JP7139797B2 - Liquid crystal composition and liquid crystal display element - Google Patents

Description

The present invention relates to a liquid crystal composition and a liquid crystal display device using the same.

As a liquid crystal display element using a liquid crystal composition exhibiting a negative dielectric anisotropy Δε, PSA or PSVA type liquid crystal TVs, liquid crystal monitors and the like are in widespread use. Patent document 1, patent document 2, patent document 3, patent document 4, patent document 5 and the like disclose various polymerizable compounds and liquid crystal compositions containing the same. Further, Patent Documents 6, 7 and 8 disclose a polymerizable compound having a biphenyl skeleton and a polymerizable compound having a terphenyl skeleton.

However, the properties of polymerizable compound-containing liquid crystal compositions that have been commonly used are insufficient for high-definition liquid crystal TVs such as 4K and 8K. Specifically, a 4K or 8K liquid crystal display element requires high-definition pixels, and an increase in wiring and light shielding areas cuts a considerable amount of UV light. For this reason, in the UV irradiation step in the manufacture of a PSA type or PSVA type liquid crystal display device, the polymerizable compound is not sufficiently polymerized and a large amount of the polymerizable compound remains. As a result, tilt formation was insufficient, resulting in deterioration of response speed and afterimages due to deterioration of orientation, and display defects such as burn-in (IS) due to the tilt change due to the gradual polymerization of the remaining polymerizable compound during driving. It is It has also been confirmed that, as a feature of the polymerizable compound, there are those whose tilt is easily changed and those whose tilt is not.

For the above reasons, PSA or PSVA type liquid crystal display elements such as high definition 4K and 8K liquid crystal televisions and liquid crystal monitors are required to have extremely high characteristics that are clearly different from conventional technologies. There is a need for liquid crystal compositions that can be stably manufactured with weak or little UV light.

JP 2016-216747 A JP 2017-14486 A Japanese Patent No. 6008065 Japanese Patent No. 6233550 Japanese Patent No. 6087815 Chinese Patent Application Publication No. 104342167 Chinese Patent Application Publication No. 104342170 WO2018/123417

The problem to be solved by the present invention is a polymerizable compound-containing liquid crystal composition capable of simultaneously achieving a high polymerization rate, large tilt formation, high tilt stability, and high voltage holding ratio (VHR), and an IS using the same. An object of the present invention is to provide a PSA type or PSVA type liquid crystal display element which is suppressed or does not occur.

As a result of intensive studies by the present inventors, the inventors have found that the above problems can be solved by a liquid crystal composition containing two or more polymerizable compounds having a specific chemical structure, and have completed the present invention.

That is, in the present invention, as the first component, the general formula (RM-13)

(Wherein, P ³ and P ⁴ are each independently represented by formulas (PG-1) to (PG-5)

(Wherein, the hydrogen atoms in the methyl group, ethyl group, n-propyl group and i-propyl group bonded to the vinyl group may be substituted with one or more fluorine atoms, and the group in which —CH ₂ — may be substituted with an oxygen atom.), S ³ and S ⁴ each independently represent a single bond or a represents an alkylene group, wherein one —CH ₂ — or two or more non-adjacent —CH ₂ — in the alkylene group may be substituted with —O—, —OCO— or —COO—; Y ¹ to Y ¹² each independently represents an alkoxy group having 1 to 5 carbon atoms, a fluorinated alkoxy group having 1 to 5 carbon atoms or a hydrogen atom, and at least one is alkoxy having 1 to 5 carbon atoms. group or a fluorinated alkoxy group having 1 to 5 carbon atoms. ) contains a polymerizable compound represented by
As the second component, general formula (RM-22) or general formula (RM-23)

(Wherein, P ⁵ , P ⁶ , P ⁷ and P ⁸ are each independently represented by formulas (PG-1) to (PG-5)

(Wherein, the hydrogen atoms in the methyl group, ethyl group, n-propyl group and i-propyl group bonded to the vinyl group may be substituted with one or more fluorine atoms, and the group in which —CH ₂ — may be substituted with an oxygen atom.), S ⁵ , S ⁶ , S ⁷ and S ⁸ each independently represent a single bond or a carbon represents an alkylene group having 1 to 5 atoms, wherein one -CH ₂ - or two or more non-adjacent -CH ₂ - in the alkylene group is -O-, -OCO- or -COO- Each of A ¹ to A ⁸ independently represents an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom, and B ¹ to B ¹² may be substituted. Each independently represents an alkyl group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom. ) to provide a liquid crystal composition containing a polymerizable compound represented by

Another object of the present invention is to provide a liquid crystal display device using the liquid crystal composition.

The liquid crystal composition of the present invention can achieve a high polymerization rate, large tilt formation, high tilt stability, and high VHR at the same time. A fine PSA type or PSVA type liquid crystal display element can be provided.

The liquid crystal composition of the present invention contains, as a first component, a polymerizable compound represented by general formula (RM-13), and as a second component, general formula (RM-22) or general formula (RM-23 ) contains a polymerizable compound represented by

In formula (RM-13), P ³ and P ⁴ are each independently represented by formula (PG-1) to formula (PG-5)

(Wherein, the hydrogen atoms in the methyl group, ethyl group, n-propyl group and i-propyl group bonded to the vinyl group may be substituted with one or more fluorine atoms, and the group One —CH ₂ — or two or more —CH ₂ — which are not adjacent to each other may be substituted with an oxygen atom.). Among them, the polymerizable groups of P ³ and P ⁴ are each independently preferably represented by formula (PG-1) or formula (PG-2), and particularly preferably represented by formula (PG-1).

S ³ and S ⁴ each independently represent a single bond or an alkylene group having 1 to 5 carbon atoms, in which one —CH ₂ — or two or more non-adjacent —CH ₂ - may be substituted with -O-, -OCO- or -COO-. Among them, S ³ and S ⁴ are preferably each independently a single bond or an unsubstituted alkylene group having 1 to 5 carbon atoms, particularly preferably a single bond.

Y ¹ to Y ¹² each independently represents an alkoxy group having 1 to 5 carbon atoms, a fluorinated alkoxy group having 1 to 5 carbon atoms, or a hydrogen atom, and at least one is an alkoxy group having 1 to 5 carbon atoms. represents an alkoxy group or a fluorinated alkoxy group having 1 to 5 carbon atoms; Among them, at least one of Y ¹ to Y ¹² is preferably an alkoxy group having 1 to 5 carbon atoms, and particularly preferably at least one of Y ¹ to Y ¹² is a methoxy group.

The number of alkoxy groups having 1 to 5 carbon atoms or fluorinated alkoxy groups having 1 to 5 carbon atoms is not particularly limited, but one or two of Y ¹ to Y ¹² are alkoxy groups or fluorine It is preferably an alkoxy group and the rest are hydrogen atoms.

When two or more of Y ¹ to Y ¹² are C 1-5 alkoxy groups or C 1-5 fluorinated alkoxy groups, two or more of those groups may be the same. , may be different from each other. Among them, it is preferable that all groups other than hydrogen atoms possessed by Y ¹ to Y ¹² are the same groups, and it is particularly preferable that all groups other than hydrogen atoms possessed by Y ¹ to Y ¹² are methoxy groups. In addition, two or more alkoxy groups or fluorinated alkoxy groups may substitute hydrogen atoms bonded to the same benzene ring in terphenyl, or may substitute hydrogen atoms bonded to different rings. When two or more hydrogen atoms bonded to different rings are substituted with an alkoxy group or a fluorinated alkoxy group, for example, the rings at both ends of the terphenyl are substituted with an alkoxy group (at positions Y ¹ and Y ⁶ as an example) and compounds substituted with

In formula (RM-22), A ¹ to A ⁸ each independently represent an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom. Among them, all of A ¹ to A ⁸ are hydrogen atoms, or one or two of A ¹ to A ⁸ are an alkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms, or a fluorine atom. more preferably, one or two of A ¹ to A ⁸ are an alkyl group having 1 to 3 carbon atoms, an alkoxy group having 1 to 3 carbon atoms or a fluorine atom, and 1 of A ¹ to A ⁸ It is particularly preferred that one or two are methyl groups, methoxy groups or fluorine atoms. When more than one of A ¹ to A ⁸ are groups or atoms other than hydrogen atoms, they may be the same groups or atoms or different groups or atoms.

In formula (RM-23), B ¹ to B ¹² each independently represent an alkyl group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom. Among them, one or two of B ¹ to B ¹² are preferably an alkyl group having 1 to 3 carbon atoms or a fluorine atom from the viewpoint of solubility, and one or two of B ¹ to B ¹² are methyl. Groups or fluorine atoms are particularly preferred. When more than one of B ¹ to B ¹² are groups or atoms other than hydrogen atoms, they may be the same groups or atoms or different groups or atoms.

In formulas (RM-22) and (RM-23), P ⁵ , P ⁶ , P ⁷ and P ⁸ are each independently a polymerizable group, and the description of the polymerizable group is given above for P ³ and the polymerizable group of ^P4 . Among them, the polymerizable groups of P ⁵ , P ⁶ , P ⁷ and P ⁸ are each independently preferably represented by formula (PG-1) or formula (PG-2), and preferably represented by formula (PG-1). is particularly preferred.

S ⁵ , S ⁶ , S ⁷ and S ⁸ each independently represent a single bond or an alkylene group having 1 to 5 carbon atoms, and one —CH ₂ — in the alkylene group or non-adjacent Two or more -CH ₂ - may be replaced with -O-, -OCO- or -COO-. Among them, S ⁵ to S ⁸ are each independently preferably a single bond or an unsubstituted alkylene group having 1 to 5 carbon atoms, more preferably a single bond.

The polymerizable compound represented by the general formula (RM-13), which is the first component, is preferably a polymerizable compound represented by the general formulas (RM-131) to (RM-156), and the general formula ( Polymerizable compounds represented by RM-131) to (RM-143) are particularly preferred.

(In the formula, P ³ , P ⁴ , S ³ and S ⁴ are the same as above.)
The polymerizable compound represented by the general formula (RM-22), which is the second component, includes general formulas (RM-221) to (RM-225), general formulas (RM-22M1) to (RM-22M9) and general Polymerizable compounds represented by formulas (RM-22O1) to (RM-22O6) are preferred, and polymerizable compounds represented by general formulas (RM-22O1) to (RM-22O6) are particularly preferred. preferable.

(In the formula, P ⁵ , P ⁶ , S ⁵ and S ⁶ are the same as above.)
The polymerizable compound represented by general formula (RM-23), which is the second component, is preferably a polymerizable compound represented by general formulas (RM-231) to (RM-255).

(In the formula, P ⁷ , P ⁸ , S ⁷ and S ⁸ are the same as above.)
The lower limit of the content of the first component in the liquid crystal composition of the present invention is preferably 0.001% by mass, preferably 0.005% by mass, and preferably 0.01% by mass. is preferably 0.02% by mass, preferably 0.03% by mass, preferably 0.1% by mass, preferably 0.2% by mass, 0.3 % by mass, preferably 0.4% by mass, and the upper limit is preferably 3% by mass, more preferably 2% by mass, and more preferably 1% by mass. preferably 0.5% by mass, more preferably 0.4% by mass, more preferably 0.3% by mass, more preferably 0.2% by mass, More preferably, it is 0.1% by mass. Hereinafter, mass % may be described as %.

The lower limit of the content of the second component in the liquid crystal composition of the present invention is preferably 0.001% by mass, preferably 0.005% by mass, and preferably 0.01% by mass. is preferably 0.02% by mass, preferably 0.03% by mass, preferably 0.1% by mass, preferably 0.2% by mass, 0.3 % by mass, preferably 0.4% by mass, and the upper limit is preferably 3% by mass, more preferably 2% by mass, and more preferably 1% by mass. It is preferably 0.5% by mass, more preferably 0.4% by mass, and even more preferably 0.3% by mass.

The lower limit of the total content of the first component and the second component in the liquid crystal composition of the present invention is preferably 0.002% by mass, preferably 0.005% by mass, and 0.005% by mass. 01% by mass, preferably 0.02% by mass, preferably 0.03% by mass, preferably 0.1% by mass, preferably 0.2% by mass is preferably 0.3% by mass, preferably 0.4% by mass, and the upper limit is preferably 6% by mass, preferably 3% by mass, and 2% by mass. More preferably, 1% by mass, more preferably 0.5% by mass, more preferably 0.4% by mass, and 0.3% by mass More preferred.

The liquid crystal composition of the present invention comprises a compound selected from the group of compounds represented by general formulas (N-01), (N-02), (N-03), (N-04) and (N-05). It is preferable to contain one type or two or more types. These compounds correspond to compounds having negative dielectric anisotropy. A “compound having negative dielectric anisotropy” means a compound in which the sign of Δε is negative and the absolute value thereof is greater than 2. The Δε of the compound is a value extrapolated from the measured value of the dielectric anisotropy of a composition obtained by adding the compound to a composition that is dielectrically neutral at 25°C.

The liquid crystal composition of the present invention contains one or more compounds selected from the group of compounds represented by general formulas (N-01), (N-02), (N-03) and (N-04). It is preferable to contain.

In the formula, R ²¹ and R ²² are each independently an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, or represents an alkenyloxy group of 8, wherein one or two or more non-adjacent -CH ₂ - in said group are each independently -CH=CH-, -C≡C-, -O-, -CO -, -COO- or -OCO-, and Z ¹ is each independently a single bond, -CH ₂ CH ₂ -, -OCH ₂ -, -CH ₂ O-, -COO- , -OCO-, -OCF ₂ -, -CF ₂ O-, -CH=CH-, -CF=CF- or -C≡C-, and m each independently represents 1 or 2;

R ²¹ is preferably an alkyl group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 5 carbon atoms, and still more preferably an alkyl group having 1 to 4 carbon atoms. However, when Z ¹ represents other than a single bond, R ²¹ is preferably an alkyl group having 1 to 3 carbon atoms.
R ²² is preferably an alkyl group having 1 to 8 carbon atoms or an alkoxy group having 1 to 8 carbon atoms, more preferably an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms. Preferred are alkoxy groups having 1 to 4 carbon atoms.
When R ²¹ and R ²² are alkenyl groups, formula (R1) to formula (R5)

(A black dot in each formula represents a carbon atom in the ring structure.), and more preferably formula (R1) or formula (R2). However, the content of the compound in which R ²¹ and R ²² are alkenyl groups should be as low as possible, preferably not included.

Z ¹ is each independently a single bond, -CH ₂ CH ₂ -, -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, - represents CH=CH-, -CF=CF- or -C≡C-, preferably a single bond, -CH ₂ CH ₂ -, -OCH ₂ - or -CH ₂ O-, and a single bond or -CH ₂ O - is more preferred.

When m is ¹ , Z1 is preferably a single bond.

When m is 2, Z ¹ is preferably -CH ₂ CH ₂ - or -CH ₂ O-.

Fluorine atoms in compounds represented by general formulas (N-01), (N-02), (N-03), (N-04) and (N-05) are substituted with chlorine atoms which are the same halogen group. It's okay to be. However, the content of the compound substituted with a chlorine atom should be as small as possible, preferably not contained.

The hydrogen atoms present on the rings of the compounds represented by the general formulas (N-01), (N-02), (N-03), (N-04) and (N-05) are fluorine atoms or chlorine Atoms may be substituted, but chlorine atoms are not preferred.

The compounds represented by the general formulas (N-01), (N-02), (N-03), (N-04) and (N-05) have a negative Δε and an absolute value greater than 3. A compound is preferred. Specifically, R ²² preferably represents an alkoxy group having 1 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms, particularly preferably an alkoxy group having 1 to 4 carbon atoms.

The liquid crystal composition of the present invention includes compounds represented by general formula (N-01), general formula (N-01-1), general formula (N-01-2), general formula (N-01-3 ) and general formula (N-01-4)

(Wherein, R ²¹ has the same meaning as described above, and R ²³ each independently represents an alkoxy group having 1 to 4 carbon atoms.) It is preferable to contain two or more kinds.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, and compounds represented by general formulas (N-01-1) to (N-01-4). It is preferable to contain one or more compounds selected from the group.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-01-1) and general formula (N-01-4) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-01-3) and general formula (N-01-4) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention is represented by general formula (N-02) as compounds represented by general formula (N-02-1), general formula (N-02-2), and general formula (N-02- 3)

(Wherein, R ²¹ has the same meaning as described above, and R ²³ each independently represents an alkoxy group having 1 to 4 carbon atoms.) It is preferable to contain two or more kinds.

The liquid crystal composition of the present invention preferably contains a polymerizable compound as the first component, a polymerizable compound as the second component, and a compound represented by general formula (N-02-1).

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-02-1) and general formula (N-02-3) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-02-1) and general formula (N-01-4) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention is represented by general formula (N-03) as a compound represented by general formula (N-03-1)

(wherein R ²¹ has the same meaning as described above, and R ²³ represents an alkoxy group having 1 to 4 carbon atoms).

The liquid crystal composition of the present invention preferably contains a polymerizable compound as the first component, a polymerizable compound as the second component, and a compound represented by general formula (N-03-1).

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-03-1) and general formula (N-01-4) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-03-1) and general formula (N-02-1) It is preferable to contain a compound represented by.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-03-1) and general formula (N-01-4) It is preferable to contain the compound represented by and the compound represented by general formula (N-02-1).

In the liquid crystal composition of the present invention, the compound represented by the general formula (N-04) is represented by the general formula (N-04-1)

(wherein R ²¹ has the same meaning as described above, and R ²³ represents an alkoxy group having 1 to 4 carbon atoms).

The liquid crystal composition of the present invention preferably contains the polymerizable compound as the first component, the polymerizable compound as the second component, and the compound represented by the general formula (N-04-1) at the same time.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-04-1) and general formula (N-01-4) It is particularly preferable to simultaneously contain the compound represented by.

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-04-1) and general formula (N-01-4) It is particularly preferable to simultaneously contain the compound represented by and the compound represented by general formula (N-02-1).

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-04-1) and general formula (N-01-4) It is particularly preferable to simultaneously contain the compound represented by and the compound represented by general formula (N-03-1).

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-04-1) and general formula (N-02-1) It is particularly preferable to simultaneously contain the compound represented by and the compound represented by general formula (N-03-1).

The liquid crystal composition of the present invention comprises a polymerizable compound as a first component, a polymerizable compound as a second component, a compound represented by general formula (N-04-1) and general formula (N-01-4) It is particularly preferable to simultaneously contain the compound represented by and the compound represented by general formula (N-02-1) and the compound represented by general formula (N-03-1).

In the liquid crystal composition of the present invention, the compound represented by general formula (N-05) is a compound selected from the group of compounds represented by formulas (N-05-1) to (N-05-3). May contain.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by the general formula (N-01) is 0%, 1%, 5%, and 10%. , 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80% is. The upper limit of the preferred content is 95%, 85%, 75%, 65%, 55%, 45%, 35%, 25%, 20% , 15%, and 10%.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by the general formula (N-02) is 0%, 1%, 5%, and 10%. , 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80% is. The upper limit of the preferred content is 95%, 85%, 75%, 65%, 55%, 45%, 35%, 25%, 20% , 15%, and 10%.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by the general formula (N-03) is 0%, 1%, 5%, and 10%. , 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80% is. The upper limit of the preferred content is 95%, 85%, 75%, 65%, 55%, 45%, 35%, 25%, 20% , 15%, and 10%.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by the general formula (N-04) is 0%, 1%, 5%, and 10%. , 20%, 30%, 40%, 50%, 55%, 60%, 65%, 70%, 75%, 80% is. The upper limit of the preferred content is 95%, 85%, 75%, 65%, 55%, 45%, 35%, 25%, 20% , 15%, and 10%.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by formula (N-05) is 0%, 2%, 5%, and 8%. Yes, 10%, 13%, 15%, 17%, 20%. Preferred upper limits of the content are 30%, 28%, 25%, 23%, 20%, 18%, 15% and 13%.

The liquid crystal composition of the present invention may further contain one or more compounds represented by general formula (N-06).

(In the formula, R ²¹ and R ²² have the same meanings as described above.)
The compound represented by the general formula (N- ₀₆ ) is effective when it is desired to adjust various physical properties. can be done.

With respect to the total amount of the liquid crystal composition of the present invention, the preferred lower limit of the content of the compound represented by formula (N-06) is 0%, 2%, 5%, and 8%. Yes, 10%, 13%, 15%, 17%, 20%. The upper limit of the preferred content is 30%, 28%, 25%, 23%, 20%, 18%, 15%, 13%, 10% and 5%.

The liquid crystal composition of the present invention has general formulas (NU-01) to (NU-08)

(In the formula, R ^NU11 , R ^NU12 , R ^NU21 , R ^NU22 , R ^NU31 , R ^NU32 , R ^NU41 , R ^NU42 , R ^NU51 , R ^NU52 , R ^NU61 , R ^NU62 , R ^NU71 , R ^NU72 , R ^NU81 and R ^NU82 each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms; , one or two or more non-adjacent -CH ₂ - in said group are each independently -CH=CH-, -C≡C-, -O-, -CO-, -COO- or -OCO may be substituted with -) contains one or more compounds selected from the group of compounds represented by

More specifically, ^RNU11 , ^RNU12 , ^RNU21 , ^RNU22 , ^RNU31 , ^RNU32 , ^RNU41 , ^RNU42 , ^RNU51 , ^RNU52 , ^RNU61 , ^RNU62 , ^RNU71 , ^RNU72 , ^RNU81 and R ^NU82 is preferably an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms, more preferably an alkyl group having 1 to 5 carbon atoms. When the response speed is important, at least one of R ^NU11 , R ^NU21 , R ^NU41 and R ^NU51 is preferably an alkenyl group having 2 to 3 carbon atoms, such as alkenyl represented by formula (R2) groups are preferred.

The compound having an alkenyl group is preferably 30% or less, preferably 25% or less, preferably 20% or less, preferably 15% or less, preferably 10% or less, based on the total amount of the liquid crystal composition of the present invention. % or less is preferable. When a high VHR is important, the content of the alkenyl group-containing compound is preferably 10% or less, preferably 5% or less, preferably 1% or less, and preferably not contained.

More specifically, R ^NU11 , R ^NU21 , R ^NU31 , R ^NU41 , R ^NU51 , R ^NU61 , R ^NU71 and R ^NU81 are particularly preferably alkyl groups having 1 to 5 carbon atoms, R ^NU12 , R ^NU22 and R ^NU32 , ^RNU42 , ^RNU52 , ^RNU62 , ^RNU72 and ^RNU82 are particularly preferably alkyl groups having 1 to 5 carbon atoms or alkoxy groups having 1 to 5 carbon atoms.

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-01) and a compound represented by general formula (NU-02).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-01) and a compound represented by general formula (NU-03).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-03) and a compound represented by general formula (NU-04).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-03) and a compound represented by general formula (NU-05).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-01) and a compound represented by general formula (NU-06).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-01) and a compound represented by general formula (NU-07).

The liquid crystal composition of the present invention preferably contains a compound represented by general formula (NU-01) and a compound represented by general formula (NU-08).

The liquid crystal composition of the present invention contains a compound represented by the general formula (NU-01), a compound represented by the general formula (NU-02), and a compound represented by the general formula (NU-04). is more preferred.

The liquid crystal composition of the present invention contains a compound represented by the general formula (NU-01), a compound represented by the general formula (NU-03), and a compound represented by the general formula (NU-05). is more preferred.

The liquid crystal composition of the present invention includes a compound represented by the general formula (NU-01), a compound represented by the general formula (NU-02), a compound represented by the general formula (NU-03), and a compound represented by the general formula ( It is more preferable to contain a compound represented by NU-05).

The content of the compound represented by the general formula (NU-01) is preferably 1 to 60% by mass, more preferably 10 to 50% by mass, and further preferably 20 to 40% by mass. preferable.

The content of the compound represented by the general formula (NU-02) is preferably 1 to 40% by mass, more preferably 5 to 25% by mass, and further preferably 5 to 20% by mass. preferable.

The content of the compound represented by the general formula (NU-03) is preferably 1 to 20% by mass, more preferably 0 to 15% by mass, and further preferably 0 to 10% by mass. preferable.

The content of the compound represented by the general formula (NU-04) is preferably 1 to 30% by mass, more preferably 3 to 20% by mass, and further preferably 3 to 10% by mass. preferable.

The content of the compound represented by the general formula (NU-05) is preferably 1 to 30% by mass, more preferably 1 to 20% by mass, and further preferably 3 to 20% by mass. preferable.

The content of the compound represented by the general formula (NU-06) is preferably 1 to 30% by mass, more preferably 3 to 20% by mass, and further preferably 3 to 10% by mass. preferable.

The content of the compound represented by the general formula (NU-07) is preferably 1 to 30% by mass, more preferably 3 to 20% by mass, and further preferably 3 to 10% by mass. preferable.

The content of the compound represented by the general formula (NU-08) is preferably 1 to 30% by mass, more preferably 3 to 20% by mass, and further preferably 3 to 10% by mass. preferable.

The liquid crystal composition of the present invention can contain one or more compounds having positive dielectric anisotropy described in paragraphs 0236 to 0509 of Patent Document 4 (Japanese Patent No. 6233550).

The composition of the present invention preferably does not contain a compound having a structure in which oxygen atoms are bonded to each other, such as a peracid (--CO--OO--) structure.

When the reliability and long-term stability of the composition are emphasized, the content of the compound having a carbonyl group is preferably 5% or less, more preferably 3% or less, relative to the total mass of the composition. Preferably, it is more preferably 1% or less, and most preferably not substantially contained.

When the stability against UV irradiation is emphasized, the content of the compound substituted with chlorine atoms is preferably 15% or less, preferably 10% or less, relative to the total mass of the composition. % or less, more preferably 5% or less, preferably 3% or less, and even more preferably not substantially contained.

It is preferable to increase the content of compounds having all 6-membered ring structures in the molecule, and the content of compounds having all 6-membered ring structures in the molecule is increased to 80% relative to the total mass of the composition. % or more, more preferably 90% or more, even more preferably 95% or more, and substantially all of the ring structures in the molecule are six-membered rings. most preferably.

In order to suppress the deterioration of the composition due to oxidation, it is preferable to reduce the content of the compound having a cyclohexenylene group as a ring structure, and the content of the compound having a cyclohexenylene group is added to the total mass of the composition. On the other hand, it is preferably 10% or less, preferably 8% or less, more preferably 5% or less, preferably 3% or less, and further preferably substantially free.

When emphasizing improvement of viscosity and improvement of TNI, it is possible to reduce the content of a compound having a 2-methylbenzene-1,4-diyl group in the molecule, in which a hydrogen atom may be substituted with a halogen. Preferably, the content of the compound having a 2-methylbenzene-1,4-diyl group in the molecule is 10% or less, preferably 8% or less, relative to the total mass of the composition. , more preferably 5% or less, preferably 3% or less, and even more preferably not substantially contained.

In the present application, "substantially not contained" means not contained except for unintentionally contained substances.

The liquid crystal composition of the present invention may contain ordinary nematic liquid crystals, smectic liquid crystals, cholesteric liquid crystals, antioxidants, ultraviolet absorbers, light stabilizers, infrared absorbers, and the like, in addition to the compounds described above.

The liquid crystal composition of the present invention preferably contains an antioxidant so as not to polymerize during heat treatment, which is one of the manufacturing processes of liquid crystal display elements. When the antioxidant is not contained, polymerization proceeds in the heat treatment before the UV irradiation step, and the desired orientation cannot be obtained.

Antioxidants include hindered phenols represented by general formulas (H-1) to (H-4).

In general formulas (H-1) to (H-3), each R ^H1 is independently an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, and 2 carbon atoms. represents an alkenyl group having 1 to 10 or an alkenyloxy group having 2 to 10 carbon atoms. More specifically, R ^{1 H1} is more preferably an alkyl group having 3 carbon atoms.

In general formula (H-4), M ^H1 is an alkylene group having 4 to 10 carbon atoms (one or two or more —CH ₂ — in the alkylene group are — O—, —CO—, —COO—, —OCO—.), —OCH ₂ —, —CH ₂ O—, —COO—, —OCO—, —CF ₂ O—, — OCF ₂ -, -CF ₂ CF ₂ -, -CH=CH-COO-, -CH=CH-OCO-, -COO-CH=CH-, -OCO-CH=CH-, -CH=CH-, - C≡C—, a single bond, a 1,4-phenylene group (any hydrogen atom in the 1,4-phenylene group may be substituted with a fluorine atom) or a trans-1,4-cyclohexylene group show.

When the liquid crystal composition of the present invention contains an antioxidant, the lower limit is preferably 10 mass ppm, preferably 20 mass ppm, preferably 50 mass ppm, and the upper limit is 10000 mass ppm, but 1000 mass ppm. is preferred, 500 mass ppm is preferred, and 100 mass ppm is preferred.

The liquid crystal composition of the present invention has a nematic phase-isotropic liquid phase transition temperature (T _NI ) of 60°C to 120°C, more preferably 70°C to 100°C, particularly preferably 70°C to 85°C. In the present invention, a temperature of 60° C. or higher is expressed as a high _TNI .

For liquid crystal television applications, the _TNI is preferably from 70 to 80°C, for mobile applications, the _TNI is preferably from 80 to 90°C, and for outdoor display applications such as PID (Public Information Display), the _TNI is from 90 to 110°C is preferred.

The liquid crystal composition of the present invention has a refractive index anisotropy (Δn) at 20° C. of 0.08 to 0.14, more preferably 0.09 to 0.13, more preferably 0.09 to 0.12. Especially preferred. More specifically, it is preferably 0.10 to 0.13 for a thin cell gap and 0.08 to 0.10 for a thick cell gap. It is particularly preferable that the liquid crystal composition of the present invention has a refractive index anisotropy (Δn) at 20° C. of 0.098 to 0.118.

The liquid crystal composition of the present invention has a rotational viscosity (γ ₁ ) at 20° C. of 50 to 160 mPa·s, preferably 55 to 160 mPa·s, more preferably 60 to 160 mPa·s, more preferably 80 mPa·s. to 150 mPa·s, preferably 90 to 140 mPa·s, preferably 90 to 130 mPa·s, and preferably 90 to 115 mPa·s.

The liquid crystal composition of the present invention has a dielectric anisotropy (Δε) at 20° C. of −1.7 to −4.0, preferably −1.7 to −3.5, more preferably −1.8 to -3.5 is more preferred, and -1.9 to -3.3 is more preferred.

The liquid crystal composition of the present invention contains a polymerizable compound of the first component and a polymerizable compound of the second component, and further general formula (N-01), general formula (N-02), general formula (N-03 ), contains one or more compounds selected from the group of compounds represented by general formula (N-04), general formula (N-05) and general formula (N-06), and further general formula (NU -01) to (NU-08) It is preferable to contain one or more compounds selected from the group of compounds represented by (NU-08), and the upper limits of the total content of these are 100% by mass and 99% by mass. , 98% by weight, 97% by weight, 96% by weight, 95% by weight, 94% by weight, 93% by weight, 92% by weight, 91% by weight, 90% by weight, 89% by weight, 88% by weight, 87% by weight, 86% by weight % by mass, preferably 85% by mass, and 84% by mass, and the lower limits of the total of these contents are 78% by mass, 80% by mass, 81% by mass, 83% by mass, 85% by mass, and 86% by mass. , 87% by weight, 88% by weight, 89% by weight, 90% by weight, 91% by weight, 92% by weight, 93% by weight, 94% by weight, 95% by weight, 96% by weight, 97% by weight, 98% by weight, 99% by weight % by mass, preferably 100% by mass.

The liquid crystal composition of the present invention contains a polymerizable compound of the first component and a polymerizable compound of the second component, and further general formula (N-01), general formula (N-02), general formula (N-03 ) and one or more compounds selected from the group of compounds represented by the general formula (N-04), and from the group of compounds represented by the general formulas (NU-01) to (NU-08) It is particularly preferable to contain one or more selected compounds, and the upper limits of the total content of these are 100% by mass, 99% by mass, 98% by mass, 97% by mass, 96% by mass, and 95% by mass. %, 94% by mass, 93% by mass, 92% by mass, 91% by mass, 90% by mass, 89% by mass, 88% by mass, 87% by mass, 86% by mass, 85% by mass, and 84% by mass. , the lower limit of the total of these contents is 78% by mass, 80% by mass, 81% by mass, 83% by mass, 85% by mass, 86% by mass, 87% by mass, 88% by mass, 89% by mass, 90% by mass %, 91% by mass, 92% by mass, 93% by mass, 94% by mass, 95% by mass, 96% by mass, 97% by mass, 98% by mass, 99% by mass, and 100% by mass.

The liquid crystal composition of the present invention can impart a sufficiently high polymerization rate and a sufficiently large pretilt angle. In addition, the liquid crystal display element using the liquid crystal composition of the present invention has a small residual amount of the polymerizable compound in the liquid crystal display element after polymerization, and is a high-definition PSA type or PSVA type liquid crystal display element such as 4K or 8K. Display defects such as IS do not occur or can be significantly suppressed. As described above, the production efficiency of high-definition PSA-type or PSVA-type liquid crystal display elements such as 4K and 8K can be significantly improved, and the industrial utility value is extremely high.
The liquid crystal composition of the present invention is suitable for producing a PSA-type or PSVA-type liquid crystal display element, and is also suitable for producing an NPS-type liquid crystal display element. It is also suitable for manufacturing a PI-less type liquid crystal display device that does not have an alignment film.

The liquid crystal composition of the present invention is also suitable for a liquid crystal display element having no alignment film, that is, a mode commonly called PI-less. For example, compounds having spontaneous orientation described in Japanese Patent Application No. 2013-552125, Japanese Patent Application No. 2014-517515, Japanese Patent No. 06081361, Japanese Patent Application No. 2015-546888, Japanese Patent Application No. 2017-12710, WO2017041893A, Japanese Patent No. 06070973, WO17/047177, etc. It is preferably used in combination with the liquid crystal composition of the invention.

The liquid crystal composition of the present invention is useful for liquid crystal display elements for active matrix driving, and can be used for liquid crystal display elements such as PSA, PSVA, PS-IPS, PS-FFS and NPS.

A liquid crystal display element of the present invention comprises: a first substrate and a second substrate arranged to face each other; a common electrode provided on the first substrate or the second substrate; It is preferable to have a pixel electrode provided on two substrates and having a thin film transistor, and a liquid crystal layer containing a liquid crystal composition provided between the first substrate and the second substrate. If necessary, an alignment film for controlling the alignment direction of liquid crystal molecules may be provided on the opposing surface side of at least one of the first substrate and/or the second substrate so as to be in contact with the liquid crystal layer. As the alignment film, a vertical alignment film, a horizontal alignment film, or the like can be appropriately selected in accordance with the drive mode of the liquid crystal display element. known alignment films can be used. Furthermore, a color filter may be appropriately provided on the first substrate or the second substrate, and a color filter may be provided on the pixel electrode or the common electrode.

The two substrates of the liquid crystal cell used in the liquid crystal display device of the present invention can be made of a flexible transparent material such as glass or plastic, and one of them can be made of an opaque material such as silicon. A transparent substrate having a transparent electrode layer can be obtained, for example, by sputtering indium tin oxide (ITO) on a transparent substrate such as a glass plate.

A color filter can be produced by, for example, a pigment dispersion method, a printing method, an electrodeposition method, a dyeing method, or the like. A method for producing a color filter by a pigment dispersion method will be described as an example. A curable coloring composition for a color filter is applied onto the transparent substrate, patterned, and cured by heating or light irradiation. By performing this process for each of the three colors of red, green, and blue, a pixel portion for a color filter can be manufactured. In addition, a pixel electrode provided with an active element such as a TFT, a thin film diode, a metal insulator metal resistivity element, or the like may be provided on the substrate.

It is preferable that the first substrate and the second substrate are opposed to each other so that the common electrode and the pixel electrode layer are inside.

A space between the first substrate and the second substrate may be adjusted via a spacer. In this case, it is preferable to adjust the thickness of the obtained light control layer to 1 to 100 μm. It is more preferably 1.5 to 10 μm, and when a polarizing plate is used, it is preferable to adjust the product of the refractive index anisotropy Δn of the liquid crystal and the cell thickness d so as to maximize the contrast. Moreover, when there are two polarizing plates, the polarizing axis of each polarizing plate can be adjusted to improve the viewing angle and contrast. Furthermore, a retardation film for widening the viewing angle can also be used. Examples of spacers include glass particles, plastic particles, alumina particles, photoresist materials, and the like. After that, a sealing agent such as an epoxy-based thermosetting composition is screen-printed on the substrates provided with a liquid crystal injection port, if necessary, and the substrates are bonded together and heated to thermally cure the sealing agent.

As a method for sandwiching the liquid crystal composition between two substrates, an ordinary vacuum injection method, an ODF method, or the like can be used.

As a method for polymerizing the polymerizable compound contained in the liquid crystal composition of the present invention, it is desirable to polymerize at an appropriate polymerization rate in order to obtain good alignment performance of the liquid crystal. A method of polymerizing by irradiating energy rays singly, in combination, or in sequence is preferred. When using ultraviolet rays, a polarized light source may be used, or a non-polarized light source may be used. In the case where the liquid crystal composition is sandwiched between two substrates and the polymerization is carried out, at least the substrate on the irradiation surface side must be given appropriate transparency to the active energy ray. In addition, after polymerizing only a specific portion using a mask during light irradiation, the orientation state of the unpolymerized portion is changed by changing the conditions such as the electric field, magnetic field, or temperature, and then the active energy ray is further irradiated. It is also possible to use a means of polymerizing by In particular, when the liquid crystal composition is exposed to ultraviolet rays, it is preferable to apply the ultraviolet rays while applying a DC electric field or an AC electric field to the liquid crystal composition. The AC electric field to be applied is preferably AC with a frequency of 1 Hz to 10 kHz, more preferably 60 Hz to 10 kHz, and the voltage is selected depending on the desired pretilt angle of the liquid crystal display element. That is, the pretilt angle of the liquid crystal display element can be controlled by the applied voltage. In the PSA type or PSVA type liquid crystal display device, it is preferable to control the pretilt angle from 80 degrees to 89.9 degrees from the viewpoint of alignment stability and contrast.
In a PSA-type or PSVA-type liquid crystal display element, IS occurs if the polymerizable compound remains as it is without being polymerized after the element is manufactured. The amount of the remaining polymerizable compound is preferably 20 ppm or less, more preferably 15 ppm or less, particularly preferably 10 ppm or less, and particularly preferably 0 or less than the detection limit.

There are no particular restrictions on the temperature during irradiation of active energy rays such as ultraviolet rays or electron beams used for polymerizing the polymerizable compound contained in the liquid crystal composition of the present invention. For example, when the liquid crystal composition of the present invention is applied to a liquid crystal display element having a substrate having an alignment film, the temperature is preferably within a range in which the liquid crystal state of the liquid crystal composition is maintained. That is, it is preferable to polymerize at 15 to 50°C.

A metal halide lamp, a high-pressure mercury lamp, an ultra-high-pressure mercury lamp, or the like can be used as a lamp for generating ultraviolet rays, and an ultra-high-pressure UV lamp manufactured by USHIO and a fluorescent type ultraviolet lamp manufactured by TOSHIBA are preferable. As for the wavelength of ultraviolet rays to be irradiated, it is preferable to irradiate ultraviolet rays in a wavelength range that is not in the absorption wavelength range of the liquid crystal composition, and if necessary, it is preferable to cut the ultraviolet rays. The intensity of the ultraviolet rays to be irradiated is preferably 0.1 mW/cm ² to 100 W/cm ² , more preferably 2 mW/cm ² to 50 W/cm ² . The energy amount of the ultraviolet rays to be irradiated can be appropriately adjusted, but is preferably 10 mJ/cm ² to 500 J/cm ² , more preferably 100 mJ/cm ² to 200 J/cm ² .

The present invention will be described in more detail with reference to examples below, but the present invention is not limited to these examples. Moreover, "%" in the compositions of the following examples and comparative examples means "% by mass". The following abbreviations are used for the description of compounds in Examples.

Each physical property value was measured based on the method described in Japan Electronics and Information Technology Industries Association standard JEITA ED-2521B revised in March 2009 issued by Japan Electronics and Information Technology Industries Association unless otherwise specified.

(side chain)
-n -C _n H _2n+1 straight-chain alkyl group having n carbon atoms n- C _n H _2n+1 - straight-chain alkyl group having n carbon atoms -On -OC _n H _2n+1 straight-chain alkoxy having n carbon atoms Group nO- C _n H _2n+1 O- Linear alkoxy group having n carbon atoms -V -CH=CH ₂
V-CH ₂ =CH-
-V1 -CH=CH-CH ₃
1V- CH ₃ -CH=CH-
-F -F
-OCF3 _-OCF3
(Connecting group)
-1O- -CH ₂ -O-
-O1- -O-CH ₂ -
-2- -CH ₂ -CH ₂ -
-COO- -COO-
-OCO- -OCO-
- single bond (ring structure)

The properties measured in the examples are as follows.

T _NI : nematic phase-isotropic liquid phase transition temperature (°C)
Δn: refractive index anisotropy at 20°C Δε: dielectric anisotropy at 20°C γ ₁ : rotational viscosity at 20°C (mPa s)
RM: Amount of residual monomer (ppm) in the liquid crystal display element after 20 minutes of irradiation with UV light at 313 nm and illuminance of 3 mW/cm ² .
Tilt: The pretilt angle (°) of the liquid crystal display element after being irradiated with UV light of 313 nm and an illuminance of 3 mW/cm ² for 2 minutes, and represents the amount of change from 90°.

IS: A value obtained by multiplying the amount of change in the pretilt angle by 100 after a liquid crystal display device was prepared after being irradiated with UV light at an illuminance of 313 nm and an illuminance of 3 mW/cm ² for 60 minutes and maintained for a certain period of time VHR: Illuminance at 313 nm A liquid crystal display element was prepared after being irradiated with UV light of 3 mW/cm ² for 60 minutes, and the voltage holding rate (%) measured at 1 V, 60 Hz, and 60°C.
(Preparation of Liquid Crystal Composition and Evaluation Results)
Liquid crystal compositions (LC-1) to (LC-4) were prepared and their physical properties were measured. Table 1 shows the component ratios and physical properties of these liquid crystal compositions.

Example 1 (E-01) to Example 4 (E-04) in which these liquid crystal compositions were mixed with the polymerizable compounds represented by the formulas (RM-131-MM) and/or (RM-22O2-MM) ), Comparative Example 1 (C-01) to Comparative Example 2 (C-02) were prepared, and the results of evaluating RM, Tilt, IS, and VHR are shown in Table 2.

In Examples 1 (E-01) to 4 (E-04), the RM was 0, which is below the detection limit, and was a sufficiently small value. Also, it was confirmed that Tilt is sufficiently large, IS is sufficiently small, and VHR is sufficiently high. From the above, it was confirmed that these examples have solved the problems of the present invention. On the other hand, it was confirmed that Comparative Example 1 (C-01) had a very large IS of 120, and Comparative Example 2 (C-02) had a large RM of 21 and a small Tilt value. From the above, it was confirmed that these comparative examples could not solve the problems of the present invention.

The polymerizable compound represented by the formula (RM-22O2-MM) included in Examples 1 (E-01) to 4 (E-04) is represented by the formula (RM-22O1-MM) A composition substituted with a polymerizable compound was prepared, and it was confirmed that the problems of the present invention were solved.

When the polymerizable compound represented by the formula (RM-22O2-MM) contained in Example 4 (E-04) was replaced with the polymerizable compound represented by the formula (RM-224-MM), A good result was obtained although slightly inferior to Example (E-04).

When the polymerizable compound represented by the formula (RM-22O2-MM) contained in Example 4 (E-04) was replaced with the polymerizable compound represented by the formula (RM-22M5-MM), A good result was obtained although slightly inferior to Example (E-04).

Furthermore, a composition obtained by adding 50 ppm of an antioxidant represented by the formula (H-2-R3) to Example 1 (E-01) was prepared to solve the problems of the present invention. confirmed. In addition, a composition obtained by adding 50 ppm of an antioxidant represented by the formula (H-3-R3) to Example 1 (E-01) was prepared to solve the problems of the present invention. confirmed. A composition in which 50 ppm of an antioxidant represented by the formula (H-4-M8) was added to Example 1 (E-01) was prepared, and it was confirmed that the problems of the present invention were solved. .

A composition in which 20 ppm of an antioxidant represented by the formula (H-2-R3) was added to Example 4 (E-04) was prepared, and it was confirmed that the problems of the present invention were solved. . Further, a composition obtained by adding 20 ppm of an antioxidant represented by the formula (H-3-R3) to Example 4 (E-04) was prepared to solve the problems of the present invention. confirmed. A composition in which 10 ppm of an antioxidant represented by the formula (H-4-M8) was added to Example 4 (E-04) was prepared, and it was confirmed that the problems of the present invention were solved. .

The liquid crystal composition described above and the formula (RM-131-MM), the following formula (RM-137-MM), the formula (RM-22O1-MM) and/or the formula (RM-22O2-MM) Example 5 (E-05) to Example 10 (E-10) were prepared by mixing the polymerizable compound, and the results of evaluating RM, Tilt, IS, and VHR are shown in Table 3.

In Examples 5 (E-05) to 10 (E-10), the RM was 0, which is below the detection limit, and was a sufficiently small value. Also, it was confirmed that Tilt is sufficiently large, IS is sufficiently small, and VHR is sufficiently high. From the above, it was confirmed that these examples have solved the problems of the present invention.

Claims (11)

As the first component, the general formula (RM-13)

(Wherein, P ³ and P ⁴ are each independently represented by formulas (PG-1) to (PG-5)

(Wherein, the hydrogen atoms in the methyl group, ethyl group, n-propyl group and i-propyl group bonded to the vinyl group may be substituted with one or more fluorine atoms, and the group in which —CH ₂ — may be substituted with an oxygen atom.), S ³ and S ⁴ each independently represent a single bond or a represents an alkylene group, wherein one —CH ₂ — or two or more non-adjacent —CH ₂ — in the alkylene group may be substituted with —O—, —OCO— or —COO—; Y ¹ to Y ¹² each independently represents an alkoxy group having 1 to 5 carbon atoms, a fluorinated alkoxy group having 1 to 5 carbon atoms or a hydrogen atom, and at least one is alkoxy having 1 to 5 carbon atoms. group or a fluorinated alkoxy group having 1 to 5 carbon atoms. ) contains a polymerizable compound represented by
As the second component, general formula (RM-22) or general formula (RM-23)

(Wherein, P ⁵ , P ⁶ , P ⁷ and P ⁸ are each independently represented by formulas (PG-1) to (PG-5)

(Wherein, the hydrogen atoms in the methyl group, ethyl group, n-propyl group and i-propyl group bonded to the vinyl group may be substituted with one or more fluorine atoms, and the group in which —CH ₂ — may be substituted with an oxygen atom.), S ⁵ , S ⁶ , S ⁷ and S ⁸ each independently represent a single bond or a carbon represents an alkylene group having 1 to 5 atoms, wherein one -CH ₂ - or two or more non-adjacent -CH ₂ - in the alkylene group is -O-, -OCO- or -COO- Each of A ¹ to A ⁸ independently represents an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom, and B ¹ to B ¹² may be substituted. Each independently represents an alkyl group having 1 to 5 carbon atoms, a fluorine atom or a hydrogen atom. ) liquid crystal composition containing a polymerizable compound represented by. Further general formula (N-01), general formula (N-02), general formula (N-03), general formula (N-04) and general formula (N-05)

(wherein R ²¹ and R ²² are each independently an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, or a represents an alkenyloxy group of ~8, wherein one or two or more non-adjacent -CH ₂ - in said group are each independently -CH=CH-, -C≡C-, -O-, -CO -, -COO- or -OCO-, and Z ¹ is each independently a single bond, -CH ₂ CH ₂ -, -OCH ₂ -, -CH ₂ O-, -COO- , -OCO-, -OCF ₂ -, -CF ₂ O-, -CH=CH-, -CF=CF- or -C≡C-, and m each independently represents 1 or 2; 2. The liquid crystal composition according to claim 1, containing one or more compounds selected from the group of compounds represented by: Further general formula (NU-01) to general formula (NU-08)

(In the formula, R ^NU11 , R ^NU12 , R ^NU21 , R ^NU22 , R ^NU31 , R ^NU32 , R ^NU41 , R ^NU42 , R ^NU51 , R ^NU52 , R ^NU61 , R ^NU62 , R ^NU71 , R ^NU72 , R ^NU81 and R ^NU82 each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxy group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms or an alkenyloxy group having 2 to 8 carbon atoms. , one or two or more non-adjacent -CH ₂ - in said group are each independently -CH=CH-, -C≡C-, -O-, -CO-, -COO- or -OCO 3. The liquid crystal composition according to claim 1, which contains one or more compounds selected from the group of compounds represented by (which may be substituted with -). As the first component, general formulas (RM-131) to (RM-143)

(Wherein, P ³ , P ⁴ , S ³ , and S ⁴ are the same as above.)
As the second component, general formulas (RM-22O1) to (RM-22O6)

4. The liquid crystal composition according to any one of claims 1 to 3, containing a polymerizable compound represented by (wherein P ⁵ , P ⁶ , S ⁵ and S ⁶ are as defined above). . Further formula (H-2-R3), formula (H-3-R3) or formula (H-4-M8)

The liquid crystal composition according to any one of claims 1 to 4, which contains an antioxidant represented by. The first component, the second component, a compound selected from the group of compounds represented by the general formulas (N-01) to the general formula (N-04), and the general formula (NU-01) to the general 6. The composition according to any one of claims 1 to 5, wherein the total content of the compounds selected from the group of compounds represented by formula (NU-08) is 80% by mass to 100% by mass with respect to the total amount of the composition. The described liquid crystal composition. The content of the first component is 0.01% by mass to 0.10% by mass relative to the total amount of the composition, and the content of the second component is 0.2% by mass to 0.2% by mass relative to the total amount of the composition. 7. The liquid crystal composition according to any one of claims 1 to 6, which is 0.5% by mass. A liquid crystal display device using the liquid crystal composition according to any one of claims 1 to 7. A liquid crystal display element for active matrix driving, using the liquid crystal composition according to any one of claims 1 to 7. A PSA-type or PSVA-type liquid crystal display device using the liquid crystal composition according to any one of claims 1 to 7. A liquid crystal display element having no alignment film, using the liquid crystal composition according to any one of claims 1 to 7.