阅读说明：本技术 液晶介质 (Liquid-crystalline medium ) 是由 M·维特克 D·克拉斯 于 2018-04-24 设计创作，主要内容包括：本发明涉及包含一种或多种式(CC)的化合物的液晶介质<Image he="157" wi="700" file="DDA0002247438160000011.GIF" imgContent="drawing" imgFormat="GIF" orientation="portrait" inline="no"></Image>其中出现的基团具有权利要求1所指示的含义,并且涉及所述液晶介质用于电光目的,特别是在用于车辆照明装置的液晶光阀中的用途,并且涉及包含该介质的液晶光阀和包括该类型的液晶光阀的用于车辆的照明装置。(The invention relates to a liquid-crystalline medium comprising one or more compounds of formula (CC) The radicals appearing therein have the meaning indicated in claim 1, and to the use of the liquid-crystalline medium for electro-optical purposes, in particular in liquid-crystal light valves for vehicle lighting devices, and to liquid-crystal light valves comprising the medium and lighting devices for vehicles comprising liquid-crystal light valves of this type.)

1. liquid-crystalline medium, characterized in that it comprises one or more compounds of the formula CC

wherein

R^CRepresents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced by And wherein in each case one or more H atoms may be replaced by F,

X^CDenotes F, Cl, halogenoalkyl, halogenoalkenyl, halogenoalkoxy or halogenoalkenyloxy having up to 6C atoms,

Z^C1，Z^C2Independently of one another represent-CH₂CH₂-or a single bond,

L^C1And L^C2Are connected with each otherindependently of each other represents H or F,

L^C3and L^C4independently of one another, H or methyl;

And is characterized in that the clearing point of the medium is 120 ℃ or higher.

2. the medium according to claim 1, wherein the total concentration of the one or more compounds of formula CC in the medium is 55% by weight or more.

3. The medium according to claim 1 or 2, wherein the medium has a birefringence in the range of 0.060 to 0.100 at 20 ℃ and a wavelength of 589.3 nm.

4. A medium according to one or more of claims 1-3, wherein the medium comprises one or more compounds of formula CP in a total concentration of 2% or less

wherein

R^PRepresents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced by And wherein in each case one or more H atoms may be replaced by F,

A^Prepresents 1, 4-cyclohexylene, in which one or two non-adjacent CH' s₂the radicals being replaced by-O-, or 1, 4-phenylene in which one or two CH groups are replaced by N,

X^PDenotes F, Cl, halogenoalkyl, halogenoalkenyl, halogenoalkoxy or halogenoalkenyloxy having up to 6C atoms,

Z^PIndependently of one another represent-CH₂CH₂-or single bond，

L^P1And L^P2Independently of one another, H or F.

5. The medium according to one or more of claims 1 to 4, wherein the medium comprises one or more compounds of formula IV-1 in a total concentration of 25% or less

wherein

R⁴¹Represents an alkyl group having up to 7 carbon atoms, and

R⁴²represents alkyl or alkoxy each having up to 7 carbon atoms,

Or

R⁴¹Represents an alkenyl group having up to 7 carbon atoms, and R⁴²Represents an alkyl or alkenyl group each having up to 7 carbon atoms,

Wherein the radical R⁴¹And R⁴²One or more H atoms in (a) may be replaced by F.

6. Medium according to one or more of claims 1 to 5, wherein the medium comprises one or more compounds of formula CC selected from the compounds CC-1 to CC-12

wherein R is^Cand X^Chave the meaning indicated in claim 1.

7. Medium according to one or more of claims 1 to 6, characterized in that it further comprises one or more compounds of the formula II in a total concentration of 40% or less,

Wherein

R²Represents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced And wherein in each case one or more H atoms may be replaced by F,

In each occurrence, the same or different representation

L²¹And L²²independently of one another, represent H or F,

L²⁵Represents a hydrogen atom or a methyl group,

X²Represents F, Cl, CN, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having 1 to 6 carbon atoms.

8. The medium according to claim 7, wherein the compound of formula II is selected from the group consisting of compounds II-1 to II-6

Wherein

R²Represents an n-alkyl group having 1 to 7 carbon atoms,

L²¹、L²²、L²³and L²⁴Independently of one another, represent H or F,

L²⁵Represents H or methyl, and

X²represents F, Cl, haloalkyl or haloalkoxy having 1 to 6 carbon atoms.

9. The medium according to one or more of claims 1 to 8, characterized in that it further comprises one or more compounds selected from the group consisting of the compounds of the formulae IIA and IIB,

wherein R is²、A²¹、A²²、L²¹、L²²and X²Has the meaning indicated in claim 7 for formula II, and L²³And L²⁴With respect to L²¹The meaning indicated in (1).

10. the medium according to one or more of claims 1 to 9, characterized in that it further comprises one or more compounds of the formula III,

Wherein R is³Has the structure shown in claim 7 for R²The meaning indicated.

Represent independently of each other at each occurrence

Z³Represents independently of one another at each occurrence-CH₂CH₂-, -COO-, trans-CH-, trans-CF-, -CH₂O-, -C.ident.C-or a single bond,

L³¹，L³²Represents a group of a compound represented by the formula H or F,

X³Represents F, Cl, CN, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having up to 6C atoms.

11. The medium according to claim 10, wherein the compound of formula III is selected from the group consisting of compounds of formulae III-1 to III-9

Wherein

R³、L³¹And L³²Having the meaning indicated in claim 10,

and

X³Denotes F, Cl, haloalkyl or haloalkoxy having up to 6C atoms.

12. Medium according to one or more of claims 1 to 11, characterized in that it further comprises one or more compounds selected from the group consisting of compounds of formulae IV-11 and IV-12

Wherein

R⁴¹And R⁴²Independently of one another, represents an n-alkyl radical having from 1 to 7 carbon atoms, and

L⁴Represents H or F.

13. Use of a liquid-crystalline medium according to one or more of claims 1 to 12 for electro-optical purposes.

14. Use according to claim 13 in liquid crystal light valves in liquid crystal displays or in lighting devices of vehicles.

15. Electro-optical component comprising a liquid-crystalline medium according to one or more of claims 1 to 12.

16. The electro-optic assembly of claim 15, wherein the assembly is a liquid crystal light valve.

17. A lighting device for a vehicle comprising the electro-optical assembly of claim 15 or 16.

18. A liquid crystal display comprising the electro-optic assembly of claim 15.

The low temperature properties of the mixtures of the prior art are also particularly disadvantageous. It is required that no crystallization and/or smectic phases occur even at low temperatures and the temperature dependence of the viscosity is as low as possible. Thus, the MLC displays of the prior art do not meet the requirements for a lighting device.

Thus, there is still a need for liquid crystal mixtures having a large operating temperature range and high light stability while having very high resistivity.

In the case of liquid crystal light valves for vehicle lighting devices, a medium is required which can promote the following advantages in the case:

Extended nematic phase range (especially for high temperatures)

Storage-stable, even at low temperatures

Switchability at low temperatures

-improved photostability.

With the media available in the prior art, it is not possible to obtain these advantages while maintaining other parameters. For example, the liquid-crystalline media of the published specifications DE 10223061 a1 and DE 102008062858 a1 have a low Δ n, but the clearing point of about 80 ℃ is too low for the application according to the invention.

The object of the present invention is to provide a medium, in particular a liquid crystal light valve for a vehicle lighting device as described above, which does not have the disadvantages described above or to a lesser extent, and preferably has both a very high clearing point and a low birefringence.

It has now been found that this object is achieved if the medium according to the invention is used in a liquid crystal module. The invention relates to a liquid-crystalline medium, characterised in that it comprises one or more compounds of formula CC

Preferably at a total concentration of 35% or more,

Wherein

R^Crepresents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced by And wherein in each case one or more H atoms may be replaced by F,

X^CDenotes F, Cl, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having up to 6C atoms,

Z^C1and Z^C2Independently of one another represent-CH₂CH₂-or a single bond,

L^C1And L^C2Independently of one another, represent H or F,

L^C3And L^C4Independently of one another, H or methyl;

And is characterized in that the clearing point of the medium is 120 ℃ or higher.

In this application, all atoms also include isotopes thereof. In particular, one or more hydrogen atoms (H) may be replaced by deuterium (D), which is particularly preferred in some embodiments; highly deuterated compounds enable or simplify analytical determination of compounds, especially at low concentrations.

in the present application, alkyl or alkoxy means a straight or branched alkyl or alkoxy group. It is preferably straight-chain, has 2, 3, 4, 5, 6 or 7 carbon atoms and therefore preferably represents ethyl, propyl, butyl, pentyl, hexyl, heptyl, ethoxy, propoxy, butoxy, pentoxy, hexyloxy or heptyloxy, furthermore methyl, octyl, nonyl, decyl, undecyl, dodecyl, tridecyl, tetradecyl, pentadecyl, methoxy, octyloxy, nonyloxy, decyloxy, undecyloxy, dodecyloxy, tridecyloxy or tetradecyloxy.

Oxaalkyl preferably denotes straight-chain 2-oxapropyl (═ methoxymethyl), 2- (═ ethoxymethyl) or 3-oxabutyl (═ 2-methoxyethyl), 2-, 3-or 4-oxapentyl, 2-, 3-, 4-or 5-oxahexyl, 2-, 3-, 4-, 5-or 6-oxaheptyl, 2-, 3-, 4-, 5-, 6-or 7-oxaoctyl, 2-, 3-, 4-, 5-, 6-, 7-or 8-oxanonyl, 2-, 3-, 4-, 5-, 6-, 7-, 8-or 9-oxadecyl.

Wherein CH₂Alkyl groups in which a group has been replaced by-CH ═ CH-may be straight-chain or branched. It is preferably straight-chain and has 2 to 10 carbon atoms. Thus, it denotes in particular vinyl, prop-1-or-2-enyl, but-1-, -2-or-3-enyl, pent-1-, -2-, -3-or-4-enyl, hex-1-, -2-, -3-, -4-or-5-enyl, hept-1-, -2-, -3-, -4-, -5-or-6-enyl, oct-1-, -2-, -3-, -4-, -5-, -6-or-7-enyl, non-1-, -2-), -3-, -4-, -5-, -6-, -7-or-8-alkenyl or-1-, -2-, -3-, -4-, -5-, -6-, -7-, -8-or-9-alkenyl.

In one of CH₂The group having been replaced by-O-and one CH₂In alkyl groups in which the group has been replaced by-CO-, these are preferably adjacent. Thus, this comprises acyloxy-CO-O-or oxycarbonyl-O-CO-. These are preferably straight-chain and have 2 to 6 carbon atoms. They therefore denote in particular acetoxy, propionyloxy, butyryloxy, pentanoyloxy, hexanoyloxy, acetoxymethyl, propionyloxymethyl, butyryloxymethyl, pentanoyloxymethyl, 2-acetoxyethyl, 2-propionyloxyethyl, 2-butyryloxyethyl, 2-acetoxypropyl, 3-propionyloxypropyl, 4-acetoxybutyl, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, propoxycarbonylmethyl, butoxycarbonylmethyl, 2- (methoxycarbonyl) ethyl, 2- (ethoxycarbonyl) ethyl, 2- (propoxycarbonyl) ethyl, 3- (methoxycarbonyl) propyl, 3- (ethoxycarbonyl) propyl or 4- (methoxycarbonyl) butyl.

Compounds containing branched side groups R are occasionally important because of their better solubility in conventional liquid crystal base materials, but in particular as chiral dopants if they are optically active. Smectic compounds of this type are suitable as components of ferroelectric materials.

Branched groups of this type typically contain no more than one branch. Preferred branched radicals R are isopropyl, 2-butyl (═ 1-methylpropyl), isobutyl (═ 2-methylpropyl), 2-methylbutyl, isopentyl (═ 3-methylbutyl), 2-methylpentyl, 3-methylpentyl, 2-ethylhexyl, 2-propylpentyl, isopropoxy, 2-methylpropoxy, 2-methylbutoxy, 3-methylbutoxy, 2-methylpentyloxy, 3-methylpentyloxy, 2-ethylhexyloxy, 1-methylhexyloxy and 1-methylheptyloxy.

In a preferred embodiment, the medium comprises one or more compounds CP

Wherein

R^PRepresents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced by And wherein in each case one or more H atoms may be replaced by F,

A^PRepresents 1, 4-cyclohexylene, in which one or two non-adjacent CH' s₂the radicals being replaced by-O-, or 1, 4-phenylene in which one or two CH groups are replaced by N,

X^Pdenotes F, Cl, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having up to 6C atoms,

Z^Pindependently of one another represent-CH₂CH₂-or a single bond,

L^P1And L^P2Independently of one another, represent H or F,

the total concentration thereof is 2% or less.

The media according to the invention particularly preferably comprise one or more compounds of the formula CP in a total concentration of 0.5% or less, very particularly preferably 0.1% or less.

in a preferred embodiment, the medium according to the invention comprises one or more compounds of the formula CP in a total concentration of from 0.01% to 2%.

In another preferred embodiment, the medium does not comprise a compound of formula CP.

The compound of formula CC is preferably selected from the compounds CC-1 to CC-12, particularly preferably from the compounds CC-1 to CC-6:

Wherein R is^CAnd X^CHave the above meanings, and are preferred

R^CRepresents an alkyl group having 1 to 7 carbon atoms in which methylene may be substituted And in which in each case one or more H atoms may be replaced by F, particularly preferably ethyl, n-propyl, n-butyl or n-pentyl,

X^CDenotes F, Cl, OCF₂H or OCH₂CF₂H。

very particularly preferred compounds of the formulae CC-1 to CC-6 are selected from the sub-formulae CC-1-1 to CC-6-10:

in a particular embodiment, the medium further comprises one or more compounds of formula I

Wherein

R¹Represents an alkyl or alkoxy group having 1 to 15 carbon atoms in which methylene may be replacedWhere one or more H atoms in these radicals may be replaced by F,

representing the same or different at each occurrence

L¹¹and L¹²independently of one another, represent H or F,

X¹Denotes F, Cl, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having up to 6C atoms,

Z¹And Z²represents-CH₂CH₂-，-CF₂CF₂-, -COO-, trans-CH-, trans-CF-, -CH₂O-or a single bond,

With the proviso that compounds of formula CC are excluded.

The compound of formula I is preferably selected from compounds of the following sub-formulae:

Wherein the radicals mentioned have the abovementioned meanings.

The compounds of the formula I are particularly preferably selected from the compounds I-4 and I-5, very particularly preferably from the following subformulae:

The medium of the invention preferably also comprises one or more compounds of the formula II

Wherein

R²Represents alkyl, alkenyl or alkoxy having 1 to 15C atoms, in which methylene may be replaced And one of them is orA plurality of H atoms may be replaced by F,

representing the same or different at each occurrence

L²¹And L²²Independently of one another, represent H or F,

L²⁵Represents H or a methyl group, preferably H,

X²Denotes F, Cl, CN, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having 1 to 6C atoms,

preferably, the total concentration is 40% or less.

The compound of the formula II is preferably selected from the group consisting of the compounds of the formulae II-1 to II-6

Wherein

R²Represents an alkyl group having 1 to 7 carbon atoms in which methylene may be substituted alternatively, where one or more H atoms may be replaced by F,

L²¹，L²²，L²³And L²⁴Independently of one another, represent H or F,

L²⁵Represents H or methyl, preferably H, and

X²represents F, Cl, haloalkyl or haloalkoxy having 1 to 6 carbon atoms.

in a particularly preferred embodiment, the compounds of the formula II are selected from the group consisting of the compounds of the formulae II-1a to II-1e

Wherein R is²Have the meanings given for formula II-1.

the medium particularly preferably comprises at least one compound of the formula II-1b, which is preferably selected from the compounds of the formulae I I-1b-1 to II-1 b-10:

In another preferred embodiment, the medium according to the invention comprises one or more compounds selected from the group consisting of the compounds of the formulae IIA and IIB,

wherein the radicals present have the meanings indicated for formula II, and are preferably

R²Represents an n-alkyl group having up to 7C atoms,

X²Denotes F, Cl, haloalkyl or haloalkoxy having up to 6C atoms,

L²¹，L²²，L²³And L²⁴Independently of one another, H or F.

X²Particularly preferably F, Cl, CF₃，OCF₃Or OCHF₂。

The compounds of the formula IIA are preferably selected from the following sub-formulae IIA-1 to IIA-7, particularly preferably from the compounds of the formula IIA-1,

Wherein the radicals mentioned have the abovementioned meanings.

The compounds of the formula IIA are particularly preferably selected from the compounds of the formulae IIA-1a to IIA-1d

Wherein R is²Has the above meaning, and X²Preferably represents F or OCF₃。

Very particular preference is given to compounds of the formulae IIA-1 d.

particularly preferred compounds of formula IIB are selected from compounds of formula IIB-1

Wherein the parameters have the above-mentioned meanings, and preferably the radicals L²¹And L²²At least one of them represents F, and X²Denotes F, Cl, CF₃Or OCF₃。

in a preferred embodiment, the medium comprises one or more compounds of the formula III,

Wherein

R³Having the formula II above for R²The meaning of what is indicated is that of,

Represent independently of each other at each occurrence

preference is given to

One or more of

To represent

L³¹And L³²Independently of one another, represent H or F,

X³Denotes F, Cl, CN, haloalkyl, haloalkenyl, haloalkoxy or haloalkenyloxy having up to 6C atoms,

Z³Represents independently of one another at each occurrence-CH₂CH₂-, -COO-, trans-CH-, trans-CF-, -CH₂O-, -C.ident.C-or a single bond, preferably one or both represent a single bond.

The compound of formula III is preferably selected from compounds of formulae III-1 to III-9:

Wherein

L³¹And L³²Independently of one another, represent H or F,

X³denotes F, Cl, haloalkyl or haloalkoxy having up to 6C atoms, and preferably denotes F or OCF₃。

The medium particularly preferably comprises one or more compounds selected from the group consisting of the compounds of the formulae III-1 and III-3.

Very particular preference is given to media which comprise one or more compounds of the following sub-formulae:

Wherein R is³Preferably represents an n-alkyl group having 1 to 7 carbon atoms.

The medium according to the invention preferably comprises one or more compounds of the formula IV

Wherein

R⁴¹And R⁴²independently of one another, have the general formula II above for R²The meaning indicated, and

Preference is given to

R⁴¹Represents an alkyl group having up to 7 carbon atoms, and

R⁴²represents alkyl or alkoxy each having up to 7 carbon atoms,

Or

R⁴¹Denotes alkenyl having up to 7C atoms,

R⁴²represents alkyl or alkenyl groups each having up to 7 carbon atoms,

Wherein the radical R⁴¹And R⁴²One or more H atoms in (a) may be replaced by F,

Represent independently of each other at each occurrence

preference is given to

One or more of

To represent

Z⁴¹And Z⁴²Represents independently of one another at each occurrence-CH₂CH₂-，-CF₂CF₂-，-CF₂CH₂-, -COO-, trans-CH-, trans-CF-, -CH₂O-，CF₂O-, -C.ident.C-or a single bond, preferably in which one or more represent a single bond, and

p represents 0, 1 or 2, preferably 0 or 1.

The compound of formula IV is preferably selected from the group consisting of compounds of formulae IV-1 to IV-13

Wherein R is⁴¹And R⁴²Has the above meaning, and L⁴Represents H or F, preferably

R⁴¹And R⁴²Independently of one another, represents an n-alkyl radical having from 1 to 7 carbon atoms, and

L⁴represents F.

The medium according to the invention particularly preferably comprises one or more compounds selected from the group consisting of the compounds of the formulae IV-5, IV-8 and IV-11.

In another preferred embodiment, the medium of the invention comprises one or more compounds of formula V

wherein

R⁵¹and R⁵²Independently of one another, have the above meanings for R in the formula II²Indicated, preferably R⁶¹Represents an alkyl group, R⁶²represents an alkyl group or an alkenyl group,

Represent independently of each other at each occurrence

Preference is given to

is represented by one or more of

Z⁵¹And Z⁵²Independently of each other, and if Z⁵¹Two occurrences, then these also represent independently of one another-CH₂CH₂-, -COO-, trans-CH-, trans-CF-, -CH₂O-or a single bond, preferably wherein one or more represent a single bond, and

r represents 0, 1 or 2, preferably 1 or 2, particularly preferably 1.

In another preferred embodiment, the medium comprises one or more compounds selected from the group consisting of compounds of formulae V-1 and V-2,

Wherein R is⁵¹And R⁵²Each have the meaning shown above in formula V and preferably represent alkyl.

The compounds of the formulae CC and I to V are prepared by Methods known per se, as described in the literature (for example in standard works, such as Houben-Weyl, Methoden der Organischen chemistry [ Methods of organic chemistry ] (Georg-Thieme-Verlag, Stuttgart), to be precise under reaction conditions which are known and suitable for the reaction in question.

the liquid-crystal mixtures according to the invention enable a significant broadening of the usable parameter range. The achievable combination of clearing point, phase width, viscosity at low temperature, thermal and UV stability and dielectric anisotropy is far superior to previous materials in the prior art.

the invention furthermore relates to electro-optical components, in particular light valves, based on the VA, IPS, FFS, TN or STN effect, which have two plane-parallel outer plates which, together with a frame, form a cell, integrated nonlinear elements on the outer plates for switching the individual pixels, and nematic liquid-crystal mixtures with positive dielectric anisotropy and high resistivity which are located in the cell, which comprise the media according to the invention, and the use of these media for electro-optical purposes.

The invention also relates to the use of the electro-optical medium or component in a lighting device of a vehicle and in a liquid crystal display, in particular a TN, STN or MLC display.

Furthermore, the invention relates to an illumination device for a vehicle and an electro-optical display comprising these components.

The vehicle lighting device according to the invention has at least one light source. The light source emits light, so that furthermore at least one screen device for influencing the light emitted by the light source is provided. The screen device is in the form of an LCD screen and therefore has at least one liquid crystal light valve which can be transilluminated from the rear. In the lighting device according to the invention, the light source may have a very wide variety of designs. It may have one or more lamps. Suitable lamps are conventional lamps in the form of incandescent bulbs or gas discharge lamps, for example. Modern lamps, such as LEDs, are also conceivable as lamps for light sources, in particular cold cathode lamps (CCFLs) for liquid crystal displays, for the purposes of the present invention. The individual lamps may be arranged differently, for example in a matrix-like manner. Of course, one or more arrangements of other optical components in the light source or in the lighting device may bring advantages. These may be, for example, one or more reflectors or one or more lenses. It is also advantageous that the liquid crystal light valve in the illumination device according to the invention has a first polarizer through which light provided by the light source enters. In addition, a second polarizer is provided through which the light exits the liquid crystal light valve. A layer comprising a liquid-crystalline medium according to the invention is arranged between the first polarizer and the second polarizer. The liquid crystal layer is for rotating a polarization plane of light passing through the liquid crystal layer according to an applied voltage. Depending on the type of design of the liquid crystal layer, the liquid crystal layer may affect the polarization rotation of light in the electric field or prevent this rotation function of light passing through. In this type of embodiment, the liquid crystal light valve, and in particular the first polarizer, is designed to be heat resistant up to a temperature of about 200 ℃. This is particularly important, especially in the case of the first polarizer, since this absorbs about 50% of the light emitted by the light source and the associated energy. The various designs of the polarizers in relation to the alignment of the liquid crystal molecules in the liquid crystal layer substantially correspond to those used in liquid crystal displays and are known to the person skilled in the art. In principle, all known configurations are suitable, and liquid crystal light valves of the TN, STN, VA, IPS or FFS type are preferred, liquid crystal light valves of the TN or STN type being particularly preferred.

it goes without saying that by a suitable choice of the components of the mixtures according to the invention, it is also possible to achieve higher clearing points (for example above 150 ℃) at higher threshold voltages or lower clearing points at lower threshold voltages, while retaining other advantageous properties. With only a corresponding only slight increase in viscosity, it is likewise possible to obtain mixtures having a greater Δ ∈ and thus a lower threshold value. Preferably, the electro-optic assembly according to the invention operates at the first Gooch-Tarry transmission minimum [ c.h.gooch and h.a.tarry, electron.lett.10, 2-4, 1974; c.h. gooch and h.a.tarry, appl.phys., volume 8, 1575-1584, 1975], wherein, in addition to particularly advantageous electro-optical properties (e.g. high steepness of the characteristic lines and low angular dependence of the contrast) (german patent 3022818), a lower dielectric constant anisotropy is sufficient at the same threshold voltage as in a similar display at the second minimum. This enables significantly higher values of resistivity to be obtained at the first minimum value using the mixtures according to the invention than in the case of mixtures comprising cyano compounds. By appropriate selection of the individual components and their weight proportions, the person skilled in the art is able to set the birefringence required for a predetermined layer thickness of the components using simple conventional methods.

measurement of Voltage Holding Ratio (HR) [ S.Matsumoto et al, Liquid Crystals51320 (1989); niwa et al, proc.sid Conference, San Francisco, 6 months 1984, page 304 (1984); weber et alHuman, Liquid Crystals5，1381(1989)]It has been shown that mixtures according to the invention comprising compounds of the formula CC and mixtures comprising compounds of the formulaCyanophenylcyclohexane of the formulaThe decrease in HR with increasing temperature is significantly less compared to a similar mixture of the ester of (a) instead of the compound of formula CC.

The UV stability of the mixtures according to the invention is also quite good, i.e. they show a significantly smaller decrease in HR when exposed to UV.

The liquid-crystal mixtures according to the invention, while maintaining the nematic phase as low as-20 ℃, preferably as low as-30 ℃, particularly preferably as low as-40 ℃, enable clearing points of 120 ℃ or more, while the dielectric anisotropy value Δ ∈ is ≧ 4, preferably ≧ 8, and enable high resistivity values to be obtained, enabling excellent light valves according to the invention to be obtained. In particular, the mixture is characterized by a low operating voltage. The TN threshold is less than 2.0V, preferably less than 1.5V, particularly preferably < 1.3V.

the clearing point of the liquid-crystal mixtures according to the invention is preferably 125 ℃ or more, preferably 130 ℃ or more, particularly preferably 135 ℃ or more, very particularly preferably 140 ℃ or more, in particular 145 ℃ or more.

The liquid-crystal mixtures according to the invention have an optical anisotropy (Δ n) of from 0.050 to 0.110, preferably from 0.060 to 0.100, particularly preferably from 0.065 to 0.090, very particularly preferably from 0.070 to 0.085.

The rotational viscosity γ of the mixture according to the invention at 20 ℃₁Preference is given to < 350 mPas, particularly preferably < 300 mPas. The nematic phase range is preferably at least 140K, in particular at least 180K. This range preferably extends at least from-40 ° to +140 °.

Other embodiments of the invention are indicated below, which are preferred individually and in combination with one another (the meanings of the acronyms used below can be taken from tables a to D shown below):

-the total concentration of compounds of formula CC in the medium is 35% or more, preferably 45% or more, particularly preferably 50% or more, very particularly preferably 55% or more, in particular 60% or more.

-the total concentration of compounds of formulae CC and I in the medium is 35% or more, preferably 45% or more, particularly preferably 50% or more, very particularly preferably 55% or more.

The medium comprises one or more compounds of formula CC in a total concentration of 34% to 100%, preferably 40% to 95%, particularly preferably 45% to 75%.

The medium comprises one or more compounds of the formulae CC and I in a total concentration of from 34% to 100%, preferably from 40% to 95%, particularly preferably from 45% to 75%.

The total concentration of compounds of the formula II in the medium is 40% or less, preferably 37% or less, particularly preferably 33% or less, very particularly preferably 30% or less, in particular 25% or less.

The total concentration of the compound of formula II in the medium, if present, is from 2% to 35%, preferably from 5% to 30%, particularly preferably from 10% to 25%.

The total concentration of the compounds of the formulae CC and II in the medium is from 35% to 100%, preferably from 60% to 90%, particularly preferably from 62 to 85%, very particularly preferably from 65% to 80%.

the total concentration of the compounds of formulae IV-1, IV-2, IV-3, IV-4, IV-5, IV-6 and IV-7 in the medium is from 3% to 25%, preferably from 5% to 18%, particularly preferably from 8% to 16%. The medium preferably comprises at least one compound of the formula IV-5.

The medium comprises one, two, three or more compounds of the formula IV-1 in a total concentration of from 0 to 25%, preferably from 0.5 to 15%, particularly preferably from 1 to 10%, very particularly preferably from 2 to 5%.

-the medium comprises one, two, three or more compounds of formula IV-1 in a total concentration of 25% or less.

The total concentration of the compounds of the formulae IV-7, IV-8, IV-9, IV-10, IV-11, IV-12 and IV-13 is from 2% to 20%, preferably from 4% to 16%, particularly preferably from 6% to 13%. The medium preferably comprises at least one compound of the formula IV-8 or IV-11, particularly preferably IV-11.

The medium comprises one or more compounds of formulae IIA and/or IIB and one or more compounds of formulae IV-11.

the medium comprises one or more compounds selected from the group consisting of compounds IIA, IIB and III, preferably selected from the group consisting of CCGU-nF, CCPU-n-F, CCCG-n-F, CCCQU-n-F, CCCQU-n-OT and CDUQU-n-F, in a total concentration of from 3% to 15%, preferably from 5% to 13%, particularly preferably from 7% to 10%.

The medium comprises one, two, three or more compounds CCU-n-O1D, preferably in a total concentration of 20 to 60%, particularly preferably 25 to 50%, very particularly preferably 30 to 40%

And/or

the total concentration of one, two, three or more compounds CCU-n-OD is preferably from 30% to 65%, particularly preferably from 40% to 60%, very particularly preferably from 45% to 55%.

the medium comprises one, two, three, four or more compounds CCG-n-F, preferably in a total concentration of 20% to 70%, particularly preferably 40% to 65%, very particularly preferably 45% to 55%.

The medium comprises one, two, three or more compounds CCU-n-F, preferably in a total concentration of 5% to 60%, particularly preferably 10% to 45%, very particularly preferably 20% to 30%.

The medium comprises three or more compounds CCG-n-F and three or more compounds of formula CCU-n-F.

The medium comprises the compound CCG-1-F.

The medium comprises one, two, three or more compounds CCP-n-Cl, preferably in a total concentration of 30 to 70%, particularly preferably 40 to 60%, very particularly preferably 45 to 55%.

the medium comprises two, three or more compounds CCEG-n-F and three or more compounds of the formula CCP-n-Cl.

The medium comprises one, two, three, four or more compounds CCEG-n-F.

the medium comprises three or more compounds CCEG-n-F and three or more compounds of formula CCU-n-F.

The medium comprises the compound CCEG-1-F.

-the medium comprises two, three or more compounds CCEG-n-F and three or more compounds of the formula CCP-n-Cl.

The medium comprises two, three or more compounds CCEP-n-F, preferably in a total concentration of from 20% to 60%, particularly preferably from 30% to 50%, very particularly preferably from 35% to 45%.

the medium comprises CCEP-1-F, preferably in a concentration of 15% to 35%, particularly preferably 20% to 30%, very particularly preferably 23% to 27%.

The medium comprises two, three or more compounds CCEU-n-F, and two, three or more compounds selected from CCEP-n-F and CCEG-n-F.

the proportion of the compound containing an unsaturated side chain (R represents alkenyl or alkynyl) in the medium is from 0 to 10%, preferably from 0.5 to 5%, particularly preferably from 1 to 2%.

The total concentration of compounds present in the medium is 100%. The concentration of the mentioned compounds in the medium is 100% or less.

It has been found that the use of one or more compounds selected from the group consisting of the compounds of the formulae CC, I, II, IIA, IIB and III to V in the liquid-crystal mixtures according to the invention leads to lower birefringence values compared to the prior art, at the same time with a broad nematic phase, very high clearing points and low smectic-nematic transition temperatures being observed, leading to an improvement in the storage stability. Particular preference is given to mixtures which, in addition to one or more compounds of the formulae CC, I and II, comprise one or more compounds of the formulae IIA and/or IIB and/or III and/or IV. All of the above compounds are colorless, stable, and readily miscible with each other and with other liquid crystal materials.

The optimum mixing ratio of the compounds of the formulae CC, I, II, IIA, IIB and III to V depends primarily on the desired properties, on the choice of the components of the formulae CC, I, II, IIA, IIB and III to V and on the choice of any other ingredients which may be present.

An appropriate mixing ratio within the above-given range can be easily determined depending on the case.

The total amount of the compounds of the formulae CC, I, II, IIA, IIB and III to V in the mixture according to the invention is not critical. Thus, to optimize various properties, the mixture may comprise one or more other components. However, the larger the observed effect on the addressing time and threshold voltage in general, the higher the total concentration of the compounds of formulae CC, I, IIA, IIB, II and III. Furthermore, the higher the clearing point, the greater the proportion of compounds of formulae IIA, IIB, III and IV.

The construction of the light valve according to the invention, consisting of a polarizer, an electrode substrate and surface-treated electrodes, corresponds to the usual design of this type of component. The term "common design" is here broadly proposed and also includes all derivatives and modifications of components, in particular also matrix display elements based on poly-silicon (poly-Si) TFTs or MIMs.

However, a significant difference between the liquid crystal light valve according to the invention and conventional displays based hitherto on twisted nematic cells consists in the choice of the liquid crystal parameters of the liquid crystal layer.

The liquid-crystal mixtures which can be used according to the invention are prepared in a manner conventional per se. In general, the desired amount of the components used in lesser amounts is dissolved in the components making up the main constituent, advantageously at elevated temperature. It is also possible to mix solutions of the components in an organic solvent, for example in acetone, chloroform or methanol, and to remove the solvent again, for example by distillation, after thorough mixing.

The dielectric may also contain other additives known to those skilled in the art and described in the literature. For example, 0-15% of a pleochroic dye or chiral dopant may be added.

C represents a crystalline phase, S represents a smectic phase, S represents_CRepresents a smectic C phase, N represents a nematic phase, and I represents an isotropic phase.

V₁₀The voltage for 10% transmission (viewing direction perpendicular to the plate surface) is indicated. t is t_ondenotes the on-time, t_offIndicating that the operating voltage corresponds to V₁₀Value 2.0 timesThe off time of the time. Δ n represents optical anisotropy, n_oRepresenting the refractive index. Δ ∈ denotes dielectric anisotropy (Δ ∈ ═ epsilon)_‖-ε_⊥In which epsilon_‖denotes the dielectric constant parallel to the longitudinal molecular axis, and_⊥Representing the dielectric constant perpendicular to the longitudinal molecular axis). Unless otherwise specifically stated, the electro-optical data were measured at a first minimum value (i.e., at a d · Δ n value of 0.5) in a TN cell at 20 ℃. Unless explicitly stated otherwise, optical data were measured at 20 ℃.

for the purposes of the present invention and the examples which follow, the structures of the liquid-crystalline compounds are indicated by acronyms and are converted into chemical formulae in accordance with the following tables A to C. All radicals C_nH_2n+1，C_mH_2m+1And C_lH_2l+1Or C_nH_2n，C_mH2_mAnd C_lH_2lAre both straight-chain alkyl or alkylene radicals having in each case n, m and l carbon atoms. Table a shows the code for the ring elements of the core of the compound, table B the bridging units and table C the symbolic meanings of the left-hand and right-hand end groups of the molecule. The acronyms consist of: the code for the ring element with the optional linker group is followed by the code for the first hyphen and left hand end group, the code for the second hyphen and right hand end group. Table D shows illustrative structures of the compounds and their respective abbreviations.

Table a: ring element

Table B: bridging unit

Table C: terminal group

Where n and m are each integers, and the three points "…" are placeholders for other abbreviations in the table.

In addition to the compounds of the formula CC, the mixtures according to the invention preferably also comprise one or more compounds of the following compounds.

The following abbreviations are used:

(n, m and z are each, independently of one another, an integer, preferably 1 to 6)

Table D

Table E shows the chiral dopants preferably used in the mixtures according to the invention.

TABLE E

In a preferred embodiment of the present invention, the medium according to the present invention comprises one or more compounds selected from the compounds of table E.

Table F shows stabilizers which can preferably be used in the mixtures according to the invention, in addition to the compounds of the formula CC. The parameter n here represents an integer of 1 to 12. In particular, the indicated phenol derivatives can be used as further stabilizers, since they act as antioxidants.

TABLE F

In a preferred embodiment of the invention, the medium according to the invention comprises one or more compounds selected from the compounds of table F, preferably in a total concentration of 0.01% to 0.2%.

The following examples are intended to illustrate the invention without limiting it. The percentage data in the context indicate weight percentages. All temperatures are expressed in degrees celsius. m.p. denotes melting point, T_(N，I)it is a clearing spot. Further, C is a crystalline state, N is a nematic phase, S is a smectic phase, and I is an isotropic phase. The data between these symbols represents the transition temperature. Δ n represents optical anisotropy (589nm, 20 ℃ C.), and Δ ε represents dielectric anisotropy (1kHz, 20 ℃ C.); flow viscosity v₂₀(mm²sec) and rotationtrans viscosity gamma₁(mPas) were determined in each case at 20 ℃.

Example M1