CN101665701A - Nematic liquid crystal composition - Google Patents

Nematic liquid crystal composition Download PDF

Info

Publication number
CN101665701A
CN101665701A CN200910093625A CN200910093625A CN101665701A CN 101665701 A CN101665701 A CN 101665701A CN 200910093625 A CN200910093625 A CN 200910093625A CN 200910093625 A CN200910093625 A CN 200910093625A CN 101665701 A CN101665701 A CN 101665701A
Authority
CN
China
Prior art keywords
compounds
crystal composition
liquid
content
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.)
Granted
Application number
CN200910093625A
Other languages
Chinese (zh)
Other versions
CN101665701B (en
Inventor
陈海光
杭德余
姜天孟
田会强
王广涛
储士红
张嫣然
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 LIQUID CRYSTAL MATERIALS SCI-TECH Co Ltd
Beijing Bayi Space LCD Technology Co Ltd
Original Assignee
BEIJING BAYI SPACE LIQUID CRYSTAL MATERIALS SCI-TECH 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 LIQUID CRYSTAL MATERIALS SCI-TECH Co Ltd filed Critical BEIJING BAYI SPACE LIQUID CRYSTAL MATERIALS SCI-TECH Co Ltd
Priority to CN 200910093625 priority Critical patent/CN101665701B/en
Publication of CN101665701A publication Critical patent/CN101665701A/en
Application granted granted Critical
Publication of CN101665701B publication Critical patent/CN101665701B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention relates to a nematic liquid crystal composition which comprises the following components: 5-50 percent of compound I, 1-60 percent of compounds II, 0-30 percent of compounds III, 5-40 percent of compounds IV, 0-50 percent of compounds V, 0-30 percent of compounds VI and 0.05-0.5 percent of optical activity components. The liquid crystal composition has excellent performance, very short total response time (ttot=ton+toff), lower voltage, high resistivity and voltage conservation rate, and can have Delta n characteristics and different threshold voltages through adjusting the content of each component. The liquid crystal composition is suitable to manufacture a TN-LCD, and is especially suitable to manufacture a TNTFT-LCD with rapid response.

Description

A kind of nematic liquid crystal composition
Technical field
The present invention relates to a kind of liquid crystal material technical field, it is little to relate to a kind of viscosity specifically, transformation temperature wide ranges, resistivity and voltage retention height, the nematic liquid crystal composition that driving voltage is low.
Background technology
Liquid-crystal display (LCD) obtains people's extensive concern as an important application of this exotic materials of liquid crystal always.Nearly decades, particularly fast development of information technology and people are to the continuous pursuit of information display mode in recent ten years, and liquid-crystal display has obtained the swiftest and the most violent development.Today, liquid-crystal display just is illustrated in face of the people with colourful form, and its many products are because its excellent characteristic makes its pursuit that becomes fashion, and processs the commodity that hand can get in the market.
Liquid-crystal display follows the discovery of liquid crystal to experience very long road for development.Austrian botanist Friedrich Reinitzer had found first kind of liquid crystal material in 1888--M-nitro benzoic acid cholesterol (cholesteryl benzoate).Manguin had invented the directed method of friction in 1917, in order to make single domain liquid crystal and research optical anisotropy.E.Bose in 1909 has set up and has collected together (Swarm) theory, and obtains people's such as L.S.Ormstein and F.Zernike experiment support (1918), after De Gennes is discussed as statistical fluctuation.G.W.Oseen and H.Zocher1933 found the continuum theory, and obtain F.C.Frank perfect (1958).M.Born (1916) and K.Lichtennecker (nineteen twenty-six) have found and have studied the dielectric anisotropy of liquid crystal.1932, W.Kast was divided into nematic phase positive and negative property two big classes in view of the above.Nineteen twenty-seven, V.Freedericksz and V.Zolinao find that nematic liquid crystal under electric field (or magnetic field) effect, deformation takes place and have voltage threshold (Freederichsz transformation).This making that is found to be liquid-crystal display provides foundation.
The nineteen sixty-eight R.Williams of U.S. RCA Corp. finds that nematic liquid crystal forms the striped farmland under electric field action, and light scattering phenomenon is arranged.G.H.Heilmeir develops into the dynamic scattering display format with being about to it, and makes first liquid-crystal display (LCD) in the world.People such as nineteen sixty-eight U.S. Heilmeir have also proposed guest-host effect (GH) pattern.Xerox company proposed Ch-N phase change memory pattern in 1969.M.F.Schiekel proposed electrically conerolled birefringence (ECB) pattern in 1971, T.L.Fergason etc. propose twisted-nematic phase (Twisted Nematic:TN) pattern, N.Clark in 1980 etc. propose ferroelectric liquid crystal mode (FLC), and 1983~1985 years people such as T.Scheffer successively propose active matrix (Active matrix:AM) mode that supertwist nematic phase (Super Twisred Nematic:STN) pattern and P.Brody proposed in 1972 and adopted again.Nagata in 1986 proposes to realize the white and black displays technology with double-deck box (DSTN); Useful again afterwards stretching polymeric membrane is realized the technology (FSTN) of white and black displays.After 1996, propose to adopt the reflective TN (RTN) and reflective STN (RSTN) pattern of single polaroid again.
At present, active matrix (active matrix) liquid-crystal display is owing to its high resolving power, high-contrast, and the slim and light characteristics of amount more and more are subjected to people's favor.Present main flow LCD is TFT (thin film transistor) liquid-crystal display that belongs to the active matrix type.
Different with the simple matrix of passive TN-LCD, STN-LCD, active matrix all is provided with a thin film transistor (TFT) on each pixel of liquid crystal display, crosstalking in the time of to overcome non-gating effectively, make the static characteristics and the number of scanning lines that show liquid crystal display irrelevant, therefore improved picture quality greatly.
The application of TFT-LCD starts to walk from small-sized consumption electronic product, and then finds its opportunity to develop in the PC industry, and especially popularizing of notebook computer promoted the demand of small-medium size panel.The TFT-LCD technique of display has the whole market share in notebook computer market at present, and the beginning vast scale is penetrated into the desktop computer monitor market.Simultaneously, TFT-LCD TV market starts and develops rapidly, and forms industry size.
In the TFT-LCD field, the division of labor of large size panel and small-medium size panel is relatively clear and definite.The Application Areas of large size TFT-LCD panel is more concentrated, mainly is indicating meter and LCD TV, small-medium size TFT-LCD panel, and Application Areas is more extensive with respect to large size, is mainly used in fields such as communication, consumer electronics, mobile office.The communications field mainly is a mobile phone, comprises Personal Handyphone System (PHS), smart mobile phone etc.Consumer electronics is used a lot, and will enrich constantly, mainly contain global positioning system (GPS) (GPS), MP3, MP4, portable electronic device (PMP), mobile DVD, digital camera, pick up camera, digital frame, PDA(Personal Digital Assistant), game machine, printer etc. are a feast for the eyes.Mobile office mainly is the super OLPC (one lap per child) that can take PC (UMPC) and be positioned at student market.In addition, Vehicular display device and medical treatment, industrial instrument are also increasing sharply to the demand of small-medium size TFT-LCD panel.
At present, the TFT-LCD product technology is ripe, has successfully solved technical barriers such as visual angle, resolving power, fullness of shade and brightness, its display performance near or surpass CRT monitor.Large size and small-medium size TFT-LCD indicating meter occupy the dominant position of flat-panel monitor gradually in field separately.
But owing to be subjected to the restriction of liquid crystal material itself, it is fast inadequately that TFT-LCD still exists response, and voltage is low inadequately, the high inadequately many defectives of electric charge conservation rate.
Therefore, it is little that the present invention proposes a kind of viscosity, the transformation temperature wide ranges, and resistivity and voltage retention height, driving voltage is low, can be used for making the nematic liquid crystal composition of the TFT of quick response with TN-LCD.
Summary of the invention
The purpose of this invention is to provide a kind of nematic liquid crystal composition, its viscosity is little, the transformation temperature wide ranges, and resistivity and voltage retention height, driving voltage is low, can be used for making the nematic liquid crystal composition of the TFT of quick response with TN-LCD.
Nematic liquid crystal composition of the present invention comprises each component of following weight percent:
(1) the I compounds of 5-50%;
(2) the II compounds of 1-60%;
(3) the III compounds of 0-30%;
(4) the IV compounds of 5-40%;
(5) the V compounds of 0-50%;
(6) the VI compounds of 0-30%.
(7) the opticity component of 0.05-0.5%.
The chemical formula of described I compounds is as follows:
Figure G2009100936256D00041
Wherein, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1, L 2And L 3Independent of each other is H or F.
The compound of Formula I representative has big Δ ε and little rotary viscosity, and has low fusing point, can effectively reduce the threshold voltage of mixed liquid crystal, reduces time of response and the low temperature mutual solubility of improving mixed liquid crystal simultaneously.
I compounds of the present invention is preferably as follows one or more in the compound of structure:
Figure G2009100936256D00042
R wherein 2Be the alkyl of 2-5 carbon atom, one of them or two non-conterminous groups can be replaced by-CH=CH-.
In the liquid-crystal composition of the present invention, the IA of I compounds, IB, IC, the content of ID compounds is respectively 0-20%, and particularly preferred content is 3-15%.
In the compound of the preferred especially following structure of I compounds of the present invention one or more:
Figure G2009100936256D00051
Figure G2009100936256D00061
I A-2 most preferably, I A-3, I A-4, I B-2, I B-3, I D-2, one or more in the compounds such as I D-4.
Described II compounds is with following chemical formulation:
Figure G2009100936256D00062
Wherein, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1, L 2And L 3Independent of each other is H or F or Cl.
This compounds has little specific refractory power anisotropy, characteristics such as low viscosity, and have moderate Δ ε and clearing point, can effectively adjust threshold voltage and widen nematic temperature range.
II compounds of the present invention is preferably as follows one or more in the compound of structure:
Figure G2009100936256D00063
Figure G2009100936256D00071
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-.
The preferred 5-45% of content of the II compounds among the present invention.
In the liquid-crystal composition of the present invention, II category-A compounds content is 0-20%; The content of II category-B compound is 0-20%; The content of II C compounds is 0-30%; The content of II D compounds is 0-40%.
In the preferred especially following compound of II compounds of the present invention one or more:
Figure G2009100936256D00072
III compounds of the present invention is with following chemical formulation:
Figure G2009100936256D00082
Wherein, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1Be H or F, W 1For-OCF 2H or-OCF 3
This compounds has big Δ ε, and higher refrigerant point and moderate viscosity can effectively reduce the threshold voltage of mixed liquid crystal.
III compounds of the present invention is preferably as follows one or more in the compound of structure:
Figure G2009100936256D00083
Figure G2009100936256D00091
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-.
The content of the III compounds among the present invention is preferably 0-20%;
In the liquid-crystal composition of the present invention, III category-A compounds content is 0-15%; The content of IIIB compounds is 0-15%; The content of IIIC compounds is 0-15%; The content of IIID compounds is 0-15%; The content of IIIE compounds is 0-15%.
In the preferred especially compound shown below of III compounds of the present invention one or more:
Figure G2009100936256D00092
Figure G2009100936256D00101
IV compounds of the present invention is as follows:
Figure G2009100936256D00102
Wherein, R 1, R 2Independent of each other is the alkyl of 0-12 carbon atom, one or two non-conterminous group can by-CH=CH-or-O-replaces, wherein,
Figure G2009100936256D00111
For
Figure G2009100936256D00112
Or
This compounds has extremely low viscosity, can effectively reduce the overall viscosity of design of mixture, thereby accelerates the time of response.
The content of IV compounds is preferably 5-35% among the present invention;
The content of any compound in the liquid-crystal composition of the present invention in the IV compounds is no more than 20%.
In the preferred compound shown below of IV compounds of the present invention one or more:
Figure G2009100936256D00121
V compounds of the present invention is shown below:
Wherein, R 1, R 2Independent of each other is the alkyl of 0-12 carbon atom, one or two non-conterminous group can by-CH=CH-or-O-replaces.
This compounds has lower viscosity and bigger K33/K11, has moderate clearing point and Δ n, and a part that can be used as mixed liquid crystal main body composition is adjusted over-all properties.
In the preferred compound shown below of V compounds of the present invention one or more:
Figure G2009100936256D00123
The content of any compound in the liquid-crystal composition of the present invention in the V compounds is no more than 20%.For adjusting the over-all properties of mixed liquid crystal, V compounds of the present invention preferred especially V-1, V-3 and V-5.
VI compounds of the present invention is shown below:
Figure G2009100936256D00131
Wherein, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-; L 1Independent of each other with L2 is F or H.
This compounds has higher clearing point, is used for widening the nematic phase upper temperature limit of mixed liquid crystal, thereby widens the operating temperature range of LCD.
In the preferred following compounds of VI compounds of the present invention one or more:
Figure G2009100936256D00132
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-.
The present invention is preferred especially but be not limited in the following compound one or more:
Figure G2009100936256D00133
The content of VI compounds is 0-30% among the present invention, and preferred content is 1-20%.
In the liquid-crystal composition of the present invention, the content of any compound of VI compounds is for being no more than 8%.
Opticity component of the present invention in addition, as S811, R811 etc., its content are 0.05-0.5%, particularly preferred is 0.07-0.15%.
Particularly preferred, described liquid-crystal composition of the present invention comprises following components in weight percentage:
(1) the I compounds of 5-50%;
(2) the II compounds of 5-45%;
(3) the III compounds of 0-20%;
(4) the IV compounds of 5-35%;
(5) the V compounds of 0-30%, wherein preferred especially V-1, V-3 and V-5,
(6) the VI compounds of 1-20%.
(7) the opticity component of 0.07-0.2%.
Nematic liquid crystal composition of the present invention, one or more that can also contain common nematic liquid crystal monomer, disc-like liquid crystal monomer, cholesteric liquid crystal monomers etc. are as the component (non-additive) among the present invention.
Liquid-crystal composition of the present invention can adopt ordinary method that two or more liquid crystalline cpds are mixed and produce, as at high temperature mixing different components and dissolved method preparation each other, wherein, liquid-crystal composition is dissolved in solvent and the mixing that is used for this compound, under reduced pressure distills out this solvent then; Liquid-crystal composition perhaps of the present invention can be according to trendy styles from Hong Kong preparation method's preparation of routine, the less component of content is dissolved under higher temperature in the bigger main ingredient of content as inciting somebody to action wherein, or component is dissolved in organic solvent under seeing each, as acetone, chloroform or methyl alcohol etc., solution is mixed obtaining after solvent is removed in the back then.
By the nematic liquid crystal composition excellent performance that the present invention obtains, have low-down overall response time (ttot=ton+toff), have lower voltage, high resistivity and voltage retention.By the adjustment to each component concentration, nematic liquid crystal composition of the present invention can have different threshold voltages and Δ n characteristic, can make client usually used four bottles or six bottles system, is convenient to use under the thick and different driving voltage at different boxes.
Above-mentioned nematic liquid-crystal composition is applicable to TN-LCD, is specially adapted to make the TNTFT-LCD of quick response.
Embodiment
Following examples are used to illustrate the present invention, but are not used for limiting the scope of the invention.
The parameter characteristic that needs in an embodiment to measure adopts following abbreviation:
Cp clearing point (nematic phase-isotropic phase transition temperature)
S → N smectic-nematic Phase temperature
η volume viscosity (mm 2/ s, 20 ℃)
Δ ε dielectric constant anisotropy (20 ℃, 1000Hz)
Δ n optical anisotropy (20 ℃, 589nm)
The character voltage of V10 threshold voltage=when relative 10% contrast gradient (V, 20 ℃)
The character voltage of V90 saturation voltage=when relative 90% contrast gradient (V, 20 ℃)
S electricity aberration inducing curve steepness=V90/V10
τ ton+toff (time of response) (ms)
Time when ton connects when reaching maximum countrast 90%
Time when toff cuts off when reaching maximum countrast 10%
In addition, in the composition of following embodiment, all ℃ to provide, " % " means " quality % " to all temperature.The distortion angle of used test box is 90 °.
Comparative Examples
Prepare a kind of liquid-crystal composition that does not contain the I compounds by the proportioning shown in the table 1, and measure its performance perameter as stated above, performance perameter also is shown in Table 1:
The proportioning of the liquid-crystal composition of table 1 Comparative Examples and performance perameter
Obviously, with the liquid-crystal composition comparison of embodiment 1, its threshold voltage is higher, and the time of response is longer.
Embodiment 1
Get composition I, II, IV, the V of following weight percent, and optically-active compound S811, the configuration liquid-crystal composition, concrete proportioning is as shown in table 2, and the character of the liquid-crystal composition of gained also sees Table 2:
The proportioning of the liquid-crystal composition of table 2 embodiment 1 and performance perameter
Figure G2009100936256D00171
Embodiment 2
Get composition I, II, III, the IV of following weight percent, VI, and optically-active compound S2011, the configuration liquid-crystal composition, concrete proportioning is as shown in table 3, and the character of the liquid-crystal composition of gained also sees Table 3:
The proportioning of the liquid-crystal composition of table 3 embodiment 2 and performance perameter
Figure G2009100936256D00181
Embodiment 3
Get composition I, II, III, IV, the V of following weight percent, VI, and optically-active compound R811, the configuration liquid-crystal composition, concrete proportioning is as shown in table 4, and the character of the liquid-crystal composition of gained also sees Table 4:
The proportioning of the liquid-crystal composition of table 4 embodiment 3 and performance perameter
Figure G2009100936256D00182
Figure G2009100936256D00191
Embodiment 4
Get composition I, II, III, IV, the V of following weight percent, VI, and optically-active compound R1011, the configuration liquid-crystal composition, concrete proportioning is as shown in table 5, and the character of the liquid-crystal composition of gained also sees Table 5:
The proportioning of the liquid-crystal composition of table 5 embodiment 4 and performance perameter
Figure G2009100936256D00192
Obviously, the threshold voltage of the liquid-crystal composition among the embodiment 1-4 reduces greatly, and the time of response accelerates greatly; Compare with the liquid-crystal composition of Comparative Examples, have obvious improvement.
Though above the present invention is described in detail with a general description of the specific embodiments, on basis of the present invention, can make some modifications or improvements it, this will be apparent to those skilled in the art.Therefore, these modifications or improvements all 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 liquid crystal composition comprises each component of following weight percent:
(1) the I compounds of 5-50%;
(2) the II compounds of 1-60%;
(3) the III compounds of 0-30%;
(4) the IV compounds of 5-40%;
(5) the V compounds of 0-50%;
(6) the VI compounds of 0-30%;
(7) the opticity component of 0.05-0.5%;
Wherein, described I compounds is suc as formula shown in the I:
Among the formula I, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1, L 2And L 3Independent of each other is H or F;
Described II compounds is represented with formula II:
Figure A2009100936250002C2
Among the formula II, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1, L 2And L 3Independent of each other is H or F or Cl;
Described III compounds is represented with formula III:
Figure A2009100936250002C3
In the formula III, R 1Be the alkyl of 0-12 carbon atom, one or two non-conterminous group can be replaced L by-CH=CH- 1Be H or F, W 1For-OCF 2H or-OCF 3
Described IV compounds shows with formula IV:
Figure A2009100936250002C4
Among the formula IV, R 1, R 2Independent of each other is the alkyl of 0-12 carbon atom, one or two non-conterminous group can by-CH=CH-or-O-replaces, wherein
Figure A2009100936250003C1
For
Figure A2009100936250003C2
Or
Figure A2009100936250003C3
Described V compounds is with shown in the formula V:
Figure A2009100936250003C4
Among the formula V, R 1, R 2Independent of each other is the alkyl of 0-12 carbon atom, one or two non-conterminous group can by-CH=CH-or-O-replaces;
Shown in the described VI compounds formula VI:
Figure A2009100936250003C5
Among the formula VI, R1 is the alkyl of 0-12 carbon atom, and one or two non-conterminous group can be replaced by-CH=CH-; L1 and L2 are independent of each other to be F or H.
2, liquid-crystal composition as claimed in claim 1 is characterized in that, one or more in the compound that described I compounds is following structure:
Figure A2009100936250003C6
Wherein, R 2Be the alkyl of 2-5 carbon atom, one of them or two non-conterminous groups can be replaced by-CH=CH-;
In the described liquid-crystal composition, IA, IB, IC, the content of ID compounds is respectively 0-20%, and particularly preferred content is 3-15%.
3, liquid-crystal composition as claimed in claim 2 is characterized in that, one or more in the compound that described I compounds is following structure:
Figure A2009100936250004C1
Figure A2009100936250005C1
IA-2 most preferably, IA-3, IA-4, IB-2, IB-3, ID-2, one or more in the ID-4 compound.
4, liquid-crystal composition as claimed in claim 1 is characterized in that, one or more in the compound that described II compounds is following structure:
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-;
In the described liquid-crystal composition, the IIA kind compound content is 0-20%; The content of IIB compounds is 0-20%; The content of IIC compounds is 0-30%; The content of IID compounds is 0-40%.
Described II compounds is preferably one or more in the following compound:
Figure A2009100936250006C1
5, liquid-crystal composition as claimed in claim 1 is characterized in that,, described III compounds is one or more in the following compound:
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-;
In the described liquid-crystal composition, the IIIA kind compound content is 0-15%; The content of IIIB compounds is 0-15%; The content of IIIC compounds is 0-15%; The content of IIID compounds is 0-15%; The content of IIIE compounds is 0-15%;
In the preferred especially compound shown below of described III compounds one or more:
Figure A2009100936250007C3
Figure A2009100936250008C1
Figure A2009100936250009C1
6, liquid-crystal composition as claimed in claim 1 is characterized in that, described IV compounds is one or more in the compound shown below:
Figure A2009100936250009C2
Figure A2009100936250010C1
Wherein, in the described liquid-crystal composition, the content of any compound in the IV compounds is no more than 20%.
7, liquid-crystal composition as claimed in claim 1 is characterized in that, described V compounds is one or more in the compound shown below:
Figure A2009100936250010C2
Wherein in the liquid-crystal composition, the content of any compound in the V compounds is no more than 20%; Described V compounds preferred especially V-1, V-3 and V-5.
8, liquid-crystal composition as claimed in claim 1 is characterized in that, described VI compounds is one or more in the following compounds:
Figure A2009100936250010C3
Figure A2009100936250011C1
R wherein 2Be the alkyl of 2-5 carbon atom, one or two non-conterminous group can be replaced by-CH=CH-;
In the preferred especially following compound of described VI compounds one or more:
Figure A2009100936250011C2
Figure A2009100936250012C1
In the described liquid-crystal composition, the content of any compound in the described VI compounds is for being no more than 8%.
9, as the arbitrary described liquid-crystal composition of claim 1-8, it is characterized in that described liquid-crystal composition comprises following components in weight percentage:
(1) the I compounds of 5-50%;
(2) the II compounds of 5-45%;
(3) the III compounds of 0-20%;
(4) the IV compounds of 5-35%;
(5) the V compounds of 0-30%, wherein preferred especially V-1, V-3 and V-5,
(6) the VI compounds of 1-20%.
(7) the opticity component of 0.07-0.2%.
10, as claim 1 or 9 described liquid-crystal compositions, it is characterized in that, described liquid-crystal composition also contain following one or more as component: disc-like liquid crystal monomer, cholesteric liquid crystal monomers.
CN 200910093625 2009-09-25 2009-09-25 Nematic liquid crystal composition Active CN101665701B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200910093625 CN101665701B (en) 2009-09-25 2009-09-25 Nematic liquid crystal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200910093625 CN101665701B (en) 2009-09-25 2009-09-25 Nematic liquid crystal composition

Publications (2)

Publication Number Publication Date
CN101665701A true CN101665701A (en) 2010-03-10
CN101665701B CN101665701B (en) 2012-12-12

Family

ID=41802484

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200910093625 Active CN101665701B (en) 2009-09-25 2009-09-25 Nematic liquid crystal composition

Country Status (1)

Country Link
CN (1) CN101665701B (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101812301A (en) * 2010-04-16 2010-08-25 北京八亿时空液晶材料科技有限公司 Liquid crystal composition
CN102559202A (en) * 2011-12-30 2012-07-11 北京八亿时空液晶科技股份有限公司 Nematic liquid crystal composition
CN102659533A (en) * 2012-04-10 2012-09-12 江苏和成显示科技股份有限公司 Indene derivative used as component of liquid crystal medium, preparation method thereof and application thereof
CN103224798A (en) * 2013-04-16 2013-07-31 西安彩晶光电科技股份有限公司 Liquid crystal composition with wide nematic phase and low refractivity
CN103242858A (en) * 2013-04-16 2013-08-14 西安彩晶光电科技股份有限公司 Liquid crystal composition with low threshold and high response speed
CN104560054A (en) * 2013-10-22 2015-04-29 江苏和成显示科技股份有限公司 Liquid crystal composition and liquid crystal display device

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE10151300A1 (en) * 2001-10-17 2003-04-30 Merck Patent Gmbh Liquid crystalline compounds
US8486298B2 (en) * 2006-09-01 2013-07-16 Merck Patent Gmbh Liquid-crystalline medium
EP2338953B1 (en) * 2007-02-02 2014-03-19 Merck Patent GmbH Liquid crystalline medium

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101812301A (en) * 2010-04-16 2010-08-25 北京八亿时空液晶材料科技有限公司 Liquid crystal composition
CN102559202A (en) * 2011-12-30 2012-07-11 北京八亿时空液晶科技股份有限公司 Nematic liquid crystal composition
CN102559202B (en) * 2011-12-30 2014-03-19 北京八亿时空液晶科技股份有限公司 Nematic liquid crystal composition
CN102659533A (en) * 2012-04-10 2012-09-12 江苏和成显示科技股份有限公司 Indene derivative used as component of liquid crystal medium, preparation method thereof and application thereof
CN102659533B (en) * 2012-04-10 2015-05-13 江苏和成显示科技股份有限公司 Indene derivative used as component of liquid crystal medium, preparation method thereof and application thereof
CN103224798A (en) * 2013-04-16 2013-07-31 西安彩晶光电科技股份有限公司 Liquid crystal composition with wide nematic phase and low refractivity
CN103242858A (en) * 2013-04-16 2013-08-14 西安彩晶光电科技股份有限公司 Liquid crystal composition with low threshold and high response speed
CN103224798B (en) * 2013-04-16 2014-09-10 西安彩晶光电科技股份有限公司 Liquid crystal composition with wide nematic phase and low refractivity
CN104560054A (en) * 2013-10-22 2015-04-29 江苏和成显示科技股份有限公司 Liquid crystal composition and liquid crystal display device

Also Published As

Publication number Publication date
CN101665701B (en) 2012-12-12

Similar Documents

Publication Publication Date Title
CN103254911B (en) Positive dielectric anisotropy liquid crystal combination with rapid response
CN108659857B (en) Liquid crystal composition having positive dielectric anisotropy and display device thereof
CN103254906B (en) Liquid crystal composition containing difluoro methoxyl ether compounds
CN108219802B (en) Liquid crystal composition and application thereof
CN101665701B (en) Nematic liquid crystal composition
CN105542794A (en) Liquid crystal composition and application thereof
CN102433130A (en) Negative dielectric anisotropic liquid crystal composition and use thereof
CN115287083B (en) Negative dielectric anisotropic liquid crystal composition and liquid crystal display device
CN101407718B (en) Nematic liquid crystal composition
CN111117659A (en) Liquid crystal composition and display device thereof
CN102140350B (en) Nematic liquid crystal composition
CN110452710A (en) A kind of liquid-crystal composition and its application
CN113667493A (en) Liquid crystal composition and liquid crystal display device
CN111117658A (en) Liquid crystal composition and display device thereof
CN103351879B (en) Positive dielectric anisotropic liquid crystal composition
CN108659856B (en) Liquid crystal composition having positive dielectric anisotropy and display device thereof
CN102140349B (en) Pyridine liquid crystal composition for TFT display
CN101608120A (en) A kind of nematic liquid crystal composition
CN111117654B (en) Liquid crystal composition and display device thereof
CN108659859B (en) Liquid crystal composition having positive dielectric anisotropy and display device thereof
CN101812301A (en) Liquid crystal composition
CN112048320B (en) Liquid crystal composition and display device thereof
CN103923662A (en) Dielectric positive liquid-crystal composition
CN111117660B (en) Liquid crystal composition and liquid crystal display device thereof
CN112048319B (en) Liquid crystal composition and display device thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C53 Correction of patent for invention or patent application
CB02 Change of applicant information

Address after: 100085 No. 5, building 1, East Road, Haidian District, Beijing, 701

Applicant after: Beijing Bayi Space LCD Materials Technology Co., Ltd.

Address before: 100085 No. 5, building 1, East Road, Haidian District, Beijing, 701

Applicant before: Beijing Bayi Space Liquid Crystal Materials Sci-tech Co., Ltd.

COR Change of bibliographic data

Free format text: CORRECT: APPLICANT; FROM: BEIJING BAYI SPACE LIQUID CRYSTAL MATERIALS SCI-TECH CO., LTD. TO: BEIJING BAYI SPACE LCD MATERIALS TECHNOLOGY CO., LTD.

C53 Correction of patent for invention or patent application
CB02 Change of applicant information

Address after: 100085 Building No. 2, building 1, ten Street, Haidian District, Beijing, 2013

Applicant after: Beijing Bayi Space LCD Materials Technology Co., Ltd.

Address before: 100085 No. 5, building 1, East Road, Haidian District, Beijing, 701

Applicant before: Beijing Bayi Space LCD Materials Technology Co., Ltd.

C14 Grant of patent or utility model
GR01 Patent grant