JP2010285499A - Liquid crystal composition containing polymerizable compound and liquid crystal display element using the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a polymerizable compound-containing liquid crystal composition which is a liquid crystal composition containing a polymerizable compound having the reduced residual amount of the polymerizable compound even when polymerization is carried out without using a photopolymerization initiator or by using an extremely small amount of an initiator, to provide a polymerizable compound-containing liquid crystal composition in which the polymerizable compound and the liquid crystal material are favorably made compatible with each other and aligning property after polymerization is further stabilized, preventing troubles in display characteristics, and further, to provide a liquid crystal display element imparted with liquid crystal aligning ability and having excellent display performance by polymerization of the polymerizable compound-containing liquid crystal composition. <P>SOLUTION: The liquid crystal composition contains, as a first component, a polymerizable compound expressed by general formula (I). The liquid crystal display element uses the liquid crystal composition. <P>COPYRIGHT: (C)2011,JPO&INPIT

Description

  The present invention relates to a liquid crystal composition containing a polymerizable compound, and further to a liquid crystal display device using the liquid crystal composition.

  A PSA (Polymer Sustained Alignment) type liquid crystal display device has a structure in which a polymer structure is formed in a cell in order to control the pretilt angle of liquid crystal molecules. Expected as an element.

  A PSA-type liquid crystal display device is manufactured by injecting a polymerizable composition comprising a liquid crystalline compound and a polymerizable compound between substrates and applying a voltage to polymerize the polymerizable compound in a state in which the liquid crystal molecules are aligned to produce liquid crystal molecules. This is done by fixing the orientation. In this case, the remaining amount of the polymerizable compound needs to be minimized because display persistence occurs in the manufactured display element due to the incomplete polymerization and the remaining polymerizable compound. However, if a large amount of a polymerization initiator is added to allow the polymerization to proceed completely, the residual polymerization initiator will reduce the voltage holding ratio of the display element, adversely affect the display quality, and suppress the decrease in voltage holding ratio. When the amount of the polymerization initiator used for polymerization is reduced, the polymerization does not proceed completely, so that the polymerizable compound remains, and the occurrence of image sticking by the remaining polymerizable compound is inevitable. In order to completely cure the polymerizable compound with a small addition amount of polymerization initiator and suppress the residue of the polymerizable compound, it is necessary to apply a large amount of energy by irradiating strong ultraviolet rays for a long time in the polymerization. This leads to an increase in the size of the apparatus and a decrease in manufacturing efficiency. Therefore, in a liquid crystal composition containing a conventional polymerizable compound, it is difficult to simultaneously reduce the residual amounts of both the uncured polymerizable compound and the polymerization initiator, and polymerization can be performed without using a polymerization initiator. There has been a demand for a liquid crystal composition containing a polymerizable compound that can be completed.

  On the other hand, the occurrence of image sticking is known to be caused by the pretilt angle of liquid crystal molecules in a liquid crystal composition containing a polymerizable compound. That is, if the polymer, which is a cured product of the polymerizable compound, is flexible, the structure of the polymer changes when the same pattern is displayed for a long time in the case where the display element is configured. As a result, the pretilt angle changes. End up. Since the change in the pretilt angle causes burn-in, a polymerizable compound that forms a polymer having a rigid structure in which the polymer structure does not change is required.

  Conventionally, in order to prevent image sticking by improving the rigidity of a polymer, a display element is configured using a polymerizable compound having a ring structure and a structure such as a 1,4-phenylene group having only a polymerizable functional group. (See Patent Document 1) and the construction of a display element using a polymerizable compound having a biaryl structure (see Patent Document 2) have been studied. However, since these polymerizable compounds have low compatibility with the liquid crystal compound, precipitation of the polymerizable compound occurs when the liquid crystal composition is prepared. Therefore, application as a practical liquid crystal composition is difficult. there were.

  Also, in order to prevent seizure by improving the rigidity of the polymer, a mixture of a bifunctional polymerizable compound and a trifunctional or higher functional polymerizable compound such as dipentaerythritol pentaacrylate and dipentaerythritol hexaacrylate It has been proposed to form a display element using a liquid crystal composition (see Patent Document 3). However, since dipentaerythritol pentaacrylate and dipentaerythritol hexaacrylate do not have a ring structure in the molecule, their affinity for liquid crystal compounds is weak and their ability to regulate alignment is weak, so sufficient alignment stability There was a problem that could not be obtained.

  From the above, the seizure characteristics of the display element, the alignment stability, the stability as a composition that does not cause precipitation, the production efficiency when preparing the PSA type liquid crystal display element, and the like required for the liquid crystal composition containing the polymerizable compound It is difficult to satisfy the characteristics, which hinders the practical application of the display element.

JP 2003-307720 A JP 2008-116931 A JP 2004-302096 A

  The problem to be solved by the present invention is that a liquid crystal composition containing a polymerizable compound reduces the residual amount of the polymerizable compound even when polymerization is carried out without using a photopolymerization initiator or in an extremely small amount used. A polymerizable compound-containing liquid crystal composition, and the polymerizable compound and the liquid crystal material are compatible with each other, the orientation after polymerization is more stable, and the display characteristics are improved. It is an object of the present invention to provide a polymerizable compound-containing liquid crystal composition that does not cause problems. Furthermore, it is providing the liquid crystal display element which the liquid crystal aligning ability was provided by polymerizing the polymeric compound containing liquid crystal composition, and was excellent in display performance.

  As a result of studying various polymerizable compounds and various non-polymerizable liquid crystal materials, the inventors of the present application have found that a liquid crystal containing a polymerizable compound having a specific structure and a polymerizable compound composed of a non-polymerizable liquid crystal material. The inventors have found that the composition can solve the above-mentioned problems and have completed the present invention.

  That is, as the first component, the general formula (I)

(In the formula, R ¹¹ is the following formula (R-1) to formula (R-15)

Any one of
S ¹¹ is an alkylene group having 1 to 12 carbon atoms in which a methylene group may be replaced with an oxygen atom, —COO—, —OCO—, or —OCOO—, or a single bond, as oxygen atoms are not directly bonded to each other. Represent,
L ¹¹ and L ¹² are each independently a single bond, —O—, —S—, —CH ₂ —, —OCH ₂ —, —CH ₂ O—, —CO—, —C ₂ H ₄ —, — ^{_{COO -, - OCO -, -}} OCOOCH 2 -, - CH 2 OCOO -, - CO-NR 111 -, - NR 111 -CO -, - SCH 2 -, - CH 2 S -, - CH = CH-COO- _{, -COO-CH = CH -,} - OCOCH = CH -, - COOC 2 H 4 -, - OCOC 2 H 4 -, - C 2 H 4 OCO -, - C 2 H 4 COO -, - OCOCH 2 _{-, - CH 2 COO -,} - CH = CH -, - CF = CH -, - CH = CF -, - CF 2 -, - CF 2 O -, - OCF 2 -, - CF 2 CH 2 -, - _{CH 2 CF 2 -, - CF} 2 CF 2 - or an -C≡C- ^{(wherein, R 111} is It represents an alkyl group having atom number 1-4.)
Z represents H, F, Cl, CN, SCN, OCF ₃ or an alkyl group having 1 to 12 carbon atoms, and the methylene group in the alkyl group is an oxygen atom, A sulfur atom, —CO—, —COO—, —OCO—, —OCOO, —CH═CH—, —C≡C— may be substituted,
Z represents alternatively -L ¹³ -S ¹² -R ¹² (wherein R ¹² has the same meaning as R ¹¹ , S ¹² has the same meaning as S ¹¹ , and L ¹³ has the same meaning as L ¹¹ ).
M ¹¹ and M ¹² are each independently 1,4-phenylene group, 1,4-cyclohexylene group, pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, naphthalene-2,6- Represents a diyl group, a tetrahydronaphthalene-2,6-diyl group or a 1,3-dioxane-2,5-diyl group, and M ¹³ represents a 1,4-phenylene group, a 1,4-cyclohexylene group, a pyridine-2. , 5-diyl group, pyrimidine-2,5-diyl group, naphthalene-2,6-diyl group, tetrahydronaphthalene-2,6-diyl group, 1,3-dioxane-2,5-diyl group, 1,3 , 5-Benzenetriyl group, 1,3,4-benzenetriyl group, 1,3,4,5-benzenetetrayl group, 1,3,5-cyclohexanetriyl group or 1,3,4-cyclohexane Tolyle The represents a hydrogen atom on M ^11, M ¹² and M ¹³ are, independently of one another, are a non or substituted by fluorine atom, a chlorine atom, a cyano group, a nitro group, an alkyl group having 1 to 8 carbon atoms, halogen An alkyl group, a halogenated alkoxy group, or an alkoxy group,
m represents 0, 1 and 2, n represents 1, 2 and 3, and when there are a plurality of Z, M ¹² and L ¹² , they may be the same or different. ) Containing one or more compounds selected from the polymerizable compounds represented by formula (II) as the second component

(In the formula, R ²¹ and R ²² each independently represent an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, and one methylene group or an adjacent group present in these groups) Two or more methylene groups which are not present may be substituted with —O— or —S—, and one or more hydrogen atoms present in these groups are substituted with fluorine atoms or chlorine atoms. It ’s okay,
M ²¹ , M ²² and M ²³ are independent of each other
(a) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(b) 1,4-phenylene group (one —CH═ present in this group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom), 3-fluoro-1 , 4-phenylene group, 3,5-difluoro-1,4-phenylene group, and
(c) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, decahydronaphthalene-2,6 -Represents a group selected from the group consisting of -diyl group and 1,2,3,4-tetrahydronaphthalene-2,6-diyl group,
o represents 0, 1 or 2;
L ²¹ and L ²² are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— , —CH═CH—, —CH═N—N═CH—, or —C≡C—, and when there are a plurality of L ²² and M ²³ , they may be the same or different. 1 or 2 or more compounds represented by general formula (IIIa), general formula (IIIb) and general formula (IIIc)

(Wherein R ³¹ , R ³² and R ³³ each independently represent an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, and one methylene group present in these groups) Alternatively, two or more methylene groups that are not adjacent to each other may be substituted with -O- or -S-, and one or more hydrogen atoms present in these groups may be replaced with a fluorine atom or a chlorine atom. May be replaced,
M ³¹ , M ³² , M ³³ , M ³⁴ , M ³⁵ , M ³⁶ , M ³⁷ , and M ³⁸ are independent of each other,
(d) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(e) a 1,4-phenylene group (one —CH═ present in the group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom), 3-fluoro-1 , 4-phenylene group, 3,5-difluoro-1,4-phenylene group, and
(f) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, 1,2,3,4 -Represents a group selected from the group consisting of a tetrahydronaphthalene-2,6-diyl group and a decahydronaphthalene-2,6-diyl group, and is included in the above group (d), group (e) or group (f) Each hydrogen atom may be substituted with a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
L ³¹ , L ³² , L ³³ , L ³⁴ , L ³⁵ , L ³⁶ , L ³⁷ and L ³⁸ are each independently a single bond, —COO—, —OCO—, —CH ₂ CH ₂ —, — (CH _{2 ) 4 -, - OCH 2 -} , - CH 2 O -, - OCF 2 -, - CF 2 O- or represents ^{-C≡C-, M 32, M 34,} M 35, M 37, M 38, L ^When there are a plurality of ³¹ , L ³³ , L ³⁵ , L ³⁶ , and L ³⁸ , they may be the same or different,
X ³¹ , X ³² , X ³³ , X ³⁴ , X ³⁵ , X ³⁶ , and X ³⁷ each independently represent a hydrogen atom or a fluorine atom,
Y ³¹ , Y ³² and Y ³³ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, Or a difluoromethoxy group,
At least one of X ³¹ , X ³² , and Y ³¹ is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, or a difluoromethoxy. Or at least one of hydrogen atoms contained in M ³¹ or M ³² represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, or a chlorine atom,
At least one of X ³³ , X ³⁴ , X ³⁵ , or Y ³² is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, A difluoromethoxy group, or at least one of hydrogen atoms contained in M ³³ , M ³⁴ , or M ³⁵ represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, or a chlorine atom,
At least one of X ³⁶ , X ³⁷ and Y ³³ is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a difluoromethoxy group Or at least one of the hydrogen atoms contained in M ³⁶ , M ³⁷ and M ³⁸ represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
p, q, r, s, and t independently represent 0, 1, or 2, but q + r and s + t are 2 or less. Or a compound selected from the group consisting of compounds represented by formula (IVa), general formula (IVb) and general formula (IVc)

(Wherein R ⁴¹ , R ⁴² , R ⁴³ , R ⁴⁴ , R ⁴⁵ and R ⁴⁶ each independently represents an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, One methylene group present in the group or two or more methylene groups not adjacent to each other may be substituted with -O- or -S-, and one or two present in these groups The above hydrogen atoms may be substituted with fluorine atoms or chlorine atoms,
M ⁴¹ , M ⁴² , M ⁴³ , M ⁴⁴ , M ⁴⁵ , M ⁴⁶ , M ⁴⁷ , M ⁴⁸ , and M ⁴⁹ are independent of each other.
(d) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(e) a 1,4-phenylene group (one —CH═ present in the group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom);
(f) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, 1,2,3,4 -Represents a group selected from the group consisting of a tetrahydronaphthalene-2,6-diyl group and a decahydronaphthalene-2,6-diyl group, and is included in the above group (d), group (e) or group (f) Each hydrogen atom may be substituted with a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
L ⁴¹ , L ⁴² , L ⁴³ , L ⁴⁴ , L ⁴⁵ , L ⁴⁶ , L ⁴⁷ , L ⁴⁸ , and L ⁴⁹ are each independently a single bond, —COO—, —OCO—, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— or —C≡C— represents M ⁴² , M ⁴³ , M ⁴⁵ , M ⁴⁶ , When there are a plurality of M ⁴⁸ , M ⁴⁹ , L ⁴¹ , L ⁴³ , L ⁴⁴ , L ⁴⁶ , L ⁴⁷ and L ⁴⁹ , they may be the same or different,
X ⁴¹ and X ⁴² each independently represents a trifluoromethyl group, a trifluoromethoxy group or a fluorine atom, and X ⁴³ , X ⁴⁴ , X ⁴⁵ , X ⁴⁶ , X ⁴⁷ and X ⁴⁸ are each independently a hydrogen atom. , A trifluoromethyl group, a trifluoromethoxy group, or a fluorine atom, wherein any one of X ⁴¹ and X ⁴² represents a fluorine atom, and any one of X ⁴³ , X ⁴⁴ , and X ⁴⁵ represents a fluorine atom Any one of X ⁴⁶ , X ⁴⁷ and X ⁴⁸ represents a fluorine atom, but X ⁴⁶ and X ⁴⁷ do not represent a fluorine atom at the same time, and X ⁴⁶ and X ⁴⁸ represent fluorine at the same time. Never represent an atom,
G represents a methylene group or —O—;
u, v, w, x, y, and z each independently represent 0, 1, or 2, but u + v, w + x, and y + z are 2 or less. And a polymerizable compound-containing liquid crystal composition characterized by containing one or more compounds selected from the group consisting of compounds represented by formula (1), and a liquid crystal display device using the liquid crystal composition. provide.

  Since the polymerizable compound which is an essential component of the present invention has excellent compatibility with other non-polymerizable liquid crystal materials, a stable liquid crystal composition can be obtained. Further, since it has a skeleton similar to a liquid crystal compound, the alignment regulating power of the liquid crystal compound is strong. In addition, the liquid crystal composition containing the polymerizable compound can polymerize the polymerizable compound without using a photopolymerization initiator or with a very small amount of addition, and an unpolymerized polymerizable compound remaining after the polymerization can be obtained. No or very little. In addition, the energy required for polymerization of the polymerizable compound can be greatly reduced. As a result, the display defects of the liquid crystal display element to which orientation is imparted by polymerizing the polymerizable compound in the liquid crystal material can be greatly reduced, and the energy cost for production can be reduced and the production efficiency can be improved. It is useful as a liquid crystal material for liquid crystal display elements.

The polymerizable compound used in the liquid crystal composition containing the polymerizable compound of the present invention is composed of a compound represented by the general formula (I). In the general formula (I), R ¹¹ represents a polymerizable group, and specific examples of the polymerizable group include the structures shown below.

  These polymerizable groups are cured by radical polymerization, radical addition polymerization, cationic polymerization, and anionic polymerization. In particular, when performing ultraviolet polymerization as a polymerization method, the formula (R-1), formula (R-2), formula (R-4), formula (R-5), formula (R-7), formula (R -11), formula (R-13) or formula (R-15) are preferred, and formula (R-1), formula (R-2), formula (R-7), formula (R-11) or formula ( R-13) is more preferable, and formula (R-1) and formula (R-2) are more preferable.

S ¹¹ represents a spacer group or a single bond, and the spacer group is preferably an alkylene group having 1 to 12 carbon atoms or a single bond, and the methylene group in the alkylene group does not directly bond oxygen atoms to each other. As an oxygen atom, -COO-, -OCO-, or -OCOO-. In order to improve the solubility, a methylene group having a certain length is preferable, but if the length is too long, the flexibility of the polymer after polymerization is increased, which causes baking. For this reason, a C1-C8 alkylene group is preferable and a C2-C6 alkylene group is more preferable.

L ¹¹ and L ¹² are each independently a single bond, —O—, —S—, —CH ₂ —, —OCH ₂ —, —CH ₂ O—, —CO—, —C ₂ H ₄ —, — ^{_{COO -, - OCO -, -}} OCOOCH 2 -, - CH 2 OCOO -, - CO-NR 111 -, - NR 111 -CO -, - SCH 2 -, - CH 2 S -, - CH = CH-COO- _{, -COO-CH = CH -,} - OCOCH = CH -, - COOC 2 H 4 -, - OCOC 2 H 4 -, - C 2 H 4 OCO -, - C 2 H 4 COO -, - OCOCH 2 _{-, - CH 2 COO -,} - CH = CH -, - CF = CH -, - CH = CF -, - CF 2 -, - CF 2 O -, - OCF 2 -, - CF 2 CH 2 -, - _{CH 2 CF 2 -, - CF} 2 CF 2 - or -C≡C- is in preferred ^{(wherein, R 11} Represents an alkyl group having 1 to 4 carbon atoms), a single _{bond, -O -., - OCH 2} -, - CH 2 O -, - CO -, - C 2 H 4 -, - COO -, - OCO _{-, - OCOOCH 2 -, -} CH 2 OCOO -, - CH = CH-COO -, - COO-CH = CH -, - OCO-CH = CH-OCO -, - COOC 2 H 4 -, - OCOC 2 H _{4 -, - C 2 H 4} OCO -, - C 2 H 4 COO -, - OCOCH 2 -, - CH 2 COO-, or -CH = CH-, more preferably a single bond, -O -, - OCH _{2 -, - CH 2 O -,} - CH = CH-COO -, - COO-CH = CH -, - OCO-CH = CH-OCO -, - COOC 2 H 4 -, - OCOC 2 H 4 -, - C _{2 H 4 OCO -, - C} 2 H 4 COO -, - OCOCH 2 -, - H ₂ COO-, or -CH = CH- is more preferable.

Z is H, F, Cl, CN, SCN, OCF ₃ , an oxygen atom is not directly bonded to each other, and a methylene group is an oxygen atom, a sulfur atom, —CO—, —COO—, —OCO—, —OCOO, — It is preferably an alkyl group having 1 to 12 carbon atoms which may be substituted with CH═CH— or —C≡C— or —L ¹³ —S ¹² —R ¹ , and further, H, F, and oxygen atoms 1 to 12 methylene groups may be substituted with oxygen atom, sulfur atom, —CO—, —COO—, —OCO—, —OCOO, —CH═CH—, —C≡C— More preferably, it is an alkyl group having the following carbon atoms, or —L ¹³ —S ¹² —R ¹² , and further, a hydrogen atom or a carbon atom that may be substituted with an oxygen atom as a methylene group in which oxygen atoms are not directly bonded to each other Number 1-12 Alkyl group, or ^-L 13 ^{-S 12 -R} 12 are more preferred. R ¹² independently represents the same meaning as R ¹¹ , S ¹² independently represents the same meaning as S ^11, and L ¹³ represents the same meaning as L ¹¹ . When Z is —S ¹² —R ¹² , S ¹¹ and S ¹² each independently represent a spacer group or a single bond, and the spacer group is an alkylene group having 2 to 12 carbon atoms, Alternatively, a single bond is preferable, and a methylene group is an alkylene group having 2 to 12 carbon atoms that may be replaced with an oxygen atom, —COO—, —OCO—, or —OCOO— as a group in which oxygen atoms are not directly bonded to each other, or A single bond is more preferable.

  m is preferably 0, 1 or 2, and more preferably 0 or 1. n is preferably 1, 2, 3 or 4, and preferably 1 or 2.

  More specifically, the compounds represented by the general formula (I) are preferably compounds represented by the following general formulas (I-1) to (I-68).

(In the formula, p and q each independently represent an integer of 0 to 12, but when 0 represents a structure in which oxygens are directly connected, one oxygen atom is removed.)
Compounds represented by general formula (I-1) to general formula (I-24) are more preferable, and compounds represented by general formula (I-1) to general formula (I-18) are more preferable.

  In the polymerizable compound-containing liquid crystal composition of the present invention, it contains at least one polymerizable compound represented by the general formula (I), preferably 1 to 5 types, preferably 1 to 3 types. It is particularly preferable to do this. If the content of the compound represented by the general formula (I) is small, the alignment regulating power for the non-polymerizable liquid crystal compound is weak, and if it is too large, the required energy during polymerization rises and polymerization that does not polymerize remains. The lower limit value is preferably 0.01% by mass, more preferably 0.03% by mass, and the upper limit value is preferably 2.0% by mass, since the amount of the active compound increases. More preferably, it is 1.0 mass%.

In the compound represented by the general formula (II) used as the second component, R ²¹ and R ²² are each independently an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms (these One methylene group present in a group or two or more methylene groups not adjacent to each other is substituted with -O- or -S-, and one or more methylene groups present in these groups The hydrogen atom includes those substituted with a fluorine atom or a chlorine atom.), Preferably an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms, or An alkenyloxy group having 3 to 6 carbon atoms is more preferable, and an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms is particularly preferable.

M ²¹ , M ²² and M ²³ are each independently a trans-1,4-cyclohexylene group (one CH ₂ group present in this group or _two non-adjacent CH ₂ groups are oxygen atoms) Including a substituted group), a 1,4-phenylene group (including one or more CH groups present in this group substituted by a nitrogen atom), 3-fluoro-1, 4-phenylene group, 3,5-difluoro-1,4-phenylene group, 1,4-cyclohexenylene group, 1,4-bicyclo [2.2.2] octylene group, piperidine-1,4-diyl group, naphthalene -2,6-diyl group, decahydronaphthalene-2,6-diyl group or 1,2,3,4-tetrahydronaphthalene-2,6-diyl group is preferred, trans-1,4-cyclohexylene group, 1 1,4-phenylene group or 1,4-bicyclo [2.2.2] octylene group is more preferable, and trans-1,4-cyclohexylene group or 1,4-phenylene group is particularly preferable. o is preferably 0, 1 or 2, and more preferably 0 or 1. L ²¹ and L ²² are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— , -CH = CH -, - CH = N-N = CH- or -C≡C-, more preferably a single _{bond, -CH 2 CH 2 -, -} (CH 2) 4 -, - OCH 2 - or -CH ₂ O— is more preferable, and a single bond or —CH ₂ CH ₂ — is still more preferable. More specifically, the general formula (II) is preferably a compound represented by the group consisting of the following general formulas (II-A) to (II-P) as a specific structure.

(Wherein R ²³ and R ²⁴ are each independently an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, or an alkenyloxy group having 3 to 10 carbon atoms) Represents a group.)
R ²³ and R ²⁴ are each independently preferably an alkyl group having 1 to 10 carbon atoms, an alkoxy group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, and an alkyl group having 1 to 5 carbon atoms or More preferred are alkoxy groups having 1 to 10 carbon atoms.

  Among the compounds represented by general formula (II-A) to general formula (II-P), general formula (II-A), general formula (II-B), general formula (II-C), and general formula (II) -E), general formula (II-H), general formula (II-I), general formula (II-I), or a compound represented by general formula (II-K) is preferred, and general formula (II-A ), General formula (II-C), general formula (II-E), general formula (II-H) or general formula (II-I) is more preferred.

  In the present invention, it contains at least one compound represented by the general formula (II), preferably 1 to 10 types, more preferably 2 to 8 types, and particularly preferably the general formula (II). Is preferably 5% by mass, more preferably 10% by mass, still more preferably 20% by mass, and particularly preferably 30% by mass. The upper limit is preferably 80% by mass, more preferably 70% by mass, and still more preferably 60% by mass.

In the compounds represented by the general formula (IIIa), general formula (IIIb) and general formula (IIIc) used as the third component, R ³¹ , R ³² and R ³³ are each independently of 1 to 10 carbon atoms. An alkyl group or an alkenyl group having 2 to 10 carbon atoms, a linear alkyl group having 1 to 15 carbon atoms or an alkenyl group having 2 to 15 carbon atoms (one methylene group present in these groups or adjacent thereto). Two or more methylene groups not substituted by —O— or —S—, and one or more hydrogen atoms present in these groups are substituted by fluorine atoms or chlorine atoms A linear alkyl group having 1 to 10 carbon atoms, a linear alkoxy group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, more preferably a straight chain having 1 to 8 carbon atoms. A chain alkyl group or an alkoxy group having 1 to 8 carbon atoms is particularly preferable. Arbitrariness.

M ³¹ , M ³² , M ³³ , M ³⁴ , M ³⁵ , M ³⁶ , M ³⁷ , and M ³⁸ are each independently a trans-1,4-cyclohexylene group (one of the groups present in this group). A methylene group or two or more methylene groups not adjacent to each other include those in which -O- or -S- is substituted.), 1,4-phenylene group (one -CH present in this group) = Or two or more non-adjacent —CH═ include those substituted with nitrogen atoms), 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine- Groups represented by 1,4-diyl group, naphthalene-2,6-diyl group, 1,2,3,4-tetrahydronaphthalene-2,6-diyl group and decahydronaphthalene-2,6-diyl group (each Groups also include those in which each hydrogen atom is replaced by a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom ), Preferably trans-1,4-cyclohexylene group, 1,4-phenylene group, 3-fluoro-1,4-phenylene group or 3,5-difluoro-1,4-phenylene group, A 1,4-cyclohexylene group or a 1,4-phenylene group is more preferred, and a trans-1,4-cyclohexylene group is particularly preferred.

L ³¹ , L ³² , L ³³ , L ³⁴ , L ³⁵ , L ³⁶ , L ³⁷ and L ³⁸ are each independently a single bond, —OCO—, —COO—, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ −, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— or —C≡C— are preferred, single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ -Or -C≡C- is more preferable, and a single bond or -CH ₂ CH ₂ -is particularly preferable. X ³¹ , X ³² , X ³³ , X ³⁴ , X ³⁵ , X ³⁶ , and X ³⁷ are each independently a hydrogen atom or a fluorine atom, and Y ³¹ , Y ³² , and Y ³³ are each independently a hydrogen atom. Represents a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a difluoromethoxy group, or an alkyl group having 1 to 12 carbon atoms. And preferably represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, or an alkyl group having 1 to 12 carbon atoms. And particularly preferably represents a fluorine atom. p, q, r, s, and t each independently represent 0, 1 or 2, but q + r and s + t represent 2 or less.

  Specifically, it is preferable to represent a structure represented by the following general formula (IIIa-1).

(Wherein R ³⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms, and L ³⁹ and L ⁴⁰ are each independently a single atom. _{bond, -CH 2 CH 2 -, -} (CH 2) 4 -, - OCH 2 -, - CH 2 O -, - OCF 2 -, - CF 2 O- or represents -C≡C-, M ³⁸ is 1,4-phenylene group or trans-1,4-cyclohexylene group, X ³² represents a hydrogen atom or a fluorine atom, p ₁ represents 0 or 1, Y ³⁴ represents a cyano group, a fluorine atom, a chlorine atom Represents a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group or a trifluoromethoxy group.)
More specifically, the following general formula (IIIa-2a) to general formula (IIIa-4d)

(Wherein R ³⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms or an alkenyl group having 2 to 8 carbon atoms, and X ³¹ and X ³² are each independently hydrogen. Y ³¹ represents a cyano group, a fluorine atom, a chlorine atom, a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group, or a trifluoromethoxy group.

(In the formula, R ³⁴ represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms or an alkenyl group having 2 to 8 carbon atoms, and Y ³¹ represents a cyano group, a fluorine atom, or a chlorine atom. Represents a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group or a trifluoromethoxy group).

  General formula (IIIb) has the following general formula as a specific structure:

(In the formula, R ³⁵ represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms or an alkenyl group having 2 to 8 carbon atoms, and Y ³⁵ represents a cyano group, a fluorine atom, or a chlorine atom. Represents a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group or a trifluoromethoxy group).
General formula (IIIc) has the following general formula as a specific structure:

(In the formula, R ³⁶ represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms or an alkenyl group having 2 to 8 carbon atoms, and Y ³⁶ represents a cyano group, a fluorine atom, or a chlorine atom. , Represents a trifluoromethyl group, a fluoromethoxy group, a difluoromethoxy group or a trifluoromethoxy group).

  It contains at least one compound selected from the group consisting of compounds represented by general formula (IIIa), general formula (IIIb) and general formula (IIIc), preferably 1 to 10 types. It is particularly preferable to contain 8 to 8 species, and the lower limit of the content of the group consisting of the compounds represented by general formula (IIIa), general formula (IIIb) and general formula (IIIc) is 5% by mass. Preferably, it is more preferably 10% by mass, preferably 20% by mass, and the upper limit is preferably 80% by mass, preferably 70% by mass, preferably 60% by mass, and further preferably 50% by mass.

In the compounds represented by general formula (IVa), general formula (IVb) and general formula (IVc), R ⁴¹ , R ⁴² , R ⁴³ , R ⁴⁴ , R ⁴⁵ and R ⁴⁶ are each independently a carbon atom. An alkyl group having 1 to 10 carbon atoms, an alkenyl group having 2 to 10 carbon atoms, a linear alkyl group having 1 to 15 carbon atoms, or an alkenyl group having 2 to 15 carbon atoms (one methylene present in these groups) A group or two or more methylene groups not adjacent to each other are substituted by —O— or —S—, and one or more hydrogen atoms present in these groups are fluorine atoms or chlorine atoms In addition, a linear alkyl group having 1 to 10 carbon atoms, a linear alkoxy group having 1 to 10 carbon atoms, or an alkenyl group having 2 to 10 carbon atoms is more preferable. A linear alkyl group having 1 to 8 or an alkoxy group having 1 to 8 carbon atoms is particularly preferred. There. M ⁴¹ , M ⁴² , M ⁴³ , M ⁴⁴ , M ⁴⁵ , M ⁴⁶ , M ⁴⁷ , M ⁴⁸ and M ⁴⁹ are each independently a trans-1,4-cyclohexylene group (1 present in this group). Methylene groups or two or more methylene groups not adjacent to each other include those in which -O- or -S- is substituted.), 1,4-phenylene group (one in this group) -CH = or two or more non-adjacent -CH = are substituted with nitrogen atoms), 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, Groups represented by piperidine-2,5-diyl group, naphthalene-2,6-diyl group, 1,2,3,4-tetrahydronaphthalene-2,6-diyl group and decahydronaphthalene-2,6-diyl group ( A hydrogen atom contained in each group is substituted with a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, or a chlorine atom, respectively. And a trans-1,4-cyclohexylene group, a 1,4-phenylene group, a 3-fluoro-1,4-phenylene group, or a 2,3-difluoro-1,4-phenylene group is more preferable. A trans-1,4-cyclohexylene group or a 1,4-phenylene group is more preferable, and a trans-1,4-cyclohexylene group is particularly preferable. L ⁴¹ , L ⁴² , L ⁴³ , L ⁴⁴ , L ⁴⁵ , L ⁴⁶ , L ⁴⁷ , L ⁴⁸ and L ⁴⁹ are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, — OCO -, - COO -, - OCH 2 -, - CH 2 O -, - OCF 2 -, - CF 2 O- or -C≡C-, more preferably a single _{bond, -CH 2 CH 2 -, -} OCH 2 - or -CH ₂ O-are more preferred. X ⁴¹ , X ⁴² , X ⁴³ , X ⁴⁴ , X ⁴⁵ , X ⁴⁶ , and X ⁴⁷ each independently represent a hydrogen atom or a fluorine atom, G represents a methylene group or —O—, and u, v, w , X, y and z each independently represent 0, 1 or 2, but u + v, w + x and y + z are each represented by 2 or less.

  In the compound represented by the general formula (IVa), it is preferable to specifically represent the structure represented by the following general formula (IVa-1).

(In the formula, R ⁴⁷ and R ⁴⁸ independently represent an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms, L ⁵⁰ , L ⁵¹ and L ⁵² are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— or — C≡C—, M ⁵⁰ represents a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and u ₁ and v ₁ each independently represents 0 or 1.)
More specifically, the following general formula (IVa-2a) to general formula (IVa-3i)

(Wherein R ⁴⁷ and R ⁴⁸ each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms). In which R ⁴⁷ and R ⁴⁸ are each independently an alkyl group having 1 to 8 carbon atoms or an alkoxyl group having 1 to 8 carbon atoms.

  In the compound represented by the general formula (IVb), specifically, a structure represented by the following general formula (IVb-1) is preferably represented.

(Wherein R ⁴⁹ and R ⁵⁰ each independently represent an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms or an alkenyl group having 2 to 8 carbon atoms, L ⁵² , L ⁵³ and L ⁵⁴ each independently represent a single _{bond, -CH 2 CH 2 -, -} (CH 2) 4 -, - OCH 2 -, - CH 2 O -, - OCF 2 -, - CF 2 O- or - C≡C—, M ⁵¹ , M ⁵² and M ⁵³ represent a 1,4-phenylene group or a trans-1,4-cyclohexylene group, and w 1 and x 1 independently represent 0, 1 or 2. W1 + x1 represents 2 or less.)
More specifically, the following general formulas (IVb-2a) to (IVb-3l)

(Wherein R ⁴⁹ and R ⁵⁰ each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms). The structure is preferred.

  In the compound represented by the general formula (IVc), specifically, it is preferable to represent a structure represented by the following general formula (IVc-1a) and general formula (IVc-1b).

(In the formula, R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms, L ⁵⁶ , L ⁵⁷ and L ⁵⁸ are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— or — C≡C—, M ⁵⁴ , M ⁵⁵ and M ⁵⁶ represent 1,4-phenylene group or trans-1,4-cyclohexylene group, and y 1 and z 1 independently represent 0, 1 or 2. However, y1 + z1 represents 2 or less.)
More specifically, the following general formulas (IVc-2a) to (IVc-2g)

(In the formula, R ⁵¹ and R ⁵² each independently represents an alkyl group having 1 to 8 carbon atoms, an alkoxyl group having 1 to 8 carbon atoms, or an alkenyl group having 2 to 8 carbon atoms.)
A compound selected from the group consisting of compounds represented by general formula (IIIa), general formula (IIIb) and general formula (IIIc) used as the third component, or general formula (IVa), general formula (IVb) and general It contains at least one compound selected from the group consisting of the compounds represented by formula (IVc), but preferably contains 2 to 10 types, particularly preferably contains 2 to 8 types, and the content rate The lower limit is preferably 5% by mass, more preferably 10% by mass, more preferably 20% by mass, and the upper limit is preferably 80% by mass, and is 70% by mass. It is preferably 60% by mass, and preferably 50% by mass.

  In the liquid crystal composition of the present invention, Δn is preferably in the range of 0.08 to 0.25.

  In the liquid crystal composition of the present invention, Δε having a positive or negative Δε can be used depending on the display mode of the liquid crystal display element. In the MVA mode liquid crystal display element, a liquid crystal composition having a negative Δε is used. In that case, Δε is preferably −1 or less, and more preferably −2 or less.

  The liquid crystal composition of the present invention has a wide liquid crystal phase temperature range (the absolute value of the difference between the liquid crystal phase lower limit temperature and the liquid crystal phase upper limit temperature), but the liquid crystal phase temperature range is preferably 100 ° C. or higher, preferably 120 ° C. or higher. Is more preferable. The upper limit temperature of the liquid crystal phase is preferably 70 ° C. or higher, and more preferably 80 ° C. or higher. Furthermore, the lower limit temperature of the liquid crystal phase is preferably −20 ° C. or lower, and more preferably −30 ° C. or lower.

  The liquid crystal composition of the present invention may contain a normal nematic liquid crystal, a smectic liquid crystal, a cholesteric liquid crystal and the like in addition to the above compounds.

  The liquid crystal composition containing the polymerizable compound of the present invention is polymerized even when no polymerization initiator is present, but may contain a polymerization initiator in order to accelerate the polymerization. Examples of the polymerization initiator include benzoin ethers, benzophenones, acetophenones, benzyl ketals, acylphosphine oxides, and the like.

  In order to improve the storage stability of the liquid crystal composition of the present invention, a stabilizer may be added. Examples of the stabilizer that can be used include hydroquinones, hydroquinone monoalkyl ethers, tert-butylcatechols, pyrogallols, thiophenols, nitro compounds, β-naphthylamines, β-naphthols, nitroso compounds, and the like. It is done. The addition amount in the case of using a stabilizer is preferably in the range of 0.005 to 1% by mass, more preferably 0.02 to 0.5% by mass, and 0.03 to 0.1% by mass with respect to the liquid crystal composition. % Is particularly preferred.

  The liquid crystal composition of the present invention is used for a liquid crystal display element that is provided with liquid crystal alignment ability by polymerization of a polymerizable compound in the liquid crystal composition and controls the amount of light transmitted using the birefringence of the liquid crystal composition. Is done. As liquid crystal display elements, AM-LCD (active matrix liquid crystal display element), TN (nematic liquid crystal display element), STN-LCD (super twisted nematic liquid crystal display element), OCB-LCD and IPS-LCD (in-plane switching liquid crystal display element) However, it is particularly useful for AM-LCDs, and can be used for transmissive or reflective liquid crystal display elements.

  The two substrates of the liquid crystal cell used in the liquid crystal display element can be made of a transparent material having flexibility such as glass or plastic, and one of them can be 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.

  The color filter can be prepared by, for example, a pigment dispersion method, a printing method, an electrodeposition method, or a dyeing method. 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 on the transparent substrate, subjected to patterning treatment, and cured by heating or light irradiation. By performing this process for each of the three colors red, green, and blue, a pixel portion for a color filter can be created. In addition, a pixel electrode provided with an active element such as a TFT, a thin film diode, or a metal insulator metal specific resistance element may be provided on the substrate.

  The said board | substrate is made to oppose so that a transparent electrode layer may become an inner side. In that case, you may adjust the space | interval of a board | substrate through a spacer. At this time, it is preferable to adjust so that the thickness of the light control layer obtained may be set to 1-100 micrometers. More preferably, the thickness is 1.5 to 10 μm. 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 that the contrast is maximized. In addition, when there are two polarizing plates, the polarizing axis of each polarizing plate can be adjusted so that the viewing angle and contrast are good. Furthermore, a retardation film for widening the viewing angle can also be used. Examples of the spacer include glass particles, plastic particles, alumina particles, and a photoresist material. Thereafter, a sealant such as an epoxy thermosetting composition is screen-printed on the substrates with a liquid crystal inlet provided, the substrates are bonded together, and heated to thermally cure the sealant.

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

  As a method for polymerizing a polymerizable compound, since rapid progress of polymerization is desirable, a method of polymerizing by irradiating active energy rays such as ultraviolet rays or electron beams is preferable. When ultraviolet rays are used, a polarized light source or a non-polarized light source may be used. Further, when the polymerization is carried out with the liquid crystal composition sandwiched between two substrates, at least the substrate on the irradiation surface side must be given appropriate transparency to the active energy rays. Moreover, after polymerizing only a specific part using a mask during light irradiation, the orientation state of the unpolymerized part is changed by changing conditions such as an electric field, a magnetic field, or temperature, and further irradiation with active energy rays is performed. Then, it is possible to use a means for polymerization. In particular, when ultraviolet exposure is performed, it is preferable to perform ultraviolet exposure while applying an alternating current to the polymerizable compound-containing liquid crystal composition. The alternating current to be applied is preferably an alternating current having a frequency of 10 Hz to 10 kHz, more preferably a frequency of 60 Hz to 10 kHz, and the voltage is selected depending on a 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 MVA mode liquid crystal display element, it is preferable to control the pretilt angle from 80 degrees to 89 degrees from the viewpoint of alignment stability and contrast.

The temperature during irradiation is preferably within a temperature range in which the liquid crystal state of the liquid crystal composition of the present invention is maintained. Polymerization is preferably performed at a temperature close to room temperature, that is, typically at a temperature of 15 to 35 ° C. As a lamp for generating ultraviolet rays, a metal halide lamp, a high-pressure mercury lamp, an ultra-high pressure mercury lamp, or the like can be used. Moreover, as a wavelength of the ultraviolet-rays to irradiate, it is preferable to irradiate the ultraviolet-ray of the wavelength range which is not the absorption wavelength range of a liquid crystal composition, and it is preferable to cut and use an ultraviolet-ray as needed. Intensity of ultraviolet irradiation is ^preferably from ^{0.1mW / cm 2 ~100W / cm 2} , 2mW / cm 2 ~50W / cm 2 is more preferable. Energy of ultraviolet light irradiation, can be appropriately adjusted, is preferably 10000 mJ / cm ² to 10, more preferably 7000mJ / cm ² to 100. When irradiating with ultraviolet rays, the intensity may be changed. The time for irradiation with ultraviolet rays is appropriately selected depending on the intensity of ultraviolet rays to be irradiated, but is preferably 10 to 600 seconds.

  EXAMPLES Hereinafter, although an Example is given and this invention is further explained in full detail, this invention is not limited to these Examples. Further, “%” in the compositions of the following examples and comparative examples means “mass%”.

The physical properties of the liquid crystal composition are expressed as follows.
T _NI : Nematic phase-isotropic liquid phase transition temperature (° C), liquid crystal phase upper limit temperature Δε: Dielectric anisotropy Δn: Refractive index anisotropy
Vth: Applied voltage (threshold voltage) at which the transmittance changes by 10% when a rectangular wave with a frequency of 1 KHz is applied
(Measurement method of residual amount of monomer after UV curing)
After injecting the liquid crystal composition into the liquid crystal cell, UV is irradiated to polymerize the polymerizable compound. Thereafter, the liquid crystal cell is disassembled to obtain an acetonitrile solution of an elution component containing a liquid crystal material, a polymer, and an unpolymerized polymerizable compound. The peak area of each component is measured by high performance liquid chromatography (column :, developing solvent: acetonitrile). The amount of the remaining polymerizable compound was determined from the peak area ratio of the liquid crystal material as an index and the peak area ratio of the unpolymerized polymerizable compound. The residual monomer amount was determined from this value and the amount of the polymerizable compound initially added. The detection limit of the remaining amount of the polymerizable compound was 1000 ppm.
Example 1
Compound selected from general formula (II), compound selected from general formula (IIIa), general formula (IIIb) and general formula (IIIc), or general formula (IVa), general formula (IVb) and general formula (IVc) A liquid crystal composition LC-1 containing a compound selected from: The constituent compounds and the ratios contained are as follows.

  Table 1 shows the physical properties of the liquid crystal composition LC-1.

  For the liquid crystal composition LC-1 99.7%, the formula (I-1-a)

A polymerizable liquid crystal composition CLC-1 was prepared by adding 0.3% of the polymerizable compound represented by the formula (II) and dissolving it uniformly. The physical properties of CLC-1 were almost the same as the physical properties of LC-1. CLC-1 was injected by a vacuum injection method into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle (crystal rotation method) of this cell, the liquid crystal cell is irradiated with ultraviolet light by a high-pressure mercury lamp through a filter that cuts ultraviolet light of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. did. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. Table 2 shows the pretilt angle of the element before and after UV irradiation and the electro-optical characteristics of the element.

  From the result of the above pretilt angle, the alignment property of the liquid crystal compound is generated by the polymerization of the polymerizable compound, and the vertically aligned liquid crystal in which the pretilt angle is fixed while the liquid crystal molecules are inclined 2.3 degrees from the vertical direction. It was found that a display element was obtained.

Further, the content of the compound represented by the general formula (I-1-a) contained in the device was analyzed by liquid chromatographic analysis, but it was not detected. Thus, the polymerizable compound represented by the general formula (I-1-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. confirmed.
(Comparative Example 1)
For the liquid crystal composition LC-1 99.7%, the formula (A)

A polymerizable liquid crystal composition CLC-A was prepared by adding 0.3% of the polymerizable compound represented by the formula (II) and dissolving it uniformly. CLC-A was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the device was 89.6 degrees, whereas the pretilt angle after the irradiation was 89.5 degrees, the pretilt angle was not changed, and the liquid crystal molecules were hardly tilted from the vertical direction. It was. As a result of analyzing the content of the compound represented by the general formula (A) contained in the element by liquid chromatographic analysis, there is no change in the content before ultraviolet irradiation, and the polymerization of the polymerizable compound (A) proceeds. It wasn't.
(Example 2)
For the liquid crystal composition LC-1 99.5%, the formula (I-1-a)
A polymerizable liquid crystal composition CLC-2 was prepared by adding 0.5% of the polymerizable compound represented by formula (II) and uniformly dissolving the compound. CLC-2 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the device was 89.7 degrees, whereas the pretilt angle after the irradiation was 86.3 degrees, and the pretilt angle was fixed while the liquid crystal molecules were tilted from the vertical direction. It was. The content of the compound represented by the general formula (I-1-a) contained in the device was analyzed by liquid chromatographic analysis, but was below the detection limit. Thus, the polymerizable compound represented by the general formula (I-1-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. confirmed.
(Example 3)
For the liquid crystal composition LC-1 99.7%, the formula (I-4-a)

A polymerizable liquid crystal composition CLC-3 was prepared by adding 0.3% of the polymerizable compound represented by formula (II) and uniformly dissolving. CLC-3 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 89.7 degrees, whereas the pretilt angle after the irradiation was 87.1 degrees, and the pretilt angle was fixed while the liquid crystal molecules were tilted from the vertical direction. It was. The content of the compound represented by the general formula (I-4-a) contained in the element was analyzed by liquid chromatographic analysis, but was below the detection limit. Thereby, the polymerizable compound represented by the general formula (I-4-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. confirmed.
Example 4
For the liquid crystal composition LC-1 99.7%, the formula (I-6-a)

A polymerizable liquid crystal composition CLC-4 was prepared by adding 0.3% of the polymerizable compound represented by formula (II) and uniformly dissolving the compound. CLC-4 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 89.6 degrees, whereas the pretilt angle after the irradiation was 87.2 degrees, and the pretilt angle was fixed while the liquid crystal molecules were tilted from the vertical direction. It was. The content of the compound represented by the general formula (I-6-a) contained in the device was analyzed by liquid chromatographic analysis, but was below the detection limit. Thus, the polymerizable compound represented by the general formula (I-6-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. confirmed.
(Example 5)
A polymerizable liquid crystal composition CLC-5 was prepared by adding 0.1% of the polymerizable compound represented by the formula (I-6-a) to 99.9% of the liquid crystal composition LC-1 and uniformly dissolving it. did. CLC-5 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 89.6 degrees, whereas the pretilt angle after the irradiation was 87.8 degrees, and the pretilt angle was fixed while the liquid crystal molecules were tilted from the vertical direction. It was. The content of the compound represented by the general formula (I-6-a) contained in the device was analyzed by liquid chromatographic analysis, but was below the detection limit. Thus, the polymerizable compound represented by the general formula (I-6-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. confirmed.
(Example 6)
Compound selected from general formula (II), compound selected from general formula (IIIa), general formula (IIIb) and general formula (IIIc), or general formula (IVa), general formula (IVb) and general formula (IVc) As an example containing a compound selected from the following, a liquid crystal composition LC-2 having the following components was prepared.

  Table 3 shows the physical properties of the liquid crystal composition LC-2.

A polymerizable liquid crystal composition CLC-6 was prepared by adding 0.3% of the polymerizable compound represented by the formula (I-1-a) to 99.7% of the liquid crystal composition LC-2 and uniformly dissolving it. did. CLC-6 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 89.5 degrees, whereas the pretilt angle after the irradiation was 87.7 degrees, which was a pretilt, and the pretilt angle was adjusted while the liquid crystal molecules were tilted from the vertical direction. It was fixed. The content of the compound represented by the formula (I-1-a) contained in the element was analyzed by liquid chromatographic analysis, but was below the detection limit. As a result, it was confirmed that the polymerizable compound represented by the formula (I-1-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. did.
(Example 7)
Compound selected from general formula (II), compound selected from general formula (IIIa), general formula (IIIb) and general formula (IIIc), or general formula (IVa), general formula (IVb) and general formula (IVc) As an example containing a compound selected from the following, a liquid crystal composition LC-3 having the following components was prepared.

  Table 4 shows the physical properties of the liquid crystal composition LC-3.

A polymerizable liquid crystal composition CLC-7 was prepared by adding 0.3% of the polymerizable compound represented by the formula (I-1-a) to 99.7% of the liquid crystal composition LC-3 and uniformly dissolving it. did. CLC-7 was injected by vacuum injection into a cell with ITO coated with a polyimide alignment film that induces homeotropic alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 89.6 degrees, whereas the pretilt angle after the irradiation was 87.3 degrees, which was a pretilt, and the pretilt angle was adjusted while the liquid crystal molecules were tilted from the vertical direction. It was fixed. The content of the compound represented by the formula (I-1-a) contained in the element was analyzed by liquid chromatographic analysis, but was below the detection limit. As a result, it was confirmed that the polymerizable compound represented by the formula (I-1-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. did.
(Example 8)
Compound selected from general formula (II), compound selected from general formula (IIIa), general formula (IIIb) and general formula (IIIc), or general formula (IVa), general formula (IVb) and general formula (IVc) As an example containing a compound selected from the following, a liquid crystal composition LC-4 having the following components was prepared.

  Table 5 shows the physical properties of the liquid crystal composition LC-4.

A polymerizable liquid crystal composition CLC-8 was prepared by adding 0.3% of the polymerizable compound represented by the formula (I-1-a) to 99.7% of the liquid crystal composition LC-4 and uniformly dissolving the compound. did. CLC-8 was injected by a vacuum injection method into a cell with ITO coated with a polyimide alignment film that induces parallel alignment with a cell gap of 3.5 μm. After measuring the pretilt angle of this cell, the liquid crystal cell was irradiated with ultraviolet rays by a high-pressure mercury lamp through a filter that cuts ultraviolet rays of 320 nm or less while applying a rectangular wave of 1.8 V at a frequency of 1 KHz. The cell surface was adjusted to have an irradiation intensity of 10 mW / cm ² and irradiated for 600 seconds to obtain a vertically aligned liquid crystal display element in which the polymerizable compound in the polymerizable liquid crystal composition was polymerized. The pretilt angle before the ultraviolet irradiation of the element was 0.1 degree, whereas the pretilt angle after the irradiation was 3.5 degrees, and the pretilt angle was given when the liquid crystal molecules were tilted from the horizontal direction. Was fixed. The content of the compound represented by the formula (I-1-a) contained in the element was analyzed by liquid chromatographic analysis, but was below the detection limit. As a result, it was confirmed that the polymerizable compound represented by the formula (I-1-a) can be polymerized without using a polymerization initiator, and the unpolymerized product remaining after the polymerization is below the detection limit. did.
(Example 9 and Comparative Example 2)
A voltage was applied to the liquid crystal display elements after polymerization prepared in Examples 1 to 6 and Comparative Example 1, and the elapsed time and the state of image sticking were visually observed. (○ indicates that no change is observed. × indicates burn-in, and the greater the number of ×, the worse the degree.)

  The liquid crystal display device manufactured in Comparative Example 1 burned in 48 hours after display, and display defects were observed over almost the entire surface after 168 hours. On the other hand, in the liquid crystal display element produced in Examples 1-6, the favorable display state was maintained even after 500 hours passed. As a result, it is possible to confirm the high reliability of the liquid crystal display element in which all the polymerizable material is polymerized and consumed, such as the compound of the present invention, and the polymer has sufficiently high rigidity without causing a decrease in the alignment regulating force. I understood it.

Claims (8)

As the first component, the general formula (I)

(In the formula, R ¹¹ is the following formula (R-1) to formula (R-15)

Any one of
S ¹¹ is an alkylene group having 1 to 12 carbon atoms in which a methylene group may be replaced with an oxygen atom, —COO—, —OCO—, or —OCOO—, or a single bond, as oxygen atoms are not directly bonded to each other. Represent,
L ¹¹ and L ¹² are each independently a single bond, —O—, —S—, —CH ₂ —, —OCH ₂ —, —CH ₂ O—, —CO—, —C ₂ H ₄ —, — ^{_{COO -, - OCO -, -}} OCOOCH 2 -, - CH 2 OCOO -, - CO-NR 111 -, - NR 111 -CO -, - SCH 2 -, - CH 2 S -, - CH = CH-COO- _{, -COO-CH = CH -,} - OCOCH = CH -, - COOC 2 H 4 -, - OCOC 2 H 4 -, - C 2 H 4 OCO -, - C 2 H 4 COO -, - OCOCH 2 _{-, - CH 2 COO -,} - CH = CH -, - CF = CH -, - CH = CF -, - CF 2 -, - CF 2 O -, - OCF 2 -, - CF 2 CH 2 -, - _{CH 2 CF 2 -, - CF} 2 CF 2 - or an -C≡C- ^{(wherein, R 111} is It represents an alkyl group having atom number 1-4.)
Z represents H, F, Cl, CN, SCN, OCF ₃ or an alkyl group having 1 to 12 carbon atoms, and the methylene group in the alkyl group is an oxygen atom, A sulfur atom, —CO—, —COO—, —OCO—, —OCOO, —CH═CH—, —C≡C— may be substituted,
Z represents alternatively -L ¹³ -S ¹² -R ¹² (wherein R ¹² has the same meaning as R ¹¹ , S ¹² has the same meaning as S ¹¹ , and L ¹³ has the same meaning as L ¹¹ ).
M ¹¹ and M ¹² are each independently 1,4-phenylene group, 1,4-cyclohexylene group, pyridine-2,5-diyl group, pyrimidine-2,5-diyl group, naphthalene-2,6- Represents a diyl group, a tetrahydronaphthalene-2,6-diyl group or a 1,3-dioxane-2,5-diyl group, and M ¹³ represents a 1,4-phenylene group, a 1,4-cyclohexylene group, a pyridine-2. , 5-diyl group, pyrimidine-2,5-diyl group, naphthalene-2,6-diyl group, tetrahydronaphthalene-2,6-diyl group, 1,3-dioxane-2,5-diyl group, 1,3 , 5-Benzenetriyl group, 1,3,4-benzenetriyl group, 1,3,4,5-benzenetetrayl group, 1,3,5-cyclohexanetriyl group or 1,3,4-cyclohexane Tolyle The represents a hydrogen atom on M ^11, M ¹² and M ¹³ are, independently of one another, are a non or substituted by fluorine atom, a chlorine atom, a cyano group, a nitro group, an alkyl group having 1 to 8 carbon atoms, halogen An alkyl group, a halogenated alkoxy group, or an alkoxy group,
m represents 0, 1 and 2, n represents 1, 2 and 3, and when there are a plurality of Z, M ¹² and L ¹² , they may be the same or different. ) Containing one or more compounds selected from the polymerizable compounds represented by formula (II) as the second component

(In the formula, R ²¹ and R ²² each independently represent an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, and one methylene group or an adjacent group present in these groups) Two or more methylene groups which are not present may be substituted with —O— or —S—, and one or more hydrogen atoms present in these groups are substituted with fluorine atoms or chlorine atoms. It ’s okay,
M ²¹ , M ²² and M ²³ are independent of each other
(a) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(b) 1,4-phenylene group (one —CH═ present in this group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom), 3-fluoro-1 , 4-phenylene group, 3,5-difluoro-1,4-phenylene group, and
(c) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, decahydronaphthalene-2,6 -Represents a group selected from the group consisting of -diyl group and 1,2,3,4-tetrahydronaphthalene-2,6-diyl group,
o represents 0, 1 or 2;
L ²¹ and L ²² are each independently a single bond, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— , —CH═CH—, —CH═N—N═CH—, or —C≡C—, and when there are a plurality of L ²² and M ²³ , they may be the same or different. 1 or 2 or more compounds represented by general formula (IIIa), general formula (IIIb) and general formula (IIIc)

(Wherein R ³¹ , R ³² and R ³³ each independently represent an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, and one methylene group present in these groups) Alternatively, two or more methylene groups that are not adjacent to each other may be substituted with -O- or -S-, and one or more hydrogen atoms present in these groups may be replaced with a fluorine atom or a chlorine atom. May be replaced,
M ³¹ , M ³² , M ³³ , M ³⁴ , M ³⁵ , M ³⁶ , M ³⁷ , and M ³⁸ are independent of each other,
(d) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(e) a 1,4-phenylene group (one —CH═ present in the group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom), 3-fluoro-1 , 4-phenylene group, 3,5-difluoro-1,4-phenylene group, and
(f) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, 1,2,3,4 -Represents a group selected from the group consisting of a tetrahydronaphthalene-2,6-diyl group and a decahydronaphthalene-2,6-diyl group, and is included in the above group (d), group (e) or group (f) Each hydrogen atom may be substituted with a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
L ³¹ , L ³² , L ³³ , L ³⁴ , L ³⁵ , L ³⁶ , L ³⁷ and L ³⁸ are each independently a single bond, —COO—, —OCO—, —CH ₂ CH ₂ —, — (CH _{2 ) 4 -, - OCH 2 -} , - CH 2 O -, - OCF 2 -, - CF 2 O- or represents ^{-C≡C-, M 32, M 34,} M 35, M 37, M 38, L ^When there are a plurality of ³¹ , L ³³ , L ³⁵ , L ³⁶ , and L ³⁸ , they may be the same or different,
X ³¹ , X ³² , X ³³ , X ³⁴ , X ³⁵ , X ³⁶ , and X ³⁷ each independently represent a hydrogen atom or a fluorine atom,
Y ³¹ , Y ³² and Y ³³ are each independently a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, Or a difluoromethoxy group,
At least one of X ³¹ , X ³² , and Y ³¹ is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, or a difluoromethoxy. Or at least one of hydrogen atoms contained in M ³¹ or M ³² represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, or a chlorine atom,
At least one of X ³³ , X ³⁴ , X ³⁵ , or Y ³² is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, A difluoromethoxy group, or at least one of hydrogen atoms contained in M ³³ , M ³⁴ , or M ³⁵ represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group, or a chlorine atom,
At least one of X ³⁶ , X ³⁷ and Y ³³ is a fluorine atom, a chlorine atom, a cyano group, a thiocyanato group, a trifluoromethoxy group, a trifluoromethyl group, a 2,2,2-trifluoroethyl group, a difluoromethoxy group Or at least one of the hydrogen atoms contained in M ³⁶ , M ³⁷ and M ³⁸ represents a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
p, q, r, s, and t independently represent 0, 1, or 2, but q + r and s + t are 2 or less. Or a compound selected from the group consisting of compounds represented by formula (IVa), general formula (IVb) and general formula (IVc)

(Wherein R ⁴¹ , R ⁴² , R ⁴³ , R ⁴⁴ , R ⁴⁵ and R ⁴⁶ each independently represents an alkyl group having 1 to 10 carbon atoms or an alkenyl group having 2 to 10 carbon atoms, One methylene group present in the group or two or more methylene groups not adjacent to each other may be substituted with -O- or -S-, and one or two present in these groups The above hydrogen atoms may be substituted with fluorine atoms or chlorine atoms,
M ⁴¹ , M ⁴² , M ⁴³ , M ⁴⁴ , M ⁴⁵ , M ⁴⁶ , M ⁴⁷ , M ⁴⁸ , and M ⁴⁹ are independent of each other.
(d) trans-1,4-cyclohexylene group (one methylene group present in this group or two or more methylene groups not adjacent to each other may be replaced by -O- or -S-) ),
(e) a 1,4-phenylene group (one —CH═ present in the group or two or more non-adjacent —CH═ may be replaced by a nitrogen atom);
(f) 1,4-cyclohexenylene group, 1,4-bicyclo (2.2.2) octylene group, piperidine-2,5-diyl group, naphthalene-2,6-diyl group, 1,2,3,4 -Represents a group selected from the group consisting of a tetrahydronaphthalene-2,6-diyl group and a decahydronaphthalene-2,6-diyl group, and is included in the above group (d), group (e) or group (f) Each hydrogen atom may be substituted with a cyano group, a fluorine atom, a trifluoromethyl group, a trifluoromethoxy group or a chlorine atom,
L ⁴¹ , L ⁴² , L ⁴³ , L ⁴⁴ , L ⁴⁵ , L ⁴⁶ , L ⁴⁷ , L ⁴⁸ , and L ⁴⁹ are each independently a single bond, —COO—, —OCO—, —CH ₂ CH ₂ —, — (CH ₂ ) ₄ —, —OCH ₂ —, —CH ₂ O—, —OCF ₂ —, —CF ₂ O— or —C≡C— represents M ⁴² , M ⁴³ , M ⁴⁵ , M ⁴⁶ , When there are a plurality of M ⁴⁸ , M ⁴⁹ , L ⁴¹ , L ⁴³ , L ⁴⁴ , L ⁴⁶ , L ⁴⁷ and L ⁴⁹ , they may be the same or different,
X ⁴¹ and X ⁴² each independently represents a trifluoromethyl group, a trifluoromethoxy group or a fluorine atom, and X ⁴³ , X ⁴⁴ , X ⁴⁵ , X ⁴⁶ , X ⁴⁷ and X ⁴⁸ are each independently a hydrogen atom. , A trifluoromethyl group, a trifluoromethoxy group, or a fluorine atom, wherein any one of X ⁴¹ and X ⁴² represents a fluorine atom, and any one of X ⁴³ , X ⁴⁴ , and X ⁴⁵ represents a fluorine atom Any one of X ⁴⁶ , X ⁴⁷ and X ⁴⁸ represents a fluorine atom, but X ⁴⁶ and X ⁴⁷ do not represent a fluorine atom at the same time, and X ⁴⁶ and X ⁴⁸ represent fluorine at the same time. Never represent an atom,
G represents a methylene group or —O—;
u, v, w, x, y, and z each independently represent 0, 1, or 2, but u + v, w + x, and y + z are 2 or less. A polymerizable compound-containing liquid crystal composition containing one or more compounds selected from the group consisting of compounds represented by formula (1): The polymerizable compound-containing liquid crystal composition according to claim 1, wherein, in the general formula (I), Z represents —L ¹³ —S ¹² —R ¹² . The polymerizable compound-containing liquid crystal composition according to claim 1 or 2, wherein in the general formula (I), R ¹¹ and R ¹² independently of each other represent the formula (R-1) or (R-2). . A liquid crystal having a structure in which a liquid crystal is sandwiched between a pair of substrates, having at least a transparent electrode and a polarizing plate, and imparting liquid crystal alignment ability by polymerizing a polymerizable compound contained in the liquid crystal composition. The polymerizable compound-containing liquid crystal composition according to claim 1, 2 or 3 used for a display element. 0.01 to 2% by mass of a compound selected from general formula (I), 5 to 70% by mass of a compound selected from general formula (II), and general formula (IIIa), general formula (IIIb) or general formula 5 to 70 mass of a compound selected from the group consisting of compounds represented by (IIIc) or a compound selected from the group consisting of compounds represented by general formula (IVa), general formula (IVb) and general formula (IVc) 5. The polymerizable compound-containing liquid crystal composition according to claim 1, wherein the content is%. The third component contains one or more compounds selected from the group consisting of compounds represented by general formula (IVa), general formula (IVb) and general formula (IVc). The polymerizable compound-containing liquid crystal composition according to 2, 3, 4, or 5. Use of the polymerizable compound-containing liquid crystal composition according to claim 1, 2, 3, 4, 5, or 6 to impart a liquid crystal alignment ability by polymerizing the polymerizable compound in the polymerizable compound-containing liquid crystal composition. A liquid crystal display element characterized by the above. The liquid crystal display element according to claim 7, wherein the dielectric anisotropy of the polymerizable compound-containing liquid crystal composition is negative.