Synthesis Example 1 below.

[0321] MA3-1 was synthesized by the synthesis method described in the literature (Liquid Crystals (2005), 32(8), 1031-1044.).

[0322] For MA4, commercially available M6BC (manufactured by Green Chemical Co., Ltd.) was used.

[0323] (Organic solvents)

[0324] THF: Tetrahydrofuran

[0325] NMP: N-methyl-2-pyrrolidone

[0326] BC: Butyl cellosolve

[0327] EDC: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride

[0328] DMAP: 4-Dimethylaminopyridine

[0329] (Polymeri...

Example Embodiment

[0331]

[0332] Synthesis of compound [MA3] (MA9 in the following formula)

[0333]

[0334] Compound [MA2] (20.00g, 65.3mmol), compound [MA9-1] (ie, compound MA3-1) (14.09g, 71.8mmol), EDC (15.02g, 78.4mmol), was added to a 500mL four-necked flask. DMAP (0.80 g, 6.53 mmol) and THF (200 g) were reacted at 23°C. Reaction tracking was performed by HPLC, and after confirming the completion of the reaction, the reaction solution was poured into distilled water (1.2 L), ethyl acetate (2 L) was added, and the water layer was removed by a liquid separation operation. After the organic layer was washed with distilled water (500 mL) three times, the organic layer was dried with magnesium sulfate. Thereafter, it was filtered and the solvent was distilled off with an evaporator to obtain compound [MA9-2] (ie, compound MA3-2) as an oily compound.

[0335] Next, pyridinium p-toluenesulfonate (labeled PPTS) (1.59 g, 6.3 mmol) and ethanol (100 g) were added to the obtained compound [MA9-2], and...

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Abstract

The present invention addresses the problem of providing a horizontal electric field drive-mode liquid crystal display element to which an alignment control function is imparted with a high efficiency and which has excellent reliability including seizing properties and a voltage retention rate. According to the liquid crystal display element, the problem can be solved by a polymer composition comprising (A) a photosensitive side chain polymer and (B) an organic solvent, wherein the (A) photosensitive side chain polymer can exhibit liquid crystallinity in a predetermined temperature range, and the lower limit and the upper limit of the temperature range in which the liquid crystallinity is exhibited are 150 DEG C or higher and 200 DEG C or higher, respectively.

Description

technical field [0001] The present invention relates to a novel polymer composition, a liquid crystal alignment film for a transverse electric field-driven liquid crystal display element using the same, and a method for manufacturing a substrate having the alignment film. Furthermore, the present invention relates to a novel method for producing a liquid crystal display element having excellent image sticking properties and reliability such as voltage retention. Background technique [0002] Liquid crystal display devices are known as display devices that are light in weight, thin in cross-section, and low in power consumption. In recent years, they have been used in large-scale television applications, etc., and have achieved remarkable development. The liquid crystal display element is constituted, for example, by sandwiching a liquid crystal layer between a pair of transparent substrates provided with electrodes. Also, in a liquid crystal display element, an organic film...

Claims

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Application Information

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IPC IPC(8): C08L101/12C08L33/10G02F1/1337
CPCC08L33/10C08L101/12G02F1/133788
Inventor 名木达哉南悟志芦泽亮一万代淳彦根木隆之川月喜弘近藤瑞穂
Owner NISSAN CHEM IND LTD
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