JP6372200B2 - Method for producing liquid crystal alignment film, photo-alignment agent, and liquid crystal display element - Google Patents

Description

  The present invention relates to a method for producing a liquid crystal alignment film, a photo-alignment agent, and a liquid crystal display element, and more particularly to a technique for imparting liquid crystal alignment to a film by a photo-alignment technique.

  Conventionally, as a liquid crystal display element, various driving methods having different electrode structures and physical properties of liquid crystal molecules to be used have been developed. For example, vertical electric field methods such as TN type, STN type, VA type, IPS type, and FFS type. Various liquid crystal display elements such as a horizontal electric field method are known. Among these, in a vertical electric field type liquid crystal display element, an electrode is formed on each of a pair of substrates arranged opposite to each other to generate an electric field in a direction perpendicular to the substrate, whereas in a horizontal electric field type liquid crystal display element, An electrode is formed on one of the pair of substrates, and an electric field is generated in a direction parallel to the substrate. Thereby, it is known that the liquid crystal display element of the horizontal electric field type can improve the contrast and viewing angle characteristics as compared with the conventional vertical electric field type.

  In the liquid crystal display element, the alignment state of liquid crystal molecules is controlled by a liquid crystal alignment film formed on a substrate. As a material for the liquid crystal alignment film, polyamic acid or polyimide is generally used from the viewpoints of various properties such as heat resistance, mechanical strength, and affinity with liquid crystal. In addition, as a method for imparting liquid crystal alignment ability to a polymer thin film formed with a liquid crystal aligning agent, a photo-alignment method using photoisomerization, photodimerization, photolysis, etc. has recently been proposed as an alternative to the rubbing method. Has been. This photo-alignment method is a method in which the radiation-sensitive organic thin film formed on the substrate is irradiated with polarized or non-polarized radiation to make the film anisotropic, thereby controlling the alignment of liquid crystal molecules. is there. According to this method, it is possible to suppress the generation of dust and static electricity in the process as compared with the conventional rubbing method, and therefore it is possible to suppress the occurrence of display defects and the decrease in yield due to dust and the like. It is. Further, there is an advantage that the liquid crystal alignment ability can be uniformly imparted to the organic thin film formed on the substrate.

  As a liquid crystal aligning agent applied to the photo-alignment method, various types have been conventionally proposed (for example, see Patent Documents 1 to 4). Patent Document 1 discloses a liquid crystal aligning agent containing a polymer having a group containing a chalcone structure in the side chain, and Patent Document 2 discloses a liquid crystal aligning agent containing a polymer having a flavonoid structure. Yes. Patent Document 3 discloses a liquid crystal aligning agent containing a polymer having an azobenzene structure or an anthracene structure, and Patent Document 4 discloses a liquid crystal aligning agent containing a low molecular weight azo compound.

JP 2003-307736 A JP 2004-163646 A JP 2002-250924 A JP 2004-83810 A

  A horizontal electric field type liquid crystal display element has a wide viewing angle characteristic and good contrast characteristics, but an afterimage (image burn-in) due to accumulation of residual charges may be a problem.

  In addition, by applying a liquid crystal alignment film obtained by the photo-alignment method to a liquid crystal display element of a horizontal electric field type, it can be expected that the above characteristics of the photo-alignment method are obtained. However, in the case of a photo-alignment method in which a chemical change is caused by irradiation with ultraviolet rays or the like, there is a general tendency that the electrical properties are inferior compared with a liquid crystal alignment film by a conventional rubbing treatment. In particular, when accompanied by photodecomposition of the polymer, there is a problem that impurity ions increase in the liquid crystal cell and the voltage holding ratio tends to decrease. In addition, it is presumed that the liquid crystal alignment film obtained by the photo-alignment method does not have sufficient liquid crystal alignment control force, and is a cause of image sticking in a horizontal electric field type liquid crystal display element. On the other hand, with the recent improvement in quality of liquid crystal panels, liquid crystal display elements that are excellent in the electrical characteristics and low afterimage properties of liquid crystal display elements are required.

  The present invention has been made in view of the above problems, and a main object of the present invention is to provide a method for manufacturing a liquid crystal alignment film that can obtain a liquid crystal display element that has a small amount of residual charge accumulation and a high voltage holding ratio. .

  The present inventors diligently studied to achieve the above-described problems of the prior art, and focused on the optical fleece rearrangement reaction as a mechanism for causing anisotropy in the film by light irradiation. This photofleece rearrangement reaction causes a skeletal change in the molecular structure by a rearrangement reaction from a phenyl ester to an aromatic hydroxyketone. And based on this point of view, the present inventors have prepared at least one polymer of polyamic acid, polyamic acid ester and polyimide having a structure in which an ester group or a thioester group is bonded to an aromatic ring in the main chain, as a liquid crystal alignment When the liquid crystal alignment film was formed by a photo-alignment method using a part of the polymer component of the agent, it was found that the above problems could be solved, and the present invention was completed. Specifically, the present invention provides the following method for producing a liquid crystal alignment film, a photoalignment agent, and a liquid crystal display element.

In one aspect, the present invention includes (A) a polymer and (B) a polymer as at least one polymer component selected from the group consisting of polyamic acid, polyamic acid ester, and polyimide, and (A) a polymer. Is a polymer having a structure (Y) represented by the following formula (1) (excluding an amide bond formed by a polymerization reaction when X ¹ is —NH—) in the main chain. The manufacturing method of the liquid crystal aligning film which includes the process of apply | coating an agent on a board | substrate and forming a coating film, and the process of irradiating the said coating film with light and setting it as a liquid crystal aligning film is provided.

（式（１）中、Ｘ^１は、硫黄原子、酸素原子又は−ＮＨ−である。「＊」はそれぞれ結合手を示す。但し、２つの「＊」のうち少なくとも一方は芳香環に結合している。）

(In Formula (1), X ¹ is a sulfur atom, an oxygen atom or —NH—. “*” Represents a bond, respectively, provided that at least one of two “*” is bonded to an aromatic ring. ing.)

  In another aspect, the present invention provides a photo-alignment agent containing the above (A) polymer and (B) polymer. In another aspect, a liquid crystal display device comprising a liquid crystal alignment film formed by using the above manufacturing method is provided.

  In a horizontal electric field type liquid crystal display element, a liquid crystal alignment film is produced using a liquid crystal alignment agent obtained by blending a polymer having a structure represented by the above formula (1) in the main chain with a polymer different from the polymer. As a result, a liquid crystal display element having a high voltage holding ratio and a small amount of residual charge can be obtained.

  Below, the liquid crystal aligning agent for photo-alignment of the present invention (hereinafter also referred to as “photo-aligning agent”) and a method for producing a liquid crystal aligning film using the photo-aligning agent will be described. First, each component of the photo-alignment agent and other components optionally blended as necessary will be described.

<Polymer component>
The photo-alignment agent of the present invention contains at least one polymer selected from the group consisting of polyamic acid, polyamic acid ester and polyimide as a polymer component. Moreover, the said polymer contains at least 2 types of polymer of (A) polymer and (B) polymer. Hereinafter, the (A) polymer and the (B) polymer will be described in order.

（式（１）中、Ｘ^１は、硫黄原子、酸素原子又は−ＮＨ−である。「＊」はそれぞれ結合手を示す。但し、２つの「＊」のうち少なくとも一方は芳香環に結合している。） [(A) Polymer]
The polymer (A) is at least one selected from the group consisting of polyamic acid, polyamic acid ester and polyimide, and is represented by the structure (Y) represented by the following formula (1) (when X ¹ is —NH— (Excluding the amide bond formed by the polymerization reaction) in the main chain.

(In Formula (1), X ¹ is a sulfur atom, an oxygen atom or —NH—. “*” Represents a bond, respectively, provided that at least one of two “*” is bonded to an aromatic ring. ing.)

As an aromatic ring couple | bonded with "*" in the said Formula (1), a benzene ring, a naphthalene ring, an anthracene ring etc. can be mentioned, for example. Among these, a benzene ring is preferable from the viewpoint of liquid crystal alignment and transparency. Of the two “*” in the above formula (1), the structure bonded to the other “*” is not particularly limited, and examples thereof include a chain hydrocarbon structure, an aliphatic ring, an aromatic ring, and a heterocyclic ring. It is done. Among these, in terms of high sensitivity to light, one of the two “*” is bonded to an aromatic ring, and the other is bonded to at least one selected from the group consisting of an aromatic ring, an aliphatic ring, and a heterocyclic ring. It is particularly preferable that two “*” are both bonded to an aromatic ring. From the viewpoint of reducing the burn-in of the liquid crystal display element, it is preferable that one of the two “*” is bonded to an aromatic ring and the other is bonded to an aliphatic ring, and the aliphatic ring is a cyclohexane ring. It is more preferable.
X ¹ is preferably a sulfur atom in terms of sensitivity to light, and is preferably an oxygen atom in terms of availability and a wide range of usable monomer options.

In the present invention, the (A) polymer is obtained by reacting a diamine with a tetracarboxylic acid derivative that is at least one selected from the group consisting of tetracarboxylic dianhydride, tetracarboxylic acid diester, and tetracarboxylic acid diester dihalide. Can be obtained. Hereinafter, (A) polyamic acid, polyamic acid ester, and polyimide as the polymer will be described.
In the present specification, the “main chain” of the polymer refers to a “trunk” portion composed of the longest chain of atoms in the polymer. However, this “trunk” portion is allowed to contain a ring structure. In this case, the atoms constituting the ring structure are bonded to other atoms constituting the “trunk” part, so that the entire ring structure exists in the main chain. Therefore, “having structure (Y) in the main chain” means that this structure constitutes a part of the main chain. However, it does not exclude that in the polymer (A), the structure (Y) is also present in a portion other than the main chain, for example, a side chain (a portion branched from the “trunk” of the polymer).

<Polyamic acid>
The polyamic acid (hereinafter also referred to as “(A) polyamic acid”) as the polymer (A) in the present invention is, for example, [i] a tetracarboxylic dianhydride (hereinafter referred to as a specific tetracarboxylic acid) having the above structure (Y). A method of reacting one or more tetracarboxylic dianhydrides including carboxylic dianhydride) with a diamine having no structure (Y); [ii] structure (Y) A method of reacting a tetracarboxylic dianhydride having no diamine with one or more diamines including a diamine having the above structure (Y) (hereinafter also referred to as a specific diamine); [iii] a specific tetra A method of reacting one or more tetracarboxylic dianhydrides containing a carboxylic dianhydride with one or more diamines containing a specific diamine; and the like.

（式（ａ）中、Ｘ^１は、硫黄原子、酸素原子又は−ＮＨ−である。Ｒ^３及びＲ^４は、それぞれ独立に、１個の酸無水物基を有する１価の有機基であり、Ｒ^３及びＲ^４のうち少なくとも一方は芳香環を有する。「−ＣＯ−Ｘ^１−」の少なくとも一方の結合手は芳香環に結合している。） [Specific tetracarboxylic dianhydride]
The specific tetracarboxylic dianhydride is a compound having a group represented by the above formula (1) and two acid anhydride groups (—CO—O—CO—). It is represented by (a).

(In Formula (a), X ¹ is a sulfur atom, an oxygen atom or —NH—. R ³ and R ⁴ are each independently a monovalent organic group having one acid anhydride group. , R ³ and R ⁴ have an aromatic ring. At least one bond of “—CO—X ¹ —” is bonded to the aromatic ring.)

The monovalent organic group of R ³ and R ^{4 in} the above formula (a) is not particularly limited as long as it has an acid anhydride group. Examples of the structure other than the acid anhydride group include a hydrocarbon group having 1 to 40 carbon atoms, a group in which a hydrogen atom of the hydrocarbon group is substituted with a halogen atom, or the like, or a carbon-carbon bond of the hydrocarbon group Between “—O—”, “—S—”, “—CO—”, “—CO—O—”, “—CO—S—”, “—SO ₂ —”, “—N = N—” , “—NH—”, “—CO—NH—” and the like.
Here, the “hydrocarbon group” in this specification may be a saturated hydrocarbon group or an unsaturated hydrocarbon group, a chain hydrocarbon group, an alicyclic hydrocarbon group, and an aromatic hydrocarbon group. The meaning includes a group. Further, the “chain hydrocarbon group” means a linear hydrocarbon group and a branched hydrocarbon group which are composed only of a chain structure without including a cyclic structure in the main chain. The “alicyclic hydrocarbon group” means a hydrocarbon group that includes only an alicyclic hydrocarbon structure as a ring structure and does not include an aromatic ring structure. However, it is not necessary to be comprised only by the structure of an alicyclic hydrocarbon, The thing which has a chain structure in the part is also included. “Aromatic hydrocarbon group” means a hydrocarbon group containing an aromatic ring structure as a ring structure. However, it is not necessary to be composed only of an aromatic ring structure, and a part thereof may include a chain structure or an alicyclic hydrocarbon structure.

（式中、「＊」は、「−Ｏ−Ｃ（＝Ｏ）−」、「−Ｓ−Ｃ（＝Ｏ）−」又は「−ＮＨ−ＣＯ−」に結合する結合手を示す。） The acid anhydride group of R ³ and R ⁴ is preferably bonded to an aromatic ring, and the aromatic ring is more preferably a benzene ring or a naphthalene ring. Specifically, R ³ and R ⁴ are each a group represented by each of the following formulas (a1-1) to (a1-3) or a group having any one of them. .

(In the formula, “*” represents a bond bonded to “—O—C (═O) —”, “—S—C (═O) —” or “—NH—CO—”).

R ³ and R ⁴ preferably have a group represented by the formula (a1-1) or the formula (a1-3) among the above from the viewpoint of enhancing the liquid crystal orientation, and the formula (a1- More preferably, it has a group represented by 1). Further, the bond in each of the above formulas (a1-1) to (a1-3) is “—O—C (═O) —”, “—S—C (═O) —” or “—NH”. It is preferably bonded to the carbonyl group of “—CO—”.

（式（ａ２）中、Ａｒ^１は、ベンゼン環又はナフタレン環であり、Ｘ^２は、−Ｏ−ＣＯ−＊^３、−Ｓ−ＣＯ−＊^３、−ＮＨ−ＣＯ−＊^３、−Ｏ−、−ＣＯ−Ｏ−＊^３、−ＣＯ−Ｓ−＊^３又は−ＣＯ−（但し、「＊^３」は、Ａｒ^１に結合する結合手を示す。）である。Ｒ^５及びＲ^７は、それぞれ独立に、シクロへキシレン基、フェニレン基又はビフェニレン基であり、これらは環部分に置換基を有していてもよい。Ｒ^６は、ｎ１＝ｎ３＝１の場合、炭素数１〜２０の２価の鎖状炭化水素基、当該鎖状炭化水素基の炭素−炭素結合間若しくは炭素原子に隣接する位置に「−Ｏ−」を含む２価の基、−Ｏ−、−Ｓ−、−ＣＯ−、−ＣＯ−Ｏ−、−ＣＯ−Ｓ−、−ＳＯ_２−、−Ｎ＝Ｎ−、−ＮＨ−又は−ＣＯ−ＮＨ−であり、ｎ１＝０又はｎ３＝０の場合、炭素数１〜２０の２価の鎖状炭化水素基又は当該鎖状炭化水素基の炭素−炭素結合間に「−Ｏ−」を含む２価の基である。ｎ１、ｎ２、ｎ３及びｍ１は、それぞれ独立に０又は１である。「＊」は結合手を示す。） When one group of R ³ and R ⁴ is a group represented by any of the above formulas (a1-1) to (a1-3), the other group is represented by the following formula (a2) And the group represented.

(In formula (a2), Ar ¹ represents a benzene ring or a naphthalene ring, and X ² represents —O—CO— * ³ , —S—CO— * ³ , —NH—CO— * ³ , —O—. , —CO—O— * ³ , —CO—S— * ³ or —CO— (where “* ³ ” represents a bond to bond to Ar ¹ ) R ⁵ and R ⁷ are Each independently represents a cyclohexylene group, a phenylene group or a biphenylene group, which may have a substituent in the ring portion, and R ⁶ has 1 to 20 carbon atoms when n1 = n3 = 1. A divalent chain hydrocarbon group, a divalent group containing “—O—” at a position between carbon-carbon bonds or adjacent to a carbon atom of the chain hydrocarbon group, —O—, —S—, — CO—, —CO—O—, —CO—S—, —SO ₂ —, —N═N—, —NH— or —CO—NH—, and n1 = 0 or Is a divalent chain hydrocarbon group having 1 to 20 carbon atoms or a divalent group containing “—O—” between carbon-carbon bonds of the chain hydrocarbon group when n3 = 0. , N2, n3 and m1 are each independently 0 or 1. “*” represents a bond.)

Ar ^{1 in the} above formula (a2) is preferably a benzene ring in terms of good liquid crystal alignment and transparency. X ² is preferably —O—CO— * ³ , —S—CO— * ³ , —CO—O— * ³ or —CO—S— * ³ in that the sensitivity to light is good. -O-CO- * ³ or -S-CO- * ³ is more preferable.

（式（３）中、ｋ及びｉは、それぞれ独立に０又は１であり、ｌは２〜９の整数であり、ｊは１〜４の整数である。「＊」はそれぞれ結合手を示す。）
式（３）において、ｊが２以上の場合、ｌ及びｉは、繰り返し単位間で同じでも異なっていてもよい。上記式（３）で表される基は、上記式（ａ２）のｎ１が０の場合にはＸ^２に対してアルカンジイル基で結合していることが好ましく、ｎ３＝０の場合には、上記式（ａ）中の−ＣＯ−Ｘ^１−に対してアルカンジイル基で結合していることが好ましい。 Examples of the divalent chain hydrocarbon group having 1 to 20 carbon atoms in R ⁶ include a methylene group, an ethylene group, a propanediyl group, a butanediyl group, a pentanediyl group, a hexanediyl group, a heptanediyl group, an octanediyl group, and a nonanediyl group. , Decanediyl group, dodecanediyl group and the like, and these are preferably linear. By making R ⁶ a highly flexible structure, it is possible to increase the heat reorientation of the alignment film during post-baking. A preferable structure of R ⁶ includes, for example, a structure represented by the following formula (3).

(In formula (3), k and i are each independently 0 or 1, l is an integer of 2 to 9, and j is an integer of 1 to 4. "*" represents a bond. .)
In Formula (3), when j is 2 or more, l and i may be the same or different between the repeating units. The group represented by the above formula (3) is preferably bonded to X ² with an alkanediyl group when n1 in the above formula (a2) is 0, and when n3 = 0, It is preferable that the alkanediyl group is bonded to —CO—X ¹ — in the above formula (a).

R ⁵ and R ⁷ are preferably a phenylene group or a biphenylene group in terms of high reactivity to light, and are preferably a cyclohexylene group in terms of reducing the burn-in of the liquid crystal display element.
When the ring portion of R ⁵ and R ⁷ has a substituent, examples of the substituent include a fluorine atom, an alkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms, and a fluoro having 1 to 3 carbon atoms. An alkyl group etc. can be mentioned. The position of the substituent may be any of the ortho position, the meta position, and the para position with respect to X ² for R ^{5 and with} respect to “—CO—X ¹ —” for R ⁷ . However, when “—CO—O—” or “—CO—S—” is bonded to the benzene ring, the substituent is preferably in the ortho position in that sensitivity to light is improved.
It is preferable that at least one of n1 and n3 is 1. n2 is preferably 1 from the viewpoint of improving liquid crystal alignment, and preferably 0 from the viewpoint of improving photoreactivity. m1 is preferably 1 in terms of enhancing the anisotropy effect due to light irradiation.

The reason why the coating film containing the polymer (A) exhibits the liquid crystal alignment ability by light irradiation is not clear, mainly due to the photofleece rearrangement reaction, or photodecomposition of the group “—CO—X ¹ —”. It is unclear whether it depends on or both. Accordingly, when “—CO—O—”, “—CO—S—” or “—CO—NH—” is bonded to the benzene ring, the sensitivity to light is increased by the presence of a substituent at the ortho position relative to the group. The reason for the increase is not clear, but if photodecomposition predominates, the introduction of substituents into the benzene ring makes rearrangement difficult, and as a result, photolysis is presumed to be promoted. Is done.

（式中、「＊」は、Ｘ^１に結合する結合手を示す。） Preferable specific examples of the group represented by the formula (a2) include, for example, groups represented by the following formulas (a2-1) to (a2-46).

(In the formula, “*” represents a bond bonded to X ^1. )

Specific examples of the specific tetracarboxylic dianhydride include, for example, compounds represented by the following formulas (a-1) to (a-37). As specific tetracarboxylic dianhydride, these 1 type can be used individually or in combination of 2 or more types.

  Of the above, the compounds represented by each of the above formulas (a-1) to (a-14) are preferable in that the sensitivity to light is high, and the above formulas (a-1) to (a-11) are preferred. The compounds represented by formula (a-13) and formula (a-14) are more preferred. In addition, the above-described formulas (a-15) to (a-24) can be obtained by imparting appropriate rigidity and flexibility to the polymer so that the reorientation of the alignment film can be increased by heating during post-baking. It is preferable that Moreover, it is preferable to set it as the compound represented by each of said Formula (a-5) and Formula (a-25)-Formula (a-29) from a photoreactive viewpoint.

[Other tetracarboxylic dianhydrides]
In the case of the above methods [i] and [iii], as the tetracarboxylic dianhydride used for the synthesis of the polyamic acid, only the specific tetracarboxylic dianhydride may be used, and the specific tetracarboxylic dianhydride may be used. Other compounds (hereinafter also referred to as “other tetracarboxylic dianhydrides”) may be used in combination. Other tetracarboxylic dianhydrides that can be used in the above methods [i] to [iii] include, for example, aliphatic tetracarboxylic dianhydrides, alicyclic tetracarboxylic dianhydrides, aromatic tetra Examples thereof include carboxylic dianhydrides.

Specific examples thereof include aliphatic tetracarboxylic dianhydrides such as 1,2,3,4-butanetetracarboxylic dianhydride, each of the following formulas (ar-6) to (ar-9): , 1,2,5,6-hexanetetracarboxylic dianhydride, 1,1,2,2-ethenetetracarboxylic dianhydride, compound represented by the following formula (ar-I) A compound represented by the following formula (ar-II);
Examples of the alicyclic tetracarboxylic dianhydride include 1,2,3,4-cyclobutanetetracarboxylic dianhydride, 2,3,5-tricarboxycyclopentylacetic acid dianhydride, 1,3,3a, 4, 5,9b-Hexahydro-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 1,3,3a, 4,5,9b- Hexahydro-8-methyl-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 3-oxabicyclo [3.2.1] octane -2,4-dione-6-spiro-3 '-(tetrahydrofuran-2', 5'-dione), 5- (2,5-dioxotetrahydro-3-furanyl) -3-methyl-3-cyclohexene- No 1,2-dicarboxylic acid 3,5,6-tricarboxy-2-carboxymethylnorbornane-2: 3,5: 6-dianhydride, 2,4,6,8-tetracarboxybicyclo [3.3.0] octane-2 : 4,6: 8-dianhydride, 4,9-dioxatricyclo [5.3.1.0 ^2,6 ] undecane-3,5,8,10-tetraone, cyclohexanetetracarboxylic dianhydride , Cyclopentanetetracarboxylic dianhydride, 1,3-dimethyl-1,2,3,4-cyclobutanetetracarboxylic dianhydride, represented by each of the following formulas (ac-1) to (ac-30) A compound to be prepared;
Examples of aromatic tetracarboxylic dianhydrides include pyromellitic dianhydride, 4,4 ′-(hexafluoroisopropylidene) diphthalic anhydride, and the following formulas (ar-1) to (ar-5): The compounds represented;
In addition to the above, tetracarboxylic dianhydrides described in JP 2010-97188 A can be used. In addition, the said other tetracarboxylic dianhydride can be used individually by 1 type or in combination of 2 or more types.

（式（ａｒ−Ｉ）及び式（ａｒ−ＩＩ）中、Ｚ^１〜Ｚ^４は、それぞれ独立に炭素数１〜２０のアルカンジイル基、脂肪族環、芳香環又は複素環であり、ｍ３〜ｍ５はそれぞれ独立に０又は１である。ただし、ｍ３〜ｍ５が同時に０になることはない。）

(In Formula (ar-I) and Formula (ar-II), Z ^{1 to} Z ⁴ are each independently an alkanediyl group having 1 to 20 carbon atoms, an aliphatic ring, an aromatic ring or a heterocyclic ring; m5 is independently 0 or 1. However, m3 to m5 are not 0 at the same time.)

A divalent group represented by “— [Z ¹ ] _m3 — [Z ² ] _m4 — [Z ³ ] _m5 —” in the above formula (ar-I), and Z ⁴ in the above formula (ar-II) are: And an alkanediyl group having 1 to 10 carbon atoms, a phenylene group, or a cyclohexylene group.
Specific examples of the compound represented by the above (ar-I) include, for example, compounds represented by the above formula (ar-6) and the following formulas (ar-10) to (ar-12). Specific examples of the compound represented by the above (ar-II) include compounds represented by the following formulas (ar-13) and (ar-14), for example.

  The other tetracarboxylic dianhydride is selected from the group consisting of an aromatic tetracarboxylic dianhydride and a tetracarboxylic dianhydride having a nitrogen atom from the viewpoint of improving the electrical characteristics of the liquid crystal display device. It is preferable to include at least one kind. When aromatic tetracarboxylic dianhydride is used as the other tetracarboxylic dianhydride, the content is 3 to 90 weights with respect to 100 parts by weight of the total tetracarboxylic dianhydride used in the synthesis. Parts, preferably 5 to 80 parts by weight.

Preferable specific examples in the case of using a tetracarboxylic dianhydride having a nitrogen atom as another tetracarboxylic dianhydride include, for example, a compound represented by the above formula (ar-I), a formula (ar-II) The compound etc. which are represented by these are mentioned. Of these, compounds represented by the above formulas (ar-6) and (ar-10) to (ar-14) are more preferable, and the above formulas (ar-6) and (ar-13) are more preferable. And a compound represented by each of formula (ar-14) is more preferred, and a compound represented by formula (ar-14) is particularly preferred.
When using the tetracarboxylic dianhydride which has a nitrogen atom as other tetracarboxylic dianhydrides, the content rate is 3 to 100 mol parts of the whole tetracarboxylic dianhydride used for synthesis. It is preferable to set it as 80 mol part, and it is more preferable to set it as 5-70 mol part.

  Further, as other tetracarboxylic dianhydrides, tetracarboxylic dianhydrides having a cyclobutane skeleton can be preferably used from the viewpoint of enhancing photosensitivity by the combined use of a photolysis reaction. 4-cyclobutanetetracarboxylic dianhydride and 1,3-dimethyl-1,2,3,4-cyclobutanetetracarboxylic dianhydride can be more preferably used. When tetracarboxylic dianhydride having a cyclobutane skeleton is used as the other tetracarboxylic dianhydride, the content ratio is 5 mol with respect to 100 mol parts of the total tetracarboxylic dianhydride used for synthesis. The amount is preferably at least part, and more preferably at least 10 parts by mole.

In the case of the above method [i], the use ratio of the specific tetracarboxylic dianhydride is based on the total amount of the tetracarboxylic dianhydride used for the synthesis of the polyamic acid from the viewpoint of sufficiently obtaining the effects of the present invention. , 50 mol% or more, preferably 60 mol% or more, more preferably 70 mol% or more.
In addition, the ratio of the specific tetracarboxylic dianhydride used in the method [iii] is 30 mol% or more with respect to the total amount of tetracarboxylic dianhydride used for the synthesis of polyamic acid. Preferably, it is more preferably 40 mol% or more, and further preferably 50 mol% or more.

  When using the tetracarboxylic dianhydride which has a structure represented by the said Formula (3), the use ratio is 1 mol% with respect to the whole quantity of the tetracarboxylic dianhydride used for the synthesis | combination of a polyamic acid. It is preferable to set it as above, more preferably 5 mol% or more, still more preferably 10 mol%. In addition, the upper limit in particular of the said usage rate is not restrict | limited, It can set arbitrarily in the range of 100 mol% or less.

（式（ｂ）中、Ｘ^１は、硫黄原子、酸素原子又は−ＮＨ−である。Ｒ^８及びＲ^９は、それぞれ独立に２価の有機基であり、Ｒ^８及びＲ^９のうち少なくとも一方は芳香環を有する。「−ＣＯ−Ｘ^１−」における少なくとも一方の結合手は芳香環に結合している。） [Specific diamine]
The specific diamine is a compound having a group represented by the above formula (1) and two primary amino groups, and is represented by, for example, the following formula (b).

(In formula (b), X ¹ is a sulfur atom, an oxygen atom or —NH—. R ⁸ and R ⁹ are each independently a divalent organic group, and at least one of R ⁸ and R ^9. Has an aromatic ring. At least one bond in “—CO—X ¹ —” is bonded to the aromatic ring.)

（式（ｂ２）中、Ａ^１は、フェニレン基、ビフェニレン基、シクロヘキシレン基、ビシクロヘキシレン基、−Ａ^３−Ａ^４−＊＊又は−Ａ^４−Ａ^３−＊＊（但し、Ａ^３はフェニレン基、Ａ^４はシクロヘキシレン基である。「＊＊」は１級アミノ基との結合手を示す。）であり、Ｘ^４は、−Ｏ−ＣＯ−＊^４、−Ｓ−ＣＯ−＊^４、−Ｏ−、−ＣＯ−Ｏ−＊^４、−ＣＯ−Ｓ−＊^４、−ＣＯ−、−Ｎ＝Ｎ−、−Ｃ＝Ｃ−又は−Ｃ≡Ｃ−（但し、「＊^４」は、Ａ^１に結合する結合手を示す。）である。Ｒ^１０は、フェニレン基、ナフチレン基、シクロへキシレン基又は窒素含有複素環基であり、これらは環部分に置換基を有していてもよい。Ｒ^１１は、炭素数１〜２０の２価の鎖状炭化水素基、又は当該鎖状炭化水素基の炭素−炭素結合間若しくは炭素原子に隣接する位置に「−Ｏ−」を含む２価の基である。Ｒ^１２は、フェニレン基、ナフチレン基又はシクロへキシレン基であり、これらは環部分に置換基を有していてもよい。ｎ４、ｎ５及びｎ６は、それぞれ独立に０又は１であり、ｍ２は０〜２の整数である。但し、Ｒ^１１が、鎖状炭化水素基の炭素原子に隣接する位置に「−Ｏ−」を含む２価の基である場合、ｎ４＝ｎ６＝１である。「＊」は結合手を示す。） Examples of the divalent organic group represented by R ⁸ and R ⁹ in the above formula (b) include a hydrocarbon group having 1 to 30 carbon atoms, a group in which a hydrogen atom of the hydrocarbon group is substituted with a halogen atom, and the like, “—O—”, “—S—”, “—CO—”, “—CO—O—”, “—CO—S—”, “—N═N—” between the carbon-carbon bonds of the hydrogen group. And the like, and groups having a heterocyclic ring. Preferable specific examples of the group “—R ⁸ —NH ₂ ” and the group “—R ⁹ —NH ₂ ” include, for example, a group represented by the following formula (b2). The group “—R ⁸ —NH ₂ ” and the group “—R ⁹ —NH ₂ ” may be the same as or different from each other.

(In the formula (b2), A ¹ represents a phenylene group, a biphenylene group, a cyclohexylene group, a bicyclohexylene group, -A ³ -A ⁴ -** or -A ⁴ -A ³ -** (where A ³ Is a phenylene group, A ⁴ is a cyclohexylene group, “**” represents a bond with a primary amino group, and X ⁴ is —O—CO— * ⁴ , —S—CO—. * ⁴ , -O-, -CO-O- * ⁴ , -CO-S- * ⁴ , -CO-, -N = N-, -C = C- or -C≡C- (however, "* ⁴ "Represents a bond bonded to A ^1. ) R ¹⁰ is a phenylene group, a naphthylene group, a cyclohexylene group or a nitrogen-containing heterocyclic group, which has a substituent in the ring portion. R ¹¹ is a divalent chain hydrocarbon group having 1 to 20 carbon atoms, or a carbon-carbon bond of the chain hydrocarbon group. R ¹² is a phenylene group, a naphthylene group, or a cyclohexylene group, and has a substituent in the ring portion. N4, n5 and n6 are each independently 0 or 1, and m2 is an integer of 0 to 2, provided that R ¹¹ is adjacent to the carbon atom of the chain hydrocarbon group. (In the case of a divalent group including “—O—”, n4 = n6 = 1. “*” Represents a bond.)

A ¹ in the above formula (b2) are, in terms of improving sensitivity to light, preferably a phenylene group or a biphenylene group, in terms of alignment control force, bi-cyclohexylene group, ^-A 3 -A 4 - ^* or It is preferably -A ⁴ -A ^3- *. X ⁴ is preferably —O—CO— * ⁴ , —S—CO— * ⁴ , —CO—O— * ⁴ or —CO—S— * ⁴ , and —O—CO— * ⁴ or — More preferably, it is S-CO- * ⁴ .
When the ring portion of R ¹⁰ and R ¹² has a substituent, examples of the substituent include a fluorine atom, an alkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms, and a fluoro having 1 to 3 carbon atoms. An alkyl group etc. can be mentioned. The position of the substituent is not particularly limited, but when “—CO—O—”, “—CO—S—” or “—CO—NH—” is bonded to the benzene ring of R ¹⁰ and R ¹² , The ortho position is preferably relative to “—CO—O—”, “—CO—S—” or “—CO—NH—”.
For R ¹¹ , the description of R ^{6 in} the above formula (a2) can be applied.
It is preferable that at least one of n4 and n6 is 1. m2 is preferably 1 or 2 from the viewpoint of suitably exhibiting anisotropy by light irradiation, and preferably 0 from the viewpoint of orientation regulating force.

Preferable specific examples of the group represented by the formula (b2) include, for example, groups represented by the following formulas (b2-1) to (b2-26).

（式中、「＊」は結合手を示す。）
上記のうち、液晶分子の配向規制力の観点では、上記式（ｂ２）で表される基を上記式（ｂ２−２４）〜式（ｂ２−２６）のそれぞれで表される基とすることが好ましい。

(In the formula, “*” indicates a bond.)
Among the above, from the viewpoint of the alignment regulating force of the liquid crystal molecules, the group represented by the above formula (b2) may be a group represented by each of the above formulas (b2-24) to (b2-26). preferable.

Specific examples of the specific diamine include 4-aminophenyl-4′-aminobenzoate (a compound represented by the following formula (b-1)) and 3,3′-dimethyl-4-aminophenyl-4′-. Aminobenzoate, 3,3 ′, 5,5′-tetramethyl-4-aminophenyl-4′-aminobenzoate, 3-methyl-4-aminophenyl-4′-aminobenzoate, represented by the following formula (b-2) ˜ Examples thereof include compounds represented by formula (b-42). In addition, as specific diamine, 1 type of these can be used individually or in combination of 2 or more types.

Among the above, diamine having a structure of “—aromatic ring—CO—X ¹ —aromatic ring—” is preferable from the viewpoint of high sensitivity to light. Specifically, the above formulas (b-1) and (b −3) to Formula (b-13), Formula (b-15) to Formula (b-20), and Formula (b-25) to Formula (b-27). Moreover, the compound represented by each of said Formula (b-28)-Formula (b-38) is preferable at the point with the high orientation control force of a liquid crystal molecule.

[Other diamines]
In the case of the above methods [ii] and [iii], as the diamine used for the synthesis of the polyamic acid, only the above-mentioned specific diamine may be used. May also be used in combination. Examples of other diamines that can be used in the methods [i] to [iii] include aliphatic diamines, alicyclic diamines, aromatic diamines, and diaminoorganosiloxanes.

  Specific examples thereof include aliphatic diamines such as metaxylylenediamine, 1,3-propanediamine, tetramethylene diamine, pentamethylene diamine, hexamethylene diamine, and the like; alicyclic diamines such as 1,4- Diaminocyclohexane, 4,4′-methylenebis (cyclohexylamine), 1,3-bis (aminomethyl) cyclohexane and the like;

  Examples of aromatic diamines include p-phenylenediamine, 4,4′-ethylenedianiline, 4,4′-diaminodiphenylmethane, 4,4′-diaminodiphenyl sulfide, 1,5-diaminonaphthalene, and 2,2′-dimethyl. -4,4'-diaminobiphenyl, 4,4'-diamino-2,2'-bis (trifluoromethyl) biphenyl, 4,4'-diaminodiphenyl ether, 2,2-bis [4- (4-aminophenoxy) ) Phenyl] propane, 2,2-bis [4- (4-aminophenoxy) phenyl] hexafluoropropane, 2,2-bis (4-aminophenyl) hexafluoropropane, 4,4 ′-(p-phenylenedi) Isopropylidene) bisaniline, 4,4 ′-(m-phenylenediisopropylidene) bisaniline, 1,4- (4-aminophenoxy) benzene, 4,4′-bis (4-aminophenoxy) biphenyl, 2,6-diaminopyridine, 3,4-diaminopyridine, 2,4-diaminopyrimidine, 3,6-diaminoacridine 3,6-diaminocarbazole, N-methyl-3,6-diaminocarbazole, N, N′-bis (4-aminophenyl) -benzidine, N, N′-bis (4-aminophenyl) -N, N '-Dimethylbenzidine, 1,4-bis- (4-aminophenyl) -piperazine, dodecanoxy-2,4-diaminobenzene, tetradecanoxy-2,4-diaminobenzene, octadecanoxy-2,5-diaminobenzene,

  Cholestanyloxy-3,5-diaminobenzene, cholestenyloxy-3,5-diaminobenzene, cholestanyloxy-2,4-diaminobenzene, cholestenyloxy-2,4-diaminobenzene, 3,5-diaminobenzoic acid Cholestanyl acid, cholestenyl 3,5-diaminobenzoate, lanostannyl 3,5-diaminobenzoate, 3,6-bis (4-aminobenzoyloxy) cholestane, 3,6-bis (4-aminophenoxy) cholestane, 4- (4′-trifluoromethoxybenzoyloxy) cyclohexyl-3,5-diaminobenzoate, 4,4′-diaminobenzophenone, 3,3′-diaminobenzophenone, {4- [2- (3,5-diaminophenoxy) -Ethoxy] -phenyl} -ethanone, 3,4-diaminobenzofe {4- [2- (3,5-diaminophenoxy) -ethoxy] -phenyl} -phenyl-methanone, {4- [2- (2,4-diaminophenoxy) -ethoxy] -phenyl} -phenyl- Methanone, {4- [2- (2,4-diaminophenoxy) -ethoxy] -phenyl} -p-toluyl-methanone, {4- [2- (2,4-diaminophenoxy) -ethoxy] -phenyl}- o-toluyl-methanone, 2,7-diaminofluorenone, 2,7-diaminofluorene, 9,9-bis (4-aminophenyl) fluorene,

のそれぞれで表される化合物などを；
ジアミノオルガノシロキサンとして、例えば、１，３−ビス（３−アミノプロピル）−テトラメチルジシロキサン、３，３’−［１，４−フェニレンビス（ジメチルシランジイル）］ビス（１−プロパンアミン）などを；それぞれ挙げることができるほか、特開２０１０−９７１８８号公報に記載のジアミンを用いることができる。その他のジアミンとしては、これらを１種単独で又は２種以上組み合わせて使用することができる。 3,5-diaminobenzoic acid, 2,4-diaminobenzoic acid, 2,5-diaminobenzoic acid, 4,4′-diaminobiphenyl-3,3′-dicarboxylic acid, 4,4′-diaminobiphenyl-2, 2'-dicarboxylic acid, 3,3'-diaminobiphenyl-4,4'-dicarboxylic acid, 3,3'-diaminobiphenyl-2,4'-dicarboxylic acid, 4,4'-diaminodiphenylmethane-3,3 ' -Dicarboxylic acid, 4,4'-diaminobiphenyl-3-carboxylic acid, 4,4'-diaminodiphenylmethane-3-carboxylic acid, 4,4'-diaminodiphenylethane-3,3'-dicarboxylic acid, 4,4 '-Diaminodiphenylethane-3-carboxylic acid, 4,4'-diaminodiphenyl ether-3,3'-dicarboxylic acid, and the following formulas (b3-1) to (b3-14)

A compound represented by each of the above;
Examples of the diaminoorganosiloxane include 1,3-bis (3-aminopropyl) -tetramethyldisiloxane, 3,3 ′-[1,4-phenylenebis (dimethylsilanediyl)] bis (1-propanamine), and the like. In addition, diamines described in JP 2010-97188 A can be used. As other diamine, these can be used individually by 1 type or in combination of 2 or more types.

  In the case of the above method [ii], the proportion of the specific diamine used is 30 mol% or more with respect to the total amount of diamine used for the synthesis of the polyamic acid, from the viewpoint of obtaining a liquid crystal display device having good sensitivity to light. Is more preferable, 40 mol% or more is more preferable, and 50 mol% or more is further more preferable. In the case of the method (iii), the proportion of the specific diamine used is preferably 20 mol% or more, more preferably 30 mol% or more, based on the total amount of diamine used for the synthesis of the polyamic acid. More preferably, it contains 40 mol% or more.

(A) The content of the structure (Y) in the polymer is preferably 1 × 10 ⁻⁵ to 1 × 10 ⁻² mol / g, and 5 × 10 ^{−5 to} 5 × 10 ⁻³ mol / g. More preferably. Therefore, it is preferable to set the types and amounts of the specific tetracarboxylic dianhydride and specific diamine to be used so that the content of the structure (Y) in the polymer (A) falls within the above range.
As the tetracarboxylic dianhydride and diamine used in the reaction, from the viewpoint of improving the sensitivity of the polymer (A) to light, the diamine used in the reaction is “-aromatic ring—CO—X ¹ —aromatic ring— A compound having a structure represented by the above formula (3) as a tetracarboxylic dianhydride used for the reaction, from the viewpoint of increasing the photoreactivity (light absorption), including a diamine having the structure of A combination comprising at least one selected from the group consisting of a compound represented by formula (a-5), a compound represented by formula (a-28) and a compound represented by formula (a-29). It is preferable. At this time, examples of the compound having the structure represented by the formula (3) include the compounds represented by the formula (a-15) to the formula (a-27), the formula (ar-1) to the formula (ar It is preferable to use a compound represented by -5).

  The specific tetracarboxylic dianhydride and the specific diamine both have the same function in that a polyamic acid having a common structure (Y) in the main chain can be obtained. Accordingly, even those not described in the following examples can be used in the present invention. Similarly, other tetracarboxylic dianhydrides and other diamines used together with specific tetracarboxylic dianhydrides or specific diamines are also used in the present invention even if they are not described in the following examples. can do.

[Molecular weight regulator]
(A) When synthesizing a polyamic acid, a terminal-modified polymer may be synthesized using an appropriate molecular weight regulator (end-capping agent) together with the tetracarboxylic dianhydride and diamine as described above. .

Examples of molecular weight regulators include acid monoanhydrides, monoamine compounds, monoisocyanate compounds, and the like. Specific examples thereof include acid monoanhydrides such as maleic anhydride, phthalic anhydride, itaconic anhydride, n-decylsuccinic anhydride, n-dodecylsuccinic anhydride, n-tetradecylsuccinic. Acid anhydride, n-hexadecyl succinic anhydride, 3- (3-trimethoxysilyl) propyl) -3,4-dihydrofuran-2,5-dione, 4,5,6,7-tetrafluoroiso Benzofuran-1,3-dione, etc .; monoamine compounds such as aniline, cyclohexylamine, n-butylamine, n-pentylamine, n-hexylamine, n-heptylamine, n-octylamine, 3- (trifluoromethoxy ) Aniline, 4- (trifluoromethoxy) aniline, triethoxysilylamine, 3-aminopropi Trimethoxysilane, 3-aminopropyltriethoxysilane, and 3-aminopropyl methoxy diethoxy silane; as monoisocyanate compounds such as phenyl isocyanate, naphthyl isocyanate and the like; may be mentioned, respectively.
The use ratio of the molecular weight regulator is preferably 20 parts by mole or less, and more preferably 10 parts by mole or less, with respect to a total of 100 parts by mole of the tetracarboxylic dianhydride and diamine used.

<Synthesis of polyamic acid>
The ratio of the tetracarboxylic dianhydride and the diamine used in the polyamic acid synthesis reaction in the present invention is such that the acid anhydride group of the tetracarboxylic dianhydride is 0. A ratio of 2 to 2 equivalents is preferable, and a ratio of 0.3 to 1.2 equivalents is more preferable.
The polyamic acid synthesis reaction is preferably carried out in an organic solvent. The reaction temperature at this time is preferably -20 ° C to 150 ° C, more preferably 0 to 100 ° C. The reaction time is preferably from 0.1 to 24 hours, more preferably from 0.5 to 12 hours.

Examples of the organic solvent include aprotic polar solvents, phenol solvents, alcohols, ketones, esters, ethers, halogenated hydrocarbons, and hydrocarbons. Specific examples of these organic solvents include aprotic polar solvents such as N-methyl-2-pyrrolidone, N, N-dimethylacetamide, N, N-dimethylformamide, dimethyl sulfoxide, γ-butyrolactone, tetramethylurea, Hexamethylphosphortriamide and the like; phenolic solvents such as phenol, m-cresol, xylenol, halogenated phenol and the like;
Examples of alcohols include methanol, ethanol, isopropyl alcohol, cyclohexanol, ethylene glycol, propylene glycol, and ethylene glycol monomethyl ether; ketones such as acetone, methyl ethyl ketone, and methyl isobutyl ketone; and esters such as ethyl lactate, Butyl lactate, methyl acetate, ethyl acetate, butyl acetate, diethyl malonate, isoamyl propionate, isoamyl isobutyrate and the like; ethers such as diethyl ether, diisopentyl ether, ethylene glycol methyl ether, ethylene glycol ethyl ether, Ethylene glycol-n-propyl ether, ethylene glycol-n-butyl ether, ethylene glycol dimethyl ether , Ethylene glycol ethyl ether acetate, diethylene glycol dimethyl ether, tetrahydrofuran, etc .; halogenated hydrocarbons such as dichloromethane, 1,2-dichloroethane, 1,4-dichlorobutane, trichloroethane, chlorobenzene, etc .; , Hexane, heptane, octane, benzene, toluene, xylene and the like;

  Among these organic solvents, one or more selected from the group consisting of an aprotic polar solvent and a phenolic solvent (first group of organic solvents), or one or more selected from the first group of organic solvents, It is preferable to use a mixture with one or more selected from the group consisting of alcohols, ketones, esters, ethers, halogenated hydrocarbons and hydrocarbons (second group organic solvent). In the latter case, the use ratio of the second group organic solvent is preferably 50% by weight or less, more preferably 40% by weight with respect to the total amount of the first group organic solvent and the second group organic solvent. % Or less, more preferably 30% by weight or less. The amount of organic solvent used (α) is such that the total amount (β) of tetracarboxylic dianhydride and diamine is 0.1 to 50% by weight based on the total amount of the reaction solution (α + β). It is preferable that

  As described above, a reaction solution obtained by dissolving polyamic acid is obtained. This reaction solution may be used as it is for the preparation of the photo-alignment agent, may be used for the preparation of the photo-alignment agent after isolating the polyamic acid contained in the reaction solution, or the isolated polyamic acid was purified. You may use for preparation of a photo-alignment agent. When polyamic acid is dehydrated and cyclized into a polyimide, the above reaction solution may be directly subjected to dehydration and cyclization reaction, or may be subjected to dehydration and cyclization reaction after isolating the polyamic acid contained in the reaction solution. Alternatively, the isolated polyamic acid may be purified and then subjected to a dehydration ring closure reaction. Isolation and purification of the polyamic acid can be performed according to known methods.

<Polyamic acid ester>
The polyamic acid ester (hereinafter also referred to as (A) polyamic acid ester) as the polymer (A) of the present invention is, for example, [I] (A) polyamic acid obtained by the above synthesis reaction and a hydroxyl group-containing compound. , A method of synthesizing by reacting an acetal esterifying agent, a halide, an epoxy group-containing compound, etc., [II] a method of reacting a tetracarboxylic acid diester and a diamine, and [III] a tetracarboxylic acid diester dihalide It can be obtained by a method of reacting with diamine.

Here, examples of the hydroxyl group-containing compound used in the method [I] include alcohols such as methanol, ethanol and propanol; phenols such as phenol and cresol. Examples of the acetal esterifying agent include N, N-dimethylformamide diethyl acetal and N, N-diethylformamide diethyl acetal. Examples of the halide include methyl bromide, ethyl bromide, stearyl bromide, methyl chloride, stearyl chloride, 1,1,1-trifluoro-2-iodoethane and the like, and as an epoxy group-containing compound, Examples thereof include propylene oxide.
The tetracarboxylic acid diester used in the method [II] can be obtained, for example, by ring-opening the tetracarboxylic dianhydride exemplified in the synthesis of the polyamic acid (A) using the above alcohols. The reaction between the tetracarboxylic acid diester and the diamine is preferably carried out in the presence of a suitable dehydration catalyst. Examples of the dehydration catalyst include 4- (4,6-dimethoxy-1,3,5-triazin-2-yl) -4-methylmorpholinium halide, carbonylimidazole, a phosphorus condensing agent, and the like.
The tetracarboxylic acid diester dihalide used in Method [III] can be obtained, for example, by reacting the tetracarboxylic acid diester obtained as described above with an appropriate chlorinating agent such as thionyl chloride.
In the above methods [II] and [III], a polyamic acid ester having the structure (Y) is obtained by using a compound having the structure (Y) in at least one of tetracarboxylic dianhydride and diamine. Can do. The polyamic acid ester may have only an amic acid ester structure, or may be a partially esterified product in which an amic acid structure and an amic acid ester structure coexist.

  As described above, a reaction solution obtained by dissolving the polyamic acid ester is obtained. This reaction solution may be used as it is for the preparation of the photo-alignment agent, and after isolation of the polyamic acid ester contained in the reaction solution, it may be used for the preparation of the photo-alignment agent, or the isolated polyamic acid ester may be used. You may use for preparation of a photoalignment agent after refine | purifying. Isolation and purification of the polyamic acid ester can be performed according to a known method.

<Polyimide>
The polyimide (A) as a polymer (hereinafter also referred to as “(A) polyimide”) contained in the photo-alignment agent of the present invention is, for example, (A) polyamic acid synthesized as described above and dehydrating and ring-closing. And can be obtained by imidization.
The above (A) polyimide may be a completely imidized product obtained by dehydrating and cyclizing all of the amic acid structure of the precursor (A) polyamic acid, and only a part of the amic acid structure is dehydrated. It may be a partially imidized product that is ring-closed and has an amic acid structure and an imide ring structure. (A) The imidation ratio of the polyimide is preferably 5% or more, more preferably 10 to 60%, still more preferably 15 to 50%. This imidation ratio represents the ratio of the number of imide ring structures to the total of the number of polyimide amic acid structures and the number of imide ring structures in percentage. Here, a part of the imide ring may be an isoimide ring.

  The polyamic acid is preferably dehydrated and closed by heating the polyamic acid, or by dissolving the polyamic acid in an organic solvent, adding a dehydrating agent and a dehydrating ring-closing catalyst to the solution, and heating the solution as necessary. . Of these, the latter method is preferred.

  In the method of imidizing a polyamic acid solution by adding a dehydrating agent and a dehydrating ring-closing catalyst, acid anhydrides such as acetic anhydride, propionic anhydride, and trifluoroacetic anhydride can be used as the dehydrating agent. It is preferable that the usage-amount of a dehydrating agent shall be 0.01-20 mol with respect to 1 mol of the amic acid structure of a polyamic acid. As the dehydration ring closure catalyst, for example, tertiary amines such as pyridine, collidine, lutidine, triethylamine and the like can be used. It is preferable that the usage-amount of a dehydration ring-closing catalyst shall be 0.01-10 mol with respect to 1 mol of dehydrating agents to be used. Examples of the organic solvent used in the dehydration ring-closing reaction include the organic solvents exemplified as those used for the synthesis of polyamic acid. The reaction temperature of the dehydration ring closure reaction is preferably 0 to 180 ° C, more preferably 10 to 150 ° C. The reaction time is preferably 1.0 to 120 hours, more preferably 2.0 to 30 hours.

  In this way, (A) a reaction solution containing polyimide is obtained. This reaction solution may be used as it is for the preparation of the photo-alignment agent, or may be used for the preparation of the photo-alignment agent after removing the dehydrating agent and the dehydration ring-closing catalyst from the reaction solution. You may use for preparation of an aligning agent, or you may use for preparation of a photo-alignment agent after refine | purifying the isolated polyimide. These purification operations can be performed according to known methods. In addition, the (A) polymer contained in the photo-alignment agent of this invention can be used individually by 1 type or in combination of 2 or more types.

[(B) Polymer]
The (B) polymer contained in the photo-alignment agent of the present invention is at least one selected from the group consisting of polyamic acid, polyamic acid ester and polyimide, and is a polymer different from the above (A) polymer. . When the polymer component of the photo-alignment agent is only the polymer (A), even when the voltage holding ratio decreases or the residual charge accumulates in the liquid crystal display element, this is improved by blending different resins. It becomes possible to do.

When the (B) polymer is a polyamic acid (hereinafter also referred to as “(B) polyamic acid”), the (B) polyamic acid is obtained by, for example, reacting a tetracarboxylic dianhydride and a diamine. Can be obtained. Here, examples of the tetracarboxylic dianhydride used for the synthesis of the polymer (B) include compounds exemplified as the tetracarboxylic dianhydride that can be used for the synthesis of the polymer (A). it can. Among them, from the viewpoint of suppressing charge transfer within and between molecules, it is preferable to include alicyclic tetracarboxylic dianhydride, and 2,3,5-tricarboxycyclopentylacetic acid dianhydride, bicyclo [3.3 .0] octane-2,4,6,8-tetracarboxylic acid 2: 4,6: 8-dianhydride, 1,3,3a, 4,5,9b-hexahydro-8-methyl-5- (tetrahydro -2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 1,3,3a, 4,5,9b-hexahydro-5- (tetrahydro-2,5 -Dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione, 1,2,3,4-cyclobutanetetracarboxylic dianhydride, cyclopentanetetracarboxylic dianhydride, and Cyclohexanetetraca More preferably contains at least one specific alicyclic tetracarboxylic acid dianhydride selected from the group consisting of carbon dianhydride.
The mixing ratio of these specific alicyclic tetracarboxylic dianhydrides (the total amount when two or more types are included) is 30 mol% with respect to the total amount of tetracarboxylic dianhydrides used in the synthesis. It is preferable to set it as the above, and it is more preferable to set it as 40 mol% or more.

  The tetracarboxylic dianhydride used for the synthesis | combination of the said (B) polyamic acid may contain the tetracarboxylic dianhydride (specific tetracarboxylic dianhydride) which has the said structure (Y). The specific tetracarboxylic dianhydride is used in proportion to the amount of tetra-carboxylic acid dianhydride used in the synthesis in order to enable introduction of a sufficient amount of components exhibiting different characteristics (for example, electrical characteristics and transparency) from the specific tetracarboxylic dianhydride. It is preferable to set it as 30 mol% or less with respect to the whole quantity of carboxylic dianhydride, and it is more preferable to set it as 20 mol% or less.

(B) As a diamine used for the synthesis | combination of a polyamic acid, the compound (specific diamine and other diamine) illustrated as a diamine which can be used for the synthesis | combination of (A) polymer can be mentioned. At this time, it is preferable to set it as 30 mol% or less with respect to the whole quantity of the diamine used for a synthesis | combination, and, as for the usage-amount of specific diamine, it is more preferable to set it as 20 mol% or less.
In addition, about the various reaction conditions in the synthesis | combination of (B) polyamic acid, the description of the said (A) polymer is applicable. Moreover, the polyamic acid ester and polyimide as (B) polymer can also be obtained according to the method described in the above (A) polymer. As the polymer (B) contained in the photo-alignment agent of the present invention, one type can be used alone, or two or more types can be used in combination.

  The polymer (B) is preferably a polymer in which the content of at least one of fluorine atoms and silicon atoms (hereinafter also referred to as “specific atom”) is different from the polymer (A). Generally, when two types of polymers with different specific atom contents are blended, the polymer with the higher specific atom content is unevenly distributed in the upper layer due to the difference in surface energy, and the lower specific atom content is It is known that this polymer tends to be unevenly distributed in the lower layer. By utilizing such an event and making the content of specific atoms different between the (A) polymer and the (B) polymer, the liquid crystal alignment film for each of the (A) polymer and the (B) polymer It is presumed that the distribution can be biased.

When at least one of the (A) polymer and (B) polymer has a specific atom (F, Si), examples of the combination include the following [1] to [4].
[1] A mode in which the (A) polymer and the (B) polymer have specific atoms, and the (A) polymer has a higher specific atom content than the (B) polymer.
[2] A mode in which (A) the polymer has a specific atom and (B) the polymer has substantially no specific atom.
[3] A mode in which the (A) polymer and the (B) polymer have a specific atom, and the (B) polymer has a higher content of the specific atom than the (A) polymer.
[4] A mode in which (B) the polymer has a specific atom and (A) the polymer has substantially no specific atom.
Among these, it is preferable that the (A) polymer has a higher specific atom content than the (B) polymer in order to suitably control the alignment of liquid crystal molecules. Specifically, the aspect [1] or [2] is preferable, and the aspect [2] is more preferable. The phrase “substantially does not have a specific atom” means that the content of the repeating unit having no specific atom or having a specific atom is 1 mol% or less with respect to all repeating units of the polymer. , Preferably 0.5 mol% or less.

In order to obtain a polymer having a specific atom, for example, in the synthesis of the polymer, [i] a method of polymerizing using a monomer containing a tetracarboxylic acid derivative having a specific atom; [ii] a monomer containing a diamine having a specific atom [Iii] A method of polymerizing using a monoamine having a specific atom as a terminal blocking agent; [iv] A polymerization using an acid monoanhydride having a specific atom as a terminal blocking agent Method, etc.
Here, as the tetracarboxylic acid derivative having a specific atom, for example, 4,4 ′-(hexafluoroisopropylidene) diphthalic anhydride, acid anhydride group-containing silicone oil (for example, trade name “X-22-2290AS”) (Shin-Etsu Silicone Co., Ltd.)) and the like; Examples of the diamine having a specific atom include 4,4′-diamino-2,2′-bis (trifluoromethyl) biphenyl, 4,4′-diamino-3, 3′-bis (trifluoromethyl) biphenyl, 2,2-bis [4- (4-aminophenoxy) phenyl] hexafluoropropane, 2,2-bis (4-aminophenyl) hexafluoropropane, 4- (4 '-Trifluoromethoxybenzoyloxy) cyclohexyl-3,5-diaminobenzoate, 1,3-bis (3-aminopropyl) -te Lamethyldisiloxane, 3,3 ′-[1,4-phenylenebis (dimethylsilanediyl)] bis (1-propanamine), etc .; monoamines having specific atoms include, for example, 3- (trifluoromethoxy) aniline 4- (trifluoromethoxy) aniline, triethoxysilylamine, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-aminopropylmethoxydiethoxysilane, etc .; acid monoanhydride having a specific atom As, for example, 3- (3-trimethoxysilyl) propyl) -3,4-dihydrofuran-2,5-dione, 4,5,6,7-tetrafluoroisobenzofuran-1,3-dione, etc. Each can be mentioned. In addition, in order to obtain the polymer which has a specific atom, 1 type in these methods [i]-[iv] may be used, and 2 or more types may be used in combination.
In the polymer having a specific atom, the content ratio of the repeating unit having the specific atom is preferably 70 mol% or less, more preferably 60 mol% or less, with respect to all the repeating units of the polymer. More preferably, it is 50 mol% or less. Moreover, it does not specifically limit about a lower limit, For example, it can be 1 mol% or more, and it is preferable to set it as 5 mol% or more.

（式（２−１）中、Ｒ^１は、ハロゲン原子、炭素数１〜１０のアルキル基又は炭素数１〜１０のアルコキシ基であり、ｒ１は０〜２の整数であり、ｒ２は０〜３の整数である。但し、ｒ１＋ｒ２≦４を満たす。「＊１」は結合手を示す。式（２−２）中、Ｒ^２は、水素原子又は炭素数１〜６のアルキル基である。「＊２」は結合手を示す。） ・ Structure (Z)
At least one of the (A) polymer and the (B) polymer has a structure represented by the following formula (2-1), a structure represented by the following formula (2-2) (however, polymerization of monomers) And at least one structure (Z) selected from the group consisting of nitrogen-containing heterocycles. By introducing such a structure (Z) into the polymer, it becomes possible to improve electrical characteristics such as voltage holding ratio and afterimage characteristics of the liquid crystal display element.

(In Formula (2-1), R ¹ is a halogen atom, an alkyl group having 1 to 10 carbon atoms, or an alkoxy group having 1 to 10 carbon atoms, r 1 is an integer of 0 to 2, and r 2 is 0 to 3 of an integer. However, satisfy r1 + r2 ≦ 4. "* 1" represents a bond in. formula (2-2), ^{R 2} is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms. “* 2” indicates a bond.)

Examples of the alkyl group having 1 to 10 carbon atoms of R ¹ include methyl group, ethyl group, propyl group, butyl group, pentyl group, hexyl group, heptyl group, octyl group, nonyl group, decanyl group and the like. These may be linear or branched. Examples of the alkoxy group having 1 to 10 carbon atoms include groups in which an alkyl group having 1 to 10 carbon atoms and an oxygen atom are bonded. Specifically, for example, a methoxy group, an ethoxy group, a propoxy group, and the like. Groups and the like. Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom.
r1 and r2 are each preferably 0 or 1.
R ² is preferably a hydrogen atom or an alkyl group having 1 to 3 carbon atoms, more preferably a hydrogen atom or a methyl group, and still more preferably a hydrogen atom.
Examples of the nitrogen-containing heterocycle include piperidine, pyrrolidine, pyridine, pyrazine, piperazine, pyrimidine, and homopiperazine. Among these, a piperidine ring or a piperazine ring is preferable, and a piperidine ring is more preferable in that the effect of relaxing the accumulated residual charge is high.
The structure (Z) is preferably a structure represented by the above formula (2-2) or a nitrogen-containing heterocycle, more preferably a nitrogen-containing heterocycle, in terms of a high effect of improving electrical characteristics. preferable.

  The structure (Z) may be introduced into either the main chain or the side chain of the polymer. In addition, the polymer which has the said structure (Z) can obtain the polymer which has a structure represented by the said Formula (2-1) by using the diamine which has a carboxyl group, for example in the case of the synthesis | combination of a polymer. it can. Further, by using a diamine represented by each of the above formulas (b3-4) and (b3-10) or a tetracarboxylic dianhydride represented by the above formula (ar-1), the above formula ( A polymer having a structure represented by 2-2) can be obtained. Diamines represented by the above formulas (b-21), (b3-1) to (b3-3), (b3-8), (b3-9), and (b3-11) to (b3-14) By using this, a polymer having a nitrogen-containing heterocyclic ring can be obtained.

The structure (Z) may be included in the (A) polymer and the (B) polymer, may be included only in the (A) polymer, or may be included only in the (B) polymer. May be. From the viewpoint of suitably performing uneven distribution of (A) polymer and (B) polymer by utilizing the difference in polarity in the coating film, one of (A) polymer and (B) polymer. It is preferable that the content ratio of the said structure (Z) is higher than the other polymer, and it is more preferable that the other polymer does not have the said structure (Z) substantially. Preferably, (B) the polymer has the structure (Z). In addition, “substantially free of structure (Z)” means that the structure does not have structure (Z) or contains the repeating unit having structure (Z) with respect to all repeating units of the polymer. The ratio is 1 mol% or less, preferably 0.5 mol% or less.
In the polymer having the structure (Z), the content ratio of the repeating unit having the structure (Z) is preferably 2 to 50 mol%, and preferably 5 to 40 mol% with respect to all the repeating units of the polymer. It is more preferable that

As preferable combinations in the polymer component of the photo-alignment agent of the present invention, for example, the following embodiments [1] to [5] are exemplified.
[1] The polymer (A) is a polymer having the structure (Y) and a specific atom, the polymer (B) has the structure (Z), and the specific atom is more than the polymer (A). The aspect which is a polymer with low content rate.
[2] The (A) polymer is a polymer having a structure (Y), a structure (Z), and a specific atom, (B) the polymer has a structure (Z), and (A) The aspect which is a polymer with the content rate of a specific atom lower than a coalescence.
[3] The (A) polymer is a mixture of a polymer having the structure (Y) and the specific atom, and a polymer having the structure (Y), the structure (Z), and the specific atom, A mode in which the coalescence is a polymer having the structure (Z) and having a specific atom content lower than that of the polymer (A).
[4] The (A) polymer is a polymer having the structure (Y) and the structure (Z), the (B) polymer has the structure (Y), and is more specific than the (A) polymer. An embodiment in which the polymer has a high atomic content.
[5] The polymer (A) is a polymer having the structure (Y) and the structure (Z), the polymer (B) has substantially no structure (Y), and (A ) An embodiment in which the specific atom content is higher than that of the polymer.
The combination of the (A) polymer and the (B) polymer is preferably an embodiment of [1], [2] or [3], and an embodiment of [1] is particularly preferable. Although it is not necessarily clear, when a coating film is formed on a substrate using the photo-alignment agent according to the aspect [1], the polymer (A) having high photoreactivity is unevenly distributed in the upper layer in the coating film. It is presumed that the polymer (B) having a high effect of improving the characteristics is unevenly distributed in the lower layer. This is presumed to show excellent liquid crystal alignment and electrical characteristics.

<Solution viscosity of polymer>
The (A) polymer and the (B) polymer preferably have a solution viscosity of 10 to 800 mPa · s, respectively, when this is a 10% by weight solution. More preferably, it has a solution viscosity of s. In addition, the solution viscosity (mPa · s) of the above polymer is based on a polymer solution having a concentration of 10% by weight prepared using a good solvent for the polymer (eg, γ-butyrolactone, N-methyl-2-pyrrolidone, etc.). The value measured at 25 ° C. using an E-type rotational viscometer.
The (A) polymer and (B) polymer preferably have a polystyrene-reduced weight average molecular weight of 500 to 500,000 as measured by gel permeation chromatography (GPC), and 1,000 to 300,000. It is more preferable that
The content ratio of the polymer (A) and the polymer (B) in the photo-alignment agent is 2/8 to 8/2 in terms of weight ratio (A / B) from the viewpoint of sufficiently obtaining the effects of the present invention. Is more preferable, and more preferably 3/7 to 7/3.

<Other ingredients>
The photo-alignment agent of the present invention may contain other components as necessary. Examples of such other components include the above-mentioned (A) polymer and other polymers other than the (B) polymer, and compounds having at least one epoxy group in the molecule (hereinafter referred to as “epoxy group-containing compound”). , Functional silane compounds, bismaleimide compounds, allyl group-containing compounds, and the like.

[Other polymers]
The above other polymers can be used for improving solution properties and electrical properties. Examples of such other polymers include polyesters, polyamides, polyorganosiloxanes, cellulose derivatives, polyacetals, polystyrene derivatives, poly (styrene-phenylmaleimide) derivatives, poly (meth) acrylates, and the like.
When other polymers are added to the photo-alignment agent, the blending ratio is preferably 20 parts by weight or less with respect to 100 parts by weight of the total polymer in the composition, and 10 parts by weight or less. It is more preferable.

のそれぞれで表される化合物、ソルビトールポリグリシジルエーテル、ペンタエリスリトールポリグリシジルエーテル、トリメチロールプロパンポリグリシジルエーテル、ヒドロキノンジグリシジルエーテル、ビスフェノールＡジグリシジルエーテル、水素化ビスフェノールＡジグリシジルエーテル、ジグリシジルテレフタレート等を好ましいものとして挙げることができる。その他、エポキシ基含有化合物としては、国際公開第２００９/０９６５９８号記載のエポキシ基含有ポリオルガノシロキサンを用いることができる。これらエポキシ化合物を光配向剤に添加する場合、その配合比率は、光配向剤中に含まれる重合体の合計１００重量部に対して、４０重量部以下が好ましく、０．１〜３０重量部がより好ましい。 [Epoxy group-containing compound]
The epoxy group-containing compound can be used to improve the adhesion and electrical properties with the substrate surface in the liquid crystal alignment film. Here, examples of the epoxy group-containing compound 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, trimethylolpropane triglycidyl ether, 2,2-dibromoneopentyl glycol diglycidyl ether, N, N, N ′, N′-tetraglycidyl-m-xylenediamine 1,3-bis (N, N-diglycidylaminomethyl) cyclohexane, N, N, N ′, N′-tetraglycidyl-4,4′-diaminodi Enirumetan, N, N-diglycidyl - benzylamine, N, N-diglycidyl - aminomethyl cyclohexane, N, N-diglycidyl - cyclohexylamine, the following formulas (e-1) ~ (e-9)

A compound represented by each of the following: sorbitol polyglycidyl ether, pentaerythritol polyglycidyl ether, trimethylolpropane polyglycidyl ether, hydroquinone diglycidyl ether, bisphenol A diglycidyl ether, hydrogenated bisphenol A diglycidyl ether, diglycidyl terephthalate, etc. It can be mentioned as a preferable one. In addition, as the epoxy group-containing compound, an epoxy group-containing polyorganosiloxane described in International Publication No. 2009/096598 can be used. When these epoxy compounds are added to the photo-alignment agent, the blending ratio is preferably 40 parts by weight or less, and 0.1 to 30 parts by weight with respect to 100 parts by weight of the total polymer contained in the photo-alignment agent. More preferred.

[Functional silane compounds]
The functional silane compound can be used for the purpose of improving the printability of the photo-alignment agent. Examples of such functional silane compounds include 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, N- (2-aminoethyl) -3-aminopropyltrimethoxysilane, and N-triethoxysilylpropyl. Examples include triethylenetriamine, N-benzyl-3-aminopropyltrimethoxysilane, N-phenyl-3-aminopropyltrimethoxysilane, glycidoxymethyltrimethoxysilane, and 3-glycidoxypropyltrimethoxysilane. it can. When these functional silane compounds are added to the photo-alignment agent, the blending ratio is preferably 2 parts by weight or less, more preferably 0.02 to 0.2 parts by weight with respect to 100 parts by weight of the total amount of the polymer.

[Bismaleimide compounds]
The bismaleimide compound can be used to improve the heat resistance and electrical properties of the liquid crystal alignment film and the wear resistance of the coating film. Examples of the bismaleimide compound include 4,4′-diphenylmethane bismaleimide, bis- (3-ethyl-5-methyl-4-maleimidophenyl) methane, and 2,2′-bis- [4- (4-maleimidophenoxy). Phenyl] propane, 4-methyl-1,3-phenylenebismaleimide, a compound represented by the following formula (ad-2), and the like. When these bismaleimide compounds are added to the liquid crystal aligning agent, the blending ratio is preferably 40 parts by weight or less, and more preferably 0.1 to 30 parts by weight with respect to 100 parts by weight of the total amount of the polymer.

[Allyl group-containing compound]
The allyl group-containing compound can be used in order to suppress an improvement in electrical characteristics and a decrease in voltage holding ratio of the liquid crystal alignment film. Examples of the allyl group-containing compound include compounds represented by the following formulas (al-1) to (al-3). When these allyl group-containing compounds are added, the blending ratio is preferably 40 parts by weight or less, more preferably 0.1 to 30 parts by weight with respect to a total of 100 parts by weight of the polymer.

  As other components, in addition to the above, additives usually added to the photo-alignment agent, for example, a compound having at least one oxetanyl group in the molecule, an antioxidant, a photosensitizer, etc. may be used. it can. In order to improve the strength of the coating film, lactams, glutaric imide compounds, hydroxypiperidone compounds and piperidine compounds as described in Japanese Patent No. 324549; described in Japanese Patent No. 5045241 Such a heterocyclic compound having at least one heterocyclic structure selected from the group consisting of oxetane, thiirane, and oxazoline; inorganic particles having a particle size of 1,000 mm or less (for example, silica particles) can be added.

<Solvent>
The liquid crystal aligning agent of the present invention is prepared as a liquid composition in which the above polymer component and other components added as needed are preferably dispersed or dissolved in an appropriate solvent.

  Examples of the organic solvent to be used include N-methyl-2-pyrrolidone, γ-butyrolactone, γ-butyrolactam, N, N-dimethylformamide, N, N-dimethylacetamide, 4-hydroxy-4-methyl-2-pentanone, Ethylene glycol monomethyl ether, butyl lactate, butyl acetate, methyl methoxypropionate, ethyl ethoxypropionate, ethylene glycol methyl ether, ethylene glycol ethyl ether, ethylene glycol-n-propyl ether, ethylene glycol-i-propyl ether , Ethylene glycol-n-butyl ether (butyl cellosolve), ethylene glycol dimethyl ether, ethylene glycol ethyl ether acetate, diethylene glycol dimethyl ether, diethylene glycol Recall diethyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monomethyl ether acetate, diethylene glycol monoethyl ether acetate, diisobutyl ketone, isoamyl propionate, isoamyl isobutyrate, diisopentyl ether, ethylene carbonate, propylene carbonate, etc. be able to. These can be used alone or in admixture of two or more.

  The solid content concentration in the photoalignment agent of the present invention (the ratio of the total weight of components other than the solvent of the photoalignment agent to the total weight of the photoalignment agent) is appropriately selected in consideration of viscosity, volatility, and the like. The range is preferably 1 to 10% by weight. That is, the photo-alignment agent of the present invention is applied to the substrate surface as described later, and preferably is heated to form a coating film that becomes a liquid crystal alignment film. At this time, the solid content concentration is 1 wt. When it is less than%, the film thickness of this coating film is too small to obtain a good liquid crystal alignment film. On the other hand, when the solid content concentration exceeds 10% by weight, it is difficult to obtain a good liquid crystal alignment film because the film thickness is excessive, and the viscosity of the photoalignment agent is increased, resulting in poor coating characteristics. It becomes.

  The particularly preferable solid content concentration range varies depending on the method used when the photo-alignment agent is applied to the substrate. For example, when the spinner method is used, the solid content concentration is particularly preferably in the range of 1.5 to 4.5% by weight. In the case of the printing method, it is particularly preferable that the solid content concentration is in the range of 3 to 9% by weight, and thereby the solution viscosity is in the range of 12 to 50 mPa · s. In the case of the inkjet method, it is particularly preferable that the solid content concentration is in the range of 1 to 5% by weight, and thereby the solution viscosity is in the range of 3 to 15 mPa · s. The temperature at the time of preparing the photo-alignment agent of the present invention is preferably 10 to 50 ° C, more preferably 20 to 30 ° C.

<Liquid crystal alignment film>
The liquid crystal alignment film in the present invention is formed using the photoalignment agent prepared as described above. The liquid crystal alignment film is preferably applied to a TN type, STN type, or lateral electric field type liquid crystal display element. In particular, application to a horizontal electric field type liquid crystal display element such as an IPS type or an FFS type is preferable because the effect of reducing the burn-in of the liquid crystal display element can be maximized.

  The liquid crystal alignment film in the present invention is a film forming process in which the photo-alignment agent of the present invention is applied onto a substrate to form a coating film, and a light irradiation process in which the formed coating film is irradiated with light to form a liquid crystal alignment film. And can be manufactured by a method including:

[Film formation process]
In this step, the coating film is formed on the substrate by coating the photo-alignment agent of the present invention on the substrate and then heating the coated surface.

When applied to a TN-type or STN-type liquid crystal display element, a pair of two substrates provided with a patterned transparent conductive film is used as a pair, and the photo-alignment agent of the present invention is formed on each transparent conductive film formation surface. Is applied to form a coating film. On the other hand, when applied to a horizontal electric field type liquid crystal display element, a pair of a substrate having an electrode made of a patterned transparent conductive film or metal film on one side and a counter substrate on which no electrode is provided, A coating film is formed by applying the photo-alignment agent of the present invention on one side of the counter substrate.
In either case, as the substrate, for example, a glass such as float glass or soda glass, a transparent substrate made of a plastic such as polyethylene terephthalate, polybutylene terephthalate, polyethersulfone, or polycarbonate can be used. As the transparent conductive film, for example, an ITO film made of In ₂ O ₃ —SnO _{2 or} a NESA (registered trademark) film made of SnO ₂ can be used. As the metal film, for example, a film made of a metal such as chromium can be used. For patterning the transparent conductive film and the metal film, for example, a patternless transparent conductive film is formed and then a pattern is formed by a photo-etching method, a sputtering method, or the like; a mask having a desired pattern is formed when forming the transparent conductive film The method used; Further, when applying the photo-alignment agent, in order to further improve the adhesion between the substrate, the conductive film or the electrode and the coating film, a functional silane compound, You may give the pretreatment which apply | coats a titanium compound etc. previously.

  Application of the photoalignment agent to the substrate can be preferably performed by a coating method such as an offset printing method, a spin coating method, a roll coater method, or an ink jet printing method. After applying the photo-alignment agent, preheating (pre-baking) is preferably performed (pre-baking step) for the purpose of preventing dripping of the applied photo-alignment agent. The pre-baking temperature is preferably 30 to 200 ° C, more preferably 40 to 150 ° C, and particularly preferably 40 to 100 ° C. The pre-bake time is preferably 0.25 to 10 minutes, and more preferably 0.5 to 5 minutes. Then, the post-baking process which bakes the coating film after a prebaking is implemented in order to remove a solvent completely and to thermally imidize the amic acid structure which exists in a polymer as needed. The post-bake temperature at this time is preferably 80 to 300 ° C, more preferably 120 to 250 ° C. The post-bake time is preferably 5 to 200 minutes, more preferably 10 to 100 minutes. The film thickness of the coating film after post-baking is preferably 0.001-1 μm, more preferably 0.005-0.5 μm.

[Light irradiation process]
In this step, liquid crystal alignment ability is imparted by irradiating polarized or non-polarized radiation to the coating film formed on the substrate. As the radiation, for example, ultraviolet rays and visible rays including light having a wavelength of 150 to 800 nm can be used. When the radiation is polarized light, it may be linearly polarized light or partially polarized light. When the radiation used is linearly polarized light or partially polarized light, irradiation may be performed from a direction perpendicular to the substrate surface, an oblique direction, or a combination thereof. When non-polarized radiation is irradiated, the irradiation direction is an oblique direction.
As a light source to be used, 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. Ultraviolet rays in a preferable wavelength region can be obtained by means of using a light source in combination with, for example, a filter or a diffraction grating.
Light irradiation is [1] a method of irradiating the coating film after the post-baking process, [2] a method of irradiating the coating film after the pre-baking process and before the post-baking process, [3] a pre-baking process, and It can be performed by a method of irradiating the coating film during heating of the coating film in at least one of the post-baking steps. The method [2] is preferred because the effect of reducing the burn-in in the liquid crystal display element is high. The amount of light irradiation is preferably 100 to 50,000 J / m ² , more preferably 300 to 20,000 J / m ² . Moreover, you may perform light irradiation with respect to a coating film, heating a coating film, in order to improve the reactivity. The temperature at the time of heating is 30-250 degreeC normally, Preferably it is 40-200 degreeC, More preferably, it is 50-150 degreeC. Thus, a liquid crystal alignment film is formed on the substrate.

<Liquid crystal display element>
The liquid crystal display element of this invention comprises the liquid crystal alignment film obtained above. The liquid crystal display element of this invention can be manufactured as follows, for example. First, a pair of substrates on which a liquid crystal alignment film is formed as described above is prepared, and a liquid crystal cell having a configuration in which liquid crystals are sandwiched between the pair of substrates is manufactured. In order to manufacture a liquid crystal cell, the following two methods are mentioned, for example. The first method is a conventionally known method. First, two substrates are arranged to face each other through a gap (cell gap) so that the respective liquid crystal alignment films face each other, and the peripheral portions of the two substrates are bonded together using a sealant, and the substrate surface and the seal are bonded. In this method, a liquid crystal cell is manufactured by injecting and filling liquid crystal into a cell gap partitioned by an agent, and then sealing an injection hole.
The second method is a method called an ODF (One Drop Fill) method. First, for example, an ultraviolet light curable sealant is applied to a predetermined place on one substrate, and liquid crystal is dropped on the surface of the liquid crystal alignment film, and then the other substrate is attached so that the liquid crystal alignment film faces each other. Then, the entire surface of the substrate is irradiated with ultraviolet light to cure the sealant, thereby manufacturing a liquid crystal cell. In any case, it is desirable to remove the flow alignment at the time of filling the liquid crystal by heating the liquid crystal cell to a temperature at which the liquid crystal used has an isotropic phase and then gradually cooling it to room temperature. And the liquid crystal display element of this invention can be obtained by bonding a polarizing plate on the outer surface of a liquid crystal cell. In addition, when the radiation is linearly polarized light, by appropriately adjusting the angle between the polarization direction of the irradiated radiation and the angle between each substrate and the polarizing plate for the two substrates on which the liquid crystal alignment film is formed, A desired liquid crystal display element can be obtained.

As the sealing agent, for example, an aluminum oxide sphere as a spacer and an epoxy resin containing a curing agent can be used.
As the liquid crystal, for example, nematic liquid crystal, smectic liquid crystal, and the like can be used, and among them, those having positive dielectric anisotropy that form nematic liquid crystal are preferable. For example, biphenyl liquid crystal, phenyl cyclohexane liquid crystal, ester liquid crystal Terphenyl liquid crystal, biphenyl cyclohexane liquid crystal, pyrimidine liquid crystal, dioxane liquid crystal, bicyclooctane liquid crystal, cubane liquid crystal and the like are used. In addition, cholesteric liquid crystals such as cholesteryl chloride, cholesteryl nonate, cholesteryl carbonate, etc .; chiral agents such as those sold under the trade names “C-15” and “CB-15” (from Merck); A ferroelectric liquid crystal such as p-decyloxybenzylidene-p-amino-2-methylbutylcinnamate may be further added and used.
Examples of the polarizing plate include a polarizing plate formed by sandwiching a polarizing film called an “H film” in which iodine is absorbed while stretching and aligning polyvinyl alcohol with a cellulose acetate protective film, and a polarizing plate made of the H film itself.

  The liquid crystal display element of the present invention has a liquid crystal alignment film formed by a photo-alignment method using the photo-alignment agent of the present invention, and therefore, when applied to a liquid crystal display element of a horizontal electric field method, High voltage holding ratio is shown. Therefore, the liquid crystal display element of the present invention can be effectively applied to various devices, such as watches, portable games, word processors, notebook computers, car navigation systems, camcorders, PDAs, digital cameras, mobile phones, smartphones. It can be suitably applied as a liquid crystal display element used in display devices such as various monitors, liquid crystal televisions, and information displays.

  EXAMPLES Hereinafter, the present invention will be described more specifically with reference to examples, but the present invention is not limited to these examples.

The weight average molecular weight of each polymer in the synthesis example, the solution viscosity of each polymer solution, and the imidization rate were measured by the following methods.
[Weight average molecular weight of polymer]
The weight average molecular weight Mw of the polymer is a polystyrene equivalent value measured by gel permeation chromatography under the following conditions.
Column: Tosoh Co., Ltd., TSKgelGRCXLII
Solvent: Tetrahydrofuran Temperature: 40 ° C
Pressure: 68 kgf / cm ²
[Solution viscosity of polymer solution]
The solution viscosity [mPa · s] of the polymer solution was measured at 25 ° C. using an E-type rotational viscometer for a solution prepared with N-methyl-2-pyrrolidone (NMP) to a polymer concentration of 10% by weight. did.
[Measurement of imidization rate]
The polyimide solution was poured into pure water, and the resulting precipitate was sufficiently dried under reduced pressure at room temperature, then dissolved in deuterated dimethyl sulfoxide, and ¹ H-NMR was measured at room temperature using tetramethylsilane as a reference substance. From the obtained ¹ H-NMR spectrum, the imidation ratio [%] was determined by the formula represented by the following formula (1).
Imidation ratio [%] = (1-A ¹ / A ² × α) × 100 (1)
(In Formula (1), A ¹ is a peak area derived from protons of NH groups appearing near a chemical shift of 10 ppm, A ² is a peak area derived from other protons, and α is a precursor of a polymer (polyamic acid). The number ratio of other protons to one proton of NH group in)

<Synthesis of polymer>
Polymers (A-1) to (A-14) and polymers (B-1) to (B-7) were synthesized using the following compounds in each synthesis example.

<Tetracarboxylic acid derivative>
・ Specific tetracarboxylic dianhydride

（式（ｔ−６）中、Ｒはエチル基である。式（ｔ−１２）中、ｍは１〜１５の整数である。） ・ Other tetracarboxylic dianhydrides and tetracarboxylic diesters

(In Formula (t-6), R is an ethyl group. In Formula (t-12), m is an integer of 1-15.)

<Diamine>
・ Specific diamine

・ Other diamines

＜（Ａ）重合体の合成＞
・ポリイミドの合成
［合成例ａ１：重合体（Ａ−１）の合成］
テトラカルボン酸二無水物として化合物（ａ−２）を１００モル部、ジアミンとして化合物（ｂ−１）を７０モル部、及び化合物（ｄ−７）を３０モル部、をＮ−メチル−２−ピロリドン（ＮＭＰ）に溶解させ、室温で６時間反応させた。これにより、固形分濃度１５％のポリアミック酸溶液を得た。次いで、得られたポリアミック酸溶液に、Ｎ−メチルピペリジン及び無水酢酸をそれぞれテトラカルボン酸二無水物の使用量に対して０．５倍モル添加して、７５℃で３時間脱水閉環反応を行った。脱水閉環後、系内の溶剤を新たなＮＭＰで溶剤置換し、イミド化率３０％のポリイミドを１５重量％含有する溶液を得た。このポリイミドを重合体（Ａ−１）とした。重合体（Ａ−１）の重量平均分子量Ｍｗは５０，０００であった。 <Monoamine>

<(A) Synthesis of polymer>
Synthesis of polyimide [Synthesis Example a1: Synthesis of Polymer (A-1)]
100 mol parts of compound (a-2) as tetracarboxylic dianhydride, 70 mol parts of compound (b-1) as diamine, and 30 mol parts of compound (d-7) as N-methyl-2- It was dissolved in pyrrolidone (NMP) and reacted at room temperature for 6 hours. As a result, a polyamic acid solution having a solid concentration of 15% was obtained. Next, N-methylpiperidine and acetic anhydride were added to the obtained polyamic acid solution in a molar amount of 0.5 times the amount of tetracarboxylic dianhydride, respectively, and a dehydration ring-closing reaction was performed at 75 ° C. for 3 hours. It was. After dehydration and ring closure, the solvent in the system was replaced with new NMP to obtain a solution containing 15% by weight of polyimide having an imidization rate of 30%. This polyimide was used as a polymer (A-1). The weight average molecular weight Mw of the polymer (A-1) was 50,000.

[Synthesis Example a7: Synthesis of Polymer (A-7)]
Except having changed the kind and quantity of the tetracarboxylic dianhydride and diamine to be used as shown in Table 1 below, the same operation as in Synthesis Example a1 was performed to synthesize a polyimide having an imidization ratio of 35%. The obtained polyimide was used as a polymer (A-7). The weight average molecular weight Mw of the polymer (A-7) was 80,000.
[Synthesis Example a10: Synthesis of Polymer (A-10)]
The same operations as in Synthesis Example a1 except that the types and amounts of tetracarboxylic dianhydride and diamine used are changed as shown in Table 1 below and that 20 mol parts of compound (m-1) is added as a monoamine. To synthesize a polyimide having an imidization ratio of 20%. The obtained polyimide was used as a polymer (A-10). The weight average molecular weight Mw of the polymer (A-10) was 95,000.

Synthesis of polyamic acid [Synthesis Example a2: Synthesis of polymer (A-2)]
50 mol parts of compound (a-2) as tetracarboxylic dianhydride, 40 mol parts of compound (a-15), 10 mol parts of compound (a-12), and compound (b-5) as diamine 80 mol parts and 20 mol parts of the compound (d-8) were dissolved in NMP and reacted at room temperature for 8 hours. As a result, a polyamic acid solution having a solid concentration of 15% was obtained. The obtained polyamic acid was used as the polymer (A-2). The weight average molecular weight Mw of the polymer (A-2) was 40,000.
[Synthesis Examples a4 to a6, a8, a14: Synthesis of Polymers (A-4) to (A-6), (A-8), (A-14)]
Except having changed the kind and quantity of the tetracarboxylic dianhydride and diamine to be used as shown in Table 1 below, the same operation as in Synthesis Example a2 was performed to obtain a polyamic acid solution having a solid content concentration of 10%. Table 1 below shows the weight average molecular weight Mw of each polymer.

[Synthesis Examples a9 and a11: Synthesis of Polymers (A-9) and (A-11)]
Synthesis Example a2 except that the type and amount of tetracarboxylic dianhydride and diamine used are changed as shown in Table 1 below, and the compound (m-1) or compound (m-2) is added as a monoamine. The same operation was performed to obtain a polyamic acid solution having a solid content concentration of 10%. Table 1 below shows the weight average molecular weight Mw of each polymer.

Synthesis of polyamic acid ester [Synthesis Example a3: Synthesis of polymer (A-3)]
70 mol parts of compound (t-3) and 30 mol parts of compound (t-8) as tetracarboxylic dianhydride, 90 mol parts of compound (b-10) as diamine, and 10 of (d-8) The molar part was dissolved in NMP and reacted at room temperature for 6 hours. Further, 80 mol parts of N, N-dimethylformamide diethyl acetal was added dropwise to this reaction solution, and then reacted at 50 ° C. for 2 hours to obtain a polyamic acid ester solution. The weight average molecular weight of the polymer (A-3) was 120,000.

[Synthesis Example a12: Synthesis of Polymer (A-12)]
30 g of compound (t-5) as tetracarboxylic dianhydride was added to 500 mL of ethanol to obtain a tetracarboxylic acid diester. The resulting precipitate was separated by filtration, washed with ethanol, and then dried under reduced pressure to obtain a tetracarboxylic acid diester powder. After 15 mol parts of the obtained tetracarboxylic acid diester (compound (t-6)), 70 mol parts of compound (a-2), and 15 mol parts of compound (t-11) were dissolved in NMP Then, 100 mol parts of the compound (b-10) as a diamine was added and dissolved. To this solution, 300 mol parts of 4- (4,6-dimethoxy-1,3,5-triazin-2-yl) -4-methylmorpholinium chloride (DMT-MM, 15 ± 2 wt% hydrate). Was added and reacted at room temperature for 4 hours to obtain a polyamic acid ester solution. The weight average molecular weight Mw of the polymer (A-12) was 40,000.

[Synthesis Example a13: Synthesis of Polymer (A-13)]
Except having changed the kind and quantity of the tetracarboxylic acid diester, tetracarboxylic dianhydride, and diamine to be used as shown in Table 1 below, the same procedure as in Synthesis Example a12 was performed to obtain a polyamic acid ester solution having a solid content concentration of 10%. Got. The weight average molecular weight Mw of the polymer (A-13) was 65,000.

<(B) Synthesis of polymer>
[Synthesis Examples b1 to b7: Synthesis of Polymers (B-1) to (B-7)]
Except having changed the kind and quantity of the tetracarboxylic dianhydride and diamine to be used as shown in Table 2 below, the same operation as in Synthesis Example a2 was performed to obtain a polyamic acid solution having a solid content concentration of 10%. The weight average molecular weight Mw of each polymer is shown in Table 2 below.

  In Tables 1 and 2, the numerical values in parentheses in each column of the compound indicate a blending ratio (mole part) with respect to a total of 100 parts by mole of the tetracarboxylic acid derivative used.

[Example 1]
<Preparation of photo-alignment agent>
In a solution containing 50 parts by weight of the polymer (A-1) obtained in Synthesis Example 1 and 50 parts by weight of the polymer (B-1) obtained in Synthesis Example 15 as a polymer component, NMP and butyl cellosolve (BC) were added and stirred sufficiently to obtain a solution having a solvent composition of NMP: BC = 70: 30 (weight ratio) and a solid content concentration of 3.0% by weight. A photoalignment agent was prepared by filtering this solution using a filter having a pore diameter of 0.45 μm.

<Manufacture of liquid crystal display elements>
A glass substrate having two metal electrodes (electrode A and electrode B) made of chromium patterned in a comb shape and capable of applying a voltage independently to the electrodes A and B was prepared. A pair of this glass substrate and a counter glass substrate on which no electrode is provided, and the photo-alignment agent prepared above is applied to the surface having the electrode of the glass substrate and one surface of the counter glass substrate using a spinner, respectively. did. Next, pre-baking is performed on an 80 ° C. hot plate for 1 minute, and then polarized ultraviolet rays 10,000 J / m ² are applied to the substrate surface on which the photo-alignment agent is applied using a Hg-Xe lamp and a Grand Taylor prism. Irradiated from the direction perpendicular to the surface. After irradiating with light, it was heated (post-baked) at 200 ° C. for 1 hour in an oven in which the inside of the chamber was replaced with nitrogen. This obtained a pair of board | substrate which has a liquid crystal aligning film with a film thickness of 0.1 micrometer.
Next, an epoxy resin adhesive containing aluminum oxide spheres having a diameter of 3.5 μm is applied to the outer periphery of the surface having one liquid crystal alignment film of the pair of substrates by screen printing, and the liquid crystal alignment film surfaces of the pair of substrates are then applied. It was made to oppose and it overlap | superposed and crimped | bonded so that the direction of each board | substrate might be reverse when irradiated with polarized ultraviolet rays, and the adhesive was thermoset at 150 degreeC over 1 hour. Next, liquid crystal “MLC-7028” manufactured by Merck was filled in the gap between the substrates from the liquid crystal injection port, and then the liquid crystal injection port was sealed with an epoxy adhesive. Furthermore, in order to remove the flow alignment at the time of liquid crystal injection, this was heated at 150 ° C. and then gradually cooled to room temperature. Next, a liquid crystal display is formed by bonding polarizing plates on both outer surfaces of the substrate so that the polarization directions thereof are orthogonal to each other and the optical axis of polarized ultraviolet light of the liquid crystal alignment film is orthogonal to the projection direction onto the substrate surface. A device was manufactured. In addition, by performing the above series of operations by changing the ultraviolet irradiation amount before pre-baking, three or more liquid crystal display elements having different ultraviolet irradiation amounts were manufactured.

<Evaluation of liquid crystal display element>
The following (1) to (5) were evaluated using the liquid crystal display device manufactured above. In addition, for the following (2) to (4), based on the result of the sensitivity evaluation similar to (1), the one having the optimum sensitivity among the three or more liquid crystal display elements having different ultraviolet irradiation amounts is used. The results of evaluation of the liquid crystal display device with the optimum sensitivity were selected.

(1) Evaluation of sensitivity to ultraviolet rays Using the liquid crystal display element produced as described above, the presence or absence of abnormal domains in the change in brightness when a voltage of 5 V was applied / released was observed with an optical microscope. It can be said that the sensitivity of the coating film to ultraviolet rays is better as the amount of ultraviolet irradiation when the liquid crystal orientation is observed (when no abnormal domain is observed) is smaller. Evaluation, when the abnormal domain was not observed in any of the amount of UV irradiation sensitivity "good", but abnormal domain was observed in the amount of ultraviolet irradiation of ^{5,000J / m 2, 7,000J / m} 2 and 10 , sensitivity if the abnormal domain was not observed in the ultraviolet irradiation amount of 000J / ^{m 2} "possible", the case where abnormal domain was observed in the amount of ultraviolet irradiation of 5,000J / ^{m 2} and 7,000J / ^{m 2} The sensitivity was “impossible”.
(2) Evaluation of voltage holding ratio Using the liquid crystal display device manufactured as described above, a voltage of 5 V was applied at 60 ° C. with an application time of 60 microseconds and a span of 167 milliseconds, and 167 milliseconds after the application release. The voltage holding ratio was measured. The measuring device used was “VHR-1” manufactured by Toyo Corporation. The voltage holding ratio of this liquid crystal display element was 99%.
(3) Measurement of charge storage amount (RDC) Using the liquid crystal display device manufactured as described above, a DC voltage of 2 V was applied at 71 ° C. for 10 minutes, then shorted for 0.2 seconds, and then opened for 10 minutes. The voltage accumulated in the liquid crystal display element when kept in the state was measured by a dielectric absorption method. The evaluation is “good (）)” when the charge accumulation amount is 0.1 V or less, “good (◯)” when the charge accumulation amount is greater than 0.1 V and 0.2 V or less, and the charge accumulation amount. Is larger than 0.2V, it was defined as “defective (Δ)”. As a result, it was possible to evaluate the charge accumulation amount of this liquid crystal display element.

(4) Evaluation of AC afterimage characteristics The AC afterimage characteristics (burn-in characteristics) were evaluated using the liquid crystal display device manufactured above. First, the liquid crystal display element was placed in an environment of 25 ° C. and 1 atmosphere, and an AC voltage of 4 V was applied to the electrode A for 2 hours without applying a voltage to the electrode B. Immediately thereafter, an AC voltage of 4 V was applied to both electrode A and electrode B. The time from when the voltage of 4V AC was started to be applied to both electrodes until the difference in light transmittance between the electrodes A and B could not be visually confirmed was measured. If this time is less than 60 seconds, the image sticking property is “good (◎)”, if it is 60 seconds or more and less than 100 seconds, the image sticking property is “good (◯)”, and if it is 100 seconds or more, the image sticking property. “Not possible (×)”. As a result, this liquid crystal display element had “good” image sticking characteristics.
(5) Evaluation of contrast after driving stress Using the apparatus in which the liquid crystal display element manufactured above is driven with an AC voltage of 10 V for 30 hours and a polarizer and an analyzer are disposed between the light source and the light amount detector, The minimum relative transmittance (%) represented by the following formula (2) was measured.
Minimum relative transmittance (%) = (β−B ⁰ ) / (B ¹⁰⁰ −B ⁰ ) × 100 (2)
(In Formula (2), B ⁰ is the transmission amount of light under a blank and crossed Nicols. B ¹⁰⁰ is the transmission amount of light under a blank and paranicols. Β is a polarizer under crossed Nicols. (This is the minimum light transmission amount with the liquid crystal display element sandwiched between the analyzers.)
The black level in the dark state is represented by the minimum relative transmittance of the liquid crystal display element, and the smaller the black level in the dark state, the better the contrast. A sample having a minimum relative transmittance of less than 0.5% was evaluated as “good”, a sample having a minimum relative transmittance of less than 0.5% and less than 1.0% was evaluated as “good”, and a sample having a minimum relative transmittance of 1.0% or more was determined as “bad”. As a result, the contrast evaluation of this liquid crystal display element was determined to be “good”.

[Examples 2, 6 to 10, 12, 13, 14, Comparative Examples 1 to 3]
A photoalignment agent was prepared in the same manner as in Example 1 except that the type of polymer used was changed as shown in Tables 3 and 4 below, and a liquid crystal display device was produced. Moreover, various evaluations of the manufactured liquid crystal display element were performed. The evaluation results are shown in Tables 3 and 4 below.
[Examples 3-5, 11, 15]
A liquid crystal display device is manufactured by preparing a photoalignment agent in the same manner as in Example 1 except that the type of polymer used is changed as shown in Tables 3 and 4 below, and the additive is added. did. Moreover, various evaluations of the manufactured liquid crystal display element were performed. The evaluation results are shown in Tables 3 and 4 below.

In Table 3 and Table 4, the numerical value in the blending amount column of the polymer indicates the blending ratio (parts by weight) of each polymer with respect to 100 parts by weight in total of the polymers used for the preparation of the photoalignment agent. The names of the additives are as follows.
[Additive]
Q-1: N, N, N ′, N′-tetraglycidyl-4,4′-diaminodiphenylmethane (the following compound (Q-1))
Q-2: The following compound (Q-2)

  As shown in Tables 3 and 4, in Examples 1 to 13, the voltage holding ratio was 99% or more, and the charge accumulation amount was small. Further, the AC afterimage characteristics, the contrast characteristics, and the sensitivity to ultraviolet rays were “good” or “good”, and various characteristics were balanced. Similar results were obtained in Examples 14 and 15. On the other hand, in Comparative Examples 1 to 3, the voltage holding ratio was as low as less than 99% and the charge accumulation amount was large.

<(A) Synthesis of polymer [2]>
Except having changed the kind and quantity of the tetracarboxylic dianhydride and diamine to be used as shown in Table 5 below, the same operation as in Synthesis Example a2 was performed to obtain a polyamic acid solution having a solid content concentration of 10% by weight. Table 5 below shows the weight average molecular weight Mw of each polymer.

表５中、化合物の各欄の括弧内の数値は、使用したテトラカルボン酸誘導体の合計１００モル部に対する配合割合（モル部）を示す。

In Table 5, the numerical value in the parenthesis in each column of the compound indicates the blending ratio (mole part) with respect to 100 mol parts in total of the tetracarboxylic acid derivative used.

<Preparation of photo-alignment agent and production and evaluation of liquid crystal display element [2]>
[Examples 16 to 21]
A liquid crystal display element was produced while preparing a photoalignment agent in the same manner as in Example 1 except that the type of polymer used was changed as shown in Table 6 below. Moreover, various evaluations of the manufactured liquid crystal display element were performed. The evaluation results are shown in Table 6 below.

表６中、重合体の配合量欄の数値は、光配向剤の調製に使用した重合体の合計１００重量部に対する各重合体の配合割合（重量部）を示す。

In Table 6, the numerical value in the blending amount column of the polymer indicates the blending ratio (parts by weight) of each polymer with respect to 100 parts by weight of the polymer used for the preparation of the photoalignment agent.

  As shown in Table 6, in Examples 16 to 21, the voltage holding ratio, the charge accumulation amount, the AC afterimage characteristics, the contrast characteristics, and the sensitivity to ultraviolet rays are all evaluated as “good” or “good”, and the balance of various characteristics. Was removed.

Claims (14)

A method of manufacturing a liquid crystal alignment film of a horizontal electric field type liquid crystal display element,
The (A) polymer and the (B) polymer are included as at least one polymer component selected from the group consisting of polyamic acid, polyamic acid ester and polyimide, and the (A) polymer is represented by the following formula (1): A step of applying a liquid crystal aligning agent, which is a polymer having a structure (Y 2 ) in the main chain, on a substrate to form a coating film;
And a step of irradiating the coating film with light to form a liquid crystal alignment film.

(In the formula (1), X ¹ is a sulfur atom or SansoHara child. "*" Indicates the respective bond. However, at least one of the two "*" is bonded to an aromatic ring. )   The manufacturing method of the liquid crystal aligning film of Claim 1 with which the content rate of the at least 1 type of specific atom of a fluorine atom and a silicon atom differs with the said (A) polymer and the said (B) polymer.   The method for producing a liquid crystal alignment film according to claim 2, wherein the (A) polymer has a higher content of the specific atom than the (B) polymer.   4. The production of the liquid crystal alignment film according to claim 2, wherein in the polymer having the specific atom, the content ratio of the repeating unit having the specific atom is 1 to 70 mol% with respect to all the repeating units of the polymer. Method.   The content ratio of the (A) polymer and the (B) polymer is 2/8 to 8/2 in weight ratio (A / B), according to any one of claims 1 to 4. A method for producing a liquid crystal alignment film. At least one of the (A) polymer and the (B) polymer has a structure represented by the following formula (2-1), a structure represented by the following formula (2-2) (however, a monomer And at least one structure (Z) selected from the group consisting of nitrogen-containing heterocycles. A method for producing a liquid crystal alignment film.

(In Formula (2-1), R ¹ is a halogen atom, an alkyl group having 1 to 10 carbon atoms, or an alkoxy group having 1 to 10 carbon atoms, r 1 is an integer of 0 to 2, and r 2 is 0 to 3 of an integer. However, satisfy r1 + r2 ≦ 4. "* 1" represents a bond in. formula (2-2), ^{R 2} is a hydrogen atom or an alkyl group having 1 to 6 carbon atoms. “* 2” indicates a bond.)   The liquid crystal aligning film of Claim 6 whose content rate of the repeating unit which has the said structure (Z) with respect to all the repeating units of the said polymer is 2-40 mol% in the polymer which has the said structure (Z). Manufacturing method. At least one of the (A) polymer and the (B) polymer has at least one specific atom of a fluorine atom and a silicon atom,
The production of the liquid crystal alignment film according to claim 6 or 7, wherein a polymer having a lower content of the specific atom among the (A) polymer and the (B) polymer has the structure (Z). Method.   The method for producing a liquid crystal alignment film according to claim 6, wherein the polymer (B) has the structure (Z). The (A) polymer has the structure (Y) and at least one specific atom of a fluorine atom and a silicon atom,
The said (B) polymer has the said structure (Z), and the content rate of the said specific atom is lower than the said (A) polymer, The liquid crystal orientation as described in any one of Claims 6-9. A method for producing a membrane.   The polymer (B) is 2,3,5-tricarboxycyclopentyl acetic acid dianhydride, bicyclo [3.3.0] octane-2,4,6,8-tetracarboxylic acid 2: 4,6: 8. Dianhydride, 1,3,3a, 4,5,9b-hexahydro-8-methyl-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1 , 3-dione, 1,3,3a, 4,5,9b-hexahydro-5- (tetrahydro-2,5-dioxo-3-furanyl) -naphtho [1,2-c] furan-1,3-dione , 1,2,3,4-cyclobutanetetracarboxylic dianhydride, cyclopentanetetracarboxylic dianhydride, and tetracarboxylic dianhydride containing at least one selected from the group consisting of cyclohexanetetracarboxylic dianhydride And Zia A polymer obtained and emissions are reacted, a method of manufacturing a liquid crystal alignment film according to any one of claims 1 to 10. The said (A) polymer is a manufacturing method of the liquid crystal aligning film as described in any one of Claims 1-11 which has a structure represented by following formula (3) in a principal chain.

(In formula (3), k and i are each independently 0 or 1, l is an integer of 2 to 9, and j is an integer of 1 to 4. "*" represents a bond. .) A photo-alignment agent for forming a liquid crystal alignment film of a horizontal electric field type liquid crystal display element,
The (A) polymer and the (B) polymer are included as at least one polymer component selected from the group consisting of polyamic acid, polyamic acid ester and polyimide, and the (A) polymer is represented by the following formula (1): A photo-alignment agent, which is a polymer having a structure (Y 2 ) represented by

(In the formula (1), X ¹ is a sulfur atom or SansoHara child. "*" Indicates the respective bond. However, at least one of the two "*" is bonded to an aromatic ring. ) A transverse electric field type liquid crystal display device comprising the liquid crystal alignment film produced by the method according to claim 1.