CN108728119A - A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application - Google Patents

A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application Download PDF

Info

Publication number
CN108728119A
CN108728119A CN201710261802.1A CN201710261802A CN108728119A CN 108728119 A CN108728119 A CN 108728119A CN 201710261802 A CN201710261802 A CN 201710261802A CN 108728119 A CN108728119 A CN 108728119A
Authority
CN
China
Prior art keywords
general formula
compound representated
liquid
crystal composition
compound
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.)
Pending
Application number
CN201710261802.1A
Other languages
Chinese (zh)
Inventor
陈卯先
陈海光
姜天孟
王杰
储士红
未欣
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 CN201710261802.1A priority Critical patent/CN108728119A/en
Publication of CN108728119A publication Critical patent/CN108728119A/en
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K19/00Liquid crystal materials
    • C09K19/04Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
    • C09K19/42Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
    • C09K19/44Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing compounds with benzene rings directly linked
    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/1303Apparatus specially adapted to the manufacture of LCDs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Nonlinear Science (AREA)
  • Materials Engineering (AREA)
  • Organic Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Liquid Crystal Substances (AREA)

Abstract

The present invention relates to field of liquid crystal display more particularly to a kind of nematic phase liquid crystal composition containing fluoroethoxy structure, the composition includes at least the compound representated by a kind of general formula I:And the compound representated by least one general formula II;Wherein, the compound representated by general formula I is the liquid-crystal compounds for containing 2,3- difluorobenzene structures, such compound has larger negative dielectric anisotropic and high clearing point;Compound representated by general formula II is the liquid-crystal compounds that two rings have 2,3-, bis- fluoro- Isosorbide-5-Nitrae-phenyl, and end uses fluoroethoxy structure, the dielectric anisotropy of liquid-crystal compounds is substantially improved.Liquid-crystal composition provided by the present invention has low rotary viscosity, good low temperature intersolubility and fast response time, is suitable for VA classes liquid crystal display device and IPS, the FFS mode liquid crystal display devices such as VA/MVA/PVA/PSVA.It is highly effective for the response time for improving liquid crystal display.

Description

A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application
Technical field
The present invention relates to a kind of liquid-crystal composition, specifically a kind of nematic phase liquid crystal composition, exactly this hair Bright provided liquid-crystal composition has negative dielectric anisotropy, more specifically in liquid-crystal composition provided by the present invention Liquid-crystal compounds containing fluoroethoxy structure belongs to liquid crystal material and its application field.
Background technology
Currently, liquid crystal is widely applied in field of information display, while the application in optical communication also achieves one Fixed progress (S.T.Wu, D.K.Yang.Reflective Liquid Crystal Displays.Wiley, 2001).It is close several Year, the application field of liquid-crystal compounds significantly widens kinds of displays part, electro-optical device, electronic component, sensor etc., Nematic liquid crystal compound obtains most commonly used application in flat-panel monitor, is especially used for tft active matrix In system.
Liquid crystal display experienced very long road for development with the discovery of liquid crystal.Austrian botanist in 1888 Friedrich Reinitzer are found that the first liquid crystal material benzoic acid cholesterol (cholesteryl benzoate). Manguin has invented rubbing within 1917, to make single domain liquid crystal and research optical anisotropy.E.Bose in 1909 Moving (Swarm) theory is established, and (1918) are supported in the experiment for obtaining L.S.Ormstein and F.Zernike et al., after It is discussed as statistical fluctuation through De Gennes.G.W.Oseen and H.Zocher founded continuum theory in 1933, and obtained F.C.Frank perfect (1958).M.Born (1916) and K.Lichtennecker (nineteen twenty-six) has found and has studied liquid crystal Dielectric anisotropy.1932, nematic phase was divided into positive and negative property two major classes by W.Kast accordingly.Nineteen twenty-seven, V.Freedericksz and V.Zolinao has found that nematic liquid crystal under electric field or magnetic fields, deforms upon and there are voltages Threshold value (Freederichsz transformations).This making for being found to be liquid crystal display provides foundation.
Nineteen sixty-eight RCA Corp. of U.S. R.Williams finds that nematic liquid crystal forms striped farmland under electric field action, and has Light scattering phenomenon.With dynamic scattering display pattern is developed into and first liquid crystal in the world is made in G.H.Heilmeir Display (LCD).Early seventies, Helfrich and Schadt have invented TN principles, and people are using TN photoelectric effect and integrate Circuit is combined, and is made display device (TN-LCD), and wide foreground has been opened up for 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 Twisred Nematic:STN) pattern And active matrix (the Active matrix that P.Brody was proposed in 1972:AM) mode is used again.Traditional TN- LCD technology has developed into STN-LCD and TFT-LCD technologies, although the number of scanning lines of STN up to 768 rows more than, work as temperature The problems such as response speed, visual angle and gray scale are remained when raising, therefore large area, high information quantity, colored display are mostly Using Active Matrix LCD At mode.TFT-LCD is widely used for direct viewing type TV, large-curtain projecting TV set, terminal Display and certain military instrument are shown, it is believed that TFT-LCD technologies have more wide application prospect.
Wherein " active matrix " includes two types:1, the OMS on the silicon wafer as substrate (partly lead by metal oxide Body) or other diodes.2, the thin film transistor (TFT) on the glass plate as substrate (TFT).
Monocrystalline silicon limits display size as substrate material, because each section display device even module assembled is tied at it Occur many problems at conjunction.Thus, second of thin film transistor (TFT) is the promising active matrix type of tool, the photoelectricity effect utilized Should be typically TN effects.TFT includes compound semiconductor, such as Cdse, or the TFT based on polycrystalline or amorphous silicon.
Negative liquid crystal is most proposed earlier than the end of the eighties in last century, is mainly used for VA patterns, major advantage is to compare Degree is high, and major defect is that visual angle is small, and the response time is slow.With the development of display technology, the technologies such as MVA, PVA, PSVA go out in succession It is existing, solve the problems, such as response time and visual angle.In recent years, as touch screen becomes the mobile device market mainstream, IPS and FFS The hard panel type display of class has inborn advantage, IPS and FFS class displays that can both use positivity liquid crystal, can also use negativity Liquid crystal, due to being bent electric field present in the class display, positivity liquid crystal is arranged along electric field line direction, curved so as to cause molecule Song, and decline in transmitance;Negative liquid crystal is arranged perpendicular to electric field line direction, thus transmitance can be substantially improved, and be current It promotes transmitance, reduce backlight power consumption the best way.But response time problem existing for negative liquid crystal is the weight currently encountered Hang-up, the FFS display response times slow 50% or more using the FFS displays of negative liquid crystal relative to positivity liquid crystal. Therefore, how to promote the response time of negative liquid crystal becomes current key problem.
Invention content
Since the response time of liquid crystal display depends on (d^2 γ 1)/Keff, (d is thickness of liquid crystal layer, and γ 1 revolves for liquid crystal Turn viscosity, Keff is effective elastic constant), therefore, rotary viscosity is reduced, thickness of liquid crystal layer is reduced and promotes elastic constant To achieve the purpose that improve the response time, thickness of liquid crystal layer depends on the design of liquid crystal display;And for liquid-crystal composition, drop Low rotary viscosity and thickness of liquid crystal are most effective.The present invention provides a kind of completely new nematic phase liquid containing fluoroethoxy structure Crystal composite can be effectively reduced the response time of liquid crystal display with low rotary viscosity.
Specifically, composition of the present invention contains the nematic phase liquid crystal composition of fluoroethoxy structure, at least wrap Containing the compound representated by a kind of general formula I:
R1Represent C1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl;A1Selected from trans- Isosorbide-5-Nitrae-hexamethylene Base or Isosorbide-5-Nitrae-phenylene.
And the compound representated by least one general formula II:
Wherein, R2Represent C1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl;A2Trans- 1 is represented, 4- cyclohexyl, 1,4- phenylenes.
Compound representated by general formula I provided by the invention is to contain the liquid-crystal compounds (end group of 2,3- difluorobenzene structures For-OCH2CH2F), such compound has larger negative dielectric anisotropic and high clearing point, is used for liquid of the present invention The negative dielectric anisotropic and clearing point of composition can be promoted in crystal composite.End group can be promoted significantly using fluoroethoxy Dielectric anisotropic, the dielectric anisotropic for can effectively promote liquid-crystal composition in liquid-crystal composition reduce polar monomer It uses, increases low viscosity monomer and use, reduce the rotary viscosity of liquid-crystal composition, promote the response time of display.
In liquid-crystal composition provided by the invention, in the case where the quality summation of its all components is 100%, general formula I The content of the compound in the composition is advisable 5~70%, and preferably 8~60% or 13~65%;More preferable 30~ 60%, 5~35%, 16~57%, 10~49% or 8~55%;Alternatively, the content of compound in the composition described in general formula I It is advisable 10~57%, preferably 10~41%, 38~57% or 29~42%;More preferable 19~34%, 49~57% or 33 ~39%;It is more advantageous to the display performance for meeting liquid crystal display at this time, reduces the response time of liquid crystal display.
Specifically, the compound representated by ideal general formula I is selected from one kind of the compound representated by Formulas I A~Formulas I B Or it is several:
Wherein, R1Represent C1~C7Straight chained alkyl, C2~C7Straight-chain alkenyl.
Preferably, the compound representated by general formula I is selected from one kind of the compound representated by Formulas I A1~IA8, IB1~IB8 Or it is several:
Wherein, when the compound representated by the general formula I selects IA2, IA3, IA4, IA5, IA6, IB2 and IB3, in the present invention Application effect in the liquid-crystal composition is especially prominent.
Liquid-crystal composition of the present invention further comprises the compound representated by least one general formula II, the general formula II Representative compound is the liquid-crystal compounds that two rings have bis- fluoro- 1,4- phenyl of 2,3-, and end uses fluoroethoxy knot Structure (- OCH2CH2F), the dielectric anisotropy of liquid-crystal compounds is substantially improved, being used for can in liquid-crystal composition of the present invention Improve the intersolubility of liquid-crystal composition and promote the negative dielectric anisotropic of liquid-crystal composition, reduces polar compound and use, increase Neutral low viscosity component uses, and realizes the viscosity for reducing liquid-crystal composition, promotes the purpose of liquid crystal display response time, The low temperature phase transition temperature for widening liquid-crystal composition simultaneously, improves the low temperature intersolubility of liquid-crystal composition.
In liquid-crystal composition provided by the invention, in the case where the quality summation of its all components is 100%, general formula II The content of the compound in the composition is advisable 1~40%, and preferably 3~35%;More preferable 5~30%, 3~20% or 10~35%;Alternatively, the content of compound in a liquid crystal composition described in general formula II is 5~30%, preferably 7~28%, 11 ~18%, 5~20%;More preferable 15~17% or 12~17%, it is more advantageous to the low temperature intersolubility of crystal composite and low at this time Rotary viscosity.
Specifically, the compound representated by ideal general formula II is one or more in IIA or IIB:
Wherein, R3Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl.
Preferably, the compound representated by general formula II is one or more in IIA1~IIA8, IIB1~IIB6:
Wherein, when the compound representated by the general formula II selects IIA2, IIA3, IIA5, IIB3, IIB4 and IIB5, at this The application effect invented in the liquid-crystal composition is especially prominent.
In addition, liquid-crystal composition provided by the present invention can also further include one or more general formula III institute's generations The compound of table:
Wherein, R3、R4C is represented each independently1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl; A3、A4Trans- 1,4- cyclohexyl or 1,4 phenylenes are represented each independently.
Compound representated by general formula III provided by the invention is twin nuclei, is added in liquid-crystal composition and helps In coordinating the compound representated by general formula I and general formula II of the present invention, further decrease liquid-crystal composition viscosity and Increase intersolubility, improve the response time of liquid crystal display and widens the low-temperature working temperature of liquid crystal display.
In liquid-crystal composition provided by the invention, in the case where the quality summation of its all components is 100%, general formula The content of compound described in III in the composition is advisable 5~70%, and preferably 15~60%;More preferable 18~56%, 15~ 35%, 30~60% or 20~45%;Alternatively, when compound described in liquid-crystal composition includes the general formula III, in group The content in object is closed 19~56%, preferably 23~50%, 18~36% or 22~43%;More preferable 21~31% or 25~ 35%;It is more advantageous to the response time for improving liquid crystal display and the operating temperature for widening liquid crystal display at this time.
Specifically, the compound representated by ideal general formula III is selected from the one or more of following compound:
Wherein, R4Represent C1~C7Straight chained alkyl;R5Represent C1~C7Straight chained alkyl, unbranched alkoxy or C2~C7's Straight-chain alkenyl.
Preferably, the compound representated by general formula III be selected from formula III A1~IIIA34, IIIB1~IIIB24, IIIC1~ The one or more of compound representated by IIIC24:
Wherein, compound selection IIIA1, IIIA2 representated by the general formula III, IIIA16, IIIA18, IIIA22, When IIIA23, IIIB18, IIIB22, IIIC2, IIIC4, IIIC15 and IIIC16, in liquid-crystal composition of the present invention Application effect is especially prominent.
Further, liquid-crystal composition provided by the present invention can also include one or more is selected from representated by general formula IV Compound:
R5、R6C is represented each independently1~C12Straight chained alkyl, wherein one or more non-conterminous CH2Can by O or CH=CH replaces.
A5Selected from lower structure:
Compound representated by general formula IV of the present invention has high clearing point and big elastic constant, is used for this hair The clearing point and elastic constant of liquid-crystal composition can be promoted in the bright liquid-crystal composition.Liquid-crystal composition provided by the invention In, in the case where the quality summation of its all components is 100%, the content of compound in the composition is 0 described in general formula IV ~45% is advisable, and preferably 0~35%;More preferable 0~25%, 1~35% or 4~30%;Alternatively, compound described in general formula IV Content in a liquid crystal composition is 0~30%, preferably 4~30% or 4~22%;More preferable 10~24% or 7~16%. It is more advantageous to the performance requirement for adapting to liquid crystal display at this time, reduces the rotary viscosity of liquid-crystal composition, promotes liquid crystal display Response time;Liquid crystal display quality problem caused by elastic constant is smaller is solved simultaneously, as image retention restores.
Preferably, the compound representated by general formula IV of the present invention is selected from one kind of formula IV A~following compounds of formula IV C Or it is a variety of:
Wherein, R5Represent C2~C10Straight chained alkyl or straight-chain alkenyl;R6Represent C1~C8Straight chained alkyl.
It is highly preferred that compound representated by general formula IV is selected from formula IV A1~IVA18, IVB1~IVB22, IVC1~IVC30 It is one or more in structure:
Wherein, the compound representated by the general formula IV selects IVA1, IVA2, IVA8, IVA12, IVA16, IVB3, IVB12 And when IVB16, the application effect in liquid-crystal composition of the present invention is especially prominent.
Further, liquid-crystal composition provided by the present invention can also include one or more is selected from representated by general formula V Compound:
Wherein, R7Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R8Represent F, C1~C12Straight chain alkane Base, unbranched alkoxy C2~C12Straight-chain alkenyl;L1、L2、L3H or F is represented each independently.
Compound representated by general formula V of the present invention has big optical anisotropy, for of the present invention The optical anisotropy of liquid-crystal composition can be promoted in liquid-crystal composition, reduce and liquid-crystal composition optical anisotropy component is provided Use, increase low viscosity monomer use, realize reduce liquid-crystal composition rotary viscosity, when promoting the response of liquid crystal display Between.
In liquid-crystal composition provided by the invention, in the case where the quality summation of its all components is 100%, general formula V The content of the compound in the composition is advisable 0~30%, preferably 0-20%;More preferable 1~20% or 5~15%; Alternatively, the content of compound in a liquid crystal composition is in 0~15%, preferably 5~15% described in general formula V;More preferable 8~ 11%, it is more advantageous to the performance requirement for adapting to liquid crystal display to liquid-crystal composition at this time, the rotation for reducing liquid-crystal composition is viscous Degree, improves the response time of liquid crystal display.
Preferably, the compound representated by general formula V is selected from one or more in lower structure;
Wherein, R7Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl, R8Represent C1~C7Straight chained alkyl, straight Chain alkoxy or C2~C7Straight-chain alkenyl.
It is highly preferred that compound representated by general formula V be selected from Formula V A1~VA4, VB1~VB24, VC1~VC14, VD1~ It is one or more in VD24:
Wherein, when the compound representated by the general formula V selects VA3, VB14, VB21, VB22, VC3 and VC4, in the present invention Application effect in the liquid-crystal composition is especially prominent.
To ensure to realize significantly more synergistic effect in composition of the present invention between each component, to effectively improve The integrated application performance of liquid crystal material is stated, the present invention has further carried out the dosage of the middle each component of the liquid crystal material excellent Choosing.
For specific, liquid-crystal composition provided by the present invention includes following components:
Compound representated by (1) 5~70% general formula I;
Compound representated by (2) 1~40% general formula II;
Compound representated by (3) 5~70% general formula IIIs;
Compound representated by (4) 0~45% general formula IV;
Compound representated by (5) 0~30% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 18~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 30~60% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~55% general formula IIIs;
Compound representated by (4) 0~25% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 30~57% general formula I;
Compound representated by (2) 5~29% general formula II;
Compound representated by (3) 18~53% general formula IIIs;
Compound representated by (4) 0~22% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 5~35% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~10% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~35% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 7~30% general formula IV;
Compound representated by (5) 0~8.5% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 13~65% general formula I;
Compound representated by (2) 15~35% general formula II;
Compound representated by (3) 15~53% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 16~57% general formula I;
Compound representated by (2) 15~30% general formula II;
Compound representated by (3) 18~49% general formula IIIs;
Compound representated by (4) 0~24% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 3~20% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 18~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 15~60% general formula I;
Compound representated by (2) 10~35% general formula II;
Compound representated by (3) 15~35% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 19~57% general formula I;
Compound representated by (2) 15~29% general formula II;
Compound representated by (3) 18~35% general formula IIIs;
Compound representated by (4) 0~24% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~55% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 30~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~49% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 30~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 35~65% general formula I;
Compound representated by (2) 10~30% general formula II;
Compound representated by (3) 15~35% general formula IIIs;
Compound representated by (4) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 38~57% general formula I;
Compound representated by (2) 11~24% general formula II;
Compound representated by (3) 18~32% general formula IIIs;
Compound representated by (4) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~50% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 1~35% general formula IV;
Compound representated by (5) 0~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~42% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 4~30% general formula IV;
Compound representated by (5) 0~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 25~60% general formula I;
Compound representated by (2) 3~25% general formula II;
Compound representated by (3) 15~45% general formula IIIs;
Compound representated by (4) 0~25% general formula IV;
Compound representated by (5) 1~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 29~57% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 18~43% general formula IIIs;
Compound representated by (4) 0~22% general formula IV;
Compound representated by (5) 5~15% general formula V.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~45% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 1~35% general formula IV.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~41% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 5~30% general formula IV.
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 25~45% general formula I;
Compound representated by (2) 3~25% general formula II;
Compound representated by (3) 20~45% general formula IIIs;
Compound representated by (4) 1~25% general formula IV;
Compound representated by (5) 1~20% general formula V.
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 29~42% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 22~43% general formula IIIs;
Compound representated by (4) 4~22% general formula IV;
Compound representated by (5) 5~15% general formula V.
In addition, in practice, it has been found that when liquid-crystal composition each component content of the present invention selects following range, answer It is especially prominent with performance:
Compound representated by (1) 50~60% general formula I;
Compound representated by (2) 20~30% general formula II;
Compound representated by (3) 15~25% general formula IIIs;
Or:
Compound representated by (1) 38~57% general formula I;
Compound representated by (2) 11~18% general formula II;
Compound representated by (3) 18~36% general formula IIIs;
Compound representated by (4) 5~15% general formula V;
It is preferred that:
Compound representated by (1) 49~57% general formula I;
Compound representated by (2) 15~17% general formula II;
Compound representated by (3) 21~31% general formula IIIs;
Compound representated by (4) 6~15% general formula V;
Or:
Compound representated by (1) 10~41% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 4~30% general formula IV;
It is preferred that:
Compound representated by (1) 19~34% general formula I;
Compound representated by (2) 7~28% general formula II;
Compound representated by (3) 23~50% general formula IIIs;
Compound representated by (4) 10~24% general formula IV;
Or:
Compound representated by (1) 29~42% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 22~43% general formula IIIs;
Compound representated by (4) 4~22% general formula IV;
Compound representated by (5) 5.5~15% general formula V;
It is preferred that:
Compound representated by (1) 33~39% general formula I;
Compound representated by (2) 12~17% general formula II;
Compound representated by (3) 25~35% general formula IIIs;
Compound representated by (4) 7~16% general formula IV;
Compound representated by (5) 8~11% general formula V.
Unless otherwise specified, the sum of the gross mass percentage of each component is 100% in liquid-crystal composition of the present invention.
Compounds of formula I provided by the present invention is that tricyclic contains 2,3- difluorobenzene class formation compounds, which is Negative dielectric anisotropic liquid crystal compound uses fluoroethoxy structure, by the study found that replacing second using fluorine in end After oxygroup, the negative dielectric anisotropic of the structure is increased dramatically, and only making exemplary part of compounds, test result is as follows:
The above comparison is it can be found that the compound of fluoroethoxy proposed by the invention has big negative dielectric respectively to different Property, the negative dielectric anisotropic of liquid-crystal composition can be effectively promoted, reducing polar monomer uses, and increases low viscosity monomer and uses, The rotary viscosity of reduction system promotes the response time.
Compound representated by general formula II of the present invention is the liquid-crystal compounds that two rings contain 2,3- difluorobenzenes, is adopted in end With fluoroethoxy structure, after the study found that replacing ethyoxyl using fluorine, negative dielectric anisotropic is increased dramatically, Only making exemplary part of compounds, test result is as follows:
The above comparison is it can be found that the compound of fluoroethoxy proposed by the invention has big negative dielectric respectively to different Property, the negative dielectric anisotropic of liquid-crystal composition can be effectively promoted, reducing polar monomer uses, and increases low viscosity monomer and uses, The rotary viscosity of reduction system promotes the response time.In addition, the compound representated by general formula III is twin nuclei, have low Rotary viscosity and excellent intersolubility feature are the essential component of fast-response liquid crystal display, the chemical combination representated by general formula IV Object is nonpolar tricyclic compound, such monomer has high clearing point and big elastic constant, is conducive to improve liquid crystal combination The elastic constant of object;Compound representated by general formula V has big optical anisotropy, for promoting the dielectric of liquid-crystal composition Anisotropy is highly effective.
The various combinations of above-mentioned five kinds of liquid-crystal compounds as described above are (wherein, representated by general formula I and general formula II Compound be essential component, remaining be optional component) combination formed liquid-crystal composition can realize ideal application Effect.It should be strongly noted that when liquid-crystal composition of the present invention is three components composition, preferably it is combined as leading to Compound representated by Formulas I+general formula II+ general formula IIIs;When liquid-crystal composition of the present invention is four components composition, reason The compound being combined as representated by general formula I+ general formulas II+ general formula IIIs+general formula IV or general formula I+ general formula II+ general formula IIIs thought+logical Compound representated by Formula V, to realize synergy of more preferably arranging in pairs or groups.
The preparation method of liquid-crystal composition of the present invention can be used conventional method and change two or more without specifically limited It closes object mixing to be produced, such as be prepared by the method for mixing different component at high temperature and being soluble in one another, wherein by liquid crystal group It closes object to be dissolved in the solvent for the compound and mix, then distills out the solvent under reduced pressure;Or it is of the present invention Liquid-crystal composition can be prepared conventionally, and the smaller component of wherein content is such as dissolved in content at a higher temperature In larger key component, or each affiliated component dissolved in organic solvent, such as acetone, chloroform or methanol, it then will be molten It is obtained after liquid mixing removal solvent.
Liquid-crystal composition provided by the present invention has low rotary viscosity, good low temperature intersolubility and fast response Time is suitable for VA classes liquid crystal display device and IPS, the FFS mode liquid crystal display devices such as VA/MVA/PVA/PSVA.For The response time for improving liquid crystal display is highly effective.
Specific implementation mode
The following examples are used to illustrate the present invention, but are not intended to limit the scope of the present invention..
Unless otherwise indicated, percentage is weight percentage in the present invention;Temperature unit is degree Celsius;Δ n represents optics Anisotropy (25 DEG C);Δ ε represents dielectric anisotropy (25 DEG C, 1000Hz);V10Threshold voltage is represented, is in relative permeability Character voltage (V, 25 DEG C) when changing 10%;γ 1 represents rotary viscosity (mPa.s, 25 DEG C);Cp represents the clear of liquid-crystal composition Bright spot (DEG C);K11、K22、K33Respectively represent splay, distortion and bend elastic constant (pN, 25 DEG C).
In following embodiment, unit structure code shown in table 1 indicates in liquid-crystal compounds.
Table 1:The group structure code of liquid-crystal compounds
By taking following compound structure as an example:
It is expressed as:3CCWO2F
It is expressed as:3PGIWO2
In following embodiment, the preparation of liquid-crystal composition is all made of heat of solution method, includes the following steps:It is pressed with balance Weight percent weighs liquid-crystal compounds, wherein weighing addition sequence without particular requirement, usually with liquid-crystal compounds fusing point by height Mixing is weighed successively to low sequence, heating stirring makes each component melt uniform at 60~100 DEG C, using filter, rotates, It finally encapsulates up to target sample.
In following embodiment, involved liquid crystal components are known compound, can such as may be used by commercially available It is provided by Beijing Bayi Space LCD Materials Technology Co., Ltd..
In following embodiment, the performance parameter of the weight percent of each component when liquid-crystal composition is shown in liquid-crystal composition Following table.
Embodiment 1
Table 2:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 2
Table 3:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 3
Table 4:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 4
Table 5:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 5
Table 6:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 6
Table 7:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 7
Table 8:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 8
Table 9:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 9
Table 10:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 10
Table 11:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 11
Table 12:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 12
Table 13:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 13
Table 14:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 14
Table 15:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 15
Table 16:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 16
Table 17:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 17
Table 18:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 18
Table 19:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 19
Table 20:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 20
Table 21:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 21
Table 22:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 22
Table 23:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 23
Table 24:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 24
Table 25:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 25
Table 26:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 26
Table 27:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 27
Table 28:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 28
Table 29:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 29
Table 30:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 30
Table 31:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 31
Table 32:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 32
Table 33:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 33
Table 34:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 34
Table 35:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 35
Table 36:The percentage of each component when performance parameter in liquid-crystal composition
Embodiment 36
Table 37:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 37
Table 38:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 38
Table 39:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 39
Table 40:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 40
Table 41:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 41
Table 42:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 42
Table 43:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 43
Table 44:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 44
Table 45:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 45
Table 46:The weight percent of each component when performance parameter in liquid-crystal composition
Embodiment 46
Table 47:The weight percent of each component when performance parameter in liquid-crystal composition
Comparative example 1
Table 48:The weight percent of each component when performance parameter in liquid-crystal composition
Compared with embodiment 1 is summarized with each performance parameter value of 1 gained liquid-crystal composition of comparative example, referring to table 49.
Table 49:The performance parameter of liquid-crystal composition compares
Δn Δε Cp γ1 K11 K22 K33
Embodiment 1 0.108 -3.8 90 80 14.8 7.4 16.8
Comparative example 1 0.108 -3.8 90 96 14.7 7.4 16.5
Known to relatively:Compared with comparative example 1, the liquid-crystal composition that embodiment 1 provides has low rotary viscosity, that is, has There is the faster response time.
As seen from the above embodiment, liquid-crystal composition provided by the present invention has low viscosity, high resistivity, suitable light Anisotropy, good low temperature intersolubility, big elastic constant and excellent photostability and thermal stability are learned, liquid can be reduced The response time of crystal display, to solve the problems, such as that liquid crystal display response speed is slow.Therefore, liquid crystal provided by the present invention Composition is suitable for VA display patterns and IPS the and FFS type TFT liquid crystal display devices such as VA/MVA/PVA/PSVA.
Although above the present invention is described in detail with a general description of the specific embodiments, On the basis of the present invention, it can be made some modifications or improvements, this will be apparent to those skilled in the art.Cause This, these modifications or improvements, belong to the scope of protection of present invention without departing from theon the basis of the spirit of the present invention.

Claims (10)

1. a kind of nematic phase liquid crystal composition containing fluoroethoxy structure, which is characterized in that include at least one general formula I institutes Compound representated by the compound of representative and at least one general formula II;
The general formula I is specially:
R1Represent C1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl;A1Selected from trans- Isosorbide-5-Nitrae-cyclohexyl or Isosorbide-5-Nitrae-phenylene;
The general formula II is specially:
Wherein, R2Represent C1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl;A2Represent trans- 1,4- rings Hexyl, 1,4- phenylenes.
2. liquid-crystal composition according to claim 1, which is characterized in that compound representated by general formula I be selected from Formulas I A~ The one or more of compound representated by IB:
Wherein, R1Represent C1~C7Straight chained alkyl, C2~C7Straight-chain alkenyl;
Preferably, the compound representated by general formula I is selected from one kind or several of the compound representated by Formulas I A1~IA8, IB1~IB8 Kind:
3. liquid-crystal composition according to claim 1 or 2, which is characterized in that compounds of formula II is selected from IIA and IIB In it is one or more:
Wherein, R3Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl;
Preferably, the compound representated by general formula II is one or more in IIA1~IIA8, IIB1~IIB6:
4. the liquid crystal according to claims 1 to 3 any one closes object, which is characterized in that also include one or more general formulas The compound of III;The general formula III is specially:
Wherein, R3、R4C is represented each independently1~C12Straight chained alkyl, unbranched alkoxy or C2~C12Straight-chain alkenyl;A3、A4 Trans- 1,4- cyclohexyl or 1,4 phenylenes are represented each independently;
Preferably, the compound representated by the general formula III is one or more in IIIA~IIIC:
Wherein, R4Represent C1~C7Straight chained alkyl;R5Represent C1~C7Straight chained alkyl, unbranched alkoxy or C2~C7Straight chain Alkenyl;
It is highly preferred that compound representated by general formula III be selected from formula III A1~IIIA34, IIIB1~IIIB24, IIIC1~ The one or more of compound representated by IIIC24:
5. according to the liquid-crystal composition described in Claims 1 to 4 any one, which is characterized in that also include one or more choosings The compound of self-drifting IV structures;The general formula IV is specially:
R5、R6C is represented each independently1~C12Straight chained alkyl, wherein one or more non-conterminous CH2It can be by O or CH= CH replaces;
A5Selected from lower structure:
Preferably, the compound representated by general formula IV is one or more in formula IV A~formula IV C:
Wherein, R5Represent C2~C10Straight chained alkyl or straight-chain alkenyl;R6Represent C1~C8Straight chained alkyl;
It is highly preferred that compound representated by general formula IV is selected from formula IV A1~IVA18, IVB1~IVB22, IVC1~IVC30 structures In it is one or more:
6. according to the liquid-crystal composition described in Claims 1 to 5 any one, which is characterized in that also include one or more choosings The compound of self-drifting V;The general formula V is specially:
Wherein, R7Represent C1~C12Straight chained alkyl or C2~C12Straight-chain alkenyl;R8Represent F, C1~C12Straight chained alkyl, straight Chain alkoxy C2~C12Straight-chain alkenyl;L1、L2、L3H or F is represented each independently;
Preferably, compounds of formula V is one or more in VA~VD;
Wherein, R7Represent C1~C7Straight chained alkyl or C2~C7Straight-chain alkenyl, R8Represent C1~C7Straight chained alkyl, straight chain alkane Oxygroup or C2~C7Straight-chain alkenyl;
It is highly preferred that the compound representated by general formula V is selected from Formula V A1~VA4, VB1~VB24, VC1~VC14, VD1~VD24 In it is one or more:
7. according to the liquid-crystal composition described in claim 1~6 any one, which is characterized in that including following components:
Compound representated by (1) 5~70% general formula I;
Compound representated by (2) 1~40% general formula II;
Compound representated by (3) 5~70% general formula IIIs;
Compound representated by (4) 0~45% general formula IV;
Compound representated by (5) 0~30% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 18~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 30~60% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~55% general formula IIIs;
Compound representated by (4) 0~25% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 30~57% general formula I;
Compound representated by (2) 5~29% general formula II;
Compound representated by (3) 18~53% general formula IIIs;
Compound representated by (4) 0~22% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 5~35% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~10% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~35% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 7~30% general formula IV;
Compound representated by (5) 0~8.5% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 13~65% general formula I;
Compound representated by (2) 15~35% general formula II;
Compound representated by (3) 15~53% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 16~57% general formula I;
Compound representated by (2) 15~30% general formula II;
Compound representated by (3) 18~49% general formula IIIs;
Compound representated by (4) 0~24% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 3~20% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 18~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 15~60% general formula I;
Compound representated by (2) 10~35% general formula II;
Compound representated by (3) 15~35% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 19~57% general formula I;
Compound representated by (2) 15~29% general formula II;
Compound representated by (3) 18~35% general formula IIIs;
Compound representated by (4) 0~24% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~55% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 30~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~49% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 30~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 35~65% general formula I;
Compound representated by (2) 10~30% general formula II;
Compound representated by (3) 15~35% general formula IIIs;
Compound representated by (4) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 38~57% general formula I;
Compound representated by (2) 11~24% general formula II;
Compound representated by (3) 18~32% general formula IIIs;
Compound representated by (4) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~50% general formula I;
Compound representated by (2) 3~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 1~35% general formula IV;
Compound representated by (5) 0~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~42% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 4~30% general formula IV;
Compound representated by (5) 0~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~60% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 0~35% general formula IV;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~57% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 0~30% general formula IV;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 25~60% general formula I;
Compound representated by (2) 3~25% general formula II;
Compound representated by (3) 15~45% general formula IIIs;
Compound representated by (4) 0~25% general formula IV;
Compound representated by (5) 1~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 29~57% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 18~43% general formula IIIs;
Compound representated by (4) 0~22% general formula IV;
Compound representated by (5) 5~15% general formula V;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 8~45% general formula I;
Compound representated by (2) 5~35% general formula II;
Compound representated by (3) 15~60% general formula IIIs;
Compound representated by (4) 1~35% general formula IV;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 10~41% general formula I;
Compound representated by (2) 7~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 5~30% general formula IV;
Preferably, the liquid-crystal composition includes following components:
Compound representated by (1) 25~45% general formula I;
Compound representated by (2) 3~25% general formula II;
Compound representated by (3) 20~45% general formula IIIs;
Compound representated by (4) 1~25% general formula IV;
Compound representated by (5) 1~20% general formula V;
It is highly preferred that the liquid-crystal composition includes following components:
Compound representated by (1) 29~42% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 22~43% general formula IIIs;
Compound representated by (4) 4~22% general formula IV;
Compound representated by (5) 5~15% general formula V.
8. according to the liquid-crystal composition described in claim 1~6 any one, which is characterized in that the liquid-crystal composition includes Following components:
Compound representated by (1) 50~60% general formula I;
Compound representated by (2) 20~30% general formula II;
Compound representated by (3) 15~25% general formula IIIs;
Or:
Compound representated by (1) 38~57% general formula I;
Compound representated by (2) 11~18% general formula II;
Compound representated by (3) 18~36% general formula IIIs;
Compound representated by (4) 5~15% general formula V;
It is preferred that:
Compound representated by (1) 49~57% general formula I;
Compound representated by (2) 15~17% general formula II;
Compound representated by (3) 21~31% general formula IIIs;
Compound representated by (4) 6~15% general formula V;
Or:
Compound representated by (1) 10~41% general formula I;
Compound representated by (2) 5~30% general formula II;
Compound representated by (3) 19~56% general formula IIIs;
Compound representated by (4) 4~30% general formula IV;
It is preferred that:
Compound representated by (1) 19~34% general formula I;
Compound representated by (2) 7~28% general formula II;
Compound representated by (3) 23~50% general formula IIIs;
Compound representated by (4) 10~24% general formula IV;
Or:
Compound representated by (1) 29~42% general formula I;
Compound representated by (2) 5~20% general formula II;
Compound representated by (3) 22~43% general formula IIIs;
Compound representated by (4) 4~22% general formula IV;
Compound representated by (5) 5.5~15% general formula V;
It is preferred that:
Compound representated by (1) 33~39% general formula I;
Compound representated by (2) 12~17% general formula II;
Compound representated by (3) 25~35% general formula IIIs;
Compound representated by (4) 7~16% general formula IV;
Compound representated by (5) 8~11% general formula V.
9. liquid-crystal composition according to claim 7 or 8, which is characterized in that each component is total in the liquid-crystal composition The sum of mass percent is 100%.
10. application of the liquid-crystal composition in liquid crystal display device described in claim 1~9 any one, preferably in fast-response Application in liquid crystal display device, more preferably in VA classes liquid crystal display device and IPS, FFS mode liquid crystal display device Using;The VA classes liquid crystal display device is preferably VA/MVA/PVA/PSVA.
CN201710261802.1A 2017-04-20 2017-04-20 A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application Pending CN108728119A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710261802.1A CN108728119A (en) 2017-04-20 2017-04-20 A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710261802.1A CN108728119A (en) 2017-04-20 2017-04-20 A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application

Publications (1)

Publication Number Publication Date
CN108728119A true CN108728119A (en) 2018-11-02

Family

ID=63933162

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710261802.1A Pending CN108728119A (en) 2017-04-20 2017-04-20 A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application

Country Status (1)

Country Link
CN (1) CN108728119A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110373210A (en) * 2019-08-07 2019-10-25 西安近代化学研究所 A kind of liquid-crystal compounds and combinations thereof containing difluoroethoxy
CN111718726A (en) * 2019-03-21 2020-09-29 北京八亿时空液晶科技股份有限公司 Liquid crystal compound with negative dielectric anisotropy as well as preparation method and application thereof
CN112080287A (en) * 2019-06-14 2020-12-15 石家庄诚志永华显示材料有限公司 Liquid crystal composition, liquid crystal display element and liquid crystal display

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1026142A1 (en) * 1997-10-24 2000-08-09 Chisso Corporation 2,3-difluorophenyl derivatives having negative value of permittivity anisotropy, liquid-crystal composition, and liquid-crystal display element
US20110240921A1 (en) * 2008-12-10 2011-10-06 Jnc Corporation Liquid crystal composition and liquid crystal display device
CN103890140A (en) * 2012-02-24 2014-06-25 Dic株式会社 Liquid crystal composition
CN103958644A (en) * 2011-09-27 2014-07-30 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same
CN104004527A (en) * 2014-05-07 2014-08-27 北京八亿时空液晶科技股份有限公司 Liquid crystal compound and its preparation method and use
CN104136575A (en) * 2011-12-21 2014-11-05 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same
CN104603235A (en) * 2012-09-11 2015-05-06 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1026142A1 (en) * 1997-10-24 2000-08-09 Chisso Corporation 2,3-difluorophenyl derivatives having negative value of permittivity anisotropy, liquid-crystal composition, and liquid-crystal display element
US20110240921A1 (en) * 2008-12-10 2011-10-06 Jnc Corporation Liquid crystal composition and liquid crystal display device
CN103958644A (en) * 2011-09-27 2014-07-30 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same
CN104136575A (en) * 2011-12-21 2014-11-05 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same
CN103890140A (en) * 2012-02-24 2014-06-25 Dic株式会社 Liquid crystal composition
CN104603235A (en) * 2012-09-11 2015-05-06 Dic株式会社 Nematic liquid crystal composition and liquid crystal display element using same
CN104004527A (en) * 2014-05-07 2014-08-27 北京八亿时空液晶科技股份有限公司 Liquid crystal compound and its preparation method and use

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111718726A (en) * 2019-03-21 2020-09-29 北京八亿时空液晶科技股份有限公司 Liquid crystal compound with negative dielectric anisotropy as well as preparation method and application thereof
CN111718726B (en) * 2019-03-21 2022-02-22 北京八亿时空液晶科技股份有限公司 Liquid crystal compound with negative dielectric anisotropy as well as preparation method and application thereof
CN112080287A (en) * 2019-06-14 2020-12-15 石家庄诚志永华显示材料有限公司 Liquid crystal composition, liquid crystal display element and liquid crystal display
CN112080287B (en) * 2019-06-14 2023-08-29 石家庄诚志永华显示材料有限公司 Liquid crystal composition, liquid crystal display element and liquid crystal display
CN110373210A (en) * 2019-08-07 2019-10-25 西安近代化学研究所 A kind of liquid-crystal compounds and combinations thereof containing difluoroethoxy
CN110373210B (en) * 2019-08-07 2021-12-21 西安近代化学研究所 Difluoroethoxy-containing liquid crystal compound and composition thereof

Similar Documents

Publication Publication Date Title
CN106883865B (en) A kind of negative dielectric anisotropy liquid crystal composition containing benzofuran and its application
CN103740377B (en) Liquid crystal composition and application thereof
CN106554783B (en) A kind of liquid-crystal composition and its application with high transmittance
CN103756686B (en) A kind of High-contrast liquid crystal composition and application thereof
CN106883864B (en) A kind of nematic phase liquid crystal composition and its application
CN107189792B (en) A kind of positive and negative mixed liquid crystal composition and its application
CN108728114A (en) Liquid crystal media and its application
CN108659860A (en) A kind of liquid-crystal composition containing fluoroethoxy compound and its application
CN111575022A (en) Negative liquid crystal composition with terminal alkene structure and application thereof
CN111607412B (en) High-gradient fast-response negative dielectric anisotropy liquid crystal composition and application thereof
CN109423301A (en) A kind of negative dielectric anisotropy liquid crystal composition and its application
CN103642502A (en) Liquid crystal composition containing compound with dioxygen heterocyclic structure and application of liquid crystal composition
CN108728119A (en) A kind of fast-response negative dielectric anisotropy liquid crystal composition and its application
CN107267157A (en) A kind of negative dielectric anisotropy liquid crystal composition and its application
CN108690637A (en) A kind of liquid-crystal composition containing fluoroethoxy compound and its application
CN110093166A (en) A kind of liquid-crystal composition containing from orientation compound and its application
CN109423303A (en) A kind of negative dielectric liquid crystal composition containing benzofuran compound and its application
CN108728113A (en) A kind of nematic phase liquid crystal composition containing fluoroethoxy structure and its application
CN108728115A (en) A kind of negative dielectric nematic phase liquid crystal composition and its application
CN109722256A (en) A kind of liquid-crystal composition and its application
CN108659861A (en) A kind of liquid-crystal composition and its application with high transmittance
CN109722255A (en) Containing 2- methyl -3,4, the liquid-crystal composition of 5- trifluoro-benzene structural compounds and its application
CN107177359B (en) Negative dielectric anisotropy liquid crystal composition containing butenyl bridged bond and application thereof
CN108690635A (en) A kind of negative dielectric anisotropy liquid crystal composition 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
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20181102