CN102352260A - Liquid crystal composition and liquid crystal lens - Google Patents
Liquid crystal composition and liquid crystal lens Download PDFInfo
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- CN102352260A CN102352260A CN2011102139053A CN201110213905A CN102352260A CN 102352260 A CN102352260 A CN 102352260A CN 2011102139053 A CN2011102139053 A CN 2011102139053A CN 201110213905 A CN201110213905 A CN 201110213905A CN 102352260 A CN102352260 A CN 102352260A
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 112
- 239000000203 mixture Substances 0.000 title claims abstract description 77
- 150000001875 compounds Chemical class 0.000 claims abstract description 104
- 125000004432 carbon atom Chemical group C* 0.000 claims description 30
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 5
- 230000004044 response Effects 0.000 abstract description 13
- 230000003287 optical effect Effects 0.000 abstract description 7
- 230000007704 transition Effects 0.000 abstract description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 10
- 230000005684 electric field Effects 0.000 description 6
- 0 CCc(c(-c1cc(*)c(*)c(O)c1)c(*)c(C)c1C2CCC(*)CC2)c1S* Chemical compound CCc(c(-c1cc(*)c(*)c(O)c1)c(*)c(C)c1C2CCC(*)CC2)c1S* 0.000 description 5
- 230000009466 transformation Effects 0.000 description 5
- -1 3,5-difluoro phenylene Chemical group 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 230000009286 beneficial effect Effects 0.000 description 3
- 230000008859 change Effects 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 239000004983 Polymer Dispersed Liquid Crystal Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- MDUQZBFHDPNORI-UHFFFAOYSA-N CCCC(CC1)CCC1c(cc1)ccc1OC Chemical compound CCCC(CC1)CCC1c(cc1)ccc1OC MDUQZBFHDPNORI-UHFFFAOYSA-N 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 210000002858 crystal cell Anatomy 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 230000036314 physical performance Effects 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Liquid Crystal Substances (AREA)
Abstract
The invention discloses a liquid crystal composition, comprising a first variety of compound shown as a general formula I, a second variety of compound shown as a general formula II, a third variety of compound shown as a general formula III and a fourth variety of compound shown as a general formula IV; the invention also provides a liquid crystal lens employing the liquid crystal composition. The liquid crystal composition of the present invention has characteristics of low nematic phase initial voltage, wide phase transition temperature scope, small viscoelastic coefficient ratio gamma 1/K11, large optical anisotropy and large dielectric anisotropy, etc., and can reduce a thickness value of a liquid crystal lens box and increase response speed of the liquid crystal lens box.
Description
Technical field
The present invention relates to technical field of liquid crystal display, particularly relate to a kind of liquid-crystal composition and liquid crystal lens thereof.
Background technology
Devices such as camera, mobile phone camera, the demonstration of 3D stereopsis, phase modulator often utilize zoom lens that image is amplified or dwindles and form images.The traditional zoom camera lens is provided with a plurality of mirror crowds (lens group), through moving along optical axis direction between the mirror crowd, with change spacing each other, thereby whole focal length is changed, but does not influence image-forming range.Yet this kind camera lens needs long mirror crowd miles of relative movement, cause the mechanism volume big, regulate slowly, focusing range is limited, cost an arm and a leg, install that to drive consumed energy big and damage easily etc.
For seeking the method that substitutes mechanical focusing; And can change focal length on a large scale; Prior art utilizes electric field to control the liquid-crystal zoom lens of focal length (Liquid Crystal lens); Form special electric field through on the electrode of band circular hole, applying voltage; Liquid crystal molecule in the electric field is deflected, thereby light is played the effect that disperses or assemble.It is actual to be a kind of simulated optical element, through between electrode, applying the specific optical lens characteristic that different voltages with different can realize easily that we want.
Wherein, column liquid crystal lens grating is a kind of device that utilizes electric field to form lens in the prior art, can realize 3D stereo display.Said column liquid crystal lens grating is through etching the strip transparent ITO electrode on transparent glass substrate; On this electrode, apply different voltages with different then and form electric field; Liquid crystal molecule in the electric field is deflected; Thereby change the incident direction of light, the variation of variation through voltage and number of electrodes simultaneously changes focal length and the pitch of column liquid crystal lens grating etc.
But because each component of liquid-crystal composition has different physicalies, so the parameters combination of each component of liquid-crystal composition has determined each performance of liquid-crystal composition.Wherein, For realizing the superiority of the column physical grating that column liquid crystal lens grating is more traditional; Need column liquid crystal lens grating under 60Hz, 120Hz or higher frequency, can freely switch,, then need a kind of liquid-crystal composition with high speed response property to this.Following relation is arranged between each variable of the liquid-crystal composition relevant with the response performance of column liquid crystal lens grating:
Relational expression one: T
On=(γ 1d
2/ k11 π
2)/[(V/Vth)
2-1]
Relational expression two: T
Off=γ 1d
2/ k11 π
2
Wherein, γ 1 is a rotary viscosity, and d is a thickness of liquid crystal layer, and K11 is the bent elastic constant of exhibition, and V is a driving voltage, and Vth is a threshold voltage.Can find out from the above-mentioned relation formula, the rotary viscosity through reducing liquid-crystal composition or improve it and open up bent elastic constant, or reduce thickness of liquid crystal layer, can shorten its time of response.Yet if reduce rotary viscosity to improve the time of response, bent elastic constant of the exhibition of liquid crystal and transformation temperature also will descend thereupon, and, increase if open up bent elastic constant, then threshold voltage and rotary viscosity will be tending towards increasing.Simultaneously, if will reduce thickness of liquid crystal layer, then the degree of birefringence of liquid-crystal composition will increase, and this can cause rotary viscosity to increase equally.Therefore, for improving the time of response, it is minimum that the equilibrium relationship between these three influence factors must reduce to.
In addition, degree of birefringence also is an important physical characteristic of liquid crystalline cpd.Common TN, STN show that degree of birefringence with liquid crystal material is generally between 0.12 to 0.20; TFT shows that degree of birefringence with liquid crystal material is generally between 0.065 to 0.135; PDLC and multistable show generally need be greater than 0.20 with the degree of birefringence of liquid crystal material, and 3D stereo display generally is greater than 0.25 with the degree of birefringence of the liquid crystal material of liquid crystal lens (Liquid Crystal lens).
Seeing that each components selection of liquid-crystal composition and proportioning have determined each performance of liquid-crystal composition; And the performance perameter of the liquid-crystal composition of prior art fails to realize comparatively ideal combination; Therefore, be necessary further optimization is done in selection of the monomer liquid crystal in the liquid-crystal composition and set of dispense ratio.
Summary of the invention
The technical problem that the present invention mainly solves provides a kind of liquid-crystal composition and liquid crystal lens thereof, fails to realize the problem of more satisfactory combination with the performance perameter of the liquid-crystal composition that solves prior art.
The invention provides a kind of liquid-crystal composition, this liquid-crystal composition comprises:
A. weight percent is the first kind compound of being represented by general formula I of 0%-70%:
Wherein, R1 and R2 are each independently-NCS,-CN,-F, with 1-10 carbon atoms or having 10 carbon atoms, an alkoxy group, K1 and K2 are each independently H or F,
are each independently
or
B. weight percent is second compounds of being represented by general formula I I of 0-50%:
Wherein, R3 and R4 be independently of one another-NCS ,-CN ,-F, have the alkyl of 0-10 carbon atom or have the alkoxyl group of 0-10 carbon atom, K3 and K4 are H or F independently of one another, Z is-COO-,-C ≡ C-or-CH2CH2-;
C. weight percent is the 3rd compounds of being represented by general formula III of 0-50%:
Wherein, R5 and R6 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K5, K6, K7, K8, K9 and K10 are each independently H or F,
are each independently
and
D. weight percent is the 4th compounds of being represented by general formula I V of 0-20%:
Wherein, R7 and R8 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K11, K12, K13, K14, K15 and K16 are each independently H or F,
is
and
where A, Y is-COO-,-C ≡ C-or-CH2CH2-.
According to a preferred embodiment of the invention, this liquid-crystal composition further comprises:
E. weight percent is the 5th compounds of being represented by general formula V of 0-50%:
Wherein, R9 and R10 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K17 and K18 are each independently H or F,
are each independently
one of them.
According to a preferred embodiment of the invention, this liquid-crystal composition further comprises:
F. weight percent is the 6th compounds of 0-5%, and the 6th compounds is selected from one or more in the following compounds:
According to a preferred embodiment of the invention, the weight percent of the 6th compounds is 0%-1%.
According to a preferred embodiment of the invention, the 5th compounds of being represented by general formula V is selected from one or more in the following compounds:
According to a preferred embodiment of the invention, the weight percent of the 5th compounds of being represented by general formula V is 0%-30%.
According to a preferred embodiment of the invention, the first kind compound of being represented by general formula I is selected from one or more in the following compounds:
According to a preferred embodiment of the invention, second compounds of being represented by general formula I I is selected from one or more in the following compounds:
and
According to a preferred embodiment of the invention, the 3rd compounds of being represented by general formula III is selected from one or more in the following compounds:
According to a preferred embodiment of the invention, the 4th compounds of being represented by general formula I V is selected from one or more in the following compounds:
According to a preferred embodiment of the invention, the weight percent of the first kind compound of being represented by general formula I is 0%-40%.
According to a preferred embodiment of the invention, the weight percent of second compounds of being represented by general formula I I is 0%-30%.
According to a preferred embodiment of the invention, the weight percent of the 3rd compounds of being represented by general formula III is 0%-30%.
According to a preferred embodiment of the invention, the weight percent of the 4th compounds of being represented by general formula I V is 0%-10%.
The present invention also provides a kind of liquid crystal lens, and this liquid crystal lens comprises liquid-crystal composition of the present invention.
The invention has the beneficial effects as follows: the performance perameter that is different from the prior art liquid-crystal composition fails to realize the problem of more satisfactory combination; Liquid-crystal composition of the present invention has the transformation temperature scope of lower nematic phase starting voltage, broad, less viscoelastic coefficient ratio γ 1/K11, bigger optical anisotropy and bigger characteristics such as dielectric anisotropy, can reduce liquid crystal lens box one-tenth-value thickness 1/10 and improve its response speed.
Embodiment
Below in conjunction with embodiment the present invention is elaborated.
Be convenient and express that the unit structure of liquid crystalline cpd hereinafter is with the listed coded representation of table 1:
Table 1: the unit structure code of liquid crystalline cpd
Compound with following structural formula is an example:
The structural formula If the codes listed in Table 1 can be expressed as means: nCPTWS.Wherein, the n in the code representes the C atomicity of left end alkyl, and for example n is 3, representes that promptly this alkyl is-C
3H
7C in the code represents cyclohexyl; P in the code represents phenylene; W in the code represents 3,5-difluoro phenylene; S in the code represents isothiocyano.
The related physical performance perameter code name and the testing conditions that need detect in an embodiment are listed below:
Tni clearing point (nematic phase-isotropic phase transition temperature);
Tcn smectic phase-nematic Phase temperature;
γ 1 rotary viscosity (20 ℃ of 20 μ m of mpa.s antiparallel testing cassete);
ε // the be parallel to specific inductivity (20 ℃ of 20 μ m of 1KHz antiparallel testing cassete) on the long axis of liquid crystal molecule direction;
ε ⊥ is perpendicular to the specific inductivity on the long axis of liquid crystal molecule direction (20 ℃ of 20 μ m of 1KHz antiparallel testing cassete);
Δ ε dielectric anisotropy (20 ℃ of 20 μ m of 1KHz antiparallel testing cassete);
Δ n optical anisotropy (20 ℃ of 8 μ m antiparallel testing cassete);
K11 opens up bent elastic constant (20 ℃ of 20 μ m antiparallel testing cassete);
K33 bend elastic constant (20 ℃ of 20 μ m antiparallel testing cassete);
Vth starting voltage (20 ℃ time liquid crystal molecule just begun to rotate required voltage);
γ 1/K11 viscoelastic coefficient ratio.
The invention provides a kind of liquid-crystal composition A, this liquid-crystal composition A comprises:
A. the first kind compound of representing by general formula I:
Wherein, R1 and R2 are each independently-NCS,-CN,-F, with 1-10 carbon atoms or having 10 carbon atoms, an alkoxy group, K1 and K2 are each independently H or F,
are each independently
or
B. second compounds of representing by general formula I I:
Wherein, R3 and R4 be independently of one another-NCS ,-CN ,-F, have the alkyl of 0-10 carbon atom or have the alkoxyl group of 0-10 carbon atom, K3 and K4 are H or F independently of one another, Z is-COO-,-C ≡ C-or-CH2CH2-;
C. the 3rd compounds of representing by general formula III:
Wherein, R5 and R6 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K5, K6, K7, K8, K9 and K10 are each independently H or F,
are each independently
and
D. the 4th compounds of representing by general formula I V:
Wherein, R7 and R8 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K11, K12, K13, K14, K15 and K16 are each independently H or F,
is
and
where A, Y is-COO-,-C ≡ C-or-CH2CH2-.
Wherein, the weight percent of the first kind compound of being represented by general formula I is 0%-70%, and special preferred weight percent is 0%-40%.The first kind compound of being represented by general formula I has extremely low viscosity, can effectively reduce the overall viscosity of liquid-crystal composition and improve its response speed.
Preferred especially in following compounds one or more of the first kind compound of representing by general formula I:
The weight percent of second compounds of being represented by general formula I I is 0-50%, and special preferred weight percent is 0%-30%.Second compounds of being represented by general formula I I has moderate degree of birefringence, relatively low rotary viscosity, and relatively low transformation temperature has certain Δ ε value simultaneously, can reduce starting voltage.
Preferred especially in following compounds one or more of second compounds of representing by general formula I I:
The weight percent of the 3rd compounds of being represented by general formula III is 0-50%, and special preferred weight percent is 0%-30%.The 3rd compounds by general formula III is represented is compared with the biphenyl acetylene compound, has higher clearing point, has bigger degree of birefringence simultaneously, can improve the Δ n of liquid-crystal composition effectively, thereby the box that reduces liquid crystal cell is thick, improves response speed.
The 3rd compounds of being represented by general formula III is selected from one or more in the following compounds:
The weight percent of the 4th compounds of being represented by general formula I V is 0-20%, and special preferred weight percent is 0%-10%.The 4th compounds of being represented by general formula I V has moderate degree of birefringence, moderate clearing point, moderate starting voltage; Especially the more important thing is higher relatively elastic constant K11; Can reduce liquid-crystal composition viscoelastic coefficient effectively, shorten its time of response.
The 4th compounds of being represented by general formula I V is selected from one or more in the following compounds:
Selectively, liquid-crystal composition A of the present invention can further include:
F. the 6th compounds, the 6th compounds is selected from one or more in the following compounds:
and
The 6th compounds is an optically active compounds, and its weight percent is 0-5%, and particularly preferred weight percent is 0%-1%.
The present invention also provides a kind of liquid-crystal composition B, and this liquid-crystal composition B comprises:
A. the first kind compound of representing by general formula I;
B. second compounds of representing by general formula I I;
C. the 3rd compounds of representing by general formula III;
D. the 4th compounds of representing by general formula I V; And
E. the 5th compounds of representing by general formula V:
Wherein, R9 and R10 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K17 and K18 are each independently H or F,
are each independently
one of them.
Wherein, The included first kind compound of representing by general formula I of liquid-crystal composition B, second compounds of representing by general formula I I, the 3rd compounds of representing by general formula III and by the 4th compounds that general formula I V representes have with liquid-crystal composition A in the included first kind compound of representing by general formula I, second compounds of representing by general formula I I, the 3rd compounds of representing by general formula III and the identical technology contents of representing by general formula I V of the 4th compounds; For for purpose of brevity, repeat no more here.
The 5th compounds weight percent of being represented by general formula V is 0-50%, and special preferred weight percent is 0%-30%.The 5th compounds of being represented by general formula V has extremely low rotary viscosity, and degree of birefringence can be too not low, and it is joined the viscoelastic coefficient ratio that can greatly reduce the liquid-crystal composition system in the liquid-crystal composition, and improves the time of response of liquid-crystal composition.
The 5th compounds of being represented by general formula V is selected from one or more in the following compounds:
Selectively; Liquid-crystal composition B of the present invention can further include f. the 6th compounds; The 6th included compounds of liquid-crystal composition B have with liquid-crystal composition A in the included identical technology contents of the 6th compounds, for the purpose of indirectly, repeat no more here.
The compound composition of the nematic liquid crystal composition of embodiment 1 to embodiment 9 sees also shown in the table 2, and wherein percentage ratio is represented weight percent.Nematic liquid crystal composition among the embodiment 1 to embodiment 5 is the specific embodiment of liquid-crystal composition A of the present invention, and the nematic liquid crystal composition among the embodiment 6 to embodiment 9 is the specific embodiment of liquid-crystal composition B of the present invention.
The compound of the nematic liquid crystal composition of table 2: embodiment 1 to embodiment 9 is formed
In the above-described embodiments; Also can add optically active compounds according to actual needs as the 6th compounds; Its content is the 0-5% of nematic liquid crystal composition weight percent; Particularly preferably be 0-1%, above-mentioned optically active compounds mainly includes but are not limited to following several chiral additives: like CB15, R-811, S-811, R-1011, S-1011 etc.
The performance perameter of the nematic liquid crystal composition of embodiment 1 to embodiment 9 please be participated in shown in the table 3.
The performance perameter of the nematic liquid crystal composition of table 3: embodiment 1 to embodiment 9
As shown in table 3; The degree of birefringence Δ n of the nematic liquid crystal composition of embodiment 1 to embodiment 9 is respectively 0.2545,0.332,0.342,0.371,0.381,0.2769,0.332,0.3654 and 0.369; All belong to bigger degree of birefringence, and chemical stability and light stability are all very high.
In addition, embodiment 1 also has following beneficial effect to the nematic liquid crystal composition of this embodiment 5:
1, starting voltage be 0.67V between the 0.86V, satisfy low starting voltage; TCN is-10 ℃, and Tni is between 110-121 ℃, and promptly the nematic phase ceiling temperature is high, lower limit temperature is low, and is lower to temperature dependency;
2, rotary viscosity γ 1 is respectively 128.6mpa.s, 132.6mpa.s, 133mpa.s, 168mpa.s and 176mpa.s, all belongs to lower rotary viscosity.
Embodiment 6 also has following beneficial effect to the nematic liquid crystal composition of this embodiment 9:
1, starting voltage be 0.67V between the 0.86V, satisfy low starting voltage; TCN is-20 ℃--10 ℃, Tni is between 85-110 ℃, and promptly the nematic phase ceiling temperature is high, lower limit temperature is low, and is lower to temperature dependency;
2, rotary viscosity γ 1 is respectively 101mpa.s, 121mpa.s, 123mpa.s and 138mpa.s, all belongs to lower rotary viscosity;
3, have very low viscoelastic coefficient ratio, γ 1/K11 is all below 12, and the viscoelastic coefficient ratio is to influence time of response very important factor.
The present invention also provides a kind of liquid crystal lens, and this liquid crystal lens comprises like arbitrary liquid-crystal composition of 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, for example through at high temperature with different compound and each other the preparation of dissolved method get.In sum; Liquid-crystal composition of the present invention has the transformation temperature scope of lower nematic phase starting voltage, broad, less viscoelastic coefficient ratio γ 1/K11, bigger optical anisotropy and bigger characteristics such as dielectric anisotropy; Can reduce liquid crystal lens box one-tenth-value thickness 1/10 and improve its response speed, make liquid crystal display product more frivolous.
Liquid-crystal composition of the present invention can be used for TN demonstration, STN demonstration, PDLC demonstration, multistable demonstration, phase modulator and camera, mobile phone camera, liquid crystal shutter 3D glasses, 3D stereo display liquid crystal crack grating, the 3D stereopsis shows with varifocal liquid crystal lens fields such as (Liquid Crystal lens).
The above only is embodiments of the invention; Be not so limit claim of the present invention; Every equivalent structure transformation that utilizes description of the present invention to do, or directly or indirectly be used in other relevant technical fields, all in like manner be included in the scope of patent protection of the present invention.
Claims (15)
1. a liquid-crystal composition is characterized in that, said liquid-crystal composition comprises:
A. weight percent is the first kind compound of being represented by general formula I of 0%-70%:
Wherein, R1 and R2 are each independently-NCS,-CN,-F, with 1-10 carbon atoms or having 10 carbon atoms, an alkoxy group, K1 and K2 are each independently H or F,
are each independently
or
B. weight percent is second compounds of being represented by general formula I I of 0-50%:
Wherein, R3 and R4 be independently of one another-NCS ,-CN ,-F, have the alkyl of 0-10 carbon atom or have the alkoxyl group of 0-10 carbon atom, K3 and K4 are H or F independently of one another, Z is-COO-,-C ≡ C-or-CH2CH2-;
C. weight percent is the 3rd compounds of being represented by general formula III of 0-50%:
Wherein, R5 and R6 are each independently-NCS,-CN,-F, having 0-10 carbon atoms or having 0-10 carbon atoms, an alkoxy group, K5, K6, K7, K8, K9 and K10 are each independently H or F,
are each independently
and
D. weight percent is the 4th compounds of being represented by general formula I V of 0-20%:
2. liquid-crystal composition according to claim 1 is characterized in that, said liquid-crystal composition further comprises:
E. weight percent is the 5th compounds of being represented by general formula V of 0-50%:
4. liquid-crystal composition according to claim 3 is characterized in that, the weight percent of said the 6th compounds is 0%-1%.
6. liquid-crystal composition according to claim 5 is characterized in that, the weight percent of said the 5th compounds of being represented by general formula V is 0%-30%.
11. liquid-crystal composition according to claim 1 is characterized in that, the weight percent of the said first kind compound of being represented by general formula I is 0%-40%.
12. liquid-crystal composition according to claim 1 is characterized in that, the weight percent of said second compounds of being represented by general formula I I is 0%-30%.
13. liquid-crystal composition according to claim 1 is characterized in that, the weight percent of said the 3rd compounds of being represented by general formula III is 0%-30%.
14. liquid-crystal composition according to claim 1 is characterized in that, the weight percent of said the 4th compounds of being represented by general formula I V is 0%-10%.
15. a liquid crystal lens is characterized in that, said liquid crystal lens comprises like claim 1,2, each described liquid-crystal composition of 5-14.
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102433133A (en) * | 2011-09-14 | 2012-05-02 | 深圳超多维光电子有限公司 | Nematic liquid crystal composition |
CN102660296A (en) * | 2012-05-16 | 2012-09-12 | 深圳超多维光电子有限公司 | Liquid crystal composition and application thereof |
CN105038816A (en) * | 2015-07-13 | 2015-11-11 | 石家庄诚志永华显示材料有限公司 | Liquid crystal composition |
CN105368465A (en) * | 2014-08-08 | 2016-03-02 | 默克专利股份有限公司 | Liquid-crystalline medium and high-frequency components comprising same |
CN105985786A (en) * | 2014-08-25 | 2016-10-05 | 深圳超多维光电子有限公司 | Liquid crystal composition and liquid crystal lens |
CN106479516A (en) * | 2016-08-31 | 2017-03-08 | 中节能万润股份有限公司 | A kind of low-voltage liquid-crystal composition and low-voltage polymer dispersion liquid crystal material |
CN106479515A (en) * | 2015-09-01 | 2017-03-08 | 深圳超多维光电子有限公司 | A kind of liquid-crystal composition and liquid crystal lens |
US20180105748A1 (en) * | 2016-10-18 | 2018-04-19 | Merck Patent Gmbh | Liquid-crystalline medium, compounds, and high-frequency components |
CN110616075A (en) * | 2019-10-15 | 2019-12-27 | 浙江晶鲸科技有限公司 | Electric control optical diffraction element based on multistable liquid crystal composition and manufacturing method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1400279A (en) * | 2001-07-27 | 2003-03-05 | 默克专利股份有限公司 | Liquid crystal mixture |
CN1536052A (en) * | 2003-04-07 | 2004-10-13 | Ĭ��ר���ɷ�����˾ | Liquid crystal mixture |
CN101323786A (en) * | 2006-12-19 | 2008-12-17 | 默克专利股份有限公司 | Liquid-crystalline medium |
CN102010718A (en) * | 2010-10-13 | 2011-04-13 | 江苏和成化学材料有限公司 | Nematic liquid crystal composition and application thereof to 3D light valve display |
-
2011
- 2011-07-28 CN CN201110213905.3A patent/CN102352260B/en active Active
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1400279A (en) * | 2001-07-27 | 2003-03-05 | 默克专利股份有限公司 | Liquid crystal mixture |
CN1536052A (en) * | 2003-04-07 | 2004-10-13 | Ĭ��ר���ɷ�����˾ | Liquid crystal mixture |
CN101323786A (en) * | 2006-12-19 | 2008-12-17 | 默克专利股份有限公司 | Liquid-crystalline medium |
CN102010718A (en) * | 2010-10-13 | 2011-04-13 | 江苏和成化学材料有限公司 | Nematic liquid crystal composition and application thereof to 3D light valve display |
Non-Patent Citations (1)
Title |
---|
SEBASTIAN GAUZA ET AL.: "High birefringence and high resistivity isothiocyanate-based nematic liquid crystal mixtures", 《LIQUID CRYSTALS》 * |
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