JP2011076065A - Method for manufacturing liquid crystal display element - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a method for manufacturing a liquid crystal display element having a wide viewing angle, a fast response speed of liquid crystal molecules and excellent in display characteristics and long-term reliability. <P>SOLUTION: The method for manufacturing the liquid crystal display element includes steps of: applying a polymer composition containing (A) at least one kind of polymer selected from a group consisting of polyamic acids and polyimide and (B) a specified compound represented by di(meth)acrylate having a biphenyl structure, on a conductive film of a pair of substrates each having the conductive film, to form a coating film; forming a liquid crystal cell by disposing the pair of substrates having the coating films formed thereon in such a manner that the coating films oppose to each other through a layer of liquid crystal molecules; and irradiating the liquid crystal cell with light while applying a voltage between the conductive films of the pair of substrates. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a method for manufacturing a liquid crystal display element. More specifically, the present invention relates to a novel method for manufacturing a liquid crystal display device having a wide viewing angle and a fast response speed.

Among liquid crystal display elements, an MVA (Multi-Domain Vertical Alignment) type panel conventionally known as a vertical alignment mode forms protrusions in the liquid crystal panel, thereby restricting the tilting direction of the liquid crystal molecules. The viewing angle is expanded. However, according to this method, the lack of transmittance and contrast due to the protrusions is unavoidable, and there is a problem that the response speed of the liquid crystal molecules is slow.
In recent years, a PSA (Polymer Sustained Alignment) mode has been proposed in order to solve the problems of the MVA type panel as described above. The PSA mode is a polymerizable compound in a gap between a pair of substrates composed of a substrate with a patterned conductive film and a substrate with a conductive film having no pattern, or between a pair of substrates composed of two substrates with a patterned conductive film. An attempt is made to control the alignment direction of the liquid crystal by expressing a pretilt angle characteristic by irradiating ultraviolet rays in a state where a voltage is applied between the conductive films while sandwiching the liquid crystal composition containing the liquid crystal and polymerizing the polymerizable compound. Technology. According to this technology, it is possible to increase the viewing angle and speed up the liquid crystal molecule response by making the conductive film into a specific configuration, and also solve the problem of lack of transmittance and contrast that was inevitable in the MVA type panel. Is done. However, in order to polymerize the polymerizable compound, it is necessary to irradiate a large amount of ultraviolet light, for example, 100,000 J / m ^2. It becomes clear that the reactive compounds remain in the liquid crystal layer, which together cause display unevenness, adversely affect the voltage holding characteristics, or cause problems in the long-term reliability of the panel. Has not reached.
On the other hand, Non-Patent Document 1 proposes a method using a liquid crystal alignment film formed from a polyimide liquid crystal aligning agent containing a reactive mesogen. According to Non-Patent Document 1, a liquid crystal display element including a liquid crystal alignment film formed by such a method is said to respond quickly to liquid crystal molecules. However, Non-Patent Document 1 does not provide any guidance on what kind of reactive mesogen should be used, and the amount of necessary ultraviolet irradiation is still large, and there are concerns about display characteristics, particularly voltage holding characteristics. Not wiped out.

JP-A-5-107544 JP 2010-97188 A

Y. -J. Lee et. al. SID 09 DIGEST, p. 666 (2009) T.A. J. et al. Scheffer et. al. , J .; Appl. Phys. vol. 48, p. 1783 (1977) F. Nakano, et. al. , JPN. J. et al. Appl. Phys. vol. 19, p. 2013 (1980)

  The present invention has been made in view of the above circumstances, and an object of the present invention is to provide a method for manufacturing a liquid crystal display element having a wide viewing angle, a high response speed of liquid crystal molecules, and excellent display characteristics and long-term reliability. To do.

According to the present invention, the above problem of the present invention is as follows.
On the conductive film of the pair of substrates having the conductive film,
(A) at least one polymer selected from the group consisting of polyamic acid and polyimide, and (B) the following formula (BI) in the molecule
^{-X 1 -Y 1 -X 2 - (} B-I)
(In Formula (BI), X ¹ and X ² are each independently a 1,4-phenylene group or a 1,4-cyclohexylene group, and Y ¹ is a single bond having 1 to 3 carbon atoms. A divalent hydrocarbon group, an oxygen atom, a sulfur atom or —COO—, wherein X ¹ and X ² are one or more alkyl groups having 1 to 4 carbon atoms and alkoxyl groups having 1 to 4 carbon atoms. , May be substituted with a fluorine atom or a cyano group.)
And at least one divalent group represented by the following formula (B-II):

(In Formula (B-II), R is a hydrogen atom or a methyl group, and Y ² and Y ³ are each independently an oxygen atom or a sulfur atom.)
Applying a polymer composition containing a compound having at least two monovalent groups represented by the formula:
A pair of substrates on which the coating film is formed are arranged to face each other so that the coating film faces through a layer of liquid crystal molecules to form a liquid crystal cell,
This is achieved by a method for manufacturing a liquid crystal display element, which includes a step of irradiating light to the liquid crystal cell in a state where a voltage is applied between conductive films of the pair of substrates.

The liquid crystal display device manufactured by the method of the present invention has a wide viewing angle, a high response speed of liquid crystal molecules, sufficient transmittance and contrast, excellent display specification, and display characteristics even when driven continuously for a long time. Will not be damaged.
In addition, according to the method of the present invention, the amount of light required for irradiation can be reduced, which contributes to a reduction in manufacturing cost of the liquid crystal display element.
Therefore, the liquid crystal display device manufactured by the method of the present invention is superior to the conventionally known liquid crystal display device in both performance and cost, and can be suitably applied to various applications.

It is explanatory drawing which shows the pattern of the transparent conductive film in the liquid crystal cell which has the patterned transparent conductive film manufactured in the Example and the comparative example. It is explanatory drawing which shows the pattern of the transparent conductive film in the liquid crystal cell which has the patterned transparent conductive film manufactured in the Example. It is explanatory drawing which shows the pattern of the transparent conductive film in the liquid crystal cell which has the patterned transparent conductive film manufactured in the Example.

<Polymer composition>
The polymer composition used in the method of the present invention is:
(A) at least one polymer selected from the group consisting of polyamic acid and polyimide, and (B) at least one divalent group represented by the above formula (BI) in the molecule and the above formula (B A compound having at least two monovalent groups represented by -II).

[(A) Polymer]
The polymer contained in the polymer composition used in the present invention is at least one selected from the group consisting of polyamic acid and polyimide.
The polyamic acid can be synthesized by, for example, reacting tetracarboxylic dianhydride and diamine, and the polyimide can be synthesized by dehydrating and ring-closing the polyamic acid to imidize.
{Tetracarboxylic acid dianhydride}
Examples of tetracarboxylic dianhydrides used to synthesize the polyamic acid include aliphatic tetracarboxylic dianhydrides, alicyclic tetracarboxylic dianhydrides, aromatic tetracarboxylic dianhydrides, and the like. be able to. Specific examples of these include aliphatic tetracarboxylic dianhydrides such as butane tetracarboxylic dianhydride;
Examples of the alicyclic tetracarboxylic dianhydride include 1,2,3,4-cyclobutanetetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentylacetic acid dianhydride, 1,3,3a, 4, 5,9b-Hexahydro-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 1,3,3a, 4,5,9b- Hexahydro-8-methyl-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 3-oxabicyclo [3.2.1] octane -2,4-dione-6-spiro-3 '-(tetrahydrofuran-2', 5'-dione), 5- (2,5-dioxotetrahydro-3-furanyl) -3-methyl-3-cyclohexene- No 1,2-dicarboxylic acid Things, 3,5,6-tricarboxy-2-carboxymethyl norbornane -2: 3,5: 6-dianhydride, 4,9-dioxatricyclo [5.3.1.0 ^{2, 6]} undecane -3,5,8,10-tetraone and the like;
Examples of the aromatic tetracarboxylic dianhydride include pyromellitic dianhydride and the like, respectively, and tetracarboxylic dianhydride described in Patent Document 2 (Japanese Patent Laid-Open No. 2010-97188). May be used.
Among these, as the tetracarboxylic dianhydride used for synthesizing the polyamic acid, only alicyclic tetracarboxylic dianhydride is used, or alicyclic tetracarboxylic dianhydride and aromatic tetra Preference is given to using mixtures with carboxylic dianhydrides. In the latter case, the ratio of the alicyclic tetracarboxylic dianhydride in the total tetracarboxylic dianhydride is preferably 20 mol% or more, and more preferably 40 mol% or more.

{Diamine}
As the diamine used for synthesizing the polyamic acid, the following formula (D ′)

(In the formula (D ′), R ^I is an alkyl group having 4 to 40 carbon atoms or a fluoroalkyl group having 4 to 40 carbon atoms, or a hydrocarbon group having 17 to 51 carbon atoms having a steroid skeleton;
Z ^I represents a single ^bond, * ^-O-, a * -COO- or ^* -OCO- (where bond marked with "*" is ^{R I} side.)
R ^II is a cyclohexylene group or a phenylene group,
n1 is 1 or 2,
However, when n1 is 2, two R ^II may be the same or different from each other,
n2 is 0 or 1;
Z ^II is ^{* -O-,} a * -COO- or ^* -OCO- (where bond marked with "*" is ^{R I} side.)
n3 is an integer of 0 to 2,
n4 is 0 or 1. )
It is preferable to use a diamine containing a diamine having a group represented by (hereinafter referred to as “specific diamine”).

As the alkyl group having 4 to 40 carbon atoms of R ¹ in the above formula (D ′), an alkyl group having 6 to 40 carbon atoms is preferable, and specifically, for example, a hexyl group, an octyl group, a decyl group, a dodecyl group, hexadecyl Groups, stearyl groups, etc .;
The fluoroalkyl group having 4 to 40 carbon atoms is preferably a fluoroalkyl group having 4 to 20 carbon atoms. Specifically, for example, a trifluoromethylpropyl group, a trifluoromethylbutyl group, a trifluoromethylhexyl group, or trifluoromethyldecyl is used. A group, a pentafluoroethylpropyl group, a pentafluoroethylbutyl group, a pentafluoroethyloctyl group, etc .;
Examples of the 17-51 hydrocarbon group having a steroid skeleton may include a cholestanyl group, a cholestenyl group, and a lanostannyl group.
The cyclohexylene group and phenylene group of R ^II in the above formula (D ′) are preferably a 1,4-cyclohexylene group and a 1,4-phenylene group, respectively. Examples of the divalent group represented by — (R ^II ) _n1 — in the above formula (D ′) include those in which n1 is 1, such as a 1,4-phenylene group, a 1,2-cyclohexylene group, and the like. ;
As a case where n1 is 2, for example, 4,4′-biphenylene group, 4,4′-bicyclohexylene group,

(In the formula, a bond marked with "*" is R ^I side.)
The groups represented by each of the above can be mentioned as preferred examples.
N3 in the formula (D ′) is preferably 2.
The specific diamine in the present invention is preferably an aromatic diamine having a group represented by the above formula (D ′). Specific examples thereof include dodecanoxy-2,4-diaminobenzene and pentadecanoxy-2,4-diamino. Benzene, hexadecanoxy-2,4-diaminobenzene, octadecanoxy-2,4-diaminobenzene, dodecanoxy-2,5-diaminobenzene, pentadecanoxy-2,5-diaminobenzene, hexadecanoxy-2,5-diaminobenzene, octadecanoxy-2 , 5-diaminobenzene, cholestanyloxy-3,5-diaminobenzene, cholestenyloxy-3,5-diaminobenzene, cholestanyl 3,5-diaminobenzoate, cholestenyl 3,5-diaminobenzoate, 3,5- Lanos diaminobenzoate Tanyl and the like can be mentioned, and it is preferable to use one or more of these. The specific diamine in the present invention is composed of hexadecanoxy-2,5-diaminobenzene, octadecanoxy-2,5-diaminobenzene, cholestanyloxy-3,5-diaminobenzene and cholestenyloxy-3,5-diaminobenzene. It is preferable to use at least one selected from the group.
As the diamine used for synthesizing the polyamic acid, only the specific diamine as described above may be used, or the specific diamine and another diamine may be used in combination.

Other diamines that can be used here are diamines having no group represented by the above formula (D ′), such as aliphatic diamines, alicyclic diamines, aromatic diamines, diaminoorganosiloxanes, and the like. Therefore, it does not correspond to the specific diamine. Specific examples thereof include aliphatic diamines such as 1,1-metaxylylenediamine, 1,3-propanediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine and the like;
Examples of alicyclic diamines include 1,4-diaminocyclohexane, 4,4′-methylenebis (cyclohexylamine), 1,3-bis (aminomethyl) cyclohexane and the like;
Examples of aromatic diamines include p-phenylenediamine, 4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenyl sulfide, 1,5-diaminonaphthalene, 2,2′-dimethyl-4,4′-diaminobiphenyl, 4,4′-diamino-2,2′-bis (trifluoromethyl) biphenyl, 2,7-diaminofluorene, 4,4′-diaminodiphenyl ether, 2,2-bis [4- (4-aminophenoxy) phenyl ] Propane, 9,9-bis (4-aminophenyl) fluorene, 2,2-bis [4- (4-aminophenoxy) phenyl] hexafluoropropane, 2,2-bis (4-aminophenyl) hexafluoropropane 4,4 ′-(p-phenylenediisopropylidene) bisaniline, 4,4 ′-(m-phenylenediisopropylene Riden) bisaniline, 1,4-bis (4-aminophenoxy) benzene, 4,4′-bis (4-aminophenoxy) biphenyl, 2,6-diaminopyridine, 3,4-diaminopyridine, 2,4-diamino Pyrimidine, 3,6-diaminoacridine, 3,6-diaminocarbazole, N-methyl-3,6-diaminocarbazole, N-ethyl-3,6-diaminocarbazole, N-phenyl-3,6-diaminocarbazole, N , N′-bis (4-aminophenyl) -benzidine, N, N′-bis (4-aminophenyl) -N, N′-dimethylbenzidine and the like;
Examples of the diaminoorganosiloxane include 1,3-bis (3-aminopropyl) -tetramethyldisiloxane, and the diamine described in Patent Document 2 (Japanese Patent Laid-Open No. 2010-97188). May be used.
The diamine used for synthesizing the polyamic acid preferably contains 2 mol% or more, more preferably 2 to 60 mol% of the specific diamine as described above, more preferably 5 to 60 mol%. It is more preferable that it is contained in an amount of ˜40 mol%, particularly preferably 10 to 30 mol%.

{Molecular weight regulator}
When synthesizing the polyamic acid, a terminal-modified polymer may be synthesized using an appropriate molecular weight regulator together with the tetracarboxylic dianhydride and dimian as described above. By using such a terminal-modified polymer, the applicability (printability) of the polymer composition can be improved without impairing the effects of the present invention.
Examples of the molecular weight regulator include acid monoanhydrides, monoamine compounds, monoisocyanate compounds, and the like. Specific examples of these acid monoanhydrides include maleic anhydride, phthalic anhydride, itaconic anhydride, n-decylsuccinic anhydride, n-dodecylsuccinic anhydride, n-tetradecylsuccinic acid. Nic acid anhydride, n-hexadecyl succinic acid anhydride, etc .;
Examples of monoamine compounds include aniline, cyclohexylamine, n-butylamine, n-pentylamine, n-hexylamine, n-heptylamine, and n-octylamine;
Examples of the monoisocyanate compound include phenyl isocyanate and naphthyl isocyanate.
It is preferable that the usage-amount of a molecular weight modifier shall be 10 weight part or less with respect to a total of 100 weight part of tetracarboxylic dianhydride and diamine to be used.

{Synthesis of polyamic acid}
The ratio of the tetracarboxylic dianhydride and the diamine used in the polyamic acid synthesis reaction is 0.2 to 2 for the tetracarboxylic dianhydride acid anhydride group to 1 equivalent of the amino group of the diamine. The ratio which becomes an equivalent is preferable, More preferably, it is the ratio which becomes 0.3-1.2 equivalent.
The polyamic acid synthesis reaction is preferably carried out in an organic solvent, preferably at -20 ° C to 150 ° C, more preferably at 0-100 ° C, preferably 0.1-24 hours, more preferably 0.5-12 hours. Done.
Here, examples of the organic solvent include N-methyl-2-pyrrolidone, N, N-dimethylacetamide, N, N-dimethylformamide, dimethylsulfoxide, γ-butyrolactone, tetramethylurea, hexamethylphosphortriamide and the like. Protic polar solvents; mention may be made of phenolic solvents such as m-cresol, xylenol, phenol, halogenated phenol. The amount of organic solvent used (a) is such that the total amount (b) of tetracarboxylic dianhydride and diamine is 0.1 to 30% by weight with respect to the total amount (a + b) of the reaction solution. It is preferable.
As described above, a reaction solution obtained by dissolving polyamic acid is obtained.
This reaction solution may be used as it is for the preparation of the liquid crystal aligning agent, may be used for the preparation of the liquid crystal aligning agent after isolating the polyamic acid contained in the reaction solution, or the isolated polyamic acid was purified. You may use for preparation of a liquid crystal aligning agent. When polyamic acid is dehydrated and cyclized into a polyimide, the above reaction solution may be directly subjected to dehydration and cyclization reaction, or may be subjected to dehydration and cyclization reaction after isolating the polyamic acid contained in the reaction solution. Alternatively, the isolated polyamic acid may be purified and then subjected to a dehydration ring closure reaction. Isolation and purification of the polyamic acid can be performed according to a known method.

{Synthesis of polyimide}
The polyimide can be obtained by dehydrating and ring-closing the polyamic acid synthesized as described above to imidize.
The polyimide in the present invention may be a completely imidized product obtained by dehydrating and cyclizing all of the amic acid structure possessed by the polyamic acid that is a precursor thereof, and by dehydrating and cyclizing only a part of the amic acid structure, A partially imidized product in which a structure and an imide ring structure coexist may be used. The polyimide in the present invention preferably has an imidization rate of 40% or more. This imidation ratio represents the ratio of the number of imide ring structures to the total of the number of polyimide amic acid structures and the number of imide ring structures in percentage.
The polyamic acid is preferably dehydrated and closed by heating the polyamic acid, or by dissolving the polyamic acid in an organic solvent, adding a dehydrating agent and a dehydrating ring-closing catalyst to the solution, and heating if necessary. . Of these, the latter method is preferred.
In the method of adding a dehydrating agent and a dehydrating ring-closing catalyst to the polyamic acid solution, for example, an acid anhydride such as acetic anhydride, propionic anhydride, or trifluoroacetic anhydride can be used as the dehydrating agent. It is preferable that the usage-amount of a dehydrating agent shall be 0.01-20 mol with respect to 1 mol of the amic acid structure of a polyamic acid. As the dehydration ring closure catalyst, for example, tertiary amines such as pyridine, collidine, lutidine, and triethylamine can be used. It is preferable that the usage-amount of a dehydration ring-closing catalyst shall be 0.01-10 mol with respect to 1 mol of dehydrating agents to be used. Examples of the organic solvent used in the dehydration ring-closing reaction include the organic solvents exemplified as those used for the synthesis of polyamic acid. The reaction temperature of the dehydration ring closure reaction is preferably 0 to 180 ° C, more preferably 10 to 150 ° C. The reaction time is preferably 1.0 to 120 hours, more preferably 2.0 to 30 hours.
In this way, a reaction solution containing polyimide is obtained. This reaction solution may be used for the preparation of the liquid crystal aligning agent as it is, or may be used for the preparation of the liquid crystal aligning agent after removing the dehydrating agent and the dehydrating ring-closing catalyst from the reaction solution. It may be used for the preparation of a liquid crystal aligning agent or may be used for the preparation of a liquid crystal aligning agent after purifying the isolated polyimide. These purification operations can be performed according to known methods.

[(B) Compound]
The compound (B) used in the present invention comprises at least one divalent group represented by the above formula (BI) and a monovalent group represented by the above formula (B-II) in the molecule. A compound having at least two. (B) It is preferable that the number of monovalent groups represented by the above formula (B-II) in the compound is two.
Examples of the divalent hydrocarbon group having 1 to 4 carbon atoms in the formula (BI) include a methylene group and a dimethylmethylene group. Examples of the divalent group represented by the formula (BI) include, for example, the following formulas (BI-1) to (BI-6):

And groups represented by each of the above. In the above formulas (BI-1) to (BI-6), the benzene ring and the cyclohexane ring are respectively an alkyl group having 1 to 4 carbon atoms, an alkoxyl group having 1 to 4 carbon atoms, a fluorine atom, or a cyano group. May be substituted.
Y ² in the above formula (B-II) is preferably an oxygen atom.
As the compound (B) used in the present invention,
Di (meth) acrylate having a biphenyl structure (the divalent group represented by the above formula (BI) is a group represented by the above formula (BI-1), and the above formula (B-II) Y ² and Y ^{3 in the above} are each an oxygen atom)
Di (meth) acrylate having a phenyl-cyclohexyl structure (the divalent group represented by the above formula (BI) is a group represented by the above formula (BI-2), and the above formula (B- Y ² and Y ³ in II) are each an oxygen atom)
Di (meth) acrylate having a 2,2-diphenylpropane structure (the divalent group represented by the above formula (BI) is a group represented by the above formula (BI-3), Y ² and Y ³ in (B-II) are each an oxygen atom.)
Di (meth) acrylate having a diphenylmethane structure (the divalent group represented by the above formula (BI) is a group represented by the above formula (BI-4), and the above formula (B-II) Y ² and Y ^{3 in the above} are each an oxygen atom)
Di-thio (meth) acrylate having a diphenylthioether structure (the divalent group represented by the above formula (BI) is a group represented by the above formula (BI-5), and the above formula (B ^{Y 2} is an oxygen atom in -II), ^{Y 3} can be cited is a sulfur atom.), and other compound (B).

Specific examples thereof include di (meth) acrylate having a biphenyl structure, such as 4′-acryloyloxy-biphenyl-4-yl-acrylate,
4′-methacryloyloxy-biphenyl-4-yl-methacrylate,
2- [4 ′-(2-acryloyloxy-ethoxy) -biphenyl-4-yloxy] -ethyl acrylate,
2- [4 ′-(2-methacryloyloxy-ethoxy) -biphenyl-4-yloxy] -ethyl methacrylate,
Bishydroxyethoxybiphenyl diacrylate,
Bishydroxyethoxybiphenyl dimethacrylate,
2- (2- {4 ′-[2- (2-acryloyloxy-ethoxy) -ethoxy] -biphenyl-4-yloxy} -ethoxy) -ethyl acrylate,
2- (2- {4 ′-[2- (2-methacryloyloxy-ethoxy) -ethoxy] -biphenyl-4-iroxy} -ethoxy) -ethyl methacrylate,
Diacrylate of biphenyl ethylene oxide adduct,
Dimethacrylate of biphenyl ethylene oxide adduct,
Diacrylate of biphenyl propylene oxide adduct,
Dimethacrylate of biphenyl propylene oxide adduct,
2- (4′-acryloyloxy-biphenyl-4-yloxy) -ethyl acrylate,
2- (4′-methacryloyloxy-biphenyl-4-yloxy) -ethyl methacrylate and the like;
Examples of di (meth) acrylate having a phenyl-cyclohexyl structure include 4- (4-acryloyloxy-phenyl) -cyclohexyl acrylate,
4- (4-methacryloyloxy-phenyl) -cyclohexyl methacrylate,
2- {4- [4- (2-acryloyloxy-ethoxy) -phenyl] -cyclohexyloxy} -ethyl acrylate,
2- {4- [4- (2-methacryloyloxy-ethoxy) -phenyl] -cyclohexyloxy} -ethyl methacrylate,
2- [2- (4- {4- [2- (2-acryloyloxy-ethoxy) -ethoxy] -phenyl} -cyclohexyloxy) -ethoxy] -ethyl acrylate,
2- [2- (4- {4- [2- (2-methacryloyloxy-ethoxy) -ethoxy] -phenyl} -cyclohexyloxy) -ethoxy] -ethyl methacrylate and the like;

Examples of di (meth) acrylates having a 2,2-diphenylpropane structure include 4- [1- (4-acryloyloxy-phenyl) -1-methyl-ethyl] -phenyl acrylate,
4- [1- (4-methacryloyloxy-phenyl) -1-methyl-ethyl] -phenyl methacrylate,
2- (4- {1- [4- (2-acryloyloxy-ethoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -ethyl acrylate,
2- (4- {1- [4- (2-methacryloyloxy-ethoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -ethyl methacrylate, bishydroxyethoxy-bisphenol A diacrylate,
Bishydroxyethoxy-bisphenol A dimethacrylate,
2- {2- [4- (1- {4- [2- (2-acryloyloxy-ethoxy) -ethoxy] -phenyl} -1-methyl-ethyl) -phenoxy] -ethoxy} -ethyl acrylate,
2- {2- [4- (1- {4- [2- (2-methacryloyloxy-ethoxy) -ethoxy] -phenyl} -1-methyl-ethyl) -phenoxy] -ethoxy} -ethyl methacrylate,
Diacrylate of ethylene oxide adduct of bisphenol A,
Dimethacrylate of ethylene oxide adduct of bisphenol A,
Diacrylate of propylene oxide adduct of bisphenol A,
Dimethacrylate of propylene oxide adduct of bisphenol A,
2- (4- {1- [4- (2-acryloyloxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -1-methyl-ethyl acrylate,
2- (4- {1- [4- (2-methacryloyloxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -1-methyl-ethyl methacrylate,
2- {2- [4- (1- {4- [2- (2-acryloyloxy-propoxy) -propoxy] -phenyl} -1-methyl-1-ethyl) -phenoxy] -1-methyl-ethoxy}- 1-methyl-ethyl acrylate,
2- {2- [4- (1- {4- [2- (2-methacryloyloxy-propoxy) -propoxy] -phenyl} -1-methyl-1-ethyl) -phenoxy] -1-methyl-ethoxy } -1-methyl-ethyl methacrylate,

3- {4- [1- (3- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenyl) -1-methyl-ethylphenoxy-2 -Hydroxy-propyl acrylate,
3- {4- [1- (3- {1- [4- (3-Methacryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenyl) -1-methyl-ethylphenoxy 2-hydroxy-propyl methacrylate,
3- (4- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -3-cyclohexyl-phenyl] -1-methyl-ethyl} -2-cyclohexyl-phenoxy) -2-hydroxy-2- Propyl acrylate,
3- (4- {1- [4- (3-Methacryloyloxy-2-hydroxy-propoxy) -3-cyclohexyl-phenyl] -1-methyl-ethyl} -2-cyclohexyl-phenoxy) -2-hydroxy- 2-propyl methacrylate,
3- (5- {1- [6- (3-acryloyloxy-2-hydroxy-propoxy) -biphenyl-3-yl] -1-methyl-ethyl} -biphenyl-2-yloxy) -2-hydroxy-propyl acrylate ,
3- (5- {1- [6- (3-Methacryloyloxy-2-hydroxy-propoxy) -biphenyl-3-yl] -1-methyl-ethyl} -biphenyl-2-yloxy) -2-hydroxy- Propyl methacrylate,
3- {4- [1- (4- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -3-methyl-phenyl] -1-methyl-ethyl} -phenyl) -1-methyl- Ethyl] -2-methyl-phenoxy} -2-hydroxy-propyl acrylate,
3- {4- [1- (4- {1- [4- (3-Methacryloyloxy-2-hydroxy-propoxy) -3-methyl-phenyl] -1-methyl-ethyl} -phenyl) -1- Methyl-ethyl] -2-methyl-phenoxy} -2-hydroxy-propyl methacrylate,
3- (4- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -2-hydroxy-propyl acrylate,

3- (4- {1- [4- (3-methacryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -2-hydroxy-propyl methacrylate,
3- [4- (1- {4- [3- (4- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy) -2- Hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -phenoxy] -2-hydroxy-propyl acrylate,
3- [4- (1- {4- [3- (4- {1- [4- (3-methacryloyloxy-2-hydroxy-propoxy) -phenyl] -1-methyl-ethyl} -phenoxy)- 2-hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -phenoxy] -2-hydroxy-propyl methacrylate,
3- {4- [1- (4- {3- [4- (1- {4- [3- (4- {1- [4- (3-acryloyloxy-2-hydroxy-propoxy) -phenyl]-) 1-methyl-ethyl} -phenoxy) -2-hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -phenoxy] -2-hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -phenoxy } -2-hydroxy-propyl acrylate,
3- {4- [1- (4- {3- [4- (1- {4- [3- (4- {1- [4- (3-methacryloyloxy-2-hydroxy-propoxy) -phenyl] ] -1-Methyl-ethyl} -phenoxy) -2-hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -phenoxy] -2-hydroxy-propoxy-]-phenyl} -1-methyl-ethyl) -Phenoxy} -2-hydroxy-propyl methacrylate,
1- (2- {4- [1- (4- {2- [2-hydroxy-3- (1-methylene-allyloxy) -propoxy] -propoxy} -phenyl) -1-methyl-ethyl] -xy} -1-methyl-ethoxy) -3- (1-methylene-allyloxy) -propan-2-ol and the like;

Examples of di (meth) acrylates having a diphenylmethane structure include 4- (4-acryloyloxy-benzyl) -phenyl acrylate,
4- (4-methacryloyloxy-benzyl) -phenyl methacrylate,
2- {4- [4- (2-acryloyloxy-ethoxy) -benzyl] -phenyl} -ethyl acrylate,
2- {4- [4- (2-methacryloyloxy-ethoxy) -benzyl] -phenyl} -ethyl methacrylate,
Diacrylate of ethylene oxide adduct of bisphenol F,
Dimethacrylate of ethylene oxide adduct of bisphenol F,
Diacrylate of propylene oxide adduct of bisphenol F,
Dimethacrylate of propylene oxide adduct of bisphenol F,
2- [2- (4- {4- [2- (2-acryloyloxy-ethoxy) -ethoxy] -benzyl} -phenoxy) -ethoxy] -ethyl acrylate,
2- [2- (4- {4- [2- (2-methacryloyloxy-ethoxy) -ethoxy] -benzyl} -phenoxy) -ethoxy] -ethyl methacrylate,
2- {4- [4- (2-acryloyloxy-propoxy) -benzyl-phenoxy} -1-methyl-ethyl acrylate,
2- {4- [4- (2-methacryloyloxy-propoxy) -benzyl-phenoxy} -1-methyl-ethyl methacrylate,
2- [2- (4- {4- [2- (2-acryloyloxy-propoxy) -propoxy] -benzyl} -phenoxy) -1-methyl-ethoxy] -1-methyl-ethylethyl acrylate,
2- [2- (4- {4- [2- (2-methacryloyloxy-propoxy) -propoxy] -benzyl} -phenoxy) -1-methyl-ethoxy] -1-methyl-ethylethyl methacrylate and the like;
Examples of di-thio (meth) acrylates having a diphenylthioether structure include 4- (4-thioacryloylsulfanyl-phenylsulfanyl) -phenyldithioacrylate,
4- (4-thiomethacryloylsulfanyl-phenylsulfanyl) -phenyldithiomethacrylate,
Bis (4-methacryloylthiophenyl) sulfide and the like;
Examples of other (B) compounds include 2,5-bis {4- (3-acryloyloxy-propoxy) -benzoic acid} toluene, respectively.

Such a compound (B) can be synthesized by appropriately combining organic chemistry methods, or can be obtained as a commercial product. (B) Examples of commercially available compounds include bishydroxyethoxy BP diacrylate and bishydroxyethoxy Bis-A diacrylate (manufactured by Honshu Chemical Industry Co., Ltd.);
Aronix M-208, M-210 (manufactured by Toagosei Co., Ltd.);
SR-349, SR-601, SR-602 (manufactured by Sartomer);
KAYARAD R-712, R-551 (manufactured by Nippon Kayaku Co., Ltd.);
NK ester BPE-100, NK ester BPE-200, NK ester BPE-500, NK ester BPE-1300, NK ester A-BPE-4 (manufactured by Shin-Nakamura Chemical Co., Ltd.), Actilane 420 (manufactured by Nippon Shibel Hegner) ):
Light ester BP-2EM, light acrylate BP-4EA, light acrylate BP-4PA, epoxy ester 3000M, epoxy ester 3000A (manufactured by Kyoeisha Chemical Co., Ltd.);
V # 540, V # 700 (manufactured by Osaka Organic Chemical Industry Co., Ltd.);
FA-321M (manufactured by Hitachi Chemical Co., Ltd.);
MPSMA (manufactured by Sumitomo Seika);
Lipoxy VR-77 (manufactured by Showa Polymer Co., Ltd.) can be exemplified.
As the compound (B) used in the present invention, it is preferable to use at least one selected from the group consisting of the compounds exemplified above.
The proportion of the compound (B) used in the polymer composition used in the present invention is preferably 1 to 100 parts by weight, and 5 to 50 parts by weight with respect to 100 parts by weight of the polymer (A). More preferably.

[Polymer composition]
The polymer composition used in the present invention is preferably prepared as a solution obtained by dissolving the polymer (A) and the compound (B) as described above in a suitable organic solvent.
Examples of the organic solvent that can be used here include N-methyl-2-pyrrolidone, γ-butyrolactone, γ-butyrolactam, N, N-dimethylformamide, N, N-dimethylacetamide, and 4-hydroxy-4-methyl. -2-pentanone, ethylene glycol monomethyl ether, butyl lactate, butyl acetate, methyl methoxypropionate, ethyl ethoxypropionate, ethylene glycol methyl ether, ethylene glycol ethyl ether, ethylene glycol-n-propyl ether, ethylene glycol -I-propyl ether, ethylene glycol-n-butyl ether (butyl cellosolve), ethylene glycol dimethyl ether, ethylene glycol ethyl ether acetate, diethylene glycol dimethyl ether Ter, diethylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether acetate, diethylene glycol monoethyl ether acetate, diisobutyl ketone, isoamyl propionate, isoamyl isobutyrate, diisopentyl ether and the like.
As the use ratio of the organic solvent, the solid content concentration of the polymer composition (the ratio of the total weight of components other than the organic solvent in the polymer composition to the total weight of the polymer composition) is 1 to 15% by weight. It is preferable to set it as the ratio which becomes 1.5 to 8 weight%.

<Method for manufacturing liquid crystal display element>
The method for producing the liquid crystal display element of the present invention comprises:
On each of the conductive films of a pair of substrates having a conductive film, a coating film is formed by applying the polymer composition as described above,
A pair of substrates on which the coating film is formed are arranged to face each other so that the coating film faces through a layer of liquid crystal molecules to form a liquid crystal cell,
A step of irradiating the liquid crystal cell with light while applying a voltage between the conductive films of the pair of substrates is characterized.
Here, as the substrate, for example, a glass such as float glass or soda glass; a transparent substrate made of a plastic such as polyethylene terephthalate, polybutylene terephthalate, polyethersulfone, or polycarbonate can be used.
As the conductive film, a transparent conductive film is preferably used. For example, a NESA film made of SnO _{2 or} an ITO film made of In ₂ O ₃ —SnO ₂ can be used. Each of the conductive films is preferably a patterned conductive film partitioned into a plurality of regions. With such a conductive film configuration, when a voltage is applied between the conductive films (described later), the direction of the pretilt angle of the liquid crystal molecules can be changed for each region by applying a different voltage for each region. This makes it possible to further widen the viewing angle characteristics.
In order to apply the polymer composition onto the conductive film of the substrate, for example, an appropriate application method such as a roll coater method, a spinner method, a printing method, or an ink jet method can be used. After coating, the coated surface is preheated (prebaked) and then baked (postbaked) to form a coating film. The pre-bake conditions are, for example, 0.1 to 5 minutes at 40 to 120 ° C., and the post-bake conditions are preferably 120 to 300 ° C., more preferably 150 to 250 ° C., preferably 5 to 200 minutes, more preferably 10 to 100 minutes. The film thickness of the coating film after post-baking is preferably 0.001-1 μm, more preferably 0.005-0.5 μm.

The coating film thus formed may be used as it is for the production of a liquid crystal cell in the next step, or may be subjected to a rubbing treatment on the coating surface as necessary prior to the production of the liquid crystal cell. The rubbing treatment can be performed by rubbing the coating film surface in a certain direction with a roll wound with a cloth made of fibers such as nylon, rayon, and cotton. Here, as described in Patent Document 1 (Japanese Patent Laid-Open No. 5-107544), a resist film is formed on a part of the coating surface after once rubbing, and is different from the previous rubbing. By performing a process of removing the resist film after performing the rubbing process in the direction and setting the rubbing direction to be different for each region, it is possible to further improve the visual field characteristics of the obtained liquid crystal display element.
Next, a pair of substrates on which the coating film has been formed are arranged to face each other with the coating film facing each other through a layer of liquid crystal molecules to form a liquid crystal cell.
The liquid crystal molecules used here are preferably nematic liquid crystals having negative dielectric anisotropy, such as dicyanobenzene liquid crystals, pyridazine liquid crystals, Schiff base liquid crystals, azoxy liquid crystals, biphenyl liquid crystals, phenyl cyclohexane liquid crystals. Etc. can be used. The thickness of the liquid crystal molecule layer is preferably 1 to 5 μm.
In order to produce a liquid crystal cell using such a liquid crystal, for example, the following two methods can be mentioned.
As a first method, two substrates are arranged to face each other through a gap (cell gap) so that the respective liquid crystal alignment films face each other, and the peripheral portions of the two substrates are bonded together using a sealant, A liquid crystal cell can be manufactured by injecting and filling liquid crystal into the cell gap defined by the substrate surface and the sealing agent and then sealing the injection hole. Alternatively, as a second method, for example, an ultraviolet light curable sealant is applied to a predetermined location on one of the two substrates on which the liquid crystal alignment film is formed, and the liquid crystal is applied onto the liquid crystal alignment film surface. After the dropping, the other substrate is bonded so that the liquid crystal alignment films face each other, and then the entire surface of the substrate is irradiated with ultraviolet light to cure the sealant, whereby a liquid crystal cell can be produced.

Thereafter, the liquid crystal cell is irradiated with light while a voltage is applied between the conductive films of the pair of substrates.
The voltage applied here can be, for example, 5 to 50 V direct current or alternating current.
As light to irradiate, for example, ultraviolet light and visible light including light having a wavelength of 150 to 800 nm can be used, but ultraviolet light including light having a wavelength of 300 to 400 nm is preferable. As a light source of irradiation light, for example, a low pressure mercury lamp, a high pressure mercury lamp, a deuterium lamp, a metal halide lamp, an argon resonance lamp, a xenon lamp, an excimer laser, or the like can be used. The ultraviolet rays in the preferable wavelength region can be obtained by means of using the light source in combination with, for example, a filter or a diffraction grating.
The amount of light irradiation is preferably 1,000 J / m ² or more and less than 100,000 J / m ² , more preferably 1,000 to 50,000 J / m ² . In the manufacture of a conventionally known PSA mode liquid crystal display element, it was necessary to irradiate light of about 100,000 J / m ^{2. In} the method of the present invention, the amount of light irradiation was set to 50,000 J / M ² or less, and even if it is 10,000 J / m ² or less, a desired liquid crystal display element can be obtained, which contributes to a reduction in manufacturing cost of the liquid crystal display element and is caused by irradiation with strong light. It is possible to avoid deterioration of electrical characteristics and long-term reliability.
And a liquid crystal display element can be obtained by bonding a polarizing plate to the outer surface of the liquid crystal cell after performing the above-mentioned treatment. As a polarizing plate used here, a polarizing plate formed by sandwiching a polarizing film called an “H film” in which iodine is absorbed while stretching and aligning polyvinyl alcohol with a cellulose acetate protective film, or a polarizing plate made of the H film itself, etc. Can be mentioned.

Synthesis example 1
110 g (0.50 mol) of 2,3,5-tricarboxycyclopentylacetic acid dianhydride as tetracarboxylic dianhydride, 43 g (0.40 mol) of p-phenylenediamine as diamine and 3 (3,5-diaminobenzoyl) 52 g (0.10 mol) of oxy) cholestane was dissolved in 830 g of N-methyl-2-pyrrolidone and reacted at 60 ° C. for 6 hours. A small amount of the obtained polyamic acid solution was collected, and N-methyl-2-pyrrolidone was added to measure the solution viscosity as a solution having a polyamic acid concentration of 10% by weight of 60 mPa · s.
Next, 1,900 g of N-methyl-2-pyrrolidone was added to the obtained polyamic acid solution, 40 g of pyridine and 51 g of acetic anhydride were added, and dehydration ring closure reaction was performed at 110 ° C. for 4 hours. After the dehydration ring-closing reaction, the solvent in the system was replaced with new N-methyl-2-pyrrolidone (pyridine and acetic anhydride used in the dehydration ring-closing reaction were removed from the system by this operation), thereby imido. A solution containing about 15% by weight of polyimide (PI-1) having a conversion rate of about 50% was obtained. A small amount of the obtained polyimide solution was taken, N-methyl-2-pyrrolidone was added, and the solution viscosity measured as a solution having a polyimide concentration of 10% by weight was 47 mPa · s.

Example 1
<Preparation of polymer composition>
(A) N-methyl-2-pyrrolidone (NMP) and butyl cellosolve (BC) are added as organic solvents to a solution containing the polyimide (PI-1) obtained in Synthesis Example 1 as a polymer, and (B) As a compound, the following formula (B-1)

20 parts by weight of the compound represented by formula (A) with respect to 100 parts by weight of the polymer, and a solvent composition having a NMP: BC = 50: 50 (weight ratio) and a solid content concentration of 6.0% by weight did. A polymer composition was prepared by filtering this solution using a filter having a pore size of 1 μm.
<Manufacture of liquid crystal cells>
Using the polymer composition prepared above, a total of six liquid crystal display elements were manufactured by changing the transparent electrode pattern (two types) and the ultraviolet irradiation amount (three levels), and evaluated as follows. .

[Manufacture of liquid crystal cell having transparent electrode without pattern]
The polymer composition prepared above was applied onto a transparent electrode surface of a glass substrate having a transparent electrode made of an ITO film using a liquid crystal alignment film printer (Nissha Printing Co., Ltd.), and hot at 80 ° C. After removing the solvent by heating (pre-baking) on the plate for 1 minute, heating (post-baking) on a hot plate at 150 ° C. for 10 minutes to form a coating film having an average film thickness of 600 mm.
The coating film was rubbed with a rubbing machine having a roll wrapped with a rayon cloth at a roll rotation speed of 400 rpm, a stage moving speed of 3 cm / sec, and a hair foot indentation length of 0.1 mm. Thereafter, ultrasonic cleaning was performed in ultrapure water for 1 minute, followed by drying in a 100 ° C. clean oven for 10 minutes to obtain a substrate having a liquid crystal alignment film. This operation was repeated to obtain a pair (two) of substrates having a liquid crystal alignment film.
Next, after applying an epoxy resin adhesive containing aluminum oxide spheres having a diameter of 5.5 μm to the outer edges of the pair of substrates having the liquid crystal alignment film, the liquid crystal alignment film surfaces are overlapped and pressure bonded. The adhesive was cured. Next, after filling nematic liquid crystal (MLC-6608, manufactured by Merck & Co., Inc.) between a pair of substrates from the liquid crystal injection port, the liquid crystal injection port is sealed with an acrylic photo-curing adhesive to produce a liquid crystal cell. did.
The above operation was repeated to produce three liquid crystal cells having unpatterned transparent electrodes. One of them was used for the evaluation of the pretilt angle described later. The remaining two liquid crystal cells were irradiated with light in a state where a voltage was applied between the conductive films by the following method, and then subjected to evaluation of a pretilt angle and a voltage holding ratio.
For two of the liquid crystal cells obtained above, an alternating current of 10 Hz is applied between the electrodes, and the liquid crystal is driven, using an ultraviolet gland irradiation device using a metal halide lamp as the light source, UV was irradiated at dose of 10,000 J / ^{m 2} or 100,000J / ^{m 2.} This irradiation amount is a value measured using a light meter that is measured on the basis of a wavelength of 365 nm.

[Evaluation of pretilt angle]
About each liquid crystal cell manufactured above, nonpatent literature 2 (TJ Scheffer et.al., J.Appl.Phys.vol.48, p.1783 (1977)) and nonpatent literature 3 (F. Of liquid crystal molecules measured by a crystal rotation method using He-Ne laser light in accordance with the method described in Nakano, et.al., JPN.J.Appl.Phys.vol.19, p.2013 (1980)). The value of the tilt angle from the substrate surface was defined as the pretilt angle.
The liquid crystal cell of not irradiated with light, the respective pre-tilt angle of the liquid crystal cell and the liquid crystal cells of the dose 100,000J / ^{m 2} of dose 10,000 J / ^{m 2} are shown in Table 1.
[Evaluation of voltage holding ratio]
For each of the liquid crystal cells produced above, a voltage of 5 V was applied at 23 ° C. with an application time of 60 microseconds and a span of 167 milliseconds, and then the voltage holding ratio after 167 milliseconds from the application release was measured. As a measuring device, VHR-1 manufactured by Toyo Corporation was used.
Table 1 shows voltage holding ratios of the liquid crystal cell with the irradiation amount of 10,000 J / m ^{2 and} the liquid crystal cell with the irradiation amount of 10,000 J / m ² .

[Manufacture of Liquid Crystal Cell Having Patterned Transparent Electrode]
The polymer composition prepared above is patterned into a slit shape as shown in FIG. 1, and a liquid crystal alignment film is printed on each electrode surface of glass substrates A and B each having an ITO electrode partitioned into a plurality of regions. Apply using a machine (Nissha Printing Co., Ltd.), heat on a hot plate at 80 ° C for 1 minute (pre-bake) to remove the solvent, then heat on a hot plate at 150 ° C for 10 minutes (post-bake) ) To form a coating film having an average film thickness of 600 mm. The coating film was subjected to ultrasonic cleaning for 1 minute in ultrapure water and then dried in a clean oven at 100 ° C. for 10 minutes to obtain a substrate having a liquid crystal alignment film. This operation was repeated to obtain a pair (two) of substrates having a liquid crystal alignment film.
Next, after applying an epoxy resin adhesive containing aluminum oxide spheres having a diameter of 5.5 μm to the outer edges of the pair of substrates having the liquid crystal alignment film, the liquid crystal alignment film surfaces are overlapped and pressure-bonded so as to face each other. The adhesive was cured. Next, after filling nematic liquid crystal (MLC-6608, manufactured by Merck & Co., Inc.) between a pair of substrates from the liquid crystal injection port, the liquid crystal injection port is sealed with an acrylic photo-curing adhesive to produce a liquid crystal cell. did.
The above operation was repeated to produce three liquid crystal cells having patterned transparent electrodes. One of them was used for evaluation of response speed as described later. For the remaining two liquid crystal cells, 10,000 J / m ² or 100,000 J / m in a state where a voltage is applied between the conductive films by the same method as in the production of the liquid crystal cell having the transparent electrode without pattern. After irradiating with light at an irradiation amount of m ² , the response speed was evaluated.
The electrode pattern used here is the same type as the electrode pattern in the PSA mode.

[Evaluation of response speed]
For each of the liquid crystal cells produced above, first, the luminance of light transmitted through the liquid crystal cell by irradiating a visible light lamp without applying a voltage was measured with a photomultimeter, and this value was defined as a relative transmittance of 0%. . Next, the transmittance when 60 V AC was applied between the electrodes of the liquid crystal cell for 5 seconds was measured in the same manner as described above, and this value was defined as a relative transmittance of 100%.
At this time, when 60 V AC was applied to each liquid crystal cell, the time until the relative transmittance shifted from 10% to 90% was measured, and this time was defined as the response speed and evaluated.
The liquid crystal cell of not irradiated with light, each of the response speed of the liquid crystal cell and the liquid crystal cells of the dose 100,000J / ^{m 2} of dose 10,000 J / ^{m 2} are shown in Table 1.

Examples 2-5
In Example 1, the polymer composition was prepared in the same manner as in Example 1 except that the type and amount of the (B) compound were as shown in Table 1, and various liquid crystal cells were prepared using this. Were manufactured and evaluated.
The evaluation results are shown in Table 1.
Comparative Example 1
In Example 1, except that the (B) compound was not used, a polymer composition was prepared in the same manner as in Example 1, and various liquid crystal cells were produced and evaluated using the polymer composition.
The evaluation results are shown in Table 1.

Comparative Example 2
<Preparation of polymer composition>
(A) Without using a polymer, the compound represented by the above formula (B-1) as a compound (B) is dissolved in N-methyl-2-pyrrolidone (NMP) and butyl cellosolve (BC) as an organic solvent. The solution was NMP: BC = 50: 50 (weight ratio) and the solid content concentration was 6.0% by weight. A polymer composition was prepared by filtering this solution using a filter having a pore size of 1 μm.
<Evaluation>
Various liquid crystal cells were produced in the same manner as in Example 1 except that the polymer composition prepared above was used, and the voltage holding ratio was evaluated. The evaluation results are shown in Table 1.
In addition, since the domain generate | occur | produced in the liquid crystal cell manufactured by this comparative example, the pretilt angle could not be evaluated and the response speed was not evaluated.
Comparative Examples 3-5
In Example 1 above, each of the polymer compositions in the same manner as in Example 1 except that each compound shown in Table 1 was used as the other compound in the amount shown in Table 1 instead of the compound (B). Were prepared, and various liquid crystal cells were produced and evaluated using the liquid crystal cells.
The evaluation results are shown in Table 1.

The abbreviations of the compound names in Table 1 have the following meanings.
B-1: Compound represented by the above formula (B-1) B-2: In the following formula (B-2), a mixture of compounds wherein n is 2-4 B-3: The following formula (B-3) A mixture of compounds wherein n is 2 to 4 B-4: a compound represented by the following formula (B-4) b-1: a compound represented by the following formula (b-1) b-2: a following formula Compound represented by (b-2) b-3: Compound represented by the following formula (b-3)

From the results of Table 1, in the method of the present invention, when the ultraviolet irradiation amount is 100,000 J / m ² (which is a value conventionally employed in the PSA mode), the degree of the pretilt angle obtained becomes excessive. It can be seen that an appropriate pretilt angle is obtained at an irradiation dose of 1,000 J / m ² or less. Moreover, even when the irradiation amount is small, a sufficiently fast response speed is obtained, and the voltage holding ratio is also excellent.
Therefore, according to the method of the present invention, the merits of the PSA mode can be realized with a small amount of light irradiation. Therefore, display unevenness due to a high amount of light irradiation, deterioration of voltage holding characteristics, and long-term reliability are insufficient. Thus, a liquid crystal display device having a wide viewing angle, a high response speed of liquid crystal molecules, a high transmittance, and a high contrast can be manufactured.

  Further, various liquid crystal cells were produced and evaluated in the same manner as in Example 1 except that the polymer compositions used in Examples 1 to 5 were used and the ITO electrode pattern of the glass substrate was changed. When any polymer composition was used, the same effects as in Examples 1 to 5 were obtained in both the pattern shown in FIG. 2 and the pattern shown in FIG.

1: ITO electrode 2: Slit part 3: Light shielding film

Claims (5)

On the conductive film of the pair of substrates having the conductive film,
(A) at least one polymer selected from the group consisting of polyamic acid and polyimide, and (B) the following formula (BI) in the molecule
^{-X 1 -Y 1 -X 2 - (} B-I)
(In Formula (BI), X ¹ and X ² are each independently a 1,4-phenylene group or a 1,4-cyclohexylene group, and Y ¹ is a single bond having 1 to 4 carbon atoms. A divalent hydrocarbon group, an oxygen atom, a sulfur atom or —COO—, wherein X ¹ and X ² are one or more alkyl groups having 1 to 4 carbon atoms and alkoxyl groups having 1 to 4 carbon atoms. , May be substituted with a fluorine atom or a cyano group.)
And at least one divalent group represented by the following formula (B-II):
(In Formula (B-II), R is a hydrogen atom or a methyl group, and Y ² and Y ³ are each independently an oxygen atom or a sulfur atom.)
Applying a polymer composition containing a compound having at least two monovalent groups represented by the formula:
A pair of substrates on which the coating film is formed are arranged to face each other so that the coating film faces through a layer of liquid crystal molecules to form a liquid crystal cell,
A method for producing a liquid crystal display element, comprising a step of irradiating the liquid crystal cell with light while applying a voltage between conductive films of the pair of substrates.   The compound (B) is a di (meth) acrylate having a biphenyl structure, a di (meth) acrylate having a phenyl-cyclohexyl structure, a di (meth) acrylate having a 2,2-diphenylpropane structure, a di (meth) having a diphenylmethane structure. 2. The method for producing a liquid crystal display device according to claim 1, which is at least one compound selected from the group consisting of acrylate and di-thio (meth) acrylate having a diphenylthioether structure.   The method for manufacturing a liquid crystal display element according to claim 1, wherein each of the conductive films is a patterned conductive film partitioned into a plurality of regions. A polymer composition used for producing the liquid crystal display element according to claim 1,
(A) at least one polymer selected from the group consisting of polyamic acid and polyimide, and (B) at least one divalent group represented by the above formula (BI) in the molecule and the above formula (B The polymer composition comprising a compound having at least two monovalent groups represented by -II). A liquid crystal display element manufactured by the method for manufacturing a liquid crystal display element according to claim 1.