WO2004072719A1 - 液晶配向剤およびそれを用いた液晶配向膜 - Google Patents

液晶配向剤およびそれを用いた液晶配向膜 Download PDF

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Publication number
WO2004072719A1
WO2004072719A1 PCT/JP2004/001362 JP2004001362W WO2004072719A1 WO 2004072719 A1 WO2004072719 A1 WO 2004072719A1 JP 2004001362 W JP2004001362 W JP 2004001362W WO 2004072719 A1 WO2004072719 A1 WO 2004072719A1
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Prior art keywords
liquid crystal
aligning agent
crystal aligning
crystal alignment
alignment film
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PCT/JP2004/001362
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English (en)
French (fr)
Japanese (ja)
Inventor
Mariko Kurosaki
Go Ono
Kio Mizuno
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Nissan Chemical Industries, Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by Nissan Chemical Industries, Ltd. filed Critical Nissan Chemical Industries, Ltd.
Priority to JP2005504963A priority Critical patent/JP4561631B2/ja
Priority to US10/545,268 priority patent/US7537812B2/en
Publication of WO2004072719A1 publication Critical patent/WO2004072719A1/ja

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    • G—PHYSICS
    • G02—OPTICS
    • G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133—Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333—Constructional arrangements; Manufacturing methods
    • G02F1/1337—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers
    • G02F1/133711—Surface-induced orientation of the liquid crystal molecules, e.g. by alignment layers by organic films, e.g. polymeric films
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02—Alignment layer characterised by chemical composition
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02—Alignment layer characterised by chemical composition
    • C09K2323/025—Polyamide
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
    • C09K2323/02—Alignment layer characterised by chemical composition
    • C09K2323/027—Polyimide

Definitions

  • the present invention relates to a liquid crystal alignment agent used for a liquid crystal display device and a liquid crystal alignment film using the same. More specifically, the present invention relates to a liquid crystal aligning agent that provides good coating uniformity even when the drying temperature at the time of forming a coating film changes, and a liquid crystal aligning film using the same.
  • liquid crystal display devices are widely used in personal computer displays and televisions as thin and lightweight display devices.
  • liquid crystal display devices have a polyamic acid-polyimide alignment.
  • Membranes are often used.
  • these liquid crystal alignment films are formed by applying a liquid crystal alignment agent in which a polyamic acid or polyimide is dissolved in an organic solvent to a substrate by flexographic printing or the like, and then performing preliminary drying and firing. At this time, it is not preferable that the coating film of the liquid crystal aligning agent has a partial thickness unevenness, which may adversely affect the display characteristics of the liquid crystal display element.
  • the solvent is a mixture of a solvent having high solubility of polyamic acid-polyimide and a solvent such as butyl sorbate. It is also known that a smooth coating film without unevenness can be obtained even when dipropylene glycol monomethyl ether is used in place of the butylacetate solvent (see Japanese Patent Application Laid-Open No. 7-109438). ). Similarly, it is known that the repellency of the repellent film can be improved even when diethylene glycol getyl ether is mixed (see Japanese Patent Application Laid-Open No. 8-28983).
  • Such a liquid crystal aligning agent is usually preliminarily dried at a temperature of 80 or higher after being applied to a substrate.
  • the liquid crystal aligning agent has been required. There is a situation in which the preliminary drying is performed at a lower temperature than before.
  • a uniform coating film may not be formed when dried at a low temperature, and a liquid crystal aligning agent capable of obtaining a uniform coating film regardless of the preliminary drying temperature has been desired. Disclosure of the invention
  • the present invention has been made in view of such circumstances, and provides a liquid crystal aligning agent that provides good coating uniformity regardless of the drying temperature after coating, and a liquid crystal aligning film that has good coating uniformity. It is in.
  • the present inventors have conducted intensive studies and have found that a liquid crystal aligning agent containing at least one polymer selected from polyamic acids or soluble polyimides and two or more specific solvents can provide a liquid crystal. It has been found that a uniform coating film can be formed regardless of the drying temperature when forming an alignment film.
  • the present invention has the following features.
  • Liquid crystal alignment characterized by containing at least one kind of polymer selected from the group consisting of polyamic acid and soluble polyimide, diethylene glycol getyl ether, and dipropylene glycol monomethyl ether. Agent.
  • liquid crystal alignment agent according to any one of the above (1) and (4), containing at least one kind of solvent.
  • liquid crystal aligning agent according to (5), wherein the content of at least one solvent selected from the group consisting of pyridones and lactones in the liquid crystal aligning agent is 390% by weight. Liquid crystal alignment agent.
  • the liquid crystal aligning agent contains at least one polymer selected from the group consisting of polyamic acid and a soluble polyimide, dimethylene glycol monoethyl ether, and dipropylene glycol monomethyl ether.
  • the polyamic acid used in the present invention is a polymer obtained by reacting diamine with an acid dianhydride
  • the soluble polyimide is a dehydration ring-closure (imimine) of the obtained polyamic acid in whole or in part.
  • Solvent-soluble polyimide obtained by The structure is not particularly limited as long as the polyamic acid is soluble polyimid as described above.
  • Examples of the diamine compound used for synthesizing the polyamic acid include the following.
  • Examples of alicyclic diamines include 1,4 diaminocyclohexane, 13-diaminocyclohexane, 4,4 'diaminodicyclohexylmethane, 44, diamino-3 3'-dimethyldicyclohexane, Examples include isophorone diamine.
  • Examples of carbocyclic aromatic diamines include o-phenylenediamine, m-phenylenediamine, p-phenylenediamine, diaminotoluenes (for example, 24 diamino toluene), and 14 diamino diamine.
  • (4-aminophenyl) phenylphosphonoxide bis (4-aminophenol) hexahexylphosphinoxide, ⁇ , ⁇ -bis (4-aminoaminophenyl) -phenylamine, ⁇ , ⁇ -Bis (4-aminophenyl: 100-methylphane, 4,4,1-diaminodiphenylurea, 1,8-diaminononaphthalene, 1,5-diaminononaphthalene, 1,5-diaminoanthraquinone , Diaminofluorenes (for example, 2,6-diaminofluorene), bis (4-aminophenyl) getylsilane, bis (4-aminophenyl) dimethylsilane, 3,4, diaminodiphenyl ether, benzidine , 2,2'-Dimethylbenzidine, 2,2-bis [4- (4-amino-phenoxy) phenyl]
  • heterocyclic diamines 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin, 2,6-diamine: nobiridin
  • 1,3,4-thiadiazole, 2,4-diamino-16-phenyl-2-s-triazine and the like are examples of aliphatic diamines, 1,2-diaminothane,
  • R represents a monovalent organic group having 5 or more carbon atoms, preferably 5 or more and 20 or less, including a long-chain alkyl group or a long-chain alkyl group or a perfluoroalkyl group.
  • these diamines can be used alone or in combination.
  • a long-chain alkyl or perfluoro group represented by a boat fork formula (1) is used. It is preferable to contain at least one of the aromatic diamines. Above all, it is particularly preferable to include 13-dia-S-no-4 (trans- 4 heptyl-six-hexyl) phenoxybenzene because of its excellent heat resistance when used as a liquid crystal alignment film.
  • the hydrate used as a raw material when synthesizing a polyamic acid is pyromellitic dianhydride as an aromatic dianhydride, 33′4,4′-biph Xnyltetracarboxylic dianhydride, 2,2 '3 3 Biphenyltetracarboxylic dianhydride, 23, 3' 4 Biphenyltetracarponic dianhydride, 3, 3 ', 4 4'-Benzophenonetetracarboxylic acid-hydrate, 2, 3 , 3 ', 4'-Benzophenone tetracarboxylic acid dianhydride, bis (3,4-dicarboxyphenyl) ether hydrate, bis (34-dicarboxyphenyl) sulfone dianhydride, 1 2 5 6 — Naph Yu Len Tetracarboxylic dianhydride and 2,3,6,7-naphthylenetetracarboxylic dianhydride.
  • Examples of the alicyclic acid dianhydride include 1,2,3,4-cyclobutanetetracarboxylic dianhydride, 1,2,3,4-cyclopentanetetracarboxylic dianhydride, 2,3,4, 5-tetrahydrofuran tetracarboxylic dianhydride, 1,2,4,5-cyclohexanetetracarboxylic dianhydride, 3,4-dicaroxy-1-cyclohexylsuccinic dianhydride, 3,4-dicarboxy-1,4 Examples thereof include 2,3,4-tetrahydro 1-naphthalene succinic dianhydride and bicyclo [3,3,0] octane-1,2,4,6,8-tetracarboxylic dianhydride.
  • acid dianhydrides can be used alone or in combination.
  • 1,2,3,4-cyclobutanetetracarboxylic dianhydride is particularly preferable because of its excellent property balance when used as a liquid crystal alignment film.
  • the polyamic acid used in the present invention is obtained by mixing the above-mentioned diamine and acid dianhydride in the presence of an organic solvent at 120 ° C. to 150 ° C., preferably at 0 t: to 80 ° C. for 30 minutes to It can be synthesized by reacting for 24 hours, preferably 1 to 10 hours.
  • the molar ratio of diamine and acid dianhydride used in the reaction is such that if the diamine is too large, the molecular weight will not increase, and if it is too small, the acid anhydride will remain and storage stability will be impaired.
  • the dianhydride is preferably 0.5 to 3.0 / 1.0 (molar ratio), and the diamine Z-acid dianhydride is preferably 0.8 to 2.0 / 1.0 (molar ratio).
  • diamine / acid dianhydride particularly preferably 1.0 to 1.2 / 1.0 (molar ratio).
  • the solvent and the concentration used in the synthesis of the polyamic acid are not particularly limited, but the solvents include N, N-dimethylformamide, N, N-dimethylacetamide, and N-methyl-2-pyrrolid. It is preferable to use dong, N-methylcaprolactam, dimethylsulfoxide, tetramethylurea, pyridine, dimethylsulfoxide, or ptyrrolactone because the resulting polymer has high solubility.
  • the concentration of polyamic acid during polymerization is increased. If it is too low, the handleability of the varnish deteriorates, and if it is too low, the molecular weight does not increase.
  • it is preferably 1 to 50% by weight, more preferably 5 to 30% by weight, and particularly preferably 8 to 20% by weight. Is good. Needless to say, a poor solvent such as butylcellsolve toluene or methanol may be added as long as the polymer is dissolved.
  • the water in the reaction system hinders the increase of the molecular weight of the polymer, it is preferable to keep the inside of the reaction system under a nitrogen atmosphere. If the reaction is performed while bubbling nitrogen into the solvent in the reaction system, the reaction is further performed. preferable.
  • the viscosity of the polyamic acid used in the present invention is high, it is difficult to handle the liquid crystal aligning agent, and if the viscosity is low, the characteristics are not stable when the alignment film is formed, so that the reduced viscosity is 0.05 to 3.0 Odl / g. And more preferably 0.1 to 2.5 dl / g (measured at a concentration of 0.5 g / d 1 in N-methyl-2-pyrrolidone at a temperature of 30).
  • the polyamic acid obtained as described above may be used as it is.
  • the polyamic acid when it is heated or catalyzed, it is completely or partially dehydrated by ring closure (imidation), and when used as a soluble polyimide, storage stability is improved. It is preferable because it excels in nature.
  • the imidization reaction for converting polyamic acid into a soluble polyimide can be performed by heating the polyamic acid solution as it is, or by adding a catalyst to the solution of the polyamic acid.
  • Chemical imidization in which the imidization reaction proceeds at a relatively low temperature, is preferable since the molecular weight of the obtained soluble polyimid is not easily reduced.
  • a polyamic acid is dissolved in an organic solvent in an amount of 0.5 to 30 moles, preferably 1 to 20 moles, of a base catalyst and 0 to 10 moles of an acid group.
  • the acid anhydride examples include acetic anhydride, trimellitic anhydride, pyromellitic anhydride and the like. Above all, acetic anhydride is preferred because purification after the reaction is facilitated.
  • the organic solvent for performing the imidization reaction the above-mentioned solvent used in the synthesis of the polyamic acid can be used.
  • the imidization rate due to chemical imidization can be controlled by adjusting the amount of catalyst and the reaction temperature.However, if the imidization rate is too low, the storage stability when using a liquid crystal aligning agent If it is too high, the solubility may be poor and may precipitate out. Therefore, the molar number of the total polyamic acid is preferably 0.1 to 99%, more preferably 5 to 90%, and more preferably 30 to 7%. 0% is particularly preferred.
  • the polyamic acid or soluble polyimide obtained as described above can be purified by injecting it into a poor solvent while stirring well and reprecipitating it.
  • the poor solvent used at this time is not particularly limited, but examples thereof include methanol, acetone, hexane, butylcellsolp, heptane, methyl ethyl ketone, methyl isobutyl ketone, ethanol, toluene, and benzene.
  • the polyamic acid or soluble polyimide obtained by the reprecipitation can be recovered by filtration and then dried at normal temperature or reduced pressure at normal temperature or under heat to obtain a powder.
  • the polyamic acid or soluble polyimide powder thus obtained can be dissolved again in a solvent containing a good solvent to form a varnish.
  • the liquid crystal aligning agent of the present invention comprises at least one polymer selected from the group consisting of a polyamic acid and a soluble polyimide obtained by the above method, diethylene glycol ethyl ether, and dipropylene glycol monomethyl. And ether.
  • a polymer selected from the group consisting of a polyamic acid and a soluble polyimide obtained by the above method, diethylene glycol ethyl ether, and dipropylene glycol monomethyl. And ether.
  • diethylene glycol diethyl ether and dipropylene glycol monomethyl ether are added little by little.
  • the polymer It is preferable because one dissolution is quick and the working efficiency is good.
  • a uniform solution is obtained by stirring at 0 to 150, preferably at room temperature to 100: 1 to 100 hours. It can be.
  • the good solvent used for dissolving the polyamic acid or the soluble polyimide is not particularly limited. Specifically, N, N-dimethylformamide, N, N-dimethylamide Cetamide, N-methyl-2-pyrrolidone, N-methylcaprolactam, dimethylsulfoxide, and carpirolactone can be exemplified. These solvents are contained in the liquid crystal aligning agent of the present invention preferably at 30 to 90% by weight, particularly preferably at 50 to 80% by weight.
  • a solvent it is preferable to include at least one selected from the group consisting of pyrrolidones and lactones because the solubility of the polymer is increased, and it is preferable to include both pyrrolidones and lactones. It is particularly preferable because the wettability when applying the liquid crystal alignment agent is good and the hygroscopicity of the coating solution can be suppressed.
  • the pyrrolidones N-methyl-12-pyrrolidone is preferable, and as the lactones, aptyrrolactone is preferable.
  • the concentration of the polymer such as polyamic acid or soluble polyimide in the liquid crystal alignment agent of the present invention is too high, it is difficult to adjust the film thickness when applied to a substrate to form a liquid crystal alignment film, and if the concentration is too low, the liquid crystal alignment film is not used. In this case, a sufficient film thickness cannot be obtained, so that the content is preferably 2 to 15% by weight, more preferably 3 to 8% by weight.
  • the liquid crystal aligning agent of the present invention needs to further contain two kinds of solvents, diethylene glycol methyl ether and dipropylene glycol monomethyl ether. . If the blending amount of the ethylene glycol getyl ether is too small, the uniformity of the coating film as a liquid crystal alignment film is reduced. If the blending amount is too large, polyamic acid-soluble polyimide is precipitated. 0.1 to 70% by weight is preferred, 1 to 50% by weight is more preferred, and 5 to 40% by weight is particularly preferred. New Also, when the amount of dipropylene glycol monomethyl ether is too small, the uniformity of the coating film as a liquid crystal alignment film is reduced, and when the amount is too large, polyamic acid and soluble polyimide are precipitated. The whole agent
  • 0.1 to 70% by weight is preferable, 1 to 50% by weight is more preferable, and 5 to 4% by weight is preferable.
  • additives such as a crosslinking agent and a force-printing agent can be added to the liquid crystal alignment agent.
  • the liquid crystal alignment agent thus obtained can be filtered and then applied to a substrate to form a liquid crystal alignment film.
  • a method of applying the composition to a substrate include a spin coating method, a flexographic printing method, and an ink jet method.
  • the flexographic printing method is preferable because the formed coating film has excellent uniformity and can be easily enlarged.
  • the substrate to be used is not particularly limited as long as it is a substrate having high transparency, and a glass substrate, a plastic substrate such as an acrylic substrate or a polycarbonate substrate, or the like can be used. Needless to say, it is preferable to use a substrate on which an I T0 electrode for driving the liquid crystal is formed from the viewpoint of simplifying the process.
  • the liquid crystal aligning agent of the present invention is uniformly coated on a substrate to improve the uniformity of the coating film
  • the liquid crystal aligning agent is preferably at room temperature to 200 ⁇ X, more preferably at 30 to 150 t: More preferably, it is preferable to perform preliminary drying at 50 to 120 for 1 to 100 minutes. This makes it possible to adjust the volatility of each component of the liquid crystal aligning agent and obtain a uniform and even coating film.
  • An alignment film can be formed.
  • the liquid crystal alignment film thus formed is used for a liquid crystal display device after being subjected to a uniaxial alignment treatment by rubbing or irradiation with polarized ultraviolet rays, or without a uniaxial alignment treatment in some applications such as a vertical alignment film.
  • NMP N-methyl-2-pyrrolidone
  • the polyimide powder obtained in Synthesis Example 1 was placed in a 100 ml eggplant flask.
  • This liquid crystal aligning agent was flexographically printed on the washed glass substrate with ITO using an alignment film printing machine (“Angstroma I” manufactured by Nissha Seizo).
  • the printed substrates were left on hot plates at 50 ° C, 65 ° and 80 ° C for 5 minutes, respectively, to perform preliminary drying of the coating film.
  • this substrate was baked for 60 minutes in an open state of 200 to obtain a substrate with a liquid crystal alignment film. No unevenness due to a change in film thickness occurred in the liquid crystal alignment film, and a uniform liquid crystal alignment film could be obtained at any of the preliminary drying temperatures.
  • the polyimide powder obtained in Synthesis Example 1 was placed in a 100 ml eggplant flask.
  • This liquid crystal aligning agent was printed on a substrate and temporarily dried in the same manner as in Example 1, and then observed. As a result, at any of the pre-drying temperatures, no unevenness was generated due to a change in the thickness of the coating film, and a uniform coating film was formed. Further, the liquid crystal alignment film obtained by firing in the same manner as in Example 1 did not show unevenness due to a change in film thickness, and a uniform liquid crystal alignment film could be obtained at any pre-drying temperature. done. (Example 3)
  • This liquid crystal aligning agent was printed on a substrate and temporarily dried in the same manner as in Example 1, and then observed. As a result, at any of the pre-drying temperatures, no unevenness was generated due to a change in the thickness of the coating film, and a uniform coating film was formed. Further, the liquid crystal alignment film obtained by firing in the same manner as in Example 1 did not show unevenness due to a change in film thickness, and a uniform liquid crystal alignment film could be obtained at any pre-drying temperature. done.
  • This liquid crystal aligning agent was printed on a substrate and temporarily dried in the same manner as in Example 1, and then observed. As a result, at any of the pre-drying temperatures, no unevenness was generated due to a change in the thickness of the coating film, and a uniform coating film was formed. Furthermore, the liquid crystal alignment film obtained by sintering in the same manner as in Example 1 did not show unevenness due to a change in film thickness, and it was possible to obtain a uniform liquid crystal alignment film at any temporary drying temperature. done.
  • This liquid crystal aligning agent was printed on a substrate and temporarily dried in the same manner as in Example 1, and then observed.
  • As a result when dried at 50 ⁇ , 65X :, unevenness due to a change in film thickness was observed, and a uniform coating film could not be obtained.
  • the unevenness due to the change in the film thickness was not eliminated, and when the preliminary drying temperature was low, a uniform liquid crystal alignment film could be obtained.
  • the preliminary drying temperature was low
  • This liquid crystal aligning agent was printed on a substrate and temporarily dried in the same manner as in Example 1, and then observed. As a result, when dried at 50 ° C. and 65, unevenness due to a change in film thickness was observed, and a uniform coating film could not be obtained. Furthermore, in the liquid crystal alignment film obtained by firing in the same manner as in Example 1, the unevenness due to the change in the film thickness was not eliminated, and when the preliminary drying temperature was low, a uniform liquid crystal alignment film could be obtained. Can not be done. table 1
  • the liquid crystal aligning agent of this invention it becomes possible to form a uniform coating film even if the temperature of preliminary drying is low, and it is possible to reduce energy cost, improve process margin, and improve yield. Become. Furthermore, the formed liquid crystal alignment film has high uniformity, and can display a good image without unevenness particularly when a large-sized liquid crystal display device is manufactured.

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  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Mathematical Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Liquid Crystal (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
PCT/JP2004/001362 2003-02-12 2004-02-10 液晶配向剤およびそれを用いた液晶配向膜 WO2004072719A1 (ja)

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US10/545,268 US7537812B2 (en) 2003-02-12 2004-02-10 Aligning agent for liquid crystal and liquid-crystal alignment film obtained with the same

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JP2006030961A (ja) * 2004-06-18 2006-02-02 Jsr Corp 垂直液晶配向剤、および垂直液晶表示素子
WO2007078153A1 (en) * 2006-01-04 2007-07-12 Lg Chem. Ltd. Composition for liquid crystal aligning, liquid crystal aligning layer prepared from the same, and liquid crystal display comprising the same
JP2008076921A (ja) * 2006-09-25 2008-04-03 Hitachi Displays Ltd 液晶表示装置
WO2009107406A1 (ja) * 2008-02-28 2009-09-03 シャープ株式会社 液晶配向膜形成用組成物及び液晶表示装置
WO2013125595A1 (ja) * 2012-02-22 2013-08-29 日産化学工業株式会社 組成物、液晶配向処理剤、液晶配向膜及び液晶表示素子
KR20140035806A (ko) * 2012-09-14 2014-03-24 제이에스알 가부시끼가이샤 액정 배향제, 액정 배향막 및 액정 표시 소자
WO2014061778A1 (ja) * 2012-10-18 2014-04-24 日産化学工業株式会社 組成物、液晶配向処理剤、液晶配向膜および液晶表示素子
WO2014061779A1 (ja) * 2012-10-18 2014-04-24 日産化学工業株式会社 組成物、液晶配向処理剤、液晶配向膜および液晶表示素子
WO2014061780A1 (ja) * 2012-10-18 2014-04-24 日産化学工業株式会社 組成物、液晶配向処理剤、液晶配向膜および液晶表示素子
WO2014061781A1 (ja) * 2012-10-18 2014-04-24 日産化学工業株式会社 組成物、液晶配向処理剤、液晶配向膜および液晶表示素子

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TWI335455B (en) * 2005-09-22 2011-01-01 Ind Tech Res Inst Liquid crystal display device
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JP5273357B2 (ja) * 2007-07-06 2013-08-28 Ｊｓｒ株式会社 液晶配向剤および液晶表示素子
KR100952965B1 (ko) 2007-08-30 2010-04-16 제일모직주식회사 액정배향제, 및 이를 이용하여 제조된 액정배향막
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KR100913605B1 (ko) 2007-12-07 2009-08-26 제일모직주식회사 액정 광배향제, 이를 포함하는 액정 광배향막, 및 이를포함하는 액정 표시 장치
KR101288558B1 (ko) 2008-12-12 2013-07-22 제일모직주식회사 액정 광배향제 및 이를 이용하여 제조된 액정 광배향막
WO2010079637A1 (ja) * 2009-01-08 2010-07-15 シャープ株式会社 液晶配向膜形成用組成物及び液晶表示装置
CN102102019A (zh) * 2009-12-16 2011-06-22 第一毛织株式会社 液晶光取向剂、液晶光取向层及其液晶显示器装置
CN102559205B (zh) 2010-12-29 2014-07-30 第一毛织株式会社 液晶取向剂、使用其制造的液晶取向膜和液晶显示器
KR101444190B1 (ko) 2011-12-19 2014-09-26 제일모직 주식회사 액정 배향제, 이를 이용한 액정 배향막 및 상기 액정 배향막을 포함하는 액정표시소자
JP5990928B2 (ja) * 2012-02-24 2016-09-14 Jsr株式会社 液晶配向剤
JP6146135B2 (ja) * 2012-08-30 2017-06-14 Jsr株式会社 液晶配向剤、液晶配向膜、液晶配向膜の製造方法及び液晶表示素子
CN103224637B (zh) * 2013-03-21 2015-02-25 京东方科技集团股份有限公司 一种液晶取向膜及其制备方法与应用
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