WO2019159886A1

WO2019159886A1 - Composition

Info

Publication number: WO2019159886A1
Application number: PCT/JP2019/004843
Authority: WO
Inventors: 辰昌葛西; 伸行幡中
Original assignee: 住友化学株式会社
Priority date: 2018-02-14
Filing date: 2019-02-12
Publication date: 2019-08-22
Also published as: TWI839166B; TW202325825A

Abstract

The invention is a composition comprising at least one compound selected from the group consisting of a non-ionic silane compound and an ionic compound, and one or more types of liquid crystal compound having a structure represented by formula (I)-1. [In formula (I)-1: Ar represents a divalent group having two or more ring structures wherein one of the two or more ring structures is a 6-membered ring bonded to L¹ and L² at position 1 and position 4 of the 6-membered ring; L¹ and L² each independently represents a single bond or a divalent linking group; G¹ and G² each independently represents a divalent aromatic group or a divalent alicyclic hydrocarbon group; and * represents a bonding partner].

Description

Composition

The present invention relates to a composition, a vertically aligned liquid crystal cured film, a laminate, an elliptically polarizing plate, and an organic EL display device.

An elliptically polarizing plate is an optical member in which a polarizing plate and a retardation plate are laminated. For example, in a device that displays an image in a planar state (for example, an organic EL display device), light reflection at an electrode constituting the device is performed. Used to prevent. In this elliptically polarizing plate, a so-called λ / 4 plate is used as the retardation plate.
As the phase difference plate used for such an elliptically polarizing plate, one showing reverse wavelength dispersion is suitable in that it exhibits the same phase difference performance in a wide wavelength range of visible light. As a retardation plate exhibiting reverse wavelength dispersion, a retardation plate comprising a horizontally aligned liquid crystal cured film obtained by polymerizing and curing a polymerizable liquid crystal compound exhibiting reverse wavelength dispersion in a horizontal direction is known. .
There is also a need for a polarizing plate with an optical compensation function having a function of compensating for the same optical performance as seen from the front direction when viewed from an oblique direction. As such a polarizing plate with an optical compensation function, a polarizing plate further comprising a vertically aligned liquid crystal cured film obtained by polymerizing and curing a polymerizable liquid crystal compound in a vertically aligned state together with a horizontally aligned liquid crystal cured film having reverse wavelength dispersion is known. It has been. Further, among these vertically aligned liquid crystal cured films, Patent Document 1 proposes a vertically aligned liquid crystal cured film using a polymerizable liquid crystal compound exhibiting reverse wavelength dispersion.

Japanese Patent Laying-Open No. 2015-57646

However, a liquid crystal compound exhibiting reverse wavelength dispersion has an unstable molecular centroid, so that a large number of alignment defects are generated with the liquid crystal compound alone, and vertical alignment is difficult. Therefore, an alignment film for vertical alignment is required for the production of a vertically aligned liquid crystal cured film. However, in that case, a process of forming an alignment film for vertical alignment is required, which causes a problem that productivity is lowered.

The present invention has been made in view of the above problems, and an object of the present invention is to provide a composition capable of forming a vertically aligned liquid crystal cured film in which the occurrence of alignment defects is suppressed without an alignment film.

As a result of intensive studies in order to solve the above problems, the present inventors have completed the present invention. That is, the present invention includes the following aspects.
[1] Formula (I) -1 below:

... (I) -1
[In the formula (I) -1, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 1 and 4 positions,
L ¹ and L ² each independently represent a single bond or a divalent linking group,
G ¹ and G ² each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and are included in the divalent aromatic group and the divalent alicyclic hydrocarbon group. Each hydrogen atom independently substituted with a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may each independently be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom,
* Represents a bond]
A composition comprising at least one liquid crystal compound having a structure represented by: and at least one selected from the group consisting of a nonionic silane compound and an ionic compound.
[2] The composition according to [1], wherein the one or more liquid crystal compounds having the structure represented by the formula (I) -1 have a maximum absorption in a wavelength range of 260 nm to 400 nm.
[3] The liquid crystal compound having the structure represented by the formula (I) -1 is represented by the following formula (I) -2:

... (I) -2
[In the formula (I) -2, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 1 and 4 positions,
L ¹ , L ² and B ¹ each independently represent a single bond or a divalent linking group,
G ¹ , G ² , and G ³ each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group and the divalent alicyclic carbon group The hydrogen atom contained in the hydrogen group is independently a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group are each independently substituted with an oxygen atom, a sulfur atom, or a nitrogen atom. You can,
* Represents a bond]
The composition according to [1] or [2], which is a liquid crystal compound having a structure represented by:
[4] The liquid crystal compound having the structure represented by the formula (I) -1 is represented by the following formula (I) -3:

... (I) -3
[In the formula (I) -3, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 1 and 4 positions,
L ¹ , L ² , B ¹ and B ² each independently represent a single bond or a divalent linking group;
G ¹ , G ² , G ³ , and G ⁴ each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group and the divalent fat The hydrogen atoms contained in the cyclic hydrocarbon group are each independently a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, Or a carbon atom contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may be independently an oxygen atom, a sulfur atom, or a nitrogen atom. May be replaced,
* Indicates a bond]
The composition according to any one of [1] to [3], which is a liquid crystal compound represented by the formula:
[5] The composition according to any one of [1] to [4], wherein the liquid crystal compound has one or more polymerizable groups.
[6] The composition according to any one of [1] to [5], wherein the nonionic silane compound is a silane coupling agent.
[7] The composition according to any one of [1] to [6], wherein the nonionic silane compound is a silane coupling agent having an alkoxysilyl group and a polar group.
[8] The composition according to any one of [1] to [7], wherein the ionic compound is entirely composed of a nonmetallic element.
[9] The composition according to any one of [1] to [8], wherein the molecular weight of the ionic compound is 100 or more and 10,000 or less.
[10] A vertically aligned liquid crystal cured film, which is a cured product of the composition according to any one of [1] to [9], wherein the liquid crystal compound contained in the composition is in the in-plane direction of the liquid crystal cured film. A vertically aligned liquid crystal cured film that is vertically aligned.
[11] The following relational expression (1):
−150 nm ≦ RthC (550) ≦ −30 nm (1)
[In relational expression (1), RthC (550) represents the retardation value in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm]
The vertically aligned liquid crystal cured film according to [10], wherein
[12] The following relational expression (2):
RthC (450) / RthC (550) ≦ 1 (2)
[In the relational expression (2), RthC (450) represents the retardation value in the thickness direction at a wavelength of 450 nm of the vertically aligned liquid crystal cured film, and RthC (550) represents the retardation in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm. Show value]
The vertically aligned liquid crystal cured film according to [10] or [11], wherein
[13] A substrate, and the vertically aligned liquid crystal cured film according to any one of [10] to [12],
A laminate in which the vertically aligned liquid crystal cured film is adjacent to the substrate.
[14] A laminate comprising the vertically aligned liquid crystal cured film according to any one of [10] to [12] and a film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film.
[15] The following relational expression (3):
ReA (450) / ReA (550) ≦ 1 (3)
[In the relational expression (3), ReA (450) represents the in-plane retardation value at a wavelength of 450 nm of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and ReA (550) In-plane retardation value at a wavelength of 550 nm of a film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film]
The laminate according to [14], wherein
[16] The following relational expression (4):
| R0 (550) -R40 (550) | ≦ 10 nm (4)
[In the relational expression (4), R0 (550) represents an in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (550) represents a horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film. Represents the retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of the oriented film]
The laminated body according to [14] or [15], wherein
[17] The following relational expression (5):
| R0 (450) -R40 (450) | ≦ 10 nm (5)
[In the relational expression (5), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, and R40 (450) is aligned in the horizontal direction with respect to the in-plane direction of the vertical alignment liquid crystal cured film. Shows the retardation value at a wavelength of 450 nm when the film is rotated 40 ° around the fast axis direction]
The laminate according to any one of claims 14 to 16, which satisfies the following conditions.
[18] The following relational expression (6):
| {R0 (450) -R40 (450)}-{R0 (550) -R40 (550)} | ≦ 3 nm (6)
[In relational expression (6), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, R0 (550) represents the in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (450) Represents a retardation value at a wavelength of 450 nm when rotated by 40 ° around the fast axis direction of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and R40 (550) is , Showing a retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of a film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film]
The laminate according to any one of [14] to [17], wherein
[19] The laminate according to any one of [14] to [18], wherein the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film is a horizontally aligned liquid crystal cured film.
[20] An elliptically polarizing plate comprising the laminate according to any one of [14] to [19] and a polarizing film.
[21] The elliptically polarizing plate according to [20], wherein the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film is a horizontally aligned liquid crystal cured film.
[22] The elliptically polarizing plate according to [20] or [21], wherein an angle formed between the slow axis of the film oriented in the horizontal direction and the absorption axis of the polarizing film is 45 ± 5 °.
[23] The polarizing film includes a horizontally aligned liquid crystal cured film in which a liquid crystal compound is horizontally aligned with respect to the film plane of the polarizing film, and the horizontally aligned liquid crystal cured film includes a dichroic dye. [20] The elliptically polarizing plate according to any one of to [22].
[24] The elliptically polarizing plate according to [23], wherein the dichroic dye has an azo group.
[25] The horizontally aligned liquid crystal cured film constituting the polarizing film is a cured film cured in a smectic phase in which the liquid crystal compound is aligned in the horizontal direction with respect to the in-plane direction of the film. [23] or [24 ] The elliptically polarizing plate as described in.
[26] An organic EL display device comprising the elliptically polarizing plate according to any one of [20] to [25].

According to the present invention, it is possible to provide a composition capable of forming a vertically aligned liquid crystal cured film in which the occurrence of alignment defects is suppressed without an alignment film.

It is a schematic sectional drawing which shows an example of the laminated constitution of the elliptically polarizing plate of this invention.

Hereinafter, embodiments of the present invention will be described in detail. In this specification, acryl and methacryl may be referred to as “(meth) acryl”. In addition, “system” is added after the compound name, and the compound and its derivatives may be collectively referred to. When the name of a polymer is expressed by adding “system” after the compound name, the repeating unit of the polymer is derived from the compound or a derivative thereof, or the chemical modification after the polymerization to the repeating unit derived from the compound or the derivative thereof, etc. It means that the polymer is subjected to.

<Composition>
The composition of the present invention (hereinafter sometimes referred to as a composition for forming a vertically aligned liquid crystal cured film) has the following formula (I) -1:

... (I) -1
[In the formula (I) -1, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 1 and 4 positions,
L ¹ and L ² each independently represent a single bond or a divalent linking group,
G ¹ and G ² each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and are included in the divalent aromatic group and the divalent alicyclic hydrocarbon group. Each hydrogen atom independently substituted with a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may each independently be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom,
* Represents a bond]
And at least one selected from the group consisting of a nonionic silane compound and an ionic compound, and includes both the nonionic silane compound and the ionic compound. Is preferred.

The composition may further contain other components as needed in addition to the one or more liquid crystal compounds represented by the formula (I) -1, the nonionic silane compound and / or the ionic compound.

The composition of the present invention can form a vertically aligned liquid crystal cured film in which the occurrence of alignment defects is suppressed without an alignment film. The reason is presumed as follows. One or more liquid crystal compounds having a structure represented by the formula (I) -1 (hereinafter sometimes referred to as a liquid crystal compound (I) -1) are represented by two Ars in the formula (I) -1 In order to represent a divalent group having the above ring structure, one of the two or more ring structures is a 6-membered ring, and binds to L ¹ and L ^{2 at} positions ¹ and 4 of the 6-membered ring. Tend to have a T-shaped structure. A compound having such a structure generally tends to exhibit reverse wavelength dispersion, and the liquid crystal compound (I) -1 usually exhibits reverse wavelength dispersion. On the other hand, since the liquid crystal compound (I) -1 has a T-shaped structure, it is usually difficult to perform vertical alignment alone. The composition of the present invention contains liquid crystal compound (I) -1 and at least one selected from the group consisting of a nonionic silane compound and an ionic compound. In the production of a liquid crystal cured film, a composition is applied to a substrate to form a coating film, and the coating film is heated and dried to form a dry film. In the dry film, a nonionic silane compound and a liquid crystal compound ( I) -1 and / or the affinity between the ionic compound and the liquid crystal compound (I) -1, the ionic compound is present on the substrate surface side and / or the substrate of the dry film The distribution is such that a nonionic silane compound is present on the opposite surface side. Since such distribution increases the vertical alignment regulating force, the liquid crystal compound (I) -1 tends to be aligned in the direction perpendicular to the substrate surface in the dry film. Therefore, the cured film can be formed while maintaining the state in which the liquid crystal compound (I) -1 is vertically aligned. Therefore, it is considered that the composition according to this embodiment can form a vertically aligned liquid crystal cured film without forming an alignment film on the substrate. At least one selected from the group consisting of nonionic silane compounds and ionic compounds includes only nonionic silane compounds, only ionic compounds, and both nonionic silane compounds and ionic compounds There are three embodiments including: Either one of the nonionic silane compound and the ionic compound has an effect of increasing the vertical alignment regulating force, but both the nonionic silane compound and the ionic compound are included from the viewpoint of further increasing the vertical alignment regulating force. It is preferable.

[1. Liquid crystal compound]
The liquid crystal compound (I) -1 is represented by the following formula (I) -1:

... (I) -1
One or more liquid crystal compounds having a structure represented by:

In formula (I) -1, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 4th and 4th positions,
L ¹ and L ² each independently represent a single bond or a divalent linking group,
G ¹ and G ² each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and are included in the divalent aromatic group and the divalent alicyclic hydrocarbon group. Each hydrogen atom independently substituted with a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may each independently be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom,
* Represents a bond.

Ar represents a divalent group having two or more ring structures. In this specification, the unit of the ring structure that Ar has is a single ring. For example, in liquid crystal compounds A, (A) -2, and (A) -3 described later, Ar has four, two, and three ring structures, respectively. In the two or more ring structures, two or more monocycles may be condensed and adjacent to each other, two or more monocycles may be bonded to each other via a chemical bond, They may be adjacent to each other without condensing or via chemical bonds. In addition, a single ring and a condensed ring (polycycle) in which a single ring is condensed may be bonded to each other via a chemical bond, and the polycycle and the polycycle may be bonded to each other via a chemical bond. A chemical bond that connects two or more rings includes, for example, a conjugated double bond (more specifically, —C═C— and —C═N— etc.) and a spatial extension of a conjugated system such as a carbonyl group. It may contain a bond or group that expands.

Examples of the monocycle include monocyclic hydrocarbon rings (more specifically, cycloalkane rings and benzene rings) and monocyclic heterocycles. Examples of monocyclic heterocycles include 5-membered heterocycles (more specifically, pyrrole ring, furan ring, thiophene ring, oxazole ring, imidazole ring, pyrazole ring, thiazole ring, triazole). Ring, pyrrolidine ring, tetrahydrofuran ring, tetrahydrothiophene ring and the like) and 6-membered heterocyclic rings (more specifically, pyridine ring, pyrazine ring, pyrimidine ring, thiazine ring, piperidine ring and the like). The polycycle is a structure having two or more ring structures, and the ring structure may be an aromatic ring or a hydrocarbon ring. Examples of the polycycle include those containing a condensed ring and a monocyclic heterocycle. The condensed ring is, for example, a ring obtained by condensing two or more of the same kind of monocycles, and a ring obtained by condensing two or more different kinds of single rings. Examples of the condensed ring include polycyclic hydrocarbon rings (more specifically, naphthalene ring, anthracene ring, and phenanthrene ring), and polycyclic heterocyclic rings (more specifically, quinoline ring, Quinoxaline ring, benzofuran ring, benzothiophene ring, fluorene ring, indole ring, carbazole ring, benzimidazole ring, benzothiazole ring, thienothiazole ring, benzoxazole ring, 1,3-benzodithiol ring, phenanthroline ring, etc.) Is mentioned. Among these condensed rings, a polycyclic structure is preferable from the viewpoint of developing reverse wavelength dispersion characteristics, and a polycyclic heterocyclic structure is more preferable.

The monocycle and polycycle may have a substituent. Examples of the substituent that the monocyclic ring and polycyclic ring may have include a hydrogen atom, an alkyl group having 1 to 20 carbon atoms, and an alkoxy group having 1 to 20 carbon atoms. Group, imino group, alkapolyenyl group, cyano group, or amino group, and a carbon atom in the substituent may be further substituted with an oxygen atom, a nitrogen atom, or a sulfur atom ( In this case, the hydrogen atom bonded to the carbon atom may be increased or decreased in accordance with the valence of the atom to be substituted). Among these substituents, the spatial spread of the conjugated system may be expanded like an imino group, alkapolyenyl group, cyano group, hydroxy group, and amino group. These substituents may be further substituted.

Examples of the 6-membered ring possessed by Ar include a benzene ring and a cyclohexane ring. The 6-membered ring may contain a hetero atom as a ring member atom. Examples of condensed rings including 6-membered rings include quinoline ring, quinoxaline ring, benzofuran ring, benzothiophene ring, fluorene ring, indole ring, carbazole ring, benzimidazole ring, benzothiazole ring, thienothiazole ring, benzoxazole ring, Examples thereof include a 1,3-benzodithiol ring and a phenanthroline ring.

Ar is preferably a divalent group containing a ring structure having one or more sulfur atoms as ring member atoms from the viewpoint of further improving the reverse wavelength dispersion of the polarizing plate. Ar preferably represents a divalent group represented by the following formula from the viewpoint of further improving the reverse wavelength dispersion. * Indicates a bond.

In the above formula, X ₁ , X ₂ , and X ₃ are each independently selected from CR _1X, R _2X , NR _3X , a sulfur atom, and an oxygen atom. R _1X , R _2X , and R _3X each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms.
U includes at least one ring structure, and examples of the ring structure include a structure including a monocyclic ring and / or a polycyclic ring described in the aforementioned paragraphs 0016 to 0018.
Y may be any substituent, but preferably contains at least one ring structure from the viewpoint of improving reverse wavelength dispersion, and the ring structure is described in the aforementioned paragraphs 0016 to 0018. Examples include a structure containing a single ring and / or a polycycle.
L ₁₀ is a divalent linking group, which is a single bond, —O—CO—O—, —N═N—, —C≡C—, —CR _a ═CR _b —, —CH═NN ═CH— or —CR _c ═N—.
L ₁₁ is a divalent linking group, which is a single bond, —CO—, —COO—, —O—CO—O—, —CO—NH—, —CH═CH—COO—, —CH═CH —OCO—, —CH ₂ CH ₂ —COO—, —CH ₂ CH ₂ —OCO—, —CH ₂ —COO—, —CH ₂ —OCO—, —N═N—, —C≡C—, —CR _{_{d = CR e -, - CH}} = N-N = CH -, - CR f = N -, - CR g = N-NR h -, - N = N-CR i R j -, - N = CR k - _{_{CR l R m -, - n}} = CR n -NR o -, - CR p = CR q -NR r -, or _{_{_{-CR s R t -N = CR u}}} - represents a. Here, R _c to R _u each independently represents a hydrogen atom or an alkyl group having 1 to 10 carbon atoms, and the carbon atom in the alkyl group may be substituted with a nitrogen atom, an oxygen atom, or a sulfur atom. Good (in this case, the number of hydrogen atoms is appropriately increased or decreased according to the valence number).
Z represents a hydrogen atom or a nonmetallic atom of Groups 14 to 16 to which a substituent may be bonded. Z is a structure that expands the spatial spread of the conjugated system (more specifically, a double bond site, a triple bond site, and an aromatic ring that satisfies the Hückel rule from the viewpoint of improving reverse wavelength dispersion. A heterocyclic ring) and at least one selected from the group consisting of atoms selected from nitrogen atoms and sulfur atoms.

Examples of the divalent linking group represented by L ¹ and L ² include an alkylene group having 1 to 4 carbon atoms, —O—, —S—, —R ^a1 OR ^a2 —, —R ^a3 COOR ^a4 —, —R ^a5 OCOR ^a6 —, R ^a7 OC═OOR ^a8 —, —N═N—, —CR ^c ═CR ^d —, and —C≡C—. Here, R ^a1 to R ^a8 each independently represents a single bond or an alkylene group having 1 to 4 carbon atoms (more specifically, a methylene group, an ethylene group, a propylene group, a butylene group, or the like), and R ^c and R ^d each independently represents an alkyl group having 1 to 4 carbon atoms (more specifically, a methyl group, an ethyl group, a propyl group, a butyl group, or the like) or a hydrogen atom.

L ¹ and L ² are each independently preferably a single bond, an alkylene group having 1 to 4 carbon atoms, —O—, —S—, —R ^a1 OR ^a2 —, —R ^a3 COOR ^a4 —, —R ^a5 OCOR ^a6 —, R ^a7 OC═OOR ^a8 —, —N═N—, —CR ^c ═CR ^d —, or —C≡C—. L ¹ and L ² are each independently more preferably a single bond, —OR ^a2-1 —, —CH ₂ —, —CH ₂ CH ₂ —, ^{—COOR a4-1} —, or OCOR ^a6-1 —. Represents. Here, R ^a2-1 , R ^a4-1 , and R ^a6-1 each independently represents a single bond, —CH ₂ —, or —CH ₂ CH ₂ —. L ¹ and L ² each independently represents a single bond, —O—, —CH ₂ CH ₂ —, —COO—, —COOCH ₂ CH ₂ —, or —OCO—.

Examples of the divalent aromatic group represented by G ¹ and G ² include a phenylenediyl group and a naphthylenediyl group. The divalent aromatic group may be substituted with a substituent such as a halogen atom (more specifically, a fluorine atom, a chlorine atom, a bromine atom, etc.) or an alkyl group having 1 to 4 carbon atoms. The divalent aromatic group may have a hetero atom (more specifically, an oxygen atom, a sulfur atom, a nitrogen atom, etc.) as a ring member atom. Examples of the divalent alicyclic hydrocarbon group represented by G ¹ and G ² include a cyclopentanediyl group, a cyclohexanediyl group, and a cycloheptanediyl group. The divalent alicyclic hydrocarbon group may be substituted with a substituent such as a halogen atom and an alkyl group having 1 to 4 carbon atoms.

In this specification, the aromatic group is a group having a planar structure having a planarity, and the number of π electrons of the cyclic structure is [4n + 2] according to the Hückel rule (n is a positive number of 1 or more). Indicates an integer). When a ring structure is formed by including hetero atoms such as -N = and S- as ring member atoms, the Hückel rule is satisfied including non-covalent electron pairs on these hetero atoms, and it has aromaticity Including cases.

G ¹ and G ² are each independently preferably a 1,4-phenylenediyl group optionally substituted with at least one substituent selected from the group consisting of a halogen atom and an alkyl group having 1 to 4 carbon atoms. 1,4-cyclohexanediyl group optionally substituted with at least one substituent selected from the group consisting of a halogen atom and an alkyl group having 1 to 4 carbon atoms, more preferably 1 substituted with a methyl group , 4-phenylenediyl group, unsubstituted 1,4-phenylenediyl group, or unsubstituted 1,4-trans-cyclohexanediyl group, particularly preferably unsubstituted 1,4-phenylenediyl group or Substituted 1,4-trans-cyclohexanediyl group. In addition, at least one of a plurality of G ¹ and G ² is preferably a divalent alicyclic hydrocarbon group, and at least one of G ¹ and G ² bonded to L ¹ or L ^2. More preferably, it is a divalent alicyclic hydrocarbon group.

The liquid crystal compound (I) -1 preferably has a maximum absorption in a wavelength range of 260 to 400 nm. When the liquid crystal compound (I) -1 has an aromatic group having a hetero atom or a structure that expands the conjugated system, the absorption in the near ultraviolet region is shifted to the longer wavelength side than the benzene ring, so that the wavelength is 260 nm or more. In this way, it is preferable to have maximum absorption in the wavelength region of 260 nm or more from the viewpoint of improving reverse wavelength dispersion. In addition, since the liquid crystal compound (I) -1 preferably has a maximum absorption in a region of a wavelength of 400 nm or less because coloring may occur when the absorption has a maximum in a wavelength region longer than the wavelength of 400 nm. Furthermore, from the viewpoint of further improving the wavelength dispersibility, it is more preferable to have a maximum absorption in a region of a wavelength of 280 nm to 400 nm, and it is more preferable to have a maximum absorption in a region of a wavelength of 300 nm to 400 nm.

Liquid crystal compound (I) -1 is represented by the following formula (I) -2:

... (I) -2
A liquid crystal compound having a structure represented by the formula (hereinafter sometimes referred to as liquid crystal compound (I) -2) is preferred.

In formula (I) -2, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 4th and 4th positions,
L ¹ , L ² and B ¹ each independently represent a single bond or a divalent linking group,
G ¹ , G ² , and G ³ each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group and the divalent alicyclic carbon group The hydrogen atom contained in the hydrogen group is independently a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group are each independently substituted with an oxygen atom, a sulfur atom, or a nitrogen atom. You can,
* Represents a bond.

Formula (I) in ^{^{-2 Ar, L 1, L 2}} , G 1, and ^{G 2} has the formula (I) in ^{^{-1 Ar, L 1, L 2}} , G 1, and ^{G 2} and respectively synonymous is there.

B ¹ is preferably a single bond, an alkylene group having 1 to 4 carbon atoms, —O—, —S—, —R ^a1 OR ^a2 —, —R ^a3 COOR ^a4 —, —R ^a5 OCOR ^a6 —, R ^a7. ^{OC = OOR a8 -, - N} = N -, - CR c = CR d -, or represents a -C≡C-. L ¹ and L ² are each independently more preferably a single bond, —OR ^a2-1 —, —CH ₂ —, —CH ₂ CH ₂ —, ^{—COOR a4-1} —, or —OCOR ^a6-1. -Represents. Here, R ^a2-1 , R ^a4-1 , and R ^a6-1 each independently represent a single bond, —CH ₂ —, or —CH ₂ CH ₂ —. L ¹ and L ² each independently represents a single bond, —O—, —CH ₂ CH ₂ —, —COO—, —COOCH ₂ CH ₂ —, or —OCO—.

Examples of the divalent aromatic group represented by G ³ include a phenylenediyl group and a naphthylylenediyl group. The divalent aromatic group may be substituted with a substituent such as a halogen atom (more specifically, a fluorine atom, a chlorine atom, a bromine atom, etc.) or an alkyl group having 1 to 4 carbon atoms. Examples of the divalent alicyclic hydrocarbon group represented by G ³ include a cyclopentanediyl group, a cyclohexanediyl group, and a cycloheptanediyl group. The divalent alicyclic hydrocarbon group may be substituted with a substituent such as a halogen atom or an alkyl group having 1 to 4 carbon atoms.

G ³ each independently preferably represents a 1,4-phenylenediyl group which may be substituted with at least one substituent selected from the group consisting of a halogen atom and an alkyl group having 1 to 4 carbon atoms, a halogen atom And a 1,4-cyclohexanediyl group optionally substituted with at least one substituent selected from the group consisting of alkyl groups having 1 to 4 carbon atoms, more preferably 1,4-cyclohexanediyl group substituted with a methyl group A phenylenediyl group, an unsubstituted 1,4-phenylenediyl group, or an unsubstituted 1,4-trans-cyclohexanediyl group, and particularly preferably an unsubstituted 1,4-phenylenediyl group or an unsubstituted 1 , 4-trans-cyclohexanediyl group.

Liquid crystal compound (I) -1 is represented by the following formula (I) -3:

... (I) -3
It is more preferable that the liquid crystal compound has a structure represented by the formula (hereinafter sometimes referred to as “liquid crystal compound (I) -3”).

In formula (I) -3, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L ¹ and L ² at the 4th and
L ¹ , L ² , B ¹ and B ² each independently represent a single bond or a divalent linking group;
G ¹ , G ² , G ³ , and G ⁴ each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group or the divalent fat The hydrogen atom contained in the cyclic hydrocarbon group is a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atom contained in the divalent aromatic group or the divalent alicyclic hydrocarbon group may be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom.
* Indicates a bond.

Formula (I) in ^{^{-3 Ar, L 1, L 2}} , G 1, and ^{G 2} has the formula (I) in ^{^{-1 Ar, L 1, L 2}} , G 1, and ^{G 2} and respectively synonymous is there. ^{B 1} and ^{G 3} in formula (I) -3 has the same meaning as ^{B 1} and ^{G 3,} respectively formula (I) in -2.

B ² is preferably a single bond, an alkylene group having 1 to 4 carbon atoms, —O—, —S—, —R ^a1 OR ^a2 —, —R ^a3 COOR ^a4 —, —R ^a5 OCOR ^a6 —, R ^a7. ^{OC = OOR a8 -, - N} = N -, - CR c = CR d -, or represents a -C≡C-. L ¹ and L ² are each independently more preferably a single bond, —OR ^a2-1 —, —CH ₂ —, —CH ₂ CH ₂ —, ^{—COOR a4-1} —, or —OCOR ^a6-1. -Represents. Here, R ^a2-1 , R ^a4-1 , and R ^a6-1 each independently represent a single bond, —CH ₂ —, or —CH ₂ CH ₂ —. L ¹ and L ² each independently represents a single bond, —O—, —CH ₂ CH ₂ —, —COO—, —COOCH ₂ CH ₂ —, or —OCO—.

Examples of the divalent aromatic group represented by G ⁴ include a phenylenediyl group or a naphthylylenediyl group. The divalent aromatic group may be substituted with a substituent such as a halogen atom (more specifically, a fluorine atom, a chlorine atom, a bromine atom, etc.) or an alkyl group having 1 to 4 carbon atoms. Examples of the divalent alicyclic hydrocarbon group represented by G ³ include a cyclopentanediyl group, a cyclohexanediyl group, and a cycloheptanediyl group. The divalent alicyclic hydrocarbon group may be substituted with a substituent such as a halogen atom or an alkyl group having 1 to 4 carbon atoms.

G ⁴ is preferably a 1,4-phenylenediyl group which may be substituted with at least one substituent selected from the group consisting of a halogen atom and an alkyl group having 1 to 4 carbon atoms, a halogen atom and 1 carbon atom. 1,4-cyclohexanediyl group optionally substituted with at least one substituent selected from the group consisting of ˜4 alkyl groups, more preferably a 1,4-phenylenediyl group substituted with a methyl group, An unsubstituted 1,4-phenylenediyl group or an unsubstituted 1,4-trans-cyclohexanediyl group, particularly preferably an unsubstituted 1,4-phenylenediyl group or an unsubstituted 1,4-trans -A cyclohexanediyl group.

The liquid crystal compound (I) -1 may have one or more polymerizable groups. In this specification, a polymerizable group means a group that can participate in a polymerization reaction by an active species such as an active radical or an acid generated from a photopolymerization initiator. Examples of the polymerizable group include an epoxy group, vinyl group, vinyloxy group, 1-chlorovinyl group, isopropenyl group, 4-vinylphenyl group, acryloyloxy group, methacryloyloxy group, oxiranyl group, and oxetanyl group. . Of these polymerizable groups, an acryloyloxy group and a methacryloyloxy group are preferable. In the present specification, the liquid crystal compound (I) -1 having a polymerizable group can form a polymer by a polymerization reaction.

Examples of the liquid crystal compound (I) -1 include liquid crystal compounds having structures represented by the formulas (A) -1 to (A) -5.

(Liquid Crystal Compound A)

... (A) -1
(Liquid crystal compound (A) -2)

... (A) -2
(Liquid crystal compound (A) -3)

... (A) -3
(Liquid crystal compound (A) -4)

... (A) -4
(Liquid crystal compound (A) -5)

... (A) -5

The content of the liquid crystal compound (I) -1 (the total of the contents when a plurality of liquid crystal compounds are included) is 50 to 99.5 parts by mass with respect to 100 parts by mass of the solid content of the composition. It is preferably 60 to 99 parts by mass, more preferably 70 to 99 parts by mass. In the present specification, the mass of the solid content of the composition means the total mass of the components excluding the solvent from the composition.

[2. Nonionic silane compound]
In this specification, the nonionic silane compound is a compound that is nonionic and contains Si element. The nonionic silane compound sufficiently improves the vertical alignment of the liquid crystal compound (I) -1 in the production of a vertically aligned liquid crystal cured film, and the vertical alignment of the liquid crystal compound (I) -1 is combined with the ionic compound. The property can be further improved. In addition, the nonionic silane compound can easily reduce the surface tension of the composition and can improve the wettability of the composition with respect to the substrate. Nonionic silane compounds include, for example, silicon polymers such as polysilanes, silicone resins such as silicone oils and silicone resins, and organic inorganic silane compounds such as silicone oligomers, silses siloxanes, and alkoxy silanes (more specifically, Include silane coupling agents and the like.

The nonionic silane compound may be a silicone monomer type or a silicone oligomer (polymer) type. Silicone oligomers are shown in the form of (monomer)-(monomer) copolymer: 3-mercaptopropyltrimethoxysilane-tetramethoxysilane copolymer, 3-mercaptopropyltrimethoxysilane-tetraethoxysilane copolymer, 3-mercapto Mercaptopropyl group-containing copolymers such as propyltriethoxysilane-tetramethoxysilane copolymer and 3-mercaptopropyltriethoxysilane-tetraethoxysilane copolymer; mercaptomethyltrimethoxysilane-tetramethoxysilane copolymer, mercaptomethyltrimethoxysilane- Tetraethoxysilane copolymer, mercaptomethyltriethoxysilane-tetramethoxysilane copolymer, and mercaptomethyltriethoxysilane-tetrae Copolymers containing mercaptomethyl groups such as xysilane copolymer; 3-methacryloyloxypropyltrimethoxysilane-tetramethoxysilane copolymer, 3-methacryloyloxypropyltrimethoxysilane-tetraethoxysilane copolymer, 3-methacryloyloxypropyltriethoxysilane- Tetramethoxysilane copolymer, 3-methacryloyloxypropyltriethoxysilane-tetraethoxysilane copolymer, 3-methacryloyloxypropylmethyldimethoxysilane-tetramethoxysilane copolymer, 3-methacryloyloxypropylmethyldimethoxysilane-tetraethoxysilane copolymer, 3-methacryloyl Oxypropylmethyldiethoxysilane-tetramethoxysilane copolymer, And copolymers containing methacryloyloxypropyl groups such as 3-methacryloxyyl propylmethyldiethoxysilane-tetraethoxysilane copolymer; 3-acryloyloxypropyltrimethoxysilane-tetramethoxysilane copolymer, 3-acryloyloxypropyltrimethoxysilane -Tetraethoxysilane copolymer, 3-acryloyloxypropyltriethoxysilane-tetramethoxysilane copolymer, 3-acryloyloxypropyltriethoxysilane-tetraethoxysilane copolymer, 3-acryloyloxypropylmethyldimethoxysilane-tetramethoxysilane copolymer, 3- Acryloyloxypropylmethyldimethoxysilane-tetraethoxysilane copolymer, 3-acryloyloxy Copolymers containing acryloyloxypropyl groups such as propylmethyldiethoxysilane-tetramethoxysilane copolymer and 3-acryloyloxypropylmethyldiethoxysilane-tetraethoxysilane copolymer; vinyltrimethoxysilane-tetramethoxysilane copolymer, vinyltrimethoxy Silane-tetraethoxysilane copolymer, vinyltriethoxysilane-tetramethoxysilane copolymer, vinyltriethoxysilane-tetraethoxysilane copolymer, vinylmethyldimethoxysilane-tetramethoxysilane copolymer, vinylmethyldimethoxysilane-tetraethoxysilane copolymer, vinylmethyldi Ethoxysilane-tetramethoxysilane copolymer and vinylmethyldiethoxysilane-tetrae Vinyl group-containing copolymers such as xysilane copolymers; 3-aminopropyltrimethoxysilane-tetramethoxysilane copolymers, 3-aminopropyltrimethoxysilane-tetraethoxysilane copolymers, 3-aminopropyltriethoxysilane-tetramethoxysilane copolymers 3-aminopropyltriethoxysilane-tetraethoxysilane copolymer, 3-aminopropylmethyldimethoxysilane-tetramethoxysilane copolymer, 3-aminopropylmethyldimethoxysilane-tetraethoxysilane copolymer, 3-aminopropylmethyldiethoxysilane-tetra Amino group-containing copolymers such as methoxysilane copolymer and 3-aminopropylmethyldiethoxysilane-tetraethoxysilane copolymer And the like. These nonionic silane compounds may be used individually by 1 type, or may be used in combination of 2 or more type. Moreover, the silane containing compound illustrated to the term of a leveling agent can also be used. Of these nonionic silane compounds, a silane coupling agent is preferable from the viewpoint of further improving the adhesion.

The silane coupling agent is selected from the group consisting of a vinyl group, an epoxy group, a styryl group, a methacryl group, an acrylic group, an amino group, an isocyanurate group, a ureido group, a mercapto group, an isocyanate group, a carboxy group, and a hydroxy group at the terminal. And a compound containing Si element having at least one functional group and at least one alkoxysilyl group or silanol group. By appropriately selecting these functional groups, the mechanical strength of the vertically aligned liquid crystal cured film is improved, the surface modification of the vertically aligned liquid crystal cured film, and the layer adjacent to the vertically aligned liquid crystal cured film (for example, the base material). It is possible to impart unique effects such as improved adhesion. The silane coupling agent is preferably a silane coupling agent having an alkoxysilyl group and another different reactive group (for example, the above functional group) from the viewpoint of further improving adhesion. Furthermore, the silane coupling agent is preferably a silane coupling agent having an alkoxysilyl group and a polar group. When the silane coupling agent has at least one alkoxysilyl group and at least one polar group in the molecule, the vertical alignment property of the liquid crystal compound is further improved, and the vertical alignment promoting effect is remarkably obtained. Examples of the polar group include an epoxy group, an amino group, an isocyanurate group, a mercapto group, a carboxy group, and a hydroxy group. The polar group may have a substituent or a protective group as appropriate in order to control the reactivity of the silane coupling agent.

Examples of the silane coupling agent include vinyltrimethoxysilane, vinyltriethoxysilane, vinyltris (2-methoxyethoxy) silane, N- (2-aminoethyl) -3-aminopropylmethyldimethoxysilane, N- (2- Aminoethyl) -3-aminopropyltrimethoxysilane, 3-aminopropyltriethoxysilane, 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropylmethyldimethoxysilane, 2- (3,4-epoxycyclohexyl) ethyltrimethoxysilane, 3-chloropropylmethyldimethoxysilane, 3-chloropropyltrimethoxysilane, 3-methacryloyloxypropyltrimethoxysilane , 3-mercaptopropyltrimethoxysilane, 3-glycidoxypropyltrimethoxysilane, 3-glycidoxypropyltriethoxysilane, 3-glycidoxypropyldimethoxymethylsilane, and 3-glycidoxypropylethoxydimethylsilane Is mentioned.

Examples of commercially available silane coupling agents include KP321, KP323, KP324, KP326, KP340, KP341, X22-161A, KF6001, KBM-1003, KBE-1003, KBM-303, KBM-402, KBM-403. , KBE-402, KBE-403, KBM-1403, KBM-502, KBM-503, KBE-502, KBE-503, KBM-5103, KBM-602, KBM-603, KBM-903, KBE-903, KBE Silane coupling agents manufactured by Shin-Etsu Chemical Co., Ltd. such as -9103, KBM-573, KBM-575, KBM-9659, KBE-585, KBM-802, KBM-803, KBE-846, and KBE-9007 Is mentioned.

The content of the nonionic silane compound is usually preferably from 0.01 to 5% by mass, more preferably from 0.05 to 4% by mass, based on the solid content of the composition, More preferably, it is ˜3 mass%. When the content of the nonionic silane compound is 0.01% by mass or more based on the solid content of the composition, the vertical alignment of the liquid crystal compound is further improved, and the content of the nonionic silane compound is solid in the composition. If it is contained in an amount of 5% by mass or less, the applicability of the composition is unlikely to decrease.

[3. Ionic compound]
The ionic compound sufficiently improves the vertical alignment of the liquid crystal compound (I) -1 in the production of a vertically aligned liquid crystal cured film, and the vertical alignment of the liquid crystal compound (I) -1 by combination with a nonionic silane compound. The property can be further improved.

Examples of the ionic compound include an onium salt (more specifically, a quaternary ammonium salt, a tertiary sulfonium salt in which a nitrogen atom has a positive charge, and a quaternary phosphonium in which a phosphorus atom has a positive charge. Salt). Of these onium salts, a quaternary onium salt is preferable from the viewpoint of further improving the vertical alignment of the liquid crystal compound (I) -1, and from the viewpoint of improving availability and mass productivity, More preferred are quaternary ammonium salts. The onium salt may have two or more quaternary onium salt sites in the molecule, and may be an oligomer or a polymer.

The molecular weight of the ionic compound is preferably 100 or more from the viewpoint of further improving the vertical alignment of the liquid crystal compound (I) -1. The molecular weight of the ionic compound is preferably 10,000 or less, more preferably 5000 or less, and still more preferably 3000 or less from the viewpoint of further improving the coating properties of the composition. The molecular weight of the ionic compound is more preferably 100 or more and 10,000 or less from the viewpoint of further improving the vertical alignment property of the liquid crystal compound (I) -1 and further improving the coating property of the composition.

Examples of the cation component of the ionic compound include inorganic cations and organic cations. Of the cationic components of these ionic compounds, organic cations are preferred from the viewpoint of suppressing the occurrence of alignment defects in the liquid crystal compound. Examples of the organic cation include an imidazolium cation, a pyridinium cation, an ammonium cation, a sulfonium cation, and a phosphonium cation.

On the other hand, ionic compounds generally have a counter anion. As an anion component used as the counter ion of the said cation component, an inorganic anion or an organic anion is mentioned, for example. Among these anion components, an organic anion is preferable from the viewpoint of suppressing the occurrence of alignment defects in the liquid crystal compound. Further, the cation and the anion do not necessarily have a one-to-one correspondence. Examples of the anion component include the following.
Chloride anion [Cl ⁻ ],
Bromide anion [Br ⁻ ],
Iodide anion [I ⁻ ],
Tetrachloroaluminate anion [AlCl ₄ ⁻ ],
Heptachlorodialuminate anion [Al ₂ Cl ₇ ⁻ ],
Tetrafluoroborate anion [BF ₄ ⁻ ],
Hexafluorophosphate anion [PF ₆ ⁻ ],
Perchlorate anion [ClO ₄ ⁻ ],
Nitrate anion [NO ₃ ⁻ ],
Acetate anion [CH ₃ COO ⁻ ],
Trifluoroacetate anion [CF ₃ COO ⁻ ],
Fluorosulfonate anion [FSO ₃ ⁻ ],
Methanesulfonate anion [CH ₃ SO ₃ ⁻ ],
Trifluoromethanesulfonate anion [CF ₃ SO ₃ ⁻ ],
p-toluenesulfonate anion [p-CH ₃ C ₆ H ₄ SO ₃ ⁻ ],
Bis (fluorosulfonyl) imide anion [(FSO ₂ ) ₂ N ⁻ ],
Bis (trifluoromethanesulfonyl) imide anion [(CF ₃ SO ₂ ) ₂ N ⁻ ],
Tris (trifluoromethanesulfonyl) methanide anion [(CF ₃ SO ₂ ) ₃ C ⁻ ],
Hexafluoroarsenate anion [AsF ₆ ⁻ ],
Hexafluoroantimonate anion [SbF ₆ ⁻ ],
Hexafluoroniobate anion [NbF ₆ ⁻ ],
Hexafluorotantalate anion [TaF ₆ ⁻ ],
Dimethyl phosphinate anion [(CH ₃ ) ₂ POO ⁻ ],
(Poly) hydrofluorofluoride anion [F (HF) _n ⁻ ] (for example, n represents an integer of 1 to 3),
Dicyanamide anion [(CN) ₂ N ⁻ ],
Thiocyan anion [SCN ⁻ ],
Perfluorobutanesulfonate anion [C ₄ F ₉ SO ₃ ⁻ ],
Bis (pentafluoroethanesulfonyl) imide anion [(C ₂ F ₅ SO ₂ ) ₂ N ⁻ ],
Perfluorobutanoate anion [C ₃ F ₇ COO ⁻ ], and (trifluoromethanesulfonyl) (trifluoromethanecarbonyl) imide anion [(CF ₃ SO ₂ ) (CF ₃ CO) N ⁻ ].

Specific examples of the ionic compound can be appropriately selected from the combination of the cation component and the anion component. Specific examples of the compound that is a combination of a cation component and an anion component include the following.

(Pyridinium salt)
N-hexylpyridinium hexafluorophosphate,
N-octylpyridinium hexafluorophosphate,
N-methyl-4-hexylpyridinium hexafluorophosphate,
N-butyl-4-methylpyridinium hexafluorophosphate,
N-octyl-4-methylpyridinium hexafluorophosphate,
N-hexylpyridinium bis (fluorosulfonyl) imide,
N-octylpyridinium bis (fluorosulfonyl) imide,
N-methyl-4-hexylpyridinium bis (fluorosulfonyl) imide,
N-butyl-4-methylpyridinium bis (fluorosulfonyl) imide,
N-octyl-4-methylpyridinium bis (fluorosulfonyl) imide,
N-hexylpyridinium bis (trifluoromethanesulfonyl) imide,
N-octylpyridinium bis (trifluoromethanesulfonyl) imide,
N-methyl-4-hexylpyridinium bis (trifluoromethanesulfonyl) imide,
N-butyl-4-methylpyridinium bis (trifluoromethanesulfonyl) imide,
N-octyl-4-methylpyridinium bis (trifluoromethanesulfonyl) imide,
N-hexylpyridinium p-toluenesulfonate,
N-octylpyridinium p-toluenesulfonate,
N-methyl-4-hexylpyridinium p-toluenesulfonate,
N-butyl-4-methylpyridinium p-toluenesulfonate, and N-octyl-4-methylpyridinium p-toluenesulfonate.

(Imidazolium salt)
1-ethyl-3-methylimidazolium hexafluorophosphate,
1-ethyl-3-methylimidazolium bis (fluorosulfonyl) imide,
1-ethyl-3-methylimidazolium bis (trifluoromethanesulfonyl) imide,
1-ethyl-3-methylimidazolium p-toluenesulfonate,
1-butyl-3-methylimidazolium methanesulfonate, etc.

(Pyrrolidinium salt)
N-butyl-N-methylpyrrolidinium hexafluorophosphate,
N-butyl-N-methylpyrrolidinium bis (fluorosulfonyl) imide,
N-butyl-N-methylpyrrolidinium bis (trifluoromethanesulfonyl) imide,
N-butyl-N-methylpyrrolidinium p-toluenesulfonate, etc.

(Ammonium salt)
Tetrabutylammonium hexafluorophosphate,
Tetrabutylammonium bis (fluorosulfonyl) imide,
Tetrahexylammonium bis (fluorosulfonyl) imide,
Trioctylmethylammonium bis (fluorosulfonyl) imide,
(2-hydroxyethyl) trimethylammonium bis (fluorosulfonyl) imide,
Tetrabutylammonium bis (trifluoromethanesulfonyl) imide,
Tetrahexylammonium bis (trifluoromethanesulfonyl) imide,
Trioctylmethylammonium bis (trifluoromethanesulfonyl) imide,
(2-hydroxyethyl) trimethylammonium bis (trifluoromethanesulfonyl) imide,
Tetrabutylammonium p-toluenesulfonate,
Tetrahexylammonium p-toluenesulfonate,
Trioctylmethylammonium p-toluenesulfonate,
(2-hydroxyethyl) trimethylammonium p-toluenesulfonate,
(2-hydroxyethyl) trimethylammonium dimethylphosphinate,
1- (3-trimethoxysilylpropyl) -1,1,1-tributylammonium bis (trifluoromethanesulfonyl) imide,
1- (3-trimethoxysilylpropyl) -1,1,1-trimethylammonium bis (trifluoromethanesulfonyl) imide,
1- (3-trimethoxysilylbutyl) -1,1,1-tributylammonium bis (trifluoromethanesulfonyl) imide,
1- (3-trimethoxysilylbutyl) -1,1,1-trimethylammonium bis (trifluoromethanesulfonyl) imide,
N-{(3-triethoxysilylpropyl) carbamoyloxyethyl)}-N, N, N-trimethylammonium bis (trifluoromethanesulfonyl) imide, and N- [2- {3- (3-trimethoxysilylpropylamino) ) -1-Oxopropoxy} ethyl] -N, N, N-trimethylammonium bis (trifluoromethanesulfonyl) imide.

(Phosphonium salt)
Tributyl (2-methoxyethyl) phosphonium bis (trifluoromethanesulfonyl) imide,
Tributylmethylphosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-trimethyl-1-[(trimethoxysilyl) methyl] phosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-trimethyl-1- [2- (trimethoxysilyl) ethyl] phosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-trimethyl-1- [3- (trimethoxysilyl) propyl] phosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-trimethyl-1- [4- (trimethoxysilyl) butyl] phosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-tributyl-1-[(trimethoxysilyl) methyl] phosphonium bis (trifluoromethanesulfonyl) imide,
1,1,1-tributyl-1- [2- (trimethoxysilyl) ethyl] phosphonium bis (trifluoromethanesulfonyl) imide, and 1,1,1-tributyl-1- [3- (trimethoxysilyl) propyl] Phosphonium bis (trifluoromethanesulfonyl) imide.

These ionic compounds may be used alone or in combination of two or more. From the viewpoint of further improving the vertical alignment of the liquid crystal compound, the ionic compound preferably has a Si element and / or an F element in the molecular structure of the cation moiety. This is because if the ionic compound has Si element and / or F element in the molecular structure of the cation site, the ionic compound can be segregated on the surface of the vertically aligned liquid crystal cured film. Of these ionic compounds, ionic compounds composed of all nonmetallic elements (more specifically, the following ionic compounds (1) to (3)) are preferred.

(Ionic compound (1))

(Ionic compound (2))

(Ionic compound (3))

As a method for improving the vertical alignment property of the liquid crystal compound, for example, there is a method of treating the surface of the substrate using a surfactant having an alkyl group having a long chain length to some extent. This method is described, for example, in “Liquid Crystal Handbook”, Chapter 2, Liquid Crystal Orientation and Physical Properties (issued by Maruzen Co., Ltd.). Thus, the method of improving the vertical alignment property of a liquid crystal compound with a surfactant can be applied to an ionic compound. That is, as a method for improving the vertical alignment property of the liquid crystal compound, for example, a method of treating the substrate surface with an ionic compound having an alkyl group having a long chain length to some extent can be mentioned. More specifically, the ionic compound preferably satisfies the following formula (10) from the viewpoint of improving the vertical alignment of the liquid crystal compound.
5 <M <16 (10)
In formula (10), M is represented by the following formula (11).
M = (the number of covalent bonds from the positively charged atom to the end of the molecular chain of the substituent having the largest number of covalent bonds from the end of the molecular chain to the end of the molecular chain among the substituents directly bonded on the positively charged atom ) ÷ (number of positively charged atoms) (11)

When two or more positively charged atoms are present in the molecule of the ionic compound, the substituent having two or more positively charged atoms is counted from the positively charged atoms considered as the base point. The number of covalent bonds to the closest other positively charged atom is defined as “the number of covalent bonds from the positively charged atom to the end of the molecular chain” described in the definition of M above. Further, when the ionic compound is an oligomer or polymer having two or more repeating units, the structural unit is considered as one molecule, and the above M is calculated. When an atom having a positive charge is incorporated in a ring structure, the number of covalent bonds leading to the atom having the same positive charge via the ring structure, or the end of a substituent bonded to the ring structure Of the number of covalent bonds, the larger number of covalent bonds is defined as “the number of covalent bonds from the positively charged atom to the end of the molecular chain” described in the definition of M above.

The content of the ionic compound is usually preferably 0.01 to 5% by mass, more preferably 0.05 to 4% by mass, and more preferably 0.1 to 3% by mass with respect to the solid content of the composition. More preferably, it is mass%. When the content of the ionic compound is 0.01% by mass or more in the solid content of the composition, the vertical alignment of the liquid crystal compound is further improved, and the content of the ionic compound is based on the solid content of the composition. When it is 5% by mass or less, the coating property of the composition is unlikely to decrease.

[4. Other ingredients]
The composition of the present invention may further contain additives such as a solvent, a photopolymerization initiator, a polymerization inhibitor, a photosensitizer, a leveling agent, and an adhesion improver as other components as necessary. Good. These additives may be used individually by 1 type, or may be used in combination of 2 or more type.

(solvent)
Since the composition of this invention is normally apply | coated to a base material etc. in the state melt | dissolved in the solvent, it is preferable that a solvent is included. Examples of the solvent include water, methanol, ethanol, ethylene glycol, isopropyl alcohol, propylene glycol, ethylene glycol methyl ether, ethylene glycol butyl ether, 1-methoxy-2-propanol, 2-butoxyethanol, and propylene glycol monomethyl ether. Alcohol solvents; ester solvents such as ethyl acetate, butyl acetate, ethylene glycol methyl ether acetate, γ-butyrolactone, propylene glycol methyl ether acetate and ethyl lactate; acetone, methyl ethyl ketone, cyclopentanone, cyclohexanone, 2-heptanone, and methyl Ketone solvents such as isobutyl ketone; aliphatic hydrocarbon solvents such as pentane, hexane, and heptane; Cycloaliphatic hydrocarbon solvents such as cyclohexane; aromatic hydrocarbon solvents such as toluene and xylene; nitrile solvents such as acetonitrile; ether solvents such as tetrahydrofuran and dimethoxyethane; chlorine-containing solvents such as chloroform and chlorobenzene Amide solvents such as dimethylacetamide, dimethylformamide, N-methyl-2-pyrrolidone (NMP), and 1,3-dimethyl-2-imidazolidinone. These solvent may be used individually by 1 type, or may be used in combination of 2 or more type. Of these solvents, alcohol solvents, ester solvents, ketone solvents, chlorine-containing solvents, amide solvents, and aromatic hydrocarbon solvents are preferable. These solvent may be used individually by 1 type, or may be used in combination of 2 or more type.

The content of the solvent is preferably 50 to 98 parts by mass, more preferably 70 to 95 parts by mass with respect to 100 parts by mass of the composition. Accordingly, the solid content in 100 parts by mass of the composition is preferably 2 to 50 parts by mass. When the solid content of the composition is 50 parts by mass or less, since the viscosity of the composition becomes low, the thickness of the vertically aligned liquid crystal cured film becomes substantially uniform, and unevenness tends not to occur in the vertically aligned liquid crystal cured film. is there. The solid content can be appropriately determined in consideration of the thickness of the vertically aligned liquid crystal cured film to be produced.

(Photopolymerization initiator)
The composition of the present invention may contain a photopolymerization initiator for the purpose of advancing the polymerization reaction. In this specification, a photoinitiator provides an active species that absorbs active energy rays and initiates a polymerization reaction. The photopolymerization initiator can be used as a curable composition that cures by radical polymerization, such as (meth) acrylate or urethane (meth) acrylate, as a curable material. In the case of using a curable composition that cures at a temperature, for example, an epoxy compound or an oxetane compound, as the curable composition, a photocationic polymerization initiator can be used.

Examples of the photopolymerization initiator include a photoradical polymerization initiator and a photocationic polymerization initiator. Examples of the photo radical polymerization initiator include benzoin compounds, benzophenone compounds, benzyl ketal compounds, α-hydroxy ketone compounds, α-amino ketone compounds, triazine compounds, and the like. Examples of the cationic photopolymerization initiator include aromatic diazonium salts, onium salts such as aromatic iodonium salts and aromatic sulfonium salts, and iron-arene complexes. Examples of the photopolymerization initiator include Irgacure (registered trademark) 907, Irgacure 184, Irgacure 651, Irgacure 819, Irgacure 250, Irgacure 369, Irgacure 379, Irgacure 127, Irgacure 2959, Irgacure 754, and Irgacure 379E. Photopolymerization initiators manufactured by BASF Japan, Inc .; photopolymerization initiators manufactured by Seiko Chemical Co., Ltd., such as Sequol BZ, Sequol Z, and Sequol BEE, kayacure BP100 (manufactured by Nippon Kayaku Co., Ltd.), And Adeka optomer SP-152, Adeka optomer SP-170, Adeka optomer N-1717, Ade Photopolymerization initiators made by ADEKA Corporation, such as Optomer N-1919, Adeka Arcles NCI-831, Adeka Arcles NCI-930; Photopolymerization made by Nippon Siebel Hegner, such as TAZ-A and TAZ-PP Initiator; Photopolymerization initiator manufactured by Sanwa Chemical Co., such as TAZ-104; Photopolymerization initiator manufactured by Nippon Kayaku Co., Ltd., such as Kayrad (registered trademark) series; Dow Chemical Co., Ltd. such as Cyracure UVI series Photopolymerization initiators manufactured by San-Apro Co., Ltd. such as CPI series; Photopolymerization initiators manufactured by Midori Chemical Co., Ltd. such as TAZ, BBI, and DTS; such as RHODORSIL (registered trademark) Examples include photopolymerization initiators manufactured by Rhodia Co., Ltd. These photoinitiators may be used individually by 1 type, or may be used in combination of 2 or more type. A photoinitiator can be suitably selected and used according to the material to be used.

Since the photopolymerization initiator can fully utilize the energy emitted from the light source and is excellent in productivity, the maximum absorption wavelength of the photopolymerization initiator is preferably 300 nm to 400 nm, more preferably 300 nm to 380 nm. Of these photopolymerization initiators, α-acetophenone polymerization initiators and oxime photopolymerization initiators are preferred.

Examples of the α-acetophenone polymerization initiator include 2-methyl-2-morpholino-1- (4-methylsulfanylphenyl) propan-1-one, 2-dimethylamino-1- (4-morpholinophenyl) -2 -Benzylbutan-1-one (2-dimethylamino-2-benzyl-1- (4-morpholinophenyl) butan-1-one) and 2-dimethylamino-1- (4-morpholinophenyl) -2- ( 4-methylphenylmethyl) butan-1-one. α-acetophenone polymerization initiators include 2-methyl-2-morpholino-1- (4-methylsulfanylphenyl) propan-1-one and 2-dimethylamino-1- (4-morpholinophenyl) -2-benzyl Butan-1-one is preferred. Commercially available products of α-acetophenone compounds include α-acetophenone polymerization initiators manufactured by BASF Japan Ltd. such as Irgacure 369, 379EG, and 907, and α-acetophenone systems manufactured by Seiko Chemical Co., Ltd. such as Seikol BEE. A polymerization initiator etc. are mentioned.

An oxime photopolymerization initiator generates radicals when irradiated with light. Polymerization of the composition in the deep part of the coating film proceeds suitably by this radical. Moreover, it is preferable to use the oxime type photoinitiator which can utilize an ultraviolet-ray with a wavelength of 350 nm or more efficiently from a viewpoint of making a polymerization reaction in the deep part of a coating film progress more efficiently. Examples of the oxime photopolymerization initiator that can efficiently use ultraviolet rays having a wavelength of 350 nm or more include triazine compounds and oxime ester type carbazole compounds. From the viewpoint of sensitivity, for example, oxime esters are more preferable. Type carbazole compounds. Examples of the oxime ester type carbazole compound include 1,2-octanedione, 1- [4- (phenylthio) -2- (O-benzoyloxime)], and ethanone, 1- [9-ethyl-6- (2 -Methylbenzoyl) -9H-carbazol-3-yl] -1- (O-acetyloxime). Examples of commercially available oxime ester type carbazole compounds include, for example, oxime ester type carbazole compounds manufactured by BASF Japan, such as Irgacure OXE-01, Irgacure OXE-02, and Irgacure OXE-03, and Adekaoptomer N-1919, An oxime ester type carbazole compound manufactured by ADEKA Corporation, such as Adeka Arcles NCI-831, can be mentioned.

The content of the photopolymerization initiator is usually 0.1 to 20 masses when the solid content (excluding the content of the solvent from the composition) contained in the composition of the present invention is 100 mass parts. Parts, preferably 0.5 to 10 parts by weight, more preferably 1 to 7 parts by weight. When the photopolymerization initiator is 0.1 to 20 parts by mass with respect to 100 parts by mass of the composition, the polymerization reaction is likely to proceed sufficiently.

(Leveling agent)
The leveling agent is used for the purpose of adjusting the coating property of the composition of the present invention, that is, for the purpose of adjusting the fluidity of the composition for coating and making the surface of the layer obtained by coating the composition flatter. It may be added to the composition. Examples of the leveling agent include a silicone leveling agent such as a silane coupling agent, a polyacrylate leveling agent, and a fluoroalkyl leveling agent. Of these leveling agents, silicone-based leveling agents and fluoroalkyl-based leveling agents are preferred from the viewpoint of further improving the vertical alignment of the liquid crystal compound.

Examples of commercially available leveling agents include DC3PA, SH7PA, DC11PA, SH28PA, SH29PA, SH30PA, ST80PA, ST86PA, SH8400, SH8700, and FZ2123; leveling agents manufactured by Toray Dow Corning Corp .; , KP326, KP340, KP341, X22-161A, KF6001, KBM-1003, KBE-1003, KBM-303, KBM-402, KBM-403, KBE-402, KBE-403, KBM-1403, KBM-502, KBM -503, KBE-502, KBE-503, KBM-5103, KBM-602, KBM-603, KBM-903, KBE-903, KBE-9103, KBM-573, KBM Leveling agents manufactured by Shin-Etsu Chemical Co., Ltd. such as 575, KBE-585, KBM-802, KBM-802, KBM-803, KBE-846, and KBE-9007; TSF400, TSF401, TSF410, TSF4300, TSF4440, TSF4445 Momentive Performance Materials Japan GK leveling agent such as TSF-4446, TSF4452, and TSF4460; Fluorinert (registered trademark) FC-72, FC-40, FC-43, and FC-3283 Leveling agents manufactured by Sumitomo 3M Co., Ltd .; Megafac® R-08, R-30, R-90, F-410, F-411, F-443, F- 445, F-470, F-4 7. Leveling agents manufactured by DIC Corporation, such as F-479, F-482, F-482, and F-556; Ftop (trade name) EF301, EF303, EF351, and EF352 Leveling agent manufactured by Mitsubishi Materials Electronic Chemical Co., Ltd .; Surflon (registered trademark) S-381, S-382, S-383, S-393, SC-101, SC-105, KH-40 Leveling agents manufactured by AGC Seimi Chemical Co., Ltd., such as SA-100; Leveling agents manufactured by Daikin Fine Chemical Laboratory, Inc., such as trade names E1830 and E5844; BM-1000, BM-1100, BYK-352, Chemie leveling agents such as BYK-353 and BYK-361N (both trade names: BM). These leveling agents may be used individually by 1 type, or may be used in combination of 2 or more type.

The content of the leveling agent is usually preferably 0.001 to 3% by mass, more preferably 0.01 to 3% by mass, and more preferably 0.1 to 3% by mass with respect to the solid content of the composition of the present invention. % Is more preferable. When the leveling agent content is 0.001 to 3 mass% with respect to the solid content of the composition, the coating property of the composition is further improved.

(Method for preparing composition for forming vertically aligned liquid crystal cured film)
The composition of the present invention comprises, for example, the liquid crystal compound (I) -1, one or both of a nonionic silane compound and an ionic compound, and an additive to be added as necessary at a predetermined temperature. By stirring or the like, these components can be obtained by dispersing or dissolving them substantially uniformly.

<Vertical alignment liquid crystal cured film>
The vertically aligned liquid crystal cured film is a cured product of the composition of the present invention, and the liquid crystal compound is aligned in a direction perpendicular to the in-plane direction. That is, the vertically aligned liquid crystal cured film includes a liquid crystal compound that is aligned in a direction perpendicular to the in-plane direction of the vertically aligned liquid crystal cured film. Further, the vertically aligned liquid crystal cured film may include a polymer of a liquid crystal compound that is aligned in a direction perpendicular to the in-plane direction of the vertically aligned liquid crystal cured film. The three-dimensional refractive index ellipsoid formed by the vertically aligned liquid crystal cured film may have biaxiality, but preferably has uniaxiality.

The vertically aligned liquid crystal cured film deteriorates the oblique reflection hue of the display including the elliptically polarizing plate including the vertically aligned liquid crystal cured film (for example, the problem that coloring such as red and blue is observed in the oblique hue of the display) )
The following relational expression (1):
−150 nm ≦ RthC (550) ≦ −30 nm (1)
[In relational expression (1), RthC (550) represents the retardation value in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm]
It is preferable to satisfy. The retardation value RthC (550) in the thickness direction of the vertically aligned liquid crystal cured film is more preferably from −100 nm to −40 nm, and more preferably from −80 nm to from the viewpoint of further suppressing the deterioration of the oblique reflection hue of the display. More preferably, it is −40 nm or less.

The retardation value RthC (550) in the thickness direction of the vertically aligned liquid crystal cured film can be adjusted by the thickness dC of the vertically aligned liquid crystal cured film. The in-plane retardation value is expressed by the following formula (1-2):
RthC (550) = [(nxC (550) + nyC (550)) / 2-nzC (550)] × dC (1-2)
[In the formula (1-2), nxC (550) represents a main refractive index at a wavelength of 550 nm in the film plane of the vertically aligned liquid crystal cured film, and nyC (550) is a direction orthogonal to the nxC (550) in the same plane. NzC (550) indicates the refractive index at a wavelength of 550 nm in the thickness direction of the vertically aligned liquid crystal cured film, and dC indicates the film thickness of the vertically aligned liquid crystal cured film.]
Therefore, in order to obtain a desired retardation value RthC (550) in the thickness direction, the three-dimensional refractive index and the film thickness dC may be adjusted. The three-dimensional refractive index depends on the molecular structure and orientation of the liquid crystal compound described above. Further, when nxC (550) = nyC (550), nxC (550) can be a refractive index in an arbitrary direction within the film plane.

The upper limit of the thickness of the vertically aligned liquid crystal cured film is preferably 3 μm or less, more preferably 2.5 μm or less, further preferably 2.0 μm or less, and particularly preferably 1.5 μm or less from the viewpoint of thinning. . The lower limit of the thickness of the vertically aligned liquid crystal cured film is preferably 0.1 μm or more, more preferably 0.3 μm or more, and further preferably 0.4 μm or more. The thickness of the vertically aligned liquid crystal cured film can be measured using an ellipsometer or a contact-type film thickness meter.

In addition, the vertically aligned liquid crystal cured film is used from the viewpoint of suppressing a decrease in ellipticity when viewed from the oblique side on the short wavelength side in the elliptically polarizing plate including the vertically aligned liquid crystal cured film.
The following relational expression (2):
RthC (450) / RthC (550) ≦ 1 (2)
[In the relational expression (2), RthC (450) represents the retardation value in the thickness direction at a wavelength of 450 nm of the vertically aligned liquid crystal cured film, and RthC (550) represents the retardation in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm. Show value]
It is preferable to satisfy. From the viewpoint of further suppressing the decrease in the ellipticity, RthC (450) / RthC (550) of the vertically aligned liquid crystal cured film is more preferably 0.95 or less, and further preferably 0.90 or less. . Further, the retardation value RthC (450) in the thickness direction of the vertically aligned liquid crystal cured film can be adjusted by the thickness dC of the vertically aligned liquid crystal cured film, similarly to RthC (550).

[Method for producing vertically aligned liquid crystal cured film]
The method for producing a vertically aligned liquid crystal cured film includes a coating film forming step in which a composition for forming a vertically aligned liquid crystal cured film is applied to a substrate, a coating film is formed on the substrate, the coating film is dried, and a dry film is formed. A dry film forming step of forming, and a cured film forming step of irradiating the dry film with active energy rays to form a vertically aligned liquid crystal cured film. The laminate produced by this production method is composed of a substrate and a vertically aligned liquid crystal cured film. The case where the liquid crystal compound has one or more polymerizable groups and the composition further contains a photopolymerization initiator will be described as an example.

(Coating film forming process)
In the coating film forming step, for example, the composition is applied to a base material using a printing apparatus to form a coating film on the base material. Examples of the application method include printing methods such as a gravure coating method, a die coating method, and a flexo method.

(Dry film formation process)
In the dry film forming step, for example, the coating film is dried using a heating device to form a dry film. After the coating film is heated and the solvent in the coating film is removed, the liquid crystal compound is vertically aligned and converted into a dry film. The heating temperature is preferably equal to or higher than the phase transition temperature of the liquid crystal compound so that the solvent can be removed.

(Curing film formation process)
In the cured film forming step, for example, using a light irradiation device, the dry film is irradiated with active energy rays (more specifically, ultraviolet rays or the like) to form a vertically aligned liquid crystal cured film. In the present invention, since the composition for forming a vertically aligned liquid crystal cured film contains a nonionic silane compound and / or an ionic compound, the liquid crystal compound exhibits a vertical alignment regulating force on the liquid crystal compound. The liquid crystal state aligned perpendicular to the substrate plane is maintained. By irradiating the dry film with active energy rays, the liquid crystal compound is photopolymerized while maintaining a vertically aligned liquid crystal state. Thereby, a vertically aligned liquid crystal cured film can be directly formed on the substrate.

(Other process: vertical alignment film formation process)
As already explained, the vertically aligned liquid crystal cured film of the present invention can be directly formed on the substrate without forming the alignment film. On the other hand, the method for producing a vertically aligned liquid crystal cured film may further include a vertical alignment film forming step of forming a vertical alignment film for the purpose of further improving the orientation of the vertically aligned liquid crystal cured film. In such a case, the vertically aligned liquid crystal cured film is indirectly formed on the substrate via the vertically aligned film.

The vertical alignment film forming process is a process executed before the coating film forming process, and forms a vertical alignment film. Here, an example of a method for forming the vertical alignment film will be described. The alignment film forming step includes, for example, a step of forming a coating film of a composition for forming a vertical alignment film, a step of forming a dry film from the coating film, and, if necessary, curing the dry film to form an alignment film. Forming.
In the coating film forming step, for example, a vertical alignment film forming composition is applied onto a substrate using a printing apparatus to form a coating film. As the composition for forming a vertical alignment film, for example, a composition containing an alignment polymer and a solvent as described later can be used. In the dry film forming step, for example, the coating film is heated using a heating device to dry the coating film, thereby forming a dry film. Further, when a step of curing by UV irradiation is required, a vertical alignment film is formed by irradiating and curing the second dry film by using a UV irradiation apparatus. When the manufacturing method of a vertical alignment liquid crystal cured film includes a vertical alignment film formation process, a vertical alignment liquid crystal cured film is formed on a vertical alignment film.

<Laminated body>
The laminated body of this invention is equipped with the said vertical alignment liquid crystal cured film. The laminate is in the in-plane direction of the base material, the vertical alignment film, the alignment film for horizontal alignment (hereinafter sometimes referred to as a horizontal alignment film), the adhesive layer, and / or the vertical alignment liquid crystal cured film described later. On the other hand, a film oriented in the horizontal direction (hereinafter sometimes referred to as a horizontally oriented film) may be further provided. As the configuration of the laminate, for example, a laminate comprising the vertical alignment liquid crystal cured film, a horizontal alignment film and a horizontal alignment film, a laminate comprising the vertical alignment liquid crystal cured film and a substrate, and the vertical alignment liquid crystal curing. A laminate including a film, a horizontal alignment film, a horizontal alignment film, and a substrate can be mentioned. However, in the present invention, since the vertically aligned liquid crystal cured film can be formed without the vertical alignment film, the laminate may not include the vertical alignment film. For example, when the laminate includes a substrate and a vertically aligned liquid crystal cured film, the vertically aligned liquid crystal cured film can be adjacent to the substrate. Moreover, the vertical alignment liquid crystal cured film adjacent to the base material produced by the above-mentioned method can transfer only the vertical alignment liquid crystal cured film through the adhesive layer, and remove the base material to produce a laminate.

〔Base material〕
As a base material, a glass base material and a film base material are mentioned, A film base material is preferable from a viewpoint of workability, and a long roll-shaped film is more preferable at the point which can be manufactured continuously. Examples of the resin constituting the film substrate include polyolefins such as polyethylene, polypropylene, and norbornene-based polymers; cyclic olefin-based resins; polyvinyl alcohol; polyethylene terephthalate; polymethacrylic acid esters; And cellulose esters such as diacetyl cellulose and cellulose acetate propionate; polyethylene naphthalate; polycarbonate; polysulfone; polyethersulfone; polyetherketone; and plastics such as polyphenylene sulfide and polyphenylene oxide. The bonding surface of the base material with the adhesive layer may be subjected to a release treatment such as a silicone treatment. As a commercially available cellulose ester base material, for example, a cellulose ester base material manufactured by Fuji Photo Film Co., Ltd. such as Fujitac Film; manufactured by Konica Minolta Opto Co., Ltd. The cellulose ester base material of this is mentioned. Such a resin can be formed into a substrate by known methods such as a solvent casting method and a melt extrusion method.

Examples of commercially available cyclic olefin resins include cyclic olefin resins manufactured by Ticona (Germany) such as “Topas (registered trademark); cyclic olefins manufactured by JSR Corporation such as“ Arton (registered trademark) ”. Type olefin resin; “ZEONOR (registered trademark)” and “ZEONEX (registered trademark)” cyclic olefin resin manufactured by Nippon Zeon Co., Ltd .; “Apel” (registered trademark) Mitsui Examples include cyclic olefin-based resins manufactured by Chemical Co., Ltd. Commercially available cyclic olefin resin base materials can also be used. Examples of commercially available cyclic olefin resin substrates include cyclic olefin resin substrates manufactured by Sekisui Chemical Co., Ltd., such as “ESCINA (registered trademark)” and “SCA40 (registered trademark)”; “ZEONOR FILM (registered trademark)”. And the cyclic olefin resin substrate made by JSR Corporation such as “Arton Film (registered trademark)”.

It is preferable that the substrate has a thickness that facilitates laminating each layer and is easy to peel off. The thickness of such a substrate is usually 5 to 300 μm, preferably 10 to 150 μm.

[Vertical alignment film]
The alignment film is a film having an alignment regulating force that aligns the liquid crystal compound of the liquid crystal cured film in a predetermined direction. Regarding the method of forming the alignment film, various alignments such as vertical alignment, horizontal alignment, hybrid alignment, and tilt alignment can be controlled depending on the type of alignment film material, rubbing conditions, and light irradiation conditions. Such processing for expressing the orientation regulating force is called orientation processing. Among these, the vertical alignment film is an alignment film having an alignment regulating force for aligning the liquid crystal compound in the vertical direction. By using the vertical alignment film, a vertically aligned liquid crystal cured film can be formed.

The vertical alignment film preferably has a solvent resistance that does not dissolve when the composition for forming a vertical alignment liquid crystal cured film is applied, and has heat resistance in heat treatment for removing the solvent and aligning the liquid crystal compound.

The vertical alignment film is preferably made of a material that lowers the surface tension of the surface of the substrate or the like. Examples of such materials include orientation polymers such as polyimide, polyamide, polyamic acid that is a hydrolyzate thereof, and fluoropolymers of perfluoroalkyl, silane compounds, and polysiloxane compounds obtained by a condensation reaction thereof. Can be mentioned. For the vertical alignment film, a composition containing such a material and a solvent, for example, the solvent exemplified in the section of the vertical alignment liquid crystal cured film, is applied on a substrate, and after the solvent is removed, the coating film is heated. Can be obtained.

In the case of using a silane compound for the vertical alignment film, the vertical alignment film is composed of Si element and C element as constituent elements from the viewpoint of easily reducing the surface tension and improving the adhesion with the layer adjacent to the vertical alignment film. The film | membrane containing the compound containing is preferable, and a silane compound can be used conveniently. As the silane compound, the nonionic silane compound described above or a silane-containing ionic compound exemplified in the section of the ionic compound can be used. By using these silane compounds, the vertical alignment is regulated. You can increase your power. These silane compounds may be used individually by 1 type, may be used in combination of 2 or more type, and may be used in mixture with other materials. When the silane compound is a nonionic silane compound, a silane compound having an alkyl group at the molecular terminal is preferable from the viewpoint of easily increasing the vertical alignment regulating force, and a silane compound having an alkyl group having 3 to 30 carbon atoms is more preferable. .

The thickness of the vertical alignment film is preferably 5 μm or less, more preferably 3 μm or less, still more preferably 2 μm or less, preferably 1 nm or more, more preferably 5 nm, from the viewpoint of expressing the alignment regulating force. Or more, more preferably 10 nm or more, and particularly preferably 30 nm or more. The film thickness of the vertical alignment film can be measured using an ellipsometer or a contact-type film thickness meter.

[Alignment film for horizontal alignment]
The horizontal alignment film has an alignment regulating force that aligns the liquid crystal compound in the horizontal direction. The horizontal alignment film can form a horizontal alignment state of the horizontal alignment liquid crystal cured film when the horizontal alignment liquid crystal cured film forming composition is formed on the horizontal alignment film. The alignment regulating force can be arbitrarily adjusted depending on, for example, the type of the alignment film, the surface state, and the rubbing conditions. It is possible. Such processing for expressing the orientation regulating force is called orientation processing.

The horizontal alignment film preferably has a solvent resistance that does not dissolve when the liquid crystal composition is applied or the like, and has heat resistance in heat treatment for removing the solvent or aligning the liquid crystal compound.

Examples of the horizontal alignment film include a rubbing alignment film, a photo alignment film, and a groove alignment film having a concavo-convex pattern and a plurality of grooves on the surface. For example, when applying to a long roll-shaped film, a photo-alignment film is preferable in that the alignment direction can be easily controlled.

A rubbing alignment film is usually formed by applying a composition containing an orientation polymer and a solvent (hereinafter sometimes referred to as a rubbing alignment film forming composition) to a substrate and removing the solvent to form a coating film. Then, the alignment regulating force can be imparted by rubbing the coating film.

Examples of the orientation polymer include polyamides and gelatins having amide bonds, polyimides having imide bonds, and polyamic acids, polyvinyl alcohols, alkyl-modified polyvinyl alcohols, polyacrylamides, polyoxazoles, polyethyleneimines, polystyrenes having imide bonds. , Polyvinyl pyrrolidone, polyacrylic acid, and polyacrylic acid esters. These orientation polymers may be used alone or in combination of two or more.

The concentration of the alignment polymer in the composition for forming a rubbing alignment film may be in a range where the alignment polymer is completely dissolved in the solvent. The content of the alignment polymer is preferably 0.1 to 20 parts by mass, and more preferably 0.1 to 10 parts by mass with respect to 100 parts by mass of the rubbing alignment film forming composition.

Examples of commercially available compositions for forming a rubbing alignment film include, for example, a composition for forming a rubbing alignment film manufactured by Nissan Chemical Industries, Ltd. such as Sanever (registered trademark), and a JSR (such as Optomer (registered trademark)). The composition for forming a rubbing alignment film manufactured by Co., Ltd. may be mentioned.

Examples of the rubbing treatment include a method in which a rubbing cloth is wound and the coating film is brought into contact with a rotating rubbing roll. If masking is performed when the rubbing treatment is performed, a plurality of regions (patterns) having different orientation directions can be formed in the alignment film.

For the photo-alignment film, a composition containing a polymer or monomer having a photoreactive group and a solvent (hereinafter sometimes referred to as a photo-alignment film-forming composition) is applied to a substrate, and the solvent is removed. It is obtained by irradiation with polarized light (preferably polarized UV) later. The photo-alignment film can arbitrarily control the direction of the alignment regulating force by selecting the polarization direction of the polarized light to be irradiated.

The photoreactive group refers to a group that generates alignment ability when irradiated with light. Specific examples include groups that are involved in photoreactions that are the origin of alignment ability, such as alignment-induced reactions, isomerization reactions, photodimerization reactions, photocrosslinking reactions, or photodecomposition reactions of molecules generated by light irradiation. As the photoreactive group, an unsaturated bond, particularly a group having a double bond is preferable, and a carbon-carbon double bond (C═C bond), a carbon-nitrogen double bond (C═N bond), and nitrogen-nitrogen. A group having at least one double bond selected from the group consisting of a double bond (N═N bond) and a carbon-oxygen double bond (C═O bond) is particularly preferred.

Examples of the photoreactive group having a C═C bond include a vinyl group, a polyene group, a stilbene group, a stilbazole group, a stilbazolium group, a chalcone group, and a cinnamoyl group. Examples of the photoreactive group having a C═N bond include groups having a structure such as an aromatic Schiff base and an aromatic hydrazone. Examples of the photoreactive group having an N = N bond include an azobenzene group, an azonaphthalene group, an aromatic heterocyclic azo group, a bisazo group, a formazan group, and a group having an azoxybenzene structure. Examples of the photoreactive group having a C═O bond include a benzophenone group, a coumarin group, an anthraquinone group, and a maleimide group. These groups may have a substituent such as an alkyl group, an alkoxy group, an aryl group, an allyloxy group, a cyano group, an alkoxycarbonyl group, a hydroxyl group, a sulfonic acid group, and a halogenated alkyl group.

A group involved in the photodimerization reaction or the photocrosslinking reaction is preferable from the viewpoint of excellent orientation. Among them, a photoreactive group involved in the photodimerization reaction is preferable, and a cinnamoyl group is preferable in that a photoalignment film having a relatively small amount of polarized light irradiation necessary for alignment and having excellent thermal stability and stability over time can be easily obtained. And chalcone groups are preferred. As the polymer having a photoreactive group, a polymer having a cinnamoyl group in which the terminal portion of the polymer side chain has a cinnamic acid structure or a cinnamic acid ester structure is particularly preferable.

Content of the polymer or monomer which has a photoreactive group can be adjusted with the kind of polymer or monomer, or the thickness of the target photo-alignment film, and it is 0.2 with respect to 100 mass parts of compositions for photo-alignment film formation. The amount is preferably at least part by mass, more preferably 0.3 to 10 parts by mass.

In order to irradiate polarized light, for example, the composition for forming a photo-alignment film applied on a substrate may be directly irradiated with polarized light after removing the solvent. The polarized light is preferably substantially parallel light. The wavelength of the polarized light to be irradiated should be in a wavelength range where the photoreactive group of the polymer or monomer having the photoreactive group can absorb light energy. Specifically, UV (ultraviolet light) having a wavelength of 250 to 400 nm is particularly preferable. Examples of the light source for irradiating the polarized light include a xenon lamp, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, a metal halide lamp, and an ultraviolet laser such as KrF and ArF. Among these light sources, a high-pressure mercury lamp, an ultrahigh-pressure mercury lamp, and a metal halide lamp are preferable because of high emission intensity of ultraviolet rays having a wavelength of 313 nm. By irradiating light from the light source through an appropriate polarizing element, polarized UV light can be irradiated. Examples of the polarizing element include a polarizing prism such as a polarizing filter, Glan Thompson, and Grand Taylor, and a wire grid. Among these polarizing elements, a wire grid is preferable from the viewpoint of increasing the area and resistance to heat.

If masking is performed when rubbing or polarized light irradiation is performed, a plurality of regions (patterns) having different liquid crystal alignment directions can be formed.

The groove alignment film is a film having a concavo-convex pattern or a plurality of grooves (grooves) on the film surface. When the composition is applied to a film having a plurality of linear grooves arranged at equal intervals, the liquid crystal compound is aligned in the direction along the groove.

As a method for obtaining a groove alignment film, a method of forming a concavo-convex pattern by performing development and rinsing after exposure through an exposure mask having a pattern-shaped slit on the photosensitive polyimide film surface, a plate having grooves on the surface A layer of a pre-curing UV curable resin is formed on the substrate, and a method of curing the resin layer after transferring the formed resin layer to the base material, and a pre-curing UV curable resin film formed on the base material, Examples include a method in which a roll-shaped master having a plurality of grooves is pressed to form irregularities and then cured.

The film thickness of the horizontal alignment film is preferably 1 μm or less, more preferably 0.5 μm or less, and even more preferably 0.3 μm or less, from the viewpoint of realizing a thin film and exhibiting alignment regulating power. The thickness of the horizontal alignment film is preferably 1 nm or more, more preferably 5 nm or more, still more preferably 10 nm or more, and particularly preferably 30 nm or more. The film thickness of the horizontal alignment film can be measured using an ellipsometer or a contact-type film thickness meter.

[Film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film]
The film that forms the laminate of the present invention and that is oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film is a retardation film. Examples of the horizontal alignment film include a stretched film and a horizontal alignment liquid crystal cured film (hereinafter also referred to as a horizontal alignment liquid crystal cured film A). The optical properties of the horizontal alignment film can be adjusted by the alignment state of the polymerizable liquid crystal compound or the stretching method. From the viewpoint of thinning the horizontal alignment film, the horizontal alignment liquid crystal cured film A is preferable.

(Horizontal alignment liquid crystal cured film A)
In this specification, the horizontal alignment liquid crystal cured film A is a liquid crystal cured film cured in a state where the polymerizable liquid crystal compound is aligned in the horizontal direction with respect to the in-plane direction of the vertical alignment liquid crystal cured film. In the horizontally aligned liquid crystal cured film A, the optical axis of the polymerizable liquid crystal compound is aligned in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film. Examples of the polymerizable liquid crystal compound include liquid crystal compound (I) -1 having at least one polymerizable group. In this specification, the horizontally aligned liquid crystal cured film included in the laminate of the present invention is referred to as a horizontally aligned liquid crystal cured film A, and the horizontally aligned liquid crystal cured film included in the polarizing film of the polarizing plate described later is horizontally aligned liquid crystal cured. These are called membranes B and are distinguished from each other.

(Method for producing horizontally aligned liquid crystal cured film A)
The horizontally aligned liquid crystal cured film A is a cured product of a composition (hereinafter sometimes referred to as a composition for forming a horizontally aligned liquid crystal cured film A). As an example of the manufacturing method of the horizontal alignment liquid crystal cured film A, the horizontal alignment liquid crystal cured film A formation composition is apply | coated on the horizontal alignment film produced previously, the application process which forms a coating film, and a coating film are dried. A dry film forming step of forming a dry film, and a cured film forming step of irradiating the dry film with active energy rays to form a horizontally aligned liquid crystal cured film.

(Stretched film)
Examples of the stretched film include a stretched film made of a polycarbonate-based resin. Examples of commercially available stretched films include stretched films manufactured by Teijin Limited such as “Pure Ace (registered trademark) WR”. The stretched film is usually obtained by stretching a base film. As a method of stretching the base film, for example, a wound body in which the base film is wound on a roll is prepared, and the base film is continuously unwound from the wound body, and the unwound base The material film is conveyed to a heating furnace. The set temperature of the heating furnace is preferably in the range of near the glass transition temperature of the base film to the glass transition temperature + 50 ° C. In the heating furnace, the base film is stretched in the transport direction or in a direction orthogonal to the transport direction. When extending | stretching, the conveyance direction and tension | tensile_strength are adjusted, an arbitrary angle is inclined, and the uniaxial stretching, biaxial stretching, or diagonally extending | stretching heat stretching process is performed. The delay axis direction of the stretched film varies depending on the stretching method, and the delay axis or the optical axis is determined according to the stretching method. The stretched film and the laminate of the present invention can be bonded via an adhesive layer.

In the laminate of the present invention, the horizontal alignment film constituting the laminate is represented by the following relational expression (3) from the viewpoint of suppressing a decrease in ellipticity on the short wavelength side in the elliptically polarizing plate provided with the laminate.
ReA (450) / ReA (550) ≦ 1 (3)
[In the relational expression (3), ReA (450) represents the in-plane retardation value at a wavelength of 450 nm of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and ReA (550) In-plane retardation value at a wavelength of 550 nm of a film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film]
It is preferable to satisfy. From the viewpoint of further suppressing the decrease in ellipticity, ReA (450) / ReA (550) is more preferably 0.95 or less, and further preferably 0.90 or less.
Similarly, from the viewpoint of improving the ellipticity of the elliptically polarizing plate provided with the laminate, the following (3) -2:
120 nm ≦ ReA (550) ≦ 170 nm (3) -2
It is preferable to satisfy. From the viewpoint of improving the ellipticity of the elliptically polarizing plate provided with the laminate, preferably 130 nm ≦ ReA (550) ≦ 160 nm.

Among the laminates described in the present invention, the laminate including the vertically aligned liquid crystal cured film and the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film is obtained from the phase difference value and the oblique direction in the front direction. From the viewpoint of reducing the difference in phase difference value of the display, that is, from the viewpoint of suppressing deterioration of the oblique reflection hue of the display including the elliptically polarizing plate including the laminate, the following relational expression (4):
| R0 (550) -R40 (550) | ≦ 10 nm (4)
[In the relational expression (4), R0 (550) represents an in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (550) represents a horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film. Represents the retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of the oriented film]
It is preferable to satisfy. From the viewpoint of further suppressing the deterioration of the oblique reflection hue, the thickness is more preferably 8 nm or less, and further preferably 4 nm or less.

Among the laminates according to the present invention, a laminate including a vertically aligned liquid crystal cured film and a film oriented in a horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film includes an elliptically polarizing plate including the laminate. From the viewpoint of suppressing deterioration of the oblique reflection hue of the display, the following relational expression (5):
| R0 (450) -R40 (450) | ≦ 10 nm (5)
[In the relational expression (5), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, and R40 (450) is aligned in the horizontal direction with respect to the in-plane direction of the vertical alignment liquid crystal cured film. Shows the retardation value at a wavelength of 450 nm when the film is rotated 40 ° around the fast axis direction]
It is preferable to satisfy. From the viewpoint of further suppressing the deterioration of the oblique reflection hue, the thickness is more preferably 8 nm or less, and further preferably 4 nm or less.

Among the laminates according to the present invention, a laminate including a vertically aligned liquid crystal cured film and a film oriented in a horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film includes an elliptically polarizing plate including the laminate. From the viewpoint of suppressing deterioration of the oblique reflection hue of the display, the following relational expression (6):
| {R0 (450) -R40 (450)}-{R0 (550) -R40 (550)} | ≦ 3 nm (6)
[In relational expression (6), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, R0 (550) represents the in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (450) Represents a retardation value at a wavelength of 450 nm when rotated by 40 ° around the fast axis direction of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and R40 (550) is , Showing a retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of a film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film]
It is preferable to satisfy. From the viewpoint of further suppressing the deterioration of the oblique reflection hue, the thickness is more preferably 2 nm or less, and further preferably 1 nm or less.

[Manufacturing method of laminate]
The manufacturing method of the laminated body of this invention includes a vertical alignment liquid crystal cured film formation process. The vertical alignment liquid crystal cured film forming step may be the above-described method for manufacturing a vertical alignment liquid crystal cured film. By the method for producing a vertically aligned liquid crystal cured film described above, a laminate composed of a substrate and a vertically aligned liquid crystal cured film, and a laminate composed of the substrate, the alignment film, and the vertically aligned liquid crystal cured film can be produced. it can.
When a laminated body is provided with the film orientated in the horizontal orientation with respect to the in-plane direction of a vertical alignment liquid crystal cured film, the manufacturing method of a laminated body further includes a stretched film bonding process or a horizontal alignment liquid crystal cured film A formation process. In the stretched film bonding step, the stretched film is bonded to, for example, a vertically aligned liquid crystal cured film using an adhesive. The manufacturing method of a laminated body provided with the horizontal alignment liquid crystal cured film A may be manufactured, for example, by bonding a vertical alignment liquid crystal cured film and a horizontal alignment liquid crystal cured film via an adhesive layer, The horizontally aligned liquid crystal cured film A may be formed on the vertically aligned liquid crystal cured film. Further, a vertically aligned liquid crystal cured film may be formed on the stretched film or on the horizontally aligned liquid crystal cured film A.

[Adhesive]
Examples of the adhesive include pressure-sensitive adhesives, dry-solidifying adhesives, and chemically reactive adhesives. Examples of the chemically reactive adhesive include an active energy ray curable adhesive.

The pressure-sensitive adhesive usually contains a polymer and may contain a solvent. Examples of the polymer include acrylic polymers, silicone polymers, polyesters, polyurethanes, and polyethers. Among these pressure-sensitive pressure-sensitive adhesives, pressure-sensitive pressure-sensitive adhesives containing acrylic polymers have excellent optical transparency, moderate wettability and cohesive strength, excellent adhesion, and weather resistance and heat resistance. It is preferable because of its high properties and the like, and is unlikely to float or peel off under heating or humidification conditions.

Examples of the acrylic polymer include (meth) acrylates in which the alkyl group in the ester moiety is an alkyl group having 1 to 20 carbon atoms such as a methyl group, an ethyl group, or a butyl group, and (meth) acrylic acid or hydroxyethyl ( A copolymer with a (meth) acrylic monomer having a functional group such as (meth) acrylate is preferred.

The pressure-sensitive adhesive containing such a copolymer has excellent adhesiveness, and even when removed after being bonded to the transfer object, it is relatively easy to cause no adhesive residue on the transfer object. This is preferable because it can be removed. The glass transition temperature of the acrylic polymer is preferably 25 ° C. or less, and more preferably 0 ° C. or less. The mass average molecular weight of such an acrylic polymer is preferably 100,000 or more.

Examples of the solvent include the solvents mentioned as the above solvent. The pressure-sensitive adhesive may contain a light diffusing agent. The light diffusing agent is an additive that imparts light diffusibility to the pressure-sensitive adhesive and may be fine particles having a refractive index different from that of the polymer contained in the pressure-sensitive adhesive. Examples of the light diffusing agent include fine particles made of an inorganic compound and fine particles made of an organic compound (polymer). Many of the polymers that pressure sensitive adhesives, including acrylic polymers, contain as an active ingredient have a refractive index of about 1.4 to 1.6, so that the light diffusion is 1.2 to 1.8. It is preferable to select appropriately from the agents. The refractive index difference between the polymer and the light diffusing agent contained in the pressure-sensitive adhesive as an active ingredient is usually 0.01 or more, and from the viewpoint of the brightness and display properties of the display device, 0.01 to 0.2. preferable. The fine particles used as the light diffusing agent are preferably spherical fine particles, or fine particles close to monodisperse, and more preferably fine particles having an average particle diameter of 2 to 6 μm. The refractive index is measured by a general minimum deviation method or Abbe refractometer.

Examples of the fine particles made of an inorganic compound include aluminum oxide (refractive index 1.76) and silicon oxide (refractive index 1.45). Examples of fine particles made of an organic compound (polymer) include melamine beads (refractive index 1.57), polymethyl methacrylate beads (refractive index 1.49), methyl methacrylate / styrene copolymer resin beads (refractive index 1). .50 to 1.59), polycarbonate beads (refractive index 1.55), polyethylene beads (refractive index 1.53), polystyrene beads (refractive index 1.6), polyvinyl chloride beads (refractive index 1.46), And silicone resin beads (refractive index 1.46). The content of the light diffusing agent is usually 3 to 30 parts by mass with respect to 100 parts by mass of the polymer.

The thickness of the pressure-sensitive pressure-sensitive adhesive is determined according to its adhesion and the like and is not particularly limited, but is usually 1 μm to 40 μm. From the viewpoint of processability and durability, the thickness is preferably 3 μm to 25 μm, and more preferably 5 μm to 20 μm. By adjusting the thickness of the pressure-sensitive adhesive layer to 5 μm to 20 μm, the brightness of the display device when viewed from the front or obliquely is maintained, and blurring or blurring of the display image occurs. Can be difficult.

The dry-solidifying adhesive may contain a solvent. As the dry solidified adhesive, for example, a polymer of a monomer having a protonic functional group such as a hydroxyl group, a carboxyl group, or an amino group and an ethylenically unsaturated group, or a urethane polymer as a main component, Furthermore, the composition containing a crosslinking agent or a curable compound such as a polyvalent aldehyde, an epoxy compound, an epoxy resin, a melamine compound, a zirconia compound, and a zinc compound is included. Examples of the polymer of a monomer having a protonic functional group such as a hydroxyl group, a carboxyl group or an amino group and an ethylenically unsaturated group include, for example, an ethylene-maleic acid copolymer, an itaconic acid copolymer, and an acrylic acid copolymer. , Acrylamide copolymer, saponified polyvinyl acetate, and polyvinyl alcohol resin.

Examples of the polyvinyl alcohol resin include polyvinyl alcohol, partially saponified polyvinyl alcohol, fully saponified polyvinyl alcohol, carboxyl group-modified polyvinyl alcohol, acetoacetyl group-modified polyvinyl alcohol, methylol group-modified polyvinyl alcohol, and amino group-modified polyvinyl alcohol. Can be mentioned. The content of the polyvinyl alcohol-based resin in the water-based adhesive is usually 1 to 10 parts by weight, preferably 1 to 5 parts by weight with respect to 100 parts by weight of water.

Examples of the urethane resin include a polyester ionomer type urethane resin. The polyester ionomer type urethane resin here is a urethane resin having a polyester skeleton, and a resin in which a small amount of an ionic component (hydrophilic component) is introduced. Since such an ionomer type urethane resin is emulsified in water without using an emulsifier and becomes an emulsion, it can be an aqueous adhesive. When a polyester ionomer type urethane resin is used, it is effective to blend a water-soluble epoxy compound as a crosslinking agent.

Examples of the epoxy resin include a polyamide epoxy resin obtained by reacting a polyalkylene polyamine such as diethylenetriamine or triethylenetetramine with a dicarboxylic acid such as adipic acid and epichlorohydrin. Examples of such commercially available polyamide epoxy resins include “Smiles Resin (registered trademark) 650” and “Smiles Resin 675” manufactured by Sumika Chemtex Co., Ltd., and “WS-525” manufactured by Japan PMC Co., Ltd. It is done. When the epoxy resin is blended, the content thereof is usually 1 to 100 parts by mass, preferably 1 to 50 parts by mass with respect to 100 parts by mass of the polyvinyl alcohol resin.

The thickness of the adhesive layer formed from the dry-solidifying adhesive is usually 0.001 to 5 μm, preferably 0.01 to 2 μm, from the viewpoint of suppressing the appearance failure. Preferably, it is 0.01 to 0.5 μm.

The active energy ray curable adhesive may contain a solvent. An active energy ray-curable adhesive is an adhesive that cures upon irradiation with an active energy ray. Examples of the active energy ray curable adhesive include a cationic polymerizable adhesive containing an epoxy compound and a cationic polymerization initiator, a radical polymerizable adhesive containing an acrylic curing component and a radical polymerization initiator, An adhesive containing both a cationic polymerizable curing component such as an epoxy compound and a radical polymerizable curing component such as an acrylic compound, and further containing a cationic polymerization initiator and a radical polymerization initiator, and these Examples thereof include an adhesive that is cured by irradiation with an electron beam without containing a polymerization initiator.

Among these active energy ray-curable adhesives, it contains radical polymerizable active energy ray-curable adhesives containing an acrylic curing component and a photoradical polymerization initiator, and epoxy compounds and photocationic polymerization initiators. Cationic polymerizable active energy ray curable adhesives are preferred. Examples of the acrylic curing component include (meth) acrylates such as methyl (meth) acrylate and hydroxyethyl (meth) acrylate, and (meth) acrylic acid. The active energy ray-curable adhesive containing an epoxy compound may further contain a compound other than the epoxy compound. Examples of compounds other than the epoxy compound include oxetane compounds and acrylic compounds.

Examples of the photo radical polymerization initiator and the photo cation polymerization initiator include the above-mentioned photo radical polymerization initiator and photo cation polymerization initiator. The content of the radical polymerization initiator and the cationic polymerization initiator is usually 0.5 to 20 parts by mass, preferably 1 to 15 parts by mass with respect to 100 parts by mass of the active energy ray-curable adhesive.

The active energy ray-curable adhesive further contains an ion trap agent, an antioxidant, a chain transfer agent, a tackifier, a thermoplastic resin, a filler, a flow regulator, a plasticizer, and an antifoaming agent. May be.

<Elliptically polarizing plate>
The elliptically polarizing plate includes the laminate and a polarizing film. The elliptically polarizing plate may further include an arbitrary layer (more specifically, a protective layer, an adhesive, etc.) as necessary. The laminate and the polarizing film are bonded via, for example, an adhesive.

FIG. 1 is a schematic cross-sectional view showing an example of the layer configuration of an elliptically polarizing plate. An elliptically polarizing plate 20 shown in FIG. 1 includes a laminate 15, an adhesive 7, a polarizing film 11, and a protective layer 13. The laminate 15 is composed of the base material 1, the horizontal alignment film 3, the horizontal alignment liquid crystal cured film A 5, the adhesive 7, and the vertical alignment liquid crystal cured film 9. The angle formed by the slow axis of the horizontally aligned liquid crystal cured film A 5 and the absorption axis of the polarizing film 11 is preferably 45 ± 5 °.

(Polarizing film)
The polarizing film is a film having a polarizing function. Examples of the polarizing film include a film containing a dichroic dye and oriented in the horizontal direction with respect to the film surface of the polarizing film (more specifically, a stretched film on which the dichroic dye is adsorbed (hereinafter referred to as polarizing film A). A horizontal alignment liquid crystal cured film containing a dichroic dye (hereinafter, the horizontal alignment liquid crystal cured film constituting the polarizing film is composed of a horizontal alignment liquid crystal cured film B and a horizontal alignment liquid crystal cured film B). The polarizing film to be used is sometimes referred to as polarizing film B). From the viewpoint of thinning the elliptically polarizing plate, a horizontally aligned liquid crystal cured film B containing a dichroic dye is preferable. The dichroic dye means a dye which exhibits absorption anisotropy and has a property that the absorbance in the major axis direction of the molecule of the dichroic dye is different from the absorbance in the minor axis direction.

(Horizontal alignment liquid crystal cured film B)
The horizontally aligned liquid crystal cured film B includes a dichroic dye and a polymerizable liquid crystal compound (hereinafter, the polymerizable liquid crystal compound forming the horizontally aligned liquid crystal cured film B may be referred to as a polymerizable liquid crystal compound (B)). Is a cured product of a composition (hereinafter, sometimes referred to as a composition for forming a polarizing film B). The horizontal alignment liquid crystal cured film B is a liquid crystal cured film that contains a dichroic dye and is cured in a state where the polymerizable liquid crystal compound (B) is aligned in the horizontal direction with respect to the in-plane direction.

The horizontally aligned liquid crystal cured film B is preferably a cured film in which the polymerizable liquid crystal compound (B) is cured in a smectic phase aligned in the horizontal direction with respect to the in-plane direction of the film. That is, when the polymerizable liquid crystal compound (B) is a thermotropic liquid crystal, it may be a thermotropic liquid crystal compound showing a nematic liquid crystal phase or a thermotropic liquid crystal compound showing a smectic liquid crystal phase. . When a polarizing function is exhibited as a cured film by a polymerization reaction, the liquid crystal state exhibited by the polymerizable liquid crystal compound is preferably a smectic phase, and a higher order smectic phase is more preferable from the viewpoint of high performance. Among them, higher-order smectic liquid crystal compounds that form a smectic B phase, a smectic D phase, a smectic E phase, a smectic F phase, a smectic G phase, a smectic H phase, a smectic I phase, a smectic J phase, a smectic K phase, or a smectic L phase. More preferred are higher-order smectic liquid crystal compounds that form a smectic B phase, a smectic F phase, or a smectic I phase. When the liquid crystal phase formed by the polymerizable liquid crystal compound (B) is a high-order smectic phase, a polarizing film having higher polarization performance can be produced. In addition, such a polarizing film having high polarization performance can obtain a Bragg peak derived from a higher-order structure such as a hexatic phase or a crystal phase in X-ray diffraction measurement. The Bragg peak is a peak derived from a periodic structure of molecular orientation, and a film having a periodic interval of 3 to 6 mm can be obtained. The horizontally aligned liquid crystal cured film B preferably contains a polymer of a polymerizable liquid crystal compound (B) polymerized in a smectic phase from the viewpoint of obtaining higher polarization characteristics. In addition, the below-mentioned polymerizable group which the polymerizable liquid crystal compound (B) has may be in an unpolymerized state or in a polymerized state in the horizontally aligned liquid crystal cured film B. That is, the horizontal alignment liquid crystal cured film B is in any state of a polymerizable liquid crystal compound (B) (monomer), an oligomer of the polymerizable liquid crystal compound (B), a polymer of the polymerizable liquid crystal compound (B), and a combination thereof. May be included. The polymerizable group of the polymerizable liquid crystal compound (B) is preferably in an unpolymerized state in the horizontally aligned liquid crystal cured film B.

Specific examples of the polymerizable liquid crystal compound (B) include a compound represented by the following formula (B1) (hereinafter also referred to as a polymerizable liquid crystal compound (B1)). The said polymerizable liquid crystal may be used independently and may be used in combination of 2 or more type.

U ¹ −V ¹ −W ¹ −X ¹ −Y ¹ −X ² −Y ² −X ³ −W ² −V ² −U ² (B1)
[In the formula (B1),
X ¹ , X ² , and X ³ each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, wherein the divalent aromatic group or the divalent fat The hydrogen atom contained in the cyclic hydrocarbon group is a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atom constituting the divalent aromatic group or the divalent alicyclic hydrocarbon group may be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom. However, at least one of X ¹ , X ² , and X ³ is an optionally substituted 1,4-phenylene group, or an optionally substituted cyclohexane-1,4- Represents a diyl group.
Y ¹ , Y ² , W ¹ and W ² each independently represent a single bond or a divalent linking group.
V ¹ and V ² each independently represents an optionally substituted alkanediyl group having 1 to 20 carbon atoms, and —CH ₂ — constituting the alkanediyl group represents —O—, — It may be substituted with CO-, -S- or NH-.
U ¹ and U ² each independently represent a polymerizable group or a hydrogen atom, and at least one of U ¹ and U ² represents a polymerizable group.

In the polymerizable liquid crystal compound (B1), at least one of X ¹ , X ² and X ³ may have a 1,4-phenylene group which may have a substituent, or a substituent. Represents a good cyclohexane-1,4-diyl group. In particular, X ¹ and X ³ preferably represent a cyclohexane-1,4-diyl group which may have a substituent, and the cyclohexane-1,4-diyl group is trans-cyclohexane- More preferably, it represents a 1,4-diyl group. Examples of the substituent which the 1,4-phenylene group which may have a substituent or the cyclohexane-1,4-diyl group which may have a substituent optionally have, for example, a methyl group , An alkyl group having 1 to 4 carbon atoms such as an ethyl group and a butyl group, a cyano group, and a halogen atom such as a chlorine atom and a fluorine atom. The 1,4-phenylene group which may have a substituent or the cyclohexane-1,4-diyl group which may have a substituent is preferably a 1,4-phenylene group or a cyclohexane. Xan-1,4-diyl group. Further, when Y ¹ and Y ² have the same structure, it is preferable that at least one of X ¹ , X ² and X ³ is a different structure. When at least one of X ¹ , X ² and X ³ has a different structure, smectic liquid crystallinity tends to be easily exhibited.

Y ¹ and Y ² are each independently a single bond, —CH ₂ CH ₂ —, —CH ₂ O—, —CH ₂ CH ₂ O—, —COO—, —OCO—, —N═N—, — CR ^a ═CR ^b —, —C≡C— or CR ^a ═N— is preferably represented, and R ^a and R ^b each independently represent a hydrogen atom or an alkyl group having 1 to 4 carbon atoms. More preferably, Y ¹ and Y ² each independently represent —CH ₂ CH ₂ —, —COO—, —OCO—, or a single bond. Further, when X ¹ , X ² and X ³ all have the same structure, it is preferable that Y ¹ and Y ² have different bonding methods. When Y ¹ and Y ² are different from each other, smectic liquid crystal properties tend to be easily exhibited.

W ¹ and W ² preferably each independently represent a single bond, —O—, —S—, —COO—, or OCO—, and more preferably each independently represents a single bond or —O—. preferable.

Examples of the alkanediyl group having 1 to 20 carbon atoms represented by V ¹ and V ² include methylene group, ethylene group, propane-1,3-diyl group, butane-1,3-diyl group, butane-1 , 4-diyl group, pentane-1,5-diyl group, hexane-1,6-diyl group, heptane-1,7-diyl group, octane-1,8-diyl group, decane-1,10-diyl group , A tetradecane-1,14-diyl group, and an icosane-1,20-diyl group. V ¹ and V ² preferably represent an alkanediyl group having 2 to 12 carbon atoms, more preferably a linear alkanediyl group having 6 to 12 carbon atoms. When V ¹ and V ² represent a linear alkanediyl group having 6 to 12 carbon atoms, the orientation of the polymerizable liquid crystal compound (B1) is improved, and smectic liquid crystallinity tends to be easily exhibited.
Examples of the substituent optionally contained in the optionally substituted alkanediyl group having 1 to 20 carbon atoms include a cyano group and halogen atoms such as a chlorine atom and a fluorine atom. The diyl group is preferably unsubstituted, and more preferably an unsubstituted and linear alkanediyl group.

U ¹ and U ² both preferably represent a polymerizable group, and more preferably both represent a photopolymerizable group. Since the polymerizable liquid crystal compound (B1) having a photopolymerizable group can be polymerized under a lower temperature condition than the thermally polymerizable group, it is advantageous in that the liquid crystal can form a polymer with a higher degree of order.

The polymerizable groups represented by U ¹ and U ² may be the same or different from each other, but are preferably the same. Examples of the polymerizable group include a vinyl group, vinyloxy group, 1-chlorovinyl group, isopropenyl group, 4-vinylphenyl group, acryloyloxy group, methacryloyloxy group, oxiranyl group, and oxetanyl group. Of these photopolymerizable groups, an acryloyloxy group, a methacryloyloxy group, a vinyloxy group, an oxiranyl group, and an oxetanyl group are preferable, and a methacryloyloxy group and an acryloyloxy group are more preferable.

Examples of such a polymerizable liquid crystal compound (B1) include polymerizable liquid crystal compounds represented by the following formulas (1-1) to (1-23).

Of the exemplified polymerizable liquid crystal compound (B1), the formula (1-2), formula (1-3), formula (1-4), formula (1-6), formula (1-7), formula (1) 1-8), at least one selected from the group consisting of compounds represented by formula (1-13), formula (1-14) and formula (1-15) is preferred. A polymeric liquid crystal compound may be used individually by 1 type, and may be used in combination of 2 or more type.

Polymerizable liquid crystal compound (B1) is, for example, Lub et al., Recl. Trav. Chim. It can be produced by a known method described in Pays-Bas, 115, 321-328 (1996), or Japanese Patent No. 4719156.

The composition for forming the polarizing film B may contain a liquid crystal compound other than the polymerizable liquid crystal compound (B) as long as the effects of the present invention are not impaired, but from the viewpoint of obtaining a polarizing film having a high degree of alignment order. The ratio of the polymerizable liquid crystal compound (B) to the total mass of all liquid crystal compounds contained in the composition for forming the polarizing film B is preferably 51% by mass or more, more preferably 70% by mass or more, and still more preferably. Is 90% by mass or more.

When the composition for forming the polarizing film B contains two or more polymerizable liquid crystal compounds (B), at least one of them may be the polymerizable liquid crystal compound (B1), and all of them are polymerizable liquid crystals. Compound (B1) may be used. By combining a plurality of polymerizable liquid crystal compounds, it may be possible to temporarily maintain liquid crystallinity even at a temperature lower than the liquid crystal-crystal phase transition temperature.

The content of the polymerizable liquid crystal compound (B) in the composition for forming a polarizing film B is preferably 40 to 99.9% by mass, more preferably 60%, based on the solid content of the composition for forming a polarizing film B. It is -99 mass%, More preferably, it is 70-99 mass%. When the content of the polymerizable liquid crystal compound (B) is within the above range, the orientation of the liquid crystal compound tends to be high. In addition, solid content means the total amount of the component remove | excluding the solvent from the composition for polarizing film B formation.

(Dichroic dye)
A dichroic dye refers to a dye having the property that the absorbance in the major axis direction of a molecule is different from the absorbance in the minor axis direction. The dichroic dye preferably has a property of absorbing visible light, and more preferably has a maximum absorption wavelength (λ _MAX ) in a wavelength range of 380 to 680 nm. Examples of the dichroic pigment include iodine and dichroic organic dyes. Examples of the dichroic organic dye include acridine dyes, oxazine dyes, cyanine dyes, naphthalene dyes, azo dyes, and anthraquinone dyes. Of these dichroic organic dyes, azo dyes are preferred. Examples of the azo dye include a monoazo dye, a bisazo dye, a trisazo dye, a tetrakisazo dye, and a stilbene azo dye. Of these azo dyes, bisazo dyes and trisazo dyes are preferable. The dichroic organic dye may be used alone or in combination of two or more. However, in order to obtain absorption in the entire visible light region, three or more kinds of dichroic dyes are used. It is preferable to use in combination, and it is more preferable to use three or more kinds of azo dyes in combination. The polyvinyl alcohol-based resin film is preferably subjected to an immersion treatment in water before the dyeing treatment.

Examples of the azo dye include a compound represented by the formula (I).
T ¹ -A ¹ (-N = NA ² ) _p -N = NA ³ -T ² (I)
[In the formula (I),
A ¹ , A ² , and A ³ each independently have a 1,4-phenylene group, a naphthalene-1,4-diyl group, or a substituent that may have a substituent. Represents a divalent heterocyclic group, and T ¹ and T ² each independently represent an electron-withdrawing group or an electron-emitting group and have a position substantially 180 ° with respect to the azo bond plane. p represents an integer of 0 to 4. When p represents an integer greater than or equal to ² , several A2 may mutually be same or different. As long as the azo dye absorbs in the visible range, the —N═N— bond may be replaced with a —C═C— bond, —COO— bond, —NHCO— bond, or —N═CH— bond. ]

Examples of the substituent that the 1,4-phenylene group, naphthalene-1,4-diyl group, and divalent heterocyclic group represented by A ¹ , A ² , and A ³ optionally have include a methyl group, an ethyl group, and the like. And an alkyl group having 1 to 4 carbon atoms such as a butyl group; an alkoxy group having 1 to 4 carbon atoms such as a methoxy group, an ethoxy group, and a butoxy group; and an alkyl group having 1 to 4 carbon atoms such as a trifluoromethyl group A fluorinated alkyl group; a cyano group; a nitro group; a halogen atom such as a chlorine atom and a fluorine atom; a substituted amino group or an unsubstituted amino group such as an amino group, a diethylamino group and a pyrrolidino group. It means an amino group having one or two alkyl groups of 1 to 6 or an amino group in which two substituted alkyl groups are bonded to each other to form an alkanediyl group having 2 to 8 carbon atoms. Substituted amino group is -NH _2.) It can be mentioned. Examples of the alkyl group having 1 to 6 carbon atoms include a methyl group, an ethyl group, and a hexyl group. Examples of the alkanediyl group having 2 to 8 carbon atoms include ethylene group, propane-1,3-diyl group, butane-1,3-diyl group, butane-1,4-diyl group, pentane-1,5- Examples thereof include a diyl group, a hexane-1,6-diyl group, a heptane-1,7-diyl group, and an octane-1,8-diyl group. For inclusion in a highly ordered liquid crystal structure such as a smectic liquid crystal, A ¹ , A ² and A ³ are either 1,4-phenylene groups which are unsubstituted or substituted with a methyl group or a methoxy group, or It preferably represents a divalent heterocyclic group, and p preferably represents an integer of 0-2. In particular, p is 1 and at least two of the three structures A ¹ , A ² and A ³ are 1,4-phenylene groups in terms of both ease of molecular synthesis and high performance. More preferred.

Examples of the divalent heterocyclic group include groups obtained by removing two hydrogen atoms from a heterocyclic ring such as quinoline, thiazole, benzothiazole, thienothiazole, imidazole, benzimidazole, oxazole, and benzoxazole. . When A ² represents a divalent heterocyclic group, a structure in which the molecular bond angle is substantially 180 ° is preferable. Specifically, a benzothiazole structure or a benzimidazole structure in which two 5-membered rings are condensed And a benzoxazole structure is more preferable.

T ¹ and T ² each independently represents an electron-withdrawing group or electron-emitting group, and preferably represents an electron-withdrawing group or electron-emitting group having a different structure, T ¹ represents an electron-withdrawing group, and T ² More preferably, it represents an electron emitting group, or T ¹ represents an electron emitting group and represents a T ² electron withdrawing group. Specifically, each of T ¹ and T ² independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, a cyano group, a nitro group, or an alkyl group having 1 to 6 carbon atoms. A substituted amino group having two or two, an amino group in which the two substituted alkyl groups are bonded to each other to form an alkanediyl group having 2 to 8 carbon atoms, and a trifluoromethyl group are preferable. In particular, in order to be included in a highly ordered liquid crystal structure such as a smectic liquid crystal, it is necessary to have a structure with a smaller excluded volume of the molecule. Group, a cyano group, a substituted amino group having one or two alkyl groups having 1 to 6 carbon atoms, and two amino groups bonded to each other to form an alkanediyl group having 2 to 8 carbon atoms Groups are preferred.

Examples of such azo dyes include azo dyes represented by the following formulas (2-1) to (2-8).

In formulas (2-1) to (2-8),
B ¹ to B ³⁰ are each independently a hydrogen atom, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, a cyano group, a nitro group, a substituted or unsubstituted amino group (substituted amino group and As defined above, the unsubstituted amino group represents a chlorine atom or a trifluoromethyl group. Further, when combined with smectic liquid crystals, from the viewpoint of obtaining high polarization performance, B ² , B ⁶ , B ⁹ , B ¹⁴ , B ¹⁸ , B ¹⁹ , B ²² , B ²³ , B ²⁴ , B ²⁷ , B ²⁸ And B ²⁹ each independently preferably represents a hydrogen atom or a methyl group, and more preferably represents a hydrogen atom.
n1 to n4 each independently represents an integer of 0 to 2.
When n1 represents 2, the plurality of B ² may be the same as or different from each other,
When n2 represents 2, the plurality of B ⁶ may be the same as or different from each other,
when n3 represents 2, the plurality of B ⁹ may be the same as or different from each other;
If n4 represents 2, a plurality of B ¹⁴ may be the same or may be different from one another.

The anthraquinone dye is preferably a compound represented by the formula (2-9).

[In the formula (2-9),
R ¹ to R ⁸ each independently represents a hydrogen atom, —R ^x , —NH ₂ , —NHR ^x , —NR ^x ₂ , —SR ^x , or a halogen atom.
R ^x represents an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 12 carbon atoms. ]

The oxazine dye is preferably a compound represented by the formula (2-10).

[In the formula (2-10),
R ⁹ to R ¹⁵ each independently represents a hydrogen atom, —R ^x , —NH ₂ , —NHR ^x , —NR ^x ₂ , —SR ^x , or a halogen atom.
R ^x represents an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 12 carbon atoms. ]

The acridine dye is preferably a compound represented by the formula (2-11).

[In the formula (2-11),
R ¹⁶ to R ²³ each independently represents a hydrogen atom, —R ^x , —NH ₂ , —NHR ^x , —NR ^x ₂ , —SR ^x , or a halogen atom.
R ^x represents an alkyl group having 1 to 4 carbon atoms or an aryl group having 6 to 12 carbon atoms. ]

In formulas (2-9), (2-10) and (2-11), examples of the alkyl group having 1 to 4 carbon atoms represented by R ^x include a methyl group, an ethyl group, a propyl group, A butyl group, a pentyl group, and a hexyl group are mentioned. In the formulas (2-9), (2-10) and (2-11), examples of the aryl group having 6 to 12 carbon atoms represented by R ^x include a phenyl group, a toluyl group, a xylyl group, And a naphthyl group.

As the cyanine dye, a compound represented by the formula (2-12) and a compound represented by the formula (2-13) are preferable.

[In the formula (2-12),
D ¹ and D ² each independently represent a group represented by any one of formulas (2-12a) to (2-12d).

n5 represents an integer of 1 to 3. ]

[In the formula (2-13),
D ³ and D ⁴ each independently represent a group represented by any one of formulas (2-13a) to (2-13h).

n6 represents an integer of 1 to 3. ]

The content of the dichroic organic dye (the total amount in the case of including a plurality of types) is usually 0.1 with respect to 100 parts by mass of the polymerizable liquid crystal compound (B) from the viewpoint of obtaining good light absorption characteristics. -30 parts by mass, preferably 1-20 parts by mass, more preferably 3-15 parts by mass. When the content of the dichroic organic dye is 0.1 parts by mass or more with respect to 100 parts by mass of the polymerizable liquid crystal compound (B), light absorption of the dichroic organic dye is sufficient, and sufficient polarization performance Tends to be obtained. When the content of the dichroic organic dye is 30 parts by mass or less with respect to 100 parts by mass of the polymerizable liquid crystal compound (B), the orientation of the polymerizable liquid crystal compound is hardly inhibited.

(Stretched film with dichroic dye adsorbed)
At least one of the stretched films on which the dichroic dye is adsorbed may be provided with a transparent protective film. A film containing a stretched film on which a dichroic dye is adsorbed as a polarizer is usually a step of uniaxially stretching a polyvinyl alcohol resin film, and the dichroism is obtained by dyeing the polyvinyl alcohol resin film with a dichroic dye. At least one surface of a polarizer produced through a step of adsorbing a dye, a step of treating a polyvinyl alcohol resin film adsorbed with a dichroic dye with an aqueous boric acid solution, and a step of washing with water after the treatment with an aqueous boric acid solution It is produced by sandwiching with a transparent protective film through an adhesive.

The polyvinyl alcohol resin is obtained by saponifying a polyvinyl acetate resin. As the polyvinyl acetate-based resin, for example, polyvinyl acetate, which is a homopolymer of vinyl acetate, or a copolymer of vinyl acetate and another monomer copolymerizable therewith is used. Examples of other monomers copolymerizable with vinyl acetate include unsaturated carboxylic acids, olefins, vinyl ethers, unsaturated sulfonic acids, and acrylamides having an ammonium group.

The degree of saponification of the polyvinyl alcohol resin is usually about 85 to 100 mol%, preferably 98 mol% or more. The polyvinyl alcohol resin may be modified, and for example, polyvinyl formal or polyvinyl acetal modified with aldehydes can also be used. The degree of polymerization of the polyvinyl alcohol resin is usually about 1,000 to 10,000, and preferably in the range of 1,500 to 5,000.

A film obtained by forming such a polyvinyl alcohol resin is used as an original film of a polarizing film. The method for forming a polyvinyl alcohol-based resin is not particularly limited, and can be formed by a known method. The film thickness of the polyvinyl alcohol-based raw film can be, for example, about 10 to 150 μm.

Uniaxial stretching of the polyvinyl alcohol-based resin film can be performed before dyeing with the dichroic dye, simultaneously with dyeing, or after dyeing. When uniaxial stretching is performed after dyeing, the uniaxial stretching may be performed before boric acid treatment or during boric acid treatment. Moreover, it is also possible to perform uniaxial stretching in these several steps. In uniaxial stretching, it may be uniaxially stretched between rolls having different peripheral speeds, or may be uniaxially stretched using a hot roll. Further, the uniaxial stretching may be dry stretching in which stretching is performed in the air, or may be wet stretching in which stretching is performed in a state where a solvent is used and a polyvinyl alcohol-based resin film is swollen. The draw ratio is usually about 3 to 8 times.

The dyeing of the polyvinyl alcohol resin film with the dichroic dye is performed, for example, by a method of immersing the polyvinyl alcohol resin film in an aqueous solution containing the dichroic dye.

When iodine is used as the dichroic dye, a method of dyeing a polyvinyl alcohol-based resin film in an aqueous solution containing iodine and potassium iodide is usually employed. The iodine content in this aqueous solution is usually about 0.01 to 1 part by mass per 100 parts by mass of water. The content of potassium iodide is usually about 0.5 to 20 parts by mass per 100 parts by mass of water. The temperature of the aqueous solution used for dyeing is usually about 20 to 40 ° C. The immersion time (dyeing time) in this aqueous solution is usually about 20 to 1,800 seconds.

On the other hand, when a dichroic organic dye is used as the dichroic dye, a method of immersing and dyeing a polyvinyl alcohol-based resin film in an aqueous solution containing a water-soluble dichroic dye is usually employed. The content of the dichroic organic dye in this aqueous solution is usually about 1 × 10 ⁻⁴ to 10 parts by mass, preferably 1 × 10 ⁻³ to 1 part by mass, more preferably 100 parts by mass of water. Is 1 × 10 ⁻³ to 1 × 10 ⁻² parts by mass. This aqueous solution may contain an inorganic salt such as sodium sulfate as a dyeing assistant. The temperature of the aqueous dichroic dye solution used for dyeing is usually about 20 to 80 ° C. The immersion time (dyeing time) in this aqueous solution is usually about 10 to 1,800 seconds.

The boric acid treatment after dyeing with a dichroic dye can usually be performed by a method of immersing the dyed polyvinyl alcohol resin film in a boric acid aqueous solution. The boric acid content in this aqueous boric acid solution is usually about 2 to 15 parts by mass, preferably 5 to 12 parts by mass, with respect to 100 parts by mass of water. When iodine is used as the dichroic dye, this boric acid aqueous solution preferably contains potassium iodide. In this case, the content of potassium iodide is usually 0.1 to 100 parts by mass of water. The amount is about 15 parts by mass, preferably 5 to 12 parts by mass. The immersion time in the boric acid aqueous solution is usually about 60 to 1,200 seconds, preferably 150 to 600 seconds, and more preferably 200 to 400 seconds. The temperature of boric acid treatment is usually 50 ° C. or higher, preferably 50 to 85 ° C., more preferably 60 to 80 ° C.

The polyvinyl alcohol resin film after the boric acid treatment is usually washed with water. The water washing treatment can be performed, for example, by a method of immersing a boric acid-treated polyvinyl alcohol resin film in water. The temperature of water in the water washing treatment is usually about 5 to 40 ° C. The immersion time is usually about 1 to 120 seconds.

After being washed with water, a drying process is performed to obtain a polarizer. The drying process can be performed using, for example, a hot air dryer or a far infrared heater. The temperature for the drying treatment is usually about 30 to 100 ° C., preferably 50 to 80 ° C. The drying treatment time is usually about 60 to 600 seconds, preferably 120 to 600 seconds. By the drying treatment, the moisture content of the polarizer is reduced to a practical level. The moisture content is usually about 5 to 20% by mass, preferably 8 to 15% by mass. When the moisture content is less than 5% by mass, the flexibility of the polarizer is lost, and the polarizer may be damaged or broken after drying. On the other hand, if the moisture content exceeds 20% by mass, the thermal stability of the polarizer may be deteriorated.

Thus, the thickness of the polarizer obtained by subjecting the polyvinyl alcohol resin film to uniaxial stretching, dyeing with a dichroic dye, boric acid treatment, washing with water and drying is preferably 5 to 40 μm.

<Organic EL display device>
The organic EL display device includes the elliptically polarizing plate. As a preferable aspect of the organic EL display device, for example, a device in which an elliptically polarizing plate is bonded to an organic EL panel through an adhesive is exemplified.

Hereinafter, the present invention will be described more specifically with reference to examples. In the examples, “%” and “part” mean mass% and mass part, respectively, unless otherwise specified.

[Preparation of liquid crystal compound]
Liquid crystal compound A was produced according to the method described in JP 2010-31223 A. Liquid crystal compound B was produced according to the method described in JP-A-2009-173893. Below, the molecular structure of the liquid crystal compound A and the liquid crystal compound B is shown, respectively.

(Liquid Crystal Compound A)

(Liquid Crystal Compound B)

[Measuring method]
(Calculation method of ratio of maximum absorption wavelength and maximum absorbance)
A 1 mg / 50 mL tetrahydrofuran solution of liquid crystal compound A was prepared and used as a measurement sample. A measurement sample was put in a measurement cell having an optical path length of 1 cm. The measurement sample was set in an ultraviolet-visible spectrophotometer (“UV-2450” manufactured by Shimadzu Corporation), and the absorption spectrum was measured. The reference was only the solvent of the measurement sample. The wavelength at which the maximum absorption was obtained was read from the obtained absorption spectrum, and this was taken as the maximum absorption wavelength λ _max . Furthermore, the maximum absorption wavelength of the liquid crystal compound A in the region of a wavelength of 260 nm or more and 400 nm or less was read from the obtained absorption spectrum. In the case where a plurality of maximum absorption wavelengths exist in the wavelength range of 260 nm to 400 nm, the wavelength having the highest absorbance among the plurality of maximum absorption wavelengths is defined as λ _max . The obtained maximum absorption wavelength is shown in Table 1.

[Preparation of ionic compound]
The ionic compound (1) was produced according to the method described in Japanese Patent Application No. 2016-514802. In addition, the ionic compound (2) and the ionic compound (3) were produced according to the method described in JP2013-28586A or JP2013-199509A. The structural formulas of the ionic compounds (1) to (3) are shown below.

(Ionic compound (1))

(Ionic compound (2))

(Ionic compound (3))

<Example 1>
[Preparation of vertically aligned liquid crystal cured film forming composition (A-1)]
Liquid crystal compound A and liquid crystal compound B were mixed at a mass ratio of 90:10 to obtain a mixture. With respect to 100 parts by mass of the resulting mixture, 1.5 parts by mass of a leveling agent (“F-556” manufactured by DIC) and 2-dimethylamino-2-benzyl-1- (4- 6 parts by mass of morpholinophenyl) butan-1-one (“Irgacure (registered trademark) 369 (Irg369)” manufactured by BASF Japan Ltd.) was added. Further, 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine (“KBE-9103” manufactured by Shin-Etsu Chemical Co., Ltd.) as a silane compound is adjusted to 0.5%. Compound (1) was further added so as to be 2.0%.

N-methyl-2-pyrrolidone (NMP) was added so that the solid content concentration was 13%. By stirring at 80 ° C. for 1 hour, a vertically aligned liquid crystal cured film forming composition (A-1) (hereinafter sometimes referred to as composition (A-1)) was obtained. The silane compound (“KBE-9103” manufactured by Shin-Etsu Chemical Co., Ltd.) reacts with the solvent in the composition (A-1) and moisture in the environment to cause hydrolysis, and the amino group which is a polar group Confirmed to generate.

[Method for producing vertically aligned liquid crystal cured film (A-1)]
Using a corona treatment device (“AGF-B10” manufactured by Kasuga Denki Co., Ltd.), an amorphous cycloolefin polymer film (COP film) (Zeon Corporation “ZF-14-23”) as a base material The corona treatment was performed once under the conditions of an output of 0.3 kW and a treatment speed of 3 m / min. Using a bar coater, the composition (A-1) was applied to the surface of the substrate subjected to the corona treatment to form a coating film. The coating film was dried at 120 ° C. for 1 minute to form a dry film. Next, using a high-pressure mercury lamp (“Unicure VB-15201BY-A” manufactured by USHIO INC.), The dry coating was irradiated with ultraviolet rays under a nitrogen atmosphere and an integrated light amount of 500 mJ / cm ^{2 at} a wavelength of 365 nm. As a result, a vertically aligned liquid crystal cured film (A-1) (film thickness: 1.0 μm) was formed.

[Optical characteristics of vertically aligned liquid crystal cured film (A-1)]
The obtained vertically aligned liquid crystal cured film (A-1) was bonded to glass via a pressure sensitive adhesive (pressure sensitive pressure sensitive adhesive 15 μm manufactured by Lintec) to prepare a sample for measuring optical properties.

(Measurement of phase difference value)
ZF-14-23, which is a base material, is an optically isotropic film having a retardation value R _F (550) of 1 nm or less at a wavelength of 550 nm, and it has been confirmed that the measured value of the sample for measuring optical properties is not affected. . Subsequently, the phase difference value was measured using a measuring device (“KOBRA-WPR” manufactured by Oji Scientific Co., Ltd.) while changing the incident angle of the light to the optical property measurement sample.

(Measurement of average refractive index)
The average refractive index at wavelengths λ = 450 nm and 550 nm was measured using a refractometer (“Multiwave Abbe Refractometer DR-M4” manufactured by Atago Co., Ltd.). Rth calculated from the obtained film thickness, average refractive index, and measurement results of a measuring instrument (“KOBRA-WPR” manufactured by Oji Scientific Instruments Co., Ltd.) are Rth (450) = − 60 nm and Rth (550) = -70 nm, and Rth (450) / Rth (550) = 0.85.

(Evaluation of orientation of alignment liquid crystal cured film)
Using a polarizing microscope (OLYMPUS "BX-51"), observation was performed under the condition of 200 times magnification, and the number of alignment defects in a visual field of 480 μm × 320 μm was counted. Here, only the number of alignment defects caused by the measurement sample was counted, and the number of defects caused by environmental foreign matters other than the optical characteristic sample was excluded and not counted. From the observation results with a polarizing microscope, the orientation of the vertically aligned liquid crystal cured film (A-1) was evaluated based on the following evaluation criteria. A, B and C were judged to have excellent orientation. As shown in Table 1, the orientation of the vertically aligned liquid crystal cured film (A-1) produced from the composition (A-1) was A.
(Evaluation criteria)
A (very good): The number of alignment defects is 0 or more and 3 or less.
B (very good): The number of alignment defects is 4 or more and 10 or less.
C (good): The number of alignment defects is 11 or more and 50 or less.
D (poor): The number of alignment defects is 51 or more, or no alignment is performed.

<Examples 2 to 9, Example 20, Example 21, and Comparative Example 1>
The base material of Example 1, 0.5% of the silane compound, and 2% of the ionic compound (2) are shown in Table 1. The compositions (A-2) of Examples 2 to 9, Example 20, Example 21, and Comparative Example 1 were prepared in the same manner as the preparation method of the composition (A-1) of Example 1, except that the amount was changed. ~ (A-9), (A-20), (A-21), and (B-1) were respectively prepared. The composition (A-1) was changed to compositions (A-2) to (A-9), (A-20), (A-21), and (B-1), and the film thickness of the coating film was further changed. Examples 2 to 9 and Examples were performed in the same manner as in the method for producing the vertically aligned liquid crystal cured film (A-1) of Example 1, except that the phase difference values shown in Table 1 were changed. 20, vertically aligned liquid crystal cured films (A-2) to (A-9), (A-20), (A-21), and (B-1) of Example 21 and Comparative Example 1 were produced. . Moreover, the sample for an optical characteristic measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. The results are shown in Table 1.

<Example 10>
The substrate was changed from a COP film (“ZF-14-23” manufactured by Nippon Zeon Co., Ltd.) to a polyethylene terephthalate with a protective layer (hereinafter sometimes referred to as “PET with a protective layer”), and when measuring optical properties A vertically aligned liquid crystal cured film (A-10) was prepared in the same manner as the method for preparing the vertically aligned liquid crystal cured film (A-1) of Example 1 except that the sample was prepared by peeling the PET substrate. . Moreover, the sample for an optical characteristic measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. The results are shown in Table 1. Hereinafter, the preparation method of PET with a protective layer is demonstrated.

(Preparation of protective layer forming composition)
50 parts of dipentaerythritol hexaacrylate (“Aronix (registered trademark) M-403” polyfunctional acrylate manufactured by Toagosei Co., Ltd.), 50 parts of acrylate resin (“Evecryl 4858” manufactured by Daicel UCB), and 2-methyl 3 parts of -1 [4- (methylthio) phenyl] -2-morpholinopropan-1-one (“Irgacure (registered trademark) 907” manufactured by Ciba Specialty Chemicals) was dissolved in 250 parts of isopropanol. Prepared. The obtained solution was used as a protective layer forming composition.

[Production of PET with protective layer]
The composition for protective layer formation was apply | coated on PET film (film thickness of 38 micrometers) using the bar coater, and the coating film was formed. The coating film was dried at 50 ° C. for 1 minute to form a dry film. Using a high pressure mercury lamp (“Unicure VB-15201BY-A” manufactured by USHIO INC.), The dried coating was irradiated with ultraviolet rays under a nitrogen atmosphere and an integrated light amount of 400 mJ / cm ^{2 at} a wavelength of 365 nm. As a result, a PET with a protective layer made of an acrylic resin was formed. In addition, it was 1 nm or less when the phase difference value in wavelength 550nm of a protective layer was measured after bonding to glass through an adhesive and peeling a PET film according to the optical property measuring method described in Example 1. The film was confirmed to be an optically isotropic film. Moreover, it was 2 micrometers when the film thickness of the formed protective layer was measured with the ellipsometer.

<Example 11>
Except that the composition of the liquid crystal compound of Example 1 was changed from 90% / 10% of the liquid crystal compound A / liquid crystal compound B to 100% of the liquid crystal compound (A) -2, the composition (A-1) of Example 1 and The composition (A-11) and the vertically aligned liquid crystal cured film (A-11) of Example 11 were prepared in the same manner as the method for preparing the vertical aligned liquid crystal cured film (A-1). The liquid crystal compound (A) -2 was prepared with reference to JP-A-2016-81035. The liquid crystal compound (A) -2 is represented by the following formula (A) -2. Moreover, the sample for a measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. Further, the ratio between the maximum absorption wavelength and the maximum absorbance of the liquid crystal compound (A) -2 was calculated in the same manner as in Example 1. The results are shown in Table 1.

... (A) -2

<Example 12>
Except that the composition of the liquid crystal compound of Example 1 was changed from Liquid Crystal Compound A / Liquid Crystal Compound B = 90% / 10% to 100% of Liquid Crystal Compound (A) -3, the composition (A-1) of Example 1 and The composition (A-12) and the vertically aligned liquid crystal cured film (A-12) of Example 12 were prepared in the same manner as the method for preparing the vertical aligned liquid crystal cured film (A-1). Liquid crystal compound (A) -3 was prepared with reference to International Patent Publication No. 2015/025793. The liquid crystal compound (A) -3 is represented by the following formula (A) -3. Moreover, the sample for an optical characteristic measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. Further, the ratio between the maximum absorption wavelength and the maximum absorbance of the liquid crystal compound (A) -3 was also calculated in the same manner as in Example 1. The results are shown in Table 1.

... (A) -3

<Example 13>
Except that the composition of the liquid crystal compound of Example 1 was changed from Liquid Crystal Compound A / Liquid Crystal Compound B = 90% / 10% to Liquid Crystal Compound (A) -4 100%, the composition (A-1) of Example 1 and The composition (A-13) and the vertically aligned liquid crystal cured film (A-13) of Example 11 were prepared in the same manner as the method for preparing the vertical aligned liquid crystal cured film (A-1). The liquid crystal compound (A) -4 was prepared with reference to JP2011-207765A. The liquid crystal compound (A) -4 is represented by the following formula (A) -4. Moreover, the sample for an optical characteristic measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. Further, the ratio between the maximum absorption wavelength and the maximum absorbance of the liquid crystal compound (A) -4 was calculated in the same manner as in Example 1. The results are shown in Table 1.

... (A) -4

<Example 14>
Except that the composition of the liquid crystal compound of Example 1 was changed from Liquid Crystal Compound A / Liquid Crystal Compound B = 90% / 10% to Liquid Crystal Compound (A) -5 100%, the composition (A-1) of Example 1 and The composition (A-14) and the vertically aligned liquid crystal cured film (A-14) of Example 14 were produced in the same manner as the method for preparing the vertical aligned liquid crystal cured film (A-1). The liquid crystal compound (A) -5 was prepared with reference to JP 2010-31223 A. The liquid crystal compound (A) -5 is represented by the following formula (A) -5. Moreover, the sample for an optical characteristic measurement was produced by the method similar to Example 1, and the phase difference value, the average refractive index, and orientation were evaluated. Further, the ratio between the maximum absorption wavelength and the maximum absorbance of the liquid crystal compound (A) -5 was also calculated in the same manner as in Example 1. The results are shown in Table 1.

... (A) -5

<Example 15>
The silane compound of Example 1 was converted from 3-triethoxysilyl-N- (1,3-dimethyl-butylidene) propylamine (“KBE-9103” manufactured by Shin-Etsu Chemical Co., Ltd.) to 3-glycidoxypropyltriethoxysilane ( Except for changing to “KBE-403” manufactured by Shin-Etsu Chemical Co., Ltd., in the same manner as in the preparation method of the composition (A-1) and the vertically aligned liquid crystal cured film (A-1) in Example 1, A composition (A-15) and a vertically aligned liquid crystal cured film (A-15) were prepared in the same manner as in Example 1. A sample for measuring optical properties was prepared in the same manner as in Example 1. The rate and orientation were evaluated and the results are shown in Table 1.

<Example 16>
[Production of Polarizing Film A]
After immersing a polyvinyl alcohol film (average polymerization degree of about 2,400, saponification degree of 99.9 mol% or more, thickness of 75 μm) in pure water at 30 ° C., the mass ratio of iodine / potassium iodide / water is 0. Iodine dyeing was carried out by dipping in a 0.02 / 2/100 aqueous solution at 30 ° C. (iodine dyeing step). The polyvinyl alcohol film which passed through the iodine dyeing process was immersed in an aqueous solution having a mass ratio of potassium iodide / boric acid / water of 12/5/100 at 56.5 ° C. to perform boric acid treatment (boric acid treatment process). ). The polyvinyl alcohol film that had undergone the boric acid treatment step was washed with pure water at 8 ° C. and then dried at 65 ° C. to obtain a polarizer (thickness 27 μm after stretching) in which iodine was adsorbed and oriented on polyvinyl alcohol. . Under the present circumstances, it extended | stretched in the iodine dyeing process and the boric-acid treatment process. The total draw ratio in such drawing was 5.3 times. The obtained polarizer and a saponified triacetyl cellulose film (“KC4UYTAC” 40 μm manufactured by Konica Minolta) were bonded together with a nip roll through an aqueous adhesive. While maintaining the tension of the obtained bonded product at 430 N / m, it was dried at 60 ° C. for 2 minutes to obtain a polarizing film A having a triacetyl cellulose film as a protective film on one side. The water-based adhesive is 100 parts of water, 3 parts of carboxyl group-modified polyvinyl alcohol (Kuraray "Kuraray Poval KL318"), water-soluble polyamide epoxy resin (Sumika Chemtex "Smiles Resin 650", solid content concentration 30 parts aqueous solution) and 1.5 parts.

[Measurement of optical properties of polarizing film A]
Optical properties of the obtained polarizing film A were measured. The measurement was carried out with a spectrophotometer (“V7100” manufactured by JASCO Corporation) with the polarizer surface of the polarizing film A obtained above as the incident surface. The absorption axis of the polarizing film coincides with the stretching direction of polyvinyl alcohol, and the obtained polarizing film has a visibility corrected single transmittance of 42.1%, a visibility corrected polarization degree of 99.996%, and a single hue a. -1.1, simple substance hue b was 3.7.

(Preparation of composition for forming horizontal alignment film)
A horizontal alignment film was formed by mixing 5 parts of a photoalignable material (weight average molecular weight: 30000) having the following structure and 95 parts of cyclopentanone as a solvent and stirring the resulting mixture at 80 ° C. for 1 hour. A composition was obtained.

[Preparation of composition for forming horizontally aligned liquid crystal cured film A]
Liquid crystal compound A and liquid crystal compound B were mixed at a mass ratio of 90:10 to obtain a mixture. For 100 parts by mass of the resulting mixture, 1.0 part of a leveling agent (“F-556” manufactured by DIC) and 2-dimethylamino-2-benzyl-1- (4-morpholinophenyl) as a polymerization initiator ) 6 parts of butan-1-one (“Irgacure (registered trademark) 369 (Irg369)” manufactured by BASF Japan Ltd.) was added. Further, N-methyl-2-pyrrolidone (NMP) was added so that the solid content concentration was 13%. The composition for horizontal alignment liquid crystal cured film A formation was obtained by stirring at 80 degreeC for 1 hour.

[Production of horizontal alignment liquid crystal cured film A]
Corona treatment was performed on a COP film (“ZF-14-50” manufactured by Nippon Zeon Co., Ltd.). Then, the composition for horizontal alignment film formation was apply | coated using the bar coater, and the coating film was formed. The coating film was dried at 80 ° C. for 1 minute to form a dry film. Using a polarized UV irradiation device (“SPOT CURE SP-9” manufactured by USHIO INC.), A polarized UV exposure is performed under conditions of an integrated light amount of 100 mJ / cm ^{2 at} a wavelength of 313 nm and an axial angle of 45 ° to form a horizontal alignment film. Obtained. When the film thickness of the obtained horizontal alignment film was measured with an ellipsometer, it was 100 nm.

Then, the horizontal alignment liquid crystal cured film A formation composition was apply | coated to the horizontal alignment film using the bar coater, and the coating film was formed. The coating film was dried at 120 ° C. for 1 minute to form a dry film. Using a high pressure mercury lamp (“Unicure VB-15201BY-A” manufactured by Ushio Electric Co., Ltd.) under a nitrogen atmosphere and with a cumulative light quantity of 500 mJ / cm ^{2 at} a wavelength of 365 nm, A horizontal alignment liquid crystal cured film A was formed to obtain a laminate comprising a substrate, a horizontal alignment film and a horizontal alignment liquid crystal cured film A. When the film thickness of the horizontal alignment liquid crystal cured film A was measured with an ellipsometer, it was 2.3 μm. Met.

[Re measurement of horizontally aligned liquid crystal cured film A]
After the laminated body which consists of a base material, a horizontal alignment film, and the horizontal alignment liquid crystal cured film A was bonded to glass through the adhesive, the COP film which is a base material was peeled. Thereby, a horizontally aligned liquid crystal cured film A for Re measurement was obtained. The in-plane retardation value ReA (λ) of the horizontally aligned liquid crystal cured film A was measured using a measuring instrument (“KOBRA-WPR” manufactured by Oji Scientific Instruments). The measurement results of the retardation value ReA (λ) at each wavelength (450 nm, 550 nm, and 650 nm) are ReA (450) = 121 nm, ReA (550) = 142 nm, ReA (650) = 146 nm, and ReA (450) / ReA (550) = 0.85.

[Measurement of R0 and R40 of a laminate comprising a horizontally aligned liquid crystal cured film A and a vertically aligned liquid crystal cured film]
The horizontally aligned liquid crystal cured film A produced by the above method and the vertically aligned liquid crystal cured film (A-1) produced by the method of Example 1 were bonded via an adhesive (pressure-sensitive adhesive 15 μm manufactured by Lintec). Then, a laminate including the horizontally aligned liquid crystal cured film A and the vertically aligned liquid crystal cured film (A-1) was produced. Furthermore, one COP film used as a base material was peeled from the laminate and bonded to glass via an adhesive to obtain a laminate for measuring a retardation value. After confirming that there is no phase difference between the COP film and the horizontal alignment film, the phase difference value R0 (λ) in the front direction of the laminate for measuring the phase difference value, and the fast axis of the horizontal alignment liquid crystal cured film A are The retardation value R40 (λ) (λ = 450 nm and 550 nm) when tilted by 40 ° as the center was measured using a measuring instrument (“KOBRA-WPR” manufactured by Oji Scientific Instruments). The measurement results are shown in Table 2. From the obtained values of R0 (λ) and R40 (λ) (λ = 450 nm and 550 nm), | R0 (550) −R40 (550) |, | R0 (450) −R40 (450) |, and | {R0 (450) -R40 (450)}-{R0 (550) -R40 (550)} | was calculated. The results are shown in Table 3.

[Evaluation of oblique reflection hue]
The laminate prepared by the above method (a laminate comprising the horizontally aligned liquid crystal cured film A and the vertically aligned liquid crystal cured film (A-1)) and the polarizing film A, the absorption axis of the polarizing film A and the horizontally aligned liquid crystal cured The film was bonded via an adhesive so that the angle formed with the slow axis of film A was 45 °, and the substrate was peeled off to produce an elliptically polarizing plate with an optical compensation function. Thereafter, it was bonded to an aluminum foil through an adhesive, and the oblique reflection hue of the elliptically polarizing plate was visually observed from the direction of 45 ° elevation and 0-360 ° azimuth. The oblique reflection hue was evaluated based on the visual observation results based on the following evaluation criteria. The results are shown in Table 3.
(Evaluation criteria)
A (good): Black color is visually confirmed.
B (poor): Obvious coloring is confirmed visually.

<Examples 17 and 18>
A retardation value measurement was performed in the same manner as in Example 16 except that the values of RthC (450) and RthC (550) were changed as shown in Table 2 by changing the thickness of the vertically aligned liquid crystal cured film. The oblique reflection hue was confirmed. The results are shown in Tables 2 and 3.

<Example 19>
The retardation value of the retardation film A was changed in the same manner as in Example 16 except that the polarizing film A was changed to a polarizing film B containing a horizontally aligned liquid crystal cured film B aligned in the horizontal direction and a dichroic dye prepared by the method shown below. Measurement and evaluation of oblique reflection hue were carried out. The results are shown in Tables 2 and 3.

[Preparation of composition for forming polarizing film B]
The following components were mixed and stirred at 80 ° C. for 1 hour to obtain a composition for forming a polarizing film B containing a polymerizable liquid crystal compound (B) and a dichroic dye. As the dichroic dye, an azo dye described in Examples of JP2013-101328A was used. The polymerizable liquid crystal compounds represented by the formulas (1-6) and (1-7) as the polymerizable liquid crystal compound (B) are described in lub et al. , Recl. Trav. Chim. It was produced according to the method described in Pays-Bas, 115, 321-328 (1996).
Polymerizable liquid crystal compound (B):

75 copies

25 parts dichroic dye 1:
Polyazo dye; Compound (1-8) 2.5 parts

Compound (1-5) 2.5 parts

Compound (1-16) 2.5 parts

A polymerization initiator;
2-dimethylamino-2-benzyl-1- (4-morpholinophenyl) butan-1-one (Irgacure 369; manufactured by Ciba Specialty Chemicals) 6 parts leveling agent;
Polyacrylate compound (“BYK-361N” manufactured by BYK-Chemie)
1.2 parts solvent; o-xylene 250 parts

[Production of Polarizing Film B]
(Production of horizontal alignment film)
Corona treatment was performed on a triacetyl cellulose film (TAC) (“KC4UY” manufactured by Konica Minolta). Subsequently, the composition for horizontal alignment film formation was apply | coated to the TAC surface which gave the corona treatment using the bar coater, and the coating film was formed. The coating film was dried at 80 ° C. for 1 minute to form a dry film. Using a polarized UV irradiation device (“SPOT CURE SP-7” manufactured by Ushio Electric Co., Ltd.), a polarized UV exposure is performed on the dried film under the conditions of an integrated light amount of 100 mJ / cm ² and an axial angle of 90 °, and horizontal alignment is performed. A membrane was obtained. It was 150 nm when the film thickness of the obtained horizontal alignment film was measured with the ellipsometer.

(Preparation of horizontal alignment liquid crystal cured film B)
Furthermore, using a bar coater, the composition for forming a polarizing film B was applied to the horizontal alignment film to form a coating film. Thereafter, the coating film was dried in a drying oven set at 120 ° C. for 1 minute. As a result, a dry coating film in which the polymerizable liquid crystal compound (B) and the dichroic dye were aligned was obtained. The dried coating film is naturally cooled to room temperature (25 ° C.) and then integrated using a high pressure mercury lamp (“Unicure VB-15201BY-A” manufactured by USHIO INC.) Under a nitrogen atmosphere at a wavelength of 365 nm and a wavelength of 365 nm. Under the condition of 1000 mJ / cm ^2, the polymerizable liquid crystal compound (B) was polymerized by irradiating ultraviolet rays to prepare a polarizing film B having a horizontally aligned liquid crystal cured film B containing a dichroic dye.

[Measurement of degree of polarization and single transmittance of polarizing film B]
The polarization degree and single transmittance of the obtained polarizing film B were measured as follows. Using a device in which the transmittance in the transmission axis direction (T ¹ ) and the transmittance in the absorption axis direction (T ² ) are set in a spectrophotometer (“UV-3150” manufactured by Shimadzu Corporation) with a folder with a polarizer. The measurement was carried out by the double beam method in a wavelength range of 2 nm steps from 380 to 680 nm. Using the following formulas (p) and (q), single transmittance and polarization degree at each wavelength were calculated. Furthermore, when the visibility correction was performed with the 2 degree visual field (C light source) of Japanese Industrial Standards JIS Z 8701, and the visibility correction single transmittance (Ty) and the visibility correction polarization degree (Py) were calculated, the single transmittance was 42% and polarization degree were 97%, and it was confirmed that it was a useful value as a polarizing film.
Single transmittance (%) = (T ¹ + T ² ) / 2 (p)
Polarization degree (%) = {(T ¹ −T ² ) / (T ¹ + T ² )} × 100 (q)

<Comparative example 2>
A sample was prepared in the same manner as in Example 16 except that the vertical alignment film and the vertical alignment liquid crystal cured film shown below were prepared, and the retardation value was measured and the oblique reflection hue was evaluated. The results are shown in Tables 2 and 3.

(Preparation of vertical alignment film forming composition (B))
0.5% polyimide (“Sun Ever SE-610” manufactured by Nissan Chemical Industries, Ltd.), 72.3% N-methyl-2-pyrrolidone, 18.1% 2-butoxyethanol, 9.1% ethyl Cyclohexane and 0.01% DPHA (manufactured by Shin-Nakamura Chemical Co., Ltd.) were mixed to prepare a vertical alignment film forming composition (B).

(Preparation of composition for forming vertical alignment liquid crystal cured film (B))
To a liquid crystal compound LC242 represented by the following formula (LC242): Paliocolor LC242 (registered trademark of BASF), 0.1 part of a leveling agent (“F-556” manufactured by DIC) and 3 parts of a polymerization initiator Irg369 were added. Then, cyclopentanone was added so that the solid content concentration would be 13%, and these were mixed to obtain a vertically aligned liquid crystal cured film forming composition (B).
Liquid crystal compound LC242: Paliocolor LC242 (registered trademark of BASF)

(Preparation of vertical alignment liquid crystal cured film)
Corona treatment was performed on a COP film (Nippon Zeon Corporation “ZF-14-23”) as a substrate. Using the bar coater, the vertical alignment film forming composition (B) was applied to the COP film that had been subjected to the corona treatment using the bar coater to form a coating film. The coating film was dried at 80 ° C. for 1 minute to obtain a vertical alignment film. The thickness of the obtained vertical alignment film was measured with an ellipsometer and found to be 0.2 μm. Subsequently, the vertically aligned liquid crystal cured film forming composition (B) was applied on the prepared vertical alignment film to form a coating film. The coating film was dried at 80 ° C. for 1 minute to form a dry film. Then, using a high-pressure mercury lamp (“Ushio VB-15201BY-A” manufactured by Ushio Electric Co., Ltd.), the dry film was irradiated with ultraviolet rays under a nitrogen atmosphere and an integrated light amount of 500 mJ / cm ^{2 at} a wavelength of 365 nm. A vertically aligned liquid crystal cured film was formed. The film thickness of the obtained vertically aligned liquid crystal cured film was 0.5 μm.

In Table 1, the “addition amount” of the column silane compound and the “addition amount” of the ionic compound respectively indicate the addition amount (unit: wt%) with respect to the composition for forming a vertically aligned liquid crystal cured film. The number of the ratio of the column liquid crystal compound and the alphabet in parentheses indicate the ratio of the added amount of the added liquid crystal compound. For example, 90/10 (A / B) indicates a mass ratio (liquid crystal compound A / liquid crystal compound B) 90/10.

The compositions (A-1) to (A-15) of Examples 1 to 15 are composed of the liquid crystal compounds A, (A) -2, (A) -3, (A) -4, and (A) -5. At least one of them, silane compound KBE-9103 or KBE-403, and any one of ionic compounds (1) to (3) were contained. Liquid crystal compounds A, (A) -2, (A) -3, (A) -4, and (A) -5 are liquid crystal compounds included in the liquid crystal compound represented by formula (I) -1. It was. Silane compounds KBE-9103 and KBE-403 were nonionic silane compounds. The evaluation of the orientation of the vertically aligned liquid crystal cured films (A-1) to (A-15) in Examples 1 to 15 was either A or B. The composition (A-20) of Example 20 contains liquid crystal compound A and an ionic compound, and the composition (A-21) of Example 21 contains liquid crystal compound A and a nonionic silane compound. It was. The orientation evaluations of the vertically aligned liquid crystal cured film (A-20) of Example (20) and the vertically aligned liquid crystal cured film (A-21) of Example (21) were both C.

The composition (B-1) of Comparative Example 1 did not contain a nonionic silane compound or an ionic compound. The evaluation of the orientation of the vertically aligned liquid crystal cured film (B-1) of Comparative Example 1 was D.

From the above, the vertically aligned liquid crystal cured films (A-1) to (A-15), (A-20), and (A-21) of Examples 1 to 15 are the aligned liquid crystal cured films (B It is clear that the orientation is excellent compared to -1). The compositions (A-1) to (A-15), (A-20), and (A-21) of Examples 1 to 15, Example 20, and Example 21 are the compositions of Comparative Example 1 ( As compared with B-1), it is clear that a vertically aligned liquid crystal cured film having excellent alignment properties can be formed without a vertically aligned film.

The elliptically polarizing plates of Examples 16 to 19 included a vertically aligned liquid crystal cured film prepared using the composition (A-1), a horizontal aligned film, a horizontal aligned liquid crystal cured film A, and a polarizing film. . The oblique reflection hues of the elliptically polarizing plates of Examples 16 to 19 were all A.

The elliptically polarizing plate of Comparative Example 2 contained a vertically aligned liquid crystal cured film prepared using the composition (B-2), a horizontal aligned film, a horizontally aligned liquid crystal cured film A, and a polarizing film. The composition (B-2) contained a liquid crystal compound LC242. Ar in the liquid crystal compound is a divalent group having one ring structure and was not included in the liquid crystal compound represented by the formula (I) -1. The oblique reflection hue of the elliptically polarizing plate of Comparative Example 2 was B.

From the above, it is clear that the elliptically polarizing plates of Examples 16 to 19 are superior in the oblique reflection hue as compared with the elliptically polarizing plate of Comparative Example 2.

DESCRIPTION OF SYMBOLS 1 ... Base material, 3 ... Horizontal alignment film, 5 ... Horizontal alignment liquid crystal cured film A, 7 ... Adhesion layer, 9 ... Vertical alignment liquid crystal cured film, 11 ... Polarizing film, 13 ... protective layer, 15 ... laminate, 20 ... elliptical polarizing plate

Claims

Formula (I) -1 below:

... (I) -1
[In the formula (I) -1, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L 1 and L 2 at the 1 and 4 positions,
L 1 and L 2 each independently represent a single bond or a divalent linking group,
G 1 and G 2 each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and are included in the divalent aromatic group and the divalent alicyclic hydrocarbon group. Each hydrogen atom independently substituted with a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may each independently be substituted with an oxygen atom, a sulfur atom, or a nitrogen atom,
* Represents a bond]
A composition comprising at least one liquid crystal compound having a structure represented by: and at least one selected from the group consisting of a nonionic silane compound and an ionic compound.
2. The composition according to claim 1, wherein the one or more liquid crystal compounds having a structure represented by the formula (I) -1 have a maximum absorption in a wavelength range of 260 nm to 400 nm.
The liquid crystal compound having the structure represented by the formula (I) -1 is represented by the following formula (I) -2:

... (I) -2
[In the formula (I) -2, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L 1 and L 2 at the 1 and 4 positions,
L 1 , L 2 and B 1 each independently represent a single bond or a divalent linking group,
G 1 , G 2 , and G 3 each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group and the divalent alicyclic carbon group The hydrogen atom contained in the hydrogen group is independently a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, or a nitro group. The carbon atoms contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group are each independently substituted with an oxygen atom, a sulfur atom, or a nitrogen atom. You can,
* Represents a bond]
The composition of Claim 1 or Claim 2 which is a liquid crystal compound which has a structure represented by these.
The liquid crystal compound having the structure represented by the formula (I) -1 is represented by the following formula (I) -3:

... (I) -3
[In the formula (I) -3, Ar represents a divalent group having two or more ring structures, and one of the two or more ring structures is a 6-membered ring, Binds L 1 and L 2 at the 1 and 4 positions,
L 1 , L 2 , B 1 and B 2 each independently represent a single bond or a divalent linking group;
G 1 , G 2 , G 3 , and G 4 each independently represent a divalent aromatic group or a divalent alicyclic hydrocarbon group, and the divalent aromatic group and the divalent fat The hydrogen atoms contained in the cyclic hydrocarbon group are each independently a halogen atom, an alkyl group having 1 to 4 carbon atoms, a fluoroalkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, a cyano group, Or a carbon atom contained in the divalent aromatic group and the divalent alicyclic hydrocarbon group may be independently an oxygen atom, a sulfur atom, or a nitrogen atom. May be replaced,
* Indicates a bond]
The composition according to any one of claims 1 to 3, which is a liquid crystal compound represented by the formula:
The composition according to any one of claims 1 to 4, wherein the liquid crystal compound has one or more polymerizable groups.
The composition according to any one of claims 1 to 5, wherein the nonionic silane compound is a silane coupling agent.
The composition according to any one of claims 1 to 6, wherein the nonionic silane compound is a silane coupling agent having an alkoxysilyl group and a polar group.
The composition according to any one of claims 1 to 7, wherein the ionic compound is entirely composed of a nonmetallic element.
The composition according to any one of claims 1 to 8, wherein the molecular weight of the ionic compound is 100 or more and 10,000 or less.
10. A vertically aligned liquid crystal cured film, which is a cured product of the composition according to claim 1, wherein the liquid crystal compound contained in the composition is aligned in a direction perpendicular to the in-plane direction of the liquid crystal cured film. Vertical alignment liquid crystal cured film.
The following relational expression (1):
−150 nm ≦ RthC (550) ≦ −30 nm (1)
[In relational expression (1), RthC (550) represents the retardation value in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm]
The vertically aligned liquid crystal cured film according to claim 10, wherein
The following relational expression (2):
RthC (450) / RthC (550) ≦ 1 (2)
[In the relational expression (2), RthC (450) represents the retardation value in the thickness direction at a wavelength of 450 nm of the vertically aligned liquid crystal cured film, and RthC (550) represents the retardation in the thickness direction of the vertically aligned liquid crystal cured film at a wavelength of 550 nm. Show value]
The vertically aligned liquid crystal cured film according to claim 10 or 11, wherein
A substrate and a vertically aligned liquid crystal cured film according to any one of claims 10 to 12,
A laminate in which the vertically aligned liquid crystal cured film is adjacent to the substrate.
A laminate comprising the vertically aligned liquid crystal cured film according to any one of claims 10 to 12 and a film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film.
The following relational expression (3):
ReA (450) / ReA (550) ≦ 1 (3)
[In the relational expression (3), ReA (450) represents the in-plane retardation value at a wavelength of 450 nm of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and ReA (550) In-plane retardation value at a wavelength of 550 nm of a film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film]
The laminated body of Claim 14 which satisfy | fills.
The following relational expression (4):
| R0 (550) -R40 (550) | ≦ 10 nm (4)
[In the relational expression (4), R0 (550) represents an in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (550) represents a horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film. Represents the retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of the oriented film]
The laminated body of Claim 14 or Claim 15 which satisfy | fills.
The following relational expression (5):
| R0 (450) -R40 (450) | ≦ 10 nm (5)
[In the relational expression (5), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, and R40 (450) is aligned in the horizontal direction with respect to the in-plane direction of the vertical alignment liquid crystal cured film. Shows the retardation value at a wavelength of 450 nm when the film is rotated 40 ° around the fast axis direction]
The laminate according to any one of claims 14 to 16, which satisfies the following conditions.
The following relational expression (6):
| {R0 (450) -R40 (450)}-{R0 (550) -R40 (550)} | ≦ 3 nm (6)
[In relational expression (6), R0 (450) represents the in-plane retardation value of the laminate at a wavelength of 450 nm, R0 (550) represents the in-plane retardation value of the laminate at a wavelength of 550 nm, and R40 (450) Represents a retardation value at a wavelength of 450 nm when rotated by 40 ° around the fast axis direction of the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film, and R40 (550) is , Showing a retardation value at a wavelength of 550 nm when rotated by 40 ° around the fast axis direction of a film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film]
The laminate according to any one of claims 14 to 17, which satisfies:
The laminate according to any one of claims 14 to 18, wherein the film oriented in the horizontal direction with respect to the in-plane direction of the vertically aligned liquid crystal cured film is a horizontally aligned liquid crystal cured film.
An elliptically polarizing plate comprising the laminate according to any one of claims 14 to 19 and a polarizing film.
The elliptically polarizing plate according to claim 20, wherein the film oriented in a horizontal direction with respect to an in-plane direction of the vertically aligned liquid crystal cured film is a horizontally aligned liquid crystal cured film.
The elliptically polarizing plate according to claim 20 or 21, wherein an angle formed by the slow axis of the horizontally oriented film and the absorption axis of the polarizing film is 45 ± 5 °.
The polarizing film includes a horizontally aligned liquid crystal cured film in which a liquid crystal compound is aligned in a horizontal direction with respect to a film plane of the polarizing film, and the horizontally aligned liquid crystal cured film includes a dichroic dye. The elliptically polarizing plate in any one.
The elliptically polarizing plate according to claim 23, wherein the dichroic dye has an azo group.
The horizontal alignment liquid crystal cured film which comprises the said polarizing film is a cured film which hardened | cured in the state of the smectic phase which the liquid crystal compound orientated in the horizontal direction with respect to the in-plane direction of a film | membrane. Elliptical polarizing plate.
An organic EL display device comprising the elliptically polarizing plate according to any one of claims 20 to 25.