CN106520138A - Liquid crystal medium and application thereof - Google Patents

Liquid crystal medium and application thereof Download PDF

Info

Publication number
CN106520138A
CN106520138A CN201510587485.3A CN201510587485A CN106520138A CN 106520138 A CN106520138 A CN 106520138A CN 201510587485 A CN201510587485 A CN 201510587485A CN 106520138 A CN106520138 A CN 106520138A
Authority
CN
China
Prior art keywords
formula
liquid crystal
represent
compound representated
chained alkyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201510587485.3A
Other languages
Chinese (zh)
Other versions
CN106520138B (en
Inventor
陈卯先
陈海光
姜天孟
储士红
王杰
未欣
张琳
田会强
苏学辉
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Beijing Bayi Space LCD Technology Co Ltd
Original Assignee
Beijing Bayi Space LCD Technology Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Beijing Bayi Space LCD Technology Co Ltd filed Critical Beijing Bayi Space LCD Technology Co Ltd
Priority to CN201510587485.3A priority Critical patent/CN106520138B/en
Publication of CN106520138A publication Critical patent/CN106520138A/en
Application granted granted Critical
Publication of CN106520138B publication Critical patent/CN106520138B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention provides a liquid crystal medium prepared from a compound containing dioxygen heterocyclic rings and 2-methyl-3,4,5-trifluoro-henyl. The liquid crystal medium has the low viscosity, the high resistance rate, the good low-temperature intersolubility, the high response speed and the excellent transmittance characteristic and can be applied to fast-response liquid crystal displaying in multiple display modes. The liquid crystal medium effectively increases the vertical dielectric, effectively improves the transmittance characteristic of a liquid crystal display, has the very low rotary viscosity gamma 1 and the high elastic constant and response speed and is suitable for a TN mode, an IPS mode and an FFS mode and especially suitable for various application of the IPS mode and the FFS mode.

Description

Liquid crystal media and its application
Technical field
The present invention relates to a kind of liquid crystal media, belongs to liquid crystal display material field, more particularly to is applied to IPS and FFS type liquid The liquid crystal media of crystal display.
Background technology
At present, liquid crystal is used widely in field of information display, while the application in optical communication also makes some progress (S.T.Wu, D.K.Yang.Reflective Liquid Crystal Displays.Wiley, 2001).In recent years, liquid-crystal compoundss Application has significantly widened kinds of displays part, electro-optical device, electronic component, sensor etc..For this purpose, having been proposed that Many different structures, particularly in nematic crystal field, nematic liquid crystal compound is obtained in flat faced display so far To most commonly used application.Particularly it is used in the system of tft active matrix.
Liquid crystal display experienced very long road for development with the discovery of liquid crystal.Austrian botanist Friedrich in 1888 Reinitzer is found that the first liquid crystal material benzoic acid cholesterol (cholesteryl benzoate).Manguin sends out within 1917 Clear rubbing, to make single domain liquid crystal and research optical anisotropy.E.Bose is established and is collected together within 1909 (Swarm) theory, and experiment support (1918) of L.S.Ormstein and F.Zernike et al. is obtained, by De Gennes It is discussed as statistical fluctuation.G.W.Oseen and H.Zocher1933 foundes continuum theory, and it is perfect to obtain F.C.Frank (1958).M.Born (1916) and K.Lichtennecker (nineteen twenty-six) have found and have studied the dielectric of liquid crystal respectively to different Property.1932, nematic phase was divided into positive and negative two big class of property by W.Kast accordingly.Nineteen twenty-seven, V.Freedericksz and V.Zolinao It was found that nematic liquid crystal deforms upon and exists voltage threshold (Freederichsz transformations) under electric field (or magnetic field) effect.This One making for being found to be liquid crystal display provides foundation.
Nineteen sixty-eight RCA Corp. of U.S. R.Williams has found that nematic liquid crystal forms striped farmland under electric field action, and has light Scattering phenomenon.G.H.Heilmeir with will its develop into dynamic scattering display pattern, and make first liquid crystal display in the world Device (LCD).Early seventies, Helfrich and Schadt have invented TN principles, and people utilize TN photoelectric effect and integrated Circuit combines, and is made display device (TN-LCD), is that wide prospect has been opened up in the application of liquid crystal.The seventies with Come, due to the development of large scale integrated circuit and liquid crystal material, application of the liquid crystal in terms of display achieves breakthrough development, 1983~1985 years T.Scheffer et al. successively propose super-twist nematic (Super TwisredNematic:STN) pattern And active matrix (the Active matrix that P.Brody was proposed in 1972:AM) mode is adopted again.Traditional TN-LCD technologies have developed into STN-LCD and TFT-LCD technologies, although the number of scanning lines of STN up to 768 rows with On, but the problems such as remaining response speed, visual angle and gray scale when the temperature increases, therefore large area, high information quantity, It is colored to show the Active Matrix LCD At mode that adopt mostly.TFT-LCD is widely used for direct viewing type TV, large screen projection electricity Depending on, terminal shows and some military instrument show, it is believed that TFT-LCD technologies have more wide application prospect.
Wherein " active matrix " includes two types:1st, on the silicon wafer as substrate OMS (metal-oxide semiconductor (MOS)) Or other diodes.2nd, on the glass plate as substrate thin film transistor (TFT) (TFT).
Monocrystal silicon limits display size as substrate material, because each several part display device even module assembled goes out in its junction Existing many problems.Thus, second thin film transistor (TFT) is that have promising active matrix type, and the photoelectric effect for being utilized is usual It is TN effects.TFT includes compound semiconductor, such as Cdse, or the TFT based on polycrystalline or amorphous silicon.
At present, for the small size for flat board and smart mobile phone display and middle display of size, in face, change (IPS) It is very interesting with fringing field switching (FFS) pattern.IPS and FFS mode are widely used in intelligent and middle size and show The reason for showing device is wide viewing angle, and relative to the low operational factor for knowing pattern in prior art, relative to IPS patterns, FFS is gathered around There is higher absorbance.Liquid crystal compound of the prior art be characterised by which by the compound with positive dielectric anisotropy and Optional neutral compound is constituted.
In a liquid crystal display, expect to contribute to the medium of the following advantage in box:
1st, wide nematic phase range (particularly downwards until low temperature)
2nd, the ability (outdoor application, automobile, avionics) for switching under extremely low temperature
3rd, the toleration (longer service life) to ultraviolet radioactive for improving
4th, low threshold voltage (saving electric energy)
5th, high-transmission rate.
The major function of liquid crystal display is to play a part of photoswitch, light after liquid crystal layer light loss to only original 6% or so, so brighter display effect will be obtained, it is necessary to increase backlight illumination, this will increase the energy consumption of backlight and reduction Backlight life.Another approach is the liquid crystal display for obtaining high absorbance, and liquid crystal media provided by the present invention is conducive to Improve the absorbance of liquid crystal display.
It has now been discovered that under IPS and FFS display patterns, with little εLiquid crystal media can effectively lift liquid crystal The light transmission rate of display, and the liquid crystal display of low driving voltage requires that liquid crystal has big △ ε (ε), therefore, Lift εBecome the key factor for lifting liquid crystal display transmitance.In liquid crystal media, liquid crystal molecule how is chosen vertical Become the index in the big liquid-crystal compoundss of the dielectric of long axis direction more of paramount importance.
In view of this, it is special to propose the present invention.
The content of the invention
The first object of the present invention be provide a kind of liquid crystal media (liquid crystal media i.e. containing dioxygen heterocycle and 2- methyl -3, The liquid-crystal composition of the compound of 4,5- trifluorophenyls, is hereafter alternatively referred to as " liquid-crystal composition "), and amazing Existing, the liquid crystal media obtained by the present invention effectively lifts the vertical dielectric of liquid crystal media, effectively improves liquid crystal display Light transmission rate, and the rotary viscosity γ 1 with very low numerical value, big elastic constant, fast response speed, it is adaptable to TN, The various applications of IPS and FFS mode, particularly IPS and FFS mode.
Specifically, liquid crystal media of the present invention includes the compound representated by least one or more of formula I:
Wherein, R1Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;
A1Represent:
A2Represent:
N and m represent 0 or 1 independently of one another.
And at least one compounds of formula II:
Wherein, R2Represent C1~C12Straight chained alkyl;R3Represent C1~C12Straight chained alkyl, wherein one or more are non-conterminous CH2Can be replaced by O, CH=CH;A3、A4Trans Isosorbide-5-Nitrae-cyclohexyl or Isosorbide-5-Nitrae-phenylene is represented independently of one another.
In order to realize more preferable coordinating effect, liquid crystal media of the present invention includes following components in percentage by weight:
1), the compound representated by 1%~60% one or more formula I;
2), the compound representated by 1%~70% one or more formula II;
3), the compound representated by 0%~40% one or more general formula III;
4), the compound representated by 0%~40% one or more formula IV;
5), the compound representated by 0%~60% one or more formula V~formula IX;
Wherein, R4Represent C1~C12Straight chained alkyl;L1Represent H or F;P=0 or 1;
A3Represent:
Wherein, R5Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R6Represent C1~C12Straight chained alkyl;
A4Represent:
Wherein, R7、R9C is represented independently of one another1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R8、R10、R11、 R12C is represented independently of one another1~C12Straight chained alkyl;X1、X2、X4F, CF is represented independently of one another3、OCF3Or OCF2H; X3Represent F, CF3、OCF3And C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;L2、L3、L4、L5、L6、 L7、L8、L9、L10、L11、L12H or F is represented independently of one another;
A5、A6Represent independently of one another:
A7Represent:
A8、A9Represent independently of one another:
More preferably, the liquid crystal media includes following components in percentage by weight:
1), the compound representated by 5%~30% one or more formula I;
2), the compound representated by 15%~60% one or more formula II;
3), the compound representated by 0%~30% one or more general formula III;
4), the compound representated by 5%~30% one or more formula IV;
5), the compound representated by 10%~50% one or more formula V~formula IX;
Preferably, the liquid crystal media includes following components in percentage by weight:
1), the compound representated by 7%~27% one or more formula I;
2), the compound representated by 42%~57% one or more formula II;
3), the compound representated by 9%~24% one or more formula IV;
4), the compound representated by 12%~29% one or more formula V~formula IX;
Or
1), the compound representated by 5%~13% one or more formula I;
2), the compound representated by 19%~45% one or more formula II;
3), the compound representated by 6.5%~26% one or more general formula III;
4), the compound representated by 6%~25% one or more formula IV;
5), the compound representated by 14%~47% one or more formula V~formula IX.
Or
1), the compound representated by the logical formula (I) of one or more of 5%~27%;
2), the compound representated by the logical formula (II) of one or more of 19%~45.5%;
3), the compound representated by the logical formula (III) of one or more of 0%~26%;
4), the compound representated by the logical formula (IV) of one or more of 6%~25%;
5), the compound representated by the logical formula V of one or more of 0%~42%~logical formula (VII)
6), the compound representated by the logical formula (VIII) of one or more of 4%~19%
7), the compound representated by the logical formula (IX) of one or more of 0%~6%.
Liquid crystal media of the present invention, it is preferable that the one kind of the compound representated by formula I in Formulas I-A~Formulas I-F or It is various:
Wherein, R1Represent C1~C7Straight chained alkyl.
Preferably, one or more in Formulas I-A-1~Formulas I-F-4 of the compound representated by formula I:
Liquid crystal media of the present invention, one or more in Formula II-A~Formula II-C of the compound representated by formula II:
Wherein, R2Represent C1~C7Straight chained alkyl;R3Represent C1~C7Straight chained alkyl, wherein one or more are non-conterminous CH2Can be replaced by O or CH=CH.
Preferably, one or more in Formula II-A-1~Formula II-C-25 of the compound representated by formula II:
Preferably, one or more in formula III-A~formula III-H of the compound described in general formula III:
Wherein, R4Represent C1~C7Straight chained alkyl.
It is highly preferred that R4Represent C2~C5Straight chained alkyl.
Liquid crystal media provided by the present invention, one or more in formula IV-A~formula IV-C of the compound described in formula IV:
Wherein, R5Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;R6Represent C1~C7Straight chained alkyl.
It is highly preferred that R5Represent C2~C5Straight chained alkyl or straight-chain alkenyl, R6Represent C1~C5Straight chained alkyl.
Liquid crystal media provided by the present invention, it is preferable that the compound described in formula V in Formula V-A~Formula V-K Plant or various:
Wherein, R7Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl.
Preferably, one or more in Formula IV-A~Formula IV-P of the compound representated by formula VI:
Wherein, R8Represent C1~C7Straight chained alkyl.
One or more in Formula VII-A~Formula VII-G of compound described in formula VII:
Wherein, R9、X3C is represented independently of one another1~C5Straight chained alkyl or C2~C5Straight-chain alkenyl.
One or more in Formula VIII-A~Formula VIII-L of compound described in formula VIII:
Wherein, R10Represent C1~C7Straight chained alkyl.
One or more in Formula IX-A~Formula IX-C of compound described in formula IX:
Wherein, R11、R12C is represented independently of one another1~C7Straight chained alkyl.
It is highly preferred that R7Represent C2~C5Straight chained alkyl or straight-chain alkenyl;R8、R9、R10、R11、R12Independently of one another Represent C2~C5Straight chained alkyl.
In liquid crystal media provided by the present invention, the compound representated by formula I contains dioxygen heterocycle structure, and the structure has strong Inductive effect, the positive dielectric anisotropy (+△ ε) of liquid-crystal compoundss can be effectively increased, and with high vertical dielectric, And intersolubility is good, the low feature of rotary viscosity, excellent combination property.
Two ring structure compounds representated by II classes formula provided by the present invention are non-polar component.Such compound is for drop The viscosity of low system, raising response speed effect are notable, are the requisite class chemical combination of liquid crystal compound for allocating quick response Thing.
The compound provided by general formula III has big positive dielectric anisotropy, is conducive to being lifted the dielectric of liquid crystal media respectively to different Property, and with good intersolubility and low rotary viscosity.
Compound representated by IV classes formula provided by the present invention is three ring non-polar conformations, and which has big elastic constant (K11、K22、K33) and low rotary viscosity, for the elastic constant for lifting liquid crystal media has positive effect.
Compound representated by V classes formula provided by the present invention is three ring polar structures, and with larger polarity, which is mutual Dissolubility is good.
Compound representated by VI classes formula provided by the present invention is three ring polar structures, and with larger polarity, which is mutual Dissolubility is good.
Compound representated by VII classes formula provided by the present invention is three structures, with big optical anisotropy, The optical anisotropy of liquid crystal media can effectively be increased.
Compound representated by VIII and IX classes formula provided by the present invention is tetracyclic structure, with big optics respectively to different Property and high clearing point performance, for lifted compositionss clearing point and optical anisotropy have remarkable result.
Positive dielectric anisotropic liquid crystals medium addition negative dielectric anisotropic composition increases display effect and sees Chinese patent earliest In CN103320142, compound I provided by the present invention is that, containing 2- methyl -3,4,5- trifluorophenyls and dioxygen are miscellaneous The compound of ring, the compound of the structure have big dielectric anisotropy and big vertical dielectric.
Two or more compounds can be mixed using conventional method by the preparation method of liquid crystal media of the present invention without particular restriction Produced, such as prepared by mixing different component method soluble in one another at high temperature, wherein, liquid crystal media is dissolved in For in the solvent of the compound and mixing, the solvent is then distilled out under reduced pressure;Or liquid crystal media of the present invention can be pressed Prepared by the method for more solito, wherein content less component is dissolved in content larger key component at a higher temperature such as In, or each affiliated component is dissolved in organic solvent, such as acetone, chloroform or methanol etc., solution mixing is removed into solvent then After obtain.
Invention also provides application of the above-mentioned liquid crystal media in liquid crystal indicator, the liquid crystal media have low viscosity, High resistivity, good low temperature intersolubility, fast response speed and excellent light transmission rate, can be used for plurality of display modes Fast-response liquid crystal display.Liquid crystal display is confined to the temperature range of liquid crystal, and liquid crystal only shows to show in the range of liquid crystalline phase Show effect, and the viscosity exponentially of liquid crystal increases during low temperature, low temperature response speed is its hard defects of liquid crystal display, so showing Effect can be substantially reduced.Liquid crystal media of the present invention overcomes these problems, with low viscosity and good cryogenic property and Excellent light transmission rate, its use in TN, IPS or FFS mode display can be obviously improved liquid crystal display and show Effect.
Specific embodiment
Following examples are used for illustrating the present invention, but are not limited to the scope of the present invention.
In the embodiment of the present invention, the preparation of liquid crystal media is adopted with the following method:
The preparation of uniform liquid crystal weighs liquid-crystalization with balance first by weight percentage using the heat of solution method for commonly using in the industry Compound, wherein weighs addition sequence without particular requirement, and the generally order with liquid-crystal compoundss fusing point from high to low weighs mixing successively, At 60-100 DEG C, heated and stirred causes each component to melt uniformly, then Jing is filtered, rotated, and finally encapsulation obtains final product target sample.
Unless otherwise stated, in context, percentage ratio is weight percentage, and all of temperature is degree Celsius being given.Using following contractings Write:
△ n be optical anisotropy (25 DEG C), Δ ε be dielectric anisotropy (25 DEG C, 1000Hz), εFor vertical dielectric (25 DEG C, 1000Hz), Cp for liquid crystal media clearing point (DEG C), γ 1 be rotary viscosity (25 DEG C, mpa.s), K11、 K22、K33Respectively splay, distortion, bend elastic constant (25 DEG C, pN).
For the ease of representing, in following examples, in liquid-crystal compoundss, code shown in unit structure table 1 is represented:
Table 1:The unit structure code of liquid-crystal compoundss
By taking following structure as an example:
The structure is represented by code listed in Table 1, then it represents that for 4CDUQKF.
For another example following structure:
The structure is represented by code listed in Table 1, then it represents that for 5CCPUF.
Embodiment 1 takes the liquid-crystal compoundss of following percentage by weight and prepares liquid crystal media in heretofore described method, specifically Performance parameter with the when liquid crystal media of gained is shown in Table 2:
The weight percent of each component when performance parameter in the liquid crystal media of 2 embodiment 1 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3DUQKF 15 △n 0.100
I 2DPUQKF 6 Δε +9.3
I 3DPUQKF 6 ε 4.3
II 3CCV 42 γ1 72
IV V2CCP1 10 Cp 80
IV VCCP1 9 K11 11.6
VIII 3CPGUOCF3 10 K22 5.8
VIII 3PPGUF 2 K33 16.2
Embodiment 2
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 3:
The weight percent of each component when performance parameter in the liquid crystal media of 3 embodiment 2 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3CDUQKF 13 △n 0.099
II 3CCV 42 Δε +12.5
III 2APUQKF 10 ε 5.5
III 3APUQKF 5 γ1 85
III 3PUQKF 10 Cp 89
IV VCCP1 6 K11 12.4
VIII 2CCPUF 5 K22 6.2
VIII 3CCPUF 5 K33 16.3
VIII 4CCPUF 4
Embodiment 3
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 4:
The weight percent of each component when performance parameter in the liquid crystal media of 4 embodiment 3 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3DCQKF 13 △n 0.095
II 3CCV 19 Δε +11.9
III 2APUQKF 5 ε 5.7
III 3APUQKF 8 Cp 91
IV VCCP1 8 γ1 120
V VCCGF 10 K11 12.6
V 2CCUF 5 K22 6.3
V 3CCUF 10 K33 16.3
V 5CCUF 5
VI 3CPGF 5
VI 5CPUF 2
VI 3CGUF 5
VIII 3CCPUF 5
Embodiment 4
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 5:
The weight percent of each component when performance parameter in the liquid crystal media of 5 embodiment 4 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 5 △n 0.100
I 4DPUQKF 2 Δε +6.3
II 3CCV 41 ε 3.4
II 5PP1 3 Cp 91
III 3PUQKF 11 γ1 72
IV 3CPP2 6 K11 12.8
V 3CCPOCF3 5 K22 6.4
V 5CCPOCF3 3 K33 15.1
VI 2CPPOCF3 6
VIII 2CCPGF 4
VIII 3CCPGF 5
VIII 4CCPGF 5
VIII 5CCPGF 4
Embodiment 5
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 6:
The weight percent of each component when performance parameter in the liquid crystal media of 6 embodiment 5 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 5 △n 0.100
I 4DPUQKF 2 Δε +6.1
II 3CCV 41 ε 3.3
II 1PP2V 4 Cp 92
III 3PUQKF 10 γ1 71
IV VCPP3 6 K11 12.6
V 3CCPOCF3 5 K22 6.3
V 5CCPOCF3 5 K33 15.8
VI 2CPPOCF3 4
VIII 2CCPGF 4
VIII 3CCPGF 5
VIII 4CCPGF 5
VIII 5CCPGF 4
Embodiment 6
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 7:
The weight percent of each component when performance parameter in the liquid crystal media of 7 embodiment 6 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3DUQKF 7 △n 0.100
I 4DUQKF 7.5 Δε +6.3
I 4DPUQKF 2 ε 3.5
II 3CCV 38.5 Cp 92
II 1PP2V 7 γ1 73
IV VCPP3 9 K11 12.6
V 3CCPGF 10 K22 6.3
VIII 2CCPGF 5 K33 15.5
VIII 3CCPGF 5
VIII 4CCPGF 5
VIII 5CCPGF 4
Embodiment 7
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 8:
The weight percent of each component when performance parameter in the liquid crystal media of 8 embodiment 7 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 7 △n 0.106
I 4DPUQKF 3 Δε +6.5
II 3CCV 26 ε 3.5
II 1PP5 7 Cp 86
III 3PUQKF 6.5 γ1 74
IV VCCP1 18 K11 12.4
V 3CCGF 12 K22 6.2
VI 3CPGF 8.5 K33 15.3
VII 3PGPF 6
VIII 3CCPGF 3
VIII 4CCPGF 3
Embodiment 8
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 9:
The weight percent of each component when performance parameter in the liquid crystal media of 9 embodiment 8 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 8 △n 0.106
I 4DPUQKF 3 Δε +6.4
II 3CCV 35 ε 3.4
II 1PP5 5 Cp 87
III 3PUQKF 9 γ1 70
IV VCCP1 13 K11 12.6
IV 3CPP1 3 K22 6.3
IV 3CPP2 3 K33 15.1
V 3CCGF 4
VII 3PGPF 6
VIII 2CCPGF 3
VIII 3CCPGF 3
VIII 4CCPGF 3
IX 3CPPC3 2
Embodiment 9
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 10:
The weight percent of each component when performance parameter in the liquid crystal media of 10 embodiment 9 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 8 △n 0.106
I 4DPUQKF 3 Δε +6.4
II 3CCV 38 ε 3.4
II 1PP5 3 Cp 86
III 3PUQKF 8.5 γ1 72
IV VCCP1 11 K11 12.5
IV 3CPP1 3 K22 6.3
IV 3CPP2 3 K33 15.4
VI 3CPGF 5.5
VII 3PGPF 6
VIII 2CCPGF 2
VIII 3CCPGF 3
VIII 4CCPGF 3
IX 3CPPC3 3
Embodiment 10
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 11:
The weight percent of each component when performance parameter in the liquid crystal media of 11 embodiment 10 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3DUQKF 5 △n 0.108
II 3CCV 36 Δε 6.6
III 3PUQKF 10 ε 3.6
IV VCCP1 13 Cp 92
IV V2CCP1 12 γ1 78
VI 3DPUF 10 K11 13.4
VIII 2CCPUF 4 K22 6.7
VIII 3CCPUF 4 K33 17.1
IX 5CPGP3 6
Embodiment 11
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 12:
The weight percent of each component when performance parameter in the liquid crystal media of 12 embodiment 11 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 3DCQKF 13 △n 0.100
II 3CCV 24 Δε +11.6
III 3PUQKF 12 ε 5.9
III 3APUQKF 14 γ1 112
IV VCCP1 9 Cp 85
V 3DCUF 10 K11 12.6
VI 3DGUF 10 K22 6.3
VIII 2CCPUF 4 K33 15.6
VIII 3CCPUF 4
Embodiment 12
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 13:
The weight percent of each component when performance parameter in the liquid crystal media of 13 embodiment 12 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 4 △n 0.099
I 4DPUQKF 3 Δε +5.9
II 3CCV 25 ε 3.2
II 3CPO1 4 γ1 70
II 5PP1 4 Cp 93
II 3CCV1 5 K11 13.8
II 3CC2 4 K22 6.9
III 3PUQKF 10 K33 16.4
III 2APUQKF 4
IV VCCP1 10
IV 3CPP2 6
IV 3CCP1 7
V 3CCPOCF3 6
VIII 3CCPGF 4
IX 3CPPC3 4
Embodiment 13
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 14:
The weight percent of each component when performance parameter in the liquid crystal media of 14 embodiment 13 of table
Classification Component Percentage by weight (%) Performance parameter Parameter value
I 4DUQKF 7 △n 0.098
II 3CCV 40 Δε +2.6
II 3CCV1 12 ε 3.0
II 5CCV1 5 γ1 54
IV VCCP1 12 Cp 80
IV V2CCP1 12 K11 13.2
VII 2PGPF 6 K22 6.6
VII 3PGPF 6 K33 15.8
Comparative example 1
Take the liquid-crystal compoundss of following percentage by weight and liquid crystal media is prepared in heretofore described method, it is concrete with when gained The performance parameter of liquid crystal media be shown in Table 15:
The weight percent of each component when performance parameter in the liquid crystal media of 15 comparative example 1 of table
Component Percentage by weight (%) Performance parameter Parameter value
3PGUQUF 6.5 △n 0.098
3APUQUF 5 Δε +2.6
3CCV 40 ε 2.6
3CCV1 12 γ1 80
1V2PP1 7 Cp 52
VCCP1 13 K11 13.6
V2CCP1 12 K22 6.8
2PGP3 4 K33 16.2
3PPGUF 0.5
Comparative example 13 and comparative example 1, its parameter such as table 16:
16 comparative example 1 of table and 13 performance parameter of embodiment
Project Comparative example 1 Embodiment 13
△n 0.098 0.098
Δε +2.6 +2.6
ε 2.6 3.0
Cp 80 80
γ1 52 54
K11 13.6 13.2
K22 6.8 6.6
K33 16.2 15.8
The vertical dielectric of embodiment 13 lifts 15% or so relative to comparative example 1, can effectively lift the transmitance of liquid crystal display Characteristic, plays transmitance and lifts 3.5% or so, its optical data such as table 17:
Chromaticity coordinates and the transmission measurement result of 17 comparative example 1 of table and embodiment 7
Project Comparative example 1 Embodiment 13
Colour temperature 7901.68 7954.82
Brightness 24.1847 25.0311
x 0.2947 0.2934
y 0.3105 0.3103
Compositionss proposed by the invention have big vertical dielectric, can effectively lift the light transmission rate of liquid crystal display, tool Body implementation is to add the compound that I classes contain dioxygen heterocycle, and which has the induced electrical polarity of big vertical direction, so tool There is big vertical dielectric;The rotary viscosity of liquid crystal media is reduced using class ii compound, is reached with this and be there is fast corresponding and height The liquid crystal media of transmitance, liquid crystal media provided by the present invention using with TN, IPS, FFS type liquid crystal display, especially fit With IPS and FFS type liquid crystal displays.
Although above the present invention is described in detail with a general description of the specific embodiments, in the present invention On the basis of, it can be made some modifications or improvements, this will be apparent to those skilled in the art.Therefore, not Deviate these modifications or improvements on the basis of present invention spirit, belong to the scope of protection of present invention.

Claims (10)

  1. It is 1. a kind of to contain dioxygen heterocycle and 2- methyl -3, the liquid crystal media of the compound of 4,5- trifluorophenyls, it is characterised in that:
    Comprising the compound representated by least one or more of formula I:
    Wherein, R1Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;
    A1Represent:
    A2Represent:
    N and m represent 0 or 1 independently of one another;
    And, the compound representated by least one formula II:
    Wherein, R2Represent C1~C12Straight chained alkyl;R3Represent C1~C12Straight chained alkyl, wherein one or more are non-conterminous CH2Can be replaced by O, CH=CH;A3、A4Trans Isosorbide-5-Nitrae-cyclohexyl or Isosorbide-5-Nitrae-phenylene is represented independently of one another.
  2. 2. liquid crystal media according to claim 1, it is characterised in that:The liquid crystal media includes following percentage by weight Component:
    1), the compound representated by 1%~60% one or more formula I;
    2), the compound representated by 1%~70% one or more formula II;
    3), the compound representated by 0%~40% one or more general formula III;
    4), the compound representated by 0%~40% one or more formula IV;
    5), the compound representated by 0%~60% one or more formula V~formula IX;
    Wherein, R4Represent C1~C12Straight chained alkyl;L1Represent H or F;P=0 or 1;
    A3It is each to represent:
    Wherein, R5Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R6Represent C1~C12Straight chained alkyl;
    A4Represent:
    Wherein, R7、R9C is represented independently of one another1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R8、R10、R11、 R12C is represented independently of one another1~C12Straight chained alkyl;X1、X2、X4F, CF is represented independently of one another3、OCF3Or OCF2H; X3Represent F, CF3、OCF3And C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;L2、L3、L4、L5、L6、 L7、L8、L9、L10、L11、L12H or F is represented independently of one another;
    A5、A6Represent independently of one another:
    A7Represent:
    A8、A9Represent independently of one another:
  3. 3. liquid crystal media according to claim 2, it is characterised in that:The liquid crystal media includes following percentage by weight Component:
    1), the compound representated by 5%~30% one or more formula I;
    2), the compound representated by 15%~60% one or more formula II;
    3), the compound representated by 0%~30% one or more general formula III;
    4), the compound representated by 5%~30% one or more formula IV;
    5), the compound representated by 10%~50% one or more formula V~formula IX;
    Preferably, the liquid crystal media includes following components in percentage by weight:
    1), the compound representated by 7%~27% one or more formula I;
    2), the compound representated by 42%~57% one or more formula II;
    3), the compound representated by 9%~24% one or more formula IV;
    4), the compound representated by 12%~29% one or more formula V~formula IX;
    Or
    1), the compound representated by 5%~13% one or more formula I;
    2), the compound representated by 19%~45% one or more formula II;
    3), the compound representated by 6.5%~26% one or more general formula III;
    4), the compound representated by 6%~25% one or more formula IV;
    5), the compound representated by 14%~47% one or more formula V~formula IX;
    Or
    1), the compound representated by the logical formula (I) of one or more of 5%~27%;
    2), the compound representated by the logical formula (II) of one or more of 19%~45.5%;
    3), the compound representated by the logical formula (III) of one or more of 0%~26%;
    4), the compound representated by the logical formula (IV) of one or more of 6%~25%;
    5), the compound representated by the logical formula V of one or more of 0%~42%~logical formula (VII)
    6), the compound representated by the logical formula (VIII) of one or more of 4%~19%
    7), the compound representated by the logical formula (IX) of one or more of 0%~6%.
  4. 4. the liquid crystal media according to any one of claim 1-3, it is characterised in that:Chemical combination representated by the formula I One or more in Formulas I-A~Formulas I-F of thing:
    Wherein, R1Represent C1~C7Straight chained alkyl;
    Preferably, one or more in Formulas I-A-1~Formulas I-F-4 of the compound representated by formula I:
  5. 5. the liquid crystal media according to any one of claim 1-4, it is characterised in that:Chemical combination representated by the formula II One or more in Formula II-A~Formula II-C of thing:
    Wherein, R2Represent C1~C7Straight chained alkyl;R3Represent C1~C7Straight chained alkyl, wherein one or more are non-conterminous CH2Can be replaced by O or CH=CH;
    Preferably, one or more in Formula II-A-1~Formula II-C-25 of the compound representated by formula II:
  6. 6. the liquid crystal media according to any one of claim 1-5, it is characterised in that:Chemical combination representated by the general formula III One or more in formula III-A~formula III-H of thing:
    Wherein, R4Represent C1~C7Straight chained alkyl;
    Preferably, R4Represent C2~C5Straight chained alkyl.
  7. 7. the liquid crystal media according to any one of claim 1-6, it is characterised in that:Chemical combination representated by the formula IV One or more in formula IV-A~formula IV-C of thing:
    Wherein, R5Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;R6Represent C1~C7Straight chained alkyl;
    Preferably, R5Represent C2~C5Straight chained alkyl or straight-chain alkenyl, R6Represent C1~C5Straight chained alkyl.
  8. 8. the liquid crystal media according to any one of claim 1-7, it is characterised in that:Compound described in formula V is selected from One or more in Formula V-A~Formula V-K:
    Wherein, R7Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;
    One or more in Formula IV-A~Formula IV-P of compound representated by the formula VI:
    Wherein, R8Represent C1~C7Straight chained alkyl;
    One or more in Formula VII-A~Formula VII-G of compound described in the formula VII:
    Wherein, R9、X3C is represented independently of one another1~C5Straight chained alkyl or C2~C5Straight-chain alkenyl;
    One or more in Formula VIII-A~Formula VIII-L of compound described in the formula VIII:
    Wherein, R10Represent C1~C7Straight chained alkyl;
    One or more in Formula IX-A~Formula IX-C of compound described in the formula IX:
    Wherein, R11、R12C is represented independently of one another1~C7Straight chained alkyl.
  9. 9. liquid crystal media according to claim 8, it is characterised in that:R7Represent C2~C5Straight chained alkyl or straight-chain alkenyl; R8、R9、R10、R11、R12C is represented independently of one another2~C5Straight chained alkyl.
  10. 10. application of the liquid crystal media in liquid crystal indicator described in any one of claim 1-9, it is characterised in that:Described Liquid crystal indicator is TN, FFS or IPS display.
CN201510587485.3A 2015-09-15 2015-09-15 Liquid crystal media and its application Active CN106520138B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201510587485.3A CN106520138B (en) 2015-09-15 2015-09-15 Liquid crystal media and its application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510587485.3A CN106520138B (en) 2015-09-15 2015-09-15 Liquid crystal media and its application

Publications (2)

Publication Number Publication Date
CN106520138A true CN106520138A (en) 2017-03-22
CN106520138B CN106520138B (en) 2019-01-29

Family

ID=58349128

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510587485.3A Active CN106520138B (en) 2015-09-15 2015-09-15 Liquid crystal media and its application

Country Status (1)

Country Link
CN (1) CN106520138B (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106916595A (en) * 2015-12-28 2017-07-04 北京八亿时空液晶科技股份有限公司 A kind of nematic phase liquid crystal composition and its application
CN106916594A (en) * 2015-12-28 2017-07-04 北京八亿时空液晶科技股份有限公司 A kind of big dielectric anisotropy liquid crystal composition and its application
JP2018502979A (en) * 2015-03-13 2018-02-01 北京八億時空液晶科技股▲ふん▼有限公司Beijing Bayi Space Lcd Technology Co.,Ltd Liquid crystal composition and use thereof
JP2018502978A (en) * 2015-01-21 2018-02-01 北京八億時空液晶科技股▲ふん▼有限公司Beijing Bayi Space Lcd Technology Co.,Ltd Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and use thereof
CN108659857A (en) * 2017-03-30 2018-10-16 江苏和成显示科技有限公司 Liquid-crystal composition with positive dielectric anisotropy and its display device

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004315819A (en) * 2003-04-11 2004-11-11 Merck Patent Gmbh Liquid crystal medium
CN104610983A (en) * 2015-01-21 2015-05-13 北京八亿时空液晶科技股份有限公司 Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and application of liquid crystal composition
CN104673323A (en) * 2015-02-04 2015-06-03 北京八亿时空液晶科技股份有限公司 Liquid crystal composition containing 2-methyl-3,4,5-trifluorophenyl liquid crystal compound and application thereof
CN104774623A (en) * 2015-03-13 2015-07-15 北京八亿时空液晶科技股份有限公司 Liquid crystal composition and applications thereof

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004315819A (en) * 2003-04-11 2004-11-11 Merck Patent Gmbh Liquid crystal medium
CN104610983A (en) * 2015-01-21 2015-05-13 北京八亿时空液晶科技股份有限公司 Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and application of liquid crystal composition
CN104673323A (en) * 2015-02-04 2015-06-03 北京八亿时空液晶科技股份有限公司 Liquid crystal composition containing 2-methyl-3,4,5-trifluorophenyl liquid crystal compound and application thereof
CN104774623A (en) * 2015-03-13 2015-07-15 北京八亿时空液晶科技股份有限公司 Liquid crystal composition and applications thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2018502978A (en) * 2015-01-21 2018-02-01 北京八億時空液晶科技股▲ふん▼有限公司Beijing Bayi Space Lcd Technology Co.,Ltd Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and use thereof
JP2018502979A (en) * 2015-03-13 2018-02-01 北京八億時空液晶科技股▲ふん▼有限公司Beijing Bayi Space Lcd Technology Co.,Ltd Liquid crystal composition and use thereof
CN106916595A (en) * 2015-12-28 2017-07-04 北京八亿时空液晶科技股份有限公司 A kind of nematic phase liquid crystal composition and its application
CN106916594A (en) * 2015-12-28 2017-07-04 北京八亿时空液晶科技股份有限公司 A kind of big dielectric anisotropy liquid crystal composition and its application
CN106916595B (en) * 2015-12-28 2019-06-28 北京八亿时空液晶科技股份有限公司 A kind of nematic phase liquid crystal composition and its application
CN108659857A (en) * 2017-03-30 2018-10-16 江苏和成显示科技有限公司 Liquid-crystal composition with positive dielectric anisotropy and its display device
CN108659857B (en) * 2017-03-30 2022-03-11 江苏和成显示科技有限公司 Liquid crystal composition having positive dielectric anisotropy and display device thereof

Also Published As

Publication number Publication date
CN106520138B (en) 2019-01-29

Similar Documents

Publication Publication Date Title
CN103740377B (en) Liquid crystal composition and application thereof
CN106554783B (en) A kind of liquid-crystal composition and its application with high transmittance
CN104673323B (en) A kind of liquid-crystal composition containing 2-methyl-3,4,5-trifluoro-benzene liquid-crystal compounds and application thereof
CN103756686B (en) A kind of High-contrast liquid crystal composition and application thereof
CN104610983B (en) Liquid crystal composition containing 2-methyl-3,4,5-trifluorobenzene liquid crystal compound and application of liquid crystal composition
CN103937508B (en) A kind of liquid-crystal composition of threshold voltage stabilization and application thereof
CN107189792B (en) A kind of positive and negative mixed liquid crystal composition and its application
CN106883865B (en) A kind of negative dielectric anisotropy liquid crystal composition containing benzofuran and its application
CN103642502B (en) A kind of liquid-crystal composition containing dioxygen heterocycle structure compound and application thereof
CN106520138B (en) Liquid crystal media and its application
CN106883864B (en) A kind of nematic phase liquid crystal composition and its application
CN104263382B (en) Containing liquid-crystal composition and the application thereof of 1,3-diox and difluoro-methoxy bridged bond compound
CN106544040A (en) A kind of liquid-crystal composition with high reliability and its application
CN104293358B (en) A kind of liquid-crystal composition containing 1,3-bis-hydride compounds and application thereof
CN106367081B (en) A kind of fast-response liquid-crystal composition and its application
CN107267157A (en) A kind of negative dielectric anisotropy liquid crystal composition and its application
CN104087313B (en) A kind of liquid-crystal composition and application thereof
CN108659860A (en) A kind of liquid-crystal composition containing fluoroethoxy compound and its application
CN108728114A (en) Liquid crystal media and its application
CN109722256A (en) A kind of liquid-crystal composition and its application
CN108690637A (en) A kind of liquid-crystal composition containing fluoroethoxy compound and its application
CN109722255A (en) Containing 2- methyl -3,4, the liquid-crystal composition of 5- trifluoro-benzene structural compounds and its application
CN108659861A (en) A kind of liquid-crystal composition and its application with high transmittance
CN107177359A (en) A kind of negative dielectric anisotropy liquid crystal composition containing cyclobutenyl bridged bond and its application
CN107345142A (en) It is a kind of containing how ring negative dielectric anisotropy liquid crystal composition and its application

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant