TW201416419A - Liquid crystal display device - Google Patents

Abstract

The object of present invention relates to a liquid crystal display device adopting a color filter using specific liquid crystal composition and specific color. The present invention provides a liquid crystal display device which prevents a decline of voltage retention (VHR) of the liquid crystal layer and increase of the ion density (ID), and solves the problem of poor displaying such as white omission, orientation irregularity, burn-in, and the like. Since the liquid crystal display device of present invention has characteristics of preventing poor displaying such as a decline of voltage retention (VHR) of the liquid crystal layer, increase of the ion density (ID), burn-in, and the like, it is especially useful for VA mode for active matrix drive, PSVA mode liquid crystal display device, and is applicable to the liquid crystal display devices such as liquid crystal TV, a monitor, a cell-phone, a smartphone, and the like.

Description

Liquid crystal display device

The present invention relates to a liquid crystal display device.

The liquid crystal display device has been used in various household electric equipment, measuring equipment, automobile panels, word processors, electronic notebooks, printers, computers, televisions, etc., starting with clocks and computers. Typical examples of the liquid crystal display method include a TN (twisted nematic) type, an STN (super twisted nematic) type, a DS (dynamic light scattering) type, a GH (guest type) type, and an IPS (in-plane). In-plane switching type, OCB (optical compensation birefringence) type, ECB (voltage controlled birefringence) type, VA (vertical alignment) type, CSH (color super series (Homeotropic) type), or FLC ( Strong ferroelectric liquid crystal). The driving method is generally from the previous static driving to the multiplex driving, and the simple matrix method, the active matrix (AM) recently driven by TFT (thin film transistor) or TFD (thin film diode). The way is mainstream.

As shown in Fig. 1, a general color liquid crystal display device has a transparent electrode serving as a common electrode between an alignment film and a substrate of one of two substrates (1) each having an alignment film (4). The layer (3a) and the color filter layer (2) are provided with a pixel electrode layer (3b) between the other alignment film and the substrate, and the substrates are disposed such that the alignment films face each other with a liquid crystal layer interposed therebetween (5).

The color filter layer is composed of a color filter including a black matrix and a red colored layer (R), a green colored layer (G), a blue colored layer (B), and A yellow colored layer (Y) is required.

When the liquid crystal material constituting the liquid crystal layer has a great influence on the electrical characteristics of the display device when impurities remain in the material, the impurities are highly managed. Further, the material for forming the alignment film is directly contacted with the liquid crystal layer, and the impurities remaining in the alignment film are moved to the liquid crystal layer, and the influence on the electrical characteristics of the liquid crystal layer is known. The characteristics of liquid crystal display devices for impurities in the alignment film material are under discussion.

On the other hand, even if a material such as an organic pigment used for a color filter layer is used, it is assumed that the influence of the same impurity as the alignment film material on the liquid crystal layer is caused. However, considering that the alignment film and the transparent electrode are interposed between the color filter layer and the liquid crystal layer, the direct influence on the liquid crystal layer is significantly reduced as compared with the alignment film material. However, the alignment film usually has a film thickness of 0.1 μm or less, and the transparent electrode is also used for the common electrode on the color filter layer side in order to increase the conductivity, and is usually 0.5 μm or less even if the film thickness is increased. Therefore, it cannot be said that the color filter layer and the liquid crystal layer are placed in a completely isolated environment, and the color filter layer passes through the alignment film and the transparent electrode, and the liquid crystal layer is formed by the impurities contained in the color filter layer. The voltage holding ratio (VHR) is lowered, and the increase in ion density (ID) causes whitening, uneven alignment, and residual image. A method for solving the display defect caused by the impurities contained in the pigment constituting the color filter is to use a pigment having a ratio of an extract derived from ethyl formate of the pigment to a specific value or less, and controlling dissolution of the liquid crystal of the impurity. (Patent Document 1); or a method of controlling liquid crystal dissolved in impurities by a pigment in a specific blue colored layer (Patent Document 2) has been studied. However, in these methods, in the simple reduction of impurities in the pigment, there is no In the recent years, even in the current state of progress in the refining technology of pigments, it is not sufficient to improve the display defects.

On the one hand, focusing on the relationship between the organic impurities contained in the color filter and the liquid crystal composition, it is revealed that the liquid crystal layer of the organic impurity is difficult to dissolve, and is represented by the hydrophobic parameter of the liquid crystal molecules contained in the liquid crystal layer. The method in which the value of the hydrophobic parameter is set to a certain value or more, or the hydrophobic parameter is related to the -OCF ₃ group at the end of the liquid crystal molecule, so that a liquid crystal composition is obtained which has a -OCF at the end of the liquid crystal molecule. A method in which a liquid crystal compound of _{3 is} contained in a certain ratio or more (Patent Document 3).

However, even in the disclosure of the cited document, the influence of the structure of the coloring material such as dyeing pigment used in the color filter on the structure of the liquid crystal material is suppressed in order to suppress the influence of the liquid crystal layer caused by impurities in the pigment. However, it has not been studied yet, and the problem of poor display of the highly-crystallized liquid crystal display device has not yet been solved.

Prior technical literature Patent literature

Patent Document 1 Japanese Patent Laid-Open Publication No. 2000-19321

Patent Document 2 Japanese Patent Laid-Open Publication No. 2009-109542

Patent Document 3 Japanese Patent Laid-Open Publication No. 2000-192040

The present invention provides a liquid crystal display device which uses a color filter which uses a specific liquid crystal composition and a specific dye and/or pigment to prevent a decrease in voltage holding ratio (VHR) of the liquid crystal layer and ion density. The increase in (ID) and the problem of poor display, such as whiteness, uneven alignment, and residual image.

In order to solve the above problems, the inventors of the present invention have studied the combination of a coloring material such as a dye pigment constituting a color filter and a liquid crystal material structure constituting a liquid crystal layer, and as a result, first discovered a liquid crystal display device. A color filter is used which uses a specific liquid crystal material structure and a pigment of a specific structure to prevent a decrease in voltage holding ratio (VHR) of the liquid crystal layer, an increase in ion density (ID), and to solve whitening, uneven alignment, and residual The invention was completed by the problem of poor display.

That is, the present invention provides a liquid crystal display device comprising: a first substrate; a second substrate; a liquid crystal composition layer sandwiched between the first substrate and the second substrate; and a color filter including a black matrix and at least RGB three-color pixel portion; a pixel electrode; and a common electrode, the liquid crystal composition layer comprising a liquid crystal composition containing 30 to 50% of a compound represented by the general formula (I)

(wherein R ¹ and R ² are each independently, and represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or 2 to 2 carbon atoms; 8 alkenyloxy, A represents 1,4-phenylene or trans-1,4-cyclohexenyl); contains 5 to 20% of the compound of the formula (II-1)

(wherein R ³ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and 25 to 45 % of the compound of the formula (II-2)

(wherein R ⁵ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁶ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and B is substituted by fluorine. 1,4-phenylene or trans-1,4-cyclohexenyl), the RGB three-color pixel portion as a coloring material, which is represented by the following formula (1) in the B pixel portion Triaryl methane pigment

(wherein R ¹ to R ⁶ each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms which may have a substituent, or an aryl group which may have a substituent; and R ¹ to R ⁶ represent a substituent which may have a substituent; In the case of an alkyl group, adjacent R ¹ and R ² , R ³ and R ⁴ , R ⁵ and R ⁶ may also be bonded to form a ring structure; X ¹ and X ² each independently represent a hydrogen atom, a halogen atom, or may have a substituent having an alkyl group having 1 to 8 carbon atoms; Z ^- represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6, selected from the group consisting of y = 0, 1, 2 or 3 a polyoxometalate anion, or an anion of at least one of (SiMoW ₁₁ O ₄₀ ) ^4- /4 heteropoly side oxymetalate anion, or a defective Dawson type phosphotungstic acid heteropoly side oxymetalate anion, The case where a molecule contains a plurality of formulas (1), which may be the same structure or different structures).

In the liquid crystal display device of the present invention, by using a color filter which uses a specific liquid crystal composition and a specific material, it is possible to prevent a decrease in the voltage holding ratio (VHR) of the liquid crystal layer and an increase in ion density (ID). It can prevent the occurrence of display defects such as whiteness, uneven alignment, and afterimages.

[Formation of the Invention]

An example of the liquid crystal display device of the present invention is shown in Fig. 2. The structure of the present invention includes a color filter layer (2) which is provided between one of the alignment films and the substrate of the two substrates (1) having the first substrate and the second substrate of the alignment film (4). The transparent electrode layer (3a) of the common electrode and the specific pigment are provided, and the pixel electrode layer (3b) is provided between the other alignment film and the substrate, and the substrates are disposed such that the alignment films face each other and are sandwiched therebetween. It is composed of a liquid crystal layer (5) of a specific liquid crystal composition.

The two substrates in the display device are bonded together by a sealing material and a sealing material disposed in the peripheral region. In many cases, a spacer column is disposed between the substrates in order to maintain the distance between the substrates. A resin formed by a spacer or photolithography.

(liquid crystal layer)

The liquid crystal layer in the liquid crystal display device of the present invention comprises a liquid crystal composition containing 30 to 50% of a compound represented by the general formula (I)

(wherein R ¹ and R ² are each independently, and represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or 2 to 2 carbon atoms; 8 alkenyloxy; A represents 1,4-phenylene or trans-1,4-cyclohexenyl); contains 5 to 20% of the compound of the formula (II-1)

(wherein R ³ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and 25 to 45% a compound of the formula (II-2)

(wherein R ⁵ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁶ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and B is substituted by fluorine. 1,4-phenylene or trans-1,4-cyclohexenyl).

In the liquid crystal display device of the present invention, the liquid crystal layer contains 30 to 50% of the compound represented by the formula (I), preferably 35 to 45%, more preferably 38 to 42%.

In the general formula (I), R ¹ and R ² each independently represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or a carbon atom. a 2 to 8 alkenyloxy group, preferably an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms or 2 to 2 carbon atoms 5 alkenyloxy, more preferably

An alkyl group having 2 to 5 carbon atoms, an alkenyl group having 2 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms or an alkenyloxy group having 2 to 4 carbon atoms, and R ¹ preferably represents an alkyl group. In this case, an alkyl group having 1, 3 or 5 carbon atoms is particularly preferred.

R ¹ and R ² may be the same or different, preferably different, and both R ¹ and R ² are alkyl groups, particularly preferably the number of carbon atoms 1, 3 or 5 which are mutually different atoms. Alkyl group.

The content of the compound of the formula (I) wherein at least one of the substituents of R ¹ and R ² is an alkyl group having 3 to 5 carbon atoms, preferably 50% or more of the compound represented by the formula (I) More preferably, it is 70% or more, and even more preferably 80% or more. Further, the content of the compound represented by the formula (I) wherein at least one of the substituents of R ¹ and R ² is an alkyl group having 3 carbon atoms is preferably 50% or more of the compound represented by the formula (I). More preferably, it is 70% or more, and even more preferably 80% or more, and the best is 100%.

A represents a 1,4-phenylene group or a trans-1,4-cyclohexenyl group, and preferably represents a trans-1,4-cyclohexenyl group. Also, A represents trans-1,4-cyclohexenyl The content of the compound represented by the formula (I) is preferably 50% or more, more preferably 70% or more, and particularly preferably 80% or more of the compound represented by the formula (I).

The compound represented by the formula (I) is specifically a compound represented by the formula (Ia) to the formula (Ik) described later.

(wherein R ¹ and R ² are each independently and represent an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, and preferably R ¹ and R in the formula (I); ^{2 the} same implementation).

In the formula (Ia) to the formula (Ik), preferred are the formula (Ia), the formula (Ib) and the formula (Ig), more preferably the formula (Ia) and the formula (Ig), The general formula (Ia) is preferably a general formula (Ib) in the case of attaching a response speed. In the case where the response speed is more important, the general formula (Ib) and the general formula (Ie) are preferred. The general formula (If) and the general formula (Ih) are particularly preferred as the diene-based compound of the formula (Ie) and the formula (If) in the case where the response speed is particularly emphasized.

From these points, the content of the compound represented by the formula (Ia) and the formula (Ig) is preferably 50% or more, more preferably 70% or more, more preferably 70% or more of the compound represented by the formula (I). It is 80% or more, and the best is 100%. Also, the general formula (Ia) The content of the compound shown is preferably 50% or more, more preferably 70% or more, still more preferably 80% or more of the compound represented by the formula (I).

The liquid crystal layer in the liquid crystal display device of the present invention contains 5 to 20% of the compound represented by the formula (II-1), preferably 10 to 15%, more preferably 12 to 14%.

In the formula (II-1), R ³ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or a carbon number of 2 to 8 The alkenyloxy group preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, more preferably an alkyl group having 2 to 5 carbon atoms or 2 to 4 carbon atoms. The alkenyl group is more preferably an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms.

R ⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms, and preferably represented by An alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, more preferably an alkyl group having 1 to 3 carbon atoms or an alkoxy group having 1 to 3 carbon atoms, still more preferably The alkyl group having 3 carbon atoms or the alkoxy group having 2 carbon atoms is particularly preferably an alkoxy group having 2 carbon atoms.

The compound represented by the formula (II-1) is specifically a compound represented by the formula (II-1a) and the formula (II-1b) described later.

(wherein R ³ represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms; and R ^4a represents an alkyl group having 1 to 5 carbon atoms).

In the formula (II-1a), R ^{3 is} preferably the same embodiment as in the formula (II-1). R ^4a represents an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 2 carbon atoms, particularly preferably an alkyl group having 2 carbon atoms.

In the formula (II-1b), R ^{3 is} preferably the same embodiment as in the formula (II-1). R ^{4a is} preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 3 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms.

Among the general formulae (II-1a) and (II-1b), in order to increase the absolute value of the dielectric anisotropy, the formula (II-1a) is preferred.

The liquid crystal layer in the liquid crystal display device of the present invention contains 25 to 45% of the compound represented by the formula (II-2), and preferably contains 30 to 40%, more preferably 31 to 36%.

In the formula (II-2), R ⁵ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or a carbon number of 2 to 8 The alkenyloxy group preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, more preferably an alkyl group having 2 to 5 carbon atoms or 2 to 4 carbon atoms. The alkenyl group is more preferably an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms.

R ⁶ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms, and preferably represents An alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, more preferably an alkyl group having 1 to 3 carbon atoms or an alkoxy group having 1 to 3 carbon atoms, still more preferably The alkyl group having 3 carbon atoms or the alkoxy group having 2 carbon atoms is particularly preferably an alkoxy group having 2 carbon atoms.

B represents a 1,4-phenylene group or a trans-1,4-cyclohexenyl group which may be substituted by fluorine, and is preferably an unsubstituted 1,4-phenylene group or a trans-1,4-cyclo ring. Hexyl group is more preferably trans-1,4-cyclohexenyl.

The compound represented by the formula (II-2), specifically, the compound of the formula (II-2a) to the formula (II-2d) described later is preferred.

(wherein R ⁵ represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms; and an alkyl group having 1 to 5 carbon atoms of R ^6a ).

In the formula (II-2a) and the formula (II-2b), R ^{5 is} preferably the same embodiment as in the formula (II-2); R ^{6a is} preferably an alkyl group having 1 to 3 carbon atoms. More preferably, it is an alkyl group having 1 or 2 carbon atoms, and particularly preferably an alkyl group having 2 carbon atoms.

In the formula (II-2c) and the formula (II-2d), R ^{5 is} preferably the same embodiment as in the formula (II-2); R ^{6a is} preferably an alkyl group having 1 to 3 carbon atoms. More preferably, it is an alkyl group having 1 or 3 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms.

Among the general formulae (II-1a) and (II-1b), in order to increase the absolute value of the dielectric anisotropy, the formula (II-1a) is preferred.

Further, in the formula (II-2), it is preferred that B represents a compound of 1,4-phenylene group and B represents a compound of trans-1,4-cyclohexenyl group, each of which contains at least one or more.

In the liquid crystal display device of the present invention, the liquid crystal layer preferably further contains a compound represented by the formula (III)

(wherein R ⁷ and R ⁸ are each independently, and represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or 2 to 2 carbon atoms; 8 alkenyloxy; D, E, F and G are each independently, meaning 1,4-phenyl or trans-1,4-cyclohexene which can be substituted by fluorine; Z ² represents a single bond, -OCH ₂ -, -OCO-, -CH ₂ O- or -COO-; n represents 0 or 1, but n represents 0, and Z ² represents -OCH ₂ -, -OCO-, -CH ₂ O- or -COO - or D, E and G represent a 1,4-phenylene group which may be substituted by fluorine). The compound represented by the formula (III) preferably contains 5 to 20%, more preferably 8 to 15%, still more preferably 10 to 13%.

In the formula (III), R ⁷ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an oxyalkylene having 2 to 8 carbon atoms. And D represents a case of trans-1,4-cyclohexene, preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, more preferably 2 carbon atoms. An alkyl group of 5 or an alkenyl group having 2 to 4 carbon atoms, more preferably an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms. And D represents a case where 1,4-phenylene group which may be substituted by fluorine, preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 4 or 5 carbon atoms, more preferably 2 to 2 carbon atoms The alkyl group of 5 or the alkenyl group having 4 carbon atoms, more preferably an alkyl group having 2 to 4 carbon atoms.

R ⁸ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms, and G represents a trans group. In the case of -1,4-cyclohexene, it is preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, more preferably an alkyl group having 2 to 5 carbon atoms or carbon. More preferably, it is an alkyl group having 2 to 4 atomic atoms, more preferably an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, particularly preferably an alkyl group having 3 carbon atoms, and G representing a fluorine atom. In the case of 1,4-phenylene, it preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 4 or 5 carbon atoms, more preferably an alkyl group having 2 to 5 carbon atoms or carbon. The alkenyl group having an atomic number of 4 is more preferably an alkyl group having 2 to 4 carbon atoms.

R ⁷ and R ⁸ represent an alkenyl group, and D or G of a bond represents a 1,4-phenylene group which may be substituted by fluorine, and in the case of an alkenyl group having 4 or 5 carbon atoms, the following structure is preferred. .

(in the formula, the right end is bonded to the ring structure)

In this case, it is preferably an alkenyl group having 4 carbon atoms.

D, E, F and G are each independently, and represent 1,4-phenylene or trans-1,4-cyclohexene which may be substituted by fluorine, and preferably represents 2-fluoro-1,4-extension. Phenyl, 2,3-difluoro-1,4-phenylene, 1,4-phenylene or trans-1,4-cyclohexene, more preferably 2-fluoro-1,4-benzene Or 2,3-difluoro-1,4-phenylene, 1,4-phenylene, particularly preferably 2,3-difluoro-1,4-phenyl or 1,4-phenyl .

Z ² represents a single bond, -OCH ₂ -, -OCO-, -CH ₂ O- or -COO-, and preferably represents a single bond, -CH ₂ O- or -COO-, more preferably a single bond.

n represents 0 or 1, and Z ² represents a substituent other than a single bond, and preferably represents 0.

When the compound represented by the formula (III) represents 0, specifically, it is preferably a compound represented by the formula (III-1a) to the formula (III-1h) described later.

(wherein R ⁷ and R ⁸ are each independently and represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, and preferably In the general formula (III), R ⁷ and R ^{8 are the} same in the same manner).

In the case where n represents 1 in the compound represented by the formula (III), specifically, the compound represented by the formula (III-2a) to the formula (III-2l) described later is preferable.

(wherein R ⁷ and R ⁸ are each independently and represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, and preferably In the general formula (III), R ⁷ and R ^{8 are the} same in the same manner).

The compound represented by the formula (II-1) and the formula (II-2) has a negative dielectric anisotropy, and the absolute value thereof is a relatively large compound, but the total content of the compounds is preferably. It is 30 to 65%, more preferably 40 to 55%, and particularly preferably 43 to 50%.

The compound represented by the formula (III), which has a dielectric anisotropy and a positive value, also contains a negative compound, but the dielectric anisotropy is negative, and the absolute value is 0.3 or more. In the case of the compound, it is preferred that the compound represented by the formula (II-1), the formula (II-2) and the formula (III) has a total content of 35 to 70%, more preferably 45 to 65%. Good for 50 to 60%.

Preferably, it contains 30 to 50% of the compound of the formula (I), and contains 35 to 70% of the compound of the formula (II-1), the formula (II-2) and the formula (III). More preferably, it contains 35 to 45% of the compound of the formula (I) and contains 45 to 65% of the compound of the formula (II-1), the formula (II-2) and the formula (III), particularly preferably 38 to 42% of the compound of the formula (I), and contains 50 to 60% of the compound of the formula (II-1), the formula (II-2) and the formula (III).

The total content of the compounds represented by the general formula (I), the general formula (II-1), the general formula (II-2) and the general formula (III) is preferably from 80 to 100%, more preferably, based on the entire composition. 90 to 100%, especially preferably 95 to 100%.

The liquid crystal layer in the liquid crystal display device of the present invention can use a nematic phase-isotropic liquid phase transfer temperature (T _ni ) in a wide range, preferably 60 to 120 ° C, more preferably 70 to 100 ° C, particularly preferably It is 70 to 85 °C.

The dielectric anisotropy is preferably -2.0 to -6.0, more preferably -2.5 to -5.0, particularly preferably -2.5 to -3.5 at 25 °C.

The refractive index anisotropy is preferably from 0.08 to 0.13, more preferably from 0.09 to 0.12 at 25 °C. More specifically, it is preferably 0.10 to 0.12 in the case of a corresponding lattice gap, and preferably 0.08 to 0.10 in the case of a lattice gap corresponding to a thickness.

The rotational viscosity ( γ 1) is preferably 150 or less, more preferably 130 or less, and particularly preferably 120 or less.

The liquid crystal layer in the liquid crystal display device of the present invention preferably has a specific value of Z as a function of rotational viscosity and refractive index anisotropy.

(where γ 1 represents rotational viscosity and Δn represents refractive index anisotropy)

Z is preferably 13,000 or less, more preferably 12,000 or less, and particularly preferably 11,000 or less.

The liquid crystal layer in the liquid crystal display device of the present invention must have a specific resistance of 10 ¹² (Ω··m) or more, preferably 10 ¹³ (Ω·m), more preferably 10 10 (Ω·m). 10 ¹⁴ (Ω‧m) or more.

In the liquid crystal display device of the present invention, in addition to the above compounds, a normal nematic liquid crystal, a matrix liquid crystal, a cholesteric liquid crystal, an antioxidant, an ultraviolet absorber, a polymerizable monomer, or the like may be contained depending on the application.

In the case of a polymerizable monomer, a difunctional monomer represented by the formula (V) is preferred.

Wherein X ¹ and X ² are each independently represented by a hydrogen atom or a methyl group, and Sp ¹ and Sp ² are each independently represented by a single bond, an alkylene group having 1 to 8 carbon atoms or -O-(CH _{2 ) s} - (wherein, s represents an integer from 2 to 7, and an oxygen atom is bonded to an aromatic ring), and Z ¹ represents -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -CF ₂ O-, -OCF ₂ -, -CH ₂ CH ₂ -, -CF ₂ CF ₂ -, -CH=CH-COO-, -CH=CH-OCO-, -COO-CH=CH-, -OCO-CH =CH-, -COO-CH ₂ CH ₂ -, -OCO-CH ₂ CH ₂ -, -CH ₂ CH ₂ -COO-, -CH ₂ CH ₂ -OCO-, -COO-CH ₂ -, -OCO- CH ₂ -, -CH ₂ -COO-, -CH ₂ -OCO-, -CY ¹ =CY ² - (wherein Y ¹ and Y ² are each independently represent a fluorine atom or a hydrogen atom), -C≡C - or a single bond, C represents 1,4-phenylene, trans-1,4-cyclohexenyl or a single bond, all of which are 1,4-phenylene, and any hydrogen atom may be fluorine Replaced by atoms).

X ¹ and X ² are each preferably a diacrylate derivative each having a hydrogen atom and a dimethacrylate derivative having a methyl group, and preferably one represents a hydrogen atom and the other represents a methyl group. Compound. The polymerization rate of these compounds is the fastest with diacrylate derivatives, the slower dimethacrylate derivatives, and the asymmetric compounds in between, which can be used according to their use. In the PSA display element, a dimethacrylate derivative is preferred.

The Sp ¹ and Sp ² systems are each independently represented by a single bond, an alkylene group having 1 to 8 carbon atoms or -O-(CH ₂ ) _s -, and at least one of the PSA display elements is preferably a single bond. More preferably, the compound which collectively represents a single bond or one of them is a single bond, and the other represents a state of an alkylene group having 1 to 8 carbon atoms or -O-(CH ₂ ) _s -. In this case, an alkyl group of 1 to 4 is preferable, and more preferably s represents 1 to 4.

Z ^{1 is} preferably -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -CF ₂ O-, -OCF ₂ -, -CH ₂ CH ₂ -, -CF ₂ CF ₂ - or The key is more preferably -COO-, -OCO- or a single bond, and particularly preferably a single bond.

The C system represents a 1,4-phenylene group, a trans-1,4-cyclohexenyl group or a single bond in which any hydrogen atom may be substituted by a fluorine atom, and is preferably a 1,4-phenylene group or single bond. C represents a ring structure other than a single bond, Z ^{1 is} preferably a linking group other than a single bond, and C is a single bond, and Z ^{1 is} preferably a single bond.

From these viewpoints, the ring structure between the general formula (V), Sp ¹ and Sp ² is, in particular, preferably the structure described later.

In the general formula (V), C represents a single bond, and in the case where the ring structure is formed by two rings, it preferably represents the following formula (Va-1) to formula (Va-5), more preferably a formula (Va). -1) to the formula (Va-3), particularly preferably the formula (Va-1).

(wherein, both ends are bonded to Sp ¹ or Sp ² ).

The polymerizable compound containing these skeletons is most suitable for the PSA type liquid crystal display device after the polymerization, and it is possible to suppress the display unevenness or not to occur at all because a good alignment state can be obtained.

From the above, in terms of the polymerizable monomer, the formula (V-1) to the formula (V-4) are particularly preferable, and the formula (V-2) is most preferable.

(wherein, Sp ² represents an alkylene group having 2 to 5 carbon atoms).

In the case where a polymerizable monomer is added, polymerization may be carried out even if the polymerization initiator is not present, and a polymerization initiator may be contained in order to promote polymerization. Examples of the polymerization initiator include benzoin ethers, benzophenones, acetophenones, benzyl ketals, and mercaptophosphine oxides. Further, in order to improve storage stability, a stabilizer may be added. Examples of the stabilizer which can be used include hydroquinones, hydroquinone monoalkyl ethers, tertiary butyl brown phenols, gallic phenols, thiophenols, nitro compounds, and β-naphthylamines. Classes, β-naphthols, nitroso compounds, and the like.

A liquid crystal layer containing a polymerizable monomer is useful for a liquid crystal display element, and is particularly useful for a liquid crystal display element for active matrix driving, and can be used for a liquid crystal display element for PSA mode, PSVA mode, VA mode, IPS mode, or ECB mode. .

A liquid crystal layer containing a polymerizable monomer, which is polymerized by ultraviolet irradiation to provide a liquid crystal alignment energy, and which utilizes birefringence of a liquid crystal composition, and is used for liquid crystal which controls the amount of light transmitted. Display component. As a liquid crystal display element, in AM-LCD (active matrix liquid crystal display element), TN (nematic liquid crystal display element), STN-LCD (super twisted nematic liquid crystal display element), OCB-LCD, and IPS-LCD (in-plane) It is useful to turn to a liquid crystal display element, and is particularly useful in an AM-LCD, and can be used for a transmissive or reflective type liquid crystal display element.

(color filter)

The color filter of the present invention is composed of a black matrix and at least RGB three-color pixel portions, and the RGB three-color pixel portion as a coloring material contains the following general formula (1) in the B pixel portion. Triaryl methane pigment

(wherein R ¹ to R ⁶ each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms which may have a substituent, or an aryl group which may have a substituent. R ¹ to R ⁶ may have a substituent. In the case of an alkyl group, adjacent R ¹ and R ² , R ³ and R ⁴ , R ⁵ and R ⁶ may also be bonded to form a ring structure; X ¹ and X ² each independently represent a hydrogen atom, a halogen atom or may have a substituent having an alkyl group having 1 to 8 carbon atoms. Z ^{- is} represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6, which is selected from an integer of y = 0, 1, 2 or 3. Heteropolyoxometalate anion, or a heteropoly side oxymetalate anion of (SiMoW ₁₁ O ₄₀ ) ⁴ / 4 or at least one of a Dawson type phosphotungstic acid heteropoly side oxymetalate anion An anion having a plurality of formulas (1) in one molecule, which may be the same structure or different structures). Further, the RGB three-color pixel portion preferably contains a diketopyrrolopyrrole pigment and/or an anionic red organic dye in the R pixel portion, and contains a metal halide phthalocyanine in the G pixel portion. At least one of the group consisting of a pigment, a phthalocyanine green dye, a mixture of a phthalocyanine blue dye and an azo yellow organic dye.

(G pixel part)

The G pixel portion preferably contains at least one selected from the group consisting of a halogenated metal phthalocyanine pigment, a phthalocyanine green dye, a mixture of a phthalocyanine blue dye and an azo yellow organic dye. In the case of a halogenated metal phthalocyanine pigment, it is selected from the group consisting of Al, Si, Sc, Ti, V, Mg, Fe, Co, Ni, Zn, Cu, Ga, Ge, Y, Zr, Nb, In, Sn And a metal halide metal phthalocyanine pigment in the group of Pb, in the case where the central metal is trivalent, one of a halogen atom, a hydroxyl group or a sulfonic acid group is bonded to the central metal thereof, or Performing side oxygen or sulfur crosslinking, in the case where the central metal has a tetravalent metal, it is preferred that the central metal has one oxygen atom bonded thereto or two halogen atoms, a hydroxyl group or a sulfonic acid which may be the same or different. A halogenated metal phthalocyanine pigment of any one of the bases. The halogenated metal phthalocyanine pigment may be exemplified by the following two groups of halogenated metal phthalocyanine pigments.

(first group)

A halogenated metal phthalocyanine pigment having a group selected from the group consisting of Al, Si, Sc, Ti, V, Mg, Fe, Co, Ni, Zn, Cu, Ga, Ge, Y, Zr, Nb, In, Sn, and Pb a metal as a central metal, a halogenated metal phthalocyanine pigment having 8 to 16 halogen atoms bonded to a benzene ring of a phthalocyanine molecule for each phthalocyanine molecule, in the center of which the center metal is trivalent, at the center thereof The metal bond has one of a halogen atom, a hydroxyl group or a sulfonic acid group (-SO ₃ H). In the case where the central metal is a tetravalent metal, one oxygen atom may be bonded to the central metal or may be the same or Any of two different halogen atoms, hydroxyl groups or sulfonic acid groups.

(second group)

a pigment comprising a halogenated metal phthalocyanine dimer: a trivalent metal selected from the group consisting of Al, Sc, Ga, Y, and In as a central metal, and each of the phthalocyanine molecules, having 8 to 16 Two molecules of a halogenated metal phthalocyanine in which a halogen atom is bonded to a benzene ring of a phthalocyanine molecule as a constituent unit, and each of the central metals of the constituent units is selected from the group consisting of an oxygen atom, a sulfur atom, and a sulfinyl group (-SO-). And a divalent atomic group in the group of sulfonyl groups (-SO ₂ -) bonded.

In the halogenated metal phthalocyanine pigment, the halogen atoms bonded to the benzene ring may be identical or different. Further, a halogen atom may be bonded to a benzene ring.

Here, each phthalocyanine molecule has 9 to 15 halogenated metal phthalocyanine pigments bonded to the benzene ring of the phthalocyanine molecule in 8 to 16 halogen atoms, and has a bright yellow color, which is most suitable for use. In the green pixel portion of the color filter. The halogenated metal phthalocyanine pigment is insoluble or poorly soluble in water or an organic solvent. Each of the halogenated metal phthalocyanine pigments includes any one of a pigment (which may be referred to as a crude pigment) which is not subjected to final processing described later, and a pigment which is subjected to final processing.

The halogenated metal phthalocyanine pigment belonging to the first group and the second group can be represented by the following formula (PIG-1).

The halogenated metal phthalocyanine pigment belonging to the first group is as follows in the general formula (PIG-1).

In the formula (PIG-1), X ₁ to X ₁₆ represent a hydrogen atom, a chlorine atom, a bromine atom or an iodine atom. The four X atoms bonded to a benzene ring may be the same or different. Among X ₁ to X ₁₆ bonded to four benzene rings, 8 to 16 are chlorine atoms, bromine atoms or iodine atoms. M represents the center metal. In the range of the above-mentioned Y and the number of the halogenated metal phthalocyanine pigments in which the number m is the same, in 16 X ₁ to X ₁₆ , the total of the chlorine atom, the bromine atom and the iodine atom is less than 8 and the pigment is blue. The total of the chlorine atoms, the bromine atoms, and the iodine atoms in the sixteen X ₁ to X ₁₆ is 8 or more. The larger the total value, the stronger the yellow color. The Y bonded to the central metal M is selected from a monovalent atomic group in a group containing a halogen atom, an oxygen atom, a hydroxyl group, and a sulfonic acid group of any one of fluorine, chlorine, bromine or iodine, and m represents a bond to the central metal M. The number of Y is an integer from 0 to 2.

The value of m is determined by the atomic price of the central metal M. The central metal M is, like Al, Sc, Ga, Y, In, in the case where the valence is trivalent, m=1, and is selected from the group consisting of fluorine, chlorine, bromine, iodine, hydroxyl, and sulfonic acid groups. One of the bases is bonded to the center metal. The central metal M, such as Si, Ti, V, Ga, Zr, Sn, in the case where the valence is tetravalent, m=2, one of the oxygen bonds to the central metal, or is selected from the group consisting of fluorine, chlorine, bromine, Two of the groups in the group of iodine, hydroxyl and sulfonic acid groups are bonded to the central metal. The center metal M is like Mg, Fe, Co, Ni, Zn, Cu, Zr, Sn, and Pb. When the valence is two, Y does not exist.

Further, the halogenated metal phthalocyanine pigment belonging to the second group is as follows in the general formula (PIG-1).

In the general formula (PIG-1), X ₁ to X ₁₆ are synonymous with the definition, and the central metal M represents a trivalent metal selected from the group consisting of Al, Sc, Ga, Y, and In; m represents 1 ;Y indicates the next atomic group.

Further, in the chemical structure of the atomic group Y, the central metal M is synonymous with the above definition, and X ₁₇ to X ₃₂ , and the general formula (PIG-1) is synonymous with the definitions of the above X ₁ to X ₁₆ . A represents a divalent atomic group selected from the group consisting of an oxygen atom, a sulfur atom, a sulfinyl group (-SO-), and a sulfonyl group (-SO ₂ -). M in the general formula (PIG-1) and M in the atomic group Y mean a bond via a divalent atomic group A.

That is, the halogenated metal phthalocyanine pigment belonging to the second group is a halogenated metal phthalocyanine dimer in which two molecules of a halogenated metal phthalocyanine are used as a constituent unit, which are bonded via the divalent atomic group.

The halogenated metal phthalocyanine pigment represented by the formula (PIG-1), specifically, the following (1) to (4).

(1) a halogenated metal phthalocyanine pigment: such as a copper halide phthalocyanine pigment, a tin halide phthalocyanine pigment, a nickel halide phthalocyanine pigment, a zinc halide phthalocyanine pigment having a color selected from the group consisting of Mg, Fe, Co, Ni, Zn, Cu a divalent metal in the group of Zr, Sn, and Pb as a central metal, and each phthalocyanine molecule is in 4 The benzene rings have a bond of 8 to 16 halogen atoms. Further, among them, it is particularly preferred that the zinc bromide phthalocyanine pigment is C.I. Pigment Green 58.

(2) a halogenated metal phthalocyanine pigment: such as a halogenated chloroaluminum phthalocyanine having a trivalent metal selected from the group consisting of Al, Sc, Ga, Y, and In as a central metal having a halogen atom in the center metal Any one of a hydroxyl group or a sulfonic acid group, and each phthalocyanine molecule has 8 to 16 halogen atoms bonded to the four benzene rings.

(3) a halogenated metal phthalocyanine pigment: such as a halogenated oxytitanium phthalocyanine or a vanadium oxyhalide phthalocyanine having a tetravalent metal selected from the group consisting of Si, Ti, V, Ge, Zr, and Sn as a central metal, The central metal has one oxygen atom or may be any of the same or different two halogen atoms, hydroxyl groups or sulfonic acid groups, and each phthalocyanine molecule has 8 to 16 halogen atoms bonded to four benzene rings. .

(4) A pigment comprising a halogenated metal phthalocyanine dimer: such as a halogenated μ-side oxy-aluminum phthalocyanine dimer, a halogenated μ-sulfur-aluminum phthalocyanine dimer, Al, Sc, Ga a trivalent metal in the group of Y and In as a central metal, and each phthalocyanine molecule has two molecules of a metal halide phthalocyanine having 8 to 16 halogen atoms bonded to four benzene rings as a constituent unit. Each of the central metals constituting the unit is bonded via a divalent atomic group selected from the group consisting of an oxygen atom, a sulfur atom, a sulfinyl group, and a sulfonyl group.

In particular, the halogenated metal phthalocyanine pigment is preferably one or more selected from the group consisting of CI Pigment Green 7, 36 and 58, and more preferably one or two selected from Green 36 and 58. . Specifically, the phthalocyanine-based green dye is preferably one or more selected from the group consisting of C.I. Solvent Green 4, the same 5, the same 7 and the same 28. In terms of phthalocyanine blue dye, specific In other words, it is preferably selected from one or more of CI solvent blue 4, the same 5, the same 25, the same 35, the same 36, the same 38, the same 58, the same 59, the same 67 and the same 70, more preferably selected One or two or more of the blue 25, the same 38, the same 67, and the same 70. In particular, the azo yellow organic dye is preferably selected from the group consisting of CI solvent yellow 2, the same 4, the same 14, the same 16, the same 18, the same 21, the same 56, the same 72, the same 82, the same 124 One or more of the same as 162 and 163, more preferably one or two selected from the group consisting of yellow 82 and the same 162.

(R pixel section)

The R pixel portion preferably contains a diketopyrrolopyrrole pigment and/or an anionic red organic dye. The diketopyrrolopyrrole pigment is, in particular, preferably selected from the group consisting of CI Pigment Red 254, 255, 264, 272, Orange 71 and 73, more preferably selected. One or more of red 254, the same 255, the same 264, and the same 272, particularly preferably CI Pigment Red 254. Specifically, the anionic red organic dye is preferably one or more selected from the group consisting of C.I. Solvent Red 124, Acid Red 52, and 289, and particularly preferably C.I. Solvent Red 124.

(B pixel section)

In the B pixel portion, a triarylmethane pigment represented by the following formula (1) is contained

(wherein R ¹ to R ⁶ each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms which may have a substituent, or an aryl group which may have a substituent. R ¹ to R ⁶ may have a substituent. In the case of an alkyl group, adjacent R ¹ and R ² , R ³ and R ⁴ , R ⁵ and R ⁶ may be bonded to form a ring structure. X ¹ and X ² are each independently represented by a hydrogen atom, a halogen atom, or An alkyl group having 1 to 8 carbon atoms which may have a substituent. Z ^{- is} represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6 and is selected from an integer of y = 0, 1, 2 or 3. The heteropoly side oxymetallate anion, or an anion of at least one of (SiMoW ₁₁ O ₄₀ ) ^4- /4 heteropoly side oxymetalate anion, or a defective Dawson type phosphotungstic acid heteropoly side oxymetallate anion. In the case where a plurality of formulas (1) are contained in one molecule, these may be the same structure or different structures).

In the general formula (1), R ¹ to R ⁶ may be the same or different. Therefore, -NRR (RR represents a combination of any of R ¹ R ² , R ³ R ⁴ , and R ⁵ R ⁶ ) may be symmetric or asymmetric

Adjacent R (R represents any one of R ¹ to R ⁶ ) is bonded to form a ring, which may be a ring crosslinked by a hetero atom. Specific examples of the ring include the following. The rings may have substituents.

Further, R ¹ to R ^{6 are} preferably independently derived from the viewpoint of chemical stability, and are a hydrogen atom, an alkyl group which may have a substituent, or an aryl group which may have a substituent.

Wherein R ¹ to R ⁶ are each independently a hydrogen atom; methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, secondary butyl, tert-butyl, pentane Any of an alkyl group such as a phenyl group, a cyclohexyl group, a hexyl group, a cyclohexyl group, a heptyl group, an octyl group or a 2-ethylhexyl group; and an aryl group such as a phenyl group or a naphthyl group is more preferred.

R ¹ to R ⁶ represent a case of an alkyl group or an aryl group, and the alkyl group or the aryl group may further have any substituent. The substituent which may further have such an alkyl group or an aryl group may, for example, be the following [Substituent Group Y].

[Substituent group Y]

Mention may be made of methyl, ethyl, propyl, isopropyl, cyclopropyl, butyl, isobutyl, secondary butyl, tert-butyl, pentyl, cyclopentyl, hexyl, cyclohexyl, heptyl. An alkyl group such as an octyl group or a 2-ethylhexyl group; an aryl group such as a phenyl group or a naphthyl group; a halogen atom such as a fluorine atom or a chlorine atom; a cyano group; a hydroxyl group; a methoxy group, an ethoxy group and a propoxy group; An alkoxy group having 1 to 8 carbon atoms such as a butoxy group; an amine group which may have a substituent such as an amine group, a diethylamino group, a dibutylamino group or an ethyl fluorenyl group; an acetamino group and a benzyl group; A mercapto group such as an alkyl group; an oxime group such as an acetoxy group or a benzyloxy group; and the like.

In the case of R ¹ to R ⁶ , an alkyl group having 1 to 8 carbon atoms which may have a substituent is more preferable, and more specifically, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, or the like may be mentioned. An unsubstituted alkyl group such as isobutyl, secondary butyl, pentyl, hexyl or 2-ethylhexyl; alkoxyalkyl group such as 2-methoxyethyl or 2-ethoxyethyl; a decyloxy group such as an ethyl ethoxyethyl group; a cyanoalkyl group such as a 2-cyanoethyl group; a fluoroalkane such as a 2,2,2-trifluoroethyl group or a 4,4,4-trifluorobutyl group; Base.

In the case where X ¹ and X ² are the above alkyl groups, it is more preferred to have any substituent. Examples of the substituent include a halogen atom such as a fluorine atom, a chlorine atom, a bromine atom or an iodine atom; an alkoxy group such as a methoxy group, an ethoxy group or a propoxy group; and the like. Specific examples of X ¹ and X ² include a halomethyl group such as a fluoromethyl group, a trifluoromethyl group, a trichloromethyl group or a 2,2,2-trifluoroethyl group; and a methoxymethyl group. Alkoxyalkyl group and the like.

In the case of X ¹ and X ² , a substituent having a moderate steric hindrance such as a hydrogen atom, a methyl group, a chlorine atom or a trifluoromethyl group which does not affect the degree of twisting is preferable. X ¹ and X ² are preferably a hydrogen atom, a methyl group or a chlorine atom, depending on the color tone and heat resistance.

The Z ^- line is represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6, which is selected from heteropoly side oxymetallate anions which are integers of y=0, 1, 2 or 3, or SiMoW ₁₁ O ₄₀ ) a heteropoly-side oxymetallate anion represented by ⁴ - 4, or an anionic triarylmethane compound of at least one of a Dawson-type phosphotungstic acid heteropolyoxymetalate anion. As the defect Dawson-type phosphotungstic acid, in particular, from the viewpoint of durability, a defect Dawson-type phosphotungstic acid heteropoly side oxymetallate anion (P ₂ W ₁₇ O ₆₁ ) ^10- /10 is preferable.

Specific examples of the triarylmethane pigment represented by the above formula (1) include, for example, the compounds described in the following Tables 1 to 7, but are not limited thereto as long as they do not exceed the scope of the present invention.

The RGB three-color pixel portion preferably contains CI solvent red 124 in the R pixel portion and a mixture of CI solvent blue 67 and CI solvent yellow 82 or the same 162 in the G pixel portion, in the B pixel portion. The triarylmethane pigment represented by the formula (1) is contained therein.

Further, the RGB three-color pixel portion preferably contains CI Pigment Red 254 in the R pixel portion as the coloring material, and one or two kinds selected from the group consisting of CI Pigment Green 7, 36, and 58 in the G pixel portion. As described above, the triarylmethane pigment represented by the above formula (1) is contained in the B pixel portion.

The RGB three-color pixel portion is preferably a coloring material, and further preferably contains, in the R pixel portion, a color selected from the group consisting of CI Pigment Red 177, 242, 166, 167, and 179; CI Pigment Orange 38, 71; CI Pigment yellow 150, the same 215, the same 185, the same 138, the same 139; CI solvent red 89; C.I. Solvent Orange 56; C.I. Organic dye pigment of at least one of Solvent Yellow 21, the same 82, the same 83:1, the same 33 and the same 162 group.

The RGB three-color pixel portion is preferably a coloring material, and further preferably contains, in the G pixel portion, a color selected from the group consisting of CI Pigment Yellow 150, the same 215, the same 185, and the same 138; CI Solvent Yellow 21, the same 82, and the same 83:1. And an organic dye pigment of at least one of the group of 33.

The RGB three-color pixel portion preferably contains, in the B pixel portion, a color selected from the group consisting of CI Pigment Violet 23; CI Basic Violet 10; CI Acid Blue 1, 90, and 83; CI Direct Blue 86. An organic dye pigment of at least one of CI Pigment Blue 15, the same 15:1, the same 15:2, the same 15:3, the same 15:4, and the same 15:6 group.

Further, the color filter is composed of a black matrix, an RGB three-color pixel portion, and a Y pixel portion, and the coloring material is preferably selected from the group consisting of CI Pigment Yellow 150, 215, and 185 as a coloring material. A yellow organic dye pigment of at least one of 138, 139; CI Solvent Yellow 21, 82, the same 83:1, the same 33, and the same 162 group.

In the color filter of the present invention, the chromaticity x and the chromaticity y of the XYZ color system under the C light source are reduced by the voltage holding ratio (VHR) of the liquid crystal layer, and the ion density (ID) is increased. Further, it is preferable to suppress the occurrence of problems such as whiteness, uneven alignment, and residual image.

The chromaticity x of the XYZ color system of the R pixel portion under the C light source is preferably 0.58 to 0.69, more preferably 0.62 to 0.68, and the chromaticity y is more preferably 0.30 to 0.36, still more preferably 0.31 to 0.35. Preferably, the chromaticity x is from 0.58 to 0.69, and the chromaticity y is from 0.30 to 0.36, more preferably the chromaticity x is from 0.62 to 0.68, and the chromaticity y is from 0.31 to 0.35.

The chromaticity x of the XYZ color system of the G pixel portion under the C light source is preferably from 0.19 to 0.35, more preferably from 0.20 to 0.26, and the chromaticity y is preferably from 0.54 to 0.76, more preferably from 0.64 to 0.74, more preferably The chromaticity x is 0.19 to 0.35, and the chromaticity y is 0.54 to 0.76, more preferably the chromaticity x is 0.20 to 0.26, and the chromaticity y is 0.64 to 0.74.

The chromaticity x of the XYZ color system of the B pixel portion under the C light source is preferably from 0.12 to 0.18, more preferably from 0.13 to 0.17, and the chromaticity y is preferably from 0.04 to 0.12, more preferably from 0.05 to 0.09, more preferably The chromaticity x is 0.12 to 0.18, and the chromaticity y is 0.04 to 0.12, more preferably the chromaticity x is 0.13 to 0.17, and the chromaticity y is 0.05 to 0.09.

The chromaticity x of the XYZ color system of the Y pixel portion under the C light source is preferably 0.46 to 0.50, more preferably 0.47 to 0.48, and the chromaticity y is preferably 0.48 to 0.53, more preferably 0.50 to 0.52, more preferably The chromaticity x is 0.46 to 0.50, and the chromaticity y is 0.48 to 0.53, more preferably the chromaticity x is 0.47 to 0.48, and the chromaticity y is 0.50 to 0.52.

Here, the XYZ color system refers to the color system recognized as the standard color system by the CIE (International Commission on Illumination) in 1931.

The chromaticity in each of the above-described pixel portions can be adjusted by changing the kind of the dye pigment to be used or the mixing ratio. For example, in the case of R pixels, an appropriate amount of a yellow dye pigment and/or an orange pigment is added to the red dye pigment; in the case of a G pixel, an appropriate amount of the yellow dye pigment is added to the green dye pigment; in the case of the B pixel, it is added to the blue dye pigment. Appropriate amount of purple dye pigment or yellow blue dye pigment can be adjusted. Further, it can be adjusted by appropriately adjusting the particle diameter of the pigment.

The color filter can be formed into a color filter pixel portion by a conventionally known method. In a representative method of the method of forming a pixel portion, there is a photolithography method in which a photocurable composition described later is applied to a surface on a side of a black matrix on which a transparent substrate for a color filter is provided, and is heated. After drying (prebaking), ultraviolet irradiation is applied through a mask to perform pattern exposure, and the photocurable compound corresponding to the pixel portion is cured, and then the unexposed portion is developed with a developing solution to remove the non-pixel portion. A method of fixing a pixel portion to a transparent substrate. In this method, a pixel portion of a hard colored film containing a photocurable composition is formed on a transparent substrate.

R pixels, G pixels, B pixels, pixels of other colors such as Y pixels can be used as needed, and each of the pixels modulates a photocurable composition described later, and by repeating the above operation, R pixels and G can be manufactured at predetermined positions. A color filter of a color pixel portion of a pixel, a B pixel, or a Y pixel.

The method of applying the photocurable composition described later to a transparent substrate such as glass may, for example, be a spin coating method, a slit coating method, a roll coating method, an ink jet method, or the like.

The drying conditions of the coating film of the photocurable composition applied to the transparent substrate vary depending on the type of each component, the blending ratio, and the like, and are usually from about 1 to 15 minutes at 50 to 150 °C. Further, it is preferable to use ultraviolet light having a wavelength range of 200 to 500 nm or visible light in the light hardening used for the photocurable composition. Various light sources that emit light in this wavelength range can be used.

Examples of the development method include a liquid-filling method, a dipping method, a spraying method, and the like. After exposure and development of the photocurable composition, the transparent substrate in which the pixel portion of the necessary color is formed is washed with water and dried. Such a place The obtained color filter is subjected to a predetermined time heat treatment (post-baking) at 90 to 280 ° C by a heating means such as a hot plate or an oven to remove volatile components in the colored coating film while The unreacted photocurable compound remaining in the hardened colored film of the photocurable composition is thermally cured, and the color filter is completed.

The coloring material for a color filter of the present invention can provide a liquid crystal display device which can prevent a decrease in the voltage holding ratio (VHR) of the liquid crystal layer and an increase in the ion density (ID) by using the liquid crystal composition of the present invention. And solve the problem of poor display, such as whiteness, uneven alignment, and residual image.

In the method for producing the photocurable composition, the dye and/or pigment composition for a color filter of the present invention, an organic solvent, and a dispersing agent are used as essential components, and these are mixed and stirred to be uniform. First, after the pigment dispersion liquid for forming the pixel portion of the color filter is prepared, a photocurable compound is added thereto, and a photocurable composition can be prepared by a thermoplastic resin or a photopolymerization initiator as needed. For the general method.

The organic solvent to be used herein may, for example, be an aromatic solvent such as toluene or xylene or methoxybenzene; ethyl acetate or propyl acetate or butyl acetate or propylene glycol monomethyl ether acetate; Acetate such as propylene glycol monoethyl ether acetate, diethylene glycol methyl ether acetate, diethylene glycol diethyl ether acetate, diethylene glycol propyl ether acetate, diethylene glycol butyl ether acetate a solvent; a propionate solvent such as ethoxyethyl propionate; an alcohol solvent such as methanol or ethanol; butyl cellosolve, propylene glycol monomethyl ether, diethylene glycol diethyl ether, diethylene glycol dimethyl ether An ether solvent such as an ether solvent, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone; an aliphatic group such as hexane a hydrocarbon solvent; a nitrogen compound solvent such as N,N-dimethylformamide, γ-butyrolactone, N-methyl-2-pyrrolidone, aniline or pyridine; γ-butyrolactone or the like a lactone solvent; a carbamate such as a mixture of methyl carbamate and ethyl urethane at 48:52.

For the dispersing agent used herein, for example, Disperbyk 130, Disperbyk 161, Disperbyk 162, Disperbyk 163, Disperbyk 170, Disperbyk 171, Disperbyk 174, Disperbyk 180, Disperbyk 182, Disperbyk 183, Disperbyk 184, Disperbyk, BYK CHEMI Corporation 185, Disperbyk 2000, Disperbyk 2001, Disperbyk 2020, Disperbyk 2050, Disperbyk 2070, Disperbyk 2096, Disperbyk 2150, Disperbyk LPN21116, Disperbyk LPN6919; Efka 46, Efka 47, Efka 452, Efka LP4008, Efka 4009, Efka LP4010, Efka Efka LP4050, LP4055, Efka 400, Efka 401, Efka 402, Efka 403, Efka 450, Efka 451, Efka 453, Efka 4540, Efka 4550, Efka LP4560, Efka 120, Efka 150, Efka 1501, Efka 1502, Efka 1503; Lubrizol's Solsperse 3000, Solsperse 9000, Solsperse 13240, Solsperse 13650, Solsperse 13940, Solsperse 17000, 18000, Solsperse 20000, Solsperse 21000, Solsperse 20000, Solsperse 24000, Solsperse 26000, Solsperse 27000, Solsperse 28000, Solsperse 32000, Solsperse 36000, Solsperse 37 000, Solsperse 38000, Solsperse 41000, Solsperse 42000, Solsperse 43000, Solsperse 46000, Solsperse 54000, Solsperse 71000; Ajinomoto Dispersing agent of Ajisper PB711, Ajisper PB821, Ajisper PB822, Ajisper PB814, Ajisper PN411, Ajisper PA111, etc., or acrylic resin, urethane resin, alkyd resin, wood rosin, rubber rosin, etc. Natural rosin such as tall oil rosin; denatured rosin such as polymerized rosin, dismutation rosin, hydrogenated rosin, oxidized rosin, maleic rosin, rosin amine, lime rosin A rosin derivative such as a rosin alkylene oxide adduct, a rosin alkyd adduct, or a rosin modified phenol, etc., which contains a liquid and water-insoluble synthetic resin at room temperature. The addition of such dispersing agents or resins also contributes to a reduction in flocculation, an improvement in pigment dispersion stability, and an increase in viscosity characteristics of the dispersion.

Further, as the dispersing aid, an organic pigment derivative such as a phthalimide methylamine derivative, a homosulfonic acid derivative, a N-(dialkylamino)methyl derivative, and the same N may be contained. a -(dialkylaminoalkyl)sulfonate decylamine derivative or the like. Of course, these derivatives may be used in combination of two or more kinds of different kinds.

The thermoplastic resin prepared by using the photocurable composition may, for example, be a urethane resin, an acrylic resin, a polyamine resin, a polyimide resin, or a styrene maleic acid resin. A styrene maleic anhydride resin or the like.

Examples of the photocurable compound include 1,6-hexanediol diacrylate, ethylene glycol diacrylate, neopentyl glycol diacrylate, triethylene glycol diacrylate, and bis(propylene oxide). 2-functional monomer such as ethoxylated bisphenol A or 3-methylpentanediol diacrylate; trimethylolpropyl propyl ester (trimethylolpropane triacrylate), neopentyl glycol triacrylate, bis[2-(methyl)propenyl oxyethyl) cis isocyanate, dineopentaerythritol hexaacrylate, dipentaerythritol pentaacrylate A polyfunctional monomer having a relatively large molecular weight, such as a polyfunctional monomer having a relatively small molecular weight such as an alcohol ester, a polyester acrylate, a polyurethane acrylate, or a polyether acrylate.

The photopolymerization initiator may, for example, be acetophenone, benzophenone, benzyldimethylketanol, benzyl peroxide or 2-chloro 9-oxosulfuric acid. , 1,3-bis(4'-azidobenzylidene)-2-propane, 1,3-bis(4'-azidobenzylidene)-2-propane-2'-sulfonic acid, 4 , 4'-diaziridine-2,2'-disulfonic acid and the like. For example, "Irgacure (trade name) - 184", "Irgacure (trade name) - 369", "Darocure (trade name) - 1173", "made by BASF", manufactured by BASF Corporation, are commercially available. "Lucariin TPO", "Kayacure (trade name) DETX" and "Kayacure (trade name) OA" manufactured by Nippon Kayaku Co., Ltd.; "Vicure 10" and "Vicure 55" manufactured by STAUFFER; "Trigonal PI" manufactured by Akzo, Sandoz "SANDORY 1000", "Deap" made by UPJOHN, "biimidazole" made by Heijin Chemical Co., Ltd., etc.

Further, a photo-sensitizer known in the art can be used in combination with the above-mentioned photopolymerization initiator. The photosensitizer may, for example, be an amine, a urea, a compound having a sulfur atom, a compound having a phosphorus atom, a compound having a chlorine atom or a nitrile or another compound having a nitrogen atom. These may be used alone or in combination of two or more.

The compounding ratio of the photopolymerization initiator is not particularly limited, and is preferably in the range of 0.1 to 30% by mass based on the mass of the compound having a photopolymerizable or photocurable functional group. At less than 0.1%, it tends to When the sensitivity of the photocuring is reduced, when the coating film is dried, the photopolymerization initiator is precipitated, and the physical properties of the coating film are deteriorated.

Using the above-mentioned respective materials, the dye and/or pigment composition for a color filter of the present invention is stirred with 300 to 1000 parts of an organic solvent and 1 to 100 parts of a dispersant per 100 parts by mass. The dye pigment liquid is obtained by dispersing into uniformity. Next, the pigment dispersion liquid is added in an amount of 3 to 20 parts per part of the pigment composition for a color filter of the present invention, and the photocurable compound is 0.05 to 3 per part. The photopolymerization initiator may be further added with an organic solvent as needed, and stirred and dispersed to be uniform, whereby a photocurable composition for forming a pixel portion of the color filter can be obtained.

As the developer, a well-known organic solvent or an aqueous alkali solution can be used. In particular, the photocurable composition contains a thermoplastic resin or a photocurable compound, and at least one of them has an acid value, and in the case of exhibiting alkali solubility, it is washed with an aqueous alkali solution in the pixel portion of the color filter. The formation has an effect.

The method of manufacturing the color filter pixel portion caused by the photolithography method is described in detail, and the color filter pixel portion modulated by the pigment composition for a color filter of the present invention is subjected to other electrodeposition methods. , transfer method, micelle electrolysis method, PVED (photovoltaic electrodeposition) method, ink inkjet method, reverse printing method, thermosetting method, etc., forming various color pixel parts to produce color Filters are also available.

(alignment film)

In the liquid crystal display device of the present invention, in order to align the liquid crystal composition on the surface of the first substrate and the second substrate that is in contact with the liquid crystal composition, the liquid crystal display device and the color filter are considered to be necessary for the alignment film. When the film is disposed between the liquid crystal layers, even if the film thickness of the alignment film is thick, it is as thin as 100 nm or less, and the interaction between the dye such as a pigment constituting the color filter and the liquid crystal compound constituting the liquid crystal layer is not completely cut off.

Further, in the liquid crystal display device which does not use the alignment film, the pigment such as the pigment constituting the color filter has a larger interaction with the liquid crystal compound constituting the liquid crystal layer.

As the alignment film material, a transparent organic material such as polyimine, polyamine, BCB (benzocyclobutene polymer), polyvinyl alcohol or the like can be used, in particular, p-phenylenediamine, 4, An aliphatic or lipid such as an aliphatic or alicyclic diamine such as 4'-diaminodiphenylmethane or a butane tetracarboxylic anhydride or 2,3,5-tricarboxycyclopentyl acetic anhydride or the like The polyamic acid synthesized by the aromatic tetracarboxylic anhydride such as a cyclic tetracarboxylic anhydride or a pyromellitic dianhydride is preferably a ruthenium imidized polyimide film. In the case of the alignment method, polishing is generally used, and in the case of use in a vertical alignment film or the like, the alignment may not be used.

In the case of the alignment film material, a material containing chalcone, cinamate, cinnamyl or azo group in the compound may be used, and may be used in combination with a material such as polyimine or polyamine. In this case, the alignment film may also be polished, or a photo-alignment technique may be used.

The alignment film is generally applied to a substrate, and the alignment film material is applied by a spin coating method or the like to form a resin film. However, a one-axis stretching method, an Iangmuir-Blodgett method, or the like may be used.

(transparent electrode)

In the liquid crystal display device of the present invention, a conductive metal oxide can be used as the material of the transparent electrode, and indium oxide (In ₂ O ₃ ) or tin oxide (SnO ₂ ) can be used as the metal oxide. Zinc oxide (ZnO), indium tin oxide (In ₂ O ₃ -SnO ₂ ), indium zinc oxide (In ₂ O ₃ -ZnO), added lanthanum titanium dioxide (Ti _1-x Nb _x O ₂ ), doped oxyfluoride tin A graphene nanobelt or a metal nanowire or the like is preferably zinc oxide (ZnO), indium tin oxide (In ₂ O ₃ -SnO ₂ ) or indium zinc oxide (In ₂ O ₃ -ZnO). In the patterning of the transparent conductive films, a photolithography method or a photomask method or the like can be used.

[Examples]

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS One of the best modes of the present invention is as follows, but the present invention is not limited to the embodiments. Moreover, "%" in the compositions of the following examples and comparative examples means "% by mass".

In the examples, the properties measured were as follows.

T _ni : nematic phase-isotropic liquid phase transfer temperature (°C)

△n: refractive index anisotropy at 25 ° C

△ ε: 25 ° C dielectric anisotropy

η: viscosity in 20 ° C (mPa ‧ s)

γ ₁ : rotational viscosity (mPa ‧ s) at 25 ° C

d _gap : the gap between the first substrate and the second substrate of the unit cell (μm)

VHR: Voltage holding ratio (%) at 70 °C

(Injecting a liquid crystal composition into a cell with a cell thickness of 3.5 μm , plus 5 V, when measured at a frame time of 200 ms and a pulse width of 64 μs , the ratio of the measured voltage to the initial applied voltage is % indicates the value)

ID: ion density (pC/cm ² ) at 70 ° C

(Injecting a liquid crystal composition into a unit cell having a cell thickness of 3.5 μm , and adding an extrapolation value of 20 V to MTR-1 (manufactured by Toyo Technica Co., Ltd.) at a frequency of 0.05 Hz)

Afterimage: The afterimage evaluation of the liquid crystal display element was performed by displaying the predetermined fixed pattern for 1000 hours in the display area, and the residual image level of the pattern was fixed when the full screen was uniformly displayed, and the following four stages of evaluation were visually performed.

◎ no residual image

○ There are very few residual images, which are also acceptable levels.

△ There is residual image, the level that cannot be tolerated

×There is a bad shadow

In addition, the following description is used for the description of the compounds in the examples.

(side chain)

-n -C _n H _2n+1 linear alkyl group having n carbon atoms

-On -OC _n H _2n+1 linear alkoxy group with n number of carbon atoms

(ring structure)

[Make color filter] [Modulation of coloring composition] [Red dye coloring composition 1]

Put 10 parts of red dye 1 (CI solvent red 124) into plastic bottles, add 55 parts of propylene glycol monomethyl ether acetate, 0.3-0.4mm ΦSEPR beads, to paint conditioner (Toyo Seiki shares) After dispersing for 4 hours, the product was filtered through a 5 μm filter to obtain a dye coloring liquid. 75.00 parts of dye coloring liquid, 5.50 parts of polyester acrylate resin (Aronics (trade name) M7100, manufactured by Toagosei Chemical Co., Ltd.), and 5.00 parts of dipentaerythritol hexaacrylate (KAYARAD (trade name) DPHA) , manufactured by Nippon Kayaku Co., Ltd.), 1.00 parts of benzophenone (KAYACURE (trade name) BP-100, manufactured by Nippon Kayaku Co., Ltd.), 13.5 parts of Ucar Ester EEP, stirred with a dispersing mixer, and 1.0 μm The filter of the pore size was filtered to obtain a red dye coloring composition 1. .

[Red dye coloring composition 2]

8 parts of red dye 1 (CI solvent red 124) and 2 parts of yellow dye 1 (CI solvent yellow 21) were used instead of the above red dye coloring composition 1 of 10 parts of red dye 1, in the same manner as above, to obtain a red dye coloring composition. Object 2.

[Red dye coloring composition 3]

10 parts of red dye 2 (C.I. Solvent Red 1) was used instead of the above red dye coloring composition 1 of 10 parts of red dye 1, and the same as above, a red dye coloring composition 3 was obtained.

[Green dye coloring composition 1]

3 parts of blue dye 1 (CI solvent blue 67) and 7 parts of yellow dye 1 (CI solvent yellow 162) were used instead of the above red dye coloring composition 1 of 10 parts of red dye 1, and the same as above, a green dye was obtained. Coloring composition 1.

[Green dye coloring composition 2]

4 parts of yellow dye 1 (CI solvent yellow 162) and 3 parts of yellow dye 3 (CI solvent yellow 82) were used instead of the above-mentioned green dye coloring composition 1 of 7 parts of yellow dye 1, in the same manner as above, to obtain a green dye coloring composition. Object 2.

[Green dye coloring composition 3]

The green dye coloring composition 3 was obtained by using 10 parts of green dye 1 (C.I. Solvent Green 7) in place of the above-mentioned green dye coloring composition 1 of 3 parts of blue dye 1 and 7 parts of yellow dye 1.

[Blue dye coloring composition 1]

The blue dye coloring composition 1 was obtained by using 10 parts of blue dye 2 (C.I. Solvent Blue 12) in place of the above-mentioned red dye coloring composition 1 of 10 parts of red dye 1.

[Yellow dye coloring composition 1]

The yellow dye coloring composition 1 was obtained by using 10 parts of yellow dye 1 (C.I. Solvent Yellow 21) in place of 10 parts of the red dye 1 of the above red dye coloring composition 1.

[Yellow dye coloring composition 2]

10 parts of yellow dye 4 (C.I. Solvent Yellow 2) was used in place of 10 parts of yellow dye 1 of the above yellow dye coloring composition 1, and the yellow dye coloring composition 2 was obtained in the same manner as above.

[Red Pigment Coloring Composition 1]

10 parts of red pigment 1 (CI Pigment Red 254, "IRGAPHOR RED BT-CF" manufactured by BASF Corporation) was placed in a plastic bottle, and 55 parts of propylene glycol monomethyl ether acetate and 7.0 parts of Disperbyk LPN21116 (made by BYK CHEMI Co., Ltd.) were added. ), 0.3-0.4mm Φ zirconia beads "ER-120S" manufactured by Saint-Gobain Co., Ltd., dispersed by a paint conditioner (manufactured by Toyo Seiki Co., Ltd.) for 4 hours, and then filtered through a filter of 1 μm to obtain a pigment dispersion liquid. . 75.00 parts of the pigment dispersion and 5.50 parts of a polyester acrylate resin (Aronics (trade name) M7100, manufactured by Toagosei Chemical Co., Ltd.), and 5.00 parts of dipentaerythritol hexaacrylate (KAYARAD (trademark) were stirred with a dispersing mixer. Name) DPHA, manufactured by Nippon Kayaku Co., Ltd.), 1.00 parts of benzophenone (KAYACURE (trade name) BP-100, manufactured by Nippon Kayaku Co., Ltd.), 13.5 parts of Ucar Ester EEP, filter with pore size of 1.0 μm Filtration was carried out to obtain a red pigment coloring composition 1.

[Red Pigment Coloring Composition 2]

In place of the above red pigment coloring composition, 6 parts of red pigment 1, 2 parts of red pigment 2 (FASTOGEN SUPER RED ATY-TR, manufactured by CI Pigment Red 177 DIC Co., Ltd.), and 2 parts of yellow pigment 2 (CI Pigment Yellow 139) were used. 10 parts of red pigment 1 was obtained in the same manner as above to obtain a red pigment coloring composition 2.

[Green Pigment Coloring Composition 1]

6 parts of green pigment 1 (C.I. Pigment Green 36, "FASTOGEN GREEN 2YK-CF" by DIC Corporation) and 4 parts of yellow pigment 1 (C.I. Pigment Yellow 150, FANCHON FAST manufactured by BAYER) YELLOW E4GN), in place of the above red pigment coloring composition 1 of 10 parts of red pigment 1, in the same manner as described above, a green pigment coloring composition 1 was obtained.

[Green Pigment Coloring Composition 2]

4 parts of green pigment 2 (CI Pigment Green 58, FDA-made FASTOGEN GREEN A110) and 6 parts of yellow pigment 3 (CI Pigment Yellow 138) were used instead of the above-mentioned green pigment coloring composition 1 of 6 parts of green pigment 1. Four parts of the yellow pigment 1 were obtained in the same manner as above to obtain a green pigment coloring composition 2.

[Blue pigment coloring composition 1]

1.80 parts of the triarylmethane pigment represented by the formula (1) (Compound No. 2 of Table 1), 2.10 parts of BYK-2164 (BYK CHEMI), 11.10 parts of propylene glycol monomethyl ether acetate, 0.3-0.4 mm Φ SEPR The beads were placed in a plastic bottle and dispersed by a paint conditioner (manufactured by Toyo Seiki Co., Ltd.) for 4 hours to obtain a pigment dispersion. 75.00 parts of a pigment dispersion liquid, 5.50 parts of a polyester acrylate resin (Aronics (trade name) M7100, manufactured by Toagosei Chemical Co., Ltd.), and 5.00 parts of dipentaerythritol hexaacrylate (KAYARAD (trade name) DPHA) , Japan Pharmaceutical Co., Ltd.), 1.00 parts of benzophenone (KAYACURE (trade name) BP-100, manufactured by Nippon Kayaku Co., Ltd.), 13.5 parts of Ucar Ester EEP (made by UNION CARBIDE), stirred with a dispersing mixer And filtered with a filter having a pore size of 1.0 μm to obtain a blue pigment coloring composition 1.

[Blue pigment coloring composition 2]

A blue pigment coloring composition 2 was obtained in the same manner as above except that the triarylmethane pigment represented by the formula (1) (Compound No. 5 of Table 1) was used instead of the above-mentioned blue pigment coloring composition 1 of the triarylmethane pigment.

[Blue pigment coloring composition 3]

The triarylmethane pigment (Table 1 Compound No. 1) represented by the formula (1) was used in place of the above-mentioned blue pigment coloring composition 1 of the triarylmethane pigment, and the blue pigment coloring composition 3 was obtained in the same manner as above.

[Blue pigment coloring composition 4]

A blue pigment coloring composition 4 was obtained in the same manner as above except that the triarylmethane pigment represented by the formula (1) (Compound No. 29 of Table 4) was used instead of the above-described blue pigment coloring composition 1 of the triarylmethane pigment.

[Yellow Pigment Coloring Composition 1]

In place of 10 parts of the red pigment 1 of the above red pigment coloring composition 1, 10 parts of yellow pigment 1 (C.I. Pigment Yellow 150, FANCHON FAST YELLOW E4GN, manufactured by LANXESS Co., Ltd.) was used, and a yellow pigment coloring composition 1 was obtained in the same manner as above.

[Production of color filter]

The glass substrate in which the black matrix was formed in advance was applied by spin coating to a red colored composition to have a film thickness of 2 μm . After drying at 70 ° C for 20 minutes, the ultraviolet rays were exposed in a stripe pattern through a mask using an exposure machine equipped with an ultrahigh pressure mercury lamp. It was spray-developed with an alkali developer for 90 seconds, washed with ion-exchanged water, and air-dried. Further, in a clean oven, post-baking was performed at 230 ° C for 30 minutes, and red pixels of a strip-shaped coloring layer were formed on the transparent substrate.

Next, it was also applied to a film thickness of 2 μm by spin coating in the same manner as the green coloring composition. After drying, the exposure machine is exposed by exposing the strip-shaped color layer to the red pixel, and a green pixel adjacent to the red pixel is formed.

Next, the blue coloring composition was similarly applied by spin coating to form a blue pixel adjacent to the red pixel and the green pixel with a film thickness of 2 μm . Thereby, a color filter having strip-shaped pixels of three colors of red, green, and blue on a transparent substrate can be obtained.

A yellow coloring composition can be formed as needed, and similarly, a blue pixel adjacent to the red pixel and the green pixel can be formed by spin coating at a film thickness of 2 μm . Thereby, a color filter having strip-shaped pixels of four colors of red, green, blue, and yellow is obtained on the transparent substrate.

Color filters 1 to 4 and comparative color filters 1 were prepared using the dye coloring composition or the pigment coloring composition shown in Table 8.

For each pixel portion of the color filter, an Olympus microscope MX-50 and an Otsuka electronic spectrophotometer MCPD-3000 microspectrophotometer were used to measure the x value and the y value in the C light source of the CIE 1931 XYZ color system. . The results are shown in Table 9 below.

(Examples 1 to 4)

An electrode structure is formed on the first and second substrates, and a vertical alignment alignment film is formed on each of the opposite sides, and then subjected to a weak grinding treatment to form a VA unit cell, and the following is sandwiched between the first substrate and the second substrate. The liquid crystal composition 1 is shown. The physical property values of the liquid crystal composition 1 are shown in Table 10. Next, liquid crystal display devices (d _gap = 3.5 μm, alignment film SE-5300) of Examples 1 to 4 were produced using the color filters 1 to 4 shown in Table 8. The VHR and ID of the obtained liquid crystal display device were measured. Moreover, the afterimage evaluation of the obtained liquid crystal display device was performed. The results are shown in Table 11.

It is understood that the liquid crystal composition 1 has a practical liquid crystal layer temperature range of 81 ° C as a liquid crystal composition for TV, has a large absolute value of dielectric anisotropy, and has low viscosity and optimum Δn.

The liquid crystal display devices of Examples 1 to 4 can realize high VHR and small ID. In addition, there is no residual image in the afterimage evaluation, or even if there is an afterimage, it is extremely small, and it is an allowable level.

(Examples 5 to 12)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 12 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 5 to 12, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 13 and 14.

Table 12

The liquid crystal display devices of Examples 5 to 12 can realize a high VHR and a small ID. In addition, there is no residual image in the afterimage evaluation, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 13 to 28)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 15 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 13 to 28, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 16 to 18.

The liquid crystal display devices of Examples 13 to 24 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 25 to 36)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 19 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 25 to 36, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 20 to 22.

The liquid crystal display devices of Examples 25 to 36 can realize high VHR and small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 37 to 48)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 23 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 37 to 48, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 24 to 26.

The liquid crystal display devices of Examples 41 to 48 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 49 to 60)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 27 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 49 to 60, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 28 to 30.

The liquid crystal display devices of Examples 49 to 60 can realize high VHR and small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 61 to 76)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 31 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 61 to 72, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 32 to 34.

The liquid crystal display devices of Examples 61 to 72 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is an allowable level.

(Examples 73 to 84)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 35 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 73 to 84, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 36 to 38.

The liquid crystal display devices of Examples 77 to 92 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 85 to 96)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 39 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 85 to 96, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 40 to 42.

The liquid crystal display devices of Examples 85 to 96 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 97 to 108)

In the same manner as in Example 1, the liquid crystal compositions shown in Table 43 were sandwiched, and the color filters shown in Table 8 were used to prepare liquid crystal display devices of Examples 97 to 108, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 44 to 46.

The liquid crystal display devices of Examples 97 to 108 can realize high VHR and small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 109 to 120)

0.3% by mass of 2-methyl-acrylic acid 4'-{2-[4-(2-propenyloxy-ethyl)-phenoxycarbonyl]-ethyl}-biphenyl was mixed in the liquid crystal composition 1. The 4-yl ester was prepared into a liquid crystal composition 28. The liquid crystal composition 31 was sandwiched between the VA unit cells used in Example 1, and a driving voltage was applied between the electrodes, and ultraviolet rays (3.0 J/cm ² ) were irradiated for 600 seconds to carry out polymerization treatment, and then, as shown in Table 8, The color filters 1 to 4 were fabricated into liquid crystal display devices of Examples 109 to 112, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Table 47.

The liquid crystal display devices of Examples 109 to 112 can realize high VHR and small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 113 to 116)

A liquid crystal composition 29 was prepared by mixing 0.3% by mass of a biphenyl methacrylate-4,4'-diyl group in the liquid crystal composition 13. The liquid crystal composition 29 was sandwiched between the VA unit cells used in Example 1, and a driving voltage was applied between the electrodes, and ultraviolet rays were irradiated (3.0 J/cm ² ) for 600 seconds to carry out polymerization treatment. Next, the color shown in Table 8 was used. The filters 1 to 4 were fabricated into liquid crystal display devices of Examples 113 to 116, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Table 48.

The liquid crystal display devices of Examples 113 to 116 can realize high VHR and small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Examples 117 to 120)

A liquid crystal composition 30 was prepared by mixing 0.3% by mass of 3-fluorobiphenyl-4,4'-diyl methacrylate in the liquid crystal composition 19. The liquid crystal composition 30 was sandwiched between the VA unit cells used in Example 1, and a driving voltage was applied between the electrodes, and ultraviolet rays (3.0 J/cm ² ) were irradiated for 600 seconds to carry out polymerization treatment, and thereafter, as shown in Table 8, The color filters 1 to 4 were prepared to prepare liquid crystal display devices of Examples 129 to 132, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Table 49.

The liquid crystal display devices of Examples 117 to 120 can realize a high VHR and a small ID. Moreover, the afterimage evaluation has no residual image, or even if there is an afterimage, it is extremely small and is a tolerable level.

(Comparative Examples 1 to 4)

The liquid crystal composition 1 shown below was sandwiched between the VA unit cells used in Example 1. The physical property values of the comparative liquid crystal compositions are shown in Table 50. Using the color filters 1 to 4 shown in Table 8, liquid crystal display devices of Comparative Examples 1 to 4 were produced, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Table 51.

In the liquid crystal display devices of Comparative Examples 1 to 4, the VHR was lower and the ID was larger as compared with the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm the occurrence of the afterimage, and is not an acceptable level.

(Comparative Examples 5 to 12)

In the same manner as in the first embodiment, the liquid crystal compositions shown in Table 52 were clamped, and the color filters 1 to 4 shown in Table 8 were used to fabricate the liquid crystal display devices of Comparative Examples 5 to 12, and the VHR and ID thereof were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 53 to 54.

In the liquid crystal display devices of Comparative Examples 5 to 12, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 13 to 24)

In the same manner as in the first embodiment, the liquid crystal compositions shown in Table 55 were clamped, and the color filters 1 to 4 shown in Table 8 were used to fabricate the liquid crystal display devices of Comparative Examples 13 to 24, and the VHR and ID thereof were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 56 to 58.

In the liquid crystal display devices of Comparative Examples 13 to 24, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 25 to 36)

In the same manner as in the first embodiment, the comparative liquid crystal compositions shown in Table 59 were sandwiched, and the color filters 1 to 4 shown in Table 8 were used to prepare liquid crystal display devices of Comparative Examples 25 to 36, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 60 to 62.

In the liquid crystal display devices of Comparative Examples 25 to 36, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 37 to 48)

In the same manner as in the first embodiment, the liquid crystal compositions shown in Table 63 were sandwiched, and the color filters 1 to 4 shown in Table 8 were used to fabricate the liquid crystal display devices of Comparative Examples 37 to 48, and the VHR and ID thereof were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 64 to 66.

In the liquid crystal display devices of Comparative Examples 37 to 48, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 49 to 60)

In the same manner as in the first embodiment, the comparative liquid crystal compositions shown in Table 67 were sandwiched, and the color filters 1 to 4 shown in Table 8 were used to prepare liquid crystal display devices of Comparative Examples 49 to 60, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 68 to 70.

In the liquid crystal display devices of Comparative Examples 49 to 60, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 61 to 72)

In the same manner as in the first embodiment, the liquid crystal compositions of Comparative Examples 61 to 72 were produced by comparing the liquid crystal compositions shown in the table 71 with the color filters 1 to 4 shown in Table 8, and the VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 72 to 74.

Comparing the liquid crystal display devices of 61 to 72, the VHR is lower and the ID is larger as compared with the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 73 to 84)

In the same manner as in the first embodiment, the comparative liquid crystal compositions shown in Table 75 were clamped, and the color filters 1 to 4 shown in Table 8 were used to prepare liquid crystal display devices of Comparative Examples 73 to 84, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 76 to 78.

Comparing the liquid crystal display devices of 73 to 84, compared with the liquid crystal display device of the present invention, the VHR is low and the ID is also increased. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 85 to 88)

In the same manner as in the first embodiment, the comparative liquid crystal compositions shown in Table 79 were sandwiched, and the color filters 1 to 4 shown in Table 8 were used to fabricate liquid crystal display devices of Comparative Examples 85 to 88, and their VHR and ID were measured. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Table 80.

Comparing the liquid crystal display devices of 85 to 88, compared with the liquid crystal display device of the present invention, the VHR is low and the ID is also increased. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

(Comparative Examples 89 to 96)

The VA unit cells used in Example 1 were each sandwiched with liquid crystal compositions 1, 2, 8, 13, 14, 19, 20 and 26, and Comparative Color Filters 1 shown in Table 1 were used to prepare Comparative Examples 89 to 96. The liquid crystal display device is measured for its VHR and ID. Moreover, the afterimage evaluation of the liquid crystal display device was performed. The results are shown in Tables 81 and 82.

In the liquid crystal display devices of Comparative Examples 89 to 96, the VHR was lower and the ID was larger than that of the liquid crystal display device of the present invention. Moreover, the afterimage evaluation can also confirm that the afterimage occurs, and is not an acceptable level.

1‧‧‧Substrate

2‧‧‧Color filter layer

2a‧‧‧Color filter layer with specific pigments

3a‧‧‧Transparent electrode layer (common electrode)

3b‧‧‧pixel electrode layer

4‧‧‧Alignment film

5‧‧‧Liquid layer

5a‧‧‧Liquid crystal layer containing specific liquid crystal composition

Fig. 1 is a view showing an example of a conventional general liquid crystal display device.

Fig. 2 is a view showing an example of a liquid crystal display device of the present invention.

Claims (16)

A liquid crystal display device comprising: a first substrate; a second substrate; a liquid crystal composition layer sandwiched between the first substrate and the second substrate; and a color filter comprising a black matrix and at least RGB three-color pixels a pixel electrode; and a common electrode comprising a liquid crystal composition containing 30 to 50% of a compound represented by the formula (I) (wherein R ¹ and R ² are each independently, and represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or 2 to 2 carbon atoms; 8 alkenyloxy; A represents 1,4-phenylene or trans-1,4-cyclohexenyl); contains 5 to 20% of the compound of the formula (II-1) (wherein R ³ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and 25 to 45 % of the compound of the formula (II-2) (wherein R ⁵ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; ⁶ represents an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 3 to 8 carbon atoms; and B is substituted by fluorine. 1,4-phenylene or trans-1,4-cyclohexenyl), the RGB three-color pixel portion contains, as a coloring material, a three-part group represented by the following formula (1) in the B pixel portion. Methane pigment (wherein R ¹ to R ⁶ each independently represent a hydrogen atom, an alkyl group having 1 to 8 carbon atoms which may have a substituent, or an aryl group which may have a substituent; and R ¹ to R ⁶ represent a substituent which may have a substituent; In the case of an alkyl group, adjacent R ¹ and R ² , R ³ and R ⁴ , R ⁵ and R ⁶ may also be bonded to form a ring structure; X ¹ and X ² each independently represent a hydrogen atom, a halogen atom, or may have a substituent having an alkyl group having 1 to 8 carbon atoms; Z ^- represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6, which is selected from an integer of y = 0, 1, 2 or 3 a poly side oxymetallate anion, or an anion of at least one of (SiMoW ₁₁ O ₄₀ ) ^4- /4 heteropoly side oxymetalate anion, or a defective Dawson type phosphotungstic acid heteropoly oxymetallate anion, in 1 The molecule contains a plurality of formulas (1), which may be the same structure or a different structure). The liquid crystal display device of claim 1, wherein the liquid crystal composition layer further contains 5 to 20% of a compound represented by the formula (III) (wherein R ⁷ and R ⁸ are each independently, and represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms or 2 to 2 carbon atoms; 8 alkenyloxy; D, E, F and G are each independently, meaning 1,4-phenyl or trans-1,4-cyclohexene which can be substituted by fluorine; Z ² represents a single bond, -OCH ₂ -, -OCO-, -CH ₂ O- or -COO-; n represents 0 or 1, but n represents 0, and Z ² represents -OCH ₂ -, -OCO-, -CH ₂ O- or -COO -, or D, E and G represent a 1,4-phenylene group which may be substituted by fluorine). The liquid crystal display device of claim 1 or 2, wherein the RGB three-color pixel portion contains, as a coloring material, a diketopyrrolopyrrole pigment and/or an anionic red organic dye in the R pixel portion; The pixel portion contains at least one selected from the group consisting of a halogenated metal phthalocyanine pigment, a phthalocyanine green dye, a mixture of a phthalocyanine blue dye and an azo yellow organic dye. The liquid crystal display device according to any one of claims 1 to 3, wherein the B pixel portion contains the triarylmethane pigment of the formula (1), and each of R ¹ to R ⁶ independently represents a hydrogen atom. a C 1 to 4 alkyl group having a substituent, or a phenyl group; X ¹ and X ² are a hydrogen atom, and Z ^{- is} represented by (P ₂ Mo _y W _18-y O ₆₂ ) ^6- /6, which is selected From a heteropoly side oxymetallate anion of y = 0, 1, 2 or 3, or a heteropoly side oxymetallate anion of (SiMoW ₁₁ O ₄₀ ) ^4- /4, or a defective Dawson type phosphotungstic acid An anion of at least one of an anion (P ₂ W ₁₇ O ₆₁ ) ^10- /10. The liquid crystal display device according to any one of claims 1 to 4, wherein the G pixel portion contains a halogenated metal phthalocyanine pigment having a selected from the group consisting of Al, Si, Sc, Ti, V, Mg, Fe. a metal of a group of Co, Ni, Zn, Cu, Ga, Ge, Y, Zr, Nb, In, Sn, and Pb as a central metal halide metal phthalocyanine pigment, in the case where the center metal is trivalent, The metal bond is bonded to any one of a halogen atom, a hydroxyl group or a sulfonic acid group, or is cross-linked with oxygen or sulfur. In the case where the central metal is a tetravalent metal, one of the central metal bonds is bonded thereto. The oxygen atom may be either of the same or different two halogen atoms, a hydroxyl group or a sulfonic acid group. The liquid crystal display device according to any one of claims 1 to 5, wherein the R pixel portion contains CI solvent red 124, and the G pixel portion contains CI solvent blue 67 and CI solvent yellow 82 or the same 162 mixture. The liquid crystal display device according to any one of claims 1 to 5, wherein the R pixel portion contains CI Pigment Red 254, and the G pixel portion contains one selected from the group consisting of CI Pigment Green 7, 36 and 58 Or more than two. The liquid crystal display device according to any one of claims 1 to 7, wherein the color filter comprises a black matrix, an RGB three-color pixel portion, and a Y pixel portion, and the coloring material is included in the Y pixel portion. A yellow organic dye pigment comprising at least one of CI Pigment Yellow 150, 215, 185, 138, 139; CI Solvent Yellow 21, 82, and 83:1, 33, and 162. The liquid crystal display device according to any one of claims 1 to 8, wherein in the formula (I), A represents a compound of 1,4-phenylene group and A represents trans-1,4-cyclohexane. The compounds of the alkenyl group each contain at least one or more. The liquid crystal display device according to any one of claims 1 to 9, wherein in the formula (II-2), B represents a compound of 1,4-phenylene group and B represents a trans-1,4-ring ring. The compound of hexenyl group each contains at least one type or more. The liquid crystal display device according to any one of claims 2 to 10, wherein the compound represented by the formula (II-1), the formula (II-2) and the formula (III) contains 35 to 70%. The liquid crystal display device according to any one of claims 1 to 11, wherein the liquid crystal composition constituting the liquid crystal composition layer is represented by the following formula (wherein, γ 1 represents a rotational viscosity, and Δn represents a refractive index anisotropy), Z is 13,000 or less, γ 1 is 150 or less, and Δn is 0.08 to 0.13. The liquid crystal display device according to any one of claims 1 to 12, wherein the liquid crystal composition constituting the liquid crystal composition layer has a nematic liquid crystal phase upper limit temperature of 60 to 120 ° C, and the nematic liquid crystal phase lower limit temperature is - Below 20 ° C, the difference between the upper limit temperature and the lower limit temperature of the nematic liquid crystal phase is from 100 to 150. The liquid crystal display device according to any one of claims 1 to 13, wherein the liquid crystal composition constituting the liquid crystal composition layer has a specific resistance of 10 ¹² (Ω‧m) or more. The liquid crystal display device according to any one of claims 1 to 14, wherein the liquid crystal composition layer is composed of a polymer obtained by polymerizing a liquid crystal composition containing a polymerizable compound represented by the general formula (V). (wherein, X ¹ and X ² are each independently represented by a hydrogen atom or a methyl group; and Sp ¹ and Sp ² are each independently represented by a single bond, an alkylene group having 1 to 8 carbon atoms or -O-(CH _{2 ) s} - (wherein, s represents an integer from 2 to 7, and an oxygen atom is bonded to an aromatic ring); Z ¹ represents -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -CF ₂ O-, -OCF ₂ -, -CH ₂ CH ₂ -, -CF ₂ CF ₂ -, -CH=CH-COO-, -CH=CH-OCO-, -COO-CH=CH-, -OCO-CH =CH-, -COO-CH ₂ CH ₂ -, -OCO-CH ₂ CH ₂ -, -CH ₂ CH ₂ -COO-, -CH ₂ CH ₂ -OCO-, -COO-CH ₂ -, -OCO- CH ₂ -, -CH ₂ -COO-, -CH ₂ -OCO-, -CY ¹ =CY ² - (wherein Y ¹ and Y ² are each independently represent a fluorine atom or a hydrogen atom), -C≡C - or a single bond; C represents 1,4-phenylene, trans-1,4-cyclohexenyl or a single bond, all of which are 1,4-phenylene, and any hydrogen atom may be fluorine Replaced by atoms). The liquid crystal display device of claim 15, wherein in the general formula (V), C represents a single bond, and Z ¹ represents a single bond.