TW202321426A - Liquid crystal aligning agent, liquid crystal alignment film, method for producing liquid crystal display element, and liquid crystal display element - Google Patents

Abstract

The present invention provides: a liquid crystal aligning agent which enables the achievement of a liquid crystal alignment film that has excellent resistance to AC afterimages and low pretilt angle characteristics; and the like. The liquid crystal aligning agent contains component (A) and component (B). Component (A): At least one polymer (A) that is selected from the group consisting of a polyimide precursor, which is a reaction product of a tetracarboxylic acid derivative component that contains a tetracarboxylic acid dianhydride represented by formula (Tc) in an amount of 100% by mole of the entire tetracarboxylic acid derivative component and a diamine component that contains a diamine represented by formula (dAL) in an amount of 60% or more of the entire diamine component, and a polyimide. Component (B): At least one polymer (B) that is selected from the group consisting of a polyimide precursor, which is a reaction product of a tetracarboxylic acid derivative component that contains a tetracarboxylic acid dianhydride represented by formula (Tf) in an amount of 5% by mole or more of the entire tetracarboxylic acid derivative component and a diamine component that contains a diamine represented by formula (dAL) and a diamine represented by formula (dn), and a polyimide. (In the formulae, the definition of each symbol is as described in the description.).

Description

Liquid crystal alignment agent, liquid crystal alignment film, manufacturing method of liquid crystal display element, and liquid crystal display element

The present invention relates to a liquid crystal alignment agent, a liquid crystal alignment film, a manufacturing method of a liquid crystal display element and a liquid crystal display element.

Liquid crystal display elements used in LCD TVs, navigators, smart phones, etc. are usually provided with a liquid crystal alignment film in the element to control the alignment state of the liquid crystal. Liquid crystal alignment film has the function of controlling the alignment of liquid crystal molecules in a certain direction in the liquid crystal display element. For example, a liquid crystal display element has a structure in which liquid crystal molecules forming a liquid crystal layer are sandwiched between liquid crystal alignment films formed on the respective surfaces of a pair of substrates. The liquid crystal molecules are aligned in a certain direction through the liquid crystal alignment film, and respond to the voltage applied to the electrodes arranged between the substrate and the liquid crystal alignment film. As a result, the liquid crystal display element displays a desired image by utilizing the alignment change due to the response of the liquid crystal molecules. So far, the liquid crystal alignment film mainly uses polyamic acid (polyamic acid) and other polyimide precursors and soluble polyimide solutions as the main components. The liquid crystal alignment agent is coated on a glass substrate and the like and calcined. Imine-based liquid crystal alignment film.

In recent years, with the high performance of liquid crystal display elements, in addition to large-screen and high-definition LCD TVs, it is also used in automotive applications (such as car navigation systems, instrument panels), surveillance cameras, and medical camera screens. For liquid crystal display elements, due to the requirement of viewing angle characteristics, transverse electric field methods such as IPS (In Plane Switching) method and FFS (Fringe Field Switching) method have been discussed (Patent Document 1, Patent Document 2). [Prior Art Literature] [Patent Document]

[Patent Document 1] WO2017-061575 Publication [Patent Document 2] WO2020-116585 Publication

(Problem to be solved by the invention)

The liquid crystal alignment film used in the liquid crystal display elements of the IPS driving method and the FFS driving method needs alignment regulation force to suppress image sticking caused by long-term AC driving (hereinafter also referred to as AC image sticking). The liquid crystal display element, which is rapidly becoming more high-definition, is gradually adopting a backlight with higher brightness than before, and the standards for display defects such as "image sticking" are becoming stricter.

Patent Document 1 describes a liquid crystal alignment film for photo-alignment suitable for liquid crystal display elements of the IPS driving method and the FFS driving method.

Also, Patent Document 2 discloses that a liquid crystal alignment film obtained from a liquid crystal alignment agent containing two kinds of polyamic acids has high resistance to AC sticking. On the other hand, the liquid crystal display elements used in the above-mentioned applications require a lower pretilt angle than before due to the need for viewing angle characteristics. full.

In view of the above circumstances, the present invention aims to provide a liquid crystal alignment agent capable of obtaining a liquid crystal alignment film having excellent resistance to AC image sticking and a low pretilt angle characteristic, the liquid crystal alignment film, and a liquid crystal display element using the liquid crystal alignment film. (How to solve the problem)

The inventors of the present invention worked diligently to achieve the above-mentioned problems. As a result, they found that forming a liquid crystal alignment film using a liquid crystal alignment agent containing a specific polymer component is effective for achieving the above-mentioned purpose, and completed the present invention.

This invention is based on this knowledge knowledge, and the following matters are made into the summary.

A liquid crystal alignment agent is characterized in that it contains the following (A) component and (B) component, (A) component: polymer (A), is selected from the tetracarboxylic dianhydride represented by the following formula (T _c ): The reaction product of 100 mol% tetracarboxylic acid derivatives of all tetracarboxylic acid derivatives and the diamine represented by the following formula (d _AL ) whose content is more than 60% of all diamines is poly At least one of the group consisting of an imide precursor and a polyimide which is an imide of the polyimide precursor, (B) component: polymer (B), selected from the following The content of the tetracarboxylic dianhydride represented by the formula (T _f ) is more than 5 mol% of the total tetracarboxylic acid derivative components, and the tetracarboxylic acid derivative components contain the diamine represented by the following formula (d _AL ) and the following formula The reaction product of the diamine component of the diamine represented by (d _n ) is at least 1 of the group consisting of a polyimide precursor and a polyimide which is an imide of the polyimide precursor kind.

[chemical 1]

R ₁₁ ~ R ₁₄ each independently represent a hydrogen atom, a halogen atom, an alkyl group with 1 to 6 carbons, an alkenyl group with 2 to 6 carbons, an alkynyl group with 2 to 6 carbons, or a fluorine atom containing 1 to 6 carbons A monovalent organic group of 6, or a phenyl group, at least one of R ₁₁ to R ₁₄ represents a group other than a hydrogen atom as defined above.

[Chem 2]

A means having a group "*11-(CH ₂ ) _n -O-*12" (*11 means an atomic bond bonded to an oxygen atom or an atomic bond bonded to a carbon atom constituting a benzene ring, *12 means an atomic bond .n is an integer from 1 to 5.) of divalent organic groups. Any hydrogen atom of the above-mentioned benzene ring bonded to the NH ₂ group may also be substituted by a monovalent group.

[Chem 3]

X _f is a tetravalent organic group having an alicyclic structure with 5 or more members.

[chemical 4]

Y represents an atomic bond selected from a heterocyclic ring containing a nitrogen atom and a group "*21-NR-*22" (*21, and *22 represent an atomic bond bonded to a carbon atom constituting an aromatic ring. However, the carbon atom is not The nitrogen atom to which R is bonded forms a ring. R represents a hydrogen atom or a monovalent organic group, and the above monovalent organic group is bonded to a carbon atom other than the carbonyl carbon and a nitrogen atom. A divalent organic group in the structure of a nitrogen atom. In addition, in the entirety of this specification, the meanings of the following terms and abbreviations are as follows. The halogen atom is a fluorine atom, chlorine atom, bromine atom, iodine atom, etc., preferably a fluorine atom. * Indicates an atomic bond. Also, Boc represents a tertiary butoxycarbonyl group. (Effect of Invention)

According to the liquid crystal alignment agent of the present invention, it is possible to obtain a liquid crystal alignment agent capable of obtaining a liquid crystal alignment film having excellent resistance to AC image sticking and low pretilt angle characteristics. Moreover, the liquid crystal display element having the liquid crystal alignment film has excellent viewing angle characteristics and high display quality.

The mechanism for obtaining the above-mentioned effects in the present invention is not necessarily clear, but it is roughly estimated as follows. That is, it is considered that by using two kinds of polymers as the polymer components used in the liquid crystal alignment agent, and using diamines with specific chain lengths in the raw material components of both polymers, it will become highly linear. Polymer, therefore, exhibits an effect of improving resistance to AC image sticking.

Also, by using two different polymer components, the two polymers are easily separated into two layers, and it is considered that high resistance to AC sticking and low pretilt angle characteristics can be achieved at the same time.

Each component contained in the liquid crystal alignment agent of the present invention and other components that can be arbitrarily blended as needed will be described below. The polymers (A) and (B) contained in the liquid crystal alignment agent of the present invention are a polyimide precursor obtained by using a tetracarboxylic acid derivative component and a diamine component, or an imide of the polyimide precursor Amides are polyimides. Among them, the polyimide precursor is a polymer that can obtain polyimide by imidizing polyamic acid, polyamic acid ester, and the like.

The polymers (A) and (B) are preferably polyimide precursors, more preferably polyamic acid, from the viewpoint of ideally obtaining the effect of the present invention. <Polymer (A)> Polyamic acid (A'), which is a polyimide precursor of the above-mentioned polymer (A), can be obtained by a polymerization reaction of a diamine component and a tetracarboxylic acid derivative component. Among the diamine components used in the production of the polymer (A) contained in the liquid crystal alignment agent of the present invention, the content of the diamine represented by the following formula (d _AL ) is 60% or more of the total diamine components. The diamine represented by the formula (d _AL ) may be used alone or in combination of two or more.

[chemical 5]

A means having a group "*11-(CH ₂ ) _n -O-*12" (*11 means an atomic bond bonded to an oxygen atom or an atomic bond bonded to a carbon atom constituting a benzene ring, *12 means an atomic bond .n is an integer from 1 to 5.) of divalent organic groups. Any hydrogen atom of the above-mentioned benzene ring bonded to the NH ₂ group may also be substituted by a monovalent group. When A in the above formula (d _AL ) is in the above-mentioned aspect, the resistance to AC image sticking is improved, and when two types of polymers are used, they are compatible with each other moderately, and low pretilt angle characteristics can be obtained.

In consideration of obtaining high liquid crystal alignment, *11 is preferably an atomic bond to an oxygen atom.

Considering the viewpoint of obtaining low pretilt angle characteristics, it is preferable that n in the group "*11-(CH ₂ ) _n -O-*12" be an integer of 2~5, and an integer of 2 or 5 is more preferable.

Regarding the two amine groups in the above formula (d _AL ), considering the viewpoint of obtaining high liquid crystal alignment, the para position relative to A is preferable.

A in the above formula (d _AL ) is preferably 1 to 18 carbons, more preferably 1 to 14 carbons, and more preferably 2 to 12 carbons in view of ideally obtaining the effects of the present invention. Valence organic base.

In the above formula (d _AL ), the monovalent group includes a halogen atom, an alkyl group with 1 to 10 carbons (more preferably 1 to 5 carbons, more preferably 1 to 3 carbons), an alkyl group with 2 to 10 carbons ( More preferably alkenyl with 2 to 5 carbons, more preferably alkenyl with 2 to 3 carbons, alkoxy with 1 to 10 carbons (more preferably 1 to 5 carbons, more preferably 1 to 3 carbons) , a fluoroalkyl group with a carbon number of 1 to 10 (more preferably a carbon number of 1 to 5, more preferably a carbon number of 1 to 3), a carbon number of 2 to 10 (more preferably a carbon number of 2 to 5, more preferably a carbon number 2~3) fluoroalkenyl group, fluoroalkoxy group with 1~10 carbons (more preferably 1~5 carbons, more preferably 1~3 carbons), carboxyl, hydroxyl, alkane with 1~10 carbons Oxycarbonyl (more preferably 2 to 5 carbons, more preferably 2 to 3 carbons), cyano, nitro, etc.

With respect to the diamine represented by the above formula (d _AL ), in view of obtaining the effects of the present invention ideally, the diamines represented by the following formulas (d _AL -1) to (d _AL -9) are preferable.

[chemical 6]

For n in the above formulas (d _AL -1)~(d _AL -2) and (d _AL -4)~(d _AL -5), considering the viewpoint of obtaining low pretilt angle characteristics, it is more ideal to be 2~5.

Considering the viewpoint of obtaining low pretilt angle characteristics, m and n in the above formula (d _AL -3) are more preferably 2 to 5 independently.

The n in the above formula (d _AL -6) is more preferably 2 to 4, and 2 or 4 are more ideal. m1 and m2 in the above formula (d _AL -6) are each independently more preferably 1 to 3, more preferably 1 to 2. Also, the total of m1, m2, and n is 3 to 16. From the viewpoint of obtaining low pretilt angle characteristics, 3 to 12 is more preferable, and 3 to 10 is more ideal.

For n in the above formulas (d _AL -7) and (d _AL -9), considering the viewpoint of obtaining low pretilt angle characteristics, it is more ideal to be 2~5.

In the above formula (d _AL -8), n is more preferably 1-4, more preferably 1-3, and more ideally 1-2. m1 and m2 in the above formula (d _AL -8) are each independently more preferably 1 to 4, more preferably 1 to 3, and more preferably 1 to 2. Also, the total of m1, m2, and n is 3 to 15, and from the viewpoint of obtaining low pretilt angle characteristics, 3 to 14 is more preferable, and 3 to 12 is more ideal.

The two amine groups in the above formulas (d _AL -1)~(d _AL -9) are preferably in the para position relative to the divalent organic group connected to the benzene ring in view of obtaining high liquid crystal alignment.

Among the constituents of the above-mentioned polymer (A), the ideal content of the diamine represented by the above formula (d _AL ) is preferably 60 mol% or more of the total diamine components used in the manufacture of the polymer (A), preferably, More than 70 mole % is more preferable, more than 80 mole % is more ideal. When other diamines described later are used in combination, the diamine represented by the above formula (d _AL ) is preferably at most 95 mol%, more preferably at most 90 mol%, and even more preferably at most 85 mol%.

As the diamine component used in the production of the polymer (A) contained in the liquid crystal alignment agent of the present invention, in addition to the above-mentioned diamines, various diamines (hereinafter also referred to as other diamines) can be used according to the characteristics of the liquid crystal alignment agent required. ). As the above-mentioned other diamines, the following can be used. Among other diamines, in view of ideally obtaining the effect of the present invention, it is preferable to have no side chain group with more than 4 carbon atoms (except for the protective group that will be detached and replaced with a hydrogen atom due to heating as described later.) good. These diamines may be used alone or in combination of two or more.

Diamine represented by the above formula (d _n ), p-phenylenediamine, 2,3,5,6-tetramethyl-p-phenylenediamine, 2,5-dimethyl-p-phenylenediamine, m-phenylenediamine, 2 ,4-Dimethyl-m-phenylenediamine, 2,5-diaminotoluene, 2,6-diaminotoluene and other phenylenediamines; 2,2'-dimethyl-4,4'-diamino Biphenyl, 3,3'-dimethyl-4,4'-diaminobiphenyl, 3,3'-dimethoxy-4,4'-diaminobiphenyl, 3,3'-bis Hydroxy-4,4'-diaminobiphenyl, 2,2'-difluoro-4,4'-diaminobiphenyl, 3,3'-difluoro-4,4'-diaminobiphenyl , 2,2'-bis(trifluoromethyl)-4,4'-diaminobiphenyl, 3,3'-bis(trifluoromethyl)-4,4'-diaminobiphenyl, 3 ,4'-Diaminobiphenyl, 4,4'-Diaminobiphenyl, 3,3'-Diaminobiphenyl, 2,2'-Diaminobiphenyl, 2,3'-Diamine 1,2-bis(6-amino-2-naphthyloxy)ethane, 1,2-bis(6-amino-2-naphthyl)ethane , 6-[2-(4-aminophenoxy)ethoxy]-2-naphthylamine, 1,5-diaminonaphthalene, 1,6-diaminonaphthalene, 1,7-diaminonaphthalene Naphthalene, 2,5-diaminonaphthalene, 2,6-diaminonaphthalene, 2,7-diaminonaphthalene and other diamines with naphthalene structure; 4,4'-diaminoazobenzene or diamine Diamines with photoalignment groups, such as diphenylacetylene (diaminotolan); diamines represented by the following formulas (h-1)~(h-5), such as diamines with amide bonds or urea bonds; 3,3 '-Diaminodiphenylmethane, 3,4'-diaminodiphenylmethane, 4,4'-diaminodiphenylmethane, 1,2-bis(4-aminophenyl)ethane Alkane, 1,2-bis(3-aminophenyl)ethane, 1,3-bis(4-aminophenyl)propane, 1,3-bis(3-aminophenyl)propane, 1, 4-bis(4-aminophenyl)butane, 1,4-bis(3-aminophenyl)butane, 1,5-bis(4-aminophenyl)pentane, 1,5- Bis(3-aminophenyl)pentane, 1,6-bis(4-aminophenyl)hexane, 1,6-bis(3-aminophenyl)hexane, 4,4'-di Aminodiphenone, 1,4-bis(4-aminophenyl)benzene, 1,3-bis(4-aminophenyl)benzene, 1,4-bis(4-aminobenzyl) Benzene, diamine represented by the following formula (d _o ): 2,4-diaminophenol, 3,5-diaminophenol, 3,5-diaminobenzyl alcohol, 2,4-diaminobenzyl alcohol , 4,6-diaminoresorcinol; 4,4'-diamino-3,3'-dihydroxybiphenyl; 2,4-diaminobenzoic acid, 2,5-diaminobenzene Formic acid, 3,5-diaminobenzoic acid, 4,4'-diaminobiphenyl-3-carboxylic acid, 4,4'-diaminodiphenylmethane-3-carboxylic acid, 1,2-bis( 4-Aminophenyl)ethane-3-carboxylic acid, 4,4'-diaminobiphenyl-3,3'-dicarboxylic acid, 4,4'-diaminobiphenyl-2,2'-di Formic acid, 3,3'-diaminobiphenyl-4,4'-dicarboxylic acid, 3,3'-diaminobiphenyl-2,4'-dicarboxylic acid, 4,4'-diaminobiphenyl Methylmethane-3,3'-dicarboxylic acid, 1,2-bis(4-aminophenyl)ethane-3,3'-dicarboxylic acid, 4,4'-diaminodiphenyl ether-3,3 Diamines with carboxyl groups such as '-dicarboxylic acid; 4-(2-(methylamino)ethyl)aniline, 4-(2-aminoethyl)aniline, 1-(4-aminophenyl)-1 ,3,3-Trimethyl-1H-indene-5-amine, 1-(4-aminophenyl)-2,3-dihydro-1,3,3-trimethyl-1H-indene -6-amine; 2-(2,4-diaminophenoxy)ethyl methacrylate and 2,4-diamino-N,N-diallylaniline, etc. Diamine; Cholesteryloxy-3,5-diaminobenzene, Cholesteryloxy-3,5-diaminobenzene, Cholesteryloxy-2,4-diaminobenzene , 3,5-diaminobenzoic acid cholestyl ester, 3,5-diaminobenzoic acid cholestyl ester, 3,5-diaminobenzoic acid lanostyl ester and 3,6-bis(4 - Diamines having a steroid skeleton such as aminobenzyloxy)cholestane; diamines represented by the following formulas (V-1) to (V-2); the following formulas (5-1) to (5-9 ) and the like have a group "-N(D)-" (D represents a protecting group that is detached by heating and replaced by a hydrogen atom, preferably tertiary butoxycarbonyl. ) of diamines (except for diamines represented by formula (d _n ).); 1,3-bis(3-aminopropyl)-tetramethyldisiloxane and other diamines with siloxane bonds; m-xylylenediamine, 1,3-propanediamine, tetramethylenediamine, pentamethylenediamine, hexamethylenediamine, 1,3-bis(aminomethyl)cyclohexane , 1,4-diaminocyclohexane, 4,4'-methylene bis(cyclohexylamine), any of the formulas (Y-1)~(Y-167) described in WO2018/117239 The ones represent diamines, etc., in which two amine groups are bonded.

[chemical 7]

[chemical 8]

When there are two or more m, each of the two or more m may be the same or different. One or more hydrogen atoms on the benzene ring may be substituted by a monovalent group. An illustration of the formula (d ₀ ) will be described later.

[chemical 9]

In formula (V-1), m and n are integers from 0 to 3 (provided that 1≦m+n≦4), j is an integer of 0 or 1, and X ¹ represents -(CH ₂ ) _a -( a is an integer from 1 to 15.), -CONH-, -NHCO-, -CO-N(CH ₃ )-, -NH-, -O-, -CH ₂ O-, -CH ₂ -OCO-, - COO-, or -OCO-. ^R1 represents a fluorine atom, an alkyl group containing a fluorine atom with 1 to 10 carbons, an alkoxy group with a fluorine atom with 1 to 10 carbons, an alkyl group with 3 to 10 carbons, and an alkoxy group with 3 to 10 carbons group, or an alkoxyalkyl group with 3 to 10 carbon atoms. In formula (V-2), X ² represents -O-, -CH ₂ O-, -CH ₂ -OCO-, -COO-, or -OCO-, and there are two m, n, X ¹ , and R ¹ , each independently has the above definition.

[chemical 10]

Specific examples of the monovalent group in the above formula (d _o ) include structures exemplified for the monovalent group in the above formula (d _AL ).

For the diamine represented by the above formula (d _o ), considering the viewpoint of making the pretilt angle low, the diamine represented by the following formula (d _o -1)~(d _o -6), 3,3'-diamine Diaminodiphenyl ether, 3,4'-diaminodiphenyl ether and 4,4'-diaminodiphenyl ether are preferred.

[chemical 11]

In the tetracarboxylic acid derivative component used in the manufacture of the polymer (A) contained in the liquid crystal alignment agent of the present invention, the content of the tetracarboxylic dianhydride represented by the above formula (T _c ) is the total tetracarboxylic acid derivative component 100 mole %.

By containing the above-mentioned specific tetracarboxylic dianhydride, the configuration at the time of imidization is restricted. The polymer (A) thus obtained has high stereoregularity, and can obtain a liquid crystal alignment film excellent in resistance to AC image sticking. In addition, since the above-mentioned specific tetracarboxylic dianhydride has a substituted structure, the polymer (A) component having high liquid crystal alignment is more likely to concentrate on the surface layer, and it is considered that the effect of the present invention can be obtained ideally. Among R ₁₁ to R ₁₄ of the formula (T _c ), specific examples of the alkyl group having 1 to 6 carbon atoms, preferably 1 to 3, include methyl, ethyl, propyl, isopropyl, n-butyl, Isobutyl, second butyl, third butyl, n-pentyl, etc. Specific examples of alkenyl groups having carbon numbers of 2 to 6, preferably 2 to 4 in the above-mentioned R ₁ to R ₄ include vinyl, propenyl, butenyl, etc., which may be linear or Branched. Specific examples of alkynyl groups with 2 to 6, preferably 2 to 3, carbon atoms in R ₁₁ to R ₁₄ above, such as ethynyl, 1-propynyl, 2-propynyl, etc. Among the above-mentioned R ₁₁ to R ₁₄ , the carbon number containing fluorine atoms is 1 to 6, preferably 1 to 3 monovalent organic groups, such as fluoromethyl, trifluoromethyl, pentafluoroethyl, pentafluoropropyl wait. For a more ideal combination of R ₁₁ ~ R ₁₄ , in view of exhibiting low pretilt angle characteristics, it is preferable that R ₁₁ and R ₁₄ have the same structure and R ₁₂ and R ₁₃ have the same structure. In addition, R ₁₁ to R ₁₄ are hydrogen atoms or methyl groups, and at least one of R ₁₁ to R ₁₄ is preferably a methyl group, and at least two of R ₁₁ to R ₁₄ are more preferably methyl groups. More preferably, R ₁₁ and R ₁₄ are methyl groups, and R ₁₂ and R ₁₃ are hydrogen atoms. <Polymer (B)> The diamine component used in the production of the polymer (B) contained in the liquid crystal alignment agent of the present invention contains the diamine represented by the above formula (d _AL ) and the diamine represented by the above formula (d _n ). amine. The diamine represented by the above formula (d _AL ) and the diamine represented by the above formula (d _n ) may be used alone or in combination of two or more.

Desirable aspects of the diamine represented by the above formula (d _AL ) used in the production of the polymer (B), and ideal aspects of the diamine represented by the above formula (d _AL ) used in the production of the polymer (A) for the same.

Among the constituents of the above-mentioned polymer (B), the content of the diamine represented by the above formula (d _AL ) is preferably 5-80 mol % of the total diamine components used in the synthesis of the polymer (B), preferably 10-70 mol %. Mole % is better, 40~60 Mole % is more ideal.

Heterocyclic rings containing nitrogen atoms in the above formula (d _n ), for example: pyrrole ring, imidazole ring, pyrazole ring, triazole ring, pyridine ring, pyrimidine ring, pyridyl ring, pyryl ring, indole ring, benzene And imidazole ring, purine ring, quinoline ring, isoquinoline ring, phenidine ring, quinoline ring, phthalein ring, three urea ring, carbazole ring, acridine ring, piperidine ring, piperidine ring, pyrrole Pyridine ring, hexamethyleneimine ring, etc. Among them, a pyridine ring, a pyrimidine ring, a pyridine ring, a piperidine ring, a piperidine ring, a quinoline ring, a carbazole ring or an acridine ring is preferable.

Monovalent organic groups of R in the above formula (d _n ), for example: alkyl groups such as methyl, ethyl, and propyl; alkenyl groups such as vinyl; cycloalkyl groups such as cyclohexyl; phenyl, methylphenyl, etc. Aryl, alkoxy (for example: methoxy, ethoxy) and the like. R is preferably a hydrogen atom or a methyl group.

Specific examples of diamines represented by the above formula (d _n ), such as: 2,6-diaminopyridine, 3,4-diaminopyridine, 2,4-diaminopyrimidine, 3,6-diaminopyridine Carbazole, N-methyl-3,6-diaminocarbazole, 1,4-bis-(4-aminophenyl)-piperone, 3,6-diaminoacridine, N-ethyl -3,6-diaminocarbazole, N-phenyl-3,6-diaminocarbazole, or diamines represented by the following formulas (d _n -1) to (d _n -3).

[chemical 12]

In formula (d _n -1), m1 and m1' are each independently an integer of 1-2. n1 is an integer from 1 to 3. R ₁ is synonymous with R of the amino group represented by the above "*21-NR-*22".

When there are a plurality of R ₁ and m1', the plurality of R1 and m1' may be the same or different.

In the formula (d _n -2), X ₂ represents a monovalent nitrogen-atom-containing heterocyclic group. Among the monovalent nitrogen-atom-containing heterocyclic groups, specific examples of nitrogen-atom-containing heterocyclic rings can be listed in the above formula Structures exemplified by nitrogen-atom-containing heterocycles in (d _n ).

n1 is an integer from 1 to 2, and n2 is an integer satisfying n1+n2=2. L ₁ and L ₂ are each independently a single bond, -CO-, an alkylene group with 1 to 6 carbons, or -O- or -CO- is inserted between the carbon-carbon bonds of the alkylene group or at the end, and A divalent organic group bonded to a nitrogen atom via a carbon atom. R represents a hydrogen atom or a methyl group.

When there are a plurality of X _{2 ,} L ₂ , and R, the plurality of X _{2 ,} L ₂ , and R may be the same or different.

In the formula (d _n -3), X ₃ represents a divalent group having a heterocyclic ring containing a nitrogen atom. Specific examples of the heterocyclic ring containing a nitrogen atom can include the heterocyclic ring containing a nitrogen atom in the above formula (d _n ) Example structure.

Ar ₃ represents a divalent aromatic ring group or a divalent nitrogen atom-containing saturated heterocyclic group. Specific examples of the aromatic ring in the divalent aromatic ring group include a benzene ring, a naphthalene ring, an anthracene ring, a pyridine ring, a pyrimidine ring, a pyridine ring, a pyrimidine ring, a trivalent ring, a pyrrole ring, and an imidazole ring. , pyrazole ring, quinoline ring, isoquinoline ring, carbazole ring, benzimidazole ring, indole ring, quinoline ring, acridine ring. Specific examples of the nitrogen-atom-containing saturated heterocyclic ring in the divalent nitrogen-atom-containing saturated heterocyclic group include piperidine ring and piperidine ring. Arbitrary hydrogen atoms of an aromatic ring group and a nitrogen atom-containing saturated heterocyclic group may be substituted with a monovalent group. Examples of the monovalent group include the structures exemplified for the monovalent group in the above formula (d _AL ), and the like.

L ₃ represents a single bond, -(CH ₂ ) _n -(n is an integer of 1 to 6.), -NR'-, -(CH ₂ ) _n -NR'-(n is an integer of 1 to 6.), -O-, -NR'-CO-, -CO-NR'-, -O-CO-, or -CO-O-, R' represents a hydrogen atom, a methyl group, or a tert-butoxycarbonyl group.

m3 and m3' are each independently an integer of 0 to 2, and any one of m3 and m3' is an integer of 1 or more.

When there are a plurality of Ar ₃ and L ₃ , the plurality of Ar ₃ and L ₃ may be the same or different.

Also, the NH ₂ groups at both ends in the formula (d _n -3) are bonded to carbon atoms constituting the aromatic ring.

Examples of ideal diamines represented by the above formulas (d _n -1) to (d _n -3) include diamines represented by the following formulas (Dp-1) to (Dp-6), and the following formulas (z-1) ~ the diamine represented by formula (z-14).

[chemical 13]

[chemical 14]

[chemical 15]

Among the constituents of the above-mentioned polymer (B), the content of the diamine represented by the above formula (d _n ) is preferably 20-95 mole % of the total diamine components used in the manufacture of the polymer (B), and 30-95 mole %. 90 mole% is better, and 40~60 mole% is more ideal.

The diamine component used in the manufacture of the polymer (B) contained in the liquid crystal alignment agent of the present invention, in addition to the above-mentioned diamines, can use various diamines (hereinafter also referred to as other diamines ( b)).

Other diamines (b) include, for example, compounds exemplified as diamines used in the production of the above-mentioned polymer (A). Among other diamines (b), it is preferable not to have a side chain group having 4 or more carbon atoms (except for the above-mentioned protecting group that is detached by heating and replaced with a hydrogen atom) in view of obtaining the effect of the present invention ideally. Diamines are preferred. The above-mentioned other diamines (b) may be used alone or in combination of two or more.

In the tetracarboxylic acid derivative component used in the production of the polymer (B) contained in the liquid crystal alignment agent of the present invention, the content of the tetracarboxylic dianhydride represented by the above formula (T _f ) is the total tetracarboxylic acid derivative component More than 5 mol%.

By containing the tetracarboxylic dianhydride represented by the above formula (T _f ), the decrease in the molecular weight of the polymer (B) is suppressed, so a liquid crystal alignment film having high liquid crystal alignment and excellent resistance to AC sticking can be obtained. In addition, the polymer (B) has a specific tetracarboxylic dianhydride that is not easily imidized, so a polymer having many hydrophilic groups such as carboxyl groups can be obtained, and the polymer (A) and the polymer (B) can be obtained. Liquid crystal alignment film with excellent two-layer separation. Therefore, the liquid crystal alignment film which has high liquid crystal alignment property as mentioned above and is excellent in the tolerance with respect to AC sticking image can be obtained.

In the aforementioned formula (T _f ), the 4-valent organic group of X _f having an alicyclic structure with more than 5 membered rings is preferably a 4-valent organic group with an alicyclic structure of 5-8 membered rings. The tetravalent organic group of the alicyclic structure of the ring is more preferable. Also, the alicyclic structure with five or more members means that when the alicyclic structure bonded by the acid anhydride group is a polycyclic structure, the number of atoms constituting the ring in each ring contained in the polycyclic structure is 5 or more. . Moreover, the aforementioned alicyclic structure only needs to be bonded to at least one of the two acid anhydride groups, and may have an alicyclic structure, a chain hydrocarbon structure, and an aromatic ring structure at the same time.

An ideal specific example of X _f includes a tetravalent organic group represented by any one of the following formulas (X _f -1) to (X _f -17). From the viewpoint of ideally obtaining the effects of the present invention, X _f is more preferably (X _f -1) to (X _f -4).

[chemical 16]

The total amount of the tetracarboxylic dianhydride represented by the above formula (T _f ) is preferably 10 moles of all the tetracarboxylic acid derivative components used in the production of the polymer (B) from the viewpoint of obtaining the effect of the present invention % or more is better, and more than 20 mol% is even better. The tetracarboxylic acid derivative component used in the manufacture of the polymer (B) contained in the liquid crystal alignment agent of the present invention, in addition to the tetracarboxylic dianhydride represented by the above formula (T _f ), can also be selected according to the characteristics of the liquid crystal alignment agent On the other hand, tetracarboxylic dianhydrides other than tetracarboxylic dianhydrides represented by the above formula (T _f ) are used (these are also collectively referred to as other tetracarboxylic dianhydrides (b)). The above-mentioned other tetracarboxylic dianhydrides (b) may be used alone or in combination of two or more.

Specific examples of other tetracarboxylic dianhydrides (b) include alicyclic tetracarboxylic dianhydrides other than tetracarboxylic dianhydrides represented by the above formula (T _f ), acyclic aliphatic tetracarboxylic dianhydrides, Or aromatic tetracarboxylic dianhydride.

Here, the alicyclic tetracarboxylic dianhydride is an acid dianhydride obtained by intramolecularly dehydrating four carboxyl groups including at least one carboxyl group bonded to an alicyclic structure. But these 4 carboxyl groups are not bonded to the aromatic ring. Moreover, it does not need to consist only of an alicyclic structure, and may have a chain hydrocarbon structure and an aromatic ring structure partly. Acyclic aliphatic tetracarboxylic dianhydride is an acid dianhydride obtained by intramolecular dehydration of 4 carboxyl groups bonded to a chain hydrocarbon structure. However, it does not need to consist only of a chain hydrocarbon structure, and may have an alicyclic structure or an aromatic ring structure partly. The aromatic tetracarboxylic dianhydride is not particularly limited as long as it is obtained by intramolecularly dehydrating four carboxyl groups including at least one carboxyl group bonded to an aromatic ring.

The non-cyclic aliphatic tetracarboxylic dianhydride, alicyclic tetracarboxylic dianhydride, or aromatic tetracarboxylic dianhydride in the above-mentioned other tetracarboxylic dianhydrides (b) is preferably the above formula (T _c ) The tetracarboxylic dianhydride represented, or the tetracarboxylic dianhydride represented by following formula (t).

[chemical 17]

In the formula, _X1 is a structure selected from the following formulas (X1-1)~(X1-10).

[chemical 18]

[chemical 19]

In the formulas (X1-9)~(X1-10), j and k are integers of 0 or 1, and _A1 and _A2 each independently represent a single bond, -O-, -CO-, -COO-, phenylene group, sulfonyl group, or amide bond. A plurality of A ₂ may each be the same or different. * Indicates an atomic bond. Desirable specific examples of the above formulas (X1-9)~(X1-10) include the following formulas (X _R -1)~(X _R -14). Considering the point of view of improving liquid crystal alignment, the above formulas (X1-9)~(X1-10) are more ideal for the above (X _R -1)~(X _R -8), (X _R -1), (X _R - 4)~(X _R -6), and (X _R -8) are more ideal.

[chemical 20]

[chem 21]

When the tetracarboxylic acid derivative component used in the manufacture of the polymer (B) contained in the liquid crystal alignment agent of the present invention contains other tetracarboxylic dianhydrides (b), the content of other tetracarboxylic dianhydrides (b) is The total tetracarboxylic acid derivative component used in the manufacture of the polymer (B) is preferably 5 mol % to 95 mol %, more preferably 10 to 90 mol %, and more preferably 20 to 80 mol %. Also, in this case, the total amount of tetracarboxylic dianhydride represented by the above formula (T _f ) is preferably 5-95 mole % of all tetracarboxylic acid derivative components, more preferably 10-90 mole %, and 20 ~80 mol % is even better.

Regarding the content ratio of the above-mentioned (A) component and (B) component, considering the viewpoint of obtaining the effect of the present invention, the content ratio of (A) component and (B) component is [(A) component]/[(B) component] The mass ratio can be 10/90~90/10, 20/80~90/10, or 20/80~80/20. ＜Manufacture of Polymer (A) and Polymer (B)＞ (Synthesis of polyamide acid) The polyimide precursor polyamic acid contained in the liquid crystal alignment agent of the present invention can be produced, for example, by the following method. In addition, not only tetracarboxylic dianhydrides but also derivatives thereof, tetracarboxylic acid dihalide compounds, tetracarboxylic Acid dialkyl ester, tetracarboxylic acid dialkyl dihalide, etc. Specifically, it can be obtained by combining the tetracarboxylic acid derivative component containing the above-mentioned tetracarboxylic dianhydride and the diamine component containing the above-mentioned diamine in the presence of an organic solvent, preferably at -20 to 150°C, more preferably 0~50°C, preferably for 0.5~24 hours, more preferably for 1~12 hours (polycondensation) reaction for synthesis.

Specific examples of the organic solvent used in the above reaction can include N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, γ-butyrolactone, N,N-dimethylformamide, N,N- Dimethylacetamide, dimethylsulfoxide, 1,3-dimethyl-2-imidazolidinone, etc. Also, when the solvent solubility of the polymer is high, methyl ethyl ketone, cyclohexanone, cyclopentanone, 4-hydroxy-4-methyl-2-pentanone, propylene glycol monomethyl ether, ethylene glycol monomethyl ether, ethyl Glycol monoethyl ether, ethylene glycol monopropyl ether, diethylene glycol monomethyl ether, or diethylene glycol monoethyl ether. These can also be used in mixture of 2 or more types.

The reaction of polyamide acid can be carried out at any concentration, preferably 1-50% by mass, more preferably 5-30% by mass. The reaction may be carried out at a high concentration in the initial stage, and a solvent may be added thereafter. During the reaction, the ratio of the total number of moles of the diamine components to the total number of moles of the tetracarboxylic acid components is preferably 0.8 to 1.2. Like the usual polycondensation reaction, the closer the molar ratio is to 1.0, the greater the molecular weight of the polyamic acid produced.

The polyamic acid obtained by the above reaction can be injected into a poor solvent while fully stirring the reaction solution to precipitate and recover the polyamic acid. In addition, the precipitation can be carried out several times, and after washing with a poor solvent, it can be dried at room temperature or by heating to obtain a refined polyamic acid powder. The poor solvent is not particularly limited, and examples thereof include water, methanol, ethanol, hexane, butylcytosol, acetone, and toluene. (Synthesis of polyamide ester) Polyamic acid esters can be utilized, for example: [I] a method of reacting polyamic acid obtained by the above method with an esterifying agent, [II] a method of reacting a tetracarboxylic acid diester with a diamine, [III] using It can be obtained by a known method such as a method of reacting a tetracarboxylic acid diester dihalide with a diamine. (Synthesis of Polyimide) Furthermore, polyimide can be obtained by ring-closing (imidizing) a polyimide precursor such as the above-mentioned polyamic acid or polyamic acid ester. Moreover, the imidization ratio referred to in this specification is the ratio of the imide group to the total amount of the imide group derived from tetracarboxylic dianhydride or its derivative, and carboxyl group (or its derivative). The imidization rate does not necessarily have to be 100%, and can be adjusted arbitrarily according to the application and purpose. [blocking agent] When synthesizing the polymers (A) and (B) in the present invention, it is also possible to use a tetracarboxylic acid derivative component containing tetracarboxylic dianhydride, a diamine component, and a suitable end-capping agent to synthesize an end-sealed polymer thing.

Capping agents such as acetic anhydride, maleic anhydride, nedylic anhydride, phthalic anhydride, itaconic anhydride, cyclohexanedicarboxylic anhydride, 3-hydroxyphthalic anhydride, trimellitic anhydride, 3-( 3-trimethoxysilyl)propyl)-3,4-dihydrofuran-2,5-dione, 4,5,6,7-tetrafluoroisobenzofuran-1,3-dione, 4 -Acid monoanhydrides such as ethynyl phthalic anhydride; Dicarbonate diester compounds such as di-tert-butyl dicarbonate and diallyl dicarbonate; Chlorine such as acryl chloride, methacryl chloride, and nicotinyl chloride Carbonyl compounds; aniline, 2-aminophenol, 3-aminophenol, 4-aminosalicylic acid, 5-aminosalicylic acid, 6-aminosalicylic acid, 2-aminobenzoic acid, 3- Aminobenzoic acid, 4-aminobenzoic acid, cyclohexylamine, n-butylamine, n-pentylamine, n-hexylamine, n-heptylamine, n-octylamine and other monoamine compounds; ethyl isocyanate, phenyl isocyanate , naphthyl isocyanate, 2-acryloxyethyl isocyanate and 2-methacryloxyethyl isocyanate and other monoisocyanate compounds such as isocyanates with unsaturated bonds; ethyl isothiocyanate, Isothiocyanate compounds such as allyl isothiocyanate, etc.

The usage ratio of the blocking agent is preferably 0.1-30 mole parts, more preferably 0.1-20 mole parts, relative to the total 100 mole parts of the diamine components used.

When recovering the produced polyamic acid from the reaction solution of polyamic acid, the reaction solution may be poured into a solvent and precipitated. Solvents used for precipitation include methanol, ethanol, isopropanol, acetone, hexane, butylcytosol, heptane, methyl ethyl ketone, methyl isobutyl ketone, toluene, benzene, water and the like. After the polyamic acid put into the solvent and precipitated is collected by filtration, it can be dried under normal pressure or reduced pressure at normal temperature or by heating. In addition, if the operation of redissolving the precipitated polymer in an organic solvent and reprecipitating it is repeated 2 to 10 times, the impurities in the polymer can be reduced. The solvent at this time includes, for example, alcohols, ketones, or hydrocarbons, and it is preferable to use three or more solvents selected from among them because the purification efficiency will be higher.

Regarding the molecular weight of the polymer (A) and polymer (B) used in the present invention, when considering the strength of the liquid crystal alignment film obtained therefrom, the workability of the film formation and the coating film property, according to GPC (Gel Permeation Chromatography) The weight average molecular weight determined by the method is ideally 5,000~1,000,000, more preferably 10,000~150,000.

The total content of the polymers contained in the liquid crystal alignment agent of the present invention can also be appropriately changed depending on the setting of the thickness of the coating film to be formed. Considering the viewpoint of forming a uniform and defect-free coating film, it is ideal to be 1% by mass or more , considering the storage stability of the solution, it is preferably 10% by mass or less. In particular, the total content of polymers is preferably 2 to 8% by mass.

The liquid crystal alignment agent of the present invention may also contain other polymers other than the polymer (A) and the polymer (B). Specific examples of other polymers include polyimide precursors other than polymer (A) and polymer (B), or polyimide, polysiloxane, polyester, polyamide, polyamide Urea, polyurethane, polyorganosiloxane, cellulose derivatives, polyacetals, polystyrene derivatives, poly(styrene-maleic anhydride) copolymers, poly(isobutylene-maleic anhydride) copolymers Polymers selected from the group consisting of poly(vinyl ether-maleic anhydride) copolymers, poly(styrene-phenylmaleimide) derivatives, and poly(meth)acrylates. Specific examples of poly(styrene-maleic anhydride) copolymers include SMA1000, 2000, 3000 (manufactured by Cray Valley), GSM301 (manufactured by Gifushellac), etc. Specific examples of poly(isobutylene-maleic anhydride) copolymers include ISOBAM-600 (made by Kuraray) is mentioned, and the specific example of a poly(vinyl ether-maleic anhydride) copolymer includes GANTREZ AN-139 (methyl vinyl ether maleic anhydride resin, manufactured by ISP Japan).

The other polymers may be used alone or in combination of two or more. The content ratio of other polymers is preferably 90 parts by mass or less, more preferably 10 to 90 parts by mass, and more preferably 20 to 80 parts by mass, based on the total of 100 parts by mass of polymers contained in the liquid crystal alignment agent.

The liquid crystal alignment agent of the present invention is preferably a liquid composition obtained by dissolving or dispersing the above-mentioned polymer (A) and polymer (B) in an organic solvent. Specifically, the organic solvent contained in the above-mentioned liquid crystal alignment agent is not particularly limited as long as the polyamic acid can be uniformly dissolved, and examples include N,N-dimethylformamide, N,N-diethylformamide Amine, N,N-Dimethylacetamide, N,N-Dimethyllactamide, N,N-Dimethylacrylamide, Tetramethylurea, N,N-Diethylformamide , N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, dimethylsulfide, γ-butyrolactone, γ-valerolactone, 1,3-dimethyl-2-imidazolidinone , methyl ethyl ketone, cyclohexanone, cyclopentanone, 3-methoxy-N,N-dimethylpropionamide, 3-butoxy-N,N-dimethylpropionamide, N-(n-propane base)-2-pyrrolidone, N-isopropyl-2-pyrrolidone, N-(n-butyl)-2-pyrrolidone, N-(tertiary butyl)-2-pyrrolidone, N-(n-pentyl)- 2-pyrrolidone, N-methoxypropyl-2-pyrrolidone, N-ethoxyethyl-2-pyrrolidone, N-methoxybutyl-2-pyrrolidone, N-cyclohexyl-2-pyrrolidone (they Also collectively referred to as "good solvent"), etc. Among them, N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, 3-methoxy-N,N-dimethylpropionamide, 3-butoxy-N,N-dimethyl Acrylamide or γ-butyrolactone is preferred. The content of the good solvent is preferably 20-99% by mass, more preferably 20-90% by mass, and particularly preferably 30-80% by mass, of all the solvents contained in the liquid crystal alignment agent.

In addition, the organic solvent contained in the liquid crystal alignment agent should be mixed with a solvent (also known as a poor solvent) that improves the coatability of the liquid crystal alignment agent and the surface smoothness of the coating film in addition to the above-mentioned solvents. . Specific examples of poor solvents used together are as follows but not limited thereto. The content of the poor solvent is preferably 1-80% by mass of the total solvent contained in the liquid crystal alignment agent, more preferably 10-80% by mass, and most preferably 20-70% by mass. The type and content of the poor solvent can be properly selected according to the coating device, coating conditions, and coating environment of the liquid crystal alignment agent.

Poor solvents, such as: diisopropyl ether, diisobutyl ether, diisobutylmethanol (2,6-dimethyl-4-heptanol), ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol Alcohol dibutyl ether, 1,2-butoxyethane, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, 4-hydroxy-4-methyl-2-pentanone, diethylene glycol methyl Diethyl ether, diethylene glycol dibutyl ether, 3-ethoxybutyl acetate, 1-methylpentyl acetate, 2-ethylbutyl acetate, 2-ethylhexyl acetate, Ethylene glycol monoacetate, ethylene glycol diacetate, propylene carbonate, ethylene carbonate, ethylene glycol monobutyl ether, ethylene glycol monoisoamyl ether, ethylene glycol monohexyl ether, propylene glycol mono Methyl ether, propylene glycol monobutyl ether, 1-(2-butoxyethoxy)-2-propanol, 2-(2-butoxyethoxy)-1-propanol, propylene glycol monomethyl ether acetic acid Ester, propylene glycol diacetate, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, dipropylene glycol dimethyl ether, ethylene glycol monobutyl ether acetate, diethylene glycol monopropyl ether, diethylene glycol monoethyl ether Ester, diethylene glycol monobutyl ether acetate, 2-(2-ethoxyethoxy) ethyl acetate, diethylene glycol acetate, n-butyl acetate, propylene glycol monoethyl ether acetate, Cyclohexyl acetate, 4-methyl-2-pentyl acetate, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, ethyl 3-methoxypropionate, 3-methoxy Propyl propionate, butyl 3-methoxypropionate, n-butyl lactate, isopentyl lactate, diethylene glycol monoethyl ether, diisobutyl ketone (2,6-dimethyl-4-heptyl ketones) etc.

Among them, diisobutylmethanol, propylene glycol monobutyl ether, propylene glycol diacetate, diethylene glycol diethyl ether, dipropylene glycol monomethyl ether, dipropylene glycol dimethyl ether, 4-hydroxy-4-methyl-2-pentane Ketone, ethylene glycol monobutyl ether, ethylene glycol monobutyl ether acetate, or diisobutyl ketone is preferred.

The ideal solvent combination of good solvent and poor solvent can include N-methyl-2-pyrrolidone and γ-butyrolactone and ethylene glycol monobutyl ether, N-methyl-2-pyrrolidone and γ-butyrolactone and Propylene glycol monobutyl ether, N,N-dimethyl lactamide and diisobutyl ketone, N-methyl-2-pyrrolidone and 3-ethoxy ethyl propionate and dipropylene glycol monomethyl ether, N-ethyl Base-2-pyrrolidone and 3-ethoxypropionate ethyl and propylene glycol monobutyl ether, N-methyl-2-pyrrolidone and 3-ethoxypropionate ethyl and diethylene glycol monopropyl ether, N- Ethyl-2-pyrrolidone and ethyl 3-ethoxypropionate and diethylene glycol monopropyl ether, N,N-dimethyl lactamide and ethylene glycol monobutyl ether, N,N-dimethyl Lactamide and Propylene Glycol Diacetate, N-Ethyl-2-Pyrrolidone and Diethylene Glycol Diethyl Ether, N-Ethyl-2-Pyrrolidone and Diethylene Glycol Monoethyl Ether and Butylseroxacetate , N-methyl-2-pyrrolidone and diethylene glycol monomethyl ether and butyl cellothreoacetate, N,N-dimethyl lactamide and diethylene glycol diethyl ether, N-methyl- 2-pyrrolidone and γ-butyrolactone and 4-hydroxy-4-methyl-2-pentanone and diethylene glycol diethyl ether, N-ethyl-2-pyrrolidone and N-methyl-2-pyrrolidone and 4 -Hydroxy-4-methyl-2-pentanone, N-ethyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol monobutyl ether, N-methyl-2-pyrrolidone and 4-Hydroxy-4-methyl-2-pentanone and diisobutyl ketone, N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and dipropylene glycol monomethyl ether, N -Methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol monobutyl ether, N-methyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and Propylene glycol diacetate, N-ethyl-2-pyrrolidone and 4-hydroxy-4-methyl-2-pentanone and dipropylene glycol dimethyl ether, gamma-butyrolactone and 4-hydroxy-4-methyl- 2-pentanone and diisobutyl ketone, γ-butyrolactone and 4-hydroxy-4-methyl-2-pentanone and propylene glycol diacetate, N-methyl-2-pyrrolidone and γ-butyrolactone Esters and propylene glycol monobutyl ether and diisobutyl ketone, N-methyl-2-pyrrolidone and γ-butyrolactone and propylene glycol monobutyl ether and diisopropyl ether, N-methyl-2-pyrrolidone and γ-butyl Lactone and propylene glycol monobutyl ether and diisobutyl carbinol, N-methyl-2-pyrrolidone and γ-butyrolactone and dipropylene glycol dimethyl ether, N-methyl-2-pyrrolidone and propylene glycol monobutyl ether and di Propylene glycol dimethyl ether, N-ethyl-2-pyrrolidone and propylene glycol monobutyl ether and dipropylene glycol monomethyl ether, N-ethyl-2-pyrrolidone and diethylene glycol diethyl ether and dipropylene glycol monomethyl ether, N-ethyl Base-2-pyrrolidone and propylene glycol monobutyl ether and propylene glycol diacetate, N-ethyl-2-pyrrolidone and propylene glycol monobutyl ether and diisobutyl ketone, N-ethyl-2-pyrrolidone and γ-butyrol Esters and diisobutyl ketone, N-ethyl-2-pyrrolidone and N,N-dimethyl lactamide and diisobutyl ketone, N-methyl-2-pyrrolidone and ethylene glycol monobutyl ether and Ethylene glycol monobutyl ether acetate, γ-butyrolactone and ethylene glycol monobutyl ether acetate and dipropylene glycol dimethyl ether, N-ethyl-2-pyrrolidone and ethylene glycol monobutyl ether acetate With propylene glycol dimethyl ether, N-methyl-2-pyrrolidone and 4-methyl-2-pentyl acetate and ethylene glycol monobutyl ether, N-ethyl-2-pyrrolidone and cyclohexyl acetate and diacetone alcohol , cyclohexanone and propylene glycol monomethyl ether, cyclopentanone and propylene glycol monomethyl ether, N-methyl-2-pyrrolidone and cyclohexanone and propylene glycol monomethyl ether, tetramethylurea and 4-hydroxy-4-methyl -2-pentanone, tetramethylurea and propylene glycol diacetate, N,N-dimethylacrylamide and propylene glycol monobutyl ether, tetramethylurea and propylene glycol monobutyl ether, tetramethylurea and cyclohexyl Ketone and propylene glycol monomethyl ether, N,N-dimethylacrylamide and propylene glycol monomethyl ether, N,N-dimethylacrylamide and ethylene glycol monobutyl ether acetate, N,N-dimethylacrylamide Dimethylacrylamide and ethylene glycol monobutyl ether, tetramethylurea and propylene glycol monomethyl ether, N,N-dimethylacrylamide and cyclohexanone and diethylene glycol diethyl ether, N,N-diethyl N,N-diethylformamide and propylene glycol monomethyl ether, N,N-diethylformamide and 4-hydroxy-4-methyl-2-pentanone, N,N-diethylformamide and propylene glycol monomethyl ether wait.

(additive ingredient) The liquid crystal alignment agent of this invention may additionally contain the said (A) component, (B) component, and components other than an organic solvent (it is also called an additive component hereafter.). These additive components, such as crosslinking compounds, functional silane compounds, metal chelate compounds, hardening accelerators, surfactants, antioxidants, sensitizers, preservatives, are used to adjust the dielectric constant and resistance of the resin film. Compounds, etc., the cross-linking compound is selected from at least one of epoxy group, oxetanyl group, azoline structure, cyclocarbonate group, blocked isocyanate group, hydroxyl group and alkoxyl group At least one of the group consisting of a crosslinkable compound (c-1) having a substituent and a crosslinkable compound (c-2) having a polymerizable unsaturated group.

Desirable specific examples of the above-mentioned crosslinkable compounds (c-1) and (c-2) include the following compounds. Compounds having epoxy groups include ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, tripropylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, Neopentyl Glycol Diglycidyl Ether, 1,6-Hexanediol Diglycidyl Ether, Glycerin Diglycidyl Ether, 2,2-Dibromoneopentyl Glycol Diglycidyl Ether, 1,3 , 5,6-tetraglycidyl-2,4-hexanediol, bisphenol A type epoxy resin such as EPIKOTE828 (manufactured by Mitsubishi Chemical Corporation), bisphenol F type epoxy resin such as EPIKOTE807 (manufactured by Mitsubishi Chemical Corporation) Resin, hydrogenated bisphenol A type epoxy resin such as YX-8000 (manufactured by Mitsubishi Chemical Corporation), epoxy resin containing a biphenyl skeleton such as YX6954BH30 (manufactured by Mitsubishi Chemical Corporation), phenol such as EPPN-201 (manufactured by Nippon Kayaku Co., Ltd.) Novolak type epoxy resin, EOCN-102S (manufactured by Nippon Kayaku Co., Ltd.), etc. (ortho, meta, para) cresol novolak type epoxy resin, tetra(glycidoxymethyl)methane, N ,N,N',N'-tetraepoxypropyl-1,4-phenylenediamine, N,N,N',N'-tetraepoxypropyl-2,2'-dimethyl-4.4' -Diaminobiphenyl, 2,2-bis[4-(N,N-diepoxypropyl-4-aminophenoxy)phenyl]propane, N,N,N',N'-tetra Epoxypropyl-4,4'-diaminodiphenylmethane and other tertiary nitrogen atoms bonded to aromatic carbon atoms; N,N,N',N'-tetraepoxypropyl-1 ,2-Diaminocyclohexane, N,N,N',N'-tetraepoxypropyl-1,3-diaminocyclohexane, N,N,N',N'-tetraepoxy Propyl-1,4-diaminocyclohexane, Bis(N,N-Diepoxypropyl-4-aminocyclohexyl)methane, Bis(N,N-Diepoxypropyl-2-methyl -4-aminocyclohexyl)methane, bis(N,N-diepoxypropyl-3-methyl-4-aminocyclohexyl)methane, 1,3-bis(N,N-diepoxy Propylaminomethyl)cyclohexane, 1,4-bis(N,N-diecidylaminomethyl)cyclohexane, 1,3-bis(N,N-diecidylaminomethyl)benzene , 1,4-bis(N,N-diepoxypropylaminomethyl)benzene, 1,3,5-paraffin(N,N-diepoxypropylaminomethyl)cyclohexane, 1,3,5 - Compounds with a tertiary nitrogen atom bonded to an aliphatic carbon atom such as (N,N-diglycidylaminomethyl)benzene, and isocyanurate such as triglycidyl isocyanurate such as TEPIC (manufactured by Nissan Chemical Co., Ltd.) Cyanurate compounds, compounds described in paragraph [0037] of JP-A-10-338880, compounds described in WO2017/170483, etc.; As a compound having an oxetanyl group, for example, 1,4-bis{[(3-ethyl-3-oxetanyl)methoxy]methyl}benzene (ARON OXETANEOXT-121(XDO) ), bis[2-(3-oxetanyl)butyl]ether (ARON OXETANEOXT-221(DOX)), 1,4-bis[(3-ethyloxetan-3-yl )methoxy]benzene (HQOX), 1,3-bis[(3-ethyloxetan-3-yl)methoxy]benzene (RSOX), 1,2-bis[(3-ethyl oxetan-3-yl)methoxy]benzene (CTOX), compounds having two or more oxetanyl groups described in paragraphs [0170] to [0175] of WO2011/132751, etc. ; Examples of compounds having an oxazoline group include compounds such as 2,2'-bis(2-oxazoline), 2,2'-bis(4-methyl-2-oxazoline), EPOCROS (trade name, Polymers and oligomers having an oxazoline group, manufactured by Nippon Shokubai Co., Ltd., compounds described in paragraph [0115] of JP-A-2007-286597, etc.; As a compound having a cyclocarbonate group, such as N,N,N',N'-tetrakis[(2-oxo-1,3-dioxolan-4-yl)methyl]-4,4' -Diaminodiphenylmethane, N,N'-bis[(2-oxo-1,3-dioxolan-4-yl)methyl]-1,3-phenylenediamine, WO2011/ Compounds described in paragraphs [0025]~[0030] and [0032] of Bulletin No. 155577; Examples of compounds having blocked isocyanate groups include CORONATEAP STABLE M, CORONATE 2503, 2515, 2507, 2513, 2555, MILLIONATEMS-50 (manufactured by Tosoh Corporation), TAKENATE B-830, B-815N, B-820NSU, B- 842N, B-846N, B-870N, B-874N, B-882N (the above are manufactured by Mitsui Chemicals Co., Ltd.), and paragraphs [0046]~[0047] of JP-A-2014-224978 have two or more Compounds with protected isocyanate groups, compounds with more than 3 protected isocyanate groups described in paragraphs [0119]~[0120] of WO2015/141598, etc.; As compounds with hydroxyl and alkoxy groups, such as N,N,N',N'-tetra(2-hydroxyethyl)adipamide, 2,2-bis(4-hydroxy-3,5-dihydroxy Methylphenyl)propane, 2,2-bis(4-hydroxy-3,5-dimethoxymethylphenyl)propane, 2,2-bis(4-hydroxy-3,5-dihydroxymethyl Phenyl)-1,1,1,3,3,3-hexafluoropropane, WO2015/072554, compound described in paragraph [0058] of JP-A-2016-118753, JP-A-2016-200798 Compounds described, compounds described in WO2010/074269, etc.; As a cross-linking compound having a polymerizable unsaturated group, for example, glycerol mono(meth)acrylate, glycerol di(meth)acrylate (1,2-, 1,3-body mixture), glycerol ginseng (meth)acrylate ) acrylate, glycerol 1,3-diglycerinic acid di(meth)acrylate, neopentylthritol tri(meth)acrylate, diethylene glycol mono(meth)acrylate, triethylene glycol mono( Meth)acrylate, tetraethylene glycol mono(meth)acrylate, pentaethylene glycol mono(meth)acrylate, hexaethylene glycol mono(meth)acrylate, and the like.

The content of the crosslinking compounds (c-1) and (c-2) contained in the liquid crystal alignment agent of the present invention is preferably 0.1 to 30 parts by mass relative to the total of 100 parts by mass of the polymer components contained in the liquid crystal alignment agent. More preferably, it is 0.1-20 mass parts, More preferably, it is 1-10 mass parts.

Examples of the compound for adjusting the dielectric constant and electrical resistance of the resin film include monoamines such as 3-picolylamine having an aromatic heterocyclic ring containing a nitrogen atom. When using a monoamine having an aromatic heterocyclic ring containing a nitrogen atom, its content is preferably 0.1-30 parts by mass, more preferably 0.1-20 parts by mass, based on 100 parts by mass of the polymer component contained in the liquid crystal alignment agent.

Ideal specific examples of functional silane compounds include 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-aminopropyldiethoxymethylsilane, 2-amine Aminopropyltrimethoxysilane, 2-aminopropyltriethoxysilane, N-(2-aminoethyl)-3-aminopropyltrimethoxysilane, N-(2-aminoethyl base)-3-aminopropylmethyldimethoxysilane, 3-ureidopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, vinyltrimethoxysilane, vinyl trimethoxysilane Ethoxysilane, 2-(3,4-epoxycyclohexyl)ethyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 3-glycidoxypropyl Trimethoxysilane, 3-glycidoxypropylmethyldiethoxysilane, 3-glycidoxypropyltriethoxysilane, p-styryltrimethoxysilane, 3-methyl Acryloxypropylmethyldimethoxysilane, 3-methacryloxypropyltrimethoxysilane, 3-methacryloxypropylmethyldiethoxysilane, 3-methyl Acryloxypropyl triethoxysilane, 3-acryloxypropyltrimethoxysilane, ginseng (3-trimethoxysilylpropyl) isocyanurate, 3-mercaptopropyl methyl Dimethoxysilane, 3-mercaptopropyltrimethoxysilane, 3-isocyanatepropyltriethoxysilane, etc. When using a functional silane compound, its content is preferably 0.1-30 mass parts with respect to 100 mass parts of polymer components contained in a liquid crystal alignment agent, More preferably, it is 0.1-20 mass parts.

The solid content concentration in the liquid crystal alignment agent (the ratio of the total mass of the components other than the solvent of the liquid crystal alignment agent to the total mass of the liquid crystal alignment agent) can be appropriately selected in consideration of viscosity, volatility, etc., preferably 1 to 10 mass % range.

The particularly desirable range of solid content concentration varies depending on the method used when coating the liquid crystal alignment agent on the substrate. For example, when the spin coating method is used, the solid content concentration is particularly preferably in the range of 1.5 to 4.5% by mass. When using the printing method, it is preferable to set the solid content concentration in the range of 3 to 9% by mass, and thereby make the solution viscosity in the range of 12 to 50mPa·s, especially preferably. When using the inkjet method, it is more preferable to set the solid content concentration in the range of 1 to 5% by mass and thereby make the solution viscosity in the range of 3 to 15 mPa·s. The temperature for preparing the polymer composition is preferably 10-50°C, more preferably 20-30°C.

The liquid crystal alignment agent described above can be effectively applied in various technical purposes, such as in liquid crystal alignment films (liquid crystal alignment films for phase difference films, scanning antennas, liquid crystal alignment films for liquid crystal array antennas, or through scattering liquid crystal dimming elements. Alignment film for liquid crystal), protective film (for example: protective film for color filter), spacer film, interlayer insulating film, anti-reflection film, wiring coating film, antistatic film, motor insulating film (flexible It can also be used in the gate insulating film of the display) and the like. [Liquid crystal alignment film and liquid crystal display element] A liquid crystal alignment film can be manufactured by using the said liquid crystal alignment agent. Moreover, the liquid crystal display element of this invention is equipped with the liquid crystal alignment film formed using the said liquid crystal alignment agent. The operation mode of the liquid crystal display device of the present invention is not particularly limited, and can be applied to, for example, TN type, STN (Super Twisted Nematic) type, vertical alignment type (including VA-MVA type, VA-PVA type, etc.), in-plane switching type (IPS type, FFS type), optical compensation bending type (OCB type) and other various operation modes.

The liquid crystal display element of the present invention, for example, can be obtained by the method including the following steps (1)~(4), the method including steps (1)~(2) and (4), the method including steps (1)~(3) , (4-2) and (4-4), or a method comprising steps (1) to (3), (4-3) and (4-4) to manufacture. <Step (1): The step of coating the liquid crystal alignment agent on the substrate> Step (1) is a step of coating the liquid crystal alignment agent of the present invention on the substrate. The specific example of step (1) is as follows.

On one side of the substrate provided with the patterned transparent conductive film, the liquid crystal alignment agent of the present invention is coated using an appropriate coating method such as roll coating method, spin coating method, printing method, inkjet method and the like. Here, the substrate is not particularly limited as long as it is highly transparent, and a glass substrate, a silicon nitride substrate, and a plastic substrate such as an acrylic substrate or a polycarbonate substrate may be used together. In addition, if the reflective liquid crystal display element is only on one side of the substrate, it can also use opaque objects such as silicon wafers. In this case, the electrodes can also use materials that reflect light such as aluminum. Also, when manufacturing IPS or FFS liquid crystal display elements, a substrate provided with electrodes made of a comb-shaped transparent conductive film or metal film and a counter substrate without electrodes are used.

For the method of coating the liquid crystal alignment agent on the substrate and forming a film, screen printing, offset printing, flexo printing, inkjet method, or spraying method, etc. can be mentioned. Among them, the coating and film-forming methods by the inkjet method can be preferably used. <Step (2): The step of calcining the coated liquid crystal alignment agent> Step (2) is a step of calcining the liquid crystal alignment agent coated on the substrate to form a film. The specific example of step (2) is as follows.

After the liquid crystal alignment agent is coated on the substrate in step (1), the solvent can be evaporated, or the polyamide acid or polyamide Thermal imidization of esters. For the drying and calcining steps after coating the liquid crystal alignment agent of the present invention, any temperature and time can be selected, and multiple times can also be performed. The temperature for calcining the liquid crystal alignment agent may be, for example, 40-180°C. Considering the point of view of reducing treatment, it can also be carried out at 40~150°C. The calcination time is not particularly limited, and examples thereof include 1 to 10 minutes or 1 to 5 minutes. When thermal imidization of polyamic acid is performed, after the above steps, a step of calcining at a temperature range of 150~300°C or 150~250°C can be added. The calcination time is not particularly limited, and may be 5 to 40 minutes, or 5 to 30 minutes.

If the calcined film is too thin, the reliability of the liquid crystal display element will be reduced, so 5~300nm is more ideal, and 10~200nm is more ideal.

<Step (3): The step of aligning the film obtained in step (2)> Step (3) is a step of performing alignment treatment on the film obtained in step (2) as the case may be. That is, in a liquid crystal display element of a horizontal alignment type such as an IPS method or an FFS method, an alignment ability-imparting treatment is performed on the coating film. On the other hand, for vertical alignment type liquid crystal display elements such as VA mode or PSA mode, the formed coating film can be directly used as a liquid crystal alignment film, but the coating film can also be subjected to alignment ability imparting treatment. The alignment treatment method of the liquid crystal alignment film includes a rubbing treatment method and a photo-alignment treatment method. As for the photo-alignment treatment method, it is possible to irradiate the surface of the above-mentioned membranous object with radiation deflected in a certain direction, and depending on the situation, preferably heat treatment at a temperature of 150-250°C to impart liquid crystal alignment (also known as liquid crystal alignment). alignment ability) method. As the radiation, ultraviolet rays or visible rays having a wavelength of 100 to 800 nm can be used. Among them, ultraviolet rays having a wavelength of 100 to 400 nm, more preferably 200 to 400 nm are preferred.

The exposure dose of the above-mentioned radiation is preferably 1~10,000mJ/cm ² . Among them, 100~5,000mJ/cm ² is preferable. In addition, when irradiating radiation, in order to improve the liquid crystal alignment, it may be irradiated while heating the above-mentioned substrate having the membranous substance at 50 to 250°C. The liquid crystal alignment film fabricated in such a manner can stably align liquid crystal molecules in a certain direction.

Also, the liquid crystal alignment film irradiated with polarized radiation as described above may be subjected to contact treatment with water or a solvent, or the liquid crystal alignment film irradiated with radiation may be heat-treated.

The solvent used in the above-mentioned contact treatment is not particularly limited as long as it dissolves the decomposed product generated from the film-like material due to radiation exposure. Specific examples include water, methanol, ethanol, 2-propanol, acetone, methyl ethyl ketone, 1-methoxy-2-propanol, 1-methoxy-2-propanol acetate, butylcylonol, Ethyl lactate, methyl lactate, diacetone alcohol, methyl 3-methoxypropionate, ethyl 3-ethoxypropionate, propyl acetate, butyl acetate, cyclohexyl acetate, etc. A solvent may be used alone or in combination of two or more.

The temperature for heat treatment of the coating film irradiated with radiation is more preferably 50 to 300°C, more preferably 120 to 250°C. The heat treatment time is preferably 1 to 30 minutes. ＜Step (4): Steps for making liquid crystal cells＞ Two substrates on which a liquid crystal alignment film was formed as described above were prepared, and liquid crystals were arranged between the two substrates facing each other. Specifically, the following two methods can be mentioned.

In the first method, two substrates are arranged facing each other through a cell gap in such a manner that the liquid crystal alignment films face each other. Then, the two substrates are bonded with a sealant on the periphery, and the liquid crystal composition is injected into the cell gap separated by the substrate surface and the sealant to make it contact the film surface, and the injection hole is sealed. .

The above-mentioned liquid crystal composition is not particularly limited, and various liquid crystal compositions containing at least one liquid crystal compound (liquid crystal molecule) and having positive or negative dielectric anisotropy can be used. Hereinafter, a liquid crystal composition having a positive dielectric anisotropy is also referred to as a positive type liquid crystal, and a liquid crystal composition having a negative dielectric anisotropy is also referred to as a negative type liquid crystal. The above liquid crystal composition may also contain a fluorine atom, a hydroxyl group, an amino group, a group containing a fluorine atom (for example: trifluoromethyl group), a cyano group, an alkyl group, an alkoxy group, an alkenyl group, an isothiocyanate group, Liquid crystal compounds of heterocycles, cycloalkanes, cycloalkenes, steroid skeletons, benzene rings, or naphthalene rings may also contain compounds with two or more rigid sites (mesogen skeletons) exhibiting liquid crystallinity in the molecule (for example: rigid Two biphenyl structures, or a double mesogen compound formed by linking two terphenyl structures with an alkyl group, etc.). The liquid crystal composition may be a liquid crystal composition in a nematic phase, a liquid crystal composition in a smectic phase, or a liquid crystal composition in a cholesteric phase. In addition, from the viewpoint of improving the alignment of liquid crystals, additives may be further added to the above-mentioned liquid crystal composition. Such additives include photopolymerizable monomers such as the following compounds having polymerizable groups; optically active compounds (for example: S-811 manufactured by Merck Co., Ltd.); antioxidants; ultraviolet absorbers; pigments; defoaming agent; polymerization initiator; or polymerization inhibitor, etc. Examples of positive liquid crystals include ZLI-2293, ZLI-4792, MLC-2003, MLC-2041, MLC-3019, and MLC-7081 manufactured by Merck & Co., Ltd. Negative liquid crystal, such as MLC-6608, MLC-6609, MLC-6610, MLC-6882, MLC-6886, MLC-7026, MLC-7026-000, MLC-7026-100, or MLC-7029 manufactured by Merck wait. Moreover, in the PSA mode, the liquid crystal containing the compound which has a polymeric group can mention MLC-3023 by Merck.

Also, the second method is a method called ODF (One Drop Fill) method. On one of the two substrates on which the liquid crystal alignment film has been formed, apply, for example, a UV-curable sealant, and then drop the liquid crystal composition on several predetermined positions on the surface of the liquid crystal alignment film. Afterwards, another substrate is bonded in such a way that the liquid crystal alignment film faces each other, and the liquid crystal composition is pressed against the entire surface of the substrate to make it contact the film surface. Then, the entire surface of the substrate is irradiated with ultraviolet light to harden the sealant. When using either method, it is advisable to further heat until the liquid crystal composition used reaches the temperature of adopting an isotropic phase, and then slowly cool down to room temperature to remove the flow alignment during liquid crystal filling.

Also, when performing rubbing treatment on the coating film, two substrates are arranged facing each other such that the rubbing directions of the respective coating films are at a predetermined angle, for example, perpendicular to or antiparallel to each other.

For the sealant, for example, an epoxy resin containing alumina balls as a curing agent and a spacer can be used. For liquid crystals, nematic liquid crystals and smectic liquid crystals can be cited, among which nematic liquid crystals are preferred, and for example, fluorine-based liquid crystals, cyano-based liquid crystals, Schiff base-based liquid crystals, and azoxy based liquid crystals can be used. Liquid crystal, biphenyl liquid crystal, phenylcyclohexane liquid crystal, ester liquid crystal, terphenyl liquid crystal, biphenyl cyclohexane liquid crystal, pyrimidine liquid crystal, dioxane liquid crystal, bicyclooctane liquid crystal, cubic liquid crystal Alkane liquid crystal, etc. In addition, cholesteric liquid crystals such as cholesteryl chloride, cholestenyl nonanoate, and cholestenyl carbonate can also be added to these liquid crystals; Manufactured) chiral reagents; p-decyloxybenzylidene p-amino-2-methylbutyl cinnamate and other ferroelectric liquid crystals are used. In addition, various substances disclosed in JP-A-2019-132952 can be used.

The above-mentioned liquid crystals are generally prepared by mixing several kinds of liquid crystals in a manner that meets the desired physical properties in accordance with the application (hereinafter, the liquid crystal components obtained by mixing multiple liquid crystals are also referred to as mixed liquid crystals.).

Among them, it is preferable to use the fluorine-based mixed liquid crystal generally used in liquid crystal display devices at present. Here, the fluorine-based mixed liquid crystal in this specification refers to a mixed liquid crystal containing one or more fluorine-based liquid crystals, and the cyano-based mixed liquid crystal refers to a mixed liquid crystal containing one or more cyano-based liquid crystals.

The above-mentioned mixed liquid crystals are generally known and commercially available. For example, fluorine-based mixed liquid crystals are sold under the trade name of ZLI-4792 for liquid crystals with positive dielectric constant anisotropy Δε (also called positive liquid crystals). Also, a liquid crystal having a negative dielectric constant anisotropy Δε (also called a negative liquid crystal) is sold by Merck Co., Ltd. under the trade name of MLC-6608. In addition, among the cyano type mixed liquid crystals, the positive liquid crystal type is sold by Chisso Petrochemical Co., Ltd. under the brand name JC-5066XX. In the present invention, a liquid crystal alignment film suitable for a liquid crystal display element using a negative liquid crystal, and a liquid crystal alignment agent provided to the liquid crystal alignment film are provided.

The liquid crystal alignment agent of the present invention is also suitable for use in liquid crystals that have a liquid crystal layer between a pair of substrates provided with electrodes, and a polymerizable compound that is polymerized by at least one of active energy rays and heat is disposed between the pair of substrates. The composition is a liquid crystal display element (PSA type liquid crystal display element) produced by applying a voltage between electrodes and polymerizing a polymerizable compound by at least one of active energy ray irradiation and heating.

In addition, the liquid crystal alignment agent of the present invention is also suitable for use in a liquid crystal layer between a pair of substrates provided with electrodes, and between the above-mentioned pair of substrates, it is suitable to arrange a polymer compound containing at least one of active energy rays and heat. A liquid crystal display element (SC-PVA mode type liquid crystal display element) manufactured through the step of applying a voltage between electrodes. <Procedure (4-2): In the case of a PSA-type liquid crystal display element> It is performed in the same manner as in (4) above except for injecting or dropping a liquid crystal composition containing a polymerizable compound. Examples of the polymerizable compound include polymerizable compounds having one or more polymerizable unsaturated groups such as acrylate groups and methacrylate groups in the molecule. <Step (4-3): In the case of SC-PVA mode liquid crystal display element> It is also possible to use a method of manufacturing a liquid crystal display element through the step of irradiating ultraviolet rays described later after performing the same procedure as in (4) above. According to this method, a liquid crystal display element excellent in response speed can be obtained with a small amount of light irradiation as in the case of manufacturing the above-mentioned PSA type liquid crystal display element. The compound having a polymerizable group may be a compound having one or more polymerizable unsaturated groups as described above in the molecule, and its content is preferably 0.1 to 30 parts by mass relative to 100 parts by mass of all polymer components, more preferably 1 to 20 parts by mass. In addition, the above-mentioned polymerizable group may be contained in a polymer used in a liquid crystal alignment agent. Examples of such a polymer include a polymer obtained by using a diamine component containing a diamine having the above-mentioned photopolymerizable group at the end for reaction. thing. <Step (4-4): Step of irradiating ultraviolet rays> The liquid crystal cell is irradiated with light in a state where a voltage is applied between the conductive films of the pair of substrates obtained in the above (4-2) or (4-3). Here, the applied voltage may be, for example, 5-50V direct current or alternating current. Also, as the light to be irradiated, for example, ultraviolet rays and visible rays including light with a wavelength of 150 to 800 nm can be used, but ultraviolet light including light with a wavelength of 300 to 400 nm is preferable. As a light source for irradiating 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 amount of light irradiation is preferably 1,000-200,000 J/m ² , more preferably 1,000-100,000 J/m ² .

In addition, if necessary, a polarizing plate can be attached to the outer surface of the liquid crystal cell to obtain a liquid crystal display element. The polarizing plate attached to the outer surface of the liquid crystal cell includes a polarizing film called "H film" that absorbs iodine while stretching polyvinyl alcohol and sandwiching it with a cellulose acetate protective film; or Polarizing plate composed of H film itself.

In addition, if necessary, a polarizing plate can be attached to the outer surface of the liquid crystal cell to obtain a liquid crystal display element. The polarizing plate attached to the outer surface of the liquid crystal cell includes a polarizing film called "H film" that absorbs iodine while stretching polyvinyl alcohol and sandwiching it with a cellulose acetate protective film; or Polarizing plate composed of H film itself.

The comb electrode substrate used in the IPS mode is the IPS substrate, which has: a substrate, and a plurality of linear electrodes formed on the substrate and arranged in a comb-like shape; and formed on the substrate by covering the linear electrodes. Liquid crystal alignment film.

In addition, the comb electrode substrate used in the FFS mode, that is, the FFS substrate, has: a substrate; a surface electrode formed on the substrate; an insulating film formed on the surface electrode; formed on the insulating film and arranged in a comb-like shape. A linear electrode; a liquid crystal alignment film formed on an insulating film to cover the linear electrode.

Fig. 1 is a schematic cross-sectional view showing an example of a transverse electric field liquid crystal display element of the present invention, which is an example of an IPS mode liquid crystal display element.

In the transverse electric field liquid crystal display element 1 illustrated in FIG. 1 , a liquid crystal 3 is sandwiched between a comb-shaped electrode substrate 2 provided with a liquid crystal alignment film 2c and an opposing substrate 4 provided with a liquid crystal alignment film 4a. The comb electrode substrate 2 has: a substrate 2a; a plurality of linear electrodes 2b formed on the substrate 2a and arranged in a comb-like shape; and a liquid crystal alignment formed on the substrate 2a to cover the linear electrodes 2b Membrane 2c. The opposite substrate 4 has: a base material 4b; and a liquid crystal alignment film 4a formed on the base material 4b. The liquid crystal alignment film 2c is, for example, the liquid crystal alignment film of the present invention. The liquid crystal alignment film 4c is also the liquid crystal alignment film of the present invention.

In this transverse electric field liquid crystal display element 1 , when a voltage is applied to the linear electrodes 2 b , an electric field is generated between the linear electrodes 2 b as shown by lines of force L .

Fig. 2 is a schematic cross-sectional view showing another example of a transverse electric field liquid crystal display element of the present invention, which is an example of an FFS mode liquid crystal display element.

In the transverse electric field liquid crystal display element 1 illustrated in FIG. 2 , a liquid crystal 3 is sandwiched between a comb-shaped electrode substrate 2 provided with a liquid crystal alignment film 2 h and an opposing substrate 4 provided with a liquid crystal alignment film 4 a. The comb electrode substrate 2 has: a base material 2d; a surface electrode 2e formed on the base material 2d; an insulating film 2f formed on the surface electrode 2e; a plurality of wires formed on the insulating film 2f and arranged in a comb shape The linear electrode 2g; the liquid crystal alignment film 2h formed on the insulating film 2f to cover the linear electrode 2g. The opposite substrate 4 has: a base material 4b; and a liquid crystal alignment film 4a formed on the base material 4b. The liquid crystal alignment film 2h is, for example, the liquid crystal alignment film of the present invention. The liquid crystal alignment film 4a is also the liquid crystal alignment film of the present invention.

In this transverse electric field liquid crystal display element 1, when a voltage is applied to the surface electrode 2e and the line electrode 2g, an electric field is generated between the surface electrode 2e and the line electrode 2g as indicated by lines of force L.

The liquid crystal alignment film of the present invention, in addition to the above-mentioned liquid crystal alignment film, can also be applied to various purposes, for example: it can be used as a liquid crystal alignment film for a retardation film, a scanning antenna, a liquid crystal alignment film for a liquid crystal array antenna, or a transmission scattering film. It is used in liquid crystal alignment film for liquid crystal dimming components. Furthermore, applications other than liquid crystal alignment films, such as: protective film (for example: protective film for color filters), spacer film, interlayer insulating film, antireflection film, wiring coating film, antistatic film, motor insulation film (gate insulating film for flexible displays) can also be used.

The liquid crystal display element of the present invention can be effectively applied in various devices, such as clocks, portable game machines, word processors, notebook computers, car navigation systems, camcorders, PDAs, digital cameras, mobile phones, Various display devices such as smart phones, various monitors, LCD TVs, and information displays. [Example]

Hereinafter, the present invention will be specifically described with examples and the like, but the present invention is not limited to these examples. In addition, the abbreviations of compounds and solvents are as follows. (Organic solvents) NMP: N-methyl-2-pyrrolidone GBL: gamma-butyrolactone BCS: Butyl Cellosu

式(DA-1)、(DA-2)及(DA-5)之二胺係含於式(d _AL)表示之二胺之範圍中。式(DA-3)之二胺係含於式(d _n)表示之二胺之範圍中。 (diamine) [Chem. 22]

The diamines of the formulas (DA-1), (DA-2) and (DA-5) are included in the range of the diamines represented by the formula (d _AL ). The diamine of the formula (DA-3) is included in the range of the diamine represented by the formula (d _n ).

式(CA-1)之四羧酸二酐係含於式(T _c)表示之四羧酸二酐之範圍中。式(CA-2)、(CA-4)之四羧酸二酐係含於式(T _f)表示之四羧酸二酐之範圍中。 (Tetracarboxylic dianhydride) [Chem. 23]

The tetracarboxylic dianhydride of formula (CA-1) is contained in the range of the tetracarboxylic dianhydride represented by formula (T _c ). Tetracarboxylic dianhydrides of formulas (CA-2) and (CA-4) are included in the range of tetracarboxylic dianhydrides represented by formula (T _f ).

(additive) AD-1: 3-Glycidoxypropyltriethoxysilane

[chem 24]

(Determination of viscosity) In the synthesis example, the viscosity of the polymer solution was measured using an E-type viscometer TVE-22H (manufactured by Toki Sangyo Co., Ltd.), with a sample volume of 1.1 mL, a conical rotor TE-1 (1°34', R24), and a temperature of 25°C. condition determination. ＜Synthesis of Polyamic Acid＞ (Synthesis Example 1) Measure 3.15g of DA-1 (11.0mmol) in a 100mL eggplant-shaped flask equipped with a stirring device and a nitrogen inlet tube, add 28.4g of NMP, and stir while feeding nitrogen to dissolve it. While stirring this diamine solution under water cooling, add 2.37g of CA-1 (10.6mmol), then add 11.6g of NMP, and stir at 40°C for 3 hours under nitrogen atmosphere to obtain a polyamic acid solution ( Viscosity: 550mPa・s) PAA-A1. (Synthesis Example 2) Measure 3.66g of DA-2 (15.0mmol) and 2.99g of DA-3 (15.0mmol) in a 100mL eggplant-shaped flask equipped with a stirring device and a nitrogen gas introduction tube, add 59.9g of NMP, and stir while feeding nitrogen gas to dissolve it. While stirring this diamine solution under water cooling, 5.63 g of CA-2 (22.5 mmol) was added, and NMP9.7 g was added, and stirred at 50° C. for 2 hours under a nitrogen atmosphere. Furthermore, 1.90 g of CA-3 (6.45 mmol) was added, and 10.8 g of NMP was added, and stirred at 50° C. for 15 hours under a nitrogen atmosphere to obtain a polyamic acid solution (viscosity: 515 mPa·s) PAA-B1. (Synthesis Example 3) 1.83g of DA-2 (7.50mmol), 0.540g of DA-4 (5.00mmol), 2.40g of DA-5 (7.50mmol), Add 77.8 g of NMP to 1.99 g of DA-6 (5.00 mmol), and dissolve it while stirring while feeding nitrogen gas. While stirring the diamine solution under water cooling, add 5.38g of CA-1 (24.0mmol), then add 11.3g of NMP, and stir for 15 hours at 40°C under nitrogen atmosphere to obtain a polyamic acid solution (viscosity: 410mPa・s)PAA-A2. (Synthesis Example 4) Measure 6.97g of DA-3 (35.0mmol) and 6.94g of DA-7 (35.0mmol) in a 200mL eggplant-shaped flask equipped with a stirring device and a nitrogen inlet tube, add 102g of NMP, and stir while feeding nitrogen gas to make It dissolves. While stirring this diamine solution under water cooling, 8.76 g of CA-2 (35.0 mmol) was added, and NMP26.4 g was added, and stirred at 50° C. for 2 hours under a nitrogen atmosphere. Furthermore, 9.54 g of CA-3 (32.4 mmol) was added, and 53.7 g of NMP was added, and stirred at 50° C. for 15 hours under a nitrogen atmosphere to obtain a polyamic acid solution (viscosity: 400 mPa·s) PAA-B2.

(Synthesis Example 5) Measure 2.49g of DA-2 (10.2mmol) and 4.74g of DA-3 (23.8mmol) in a 100mL eggplant-shaped flask equipped with a stirring device and a nitrogen inlet tube, add 58.5g of NMP, and stir while feeding nitrogen gas to dissolve it. While stirring this diamine solution under water cooling, 3.81 g of CA-4 (17.0 mmol) was added, and NMP4.1 g was added, and stirred at 50° C. for 2 hours under a nitrogen atmosphere. Furthermore, add 4.35g of CA-3 (14.8mmol), then add 24.7g of NMP, and stir at 50°C for 15 hours under nitrogen atmosphere to obtain a solution of polyamic acid (viscosity: 298mPa·s) PAA-B3 . The types and amounts of diamine components and tetracarboxylic acid derivative components used in Synthesis Examples 1 to 5 are summarized in Table 1. In Table 1, the values in parentheses represent the usage amount (mol parts) of the monomers relative to the total of 100 mol parts in each component.

[Table 1] Synthesis example Polymer name Polymer type Tetracarboxylic acid derivatives Diamine component 1 PAA-A1 Polyamide CA-1(100) DA-1(100) 2 PAA-B1 Polyamide CA-2(77)CA-3(23) DA-2(50) DA-3(50) 3 PAA-A2 Polyamide CA-1(100) DA-2(30) DA-4(20) DA-5(30) DA-6(20) 4 PAA-B2 Polyamide CA-2(52) CA-3(48) DA-3(50) DA-7(50) 5 PAA-B3 Polyamide CA-3(47)CA-4(53) DA-2(30) DA-3(70)

＜Preparation of liquid crystal alignment agent＞ (Examples 1 to 3, and Comparative Example 1) The solutions of polyamic acid obtained in Synthesis Examples 1 to 5 were weighed to form a combination of polymer 1 and polymer 2 shown in the following table, and mixed. Then NMP, GBL, BCS, the GBL solution containing 1% by weight of AD-1, and the NMP solution containing 10% by weight of AD-2 were added while stirring in such a way as to form the composition shown in Table 2 below, and then Stir at room temperature for 2 hours to obtain the liquid crystal alignment agents (1) to (3) of Examples 1 to 3 and the liquid crystal alignment agent (R1) of Comparative Example 1. The specifications of the liquid crystal alignment agents obtained in Examples 1-3 and Comparative Example 1 are shown in Table 2.

[Table 2] Liquid crystal alignment agent Polymer 1 Polymer 2 Organic solvents additive solution NMP GBL BCS AD-1 AD-2 Example 1 (1) PAA-A1 1.50g PAA-B1 2.80g 5.40g 5.40g 4.00g 0.600g 0.300g Example 2 (2) PAA-A2 1.50g PAA-B1 2.80g 5.40g 5.40g 4.00g 0.600g 0.300g Example 3 (3) PAA-A1 1.50g PAA-B3 2.80g 5.40g 5.40g 4.00g 0.600g 0.300g Comparative example 1 (R1) PAA-A2 1.50g PAA-B2 2.80g 5.40g 5.40g 4.00g 0.600g 0.300g

Using the liquid crystal alignment agents obtained above, FFS mode liquid crystal cells were produced according to the procedure shown below, and the pretilt angle and image sticking characteristics due to long-term AC driving were evaluated. [Production of FFS mode liquid crystal cell] First, an electrode-attached glass substrate with a size of 30 mm×35 mm and a thickness of 0.7 mm was prepared. Form the IZO electrode with a solid pattern on the substrate as the counter electrode of the first layer, and form a film by CVD (chemical vapor deposition) method as the second layer on the counter electrode of the first layer SiN (silicon nitride) film. The thickness of the SiN film of the second layer is 500nm which functions as an interlayer insulating film. On the SiN film of the second layer, a comb-shaped pixel electrode formed by patterning the IZO film of the third layer is arranged to form two pixels of the first pixel and the second pixel. The dimensions are 10mm in length and 5mm in width. At this time, the counter electrode of the first layer and the pixel electrode of the third layer are electrically insulated by the function of the SiN film of the second layer. The pixel electrode on the third layer has a comb-tooth shape in which multiple electrode elements with a width of 3 μm bent at an inner angle of 160° are arranged in parallel at intervals of 6 μm. One pixel connects multiple electrode elements. The line of the bending part is the boundary, and each has a first zone and a second zone.

Then filter the liquid crystal alignment agents (1)~(3) and (R1) obtained in the above-mentioned Examples 1-3 and Comparative Example 1 with a filter with a pore size of 1.0 μm, and then apply it on the substrate with electrodes prepared above by spin coating (1st glass substrate) and the surface of the glass substrate (2nd glass substrate) which formed the ITO film on the back surface and has the columnar spacer of height 4 micrometers. Then, after drying on a hot plate at 80° C. for 2 minutes, firing was performed at 230° C. for 20 minutes to obtain a polyimide film with a film thickness of 60 nm on each substrate. After rubbing the liquid crystal alignment film with a rayon cloth (roller diameter: 140mm, roll speed: 1000rpm, moving speed: 30mm/sec, push-in length: 0.3mm), it was irradiated with ultrasonic waves for 1 minute in pure water. Wash and remove water droplets by blowing air, then dry at 80°C for 10 minutes to obtain a substrate with a liquid crystal alignment film. Use the above two substrates with liquid crystal alignment film, combine them in such a way that their respective rubbing directions are antiparallel, keep the liquid crystal injection port and seal the surrounding, and make a void cell with a cell gap of 4 μm. The ghost cells were vacuum-injected into liquid crystal MLC-7026-100 (manufactured by Merck & Co., negative-type liquid crystal) at room temperature, and the injection port was sealed to prepare a liquid crystal cell with antiparallel alignment. The obtained liquid crystal cells constituted an FFS mode liquid crystal display element. Thereafter, the liquid crystal cell was heated at 120° C. for 1 hour, left overnight at 23° C., and used in the following evaluations. <Evaluation of pretilt angle> Using AxoScan Mueller matrix polarimeter (Mueller matrix polarimeter) manufactured by OPTOMETRICS, the pretilt angle of the said liquid crystal cell was evaluated. The viewing angle characteristics are better as the pretilt angle is lower. Specifically, when the pretilt angle is less than 2.0°, it is defined and rated as "good", and when it is more than 2.0°, it is defined and rated as "poor". <Evaluation of afterimage characteristics due to long-term AC driving> Using the above-mentioned liquid crystal cell, under the irradiation of high-brightness backlight (30,000cd/m ² ), AC voltage of ±5.5V was applied at a frequency of 30Hz for 72 hours. Thereafter, the pixel electrode and the counter electrode of the liquid crystal cell are short-circuited.

After placing the liquid crystal cell at 23°C for one night, arrange the liquid crystal cell between two polarizers whose polarization axes are perpendicular to each other, turn on the backlight with no voltage applied, and adjust the arrangement angle of the liquid crystal cell so that the brightness of the transmitted light becomes minimum. Also, calculate and define the rotation angle when the liquid crystal cell is rotated from the angle at which the second region of the first pixel becomes darkest to the angle at which the first region becomes darkest is angle Δθ1, and the second pixel is also compared with the second area and the first area and calculate the angle Δθ2. The average value of these Δθ1 and Δθ2 is defined as the angle Δθ of the liquid crystal cell, and the smaller the value is, the better the liquid crystal alignment is defined and evaluated. Specifically, when this angle Δθ is less than 0.4°, the afterimage characteristic is excellent, that is, defined and evaluated as "good", and when it is more than 0.4°, it is defined and evaluated as "poor".

The evaluation results of the liquid crystal display elements using the liquid crystal alignment agents of Examples 1 to 3 and Comparative Example 1 are shown in Table 3 below.

[table 3] Liquid crystal alignment agent Polymer 1 Polymer 2 Pretilt Angle(˚) Δθ(°) Example 1 (1) PAA-A1 PAA-B1 1.8 (good) 0.18 (good) Example 2 (2) PAA-A2 PAA-B1 1.9 (good) 0.22 (good) Example 3 (3) PAA-A1 PAA-B3 1.8 (good) 0.20(good) Comparative example 1 (R1) PAA-A2 PAA-B2 2.4 (bad) 0.41 (bad)

As shown in the above table, the liquid crystal display element using the liquid crystal alignment agent of Comparative Example 1 has poor pretilt angle and afterimage characteristics. and afterimage characteristics were good. From the above, it can be said that the liquid crystal display element using the liquid crystal alignment agent of the present invention has a small pretilt angle and good image sticking characteristics.

In addition, the entire contents of the specification, claims, drawings, and abstract of Japanese Patent Application No. 2021-115167 filed on July 12, 2021 are hereby cited and cited as the disclosure content of the specification of the present invention.

1: Transverse electric field liquid crystal display element 2: Comb electrode substrate 2a, 4b, 2d: substrate 2b, 2g: wire electrodes 2c, 2h, 4a: Liquid crystal alignment film 2e: surface electrode 2f: insulating film 3: LCD 4: Facing the substrate L: power line

Fig. 1 shows a schematic cross-sectional view of an example of a transverse electric field liquid crystal display element of the present invention. Fig. 2 shows a schematic cross-sectional view of another example of the transverse electric field liquid crystal display element of the present invention.

1: Transverse electric field liquid crystal display element

2: Comb electrode substrate

2a, 4b: Substrate

2b: Wire electrode

2c, 4a: Liquid crystal alignment film

3: LCD

4: Facing the substrate

L: power line

Claims (14)

A liquid crystal alignment agent is characterized in that it contains the following (A) component and (B) component, (A) component: polymer (A), is selected from the tetracarboxylic dianhydride represented by the following formula (T _c ): The reaction product of 100 mol% tetracarboxylic acid derivatives of all tetracarboxylic acid derivatives and the diamine represented by the following formula (d _AL ) whose content is more than 60% of all diamines is poly At least one of the group consisting of an imide precursor and a polyimide which is an imide of the polyimide precursor, (B) component: polymer (B), selected from the following The content of the tetracarboxylic dianhydride represented by the formula (T _f ) is more than 5 mol% of the total tetracarboxylic acid derivative components, and the tetracarboxylic acid derivative components contain the diamine represented by the following formula (d _AL ) and the following formula The reaction product of the diamine component of the diamine represented by (d _n ) is at least 1 of the group consisting of a polyimide precursor and a polyimide which is an imide of the polyimide precursor kind,

R ₁₁ ~ R ₁₄ each independently represent a hydrogen atom, a halogen atom, an alkyl group with 1 to 6 carbons, an alkenyl group with 2 to 6 carbons, an alkynyl group with 2 to 6 carbons, or a fluorine atom containing 1 to 6 carbons A monovalent organic group of 6, or a phenyl group, at least one of R ₁₁ to R ₁₄ represents a group other than a hydrogen atom in the above definition,

A means having a group "*11-(CH ₂ ) _n -O-*12, where *11 means an atomic bond bonded to an oxygen atom or an atomic bond bonded to a carbon atom constituting a benzene ring, and *12 means an atomic bond bond, n is an integer from 1 to 5", any hydrogen atom of the benzene ring bonded to the NH ₂ group can also be substituted by a 1-valent group,

_Xf is a 4-valent organic group having an alicyclic structure with 5 or more members,

Y represents a heterocyclic ring selected from a nitrogen-containing atom and a group "*21-NR-*22, wherein, *21 and *22 represent an atomic bond bonded to a carbon atom constituting an aromatic ring, but the carbon atom is not It forms a ring with the nitrogen atom to which R is bonded, and R represents a hydrogen atom or a monovalent organic group, and the monovalent organic group is composed of a carbon atom other than carbonyl carbon and a nitrogen atom. A divalent organic group in the structure of a nitrogen atom. The liquid crystal alignment agent according to Claim 1, wherein A in the formula (d _AL ) is a divalent organic group with 1 to 18 carbon atoms. The liquid crystal alignment agent according to Claim 1 or 2, wherein the content of the diamine represented by the formula (d _AL ) in the constituents of the polymer (B) is all diamine used in the manufacture of the polymer (B). 5~80 mol% of the amine component. The liquid crystal alignment agent according to any one of claims 1 to 3, wherein the content of the diamine represented by the above formula (d _n ) in the constituents of the polymer (B) is the production of the polymer (B) 20~95 mol% of all diamine components used in The liquid crystal alignment agent according to any one of claims 1 to 4, wherein, in the formula (d _AL ), *11 is an atomic bond bonded to an oxygen atom. The liquid crystal alignment agent according to any one of claims 1 to 5, wherein the diamine represented by the formula (d _AL ) is a diamine represented by the following formula (d _AL -1)~(d _AL -9),

. The liquid crystal alignment agent according to any one of claims 1 to 6, wherein the diamine represented by the formula (d _n ) is selected from 2,6-diaminopyridine, 3,4-diaminopyridine, 2, 4-diaminopyrimidine, 3,6-diaminocarbazole, N-methyl-3,6-diaminocarbazole, 1,4-bis-(4-aminophenyl)-piperone, 3,6-diaminoacridine, N-ethyl-3,6-diaminocarbazole, N-phenyl-3,6-diaminocarbazole, and the following formula (d _n -1)~ At least one diamine in the group consisting of diamines represented by (d _n -3),

In the formula (d _n -1), m1 and m1' are each independently an integer of 1 to 2, n1 is an integer of 1 to 3, R ₁ and "*21-NR-* in the above formula (d _n ) R in the amino group represented by 22" is synonymous. When there are multiple R ₁ and m1', the multiple R ₁ and m1' can be the same or different. In formula (d _n -2), X ₂ represents 1 A heterocyclic group containing a nitrogen atom, n1 is an integer of 1~2, n2 is an integer satisfying n1+n2=2, L ₁ and L ₂ each independently represent a single bond, -CO-, carbon number 1~ An alkylene group of 6, or a divalent organic group with -O- or -CO- inserted between the carbon-carbon bonds or at the end of the alkylene group with a carbon number of 1 to 6 and bonded to a nitrogen atom through a carbon atom, R Represents a hydrogen atom or a methyl group. When there are multiple X _{2 ,} L ₂ , and R, the multiple X _{2 ,} L ₂ , and R can be the same or different. In formula (d _n -3), X ₃ represents A divalent group of a heterocyclic nitrogen atom, Ar ₃ represents a divalent aromatic ring group, or a divalent saturated heterocyclic group containing a nitrogen atom; any hydrogen of an aromatic ring group, and a saturated heterocyclic group containing a nitrogen atom Atoms can also be substituted by monovalent groups, L ₃ represents a single bond, -(CH ₂ ) _n -, -NR'-, -(CH ₂ ) _n -NR'-, -O-, -NR'-CO-, -CO-NR'-, -O-CO-, or -CO-O-, R'represents a hydrogen atom, methyl, or tertiary butoxycarbonyl, n is an integer from 1 to 6, m3, and m3' Each independently is an integer of 0~2, and any one of m3 and m3' is an integer of 1 or more, when there are multiple Ar ₃ and L ₃ , the multiple Ar ₃ and L ₃ may be the same or different, but The NH ₂ groups at both ends of the formula (d _n -3) are bonded to the carbon atoms constituting the aromatic ring. The liquid crystal alignment agent according to claim 7, wherein the diamines represented by the formulas (d _n -1) ~ (d _n -3) are selected from the diamines represented by the following formulas (Dp-1) ~ (Dp-6) , and the diamines in the diamines represented by the following formula (z-1) ~ formula (z-14),

. The liquid crystal alignment agent according to any one of claims 1 to 8, wherein X _f of the formula (T _f ) is represented by any one of the following formulas (X _f -1)~(X _f -17) 4-valent organic group,

* Indicates an atomic bond. The liquid crystal alignment agent according to any one of Claims 1 to 9, wherein the content ratio of the (A) component to the (B) component is based on the mass ratio of [(A) component]/[(B) component], It is 10/90~90/10. The liquid crystal alignment agent according to any one of claims 1 to 10, wherein the liquid crystal alignment agent further contains a compound selected from crosslinking compounds, functional silane compounds, metal chelate compounds, hardening accelerators, surfactants, anti- At least one additive component in the group consisting of an oxidant, a sensitizer, a preservative, and a compound for adjusting the dielectric constant and resistance of the resin film, The cross-linking compound is selected from having at least one substituent selected from epoxy group, oxetanyl group, oxazoline structure, cyclocarbonate group, blocked isocyanate group, hydroxyl group and alkoxy group At least one of the group consisting of a crosslinking compound (c-1) and a crosslinking compound (c-2) having a polymerizable unsaturated group. A liquid crystal alignment film formed by using the liquid crystal alignment agent according to any one of claims 1 to 11. A liquid crystal display element comprising the liquid crystal alignment film according to claim 12. A method for manufacturing a liquid crystal display element, comprising the following steps (1) to (3), Step (1): Coating the liquid crystal alignment agent according to any one of claims 1 to 11 on the substrate, Step (2): calcining the coated liquid crystal alignment agent to obtain a film, Step (3): performing alignment treatment on the film obtained in step (2).

Images