JP6859626B2 - Liquid crystal composition and liquid crystal display element - Google Patents

Description

The present invention relates to a liquid crystal composition, a liquid crystal display device containing the composition, and the like. In particular, it relates to a liquid crystal composition having a positive dielectric anisotropy, and an AM (active matrix) device containing the composition and having a mode of TN, OCB, IPS, FFS, or FPA.

In liquid crystal display elements, the classification based on the operation mode of liquid crystal molecules is PC (phase change), TN (twisted nematic), STN (super twisted nematic), ECB (electrically controlled birefringence), OCB (optically compensated bend), IPS. (In-plane switching), VA (vertical alignment), FFS (fringe field switching), FPA (field-induced photo-reactive alignment) and other modes. The classifications based on the drive method of the element are PM (passive matrix) and AM (active matrix). PM is classified into static and multiplex, and AM is classified into TFT (thin film transistor), MIM (metal insulator metal) and the like. The classification of TFTs is amorphous silicon and polycrystal silicon. The latter is classified into a high temperature type and a low temperature type according to the manufacturing process. The classification based on the light source is a reflective type that uses natural light, a transmissive type that uses a backlight, and a semi-transmissive type that uses both natural light and a backlight.

The liquid crystal display element contains a liquid crystal composition having a nematic phase. This composition has suitable properties. By improving the characteristics of this composition, an AM element having good characteristics can be obtained. The relationships in these properties are summarized in Table 1 below. The properties of the composition will be further described based on commercially available AM devices. The temperature range of the nematic phase is related to the temperature range in which the device can be used. The preferred upper limit temperature of the nematic phase is about 70 ° C. or higher, and the preferred lower limit temperature of the nematic phase is about −10 ° C. or lower. The viscosity of the composition is related to the response time of the device. A short response time is preferred for displaying moving images on the device. A shorter response time of even 1 millisecond is desirable. Therefore, a small viscosity in the composition is preferred. Small viscosities at low temperatures are more preferred. The elastic constant of the composition is related to the contrast of the device. In order to increase the contrast in the device, a large elastic constant in the composition is more preferable.

The optical anisotropy of the composition is related to the contrast ratio of the device. Depending on the mode of the device, a large optical anisotropy or a small optical anisotropy, that is, an appropriate optical anisotropy is required. The product (Δn × d) of the optical anisotropy (Δn) of the composition and the cell gap (d) of the device is designed to maximize the contrast ratio. The appropriate product value depends on the type of operating mode. For devices in modes such as TN, a suitable value is about 0.45 μm. In this case, a composition having a large optical anisotropy is preferable for a device having a small cell gap. The large permittivity anisotropy in the composition contributes to the low threshold voltage, low power consumption and large contrast ratio in the device. Therefore, a large dielectric anisotropy is preferred. A large resistivity in the composition contributes to a large voltage retention and a large contrast ratio in the device. Therefore, a composition having a large resistivity at an initial stage not only at room temperature but also at a temperature close to the upper limit temperature of the nematic phase is preferable. After long-term use, a composition having a large resistivity not only at room temperature but also at a temperature close to the upper limit temperature of the nematic phase is preferable. The stability of the composition against ultraviolet light and heat is related to the life of the liquid crystal display device. When these stability is high, the life of this device is long. Such characteristics are preferable for AM elements used in liquid crystal projectors, liquid crystal televisions, and the like.

In the AM device having the TN mode, a composition having a positive dielectric anisotropy is used. In the AM device having the VA mode, a composition having a negative dielectric anisotropy is used. In an AM device having an IPS mode or an FFS mode, a composition having positive or negative dielectric anisotropy is used. In a polymer sustained alignment (PSA) type AM device, a composition having positive or negative dielectric anisotropy is used.

International Publication No. 1996/11897 Japanese Unexamined Patent Publication No. 2008-38018 International Publication No. 2010/67661

One object of the present invention is a high upper limit temperature of the nematic phase, a lower lower limit temperature of the nematic phase, a small viscosity, an appropriate optical anisotropy, a large dielectric anisotropy, a large dielectric constant in the minor axis direction of a liquid crystal molecule, and the like. It is an object of the present invention to provide a liquid crystal composition satisfying at least one of properties such as high specific resistance, high stability against ultraviolet rays, high stability against heat, and a large elastic constant. Another object is to provide a liquid crystal composition having an appropriate balance between at least two of these properties. Another object is to provide a liquid crystal display device containing such a composition. Another object is to provide an AM device with characteristics such as short response time, high voltage retention, low threshold voltage, high contrast ratio, long life.

式（１）および式（２）において、Ｒ^１は、炭素数１から１２のアルキルまたは炭素数２から１２のアルケニルであり、これらの基において、少なくとも１つの−ＣＨ_２−は、−Ｏ−で置き換えられてもよく；Ｒ^２およびＲ^３は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルであり；環Ａは、１，４−シクロヘキシレンまたは１，４−シクロヘキセニレンであり；環Ｂは、１，４−シクロヘキシレン、１，４−シクロヘキセニレン、１，４−フェニレン、２−フルオロ−１，４−フェニレン、２，３−ジフルオロ−１，４−フェニレン、２，６−ジフルオロ−１，４−フェニレン、ピリミジン−２，５−ジイル、１，３−ジオキサン−２，５−ジイル、またはテトラヒドロピラン−２，５−ジイルであり；Ｚ^１およびＺ^２は独立して、単結合、エチレン、メチレンオキシ、カルボニルオキシ、またはジフルオロメチレンオキシであり；Ｘ^１およびＸ^２は独立して、水素またはフッ素であり；Ｙ^１は、フッ素、塩素、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルコキシ、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルオキシであり；ａは、０、１、２、または３であり；ここで、ａが１かつＺ^２がジフルオロメチレンオキシであるとき、環Ｂは、１，４−フェニレン、２−フルオロ−１，４−フェニレン、２，３−ジフルオロ−１，４−フェニレン、２，６−ジフルオロ−１，４−フェニレン、ピリミジン−２，５−ジイル、１，３−ジオキサン−２，５−ジイル、またはテトラヒドロピラン−２，５−ジイルであり；ｎは、１、２、または３である。 In the present invention, at least one compound selected from the group of compounds represented by the formula (1) as the first component, and at least one selected from the group of compounds represented by the formula (2) as the second component. The present invention relates to a liquid crystal composition containing one compound and having a nematic phase, and a liquid crystal display element containing this composition.

In formulas (1) and (2), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, at least one −CH ₂ − is −O−. ^{R 2} and R ³ may be independently replaced by an alkyl having 1 to 12 carbons, an alkoxy having 1 to 12 carbons, an alkenyl having 2 to 12 carbons, and at least one hydrogen being fluorine or chlorine. An alkyl having 1 to 12 carbon atoms replaced, or an alkenyl having 2 to 12 carbon atoms in which at least one hydrogen has been replaced with fluorine or chlorine; ring A is 1,4-cyclohexylene or 1,4-cyclohexyl. Senilene; Ring B is 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4- Phenylene, 2,6-difluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ¹ and Z ² is independently single-bonded, ethylene, methyleneoxy, carbonyloxy, or difluoromethyleneoxy; X ¹ and X ² are independently hydrogen or fluorine; Y ¹ is fluorine, chlorine, at least 1 One hydrogen is replaced with fluorine or chlorine, alkyl with 1 to 12 carbons, at least one hydrogen is replaced with fluorine or chlorine, alkoxy with 1 to 12 carbons, or at least one hydrogen is replaced with fluorine or chlorine. It is an alkenyloxy having 2 to 12 carbon atoms; a is 0, 1, 2, or 3; where a is 1 and Z ² is difluoromethyleneoxy, the ring B is 1,4. -Phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyrimidin-2,5-diyl, 1,3-dioxane -2,5-diyl, or tetrahydropyran-2,5-diyl; n is 1, 2, or 3.

The advantages of the present invention are high upper limit temperature of nematic phase, lower lower limit temperature of nematic phase, small viscosity, appropriate optical anisotropy, large permittivity anisotropy, large permittivity of liquid crystal molecules in the minor axis direction, large ratio. It is an object of the present invention to provide a liquid crystal composition that satisfies at least one of properties such as resistance, high stability against ultraviolet rays, high stability against heat, and a large elastic constant. Another advantage is to provide a liquid crystal composition having an appropriate balance between at least two of these properties. Another advantage is to provide a liquid crystal display device containing such a composition. Another advantage is to provide an AM device with characteristics such as short response time, high voltage retention, low threshold voltage, high contrast ratio, long life.

The usage of terms in this specification is as follows. The terms "liquid crystal composition" and "liquid crystal display element" may be abbreviated as "composition" and "element", respectively. "Liquid crystal display element" is a general term for a liquid crystal display panel and a liquid crystal display module. The "liquid crystal compound" is composed for the purpose of adjusting characteristics such as a temperature range, viscosity, and dielectric constant anisotropy of a compound having a liquid crystal phase such as a nematic phase and a smectic phase, and a nematic phase having no liquid crystal phase. It is a general term for compounds that are mixed with substances. This compound has a six-membered ring such as 1,4-cyclohexylene or 1,4-phenylene, and its molecular structure is rod-like. A "polymerizable compound" is a compound added for the purpose of forming a polymer in a composition. Liquid crystal compounds with alkenyl are not polymerizable in that sense.

The liquid crystal composition is prepared by mixing a plurality of liquid crystal compounds. Additives such as optically active compounds, antioxidants, ultraviolet absorbers, dyes, defoamers, polymerizable compounds, polymerization initiators, polymerization inhibitors, and polar compounds are added to the liquid crystal composition as needed. To. The proportion of the liquid crystal compound is expressed as a weight percentage (% by weight) based on the weight of the liquid crystal composition containing no additive even when the additive is added. The ratio of the additive is expressed as a weight percentage (% by weight) based on the weight of the liquid crystal composition containing no additive. That is, the ratio of the liquid crystal compound or the additive is calculated based on the total weight of the liquid crystal compound. Parts per million (ppm) by weight may also be used. The proportions of polymerization initiators and polymerization inhibitors are exceptionally expressed based on the weight of the polymerizable compound.

The "upper limit temperature of the nematic phase" may be abbreviated as the "upper limit temperature". The "lower limit temperature of the nematic phase" may be abbreviated as the "lower limit temperature". "Large resistivity" means that the composition has a large resistivity not only at room temperature but also at a temperature close to the upper limit temperature of the nematic phase in the initial stage, and after long-term use, it reaches the upper limit temperature of the nematic phase as well as room temperature. It means that it has a large resistivity even at a close temperature. "Large voltage retention" means that the device has a large voltage retention not only at room temperature but also at a temperature close to the upper limit temperature of the nematic phase at the initial stage, and after long-term use, not only the room temperature but also the upper limit temperature of the nematic phase. It means that it has a large voltage retention even at a temperature close to. The characteristics of the composition or device may be examined before and after the aging test (including the accelerated deterioration test). The expression "increase the dielectric anisotropy" means that when the composition has a positive dielectric anisotropy, its value increases positively, and the composition has a negative dielectric anisotropy. When it is a thing, it means that its value increases negatively.

The compound represented by the formula (1) may be abbreviated as "compound (1)". At least one compound selected from the group of compounds represented by the formula (1) may be abbreviated as "Compound (1)". "Compound (1)" means one compound represented by the formula (1), a mixture of two compounds, or a mixture of three or more compounds. The same applies to compounds represented by other formulas. The expression "at least one'A'" means that the number of'A'is arbitrary. The expression "at least one'A'may be replaced by'B'" is that when the number of'A's is 1, the position of the'A'is arbitrary and the number of'A's is 2. When there is more than one, their positions can be selected without limitation. This rule also applies to the expression "at least one'A'has been replaced by a'B'".

Expressions such as "at least one -CH _2- may be replaced by -O-" are used herein. In this case, −CH ₂ −CH ₂ −CH ₂₋ may be converted to −O−CH ₂₋ O− by replacing the non-adjacent −CH _{2− with −O−.} However, the adjacent −CH ₂₋ is not replaced by −O−. This is because -O-O-CH _2- (peroxide) is produced by this replacement. That is, this expression includes both "one -CH _2- may be replaced by -O-" and "at least two non-adjacent -CH _2- may be replaced by -O-". means. This rule applies not only to the replacement with -O-, but also to the replacement with divalent groups such as -CH = CH- and -COO-.

In the chemical formulas of the component compounds, with symbols of terminal groups R ¹ to a plurality of compounds. In these compounds, two groups represented by any two of R ¹ may be may be the same or different. For example, there are cases where ^{R 1 of} compound (1-1) ^{is ethyl and R 1} of compound (1-2) is ethyl. ^{In some cases, R 1 of} compound (1-1) ^{is ethyl and R 1} of compound (1-2) is propyl. This rule also applies to symbols such as other end groups. In equation (1), when the subscript'a'is 2, there are two rings B. In this compound, the two rings represented by the two rings B may be the same or different. This rule also applies to any two rings B when the subscript'a'is greater than 2. This rule, Z ^3, applies to such rings C.

2-Fluoro-1,4-phenylene means the following two divalent groups. In the chemical formula, fluorine may be left-facing (L) or right-facing (R). This rule also applies to asymmetric divalent groups generated by removing two hydrogens from the ring, such as tetrahydropyran-2,5-diyl. This rule also applies to divalent binding groups such as carbonyloxy (-COO- or -OCO-).

The alkyl of the liquid crystal compound is linear or branched and does not contain cyclic alkyl. Linear alkyl is preferred over branched alkyl. The same applies to terminal groups such as alkoxy and alkenyl. The configuration for 1,4-cyclohexylene is preferably trans over cis in order to raise the upper temperature limit.

The present invention includes the following items.

式（１）および式（２）において、Ｒ^１は、炭素数１から１２のアルキルまたは炭素数２から１２のアルケニルであり、これらの基において、少なくとも１つの−ＣＨ_２−は、−Ｏ−で置き換えられてもよく；Ｒ^２およびＲ^３は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルであり；環Ａは、１，４−シクロヘキシレンまたは１，４−シクロヘキセニレンであり；環Ｂは、１，４−シクロヘキシレン、１，４−シクロヘキセニレン、１，４−フェニレン、２−フルオロ−１，４−フェニレン、２，３−ジフルオロ−１，４−フェニレン、２，６−ジフルオロ−１，４−フェニレン、ピリミジン−２，５−ジイル、１，３−ジオキサン−２，５−ジイル、またはテトラヒドロピラン−２，５−ジイルであり；Ｚ^１およびＺ^２は独立して、単結合、エチレン、メチレンオキシ、カルボニルオキシ、またはジフルオロメチレンオキシであり；Ｘ^１およびＸ^２は独立して、水素またはフッ素であり；Ｙ^１は、フッ素、塩素、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルコキシ、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルオキシであり；ａは、０、１、２、または３であり；ここで、ａが１かつＺ^２がジフルオロメチレンオキシであるとき、環Ｂは、１，４−フェニレン、２−フルオロ−１，４−フェニレン、２，３−ジフルオロ−１，４−フェニレン、２，６−ジフルオロ−１，４−フェニレン、ピリミジン−２，５−ジイル、１，３−ジオキサン−２，５−ジイル、またはテトラヒドロピラン−２，５−ジイルであり；ｎは、１、２、または３である。 Item 1. Contains at least one compound selected from the group of compounds represented by the formula (1) as the first component and at least one compound selected from the group of compounds represented by the formula (2) as the second component. A liquid crystal composition having a nematic phase.

In formulas (1) and (2), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, at least one −CH ₂ − is −O−. ^{R 2} and R ³ may be independently replaced by an alkyl having 1 to 12 carbons, an alkoxy having 1 to 12 carbons, an alkenyl having 2 to 12 carbons, and at least one hydrogen being fluorine or chlorine. An alkyl having 1 to 12 carbon atoms replaced, or an alkenyl having 2 to 12 carbon atoms in which at least one hydrogen has been replaced with fluorine or chlorine; ring A is 1,4-cyclohexylene or 1,4-cyclohexyl. Senilene; Ring B is 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4- Phenylene, 2,6-difluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ¹ and Z ² is independently single-bonded, ethylene, methyleneoxy, carbonyloxy, or difluoromethyleneoxy; X ¹ and X ² are independently hydrogen or fluorine; Y ¹ is fluorine, chlorine, at least 1 One hydrogen is replaced with fluorine or chlorine, alkyl with 1 to 12 carbons, at least one hydrogen is replaced with fluorine or chlorine, alkoxy with 1 to 12 carbons, or at least one hydrogen is replaced with fluorine or chlorine. It is an alkenyloxy having 2 to 12 carbon atoms; a is 0, 1, 2, or 3; where a is 1 and Z ² is difluoromethyleneoxy, the ring B is 1,4. -Phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyrimidin-2,5-diyl, 1,3-dioxane -2,5-diyl, or tetrahydropyran-2,5-diyl; n is 1, 2, or 3.

式（１−１）から式（１−１０）において、Ｒ^１は、炭素数１から１２のアルキルまたは炭素数２から１２のアルケニルであり、これらの基において、少なくとも１つの−ＣＨ_２−は、−Ｏ−で置き換えられてもよく；Ｘ^１、Ｘ^２、Ｘ^３、Ｘ^４、Ｘ^５、およびＸ^６は独立して、水素またはフッ素であり；Ｙ^１は、フッ素、塩素、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルコキシ、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルオキシであり；ｎは、１、２、または３である。 Item 2. Item 2. The liquid crystal composition according to Item 1, which contains at least one compound selected from the group of compounds represented by formulas (1-1) to (1-10) as a first component.

In formulas (1-1) to (1-10), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, at least one −CH ₂ − is. , -O- may be replaced; X ¹ , X ² , X ³ , X ⁴ , X ⁵ , and X ⁶ are independently hydrogen or fluorine; Y ¹ is fluorine, chlorine, at least 1 Alkyl with 1 to 12 carbon atoms in which one hydrogen is replaced with fluorine or chlorine, alkoxy with 1 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine, or at least one hydrogen is replaced with fluorine or chlorine. It is an alkenyloxy having 2 to 12 carbon atoms; n is 1, 2, or 3.

Item 3. Item 2. The liquid crystal composition according to Item 1 or 2, wherein the ratio of the first component is in the range of 3% by weight to 30% by weight, and the ratio of the second component is in the range of 10% by weight to 80% by weight.

式（３）において、Ｒ^４は、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、または炭素数２から１２のアルケニルであり；環Ｃは、１，４−シクロヘキシレン、１，４−フェニレン、２−フルオロ−１，４−フェニレン、２，３−ジフルオロ−１，４−フェニレン、２，６−ジフルオロ−１，４−フェニレン、ピリミジン−２，５−ジイル、１，３−ジオキサン−２，５−ジイル、またはテトラヒドロピラン−２，５−ジイルであり；Ｚ^３は、単結合、エチレン、カルボニルオキシ、またはジフルオロメチレンオキシであり；Ｘ^７およびＸ^８は独立して、水素またはフッ素であり；Ｙ^２は、フッ素、塩素、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルキル、少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数１から１２のアルコキシ、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルオキシであり；ｂは、１、２、３、または４である。 Item 4. Item 6. The liquid crystal composition according to any one of Items 1 to 3, which contains at least one compound selected from the group of compounds represented by the formula (3) as a third component.

In formula (3), R ⁴ is an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, or an alkenyl having 2 to 12 carbon atoms; ring C is 1,4-cyclohexylene, 1, 1. 4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyrimidin-2,5-diyl, 1,3- Dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ³ is a single bond, ethylene, carbonyloxy, or difluoromethyleneoxy; X ⁷ and X ⁸ are independently hydrogen. Or fluorine; Y ² is fluorine, chlorine, an alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, and 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine. Aalkoxy, or an alkenyloxy having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine; b is 1, 2, 3, or 4.

式（３−１）から式（３−３５）において、Ｒ^４は、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、または炭素数２から１２のアルケニルである。 Item 5. Item 2. The liquid crystal composition according to any one of Items 1 to 4, which contains at least one compound selected from the group of compounds represented by the formulas (3-1) to (3-35) as the third component. Stuff.

In the formula (3-35) from equation (3-1), ^{R 4} is an alkenyl alkyl of 1 to 12 carbons, alkoxy having 1 to 12 carbons, or 2 to 12 carbons.

Item 6. The liquid crystal composition according to claim 4 or 5, wherein the proportion of the third component is in the range of 10% by weight to 70% by weight.

式（４）において、Ｒ^５およびＲ^６は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルであり；環Ｄおよび環Ｅは独立して、１，４−シクロヘキシレン、１，４−フェニレン、２−フルオロ−１，４−フェニレン、または２，５−ジフルオロ−１，４−フェニレンであり；Ｚ^４は、単結合、エチレン、またはカルボニルオキシであり；ｃは、１、２、または３であり；ｃが１であるとき、環Ｅは、１，４−フェニレン、２−フルオロ−１，４−フェニレン、または２，５−ジフルオロ−１，４−フェニレンである。 Item 7. Item 6. The liquid crystal composition according to any one of Items 1 to 6, further containing at least one compound selected from the group of compounds represented by the formula (4) as the fourth component.

In formula (4), R ⁵ and R ⁶ are independently an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, or at least one hydrogen being fluorine or chlorine. It is a replaced alkenyl with 2 to 12 carbon atoms; rings D and E are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, or 2,5. -Difluoro-1,4-phenylene; Z ⁴ is single bond, ethylene, or carbonyloxy; c is 1, 2, or 3; when c is 1, ring E is 1 , 4-Phenylene, 2-Fluoro-1,4-Phenylene, or 2,5-Difluoro-1,4-Phenylene.

式（４−１）から式（４−１２）において、Ｒ^５およびＲ^６は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、または少なくとも１つの水素がフッ素または塩素で置き換えられた炭素数２から１２のアルケニルである。 Item 8. Item 2. The liquid crystal composition according to any one of Items 1 to 7, which contains at least one compound selected from the group of compounds represented by the formulas (4-1) to (4-12) as the fourth component. Stuff.

In the formula (4-12) from equation (4-1), independently of ^{R 5} and ^{R 6,} alkyl of 1 to 12 carbons, alkoxy having 1 to 12 carbons, from 2 to 12 carbons, alkenyl or, An alkoxy having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine.

Item 9. Item 7. The liquid crystal composition according to Item 7 or 8, wherein the proportion of the fourth component is in the range of 5% by weight to 60% by weight.

式（５）において、Ｒ^７およびＲ^８は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、または炭素数２から１２のアルケニルオキシであり；環Ｆおよび環Ｉは独立して、１，４−シクロヘキシレン、１，４−シクロヘキセニレン、１，４−フェニレン、少なくとも１つの水素がフッ素または塩素で置き換えられた１，４−フェニレン、またはテトラヒドロピラン−２，５−ジイルであり；環Ｇは、２，３−ジフルオロ−１，４−フェニレン、２−クロロ−３−フルオロ−１，４−フェニレン、２，３−ジフルオロ−５−メチル−１，４−フェニレン、３，４，５−トリフルオロナフタレン−２，６−ジイル、または７，８−ジフルオロクロマン−２，６−ジイルであり；Ｚ^５およびＺ^６は独立して、単結合、エチレン、カルボニルオキシ、またはメチレンオキシであり；ｄは、１、２、または３であり、ｅは、０または１であり、ｄとｅとの和は３以下である。 Item 10. Item 6. The liquid crystal composition according to any one of Items 1 to 9, which contains at least one compound selected from the group of compounds represented by the formula (5) as the fifth component.

In formula (5), R ⁷ and R ⁸ are independently composed of an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, or an alkenyloxy having 2 to 12 carbon atoms. Yes; Rings F and I are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one hydrogen is replaced with fluorine or chlorine. , Or tetrahydropyran-2,5-diyl; ring G is 2,3-difluoro-1,4-phenylene, 2-chloro-3-fluoro-1,4-phenylene, 2,3-difluoro-5. - methyl-1,4-phenylene, 3,4,5-trifluoro-2,6-diyl or 7,8-be difluorochroman-2,6-diyl; ^{Z 5} and ^{Z 6} are each independently , Single bond, ethylene, carbonyloxy, or methyleneoxy; d is 1, 2, or 3, e is 0 or 1, and the sum of d and e is 3 or less.

式（５−１）から式（５−２２）において、Ｒ^７およびＲ^８は独立して、炭素数１から１２のアルキル、炭素数１から１２のアルコキシ、炭素数２から１２のアルケニル、または炭素数２から１２のアルケニルオキシである。 Item 11. Item 2. The liquid crystal composition according to any one of Items 1 to 10, which contains at least one compound selected from the group of compounds represented by the formulas (5-1) to (5-22) as the fifth component. Stuff.

In formulas (5-1) to (5-22), R ⁷ and R ⁸ are independently alkyl with 1 to 12 carbon atoms, alkoxy with 1 to 12 carbon atoms, alkenyl with 2 to 12 carbon atoms, or It is an alkoxyoxy having 2 to 12 carbon atoms.

Item 12. Item 2. The liquid crystal composition according to Item 10 or 11, wherein the proportion of the fifth component is in the range of 2% by weight to 30% by weight.

Item 13. The upper limit temperature of the nematic phase is 70 ° C. or higher, the optical anisotropy at a wavelength of 589 nm (measured at 25 ° C.) is 0.07 or higher, and the dielectric anisotropy at a frequency of 1 kHz (measured at 25 ° C.) is 2. The liquid crystal composition according to any one of Items 1 to 12, which is the above.

Item 14. A liquid crystal display device containing the liquid crystal composition according to any one of Items 1 to 13.

Item 15. Item 14. The liquid crystal display element according to Item 14, wherein the operation mode of the liquid crystal display element is TN mode, ECB mode, OCB mode, IPS mode, FFS mode, or FPA mode, and the drive method of the liquid crystal display element is the active matrix method. ..

Item 16. Use of the liquid crystal composition according to any one of Items 1 to 13 in a liquid crystal display device.

The present invention also includes the following sections. (A) The above composition further containing at least one of additives such as an optically active compound, an antioxidant, an ultraviolet absorber, a dye, an antifoaming agent, a polymerizable compound, a polymerization initiator, a polymerization inhibitor, and a polar compound. Stuff. (B) AM device containing the above composition. (C) The above-mentioned composition further containing a polymerizable compound, and a polymer-supported orientation (PSA) type AM device containing this composition. (D) A polymer-supported orientation (PSA) type AM device containing the above composition and in which the polymerizable compound in the composition is polymerized. (E) A device containing the above composition and having a mode of PC, TN, STN, ECB, OCB, IPS, VA, FFS, or FPA. (F) A transmissive device containing the above composition. (G) Use of the above composition as a composition having a nematic phase. (H) Use as an optically active composition by adding an optically active compound to the above composition.

The composition of the present invention will be described in the following order. First, the composition of the composition will be described. Secondly, the main properties of the constituent compounds and the main effects of this compound on the composition will be described. Third, the combination of ingredients in the composition, the preferred proportions of the ingredients and the rationale thereof will be described. Fourth, preferable forms of the component compounds will be described. Fifth, preferred component compounds are shown. Sixth, additives that may be added to the composition will be described. Seventh, a method for synthesizing a component compound will be described. Finally, the use of the composition will be described.

First, the composition of the composition will be described. The compositions of the present invention are classified into composition A and composition B. The composition A includes a liquid crystal compound selected from the compound (1), the compound (2), the compound (3), the compound (4), and the compound (5), as well as other liquid crystal compounds, additives, and the like. May be further contained. The "other liquid crystal compound" is a liquid crystal compound different from the compound (1), the compound (2), the compound (3), the compound (4), and the compound (5). Such compounds are mixed into the composition for the purpose of further adjusting the properties. Additives include optically active compounds, antioxidants, UV absorbers, dyes, defoamers, polymerizable compounds, polymerization initiators, polymerization inhibitors, polar compounds and the like.

The composition B is substantially composed of only a liquid crystal compound selected from the compound (1), the compound (2), the compound (3), the compound (4), and the compound (5). "Substantially" means that the composition may contain additives but does not contain other liquid crystal compounds. Composition B has a smaller number of components than composition A. The composition B is preferable to the composition A from the viewpoint of reducing the cost. Composition A is preferable to composition B from the viewpoint that the properties can be further adjusted by mixing other liquid crystal compounds.

Secondly, the main properties of the constituent compounds and the main effects of this compound on the composition will be described. The main properties of the component compounds are summarized in Table 2 based on the effects of the present invention. In the symbols in Table 2, L means large or high, M means medium, and S means small or low. The symbols L, M, and S are classifications based on qualitative comparisons between the constituent compounds, and 0 (zero) means that the value is close to zero.

When the component compound is mixed with the composition, the main effects of the component compound on the properties of the composition are as follows. Compound (1) increases the dielectric anisotropy. Compound (2) lowers the viscosity or lowers the lower limit temperature. Compound (3) increases the dielectric anisotropy. Compound (4) raises the upper limit temperature or lowers the lower limit temperature. Compound (5) increases the dielectric constant in the minor axis direction.

Thirdly, the combination of components in the composition, the preferable ratio of the component compounds, and the rationale thereof will be described. Preferred combinations of components in the composition are 1st component + 2nd component, 1st component + 2nd component + 3rd component, 1st component + 2nd component + 4th component, 1st component + 2nd component + 1st component. Five components, first component + second component + third component + fourth component, first component + second component + third component + fifth component, first component + second component + fourth component + fifth component , Or the first component + the second component + the third component + the fourth component + the fifth component. A more preferable combination is the first component + the second component + the third component + the fourth component.

The preferable ratio of the first component is about 3% by weight or more in order to increase the dielectric anisotropy, and about 30% by weight or less in order to lower the lower limit temperature. A more preferred proportion is in the range of about 3% by weight to about 20% by weight. A particularly preferred proportion is in the range of about 3% by weight to about 15% by weight.

The preferred proportion of the second component is about 10% by weight or more to reduce the viscosity and about 80% by weight or less to increase the dielectric anisotropy. A more preferred proportion is in the range of about 15% by weight to about 75% by weight. A particularly preferred proportion is in the range of about 20% by weight to about 70% by weight.

The preferable ratio of the third component is about 10% by weight or more in order to increase the dielectric anisotropy, and about 70% by weight or less in order to lower the lower limit temperature. A more preferred proportion is in the range of about 15% by weight to about 65% by weight. A particularly preferred proportion is in the range of about 15% by weight to about 60% by weight.

The preferable ratio of the fourth component is about 5% by weight or more in order to raise the upper limit temperature or lower the viscosity, and about 60% by weight or less in order to raise the dielectric anisotropy. A more preferred ratio is in the range of about 5% by weight to about 50% by weight. A particularly preferable ratio is in the range of about 10% by weight to about 40% by weight.

The preferable ratio of the fifth component is about 2% by weight or more in order to increase the dielectric constant of the liquid crystal molecule in the minor axis direction, and about 30% by weight or less in order to lower the lower limit temperature. A more preferred ratio is in the range of about 2% by weight to about 20% by weight. A particularly preferable ratio is in the range of about 2% by weight to about 10% by weight.

Fourth, preferable forms of the component compounds will be described. In formulas (1), (2), formula (3), formula (4), and formula (5), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms. Under the basis of, at least one −CH ₂₋ may be replaced by −O−. Preferred R ¹ is an alkyl having 1 to 12 carbon atoms to improve stability against ultraviolet rays and heat. R ² and R ³ are independently from alkyl with 1 to 12 carbons, alkoxy with 1 to 12 carbons, alkenyl with 2 to 12 carbons, and 1 carbon with at least one hydrogen replaced by fluorine or chlorine. Twelve alkyl, or alkenyl with 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine. Preferred R ² or R ³ is an alkenyl having 2 to 12 carbon atoms to reduce the viscosity and an alkyl having 1 to 12 carbon atoms to increase stability against ultraviolet rays and heat. R ⁴ is alkenyl alkyl of 1 to 12 carbons, alkoxy having 1 to 12 carbons, or 2 to 12 carbons. Preferred R ⁴ is alkyl having 1 to 12 carbons for increasing the stability to ultraviolet light and heat. R ⁵ and R ⁶ are independently alkyl with 1 to 12 carbons, alkoxy with 1 to 12 carbons, alkenyl with 2 to 12 carbons, or 2 carbons in which at least one hydrogen is replaced with fluorine or chlorine. To 12 alkenyl. Preferred R ⁵ and R ⁶ is alkenyl having 2 to 12 carbons for decreasing the viscosity, and alkyl having 1 to 12 carbons for increasing the stability to ultraviolet light and heat. R ⁷ and R ⁸ are independently alkyls with 1 to 12 carbons, alkoxys with 1 to 12 carbons, alkenyl with 2 to 12 carbons, or alkenyloxys with 2 to 12 carbons. Preferred R ⁷ or R ⁸ is an alkyl having 1 to 12 carbon atoms to increase stability against ultraviolet rays and heat, and an alkoxy having 1 to 12 carbon atoms to increase the dielectric constant in the minor axis direction.

Preferred alkyls are methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, or octyl. More preferred alkyls are methyl, ethyl, propyl, butyl, or pentyl to reduce viscosity.

Preferred alkoxys are methoxy, ethoxy, propoxy, butoxy, pentyloxy, hexyloxy, or heptyloxy. More preferred alkoxys are methoxy or ethoxy to reduce the viscosity.

Preferred alkenyl is vinyl, 1-propenyl, 2-propenyl, 1-butenyl, 2-butenyl, 3-butenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, or 5-hexenyl. More preferred alkenyl is vinyl, 1-propenyl, 3-butenyl, or 3-pentenyl to reduce the viscosity. The preferred configuration of -CH = CH- in these alkenyl depends on the position of the double bond. In alkenyl such as 1-propenyl, 1-butenyl, 1-pentenyl, 1-hexenyl, 3-pentenyl, 3-hexenyl, trans is preferable for lowering the viscosity. Sis is preferred for alkenyl such as 2-butenyl, 2-pentenyl, 2-hexenyl. In these alkenyl, linear alkenyl is preferable to branching.

Preferred alkenyloxys are vinyloxy, allyloxy, 3-butenyloxy, 3-pentenyloxy, or 4-pentenyloxy. More preferred alkenyloxy are allyloxy or 3-butenyloxy to reduce the viscosity.

Preferred examples of alkyl in which at least one hydrogen is replaced with fluorine or chlorine are fluoromethyl, 2-fluoroethyl, 3-fluoropropyl, 4-fluorobutyl, 5-fluoropentyl, 6-fluorohexyl, 7-fluoroheptyl. , Or 8-fluorooctyl. More preferred examples are 2-fluoroethyl, 3-fluoropropyl, 4-fluorobutyl, or 5-fluoropentyl to increase the dielectric anisotropy.

Preferred examples of alkenyl in which at least one hydrogen is replaced with fluorine or chlorine are 2,2-difluorovinyl, 3,3-difluoro-2-propenyl, 4,4-difluoro-3-butenyl, 5,5-difluoro. -4-pentenyl, or 6,6-difluoro-5-hexenyl. A more preferred example is 2,2-difluorovinyl or 4,4-difluoro-3-butenyl to reduce the viscosity.

または

であり、好ましくは

である。 Ring A is 1,4-cyclohexylene or 1,4-cyclohexenylene. The preferred ring A is 1,4-cyclohexylene. Ring B, 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6- Difluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl. Preferred ring B is 1,4-cyclohexylene to increase the upper temperature limit, 1,4-phenylene to increase the optical anisotropy, and 2-fluoro-1 to increase the dielectric anisotropy. , 4-Phenylene or 2,6-difluoro-1,4-phenylene. Tetrahydropyran-2,5-diyl is

Or

And preferably

Is.

Ring C is 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene. , Pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl. Preferred ring C is 1,4-cyclohexylene to increase the upper temperature limit, 1,4-phenylene to increase the optical anisotropy, and 2,6-difluoro to increase the dielectric anisotropy. -1,4-Phenylene.

Rings D and E are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, or 2,5-difluoro-1,4-phenylene. Preferred ring D or ring E is 1,4-cyclohexylene for lowering the viscosity or raising the upper temperature limit and 1,4-phenylene for lowering the lower limit temperature.

Rings F and I are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one hydrogen is replaced with fluorine or chlorine, or Tetrahydropyran-2,5-diyl. Preferred ring F or ring I is 1,4-cyclohexylene to reduce viscosity, tetrahydropyran-2,5-diyl to increase dielectric anisotropy, and to increase optical anisotropy. It is 1,4-phenylene. Ring G is 2,3-difluoro-1,4-phenylene, 2-chloro-3-fluoro-1,4-phenylene, 2,3-difluoro-5-methyl-1,4-phenylene, 3,4. 5-Trifluoronaphthalene-2,6-diyl, or 7,8-difluorochroman-2,6-diyl. The preferred ring G is 2,3-difluoro-1,4-phenylene to reduce the viscosity, 2-chloro-3-fluoro-1,4-phenylene to reduce the optical anisotropy, and the dielectric constant. 7,8-Difluorochroman-2,6-diyl to increase anisotropy.

Z ¹ and Z ² are independently single bonds, ethylene, methyleneoxy, carbonyloxy, or difluoromethyleneoxy. Preferred Z ¹ or Z ² is a single bond to reduce viscosity and difluoromethyleneoxy to increase dielectric anisotropy. Z ³ is a single bond, ethylene, carbonyloxy, or difluoromethyleneoxy. Preferred Z ³ is a single bond to reduce the viscosity and difluoromethyleneoxy to increase the dielectric anisotropy. Z ⁴ is a single bond, ethylene, or carbonyloxy. Preferred Z ⁴ is a single bond to reduce viscosity. Z ⁵ and Z ⁶ are independently single bonds, ethylene, carbonyloxy, or methyleneoxy. Preferred Z ⁵ or Z ⁶ is a single bond to reduce the viscosity, ethylene to lower the lower limit temperature, and methyleneoxy to increase the dielectric anisotropy.

X ¹ , X ² , X ³ , X ⁴ , X ⁵ , X ⁶ , X ⁷ , and X ⁸ are independently hydrogen or fluorine. Preferred X ¹ , X ² , X ³ , X ⁴ , X ⁵ , X ⁶ , X ⁷ , or X ⁸ are fluorine to increase the dielectric anisotropy.

Y ¹ and Y ² are fluorine, chlorine, alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, and alkoxy having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine. , Or an alkenyloxy having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine. Preferred Y ¹ or Y ² is fluorine to lower the lower limit temperature.

a is 0, 1, 2, or 3. Preferred a is 0 or 1 to lower the lower limit temperature and 2 or 3 to raise the upper limit temperature. b is 1, 2, 3, or 4. Preferred b is 2 for lowering the lower limit temperature and 3 for raising the upper limit temperature. c is 1, 2, or 3. The preferred c is 1 for lowering the viscosity and 2 or 3 for raising the upper temperature limit. d is 1, 2, or 3, e is 0 or 1, and the sum of d and e is 3 or less. The preferred d is 1 for lowering the viscosity and 2 or 3 for raising the upper temperature limit. Preferred e is 0 to lower the viscosity and 1 to lower the lower limit temperature. n is 1, 2, or 3. Preferred n is 1 or 2 to increase the dielectric anisotropy.

Fifth, preferred component compounds are shown. Preferred compounds (1) are compounds (1-1) to compounds (1-10) according to Item 2. In these compounds, at least one of the first components is preferably compounds (1-3), (1-5), (1-6) or (1-8). At least two of the first components are compound (1-3) and compound (1-6), compound (1-3) and compound (1-8), or compound (1-6) and compound (1-8). Is preferable.

Preferred compounds (3) are compounds (3-1) to compounds (3-35) according to Item 5. In these compounds, at least one of the third components is compound (3-4), compound (3-12), compound (3-14), compound (3-15), compound (3-17), compound ( 3-18), compound (3-23), compound (3-24), compound (3-27), compound (3-29), or compound (3-30) is preferred. At least two of the third components are compound (3-12) and compound (3-15), compound (3-14) and compound (3-27), compound (3-18) and compound (3-24), It is preferably a combination of compound (3-18) and compound (3-29), compound (3-24) and compound (3-29), or compound (3-29) and compound (3-30).

Preferred compounds (4) are compounds (4-1) to compounds (4-12) according to Item 8. In these compounds, at least one of the fourth components is compound (4-2), compound (4-4), compound (4-5), compound (4-6), compound (4-8), or compound. (4-12) is preferable. At least two of the fourth components are compound (4-2) and compound (4-4), compound (4-2) and compound (4-6), or compound (4-4) and compound (4-6). Is preferable.

Preferred compounds (5) are compounds (5-1) to compounds (5-22) according to Item 11. In these compounds, at least one of the fifth components is compound (5-1), compound (5-3), compound (5-4), compound (5-6), compound (5-8), or compound. (5-10) is preferable. At least two of the fifth components are compound (5-1) and compound (5-6), compound (5-3) and compound (5-6), compound (5-3) and compound (5-10), It is preferably a combination of compound (5-4) and compound (5-6), compound (5-4) and compound (5-8), or compound (5-6) and compound (5-10).

Sixth, additives that may be added to the composition will be described. Such additives include optically active compounds, antioxidants, UV absorbers, dyes, defoamers, polymerizable compounds, polymerization initiators, polymerization inhibitors, polar compounds and the like. An optically active compound is added to the composition for the purpose of inducing the helical structure of the liquid crystal to give a twist angle. Examples of such compounds are compound (6-1) to compound (6-5). The preferred proportion of the optically active compound is about 5% by weight or less. A more preferred proportion is in the range of about 0.01% by weight to about 2% by weight.

Antioxidants are composed to prevent a decrease in resistivity due to heating in the atmosphere, or to maintain a large voltage retention not only at room temperature but also at temperatures close to the upper limit temperature after long-term use of the device. It is added to the thing. A preferred example of the antioxidant is compound (7) in which t is an integer of 1 to 9.

In compound (7), the preferred t is 1, 3, 5, 7, or 9. A more preferable t is 7. Since the compound (7) having t of 7 has low volatility, it is effective in maintaining a large voltage holding ratio not only at room temperature but also at a temperature close to the upper limit temperature after the device has been used for a long time. The preferable ratio of the antioxidant is about 50 ppm or more in order to obtain the effect, and is about 600 ppm or less so as not to lower the upper limit temperature or raise the lower limit temperature. A more preferred ratio is in the range of about 100 ppm to about 300 ppm.

Preferred examples of the UV absorber are benzophenone derivatives, benzoate derivatives, triazole derivatives and the like. Light stabilizers such as sterically hindered amines are also preferred. The preferable ratio of these absorbents and stabilizers is about 50 ppm or more in order to obtain the effect, and about 10,000 ppm or less so as not to lower the upper limit temperature or raise the lower limit temperature. A more preferred ratio is in the range of about 100 ppm to about 10000 ppm.

Dichroic dyes such as azo dyes, anthraquinone dyes and the like are added to the composition to accommodate devices in GH (guest host) mode. The preferred proportion of dye is in the range of about 0.01% by weight to about 10% by weight. To prevent foaming, a defoaming agent such as dimethyl silicone oil or methyl phenyl silicone oil is added to the composition. The preferable ratio of the defoaming agent is about 1 ppm or more in order to obtain the effect, and about 1000 ppm or less in order to prevent display defects. A more preferred ratio is in the range of about 1 ppm to about 500 ppm.

Polymerizable compounds are added to the composition to accommodate polymer-supported orientation (PSA) type devices. Preferred examples of the polymerizable compound are compounds having a polymerizable group such as acrylate, methacrylate, vinyl compound, vinyloxy compound, propenyl ether, epoxy compound (oxylane, oxetane), vinyl ketone and the like. A more preferred example is a derivative of acrylate or methacrylate. The preferable ratio of the polymerizable compound is about 0.05% by weight or more in order to obtain the effect, and about 10% by weight or less in order to prevent display defects. A more preferred ratio is in the range of about 0.1% by weight to about 2% by weight. The polymerizable compound is polymerized by irradiation with ultraviolet rays. Polymerization may be carried out in the presence of an initiator such as a photopolymerization initiator. Appropriate conditions for polymerization, the appropriate type of initiator, and the appropriate amount are known to those of skill in the art and are described in the literature. For example, the photoinitiators Irgacure651®, Irgacure184® (registered trademark; BASF), or Darocur1173® are suitable for radical polymerization. The preferred proportion of photopolymerization initiator is in the range of about 0.1% by weight to about 5% by weight based on the weight of the polymerizable compound. A more preferred ratio is in the range of about 1% by weight to about 3% by weight.

When storing the polymerizable compound, a polymerization inhibitor may be added to prevent polymerization. The polymerizable compound is usually added to the composition without removing the polymerization inhibitor. Examples of polymerization inhibitors are hydroquinone, hydroquinone derivatives such as methylhydroquinone, 4-tert-butylcatechol, 4-methoxyphenol, phenothiazine and the like.

Seventh, a method for synthesizing a component compound will be described. These compounds can be synthesized by known methods. An example of the synthesis method. The method for synthesizing compound (1) is described in the section of Examples. Compound (2) is synthesized by the method described in JP-A-59-176221. Compound (3-2) and compound (3-8) are synthesized by the method described in JP-A-2-233626. Compound (4-6) is synthesized by the method described in JP 2006-503130. Compound (5-1) and compound (5-6) are synthesized by the method published in JP-A-2-503441. Antioxidants are commercially available. The compound of formula (7) where t is 1 can be obtained from Sigma-Aldrich Corporation. Compound (7) and the like having t of 7 are synthesized by the method described in US Pat. No. 3,660,505.

Compounds for which synthetic methods were not described are Organic Syntheses, John Wiley & Sons, Inc, Organic Reactions, John Wiley & Sons, Inc, and Comprehensive Organic. It can be synthesized by the methods described in books such as Synthesis, Pergamon Press) and New Experimental Chemistry Course (Maruzen). The composition is prepared from the compound thus obtained by a known method. For example, the constituent compounds are mixed and dissolved by heating.

Finally, the use of the composition will be described. The compositions of the present invention mainly have a lower limit temperature of about −10 ° C. or lower, an upper limit temperature of about 70 ° C. or higher, and an optical anisotropy in the range of about 0.07 to about 0.20. The device containing this composition has a large voltage holding ratio. This composition is suitable for AM devices. This composition is particularly suitable for transmissive AM devices. Compositions with optical anisotropy in the range of about 0.08 to about 0.25, and even from about 0.10, by controlling the proportions of the constituent compounds or by mixing other liquid crystal compounds. A composition having an optical anisotropy in the range of about 0.30 may be prepared. This composition can be used as a composition having a nematic phase, or can be used as an optically active composition by adding an optically active compound.

This composition can be used for AM devices. It can also be used for PM elements. This composition can be used for AM and PM devices having modes such as PC, TN, STN, ECB, OCB, IPS, FFS, VA, FPA. Use on AM devices with TN, OCB, IPS or FFS modes is particularly preferred. In an AM device having an IPS mode or an FFS mode, the arrangement of liquid crystal molecules may be parallel to or perpendicular to the glass substrate when no voltage is applied. These elements may be reflective, transmissive or transflective. Use for transmissive devices is preferred. It can also be used for non-crystalline silicon-TFT elements or polycrystalline silicon-TFT elements. It can also be used for an NCAP (nematic curvilinear aligned phase) type device produced by microencapsulating this composition and a PD (polymer dispersed) type device in which a three-dimensional network polymer is formed in the composition.

The present invention will be described in more detail by way of examples. The present invention is not limited by these examples. The present invention includes a mixture of the composition of Example 1 and the composition of Example 2. The present invention also includes a mixture of at least two of the compositions of the Examples. The synthesized compound was identified by a method such as NMR analysis. The properties of the compounds and compositions were measured by the methods described below.

NMR analysis: A DRX-500 manufactured by Bruker Biospin was used for the measurement. ^{1 In the 1} H-NMR measurement, the sample _{was dissolved in a deuterated solvent such as CDCl 3,} and the measurement was carried out at room temperature under the conditions of 500 MHz and 16 times of integration. Tetramethylsilane was used as an internal standard. ^{19 In the} F-NMR measurement, CFCl ₃ was used as an internal standard, and the number of integrations was 24. In the description of the nuclear magnetic resonance spectrum, s means singlet, d means doublet, t means triplet, q means quartet, quin means quintet, sex means sextet, m means multiplet, and br means broad.

Gas chromatograph analysis: A GC-14B type gas chromatograph manufactured by Shimadzu Corporation was used for the measurement. The carrier gas is helium (2 mL / min). The sample vaporization chamber was set to 280 ° C. and the detector (FID) was set to 300 ° C. A capillary column DB-1 (length 30 m, inner diameter 0.32 mm, film thickness 0.25 μm; fixed liquid phase was dimethylpolysiloxane; non-polar) manufactured by Agilent Technologies Inc. was used for separation of the component compounds. The column was held at 200 ° C. for 2 minutes and then warmed to 280 ° C. at a rate of 5 ° C./min. The sample was prepared in an acetone solution (0.1% by weight), and then 1 μL thereof was injected into the sample vaporization chamber. The recorder is a C-R5A type Chromatopac manufactured by Shimadzu Corporation, or an equivalent product thereof. The obtained gas chromatogram showed the peak retention time and peak area corresponding to the constituent compounds.

Chloroform, hexane or the like may be used as the solvent for diluting the sample. The following capillary columns may be used to separate the constituent compounds. HP-1 (length 30 m, inner diameter 0.32 mm, film thickness 0.25 μm) manufactured by Agilent Technologies Inc., Rtx-1 (length 30 m, inner diameter 0.32 mm, film thickness 0.25 μm) manufactured by Restek Corporation, BP-1 manufactured by SGE International Pty. Ltd (length 30 m, inner diameter 0.32 mm, film thickness 0.25 μm). A capillary column CBP1-M50-025 (length 50 m, inner diameter 0.25 mm, film thickness 0.25 μm) manufactured by Shimadzu Corporation may be used for the purpose of preventing overlapping of compound peaks.

The proportion of the liquid crystal compound contained in the composition may be calculated by the following method. A mixture of liquid crystal compounds is detected by gas chromatography (FID). The area ratio of the peak in the gas chromatogram corresponds to the ratio (weight ratio) of the liquid crystal compound. When the capillary column described above is used, the correction coefficient of each liquid crystal compound may be regarded as 1. Therefore, the proportion (% by weight) of the liquid crystal compound can be calculated from the area ratio of the peak.

Measurement sample: When measuring the characteristics of the composition, the composition was used as it was as a sample. When measuring the properties of the compound, a sample for measurement was prepared by mixing this compound (15% by weight) with the mother liquid crystal (85% by weight). From the values obtained by the measurement, the characteristic values of the compound were calculated by the extrapolation method. (Extrapolated value) = {(Measured value of sample) −0.85 × (Measured value of mother liquid crystal)} /0.15. When the smectic phase (or crystal) precipitates at this ratio at 25 ° C., the ratio of the compound to the mother liquid crystal is 10% by weight: 90% by weight, 5% by weight: 95% by weight, 1% by weight: 99% by weight, in that order. changed. The values of upper temperature, optical anisotropy, viscosity, and permittivity anisotropy for the compound were determined by this extrapolation method.

The following mother liquid crystal was used. The ratio of the component compounds is shown in% by weight.

Measurement method: The characteristics were measured by the following method. Many of these are methods described in the JEITA standard (JEITA ED-2521B) deliberated and enacted by the Japan Electronics and Information Technology Industries Association (hereinafter referred to as JEITA), or modified. It was a method. A thin film transistor (TFT) was not attached to the TN element used for the measurement.

(1) Upper limit temperature of nematic phase (NI; ° C.): A sample was placed on a hot plate of a melting point measuring device equipped with a polarizing microscope and heated at a rate of 1 ° C./min. The temperature when a part of the sample changed from the nematic phase to the isotropic liquid was measured.

(2) Minimum Temperature of a Nematic Phase _{(T C;} ° C.): A sample having a nematic phase was put in a glass bottle, 0 ℃, -10 ℃, -20 ℃, -30 ℃, and -40 ℃ for 10 days in a freezer After storage, the liquid crystal phase was observed. _{For example, TC} was described as <-20 ° C. when the sample remained in the nematic phase at −20 ° C. and changed to a crystalline or smectic phase at −30 ° C.

(3) Viscosity (bulk viscosity; η; measured at 20 ° C.; mPa · s): An E-type rotational viscometer manufactured by Tokyo Keiki Co., Ltd. was used for the measurement.

(4) Viscosity (rotational viscosity; γ1; measured at 25 ° C.; mPa · s): The measurement was carried out according to the method described in M. Imai et al., Molecular Crystals and Liquid Crystals, Vol. 259, 37 (1995). I obeyed. The sample was placed in a TN device having a twist angle of 0 ° and a distance (cell gap) between the two glass substrates of 5 μm. A stepwise application was applied to this device in 0.5 V increments in the range of 16 V to 19.5 V. After no application for 0.2 seconds, application was repeated under the conditions of only one square wave (square pulse; 0.2 seconds) and no application (2 seconds). The peak current and peak time of the transient current generated by this application were measured. The value of rotational viscosity was obtained from these measured values and the calculation formula (8) described on page 40 in the paper by M. Imai et al. The value of the dielectric anisotropy required for this calculation was obtained by the method described below using the element whose rotational viscosity was measured.

(5) Optical anisotropy (refractive index anisotropy; Δn; measured at 25 ° C.): The measurement was performed using light having a wavelength of 589 nm and using an Abbe refractometer with a polarizing plate attached to the eyepiece. After rubbing the surface of the main prism in one direction, the sample was dropped onto the main prism. The refractive index n‖ was measured when the direction of polarization was parallel to the direction of rubbing. The refractive index n⊥ was measured when the direction of polarization was perpendicular to the direction of rubbing. The value of optical anisotropy was calculated from the equation of Δn = n ‖ −n ⊥.

(6) Dielectric constant anisotropy (Δε; measured at 25 ° C.): The sample was placed in a TN element having a distance (cell gap) between two glass substrates of 9 μm and a twist angle of 80 degrees. A sine wave (10 V, 1 kHz) was applied to this device, and after 2 seconds, the permittivity (ε ‖) of the liquid crystal molecule in the long axis direction was measured. A sine wave (0.5 V, 1 kHz) was applied to this device, and after 2 seconds, the permittivity (ε⊥) of the liquid crystal molecule in the minor axis direction was measured. The value of permittivity anisotropy was calculated from the equation Δε ＝ ε‖−ε⊥.

(7) Threshold voltage (Vth; measured at 25 ° C.; V): An LCD5100 type luminance meter manufactured by Otsuka Electronics Co., Ltd. was used for the measurement. The light source was a halogen lamp. The sample was placed in a normally white mode TN element in which the distance (cell gap) between the two glass substrates was 0.45 / Δn (μm) and the twist angle was 80 degrees. The voltage (32 Hz, square wave) applied to this device was gradually increased by 0.02 V from 0 V to 10 V. At this time, the element was irradiated with light from the vertical direction, and the amount of light transmitted through the element was measured. A voltage-transmittance curve was created in which the transmittance was 100% when the amount of light was maximum and the transmittance was 0% when the amount of light was minimum. The threshold voltage is expressed as the voltage when the transmittance reaches 90%.

(8) Voltage retention rate (VHR-1; measured at 25 ° C.;%): The TN element used for the measurement had a polyimide alignment film, and the distance (cell gap) between the two glass substrates was 5 μm. .. This device was sealed with an adhesive that cures with ultraviolet light after the sample was placed. A pulse voltage (60 microseconds at 5 V) was applied to the TN element to charge it. The decaying voltage was measured with a high-speed voltmeter for 16.7 milliseconds, and the area A between the voltage curve and the horizontal axis in a unit period was determined. Area B was the area when there was no attenuation. The voltage holding ratio is expressed as a percentage of the area A with respect to the area B.

(9) Voltage retention rate (VHR-2; measured at 80 ° C.;%): The voltage retention rate was measured by the same procedure as above except that the voltage retention rate was measured at 80 ° C. instead of 25 ° C. The obtained value was represented by VHR-2.

(10) Voltage retention rate (VHR-3; measured at 25 ° C.;%): After irradiation with ultraviolet rays, the voltage retention rate was measured to evaluate the stability against ultraviolet rays. The TN device used for the measurement had a polyimide alignment film, and the cell gap was 5 μm. A sample was injected into this device and irradiated with light for 20 minutes. The light source was an ultra-high pressure mercury lamp USH-500D (manufactured by Ushio, Inc.), and the distance between the element and the light source was 20 cm. In the VHR-3 measurement, the voltage decayed for 16.7 milliseconds was measured. Compositions with large VHR-3 have great stability to UV light. VHR-3 is preferably 90% or more, more preferably 95% or more.

(11) Voltage retention rate (VHR-4; measured at 25 ° C.;%): After heating the TN element into which the sample was injected in a constant temperature bath at 80 ° C. for 500 hours, the voltage retention rate was measured and stability against heat was measured. Was evaluated. In the VHR-4 measurement, the voltage decayed for 16.7 milliseconds was measured. Compositions with large VHR-4 have great stability to heat.

(12) Response time (τ; measured at 25 ° C.; ms): An LCD5100 type luminance meter manufactured by Otsuka Electronics Co., Ltd. was used for the measurement. The light source was a halogen lamp. The low-pass filter was set to 5 kHz. The sample was placed in a normally white mode TN element in which the distance (cell gap) between the two glass substrates was 5.0 μm and the twist angle was 80 degrees. A square wave (60 Hz, 5 V, 0.5 seconds) was applied to this device. At this time, the element was irradiated with light from the vertical direction, and the amount of light transmitted through the element was measured. It was considered that the transmittance was 100% when the amount of light was maximum, and the transmittance was 0% when the amount of light was minimum. The rise time (τr: rise time; millisecond) is the time required for the transmittance to change from 90% to 10%. The fall time (τf: fall time; millisecond) is the time required for the transmittance to change from 10% to 90%. The response time was expressed as the sum of the rise time and the fall time obtained in this way.

(13) Elastic constant (K; measured at 25 ° C.; pN): An HP4284A type LCR meter manufactured by Yokogawa Hewlett-Packard Co., Ltd. was used for the measurement. The sample was placed in a horizontally oriented element in which the distance (cell gap) between the two glass substrates was 20 μm. A charge of 0 to 20 volts was applied to this device, and the capacitance and applied voltage were measured. Fitting the measured capacitance (C) and applied voltage (V) values using the "Liquid Crystal Device Handbook" (Nikkan Kogyo Shimbun), equations (2.98) and (2.11) on page 75. Then, the values of K11 and K33 were obtained from the formula (2.99). Next, K22 was calculated using the values of K11 and K33 obtained earlier in the formula (3.18) on page 171 of the same. The elastic constant was represented by the average value of K11, K22, and K33 thus obtained.

(14) Specific resistance (ρ; measured at 25 ° C.; Ωcm): 1.0 mL of the sample was injected into a container equipped with an electrode. A DC voltage (10 V) was applied to this container, and the DC current after 10 seconds was measured. The specific resistance was calculated from the following formula. (Specific resistance) = {(voltage) x (electrical capacity of container)} / {(DC current) x (vacuum permittivity)}.

(15) Spiral pitch (P; measured at room temperature; μm): The spiral pitch was measured by the wedge method. See "LCD Handbook", page 196 (published in 2000, Maruzen). The sample was injected into a wedge-shaped cell, allowed to stand at room temperature for 2 hours, and then the spacing of the dispersion lines (d2-d1) was observed with a polarizing microscope (Nikon Corporation, trade name MM40 / 60 series). The spiral pitch (P) was calculated from the following equation in which the angle of the wedge cell was expressed as θ. P = 2 × (d2-d1) × tan θ.

(16) Dielectric constant in the minor axis direction (ε⊥; measured at 25 ° C.): The sample was placed in a TN element having a distance (cell gap) between two glass substrates of 9 μm and a twist angle of 80 degrees. .. A sine wave (0.5 V, 1 kHz) was applied to this device, and after 2 seconds, the permittivity (ε⊥) of the liquid crystal molecule in the minor axis direction was measured.

Compound (1-3) was synthesized by the method described below. Solmix A-11 is a mixture of ethanol (85.5%), methanol (13.4%) and isopropyl alcohol (1.1%), and was obtained from Japan Alcohol Trading Co., Ltd.

Step 1 Under a nitrogen atmosphere, compound (T-1) (25.00 g), compound (T-2) (6.164 g), potassium carbonate (12.08 g), tetrabutylammonium bromide (TBAB) (4. 03 g) and 1,4-dioxane (200 ml) were placed in a reactor, and the mixture was heated under reflux for 8 hours. The reaction mixture was poured into water and the aqueous layer was extracted with toluene. The combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. This solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (toluene / ethyl acetate = 10/1, volume ratio). Further, purification was performed by recrystallization from Solmix A-11 to obtain compound (T-3) (12.82 g, 62%).
Step 2 Under a nitrogen atmosphere, compound (T-3) (12.82 g), formic acid (38.4 ml), TBAB (2.27 g), and toluene (128 ml) were placed in a reactor and stirred at room temperature for 3 hours. did. The reaction mixture was poured into water and returned to neutral with baking soda. The aqueous layer was extracted with toluene, the combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. This solution is concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (toluene / ethyl acetate = 10/1, volume ratio) to obtain compound (T-4) (11.17 g, yield 99%). It was.

Step 3 Under a nitrogen atmosphere, (methoxymethyl) triphenylphosphonium chloride (12.30 g) and THF (100 ml) were placed in a reactor and cooled to −40 ° C. Potassium t-butoxide (4.03 g) was added thereto, and the mixture was stirred at -40 ° C for 1 hour. Next, a solution of compound (T-4) (10.41 g) in THF (40 ml) was slowly added dropwise, and after the addition, the mixture was stirred for 3 hours while returning to room temperature. The reaction mixture was poured into water and the aqueous layer was extracted with toluene. The combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. This solution was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (toluene / heptane = 2/1, volume ratio) to obtain compound (T-5). The obtained compound (T-5), 5% palladium carbon (0.31 g), toluene (100 ml), and IPA (100 ml) were placed in a reactor and stirred under a hydrogen atmosphere for 12 hours. After removing the catalyst by filtration, the mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate / heptane = 1/10, volume ratio). Further, purification was performed by recrystallization from Solmix A-11 to obtain compound (1-3) (3.71 g, yield 33%).

^{1 1} H-NMR (ppm; CDCl ₃ ): δ6.98-6.92 (m, 2H), 6.85-6.82 (m, 2H), 3.35 (s, 3H), 3.24 ( d, J = 6.3Hz, 2H), 2.50 (tt, J = 12.2Hz, J = 3.1Hz, 1H), 1.97-1.90 (m, 4H), 1.69-1 .60 (m, 1H), 1.46-1.37 (m, 2H), 1.17-1.08 (m, 2H).

Examples of the composition are shown below. The component compounds are represented by symbols based on the definitions in Table 3 below. In Table 3, the molecular configuration for 1,4-cyclohexylene is trance. The number in parentheses after the symbolized compound represents the chemical formula to which the compound belongs. The symbol (-) means other liquid crystal compounds. The proportion (percentage) of the liquid crystal compound is a weight percentage (% by weight) based on the weight of the liquid crystal composition. Finally, the characteristic values of the composition are summarized.

[Comparative Example 1]
Example 35 was selected from the compositions disclosed in WO 1996/11897. The rationale is that this composition contains compound (2), compound (3), compound (4-1), compound (4-4), and compound (4-5) and has the lowest bulk viscosity. .. The components and properties of this composition were as follows.
3-HBXB (F, F) -F (3) 10%
5-HBXB (F, F) -F (3) 10%
2-HB (F) -C (-) 7%
3-HB (F) -C (-) 10%
3-HHB-F (3) 5%
3-HB-O2 (4-1) 10%
5-HH-V (2) 5%
3-HH-2V (2) 5%
2-BTB-O1 (-) 8%
V-HHB-1 (4-4) 8%
V-HBB-2 (4-5) 5%
1V2-HBB-2 (4-5) 5%
3-HHB-O1 (4-4) 4%
3-H2BTB-2 (-) 4%
3-H2BTB-3 (-) 4%
NI = 71.6 ° C.; η = 16.9 mPa · s; Δn = 0.121; Δε = 6.1; Vth = 1.81 V.

[Example 1]
1O1-HB (F, F) XB (F, F) -F (1-3) 5%
1O1-HHB (F, F) XB (F, F) -F (1-5) 5%
3-HH-V (2) 40%
3-HH-V1 (2) 6%
5-HH-V (2) 4%
3-BB (F, F) XB (F, F) -F (3-18) 9%
3-HBBXB (F, F) -F (3-23) 9%
3-HBB (F, F) XB (F, F) -F (3-24) 4%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 6%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 2%
V-HHB-1 (4-4) 5%
V2-HHB-1 (4-4) 5%
NI = 74.2 ° C; Tc <-20 ° C; η = 10.2 mPa · s; Δn = 0.093; Δε = 7.6; Vth = 1.55 V; γ1 = 50.0 mPa · s.

[Example 2]
2O1-HBBXB (F, F) -F (1-6) 3%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 3%
3-HH-V (2) 39%
5-HHB (F, F) -F (3-2) 5%
3-HHEB (F, F) -F (3-3) 6%
2-HBB (F, F) -F (3-8) 3%
3-HB (F) B (F, F) -F (3-9) 5%
3-HBEB (F, F) -F (3-10) 3%
3-GB (F, F) XB (F, F) -F (3-14) 4%
3-BBXB (F, F) -F (3-17) 4%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 4%
V2-B (2F, 3F) BXB (F, F) -F (3-33) 3%
V-HHB-1 (4-4) 4%
V2-HHB-1 (4-4) 6%
1V-HBB-2 (4-5) 5%
5-B (F) BB-3 (4-7) 3%
NI = 74.1 ° C; Tc <-20 ° C; η = 10.5 mPa · s; Δn = 0.100; Δε = 6.4; Vth = 1.69 V; γ1 = 51.6 mPa · s.

[Example 3]
1O1-HB (2F, 3F) XB (F, F) -F (1-4) 2%
1O1-HBB (F, F) XB (F, F) -F (1-6) 2%
2O2-HB (F, F) XB (F) B (F, F) -F (1-8) 2%
2-HH-3 (2) 14%
3-HH-V (2) 30%
3-HHB (F, F) -F (3-2) 3%
4-HHEB (F, F) -F (3-3) 3%
3-HHXB (F, F) -F (3-4) 2%
5-HB (F) B (F, F) -F (3-9) 4%
2-GB (F, F) XB (F, F) -F (3-14) 3%
3-BB (F) B (F, F) -CF3 (3-16) 3%
3-HHBB (F, F) -F (3-19) 4%
3-BB (F) B (F, F) XB (F) -F (3-28) 5%
4-BB (F) B (F, F) XB (F) -F (3-28) 5%
3-HB (2F, 3F) BXB (F, F) -F (3-34) 3%
3-BB (2F, 3F) BXB (F, F) -F (3-35) 3%
1-BB-3 (4-2) 3%
V2-HHB-1 (4-4) 3%
1V-HBB-2 (4-5) 4%
3-HHEBH-4 (4-10) 2%
NI = 74.7 ° C; Tc <-20 ° C; η = 11.7 mPa · s; Δn = 0.099; Δε = 6.8; Vth = 1.62 V; γ1 = 57.5 mPa · s.

[Example 4]
1O1-HHB (F, F) -F (1-1) 2%
2O1-HBBXB (F, F) -F (1-6) 2%
1O1-HB (F, F) XB (F) B (F, F) -OCF3 (1-8) 2%
3-HH-V (2) 37%
3-HH-V1 (2) 5%
4-HH-V (2) 4%
5-HHEB (F, F) -F (3-3) 5%
5-GHB (F, F) -F (3-7) 3%
2-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -F (3-15) 3%
3-HHBB (F, F) -F (3-19) 2%
3-BB (F) B (F, F) XB (F) -F (3-28) 5%
4-BB (F) B (F, F) XB (F) -F (3-28) 4%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 5%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 2%
3-BB (2F, 3F) XB (F, F) -F (3-32) 3%
1-BB-5 (4-2) 2%
V2-BB-1 (4-2) 2%
3-HHB-1 (4-4) 5%
3-BB (F) B-2V (4-6) 2%
5-HBB (F) B-2 (4-12) 2%
NI = 75.4 ° C; Tc <-20 ° C; η = 12.6 mPa · s; Δn = 0.108; Δε = 6.8; Vth = 1.63 V; γ1 = 61.6 mPa · s.

[Example 5]
1O1-HBB (F, F) -F (1-2) 2%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 4%
1O1-chBB (F, F) XB (F, F) -F (1-10) 2%
2-HH-3 (2) 25%
3-HH-V (2) 15%
3-HHB (F, F) -F (3-2) 3%
2-HBB (F, F) -F (3-8) 3%
3-HB (F) B (F, F) -F (3-9) 5%
3-GB (F, F) XB (F, F) -F (3-14) 3%
2-BB (F, F) XB (F, F) -F (3-18) 3%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 2%
5-BB (F) B (F, F) XB (F) B (F, F) -F (3-31) 3%
3-HB-O2 (4-1) 3%
V-HHB-1 (4-4) 5%
V2-HHB-1 (4-4) 6%
3-HBB-2 (4-5) 5%
3-BB (F) B-2V (4-6) 5%
5-HBB (F) B-2 (4-12) 3%
NI = 74.4 ° C; Tc <-20 ° C; η = 10.0 mPa · s; Δn = 0.105; Δε = 6.4; Vth = 1.68 V; γ1 = 49.0 mPa · s.

[Example 6]
1O1-HB (F, F) XB (F, F) -F (1-3) 2%
1O1-HHB (F, F) XB (F, F) -F (1-5) 3%
1O1-chBB (F, F) -F (1-9) 5%
3-HH-V (2) 33%
3-HH-V1 (2) 10%
1-HHB (F, F) -F (3-2) 3%
3-HBB (F, F) -F (3-8) 3%
3-BB (F, F) XB (F, F) -F (3-18) 3%
4-HHB (F) B (F, F) -F (3-20) 3%
5-GB (F) B (F) B (F) -F (3-21) 4%
3-GB (F) B (F, F) XB (F, F) -F (3-27) 3%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 2%
3-BB (F, F) XB (F) B (F, F) -F (3-30) 3%
3-HB-O2 (4-1) 2%
1-BB-5 (4-2) 3%
1V2-BB-1 (4-2) 2%
V2-HHB-1 (4-4) 3%
3-HBB-2 (4-5) 3%
V-HBB-2 (4-5) 3%
5-B (F) BB-3 (4-7) 2%
3-HBB (2F, 3F) -O2 (5-10) 2%
NI = 74.6 ° C; Tc <-20 ° C; η = 12.7 mPa · s; Δn = 0.109; Δε = 6.6; Vth = 1.65 V; γ1 = 62.3 mPa · s.

[Example 7]
1O1-HB (F, F) XB (F, F) -F (1-3) 5%
1O1-HBBXB (F, F) -F (1-6) 2%
2O1-HBBXB (F, F) -F (1-6) 2%
3-HH-V (2) 25%
4-HH-V (2) 5%
5-HH-V (2) 7%
1-HHXB (F, F) -F (3-4) 6%
3-HB (F) B (F, F) -F (3-9) 3%
V-HB (F) B (F, F) -F (3-9) 3%
3-HBEB (F, F) -F (3-10) 3%
2-HHBB (F, F) -F (3-19) 3%
5-GB (F) B (F, F) XB (F) -F (3-26) 3%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 5%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 4%
V2-BB-1 (4-2) 9%
3-HHB-3 (4-4) 5%
V2-HHB-1 (4-4) 6%
3-BB (F) B-5 (4-6) 2%
V2-BB2B-1 (4-8) 2%
NI = 71.1 ° C; Tc <-20 ° C; η = 11.4 mPa · s; Δn = 0.105; Δε = 6.8; Vth = 1.62 V; γ1 = 56.1 mPa · s.

[Example 8]
1O1-HB (F, F) XB (F, F) -F (1-3) 3%
1O1-HBBXB (F, F) -F (1-6) 3%
3-HH-V (2) 33%
3-HH-V1 (2) 5%
3-HH-VFF (2) 7%
5-HHB (F, F) -F (3-2) 5%
2-HBEB (F, F) -F (3-10) 3%
3-GB (F, F) XB (F, F) -F (3-14) 2%
3-BB (F) B (F, F) -F (3-15) 2%
3-BB (F) B (F, F) -CF3 (3-16) 2%
2-HHB (F) B (F, F) -F (3-20) 3%
3-HHB (F) B (F, F) -F (3-20) 2%
3-HBBXB (F, F) -F (3-23) 6%
3-dhBB (F, F) XB (F, F) -F (3-25) 3%
4-GB (F) B (F, F) XB (F) -F (3-26) 3%
3-BB (F) B (F, F) XB (F) -F (3-28) 4%
3-HB-O2 (4-1) 3%
V2-HHB-1 (4-4) 4%
1-BB (F) B-2V (4-6) 3%
5-B (F) BB-2 (4-7) 2%
3-HB (F) HH-5 (4-9) 2%
NI = 81.8 ° C; Tc <-20 ° C; η = 12.4 mPa · s; Δn = 0.105; Δε = 6.8; Vth = 1.61 V; γ1 = 60.9 mPa · s.

[Example 9]
1O1-HHB (F, F) XB (F, F) -F (1-5) 3%
1O1-HBBXB (F, F) -F (1-6) 2%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 3%
3-HH-V (2) 23%
3-HH-V1 (2) 5%
4-HH-V (2) 5%
3-HHXB (F, F) -CF3 (3-5) 3%
3-HB (F) B (F, F) -F (3-9) 2%
3-HBEB (F, F) -F (3-10) 3%
3-GB (F, F) XB (F) -F (3-13) 2%
3-BB (F) B (F, F) -F (3-15) 2%
3-HBB (F, F) XB (F, F) -F (3-24) 3%
3-BB (F) B (F, F) XB (F) -F (3-28) 5%
4-BB (F) B (F, F) XB (F) -F (3-28) 4%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
3-HB-O2 (4-1) 6%
7-HB-1 (4-1) 4%
V2-BB-1 (4-2) 7%
V-HHB-1 (4-4) 3%
V2-HHB-1 (4-4) 6%
2-BB (F) B-2V (4-6) 3%
5-HB (F) BH-3 (4-11) 3%
NI = 75.8 ° C; Tc <-20 ° C; η = 12.2 mPa · s; Δn = 0.112; Δε = 6.8; Vth = 1.63 V; γ1 = 60.0 mPa · s.

[Example 10]
1O1-HB (F, F) XB (F, F) -F (1-3) 3%
1O1-HBB (F, F) XB (F, F) -F (1-6) 3%
2-HH-5 (2) 3%
3-HH-V (2) 31%
3-HH-V1 (2) 7%
5-GHB (F, F) -F (3-7) 3%
2-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -CF3 (3-16) 3%
4-GB (F) B (F, F) XB (F, F) -F (3-27) 3%
3-BB (F) B (F, F) XB (F) -F (3-28) 3%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
3-BB (F, F) XB (F) B (F, F) -F (3-30) 3%
1V2-BB-1 (4-2) 6%
V-HHB-1 (4-4) 7%
V2-HHB-1 (4-4) 5%
V-HBB-2 (4-5) 2%
5-B (F) BB-2 (4-7) 2%
V2-BB2B-1 (4-8) 2%
1-BB2B-2V (4-8) 2%
NI = 75.5 ° C.; Tc <-20 ° C.; η = 11.5 mPa · s; Δn = 0.117; Δε = 7.7; Vth = 1.53 V; γ1 = 56.3 mPa · s.

[Example 11]
1O1-HBBXB (F, F) -F (1-6) 2%
2O1-HBBXB (F, F) -F (1-6) 2%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 3%
2-HH-3 (2) 10%
3-HH-V (2) 28%
3-HH-V1 (2) 6%
1V2-HH-3 (2) 2%
3-HHB (F, F) -F (3-2) 5%
3-HHXB (F, F) -F (3-4) 5%
2-HGB (F, F) -F (3-6) 3%
3-HGB (F, F) -F (3-6) 2%
3-GHB (F, F) -F (3-7) 3%
5-GHB (F, F) -F (3-7) 3%
5-HBEB (F, F) -F (3-10) 3%
3-BB (F) B (F, F) -F (3-15) 2%
3-HHBB (F, F) -F (3-19) 2%
3-HBBXB (F, F) -F (3-23) 2%
5-HBBXB (F, F) -F (3-23) 3%
4-BB (F) B (F, F) XB (F) -F (3-28) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
7-HB-1 (4-1) 2%
3-HHB-3 (4-4) 2%
1-BB (F) B-2V (4-6) 2%
3-BB (F) B-2V (4-6) 2%
NI = 74.8 ° C; Tc <-20 ° C; η = 12.3 mPa · s; Δn = 0.092; Δε = 6.4; Vth = 1.67 V; γ1 = 60.4 mPa · s.

[Example 12]
1O1-HHB (F, F) -F (1-1) 3%
1O1-HHB (F, F) XB (F, F) -F (1-5) 3%
2-HH-3 (2) 26%
2-HH-5 (2) 4%
3-HH-V (2) 6%
1V2-HH-1 (2) 3%
2-HGB (F, F) -F (3-6) 3%
3-HGB (F, F) -F (3-6) 3%
5-HGB (F, F) -F (3-6) 4%
3-HB (F) B (F, F) -F (3-9) 3%
5-HB (F) B (F, F) -F (3-9) 3%
2-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -F (3-15) 3%
3-BB (F, F) XB (F, F) -F (3-18) 4%
3-HHB (F) B (F, F) -F (3-20) 2%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 4%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
2-HHB-1 (4-4) 2%
V-HHB-1 (4-4) 3%
V2-HHB-1 (4-4) 5%
3-HBB-2 (4-5) 5%
5-B (F) BB-2 (4-7) 3%
1O1-HBBH-5 (-) 2%
NI = 72.1 ° C; Tc <-20 ° C; η = 12.3 mPa · s; Δn = 0.096; Δε = 6.4; Vth = 1.69 V; γ1 = 60.3 mPa · s.

[Example 13]
1O1-HB (2F, 3F) XB (F, F) -F (1-4) 3%
1O1-HBBXB (F, F) -F (1-6) 3%
3-HH-V (2) 27%
3-HH-V1 (2) 7%
2-HGB (F, F) -F (3-6) 3%
3-HGB (F, F) -F (3-6) 3%
3-HB (F) B (F, F) -F (3-9) 4%
5-HBEB (F, F) -F (3-10) 3%
3-BB (F) B (F, F) -F (3-15) 5%
3-BBXB (F, F) -F (3-17) 3%
4-HHBB (F, F) -F (3-19) 3%
3-HBBXB (F, F) -F (3-23) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 5%
3-B (2F, 3F) BXB (F, F) -F (3-33) 3%
1V2-BB-1 (4-2) 5%
V-HHB-1 (4-4) 5%
V2-HHB-1 (4-4) 5%
V-HBB-2 (4-5) 6%
3-BB (F) B-5 (4-6) 4%
NI = 79.3 ° C; Tc <-20 ° C; η = 12.2 mPa · s; Δn = 0.116; Δε = 6.3; Vth = 1.72 V; γ1 = 60.0 mPa · s.

[Example 14]
1O1-HHB (F, F) -F (1-1) 2%
1O1-HBB (F, F) -F (1-2) 2%
1O1-HHB (F, F) XB (F, F) -F (1-5) 2%
3-HH-V (2) 37%
3-HH-V1 (2) 10%
3-HHXB (F, F) -CF3 (3-5) 5%
4-GHB (F, F) -F (3-7) 3%
3-GB (F) B (F) -F (3-11) 8%
2-BB (F, F) XB (F, F) -F (3-18) 3%
2-HHBB (F, F) -F (3-19) 3%
3-HHBB (F, F) -F (3-19) 3%
5-GB (F) B (F, F) XB (F, F) -F (3-27) 3%
3-BB (F) B (F, F) XB (F) -F (3-28) 7%
3-HB-O2 (4-1) 5%
V2-HHB-1 (4-4) 4%
2-BB (F) B-5 (4-6) 3%
NI = 74.2 ° C; Tc <-20 ° C; η = 11.7 mPa · s; Δn = 0.094; Δε = 6.3; Vth = 1.71 V; γ1 = 57.2 mPa · s.

[Example 15]
1O1-HB (F, F) XB (F, F) -F (1-3) 3%
1O1-HBBXB (F, F) -F (1-6) 3%
2-HH-3 (2) 8%
3-HH-V (2) 33%
3-HHXB (F, F) -F (3-4) 5%
5-HB (F) B (F, F) -F (3-9) 4%
3-GB (F, F) XB (F, F) -F (3-14) 4%
3-HHB (F) B (F, F) -F (3-20) 3%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 4%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 6%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 5%
5-HB-O2 (4-1) 5%
V-HHB-1 (4-4) 5%
V2-HHB-1 (4-4) 5%
1V-HBB-2 (4-5) 3%
5-B (F) BB-2 (4-7) 2%
5-B (F) BB-3 (4-7) 2%
NI = 76.7 ° C; Tc <-20 ° C; η = 10.7 mPa · s; Δn = 0.103; Δε = 7.4; Vth = 1.56 V; γ1 = 52.7 mPa · s.

[Example 16]
1O1-HBB (F, F) XB (F, F) -F (1-6) 3%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 3%
3-HH-4 (2) 7%
3-HH-V (2) 29%
3-HH-V1 (2) 8%
4-HHEB (F, F) -F (3-3) 3%
1-HHXB (F, F) -F (3-4) 3%
3-GB (F, F) XB (F, F) -F (3-14) 4%
3-BBXB (F, F) -F (3-17) 3%
2-BB (F, F) XB (F, F) -F (3-18) 3%
3-BB (F, F) XB (F, F) -F (3-18) 3%
2-HHBB (F, F) -F (3-19) 2%
4-HHB (F) B (F, F) -F (3-20) 3%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 4%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
3-HHEH-3 (4-3) 2%
V-HHB-1 (4-4) 5%
V2-HHB-1 (4-4) 7%
2-BB (F) B-3 (4-6) 3%
5-B (F) BB-2 (4-7) 2%
NI = 79.6 ° C; Tc <-20 ° C; η = 11.9 mPa · s; Δn = 0.099; Δε = 7.0; Vth = 1.58 V; γ1 = 58.4 mPa · s.

[Example 17]
1O1-HB (F, F) XB (F, F) -F (1-3) 3%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 2%
1O1-HB (F, F) XB (F) B (F, F) -OCF3 (1-8) 2%
3-HH-V (2) 35%
3-HH-V1 (2) 8%
1V2-HH-3 (2) 3%
3-HHEB (F, F) -F (3-3) 3%
5-HHEB (F, F) -F (3-3) 4%
3-HHXB (F, F) -F (3-4) 6%
3-GB (F) B (F, F) -F (3-12) 3%
5-GB (F) B (F, F) -F (3-12) 3%
3-GB (F) B (F) B (F) -F (3-21) 3%
3-BB (F) B (F, F) XB (F) -F (3-28) 4%
4-BB (F) B (F, F) XB (F) -F (3-28) 6%
1-BB-3 (4-2) 3%
V-HHB-1 (4-4) 4%
3-HBB-2 (4-5) 5%
V2-BB2B-1 (4-8) 3%
NI = 76.8 ° C; Tc <-20 ° C; η = 11.3 mPa · s; Δn = 0.100; Δε = 6.3; Vth = 1.72 V; γ1 = 55.7 mPa · s.

[Example 18]
1O1-HBBXB (F, F) -F (1-6) 2%
2O1-HBBXB (F, F) -F (1-6) 2%
1O1-HBB (2F, 3F) XB (F, F) -F (1-7) 3%
2-HH-3 (2) 14%
3-HH-V (2) 26%
5-HH-V (2) 4%
4-HHB (F, F) -F (3-2) 3%
5-HHB (F, F) -F (3-2) 3%
2-HBEB (F, F) -F (3-10) 4%
2-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -F (3-15) 3%
3-BB (F) B (F, F) -CF3 (3-16) 3%
2-dhBB (F, F) XB (F, F) -F (3-25) 3%
3-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
5-BB (F) B (F, F) XB (F, F) -F (3-29) 3%
3-HB-O2 (4-1) 6%
3-HHB-1 (4-4) 3%
VFF-HHB-1 (4-4) 2%
V-HBB-2 (4-5) 3%
3-BB (F) B-5 (4-6) 2%
3-HHEBH-3 (4-10) 2%
NI = 72.8 ° C; Tc <-20 ° C; η = 11.7 mPa · s; Δn = 0.100; Δε = 6.7; Vth = 1.64V; γ1 = 57.2 mPa · s.

[Example 19]
1O1-HB (F, F) XB (F, F) -F (1-3) 3%
1O1-HB (F, F) XB (F) B (F, F) -F (1-8) 3%
2-HH-3 (2) 9%
3-HH-V (2) 32%
3-HH-V1 (2) 5%
1V2-HH-3 (2) 3%
1-HHB (F, F) -F (3-2) 2%
2-HHB (F, F) -F (3-2) 3%
3-HHB (F, F) -F (3-2) 3%
3-HBB (F, F) -F (3-8) 3%
5-HBB (F, F) -F (3-8) 3%
V-HB (F) B (F, F) -F (3-9) 3%
3-GB (F, F) XB (F) -F (3-13) 3%
3-GBB (F) B (F, F) -F (3-22) 2%
4-BB (F) B (F, F) XB (F) -F (3-28) 5%
4-BB (F) B (F, F) XB (F, F) -F (3-29) 5%
5-BB (F) B (F, F) XB (F) B (F, F) -F (3-31) 3%
3-HHB-O1 (4-4) 2%
V-HHB-1 (4-4) 2%
V2-HHB-1 (4-4) 2%
2-BB (F) B-2V (4-6) 2%
3-HHEBH-5 (4-10) 2%
NI = 72.5 ° C; Tc <-20 ° C; η = 11.8 mPa · s; Δn = 0.093; Δε = 6.3; Vth = 1.73 V; γ1 = 57.8 mPa · s.

[Example 20]
1O1-HBBXB (F, F) -F (1-6) 3%
1O1-HBB (F, F) XB (F, F) -F (1-6) 3%
2-HH-3 (2) 27%
3-HH-4 (2) 3%
3-HH-5 (2) 3%
3-HH-V1 (2) 8%
5-HXB (F, F) -F (3-1) 3%
3-HB (F) B (F, F) -F (3-9) 3%
3-GB (F, F) XB (F, F) -F (3-14) 4%
3-BB (F) B (F, F) -F (3-15) 3%
3-BB (F, F) XB (F, F) -F (3-18) 8%
3-HHBB (F, F) -F (3-19) 4%
5-HHBB (F, F) -F (3-19) 2%
2-HHB (F) B (F, F) -F (3-20) 3%
3-HHB (F) B (F, F) -F (3-20) 3%
5-GB (F) B (F, F) XB (F, F) -F (3-27) 2%
3-HB-O2 (4-1) 3%
V-HHB-1 (4-4) 3%
V2-HHB-1 (4-4) 3%
3-HBB-2 (4-5) 5%
2-BB (F) B-5 (4-6) 2%
1-BB2B-2V (4-8) 2%
NI = 74.0 ° C; Tc <-20 ° C; η = 11.4 mPa · s; Δn = 0.095; Δε = 6.6; Vth = 1.64V; γ1 = 56.1 mPa · s.

The bulk viscosity of the composition of Comparative Example 1 was 16.9 mPa · s. On the other hand, the bulk viscosities of the compositions of Examples 1 to 20 were 10.0 to 12.7 mPa · s. As described above, the composition of the example has a smaller bulk viscosity than the composition of the comparative example. Therefore, it is concluded that the liquid crystal composition of the present invention has excellent properties.

The liquid crystal composition of the present invention can be used for liquid crystal projectors, liquid crystal televisions and the like.

Claims (16)

At least one compound selected from the group of compounds represented by the formula (1) as the first component, at least one compound selected from the group of compounds represented by the formula (2) as the second component, and the first component. A liquid crystal composition containing at least one compound selected from the group of compounds represented by the formula (3) as three components and having a nematic phase.

In formulas (1) and (2), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, at least one −CH ₂ − is −O−. ^{R 2} and R ³ may be independently replaced by an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, and at least one hydrogen being fluorine or chlorine. An alkyl having 1 to 12 carbon atoms replaced, or an alkenyl having 2 to 12 carbon atoms in which at least one hydrogen has been replaced with fluorine or chlorine; ring A is 1,4-cyclohexylene or 1,4-cyclohexylene. It is senylene; ring B is 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4- Phenylene, 2,6-difluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ¹ and Z ² is independently a single bond, ethylene, methyleneoxy, carbonyloxy or difluoromethyleneoxy, wherein at least one of Z ¹ and Z ² is located at difluoromethyleneoxy; X ¹ and X ² are independently , Hydrogen or fluorine; Y ¹ is fluorine, chlorine, alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, and 1 carbon number in which at least one hydrogen is replaced by fluorine or chlorine. To 12 alkoxys, or alkenyloxys having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine; a is 0, 1, 2, or 3; where a is 1 and When Z ² is difluoromethyleneoxy, ring B is 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1, 4-phenylene, pyrimidine-2,5-diyl, it is a 1,3-dioxane-2,5-diyl or tetrahydropyran-2,5-diyl,; n is 1, 2 or 3 der, Ri;
In formula (3), R ⁴ is an alkyl having 1 to 12 carbons, an alkoxy having 1 to 12 carbons, or an alkenyl having 2 to 12 carbons; ring C is 1,4-cyclohexylene, 1, 4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1,4-phenylene, pyrimidin-2,5-diyl, 1,3- Dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ³ is a single bond, ethylene, carbonyloxy, or difluoromethyleneoxy; X ⁷ and X ⁸ are independently hydrogen. Or fluorine; Y ² is fluorine, chlorine, an alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, and 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine. be alkoxy or at least one hydrogen having 2 to 12 carbons are replaced by fluorine or chlorine alkenyloxy; b is an 1, 2, 3 or 4,; provided, R ⁴ is C 1 -C To 10 alkyl, 1 to 9 carbon alkoxy, or 2 to 10 carbon alkenyl, and ring C is 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4- It is phenylene, or pyrimidin-2,5-diyl, and Z ³ is a single bond, ethylene, or carbonyloxy, and X ⁷ is hydrogen or fluorine, and X ⁸ is hydrogen and Y ² is an alkyl with 1 to 10 carbon atoms in which at least one hydrogen is replaced with fluorine, an alkoxy having 1 to 9 carbon atoms in which at least one hydrogen is replaced with fluorine, or at least one hydrogen is replaced with fluorine. Excludes compounds represented by the formula (3), which are alkenyloxy having 2 to 9 carbon atoms and have b of 1, 2, or 3 . The first component according to claim 1, wherein the first component contains at least one compound selected from the group of compounds represented by the formulas (1-3) to (1-8) and the formula (1-10). Liquid crystal composition.

In formulas (1-3) to (1-8) and (1-10), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, At least one -CH _2- may be replaced by -O-; X ¹ , X ² , X ³ , X ⁴ , X ⁵ , and X ⁶ are independently hydrogen or fluorine; Y ¹ Fluorine, chlorine, alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, alkoxy having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, or at least one Hydrogen is an alkenyloxy having 2 to 12 carbon atoms in which fluorine or chlorine has been replaced; n is 1, 2, or 3. The liquid crystal composition according to claim 1 or 2, wherein the ratio of the first component is in the range of 3% by weight to 30% by weight, and the ratio of the second component is in the range of 10% by weight to 80% by weight. The liquid crystal according to any one of claims 1 to 3 , which contains at least one compound selected from the group of compounds represented by formulas (3-1) to (3-35) as a third component. Composition.

In formula (3-35) from equation (3-1), ^{R 4} is an alkenyl alkyl of 1 to 12 carbons, alkoxy having 1 to 12 carbons, or 2 to 12 carbons. The liquid crystal composition according to any one of claims 1 to 4, wherein the proportion of the third component is in the range of 10% by weight to 70% by weight. The liquid crystal composition according to any one of claims 1 to 5 , further containing at least one compound selected from the group of compounds represented by the formula (4) as a fourth component.

In formula (4), R ⁵ and R ⁶ are independently an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, or at least one hydrogen being fluorine or chlorine. It is a replaced alkenyl with 2 to 12 carbon atoms; rings D and E are independently 1,4-cyclohexylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, or 2,5. -Difluoro-1,4-phenylene; Z ⁴ is single bond, ethylene, or carbonyloxy; c is 1, 2, or 3; when c is 1, ring E is 1 , 4-Phenylene, 2-Fluoro-1,4-Phenylene, or 2,5-Difluoro-1,4-Phenylene. The liquid crystal according to any one of claims 1 to 6 , which contains at least one compound selected from the group of compounds represented by the formulas (4-1) to (4-12) as the fourth component. Composition.

In the formula (4-12) from equation (4-1), independently of ^{R 5} and ^{R 6,} alkyl of 1 to 12 carbons, alkoxy having 1 to 12 carbons, from 2 to 12 carbons, alkenyl or, An alkoxy having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine. The liquid crystal composition according to claim 6 or 7 , wherein the proportion of the fourth component is in the range of 5% by weight to 60% by weight. The liquid crystal composition according to any one of claims 1 to 8 , which contains at least one compound selected from the group of compounds represented by the formula (5) as a fifth component.

In formula (5), R ⁷ and R ⁸ are independently composed of an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, or an alkenyloxy having 2 to 12 carbon atoms. Yes; Rings F and I are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one hydrogen is replaced with fluorine or chlorine. , Or tetrahydropyran-2,5-diyl; ring G is 2,3-difluoro-1,4-phenylene, 2-chloro-3-fluoro-1,4-phenylene, 2,3-difluoro-5. - methyl-1,4-phenylene, 3,4,5-trifluoro-2,6-diyl or 7,8-be difluorochroman-2,6-diyl; ^{Z 5} and ^{Z 6} are each independently , Single bond, ethylene, carbonyloxy, or methyleneoxy; d is 1, 2, or 3, e is 0 or 1, and the sum of d and e is 3 or less. The liquid crystal according to any one of claims 1 to 9 , which contains at least one compound selected from the group of compounds represented by formulas (5-1) to (5-22) as a fifth component. Composition.

In formulas (5-1) to (5-22), R ⁷ and R ⁸ are independently alkyl with 1 to 12 carbon atoms, alkoxy with 1 to 12 carbon atoms, alkenyl with 2 to 12 carbon atoms, or It is an alkoxyoxy having 2 to 12 carbon atoms. The liquid crystal composition according to claim 9 or 10 , wherein the proportion of the fifth component is in the range of 2% by weight to 30% by weight. At least one compound selected from the group of compounds represented by the formula (1) as the first component, at least one compound selected from the group of compounds represented by the formula (2) as the second component, and the first component. A liquid crystal composition containing at least one compound selected from the group of compounds represented by the formula (5) as five components and having a nematic phase.

In formulas (1) and (2), R ¹ is an alkyl having 1 to 12 carbon atoms or an alkenyl having 2 to 12 carbon atoms, and in these groups, at least one −CH ₂ − is −O−. ^{R 2} and R ³ may be independently replaced by an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, and at least one hydrogen being fluorine or chlorine. An alkyl having 1 to 12 carbon atoms replaced, or an alkenyl having 2 to 12 carbon atoms in which at least one hydrogen has been replaced with fluorine or chlorine; ring A is 1,4-cyclohexylene or 1,4-cyclohexylene. It is senylene; ring B is 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4- Phenylene, 2,6-difluoro-1,4-phenylene, pyrimidine-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; Z ¹ and Z ² is independently a single bond, ethylene, methyleneoxy, carbonyloxy or difluoromethyleneoxy, wherein at least one of Z ¹ and Z ² is located at difluoromethyleneoxy; X ¹ and X ² are independently , Hydrogen or fluorine; Y ¹ is fluorine, chlorine, alkyl having 1 to 12 carbon atoms in which at least one hydrogen is replaced by fluorine or chlorine, and 1 carbon number in which at least one hydrogen is replaced by fluorine or chlorine. To 12 alkoxys, or alkenyloxys having 2 to 12 carbon atoms in which at least one hydrogen is replaced with fluorine or chlorine; a is 0, 1, 2, or 3; where a is 1 and When Z ² is difluoromethyleneoxy, ring B is 1,4-phenylene, 2-fluoro-1,4-phenylene, 2,3-difluoro-1,4-phenylene, 2,6-difluoro-1, They are 4-phenylene, pyrimidin-2,5-diyl, 1,3-dioxane-2,5-diyl, or tetrahydropyran-2,5-diyl; n is 1, 2, or 3;
In formula (5), R ⁷ and R ⁸ are independently composed of an alkyl having 1 to 12 carbon atoms, an alkoxy having 1 to 12 carbon atoms, an alkenyl having 2 to 12 carbon atoms, or an alkenyloxy having 2 to 12 carbon atoms. Yes; Rings F and I are independently 1,4-cyclohexylene, 1,4-cyclohexenylene, 1,4-phenylene, 1,4-phenylene in which at least one hydrogen is replaced with fluorine or chlorine. , Or tetrahydropyran-2,5-diyl; ring G is 2,3-difluoro-1,4-phenylene, 2-chloro-3-fluoro-1,4-phenylene, 2,3-difluoro-5. - methyl-1,4-phenylene, 3,4,5-trifluoro-2,6-diyl or 7,8-be difluorochroman-2,6-diyl; ^{Z 5} and ^{Z 6} are each independently , Single bond, ethylene, carbonyloxy, or methyleneoxy; d is 1, 2, or 3, e is 0 or 1, and the sum of d and e is 3 or less. The upper limit temperature of the nematic phase is 70 ° C. or higher, the optical anisotropy at a wavelength of 589 nm (measured at 25 ° C.) is 0.07 or higher, and the dielectric anisotropy at a frequency of 1 kHz (measured at 25 ° C.) is 2. The liquid crystal composition according to any one of claims 1 to 12, which is the above. A liquid crystal display device containing the liquid crystal composition according to any one of claims 1 to 13. The liquid crystal display according to claim 14, wherein the operation mode of the liquid crystal display element is TN mode, ECB mode, OCB mode, IPS mode, FFS mode, or FPA mode, and the drive method of the liquid crystal display element is an active matrix method. element. Use of the liquid crystal composition according to any one of claims 1 to 13 in a liquid crystal display device.