JPH05230033A - Liquid crystal compound - Google Patents

Abstract

PURPOSE:To provide a new pyrimidine ring-containing liquid crystal compound expectable in the application to new electro-optic elements, liquid crystal displays, etc., using a liquid crystal phase S*(3) exhibiting a three stable state and excellent in the light leakage rate. CONSTITUTION:A compound of formula I (R1 is 8-12C linear alkyl or alkoxy; R2 is 6-8C linear alkyl; (t) is H, F; * is asymmetric carbon), e.g. 4-(1,1,1- trifluoro-2-octyloxycarbonyl)phenyl-2-(4-n-nonylphenyl)pyrimidin-5-yl- carboxylate. The compound of formula I wherein (t) is H is obtained by condensing a 2-(4-alkyl or alkoxy-phenyl)pyrimidin-5-ylcarboxylic acid chloride of formula II with an optically active 4-hydroxybenzoic acid-1,1,1-trifluoro-2-alkyl ester of formula III.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a liquid crystal substance suitable for use in an electro-optical device utilizing the response of a chiral smectic liquid crystal to an electric field, particularly a ferroelectric liquid crystal substance containing a pyrimidine ring and an optical tristable state. The present invention also relates to a liquid crystal substance having excellent light leakage rate.

[0002]

2. Description of the Related Art Liquid crystal display devices have 1) low voltage operability and 2)
It has excellent features such as low power consumption, 3) thin display, 4) light receiving type, etc., so far, TN method, STN method,
A guest-host method has been developed and put into practical use. However, a nematic liquid crystal that is widely used at present has a response speed of several mse.
It has a drawback that it is as slow as c to several tens of msec, and is subject to various restrictions in application. In order to solve these problems, an STN method and an active matrix method using a thin layer transistor have been developed, but the STN type display element has excellent display quality such as display contrast and viewing angle. However, there are problems that high precision is required for controlling the cell gap and the tilt angle, and that the response is rather slow. Therefore, there has been a demand for the development of a new liquid crystal display system having excellent responsiveness, and an attempt has been made to develop a ferroelectric liquid crystal capable of realizing an ultra-high speed device having an optical response time as short as μsec. Ferroelectric liquid crystal has 1
In 975, DOBAMBC (p-decyloxybenzylidene-p-amino-2-methylbutyl cinnamate) was first synthesized by Meyor et al. (Le Jour).
nal de Physique, vol. 36, 1975, L
-69). In addition, 1980, Clark and Laga
Since the characteristics of display devices such as high-speed submicrosecond response of DOBAMBC and memory characteristics have been reported by WALL, ferroelectric liquid crystals have attracted great attention [N. A. Clark, et al. , Appl.
Phys. Lett. 36.899 (1980)]. However, their method has many technical problems for practical use, and there is no material showing ferroelectric liquid crystal at room temperature,
An effective and practical method for controlling the alignment of liquid crystal molecules, which is indispensable for display, has not been established. Since this report, various attempts have been made from both sides of liquid crystal materials / devices, and a display device utilizing switching between twisted two states has been prototyped. However, high contrast and proper threshold characteristics have not been obtained. From this point of view, other switching methods were also searched, and a transient scattering method was proposed. Then, in 1988, the inventors of the present invention reported a three-state switching method for a liquid crystal having three stable states [A. D.
L. Chandani, T .; Hagiwara, Y. S
uzuki et al. , Japan. J. ofApp
l. Phys. , 27, (5), L729-L732
(1988)]. The “having three states” means a liquid crystal electro-optical device in which a ferroelectric liquid crystal is sandwiched between a first electrode substrate and a second electrode substrate which is arranged with a predetermined gap therebetween. A voltage for forming an electric field is applied to the first and second electrode substrates, and when a voltage is applied as the triangular wave shown in FIG. 1A, the ferroelectric liquid crystal shows no electric field as shown in FIG. 1D. At times, the molecular orientation has a first stable state (2 in FIG. 1D), and when an electric field is applied, the molecular orientation is different from the first stable state with respect to one electric field direction. 1) and further has a third molecular orientation stable state (3 in FIG. 1D) different from the first and second stable states with respect to the other electric field direction. A liquid crystal compound having a liquid crystal phase S * (3) exhibiting a tristable state in a phase series is disclosed in JP-A-1-
316367, JP-A-1-316372, JP-A-1
-316339, JP-A-2-28128, and JP-A-1-213390 of Ichihashi, etc., and as a liquid crystal electro-optical device utilizing the tristable state, the present applicant has JP-A-2-40625 and JP-A-2-40625. Although new proposals are made in JP-A-2-153322 and JP-A-2-173724, the liquid crystal compound of the present invention is unknown. In addition, there is no disclosure about a liquid crystal exhibiting a good memory effect and tristable state. The three-state switching method applies the clear threshold characteristic and the hysteresis characteristic to the driving voltage, which is indicated by the liquid crystal phase S * (3) that exhibits a tristable state that is basically different from the conventional bistable state in the liquid crystal molecule alignment. Therefore, it is considered to be an epoch-making driving method that can realize large-screen moving image display by the simple matrix method. Furthermore, the performance of a display device using a liquid crystal exhibiting a tristable state largely depends on the shape of hysteresis, which is a physical property peculiar to the tristable state liquid crystal. With the hysteresis having the shape shown in FIG. 2, an ideal dark state can be realized at 0V, but light leakage occurs when the voltage is increased from 0V to V ₁ or reduced from 0V to −V ₁ . It can be said that a liquid crystal exhibiting a tristable state having such a hysteresis has a poor memory effect in the dark state. Then, this phenomenon brings about a reduction in the contrast of the display element. On the other hand, in the hysteresis as shown in FIG. 3, the ideal dark state realized by 0 V is the voltage V ₃ or the voltage −V _3.
The memory effect in the dark state is good. Then, the contrast of the display element becomes good. However, in reality, it is difficult to obtain a liquid crystal compound having an ideal hysteresis curve as shown in FIG. 3, and the hysteresis curve as shown in FIG. 4 is obtained, and the bias voltage Vb ₀ = (V ₂ + V ₃ ). When (C) ÷ (D) × 100 when ÷ 2 is expressed as a light leakage rate (%), most liquid crystal compounds have a light leakage rate in the range of 5 to 10%, and in the range of 0 to 5%. It was very difficult to find a liquid crystal compound having a light leakage rate.

[0003]

[Objective] The object of the present invention is to provide a liquid crystal phase S * exhibiting a tristable state.
The point is to provide a novel liquid crystal compound containing a pyrimidine ring, which can be expected to be applied to a new electro-optical element using (3), a liquid crystal display, and the like and has an excellent light leakage rate.

[0004]

[Structure] The present invention has the general formula

[Chemical 2] (In the formula, R ₁ is a linear alkyl group or alkoxy group having 8 to 12 carbon atoms, R ₂ is a linear alkyl group having 6 to 8 carbon atoms,
t is hydrogen or fluorine, and * represents an asymmetric carbon), and relates to a liquid crystal compound having an excellent light leakage rate in the tristable state.

An example of a typical method for producing the compound of the present invention will be explained. 2- (4-alkyl or alkoxy-phenyl) pyrimidin-5-yl-carboxylic acid is reacted with excess thionyl chloride to give 2- (4 -Alkyl or alkoxy-phenyl) pyrimidin-5-yl-carboxylic acid chloride (1) was obtained. Then, this is condensed with optically active 4-hydroxybenzoic acid 1,1,1-trifluoro-2-alkyl ester (2) to give 4- (1,1,1-tolufluoro-2-alkyloxycarbonyl) phenyl.
2- (4-Alkyl or alkoxyphenyl) pyrimidin-5-yl-carboxylate is obtained.

[Chemical 3]

[0006]

【Example】

Example 1 4- (1,1,1-trifluoro-2-octyloxycarbonyl) phenyl 2- (4-n-nonylphenyl)
Synthesis of pyrimidin-5-yl-carboxylate

[Chemical 4] After heating 1.6 g of 2- (4-n-nonylphenyl) pyrimidin-5-yl-carboxylic acid under reflux with excess thionyl chloride for 4 hours, unreacted thionyl chloride was distilled off to give 2- (4- n-Nonylphenyl) pyrimidin-5-yl-carboxylic acid chloride was obtained. Then, optically active 4-hydroxybenzoic acid 1,1,1-trifluoro-2-octyl ester (1.52 g) and triethylamine (1.52 g) were dissolved in 10 ml of chloroform to synthesize 2 previously.
A solution of-(4-n-nonylphenyl) -5-yl-carboxylic acid chloride dissolved in 20 ml of chloroform was added dropwise little by little, and the mixture was stirred at room temperature overnight. After the reaction mixture was put into water to make the liquid neutral, only the chloroform layer was extracted. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization to obtain 1.2 g of the desired product. Specific rotation [α] D ²⁰ + 31.14 ° (C: 2.030
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2928,2854,1740,1586,1436,1264,1212,1182,1163,1093,
1025,794 The phase transition temperature (° C) by observation with a polarization microscope equipped with a hot stage is as follows.

[Table 1] However, S * (3) indicates an optical tristable state phase.

Example 2 Synthesis of 4- (1,1,1-trifluoro-2-octyloxycarbonyl) phenyl 2- (4-n-nonyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 5] 2- (4-n-nonyloxyphenyl) pyrimidine-5
-Yl-carboxylic acid 1.0 g was heated under reflux with excess thionyl chloride for 4 hours, then unreacted thionyl chloride was distilled off to give 2- (4-n-nonyloxyphenyl) pyrimidin-5-yl-carboxylic acid. An acid chloride was obtained. Next, 0.91 g of optically active 4-hydroxybenzoic acid 1,1,1-trifluoro-2-octyl ester and 0.94 g of triethylamine were dissolved in 10 ml of chloroform to synthesize 2- (4-n-) previously synthesized. Nonyloxyphenyl) -5
A solution of -yl-carboxylic acid chloride dissolved in 12 ml of chloroform was added dropwise little by little, and the mixture was stirred at room temperature overnight. After the reaction mixture was put into water to make the liquid neutral, only the chloroform layer was extracted. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization to obtain 1.4 g of the desired product. Specific rotation [α] D ²⁰ + 30.50 ° (C: 2,000
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2931,2856,1741,1606,1589,1437,1277,1260,1204,1179,
1094, 1021, 803 The phase transition temperatures (° C) observed by a polarization microscope with a hot stage are as follows.

[Table 2] However, S * (3) indicates an optical tristable state phase.

Example 3 Synthesis of 4- (1,1,1-trifluoro-2-decyloxycarbonyl) phenyl 2- (4-n-nonyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 6] 2- (4-n-nonyloxyphenyl) pyrimidine-5
-Yl-carboxylic acid 1.0 g was heated under reflux with excess thionyl chloride for 4 hours, then unreacted thionyl chloride was distilled off to give 2- (4-n-nonyloxyphenyl) pyrimidin-5-yl-carboxylic acid. An acid chloride was obtained. Then, 0.99 g of optically active 4-hydroxybenzoic acid 1,1,1-trifluoro-2-decyl ester and 0.94 g of triethylamine were dissolved in 10 ml of chloroform to synthesize 2- (4-n-) previously synthesized. Nonyloxyphenyl) -5
A solution of -yl-carboxylic acid chloride dissolved in 12 ml of chloroform was added dropwise little by little, and the mixture was stirred at room temperature overnight. After the reaction mixture was put into water to make the liquid neutral, only the chloroform layer was extracted. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization to obtain 1.1 g of the desired product. Specific rotation [α] D ²⁰ + 30.41 ° (C: 2.045
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2927,2855,1733,1608,1582,1434,1263,1214,1163,1092,
1017,801 Phase transition temperature (° C) observed by polarized microscope with hot stage is as follows.

[Table 3] However, S * (3) indicates an optical tristable state phase.

Example 4 Synthesis of 4- (1,1,1-trifluoro-2-octyloxycarbonyl) phenyl 2- (4-n-decyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 7] 4- (5-n-decyloxyphenyl) pyrimidin-5-yl-carboxylic acid 1.2 in a 100 ml round bottom flask.
8 g, optically active 2-fluoro-4-hydroxybenzoic acid 1,1,1-trifluoro-2-octyl ester 1.1 g, 4-dimethylaminopyridine 0.03 g and chloroform 35 ml were put and stirred. 0.82 g of N, N'-dicyclohexylcarbodiimide was added to this mixture.
Was added and reacted at room temperature all day and night. After the reaction was completed, the white insoluble matter was filtered off. The chloroform layer was thoroughly washed with diluted hydrochloric acid and water, dried, and then the organic solvent was removed under reduced pressure. The obtained crude product was purified by column chromatography and recrystallization to obtain 1.7 g of the desired product. Specific rotation [α] D ²⁰ + 31.06 ° (C: 2.015
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2930,2854,1744,1584,1434,1388,1332,1260,1203,1169,
1090,1018,803 The phase transition temperature (° C) by observation with a polarizing microscope equipped with a hot stage is as follows.

[Table 4] However, S * (3) indicates an optical tristable state phase.

Example 5 Synthesis of 4- (1,1,1-trifluoro-2-decyloxycarbonyl) phenyl 2- (4-n-decyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 8] 4- (5-n-decyloxyphenyl) pyrimidin-5-yl-carboxylic acid 1.1 in a 100 ml round bottom flask.
7 g, optically active 2-fluoro-4-hydroxybenzoic acid 1,1,1-trifluoro-2-decyl ester 1.
1 g, 4-dimethylaminopyridine 0.03 g and chloroform 40 ml were added and stirred. N in this mixture
0.75 g of N'-dicyclohexylcarbodiimide was added, and the mixture was reacted overnight at room temperature. After the reaction was completed, the white insoluble matter was filtered off. The chloroform layer was thoroughly washed with diluted hydrochloric acid and water, dried, and then the organic solvent was removed under reduced pressure. The obtained crude product was purified by column chromatography and recrystallization to obtain 1.5 g of the desired product. Specific rotation [α] D ²⁰ + 30.60 ° (C: 2.01 C
HCI ₃ ) Infrared absorption spectrum (KBr method) (cm ^-1 ) 2922,2853,1733,1609,1586,1440,1266,1218,1165,1095,
1019,799 The phase transition temperature (° C) observed by a polarizing microscope with a hot stage is as follows.

[Table 5] However, S * (3) indicates an optical tristable state phase.

Example 6 Synthesis of 4- (1,1,1-trifluoro-2-octyloxycarbonyl) phenyl 2- (4-n-undecyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 9] After heating 1.0 g of 2- (4-n-undecyloxyphenyl) pyrimidin-5-yl-carboxylic acid under reflux with excess thionyl chloride for 4 hours, unreacted thionyl chloride was distilled off to give 2- ( 4-n-undecyloxyphenyl)
Pyrimidin-5-yl-carboxylic acid chloride was obtained. Next, 0.85 g of optically active 4-hydroxybenzoic acid 1,1,1-trifluoro-2-octyl ester and 0.85 g of triethylamine were dissolved in 20 ml of chloroform to synthesize 2- (4-n-) previously synthesized. A solution of undecyloxyphenyl) -5-yl-carboxylic acid chloride dissolved in 20 ml of chloroform was added dropwise little by little, and the mixture was stirred at room temperature overnight. After the reaction mixture was put into water to make the liquid neutral, only the chloroform layer was extracted. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization to obtain 1.3 g of the desired product. Specific rotation [α] D ²⁰ + 30.82 ° (C: 2.025
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2924,2864,1735,1609,1583,1435,1264,1214,1163,1091,
800 The phase transition temperature (° C) observed by a polarizing microscope with a hot stage is as follows.

[Table 6] However, S * (3) indicates an optical tristable state phase.

Example 7 Synthesis of 4- (1,1,1-trifluoro-2-decyloxycarbonyl) phenyl 2- (4-n-undecyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 10] After heating 1.0 g of 2- (4-n-undecyloxyphenyl) pyrimidin-5-yl-carboxylic acid with an excess of thionyl chloride under reflux for 5 hours, unreacted thionyl chloride was distilled off to give 2- ( 4-n-undecyloxyphenyl)
Pyrimidin-5-yl-carboxylic acid chloride was obtained. Next, 0.93 g of 1,1,1-trifluoro-2-decyl ester of optically active 4-hydroxybenzoic acid and 0.85 g of triethylamine were dissolved in 10 ml of chloroform to synthesize 2- (4-n-) previously synthesized. Undecyloxyphenyl) pyrimidin-5-yl-carboxylic acid chloride
Add the solution dissolved in ml of chloroform little by little,
Stirred overnight at room temperature. After the reaction mixture was put into water to make the liquid neutral, only the chloroform layer was extracted. After drying over anhydrous magnesium sulfate, the solvent was distilled off, and the residue was purified by silica gel column chromatography and recrystallization to obtain 1.4 g of the desired product. Specific rotation [α] D ²⁰ + 28.70 ° (C: 2.290
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2924,2854,1734,1609,1583,1435,1334,1265,1214,1164,
1093,1020,800 The phase transition temperature (° C) observed by a polarization microscope with a hot stage is as follows.

[Table 7] However, S * (3) indicates an optical tristable state phase.

Example 8 3-Fluoro-4- (1,1,1-trifluoro-2-
Synthesis of decyloxycarbonyl) phenyl 2- (4-n-decyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 11] 2- (4-n-decyloxyphenyl) pyrimidin-5-yl-carboxylic acid 1.0 in a 100 ml round bottom flask.
3 g, optically active 2-fluoro-4-hydroxybenzoic acid 1,1,1-trifluoro-2-decyl ester 1.
05 g, 4-dimethylaminopyridine 0.03 g and chloroform 45 ml were added and stirred. 0.66 g of N, N'-dicyclohexylcarbodiimide was added to this mixture.
Was added and reacted at room temperature all day and night. After the reaction was completed, the white insoluble matter was filtered off. The chloroform layer was washed well with diluted hydrochloric acid and water, dried, and then the organic solvent was removed under reduced pressure. The obtained crude product was purified by silica gel column chromatography and recrystallization to obtain 1.1 g of the desired product. Specific rotation [α] D ²⁰ + 26.65 ° (C: 2.045
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ^-1 ) 2924,2855,1729,1684,1438,1286,1169,1127,1088,800 The phase transition temperature (° C) by the observation with a polarization microscope with a hot stage is as follows. Is the street.

[Table 8] However, S * (3) indicates an optical tristable state phase.

Example 9 3-Fluoro-4- (1,1,1-trifluoro-2-
Octyloxycarbonyl) phenyl 2- (4-n-
Synthesis of nonyloxyphenyl) pyrimidin-5-yl-carboxylate

[Chemical 12] 2- (4-n-nonyloxyphenyl) pyrimidin-5-yl-carboxylic acid 1.1 in a 100 ml round bottom flask.
0 g, optically active 2-fluoro-4-hydroxybenzoic acid 1,1,1-trifluoro-2-octyl ester 0.96 g, 4-dimethylaminopyridine 0.03 g and chloroform 45 ml were added and stirred. To this mixture was added N, N'-dicyclohexylcarbodiimide 0.69.
g was added, and the mixture was reacted overnight at room temperature. After the reaction was completed, the white insoluble matter was filtered off. The chloroform layer was washed well with diluted hydrochloric acid and water, dried, and then the organic solvent was removed under reduced pressure. The obtained crude product was purified by silica gel column chromatography and recrystallization to obtain 1.1 g of the desired product. Specific rotation [α] D ²⁰ + 27.82 ° (C: 2.130
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ⁻¹ ) 2927,2856,1744,1618,1584,1436,1260,1169,1125,1081,
1023,800 The phase transition temperature (° C) observed by a polarization microscope with a hot stage is as follows.

[Table 9] However, S * (3) indicates an optical tristable state phase.

Example 10 3-Fluoro-4- (1,1,1-trifluoro-2-
Synthesis of decyloxycarbonyl) phenyl 2- (4-n-undecylphenyl) pyrimidin-5-yl-carboxylate

[Chemical 13] In a 100 ml round bottom flask, 1.02 of 2- (4-n-undecylphenyl) pyrimidin-5-yl-carboxylic acid.
g, optically active 2-fluoro-4-hydroxybenzoic acid
1,1,1-trifluoro-2-decyl ester 1.0
5 g, 4-dimethylaminopyridine 0.03 g and chloroform 45 ml were added and stirred. N in this mixture
0.66 g of N'-dicyclohexylcarbodiimide was added, and the mixture was reacted overnight at room temperature. After the reaction was completed, the white insoluble matter was filtered off. The chloroform layer was washed well with diluted hydrochloric acid and water, dried, and then the organic solvent was removed under reduced pressure. The obtained crude product was purified by silica gel column chromatography and recrystallization to obtain 1.4 g of the desired product. Specific rotation [α] D ²⁰ + 28.70 ° (C: 2.290
CHCl ₃ ) Infrared absorption spectrum (KBr method) (cm ^-1 ) 2923,2853,1747,1586,1434,1250,1178,1128,1087 The phase transition temperature (° C) by the observation with a polarization microscope with a hot stage is as follows. Is.

[Table 10] However, S * (3) indicates an optical tristable state phase.

Comparative example

[Chemical 14]

[Table 11]

Example 11 A rubbing-treated polyimide alignment film was formed on an ITO electrode substrate.
The liquid crystal cell having a cell thickness of 1.6 μm in Example 1 was obtained in each example.
Each of the liquid crystal compounds thus obtained is put into the Isotropic phase.
And filled to prepare a liquid crystal thin film cell. Created liquid crystal cell
Photomultiplier with two polarizing plates orthogonal to each other
Length of a polarized light microscope with a DC voltage of -40V applied
The polarizer was placed so that the axial direction and the polarizer overlap. This liquid crystal cell
To the SA phase with a temperature gradient of 0.1 to 1.0 ° C / 1 minute
Gradually cooled. Further cooling, temperature at which S * (3) phase is taken
± 40V, 1Hz triangular wave voltage is applied in degrees range
did. From the resulting hysteresis curve,
The threshold voltage was calculated. V₁: Relative light transmittance of 10 when voltage is reduced from bright state
% Voltage V₂: Relative light transmittance 90 when voltage is reduced from bright state
% Voltage V₃: Relative light transmittance of 10 when voltage is increased from dark state
% Voltage V_Four: Relative light transmittance 90 when voltage is increased from dark state
% Voltage and the parameters of the threshold characteristic and the width of hysteresis.
Then, the drive margin M shown by the following equation was obtained. When the driving margin M ≧ 2 or more, an appropriate threshold characteristic and
The width of the sterisis is obtained and the contrast is improved. Well
Further, in the hysteresis curve as shown in FIG. 3, the bias voltage Vbo = (V₂+ V₃) / 2 relative light transmittance in the dark state [(C) in FIG. 4] and in the bright state
Ratio (C) / (D) × 1 of relative light transmittance [(D) in FIG. 4]
00 was determined as the light leakage rate. In addition, TCA is SA
Is the temperature at which the S * (2) phase transitions to the S * (3) phase
Where T is the measured temperature. The results are shown in the table below.
You

[Table 12]

[0018]

[Discussion] As for the light leakage rate, compared with the compound of the comparative example, Example 1 has about 4.75 times, Example 2 has about 2.48 times, and Examples 3, 4, 6, 7, 7, and 10 are improved by about 3.35 times, and those of the ninth embodiment are improved by about 1.58 times, and those of the fifth embodiment are improved. Also, the driving margins of Examples 1 and 5 are approximately 5.66 times, those of Example 2 are approximately 8.68 times, those of Example 3 are approximately 6.58 times, and those of Example 4 are also About 8.29
Example 5 and 8 are about 5.66 times, Example 6 is about 4.21 times, Example 7 is about 4.47 times, Example 9 is about 2.10. In the case of Example 10, it is improved by about 6.84 times. Further, the working voltage of Examples 2, 6 and 7 has an excellent effect of being extremely low.

[0019]

[Effect] Since the novel liquid crystals of the present invention all show stable three states and exhibit an excellent light leakage rate, a display device having excellent contrast can be provided.

[Brief description of drawings]

FIG. 1 shows optical response characteristics of a triangular wave to which A is applied, B is a commercially available nematic liquid crystal, C is a two-state liquid crystal, and D is a three-state liquid crystal.

FIG. 2 shows poor hysteresis of dark memory effect for a tri-state liquid crystal.

FIG. 3 shows an ideal hysteresis with good memory effect in the dark area for a three-state liquid crystal.

FIG. 4 shows hysteresis for explaining the light leakage rate.

 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Yoshikazu Suzuki 3-5 Kasumigaseki, Chiyoda-ku, Tokyo Within Showa Shell Sekiyu (72) Inventor Nobuhiro Okabe 3-5-5 Kasumigaseki, Chiyoda-ku, Tokyo Showa Shell Sekiyu Co., Ltd. (72) Inventor Hitoshi Suenaga 5-41 Senmon, Itami-shi, Hyogo Teikoku Chemical Industry Co., Ltd. Itami Factory (72) Inventor Yasuhiro Hasegawa 5-41 Senmon, Itami-shi, Hyogo Teikoku Kagaku Sangyo Itami Factory Co., Ltd.

Claims (1)

[Claims] 1. A general formula: (In the formula, R ₁ is a linear alkyl group or alkoxy group having 8 to 12 carbon atoms, R ₂ is a linear alkyl group having 6 to 8 carbon atoms,
t is hydrogen or fluorine, and * represents an asymmetric carbon), which is an optically active liquid crystal compound exhibiting a tristable state with an excellent light leakage rate.