TW201444917A - Liquid crystal alignment agent, liquid crystal alignment film, liquid crystal display element, polyamic acid and imidized polymer thereof and diamine compound - Google Patents

Abstract

The invention provides a liquid crystal alignment agent, which is characterized by: containing at least one polymer selected from a group consisted of a polyamic acid and an imidized polymer thereof which have a structure represented by formula (1) below on a main chain. (In the formula (1), existed two X respectively and independently is an oxygen atom, a sulfur atom, an ester bond, a thioester bond, an amide bond, -NH-, -C(=O)-, divalent saturated aliphatic groups having carbon quantity from 1 to 10 or divalent unsaturated aliphatic groups having carbon quantity from 2 to 10; existed two Y respectively and independently is a single bond, an oxygen atom, a sulfur atom, an ester bond or a thioester bond; R is a methylene group, or alkylene groups having carbon quantity from 2 to 12 which may be interrupted by the oxygen atom on a way; besides, ''*'' represents a bonding).

Description

Liquid crystal alignment agent, liquid crystal alignment film, liquid crystal display element, polylysine and its ruthenium iodide polymer and diamine compound

This invention relates to a liquid crystal alignment agent.

In a liquid crystal display element widely used in televisions, mobile devices, various monitors, and the like, a liquid crystal alignment film is used in order to align liquid crystal molecules in a liquid crystal cell. A method of imparting a liquid crystal alignment ability to the liquid crystal alignment film has previously known a method of rubbing an organic film, a method of obliquely vaporizing ruthenium oxide, a method of forming a monomolecular film having a long-chain alkyl group, and the like.

The optical alignment method can achieve uniform liquid crystal alignment without generating static electricity and dust, and can also closely control the alignment direction of the liquid crystal. Therefore, research has been actively conducted in recent years (Patent Documents 1 to 3).

However, the liquid crystal alignment film formed by using the previously known liquid crystal alignment film material and using the photoalignment method has a self-contradictory relationship in obtaining high contrast and achieving good afterimage characteristics, and these two characteristics cannot be sufficiently improved. Therefore, it is impossible to simultaneously It satisfies the requirements for display of high-definition images and high-level dynamic image reproduction display in recent years.

[Previous Technical Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open No. Hei 6-287453

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2003-307736

[Patent Document 3] Japanese Patent Laid-Open No. Hei 9-297313

[Patent Document 4] Japanese Patent Laid-Open Publication No. 2010-97188

The present invention has been made to solve the above-described situation.

Accordingly, an object of the present invention is to provide a liquid crystal alignment agent which can provide a liquid crystal alignment property by a photo-alignment method and which is excellent in characteristics such as electrical characteristics, particularly high contrast and good disability. A liquid crystal alignment film like a characteristic.

According to the present invention, the object and an advantage of the present invention are attained by a liquid crystal alignment agent characterized by containing a structure selected from the group consisting of the following formula (1) in the main chain. At least one polymer of the group consisting of polylysine and its quinone imidized polymer.

[Chemical 1]

(In the formula (1), two of X are independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond, a guanamine bond, -NH-, -C(=O)-, and a carbon number of 1 to 10; a divalent saturated aliphatic group or a divalent unsaturated aliphatic group having 2 to 10 carbon atoms; wherein two Y atoms are each independently a single bond, an oxygen atom, a sulfur atom, an ester bond or a thioester bond; R is a sub A methyl group, or an alkyl group having 2 to 12 carbon atoms interrupted by an oxygen atom in the middle; and "*" means a bond.)

The liquid crystal alignment agent of the present invention can form a liquid crystal alignment film having good liquid crystal alignment by a photo-alignment method. The liquid crystal alignment film formed of the liquid crystal alignment agent of the present invention is excellent not only in electrical characteristics represented by the voltage holding ratio but also in high contrast and good afterimage characteristics (burning characteristics), and thus the liquid crystal display element including the liquid crystal alignment film can be used. Suitable for a variety of uses.

The use of the liquid crystal display element including the liquid crystal alignment film formed of the liquid crystal alignment agent of the present invention is exemplified as follows: a television, a portable game, a word processor (word Processor), note type personal computer, car navigation system, camcorder, personal digital assistant, digital camera, mobile phone, various surveillance And so on.

101‧‧‧electrode A

102‧‧‧Electrode B

FIG. 1 is an explanatory view showing a pattern of an electrode used in a liquid crystal display element for evaluating afterimage characteristics.

The liquid crystal alignment agent of the present invention contains at least 1 selected from the group consisting of polylysine having a structure represented by the above formula (1) and a quinone imidized polymer thereof in the main chain as described above. A polymer (hereinafter referred to as "specific polymer").

Here, the main chain of the polymer means a portion of the polymer which contains the "backbone" of the longest atomic chain. The backbone is allowed to contain a ring structure. In this case, the entire structure of the ring exists on the main chain. The structure represented by the above formula (1) in the main chain means that the structure constitutes a part of the main chain. The essential condition of the specific polymer of the present invention is that the structure represented by the formula (1) exists in the main chain, but it is not prohibited to overlap the structure in a portion other than the main chain, for example, a side chain (from the backbone of the polymer) "The part of the upper branch).

When X or Y in the formula (1) is an ester bond or a thioester bond, and X is a guanamine bond, the bonding direction may be either direction.

Examples of the divalent saturated aliphatic group having 1 to 10 carbon atoms in X include a methylene group, a 2,2-dipropyl group, and an alkylene group having 2 to 10 carbon atoms. The carbon number of the alkylene group is preferably 2 to 4, and more preferably 2. The divalent unsaturated aliphatic group having 2 to 10 carbon atoms in X is preferably a (poly)alkenyl group having 2 to 10 carbon atoms. The (poly)alkenyl group preferably has 2 to 4 carbon atoms. Specific examples thereof include -CH=CH-, -CH=CH-CH ₂ -, -CH ₂ -CH=CH-CH ₂ -, -CH=CH-CH=CH-, and the like.

X is a saturated aliphatic group or an unsaturated aliphatic group, and when the group is asymmetrical to the left and right, the bonding direction may be either direction.

Preferably, as X, two X are each independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond, -NH-, -CH ₂ -CH ₂ - or -CH=CH-, more preferably an ester bond or sulfur. Ester bond, -NH-, -CH ₂ -CH ₂ - or -CH=CH-. Y is preferably an oxygen atom.

R in the formula (1) is a site which imparts flexibility to a main chain of a specific polymer. Therefore, the R is preferably a group represented by the formula: -(CH ₂ ) _n - or -(CR'H-CH ₂ )-(O-CR'H-CH ₂ ) _m -

(wherein R' is independently a hydrogen atom, a methyl group or an ethyl group; n is an integer from 1 to 12; m is an integer from 1 to 3)

Here, it is understood from the definition of R in the formula (1) that the upper limit of the carbon number in the formula is limited to 12.

R' in the formula is preferably a hydrogen atom; n is preferably 2-8, more preferably 4-6; m is preferably 1 or 2.

The four pendant phenyl groups present in the formula (1) are each independently preferably a 1,3-phenylene group or a 1,4-phenylene group, and more preferably a 1,4-phenylene group.

The structure represented by the formula (1) is, for example, a structure represented by the following formula (1-1) to formula (1-12).

[Chemical 2]

(In the above formula (1-1) to formula (1-12), n is an integer of 2 to 12, and m is 1 or 2.)

n in the formula (1-1), the formula (1-3), the formula (1-5), the formula (1-7), the formula (1-9), and the formula (1-11) is preferably 2~ 8, more preferably 4 to 6.

The specific polymer of the present invention is at least one polymer selected from the group consisting of polylysine having a structure represented by the formula (1) in the main chain and its quinone imidized polymer. The remaining structure is arbitrary, and may be a polymer obtained by any of the synthetic methods.

The specific polymer of the present invention may be, for example, a polyamic acid obtained by reacting a tetracarboxylic dianhydride containing a tetracarboxylic dianhydride having the structure represented by the above formula (1) with a diamine. And one or more polymers selected from the group consisting of ruthenium imidized polymers; or may be selected from the group consisting of tetracarboxylic dianhydrides and diamines having the structure represented by the formula (1) Diamine

One or more polymers selected from the group consisting of polylysine and its quinone imidized polymer obtained by the reaction. Among these polymers, the latter is preferable from the viewpoint of easiness of synthesis of a raw material monomer.

[tetracarboxylic dianhydride]

Examples of the tetracarboxylic dianhydride used for the synthesis of the specific polymer of the present invention include aliphatic tetracarboxylic dianhydride, alicyclic tetracarboxylic dianhydride, and aromatic tetracarboxylic dianhydride. Specific examples of the tetracarboxylic dianhydride include aliphatic butane tetracarboxylic dianhydride: butane tetracarboxylic dianhydride; and alicyclic tetracarboxylic dianhydride: 1, 2, 3, and 4 - cyclobutane tetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentyl acetic 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-1,2-dicarboxylic anhydride, 3,5,6-tricarboxy-2-carboxymethylnorbornane-2:3,5:6-dianhydride, 2,4,6, 8-tetracarboxybicyclo[3.3.0]octane-2:4,6:8-dianhydride, 4,9-dioxatricyclo[5.3.1.0 ^2,6 ]undecane-3,5,8 Examples of the aromatic tetracarboxylic dianhydride include pyromellitic dianhydride and a compound represented by the following formula (T1). In addition, Patent Document 4 (Japanese Patent) can be used. The tetracarboxylic dianhydride described in JP-A-2010-97188.

(In the formula (T1), Z is independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond or -NH- in the case where a plurality of Z are present; and R ¹ is independently carbon in the presence of a plurality of a number of 6 to 18 aryl groups or a carbon number of 2 to 6 alkyl groups; and, n1 is an integer of 0 to 2.)

Z in the formula (T1) is preferably an oxygen atom or an ester bond. Examples of the aryl group of R ¹ include a stretching phenyl group, a stretching naphthyl group, a stretching biphenyl group, and the like; and an alkyl group, for example, a 1,2-extended ethyl group, a 1,2-extended propyl group, and 1,3 - stretch propyl and so on. R ¹ is preferably an extended aryl group, and in the case where a plurality of aryl groups are present, it is particularly preferably independently 1,4-phenylene, 2,6-anthranyl or 4,4′-extended biphenyl. N1 is preferably 0 or 1.

Specific examples of the compound represented by the formula (T1) include a compound represented by the following formula (T-1) and formula (T-2), and the like.

The tetracarboxylic dianhydride for synthesizing the specific polymer of the present invention preferably contains the compound represented by the above formula (T1), and preferably contains the formula of 20 mol% or more with respect to all of the tetracarboxylic dianhydride. The compound represented by (T1) more preferably contains 50 mol% or more, and particularly preferably contains 80 mol% or more.

[diamine]

The diamine used for the synthesis of the specific polymer of the present invention is preferably a diamine containing the structure represented by the above formula (1). The diamine having a structure represented by the above formula (1) is, for example, a compound represented by the following formula (A1) (hereinafter referred to as "specific diamine").

(In the formula (A1), X, Y and R have the same meanings as in the formula (1), respectively.)

The bonding direction of the four phenyl groups present in the formula (A1) is the same as the bonding direction described above for the phenyl group in the formula (1).

In a preferred embodiment of the specific diamine of the present invention, for example, in the structures represented by the formulas (1-1) to (1-12), the direct bonds are respectively indicated by the two binding bonds represented by "*". A compound obtained by combining two amine groups, and the like.

The diamine used to synthesize the specific polymer of the present invention may use only a specific diamine, or Other diamines can also be used in combination with a specific diamine.

Other diamines which may be used herein may be classified, for example, as diamines having a pretilt-expressing group and diamines having no pretilt-expressing group.

The diamine having a pretilt-exhibiting group is preferably an aromatic diamine having a pretilt-expressing group, and specific examples thereof include dodecyloxy-2,4-diaminobenzene and tetradecyloxy group. -2,4-diaminobenzene, pentadecyloxy-2,4-diaminobenzene, hexadecyloxy-2,4-diaminobenzene, octadecyloxy-2,4- Diaminobenzene, dodecyloxy-2,5-diaminobenzene, tetradecyloxy-2,5-diaminobenzene, pentadecyloxy-2,5-diaminobenzene, Hexadecyloxy-2,5-diaminobenzene, octadecyloxy-2,5-diaminobenzene, cholestyloxy-3,5-diaminobenzene, cholesteryloxy Base-3,5-diaminobenzene, cholestyloxy-2,4-diaminobenzene, cholesteryloxy-2,4-diaminobenzene, 3,5-diaminobenzene Cholesteryl formate, cholesteryl 3,5-diaminobenzoate, lanosteryl 3,5-diaminobenzoic acid, 3,6-bis(4-aminobenzidineoxy) Cholesterol, 3,6-bis(4-aminophenoxy)cholestane, 1,1-bis(4-((aminophenyl)methyl)phenyl)-4-butyl Cyclohexane, 1,1-bis(4-((aminophenyl)methyl)phenyl)-4-heptylcyclohexane, 1,1-bis(4-((aminophenoxy)) Methyl)phenyl)-4-g Cyclohexane, 1,1-bis(4-((aminophenyl)methyl)phenyl)-4-(4-heptylcyclohexyl)cyclohexane, N-(2,4-diamino) Phenyl)-4-(4-heptylcyclohexyl)benzamide, a compound represented by the following formula (A-1), and the like.

[Chemistry 7]

(In the formula (A-1), X ^I and X ^II are a single bond, *-O-, *-COO- or *-OOC-, respectively (wherein the bond with "*" is oriented toward the formula (AI) R ^I is a single bond, a methylene group or an alkylene group having a carbon number of 2 or 3; a is 0 or 1, and b is an integer of 0 to 2, but a and b are not simultaneously 0; An integer from 1 to 20.)

The divalent group represented by X ^I -R ^I -X ^II - in the formula (A-1) is preferably a methylene group, an alkylene group having 2 or 3 carbon atoms, *-O-, *-COO - or *-O-CH ₂ CH ₂ -O- (wherein the bond with "*" is bonded to the diaminophenyl group). When c is 3 or more in the group -C _c H _2c+1 , the group is preferably linear. The two amine groups in the diaminophenyl group are preferably located at the 2,4-position or the 3,5-position relative to other groups. Specific examples of the compound represented by the formula (A-1) are preferably, for example, the following formula (A-1-1-1), formula (A-1-1-2), and formula (A-1-2). ) Compounds represented separately.

[化8]

(In the formula, "positive" means linear)

Examples of the diamine having no pretilt-exhibiting group include an aliphatic diamine, an alicyclic diamine, an aromatic diamine, a diamine-based organodecane, and the like which do not have a pretilt expression group.

Among the diamines having no pretilt-exhibiting group, examples of the aliphatic diamine include 1,1-m-xylylenediamine, 1,3-propanediamine, tetramethylenediamine, and pentamethylene. An amine, hexamethylenediamine or the like; an alicyclic diamine, for example, 1,4-diaminocyclohexane, 4,4'-methylenebis(cyclohexylamine), 1,3-double (Aminomethyl)cyclohexane; etc.; as an aromatic diamine which does not have a pre-tilt-representation group, for example, an aromatic diamine is, for example, o-phenylenediamine, m-phenylenediamine, 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-diaminopurine, 4,4'-diaminodiphenyl Ether, 2,2-bis[4-(4-aminophenoxy)phenyl]propane, 9,9-bis(4-aminophenyl)anthracene, 2,2-bis[4-(4- Aminophenoxy)phenyl]hexafluoropropane, 2,2-bis(4-aminophenyl)hexafluoropropane, 4,4'-(p-phenylenediphenylene)diphenylamine, 4 , 4'-(meta-phenyldiisopropylidene)diphenylamine, 1,4-bis(4-aminophenoxy)benzene, 4,4'-bis(4-aminophenoxy) Benzene, 2,6-diamine Pyridine, 3,4-diaminopyridine, 2,4-diaminopyrimidine, 3,6-diaminoacridine, 3,6-diaminocarbazole, N-methyl-3,6-di Aminocarbazole, N-ethyl-3,6-diaminocarbazole, N-phenyl-3,6-diaminocarbazole, N,N'-bis(4-aminophenyl)- Benzidine, N,N'-bis(4-aminophenyl)-N,N'-dimethylbenzidine, 1,4-bis-(4-aminophenyl)-piperazine, 3,5 -diaminobenzoic acid, 4-(4'-trifluoromethoxybenzylideneoxy)cyclohexyl-3,5-diaminobenzoate, 4-(4'-trifluoromethylbenzene Methoxyoxy)cyclohexyl-3,5-diaminobenzoic acid ester, 2,4-diamino-N,N-diallylaniline, 4-aminobenzylamine, 3-amino Benzylamine, 1-(2,4-diaminophenyl)piperazine-4-carboxylic acid, 4-(morpholin-4-yl)benzene-1,3-diamine, 1,3-double ( N-(4-aminophenyl)piperidinyl)propane, α-amino-ω-aminophenylalkylene, 4-(2-aminoethyl)aniline, represented by the following formula (N) Compound, etc.

Examples of the diamine-based organosiloxane having no pretilt-expressing group include, for example, 1,3-bis(3-aminopropyl)-tetramethyldioxane; The tetracarboxylic dianhydride described in Patent Document 4 (Japanese Patent Laid-Open Publication No. 2010-97188) can also be used.

The diamine used for the synthesis of the specific polymer of the present invention preferably contains 5 mol% or more of the specific diamine as described above with respect to the entire diamine, more preferably 10 mol% or more, and particularly preferably 30 Mole%~80% by mole.

The liquid crystal alignment agent of the present invention is particularly suitable for forming a Twisted Nematic (TN) type, a Super Twisted Nematic (STN) type, and an In Plane Switching (IPS) by a photoalignment method. A liquid crystal alignment film in a so-called horizontal alignment type liquid crystal display element such as a Fringe Field Switching (FFS) type. Therefore, it is preferable to limit the use ratio of the diamine having a pretilt expression group among the diamines used to a certain value or less. The ratio of use of the diamine having a pretilt-exhibiting group is preferably 20 mol% or less with respect to all diamines used, and more preferably 10 mol% or less, and particularly preferably It is 5 mol% or less.

<Synthesis of specific polymers>

The polyamic acid which is a specific polymer of the present invention can be obtained by reacting the tetracarboxylic dianhydride and the diamine as described above with a blocking agent which is optionally used.

The ruthenium iodide polymer which is a specific polymer of the present invention can be obtained by subjecting polylysine obtained in the above manner to dehydration ring closure and ruthenium imidization.

Examples of the blocking agent include carboxylic acid monoanhydrides such as maleic anhydride, phthalic anhydride, and itaconic anhydride; and monoamines such as aniline, cyclohexylamine, and n-butylamine; A monoisocyanate compound such as phenyl isocyanate or naphthyl isocyanate.

The ratio of the tetracarboxylic dianhydride to the diamine to be used in the synthesis reaction of the polyamic acid is preferably 1 equivalent to the amine group of the diamine, and the number of equivalents of the acid anhydride group of the tetracarboxylic dianhydride is 0.2 equivalent to 2 equivalents. The ratio is more preferably 0.3 to 1.2 equivalents. In the case of using a blocking agent, the use ratio of the blocking agent is preferably 20 parts by weight or less based on 100 parts by weight of the total of the tetracarboxylic dianhydride and the diamine.

The synthesis reaction of polylysine is preferably carried out in an organic solvent at a temperature of preferably -20 ° C to 150 ° C, more preferably 0 ° C to 100 ° C, preferably 0.1 to 24 hours, more preferably carried out. 0.5 hours to 12 hours.

Examples of the organic solvent which can be used in the synthesis of polyamic acid include an aprotic polar solvent, phenol and a derivative thereof, an alcohol, a ketone, an ester, an ether, a halogenated hydrocarbon, and a hydrocarbon. Among these organic solvents, at least one selected from the group consisting of an aprotic polar solvent and a phenol and a derivative thereof (the first group of organic solvents) is preferably used, or is selected from the first group. A mixture of at least one of the organic solvents and at least one selected from the group consisting of alcohols, ketones, esters, ethers, halogenated hydrocarbons, and hydrocarbons (organic solvents of the second group). In the latter case, the use ratio of the organic solvent of the second group is preferably 50% by weight or less, and more preferably 40% by weight or less based on the total of the organic solvent of the first group and the organic solvent of the second group. It is especially preferably 30% by weight or less.

It is particularly preferred to use a group selected from the group consisting of N-methyl-2-pyrrolidone, N,N-dimethylacetamide, N,N-dimethylformamide, dimethyl hydrazine, γ-butyrolactone, four Methyl urea, Hexamethylphosphonium triamine, m-cresol, xylenol, 3-methoxy-N,N-dimethylpropanamide, 3-butoxy-N,N-dimethylpropanamide and At least one of the group consisting of halogenated phenols.

The amount (a) of the organic solvent used is preferably a total amount of the tetracarboxylic dianhydride and the diamine (and, in the case of being, a blocking agent), and (b) the total amount of the polymerization reaction solution (a+b). The proportion (b/(a+b)) in the amount is 0.1% by weight to 50% by weight.

A solution containing polylysine was obtained in the above manner. The solution may be provided directly or, if necessary, the polylysine may be isolated by a known method. After purification, it is supplied to the next oxime imidization reaction or the preparation of the liquid crystal alignment agent of the present invention.

In the case of using a ruthenium iodide polymer of polylysine as the specific polymer of the present invention, the ruthenium imidation ratio of the ruthenium iodide polymer is preferably selected from the viewpoint of ensuring good electrical characteristics. It is 30% or more, more preferably 50% or more, and particularly preferably 65% or more. On the other hand, from the viewpoint of ensuring the solubility of the specific polymer of the ruthenium iodide polymer and improving the coatability of the obtained liquid crystal alignment agent, the sulfhydrylation ratio is preferably 99% or less, and more preferably Set to 80% or less.

In order to subject the polylysine obtained in the above manner to dehydration ring closure and imidization, it is preferably carried out by the following method: (i) a method of heating polylysine; or (ii) a polylysine A method of dissolving in an organic solvent, adding a dehydrating agent and a dehydration ring-closing catalyst to the solution, and heating as needed.

The reaction temperature in the method (i) for heating poly-proline is preferred It is 50 ° C to 200 ° C, more preferably 60 ° C to 170 ° C. When the reaction temperature is less than 50 ° C, the dehydration ring closure reaction does not proceed sufficiently, and if the reaction temperature exceeds 200 ° C, the molecular weight of the obtained ruthenium iodide polymer decreases. The reaction time is preferably from 1.0 to 24 hours, more preferably from 1.0 to 12 hours.

On the other hand, in the method of (ii) adding a dehydrating agent and a dehydration ring-closure catalyst to a solution of poly-proline, the dehydrating agent may be, for example, an acid anhydride such as acetic anhydride, propionic anhydride or trifluoroacetic anhydride. The amount of the dehydrating agent to be used depends on the desired ruthenium iodide ratio, and is preferably from 0.01 mol to 20 mol based on 1 mol of the proline structure of the polyglycolic acid. Further, as the dehydration ring-closing catalyst, for example, a tertiary amine such as pyridine, trimethylpyridine, dimethylpyridine or triethylamine can be used. The amount of the dehydration ring-closure catalyst to be used is preferably 0.01 mol to 10 mol with respect to 1 mol of the dehydrating agent to be used. The more the amount of the dehydrating agent and the dehydration ring-closing agent used, the more the sulfhydrylation rate is increased. The organic solvent used for the dehydration ring-closure reaction is exemplified as an organic solvent exemplified as the organic solvent used in the synthesis of polyglycine. The reaction temperature of the dehydration ring closure reaction is preferably from 0 ° C to 180 ° C, more preferably from 10 ° C to 150 ° C. The reaction time is preferably from 1.0 to 120 hours, more preferably from 2.0 to 30 hours. A solution of a ruthenium imidized polymer containing polylysine was obtained in the above manner. The solution may be provided directly or, as needed, the ruthenium iodide polymer may be isolated by a known method. After purification, it is supplied to the preparation of the liquid crystal alignment agent of the present invention.

<Other ingredients>

The liquid crystal alignment agent of the present invention contains the specific polymer as described above as an essential component, and it is preferred that the composition is a solution composition dissolved in a solvent to be described later. It contains other ingredients as needed.

Examples of such other components include other polymers, compounds having at least one epoxy group in the molecule (hereinafter referred to as "epoxy compounds"), and functional decane compounds.

[Other polymers]

The other polymer is a polymer other than the specific polymer, and can be used to improve solution characteristics (coatability) and electrical characteristics of the liquid crystal alignment agent of the present invention.

Examples of the other polymer include polylysine which does not have the structure represented by the above formula (1) in the main chain, ruthenium iodide polymer of the polyglycine, polyphthalate, polyester, Polyamide, polyoxyalkylene, cellulose derivative, polyacetal, polystyrene derivative, poly(styrene-phenylmethylene iodide) derivative, poly(meth)acrylate, etc. .

The ratio of use of the other polymer is preferably 50% by weight or less, and more preferably 30% by weight or less based on 100 parts by weight of the specific polymer.

[epoxy compound]

Examples of the epoxy compound include ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, tripropylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, and neopentyl glycol. Diglycidyl ether, 1,6-hexanediol diglycidyl ether, glycerol diglycidyl ether, trimethylolpropane triglycidyl ether, 2,2-dibromoneopentyl glycol diglycidyl ether, N, N,N',N'-tetraglycidyl-m-xylylenediamine, 1,3-bis(N,N-diglycidylaminomethyl)cyclohexane, N,N,N',N '-tetraglycidyl-4,4'-diaminodiphenylmethane, N,N-diglycidyl-benzylamine, N,N-diglycidyl-aminomethylcyclohexane, N,N-diglycidyl-cyclohexylamine, etc. As a preferred compound.

The compounding ratio of these epoxy compounds is preferably 40 parts by weight or less, more preferably 0.1 parts by weight to 30 parts by weight, based on 100 parts by weight of the specific polymer.

[functional decane compound]

Examples of the functional decane compound include 3-aminopropyltrimethoxydecane, 3-aminopropyltriethoxydecane, 2-aminopropyltrimethoxydecane, and 2-aminopropyl group. Triethoxy decane, N-(2-aminoethyl)-3-aminopropyltrimethoxydecane, N-(2-aminoethyl)-3-aminopropylmethyldimethoxy Baseline, 3-ureidopropyltrimethoxydecane, 3-ureidopropyltriethoxydecane, N-ethoxycarbonyl-3-aminopropyltrimethoxydecane, N-ethoxycarbonyl 3-aminopropyltriethoxydecane, N-triethoxydecylpropyltriethylamine, N-trimethoxydecylpropyltriethylamine, 10-trimethoxy Base alkyl-1,4,7-triazadecane, 10-triethoxydecyl-1,4,7-triazadecane, 9-trimethoxydecyl-3,6-di Azaindenyl acetate, 9-trimethoxydecyl-3,6-diazadecyl acetate, 9-triethoxydecyl-3,6-diazaindolyl acetate , 9-trimethoxydecyl-3,6-diazepine, methyl 9-triethoxydecyl-3,6-diazepine, N-benzyl-3-amine Propyltrimethoxydecane, N-benzyl-3- Aminopropyltriethoxydecane, N-phenyl-3-aminopropyltrimethoxydecane, N-phenyl-3-aminopropyltriethoxydecane, and the like.

The compounding ratio of these functional decane compounds is preferably 2 parts by weight or less, more preferably 0.02 parts by weight to 0.2 parts by weight, based on 100 parts by weight of the specific polymer.

<Liquid alignment agent>

The liquid crystal alignment agent of the present invention is composed of a specific polymer as described above and optionally The other components which are optionally formulated are preferably dissolved and contained in a solvent.

The solvent which can be used for the liquid crystal alignment agent of the present invention is preferably an organic solvent, and examples thereof include N-methyl-2-pyrrolidone, γ-butyrolactone, γ-butylide, and N,N-dimethyl group. Formamide, N,N-dimethylacetamide, 4-hydroxy-4-methyl-2-pentanone, ethylene glycol monomethyl ether, butyl lactate, butyl acetate, methoxypropionate Ester, ethyl ethoxypropionate, ethylene glycol methyl ether, ethylene glycol ether, ethylene glycol-n-propyl ether, ethylene glycol-isopropyl ether, ethylene glycol-n-butyl ether (butyl cellosolve), Ethylene glycol dimethyl ether, ethylene glycol ethyl ether acetate, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol single Methyl ether acetate, diethylene glycol monoethyl ether acetate, diisobutyl ketone, isoamyl propionate, isoamyl isobutyrate, diisoamyl ether, ethylene carbonate, propylene carbonate, etc. . These solvents may be used singly or in combination of two or more.

The solid content concentration in the liquid crystal alignment agent of the present invention (the ratio of the total weight of the components other than the solvent of the liquid crystal alignment agent to the total weight of the liquid crystal alignment agent) is appropriately selected in consideration of viscosity, volatility, and the like, and is preferably selected. It is in the range of 1% by weight to 10% by weight. In other words, the liquid crystal alignment agent of the present invention is applied to the surface of the substrate as described later, and is preferably formed into a coating film to be a liquid crystal alignment film by heating. However, when the solid content concentration is less than 1% by weight, the film thickness of the coating film is When the solid content concentration exceeds 10% by weight, the film thickness of the coating film becomes too large to obtain a good liquid crystal alignment film, and the liquid crystal alignment agent is too small to obtain a good liquid crystal alignment film. The viscosity is increased and the coating characteristics are poor.

A particularly preferred range of solid component concentration is based on coating a liquid crystal alignment on a substrate The method used in the agent differs. For example, in the case of using the rotator method, the solid content concentration is particularly preferably in the range of 1.5% by weight to 4.5% by weight. In the case of using the printing method, it is particularly preferable to set the solid content concentration to a range of 3% by weight to 9% by weight, thereby setting the solution viscosity to 12 mPa. s~50mPa. The scope of s. In the case of using the inkjet method, it is particularly preferable to set the solid content concentration to a range of 1% by weight to 5% by weight, thereby setting the solution viscosity to 3 mPa. s~15mPa. The scope of s.

The temperature at which the liquid crystal alignment agent of the present invention is prepared is preferably from 10 ° C to 45 ° C, more preferably from 20 ° C to 30 ° C.

<Method of Forming Liquid Crystal Alignment Film>

The liquid crystal alignment film can be formed using the liquid crystal alignment agent of the present invention. That is, a liquid crystal alignment film can be formed by forming a coating film by applying the liquid crystal alignment agent of the present invention on a substrate, and irradiating the coating film with light.

The liquid crystal alignment agent of the present invention can be applied, for example, to a liquid crystal display element having a suitable liquid crystal cell such as a TN type, an STN type, an IPS type, an FFS type, a VA type, or an MVA type. However, in terms of maximizing the advantageous effects of the present invention, it is preferably applied to a liquid crystal display element having a so-called horizontal alignment type liquid crystal cell such as a TN type, an STN type, an IPS type, or an FFS type.

In the case where a liquid crystal alignment film formed of the liquid crystal alignment agent of the present invention is applied to a TN type or STN type liquid crystal display element, the substrate is formed by using two substrates provided with a patterned transparent conductive film as a pair. The liquid crystal alignment agent is applied to the surface of each of the substrates on which the transparent conductive film is formed. On the other hand, in the case where the liquid crystal alignment film is applied to an IPS type or FFS type liquid crystal display element, The substrate is a substrate having a transparent conductive film on one surface or a metal film patterned into a comb-shaped electrode, and a pair of opposite substrates not provided with an electrode, and the liquid crystal alignment agent is applied to the formation surface of the comb-shaped electrode. And one side of the opposite substrate.

In any of the cases, the substrate may be, for example, glass such as float glass or soda glass; including polyethylene terephthalate, polybutylene terephthalate, polyether oxime, poly A transparent substrate of plastic such as carbonate. For example, the transparent conductive film of indium tin containing In ₂ O ₃ -SnO ₂ oxide (Indium Tin Oxide, ITO) film, comprising SnO Naisai (NESA) ₂ (registered trademark) film. As the metal film, for example, a film containing a metal such as chromium can be used. When the transparent conductive film and the metal film are patterned, the following method can be utilized: for example, after forming a transparent conductive film without a pattern, the light is utilized. A method of forming a pattern by an etching method, a sputtering method, or the like; a method of using a mask having a desired pattern when forming a transparent conductive film, or the like.

When a liquid crystal alignment agent for photoalignment is applied onto a substrate, functional decane may be preliminarily coated on the substrate, the transparent conductive film or the metal film in order to improve the adhesion between the substrate, the transparent conductive film or the metal film and the coating film. a compound, a titanate compound, or the like.

The application of the liquid-aligning liquid crystal alignment agent on the substrate is preferably carried out by an appropriate coating method such as an offset printing method, a spin coating method, a roll coater method, or an inkjet printing method, and then the coated surface is heated (prebaking) ), thereby forming a coating film. The prebaking conditions are, for example, from 0.1 to 5 minutes at 40 ° C to 120 ° C.

Then, by applying light irradiation to the coating film formed as described above, the liquid crystal alignment ability is imparted to the coating film to form a liquid crystal alignment film. Here, light can be used, for example. Ultraviolet rays and visible rays containing light having a wavelength of 150 nm to 800 nm are preferably ultraviolet rays containing light having a wavelength of 200 nm to 400 nm. The irradiation light may be polarized light or non-polarized light, and is preferably polarized light. As the light source, for example, a low pressure mercury lamp, a high pressure mercury lamp, a xenon lamp, a metal halide lamp, an argon resonance lamp, a xenon lamp, an Hg-Xe lamp, an excimer laser or the like can be used. The light of the preferred wavelength region can be obtained by a method in which the light source is used in combination with, for example, a filter, a diffraction grating, or the like.

The irradiation amount of light is preferably from 400 J/m ² to 50,000 J/m ² , and more preferably from 1,000 J/m ² to 10,000 J/m ² .

The coating film which imparts the alignment ability to the liquid crystal by light irradiation in the above manner is preferably used after further heating (post-baking). The post-baking condition is preferably from 120 ° C to 300 ° C, more preferably from 150 ° C to 250 ° C, more preferably from 5 minutes to 200 minutes, still more preferably from 10 minutes to 100 minutes.

The film thickness of the liquid crystal alignment film formed of the liquid crystal alignment agent of the present invention is preferably 0.001 μm to 1 μm, and more preferably 0.005 μm to 0.5 μm.

<Liquid crystal display element>

A substrate on which a liquid crystal alignment film is formed by the method of the present invention and in the above manner can be used, for example, a liquid crystal display element is manufactured in the following manner.

A pair of substrates in which the liquid crystal alignment film is formed as described above is prepared, and a liquid crystal cell having a liquid crystal sandwiched between the pair of substrates is manufactured.

As the liquid crystal, for example, a nematic liquid crystal, a smectic liquid crystal, or the like can be used. A liquid crystal having positive dielectric anisotropy for forming a nematic liquid crystal is preferable, and for example, a biphenyl liquid crystal or a phenyl ring can be used. A hexane liquid crystal, an ester liquid crystal, a terphenyl liquid crystal, a biphenyl cyclohexane liquid crystal, a pyrimidine liquid crystal, a dioxane liquid crystal, a bicyclooctane liquid crystal, a cubane liquid crystal, or the like. Further, a cholesteric liquid crystal such as cholesteryl chloride, cholesteryl nonanoate, or cholesteryl carbonate may be added to the liquid crystal (for example). Cholesteric liquid crystal; a chiral agent sold under the trade names "C-15", "CB-15" (above manufactured by Merck); p-methoxybenzylidene-p-amino- A ferroelectric liquid crystal such as p-decyloxybenzylidene-p-amino-2-methylbutylcinnamate.

In the case of manufacturing a liquid crystal cell, for example, a method in which two liquid crystal substrates are opposed to each other via a gap (cell gap) is disposed, and the peripheral portions of the two substrates are bonded together by a sealant. a method of sealing an injection hole after injecting a liquid crystal into a cell gap of a substrate surface and a sealant; and coating a predetermined number of portions on one of the two substrates on which the liquid crystal alignment film is formed, for example, photocurable Further, after the liquid crystal is dropped onto a predetermined number of portions of the liquid crystal alignment film surface, the sealing agent is bonded to the other substrate so as to face the liquid crystal alignment film, and then the entire surface of the substrate is irradiated with ultraviolet light to harden the sealing agent. Method (liquid crystal dropping method, ODF method = One Drop Fill method) and the like. As the sealant, for example, an epoxy resin or the like containing an alumina ball as a spacer and a curing agent can be used.

In the case of using any of the above methods, it is preferred to sequentially remove the liquid crystal cell until the liquid crystal used becomes a temperature of the isotropic phase, and then slowly cool to room temperature to remove the liquid alignment during liquid crystal filling. .

Next, a liquid crystal display element can be manufactured by bonding a polarizing plate to the outer surface of the liquid crystal cell. Here, the desired liquid crystal display element can be obtained by appropriately adjusting the angle of the polarizing plate in the two substrates on which the liquid crystal alignment film is formed. The polarizing plate may be a polarizing plate in which a polarizing film called "H film" is sandwiched between a cellulose acetate protective film, or a polarizing plate including the H film itself, and the "H film" is a side. The vinyl alcohol is extended to a polarizing film which is made to absorb iodine.

The liquid crystal display element manufactured in the above manner is excellent in display characteristics, electrical characteristics, and the like.

[Examples]

Hereinafter, the present invention will be specifically described by way of examples, but the invention is not limited to the examples.

The solution viscosity of each polymer solution in the synthesis example of the following polymer is a value measured at 25 ° C using the E-type rotational viscometer for the polymer solution indicated in each synthesis example.

<Synthesis Example of Specific Diamine>

The following synthesis examples are repeated on the following scale as necessary to ensure the necessary amount in the synthesis of the following polymers.

Synthesis Example A-1

The compound (A-1-1) was synthesized according to the following Scheme 1.

(1) Synthesis of Compound (A-1-1a)

105.0 mmol (15.98 g) of methyl 4-hydroxybenzoate, 50.0 mmol (10.80 g) of 1,4-dibromobutane, and 120.0 mmol (16.59 g) of potassium carbonate were added to the reaction vessel. 100 mL of N,N-dimethylacetamide was mixed, and the reaction was carried out for 6 hours while stirring at 80 °C. In the middle of the reaction, the formation of crystals was observed in the reaction system.

After completion of the reaction, 500 mL of ethyl acetate and 300 mL of distilled water were added to the reaction mixture in this order to carry out liquid separation washing. After washing, the recovered organic layer was placed under reduced pressure to remove the solvent, and the total amount of the obtained solid was recovered, washed with ethanol, and dried under reduced pressure to obtain a white crystalline compound (A- 1-1a) 44.4 mmol (15.91 g) (yield 88.8%).

(2) Synthesis of Compound (A-1-1b)

The entire amount of the obtained compound (A-1-1a) (44.4 mmol (15.91 g)), lithium hydroxide monohydrate 133.2 mmol (5.59 g), methanol 60 mL, ethanol 40 mL, and distilled water 30 mL were placed in a reaction container. The mixture was mixed, and the reaction was carried out for 3 hours while stirring at 80 °C. After completion of the reaction, 1 N hydrochloric acid was added to the reaction mixture to make the liquid acidic, and the resulting powder was collected by filtration. This powder was separately washed with distilled water and ethanol, and dried under reduced pressure to obtain 41.6 mmol (13.73 g) of compound (A-1-1b) (yield: 93.6%).

(3) Synthesis of Compound (A-1-1c)

The entire amount of the obtained compound (A-1-1b) (41.6 mmol (13.73 g)), thionyl chloride 35 mL, and N,N-dimethylformamide were placed in a reaction vessel. The mixture was mixed and reacted at 80 ° C for 1 hour while stirring. After the end of the reaction, the reaction mixture was placed under reduced pressure of a water jet to remove unreacted sulfoxide. Add 100 mL of tetrahydrofuran to the resulting solution, It is used as solution <1>.

In a separate reaction vessel, 87.3 mmol (12.14 g) of 4-nitrophenol, 124.7 mmol (17.3 mL) of triethylamine, and 150 mL of tetrahydrofuran were charged, and the mixture was stirred under ice bath. The solution <1> was added dropwise thereto over 1 hour, and the reaction was carried out for 4 hours while stirring at 25 °C. After completion of the reaction, 500 mL of ethyl acetate was added to the reaction mixture, followed by washing with 1 N hydrochloric acid and distilled water. At this time, the powder floated on the side of the organic layer.

The powder was collected by filtration and recovered, and dried under reduced pressure to give the compound (A-1-1c) (36.9 mol (21.15 g)) (yield 88.8%).

(4) Synthesis of Compound (A-1-1)

36.9 mol (21.15 g) of the obtained compound (A-1-1c), 738 mmol (48.3 g) of zinc, 147.6 mmol (7.75 g) of ammonium chloride, 332 mL of tetrahydrofuran, and ethanol were added to the reaction vessel under a nitrogen atmosphere. 37 mL was mixed and stirred under an ice bath. After 18.5 mL of distilled water was added dropwise thereto, the mixture was stirred at 25 ° C for 8 hours and at 70 ° C for 1 hour to carry out a reaction. After the completion of the reaction, the insoluble components such as the produced inorganic salt are removed by filtration from the reaction mixture. The organic layer obtained by adding 1,850 mL of ethyl acetate to the filtrate was washed four times with 738 mL of distilled water. After the washed organic layer was filtered, the solvent was removed under reduced pressure to obtain a powder. The powder was washed successively with ethanol and ethyl acetate, and the solvent was completely removed under reduced pressure to obtain 21.0 mmol (10.7 g) of compound (A-1-1) (yield: 56.8%).

Synthesis Example A-2

The compound (A-8-1) was synthesized according to the following Scheme 2.

(Ts in the formula (A-8-1b) is a toluenesulfonyl group.)

(1) Synthesis of Compound (A-8-1a)

In a 200 mL three-necked flask equipped with a nitrogen gas introduction tube, a reflux tube, and a thermometer, 20 g of 4-nitrophenylacetic acid, 10 g of p-hydroxybenzaldehyde, and 5 mL of piperidine were placed, and the reaction was carried out at 140 ° C for 1 hour. Then, add 75 mL of ethanol and water to it. 25 mL and 0.5 mL of acetic acid were reacted under reflux for 2 hours. After completion of the reaction, the formed precipitate was collected by filtration and recrystallized using isopropyl alcohol to obtain 17 g of a reddish brown compound (A-8-1a).

(2) Synthesis of Compound (A-8-1c)

14 g of the obtained compound (A2-8-1a), 20 g of potassium carbonate, and 460 mL of acetonitrile were placed in a 1 L three-necked flask equipped with a reflux tube and a nitrogen gas introduction tube, and the reaction was carried out for 30 minutes under reflux. Then, 12 g of the compound (A-8-1b) was added thereto, and the reaction was carried out under reflux for 24 hours. After completion of the reaction, the reaction mixture was poured into 1 L of ethyl acetate to suspend it, and the mixture was washed once with 500 mL of diluted hydrochloric acid, and washed three times with 500 mL of water, and then decompressed from the organic layer. The solvent was removed, the obtained yellow crystals were collected by filtration, and the solvent was completely removed under reduced pressure, whereby 14 g of compound (A-8-1c) was obtained.

(3) Synthesis of Compound (A-8-1)

13 g of the obtained compound (A-8-1c), 1.3 g of 5% by weight of palladium carbon powder, 250 mL of tetrahydrofuran, 35 mL of ethanol, and 80% by weight were placed in a 1 L three-necked flask equipped with a reflux tube, a nitrogen gas introduction tube, and a thermometer. 12 mL of hydrazine monohydrate was reacted under reflux for 6 hours. After completion of the reaction, 500 mL of ethyl acetate was added to the filtrate obtained by filtering the reaction mixture, and the mixture was washed three times with 500 mL of water. The organic layer after washing was concentrated, and the precipitated white crystals were collected by filtration, and the solvent was completely removed under reduced pressure to obtain 9.5 g of white crystals of compound (A-8-1).

<Synthesis of Polymer>

The abbreviations of the tetracarboxylic dianhydride used in the synthesis examples of the following polymers are respectively The following meanings.

Compound (T-1): a compound represented by the formula (T-1)

Compound (T-2): a compound represented by the formula (T-2)

Synthesis Example P-1

9.3 g of the compound (T-1) as a tetracarboxylic dianhydride and 10.7 g of the compound (A-1-1) obtained in the above Synthesis Example A-1 as a diamine were dissolved in N-methyl-2- In 80 g of pyrrolidone, the reaction was carried out for 4 hours at room temperature, whereby a solution containing 20% by weight of poly-proline (PA-1) was obtained. The solution has a solution viscosity of 2,700 mPa. s.

Synthesis Example P-2

7.4 g of the compound (T-2) as a tetracarboxylic dianhydride and 13.6 g of the compound (A-1-1) obtained in the synthesis example A-1 as a diamine were dissolved in N-methyl-2- In 80 g of pyrrolidone, the reaction was carried out for 4 hours at room temperature, whereby a solution containing 20% by weight of polyglycine (PA-2) was obtained. The solution has a solution viscosity of 1,900 mPa. s.

Synthesis Example P-3

9.5 g of the compound (T-1) as a tetracarboxylic dianhydride and 10.5 g of the compound (A-8-1) obtained in the above Synthesis Example A-1 as a diamine were dissolved in N-methyl-2- In 80 g of pyrrolidone, the reaction was carried out for 4 hours at room temperature, whereby a solution containing 20% by weight of polyglycine (PA-3) was obtained. The solution has a solution viscosity of 3,000 mPa. s.

Comparative Synthesis Example R-1

13.3 g of the compound (T-1) as a tetracarboxylic dianhydride and 6.7 g of 4-aminobenzoic acid-4-aminophenyl ester as a diamine were dissolved in 80 g of N-methyl-2-pyrrolidone. The reaction was carried out for 4 hours at room temperature, thereby obtaining 20% by weight of polydecylamine. A solution of acid (R-1). The solution has a solution viscosity of 1,500 mPa. s.

Comparative Synthesis Example R-2

13.6 g of a compound (T-1) as a tetracarboxylic dianhydride and 6.4 g of 1,2-bis(4-aminophenyl)ethane as a diamine were dissolved in 80 g of N-methyl-2-pyrrolidone The reaction was carried out for 4 hours at room temperature, whereby a solution containing 20% by weight of poly-proline (R-2) was obtained. The solution has a solution viscosity of 2,900 mPa. s.

<Preparation and evaluation of liquid crystal alignment agent>

Example 1

1. Preparation of liquid crystal alignment agent

In a solution containing the poly-proline (PA-1) obtained in the synthesis example (P-1), N-methyl-2-pyrrolidone (NMP) and butyl cellosolve (BC) were added and stirred well. A solution having a solvent composition of NMP: BC = 60: 40 (weight ratio) and a solid content concentration of 2.5% by mass was prepared. This solution was filtered using a filter having a pore size of 1 μm, thereby preparing a liquid crystal alignment agent.

2. Evaluation of liquid crystal alignment agent

(1) Production of liquid crystal cell for liquid crystal alignment, voltage retention, and contrast evaluation

The prepared liquid crystal alignment agent was applied to each of the transparent electrode faces of two (a pair of) glass substrates having a transparent electrode including an ITO film by using a spinner so as to have a film thickness of 0.1 μm, and then at 80 ° C. The film was formed by heating (prebaking) for 1 minute. Using the Hg-Xe lamp, the surface of the coating film was irradiated with ultraviolet rays containing a polarized light of 254 nm from the normal direction of the substrate by the irradiation amount shown in Table 1, and then After heating (post-baking) in a clean oven at 230 ° C for 1 hour, a liquid crystal alignment film was formed on each of two (one pair) substrates.

Then, one of the pair of substrates subjected to the light irradiation treatment is applied by screen printing so that the liquid crystal injection port remains in the outer peripheral edge portion of the surface on which the liquid crystal alignment film is formed. The epoxy resin binder of the alumina ball having a diameter of 5.5 μm is laminated and crimped so that the liquid crystal alignment film forming surface faces each other and the projection direction of the polarized light at the time of light irradiation faces the substrate surface. The adhesive was thermally hardened by heating at 150 ° C for 1 hour.

Then, a nematic liquid crystal (MLC-7028, manufactured by Merck & Co., Inc.) was filled between the pair of substrates from the liquid crystal injection port, and then the liquid crystal injection port was sealed with an epoxy-based adhesive. Further, in order to remove the flow alignment at the time of liquid crystal injection, it was heated to 150 ° C and then slowly cooled to room temperature, thereby producing a liquid crystal cell.

(2) Evaluation of liquid crystal alignment

For the manufactured liquid crystal cell, use a polarizing microscope to observe when turned on. Turns off (ON.OFF) (applies and releases) the presence or absence of an abnormal region when the AC voltage is 5V.

When the abnormal region was not observed, it was evaluated that the liquid crystal alignment property was "good", and even when only one abnormal region was observed in the display region, the liquid crystal alignment "defect" was evaluated. As a result, the liquid crystal alignment property of the liquid crystal cell was judged. It is "good".

(3) Evaluation of voltage retention rate

With respect to the manufactured liquid crystal cell, after applying a voltage of 5 V with an application time of 60 μsec and a span of 167 msec, the voltage holding ratio after 167 msec from the application release was measured, and as a result, the voltage holding ratio of the liquid crystal cell was 98. %.

The type name "VHR-1" manufactured by Toyo Technica Co., Ltd. was used as a measuring device for voltage holding ratio.

(4) Evaluation of contrast

The contrast after driving the manufactured liquid crystal cell for 30 hours was ascertained.

Using a device in which a polarizer and an analizer are disposed between the light source and the light amount detector, the manufactured liquid crystal cell is disposed between the polarizer and the analyzer, and the cross-cut is found The light transmittance β under the crossed nicols is substituted into the following mathematical expression (1) to calculate the minimum relative transmittance (%).

Minimum relative transmittance (%) = (β-B0) / (B100 - B0) × 100 (1)

(In the formula (1), B0 is the light transmission amount of the blank under the crossed nibble; B100 is the light transmission amount of the blank under the parallel nicols; and β is under the orthogonal nibble, The amount of light transmitted by measuring the state of the liquid crystal cell is arranged between the polarizer and the analyzer.)

The minimum relative transmittance calculated by the above formula (1) indicates the degree of the black level in the dark state, and the smaller the value of the minimum relative transmittance, the more excellent the contrast can be evaluated.

The case where the minimum relative transmittance was less than 0.5% was evaluated as "good", the case where 0.5% to 1.0% was evaluated as "consistency", and the case where the minimum transmittance was more than 1.0% was evaluated as "poor". The minimum relative transmittance of the liquid crystal cell 0.3%, so the contrast is judged as "good".

(5) Manufacture of liquid crystal cell for evaluation of afterimage characteristics

A liquid crystal for evaluation of afterimage characteristics was produced in the same manner as in the above-mentioned "(2) Liquid crystal alignment, voltage retention, and production of liquid crystal cells for contrast evaluation", except for using a pair of substrates having the following configuration. In the unit (FFS type liquid crystal cell), a polarizing plate was bonded to both surfaces of the substrate to form a liquid crystal display element.

Here, the electrode substrate uses a glass substrate on which two system electrodes (electrode A (101) and electrode B (102)) are formed, and the two-system electrodes (electrode A (101) and electrode B (102)) have the structure shown in FIG. The comb-tooth pattern is shown to include chromium; the counter substrate is a glass substrate on which no electrode is formed. A liquid crystal alignment agent is applied to one surface of the electrode formation surface of the electrode substrate and the counter substrate.

(6) Evaluation of afterimage characteristics (burning)

The produced liquid crystal display element was placed in an environment of 25 ° C and 1 atm, and no voltage was applied to the electrode B, and a combined voltage of an alternating current voltage of 3.5 V and a direct current voltage of 5 V was applied to the electrode A for 2 hours. Immediately after the lapse of 2 hours, an alternating voltage of 4 V was applied to both of the electrode A and the electrode B. Next, the time from the time when the alternating voltage was applied to the two electrodes was 4 V until the difference in light transmittance between the electrodes was not confirmed by visual observation. When the time is less than 100 seconds, the afterimage characteristics are evaluated as "good"; when the time is 100 seconds or longer and less than 150 seconds, the afterimage characteristics are evaluated as "OK"; In the case of 150 seconds or longer, the afterimage characteristics were evaluated as "poor", and as a result, the afterimage characteristics of the liquid crystal display element were "good".

Example 2 to Example 4 and Comparative Example 1 and Comparative Example 2

In addition to using a solution containing a polylysine of the type shown in Table 1 instead of a solution containing poly-proline (PA-1), and "2. (1) liquid crystal alignment, voltage retention, and contrast evaluation The amount of the polarized ultraviolet ray irradiation in the "manufacture of the liquid crystal cell used" and "2. (5) Manufacture of the liquid crystal cell for evaluation of afterimage characteristics" are the same as those in the first embodiment except that they are as described in Table 1. In the manner of preparing a liquid crystal alignment agent, various evaluations were carried out using the liquid crystal alignment agent.

The evaluation results are shown in Table 1.

As can be easily understood from the above Table 1, it is verified that the liquid crystal alignment agent of the present invention containing the polymer having the structure represented by the formula (1) in the main chain is subjected to the photoalignment method thereto, A liquid crystal alignment film excellent in both contrast and afterimage characteristics, in addition to excellent liquid crystal alignment and voltage retention.

101‧‧‧electrode A

102‧‧‧Electrode B

Claims (9)

A liquid crystal alignment agent containing at least one selected from the group consisting of polylysine having a structure represented by the following formula (1) in the main chain and a ruthenium iodide polymer thereof polymer: (In the formula (1), two of X are independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond, a guanamine bond, -NH-, -C(=O)-, and a carbon number of 1 to 10; a divalent saturated aliphatic group or a divalent unsaturated aliphatic group having 2 to 10 carbon atoms; wherein two Y atoms are each independently a single bond, an oxygen atom, a sulfur atom, an ester bond or a thioester bond; R is a sub A methyl group, or an alkyl group having 2 to 12 carbon atoms interrupted by an oxygen atom in the middle; and "*" means a bond). The liquid crystal alignment agent according to claim 1, wherein R in the formula (1) is a group represented by the following formula: -(CH ₂ ) _n - or -(CR'H-CH ₂ )-(O-CR'H-CH ₂ ) _m - (wherein R' is a hydrogen atom, a methyl group or an ethyl group; n is an integer of 1 to 12; m is an integer of 1 to 3). The liquid crystal alignment agent according to claim 1, wherein the polymer is a polyfluorene obtained by reacting a tetracarboxylic dianhydride with a diamine containing a compound represented by the following formula (A1). At least one polymer of the group consisting of aminic acid and its quinone imidized polymer: (In the formula (A1), X, Y and R have the same meanings as in the formula (1), respectively). The liquid crystal alignment agent according to claim 3, wherein the tetracarboxylic dianhydride comprises a compound represented by the following formula (T1): [Chemical 4] (In the formula (T1), Z is independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond or -NH- in the case where a plurality of Z are present; and R ¹ is independently carbon in the presence of a plurality of The number of 6 to 18 aryl groups or carbon number 2 to 6 alkyl groups; and, n1 is an integer of 0 to 2). A liquid crystal alignment film which is formed by the liquid crystal alignment agent according to any one of claims 1 to 4. A liquid crystal display element comprising the liquid crystal alignment film according to item 5 of the patent application. A polyproline which is obtained by reacting a tetracarboxylic dianhydride with a diamine comprising a compound represented by the following formula (A1): (In the formula (A1), two of X are independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond, a guanamine bond, -NH-, -C(=O)-, and a carbon number of 1 to 10; a divalent saturated aliphatic group or a divalent unsaturated aliphatic group having 2 to 10 carbon atoms; and a plurality of Y groups are each independently a single bond, an oxygen atom, a sulfur atom, an ester bond or a thioester bond; R is a sub A methyl group, or a 2 to 12 carbon alkyl group interrupted by an oxygen atom in the middle). A quinone imidized polymer which is a ruthenium iodide polymer of polyglycine as described in claim 7 of the patent application. A diamine compound represented by the following formula (A1): (In the formula (A1), two of X are independently an oxygen atom, a sulfur atom, an ester bond, a thioester bond, a guanamine bond, -NH-, -C(=O)-, and a carbon number of 1 to 10; a divalent saturated aliphatic group or a divalent unsaturated aliphatic group having 2 to 10 carbon atoms; and a plurality of Y groups are each independently a single bond, an oxygen atom, a sulfur atom, an ester bond or a thioester bond; R is a sub A methyl group, or a 2 to 12 carbon alkyl group interrupted by an oxygen atom in the middle).