JPWO2017057557A1 - Liquid crystal display element and manufacturing method thereof - Google Patents

Abstract

Prevents the formation of dripping marks during production without deteriorating various characteristics as liquid crystal display elements such as dielectric anisotropy, viscosity, nematic phase upper limit temperature, rotational viscosity (γ1), and the seizure characteristics of liquid crystal display elements. The present invention provides a liquid crystal display element with excellent high-speed response by improving the fall time of liquid crystal and a method for manufacturing the same. The liquid crystal display element 10 of the present invention has a liquid crystal composition layer 13 sandwiched between a first substrate 11 and a second substrate 12, and vertical alignment films 16 and 17 containing a polymer of a polymerizable compound. The vertical alignment films 16 and 17 are polymers of two or more polymerizable compounds represented by the following general formula (1), and one or more of the two or more polymerizable compounds are bifunctional. It is characterized by including a polymer which is a polymerizable compound. [Chemical 1]

Description

  The present invention relates to a liquid crystal display element useful as a constituent member for a liquid crystal TV and the like, and a method for manufacturing the same.

  Liquid crystal display elements are used in various measuring instruments, automobile panels, word processors, electronic notebooks, printers, computers, televisions, watches, advertisement display boards, as well as watches and calculators. Typical liquid crystal display methods include TN (twisted nematic) type, STN (super twisted nematic) type, vertical alignment type (vertical alignment; VA) using TFT (thin film transistor), and IPS. (In-plane switching) type. The liquid crystal composition used in these liquid crystal display elements is stable against external factors such as moisture, air, heat, and light, and exhibits a liquid crystal phase in the widest possible temperature range centering on room temperature. It is required to be viscous and have a low driving voltage. Furthermore, the liquid crystal composition is composed of several to several tens of kinds of compounds in order to optimize dielectric anisotropy (Δε), refractive index anisotropy (Δn), etc. for each liquid crystal display element. It is composed of

In the VA type display, a liquid crystal composition having a negative Δε is used, which is widely used for liquid crystal TVs and the like. On the other hand, in all driving methods, low voltage driving, high-speed response, and a wide operating temperature range are required. That is, the absolute value of Δε is large, the viscosity (η) is small, and a high nematic phase-isotropic liquid phase transition temperature (T _ni ) is required. Further, from the setting of Δn × d, which is the product of Δn and the cell gap (d), it is necessary to adjust Δn of the liquid crystal composition to an appropriate range according to the cell gap. In addition, when applying a liquid crystal display element to a television or the like, since high-speed response is important, a liquid crystal composition having a low rotational viscosity (γ ₁ ) is required.

  On the other hand, in order to improve the viewing angle characteristics of a VA display, an MVA (multi-domain vertical alignment) type that divides the alignment direction of liquid crystal molecules in a pixel into a plurality of parts by providing a protrusion structure on the substrate. Liquid crystal display elements have been widely used. Although the MVA type liquid crystal display element is excellent in view angle characteristics, the response speed of liquid crystal molecules is different between the vicinity of the protrusion structure on the substrate and the part away from the protrusion structure, and the liquid crystal having a slow response speed away from the protrusion structure. There is a problem that the response speed as a whole is insufficient due to the influence of molecules, and there is a problem of a decrease in transmittance due to the protruding structure. In order to solve this problem, PSA is a method for providing a uniform pretilt angle in a divided pixel without providing a non-transparent protrusion structure in a cell, unlike a normal MVA liquid crystal display element. Liquid crystal display elements (including polymer sustained alignment, including PS liquid crystal display elements (polymer stabilized)) have been developed. A PSA liquid crystal display element is obtained by adding a small amount of a reactive monomer to a liquid crystal composition, introducing the liquid crystal composition into a liquid crystal cell, and then irradiating active energy rays while applying a voltage between the electrodes. It is produced by polymerizing the reactive monomer. Therefore, an appropriate pretilt angle can be given in the divided pixels, and as a result, high contrast can be achieved by improving the transmittance and high speed response by giving a uniform pretilt angle (see, for example, Patent Document 1). However, in a PSA liquid crystal display element, it is necessary to add a reactive monomer to the liquid crystal composition, and in an active matrix liquid crystal display element that requires a high voltage holding ratio, there are many problems and display defects such as burn-in are caused. There were also problems that occurred.

However, the lateral electric field type liquid crystal display device exhibiting such good display characteristics has a problem that the white display appears to be colored blue or yellow when the liquid crystal panel is viewed from an inclined angle.

  As a method of improving the drawbacks of PSA liquid crystal display elements and providing a uniform pretilt angle to liquid crystal molecules without introducing foreign substances other than the liquid crystal material into the liquid crystal composition, a reactive monomer is mixed into the alignment film material. Then, after introducing the liquid crystal composition into the liquid crystal cell, a method of polymerizing the reactive monomer in the alignment film by applying active energy rays while applying a voltage between the electrodes has been developed (for example, Patent Document 2, 3 and 4).

On the other hand, with the increase in the screen size of the liquid crystal display element, the manufacturing method of the liquid crystal display element has also undergone great changes. That is, in the case of manufacturing a large panel, the conventional vacuum injection method requires a lot of time for the manufacturing process. Therefore, in the manufacture of a large panel, a manufacturing method using an ODF (one-drop-fill) method is mainly used. (For example, see Patent Document 5). Since this method can shorten the injection time compared with the vacuum injection method, it has become the mainstream method for manufacturing liquid crystal display elements. However, a phenomenon in which a drop mark in which a liquid crystal composition is dropped remains in the liquid crystal display element in a dropped shape after the liquid crystal display element is produced has become a new problem. In addition, a dripping mark is defined as a phenomenon in which a mark in which a liquid crystal composition is dripped appears white when displaying black. In particular, in the method in which a reactive monomer is added to the alignment film material described above to give a pretilt angle to the liquid crystal molecules, the reactive monomer that is a foreign substance is present in the alignment film when the liquid crystal composition is dropped onto the substrate. Therefore, the problem of dripping marks is likely to occur. In general, the occurrence of dripping marks is often caused by the selection of a liquid crystal material, and the cause is not clear.

  As a method for suppressing the drop mark, the polymerizable compound mixed in the liquid crystal composition is polymerized to form a polymer layer in the liquid crystal composition layer, thereby suppressing the drop mark generated in relation to the alignment control film. Is disclosed (see, for example, Patent Document 6). However, in this method, like the PSA method, there is a problem of display burn-in caused by the reactive monomer added to the liquid crystal composition, and the effect of suppressing dripping marks is insufficient. There has been a demand for the development of a liquid crystal display element that does not easily cause image sticking or dripping marks while maintaining basic characteristics as a display element.

JP 2002-357830 A JP 2010-107536 A US Patent Application Publication No. 2011/261295 JP 2011-227284 A JP-A-6-235925 JP 2006-58755 A

The present invention has been made in view of the above circumstances, and has various characteristics as a liquid crystal display device such as dielectric anisotropy, viscosity, nematic phase upper limit temperature, rotational viscosity (γ ₁ ), and image sticking of the liquid crystal display device. An object of the present invention is to provide a liquid crystal display element having excellent high-speed response by preventing generation of dripping marks during production and improving the fall time of liquid crystal without deteriorating characteristics.

  In order to solve the above problems, the present inventors have studied a combination of various liquid crystal compositions and a method for imparting a pretilt angle in a liquid crystal display element. As a result, a reactive monomer is contained in the vertical alignment film, and the liquid crystal By introducing a composition into a liquid crystal cell and then polymerizing a reactive monomer in an alignment film by irradiating active energy rays while applying a voltage between electrodes, the above-mentioned problem is achieved by combining specific liquid crystal compositions. It was found that the problem can be solved, and the present invention has been completed.

  That is, the present invention provides a liquid crystal composition in which a liquid crystal display element is sandwiched between a first substrate having a common electrode, a second substrate having a pixel electrode, and the first substrate and the second substrate. A liquid crystal that controls a liquid crystal molecule in the liquid crystal composition layer by applying an electric field substantially perpendicularly to the first substrate and the second substrate between the common electrode and the pixel electrode. A display element, wherein at least one of the first substrate and the second substrate indicates the orientation direction of the liquid crystal molecules in the liquid crystal composition layer, and the liquid crystal in the first substrate and the second substrate. It has a vertical alignment film that is controlled substantially perpendicular to the surface adjacent to the composition layer, and the vertical alignment film is a polymer of two or more polymerizable compounds represented by the following general formula (1) Polymerization in which at least one of the two or more polymerizable compounds is a bifunctional polymerizable compound A liquid crystal display element characterized by containing the.

In addition, the present invention provides at least one of a first substrate having a common electrode and a second substrate having a pixel electrode, two or more polymerizable compounds represented by the following general formula (1), and a vertical alignment material After forming an alignment film by applying an alignment material containing and heating, a liquid crystal composition is sandwiched between the first substrate and the second substrate, and a voltage is applied between the common electrode and the pixel electrode. And irradiating active energy rays in an aligned state to polymerize the polymerizable compound in the alignment film,
One or more of the two or more polymerizable compounds represented by the general formula (1) is a method for producing a liquid crystal display element which is a bifunctional polymerizable compound.

(In the formula, P ² represents a polymerizable functional group, S ¹ represents an alkylene group having 1 to 18 carbon atoms (the hydrogen atom in the alkylene group is one or more halogen atoms, CN group, or polymerized). It may be substituted by an alkyl group having 1 to 8 carbon atoms having a sexual functional groups, independently of each one CH ₂ group or not adjoining two or more CH ₂ groups existing in the groups to each other And X ¹ is —O—, —S—, —OCH ₂ —, —CH ₂ O, which may be replaced by —O—, —COO—, —OCO— or —OCO—O—. -, -CO-, -COO-, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -SCH _{2- , -CH 2 S -, - CF} 2 O -, - OCF 2 -, - CF 2 S -, - SCF 2 -, - CH = H-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—, —CH═CH—, — N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C— or a single bond (where P ² —S ¹ and S ¹ —X ¹ are —O -O-, -O-NH-, -S-S- and -O-S- groups are not included.), Q1 represents 0 or 1, MG represents a mesogenic group, R ² represents a hydrogen atom, Represents a halogen atom, a cyano group, or a linear or branched alkyl group having 1 to 12 carbon atoms, and the alkyl group is linear; May be branched, the alkyl group is one -CH ₂ - or nonadjacent two or more -CH ₂ - are each independently -O -, - S -, - CO -, - COO -, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -CH = CH-COO-, -CH = CH —OCO—, —COO—CH═CH—, —OCO—CH═CH—, —CH═CH—, —CF═CF— or —C≡C— may be substituted, or R ² may be Formula (1-a)

(Wherein P ³ represents a polymerizable functional group, S ² represents the same as defined in S ¹ , and X ² represents the same as defined in X ¹ ( Provided that P ³ —S ² and S ² —X ² do not include —O—O—, —O—NH—, —S—S— and —O—S— groups.), Q ² is 0 Or represents 1), and the mesogenic group represented by MG is represented by the general formula (1-b).

(In the formula, B ¹ , B ² and B ³ are each independently 1,4-phenylene group, 1,4-cyclohexylene group, 1,4-cyclohexenyl group, tetrahydropyran-2,5-diyl group. 1,3-dioxane-2,5-diyl group, tetrahydrothiopyran-2,5-diyl group, 1,4-bicyclo (2,2,2) octylene group, decahydronaphthalene-2,6-diyl group Pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine-2,5-diyl group, thiophene-2,5-diyl group-, 1,2,3,4-tetrahydronaphthalene-2 , 6-diyl group, 2,6-naphthylene group, phenanthrene-2,7-diyl group, 9,10-dihydrophenanthrene-2,7-diyl group, 1,2,3,4,4a, 9,10a- Octahydrophenane Len-2,7-diyl group, 1,4-naphthylene group, benzo [1,2-b: 4,5-b ′] dithiophene-2,6-diyl group, benzo [1,2-b: 4, 5-b ′] diselenophen-2,6-diyl group, [1] benzothieno [3,2-b] thiophene-2,7-diyl group, [1] benzoselenopheno [3,2-b] selenophene-2 , 7-diyl group, or fluorene-2,7-diyl group, and one or more F, Cl, CF ₃ , OCF ₃ , CN groups, alkyl groups having 1 to 8 carbon atoms, carbon atoms as substituents An alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, Alkenyloxy group having 2 to 8 carbon atoms, carbon atoms 8 alkenoyl group, alkenoyloxy group having from 2 to 8 carbon atoms, or the general formula (1-c)

(Wherein P ⁴ represents a polymerizable functional group, S ³ represents the same as defined in S ¹ , and X ³ represents —O—, —COO—, —OCO—, —OCH, ₂ —, —CH ₂ O—, —CH ₂ CH ₂ OCO—, —COOCH ₂ CH ₂ —, —OCOCH ₂ CH ₂ —, or a single bond, q ³ represents 0 or 1, and q ⁴ represents 0. Or 1 (wherein, P ⁴ —S ³ and S ³ —X ³ do not include —O—O—, —O—NH—, —S—S— and —O—S— groups). )), R1 represents 0, 1, 2 or 3, and Z1 and Z2 are each independently —COO—, —OCO—, —CH ₂ CH ₂ —, —OCH ₂ —. , —CH ₂ O—, —CH═CH—, —C≡C—, —CH═CHCOO—, —OCOCH═CH—, —CH ₂ CH ₂ COO—, —CH ₂ CH ₂ OC _{O -, - COOCH 2 CH 2} -, - OCOCH 2 CH 2 -, - C = N -, - N = C -, - CONH -, - NHCO -, - C (CF 3) 2 -, - OCH 2 CH ₂ O— represents an alkyl group having 2 to 10 carbon atoms which may have a halogen atom or a single bond, and when r1 is 0 or 1, when B1 and a plurality of Z1 are present, they are the same. Or different. However, in the case of r1 is 0 ^{Z 2} is not a single bond, ^{Z 1} and ^{Z 2} is not a single bond when it has one general formula (1-c) as the substituent of ^{B 1} or ^{B 3.} ).

According to the present invention, it has excellent high-speed response as a liquid crystal display element, little occurrence of image sticking, and little occurrence of dripping marks at the time of production thereof, so that it can be effectively used as a display element for liquid crystal TVs, monitors and the like. .

  In addition, according to the present invention, it is possible to manufacture an efficient liquid crystal display element in which dripping marks are hardly generated.

It is a schematic perspective view which shows one Embodiment of the liquid crystal display element of this invention. It is a schematic plan view which shows an example of the slit electrode (comb-shaped electrode) used for the liquid crystal display element of this invention. It is a figure which shows the definition of the pretilt angle in the liquid crystal display element of this invention.

  Embodiments of a liquid crystal display element and a method for manufacturing the same according to the present invention will be described.

  Note that this embodiment is specifically described in order to better understand the gist of the invention, and does not limit the present invention unless otherwise specified.

[Liquid crystal display element]
The liquid crystal display element of the present invention is a liquid crystal display element having a liquid crystal composition layer sandwiched between a pair of substrates, and a voltage is applied to the liquid crystal composition layer to displace the liquid crystal molecules in the liquid crystal composition layer. This is based on the principle of acting as an optical switch by transferring, and a well-known and conventional technique can be used in this respect.

  In a normal vertical alignment liquid crystal display element in which two substrates have electrodes for transferring the Fredericks of liquid crystal molecules, a method of applying a charge vertically between the two substrates is generally employed. In this case, one electrode is a common electrode and the other electrode is a pixel electrode. The most typical embodiment of this scheme is shown below.

  FIG. 1 is a schematic perspective view showing an embodiment of the liquid crystal display element of the present invention.

  The liquid crystal display element 10 of this embodiment includes a first substrate 11, a second substrate 12, a liquid crystal composition layer 13 sandwiched between the first substrate 11 and the second substrate 12, and a first The common electrode 14 provided on the surface of the substrate 11 facing the liquid crystal composition layer 13, the pixel electrode 15 provided on the surface of the second substrate 12 facing the liquid crystal composition layer 13, and the common electrode 14, a vertical alignment film 16 provided on the surface facing the liquid crystal composition layer 13, a vertical alignment film 17 provided on the surface of the pixel electrode 15 facing the liquid crystal composition layer 13, and the first substrate 11 and a color filter 18 provided between the common electrode 14.

  As the first substrate 11 and the second substrate 12, a glass substrate or a plastic substrate is used. As the plastic substrate, a substrate made of a resin such as acrylic resin, methacrylic resin, polyethylene terephthalate, polycarbonate, or cyclic olefin resin is used.

  The common electrode 14 is usually made of a transparent material such as indium-added tin oxide (ITO).

  The pixel electrode 15 is usually made of a transparent material such as indium-added tin oxide (ITO). The pixel electrodes 15 are arranged in a matrix on the second substrate 12. The pixel electrode 15 is controlled by a drain electrode of an active element typified by a TFT switching element, and the TFT switching element has a gate line as an address signal line and a source line as a data line in a matrix. Here, the configuration of the TFT switching element is not shown.

  In order to improve viewing angle characteristics, when pixel division is performed to divide the direction in which the liquid crystal molecules in the pixel fall into several regions, slits having striped or V-shaped patterns (electrode formation) are formed in each pixel. A pixel electrode having a portion that is not provided) may be provided.

  FIG. 2 is a schematic plan view showing a typical form of a slit electrode (comb electrode) when the inside of a pixel is divided into four regions. The slit electrode has comb-like slits in four directions from the center of the pixel, so that the liquid crystal molecules in each pixel that are substantially perpendicularly aligned with respect to the substrate when no voltage is applied are applied with voltage application. The liquid crystal molecules are directed in four different directions, approaching horizontal alignment. As a result, the orientation direction of the liquid crystal in the pixel can be divided into a plurality of parts, so that the viewing angle characteristic is extremely wide.

  As a method for dividing the pixel, in addition to a method of providing a slit in the pixel electrode, a method of providing a structure such as a linear protrusion in the pixel, a method of providing an electrode other than the pixel electrode and the common electrode, and the like are used. . Although the alignment direction of the liquid crystal molecules can be divided by these methods, a configuration using a slit electrode is preferable from the viewpoint of transmittance and ease of production. Since the pixel electrode provided with the slit does not have a driving force for the liquid crystal molecules when no voltage is applied, the pretilt angle cannot be given to the liquid crystal molecules. However, when the alignment film material used in the present invention is used in combination, a pretilt angle can be given, and a wide viewing angle by pixel division can be achieved by combining with a slit electrode obtained by pixel division.

  In the present invention, having a pretilt angle means that the liquid crystal molecules are perpendicular to the substrate surface (the surface adjacent to the liquid crystal composition layer 13 in the first substrate 11 and the second substrate 12) in the state where no voltage is applied. The director is slightly different.

  Since the liquid crystal display element of the present invention is a vertical alignment (VA) type liquid crystal display element, the director of the liquid crystal molecules is aligned substantially perpendicular to the substrate surface when no voltage is applied. In order to vertically align liquid crystal molecules, a vertical alignment film is generally used. As a material for forming the vertical alignment film (vertical alignment film material), polyimide, polyamide, polysiloxane, or the like is used. Among these, polyimide is preferable. The vertical alignment film material may contain a mesogenic site, but unlike a polymerizable compound described later, it is preferable that the material does not contain a mesogenic site. When the vertical alignment film material includes a mesogenic part, image sticking or the like due to disorder of the molecular arrangement may occur due to repeated application of voltage. When the vertical alignment film is made of polyimide, it is preferable to use a polyimide solution in which a mixture of tetracarboxylic dianhydride and diisocyanate, polyamic acid, or polyimide is dissolved or dispersed in a solvent. In this case, the polyimide in the polyimide solution is used. The content of is preferably 1% by mass or more and 10% by mass or less, more preferably 3% by mass or more and 5% by mass or less, and still more preferably 10% by mass or less.

  On the other hand, when a polysiloxane-based vertical alignment film is used, the polysiloxane produced by mixing and heating an alkoxy group-containing silicon compound, an alcohol derivative, and an oxalic acid derivative at a predetermined blending ratio was dissolved. A polysiloxane solution can be used.

  In the liquid crystal display element of the present invention, the vertical alignment film formed of polyimide or the like includes a polymer formed by polymerization of a polymerizable compound having a reactive group. This polymerizable compound imparts a function of fixing the pretilt angle of the liquid crystal molecules. That is, it is possible to tilt the director of the liquid crystal molecules in the pixel in different directions when a voltage is applied, using a slit electrode or the like. However, even in the configuration using the slit electrode, the liquid crystal molecules are aligned almost perpendicularly to the substrate surface when no voltage is applied, and no pretilt angle is generated.

  In the case of the above-described PSA method, an appropriate pretilt angle is obtained by applying a voltage between the electrodes and irradiating ultraviolet rays or the like in a state where the liquid crystal molecules are slightly tilted to polymerize the reactive monomer in the liquid crystal composition. Is granted.

  Also in the liquid crystal display element of the present invention, as in the PSA method, a voltage is applied between the electrodes and the liquid crystal molecules are slightly tilted to irradiate ultraviolet rays or the like to give a pretilt angle. In contrast, the liquid crystal composition does not contain a polymerizable compound. In the present invention, the polymerizable compound having a reactive group is previously contained in the vertical alignment film material such as polyimide, and after sandwiching the liquid crystal composition between the substrates, the polymerizable compound is added while applying a voltage. Curing imparts a pretilt angle, which is essentially different from the PSA method in that it does not utilize phase separation of the polymerizable compound.

  In the present invention, “substantially vertical” means a state in which a director of liquid crystal molecules that are vertically aligned is slightly tilted from the vertical direction to give a pretilt angle. When the pretilt angle is 90 ° in the case of complete vertical alignment and 0 ° in the case of homogeneous alignment (orientation horizontally on the substrate surface), the substantially vertical is preferably 89 to 85 °, preferably 89 to 87 °. It is more preferable that

  The vertical alignment film containing a polymer of a polymerizable compound is formed by the effect of the polymerizable compound mixed in the vertical alignment film material. Therefore, it is presumed that the vertical alignment film and the polymerizable compound are intertwined in a complicated manner to form a kind of polymer alloy, but the exact structure cannot be shown.

(Polymerizable compound)
The vertical alignment film in the present invention is a polymer of two or more polymerizable compounds represented by the following general formula (1), and at least one of the two or more polymerizable compounds is a bifunctional polymerization. A polymer which is a functional compound.

As the polymerizable compound, any of a monofunctional polymerizable compound having one reactive group and a polyfunctional polymerizable compound having two or more reactive groups such as bifunctional or trifunctional may be used. However, a polymerizable compound represented by the following general formula (1) is preferable, a polyfunctional polymerizable compound is preferable, and a bifunctional polymerizable compound is preferable, and a polymerizable group and a mesogenic group are preferably used. Those having some kind of linking group are preferred. By containing such a polymerizable compound, various properties such as dielectric anisotropy, viscosity, nematic phase upper limit temperature, rotational viscosity (γ ₁ ) and the like of the liquid crystal contained in the liquid crystal display element can be improved. It is possible to prevent the occurrence of dripping marks during the production without deteriorating the image sticking characteristics of the liquid crystal display element due to the alignment film containing. This is thought to be because the reactivity of the polymerizable compound increases and the residual monomer decreases. Moreover, the light transmittance of a liquid crystal display element can be improved by including a polyfunctional polymerizable compound, and response speed, such as fall time of a liquid crystal, can be improved. This is presumably because the polymer structure after polymerization becomes rigid and the alignment regulating force increases. A polymerizable compound having a structure containing a mesogenic moiety can increase the alignment regulating force, and thus can be a liquid crystal display device having high transmittance and excellent high-speed response. A monofunctional or bifunctional polymerizable compound is preferable because the alignment structure after polymerization is less likely to be disturbed and the alignment regulating force can be kept large. Therefore, the monofunctional or polyfunctional polymerizable compound of the general formula (1) is added to the bifunctional polymerizable compound of the general formula (1) having both high reactivity, rigidity and orientation of the polymer. It is preferable to optimize the reactivity and the alignment regulating force.

  As the reactive group in the polymerizable compound, a reactive group having a polymerizable property by light is particularly preferable since the reaction of the polymerizable compound can be suppressed during the thermal polymerization of the vertical alignment film material. In addition, it is not preferable that the polymerizable compound having a reactive group is decomposed or unexpected thermal polymerization occurs during the thermal polymerization of the vertical alignment film. In order to avoid such a phenomenon, the mesogenic site is not provided. The structure represented by the general formula (1) is preferable, and those having a linking group between the polymerizable group and the mesogenic moiety are preferable.

(In the formula, P ² represents a polymerizable functional group, S ¹ represents an alkylene group having 1 to 18 carbon atoms (the hydrogen atom in the alkylene group is one or more halogen atoms, CN group, or polymerized). It may be substituted by an alkyl group having 1 to 8 carbon atoms having a sexual functional groups, independently of each one CH ₂ group or not adjoining two or more CH ₂ groups existing in the groups to each other And X ¹ is —O—, —S—, —OCH ₂ —, —CH ₂ O, which may be replaced by —O—, —COO—, —OCO— or —OCO—O—. -, -CO-, -COO-, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -SCH _{2- , -CH 2 S -, - CF} 2 O -, - OCF 2 -, - CF 2 S -, - SCF 2 -, - CH = H-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—, —CH═CH—, — N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C— or a single bond (where P ² —S ¹ and S ¹ —X ¹ are —O -O-, -O-NH-, -S-S- and -O-S- groups are not included.), Q1 represents 0 or 1, MG represents a mesogenic group, R ² represents a hydrogen atom, Represents a halogen atom, a cyano group, or a linear or branched alkyl group having 1 to 12 carbon atoms, and the alkyl group is linear; May be branched, the alkyl group is one -CH ₂ - or nonadjacent two or more -CH ₂ - are each independently -O -, - S -, - CO -, - COO -, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -CH = CH-COO-, -CH = CH —OCO—, —COO—CH═CH—, —OCO—CH═CH—, —CH═CH—, —CF═CF— or —C≡C— may be substituted, or R ² may be Formula (1-a)

(Wherein P ³ represents a polymerizable functional group, S ² represents the same as defined in S ¹ , and X ² represents the same as defined in X ¹ ( Provided that P ³ —S ² and S ² —X ² do not include —O—O—, —O—NH—, —S—S— and —O—S— groups.), Q ² is 0 Or 1).
The mesogenic group represented by the above MG has the general formula (1-b)

(In the formula, B ¹ , B ² and B ³ are each independently 1,4-phenylene group, 1,4-cyclohexylene group, 1,4-cyclohexenyl group, tetrahydropyran-2,5-diyl group. 1,3-dioxane-2,5-diyl group, tetrahydrothiopyran-2,5-diyl group, 1,4-bicyclo (2,2,2) octylene group, decahydronaphthalene-2,6-diyl group Pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine-2,5-diyl group, thiophene-2,5-diyl group-, 1,2,3,4-tetrahydronaphthalene-2 , 6-diyl group, 2,6-naphthylene group, phenanthrene-2,7-diyl group, 9,10-dihydrophenanthrene-2,7-diyl group, 1,2,3,4,4a, 9,10a- Octahydrophenane Len-2,7-diyl group, 1,4-naphthylene group, benzo [1,2-b: 4,5-b ′] dithiophene-2,6-diyl group, benzo [1,2-b: 4, 5-b ′] diselenophen-2,6-diyl group, [1] benzothieno [3,2-b] thiophene-2,7-diyl group, [1] benzoselenopheno [3,2-b] selenophene-2 , 7-diyl group, or fluorene-2,7-diyl group, and one or more F, Cl, CF ₃ , OCF ₃ , CN groups, alkyl groups having 1 to 8 carbon atoms, carbon atoms as substituents An alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, Alkenyloxy group having 2 to 8 carbon atoms, carbon atoms 8 alkenoyl group, alkenoyloxy group having from 2 to 8 carbon atoms, and / or the general formula (1-c)

(Wherein P ⁴ represents a polymerizable functional group,
S ³ represents the same as defined in S ¹ , and X ³ represents —O—, —COO—, —OCO—, —OCH ₂ —, —CH ₂ O—, —CH ₂ CH _{2. OCO -, - COOCH 2 CH 2} -, - OCOCH 2 CH 2 -, or a single bond, ^{q 3} is 0 or 1, ^{q 4} represents 0 or 1. (However, P ⁴ —S ³ and S ³ —X ³ do not include —O—O—, —O—NH—, —S—S—, and —O—S— groups). even if well, r1 represents 0, 1, 2 or 3, Z1 and Z2 each independently, -COO -, - OCO -, - CH 2 CH 2 -, - OCH 2 -, - CH 2 O —, —CH═CH—, —C≡C—, —CH═CHCOO—, —OCOCH═CH—, —CH ₂ CH ₂ COO—, —CH ₂ CH ₂ OCO—, —COOCH ₂ CH ₂ —, — OCOCH ₂ CH ₂ —, —C═N—, —N═C—, —CONH—, —NHCO—, —C (CF ₃ ) ₂ —, —OCH ₂ CH ₂ O—, and a halogen atom Represents a good alkyl group having 2 to 10 carbon atoms or a single bond, and when r1 is 0 or 1, when B1 and a plurality of Z1 are present, Each may be the same or different. However, in the case of r1 is 0 ^{Z 2} is not a single bond, ^{Z 1} and ^{Z 2} is not a single bond when it has one general formula (1-c) as the substituent of ^{B 1} or ^{B 3.} ).

P ² , P ³ and P ⁴ each independently represent a substituent selected from a polymerizable group represented by the following formula (P-2-1) to formula (P-2-20). preferable.

  Among these polymerizable functional groups, from the viewpoint of increasing the polymerizability, the formulas (P-2-1), (P-2-2), (P-2-7), (P-2-12), ( P-2-13) is preferable, and formulas (P-2-1) and (P-2-2) are more preferable.

(Monofunctional polymerizable liquid crystal compound)
Of the compounds represented by the general formula (1), the monofunctional polymerizable liquid crystal compound having one polymerizable functional group in the molecule is preferably a compound represented by the following general formula (1-1).

In the formula, P ² , S ¹ , X ¹ , q1 and MG each represent the same definition as in the general formula (1), and R ²¹ represents a hydrogen atom, a halogen atom, a cyano group, or the number of carbon atoms. 1 to 12 straight-chain or branched alkyl group, or straight-chain or branched alkenyl group having 1 to 12 carbon atoms, one —CH ₂ — of the alkyl group or the alkenyl group or _two not adjacent to each other more -CH ₂ - are each independently -O -, - S -, - CO -, - COO -, - OCO -, - CO-S -, - S-CO -, - OCO-O- , —CO—NH—, —NH—CO—, —NH—, —N (CH ₃ ) —, —CH═CH—COO—, —CH═CH—OCO—, —COO—CH═CH—, — Set by OCO—CH═CH—, —CH═CH—, —CF═CF— or —C≡C—. In addition, one or more hydrogen atoms of the alkyl group or the alkenyl group may be substituted with a halogen atom or a cyano group. Or different. Examples of the general formula (1-1) include compounds represented by the following general formulas (1-1-A) to (1-1-D), but are not limited to the following general formulas. is not.

In the formula, P ² , S ¹ , X ¹ , and q ¹ each represent the same definition as in the general formula (1), and B 11, B 12, B 13, B 2, and B 3 represent the general formula (1- b) represents the same definition as B1-B3, and may be the same or different,
Z11, Z12, Z13, and Z2 represent the same definitions as Z1 and Z2 in the general formula (1-c), and may be the same or different, and R ²¹ is a hydrogen atom, Represents a halogen atom, a cyano group, a linear or branched alkyl group having 1 to 12 carbon atoms, or a linear or branched alkenyl group having 1 to 12 carbon atoms, and one —CH of the alkyl group or the alkenyl group _2- or two or more non-adjacent —CH ₂ — are each independently —O—, —S—, —CO—, —COO—, —OCO—, —CO—S—, —S—CO. -, - O-COO -, - CO-NH -, - NH-CO -, - NH -, - N (CH 3) -, - CH = CH-COO -, - CH = CH-OCO-, -COO-CH = CH-, -OCO-CH = CH-, -CH = CH-, -CF = CF- or -C≡C- may be substituted, and one or more hydrogen atoms of the alkyl group or alkenyl group may be substituted by a halogen atom or a cyano group. When a plurality of substitutions are made, they may be the same or different.

  As the compounds represented by the general formulas (1-1-A) to (1-1-D), compounds represented by the following formulas (1-1-1) to (1-1-30) However, the present invention is not limited to these examples.

In the formula, R ^c represents a hydrogen atom or a methyl group, m represents an integer of 0 to 18, n represents 0 or 1, and R ²¹ represents the above general formulas (1-1-A) to (1- 1-D) represents the same definition, but R ²¹ represents a hydrogen atom, a halogen atom, a cyano group, a linear alkyl group having 1 to 6 carbon atoms, or a linear alkenyl group having 1 to 6 carbon atoms, Alternatively, one in which one —CH ₂ — of the alkyl group or alkenyl group is substituted by —O—, —CO—, —COO—, —OCO—, is preferable, and the cyclic group has 1 as a substituent. 1 or more F, Cl, CF ₃ , OCF ₃ , CN group, alkyl group having 1 to 8 carbon atoms, alkoxy group having 1 to 8 carbon atoms, alkanoyl group having 1 to 8 carbon atoms, 1 carbon atom -8 alkanoyloxy groups, alkoxycals having 1 to 8 carbon atoms Nyl group, alkenyl group having 2 to 8 carbon atoms, alkenyloxy group having 2 to 8 carbon atoms, alkenoyl group having 2 to 8 carbon atoms, and alkenoyloxy group having 2 to 8 carbon atoms. Also good.

The total content of the monofunctional polymerizable liquid crystal compound having one polymerizable functional group in the molecule is preferably 0 to 90% by mass in the total amount of the polymerizable liquid crystal compound to be used, and 0 to 85% by mass. % Is more preferable, and 0 to 80% by mass is particularly preferable. When placing importance on the orientation of the optical anisotropic body, the lower limit value is preferably 5% by mass or more, more preferably 10% by mass or more, and when emphasizing the hardness of the coating film, the upper limit value. Is preferably 80% by mass or less, and more preferably 70% by mass or less.

(Bifunctional polymerizable liquid crystal compound)
Among the compounds represented by the general formula (1), the following general formula (1-2) is used as a polyfunctional polymerizable liquid crystal compound (bifunctional polymerizable liquid crystal compound) having two polymerizable functional groups in the molecule. The compound represented by these is preferable.

In the formula, P ² , S ¹ , X ¹ , q ¹ , MG, X ² , S ² , q ² , and P ³ represent the same definitions as in the general formulas (1) and (1-a), respectively. Examples of the general formula (1-2) include compounds represented by the following general formulas (1-2-A) to (1-2-D), but are not limited to the following general formulas. is not.

In the formula, P ² , S ¹ , X ¹ , q ¹ , MG, X ² , S ² , q ² , P ³ represent the same definitions as in the general formulas (1) and (1-a),
B11, B12, B13, B2, and B3 represent the same definitions as B1 to B3 in the general formula (1-b), and may be the same or different,
Z11, Z12, Z13, and Z2 represent the same definitions as Z1 and Z2 in the general formula (1-c), and may be the same or different.

  Of the compounds represented by the general formulas (1-2-A) to (1-2-D), they are represented by the following general formulas (1-2-4) to (1-232). It is preferable to use a compound having three or more ring structures in the compound because the orientation of the obtained optical anisotropic body is good and the curability is good, and the general formula having three ring structures in the compound is preferable. It is particularly preferable to use the compounds represented by (1-2-4), (1-2-5), (1-2-6) to (1-2-13).

  As the compounds represented by the general formulas (1-2-A) to (1-2-D), compounds represented by the following formulas (1-2-1) to (1-232) However, the present invention is not limited to these examples.

In the formula, each of R ^d and R ^e independently represents a hydrogen atom or a methyl group, and the cyclic group has one or more F, Cl, CF ₃ , OCF ₃ , CN groups, or carbon atoms as a substituent. An alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, carbon You may have a C2-C8 alkenyl group, a C2-C8 alkenyloxy group, a C2-C8 alkenoyl group, and a C2-C8 alkenoyloxy group. m1 and m2 each independently represent an integer of 0 to 18, and n1, n2, n3, and n4 each independently represent 0 or 1.

  The liquid crystal compound having two polymerizable functional groups can be used singly or in combination of two or more, but preferably 1 to 6 types, more preferably 2 to 6 types.

  The total content of the bifunctional polymerizable liquid crystal compound having two polymerizable functional groups in the molecule is preferably 10 to 100% by mass in the total amount of the polymerizable liquid crystal compound used, and is preferably 15 to 85% by mass. % Content is more preferable, and 20 to 80% by mass is particularly preferable. When importance is attached to the rigidity and high reactivity of the cured product, the lower limit is preferably 30% by mass or more, more preferably 50% by mass or more, and the orientation of the optical anisotropic body is important. The upper limit is preferably 85% by mass or less, and more preferably 80% by mass or less.

(Polyfunctional polymerizable liquid crystal compound)
As the polyfunctional polymerizable liquid crystal compound having three or more polymerizable functional groups, it is preferable to use a compound having three polymerizable functional groups. Of the compounds represented by the general formula (1), the polyfunctional polymerizable liquid crystal compound having three polymerizable functional groups in the molecule is preferably a compound represented by the following general formula (1-3).

In the formula, P ² , S ¹ , X ¹ , q ¹ , MG, X ² , S ² , q ² , P ³ , X ³ , q 3, S ³ , q ⁴ , P ⁴ , q 5 are each represented by the above general formula (1 ) Represents the same definition. Examples of the general formula (1-3) include compounds represented by the following general formulas (1-3-A) to (1-3-P), but are not limited to the following general formulas. is not.

In the formula, P ² , S ¹ , X ¹ , q ¹ , MG, X ² , S ² , q ² , P ³ , X ³ , q 3, S ³ , P ⁴ , X ⁴ , S ⁴ , q ⁴ , X ⁵ , S ⁵ and q5 represent the same definitions as in the general formulas (1) and (1-a),
B11, B12, B13, B2, and B3 represent the same definitions as B1 to B3 in the general formula (1-b), and may be the same or different,
Z11, Z12, Z13, and Z2 represent the same definitions as Z1 and Z2 in the general formula (1-c), and may be the same or different.

  As the compounds represented by the general formulas (1-3-A) to (1-3-P), compounds represented by the following formulas (1-3-1) to (1-3-14) However, the present invention is not limited to these examples.

In the formula, R ^f , R ^g, and R ^h each independently represent a hydrogen atom or a methyl group, and R ⁱ , R ^j, and R ^k are each independently a hydrogen atom, a halogen atom, or a carbon number of 1 to 6 An alkyl group, an alkoxy group having 1 to 6 carbon atoms, a cyano group, and when these groups are an alkyl group having 1 to 6 carbon atoms or an alkoxy group having 1 to 6 carbon atoms, all are unsubstituted, Alternatively, the cyclic group may be substituted with one or two or more halogen atoms, and the cyclic group has one or more F, Cl, CF ₃ , OCF ₃ , CN groups, 1 to 8 carbon atoms as a substituent. An alkyl group, an alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, and 2 to 2 carbon atoms. 8 alkenyl groups, carbon atoms Number 2-8 alkenyloxy group, alkenoyl group having 2 to 8 carbon atoms, which may have a alkenoyloxy group having from 2 to 8 carbon atoms.
m4 to m9 each independently represents an integer of 0 to 18, and n4 to n9 each independently represents 0 or 1.

  The polyfunctional polymerizable liquid crystal compound having three or more polymerizable functional groups can be used alone or in combination of two or more.

  The total content of the polyfunctional polymerizable liquid crystal compound having three or more polymerizable functional groups in the molecule is preferably 0 to 80% by mass in the total amount of the polymerizable liquid crystal compound to be used. More preferably, it is contained in an amount of 0 to 40% by mass. When importance is attached to the rigidity of the optical anisotropic body, the lower limit value is preferably 10% by mass or more, more preferably 20% by mass or more, and particularly preferably 30% by mass or more. When emphasizing low curing shrinkage, the upper limit is preferably 50% by mass or less, more preferably 35% by mass or less, and particularly preferably 20% by mass or less.

(Liquid crystal composition)
In the liquid crystal composition of the present invention, the first component preferably contains 25 to 70% by mass, more preferably 30 to 60% by mass of a compound represented by the following general formula (I), 35 It is more preferable to contain -50 mass%, and it is most preferable to contain 38-47 mass%.

(In the formula, R ¹ and R ² are each independently 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 represents an alkenyloxy group, A represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and l represents 1 or 2, but when l is 2, two A's are the same. Or different.)
In the general formula (I), R ¹ and R ² are each independently 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 carbon. Represents an alkenyloxy group having 2 to 8 atoms,
It preferably represents 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 an alkenyloxy group having 2 to 5 carbon atoms,
More preferably, it represents 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,
It is particularly preferable to represent an alkyl group having 2 to 5 carbon atoms and an alkenyl group having 2 to 4 carbon atoms. When R ¹ represents an alkyl group, an alkyl group having 1, 3 or 5 carbon atoms is particularly preferred. In the case where R ¹ represents an alkenyl group, the following structures are preferred.

(In the formula, it shall be bonded to the ring structure at the right end.)
In the above structure, a vinyl group or 1-propenyl group which is an alkenyl group having 2 or 3 carbon atoms is more preferable.

In the above general formula (I), R ¹ and R ² may be the same or different, but are preferably different. When R ¹ and R ² are both alkyl groups, they are different from each other. Particularly preferred are alkyl groups of 1, 3 or 5 carbon atoms.
The content of the compound represented by the above general formula (I), wherein at least one substituent of R ¹ and R ² is an alkyl group having 3 to 5 carbon atoms, is represented by the above general formula (I). It is preferably 50% by mass or more in the compound, more preferably 70% by mass or more, and further preferably 80% by mass or more.

In addition, the content of the compound represented by the general formula (I) in which at least one substituent of R ¹ and R ² is an alkyl group having 3 carbon atoms is represented by the general formula (I). It is preferably 50% by mass or more in the compound, more preferably 70% by mass or more, further preferably 80% by mass or more, and most preferably 100%.

  In the above general formula (I), A represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and preferably represents a trans-1,4-cyclohexylene group. Further, the content of the compound represented by the above general formula (I) in which A represents a trans-1,4-cyclohexylene group is 50% by mass or more in the compound represented by the above general formula (I). Preferably, it is 70% by mass or more, and more preferably 80% by mass or more.

  Specifically, the compound represented by the general formula (I) is preferably a compound represented by the following general formula (Ia) to general formula (Ik).

(In the formula, R ¹ and R ² each independently represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, and R ¹ and R ² in the general formula (I)) Similar embodiments are preferred.)
In general formula (Ia) to general formula (Ik), general formula (Ia), general formula (Ib) and general formula (Ig) are preferable, general formula (Ia) and general formula (Ig) are more preferable, and response The general formula (Ia) is particularly preferable in order to improve the balance of speed, seizure characteristics reduction, and drop mark suppression, but the general formula (Ib) is also preferable when the response speed is important. When importance is attached to speed, general formula (Ib), general formula (Ie), general formula (If) and general formula (Ih) are preferred, and dialkenyl compounds of general formula (Ie) and general formula (If) are particularly preferred This is preferable when the response speed is important.

  From these points, it is preferable that the content of the compound represented by the general formula (Ia) and the general formula (Ig) is 50% by mass or more in the compound represented by the general formula (I). More preferably, it is 70 mass% or more, More preferably, it is 80 mass% or more, Most preferably, it is 100 mass%. Moreover, it is preferable that content of the compound represented by the said general formula (Ia) is 50 mass% or more in the compound represented by the said general formula (I), and it is more preferable that it is 70 mass% or more. Preferably, it is 80 mass% or more.

  In the liquid crystal composition of the present invention, as the second component, the following general formula (II)

(In the formula, 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, 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 B and D are Each independently represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and Z ² represents a single bond, —OCH ₂ —, —OCO—, —CH ₂ O— or —COO—. , M represents 0, 1 or 2, but when m is 2, the two Bs may be the same or different.

  M in the formula is preferably 1 or 2.

  Specifically, the compound represented by the general formula (II) in which m is 1 is represented by the following general formula (II-1), general formula (II-1 ′) and general formula (II-2). The compound which is made is mentioned.

(In the formula, 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, 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.
In the above general formula (II-1) and general formula (II-2), R ³ is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, or an alkoxy group having 1 to 8 carbon atoms. Or an alkenyloxy group having 2 to 8 carbon atoms, preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and an alkyl group having 2 to 5 carbon atoms or More preferably, it represents an alkenyl group having 2 to 4 carbon atoms, more preferably represents an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, and represents an alkyl group having 3 carbon atoms. Is particularly preferred.

In the above general formula (II-1) and general formula (II-2), R ⁴ is an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 4 to 8 carbon atoms, or an alkoxy group having 1 to 8 carbon atoms. Or an alkenyloxy group having 3 to 8 carbon atoms, preferably an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, and an alkyl group having 1 to 3 carbon atoms or More preferably, it represents an alkoxy group having 1 to 3 carbon atoms, more preferably represents an alkyl group having 3 carbon atoms or an alkoxy group having 2 carbon atoms, and particularly represents an alkoxy group having 2 carbon atoms. preferable.

  The compounds represented by the above general formula (II-1) and general formula (II-2) are specifically the compounds represented by the following general formula (II-1a) and general formula (II-1b) Is preferred.

(In the formula, 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 general formula (II-1a), R ⁴ is preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 2 carbon atoms, and particularly preferably an alkyl group having 2 carbon atoms.

In the general formula (II-1b), R ⁴ is preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 3 carbon atoms, and particularly preferably an alkyl group having 3 carbon atoms.

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

In the general formula (II-2a), R ⁴ is preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 2 carbon atoms, and particularly preferably an alkyl group having 2 carbon atoms.

In the general formula (II-2b), R ⁴ is preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 3 carbon atoms, and particularly preferably an alkyl group having 3 carbon atoms.

  Among the general formulas (II-2a) and (II-2b), the general formula (II-2a) is preferable in order to increase the absolute value of the dielectric anisotropy.

  In the liquid crystal composition of the present invention, the compound represented by General Formula (II-1) and General Formula (II-2) is preferably contained in an amount of 5 to 30% by mass, more preferably 10 to 25% by mass. Preferably, the content is 12 to 20% by mass.

  Specific examples of the compound represented by the general formula (II) in which m is 1 include compounds represented by the following general formula (II-3).

(In the formula, 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, 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; A 4-phenylene group or a trans-1,4-cyclohexylene group, and Z ² represents a single bond, —OCH ₂ —, —OCO—, —CH ₂ O— or —COO—.
In the general formula (II-3), R ⁵ is 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 8 carbon atoms. An alkenyloxy group, preferably an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, preferably an alkyl group having 2 to 5 carbon atoms or alkenyl having 2 to 4 carbon atoms It is more preferably a group, more preferably an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, and particularly preferably an alkyl group having 3 carbon atoms.

In the general formula (II-3), R ⁶ is 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 3 to 8 carbon atoms. An alkenyloxy group, preferably an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, preferably an alkyl group having 1 to 3 carbon atoms or an alkoxy group having 1 to 3 carbon atoms It is more preferable to represent a group, more preferably an alkyl group having 3 carbon atoms or an alkoxy group having 2 carbon atoms, and particularly preferably an alkoxy group having 2 carbon atoms.

  In the general formula (II-3), B represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group which may be fluorine-substituted, but an unsubstituted 1,4-phenylene group or A trans-1,4-cyclohexylene group is preferred, and a trans-1,4-cyclohexylene group is more preferred.

In the above general formula (II-3), Z ² represents a single bond, —OCH ₂ —, —OCO—, —CH ₂ O— or —COO—, but may represent a single bond or —CH ₂ O—. Preferably, it represents a single bond.

  Specifically, the compound represented by the general formula (II-3) is preferably a compound represented by the following general formula (II-3a) to general formula (II-3f).

(In the formula, R ⁵ represents an alkyl group having 1 to ⁵ carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and R ^6a represents an alkyl group having 1 to 5 carbon atoms. Preferred is the same embodiment as R ⁵ and R ⁶ in 3).
In General Formula (II-3a) to General Formula (II-3f), R ⁵ is preferably the same embodiment as in General Formula (II-3).
In General Formula (II-3a) to General Formula (II-3f), R ^6a is preferably an alkyl group having 1 to 3 carbon atoms, more preferably an alkyl group having 1 or 2 carbon atoms, and 2 carbon atoms. Are particularly preferred.

  Among general formulas (II-3a) to (II-3f), in order to increase the absolute value of dielectric anisotropy, general formula (II-3a) or general formula (II-3e) is Preferably, in the composition having a large Δn, the general formula (II-3b) is preferable.

  In the liquid crystal composition of the present invention, the compound represented by the general formula (II-3) is preferably contained in an amount of 20 to 45% by mass, more preferably 25 to 40% by mass, and more preferably 28 to 38% by mass. More preferably.

  In the liquid crystal composition of the present invention, as the third component, a compound represented by the following general formula (III) can also be contained.

(In the formula, R ⁷ and R ⁸ are each independently 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 represents an alkenyloxy group, Y ¹ and Y ² each independently represent a hydrogen atom or a fluorine atom, and E, F and G each independently represent a 1,4-phenylene group or trans-1,4 - cyclohexylene, ^{Z 3} is a single _{bond, -OCH 2 -, - OCO -} , - CH 2 O- or represents -COO-, n represents 0 or 1).
In the general 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 alkenyloxy having 2 to 8 carbon atoms. Represents a group,
When E represents trans-1,4-cyclohexylene, it preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and an alkyl group or carbon having 2 to 5 carbon atoms. More preferably, it represents an alkenyl group having 2 to 4 atoms, more preferably represents an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, and represents an alkyl group having 3 carbon atoms. Particularly preferred,
When E represents a 1,4-phenylene group which may be substituted with fluorine, it preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 4 or 5 carbon atoms, More preferably, it represents a 5 alkyl group or an alkenyl group having 4 carbon atoms, and more preferably represents an alkyl group having 2 to 4 carbon atoms.

In the general formula (III), R ⁸ is 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 having 3 to 8 carbon atoms. Represents a group,
When G represents trans-1,4-cyclohexylene, it preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and an alkyl group or carbon having 2 to 5 carbon atoms. More preferably, it represents an alkenyl group having 2 to 4 atoms, more preferably represents an alkyl group having 3 to 5 carbon atoms or an alkenyl group having 2 carbon atoms, and represents an alkyl group having 3 carbon atoms. Particularly preferred,
When G represents a 1,4-phenylene group optionally substituted with fluorine, it preferably represents an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 4 or 5 carbon atoms, More preferably, it represents a 5 alkyl group or an alkenyl group having 4 carbon atoms, and more preferably represents an alkyl group having 2 to 4 carbon atoms.

In the general formula (III), when R ⁷ and R ⁸ represent an alkenyl group, and F or G to be bonded represents a 1,4-phenylene group which may be fluorine-substituted, the number of carbon atoms is 4 or 5. As the alkenyl group, a structure represented by the following formula is preferable.

(In the formula, it shall be bonded to the ring structure at the right end.)
Also in this case, an alkenyl group having 4 carbon atoms is more preferable.

In the above general formula (III), Y ¹ and Y ² each independently represent a hydrogen atom or a fluorine atom, and any ^one of Y ¹ and Y ² preferably represents a fluorine atom, and has an anisotropic dielectric constant. When importance is attached to the absolute value of sex, it is preferable that both Y ¹ and Y ² represent a fluorine atom.
In the above general formula (III), E, F and G each independently represent a fluorine-substituted 1,4-phenylene group or trans-1,4-cyclohexylene. , 4-phenylene group or trans-1,4-cyclohexylene is preferred.
In formula (III), ^{Z 2} is a single _{bond, -OCH 2 -, - OCO -} , - CH 2 O- or represents a -COO-, represents a single bond, _-CH 2 O-or -COO- It is preferable that it represents a single bond.
In the above general formula (III), n represents 0 or 1, but preferably represents 0 when Z ³ represents a substituent other than a single bond.
When n represents 0, the compound represented by the general formula (III) is specifically preferably a compound represented by the following general formula (III-1a) to general formula (III-1h).

(Wherein R ⁷ and R ⁸ each independently represents 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, An embodiment similar to R ⁷ and R ⁸ in (III) is preferred.)
When n represents 1, the compound represented by the general formula (III) is specifically preferably a compound represented by the following general formula (III-2a) to general formula (III-2l).

(Wherein R ⁷ and R ⁸ each independently represents 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, An embodiment similar to R ⁷ and R ⁸ in (III) is preferred.)

  In the liquid crystal composition of the present invention, the compound represented by the general formula (III) is preferably contained in an amount of 5 to 20% by mass, more preferably 8 to 15% by mass, and more preferably 10 to 13% by mass. Is more preferable.

The liquid crystal composition in the present invention is composed of a combination of compounds represented by the above general formulas (I) to (III), and the following contents are preferable as these combinations.
The compounds represented by the general formula (II-1), general formula (II-2) and general formula (II-1 ′) all have negative dielectric anisotropy, and their absolute values are relatively Although it is a large compound, the total content of these compounds in the liquid crystal composition is preferably 30 to 65% by mass, more preferably 40 to 55% by mass, and particularly preferably 43 to 50% by mass.

The compound represented by the general formula (III) includes both a positive compound and a negative compound with respect to dielectric anisotropy, but the dielectric anisotropy is negative and the absolute value thereof is 0. When three or more compounds are used, the compounds represented by formula (II-1), formula (II-2), formula (II-1 ′) and formula (III) in the liquid crystal composition are used. The total content is preferably 35 to 70% by mass, more preferably 45 to 65% by mass, and particularly preferably 50 to 60% by mass.
Moreover, it is preferable that the liquid-crystal composition in this invention contains 30-50 mass% of compounds represented by the said general formula (I), General formula (II-1), General formula (II-2), General It is preferable to contain 35 to 70% by mass of the compound represented by the formula (II-1 ′) and the general formula (III),
More preferably, the compound represented by the general formula (I) is contained in an amount of 35 to 45% by mass. The general formula (II-1), the general formula (II-2), the general formula (II-1 ′), and the general formula More preferably, it contains 45 to 65% by mass of the compound represented by the formula (III),
It is particularly preferable to contain 38 to 42% by mass of the compound represented by the above general formula (I). General formula (II-1), general formula (II-2), general formula (II-1 ′) and general It is particularly preferable to contain 50 to 60% by mass of the compound represented by the formula (III).
Further, the total content of the compounds represented by the general formula (II-1), the general formula (II-2), the general formula (II-1 ′) and the general formula (III) is based on the whole liquid crystal composition. 80-100 mass% is preferable, 90-100 mass% is more preferable, 95-100 mass% is especially preferable.

  The liquid crystal composition in the present invention can use a nematic phase-isotropic liquid phase transition temperature (Tni) in a wide range, but the nematic phase-isotropic liquid phase transition temperature (Tni) is 60. It is preferable that it is -120 degreeC, It is more preferable that it is 70-100 degreeC, It is especially preferable that it is 70-85 degreeC.

  The dielectric anisotropy of the liquid crystal composition in the invention is preferably −2.0 to −6.0, more preferably −2.5 to −5.0 at 25 ° C., − Particularly preferred is 2.5 to -3.5.

  The refractive index anisotropy of the liquid crystal composition in the present invention is preferably 0.08 to 0.13 at 25 ° C., more preferably 0.09 to 0.12. More specifically, in the case of corresponding to a thin cell gap, the refractive index anisotropy of the liquid crystal composition in the present invention is preferably 0.10 to 0.12 at 25 ° C., and corresponds to a thick cell gap. In this case, the refractive index anisotropy of the liquid crystal composition in the present invention is preferably 0.08 to 0.10 at 25 ° C.

[Method of manufacturing liquid crystal display element]
Next, with reference to FIG. 1, the manufacturing method of the liquid crystal display element of this invention is demonstrated.

  An alignment material containing a polymerizable compound having a reactive group and a vertical alignment material is applied to the surface of the first substrate 11 on which the common electrode 14 is formed and the surface of the second substrate 12 on which the pixel electrode 15 is formed. Then, the vertical alignment films 16 and 17 are formed by heating.

  Here, first, a polymer compound precursor (polymerizable compound) to be the first polymer compound, a polymerizable compound of the compounds represented by the above general formula (VI) and general formula (V), and further necessary In response, an alignment material containing a compound having photopolymerizability and photocrosslinkability is prepared.

  When the first polymer compound is polyimide, examples of the polymer compound precursor include a mixture of tetracarboxylic dianhydride and diisocyanate, polyamic acid, and a polyimide solution in which polyimide is dissolved or dispersed in a solvent. Etc. The polyimide content in the polyimide solution is preferably 1% by mass or more and 10% by mass or less, and more preferably 3% by mass or more and 5% by mass or less.

When the first polymer compound is polysiloxane, examples of the polymer compound precursor include a silicon compound having an alkoxy group, a silicon compound having a halogenated alkoxy group, alcohol, and oxalic acid. Examples thereof include a polysiloxane solution prepared by synthesizing polysiloxane by mixing at a quantitative ratio and heating, and dissolving it in a solvent.
In addition, you may add the compound which has photocrosslinkability, a photoinitiator, a solvent, etc. to alignment material as needed.

  In the case where the first polymer compound is a solution in which a polymer is dissolved in a solvent such as polyacrylate or polyvinyl alcohol, it is not necessary to add a reaction aid in particular, and the polymerizability represented by the above general formula (1) Prepare a mixture solution with the compound.

  In addition, you may add the compound which has photocrosslinkability, a photoinitiator, a solvent, etc. to alignment material as needed.

  In general, the polymerizable compound of the present invention is polymerized by irradiation with light such as ultraviolet rays. Examples of the photopolymerization initiator used in the case of light irradiation include 2-hydroxy-2-methyl-1-phenylpropan-1-one (“Darocur 1173” manufactured by Merck), 1-hydroxycyclohexyl phenyl ketone (BASF) “Irgacure 184”), 1- (4-isopropylphenyl) -2-hydroxy-2-methylpropan-1-one (“Darocur 1116” manufactured by Merck & Co.), 2-methyl-1-[(methylthio) phenyl] -2-Molyphorinopropane-1 (“Irgacure 907” manufactured by BASF). Benzylmethylketal ("Irgacure 651" manufactured by BASF). A mixture of 2,4-diethylthioxanthone (“Kayacure DETX” manufactured by Nippon Kayaku Co., Ltd.) and ethyl p-dimethylaminobenzoate (“Kayacure EPA” manufactured by Nippon Kayaku Co., Ltd.), isopropylthioxanthone (“Kantacure” manufactured by Word Prekinsop Co., Ltd.) -ITX ") and a mixture of ethyl p-dimethylaminobenzoate, acylphosphine oxide (" Lucirin TPO "manufactured by BASF), and the like. 10 mass% or less is preferable with respect to a polymeric compound, and, as for the usage-amount of a photoinitiator, 0.5-5 mass% is especially preferable.

  In addition, a liquid crystal compound that generates radicals by light can also be used. As such a liquid crystal compound, a compound having an aryloxycarbonyl skeleton can be used, which is preferable without deteriorating the electrical characteristics of the liquid crystal display element. The radical generation mechanism of a compound having an aryloxycarbonyl skeleton by light is shown below. Ring A is 1,4-phenylene group, 1,4-cyclohexylene group, anthracene-2,6-diyl group, phenanthrene-2,7-diyl group, pyridine-2,5-diyl group, pyrimidine-2,5. -Represents a diyl group or naphthalene-2,6-diyl group, and the hydrogen atom present in ring A may be substituted with a halogen atom or an alkoxyl group.

As the compound having an aryloxycarbonyl skeleton, a compound represented by the following general formula (1 ') is preferable.

In the formula, rings A, B and C are 1,4-phenylene group, 1,4-cyclohexylene group, anthracene-2,6-diyl group, phenanthrene-2,7-diyl group, pyridine-2,5-diyl. Represents a group, pyrimidine-2,5-diyl group, naphthalene-2,6-diyl group, and hydrogen atoms present in rings A, B, and C may be substituted with a halogen atom or an alkoxyl group. X ^{1 to} X ⁵ each independently represents a single bond, —O—, —CO—, —OCO— or —COO—, and Z ¹ and Z ² represent —COO—, —OCO— and —CH ₂ CH. ₂ —, —CH═CH—, —C≡C—, —CF═CF—, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF _{2 -, - CF 2 O -,} - OCF 2 -, - COO -, - OCO-, or an -OCH ₂ CH ₂ O-. However, at least ^one of X ^{1 to} X ⁵ and Z ^{1 to} Z ² is —COO—, —OCO—, or —OCH ₂ CH ₂ O—, and —COO— and —OCO— The oxygen atom not contained in the carbonyl group is 1,4-phenylene group, anthracene-2,6-diyl group, phenanthrene-2,7-diyl group, pyridine-2,5-diyl group, pyrimidine-2,5- Bonded to diyl group and naphthalene-2,6-diyl group. R ^{1 to} R ⁵ each independently represent hydrogen or an alkylene group having 1 to 12 carbon atoms, and one or two or more hydrogen atoms in hydrogen or the alkyl may be substituted with -P. , One or more methylene groups in the alkyl are each independently substituted with —CH═CH—, —CO—, —O—, P—, as oxygen atoms are not directly bonded to each other. P may represent a polymerizable group. n1 to n3 represent 0, 1, 2, 3 or 4, and n represents 0, 1, 2 or 3. In addition, when the compound contained in the said general formula (1 ') corresponds to above-described general formula (I), the said compound can be used as a polymeric compound represented by the said general formula (I). .

  The liquid crystalline compound that generates radicals by light is preferably contained in an amount of 0.1 to 10% by mass, and preferably 0.5 to 5% by mass, based on the total weight of the polymerizable composition and the liquid crystal composition. More preferably, it is particularly preferably 1.0 to 3% by mass.

  The liquid crystalline compound having a function of generating radicals by light may or may not have a polymerizable functional group, but from the viewpoint of ensuring the stability and reliability of the device. Preferably it is. In this case, the number of polymerizable functional groups contained in one molecule is preferably 1 to 6, more preferably 2 to 3, and particularly preferably 2. Such a compound is preferably 0.1 to 10% by mass, more preferably 1.5 to 9% by mass based on the total weight of the polymerizable composition and the liquid crystal composition, It is particularly preferable to contain 8% by mass. Further, the liquid crystalline compound having a function of generating radicals by light preferably has no polymerizable functional group from the viewpoint of realizing a low driving voltage of the liquid crystal display element. In this case, the maximum addition amount concentration in the polymerizable liquid crystal composition is preferably 10% by mass or less, preferably 7% by mass or less, and preferably 5% by mass or less. If the amount added is large, the stability and reliability of the liquid crystal display element and the voltage holding ratio tend to deteriorate. Further, as the liquid crystalline compound having a function of generating radicals by light, a compound having a polymerizable functional group and a compound having no polymerizable functional group may be used in combination.

  Specifically, the following compounds are preferable.

  After adjusting the alignment material, the alignment material is applied or printed on each of the first substrate 11 and the second substrate 12 so as to cover the common electrode 14 and the pixel electrode 15 and the slit portion (not shown). Then, heat treatment is performed. As a result, the polymer compound precursor contained in the applied or printed alignment material is polymerized and cured to become the first polymer compound, and the first alignment compound and the polymerizable compound are mixed. 16, 17 are formed.

  Here, when heat-processing, the temperature is preferable 80 degreeC or more, and 150-200 degreeC is more preferable.

  Note that the orientation control unit including the first polymer compound is formed at this stage. Thereafter, a process such as rubbing may be performed as necessary.

  Next, the first substrate 11 and the second substrate 12 are overlapped, and a liquid crystal composition layer 13 containing liquid crystal molecules is sealed between them.

  Specifically, spacer protrusions for securing a cell gap with respect to the surface on which the vertical alignment films 16 and 17 are formed on either one of the first substrate 11 and the second substrate 12, for example, In addition to spraying plastic beads or the like, for example, the seal portion is printed using an epoxy adhesive or the like by a screen printing method.

  Thereafter, the first substrate 11 and the second substrate 12 are bonded together through spacer protrusions and a seal portion so that the vertical alignment films 16 and 17 are opposed to each other, and a liquid crystal composition containing liquid crystal molecules is injected. To do.

  Thereafter, the liquid crystal composition is sealed between the first substrate 11 and the second substrate 12 by curing the seal portion by heating or the like.

  Next, a voltage is applied between the common electrode 14 and the pixel electrode 15 using voltage applying means. A voltage is applied with the magnitude | size of 1-30 (V), for example. Thereby, the surface adjacent to the liquid crystal composition layer 13 in the first substrate 11 (surface facing the liquid crystal composition layer 13) and the surface adjacent to the liquid crystal composition layer 13 in the second substrate 12 (liquid crystal composition). An electric field in a direction forming a predetermined angle with respect to the surface facing the physical layer 13 is generated, and the liquid crystal molecules 19 are oriented in a predetermined direction with respect to the normal direction of the first substrate 11 and the second substrate 12. It will be. At this time, the tilt angle of the liquid crystal molecules 19 is approximately equal to the pretilt θ given to the liquid crystal molecules 19 in a process described later. Therefore, the magnitude of the pretilt θ of the liquid crystal molecules 19 can be controlled by appropriately adjusting the magnitude of the voltage (see FIG. 3).

  Furthermore, the polymerizable compound in the vertical alignment films 16 and 17 is polymerized by irradiating the liquid crystal composition layer 13 with, for example, ultraviolet light UV from the outside of the first substrate 11 with the voltage applied. To produce a second polymer compound.

In this case, the intensity of the ultraviolet light UV to be irradiated may or may not be constant, and the irradiation time at each intensity when the irradiation intensity is changed is arbitrary, but two or more stages of irradiation processes are performed. When employed, it is preferable to select an irradiation intensity in the irradiation process in the second stage and after that which is weaker than the irradiation intensity in the first stage, and the total irradiation time in the second stage and after is more than the irradiation time in the first stage. It is preferable that the total irradiation energy amount is long and long. When the irradiation intensity is changed discontinuously, it is desirable that the average irradiation light intensity in the first half of the entire irradiation process time is stronger than the average irradiation intensity in the second half, and the intensity immediately after the start of irradiation is the strongest. More desirably, it is further preferable that the irradiation intensity always decreases to a certain value as the irradiation time elapses. In this case, the ultraviolet UV intensity is preferably ² mW / cm ^{−2 to} 100 mW / cm ^−2, but the first stage in the case of multi-stage irradiation or the entire irradiation process in the case of changing the irradiation intensity discontinuously. it highest illumination intensity is ^{10mW / cm -2 ~100mW / cm -2} , and a minimum irradiation intensity when changing the second stage or later, or discontinuously irradiation intensity in the case of multi-stage irradiation 2 mW / cm ^- It is more preferably ^{2 to} 50 mW / cm ⁻² . Further, the total irradiation energy amount is preferably 1J to 300J, preferably 10J to 300J, more preferably 50J to 250J, and further preferably 100J to 250J.

  In this case, the applied voltage may be alternating current or direct current.

  As a result, an alignment regulating portion (not shown) including the second polymer compound fixed to the alignment control portions of the vertical alignment films 16 and 17 is formed. This alignment regulating part has a function of imparting a pretilt θ to the liquid crystal molecules 19 located in the vicinity of the interface between the liquid crystal composition layer 13 and the vertical alignment films 16 and 17 in the non-driven state. Here, although the ultraviolet light UV is irradiated from the outside of the first substrate 11, it may be irradiated from the outside of the second substrate 12, and both the first substrate 11 and the second substrate 12 may be irradiated. Irradiation may be performed from the outside of the substrate.

  Thus, in the liquid crystal display element of the present invention, the liquid crystal molecules 19 in the liquid crystal composition layer 13 have a predetermined pretilt θ. As a result, the response speed to the drive voltage can be greatly improved as compared with a liquid crystal display element that has not been subjected to any pretilt processing and a liquid crystal display device having the liquid crystal display element.

  In the liquid crystal display element of the present invention, a non-photosensitive polyimide precursor is preferable as the polymer compound precursor constituting the vertical alignment films 16 and 17.

  The total content of the polymerizable compounds, particularly the compounds represented by the general formula (VI) and the general formula (V) in the polymer compound precursor is preferably 0.5 to 4% by mass. 1 to 2% by mass is more preferable.

  EXAMPLES Hereinafter, although an Example and a comparative example demonstrate this invention further more concretely, this invention is not limited to a following example. Further, “%” in the compositions of the following Examples and Comparative Examples means “mass%”.

In the following Examples and Comparative Examples, Tni, Δn, Δε, η , γ 1 respectively are defined as follows.

T _ni : Nematic phase-isotropic liquid phase transition temperature (° C.)
Δn: refractive index anisotropy at 25 ° C. Δε: dielectric anisotropy at 25 ° C. η: viscosity at 20 ° C. (mPa · s)
γ ₁ : rotational viscosity at 25 ° C. (mPa · s)
In the following examples and comparative examples, the burn-in, drop marks, and contrast of liquid crystal display elements were evaluated by the following methods.
(Burn in)
The burn-in evaluation of the liquid crystal display element is based on the following four-level evaluation of the afterimage level of the fixed pattern when the predetermined fixed pattern is displayed in the display area for 1000 hours and then the entire screen is uniformly displayed. went.
◎: No afterimage ○: Level of afterimage is slightly acceptable but acceptable △: Level of afterimage is unacceptable ×: Image retention is quite poor (drop mark)
Evaluation of the drop marks of the liquid crystal display device was performed by the following four-stage evaluation of the drop marks that appeared white when the entire surface was displayed in black.
◎: No afterimage ○: Even if there is very little afterimage, acceptable level Δ: Afterimage is unacceptable level ×: Afterimage is quite poor
(Side chain)
-N _represents -C _{n H 2n + 1} (straight-chain alkyl group having a carbon number of n).
-On _represents -OC _{n H 2n + 1} (straight-chain alkoxy group having carbon atoms n).
(Ring structure)

Example 1
A first substrate (common electrode substrate) having a transparent electrode layer and a color filter layer made of a transparent common electrode, and a second substrate (pixel) having a pixel electrode layer having a transparent pixel electrode driven by an active element Electrode substrate).

  In the pixel electrode substrate, each pixel electrode was obtained by etching ITO so that a slit having no electrode was present in the pixel electrode in order to divide the alignment of liquid crystal molecules.

  A vertical alignment film material containing a polyimide precursor and a polymerizable compound is applied to each of the common electrode substrate and the pixel electrode substrate by a spin coating method, and the coating film is heated at 200 ° C. The polyimide precursor was cured to form a 100 nm vertical alignment film on the surface of each substrate. At this stage, the polymerizable compound having a reactive group is not cured in the vertical alignment film.

  As a material for forming a vertical alignment film, a polymerizable compound represented by the following formula (E-2-1) and a polyimide solution containing 3% of a polyimide precursor (trade name: JALS2131-R6, manufactured by JSR) and The polymerizable compound represented by the formula (E-2-2) was added so that the content of each of the polyimide precursors was 1%, and further, 5% photoinitiator Irgacure with respect to the polymerizable compound. What added 907 (made by BASF) was used.

  A liquid crystal composition containing a compound represented by the following chemical formula was sandwiched between the common electrode substrate and the pixel electrode substrate on which the vertical alignment film was formed, and then the sealing material was cured to form a liquid crystal composition layer. At this time, using a spacer having a thickness of 4 μm, the thickness of the liquid crystal composition layer was set to 4 μm.

  In the chemical formula shown below, the compound belonging to the group (I) is a compound represented by the general formula (I), and the compound belonging to the group (II) is represented by the general formula (II). It is a compound.

  The obtained liquid crystal display element was irradiated with ultraviolet rays in a state where a rectangular alternating electric field was applied, and the polymerizable compound having the reactive group was cured. As the irradiation apparatus, UIS-S2511RZ manufactured by USHIO INC. And USH-250BY manufactured by USHIO ELECTRIC CO., LTD. Are used as UV lamps, and the liquid crystal display device is irradiated with UV rays at 20 mW for 10 minutes. Got. By this step, a vertical alignment film containing a polymer of a polymerizable compound having a reactive group is formed, and a pretilt angle is imparted to the liquid crystal molecules in the liquid crystal composition layer.

  Here, the pretilt angle is defined as shown in FIG. In the case of complete vertical alignment, the pretilt angle (θ) is 90 °, and when the pretilt angle is given, the pretilt angle (θ) is smaller than 90 °.

  The liquid crystal display element of Example 1 has pretilt angles in different directions in the four sections according to the slits of the pixel electrode as shown in FIG. 2, and the AC electric field is turned off after the polymerizable compound is cured. The pretilt angle was maintained. The pretilt angle maintained was 87 °.

  As shown in Table 1, the liquid crystal display element of Example 1 obtained in this way showed excellent response speed, hardly caused drop marks, and was also excellent in terms of image sticking.

(Example 2)
As a vertical alignment film forming material, a polymerizable compound represented by formula (E-2-3) and a formula (E) are added to a polyimide solution containing 3% of a polyimide precursor (trade name: JALS2131-R6, manufactured by JSR). A liquid crystal display element of Example 2 was obtained in the same manner as in Example 1 except that the polymerizable compound represented by (1-1) was used as a solution having a content of 1% in the polyimide precursor. It was.

For the liquid crystal display element of Example 2, image sticking and dropping marks were measured in the same manner as Example 1. The results are shown in Table 2.
As a result, the liquid crystal display element of Example 2 is slightly inferior to the liquid crystal display element of Example 1, but exhibits an excellent response speed, hardly causes dripping marks, and is excellent in terms of image sticking. It became clear.

(Example 3)
As a vertical alignment film forming material, a polymerizable compound and a formula represented by the following formula (E-2-4) are added to a polyimide solution containing 3% of a polyimide precursor (trade name: JALS2131-R6, manufactured by JSR). In the same manner as in Example 1, except that a polymerizable compound represented by (E-3-1) was used in a solution in which the content of the polyimide precursor was 2% and 1%, respectively. A liquid crystal display element was obtained.

For the liquid crystal display element of Example 3, image sticking and dropping marks were measured in the same manner as in Example 1. The results are shown in Table 3.
As a result, the liquid crystal display element of Example 3 is slightly inferior to the liquid crystal display element of Example 1, but exhibits an excellent response speed, hardly causes dripping marks, and is excellent in terms of image sticking. It became clear.

Example 4
A liquid crystal composition having the composition shown in Table 4 was prepared, and a liquid crystal display device of Example 4 was obtained in the same manner as Example 1 except that the liquid crystal composition was used.
For the liquid crystal display element of Example 4, image sticking and dropping marks were measured in the same manner as in Example 1. The results are shown in Table 4.

  As a result, the liquid crystal display element of Example 4 is slightly inferior to the liquid crystal display element of Example 1, but exhibits a relatively excellent response speed, hardly causes dripping marks, and is excellent in terms of image sticking. It became clear.

(Example 5)
A liquid crystal composition having the composition shown in Table 5 was prepared, and a liquid crystal display device of Example 5 was obtained in the same manner as Example 1 except that the liquid crystal composition was used.
For the liquid crystal display element of Example 5, image sticking, dropping marks and response speed were measured in the same manner as in Example 1. The results are shown in Table 5.

  As a result, the liquid crystal display element of Example 5 is slightly inferior to the liquid crystal display element of Example 1, but exhibits a relatively excellent response speed, hardly causes dripping marks, and is excellent in terms of image sticking. It became clear.

(Example 6)
A liquid crystal composition having the composition shown in Table 6 was prepared, and a liquid crystal display element of Example 6 was obtained in the same manner as in Example 1 except that the liquid crystal composition was used.
For the liquid crystal display element of Example 6, image sticking and dropping marks were measured in the same manner as in Example 1. The results are shown in Table 6.

  As a result, although the liquid crystal display element of Example 6 is slightly inferior to the liquid crystal display element of Example 1, it exhibits a relatively excellent response speed, hardly causes dripping marks, and is excellent in terms of image sticking. It became clear.

(Example 7)
A liquid crystal display device of Example 7 was prepared in the same manner as in Example 1 except that the polymerizable compound RV-3 was used in place of the photoinitiator Irgacure 907 and a solution having a content of 1% in the polyimide precursor was used. Obtained.

  For the liquid crystal display element of Example 7, image sticking and dropping marks were measured in the same manner as in Example 1. The results are shown in Table 7. As a result, it became clear that the liquid crystal display element of Example 7 showed excellent response speed, hardly caused drop marks, and was excellent in terms of image sticking, similar to the liquid crystal display element of Example 1. .

(Example 8)
The liquid crystal display element of Example 8 was prepared in the same manner as in Example 2 except that the polymerizable compound RV-3 was used in place of the photoinitiator Irgacure 907 and a solution having a content of 1% in the polyimide precursor was used. Obtained.
For the liquid crystal display element of Example 8, image sticking and dropping marks were measured in the same manner as in Example 2. The results are shown in Table 8. As a result, it became clear that the liquid crystal display element of Example 8 showed an excellent response speed as in the liquid crystal display element of Example 2, hardly caused drop marks, and was excellent in terms of image sticking. .

Example 9
A liquid crystal display device of Example 9 was prepared in the same manner as in Example 3 except that the polymerizable compound RV-3 was used in place of the photoinitiator Irgacure 907 and a solution having a content of 1% in the polyimide precursor was used. Obtained.
For the liquid crystal display element of Example 9, image sticking and dropping marks were measured in the same manner as in Example 3. The results are shown in Table 8. As a result, it became clear that the liquid crystal display element of Example 8 showed an excellent response speed as in the liquid crystal display element of Example 3, was less likely to cause drip marks, and was excellent in terms of image sticking. .

(Comparative Example 1)
As the polymerizable compound, a compound represented by the following formula (C-1-1) that does not satisfy the general formula (1) was used in place of the compound represented by the formula (E-2-1). A liquid crystal display element of Comparative Example 1 was obtained in the same manner as Example 1.

  For the liquid crystal display element of Comparative Example 1, image sticking, dripping marks and response speed were measured in the same manner as in Example 1. The results are shown in Table 10.

  As a result, the liquid crystal display device prepared in Comparative Example 1 was inferior in dropping mark evaluation, image sticking evaluation, and response speed as compared with Example 1.

(Comparative Example 2)
As a polymerizable compound, it replaces with the compound represented by Formula (E-2-1) and Formula (E-2-2), and is represented by Formula (C-2-1) and Formula (E-1-1). A liquid crystal display element of Comparative Example 2 was obtained in the same manner as in Example 1 except that each of the above compounds was used.

  For the liquid crystal display element of Comparative Example 2, image sticking, dripping marks and response speed were measured in the same manner as in Example 1. The results are shown in Table 11.

  As a result, the liquid crystal display element prepared in Comparative Example 2 was inferior in dropping mark evaluation, image sticking evaluation, and response speed as compared with Example 1.

(Comparative Example 3)
As a polymerizable compound, it replaces with the compound represented by Formula (E-2-1) and Formula (E-2-2), and is represented by Formula (E-3-1) and Formula (E-1-1). A liquid crystal display device of Comparative Example 3 was obtained in the same manner as in Example 1 except that each of the above compounds was used.

  For the liquid crystal display element of Comparative Example 3, image sticking, dripping marks and response speed were measured in the same manner as in Example 1. The results are shown in Table 12.

As a result, the liquid crystal display device prepared in Comparative Example 3 was inferior in response speed as compared with Example 1.

DESCRIPTION OF SYMBOLS 10 ... Liquid crystal display element, 11 ... 1st board | substrate, 12 ... 2nd board | substrate, 13 ... Liquid crystal composition layer, 14 ... Common electrode, 15 ... Pixel electrode, 16 ... vertical alignment film, 17 ... vertical alignment film, 18 ... color filter, 19 ... liquid crystal molecule.

Claims (12)

A first substrate having a common electrode; a second substrate having a pixel electrode; and a liquid crystal composition layer sandwiched between the first substrate and the second substrate, and the common electrode A liquid crystal display element that applies an electric field substantially perpendicularly to the first substrate and the second substrate between the pixel electrodes to control liquid crystal molecules in the liquid crystal composition layer,
The orientation direction of the liquid crystal molecules in the liquid crystal composition layer is adjacent to at least one of the first substrate and the second substrate with respect to the liquid crystal composition layer in the first substrate and the second substrate. A vertical alignment film that is controlled substantially perpendicular to the surface, and the vertical alignment film is a polymer of two or more polymerizable compounds represented by the following general formula (1). One or more of the polymerizable compounds include a polymer that is a bifunctional polymerizable compound.

(In the formula, P ² represents a polymerizable functional group, S ¹ represents an alkylene group having 1 to 18 carbon atoms (the hydrogen atom in the alkylene group is one or more halogen atoms, CN group, or polymerized). It may be substituted by an alkyl group having 1 to 8 carbon atoms having a sexual functional groups, independently of each one CH ₂ group or not adjoining two or more CH ₂ groups existing in the groups to each other And X ¹ is —O—, —S—, —OCH ₂ —, —CH ₂ O, which may be replaced by —O—, —COO—, —OCO— or —OCO—O—. -, -CO-, -COO-, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -SCH _{2- , -CH 2 S -, - CF} 2 O -, - OCF 2 -, - CF 2 S -, - SCF 2 -, - CH = H-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—, —CH═CH—, — N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C— or a single bond (where P ² —S ¹ and S ¹ —X ¹ are —O -O-, -O-NH-, -S-S- and -O-S- groups are not included.), Q1 represents 0 or 1, MG represents a mesogenic group, R ² represents a hydrogen atom, Represents a halogen atom, a cyano group, or a linear or branched alkyl group having 1 to 12 carbon atoms, and the alkyl group is linear; May be branched, the alkyl group is one -CH ₂ - or nonadjacent two or more -CH ₂ - are each independently -O -, - S -, - CO -, - COO -, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -CH = CH-COO-, -CH = CH —OCO—, —COO—CH═CH—, —OCO—CH═CH—, —CH═CH—, —CF═CF— or —C≡C— may be substituted, or R ² may be Formula (1-a)

(Wherein P ³ represents a polymerizable functional group, S ² represents the same as defined in S ¹ , and X ² represents the same as defined in X ¹ ( Provided that P ³ —S ² and S ² —X ² do not include —O—O—, —O—NH—, —S—S— and —O—S— groups.), Q ² is 0 Or 1).
The mesogenic group represented by the above MG has the general formula (1-b)

(In the formula, B ¹ , B ² and B ³ are each independently 1,4-phenylene group, 1,4-cyclohexylene group, 1,4-cyclohexenyl group, tetrahydropyran-2,5-diyl group. 1,3-dioxane-2,5-diyl group, tetrahydrothiopyran-2,5-diyl group, 1,4-bicyclo (2,2,2) octylene group, decahydronaphthalene-2,6-diyl group Pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine-2,5-diyl group, thiophene-2,5-diyl group-, 1,2,3,4-tetrahydronaphthalene-2 , 6-diyl group, 2,6-naphthylene group, phenanthrene-2,7-diyl group, 9,10-dihydrophenanthrene-2,7-diyl group, 1,2,3,4,4a, 9,10a- Octahydrophenane Len-2,7-diyl group, 1,4-naphthylene group, benzo [1,2-b: 4,5-b ′] dithiophene-2,6-diyl group, benzo [1,2-b: 4, 5-b ′] diselenophen-2,6-diyl group, [1] benzothieno [3,2-b] thiophene-2,7-diyl group, [1] benzoselenopheno [3,2-b] selenophene-2 , 7-diyl group, or fluorene-2,7-diyl group, and one or more F, Cl, CF ₃ , OCF ₃ , CN groups, alkyl groups having 1 to 8 carbon atoms, carbon atoms as substituents An alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, Alkenyloxy group having 2 to 8 carbon atoms, carbon atoms 8 alkenoyl group, alkenoyloxy group having from 2 to 8 carbon atoms, or the general formula (1-c)

(Wherein P ⁴ represents a polymerizable functional group, S ³ represents the same as defined in S ¹ , and X ³ represents —O—, —COO—, —OCO—, —OCH, ₂ —, —CH ₂ O—, —CH ₂ CH ₂ OCO—, —COOCH ₂ CH ₂ —, —OCOCH ₂ CH ₂ —, or a single bond, q ³ represents 0 or 1, and q ⁴ represents 0. Or 1 (wherein, P ⁴ —S ³ and S ³ —X ³ do not include —O—O—, —O—NH—, —S—S— and —O—S— groups). )), R1 represents 0, 1, 2 or 3, and Z1 and Z2 are each independently —COO—, —OCO—, —CH ₂ CH ₂ —, —OCH ₂ —. , —CH ₂ O—, —CH═CH—, —C≡C—, —CH═CHCOO—, —OCOCH═CH—, —CH ₂ CH ₂ COO—, —CH ₂ CH ₂ OC _{O -, - COOCH 2 CH 2} -, - OCOCH 2 CH 2 -, - C = N -, - N = C -, - CONH -, - NHCO -, - C (CF 3) 2 -, - OCH 2 CH ₂ O— represents an alkyl group having 2 to 10 carbon atoms which may have a halogen atom or a single bond, and when r1 is 0 or 1, when B1 and a plurality of Z1 are present, they are the same. Or different. However, in the case of r1 is 0 ^{Z 2} is not a single bond, ^{Z 1} and ^{Z 2} is not a single bond when it has one general formula (1-c) as the substituent of ^{B 1} or ^{B 3.} )   The liquid crystal display element according to claim 1, comprising a plurality of pixels, and two or more regions having different pretilt angles in the pixels.   The liquid crystal display element according to claim 1, wherein the vertical alignment film includes a polyimide structure.   2. The liquid crystal display element according to claim 1, wherein the vertical alignment film is provided on a surface adjacent to the liquid crystal composition layer in the first substrate and the second substrate, and a color filter layer is provided on the first substrate. .   The liquid crystal display according to claim 1, wherein the pixel electrode has slits in a comb shape in four directions from the center of the pixel, and has four regions in which liquid crystal molecules in the liquid crystal composition layer are aligned in different directions. element.   The liquid crystal display element according to claim 1, wherein the liquid crystal composition layer is formed by a dropping method. The liquid crystal composition constituting the liquid crystal composition layer has the following general formula (I)

(In the formula, R ¹ and R ² are each independently 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 represents an alkenyloxy group, A represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and l represents 1 or 2, but when l is 2, two A's are the same. And may be different from each other) and a compound represented by the following general formula (II):

(In the formula, 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, 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 B and D are Each independently represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and Z ² represents a single bond, —OCH ₂ —, —OCO—, —CH ₂ O— or —COO—. , M represents 0, 1 or 2, but when m is 2, two Bs may be the same or different.) The liquid crystal display according to claim 1, element.   The said liquid crystal composition contains 30-60 mass% of compounds represented by the said general formula (I), and contains 30-65 mass% of compounds represented by the said general formula (II). Liquid crystal display element. The liquid crystal composition has the following general formula (III)

(In the formula, R ⁷ and R ⁸ are each independently 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 represents an alkenyloxy group, Y ¹ and Y ² each independently represent a hydrogen atom or a fluorine atom, and E, F and G each independently represent a 1,4-phenylene group or trans-1,4 -Represents cyclohexylene, Z ³ represents a single bond, —OCH ₂ —, —OCO—, —CH ₂ O— or —COO—, and n represents 0 or 1). The liquid crystal display element of Claim 7 or 8 containing 20 mass%. An alignment material containing two or more polymerizable compounds represented by the following general formula (1) and a vertical alignment material on at least one of the first substrate having a common electrode and the second substrate having a pixel electrode: After applying and heating to form an alignment film, the liquid crystal composition is sandwiched between the first substrate and the second substrate, and a voltage is applied between the common electrode and the pixel electrode for alignment. By irradiating active energy rays in a state, a method for producing a liquid crystal display element that polymerizes a polymerizable compound in the alignment film,
The manufacturing method of the liquid crystal display element whose 1 or more types is a bifunctional polymeric compound among the 2 or more types of polymeric compounds represented by the said General formula (1).

(In the formula, P ² represents a polymerizable functional group, S ¹ represents an alkylene group having 1 to 18 carbon atoms (the hydrogen atom in the alkylene group is one or more halogen atoms, CN group, or polymerized). It may be substituted by an alkyl group having 1 to 8 carbon atoms having a sexual functional groups, independently of each one CH ₂ group or not adjoining two or more CH ₂ groups existing in the groups to each other And X ¹ is —O—, —S—, —OCH ₂ —, —CH ₂ O, which may be replaced by —O—, —COO—, —OCO— or —OCO—O—. -, -CO-, -COO-, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -SCH _{2- , -CH 2 S -, - CF} 2 O -, - OCF 2 -, - CF 2 S -, - SCF 2 -, - CH = H-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—, —CH═CH—, — N═N—, —CH═N—N═CH—, —CF═CF—, —C≡C— or a single bond (where P ² —S ¹ and S ¹ —X ¹ are —O -O-, -O-NH-, -S-S- and -O-S- groups are not included.), Q1 represents 0 or 1, MG represents a mesogenic group, R ² represents a hydrogen atom, Represents a halogen atom, a cyano group, or a linear or branched alkyl group having 1 to 12 carbon atoms, and the alkyl group is linear; May be branched, the alkyl group is one -CH ₂ - or nonadjacent two or more -CH ₂ - are each independently -O -, - S -, - CO -, - COO -, -OCO-, -CO-S-, -S-CO-, -O-CO-O-, -CO-NH-, -NH-CO-, -CH = CH-COO-, -CH = CH —OCO—, —COO—CH═CH—, —OCO—CH═CH—, —CH═CH—, —CF═CF— or —C≡C— may be substituted, or R ² may be Formula (1-a)

(Wherein P ³ represents a polymerizable functional group, S ² represents the same as defined in S ¹ , and X ² represents the same as defined in X ¹ ( Provided that P ³ —S ² and S ² —X ² do not include —O—O—, —O—NH—, —S—S— and —O—S— groups.), Q ² is 0 Or 1).
The mesogenic group represented by the above MG has the general formula (1-b)

(In the formula, B ¹ , B ² and B ³ are each independently 1,4-phenylene group, 1,4-cyclohexylene group, 1,4-cyclohexenyl group, tetrahydropyran-2,5-diyl group. 1,3-dioxane-2,5-diyl group, tetrahydrothiopyran-2,5-diyl group, 1,4-bicyclo (2,2,2) octylene group, decahydronaphthalene-2,6-diyl group Pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, pyrazine-2,5-diyl group, thiophene-2,5-diyl group-, 1,2,3,4-tetrahydronaphthalene-2 , 6-diyl group, 2,6-naphthylene group, phenanthrene-2,7-diyl group, 9,10-dihydrophenanthrene-2,7-diyl group, 1,2,3,4,4a, 9,10a- Octahydrophenane Len-2,7-diyl group, 1,4-naphthylene group, benzo [1,2-b: 4,5-b ′] dithiophene-2,6-diyl group, benzo [1,2-b: 4, 5-b ′] diselenophen-2,6-diyl group, [1] benzothieno [3,2-b] thiophene-2,7-diyl group, [1] benzoselenopheno [3,2-b] selenophene-2 , 7-diyl group, or fluorene-2,7-diyl group, and one or more F, Cl, CF ₃ , OCF ₃ , CN groups, alkyl groups having 1 to 8 carbon atoms, carbon atoms as substituents An alkoxy group having 1 to 8 carbon atoms, an alkanoyl group having 1 to 8 carbon atoms, an alkanoyloxy group having 1 to 8 carbon atoms, an alkoxycarbonyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, Alkenyloxy group having 2 to 8 carbon atoms, carbon atoms 8 alkenoyl group, alkenoyloxy group having from 2 to 8 carbon atoms, and / or the general formula (1-c)

(Wherein P ⁴ represents a polymerizable functional group,
S ³ represents the same as defined in S ¹ , and X ³ represents —O—, —COO—, —OCO—, —OCH ₂ —, —CH ₂ O—, —CH ₂ CH _{2. OCO -, - COOCH 2 CH 2} -, - OCOCH 2 CH 2 -, or a single bond, ^{q 3} is 0 or 1, ^{q 4} represents 0 or 1. (However, P ⁴ —S ³ and S ³ —X ³ do not include —O—O—, —O—NH—, —S—S—, and —O—S— groups). even if well, r1 represents 0, 1, 2 or 3, Z1 and Z2 each independently, -COO -, - OCO -, - CH 2 CH 2 -, - OCH 2 -, - CH 2 O —, —CH═CH—, —C≡C—, —CH═CHCOO—, —OCOCH═CH—, —CH ₂ CH ₂ COO—, —CH ₂ CH ₂ OCO—, —COOCH ₂ CH ₂ —, — OCOCH ₂ CH ₂ —, —C═N—, —N═C—, —CONH—, —NHCO—, —C (CF ₃ ) ₂ —, —OCH ₂ CH ₂ O—, and a halogen atom Represents a good alkyl group having 2 to 10 carbon atoms or a single bond, and when r1 is 0 or 1, when B1 and a plurality of Z1 are present, Each may be the same or different. However, in the case of r1 is 0 ^{Z 2} is not a single bond, ^{Z 1} and ^{Z 2} is not a single bond when it has one general formula (1-c) as the substituent of ^{B 1} or ^{B 3.} ) The method of manufacturing a liquid crystal display element according to claim 10, wherein the active energy ray is ultraviolet light, the intensity thereof is ² mW / cm ^{−2 to} 100 mW / cm ⁻² , and the total irradiation energy amount is 1 J to 300 J.   The liquid crystal composition contains 30 to 50% by mass of the compound represented by the general formula (I) and 30 to 50% by mass of the compound represented by the general formula (II). The manufacturing method of the liquid crystal display element of description.

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