CN105505404B - Liquid-crystal composition and its display device - Google Patents

Liquid-crystal composition and its display device Download PDF

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Publication number
CN105505404B
CN105505404B CN201410559742.8A CN201410559742A CN105505404B CN 105505404 B CN105505404 B CN 105505404B CN 201410559742 A CN201410559742 A CN 201410559742A CN 105505404 B CN105505404 B CN 105505404B
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compound
liquid
crystal composition
gross weight
group
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CN105505404A (en
Inventor
马文阳
韩文明
徐海彬
施红萍
马定福
李鹏飞
丁文全
戴慧娟
刘云云
贺迪
姚丽芳
张鹤鸣
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Jiangsu Hecheng Display Technology Co Ltd
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Jiangsu Hecheng Display Technology Co Ltd
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Abstract

The invention discloses a kind of liquid-crystal composition and its display device.The liquid-crystal composition is included:The compound of one or more formulas I;The compound of one or more formulas II;The compound of one or more general formula IIIs;And the compound of one or more general formulae IVs.Liquid-crystal composition provided by the present invention, with suitable optical anisotropy, suitable dielectric anisotropy, higher clearing point, higher nematic phase temperature upper limit, preferably faster response speed, anti-UV stability and preferable high-temperature stability, suitable for liquid crystal display device, make the liquid crystal display device that there is quick response, reliability is high, and the characteristic of normal work is capable of in rugged environment.

Description

Liquid-crystal composition and its display device
Technical field
It is more particularly to a kind of that there is suitable optical anisotropy, suitable Jie the present invention relates to a kind of liquid-crystal composition Electrical anisotropy, higher clearing point, faster response speed, the liquid of preferable anti-UV stability and preferable high-temperature stability Crystal composite, and the liquid crystal display device comprising the liquid-crystal composition.
Background technology
Liquid crystal material is the not only mobility with liquid but also anisotropic organic with crystal at a certain temperature The mixture of bar-shaped micromolecular compound.Liquid crystal display cells be optical anisotropy in itself that have using liquid crystal material and Dielectric anisotropy has been widely used at present come what is be operated.Utilize the different characteristic of liquid crystal material and work Mode, can design device to a variety of mode of operations, and what wherein conventional display was generally used has (the distortion of TN patterns Nematic-mode, liquid crystal compound has the nematic structure of about 90 degree of torsion resistance), STN mode (supertwisted nematic mode), SBE Pattern (SBE), ecb mode (electrically conerolled birefringence), VA patterns (vertical arrangement), IPS (being changed in face) etc., also have Many improved modes made according to any of the above pattern.
For liquid crystal display, possess good chemically and thermally stability, it is good to electric field and electromagnetic radiation Stability, appropriate optical anisotropy, the liquid-crystal compounds and liquid crystal of faster response speed and relatively low threshold voltage are situated between Matter meets current needs.Mixture due to liquid crystal usually as various ingredients is used, dissolving each other each other between each component Then it is particularly important, and according to different battery types and application field, liquid crystal has to meet different requirements, such as conductance Rate, dielectric anisotropy and optical anisotropy etc., but when significantly having the drawback that longer response in the prior art Between, low resistivity and operating voltage is excessively high, such as EP0673986, DE19528106, DE19528107.In addition, low temperature is stored Less stable is also the defect of existing many liquid crystal materials.For the liquid crystal display of active array addressing, liquid crystal is situated between Matter will also have high voltage to keep ratio, and good light, heat endurance.Especially, for using Vehicle-carrying type steel and its The display that his open air is used, the nematic temperature range especially with non-constant width.
A series of compounds with liquid crystal Jie's phase disclosed so far do not include meeting all these aspect requirements Monomeric compound, therefore, liquid crystal material field it is necessary to have improve performance novel liquid crystalline compositions.Especially, for For many application types, liquid-crystal composition must have suitable wide nematic phase range, appropriate refractive index, dielectric respectively to different The performance such as property, low temperature storage stability, anti-UV stability.
The content of the invention
Goal of the invention:The technical problem to be solved in the invention is to provide a kind of liquid-crystal composition, with faster response Speed, the preferably characteristic such as anti-UV stability and preferable high-temperature stability, it is adaptable in liquid crystal display device, make the liquid crystal Display device energy quick response, and can be good in rugged environment display, normal work.In addition, what the present invention was provided Liquid-crystal composition also has suitable optical anisotropy, suitable dielectric anisotropy and higher clearing point.
The technical solution used in the present invention is:
A kind of liquid-crystal composition, the liquid-crystal composition is included:
One or more are selected from the compound by formula I
One or more are selected from the compound by formula II
One or more are selected from the compound by general formula III
And
One or more are selected from the compound by general formulae IV
Wherein,
R1、R2、R3、R4And R5It is identical or different, alkyl or alkoxy that carbon number is 1 to 5 are represented independently of one another, or Carbon number is 2 to 5 alkenyl;
X1Expression-OCF3Or-CF3
X2Represent F or-OCF3
L1And L2It is identical or different, H or F is represented independently of one another;
WithIt is identical or different, represent independently of one anotherOrIt is describedUpper one or more H can be replaced by F;
M represents 1 or 2;
N represents 0,1 or 2.
In embodiments of the invention, the compound of the formula I accounts for the 1-30% of the liquid-crystal composition gross weight; The compound of the formula II accounts for the 1-25% of the liquid-crystal composition gross weight;The compound of the general formula III accounts for the liquid crystal The 10-45% of composition total weight;And the compound of the general formulae IV accounts for the 35-60% of the liquid-crystal composition gross weight.
In some embodiments of the present invention, the compound of preferably described formula I be selected from by following compound group into One or more compounds in group:
And
In some embodiments of the present invention, the compound of preferably described formula II be selected from by following compound group into One or more compounds in group:
And
In some embodiments of the present invention, the compound of preferably described general formula III be selected from by following compound group into One or more compounds in group:
And
Wherein,
R3The alkyl that carbon number is 2 to 5 is represented independently of one another.
In some embodiments of the present invention, the compound of preferably described general formulae IV be selected from by following compound group into One or more compounds in group:
And
Wherein,
R4And R5It is identical or different, the alkyl that carbon number is 1 to 5 is represented independently of one another.
As particularly preferred scheme, the compound of the particularly preferred general formula III -1 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -2 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -3 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -4 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -5 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -6 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -7 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -8 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -9 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -10 be selected from by following compound group into One or more compounds in group:
And
As particularly preferred scheme, the compound of the particularly preferred general formula III -11 be selected from by following compound group into One or more compounds in group:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -1 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -2 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -3 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -4 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -5 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -6 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -7 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -8 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -9 be selected from by following compound group into group Middle one or more compounds:
And
As particularly preferred scheme, the compound of the particularly preferred general formulae IV -10 be selected from by following compound group into One or more compounds in group:
And
More preferably, the compound of the formula I accounts for the 5-30% of the liquid-crystal composition gross weight;The change of the formula II Compound accounts for the 4-20% of the liquid-crystal composition gross weight;The compound of the general formula III accounts for the liquid-crystal composition gross weight 10-40%;And the compound of the general formulae IV accounts for the 40-55% of the liquid-crystal composition gross weight.
The present invention also provides a kind of liquid crystal display, and the liquid crystal display includes the liquid crystal combination provided of the present invention Thing.
The present invention uses above-mentioned technical proposal, and compared to the prior art acquired technological progress has:
Liquid-crystal composition provided by the present invention have suitable optical anisotropy, suitable dielectric anisotropy, compared with High clearing point, higher nematic phase temperature upper limit, faster response speed, preferable anti-UV stability and preferable high temperature Stability, it is adaptable in liquid crystal display device, makes the liquid crystal display device have quick response, and can in rugged environment The characteristic of normal work.
In the present invention unless otherwise specified, described ratio is weight ratio, and all temperature are degree celsius temperature, institute The box thickness that the test for the response time data stated is selected is 7 μm.
Brief description of the drawings
Fig. 1 is the MS figures of chemical compounds I -6.
Embodiment
Illustrate the present invention below with reference to specific embodiment.It should be noted that the following examples are the present invention Example, only for illustrating the present invention, and be not limited to the present invention.In the case of without departing from present subject matter or scope, Other combinations and the various improvement in present inventive concept can be carried out.
For ease of expressing, in following embodiment, the unit structure of liquid-crystal composition is represented with the code listed by table 1:
The group structure code of the liquid-crystal compounds of table 1
By taking the compound of following structural formula as an example:
Structural formula code as listed by with table 2 is represented, then can be expressed as:N in nCPUF, code represents the C of left end alkyl Atomicity, such as n are " 3 ", that is, it is-C to represent the alkyl3H7;C in code represents cyclohexyl.
In following examples test event to write a Chinese character in simplified form code name as follows:
Cp(℃):Clearing point (nematic-isotropic phase transition temperature)
Δn:Optical anisotropy (589nm, 20 DEG C)
Δε:Dielectric anisotropy (1KHz, 25 DEG C)
η:Kinematic viscosity (mm2·s-1, 25 DEG C, unless otherwise indicated)
VHR (initial):Voltage retention (%)
Voltage retention (%) after VHR (UV) sunshine irradiation 20min
VHR(150℃):The voltage retention (%) measured after 150 DEG C of deterioration 1h
τon:Until the time (ms) when reaching transmitance 90%
τoff:Until reaching the time (ms) when transmitance 10% is cut off
τ:Ton+Toff (response time) (ms)
Wherein, optical anisotropy using abbe's refractometer under sodium lamp (589nm) light source, 20 DEG C test;Dielectric Testing cassete is TN90 types, and box is thick 7 μm.
Δ ε=ε ∥-ε ⊥, wherein, ε ∥ are the dielectric constant parallel to molecular axis, and ε ⊥ are the dielectric perpendicular to molecular axis Constant, test condition:25 DEG C, 1KHz, testing cassete be TN90 types, box is thick 7 μm.
VHR (initial) is obtained using TOYO6254 type liquid crystal evaluation of physical property system testings;Test temperature is 60 DEG C, test electricity Press as 5V, the testing time is 166.7ms;VHR (150 DEG C) is to use TOYO6254 type liquid crystal after liquid crystal is deteriorated into 1h at 150 DEG C Evaluation of physical property system testing is obtained;Test temperature is 60 DEG C, and test voltage is 5V, and the testing time is 166.7ms;VHR (UV) is to make Obtained with TOYO6254 type liquid crystal evaluation of physical property system testings;Test temperature is 60 DEG C, and test voltage is 5V, and the testing time is 166.7ms, the solar irradiation time is 20min.
Each composition used below in an example, can be synthesized, or pass through by known method Commercial sources are obtained.These synthetic technologys are conventional, and resulting each liquid-crystal compounds meets electrical type compound mark after tested It is accurate.
According to the proportioning of each liquid-crystal composition as defined in following examples, liquid-crystal composition is prepared.The liquid-crystal composition Preparation be to be carried out according to the conventional method of this area, such as take heating, ultrasonic wave, the mode that suspends mixed according to regulation ratio Close and be made.
Compound preparation example
The compound of formula I uses available commercial raw material, is obtained by the suzuki methods being coupled, synthetic route is such as Under:
Wherein, R1Represent the alkyl that carbon number is 1 to 5.Compound A and compound B can be obtained by commercial sources.
The compound of following structural formula is prepared by the above method:
Work as R1=C2H5When, the compound of following structural formula is obtained by the above method:
Work as R1=C3H7When, the compound of following structural formula is obtained by the above method:
Work as R1=C4H9When, the compound of following structural formula is obtained by the above method:
Work as R1=C5H11When, the compound of following structural formula is obtained by the above method:
The compound liquid crystal property parameter of table 2
Compound Δn Cp Δε
Ⅰ-5 0.20 235 7.3
Ⅰ-6 0.23 252 7.2
Ⅰ-7 0.22 263 7.0
Ⅰ-8 0.23 281 7.0
The MS figures of chemical compounds I -6 are shown in Fig. 1.
Reference examples 1
The liquid-crystal composition of reference examples 1 is configured to by each compound and percetage by weight listed in table 3, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 3 and its test performance
Embodiment 1
The liquid-crystal composition of embodiment 1 is configured to by each compound and percetage by weight listed in table 4, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 4 and its test performance
It is close in optical anisotropy, dielectric anisotropy and clearing point from above example 1 and reference examples 1 In the case of, liquid-crystal composition of the invention has lower kinematic viscosity, faster response speed, and in high temperature and UV illumination There is higher voltage retention afterwards.
Reference examples 2
The liquid-crystal composition of reference examples 2 is configured to by each compound and percetage by weight listed in table 5, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 5 and its test performance
Embodiment 2
The liquid-crystal composition of embodiment 2 is configured to by each compound and percetage by weight listed in table 6, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 6 and its test performance
It is close in optical anisotropy, dielectric anisotropy and clearing point from above example 2 and reference examples 2 In the case of, liquid-crystal composition of the invention has lower kinematic viscosity, faster response speed, and in high temperature and UV illumination There is higher voltage retention afterwards.
Reference examples 3
The liquid-crystal composition of reference examples 3 is configured to by each compound and percetage by weight listed in table 7, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 7 and its test performance
Embodiment 3
The liquid-crystal composition of embodiment 3 is configured to by each compound and percetage by weight listed in table 8, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 8 and its test performance
It is close in optical anisotropy, dielectric anisotropy and clearing point from above example 3 and reference examples 3 In the case of, liquid-crystal composition of the invention has lower kinematic viscosity, faster response speed, and in high temperature and UV illumination There is higher voltage retention afterwards.
Reference examples 4
The liquid-crystal composition of reference examples 4 is configured to by each compound and percetage by weight listed in table 9, it is filled in liquid Performance test is carried out between crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 9 and its test performance
Embodiment 4
The liquid-crystal composition of embodiment 4 is configured to by each compound and percetage by weight listed in table 10, it is filled in Performance test is carried out between liquid crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 10 and its test performance
It is close in optical anisotropy, dielectric anisotropy and clearing point from above example 4 and reference examples 4 In the case of, liquid-crystal composition of the invention has lower kinematic viscosity, faster response speed, and in high temperature and UV illumination There is higher voltage retention afterwards.
Reference examples 5
The liquid-crystal composition of reference examples 5 is configured to by each compound and percetage by weight listed in table 11, it is filled in Performance test is carried out between liquid crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 11 and its test performance
Embodiment 5
The liquid-crystal composition of embodiment 5 is configured to by each compound and percetage by weight listed in table 12, it is filled in Performance test is carried out between liquid crystal display two substrates, test data is as shown in the table:
The liquid crystal combination composition formula of table 12 and its test performance
From embodiment 5 and comparative example 5, in optical anisotropy, the dielectric anisotropy situation close with clearing point Under, liquid-crystal composition of the invention has lower kinematic viscosity, faster response speed, and has after high temperature and UV illumination There is higher voltage retention.
The technical concepts and features of embodiment of above only to illustrate the invention, its object is to allow be familiar with technique People understands present invention and is carried out, and it is not intended to limit the scope of the present invention, all real according to spirit of the invention The equivalent change or modification that matter is done, should all cover within the scope of the present invention.

Claims (11)

1. a kind of liquid-crystal composition, it is characterised in that the liquid-crystal composition is included:
One or more are selected from the compound by formula I
One or more are selected from the compound by formula II
One or more are selected from the compound by general formula III
And
One or more are selected from the compound by general formulae IV
Wherein,
R1、R2、R3、R4And R5It is identical or different, alkyl or alkoxy that carbon number is 1 to 5, or carbon original are represented independently of one another Subnumber is 2 to 5 alkenyl;
X1Expression-OCF3Or-CF3
X2Represent F or-OCF3
L1And L2It is identical or different, H or F is represented independently of one another;
It is identical or different, represent independently of one another It is describedUpper one or more H can be replaced by F;
M represents 1 or 2;
N represents 0,1 or 2.
2. liquid-crystal composition according to claim 1, it is characterised in that the compound of the formula I accounts for the liquid crystal group The 1-30% of compound gross weight;The compound of the formula II accounts for the 1-25% of the liquid-crystal composition gross weight;The formula III compound accounts for the 10-45% of the liquid-crystal composition gross weight;And the compound of the general formulae IV accounts for the liquid crystal group The 35-60% of compound gross weight.
3. liquid-crystal composition according to claim 1, it is characterised in that the compound of the formula I is selected from by followingization One or more compounds in the group of compound composition:
And
4. liquid-crystal composition according to claim 1, it is characterised in that the compound of the formula II is selected from by followingization One or more compounds in the group of compound composition:
And
5. liquid-crystal composition according to claim 1, it is characterised in that the compound of the general formula III is selected from by followingization One or more compounds in the group of compound composition:
And
Wherein,
R3The alkyl that carbon number is 2 to 5 is represented independently of one another.
6. liquid-crystal composition according to claim 1, it is characterised in that the compound of the general formulae IV is selected from by followingization One or more compounds in the group of compound composition:
And
Wherein,
R4And R5It is identical or different, the alkyl that carbon number is 1 to 5 is represented independently of one another.
7. liquid-crystal composition according to claim 5, it is characterised in that the compound of the general formula III -1 is selected from by following Compound group into group in one or more compounds:
And
The compound of the general formula III -2 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -3 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -4 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -5 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -6 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -7 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -8 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -9 selected from by following compound group into group in one or more compounds:
And
The compound of the general formula III -10 selected from by following compound group into group in one or more compounds:
And
And
The compound of the general formula III -11 selected from by following compound group into group in one or more compounds:
And
8. liquid-crystal composition according to claim 6, it is characterised in that the compound of the general formulae IV -1 is selected from by following Compound group into group in one or more compounds:
And
The compound of the general formulae IV -2 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -3 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -4 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -5 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -6 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -7 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -8 selected from by following compound group into group in one or more compounds:
And
The compound of the general formulae IV -9 selected from by following compound group into group in one or more compounds:
And
And
The compound of the general formulae IV -10 selected from by following compound group into group in one or more compounds:
And
9. the liquid-crystal composition according to claim any one of 1-8, it is characterised in that the compound of the formula I accounts for institute State the 5-30% of liquid-crystal composition gross weight;The compound of the formula II accounts for the 4-20% of the liquid-crystal composition gross weight; The compound of the general formula III accounts for the 10-40% of the liquid-crystal composition gross weight;And the compound of the general formulae IV accounts for institute State the 40-55% of liquid-crystal composition gross weight.
10. liquid-crystal composition according to claim 9, it is characterised in that the liquid-crystal composition is included:
Account for the compound ii -1 of the liquid-crystal composition gross weight 5%;
Account for the chemical compounds I -1 of the liquid-crystal composition gross weight 5%;
Account for the compounds Ⅳ -10-1 of the liquid-crystal composition gross weight 5%;
Account for the chemical compounds I -6 of the liquid-crystal composition gross weight 5%;
Account for the compound III -1-2 of the liquid-crystal composition gross weight 5%;
Account for the compound III -5-2 of the liquid-crystal composition gross weight 2%;
Account for the compound III -4-2 of the liquid-crystal composition gross weight 10%;
Account for the compound III -9-2 of the liquid-crystal composition gross weight 5%;
Account for the compound III -11-1 of the liquid-crystal composition gross weight 10%;
Account for the compounds Ⅳ -1-1 of the liquid-crystal composition gross weight 10%;
Account for the compounds Ⅳ -1-3 of the liquid-crystal composition gross weight 8%;And
Account for the compounds Ⅳ -2-1 of the liquid-crystal composition gross weight 30%;
Or described liquid-crystal composition is included:
Account for the compound III -2-1 of the liquid-crystal composition gross weight 5%;
Account for the compound III -7-1 of the liquid-crystal composition gross weight 10%;
Account for the compounds Ⅳ -1-4 of the liquid-crystal composition gross weight 10%;
Account for the compound ii -3 of the liquid-crystal composition gross weight 10%;
Account for the compound ii -2 of the liquid-crystal composition gross weight 10%;
Account for the chemical compounds I -5 of the liquid-crystal composition gross weight 10%;
Account for the compounds Ⅳ -2-1 of the liquid-crystal composition gross weight 35%;
Account for the compounds Ⅳ -5-1 of the liquid-crystal composition gross weight 5%;And
Account for the compounds Ⅳ -6-1 of the liquid-crystal composition gross weight 5%;
Or described liquid-crystal composition is included:
Account for the compounds Ⅳ -3-2 of the liquid-crystal composition gross weight 5%;
Account for the compounds Ⅳ -4-2 of the liquid-crystal composition gross weight 10%;
Account for the chemical compounds I -2 of the liquid-crystal composition gross weight 10%;
Account for the compound ii -4 of the liquid-crystal composition gross weight 5%;
Account for the compound III -5-2 of the liquid-crystal composition gross weight 10%;
Account for the compound III -4-2 of the liquid-crystal composition gross weight 10%;
Account for the compound III -10-4 of the liquid-crystal composition gross weight 6%;
Account for the compound III -3-2 of the liquid-crystal composition gross weight 5%;And
Account for the compounds Ⅳ -2-1 of the liquid-crystal composition gross weight 39%;
Or described liquid-crystal composition is included:
Account for the chemical compounds I -3 of the liquid-crystal composition gross weight 2%;
Account for the compound ii -2 of the liquid-crystal composition gross weight 10%;
Account for the compound III -7-1 of the liquid-crystal composition gross weight 8%;
Account for the compound III -9-2 of the liquid-crystal composition gross weight 5%;
Account for the compound III -11-1 of the liquid-crystal composition gross weight 10%;
Account for the compounds Ⅳ -1-3 of the liquid-crystal composition gross weight 10%;
Account for the chemical compounds I -8 of the liquid-crystal composition gross weight 13%;
Account for the compound III -6-2 of the liquid-crystal composition gross weight 2%;And
Account for the compounds Ⅳ -2-1 of the liquid-crystal composition gross weight 40%;
Or described liquid-crystal composition is included:
Account for the chemical compounds I -5 of the liquid-crystal composition gross weight 7%;
Account for the chemical compounds I -6 of the liquid-crystal composition gross weight 8%;
Account for the chemical compounds I -1 of the liquid-crystal composition gross weight 7%;
Account for the chemical compounds I -2 of the liquid-crystal composition gross weight 8%;
Account for the compound ii -3 of the liquid-crystal composition gross weight 4%;
Account for the compound III -6-1 of the liquid-crystal composition gross weight 3%;
Account for the compound III -6-2 of the liquid-crystal composition gross weight 4%;
Account for the compound III -7-1 of the liquid-crystal composition gross weight 3%;
Account for the compound III -7-2 of the liquid-crystal composition gross weight 4%;And
Account for the compounds Ⅳ -2-1 of the liquid-crystal composition gross weight 52%.
11. a kind of liquid crystal display, it is characterised in that it includes the liquid-crystal composition described in claim any one of 1-10.
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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02237949A (en) * 1988-07-05 1990-09-20 Seiko Epson Corp Liquid crystal compound
EP1310542A1 (en) * 2001-11-07 2003-05-14 MERCK PATENT GmbH Liquid crystalline compound, medium and display
CN101475811A (en) * 2007-04-13 2009-07-08 默克专利股份有限公司 Liquid crystal medium
CN101772561A (en) * 2007-08-31 2010-07-07 智索株式会社 Liquid crystal composition and liquid crystal display element
CN103725293A (en) * 2006-09-01 2014-04-16 默克专利股份有限公司 Liquid-crystalline medium

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02237949A (en) * 1988-07-05 1990-09-20 Seiko Epson Corp Liquid crystal compound
EP1310542A1 (en) * 2001-11-07 2003-05-14 MERCK PATENT GmbH Liquid crystalline compound, medium and display
CN103725293A (en) * 2006-09-01 2014-04-16 默克专利股份有限公司 Liquid-crystalline medium
CN101475811A (en) * 2007-04-13 2009-07-08 默克专利股份有限公司 Liquid crystal medium
CN101772561A (en) * 2007-08-31 2010-07-07 智索株式会社 Liquid crystal composition and liquid crystal display element

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