KR20150070288A

KR20150070288A - Composition, liquid crystal aligning agent, liquid crystal alignment film, and liquid crystal display element

Info

Publication number: KR20150070288A
Application number: KR1020157012504A
Authority: KR
Inventors: 노리토시 미키; 준 하시모토; 고헤이 고토; 가즈요시 호사카
Original assignee: 닛산 가가쿠 고교 가부시키 가이샤
Priority date: 2012-10-18
Filing date: 2013-10-18
Publication date: 2015-06-24
Also published as: TW201430054A; CN104854193A; JP5950137B2; CN104854193B; TWI542632B; JPWO2014061779A1; WO2014061779A1; KR20170027886A

Abstract

A composition comprising the following components (A), (B) and (C). Component (A): At least one solvent selected from the following formula [1a] or formula [1b].

(In the formula [1a], X ¹ represents an alkyl group having 1 to 3 carbon atoms, and in the formula [1b], X ² represents an alkyl group having 1 to 3 carbon atoms. Component (B): at least one polymer selected from a polyimide precursor or polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component. (C): Polysiloxane obtained by polycondensation of an alkoxysilane containing any one of alkoxysilanes represented by the following formula [A1], formula [A2] or formula [A3].

Description

TECHNICAL FIELD [0001] The present invention relates to a composition, a liquid crystal alignment treatment agent, a liquid crystal alignment film and a liquid crystal display element,

The present invention relates to a composition used for forming a resin film, a liquid crystal alignment treatment agent used in the production of a liquid crystal display element, a liquid crystal alignment film obtained from the liquid crystal alignment treatment agent, and a liquid crystal display element using the liquid crystal alignment film.

The resin film made of an organic material such as a polymer material is widely used as an interlayer insulating film or a protective film in an electronic device, with attention being paid to ease of formation and insulation performance. Among them, in a liquid crystal display element well known as a display device, a resin film made of an organic material is used as a liquid crystal alignment film.

At present, a polyimide-based organic film having excellent durability is used as a resin film used industrially. This polyimide-based organic film is formed of a composition containing a polyimide precursor polyamide acid or polyimide. That is, the polyimide-based organic film is formed by applying a composition containing polyamic acid or polyimide to the substrate, followed by a firing process. At that time, usually, these compositions use a solvent having a high boiling point such as N-methyl-2-pyrrolidone (also referred to as NMP) or? -Butyrolactone (also referred to as? -BL) It is necessary to sinter at a high temperature of about 300 DEG C (see, for example, Patent Document 1).

In recent years, a resin film formed of a composition containing a polyimide-based polymer (polyimide precursor and polyimide) and a polysiloxane is used for an interlayer insulating film, a protective film, and a liquid crystal alignment film. In particular, a liquid crystal alignment treatment agent and a liquid crystal alignment film containing a polyimide-based polymer and a polysiloxane have been proposed in order to improve reliability accompanying long-term driving of a liquid crystal display element (see, for example, Patent Document 2).

Japanese Laid-Open Patent Publication No. 09-278724 Japanese Laid-Open Patent Publication No. 2010-097007

When a liquid crystal alignment film containing a polyimide-based polymer is used to form a liquid crystal alignment film, the firing process is required to be fired at a high temperature even in the process for producing the liquid crystal display device for the reasons described above. This is because, even in the case of a liquid crystal alignment treatment agent containing a polyimide-based polymer and a polysiloxane, baking at a high temperature is required because NMP or? -BL is used as a solvent for dissolving a polyimide-based polymer. However, when a substrate of a liquid crystal display element is replaced by a thin and lightweight plastic substrate having low heat resistance instead of a usual glass substrate, firing at a lower temperature is required. Similarly, in order to suppress deterioration of color characteristics of a color filter of a liquid crystal display element accompanied by firing at a high temperature, and further to reduce the energy cost in the production of a liquid crystal display element, do.

In addition, a liquid crystal alignment treatment agent obtained from a polymer solution in which a polyimide-based polymer is dissolved and a polysiloxane in NMP or? -BL, which are commonly used solvents, is used in combination with NMP or? -BL having high polarity and polysiloxane having high hydrophobicity The sex is getting worse. As a result, when this liquid crystal alignment treatment agent is applied to the substrate, pinholes accompanying cratering are likely to be generated on the liquid crystal alignment film. That is, in a liquid crystal alignment treatment agent containing a conventional polyimide-based polymer and a polysiloxane, alignment defects accompanying pinholes are apt to occur.

The liquid crystal alignment film is formed by applying a liquid crystal alignment treatment agent to a substrate and then firing the coating film. At this time, for the purpose of raising the coating film property (also referred to as coatability) of the liquid crystal alignment film, that is, for suppressing the occurrence of pinholes accompanying cratering, it is required to improve the wetting and diffusing property of the liquid crystal alignment treatment agent .

The resin film obtained from the composition containing the polyimide-based polymer and the polysiloxane is excellent in the chemical stability of the resin film obtained from the composition containing no polysiloxane, and in addition to the liquid crystal alignment film, It is also used as an insulating film or a protective film. Also in these films, it is necessary to form a resin film by baking at a low temperature and to improve the coating property of the resin film. By performing firing at a low temperature, the energy cost in manufacturing can be reduced. Further, by the improvement of the coating property, occurrence of pinholes accompanying cratering on the resin coating can be suppressed.

Therefore, the present invention aims to provide a composition having the above characteristics. That is, the object of the present invention is to provide a composition capable of forming a resin coating film by firing at a low temperature in a composition containing a polyimide-based polymer and a polysiloxane. It is another object of the present invention to provide a composition capable of suppressing occurrence of pinholes accompanying cratering when forming a resin film.

It is another object of the present invention to provide a liquid crystal alignment treatment agent capable of forming a liquid crystal alignment film by firing at a low temperature in the liquid crystal alignment treatment agent using the above-described composition. It is another object of the present invention to provide a liquid crystal alignment treatment agent capable of suppressing generation of pinholes accompanying cratering when forming a liquid crystal alignment film.

It is another object of the present invention to provide a liquid crystal alignment film corresponding to the above-described requirement. That is, it is an object of the present invention to provide a liquid crystal alignment film which can be formed by firing at a low temperature, and to provide a liquid crystal alignment film capable of suppressing alignment defects accompanying pinholes.

Another object of the present invention is to provide a liquid crystal display element provided with a liquid crystal alignment film corresponding to the above-described requirements.

As a result of intensive studies, the present inventors have found that a polyimide precursor obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component, or a polyimide precursor obtained by reacting at least one Of a polymer and a polysiloxane having a specific structure are very effective for achieving the above object, and have completed the present invention.

That is, the present invention has the following points.

(1) A composition comprising the following components (A), (B) and (C).

Component (A): At least one solvent selected from the following formula [1a] or formula [1b].

[Chemical Formula 1]

(In the formula [1a], X ¹ represents an alkyl group having 1 to 3 carbon atoms, and in the formula [1b], X ² represents an alkyl group having 1 to 3 carbon atoms.

Component (B): at least one polymer selected from a polyimide precursor or polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component.

(C): Polysiloxane obtained by polycondensation of an alkoxysilane containing any one of alkoxysilanes represented by the following formula [A1], formula [A2] or formula [A3].

(2)

Wherein A ¹ is an aliphatic hydrocarbon, a benzene ring, a cyclohexane ring, an organic group having 8 to 35 carbon atoms having a heterocyclic or steroid structure, A ² is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, represents, a ³ is. However, each represents an alkyl group of a carbon number of 1 ~ 5, m is an integer of 1 or 2, n is an integer of 0 ~ 2, p represents an integer of 0 ~ 3 m + n + P is 4).

(3)

Wherein B ¹ represents an organic group having 2 to 12 carbon atoms and having a vinyl group, an epoxy group, an amino group, a mercapto group, an isocyanate group, a methacryl group, an acryl group, a ureide group or a cinnamoyl group, B ² each represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, B ³ each represent an alkyl group having 1 to 5 carbon atoms, m represents an integer of 1 or 2, n represents an integer of 0 to 2, p represents Represents an integer of 0 to 3, provided that m + n + p is 4).

[Chemical Formula 4]

(In the formula [A3], D ¹ is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, D ² is an alkyl group having 1 to 5 carbon atoms, and n is an integer of 0 to 3).

(2) The composition according to the above (1), wherein the component (A) is 50 to 100 mass% of the total solvent contained in the composition.

(3) The composition according to the above (1) or (2), wherein the diamine compound having a carboxyl group as the component (B) is a diamine compound having a structure represented by the following formula [2].

[Chemical Formula 5]

(In the formula [2], a represents an integer of 0 to 4).

(4) The composition according to the above (1) or (2), wherein the diamine compound having a carboxyl group as the component (B) is a diamine compound having a structure represented by the following formula [2a].

[Chemical Formula 6]

(In the formula [2a], a represents an integer of 0 to 4, and n represents an integer of 1 to 4).

(5) The composition according to the above (3) or (4), wherein the diamine compound having a carboxyl group is contained in an amount of 20 mol% to 100 mol% in the total diamines used in the component (B).

(6) The process according to any one of (1) to (5) above, wherein the diamine component of the component (B) contains at least one kind of diamine compound selected from the structures represented by the following formula [ &Lt; / RTI >

(7)

(In the formula [2b], Y represents a structure represented by the following formula [2b-1], formula [2b-2], formula [2b-3], formula [2b-4] m represents an integer of 1 to 4).

[Chemical Formula 8]

(Wherein a is an integer of 0 to 4, and Y ¹ is a single bond, - (CH ₂ ) _a - (a is an integer of 1 to 15) in the formula [2b-2] , -O-, -CH ₂ represents an O-, -COO- or -OCO-, Y ² is a single bond or - (CH ₂₎ _b - represents a (b is an integer of 1 ~ 15), Y ³ is a single _{bond, - (CH 2) c -} (c is an integer from 1 to 15), represents an -O-, -CH ₂ O-, -COO- or -OCO-, Y ⁴ is a benzene ring, a cyclohexane ring Or a divalent cyclic group selected from a heterocyclic ring or a divalent organic group having 12 to 25 carbon atoms and having a steroid skeleton, and any hydrogen atom on the cyclic group may be replaced by an alkyl group having 1 to 3 carbon atoms, an alkoxyl group having 1 to 3 carbon atoms carbon atoms and may be substituted with 1-3 fluorine-containing alkyl group, fluorine-containing alkoxy group of 1 to 3 carbon atoms or a fluorine atom of, Y ⁵ is a divalent cyclic group selected from benzene ring, a cyclohexane ring or a heterocyclic ring , And any hydrogen atom on the cyclic group may be substituted with an alkyl group having 1 to 3 carbon atoms, an alkoxyl group having 1 to 3 carbon atoms, a fluorine-containing alkyl group having 1 to 3 carbon atoms, a fluoro-containing alkoxyl group having 1 to 3 carbon atoms, may be, n represents an integer of 0 ~ 4, Y ⁶ is a fluorine-containing alkoxyl group having 1 to 18 alkyl group, having 1 to 18 fluorine-containing alkyl group, having 1 to 18 carbon atoms, an alkoxyl group or a C 1 to 18 of the represents the formula [2b-3] of the, Y ⁷ represents an alkyl group of a carbon number of 8 to 22, formula [2b-4] of, Y ⁸ and Y ⁹ are each independently a monovalent hydrocarbon group having 1 to 6 carbon atoms, formula [ 2b-5], Y ¹⁰ represents an alkyl group having 1 to 8 carbon atoms.

(7) The composition according to any one of (1) to (6), wherein the tetracarboxylic acid dianhydride component of the component (B) is a compound represented by the following formula [3].

[Chemical Formula 9]

(In the formula [3], Z ¹ is a group of at least one structure selected from the following formulas [3a] to [3j]).

[Chemical formula 10]

(Formula [3a] of, Z ² ~ Z ⁵ represents a hydrogen atom, a methyl group, a chlorine atom or a benzene ring, and also the same or different and wherein [3g], Z ⁶ and Z ⁷ represents a hydrogen atom or a methyl group And may be the same or different from each other).

(8) The positive resist composition as described in the above item (1), wherein the alkoxysilane represented by the formula (A2) of the component (C) is at least one selected from the group consisting of allyltriethoxysilane, allyltrimethoxysilane, diethoxymethylvinylsilane, dimethoxymethylvinylsilane, (Trimethoxysilyl) propyl methacrylate, 3- (trimethoxysilyl) propyl acrylate or 3- (trimethoxysilyl) propyl methacrylate, vinyltriethoxysilane, The composition according to any one of the above (1) to (7), wherein the composition is at least one selected from the group consisting of propyl methacrylate.

(9) The positive resist composition as described in any one of the above items (1) to (4), wherein the alkoxysilane represented by the formula [A2] of the component (C) is at least one member selected from the group consisting of 3-glycidyloxypropyl (dimethoxy) methylsilane, 3-glycidyloxypropyl (1) to (7) above, wherein the silane coupling agent is at least one selected from the group consisting of a silane coupling agent, a silane coupling agent, a silane coupling agent, a silyloxypropyltrimethoxysilane, and a 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane. Composition.

(10) The positive resist composition as described in any of (1) to (9) above, wherein the polysiloxane of the component (C) is a polysiloxane obtained by polycondensation of the alkoxysilane represented by the formula [A1], the formula [A2] Lt; RTI ID = 0.0 > 1, < / RTI >

(11) The liquid crystal composition according to the above (1), wherein as the component (D), at least one solvent selected from the group consisting of N-methyl-2-pyrrolidone, N- The composition according to any one of the above (10) to (10).

(12) A positive resist composition comprising, as the component (E), 1-hexanol, cyclohexanol, 1,2-ethanediol, (1) to (11), wherein the solvent is at least one solvent selected from the group consisting of ethylene glycol monoethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol isopropyl ether and diethylene glycol monobutyl ether. A composition according to any one of the preceding claims.

(13) A resin film obtained from the composition according to any one of (1) to (12).

(14) A liquid crystal alignment treatment agent obtained from the composition according to any one of (1) to (12).

(15) A liquid crystal alignment film obtained by using the liquid crystal alignment treatment agent according to (14) above.

(16) A liquid crystal alignment film obtained by the ink jet method using the liquid crystal alignment treatment agent described in (14) above.

(17) A liquid crystal display element having the liquid crystal alignment film according to (15) or (16) above.

(18) A liquid crystal composition comprising a liquid crystal layer between a pair of substrates provided with electrodes, and containing a polymerizable compound polymerized by at least one of active energy rays and heat between the pair of substrates, (15) or (16) above, wherein the liquid crystal alignment film is used for a liquid crystal display device manufactured by a process of polymerizing the polymerizable compound while applying a voltage between the electrodes.

(19) A liquid crystal display element having the liquid crystal alignment film according to (18).

(20) A liquid crystal alignment film comprising a liquid crystal layer between a pair of substrates provided with electrodes and containing a polymerizable group polymerized by at least one of active energy rays and heat between the pair of substrates The liquid crystal alignment film according to (15) or (16) above, which is used for a liquid crystal display device manufactured through a step of polymerizing the polymerizable group while applying a voltage between the electrodes.

(21) A liquid crystal display element having the liquid crystal alignment film according to (20) above.

A solvent having a specific structure of the present invention, at least one polymer selected from a polyimide precursor or a polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component, and a polysiloxane Can form a resin coating film by firing at a low temperature. In addition, the composition of the present invention can suppress the generation of pinholes accompanying cratering on the resin coating when coating the substrate.

The liquid crystal alignment treatment agent comprising the composition of the present invention can form a liquid crystal alignment film by firing at a low temperature. This liquid crystal alignment treatment agent can suppress the occurrence of pinholes accompanying cratering on the liquid crystal alignment film when the substrate is applied. Therefore, the liquid crystal display element having the liquid crystal alignment film thus obtained is free from alignment defects and becomes a highly reliable liquid crystal display element.

As a result of intensive studies, the present inventors have obtained the following findings and have completed the present invention.

The present invention relates to a composition containing the following components (A), (B) and (C), a liquid crystal alignment treatment agent, a resin film obtained by using the composition, a liquid crystal alignment film obtained by using the liquid crystal alignment treatment agent, , And a liquid crystal display element having the liquid crystal alignment film.

Component (A): At least one solvent (also referred to as a specific solvent) selected from the following formula [1a] or formula [1b].

(11)

(In the formula [1a], X ¹ represents an alkyl group having 1 to 4 carbon atoms, and in the formula [1b], X ² represents an alkyl group having 1 to 4 carbon atoms.

Component (B): at least one polymer (also referred to as a specific polymer) selected from a polyimide precursor or polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component.

(C): Polysiloxane (also referred to as a specific polysiloxane) obtained by polycondensation of an alkoxysilane containing any one of alkoxysilanes represented by the following formula [A1], formula [A2] or formula [A3].

[Chemical Formula 12]

[Chemical Formula 13]

[Chemical Formula 14]

The specific solvent of the present invention usually has a lower boiling point than NMP or? -BL, which is a solvent used in a composition containing a polyimide-based polymer, and can dissolve a specific polymer of the present invention. The specific polysiloxane of the present invention can be dissolved not only in a solvent having a high boiling point such as NMP or? -BL, but also in a specific solvent, a general alcohol solvent or a glycol solvent of the present invention. Therefore, the composition of the present invention can form a resin coating by firing at a low temperature.

Further, since the composition of the present invention is not a solvent having a high polarity such as NMP or? -BL, even when a polymer solution of a specific polysiloxane or a specific polysiloxane is mixed into a polymer solution prepared by dissolving a specific polymer in a specific solvent, The compatibility of the solvent with the polymer solution of the specific polysiloxane or the specific polysiloxane is improved. Therefore, when this composition is applied to a substrate, generation of pinholes accompanying cratering on the resin coating can be suppressed.

In addition, the specific solvent of the present invention usually has a lower surface tension as a solvent than a solvent such as NMP or? -BL used in a composition having a polyimide-based polymer. Therefore, the composition using a specific solvent has a high wetting property to the substrate. Therefore, occurrence of pinholes accompanying cratering on the resin coating can be suppressed.

In view of the above, the composition of the present invention can form a resin coating by firing at a low temperature, and can suppress the occurrence of pinholes accompanying cratering on the resin coating when the coating is applied to the substrate. In addition, the liquid crystal alignment treatment agent obtained from the composition of the present invention can also achieve the above-mentioned effects for the same reason.

Hereinafter, embodiments of the present invention will be described in detail.

The specific solvent as the component (A) of the present invention is at least one solvent selected from the following formula [1a] or formula [1b].

[Chemical Formula 15]

(In the formula [1a], X ¹ represents an alkyl group having 1 to 3 carbon atoms).

(In the formula [1b], X ² represents an alkyl group having 1 to 3 carbon atoms.)

Specifically, the structures represented by the following formulas [1a-1] to [1a-4] and the formulas [1b-1] to [1b-4] can be mentioned.

[Chemical Formula 16]

[Chemical Formula 17]

Among them, the formula [1a-1], the formula [1b-1], the formula [1b-2] or the formula [1b-3] are preferable in view of the boiling point and the availability of the solvent.

The specific solvent of the present invention is capable of forming a resin film or a liquid crystal alignment film by firing at the above-described low temperature and further enhancing the wet diffusibility of the substrate. Therefore, it is preferable that the specific solvent is contained in the composition or the liquid crystal alignment treatment agent Is preferably 50 to 100% by mass of the entire solvent. Among these, 55 to 100 mass% is preferable. More preferred is 55 to 95 mass%.

The effect of the present invention, that is, the effect of the present invention, that is, the resin coating or the liquid crystal alignment film can be formed by firing at a low temperature, the more the amount of the specific solvent of the present invention is in the whole solvent in the composition or the liquid crystal alignment treatment agent using the composition. The wetting and diffusing property of the coating solution is enhanced, and a resin coating film or liquid crystal alignment film excellent in coating property can be obtained.

&Lt; Specific polymer &

The specific polymer as the component (B) of the present invention is at least one polymer selected from a polyimide precursor or polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component.

The polyimide precursor has a structure represented by the following formula [A].

[Chemical Formula 18]

(Wherein [A] of, R ¹ is a tetravalent organic group, R ² is a divalent organic group having a carboxyl group, A ¹ and A ² represents a hydrogen atom or an alkyl group having 1 to 8 carbon atoms, the same or different and each And A ³ and A ^{4 each} represent a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, or an acetyl group, which may be the same or different, and n represents a positive integer).

The diamine component is a diamine compound having two primary or secondary amino groups in the molecule. Examples of the tetracarboxylic acid component include a tetracarboxylic acid compound, a tetracarboxylic acid dianhydride, a dicarboxylic acid dihalide compound, A dicarboxylic acid dialkyl ester compound or a dialkyl ester dihalide compound.

The specific polymer of the present invention can be obtained by relatively easily obtaining a diamine compound having a carboxyl group represented by the following formula [B] and a tetracarboxylic acid dianhydride represented by the following formula [C] D] or a polyimide obtained by imidizing the polyamic acid is preferable.

[Chemical Formula 19]

(In the formulas [B] and [C], R ¹ and R ² are as defined in formula [A].

[Chemical Formula 20]

(In formula [D], R ¹ and R ² are as defined in formula [A]).

In addition, the polymers of the usual synthesis techniques, equation [D] obtained in the above-mentioned formula [A] represented by A ¹ and A carbon number of alkyl group of 1-8 of Figure ^2, and the equation [A] represented by A ³ and A ⁴ An alkyl group having 1 to 5 carbon atoms or an acetyl group may be introduced.

The diamine compound having a carboxyl group of the present invention is a diamine compound having a structure represented by the following formula [2] in the molecule.

[Chemical Formula 21]

In the formula [2], a represents an integer of 0 to 4. Of these, an integer of 0 or 1 is preferable in view of availability of raw materials and ease of synthesis.

Specific examples of the diamine compound having a structure represented by the formula [2] include a structure represented by the following formula [2a].

[Chemical Formula 22]

In formula [2a], a represents an integer of 0 to 4. Among them, 0 or 1 is preferable from the viewpoint of availability of raw materials and easiness of synthesis.

In the formula [2a], n represents an integer of 1 to 4. Among them, 1 is preferable from the viewpoint of easiness of synthesis.

The method for producing the diamine compound represented by the formula [2a] of the present invention is not particularly limited, but preferred examples include the following.

As an example, the diamine compound represented by the formula [2a] is obtained by synthesizing a dinitro compound represented by the following formula [2a-A], reducing the nitro group and converting it into an amino group.

(23)

(In the formula [2a-A], a represents an integer of 0 to 4, and n represents an integer of 1 to 4).

The method for reducing the dinitro group of the dinitro compound represented by the formula [2a-A] is not particularly limited, and typically, a solvent such as palladium (II) acetate, toluene, tetrahydrofuran, dioxane or alcohol- Hydrazine or hydrogen chloride using carbon, platinum oxide, Raney nickel, platinum black, rhodium-alumina or platinum sulfide carbon as a catalyst.

Examples of the diamine compound having a carboxyl group of the present invention include structures represented by the following formulas [2a-1] to [2a-4].

&Lt; EMI ID =

In the formula ^[2a-1], A 1 represents a single _{bond, -CH 2 -, -C 2 H} 4 -, -C (CH 3) 2 -, -CF 2 -, -C (CF 3) 2 -, - O-, -CO-, -NH-, -N ( CH 3) -, -CONH-, -NHCO-, -CH 2 O-, -OCH 2 -, -COO-, -OCO-, -CON (CH ₃₎ - or -N (CH ₃₎ represents a CO-. Among them, a single bond, -CH ₂ -, -C (CH ₃ ) ₂ -, -O-, -CO-, -NH-, -N (CH ₃ ) -, -CONH- , -NHCO-, -COO- or -OCO-. More preferred is a single bond, -CH ₂ -, -C (CH ₃ ) ₂ -, -O-, -CO-, -NH- or -N (CH ₃ ) -.

In the formula [2a-1], m ¹ and m ² each represent an integer of 0 to 4, and m ¹ + m ² represents an integer of 1 to 4. In particular, m ¹ + m ² is 1 or 2 are preferred.

In the formula [2a-2], m ³ and m ⁴ each represent an integer of 1 to 5. Among them, 1 or 2 is preferable from the viewpoint of ease of synthesis.

In the formula [2a-3], A ² represents a linear or branched alkyl group having 1 to 5 carbon atoms. Among them, a linear alkyl group having 1 to 3 carbon atoms is preferable.

In the formula [2a-3], m ⁵ represents an integer of 1-5. Among them, 1 or 2 is preferable.

In the formula [2a-4], A ³ is a single _{bond, -CH 2 -, -C 2 H} 4 -, -C (CH 3) 2 -, -CF 2 -, -C (CF 3) 2 -, - O-, -CO-, -NH-, -N ( CH 3) -, -CONH-, -NHCO-, -CH 2 O-, -OCH 2 -, -COO-, -OCO-, -CON (CH ₃₎ - or -N (CH ₃₎ represents a CO-. Among them, a single bond, -CH ₂ -, -C (CH ₃ ) ₂ -, -O-, -CO-, -NH-, -CONH-, -NHCO-, -CH ₂ O-, -OCH ₂ - , -COO-, or -OCO-. More preferred is, -O-, -CO-, -NH-, -CONH- , -NHCO-, -CH 2 O-, -OCH 2 - is, -COO- or -OCO-.

In the formula [2a-4], m ⁶ represents an integer of 1 to 4. Among them, 1 is preferable from the viewpoint of easiness of synthesis.

The diamine compound having a carboxyl group of the present invention is preferably 20 mol% to 100 mol%, more preferably 30 mol% to 100 mol%, of the total diamine component.

The above-mentioned diamine compound having a carboxyl group can be used in one kind or two or more kinds depending on the solubility of the specific polymer of the present invention in the solvent, the coating property of the composition, the orientation of the liquid crystal when the liquid crystal alignment film is used, Or a mixture of two or more of them may be used.

&Lt; Second diamine compound >

As the diamine component for producing the specific polymer of the present invention, a diamine compound (also referred to as a second diamine compound) represented by the following formula [2b] may be used as the second diamine compound.

(25)

(In the formula [2b], Y represents a structure represented by the following formula [2b-1], formula [2b-2], formula [2b-3], formula [2b-4] and m represents an integer of 0 to 4).

(26)

In the formula [2b-1], a represents an integer of 0 to 4. Of these, an integer of 0 or 1 is preferable in view of availability of raw materials and ease of synthesis.

Y ¹ is a single bond, - (CH ₂ ) _a - (a is an integer of 1 to 15), -O-, -CH ₂ O-, -COO-, or -OCO- in the formula [2b-2] . Among them, a single bond, - (CH ₂ ) _a - (a is an integer of 1 to 15), -O-, -CH ₂ O- or -COO- is preferable in view of availability of raw materials and ease of synthesis desirable. More preferably, it is a single bond, - (CH ₂ ) _a - (a is an integer of 1 to 10), -O-, -CH ₂ O- or -COO-.

In the formula [2b-2], Y ² represents a single bond or - (CH ₂ ) _b - (b is an integer of 1 to 15). Among them, a single bond or - (CH ₂ ) _b - (b is an integer of 1 to 10) is preferable.

In formula [2b-2], Y ³ represents a single bond, - (CH ₂ ) _c - (c is an integer of 1 to 15), -O-, -CH ₂ O-, -COO- or -OCO- . Among them, a single bond, - (CH ₂ ) _c - (c is an integer of 1 to 15), -O-, -CH ₂ O- or -COO- is preferable from the viewpoint of easiness of synthesis. More preferably, it is a single bond, - (CH ₂ ) _c - (c is an integer of 1 to 10), -O-, -CH ₂ O- or -COO-.

In the formula [2b-2], Y ⁴ is a divalent cyclic group selected from a benzene ring, a cyclohexane ring or a heterocyclic ring, and any hydrogen atom on the cyclic group may be an alkyl group having 1 to 3 carbon atoms, An alkoxyl group having 1 to 3 carbon atoms, a fluorine-containing alkyl group having 1 to 3 carbon atoms, a fluoro-containing alkoxyl group having 1 to 3 carbon atoms, or a fluorine atom. Y ⁴ may be a divalent organic group selected from organic groups having 12 to 25 carbon atoms and having a steroid skeleton. Among them, an organic group having 12 to 25 carbon atoms having a benzene ring, a cyclohexane ring, or a steroid skeleton is preferable from the viewpoint of ease of synthesis.

In formula [2b-2], Y ⁵ represents a divalent cyclic group selected from a benzene ring, a cyclohexane ring or a heterocyclic ring, and any hydrogen atom on the cyclic group may be substituted with an alkyl group having 1 to 3 carbon atoms, An alkoxyl group having 1 to 3 carbon atoms, a fluorine-containing alkyl group having 1 to 3 carbon atoms, a fluoro-containing alkoxyl group having 1 to 3 carbon atoms, or a fluorine atom. Among them, a benzene ring or a cyclohexane ring is preferable.

In the formula [2b-2], n represents an integer of 0 to 4. Among them, from the viewpoint of availability of raw materials and easiness of synthesis, 0 to 3 is preferable. More preferred is 0 to 2.

In the formula [2b-2], Y ⁶ represents an alkyl group having 1 to 18 carbon atoms, a fluorine-containing alkyl group having 1 to 18 carbon atoms, an alkoxyl group having 1 to 18 carbon atoms, or a fluorinated alkoxyl group having 1 to 18 carbon atoms. Among them, an alkyl group having 1 to 18 carbon atoms, a fluorine-containing alkyl group having 1 to 10 carbon atoms, an alkoxyl group having 1 to 18 carbon atoms, or a fluorinated alkoxyl group having 1 to 10 carbon atoms is preferable. More preferably an alkyl group having 1 to 12 carbon atoms or an alkoxyl group having 1 to 12 carbon atoms. And particularly preferably an alkyl group having 1 to 9 carbon atoms or an alkoxyl group having 1 to 9 carbon atoms.

Preferable combinations of Y ¹ , Y ² , Y ³ , Y ⁴ , Y ⁵ , Y ⁶ and n in the formula [2b-2] for constituting the substituent Y in the formula [2b] (2-1) to (2-629) listed in Tables 6 to 47 of Tables 13 to 34 of International Patent Application No. 132751 (published on October 27, 2011). In each table of the International Publication, Y ¹ to Y ⁶ in the present invention are represented as Y ¹ to Y ⁶ , and Y ¹ to Y ⁶ are read in place of Y ¹ to Y ⁶ .

In the formula [2b-3], Y ⁷ represents an alkyl group of a carbon number of 8 to 22.

In the formula [2b-4], Y ⁸ and Y ⁹ each independently represent a hydrocarbon group having 1 to 6 carbon atoms.

In the formula [2b-5], Y ¹⁰ represents an alkyl group having 1 to 8 carbon atoms.

The method for producing the diamine compound represented by the formula [2b] of the present invention is not particularly limited, and preferable examples include the following.

As an example, the diamine compound represented by the formula [2b] can be obtained by synthesizing a dinitro compound represented by the following formula [2b-A], reducing the nitro group and converting it into an amino group.

(27)

(Wherein Y is at least one selected from the above-mentioned formula [2b-1], formula [2b-2], formula [2b-3], formula [2b-4] or formula [2b-5] And m represents an integer of 0 to 4).

The method for reducing the dinitro group of the dinitro compound represented by the formula [2b-A] is not particularly limited, and typically, a solvent such as palladium (II) acetate, toluene, tetrahydrofuran, dioxane or alcohol- Hydrazine or hydrogen chloride using carbon as a catalyst, platinum oxide, Raney nickel, platinum black, rhodium-alumina or platinum sulfide carbon as a catalyst.

Specific structures of the second diamine compound represented by the formula [2b] of the present invention are shown below, but the present invention is not limited to these examples.

Namely, examples of the second diamine represented by the formula [2b] include m-phenylenediamine, 2,4-dimethyl-m-phenylenediamine, 2,6-diaminotoluene, 2,4- Diaminobenzyl alcohol, 2,4,6-diaminobenzyl alcohol, 4,6-diaminoresorcinol, and the like represented by the following formulas [2b-6] to [2b-46] Diamine compound of the structure

(28)

(In the formula [2b-6] ~ formula [2b-9], A ¹ is an alkyl group or a fluorine-containing alkyl group having a carbon number of 1 to 22).

[Chemical Formula 29]

(30)

(31)

(32)

(33)

(34)

(35)

(36)

(37)

(38)

[Chemical Formula 39]

(40)

(Wherein R ¹ represents -O-, -OCH ₂ -, -CH ₂ O-, -COOCH ₂ - or CH ₂ OCO-, and R ² represents a carbon number An alkyl group having 1 to 22 carbon atoms, an alkoxy group, a fluorine-containing alkyl group or a fluorine-containing alkoxy group).

(41)

(Wherein R ³ is -COO-, -OCO-, -COOCH ₂ -, -CH ₂ OCO-, -CH ₂ O-, -OCH ₂ - or - (CH ₂₎ CH ₂ -, and R ⁴ represents an alkyl group, an alkoxy group, a fluorine-containing alkyl group or a fluorine-containing alkoxy group having 1 to 22 carbon atoms.

(42)

(Formula [2b-40] and formula [2b-41] of, R ⁵ is _{-COO-, -OCO-, -COOCH 2 -,} -CH 2 OCO-, -CH 2 O-, -OCH 2 -, - CH ₂ - or -O-, and R ⁶ is a fluorine group, a cyano group, a trifluoromethane group, a nitro group, an azo group, a formyl group, an acetyl group, an acetoxy group or a hydroxyl group.

(43)

(Formula [2b-42] and formula [2b-43] of, R ⁷ represents an alkyl group having a carbon number of 3 to 12. In addition, the 1,4-cis-cyclohexylene-trans reason, each trans isomer is preferred) .

(44)

(In the formula [2b-44] and the formula [2b-45], R ⁸ represents an alkyl group having 3 to 12 carbon atoms, and the cis- trans isomer of 1,4-cyclohexylene is preferably a trans isomer) .

[Chemical Formula 45]

(In the formula [2b-46], B ⁴ represents an alkyl group having 3 to 20 carbon atoms which may be substituted with a fluorine atom, B ³ represents a 1,4-cyclohexylene group or a 1,4-phenylene group, B ² Represents an oxygen atom or -COO- * (provided that a bonding hand to which " * " is bonded is bonded to B ³ ), B ¹ represents an oxygen atom or -COO- * CH ₂ ) a ² ), a ¹ represents an integer of 0 or 1, a ² represents an integer of 2 to 10, and a ³ represents an integer of 0 or 1.

Among the second diamine compounds of the present invention, the composition using the diamine compound having the structure represented by the formula [2b-2] in which the substituent Y in the formula [2b] is used can increase the hydrophobicity of the resin film. Further, when the liquid crystal alignment film is used, the pretilt angle of the liquid crystal can be increased. Among these diamine compounds, diamine compounds represented by the formulas [2b-28] to [2b-39] or the formulas [2b-42] to [2b-46] are used . More preferred are diamine compounds represented by the formulas [2b-24] to [2b-39] or the formulas [2b-42] to [2b-46]. In order to further enhance these effects, it is preferable that these diamine compounds are contained in an amount of not less than 5 mol% and not more than 80 mol% of the total diamine component. More preferably, these diamine compounds are contained in an amount of not less than 5 mol% and not more than 60 mol% of the total diamine component from the viewpoints of coating properties of the composition and the liquid crystal alignment treatment agent and electrical characteristics as a liquid crystal alignment film. Particularly preferably, it is 10 mol% or more and 60 mol% or less of the total diamine component.

The second diamine compound of the present invention may contain one or two or more kinds of monomers selected depending on the solubility or coating properties of the specific polymer of the present invention, the orientation of the liquid crystal when the liquid crystal alignment film is used, the voltage retention rate, Or more.

Specific polymers of the present invention may contain a diamine compound having a carboxyl group in the molecule represented by the formula [2a], a formula [2a-1] to a formula [2a-4] ], Other diamine compounds (also referred to as other diamine compounds) can be used as the diamine component.

Specific examples of other diamine compounds are shown below, but the present invention is not limited to these examples.

Examples of other diamine compounds include 4,4'-diaminobiphenyl, 3,3'-dimethyl-4,4'-diaminobiphenyl, 3,3'-dimethoxy-4,4'-diamino Biphenyl, 3,3'-dihydroxy-4,4'-diaminobiphenyl, 3,3'-dicarboxy-4,4'-diaminobiphenyl, 3,3'-difluoro- , 4'-biphenyl, 3,3'-trifluoromethyl-4,4'-diaminobiphenyl, 3,4'-diaminobiphenyl, 3,3'-diaminobiphenyl, 2,2 Diaminobiphenyl, 2,3'-diaminobiphenyl, 4,4'-diaminodiphenylmethane, 3,3'-diaminodiphenylmethane, 3,4'-diaminodiphenylmethane, Diaminodiphenylmethane, 2,2'-diaminodiphenylmethane, 2,3'-diaminodiphenylmethane, 4,4'-diaminodiphenyl ether, 3,3'-diaminodiphenyl ether, 3,4'- Aminodiphenyl ether, 2,2'-diaminodiphenyl ether, 2,3'-diaminodiphenyl ether, 4,4'-sulfonyldiamine, 3,3'-sulfonyldiamine, bis Bis (3-aminophenyl) silane, dimethyl-bis (4-aminophenyl) silane, dimethyl- (3-aminophenyl) silane, 4,4'-thiodianiline, 3,3'-thiodianiline, 4,4'-diaminodiphenylamine, 3,3'-diaminodiphenylamine, 3 , 4'-diaminodiphenylamine, 2,2'-diaminodiphenylamine, 2,3'-diaminodiphenylamine, N-methyl (4,4'-diaminodiphenyl) amine, N- (3,3'-diaminodiphenyl) amine, N-methyl (3,4'-diaminodiphenyl) amine, N-methyl (2,2'- diaminodiphenyl) Diaminodiphenyl) amine, 4,4'-diaminobenzophenone, 3,3'-diaminobenzophenone, 3,4'-diaminobenzophenone, 1,4-diaminonaphthalene, Diaminobenzophenone, 1,5-diaminonaphthalene, 1,6-diaminonaphthalene, 1,7-diaminonaphthalene, 1,8-diamino Naphthalene, 2,5-diaminonaphthalene, 2,6-diaminonaphthalene, 2,7-diaminonaphthalene, 2,8-diaminonaphthalene, 1,2- Bis (3-aminophenyl) ethane, 1,3-bis (4-aminophenyl) Bis (3-aminophenyl) propane, 1,4-bis (4-aminophenyl) butane, 1,4- Aminophenoxy) benzene, 1,4-bis (4-aminophenoxy) benzene, 1,4-bis (4-aminophenyl) benzene, 1,4-bis (4-aminobenzyl) benzene, 1,3- Phenylene bis (methylene)] dianiline, 3, 4 '- [1,3-phenylenebis (methylene)] dianiline, 3,4' - [ 4'- [1,3-phenylenebis (methylene)] dianiline, 3,3 '- [1,4-phenylenebis (methylene)] dianiline, 3,3' - [ Phenylene] methanone], 1,4-phenylenebis [(4-aminophenyl) methanone], 1,4-phenylenebis [ Bis (4-aminophenyl) methanone], 1,3-phenylenebis [(3-aminophenyl) methanone], 1,4-phenylenebis (3-aminobenzo Aminobenzoate), bis (4-aminophenyl) terephthalate, bis (3-aminophenyl) Bis (4-aminophenyl) isophthalate, bis (3-aminophenyl) isophthalate, N, N ' (1,3-phenylene) bis (4-aminobenzamide), N, N ' Aminophenyl) terephthalamide, N, N'-bis (4-aminophenyl) terephthalamide, N, N'- (Aminophenyl) isophthalamide, N, N'-bis (3-aminophenyl) isophthalamide, 9,10- Bis [4- (4-aminophenoxy) phenyl] hexafluoropropane, 2,2 '-bis [ - bis (4-aminophenyl) hexaflue Bis (3-aminophenyl) hexafluoropropane, 2,2'-bis (3-amino-4-methylphenyl) hexafluoropropane, 2,2'- Bis (4-aminophenoxy) propane, 2,2'-bis (3-aminophenoxy) propane, Propane, 1,4-bis (4-aminophenoxy) butane, 1,4-bis (3-aminophenoxy) butane, 1,5- Bis (3-aminophenoxy) pentane, 1,6-bis (3-aminophenoxy) pentane, Heptane, 1,8-bis (4-aminophenoxy) octane, 1,8-bis (3-aminophenoxy) heptane, ) Octane, 1,9-bis (4-aminophenoxy) nonane, 1,9-bis (3-aminophenoxy) -Aminophenoxy) decane, 1,11- (4-aminophenoxy) undecane, 1,11- (3-aminophenoxy) undecane, 1,12- Dodecane, 1,12- (3-aminophenoxy) dodecane, bis (4-aminocyclohexyl) methane, bis (4-amino-3-methylcyclohexyl) Diaminobutane, 1,5-diaminopentane, 1,6-diaminohexane, 1,7-diaminoheptane, 1,8-diaminooctane, 1,9- 1,10-diaminodecane, 1,11-diaminoundecane, 1,12-diaminododecane, and the like.

As other diamine compounds, those having an alkyl group, a fluorine-containing alkyl group, an aromatic ring, an aliphatic ring or a heterocyclic ring in the diamine side chain, and those having a polycyclic substituent composed of these may also be cited. Specifically, the diamine compounds represented by the following formulas [DA1] to [DA13] can be exemplified.

(46)

(47)

(48)

(Wherein [DA1] ~ formula [DA6] of, A ¹ is -COO-, -OCO-, -CONH-, -NHCO-, -CH 2 - represents, -O-, -CO- or -NH-, A ² represents a linear or branched alkyl group having 1 to 22 carbon atoms or a linear or branched fluorine-containing alkyl group having 1 to 22 carbon atoms.

(49)

(In the formula [DA7], p represents an integer of 1 to 10).

As other diamine compounds, diamine compounds represented by the following formulas [DA8] to [DA13] may be used as long as they do not impair the effect of the present invention.

(50)

(51)

(In the formula [DA10], m represents an integer of 0 to 3, and in the formula [DA13], n represents an integer of 1 to 5).

In addition, as long as the effect of the present invention is not impaired, a diamine compound represented by the following formula [DA14] may be used.

(52)

(Wherein [DA14] of, A ¹ is _{-O-, -NH-, -N (CH 3} ) -, -CONH-, -NHCO-, -CH 2 O-, -OCO-, -CON (CH 3) - or -N (CH ₃₎ is a divalent organic group selected from CO-, a ² is a single bond, C 1 -C 20 aliphatic hydrocarbon group, non-aromatic cyclic hydrocarbon group or an aromatic hydrocarbon group, a ³ is a single -NH-, -N (CH ₃ ) -, -CONH-, -NHCO-, -COO-, -OCO-, -CON (CH ₃ ) -, -N (CH ₃ ) Or -O (CH ₂ ) _m - (m is an integer of 1 to 5), A ⁴ is a nitrogen-containing aromatic heterocyclic ring, and n is an integer of 1 to 4.

In addition, as other diamine compounds, diamine compounds represented by the following formulas [DA15] and [DA16] may be used.

(53)

The other diamine compounds may be used alone or in combination of two or more kinds, depending on the solubility of the specific polymer of the present invention in the solvent, the coating property of the composition, the orientation of the liquid crystal when the liquid crystal alignment film is used, Two or more kinds may be mixed and used.

&Lt; Tetracarboxylic acid dianhydride component >

As the tetracarboxylic acid dianhydride component for producing a specific polymer of the present invention, a tetracarboxylic acid anhydride or a tetracarboxylic acid derivative (also referred to as a specific tetracarboxylic acid dianhydride component) represented by the following formula [3] .

(54)

In the formula [3], Z ¹ is a group of at least one structure selected from the following formulas [3a] to [3j].

(55)

In the formula [3a], Z ² to Z ⁵ represent a hydrogen atom, a methyl group, a chlorine atom or a benzene ring, and may be the same or different.

In the formula [3g], Z ⁶ and Z ⁷ each represent a hydrogen atom or a methyl group, and may be the same or different.

Among the structures represented by the formula [3], which is a specific tetracarboxylic acid dianhydride component of the present invention, Z ¹ is preferably a tetracarboxylic acid dianhydride represented by the formula [3a], the formula [ 3c], the formula [3d], the formula [3e], the formula [3f] or the formula [3g]. More preferred is a structure represented by the formula [3a], the formula [3e], the formula [3f] or the formula [3g].

The specific tetracarboxylic acid component of the present invention is preferably at least 1 mol% of the total tetracarboxylic acid component. More preferably, it is at least 5 mol%, particularly preferably at least 10 mol%.

When the specific tetracarboxylic acid dianhydride component having the structure of the formula [3e], the formula [3f] or the formula [3g] is used, the amount of the tetracarboxylic acid dianhydride component to be used is preferably 20 mol% or more of the total amount of the tetracarboxylic acid dianhydride component A desired effect can be obtained. Preferably, it is at least 30 mol%. The tetracarboxylic acid dianhydride component may be a tetracarboxylic acid dianhydride component having the structure of the formula [3e], the formula [3f] or the formula [3g].

In the specific polymer of the present invention, other tetracarboxylic acid dianhydride components other than the specific tetracarboxylic acid dianhydride component may be used as long as the effect of the present invention is not impaired.

As other tetracarboxylic acid dianhydride components, tetracarboxylic acid compounds, tetracarboxylic acid dianhydrides, dicarboxylic acid dihalide compounds, dicarboxylic acid dialkyl ester compounds or dialkyl ester dihalide compounds shown below may be used. .

Namely, at least one of pyromellitic acid, 2,3,6,7-naphthalenetetracarboxylic acid, 1,2,5,6-naphthalenetetracarboxylic acid, 1,4,5,8-naphthalenetetracarboxylic acid, 2, 3,6 '-anthracene tetracarboxylic acid, 1,2,5,6-anthracene tetracarboxylic acid, 3,3', 4,4'-biphenyltetracarboxylic acid, 2,3,3 ' (3,4-dicarboxyphenyl) ether, 3,3 ', 4,4'-benzophenonetetracarboxylic acid, bis (3,4-dicarboxyphenyl) sulfone, Bis (3,4-dicarboxyphenyl) methane, 2,2-bis (3,4-dicarboxyphenyl) propane, 1,1,1,3,3,3-hexafluoro-2,2-bis Dicarboxyphenyl) propane, bis (3,4-dicarboxyphenyl) dimethylsilane, bis (3,4-dicarboxyphenyl) diphenylsilane, 2,3,4,5-pyridine tetracarboxylic acid , 2,6-bis (3,4-dicarboxyphenyl) pyridine, 3,3 ', 4,4'-diphenylsulfonetetracarboxylic acid, 3,4,9,10-perylenetetracarboxylic acid or 1,3-diphenyl-1,2,3,4-cyclobutane tetracarboxylic acid The can.

The specific tetracarboxylic acid dianhydride component and the other tetracarboxylic acid component can be used in a wide range depending on the solubility of the specific polymer of the present invention in the solvent or the coating property of the composition, the orientation of the liquid crystal in the case of a liquid crystal alignment film, Depending on the characteristics of charge, etc., one kind or two or more kinds may be mixed and used.

&Lt; Process for producing specific polymer &

In the present invention, a method of synthesizing a specific polymer is not particularly limited. It is usually obtained by reacting a diamine component and a tetracarboxylic acid dianhydride component. Generally, a polyamic acid is reacted with at least one tetracarboxylic acid dianhydride component selected from the group consisting of tetracarboxylic acid and its derivatives and a diamine component composed of one or more kinds of diamine compounds, . Specifically, there are a method of polycondensing a tetracarboxylic acid dianhydride and a primary or secondary diamine compound to obtain a polyamic acid, a method of dehydrating polycondensation reaction of a tetracarboxylic acid and a primary or secondary diamine compound, A method of obtaining an acid or a method of polycondensing a dicarboxylic acid dihalide and a primary or secondary diamine compound to obtain a polyamic acid is used.

To obtain the polyamide acid alkyl ester, polycondensation of a tetracarboxylic acid in which a carboxylic acid group is dialkyl esterified with a primary or secondary diamine compound, a method in which a carboxylic acid group is dialkyl esterified and a dicarboxylic acid dihalide And a primary or secondary diamine compound, or a method of converting a carboxyl group of a polyamic acid into an ester is used.

To obtain the polyimide, a method of converting the above polyamic acid or polyamide acid alkyl ester into a polyimide by ring closure is used.

The reaction of the diamine component and the tetracarboxylic acid component is usually carried out in an organic solvent with the diamine component and the tetracarboxylic acid component. The organic solvent to be used at this time is not particularly limited as long as it dissolves the specific solvent which is the component (A) of the present invention or the produced polyimide precursor.

Examples of the solvent other than the specific solvent of the present invention include the following solvents.

That is, it is preferable to use a solvent such as N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, 3-dimethyl-imidazolidinone, methyl ethyl ketone, cyclohexanone, cyclopentanone or 4-hydroxy-4-methyl-2-pentanone.

These may be used alone or in combination. Further, a solvent that does not dissolve the polyimide precursor may be used in combination with the solvent insofar as the resulting polyimide precursor does not precipitate. In addition, water in the organic solvent inhibits the polymerization reaction and further causes hydrolysis of the resulting polyimide precursor, and therefore, the organic solvent is preferably dehydrated and dried.

When the diamine component and the tetracarboxylic acid component are reacted in an organic solvent, a method in which the solution in which the diamine component is dispersed or dissolved in an organic solvent is stirred to add the tetracarboxylic acid component as it is or after dispersed or dissolved in an organic solvent , A method of adding a diamine component to a solution in which a tetracarboxylic acid component is dispersed or dissolved in an organic solvent, a method of alternately adding a tetracarboxylic acid component and a diamine component, and the like. May be used. When a plurality of diamine components or tetracarboxylic acid components are used in the reaction, they may be reacted in a preliminarily mixed state, or they may be reacted individually in sequence, or the low molecular weight compounds reacted individually may be mixed and reacted, . The polymerization temperature at that time may be any temperature between -20 DEG C and 150 DEG C, preferably between -5 DEG C and 100 DEG C. The reaction can be carried out at an arbitrary concentration, but if the concentration is too low, it becomes difficult to obtain a polymer having a high molecular weight. If the concentration is too high, the viscosity of the reaction liquid becomes too high, and uniform stirring becomes difficult. Therefore, the content is preferably 1 to 50% by mass, and more preferably 5 to 30% by mass. The reaction is carried out at a high concentration in the initial stage, and then an organic solvent can be added.

In the polymerization reaction of the polyimide precursor, the ratio of the total molar number of the diamine component to the total molar number of the tetracarboxylic acid component is preferably 0.8 to 1.2. As in the case of the usual polycondensation reaction, the closer the molar ratio is to 1.0, the larger the molecular weight of the resulting polyimide precursor.

The polyimide of the present invention is a polyimide obtained by ring closure of the above-mentioned polyimide precursor. In this polyimide, the closed rate (also referred to as imidization rate) of the amide acid group does not necessarily have to be 100% Can be adjusted arbitrarily.

Examples of the method of imidizing the polyimide precursor include heat imidization for directly heating the solution of the polyimide precursor or catalyst imidization for adding a catalyst to a solution of the polyimide precursor.

When the polyimide precursor is thermally imidized in a solution, the temperature is preferably 100 占 폚 to 400 占 폚, preferably 120 占 폚 to 250 占 폚, and the water generated by the imidization reaction is preferably removed while removing it from the system.

The catalyst imidation of the polyimide precursor can be carried out by adding a basic catalyst and an acid anhydride to the polyimide precursor solution and stirring at -20 to 250 ° C, preferably 0 to 180 ° C. The amount of the basic catalyst is 0.5 to 30 moles, preferably 2 to 20 moles, of the amide group, and the amount of the acid anhydride is 1 to 50 moles, preferably 3 to 30 moles, of the amide group. Examples of the basic catalyst include pyridine, triethylamine, trimethylamine, tributylamine, trioctylamine, and the like. Of these, pyridine is preferred because it has a suitable basicity for promoting the reaction. Examples of the acid anhydride include acetic anhydride, trimellitic anhydride, and pyromellitic anhydride. Of these, use of acetic anhydride is preferable because purification after completion of the reaction is facilitated. The imidization rate by the catalyst imidization can be controlled by adjusting the catalyst amount, the reaction temperature, and the reaction time.

When the polyimide precursor or the polyimide is recovered from the polyimide precursor or polyimide reaction solution, the reaction solution may be put into a solvent and precipitated. Examples of the solvent used in the precipitation include methanol, ethanol, isopropyl alcohol, acetone, hexane, butyl cellosolve, heptane, methyl ethyl ketone, methyl isobutyl ketone, toluene, benzene and water. The polymer precipitated by charging into the solvent can be recovered by filtration and then dried under normal pressure or reduced pressure at room temperature or by heating. In addition, by repeating the operation of re-dissolving the polymer recovered and precipitated in the organic solvent and re-precipitating and recovering the polymer 2 to 10 times, impurities in the polymer can be reduced. As the solvent at this time, for example, alcohols, ketones or hydrocarbons can be exemplified, and when three or more solvents selected from these solvents are used, the purification efficiency is further improved, which is preferable.

The molecular weight of the specific polymer of the present invention is preferably from 5,000 to 1,000,000 as measured by a gel permeation chromatography (GPC) method in consideration of the strength of the resin film or the liquid crystal alignment film obtained therefrom, , And more preferably from 10,000 to 150,000.

The specific polysiloxane as the component (C) of the present invention is a polysiloxane obtained by polycondensation of an alkoxysilane containing any one of the alkoxysilanes represented by the above-mentioned formula [A1], formula [A2] or formula [A3].

The alkoxysilane represented by the formula [A1] of the present invention is an alkoxysilane represented by the following formula [A1].

(56)

In the formula [A1], A ¹ is an organic group having 8 to 35 carbon atoms and having an aliphatic hydrocarbon, a benzene ring, a cyclohexane ring, a heterocyclic ring or a steroid structure.

In the formula [A1], A ² are each a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. Among them, a hydrogen atom or an alkyl group having 1 to 3 carbon atoms is preferable.

In the formula [A1], A ³ is an alkyl group having 1 to 5 carbon atoms. Among them, an alkyl group having 1 to 3 carbon atoms is preferable in view of reactivity of polycondensation.

In the formula [A1], m is an integer of 1 or 2. Among them, 1 is preferable in terms of synthesis.

In the formula [A1], n is an integer of 0 to 2.

In the formula [A1], p is an integer of 0 to 3. Among them, an integer of 1 to 3 is preferable in view of the reactivity of polycondensation. More preferably 2 or 3.

In the formula [A1], m + n + p is an integer of 4.

Specific examples of the alkoxysilane represented by the formula [A1] include octyltrimethoxysilane, octyltriethoxysilane, decyltrimethoxysilane, dodecyltrimethoxysilane, dodecyltriethoxysilane, hexadecyltrimethoxysilane , Hexadecyltriethoxysilane, pentyltriethoxysilane, heptadecyltrimethoxysilane, heptadecyltriethoxysilane, octadecyltrimethoxysilane, octadecyltriethoxysilane, nonadecyltrimethoxysilane, nona Stearylethyltrimethoxysilane, p-styrylethyltrimethoxysilane, 1- (2-ethylhexyl) -trimethoxysilane, pentyltriethoxysilane, pentafluorophenyltrimethoxysilane, m- Naphthyltriethoxysilane, 1-naphtyltrimethoxysilane, triethoxy-1H, 1H, 2H, 2H-tridecafluoro-n-octylsilane, dimethoxydiphenylsilane, dimethoxymethylphenylsilane or triethoxy Phenyl silane, and the like.

In addition, alkoxysilanes represented by the following formulas [A1-1] to [A1-32] may be used.

(57)

(58)

[Chemical Formula 59]

(60)

(61)

(62)

(63)

&Lt; EMI ID =

(65)

(Wherein [A1-1] ~ formula [A1-18], R ¹ represents an alkyl group having 1 to 5 carbon atoms each).

(66)

(In the formulas [A1-19] to formula [A1-22], R ¹ represents an alkyl group having 1 to 5 carbon atoms, and R ² each represent -O-, -COO-, -OCO-, -CONH-, _{NHCO-, -CON (CH 3) -} , -N (CH 3) CO-, -OCH 2 -, -CH 2 O-, -COOCH 2 - or denotes a -CH ₂ OCO-, R ³ are each C 1 An alkyl group, an alkoxy group, a fluorine-containing alkyl group or a fluorine-containing alkoxy group).

(67)

(Wherein [A1-23] and formula [A1-24] of, R ¹ each represent an alkyl group of a carbon number of 1 ~ 5, R ² are each -O-, -COO-, -OCO-, -CONH-, - _{NHCO-, -CON (CH 3) -} , -N (CH 3) CO-, -OCH 2 -, -CH 2 O-, -COOCH 2 - or denotes a -CH ₂ OCO-, R ³ are each C 1 An alkoxy group, a fluorine-containing alkyl group, a fluorine-containing alkoxy group, a fluorine group, a cyano group, a trifluoromethane group, a nitro group, an azo group, a formyl group, an acetyl group, an acetoxy group or a hydroxyl group.

(68)

(69)

(Wherein [A1-25] ~ formula [A1-31] of, R ¹ each represent an alkyl group of a carbon number of 1 ~ 5, R ² are each -O-, -COO-, -OCO-, -CONH-, - _{NHCO-, -CON (CH 3) -} , -N (CH 3) CO-, -OCH 2 -, -CH 2 O-, -COOCH 2 - or denotes a -CH ₂ OCO-, R ³ are each C 1 An alkyl group, an alkoxy group, a fluorine-containing alkyl group or a fluorine-containing alkoxy group).

(70)

(In the formula [A1-32], R ¹ represents an alkyl group of 1 to 5 carbon atoms, B ⁴ represents an alkyl group of 3 to 20 carbon atoms which may be substituted with a fluorine atom, B ³ represents 1,4-cyclohexylene And B ² represents an oxygen atom or a COO- * group, provided that a bonding hand to which "*" is bonded is bonded to B ^3, and B ¹ represents an oxygen atom or COO- * (However, the combined hand giving "*" is combined with (CH ₂ ) a ² ). A ¹ represents an integer of 0 or 1, a ² represents an integer of 2 to 10, and a ³ represents an integer of 0 or 1).

The alkoxysilane represented by the above formula [A1] can be suitably selected depending on the strength of the resin film or the liquid crystal alignment film, the workability at the time of film formation, furthermore, the properties such as liquid crystal alignment property, voltage holding ratio, , One kind or two or more kinds may be mixed and used.

The alkoxysilane represented by the formula [A2] of the present invention is an alkoxysilane represented by the following formula [A2].

(71)

In formula [A2], B ¹ is an organic group having 2 to 12 carbon atoms and having a vinyl group, an epoxy group, an amino group, a mercapto group, an isocyanate group, a methacrylic group, an acrylic group, a ureide group or a cinnamoyl group. Among them, a vinyl group, an epoxy group, an amino group, a methacrylic group, an acrylic group or an ureide group is preferable in view of easiness of obtaining. More preferably a methacryl group, an acrylic group or a ureide group.

In the formula [A2], B ² is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms. Among them, a hydrogen atom or an alkyl group having 1 to 3 carbon atoms is preferable.

In the formula [A2], B ³ is an alkyl group having 1 to 5 carbon atoms. Among them, an alkyl group having 1 to 3 carbon atoms is preferable in view of reactivity of polycondensation.

In the formula [A2], m is an integer of 1 or 2. Among them, 1 is preferable in terms of synthesis.

In the formula [A2], n is an integer of 0 to 2.

In the formula [A2], p is an integer of 0 to 3. Among them, an integer of 1 to 3 is preferable in view of the reactivity of polycondensation. More preferably 2 or 3.

In the formula [A2], m + n + p is an integer of 4.

Specific examples of the alkoxysilane represented by the formula [A2] include allyltriethoxysilane, allyltrimethoxysilane, diethoxymethylvinylsilane, dimethoxymethylvinylsilane, triethoxyvinylsilane, vinyltrimethoxysilane, vinyltris (2-methoxyethoxy) silane, m-styrylethyltriethoxysilane, p-styrylethyltriethoxysilane, m-styrylmethyltriethoxysilane, p-styrylmethyltriethoxysilane, (3-glycidyloxypropyl) methylsilane, 3-glycidyloxypropyl (dimethoxy) methylsilane, 3 (trimethylsilyl) 3- (2-aminoethylamino) propyldimethoxymethylsilane, 3- (2-aminoethyl) ethyltrimethoxysilane, 2- Amino) propyltriethoxysilane, 3- (2-aminoethylamino) propyltrimethoxysilane, 3-aminopropyldiethoxymethylsilane, 3- (Methoxy) methylsilane, 3-aminopropyltrimethoxysilane, trimethoxy [3- (phenylamino) propyl] silane, 3-mercaptopropyl (Triethoxysilyl) propyl methacrylate, 3- (trimethoxysilyl) propyl methacrylate, 3- (trimethoxysilyl) propyl methacrylate, 3- (trimethoxysilyl) propyl acrylate, 3- (trimethoxysilyl) propyl acrylate, 3- (triethoxysilyl) ethyl methacrylate, 3- 3- (trimethoxysilyl) ethyl acrylate, 3- (trimethoxysilyl) ethyl acrylate, 3- (triethoxysilyl) methyl methacrylate, 3- Acrylate, 3- (triethoxysilyl) methyl acrylate, 3- (trimethoxysilyl) methyl acrylate, (R) -N-1-phenylethyl-N'-triethoxysilylpropylurea, γ-ureido propyltrimethoxysilane, γ-ureidopropyltripropoxysilane, 3- (trimethoxysilyl) propyl] urea, bis [3- (tripropoxysilyl) propyl] urea, 1- [3 - (trimethoxysilyl) propyl] urea, and the like.

The alkoxysilane represented by the above-mentioned formula [A2] can be suitably selected depending on the strength of the resin film or the liquid crystal alignment film, the workability at the time of film formation, furthermore, the properties such as liquid crystal alignment property, voltage retention rate, , One kind or two or more kinds may be mixed and used.

The alkoxysilane represented by the formula [A3] of the present invention is an alkoxysilane represented by the following formula [A].

(72)

In the formula [A3], D ¹ is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, and they may be substituted with a halogen atom, a nitrogen atom, an oxygen atom or a sulfur atom. Among them, a hydrogen atom or an alkyl group having 1 to 3 carbon atoms is preferable.

In the formula [A3], D ² is an alkyl group having 1 to 5 carbon atoms. Among them, an alkyl group having 1 to 3 carbon atoms is preferable in view of reactivity of polycondensation.

In the formula [A3], n is an integer of 0 to 3.

Specific examples of the alkoxysilane represented by the formula [A3] include tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, tetrabutoxysilane, methyltrimethoxysilane, methyltriethoxysilane, ethyltrimethoxysilane, (Trimethylsilyl) silane, dibutyldimethylsilane, dibutoxydimethylsilane, dibutoxydimethylsilane, (chloromethyl) triethoxysilane, ethyltriethoxysilane, propyltrimethoxysilane, propyltriethoxysilane, methyltripropoxysilane, dimethyldimethoxysilane, dimethyldiethoxysilane, But are not limited to, ethoxysilane, 3-chloropropyldimethoxymethylsilane, 3-chloropropyltriethoxysilane, 2-cyanoethyltriethoxysilane, trimethoxy (3,3,3-trifluoropropyl) Trimethoxysilane, 3-trimethoxysilylpropyl chloride and the like.

Examples of the alkoxysilane of the formula [A3] wherein n is 0 include tetramethoxysilane, tetraethoxysilane, tetrapropoxysilane, and tetrabutoxysilane.

The alkoxysilane represented by the above-mentioned formula [A3] is preferably used in an amount of from 0.01 to 10 parts by weight, based on the strength of the resin coating film or the liquid crystal alignment film, the workability at the time of film formation, furthermore, the liquid crystal alignment property, , One kind or two or more kinds may be mixed and used.

The specific polysiloxane of the present invention is a polysiloxane obtained by polycondensation of an alkoxysilane containing any one of the alkoxysilanes represented by the above-mentioned formula [A1], formula [A2] or formula [A3] Is preferably a polysiloxane obtained by polycondensation of an alkoxysilane. That is, the alkoxysilane containing two kinds of the above-mentioned formula [A1] and the formula [A2], the formula [A1] and the formula [A3] or the formula [A2] and the formula [A3] ], The formula [A2] and the formula [A3]. Among them, alkoxysilane containing two kinds of the above-mentioned formula [A1] and the formula [A2], the above-mentioned formula [A1] and the formula [A3], or the alkoxysilane of the above formula [A1], the formula [A2] Alkoxysilanes containing three species are preferable.

The alkoxysilane represented by the formula [A1], the formula [A2] or the formula [A3] is used for obtaining the specific polysiloxane of the present invention.

The alkoxysilane represented by the formula [A1] is preferably 1 to 40 mol%, more preferably 1 to 30 mol%, of all the alkoxysilanes. The alkoxysilane represented by the formula [A2] is preferably 1 to 70 mol%, more preferably 1 to 60 mol%, of all the alkoxysilanes. The alkoxysilane represented by the formula [A3] is preferably 1 to 99 mol%, more preferably 1 to 80 mol%, of all the alkoxysilanes.

The method for obtaining the specific polysiloxane used in the present invention is not particularly limited. The specific polysiloxane in the present invention is obtained by polymerizing an alkoxysilane containing any one of the alkoxysilanes represented by the above-mentioned formula [A1], formula [A2] or formula [A3] in an organic solvent, Can be obtained by polymerizing a plurality of alkoxysilanes among the alkoxysilanes represented by the formulas [A1], [A2] and [A3] in an organic solvent. The specific polysiloxane of the present invention is obtained as a solution in which an alkoxysilane is polycondensed and uniformly dissolved in an organic solvent.

The method of polycondensation of the specific polysiloxane of the present invention is not particularly limited. Among them, for example, a method of subjecting an alkoxysilane to a hydrolysis and polycondensation reaction in a specific solvent, an alcohol solvent or a glycol solvent of the present invention. At this time, the hydrolysis-polycondensation reaction may be partially hydrolyzed or completely hydrolyzed. In the case of completely hydrolyzing, in theory, 0.5-fold molar amount of water of all alkoxy groups in the alkoxysilane may be added, but it is usually preferable to add an excess amount of water in excess of 0.5-fold molar amount. In order to obtain the specific polysiloxane of the present invention, the amount of water used in the hydrolysis and polycondensation reaction may be appropriately selected according to the purpose, but is preferably 0.5 to 2.5 times the molar amount of all the alkoxy groups in the alkoxysilane.

For the purpose of accelerating the hydrolysis and polycondensation reaction, an acidic compound such as hydrochloric acid, sulfuric acid, nitric acid, acetic acid, formic acid, oxalic acid, maleic acid or fumaric acid, ammonia, methylamine, ethylamine, ethanolamine or triethylamine Or a catalyst such as a metal salt such as hydrochloric acid, nitric acid or nitric acid can be used. In addition, the hydrolysis-polycondensation reaction may be promoted by heating the solution in which the alkoxysilane is dissolved. At that time, the heating temperature and the heating time can be appropriately selected depending on the purpose. For example, heating and stirring at 50 DEG C for 24 hours, and then heating and stirring for 1 hour under reflux.

As another method of polycondensation, there is a method of heating a mixture of alkoxysilane, organic solvent and oxalic acid to perform polycondensation reaction. Specifically, oxalic acid is added to a specific solvent or alcohol solvent of the present invention in advance to prepare a solution of oxalic acid, and then the solution is heated to mix the alkoxysilane. At this time, the amount of oxalic acid to be used in the above reaction is preferably 0.2 to 2.0 mol per 1 mol of all alkoxy groups in the alkoxysilane. This reaction can be carried out at a temperature of the solution of 50 to 180 ° C, but is preferably carried out for several tens of minutes to several tens of hours under reflux so as not to evaporate or volatilize the solvent.

In the case of using a plurality of alkoxysilanes represented by the above formulas [A1], [A2] and [A3] in the polycondensation reaction for obtaining the specific polysiloxane of the present invention, Or may be reacted while sequentially adding a plurality of kinds of alkoxysilanes.

The solvent used in the polycondensation reaction of the alkoxysilane is not particularly limited as long as it dissolves the alkoxysilane. In addition, a solvent in which the alkoxysilane is not dissolved may be any one that dissolves along with the progress of the polycondensation reaction of the alkoxysilane. As the solvent used in the polycondensation reaction, an alcohol is generally generated by a polycondensation reaction of an alkoxysilane, and therefore an organic solvent having good compatibility with an alcohol solvent, a glycol solvent, a glycol ether solvent or an alcohol is used . Specific examples of the solvent to be used in the polycondensation reaction include alcohol solvents such as methanol, ethanol, propanol, butanol or diacetone alcohol, alcohols such as ethylene glycol, diethylene glycol, propylene glycol, dipropylene glycol, hexylene glycol, Butanediol, 1,3-butanediol, 2,3-butanediol, 1,2-pentanediol, 1,3-pentanediol, 1,4-pentanediol, Glycol solvents such as ethylene glycol monomethyl ether, ethylene glycol monoethyl ether, ethylene glycol monopropyl ether , Ethylene glycol monobutyl ether, ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dipropyl ether, ethylene glycol dibutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether , Diethylene glycol monobutyl ether, diethylene glycol dimethyl ether, diethylene glycol diethyl ether, diethylene glycol dipropyl ether, diethylene glycol dibutyl ether, propylene glycol monomethyl ether, propylene glycol monoethyl ether, propylene glycol monopropyl Glycol ether solvents such as ether, propylene glycol monobutyl ether, propylene glycol dimethyl ether, propylene glycol diethyl ether, propylene glycol dipropyl ether or propylene glycol dibutyl ether, N-methyl-2-pyrrolidone, An alcohol such as n-butanol, 2-pyrrolidone,? -Butyrolactone, N, N-dimethylformamide, N, N-dimethylacetamide, dimethylsulfoxide, tetramethylurea, hexamethylphosphotriapamide or m- Organic solvents with good hygroscopicity can be mentioned.

Among them, it is preferable to use the specific solvent of the present invention when adjusting the composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention. In the present invention, at the time of the polycondensation reaction, one or two or more kinds of the above-mentioned solvents may be mixed and used.

Solution polymerization of a specific polysiloxane obtained by the above method, it is preferred that (also referred to as SiO ₂ in terms of concentration) the total alkoxy silane is in terms of a silicon atom having a SiO ₂ concentration of injected as a raw material, 20 mass% or less. In particular, it is preferably 5 to 15% by mass. By selecting an arbitrary concentration in this concentration range, the generation of gel in the solution can be suppressed, and a uniform polycondensation solution of the specific polysiloxane can be obtained.

In the present invention, the polycondensation solution of the specific polysiloxane obtained by the above method may be directly used as the solution of the specific polysiloxane of the component (C) of the present invention. If necessary, the polycondensation solution of the specific polysiloxane obtained by the above- Or may be diluted by adding a solvent or replaced with another solvent to obtain a solution of the specific polysiloxane of the component (C).

The solvent (also referred to as an addition solvent) to be used for diluting by adding the above solvent may be a solvent used for a polycondensation reaction, a specific solvent of the present invention, or other solvent. The addition solvent is not particularly limited as long as the specific polysiloxane is uniformly dissolved, and one or more kinds of the addition solvent may be arbitrarily selected and used. Examples of such an addition solvent include ketone solvents such as acetone, methyl ethyl ketone or methyl isobutyl ketone, ester solvents such as methyl acetate, ethyl acetate or ethyl lactate, etc., in addition to the solvent used in the above polycondensation reaction .

In the present invention, it is preferable that the specific polysiloxane of the component (C) is subjected to distillation at a normal pressure or a reduced pressure to remove the alcohol generated during the polycondensation reaction of the specific polysiloxane before mixing with the specific polymer of the component (B).

The composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention is a coating solution for forming a resin coating or a liquid crystal alignment layer (collectively referred to as a resin coating), and is a coating solution for forming a resin coating containing a specific solvent, a specific polymer and a specific polysiloxane Coating solution. Among them, the polymer of the present invention in the composition or the liquid crystal alignment treatment agent using the composition is a specific polymer and a specific polysiloxane.

The content of the specific polysiloxane in the composition of the invention or the liquid crystal alignment treatment agent using the composition is preferably 0.1 to 90 parts by mass with respect to 100 parts by mass of the specific polymer component. Among them, from the viewpoint of the stability of the composition or the liquid crystal alignment treatment agent, 1 to 70 parts by mass is more preferable relative to 100 parts by mass of the specific polymer. Particularly preferably 5 to 60 parts by mass.

In the composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention, all of the polymer components may be the polymer of the present invention, and the polymer of the present invention may be mixed with other polymers. At that time, the content of the other polymer is 0.5% by mass to 15% by mass, preferably 1% by mass to 10% by mass, of the polymer of the present invention. As the other polymer, there may be mentioned a diamine compound having a carboxyl group, a second diamine compound, or a polyimide precursor or polyimide not using a specific tetracarboxylic acid component. Further, polymers other than polyimide precursors and polyimides, specifically, acrylic polymers, methacrylic polymers, polystyrenes, polyamides, and the like can be given.

The organic solvent in the composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention preferably has an organic solvent content of 70 to 99.9 mass% from the viewpoint of forming a uniform resin film by coating. This content can be appropriately changed depending on the film thickness of the intended resin film or liquid crystal alignment film.

All of the organic solvents in the organic solvent used in the composition of the present invention or the liquid crystal alignment treatment agent using the same may be any of the specific solvents of the present invention, and even if other organic solvents are mixed in the organic solvent of the present invention do. At this time, the specific solvent of the present invention is preferably 50 to 100% by mass of the total solvent contained in the composition or the liquid crystal alignment treatment agent. Among these, 55 to 100 mass% is preferable. More preferred is 55 to 95 mass%.

The other organic solvent is not particularly limited as long as it is an organic solvent capable of dissolving a specific polymer and a specific polysiloxane. Specific examples thereof are given below.

Examples of the solvent include N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, N- 1,3-dimethyl-imidazolidinone, methyl ethyl ketone, cyclohexanone, cyclopentanone or 4-hydroxy-4-methyl-2-pentanone.

Among them, it is preferable to use N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone or? -Butyrolactone (also referred to as component (D)).

These components (D) are preferably contained in an amount of 1 to 50% by mass of the entire organic solvent contained in the composition or the liquid crystal alignment treatment agent using the composition. Among them, 1 to 40% by mass is preferable. The content is more preferably from 1 to 30% by mass, and still more preferably from 5 to 30% by mass.

The composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention can be used in an organic solvent for improving the coating film property or surface smoothness of the resin film or liquid crystal alignment film when the composition or the liquid crystal alignment treatment agent using the composition is applied, , That is, a poor solvent can be used.

Specific examples of the poor solvent for improving the coating film property and surface smoothness of the resin coating film or liquid crystal alignment film are shown below.

Butanol, isobutyl alcohol, tert-butyl alcohol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, Butanol, neopentyl alcohol, 1-hexanol, 2-methyl-1-pentanol, 2-methyl- Butanol, 1-heptanol, 2-heptanol, 3-heptanol, 1-octanol, 2-octanol, 2-ethyl-1-hexanol, cyclohexanol, 1-methylcyclohexanol, 1,3-propanediol, 1,2-butanediol, 1,3-butanediol, 1,4-butanediol, 1,3-propanediol, Butanediol, 1,5-pentanediol, 2-methyl-2,4-pentanediol, 2-ethyl-1,3-hexanediol, dipropyl ether, dibutyl ether, dihexyl ether, dioxane, Ethylene glycol dimethyl ether, ethylene glycol diethyl ether, ethylene glycol dibutyl ether, 1,2-butoxyethane, diethylene glycol dimethyl ether, Ethylene glycol diethyl ether, diethylene glycol methyl ethyl ether, diethylene glycol dibutyl ether, 2-pentanone, 3-pentanone, 2-hexanone, 2-heptanone, 4- (2-ethylhexyl) acetate, ethylene glycol monoacetate, ethylene glycol diacetate, propylene carbonate, ethylene carbonate, 2- (methoxymethoxy) ethanol, ethylene glycol monobutyl Diethylene glycol monoethyl ether, diethylene glycol monoethyl ether, diethylene glycol monoethyl ether, ethylene glycol monohexyl ether, ethylene glycol monohexyl ether, 2- (hexyloxy) ethanol, furfuryl alcohol, diethylene glycol, diethylene glycol monomethyl ether, Propyl ether, diethylene glycol isopropyl ether, diethylene glycol monobutyl ether, propylene glycol, propylene glycol monobutyl ether, 1- (butoxyethoxy) Propylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, ethylene glycol monomethyl ether acetate, dipropylene glycol monomethyl ether, dipropylene glycol monoethyl ether, tripropylene glycol monomethyl ether, ethylene glycol monomethyl ether acetate, ethylene glycol monoethyl ether acetate, Diethylene glycol monoethyl ether acetate, diethylene glycol monobutyl ether acetate, 2- (2-ethoxyethoxy) ethyl acetate, diethylene glycol acetate, triethylene glycol monoacetate, triethylene glycol monoacetate, triethylene glycol monoacetate, triethylene glycol monoacetate, monobutyl ether acetate, ethylene glycol monoacetate, ethylene glycol diacetate, Propylene glycol monomethyl ether, ethylene glycol, triethylene glycol monomethyl ether, triethylene glycol monoethyl ether, methyl lactate, ethyl lactate, methyl acetate, ethyl acetate, n-butyl acetate, propylene glycol monoethyl ether acetate, methyl pyruvate, Methoxypropionate, methyl 3-methoxypropionate, methyl 3-methoxypropionate, methyl 3-ethoxypropionate, ethyl 3-methoxypropionate, 3-ethoxypropionic acid, 3- A solvent such as lactic acid methyl ester, lactic acid ethyl ester, n-propyl lactic acid ester, n-butyl lactic acid ester or lactic acid diisobutyl ester is low in surface tension.

Among them, 1-hexanol, cyclohexanol, 1,2-ethanediol, 1,2-propanediol, propylene glycol monobutyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, diethylene glycol monoethyl Ether, diethylene glycol monopropyl ether, diethylene glycol isopropyl ether or diethylene glycol monobutyl ether (also referred to as component (E)) is preferably used.

These components (E) are preferably contained in an amount of 1 to 50% by mass based on the total amount of the organic solvent contained in the composition or the liquid crystal alignment treatment agent using the composition. In particular, it is preferably 1 to 45% by mass. The content is more preferably 5 to 45% by mass, and still more preferably 5 to 40% by mass.

As long as the effect of the present invention is not impaired, the composition of the present invention or the liquid crystal alignment treatment agent using the composition may contain a crosslinkable compound having an epoxy group, an isocyanate group, an oxetane group or a cyclocarbonate group, a hydroxyl group, a hydroxyalkyl group and a lower alkoxyalkyl group , Or a crosslinkable compound having at least one kind of substituent selected from the group consisting of a polymerizable unsaturated bond may be introduced. These substituent groups and polymerizable unsaturated bonds need to have two or more in the crosslinkable compound.

Examples of the crosslinkable compound having an epoxy group or an isocyanate group include bisphenol acetone glycidyl ether, phenol novolak epoxy resin, cresol novolak epoxy resin, triglycidyl isocyanurate, tetraglycidylaminodiphenylene, (Aminoethyl) cyclohexane, tetraphenyl glycidyl ether ethane, triphenyl glycidyl ether ethane, bisphenol hexafluoroacetate di Glycidyl ether, 1,3-bis (1- (2,3-epoxypropoxy) -1-trifluoromethyl-2,2,2-trifluoromethyl) benzene, 4,4- 2- (4- (2,3-epoxypropoxy) phenyl) -2- (4-methylphenyl) Bis (4- (1- (4- (2,3-epoxypropoxy) phenyl) ethyl) phenyl) propane or 1,3- ) Phenyl) -1- ( 1-methylethyl) phenyl) ethyl) phenoxy) -2-propanol, and the like.

The crosslinkable compound having an oxetane group is a crosslinkable compound having at least two oxetane groups represented by the following formula [4].

(73)

Specifically, it is a crosslinkable compound represented by the following formulas [4-1] to [4-11].

&Lt; EMI ID =

(In the formula [4-1], n represents an integer of 1 to 3).

(75)

[Formula 76]

[Formula 77]

(4-7), n represents an integer of 1 to 3, and n in the formula [4-8] represents an integer of 1 to 3, and n in the formula [4-9] Lt; / RTI >

(78)

(In the formula [4-11], n represents an integer of 1 to 10).

The crosslinkable compound having a cyclocarbonate group is a crosslinkable compound having at least two cyclocarbonate groups represented by the following formula [5].

(79)

Specifically, it is a crosslinkable compound represented by the following formulas [5-1] to [5-37].

(80)

[Formula 81]

(82)

(83)

(84)

(85)

&Lt; EMI ID =

[Chemical Formula 87]

[Formula 88]

(89)

(90)

[Formula 91]

(In the formula [5-24], n represents an integer of 1 to 10, and in the formula [5-25], n represents an integer of 1 to 10).

&Lt; EMI ID =

&Lt; EMI ID =

(94)

&Lt; EMI ID =

&Lt; EMI ID =

(In the formula [5-36], n represents an integer of 1 to 100, and in the formula [5-37], n represents an integer of 1 to 10).

Also, a polysiloxane having at least one structure represented by the following formulas [5-38] to [5-40] may be used.

[Formula 97]

(Wherein R ₁ , R ₂ , R ₃ , R ₄ and R ₅ each independently represent a structure represented by the formula [5], a hydrogen atom, a hydroxyl group, a carbon number An alkyl group, an alkoxyl group, an aliphatic ring or an aromatic ring of 1 to 10 carbon atoms, and at least one of them represents a structure represented by the formula [5].

More specifically, the compounds of the following formulas [5-41] and [5-42] can be mentioned.

(98)

(In the formula [5-42], n represents an integer of 1 to 10).

Examples of the crosslinkable compound having at least one substituent selected from the group consisting of a hydroxyl group and an alkoxyl group include an amino resin having a hydroxyl group or an alkoxyl group such as a melamine resin, Formaldehyde resin, succinamide-formaldehyde resin or ethylene urea-formaldehyde resin, and the like. Specifically, a melamine derivative in which the hydrogen atom of the amino group is substituted with a methylol group or an alkoxymethyl group, or a benzoguanamine derivative or glycoluril can be used. The melamine derivative or the benzoguanamine derivative may be present as a dimer or trimer. These groups preferably have 3 to 6 on average of methylol groups or alkoxymethyl groups per one triazine ring.

Examples of such melamine derivatives or benzoguanamine derivatives include MX-750 in which a methoxymethyl group is substituted on average 3.7 per 1 triazine ring of a commercial product, MW- Methomethylated melamines such as Cymel 235, 236, 238, 212, 253, and 309 (manufactured by Sanwa Chemical Co., Ltd.) or Cymel 300, 301, 303, 350, 370, 771, 325, 327, 703, 254, methoxymethylated butoxymethylated melamines such as Cymel 506 and 508, carboxyl-containing methoxymethylated isobutoxymethylated melamines such as Cymel 1141, methoxymethylated ethoxymethylated melamine such as Cymel 1123, Guanamine, methoxymethylated butoxymethylated benzoguanamine such as Cymel 1123-10, butoxymethylated benzoguanamine such as Cymel 1128, carboxyl-containing methoxymethylated ethoxymethylated benzylamine such as Cymel 1125-80 Guanamine may include (or more, mid, manufactured by Mitsui between Ana). Examples of glycoluril include butoxymethylated glycoluril such as Cymel 1170, methylol glycoluryl such as Cymel 1172, and methoxymethylolglycoluril such as Powderlink 1174, and the like.

Examples of the benzene or phenolic compound having a hydroxyl group or an alkoxyl group include 1,3,5-tris (methoxymethyl) benzene, 1,2,4-tris (isopropoxymethyl) benzene, 4-bis (sec-butoxymethyl) benzene, or 2,6-dihydroxymethyl-p-tert-butylphenol.

More specifically, there are listed crosslinkable compounds represented by the formulas [6-1] to [6-48], which are listed on pages 62 to 66 of International Publication WO2011 / 132751 have.

Examples of the crosslinkable compound having a polymerizable unsaturated bond include trimethylolpropane tri (meth) acrylate, pentaerythritol tri (meth) acrylate, dipentaerythritol penta (meth) acrylate, tri (meth) Acryloyloxyethoxy trimethylol propane or glycerin polyglycidyl ether poly (meth) acrylate, and also crosslinking compounds having three polymerizable unsaturated groups in the molecule, such as ethylene glycol di (meth) acrylate, diethylene Acrylate, propylene glycol di (meth) acrylate, polypropylene glycol di (meth) acrylate, butylene glycol di (meth) acrylate, diethylene glycol di (Meth) acrylate, neopentyl glycol di (meth) acrylate, ethylene oxide bisphenol A type di (meth) acrylate, propylene (Meth) acrylate, glycerin di (meth) acrylate, pentaerythritol di (meth) acrylate, ethylene glycol diglycidyl ether di (Meth) acrylate such as di (meth) acrylate, diethylene glycol diglycidyl ether di (meth) acrylate, phthalic acid diglycidyl ester di (meth) acrylate or hydroxypivalic acid neopentyl glycol di (Meth) acrylate, 2-hydroxypropyl (meth) acrylate, 2-hydroxybutyl (meth) acrylate, 2-phenoxy 2-hydroxypropyl (meth) acrylate, glycerin mono (meth) acrylate, 2-hydroxypropyl Rate, 2 A crosslinkable compound having one polymerizable unsaturated group such as - (meth) acryloyloxyethyl phosphate ester or N-methylol (meth) acrylamide.

In addition, a compound represented by the following formula [7] may be used.

[Formula 99]

(Wherein E ₁ represents a group selected from the group consisting of a cyclohexane ring, a bicyclohexane ring, a benzene ring, a biphenyl ring, a terphenyl ring, a naphthalene ring, a fluorene ring, an anthracene ring or a phenanthrene ring) And E ₂ represents a group selected from the following formula [7a] or formula [7b], and n represents an integer of 1 to 4).

(100)

The above compound is an example of a crosslinkable compound, but is not limited thereto. The crosslinkable compound used in the composition of the present invention or the liquid crystal alignment treatment agent using the composition may be of one kind, or may be a combination of two or more kinds.

The content of the crosslinkable compound in the composition of the present invention or the liquid crystal alignment treatment agent using it is preferably 0.1 to 150 parts by mass with respect to 100 parts by mass of all the polymer components. More preferably from 0.1 to 100 parts by mass, particularly preferably from 1 to 50 parts by mass, per 100 parts by mass of all the polymer components, in order for the crosslinking reaction to proceed and to exhibit the intended effect.

As a compound for promoting charge transfer in the liquid crystal alignment film and promoting charge leakage of the liquid crystal cell using the liquid crystal alignment film when the liquid crystal alignment treatment agent using the composition of the present invention is used as a liquid crystal alignment film, It is preferable to add a nitrogen-containing heterocyclic amine compound represented by the formula [M1] to the formula [M156], which is disclosed on pages 69 to 73 of Published Dec. 27, 2011. The amine compound may be added directly to the composition, but it is preferable to add the amine compound in an appropriate solvent at a concentration of 0.1% by mass to 10% by mass, preferably 1% by mass to 7% by mass. This solvent is not particularly limited as long as it is an organic solvent capable of dissolving the above-mentioned polymer.

The composition of the present invention or the liquid crystal alignment treatment agent using the composition can improve the uniformity of the film thickness or the surface smoothness of the resin film or the liquid crystal alignment film when the composition or the liquid crystal alignment treatment agent using the composition is applied, May be used. Further, a compound for improving the adhesion of the resin film or the liquid crystal alignment film to the substrate may be used.

Examples of the compound which improves the uniformity of the film thickness or the surface smoothness of the resin coating film or the liquid crystal alignment film include a fluorinated surfactant, a silicon surfactant and a nonionic surfactant.

More specifically, for example, EF301, EF303 and EF352 (manufactured by Tohchem Products Corporation), Megafac F171, F173 and R-30 (manufactured by Dainippon Ink and Chemicals, Inc.), Florad FC430 and FC431 (Available from Asahi Glass Co., Ltd.), Asahi Guard AG710, Surfron S-382, SC101, SC102, SC103, SC104, SC105 and SC106 (manufactured by Asahi Glass Co., Ltd.). The ratio of these surfactants to be used is preferably 0.01 to 2 parts by mass, more preferably 0.01 to 1 part by mass based on 100 parts by mass of all the polymer components contained in the composition or the liquid crystal alignment treatment agent.

Specific examples of the compound that improves the adhesion between the resin film or the liquid crystal alignment film and the substrate include the following functional silane-containing compounds and epoxy group-containing compounds.

For example, 3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 2-aminopropyltrimethoxysilane, 2-aminopropyltriethoxysilane, N- (2-aminoethyl) -3 3-aminopropylmethyldimethoxysilane, 3-ureidopropyltrimethoxysilane, 3-ureidopropyltriethoxysilane, N-ethoxy (3-aminopropyl) Aminopropyltriethoxysilane, N-trimethoxysilylpropyltriethoxysilane, N-trimethoxysilylpropyltriethoxysilane, N-trimethoxysilylpropyltriethoxysilane, N-trimethoxysilylpropyltriethoxysilane, Amine, 10-trimethoxysilyl-1,4,7-triazadecane, 10-triethoxysilyl-1,4,7-triazadecane, 9-trimethoxysilyl-3,6-diazanonyl Acetate, 9-triethoxysilyl-3,6-diazanonyl acetate, N-benzyl-3-aminopropyltrimethoxysilane, N-benzyl-3-aminopropyltriethoxysilane, N- Bis (oxyethylene) -3-aminopropyltrimethoxysilane, N-phenyl-3-aminopropyltriethoxysilane, N- Aminopropyltriethoxysilane, ethylene glycol diglycidyl ether, polyethylene glycol diglycidyl ether, propylene glycol diglycidyl ether, tripropylene glycol diglycidyl ether, polypropylene glycol diglycidyl ether, neo Pentyl glycol diglycidyl ether, 1,6-hexanediol diglycidyl ether, glycerin diglycidyl ether, 2,2-dibromoneopentyl glycol diglycidyl ether, 1,3,5,6 Tetraglycidyl-2,4-hexanediol, N, N, N ', N', -tetraglycidyl-m-xylylenediamine, 1,3-bis (N, N-diglycidylamino Methyl) cyclohexane or N, N, N ', N', -tetraglycidyl-4,4'-diaminodiphenylmethane and the like.

When a compound which adheres to these substrates is used, it is preferably 0.1 to 30 parts by mass, more preferably 1 to 20 parts by mass, based on 100 parts by mass of all the polymer components contained in the composition or the liquid crystal alignment treatment agent using the same. If the amount is less than 0.1 part by mass, the effect of improving the adhesion can not be expected. If the amount is more than 30 parts by mass, the storage stability of the composition or the liquid crystal alignment treatment agent using the composition may be deteriorated.

The composition of the present invention or the liquid crystal alignment treatment agent using the composition of the present invention may contain, in addition to the compound for improving the uniformity of the film thickness of the poor solvent, the crosslinkable compound, the resin film or the liquid crystal alignment film, If the effect is not hindered, a dielectric material or a conductive material may be added for the purpose of changing electrical characteristics such as dielectric constant and conductivity of the resin film or the liquid crystal alignment film.

&Lt; Resin Coating >

The composition of the present invention can be used as a resin film after being coated and baked on a substrate. As the substrate to be used at this time, a plastic substrate such as a glass substrate, a silicon wafer, an acrylic substrate, or a polycarbonate substrate may be used depending on the intended device. The method of applying the composition is not particularly limited, but a method of industrially performing the method by dip coating, roll coating, slit coating, spinner coating, spray coating, screen printing, offset printing, It is common. They may be used according to the purpose.

After the composition is applied onto the substrate, it is heated to 50 to 250 DEG C, preferably 80 to 200 DEG C, more preferably 80 to 200 DEG C, by heating means such as a hot plate, a heat circulation type oven or an IR (infrared) The solvent can be evaporated at 150 ° C to form a resin film. The thickness of the resin film after firing can be adjusted to 0.01 to 100 탆, depending on the purpose.

The liquid crystal alignment treatment agent using the composition of the present invention can be used as a liquid crystal alignment film after being applied and baked on a substrate and subjected to an orientation treatment by rubbing treatment, light irradiation, or the like. Further, in the case of vertical alignment application, etc., it can be used as a liquid crystal alignment film without alignment treatment. The substrate to be used at this time is not particularly limited as long as it is a substrate having high transparency. In addition to the glass substrate, a plastic substrate such as an acrylic substrate or a polycarbonate substrate can also be used. From the viewpoint of simplification of the process, it is preferable to use a substrate on which an ITO electrode or the like for liquid crystal driving is formed. In a reflective liquid crystal display device, an opaque substrate such as a silicon wafer can be used as long as it is a substrate on only one side. As the electrode in this case, a material that reflects light such as aluminum can also be used.

The method of applying the liquid crystal alignment treatment agent is not particularly limited, but industrially, a method of screen printing, offset printing, flexographic printing, or inkjet printing is generally used. Other coating methods include a dipping method, a roll coater method, a slit coater method, a spinner method, and a spraying method, and they may be used depending on the purpose.

After the liquid crystal alignment treatment agent is applied onto the substrate, it is heated to 50 to 250 ° C, preferably 80 to 200 ° C, more preferably to 80 to 200 ° C by heating means such as a hot plate, a heat circulation type oven, or an IR (infrared) The liquid crystal alignment layer can be formed by evaporating the solvent at 80 to 150 ° C. When the thickness of the liquid crystal alignment film after firing is too large, the power consumption of the liquid crystal display element is disadvantageously deteriorated. When too thin, the reliability of the liquid crystal display element may deteriorate, so that the thickness is preferably 5 to 300 nm, 10 to 100 nm. When the liquid crystal is horizontally or tilted, the fired liquid crystal alignment film is treated by rubbing, polarized ultraviolet irradiation, or the like.

In the liquid crystal display element of the present invention, a substrate on which a liquid crystal alignment film is formed from the liquid crystal alignment treatment agent of the present invention is formed by the above-mentioned technique, and then a liquid crystal cell is produced by a known method to form a liquid crystal display element.

As a manufacturing method of the liquid crystal cell, a pair of substrates on which a liquid crystal alignment film is formed is prepared, a spacer is spread on the liquid crystal alignment film of the substrate of the one chamber, and the substrates of the other chamber are bonded ), A method of sealing the liquid crystal by injecting the liquid crystal under reduced pressure, or a method in which liquid crystal is dropped on the surface of the liquid crystal alignment film on which the spacer is sprayed, and the substrate is then subjected to sealing.

Further, the liquid crystal alignment treatment agent of the present invention is a liquid crystal alignment treatment agent comprising a liquid crystal layer between a pair of substrates provided with electrodes, a polymerizable compound which is polymerized by at least one of active energy rays and heat between a pair of substrates And a method of polymerizing a polymerizable compound by at least one of irradiation of an active energy ray and heating while applying a voltage between electrodes is preferably used for a liquid crystal display device. As the active energy ray, ultraviolet ray is preferable. The ultraviolet ray has a wavelength of 300 to 400 nm, preferably 310 to 360 nm. In the case of polymerization by heating, the heating temperature is 40 to 120 占 폚, preferably 60 to 80 占 폚. In addition, irradiation with ultraviolet rays and heating may be simultaneously performed.

The liquid crystal display element described above controls the pretilt of liquid crystal molecules by a PSA (Polymer Sustained Alignment) method. In the PSA system, a small amount of a photopolymerizable compound such as a photopolymerizable monomer is mixed in a liquid crystal material, and after a liquid crystal cell is assembled, a predetermined voltage is applied to the liquid crystal layer, And controls the pretilt of the liquid crystal molecules by the produced polymer. Since the alignment state of the liquid crystal molecules when the polymer is produced is stored even after the voltage is removed, the pretilt of the liquid crystal molecules can be adjusted by controlling the electric field or the like formed on the liquid crystal layer. In the PSA method, since the rubbing treatment is not required, it is suitable for forming a vertical alignment type liquid crystal layer which is difficult to control the pretilt by the rubbing treatment.

That is, the liquid crystal display element of the present invention can be obtained by obtaining a substrate on which a liquid crystal alignment film is formed from the liquid crystal alignment treatment agent of the present invention by the above-mentioned technique, preparing a liquid crystal cell, The orientation of the liquid crystal molecules can be controlled.

For example, a pair of substrates on which a liquid crystal alignment film is formed is prepared. Spacers are sprayed on the liquid crystal alignment film of the substrate of the single chamber to make the liquid crystal alignment film face inward, A method in which liquid crystal is injected under reduced pressure, or a method in which a liquid crystal is dropped on the surface of a liquid crystal alignment film on which a spacer is spread, and then a substrate is bonded by sealing.

The liquid crystal is mixed with a polymerizable compound which is polymerized by irradiation with heat or ultraviolet rays. Examples of the polymerizable compound include compounds having at least one polymerizable unsaturated group such as an acrylate group or a methacrylate group in the molecule. At that time, the polymerizable compound is preferably 0.01 to 10 parts by mass, more preferably 0.1 to 5 parts by mass, per 100 parts by mass of the liquid crystal component. When the amount of the polymerizable compound is less than 0.01 part by mass, the polymerizable compound is not polymerized and the orientation of the liquid crystal can not be controlled. When the amount is larger than 10 parts by mass, the amount of unreacted polymerizable compound increases, .

After the liquid crystal cell is fabricated, the polymerizable compound is polymerized by applying heat or ultraviolet rays while applying alternating current or direct current voltage to the liquid crystal cell. Thereby, the orientation of the liquid crystal molecules can be controlled.

In addition, the liquid crystal alignment treatment agent of the present invention comprises a liquid crystal layer between a pair of substrates provided with electrodes, and a polymerizable group which is polymerized by at least one of active energy rays and heat between the pair of substrates And a liquid crystal display device manufactured by a process of applying a voltage between electrodes. As the active energy ray, ultraviolet ray is preferable. The ultraviolet ray has a wavelength of 300 to 400 nm, preferably 310 to 360 nm. In the case of polymerization by heating, the heating temperature is 40 to 120 占 폚, preferably 60 to 80 占 폚. In addition, irradiation with ultraviolet rays and heating may be simultaneously performed.

In order to obtain a liquid crystal alignment film containing a polymerizable group polymerized by at least one of an active energy ray and heat, a method of adding a compound containing the polymerizable group to a liquid crystal alignment treatment agent, a method of using a polymer component containing a polymerizable group Method. Since the liquid crystal alignment treatment agent of the present invention contains a specific compound having a double bonding site that reacts by irradiation with heat or ultraviolet rays, the orientation of the liquid crystal molecules can be controlled by at least one of irradiation of ultraviolet rays and heating have.

One example of manufacturing a liquid crystal cell is to prepare a pair of substrates on which a liquid crystal alignment film is formed and spray a spacer on the liquid crystal alignment film of the substrate of the single chamber to make the liquid crystal alignment film face inward, , A method of sealing the liquid crystal by injecting it under a reduced pressure, or a method of dropping liquid crystal on the surface of the liquid crystal alignment film spreading the spacer and then sealing the substrate by bonding.

After the liquid crystal cell is manufactured, the alignment of the liquid crystal molecules can be controlled by applying heat or ultraviolet rays while applying alternating current or direct current voltage to the liquid crystal cell.

As described above, the liquid crystal display device manufactured using the liquid crystal alignment treatment agent of the present invention is excellent in reliability, and can be preferably used for a liquid crystal television with high precision on a large screen.

Example

Hereinafter, the present invention will be described in more detail by way of examples, but the present invention is not limited thereto.

Abbreviations used in Synthesis Examples, Examples and Comparative Examples are as follows.

(Diamine compound having a carboxyl group)

A1: 3,5-diaminobenzoic acid (diamine compound represented by the following formula [A1]):

A2: 2,5-diaminobenzoic acid (diamine compound represented by the following formula [A2]):

(101)

(Second diamine compound)

B1: 1,3-diamino-4- [4- (trans-4-n-heptylcyclohexyl) phenoxy] benzene (diamine compound represented by the following formula [B1]

B2: 1,3-diamino-4- [4- (trans-4-n-heptylcyclohexyl) phenoxymethyl] benzene (diamine compound represented by the following formula [B2]

B3: 1,3-Diamino-4- {trans 4- (trans-4-n-pentylcyclohexyl) cyclohexyl] phenoxy} benzene (diamine compound represented by the following formula [B3]

B4: diamine compound represented by the following formula [B4]

B5: 1,3-Diamino-4-octadecyloxybenzene (diamine compound represented by the following formula [B5]):

B6: diamine compound represented by the following formula [B6]

&Lt; EMI ID =

&Lt; EMI ID =

&Lt; EMI ID =

(Other diamine compounds)

C1: p-phenylenediamine (diamine compound represented by the following formula [C1]):

C2: m-phenylenediamine (diamine compound represented by the following formula [C2]):

&Lt; EMI ID =

(Tetracarboxylic acid component)

D1: 1,2,3,4-Cyclobutane tetracarboxylic acid dianhydride (tetracarboxylic acid dianhydride represented by the following formula [D1]):

D2: bicyclo [3,3,0] octane-2,4,6,8-tetracarboxylic acid dianhydride (tetracarboxylic acid dianhydride represented by the following formula [D2]

D3: tetracarboxylic acid dianhydride represented by the following formula [D3]

D4: tetracarboxylic acid dianhydride represented by the following formula [D4]

&Lt; EMI ID =

(Alkoxysilane monomer)

MPMS: 3-methacryloxypropyltrimethoxysilane (alkoxysilane monomer represented by the formula [A2] of the present invention)

UPS: 3-ureide propyltriethoxysilane (alkoxysilane monomer represented by the formula [A2] of the present invention)

TEOS: tetraethoxysilane (alkoxysilane monomer represented by the formula [A3] of the present invention)

(Component (A) (specific solvent) of the present invention)

PGME: Propylene glycol monomethyl ether (solvent represented by the formula [1a-1] of the present invention)

MCS: Ethylene glycol monomethyl ether (solvent represented by the formula [1b-1] of the present invention)

ECS: ethylene glycol monoethyl ether (solvent represented by the formula [1b-2] of the present invention)

PCS: ethylene glycol monopropyl ether (solvent represented by the formula [1b-3] of the present invention)

&Lt; EMI ID =

(Component (D) of the present invention (other organic solvent))

NMP: N-methyl-2-pyrrolidone

NEP: N-ethyl-2-pyrrolidone

? -BL:? -butyrolactone

(Component (E) (other organic solvent) of the present invention)

BCS: ethylene glycol monobutyl ether

(Measurement of molecular weight of polyimide precursor and polyimide)

The molecular weights of the polyimide precursor and the polyimide in the synthesis examples were measured using a gel permeation chromatography (GPC) apparatus (GPC-101) (manufactured by Showa Denko K.K.), a column (KD-803, KD-805 Manufactured by Mitsui Chemicals, Inc.).

Column temperature: 50 ° C

Eluent: 30 mmol / l (liter) of lithium bromide-hydrate (LiBr.H ₂ O), 30 mmol / l of phosphoric anhydride crystal (o-phosphoric acid) as an additive, N, N'-dimethylformamide 10 ml / l of hydrofuran (THF)

Flow rate: 1.0 ml / min

Standard samples for preparing a calibration curve: TSK standard polyethylene oxide (molecular weight: about 900,000, 150,000, 100,000 and 30,000) (manufactured by Toso Co., Ltd.) and polyethylene glycol (molecular weight: about 12,000, 4,000 and 1,000) by Polymer Laboratories.

(Measurement of imidization ratio of polyimide)

The imidization rate of the polyimide in the synthesis example was measured in the following manner. (DMSO-d6, 0.05 mass% TMS (tetramethylsilane) mixture) of polyimide powder was placed in an NMR (nuclear magnetic resonance) sample tube (NMR sampling tube standard, Product) (0.53 ml) was added, and completely dissolved by ultrasonic wave. This solution was subjected to proton NMR measurement at 500 MHz using an NMR measuring instrument (JNW-ECA500) (manufactured by Nippon Denshoku KK). A proton originating from a structure which does not change before and after imidization is defined as a reference proton and the peak value of the proton is calculated by integrating the proton peak derived from the NH group of the amide acid appearing in the vicinity of 9.5 ppm to 10.0 ppm Value obtained by the following equation.

Imidization ratio (%) = (1 -? X / y) x 100

In the above formula, x is the proton peak integrated value derived from the NH group of the amide acid, y is the peak integrated value of the reference proton, and? Is the NH of the amide acid in the case of the polyamic acid (the imidization rate is 0% The ratio of the number of reference protons to one protopertone.

&Quot; Synthesis of specific polymer (polyimide precursor and polyimide) which is component (B) of the present invention "

&Lt; Synthesis Example 1 &

(3.12 g, 15.9 mmol) and A1 (2.42 g, 15.9 mmol) were mixed in PGME (49.9 g) and reacted at 40 ° C for 8 hours to obtain a polyamic acid solution (1) having a resin solid concentration of 10.0 mass% . The polyamic acid had a number average molecular weight of 10,100 and a weight average molecular weight of 23,500.

&Lt; Synthesis Example 2 &

D1 (1.65 g, 8.41 mmol) and NMP (22.2 g) were added to the reaction mixture at 80 ° C for 5 hours, And the mixture was allowed to react at 40 DEG C for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (6.52 g) and pyridine (5.05 g) were added as an imidation catalyst and the reaction was carried out at 90 ° C for 4 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (2). The imidization ratio of this polyimide was 55%, and the number average molecular weight was 12,200 and the weight average molecular weight was 33,000.

&Lt; Synthesis Example 3 &

D2 (1.82 g, 7.27 mmol), B1 (2.30 g, 6.04 mmol) and A1 (0.92 g, 6.05 mmol) were mixed in PGME (29.7 g) 4.84 mmol) and PGME (24.3 g) were added and reacted at 40 占 폚 for 8 hours to obtain a polyamic acid solution (3) having a resin solid content concentration of 10.0 mass%. The number average molecular weight of the polyamic acid was 12,500 and the weight average molecular weight was 34,100.

&Lt; Synthesis Example 4 &

D2 (3.83 g, 15.3 mmol), B1 (4.86 g, 12.8 mmol) and A1 (1.94 g, 12.8 mmol) were mixed in NMP (20.8 g) 10.2 mmol) and NMP (17.0 g) were added and reacted at 40 占 폚 for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (5.16 g) and pyridine (4.00 g) were added as imidation catalysts and reacted at 80 ° C for 2 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (4). The imidization ratio of the polyimide was 61%, the number average molecular weight was 15,200, and the weight average molecular weight was 38,300.

&Lt; Synthesis Example 5 &

C (0.33 g, 3.05 mmol) was mixed in NMP (24.2 g) and stirred at 80 < 0 > C for 5 h After the reaction, D1 (1.20 g, 6.12 mmol) and NMP (19.8 g) were added and reacted at 40 ° C for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

To the resulting polyamic acid solution (40.0 g) was added NMP and diluted to 6 mass%. Acetic anhydride (5.33 g) and pyridine (4.13 g) were added as imidation catalysts and reacted at 80 ° C for 2 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (5). The imidization ratio of the polyimide was 58%, the number average molecular weight was 16,100, and the weight average molecular weight was 39,100.

&Lt; Synthesis Example 6 &

(2.19 g, 14.0 mmol) and B6 (1.14 g, 5.61 mmol) were mixed in NMP (21.7 g) and heated to 80 < 0 > C for 5 hours After the reaction, D1 (1.65 g, 8.41 mmol) and NMP (17.8 g) were added and reacted at 40 ° C for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (5.50 g) and pyridine (4.25 g) were added as imidation catalysts and reacted at 80 ° C for 3 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol, and dried at 100 ° C under reduced pressure to obtain a polyimide powder (6). The imidization ratio of the polyimide was 51%, the number average molecular weight was 17,900, and the weight average molecular weight was 41,200.

&Lt; Synthesis Example 7 &

(2.63 g, 17.3 mmol) and C2 (0.31 g, 2.87 mmol) were mixed in NMP (22.2 g) and heated to 80 < 0 > C for 5 h After the reaction, D1 (1.70 g, 8.67 mmol) and NMP (18.2 g) were added and reacted at 40 占 폚 for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute the solution to 6 mass%, acetic anhydride (5.64 g) and pyridine (4.38 g) were added as imidation catalysts and reacted at 80 ° C for 3 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol, and dried at 100 ° C under reduced pressure to obtain a polyimide powder (7). The imidization ratio of the polyimide was 60%, the number average molecular weight was 18,900, and the weight average molecular weight was 42,900.

&Lt; Synthesis Example 8 &

D2 (6.28 g, 25.1 mmol), B4 (2.32 g, 4.71 mmol) and A1 (4.06 g, 26.7 mmol) were mixed in NMP (22.9 g) 6.27 mmol) and NMP (18.7 g) were added and reacted at 40 占 폚 for 6 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

To the resulting polyamic acid solution (40.0 g) was added NMP and diluted to 6 mass%. Acetic anhydride (5.77 g) and pyridine (4.47 g) were added as an imidization catalyst and reacted at 80 ° C for 3.5 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (8). The imidization ratio of the polyimide was 45%, the number average molecular weight was 15,100, and the weight average molecular weight was 36,500.

&Lt; Synthesis Example 9 &

(3.3 g, 8.72 mmol) and A1 (3.09 g, 20.3 mmol) were mixed in NMP (38.8 g) and reacted at 40 ° C for 5 hours to obtain a resin solid concentration of 25.0 mass % Polyamic acid solution.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (5.74 g) and pyridine (4.45 g) were added as an imidation catalyst and reacted at 80 ° C for 3 hours. The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (9). The imidization ratio of the polyimide was 60%, the number average molecular weight was 13,100, and the weight average molecular weight was 36,200.

&Lt; Synthesis Example 10 &

A mixture of D3 (6.54 g, 29.2 mmol), B5 (3.30 g, 8.76 mmol), B6 (1.19 g, 5.85 mmol) and A2 (2.22 g, 14.6 mmol) in NMP (39.7 g) To obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (5.62 g) and pyridine (4.36 g) were added as an imidation catalyst and reacted at 80 ° C for 3 hours. The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 占 폚 to obtain a polyimide powder (10). The imidization ratio of this polyimide was 55%, and the number average molecular weight was 12,100 and the weight average molecular weight was 32,900.

&Lt; Synthesis Example 11 &

(2.40 g, 15.8 mmol) were mixed in NMP (22.6 g), and the mixture was stirred at 80 占 폚 for 5 hours After the reaction, D1 (2.25 g, 11.5 mmol) and NMP (18.5 g) were added and reacted at 40 DEG C for 5.5 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (6.45 g) and pyridine (3.35 g) were added as imidation catalysts and reacted at 40 ° C for 1.5 hours. The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (11). The imidization ratio of the polyimide was 59%, the number average molecular weight was 19,100, and the weight average molecular weight was 40,600.

&Lt; Synthesis Example 12 &

B6 (1.65 g, 8.12 mmol) and A1 (1.64 g, 10.8 mmol) were mixed in NMP (21.6 g) and heated at 80 < 0 > C for 5 h After the reaction, D1 (2.65 g, 13.5 mmol) and NMP (17.7 g) were added and reacted at 40 DEG C for 5.5 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

NMP was added to the obtained polyamic acid solution (40.0 g) to dilute to 6 mass%, acetic anhydride (6.33 g) and pyridine (3.27 g) were added as imidation catalysts and reacted at 40 ° C for 1.5 hours. The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol and dried under reduced pressure at 100 ° C to obtain a polyimide powder (12). The imidization ratio of this polyimide was 55%, the number average molecular weight was 17,800, and the weight average molecular weight was 39,100.

&Lt; Synthesis Example 13 &

(2.85 g, 14.5 mmol) were mixed in NMP (15.2 g) and reacted at 40 DEG C for 8 hours to obtain a polyamic acid solution (13) having a resin solid content concentration of 25.0 mass% . The polyamic acid had a number average molecular weight of 18,100 and a weight average molecular weight of 35,200.

&Lt; Synthesis Example 14 &

D2 (4.11 g, 16.4 mmol), B1 (5.22 g, 13.7 mmol) and A1 (2.09 g, 13.7 mmol) were mixed in NMP (22.4 g) 11.0 mmol) and NMP (18.3 g) were added and reacted at 40 DEG C for 6 hours to obtain a polyamic acid solution (14) having a resin solid content concentration of 25.0 mass%. The polyamic acid had a number average molecular weight of 19,100 and a weight average molecular weight of 45,800.

&Lt; Synthesis Example 15 &

(2.10 g, 13.4 mmol) were dissolved in NMP (20.9 g) and reacted at 80 ° C for 5 hours. 10.7 mmol) and NMP (17.1 g) were added and reacted at 40 DEG C for 5.5 hours to obtain a polyamic acid solution having a resin solid content concentration of 25.0 mass%.

To the resulting polyamic acid solution (40.0 g) was added NMP and diluted to 6 mass%. Acetic anhydride (5.40 g) and pyridine (4.18 g) were added as imidation catalysts and reacted at 80 ° C for 3 hours . The reaction solution was poured into methanol (650 ml), and the resulting precipitate was separated by filtration. The precipitate was washed with methanol, and dried at 100 ° C under reduced pressure to obtain a polyimide powder (15). The imidization rate of the polyimide was 60%, the number average molecular weight was 16,000, and the weight average molecular weight was 39,200.

Specific polymers of the present invention (polyimide precursor and polyimide) are shown in Table 1.

* 1: Polyamide acid.

&Quot; Synthesis of alkoxysilane monomer represented by formula [A1] of the present invention "

&Lt; Synthesis Example 16 &

(108)

Compound (1) (30.0 g), potassium carbonate (25.2 g) and DMF (120 g) were charged into a 500 ml four-necked flask equipped with a magnetic stirrer and allyl bromide (22.1 g) did. Thereafter, the mixture was stirred at 50 占 폚 for 11 hours. The reaction solution was diluted with ethyl acetate (500 g), and the organic phase was washed three times with pure water (200 g). The organic phase was dried over sodium sulfate, filtered and the filtrate was concentrated to dryness to give compound (2) (yield: 34.8 g, yield: 100%).

Compound (2) (20.0 g) and toluene (120 g) were poured into a 300 ml four-necked flask equipped with a magnetic stirrer and stirred at 25 占 폚. Next, 700 쨉 l of a Karstedt catalyst (0.1 mol / l xylene solution of platinum (0) -1,1,3,3-tetramethyldisiloxane complex) (700 쨉 l) was added, and trimethoxysilane (12.4 ml ). After stirring at 25 DEG C for 29 hours, the reaction solution was concentrated to dryness to obtain an amorphous substance. This was subjected to distillation under reduced pressure to distill out under the conditions of an external temperature of 245 ° C and a pressure of 0.8 torr to obtain an alkoxysilane monomer (A) (yield: 12.2 g, yield: 43%) represented by the formula [A1] .

&Quot; Synthesis of specific polysiloxane which is component (C) of the present invention "

&Lt; Synthesis Example 17 &

PGME (28.3 g), TEOS (32.5 g), the alkoxysilane monomer (A) (4.10 g) obtained in Synthesis Example 16 and MPMS (7.45 g) were placed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube The solution of the alkoxysilane monomer was adjusted by mixing. To this solution, a solution prepared by previously mixing PGME (14.2 g), water (10.8 g) and oxalic acid (0.70 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes. Then, a mixed solution of a methanol solution (1.20 g) having a UPS content of 92 mass% and PGME (0.90 g) was added. After refluxing for another 30 minutes, the solution was allowed to cool to obtain a polysiloxane solution (1) having a SiO ₂ concentration of 12 mass%.

&Lt; Synthesis Example 18 &

MCS (28.3 g), TEOS (32.5 g), the alkoxysilane monomer (A) (4.10 g) obtained in Synthesis Example 16 and MPMS (7.45 g) were placed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube And mixed to prepare a solution of the alkoxysilane monomer. To this solution, a solution prepared by previously mixing MCS (14.2 g), water (10.8 g) and oxalic acid (0.70 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes. Then, a mixed solution of a methanol solution (1.20 g) having a UPS content of 92 mass% and MCS (0.90 g) was added. After refluxing for another 30 minutes, the solution was cooled to obtain a polysiloxane solution (2) having a SiO ₂ concentration of 12 mass%.

&Lt; Synthesis Example 19 &

ECS (28.3 g), TEOS (32.5 g), the alkoxysilane monomer (A) (4.10 g) obtained in Synthesis Example 16 and MPMS (7.45 g) were placed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube And mixed to prepare a solution of the alkoxysilane monomer. To this solution, a solution prepared by previously mixing ECS (14.2 g), water (10.8 g) and oxalic acid (0.70 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes, and then a mixed solution of a methanol solution (1.20 g) having a UPS content of 92 mass% and ECS (0.90 g) adjusted in advance was added. It was again refluxed for 30 minutes, bangraeng to SiO ₂ in terms of the concentration to obtain a polysiloxane solution 3 of 12% by mass.

&Lt; Synthesis Example 20 &

PCS (28.3 g), TEOS (32.5 g), the alkoxysilane monomer (A) (4.10 g) obtained in Synthesis Example 16 and MPMS (7.45 g) were placed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube And mixed to prepare a solution of the alkoxysilane monomer. To this solution, a solution prepared by previously mixing PCS (14.2 g), water (10.8 g) and oxalic acid (0.70 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes. Then, a mixed solution of methanol solution (1.20 g) having a UPS content of 92% by mass and PCS (0.90 g) was added. It was again refluxed for 30 minutes, bangraeng to SiO ₂ in terms of the concentration to obtain a polysiloxane solution (4) of 12% by mass.

&Lt; Synthesis Example 21 &

PGME (25.4 g), TEOS (20.0 g), the alkoxysilane monomer (A) (8.20 g) obtained in Synthesis Example 16 and MPMS (19.9 g) were placed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube And mixed to prepare a solution of the alkoxysilane monomer. To this solution, a solution prepared by previously mixing PGME (12.7 g), water (10.8 g) and oxalic acid (1.10 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes. Then, a mixed solution of a methanol solution (1.20 g) having a UPS content of 92 mass% and PGME (0.90 g) was added. After refluxing for another 30 minutes, the solution was cooled to obtain a polysiloxane solution (5) having a concentration of 12 mass% in terms of SiO ₂ .

&Lt; Synthesis Example 22 >

PGME (29.2 g), TEOS (38.8 g) and the alkoxysilane monomer (A) (4.10 g) obtained in Synthesis Example 16 were mixed in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube to obtain an alkoxysilane monomer Was prepared. To this solution, a solution prepared by previously mixing PGME (14.6 g), water (10.8 g) and oxalic acid (0.50 g) as a catalyst was added dropwise at 25 占 폚 over 30 minutes and further stirred at 25 占 폚 for 30 minutes did. Thereafter, the mixture was heated using an oil bath and refluxed for 30 minutes. Then, a mixed solution of a methanol solution (1.20 g) having a UPS content of 92 mass% and PGME (0.90 g) was added. It was again refluxed for 30 minutes, bangraeng to SiO ₂ in terms of the concentration to obtain a polysiloxane solution (6) of 12 mass%.

&Lt; Synthesis Example 23 >

A solution of alkoxy silane monomer was prepared by mixing PGME (31.6 g) and TEOS (41.7 g) in a 200 ml four-neck reaction flask equipped with a thermometer and a reflux tube. A solution prepared by previously mixing PGME (15.8 g), water (10.8 g) and oxalic acid (0.20 g) as a catalyst was added dropwise to this solution over 25 minutes at 25 占 폚 and further stirred at 25 占 폚 for 30 minutes at room temperature . Then, after heated using an oil bath reflux for 60 minutes, bangraeng to SiO ₂ in terms of the concentration to obtain a polysiloxane solution 7, a 12 mass%.

The specific polysiloxane (polysiloxane solution) of the present invention is shown in Table 2.

&Quot; Composition of the present invention and production of liquid crystal alignment treatment agent "

In the following Examples 1 to 27 and Comparative Examples 1 to 7, production examples of the composition are described. These compositions are also used for evaluation of a liquid crystal alignment treatment agent.

The composition of the present invention and the liquid crystal alignment treatment agent are shown in Tables 3 to 5.

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " Evaluation of inkjet application property of liquid crystal alignment treatment agent ", " Evaluation of inkjet application property of liquid crystal alignment treatment agent & ), Evaluation of liquid crystal orientation (normal cell), production of liquid crystal cell, evaluation of liquid crystal orientation (PSA cell), and evaluation of voltage holding ratio. The conditions are as follows.

&Quot; Evaluation of applicability of composition and liquid crystal alignment treatment agent "

The composition obtained in Examples and Comparative Examples of the present invention was subjected to pressure filtration with a membrane filter having a pore diameter of 1 占 퐉 to evaluate the applicability. For application, a spin coater (1H-D7) (manufactured by Mikasa) was used. The application was performed by spin-coating the ITO surface of a substrate (40 mm long × 30 mm wide, 0.7 mm thick) on which a 30 × 40 mm ITO electrode cleaned with pure water and IPA (isopropyl alcohol) was formed, And the drying was carried out on a hot plate at 80 DEG C for 5 minutes.

Then, evaluation of the pinhole of the obtained resin coating was carried out. The pinholes of the resin coatings were evaluated by visually observing the resin coatings under a sodium lamp. Specifically, the number of pinholes identified on the resin coating was counted, and the smaller the number of pinholes, the better the evaluation was.

In addition, the compositions obtained in Examples and Comparative Examples of the present invention can be used for a liquid crystal alignment treatment agent. As a result, the coating properties of the resin coatings obtained in this example and the comparative example also resulted in the printing property of the liquid crystal alignment film.

Tables 6 to 8 show the number of pinholes of the resin film (liquid crystal alignment film) obtained in Examples and Comparative Examples.

Evaluation of inkjet application property of liquid crystal alignment treatment agent "

Evaluation of inkjet application property was performed using a solution obtained by pressure filtration of the liquid crystal alignment treatment agent (9) obtained in Example 9 of the present invention and the liquid crystal alignment treatment agent (16) obtained in Example 16 with a membrane filter having a pore diameter of 1 占 퐉 . For the ink-jet applicator, HIS-200 (manufactured by Hitachi Plant Technologies Co., Ltd.) was used. The coating was carried out on an ITO (indium tin oxide) -evaporated substrate cleaned with pure water and IPA (isopropyl alcohol) with a coating area of 70 x 70 mm, a nozzle pitch of 0.423 mm, a scan pitch of 0.5 mm, a coating speed of 40 mm / sec, the time from application to drying was 60 seconds, and drying was carried out on a hot plate at 70 DEG C for 5 minutes.

The evaluation of the pinhole of the obtained liquid crystal alignment film was carried out under the same conditions as " Evaluation of applicability of composition and liquid crystal alignment treatment agent ".

Table 6 and Table 7 show the number of pinholes of the liquid crystal alignment film obtained in the examples.

&Quot; Fabrication of liquid crystal cell (ordinary cell) "

The liquid crystal alignment treatment agent obtained in Examples and Comparative Examples of the present invention was press-filtered with a membrane filter having a pore diameter of 1 占 퐉 to prepare a 30 占 40 mm ITO electrode cleaned with pure water and IPA (isopropyl alcohol) The ITO surface of the substrate (40 mm in length x 30 mm in width and 0.7 mm in thickness) was spin-coated and heat-treated on a hot plate at 100 DEG C for 5 minutes to obtain an ITO substrate on which a polyimide liquid crystal alignment film with a thickness of 100 nm was formed . The coated surface of the ITO substrate was rubbed with a rayon cloth with a rubbing apparatus having a roll diameter of 120 mm under the conditions of a roll rotation number of 1000 rpm, a roll advancing speed of 50 mm / sec, and an indentation amount of 0.1 mm.

Two pieces of the ITO substrate on which the obtained liquid crystal alignment film was formed were prepared, and a sealing agent (XN-1500T) (manufactured by Mitsui Chemicals) was printed by combining the liquid crystal alignment film face inside with spacers of 6 m in between. Subsequently, the other substrate and the liquid crystal alignment film surface were faced to each other, and the sealant was cured by heat treatment in a thermocycling type clean oven at 120 캜 for 90 minutes to prepare empty cells. A liquid crystal was injected into this empty cell by a low pressure injection method and the injection port was sealed to obtain a liquid crystal cell (ordinary cell).

The liquid crystal alignment treatment agent (1) to the liquid crystal alignment treatment agent (3) obtained in Examples 1 to 3 and the liquid crystal alignment treatment agent (28) obtained in Comparative Examples 1 to 3, For the cell, a nematic liquid crystal (MLC-2003) (manufactured by Merck Japan) was used for the liquid crystal.

The liquid crystal alignment treatment agents (4) to (8) obtained in Examples 4 to 8, the liquid crystal alignment treatment agents (10) to (15) obtained in Examples 10 to 15, In the liquid crystal cell using the liquid crystal alignment treatment agent (17) to the liquid crystal alignment treatment agent (27) obtained in Example 17 and the liquid crystal alignment treatment agent (31) to the liquid crystal alignment treatment agent (34) obtained in Comparative Examples 4 to 7, Enematic liquid crystal (MLC-6608) (Merck Japan) was used.

&Quot; Evaluation of liquid crystal alignment property (normal cell) "

The liquid crystal alignability was evaluated using the liquid crystal cell obtained in the above " Fabrication of liquid crystal cell (normal cell) ". The liquid crystal alignability was confirmed by observing the liquid crystal cell with a polarizing microscope (ECLIPSE E600WPOL) (Nikon Corporation) to determine whether there was an alignment defect. Concretely, it was said that the alignment defect was not seen in the evaluation (excellent in Tables 6 to 8).

Tables 6 to 8 show the results of the liquid crystal alignment properties obtained in Examples and Comparative Examples.

&Quot; Production of liquid crystal cell and evaluation of liquid crystal orientation property (PSA cell) "

The liquid crystal alignment treatment agent 7 obtained in Example 7, the liquid crystal alignment treatment agent 12 obtained in Example 12, the liquid crystal alignment treatment agent 14 obtained in Example 14 and the liquid crystal alignment treatment agent 26 obtained in Example 26 were changed in pore diameter (40 mm in length x 30 mm in width) having an ITO electrode with a pattern interval of 20 탆 formed in a center of 10 × 10 mm, which was cleaned with pure water and IPA (isopropyl alcohol) using a solution obtained by pressure filtration with a 1 μm membrane filter. (length 40 mm x width 30 mm, thickness 0.7 mm) on which ITO electrodes having a size of 10 mm x 40 mm were formed and a heat treatment was performed on a hot plate at 100 DEG C for 5 minutes To obtain a polyimide coating film having a film thickness of 100 nm. After the coated film surface was cleaned with pure water, the substrate was heat-treated at 100 ° C for 15 minutes in a thermocycling type clean oven to obtain a substrate having a liquid crystal alignment film formed thereon.

The substrate on which this liquid crystal alignment film was formed was assembled with spacers of 6 占 퐉 interposed therebetween with the liquid crystal alignment film surface on the inner side, and the periphery was bonded with a sealant to prepare empty cells. The polymerizable compound (1) represented by the following formula was dissolved in 100 mass% of a nematic liquid crystal (MLC-6608) in a nematic liquid crystal (MLC-6608) , And 0.3% by mass of the polymerizable compound (1) were injected into the liquid crystal cell, and the injection port was sealed to obtain a liquid crystal cell.

(109)

A wavelength of 350 nm or less was cut using a metal halide lamp having an illuminance of 60 mW while applying an AC voltage of 5 V to the obtained liquid crystal cell and irradiated with ultraviolet rays of 20 J / cm 2 in terms of 365 nm, (PSA cell) in which the alignment direction of the liquid crystal cell was controlled. The temperature in the irradiator when the liquid crystal cell was irradiated with ultraviolet rays was 50 占 폚.

The response speed of the liquid crystal before the ultraviolet irradiation and after the ultraviolet irradiation of the liquid crystal cell were measured. The response speed was measured from T90 to T10 from a transmittance of 90% to a transmittance of 10%.

It was confirmed that the PSA cell obtained in the Example had a higher response speed of the liquid crystal cell after ultraviolet irradiation than in the liquid crystal cell before the ultraviolet irradiation, and thus the alignment direction of the liquid crystal was controlled. It was confirmed that the liquid crystal was uniformly aligned with any liquid crystal cell by observation with a polarizing microscope (ECLIPSE E600WPOL) (manufactured by Nikon Corporation).

Evaluation of voltage holding ratio "

A voltage of 1 V was applied for 60 占 퐏 at a temperature of 80 占 폚 to the liquid crystal cell obtained in the above-mentioned "production of a liquid crystal cell (normal cell)", and the voltage after 16.67 ms and after 50 ms was measured. Was calculated as a voltage holding ratio (also referred to as VHR). The measurement was carried out by setting the voltage: ± 1 V, the pulse width: 60 μs, the flame period: 16.67 ms, or 50 ms using a voltage sustaining rate measuring apparatus (VHR-1) (manufactured by Toyota Corporation).

Table 9 shows the results of the voltage holding ratio obtained in Examples and Comparative Examples.

&Lt; Example 1 >

PGME (10.5 g) was added to polyamic acid solution (1) (12.0 g) having a resin solid content concentration of 10.0% by mass obtained by the synthetic method of Synthesis Example 1, and the mixture was stirred at 25 占 폚 for 1 hour. To this solution, a polysiloxane solution 7 (2.50 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (1). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (1) was also used for evaluation as the liquid crystal alignment treatment agent (1).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property of liquid crystal alignment treatment agent " in the above- Evaluation (normal cell) "

&Lt; Example 2 >

PGME (10.5 g) and? -BL (1.27 g) were added to polyamic acid solution (1) (10.5 g) having a resin solid content concentration of 10.0% by mass obtained by the synthetic method of Synthesis Example 1, Lt; / RTI > To this solution, a polysiloxane solution 7 (4.71 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (2). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (2) was also used for evaluation as the liquid crystal alignment treatment agent (2).

&Lt; Example 3 >

PGME (28.0 g) and NMP (4.20 g) were added to the polyimide powder (2) (1.34 g) obtained by the synthetic method of Synthesis Example 2 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution 7 (11.2 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (3). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (3) was also used for evaluation as the liquid crystal alignment treatment agent (3).

Evaluation of the coating property of the composition and the liquid crystal alignment treatment agent ", " preparation of the liquid crystal cell (normal cell) ", and " evaluation of the liquid crystal alignment property of the liquid crystal alignment treatment agent " in the above- Evaluation (normal cell) "

PGME (11.8 g) was added to polyamic acid solution (3) (13.5 g) having a resin solid content concentration of 10.0% by mass obtained by the synthetic method of Synthesis Example 3, and the mixture was stirred at 25 占 폚 for 1 hour. To this solution, a polysiloxane solution (5) (2.81 g) having a SiO ₂ concentration of 12% by mass obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (4). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (4) was also used for evaluation as the liquid crystal alignment treatment agent (4).

Evaluation of the coating property of the composition and the liquid crystal alignment treatment agent ", " preparation of the liquid crystal cell (normal cell) ", " evaluation of the liquid crystal alignment property of the liquid crystal alignment treatment agent " Evaluation (normal cell) " and " evaluation of voltage holding ratio ".

&Lt; Example 5 >

PGME (10.1 g) and? -BL (2.66 g) were added to polyamic acid solution (3) (8.50 g) having a resin solid content concentration of 10.0% by mass obtained by the synthetic method of Synthesis Example 3, Lt; / RTI > To this solution, a polysiloxane solution (1) (7.08 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 17 was added and stirred at 25 캜 for 2 hours to obtain a composition (5). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (5) was also used for evaluation as the liquid crystal alignment treatment agent (5).

&Lt; Example 6 >

PGFE (3.56 g),? -BL (2.61 g) and BCS (5.22 g) were added to polyamic acid solution (3) (15.0 g) having a resin solid content concentration of 10.0% by mass obtained by the synthetic method of Synthesis Example 3 , And the mixture was stirred at 25 占 폚 for 1 hour. To this solution, a polysiloxane solution 5 (1.39 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by a synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (6). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (6) was also used for the evaluation as the liquid crystal alignment treatment agent (6).

&Lt; Example 7 >

PGME (35.0 g) was added to the polyimide powder (4) (1.65 g) obtained by the synthetic method of Synthesis Example 4 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (1) (9.17 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 17 was added and stirred at 25 캜 for 2 hours to obtain a composition (7). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (7) was also used for the evaluation as the liquid crystal alignment treatment agent (7).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", " evaluation of liquid crystal alignment property of liquid crystal alignment treatment agent ", and " Evaluation of liquid crystal alignment (PSA cell) " and " evaluation of voltage holding ratio ".

&Lt; Example 8 >

PCS (23.6 g) and? -BL (8.33 g) were added to the polyimide powder (4) (1.33 g) obtained by the synthetic method of Synthetic Example 4 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution was added a polysiloxane solution (4) (11.1 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20, and the mixture was stirred at 25 캜 for 2 hours to obtain a composition (8). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (8) was also used for evaluation as the liquid crystal alignment treatment agent (8).

&Lt; Example 9 >

PCS (36.8 g) and? -BL (11.0 g) were added to the polyimide powder (4) (1.00 g) obtained by the synthetic method of Synthetic Example 4 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (4) (8.33 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (9). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (9) was also used for evaluation as the liquid crystal alignment treatment agent (9).

Using the obtained liquid crystal alignment treatment agent (9), " Evaluation of inkjet application property of liquid crystal alignment treatment agent "

&Lt; Example 10 >

PCS (14.7 g),? -BL (4.28 g) and BCS (12.9 g) were added to the polyimide powder (4) (1.23 g) obtained by the synthetic method of Synthetic Example 4 and stirred at 70 ° C for 24 hours . To this solution, a polysiloxane solution (4) (12.5 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (10). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (10) was also used for evaluation as the liquid crystal alignment treatment agent (10).

Evaluation of the coating property of the composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property of the liquid crystal alignment treatment agent " in the above- Evaluation (normal cell) "

&Lt; Example 11 >

MCS (20.8 g), NEP (6.17 g) and BCS (10.3 g) were added to the polyimide powder (5) (2.10 g) obtained by the synthetic method of Synthesis Example 5 and dissolved by stirring at 70 ° C for 24 hours . To this solution, a polysiloxane solution (2) (4.38 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 18 was added and stirred at 25 캜 for 2 hours to obtain a composition (11). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (11) was also used for evaluation as the liquid crystal alignment treatment agent (11).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property (evaluation of liquid crystal alignment property) " were carried out under the above- (Normal cell) ".

&Lt; Example 12 >

PGME (24.6 g),? -BL (13.3 g) and BCS (4.44 g) were added to the polyimide powder (5) (2.55 g) obtained by the synthetic method of Synthesis Example 5 and stirred at 70 ° C for 24 hours . To this solution, a polysiloxane solution 6 (2.36 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 22 was added and stirred at 25 캜 for 2 hours to obtain a composition (12). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (12) was also used for evaluation as the liquid crystal alignment treatment agent (12).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", " evaluation of liquid crystal alignment property (Normal cell) " and " production of liquid crystal cell and evaluation of liquid crystal orientation property (PSA cell) ".

&Lt; Example 13 >

To polyimide powder (6) (1.35 g) obtained by the synthetic method of Synthesis Example 6, PGME (32.4 g) was added and dissolved by stirring at 70 캜 for 24 hours. To this solution, a polysiloxane solution (5) (11.3 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain Composition (13). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (13) was also used for evaluation as the liquid crystal alignment treatment agent (13).

&Lt; Example 14 >

PGME (33.2 g) and? -BL (4.11 g) were added to the polyimide powder (6) (2.10 g) obtained by the synthetic method of Synthesis Example 6 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution 7 (4.38 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (14). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (14) was also used for evaluation as the liquid crystal alignment treatment agent (14).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " manufacture of liquid crystal cell (normal cell) ", " evaluation of liquid crystal orientation property ", and evaluation of liquid crystal alignment property were carried out under the above- (Normal cell) " and " production of liquid crystal cell and evaluation of liquid crystal orientation property (PSA cell) ".

&Lt; Example 15 >

PCS (21.9 g), NEP (7.83 g) and BCS (3.92 g) were added to the polyimide powder (6) (1.75 g) obtained by the synthetic method of Synthesis Example 6 and dissolved by stirring at 70 ° C for 24 hours . To this solution, a polysiloxane solution 4 (6.25 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (15). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (15) was also used for evaluation as the liquid crystal alignment treatment agent (15).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property (Normal cell) ".

&Lt; Example 16 >

PCS (25.7 g), NEP (8.27 g) and BCS (4.14 g) were added to the polyimide powder (6) (1.05 g) obtained by the synthetic method of Synthesis Example 6 and dissolved by stirring at 70 캜 for 24 hours . To this solution, a polysiloxane solution (4) (3.75 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (16). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (16) was also used for evaluation as the liquid crystal alignment treatment agent (16).

Using the obtained liquid crystal alignment treatment agent 16, " Evaluation of inkjet application property of liquid crystal alignment treatment agent " under the above-described conditions was performed.

&Lt; Example 17 >

ECS (20.9 g), NMP (8.26 g) and BCS (8.26 g) were added to the polyimide powder (7) (2.11 g) obtained by the synthetic method of Synthetic Example 7 and dissolved by stirring at 70 캜 for 24 hours . To this solution, a polysiloxane solution (3) (4.40 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 19 was added and stirred at 25 캜 for 2 hours to obtain Composition (17). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (17) was also used for the evaluation as the liquid crystal alignment treatment agent (17).

Evaluation of composition and coating property of liquid crystal alignment treatment agent ", " production of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property ", under the conditions described above, using the obtained composition (17) (Normal cell) ".

&Lt; Example 18 >

PGME (37.9 g) and? -BL (4.44 g) were added to the polyimide powder (8) (2.55 g) obtained by the synthetic method of Synthesis Example 8 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution 6 (2.36 g) having a SiO ₂ concentration of 12% by mass obtained by the synthetic method of Synthesis Example 22 was added and stirred at 25 캜 for 2 hours to obtain a composition (18). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (18) was also used for evaluation as the liquid crystal alignment treatment agent (18).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property ", under the above-described conditions, using composition 18 and liquid crystal alignment treatment agent 18. [ (Normal cell) ".

&Lt; Example 19 >

MCS (27.8 g),? -BL (1.96 g) and BCS (3.92 g) were added to the polyimide powder (8) (1.75 g) obtained by the synthetic method of Synthetic Example 8 and stirred at 70 ° C for 24 hours . To this solution, a polysiloxane solution (2) (6.25 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 18 was added and stirred at 25 캜 for 2 hours to obtain a composition (19). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. This composition (19) was also used for evaluation as the liquid crystal alignment treatment agent (19).

&Lt; Example 20 >

PGME (26.5 g) and? -BL (3.85 g) were added to the polyimide powder (9) (1.35 g) obtained by the synthetic method of Synthesis Example 9 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (5) (9.20 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (20). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (20) was also used for evaluation as the liquid crystal alignment treatment agent (20).

&Lt; Example 21 >

PCS (22.2 g),? -BL (7.92 g) and BCS (3.96 g) were added to the polyimide powder (9) (1.77 g) obtained by the synthetic method of Synthesis Example 9 and stirred at 70 ° C for 24 hours . To this solution, a polysiloxane solution (4) (6.32 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain Composition (21). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (21) was also used for the evaluation as the liquid crystal alignment treatment agent (21).

&Lt; Example 22 >

PCS (23.3 g) and NMP (9.94 g) were added to the polyimide powder (10) (1.65 g) obtained by the synthetic method of Synthesis Example 10 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (4) (7.40 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (22). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (22) was also used for evaluation as the liquid crystal alignment treatment agent (22).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " production of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property (evaluation of liquid crystal alignment property) " were carried out under the conditions described above by using the obtained composition (22) (Normal cell) ".

&Lt; Example 23 >

PGME (30.8 g) and? -BL (3.82 g) were added to the polyimide powder (11) (1.95 g) obtained by the synthetic method of Synthesis Example 11 and dissolved by stirring at 70 占 폚 for 24 hours. To the solution, a solution of a polysiloxane in terms of SiO ₂ concentration obtained in the synthesis method of Synthesis Example 17 12% by weight (1) was added (4.06 g) and stirred for 2 hours at 25 ℃, to obtain a composition (23). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (23) was also used for evaluation as the liquid crystal alignment treatment agent (23).

&Lt; Example 24 >

PGME (32.3 g) and? -BL (4.25 g) were added to the polyimide powder (11) (1.90 g) obtained by the synthetic method of Synthesis Example 11 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution 6 (6.79 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 22 was added and stirred at 25 캜 for 2 hours to obtain a composition (24). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (24) was also used for evaluation as the liquid crystal alignment treatment agent (24).

&Lt; Example 25 >

PCS (25.4 g),? -BL (3.88 g) and BCS (7.76 g) were added to the polyimide powder (11) (2.23 g) obtained by the synthetic method of Synthesis Example 11 and stirred at 70 占 폚 for 24 hours . To this solution, a polysiloxane solution (4) (2.06 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 20 was added and stirred at 25 캜 for 2 hours to obtain a composition (25). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (25) was also used for evaluation as the liquid crystal alignment treatment agent (25).

&Lt; Example 26 >

PGME (25.5 g) and? -BL (3.82 g) were added to the polyimide powder (12) (1.22 g) obtained by the synthetic method of Synthesis Example 12 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (5) (10.2 g) having a concentration of 12% by mass in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (26). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. This composition (26) was also used for evaluation as the liquid crystal alignment treatment agent (26).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", " evaluation of liquid crystal alignment property ", and evaluation of liquid crystal alignment property were carried out under the above- (Normal cell) " and " production of liquid crystal cell and evaluation of liquid crystal orientation property (PSA cell) ".

&Lt; Example 27 >

MCS (28.4 g),? -BL (2.18 g) and BCS (10.9 g) were added to the polyimide powder (12) (2.50 g) obtained by the synthetic method of Synthesis Example 12 and stirred at 70 占 폚 for 24 hours . To this solution, a polysiloxane solution (2) (2.31 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 18 was added and stirred at 25 캜 for 2 hours to obtain a composition (27). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (27) was also used for the evaluation as the liquid crystal alignment treatment agent (27).

&Lt; Comparative Example 1 &

NMP (28.4 g) was added to polyamic acid solution 13 (7.70 g) having a resin solid content concentration of 25.0% by mass obtained by the synthetic method of Synthesis Example 13, and the mixture was stirred at 25 占 폚 for 1 hour. To this solution, a polysiloxane solution 7 (4.01 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (28). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (28) was also used for evaluation as the liquid crystal alignment treatment agent (28).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", and " evaluation of liquid crystal alignment property (evaluation of liquid crystal alignment property) " were carried out under the conditions described above by using the obtained composition (28) (Normal cell) ".

&Lt; Comparative Example 2 &

To polyamic acid solution 13 (7.75 g) having a resin solid content concentration of 25.0% by mass obtained by the synthetic method of Synthesis Example 13,? -BL (28.6 g) was added and stirred at 25 占 폚 for 1 hour. To the solution, a solution of the polysiloxane to the SiO ₂ in terms of the concentration obtained by the synthesis method of Synthesis Example 23 12% by weight was added to (7) (4.04 g) and stirred for 2 hours at 25 ℃, to obtain a composition (29). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. This composition (29) was also used for evaluation as the liquid crystal alignment treatment agent (29).

&Lt; Comparative Example 3 &

NMP (17.6 g) and BCS (6.36 g) were added to polyamic acid solution 13 (6.50 g) having a resin solid content concentration of 25.0% by mass obtained by the synthetic method of Synthesis Example 13 and stirred at 25 占 폚 for 1 hour . To this solution, a polysiloxane solution 7 (3.39 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 23 was added and stirred at 25 캜 for 2 hours to obtain a composition (30). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (30) was also used for evaluation as the liquid crystal alignment treatment agent (30).

&Lt; Comparative Example 4 &

NMP (29.9 g) was added to the polyamic acid solution 14 (8.12 g) having a resin solid content concentration of 25.0% by mass obtained by the synthetic method of Synthesis Example 14, and the mixture was stirred at 25 占 폚 for 1 hour. To this solution, a polysiloxane solution (5) (4.23 g) having a SiO ₂ concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (31). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. This composition (31) was also used for evaluation as the liquid crystal alignment treatment agent (31).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " preparation of liquid crystal cell (normal cell) ", " evaluation of liquid crystal alignment property ", and evaluation of liquid crystal alignment property were conducted under the above- (Normal cell) " and " evaluation of voltage holding ratio ".

&Lt; Comparative Example 5 &

NMP (21.9 g) and BCS (7.93 g) were added to polyamic acid solution 14 (8.10 g) having a resin solid content concentration of 25.0% by mass obtained by the synthetic method of Synthesis Example 14 and stirred at 25 占 폚 for 1 hour . To this solution, a polysiloxane solution (5) (4.22 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 21 was added and stirred at 25 캜 for 2 hours to obtain a composition (32). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (32) was also used for evaluation as the liquid crystal alignment treatment agent (32).

&Lt; Comparative Example 6 >

NMP (35.0 g) was added to the polyimide powder (4) (1.65 g) obtained by the synthetic method of Synthesis Example 4 and dissolved by stirring at 70 占 폚 for 24 hours. To this solution, a polysiloxane solution (1) (9.17 g) having a concentration of 12 mass% in terms of SiO ₂ obtained by the synthetic method of Synthesis Example 17 was added and stirred at 25 캜 for 2 hours to obtain a composition (33). No abnormality such as turbidity or generation of precipitates was observed in this composition, and it was confirmed that the solution was a homogeneous solution. The composition (33) was also used for evaluation as the liquid crystal alignment treatment agent (33).

Evaluation of coating property of composition and liquid crystal alignment treatment agent ", " manufacture of liquid crystal cell (normal cell) ", " evaluation of liquid crystal alignment property ", and evaluation of liquid crystal alignment property were carried out under the above- (Normal cell) " and " evaluation of voltage holding ratio ".

&Lt; Comparative Example 7 &

PGME (32.9 g) was added to the polyimide powder (15) (1.55 g) obtained by the synthetic method of Synthesis Example 15, and the mixture was stirred at 70 占 폚 for 24 hours. Since the polyimide powder remained dissolved in the solution, the polyimide powder was stirred at 70 DEG C for 12 hours, but the polyimide powder could not be completely dissolved.

Therefore, the composition 34 and the liquid crystal alignment treatment agent 34 could not be produced.

* 2: Represents the proportion of the polymer in the composition (liquid crystal alignment treatment agent).

* 3: Represents the ratio of the polymer in the composition (liquid crystal alignment treatment agent).

* 4: Represents the proportion of the polymer in the composition (liquid crystal alignment treatment agent).

* 5: Represents the solvent component contained in the polysiloxane solution.

* 6: Since the polyimide powder was not completely dissolved, the composition and the liquid crystal alignment treatment agent could not be adjusted.

* 7: 15 to 24 alignment defects were confirmed.

* 8: More than 25 alignment defects were identified.

As can be seen from the above results, the compositions of the examples of the present invention exhibited a uniform coating film property that did not cause pinholes accompanied by cratering when applied to a substrate, as compared with the composition of the comparative example. Concretely, the comparison in the composition using the same polyimide precursor or the solvent-soluble polyimide, that is, the comparison between Example 1 and Comparative Example 1, Comparative Example 2 or Comparative Example 3, the comparison between Example 4 and Comparative Example 4, A comparison of Example 5, and a comparison of Example 7 and Comparative Example 6.

The liquid crystal alignment film obtained from the liquid crystal alignment treatment agent using the composition of the present invention was also able to obtain the same results. Specifically, the comparison of the liquid crystal alignment treatment agent using the same polyimide precursor or the solvent-soluble polyimide, that is, the comparison between Example 1 and Comparative Example 1, Comparative Example 2 or Comparative Example 3, the comparison between Example 4 and Comparative Example 4 Or a comparison of Comparative Example 5, and a comparison of Example 7 and Comparative Example 6. Particularly, even in the case of a liquid crystal alignment treatment agent using a polyimide precursor or a solvent-soluble polyimide obtained by using a diamine compound having a side chain as a diamine component, a uniform coating film characteristic without pinholes was exhibited as described above.

Further, in the evaluation of the liquid crystal alignability of the liquid crystal cell, the liquid crystal cell obtained from the liquid crystal alignment treatment agent using the composition of the present invention showed no alignment defects due to pinholes as compared with the liquid crystal cell obtained from the liquid crystal alignment treatment agent using the composition of the comparative example , Uniform liquid crystal alignability was obtained. Specifically, the comparison of the liquid crystal alignment treatment agent using the same polyimide precursor or the solvent-soluble polyimide, that is, the comparison between Example 1 and Comparative Example 1, Comparative Example 2 or Comparative Example 3, the comparison between Example 4 and Comparative Example 4 Or a comparison of Comparative Example 5, and a comparison of Example 7 and Comparative Example 6.

In addition, in evaluating the voltage holding ratio, the liquid crystal cell obtained from the liquid crystal alignment treatment agent using the composition of the present invention showed a higher value than the liquid crystal cell obtained from the liquid crystal alignment treatment agent using the composition of the comparative example. Concretely, the liquid crystal alignment treatment agent using the same polyimide precursor or solvent-soluble polyimide, that is, the comparison between Example 4 and Comparative Example 4, and the comparison between Example 7 and Comparative Example 6 are compared.

Industrial availability

The composition of the present invention can provide a resin coating which exhibits uniform coating film properties without pinholes caused by cratering when coating the substrate. In the liquid crystal alignment treatment agent using the composition of the present invention, the same result can be obtained.

In addition, the liquid crystal alignment treatment agent of the present invention can obtain a liquid crystal cell in which alignment defects due to pinholes accompanying cratering do not occur. Particularly, the same result can be obtained even with a liquid crystal alignment treatment agent using a polyimide precursor obtained by using a diamine compound having a side chain as a diamine component or a solvent-soluble polyimide.

The liquid crystal alignment treatment agent of the present invention is a liquid crystal display element that performs switching between the transmissive state of liquid crystal (also referred to as a transparent state) and the scattered state, that is, a polymer dispersed liquid crystal (PDLC) And is also useful for a liquid crystal display device using a polymer network liquid crystal (PNLC (Polymer Network Liquid Crystal)).

Particularly, it is useful for a reverse type device which becomes transparent when no voltage is applied and is in a scattering state when voltage is applied. This reverse type device is a liquid crystal display for display using a glass substrate or a plastic substrate such as PET (polyethylene terephthalate) or an acrylic substrate, and further, a dimmer window for controlling the transmission and blocking of light, A shutter device, a dimmer window of a transportation vehicle such as a car, and a back plate of a transparent display.

In addition, the liquid crystal alignment treatment agent of the present invention can exhibit a high voltage holding ratio even at a low temperature.

Therefore, the liquid crystal display element having the liquid crystal alignment film obtained from the liquid crystal alignment treatment agent of the present invention has excellent reliability and can be preferably used for a liquid crystal television with high precision on a large screen, and is suitable for use as a TN device, STN device, TFT liquid crystal device, And is useful for an alignment type liquid crystal display element.

Further, the liquid crystal alignment film obtained from the liquid crystal alignment treatment agent of the present invention is also useful for a liquid crystal display element which needs to irradiate ultraviolet rays when a liquid crystal display element is manufactured. That is, a liquid crystal composition containing a liquid crystal layer between a pair of substrates provided with electrodes and containing a polymerizable compound polymerized by at least one of active energy rays and heat is disposed between the pair of substrates And a liquid crystal display element manufactured through a process of polymerizing the polymerizable compound while applying a voltage between the electrodes and further comprising a liquid crystal layer between a pair of substrates provided with electrodes, It is also applicable to a liquid crystal display device manufactured by arranging a liquid crystal alignment film containing a polymerizable group polymerized in at least one of active energy ray and heat between substrates and polymerizing the polymerizable group while applying a voltage between the electrodes Do.

Claims

A composition comprising the following components (A), (B) and (C).
Component (A): At least one solvent selected from the following formula [1a] or formula [1b].
[Chemical Formula 1]

(In the formula [1a], X ¹ represents an alkyl group having 1 to 3 carbon atoms, and in the formula [1b], X ² represents an alkyl group having 1 to 3 carbon atoms.
Component (B): at least one polymer selected from a polyimide precursor or polyimide obtained by reacting a diamine component containing a diamine compound having a carboxyl group and a tetracarboxylic acid dianhydride component.
(C): Polysiloxane obtained by polycondensation of an alkoxysilane containing any one of alkoxysilanes represented by the following formula [A1], formula [A2] or formula [A3].
(2)

Wherein A ¹ is an aliphatic hydrocarbon, a benzene ring, a cyclohexane ring, an organic group having 8 to 35 carbon atoms having a heterocyclic or steroid structure, A ² is a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, represents, a ³ is. However, each represents an alkyl group of a carbon number of 1 ~ 5, m is an integer of 1 or 2, n is an integer of 0 ~ 2, p represents an integer of 0 ~ 3 m + n + P is 4).
(3)

Wherein B ¹ represents an organic group having 2 to 12 carbon atoms and having a vinyl group, an epoxy group, an amino group, a mercapto group, an isocyanate group, a methacryl group, an acryl group, a ureide group or a cinnamoyl group, B ² each represent a hydrogen atom or an alkyl group having 1 to 5 carbon atoms, B ³ each represent an alkyl group having 1 to 5 carbon atoms, m represents an integer of 1 or 2, n represents an integer of 0 to 2, p represents Represents an integer of 0 to 3, provided that m + n + p is 4).
[Chemical Formula 4]

The method according to claim 1,
Wherein the component (A) is 50 to 100% by mass of the total solvent contained in the composition.

3. The method according to claim 1 or 2,
Wherein the diamine compound having a carboxyl group as the component (B) is a diamine compound having a structure represented by the following formula [2].
[Chemical Formula 5]

(In the formula [2], a represents an integer of 0 to 4).

3. The method according to claim 1 or 2,
Wherein the diamine compound having a carboxyl group as the component (B) is a diamine compound having a structure represented by the following formula [2a].
[Chemical Formula 6]

The method according to claim 3 or 4,
Wherein the diamine compound having a carboxyl group is 20 mol% to 100 mol% of all the diamines used in the component (B).

6. The method according to any one of claims 1 to 5,
Wherein the diamine component of the component (B) contains at least one diamine compound selected from the group consisting of the following formula (2b).
(7)

(In the formula [2b], Y represents a structure represented by the following formula [2b-1], formula [2b-2], formula [2b-3], formula [2b-4] m represents an integer of 1 to 4).
[Chemical Formula 8]

7. The method according to any one of claims 1 to 6,
Wherein the tetracarboxylic acid dianhydride component of the component (B) is a compound represented by the following formula [3].
[Chemical Formula 9]

(In the formula [3], Z ¹ is a group of at least one structure selected from the following formulas [3a] to [3j]).
[Chemical formula 10]

8. The method according to any one of claims 1 to 7,
Wherein the alkoxysilane represented by the formula [A2] of the component (C) is at least one selected from the group consisting of allyltriethoxysilane, allyltrimethoxysilane, diethoxymethylvinylsilane, dimethoxymethylvinylsilane, triethoxvinylsilane, vinyltrimethoxy Silane, vinyltris (2-methoxyethoxy) silane, 3- (triethoxysilyl) propyl methacrylate, 3- (trimethoxysilyl) propyl acrylate or 3- (trimethoxysilyl) Lt; RTI ID = 0.0 > 1, < / RTI >

8. The method according to any one of claims 1 to 7,
Wherein the alkoxysilane represented by the formula [A2] of the component (C) is at least one member selected from the group consisting of 3-glycidyloxypropyl (dimethoxy) methylsilane, 3- glycidyloxypropyl (diethoxy) methylsilane, 3-glycidyloxy Propyl trimethoxy silane or 2- (3,4-epoxycyclohexyl) ethyl trimethoxy silane.

10. The method according to any one of claims 1 to 9,
Wherein the polysiloxane of the component (C) is a polysiloxane obtained by polycondensation of an alkoxysilane represented by the formula [A1], the formula [A2] and the formula [A3].

11. The method according to any one of claims 1 to 10,
(D), at least one solvent selected from the group consisting of N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone and? -Butyrolactone.

12. The method according to any one of claims 1 to 11,
As the component (E), at least one member selected from the group consisting of 1-hexanol, cyclohexanol, 1,2-ethanediol, 1,2-propanediol, propylene glycol monobutyl ether, ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, Glycol monoethyl ether, diethylene glycol monopropyl ether, diethylene glycol isopropyl ether, or diethylene glycol monobutyl ether.

A resin film obtained from the composition according to any one of claims 1 to 12.

A liquid crystal alignment treatment agent characterized by being obtained from the composition according to any one of claims 1 to 12.

A liquid crystal alignment film obtained by using the liquid crystal alignment treatment agent according to claim 14.

A liquid crystal alignment film obtained by an ink jet method using the liquid crystal alignment treatment agent according to claim 14.

A liquid crystal display element having the liquid crystal alignment layer according to claim 15 or 16.

17. The method according to claim 15 or 16,
A liquid crystal composition containing a liquid crystal layer between a pair of substrates provided with electrodes and containing a polymerizable compound polymerized by at least one of active energy rays and heat is disposed between the pair of substrates, Wherein the polymerizable compound is used in a liquid crystal display device manufactured through a process of polymerizing the polymerizable compound while applying a voltage between the electrodes.

A liquid crystal display element having the liquid crystal alignment film according to claim 18.

17. The method according to claim 15 or 16,
A liquid crystal alignment film comprising a liquid crystal layer between a pair of substrates provided with electrodes and including a polymerizable group polymerized by at least one of active energy rays and heat between the pair of substrates is disposed, Wherein the liquid crystal alignment layer is used in a liquid crystal display device manufactured through a process of polymerizing the polymerizable group while applying a voltage between the electrodes.

A liquid crystal display element having the liquid crystal alignment film according to claim 20.