Process for the purification of a liquid-crystal mixture

Abstract

In a process for the purification of a liquid-crystal mixture (7), the liquid-crystal mixture (7) is passed through a first electrodialysis cell (2) and a concentrate solution (14) is passed through a second electrodialysis cell (8) which is adjacent to the first electrodialysis cell (2) and is separated by an ion-exchanger membrane (9), and an electric field transverse to a direction of passage of the liquid-crystal mixture (7) through the first electrodialysis cell (2) is generated with the aid of an anode/cathode arrangement (15, 16) arranged outside the electrodialysis cells (2, 8) so that ionized constituents of the liquid-crystal mixture (7) are discharged at the ion-exchanger membrane (9) and removed from the liquid-crystal mixture (7).

Claims

1. Process for the purification of a liquid-crystal mixture (7), which comprises passing the liquid-crystal mixture (7) through a first electrodialysis cell (2), passing a concentrate solution (14) through a second electrodialysis cell (8) which is adjacent to the first electrodialysis cell (2) with the first and second electrodialysis cells separated by an ion-exchanger membrane (9), and, with the aid of an anode/cathode arrangement (15, 16) arranged outside the electrodialysis cells (2, 8), generating an electric field transverse to a direction of passage of the liquid-crystal mixture (7) through the first electrodialysis cell (2) so that ionised constituents of the liquid-crystal mixture (7) are discharged at the ion-exchanger membrane (9) and removed from the liquid-crystal mixture (7).

2. Process according to claim 1, which comprises passing the liquid-crystal mixture (7) through the first electrodialysis cell (2) multiple times.

3. Process according to claim 1, which comprises passing the liquid-crystal mixture (7) successively through a plurality of electrodialysis cells having an arrangement, comparable to the first electrodialysis cell (2), of an ion-exchanger membrane (9) and an adjacent second electrodialysis cell (8) and an electric field.

4. Process according to claim 1, which comprises passing the liquid-crystal mixture (7) through the first electrodialysis cell (2) over a period of more than one hour.

5. Process according to claim 1, wherein the concentrate solution (14) used is deionised water.

6. Process according to claim 1, wherein the ion-exchanger membrane (9) used is a membrane having a breakdown voltage of greater than 10 volts and an electric potential difference which effects the greatest possible drop in voltage at the ion-exchanger membrane (9), but which is below the breakdown voltage, is pre-specified with the aid of the anode/cathode arrangement (15, 16).

7. Process according to claim 6, wherein the ion-exchanger membrane (9) used is a membrane having a breakdown voltage of greater than 80 volts.

8. Process according to claim 6, wherein the ion-exchanger membrane (9) used is a membrane having a breakdown voltage of greater than 400 volts.

9. Process according to claim 1, wherein the anode (15) and the cathode (16) are flushed with transformer oil (19) while the process is being carried out.

10. Process according to claim 1, wherein low-pulsation pumps are used to convey the liquid-crystal mixture (7) and the concentrate solution (14).

11. Process according to claim 1, further comprising thoroughly mixing and homogenizing the liquid-crystal mixture (7) before introducing it into the first electrodialysis cell (2).

12. Process according to claim 1, which comprises passing the liquid-crystal mixture (7) through the first electrodialysis cell (2) over a period of more than four hours.

13. Process according to claim 1, wherein the ion-exchange membrane (9) is a cation-exchanger membrane and the anode and the cathode are separated from the first and second electrodialysis cells by anion-exchanger membranes.

Description

BRIEF DESCRIPTION OF THE FIGURES

(1) FIG. 1 shows a diagrammatic representation of a purification process according to the invention which is carried out with the aid of a suitable electrodialysis device, and

(2) FIG. 2 shows a diagrammatic representation of a change in a specific resistance of a liquid-crystal mixture over time over the duration of performance of the purification process.

(3) A purification device 1, depicted by way of example in FIG. 1, by means of which the process according to the invention for the purification of a liquid-crystal mixture can be carried out has a first electrodialysis cell 2 having a supply line 3 and a discharge line 4, which are connected to a liquid-crystal mixture reservoir 5. With the aid of a gear pump 6, an amount of fluid of a liquid-crystal mixture 7 can be conveyed out of the liquid-crystal mixture reservoir 5, through the first electrodialysis cell 2 and back into the liquid-crystal mixture reservoir 5, so that a circuit is produced and the liquid-crystal mixture 7 is passed continuously through the first electrodialysis cell 2. In the representation in accordance with FIG. 1, the liquid-crystal mixture 7 flows through the first electrodialysis cell 2 in a direction of passage running from top to bottom.

(4) A second electrodialysis cell 8, which is adjacent to the first electrodialysis cell 2, is separated from the first electrodialysis cell 2 by a suitable anion-exchanger membrane 9. The second electrodialysis cell 8 likewise has a supply line 10 and a discharge line 11, which are connected to a concentrate-solution reservoir 12, so that a concentrate solution 14 can be passed through the second electrodialysis cell 8 with the aid of a gear pump 13. The concentrate solution 14 used is deionised water.

(5) The first electrodialysis cell 2 and the second electrodialysis cell 8 are arranged between an anode 15 and a cathode 16 in such a way that an electric field transverse to the direction of passage of the liquid-crystal mixture 7 in the first electrodialysis cell 2 can be generated by means of this anode/cathode arrangement.

(6) The anode 15 and the cathode 16 are separated from the first electrodialysis cell 2 and from the second electrodialysis cell 8 in each case by a cation-exchanger membrane 17 and can be flushed continuously or on demand with transformer oil 19 with the aid of a transformer-oil circuit 18.

(7) All components which come into contact with the liquid-crystal mixture 7, such as, for example, the electrodialysis cells 2 and 8, the ion-exchanger membranes 9 and 17, the spacers and the tubes used for the supply lines 3 and 10 and the discharge lines 4 and 11, are made from an inert polymer or provided with a corresponding coating. A suitable inert polymer is, for example, PFA or PTFE.

(8) In order to carry out the purification process, a potential difference of, for example, 80 volts or 120 volts is generated between the anode 15 and the cathode 16 with the aid of a direct-voltage source. The gear pumps 6 and 13 are started and effect uniform passage of the liquid-crystal mixture 7 through the first electrodialysis cell 2 and of the concentrate solution 14 through the second electrodialysis cell 8. While the liquid-crystal mixture 7 flows through the first electrodialysis cell 2, ionised impurities are diverted by the electric field either in the direction of the second electrodialysis cell 8 at the anion-exchanger membrane 9, or, in the case of an opposite charge sign of the ionised impurity, in the direction of the cathode 16 at the cation-exchanger membrane 17 and are thereby removed from the liquid-crystal mixture 7 flowing through.

(9) The liquid-crystal mixture can be passed through the first electrodialysis cell 2 over a sufficiently long period. While the purification process is being carried out, samples can be taken continuously or at time intervals in order to determine and monitor the purification of the liquid-crystal mixture 7 that has already been achieved.

(10) FIG. 2 depicts diagrammatically a specific resistance ρ in the unit ohm×cm determined while the purification process for a liquid-crystal mixture 7 is being carried out, as a function of the purification duration t in the unit hours. The specific resistance ρ is a measure of the proportion of dissolved ions in the liquid-crystal mixture 7 and thus at least indirectly a measure of the proportion of ionised impurities present in the liquid-crystal mixture 7. The greater the specific resistance ρ, the smaller the proportion of ionised impurities and the higher the purity of the liquid-crystal mixture 7. It has been found that the specific resistance ρ of a typical liquid-crystal mixture 7 increases by about a factor of 10 after only one hour and by about a factor of 40 after about four hours.

(11) The purification process according to the invention can be carried out using standard laboratory electrodialysis devices and merely requires continuous operation of the gear pumps. Correspondingly, the purification process can be carried out using simple equipment and inexpensively and facilitates very efficient purification of the liquid-crystal mixture 7. The efficiency can be increased further by additionally carrying out further purification processes based on other methods beforehand.

(12) The purification process described above is particularly suitable for liquid-crystal mixtures comprising at least two organic substances, preferably mesogenic, in particular liquid-crystalline substances, where the organic substances are preferably selected from the compounds of the general formula I,

(13) ##STR00001## in which R.sup.1 and R.sup.2 each, independently of one another, denote H, an alkyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF.sub.3 or at least monosubstituted by halogen, where, in addition, one or more CH.sub.2 groups in these radicals may be replaced by —O—, —S—,

(14) ##STR00002## —C≡C—, —CH═CH—, —CF.sub.2O—, —OCF.sub.2—, —OC—O— or —O—CO— in such a way that O atoms are not linked directly to one another, and one of the radicals R.sup.1 and R.sup.2 also denotes F, Cl, CN, SF.sub.5, NCS, SCN, OCN, rings A, B, C, D and E each, independently of one another, denote

(15) ##STR00003## ##STR00004## ##STR00005## ##STR00006## r, s and t each, independently of one another, denote 0, 1, 2 or 3, where r+s+t≦3, Z.sup.1-4 each, independently of one another, denote —CO—O—, —O—CO—, —CF.sub.2O—, —OCF.sub.2—, —CH.sub.2O—, —OCH.sub.2—, —CH.sub.2CH.sub.2—, —(CH.sub.2).sub.4—, —CH═CH—CH.sub.2O, —C.sub.2F.sub.4—, —CH.sub.2CF.sub.2—, —CF.sub.2CH.sub.2—, —CF═CF—, —CH═CF—, —CF═CH—, —CH═CH—, —C≡C— or a single bond, and L.sup.1 and L.sup.2 each, independently of one another, denote H or F.

(16) In the case where r+s+t=0, Z.sup.1 and Z.sup.4 are preferably selected in such a way that, if they do not denote a single bond, they are not linked to one another via two O atoms.

(17) The liquid-crystal mixtures employed comprising the individual mesogenic substances may additionally also comprise one or more polymerisable compounds, so-called reactive mesogens (RMs), for example as disclosed in U.S. Pat. No. 6,861,107, in concentrations of, preferably, 0.1-5% by weight, particularly preferably 0.2-2% by weight, based on the mixture. Mixtures of this type can be used for so-called polymer stabilised VA (PS-VA) modes, negative IPS (PS-IPS) or negative FFS (PS-FFS) modes, in which polymerisation of the reactive mesogens is intended to take place in the liquid-crystalline mixture. The prerequisite for this is that the liquid-crystal mixture does not itself comprise any individual polymerisable substances.

(18) The prerequisite for this is that the liquid-crystal mixture itself does not comprise any polymerisable components which likewise polymerise under the conditions where the compounds of the formula M polymerise.

(19) The polymerisation is preferably carried out under the following conditions:

(20) The polymerisable components are polymerised in a cell using a UV-A lamp of defined intensity for a defined period and applied voltage (typically 10 V to 30 V alternating voltage, frequencies in the range from 60 Hz-1 kHz). The UV-A light source employed is typically a metal-halide vapour lamp or high-pressure mercury lamp having an intensity of 50 mW/cm.sup.2. These are conditions where, for example, liquid-crystalline compounds containing an alkenyl or alkenyloxy side chain, such as, for example, the compound of the formula

(21) ##STR00007##
do not polymerise.

(22) The polymerisable mesogenic or liquid-crystalline compounds, also known as “reactive mesogens” (RMs), are preferably selected from the compounds of the formula II
R.sup.a-A.sup.1-(Z.sup.1-A.sup.2).sub.m-R.sup.b  II
in which the individual radicals have the following meanings: A.sup.1 and A.sup.2 each, independently of one another, denote an aromatic, heteroaromatic, alicyclic or heterocyclic group, preferably having 4 to 25 C atoms, which may also contain fused rings and which is optionally mono- or polysubstituted by L, Z.sup.1 on each occurrence, identically or differently, denotes —O—, —S—, —CO—, —CO—O—, —OCO—, —O—CO—O—, —OCH.sub.2—, —CH.sub.2O—, —SCH.sub.2—, —CH.sub.2S—, —CF.sub.2O—, —OCF.sub.2—, —CF.sub.2S—, —SCF.sub.2—, —(CH.sub.2).sub.n—, —CF.sub.2CH.sub.2—, —CH.sub.2CF.sub.2—, —(CF.sub.2).sub.n—, —CH═CH—, —CF═CF—, —C≡C—, —CH═CH—COO—, —OCO—CH═CH—, CR.sup.0R.sup.00 or a single bond, L, R.sup.a and R.sup.b each, independently of one another, denote H, halogen, SF.sub.5, NO.sub.2, a carbon group or hydrocarbon group, where the compounds contain at least one radical L, R.sup.a and R.sup.b which denotes or contains a P-Sp-group, R.sup.0 and R.sup.00 each, independently of one another, denote H or alkyl having 1 to 12 C atoms, P denotes a polymerisable group, Sp denotes a spacer group or a single bond, m denotes 0, 1, 2, 3 or 4, n denotes 1, 2, 3 or 4.

(23) The polymerisable compounds may contain one polymerisable group (monoreactive) or two or more (di- or multireactive), preferably two, polymerisable groups.

(24) Above and below, the following meanings apply:

(25) The term “mesogenic group” is known to the person skilled in the art and is described in the literature, and denotes a group which, due to the anisotropy of its attracting and repelling interactions, essentially contributes to causing a liquid-crystal (LC) phase in low-molecular-weight or polymeric substances. Compounds containing mesogenic groups (mesogenic compounds) do not necessarily have to have an LC phase themselves. It is also possible for mesogenic compounds to exhibit LC phase behaviour only after mixing with other compounds and/or after polymerisation. Typical mesogenic groups are, for example, rigid rod- or disc-shaped units. An overview of the terms and definitions used in connection with mesogenic or LC compounds is given in Pure Appl. Chem. 73(5), 888 (2001) and C. Tschierske, G. Pelzl, S. Diele, Angew. Chem. 2004, 116, 6340-6368.

(26) The term “spacer group”, also referred to as “Sp” above and below, is known to the person skilled in the art and is described in the literature, see, for example, Pure Appl. Chem. 73(5), 888 (2001) and C. Tschierske, G. Pelzl, S. Diele, Angew. Chem. 2004, 116, 6340-6368. Unless indicated otherwise, the term “spacer group” or “spacer” above and below denotes a flexible group which connects the mesogenic group and the polymerisable group(s) in a polymerisable mesogenic compound (“RM”) to one another. Sp preferably denotes a single bond or a 1-16 C alkylene, in which one or more CH.sub.2 groups may be replaced by —O—, —CO—, —COO— or —OCO— in such a way that two O atoms are not connected directly to one another.

(27) The term “organic group” denotes a carbon or hydrocarbon group.

(28) The term “carbon group” denotes a mono- or polyvalent organic group containing at least one carbon atom which either contains no further atoms (such as, for example, —C≡C—) or optionally contains one or more further atoms, such as, for example, N, O, S, P, Si, Se, As, Te or Ge (for example carbonyl, etc.). The term “hydrocarbon group” denotes a carbon group which additionally contains one or more H atoms and optionally one or more heteroatoms, such as, for example, N, O, S, P, Si, Se, As, Te or Ge.

(29) “Halogen” denotes F, Cl, Br or I.

(30) The terms “alkyl”, “aryl”, “heteroaryl”, etc., also encompass polyvalent groups, for example alkylene, arylene, heteroarylene, etc.

(31) The term “alkyl” in this application encompasses straight-chain and branched alkyl groups having 1 to 9 carbon atoms, preferably the straight-chain groups methyl, ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl and nonyl. Groups having 1 to 5 carbon atoms are particularly preferred.

(32) The term “alkenyl” in this application encompasses straight-chain and branched alkenyl groups having 2 to 9 carbon atoms, preferably the straight-chain groups having 2 to 7 carbon atoms. Particularly preferred alkenyl groups are C.sub.2-C.sub.7-1E-alkenyl, C.sub.4-C.sub.7-3E-alkenyl, C.sub.5-C.sub.7-4-alkenyl, C.sub.6-C.sub.7-5-alkenyl and C.sub.7-6-alkenyl, in particular C.sub.2-C.sub.7-1E-alkenyl, C.sub.4-C.sub.7-3E-alkenyl and C.sub.5-C.sub.7-4-alkenyl. Examples of preferred alkenyl groups are vinyl, 1E-propenyl, 1E-butenyl, 1E-pentenyl, 1E-hex-enyl, 1E-hept-enyl, 3-butenyl, 3E-pentenyl, 3E-hexenyl, 3E-heptenyl, 4-pentenyl, 4Z-hexenyl, 4E-hexenyl, 4Z-hep-tenyl, 5-hexenyl, 6-heptenyl and the like. Groups having up to 5 carbon atoms are particularly preferred.

(33) The term “fluoroalkyl” in this application encompasses straight-chain groups having a terminal fluorine, i.e. fluoromethyl, 2-fluoroethyl, 3-fluoropropyl, 4-fluoro-butyl, 5-fluoro-pentyl, 6-fluorohexyl and 7-fluoroheptyl. However, other positions of the fluorine are not excluded.

(34) The term “oxaalkyl” or “alkoxy” in this application encompasses straight-chain radicals of the formula C.sub.nH.sub.2n+1-O—(CH.sub.2).sub.m, in which n and m each, independently of one another, denote 1 to 6. Preferably, n=1 and m=1 to 6.

(35) The term “aryl” denotes an aromatic carbon group or a group derived therefrom. The term “heteroaryl” denotes “aryl” in accordance with the above definition containing one or more heteroatoms.

(36) The polymerisable group P is a group which is suitable for a polymerisation reaction, such as, for example, free-radical or ionic chain polymerisation, polyaddition or polycondensation, or for a polymer-analogous reaction, for example addition or condensation onto a main polymer chain. Particular preference is given to groups for chain polymerisation, in particular those containing a C═C double bond or a —C≡C— triple bond, and groups which are suitable for polymerisation with ring opening, such as, for example, oxetane or epoxide groups.

(37) The polymerisable compounds are prepared analogously to processes which are known to the person skilled in the art and are described in standard works of organic chemistry, such as, for example, in Houben-Weyl, Methoden der organischen Chemie [Methods of Organic Chemistry], Thieme-Verlag, Stuttgart.

(38) Typical and preferred reactive mesogens (RMs) are described, for example, in WO 93/22397, EP 0 261 712, DE 195 04 224, WO 95/22586, WO 97/00600, U.S. Pat. No. 5,518,652, U.S. Pat. No. 5,750,051, U.S. Pat. No. 5,770,107 and U.S. Pat. No. 6,514,578. Very particularly referred reactive mesogens are shown on Table E.

(39) The process is used for the preparation of a mixture consisting of organic compounds, one or more of which are preferably mesogenic, preferably liquid-crystalline, per se. The mesogenic compounds preferably include one or more liquid-crystalline compounds. The process product is preferably a homogeneous, liquid-crystalline mixture. In the broader sense, the process also encompasses the preparation of mixtures which consist of organic substances in the homogeneous liquid phase and comprise additives which are insoluble therein (for example small particles). The process can thus also be used for the preparation of suspension-like or emulsion-like mixtures based on a continuous homogeneous organic phase. However, process variants of this type are generally less preferred.

(40) By means of suitable additives, the liquid-crystal mixtures comprising at least two compounds of the formula I can be modified in such a way that they can be employed in any type of LCD display that has been disclosed to date, for example, ECB, VAN, IPS, FFS, TN, TN-TFT, STN, OCB, GH, PS-IPS, PS-FFS, PM-VA, PVA, PSA, PS-VA or ASM-VA displays.

(41) The liquid-crystal mixtures may also comprise further additives known to the person skilled in the art and described in the literature, such as, for example, UV stabilisers, such as, for example, Tinuvin®, for example Tinuvin® 770, from BASF, antioxidants, such as, for example, Irganox®, for example Irganox® 1076 (octadecyl 3-(3,5-di-tert.butyl-4-hydroxyphenyl)propionate), from BASF, free-radical scavengers, nanoparticles, microparticles, one or more dopants, etc. For example, 0-15% of pleochroic dyes may be added, furthermore conductive salts, preferably ethyldimethyldodecylammonium 4-hexoxybenzoate, tetrabutylammonium tetraphenylboranate or complex salts of crown ethers (cf., for example, Haller et al., Mol. Cryst. Liq. Cryst. Volume 24, pages 249-258 (1973)) in order to improve the conductivity, or substances can be added in order to modify the dielectric anisotropy, the viscosity and/or the alignment of the nematic phases. Substances of this type are described, for example, in DE-A 22 09 127, 22 40 864, 23 21 632, 23 38 281, 24 50 088, 26 37 430 and 28 53 728.

(42) Suitable stabilisers and dopants which can be combined with the compounds of the formula I in the electrodialysis cell during the preparation of the liquid-crystal mixtures are indicated below in Tables C and D.

(43) The following examples are intended to explain the invention without limiting it. Above and below, percent data denote percent by weight; all temperatures are indicated in degrees Celsius.

(44) Throughout the patent application, 1,4-cyclohexylene rings and 1,4-phenylene rings are depicted as follows:

(45) ##STR00008##

(46) The cyclohexylene rings are trans-1,4-cyclohexylene rings.

(47) In the present application and in the following examples, the structures of the liquid-crystal compounds are indicated by means of acronyms, with the transformation into chemical formulae taking place in accordance with Tables A and B below. All radicals C.sub.nH.sub.2n+1 and C.sub.mH.sub.2m+1 are straight-chain alkyl radicals having n and m C atoms respectively; n, m, k and z are integers and preferably denote 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12. The term “(O)C.sub.mH.sub.2m-1” means OC.sub.mH.sub.2m+1 or C.sub.mH.sub.2m+1. The coding in Table B is self-evident.

(48) In Table A, only the acronym for the parent structure is indicated. In individual cases, this is followed, separated from the acronym for the parent structure by a dash, by a code for the substituents R.sup.1*, R.sup.2*, L.sup.1* and L.sup.2*:

(49) TABLE-US-00001 Code for R.sup.1*, R.sup.2*, L.sup.1*, L.sup.2*, L.sup.3* R.sup.1* R.sup.2* L.sup.1* L.sup.2* nm C.sub.nH.sub.2n+1 C.sub.mH.sub.2m+1 H H nOm C.sub.nH.sub.2n+1 OC.sub.mH.sub.2m+1 H H nO.m OC.sub.nH.sub.2n+1 C.sub.mH.sub.2m+1 H H n C.sub.nH.sub.2n+1 CN H H nN.F C.sub.nH.sub.2n+1 CN F H nN.F.F C.sub.nH.sub.2n+1 CN F F nF C.sub.nH.sub.2n+1 F H H nCl C.sub.nH.sub.2n+1 Cl H H nOF OC.sub.nH.sub.2n+1 F H H nF.F C.sub.nH.sub.2n+1 F F H nF.F.F C.sub.nH.sub.2n+1 F F F nOCF.sub.3 C.sub.nH.sub.2n+1 OCF.sub.3 H H nOCF.sub.3.F C.sub.nH.sub.2n+1 OCF.sub.3 F H n-Vm C.sub.nH.sub.2n+1 —CH═CH—C.sub.mH.sub.2m+1 H H nV-Vm C.sub.nH.sub.2n+1—CH═CH— —CH═CH—C.sub.mH.sub.2m+1 H H

(50) Preferred mesogenic or liquid-crystalline substances which are suitable for the preparation of liquid-crystal mixtures and can be used in the purification process according to the invention are listed, in particular, in Tables A and B:

(51) TABLE-US-00002 TABLE A PYP 0 PYRP BCH CBC CCH CCP CPTP CEPTP ECCP CECP EPCH 0 PCH CH PTP CCPC CP BECH EBCH CPC B FET-nF 0 CGG CGU CFU

(52) TABLE-US-00003 TABLE B (n = 1-15; (O)C.sub.nH.sub.2n+1 means C.sub.nH.sub.2n+1 or OC.sub.nH.sub.2n+1) APU-n-OXF ACQU-n-F CPU-n-OXF APUQU-n-F BCH-n.Fm CFU-n-F CBC-nmF 0 CCP-nOCF.sub.3 CCZU-n-F ECCP-nm ECCP-nF.F PGP-n-m CGU-n-F CGUQU-n-F CLUQU-n-F CDUQU-n-F CDU-n-F 0 DCU-n-F CGG-n-F CPZG-n-OT CC-nV-Vm GPP-n-m CCP-Vn-m CCG-V-F CCP-nV-m CC-n-V CCQU-n-F 0 CC-n-Vm CPPC-nV-Vm CCQG-n-F CQU-n-F CP-1V-m CP-2V-m CP-V2-m CP-1V-N CP-V2-N CCP-nF 0 CCP-nF.F BCH-nF.F.F CCP-nF.F.F Dec-U-n-F CWCU-n-F CPGP-n-m CWCG-n-F CCOC-n-m CPTU-n-F GPTU-n-F 0 PQU-n-F PUQU-n-F PGU-n-F CGZP-n-OT PGU-n-OXF CCGU-n-F CUQU-n-F CCCQU-n-F CPGU-n-OT CPGU-n-F 0 CVCP-1V-OT GGP-n-Cl PP-nV-Vm PP-1-nVm CWCQU-n-F PPGU-n-F PGUQU-n-F GPQU-n-F MPP-n-F PGP-n-kVm 00 PP-n-kVm 01 PCH-nCl 02 GP-n-Cl 03 GGP-n-F 04 PGIGI-n-F 05 AIK-n-F 06 BCH-nm 07 BCN-nm 08 CY-n-Om 09 CP(F,Cl)n-Om 0 CP(Cl,F)-n-Om CCY-n-Om CCY-n-m CCP(Cl,F)-n-Om CCP(F,Cl)n-Om CCY-V-m CCY-Vn-m CCY-n-OmV CBC-nm CCP-V-m 0 CCP-n-m CPYC-n-m CYYC-n-m CCYY-n-(O)m CCY-n-O2V CY-n-m CCH-nm CCH-nOm CEY-n-Om CC-n-V1 0 CY-n-OV CC-2V-V2 CVC-n-m CC-n-mV CP-nOmFF CH-nm CEY-V-n CVY-V-n CY-V-On CY-n-OC(CH.sub.3)═CH.sub.2 0 CY-1V-On CY-V1-On CY-n-O1V CCN-nm CCPC-nm CCY-n-zOm CPY-n-m CPY-n-Om CPY-1V-Om CPY-V-Om 0 CPP(Cl,F)-n-(O)m CQY-n-(O)m CPP(F,Cl)n—(O)m CQIY-n-(O)m PGIY-n-Om CCQY-n-(O)m CCQIY-n-(O)m CPQY-n-(O)m CPQIY-n-(O)m CPYG-n-(O)m 0 CCY-V-Om D-nOmFF CY-nV-(O)m PCH-nm PCH-nOm CY-nV-OmV DPGU-n-F DPGU-n-OT PP-n-m PYP-n-mV 0 CYLI-n-m CENap-n-Om LY-n-(O)m CCNap-n-Om CNap-n-Om YPY-n-mV CETNap-n-Om CTNap-n-Om CK-n-F YPY-n-m 0 LYLI-n-m C-DFDBF-n-(O)m CPYG-n-(O)m DFDBC-n(O)-(O)m HP-nN.F CCY-V2-(O)m CCY-1V2-(O)m CCY-3V-(O)m PYP-nF MEnN.F 0 MUQU-n-F NUQU-n-F CCY-V2-(O)m CCY-1V2-(O)m CCY-3V-(O)m CCVC-n-V COChrom-n-Om COChrom-n-m CCOChrom-n-Om CCOChrom-n-m 00 CONaph-n-Om 01 CCONaph-n-Om 02 CLY-n-Om 03 CLY-n-m 04 LYLI-n-m 05 CYLI-n-m 06 LY-n-(O)m 07 COYOICC-n-m 08 COYOIC-n-V 09 CCOY-V-O2V 0 CCOY-V-O3V COY-n-Om CCOY-n-Om PYP-n-m PYP-n-Om YPY-n-m YPY-n-mV Y-nO-Om Y-n-Om PY-n-m 0 PY-n-Om PY-V2-Om PY-3V-Om PY-V-Om PY-1V-Om PY-1V2-Om C-DFDBF-n-(O)m DFDBC-n(O)-(O)m B-nO-Om DFDBC-n(O)-(O)m 0 CPU-n-VT CPU-n-AT DGUQU-n-F C-n-V C-n-XF C-n-m CC-n-2V1 BCH-nF BCH-nF.F 0 PY-n-m PY-n-Om PTP-nOmFF CPTP-nOmFF PPTUI-n-m CPTP-nOm CPTP-nm PTP-nOm PTP-nm Y-nO-Om 0 Y-nO-OmV Y-nO-OmVm′

(53) Particular preference is given to liquid-crystalline mixtures which comprise at least one, two, three, four or more compounds from Table B besides one or more compounds of the formula I.

(54) TABLE-US-00004 TABLE C 0

(55) Table C indicates possible dopants, which are generally added to the liquid-crystalline mixtures. The mixtures preferably comprise 0-10% by weight, in particular 0.01-5% by weight and particularly preferably 0.01-3% by weight, of dopants.

(56) TABLE-US-00005 TABLE D STAB-1 STAB-2 STAB-3 STAB-4 STAB-5 0 STAB-6 STAB-7 STAB-8 STAB-9 STAB-10 STAB-11 STAB-12 STAB-13 STAB-14 STAB-15 0 STAB-16 STAB-17 STAB-18 STAB-19 STAB-20 STAB-21 STAB-22 STAB-23 STAB-24 STAB-25 0 STAB-26 STAB-27 STAB-28 STAB-29 STAB-30 STAB-31 STAB-32 STAB-33 STAB-34 STAB-35 00 STAB-36 01 STAB-37 02 STAB-38

(57) Stabilisers, which can be added, for example, to the liquid-crystalline mixtures in amounts of 0-10% by weight, are shown below.

(58) (n=1-12)

(59) Suitable polymerisable compounds (reactive mesogens) for use in the mixtures according to the invention, preferably in PSA and PS-VA applications or PS-IPS/FFS applications, are shown below in Table E:

(60) TABLE-US-00006 TABLE E 03 RM-1 04 RM-2 05 RM-3 06 RM-4 07 RM-5 08 RM-6 09 RM-7 0 RM-8 RM-9 RM-10 RM-11 RM-12 RM-13 RM-14 RM-15 RM-16 RM-17 0 RM-18 RM-19 RM-20 RM-21 RM-22 RM-23 RM-24 RM-25 RM-26 RM-27 0 RM-28 RM-29 RM-30 RM-31 RM-32 RM-33 RM-34 RM-35 RM-36 RM-37 0 RM-38 RM-39 RM-40 RM-41 RM-42 RM-43 RM-44 RM-45 RM-46 RM-47 0 RM-48 RM-49 RM-50 RM-51 RM-52 RM-53 RM-54 RM-55 RM-56 RM-57 0 RM-58 RM-59 RM-60 RM-61 RM-62 RM-63 RM-64 RM-65 RM-66 RM-67 0 RM-68 RM-69 RM-70 RM-71 RM-72 RM-73 RM-74 RM-75 RM-76 RM-77 0 RM-78 RM-79 RM-80 RM-81 RM-82 RM-83 RM-84 RM-85 RM-86 RM-87 0 RM-88 RM-89 RM-90 RM-91 RM-92 RM-93 RM-94 RM-95

(61) Table E shows example compounds which can preferably be used as reactive mesogenic compounds in the liquid-crystalline mixtures according to the invention. If the liquid-crystalline mixtures comprise one or more reactive compounds, they are preferably employed in amounts of 0.01-5% by weight. It may be necessary also to add an initiator or a mixture of two or more initiators for the polymerisation. The initiator or the initiator mixture is preferably added in amounts of 0.001-2% by weight, based on the mixture. A suitable initiator is, for example, Irgacure (BASF) or Irganox (BASF).

(62) Suitable polymerisable compounds (reactive mesogens) for use in the mixtures according to the invention, preferably in PSA and PS-VA applications or PS-IPS/FFS applications, are shown below in Table E:

(63) In a preferred embodiment, the liquid-crystalline mixtures comprise one or more compounds selected from the group of the compounds from Table E.

EXAMPLES

(64) The following working examples are intended to explain the invention without restricting it.

(65) Above and below, percent data denote percent by weight. All temperatures are indicated in degrees Celsius. m.p. denotes melting point, cl.p.=clearing point. Furthermore, C=crystalline state, N=nematic phase, S=smectic phase and I=isotropic phase. The data between these symbols represent the transition temperatures. Furthermore, V.sub.o denotes threshold voltage, capacitive [V] at 20° C. Δπ denotes the optical anisotropy measured at 20° C. and 589 nm Δ∈ denotes the dielectric anisotropy at 20° C. and 1 kHz cl.p. denotes clearing point [° C.] K.sub.1 denotes elastic constant, “splay” deformation at 20° C., [pN] K.sub.3 denotes elastic constant, “bend” deformation at 20° C., [pN] γ.sub.1 denotes rotational viscosity measured at 20° C. [mPa.Math.s], determined by the rotation method in a magnetic field LTS denotes low-temperature stability (nematic phase), determined in test cells.

(66) The following examples are intended to explain the invention without limiting it.

(67) Above and below, percentages denote percent by weight. All temperatures are indicated in degrees Celsius.

WORKING EXAMPLES

Example 1

(68) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(69) TABLE-US-00007 CCH-35 9.47% CCH-501 4.99% CCY-2-1 9.47% CCY-3-1 10.47% CCY-3-O2 10.47% CCY-5-O2 9.47% CPY-2-O2 11.96% CY-3-O4 8.97% CY-5-O4 10.97% RM-1 0.30% PCH-53 13.46%
is purified using the process according to the invention.

Example 2

(70) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(71) TABLE-US-00008 BCH-32 7.48% CCH-23 21.93% CCH-34 3.49% CCY-3-O3 6.98% CCY-4-O2 7.98% CPY-2-O2 10.97% CPY-3-O2 10.97% CY-3-O2 15.45% RM-1 0.30% PCH-301 12.46% PCH-302 1.99%
is purified using the process according to the invention.

Example 3

(72) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(73) TABLE-US-00009 CC-3-V1 7.98% CCH-23 17.95% CCH-34 3.99% CCH-35 6.98% CCP-3-1 4.99% CCY-3-O2 12.46% CPY-2-O2 7.98% CPY-3-O2 10.97% CY-3-O2 15.45% RM-1 0.30% PY-3-O2 10.97%
is purified using the process according to the invention.

Example 4

(74) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(75) TABLE-US-00010 CC-3-V1 8.97% CCH-23 12.96% CCH-34 6.23% CCH-35 7.73% CCP-3-1 3.49% CCY-3-O2 12.21% CPY-2-O2 6.73% CPY-3-O2 11.96% CY-3-O2 11.47% RM-1 0.30% PP-1-2V1 4.24% PY-3-O2 13.71%
is purified using the process according to the invention.

Example 5

(76) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(77) TABLE-US-00011 CBC-33 3.50% CC-3-V 38.00% CC-3-V1 10.00% CCP-V-1 3.00% CCP-V2-1 9.00% PGP-2-3 5.00% PGP-2-4 5.00% PGU-2-F 8.00% PGU-3-F 9.00% PUQU-3-F 9.50%
is purified using the process according to the invention.

Example 6

(78) A liquid-crystalline mixture, for example for IPS or FFS applications, of the composition

(79) TABLE-US-00012 APUQU-3-F 4.50% CC-3-V 44.00% CC-3-V1 12.00% CCP-V-1 11.00% CCP-V2-1 9.00% PGP-2-3 6.00% PGUQU-3-F 6.00% PP-1-2V1 7.00% PPGU-3-F 0.50%
is purified using the process according to the invention.

Example 7

(80) A liquid-crystalline mixture, for example for IPS or FFS applications, of the composition

(81) TABLE-US-00013 APUQU-3-F 8.00% CBC-33 3.00% CC-3-V 34.00% CC-3-V1 2.50% CCGU-3-F 4.00% CCP-30CF.sub.3 4.00% CCP-3F.F.F 4.50% CCP-50CF.sub.3 3.00% CCP-V-1 10.00% CCQU-3-F 10.00% CPGU-3-OT 6.00% PGUQU-3-F 4.00% PUQU-3-F 7.00%
is purified using the process according to the invention.

Example 8

(82) A liquid-crystalline mixture, for example for IPS or FFS applications, of the composition

(83) TABLE-US-00014 APUQU-2-F 5.00% APUQU-3-F 7.50% BCH-3F.F.F 7.00% CC-3-V 40.50% CC-3-V1 6.00% CCP-V-1 9.50% CPGU-3-OT 5.00% PGP-2-3 6.00% PGP-2-4 6.00% PPGU-3-F 0.50% PUQU-3-F 7.00%
is purified using the process according to the invention.

Example 9

(84) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(85) TABLE-US-00015 APUQU-2-F 8.00% APUQU-3-F 8.00% BCH-32 7.00% CC-3-V 43.00% CCP-V-1 9.00% PGP-2-3 7.00% PGP-2-4 6.00% PUQU-2-F 5.00% PUQU-3-F 7.00%
is purified using the process according to the invention.

Example 10

(86) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(87) TABLE-US-00016 BCH-5F.F 8.00% CBC-33F 3.00% CC-3-V 22.00% CCGU-3-F 6.00% CCP-3F.F.F 8.00% CCP-5F.F.F 4.00% CCP-V-1 13.00% CCP-V2-1 11.00% CCQU-3-F 5.00% CCQU-5-F 4.00% PUQU-3-F 16.00%
is purified using the process according to the invention.

Example 11

(88) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(89) TABLE-US-00017 CBC-33F 3.00% CBC-53F 3.00% CC-3-V 17.00% CC-3-V1 4.00% CCP-3F.F.F 8.00% CCPC-33 3.00% CCPC-34 3.00% CCP-V-1 5.00% CCP-V2-1 2.00% CCQU-2-F 1.50% CCQU-3-F 10.00% CCQU-5-F 10.00% CGU-3-F 6.00% PGP-2-3 7.50% PP-1-2V1 7.00% PUQU-3-F 10.00%
is purified using the process according to the invention.

Example 12

(90) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(91) TABLE-US-00018 APUQU-2-F 1.00% BCH-3F.F.F 15.00% CC-3-V 33.50% CC-3-V1 2.00% CCGU-3-F 1.00% CCPC-33 2.00% CCP-V-1 4.50% BCH-2F 5.00% BCH-3F 5.00% PGP-2-3 8.50% PGUQU-3-F 7.80% PP-1-2V1 11.00% PPGU-3-F 0.20% PUQU-3-F 3.50%
is purified using the process according to the invention.

Example 13

(92) A liquid-crystalline mixture, for example for IPS or FFS applications, of the composition

(93) TABLE-US-00019 APUQU-2-F 2.00% APUQU-3-F 6.00% CC-3-V 42.00% CCP-3-1 3.00% CCP-3-3 3.00% CCP-3F.F.F 8.00% CCP-V-1 1.50% CCQU-3-F 7.00% CCQU-5-F 3.00% CPGU-3-OT 6.50% PGUQU-3-F 5.00% PGUQU-4-F 4.00% PGUQU-5-F 4.00% PPGU-3-F 0.50% PUQU-3-F 4.50%
is purified using the process according to the invention.

Example 14

(94) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(95) TABLE-US-00020 CC-3-V 49.50% CCP-3-1 1.50% CCP-V-1 6.00% CPGU-3-OT 7.00% PGP-2-3 8.50% PGP-2-4 5.50% PGUQU-3-F 7.00% PGUQU-4-F 4.00% PP-1-2V1 2.50% PPGU-3-F 0.50% PUQU-3-F 8.00%
is purified using the process according to the invention.

Example 15

(96) A liquid-crystalline mixture, for example for VA applications, of the composition

(97) TABLE-US-00021 BCH-32 6.00% CCH-23 18.00% CCH-34 8.00% CCP-3-1 12.00% CCP-3-3 3.00% CCY-3-O2 6.00% CPY-2-O2 6.00% CPY-3-O2 7.00% CY-3-O2 14.00% CY-3-O4 8.00% CY-5-O2 9.00% PYP-2-3 3.00%
is purified using the process according to the invention.

Example 16

(98) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(99) TABLE-US-00022 CC-3-V1 7.98% CCH-23 17.95% CCH-34 3.99% CCH-35 6.98% CCP-3-1 4.99% CCY-3-O2 12.46% CPY-2-O2 7.98% CPY-3-O2 10.97% CY-3-O2 15.45% RM-17 0.30% PY-3-O2 10.97%
is purified using the process according to the invention.

Example 17

(100) A liquid-crystalline mixture, for example for VA applications, of the composition

(101) TABLE-US-00023 CC-3-V 29.50% PP-1-3 11.00% PY-3-O2 12.00% CCP-3-1 9.50% CCOY-2-O2 18.00% CCOY-3-O2 13.00% GPP-5-2 7.00%
is purified using the process according to the invention.

(102) Mixture Examples 1 to 17 may additionally also comprise one or more, for example one or two, stabiliser(s) and/or a dopant from Tables C and D.

Example 18

(103) A liquid-crystalline mixture, for example for TN applications, of the composition

(104) TABLE-US-00024 BCH-3F.F 7.50% BCH-5F.F 7.50% CC-3-V 35.00% CCGU-3-F 4.00% CCP-3F.F.F 12.00% CCPC-33 3.00% CCP-V-1 10.00% PGP-2-4 4.00% PPGU-3-F 1.00% PUQU-3-F 16.00%
is purified using the process according to the invention.

Example 19

(105) A liquid-crystalline mixture, for example for TN applications, of the composition

(106) TABLE-US-00025 BCH-2F.F 4.00% BCH-3F.F.F 8.50% CC-3-V1 8.00% CC-4-V 10.00% CCG-V-F 8.00% CCP-20CF.sub.3 7.00% CCP-2F.F.F 8.00% CCP-30CF.sub.3 5.00% CCP-3-1 3.00% CCPC-33 2.50% CCP-V-1 11.50% CCQU-3-F 5.00% CDU-2-F 7.00% CDU-3-F 7.00% PUQU-3-F 5.50%
is purified using the process according to the invention.

Example 20

(107) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(108) TABLE-US-00026 BCH-32 7.48% CCH-23 21.93% CCH-34 3.49% CCY-3-O3 6.98% CCY-4-O2 7.98% CPY-2-O2 10.97% CPY-3-O2 10.97% CY-3-O2 15.45% RM-1 0.30% PCH-301 12.46% PCH-302 1.99%
is purified using the process according to the invention.

Example 21

(109) A liquid-crystalline mixture, for example for VA applications, of the composition

(110) TABLE-US-00027 BCH-32 8.50% CC-3-V 24.00% CC-3-V1 5.00% CCP-V-1 2.00% CCY-3-1 2.50% CCY-3-O1 7.00% CCY-3-O2 6.50% CCY-3-O3 4.00% CCY-4-O2 4.00% CPY-2-O2 7.50% CPY-3-O2 10.00% CY-3-O2 3.50% PY-3-O2 8.50% PYP-2-3 4.00% PYP-2-4 3.00%
is purified using the process according to the invention.

Example 22

(111) A liquid-crystalline mixture, for example for FFS applications, of the composition

(112) TABLE-US-00028 APUQU-2-F 4.00% CC-3-V 26.50% CC-3-V1 7.00% CCGU-3-F 1.50% CCP-2F.F.F 1.50% CCP-30CF.sub.3 8.00% CCP-3-1 2.00% CCP-V-1 10.00% CCP-V2-1 7.00% CDU-2-F 5.00% CPGU-3-OT 4.50% PGU-3-F 3.00% PGUQU-3-F 3.00% PGUQU-4-F 3.00% PPGU-3-F 1.50% PUQU-3-F 12.50%
is purified using the process according to the invention.

Example 23

(113) A liquid-crystalline mixture, for example for FFS applications, of the composition

(114) TABLE-US-00029 BCH-3F.F 7.00% CBC-33 3.00% CC-3-V 25.00% CCGU-3-F 6.00% CCP-30CF.sub.3 8.00% CCP-3-1 4.50% CCP-V-1 13.50% CCP-V2-1 6.00% CCQU-3-F 8.00% CPGP-5-2 3.00% DPGU-4-F 2.50% PPGU-3-F 1.00% PUQU-3-F 4.50% Y-4O-O4 8.00%
is purified using the process according to the invention.

Example 24

(115) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(116) TABLE-US-00030 CC-3-V1 10.22% CCH-23 18.44% Irganox ® 1076 0.01% RM-1 0.30% PY-3-O2 12.96% PP-1-2V1 3.74% CY-3-O2 11.47% CPY-3-O2 9.72% CPY-2-O2 5.98% CCY-3-O2 11.96% CCY-3-1 2.49% CCP-3-1 5.98% CCH-35 6.73%
is purified using the process according to the invention.

Example 25

(117) A liquid-crystalline mixture, for example for TN applications, of the composition

(118) TABLE-US-00031 APUQU-2-F 2.00% BCH-3F.F 9.00% BCH-3F.F.F 9.00% CC-3-V1 5.00% CC-4-V 6.00% CCGU-3-F 7.50% CCG-V-F 15.50% CCP-2F.F.F 8.50% CCP-30CF.sub.3 6.00% CCP-3-1 2.00% CCP-3F.F.F 10.00% CCQU-3-F 9.50% CCQU-5-F 9.00% PPGU-3-F 1.00%
is purified using the process according to the invention.

Example 26

(119) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(120) TABLE-US-00032 RM-1 0.199% Irganox ® 1076 0.001% PYP-2-4 8.98% PYP-2-3 8.98% PCH-53 2.99% PCH-301 5.99% CY-3-O4 20.46% CPY-3-O2 4.49% CPY-2-O2 9.98% CCY-4-O2 6.99% CCY-3-O3 7.98% CCY-3-O2 6.99% CCH-35 5.99% BCH-52 3.99% CCH-34 5.99%
is purified using the process according to the invention.

Example 27

(121) A liquid-crystalline mixture, for example for FFS applications, of the composition

(122) TABLE-US-00033 CDUQU-3-F 3.00% CCP-V-1 13.50% CCP-3-3 2.50% CC-3-V 44.00% APUQU-2-F 4.50% CPGU-3-OT 4.00% PUQU-2-F 5.00% PGU-2-F 6.00% PGU-3-F 6.00% PGUQU-3-F 3.50% PGUQU-4-F 3.50% PPGU-3-F 0.50% DPGU-4-F 4.00%
is purified using the process according to the invention.

Example 28

(123) A liquid-crystalline mixture, for example for FFS applications, of the composition

(124) TABLE-US-00034 BCH-3F.F 15.00% BCH-3F.F.F 8.00% CC-3-V 10.00% CC-3-V1 10.50% CC-4-V 10.50% CCP-30CF.sub.3 10.00% CCP-V-1 15.00% CDUQU-3-F 6.50% PGP-2-2V 1.00% PGU-2-F 8.00% PPGU-3-F 1.00% PUQU-3-F 4.50%
is purified using the process according to the invention.

Example 29

(125) A liquid-crystalline mixture, for example for FFS applications, of the composition

(126) TABLE-US-00035 PUQU-3-F 14.00% PPGU-3-F 1.00% PGP-2-2V 4.50% DPGU-4-F 3.00% CPGU-3-OT 3.00% STAB-37 0.01% CCP-V-1 14.00% CCP-30CF.sub.3 6.00% CC-3-V1 5.50% CC-3-V 38.99% APUQU-2-F 4.00% CCY-3-O2 6.00%
is purified using the process according to the invention.

Example 30

(127) A liquid-crystalline mixture, for example for VA applications, of the composition

(128) TABLE-US-00036 CLY-3-O2 10.00% CCY-3-O2 9.25% CCH-35 8.00% CC-3-V1 10.00% CC-3-V 27.50% CPY-3-O2 11.75% PYP-2-4 0.50% PY-4-O2 9.00% PY-3-O2 14.00%
is purified using the process according to the invention.

Example 31

(129) A liquid-crystalline mixture, for example for PVA applications, of the composition

(130) TABLE-US-00037 CCH-23 12.00% CCH-34 10.00% CCP-3-1 7.00% CCY-3-1 10.00% CCY-3-O2 9.00% CCY-3-O3 9.00% CCY-4-O2 9.00% CPGP-4-3 2.00% CPY-2-O2 8.00% CPY-3-O2 8.00% CY-3-O4 4.50% PCH-301 10.00% PYP-2-3 1.50%
is purified using the process according to the invention.

Example 32

(131) A liquid-crystalline mixture, for example for FFS applications, of the composition

(132) TABLE-US-00038 CC-3-V 33.00% CCY-3-O1 5.00% CCY-3-O2 6.50% CCY-4-O2 8.00% CCY-5-O2 3.50% CPY-2-O2 9.00% CPY-3-O2 9.00% CY-3-O2 10.00% CY-5-O2 2.00% PY-3-O2 9.00% PYP-2-3 5.00%
is purified using the process according to the invention.

Example 33

(133) A liquid-crystalline mixture, for example for FFS applications, of the composition

(134) TABLE-US-00039 CC-3-V 44.50% CC-3-V1 5.50% CCP-30CF.sub.3 8.00% CCP-V-1 8.00% CCQU-3-F 5.00% PGP-2-3 4.00% PGP-2-4 5.00% PGUQU-3-F 3.00% PGUQU-4-F 9.00% PGUQU-5-F 5.50% PUQU-3-F 2.50%
is purified using the process according to the invention.

Example 34

(135) A liquid-crystalline mixture, for example for FFS applications, of the composition

(136) TABLE-US-00040 APUQU-2-F 5.00% APUQU-3-F 5.00% CC-3-V 40.00% CC-3-V1 4.50% CCGU-3-F 3.50% CCP-30CF.sub.3 5.50% CCP-V-1 10.50% CCQU-3-F 5.50% CPGU-3-OT 3.00% PGUQU-4-F 6.00% PGUQU-5-F 4.50% PUQU-3-F 7.00%
is purified using the process according to the invention.

Example 35

(137) A liquid-crystalline mixture, for example for FFS applications, of the composition

(138) TABLE-US-00041 CC-3-V 23.50% CC-3-V1 9.00% CCGU-3-F 5.00% CCP-30CF.sub.3 8.00% CCP-50CF.sub.3 6.00% CCP-V-1 12.00% CCP-V2-1 5.00% CPGP-4-3 3.00% PCH-301 5.00% PGP-1-2V 7.50% PGP-2-2V 8.00% PUQU-3-F 8.00%
is purified using the process according to the invention.

Example 36

(139) A liquid-crystalline mixture, for example for IPS applications, of the composition

(140) TABLE-US-00042 APUQU-2-F 5.00% APUQU-3-F 8.00% CC-3-V 36.00% CC-3-V1 5.00% CCP-V-1 8.00% CCQU-3-F 9.50% PGP-2-2V 3.00% PGUQU-3-F 4.00% PGUQU-4-F 8.00% PGUQU-5-F 5.00% PUQU-3-F 8.50%
is purified using the process according to the invention.

Example 37

(141) A liquid-crystalline mixture, for example for IPS applications, of the composition

(142) TABLE-US-00043 APUQU-2-F 7.00% APUQU-3-F 7.00% CC-3-2V1 4.50% CC-3-V 32.00% CC-3-V1 11.00% CCP-30CF.sub.3 7.50% CCP-50CF.sub.3 1.50% DGUQU-4-F 8.00% DPGU-4-F 5.00% PGUQU-3-F 3.00% PGUQU-4-F 8.00% PGUQU-5-F 2.00% PP-1-2V1 2.00% PUQU-3-F 1.50%
is purified using the process according to the invention.

Example 38

(143) A liquid-crystalline mixture, for example for PS-VA applications, of the composition

(144) TABLE-US-00044 CCH-23 13.97% CCH-34 11.98% CCP-3-1 2.99% CCY-3-1 7.98% CCY-3-O2 11.98% CCY-3-O3 11.98% CCY-4-O2 9.98% CPY-2-O2 2.99% CPY-3-O2 9.98% PCH-301 9.98% PYP-2-3 5.99% RM-1 0.20%
is purified using the process according to the invention.

Example 39

(145) A liquid-crystalline mixture, for example for FFS applications, of the composition

(146) TABLE-US-00045 CC-3-V 29.00% CCY-3-O1 3.50% CCY-3-O2 9.00% CCY-4-O2 9.00% CCY-5-O2 3.00% CPY-3-O2 9.50% CY-3-O2 13.00% CY-5-O2 2.00% PY-3-O2 10.00% PYP-2-3 2.50% CPY-2-O2 9.50%
is purified using the process according to the invention and 0.005% of STAB-35 is subsequently added.

Example 40

(147) A liquid-crystalline mixture, for example for PS-IPS applications, of the composition

(148) TABLE-US-00046 APUQU-2-F 2.99% APUQU-3-F 5.99% BCH-2F.F 2.00% BCH-3F.F 7.48% CC-3-V 25.44% CC-3-V1 5.98% CCP-V-1 12.97% CCP-V2-1 5.98% CCQU-3-F 7.98% CCQU-5-F 3.98% PGUQU-3-F 4.99% PPGU-3-F 0.50% PUQU-3-F 13.47% RM-35 0.25%
is purified using the process according to the invention.

Example 41

(149) A liquid-crystalline mixture, for example for PS-IPS applications, of the composition

(150) TABLE-US-00047 APUQU-2-F 2.99% APUQU-3-F 5.99% BCH-2F.F 2.00% BCH-3F.F 7.48% CC-3-V 25.44% CC-3-V1 5.98% CCP-V-1 12.97% CCP-V2-1 5.99% CCQU-3-F 7.98% CCQU-5-F 3.98% PGUQU-3-F 4.98% PPGU-3-F 0.50% PUQU-3-F 13.47% RM-41 0.25%
is purified using the process according to the invention.

Example 42

(151) A liquid-crystalline mixture, for example for TN applications, of the composition

(152) TABLE-US-00048 PPGU-3-F 0.50% PP-1-2V1 1.50% PGUQU-4-F 4.00% PGUQU-3-F 5.00% PGP-2-5 2.00% PGP-2-4 5.00% PUQU-3-F 6.00% PCH-302 6.00% CPGP-5-3 6.00% CPGP-5-2 6.00% CC-3-V 30.00% BCH-3F.F.F 12.00% BCH-3F.F 10.00% PGP-2-3 6.00%
is purified using the process according to the invention.

Example 43

(153) A liquid-crystalline mixture, for example for TN-TFT applications, of the composition

(154) TABLE-US-00049 CC-3-V 29.00% CCGU-3-F 4.00% CCG-V-F 5.00% CCP-2F.F.F 5.00% CCP-3F.F.F 8.00% CCPC-33 3.00% CCPC-34 3.00% CCPC-35 1.50% CCP-V-1 10.00% CCP-V2-1 11.00% CCQU-2-F 1.50% CCQU-3-F 8.00% PUQU-3-F 11.00%
is purified using the process according to the invention.

Example 44

(155) A liquid-crystalline mixture, for example for FFS applications, of the composition

(156) TABLE-US-00050 BCH-32 4.50% CC-3-V 23.50% CCH-301 4.00% CCY-3-O2 4.00% CCY-3-O3 7.00% CCY-4-O2 8.00% CLY-3-O2 8.00% CPY-2-O2 7.00% CPY-3-O2 11.00% CY-3-O2 11.00% PY-3-O2 12.00%
is purified using the process according to the invention.

Example 45

(157) A liquid-crystalline mixture, for example for IPS applications, of the composition

(158) TABLE-US-00051 APUQU-2-F 2.50% APUQU-3-F 4.50% CC-3-V 42.00% CCGU-3-F 4.00% CCP-30CF.sub.3 5.00% CCP-3-1 3.00% CCP-V-1 10.00% CCP-V2-1 2.50% CCQU-3-F 6.00% CPGU-3-OT 5.00% PGUQU-3-F 4.50% PGUQU-4-F 3.50% PPGU-3-F 0.50% PUQU-3-F 7.00%
is purified using the process according to the invention.

Example 46

(159) A liquid-crystalline mixture, for example for IPS applications, of the composition

(160) TABLE-US-00052 BCH-32 2.99% CCH-303 1.49% CCH-34 12.93% CCH-501 5.97% CCY-2-1 5.97% CCY-3-1 5.97% CCY-3-O2 5.97% CCY-3-O3 5.97% CCY-4-O2 5.97% CCY-5-O2 2.99% CPY-2-O2 6.97% CPY-3-O2 6.97% CY-3-O2 14.93% CY-5-O2 9.46% PCH-302 4.98% RM-41 0.30% S-4011 0.17%
is purified using the process according to the invention.

Example 47

(161) A liquid-crystalline mixture, for example for PM-VA applications, of the composition

(162) TABLE-US-00053 CPY-3-O2 8.00% CPY-2-O2 8.00% CH-43 3.00% CH-35 3.00% CH-33 3.00% CCY-5-O2 5.50% CCY-4-O2 6.50% CCY-3-O3 6.50% CCY-3-O2 6.50% CCPC-35 5.00% CCPC-34 5.00% CCPC-33 5.00% CC-4-V 4.50% CY-3-O4 15.50% Y-4O-O4 15.00%
is purified using the process according to the invention.

Example 48

(163) A liquid-crystalline mixture, for example for PS-FFS applications, of the composition

(164) TABLE-US-00054 APUQU-2-F 2.49% APUQU-3-F 6.98% CC-3-V 24.94% CC-3-V1 7.98% CCGU-3-F 3.49% CCP-30CF.sub.3 4.99% CCP-V-1 5.99% CCP-V2-1 13.97% CCQU-3-F 9.98% PCH-302 6.48% PGUQU-3-F 3.99% PGUQU-4-F 3.99% PPGU-3-F 0.49% PUQU-3-F 3.99% RM-41 0.25%
is purified using the process according to the invention.

Example 49

(165) A liquid-crystalline mixture, for example for FFS applications, of the composition

(166) TABLE-US-00055 APUQU-2-F 3.50% APUQU-3-F 6.00% CC-3-V 45.50% CCP-30CF.sub.3 5.00% CCP-3-1 3.00% CCP-V2-1 8.50% CPGU-3-OT 6.00% PGUQU-3-F 5.00% PGUQU-4-F 5.00% PPGU-3-F 0.50% PUQU-3-F 12.00%
is purified using the process according to the invention.

Example 50

(167) A liquid-crystalline mixture, for example for FFS applications, of the composition

(168) TABLE-US-00056 APUQU-2-F 4.00% APUQU-3-F 6.00% CC-3-V 45.00% CCP-20CF.sub.3 4.00% CCP-30CF.sub.3 4.00% CCP-40CF.sub.3 2.50% CPGP-5-2 7.00% CPGP-5-3 7.00% PGP-2-3 5.50% PGP-2-4 5.00% PPGU-3-F 0.50% PUQU-3-F 9.50%
is purified using the process according to the invention.

Example 51

(169) A liquid-crystalline mixture, for example for TN applications, of the composition

(170) TABLE-US-00057 CC-3-V 49.50% CCP-3-1 1.50% CCP-V-1 6.00% CPGU-3-OT 7.00% PGP-2-3 8.50% PGP-2-4 5.50% PGUQU-3-F 7.00% PGUQU-4-F 4.00% PP-1-2V1 2.50% PPGU-3-F 0.50% PUQU-3-F 8.00%
is purified using the process according to the invention.

Example 52

(171) A liquid-crystalline mixture, for example for PA-VA applications, of the composition

(172) TABLE-US-00058 BCH-32 6.00% CCH-23 18.00% CCH-34 8.00% CCP-3-1 12.00% CCP-3-3 3.00% CCY-3-O2 6.00% CPY-2-O2 6.00% CPY-3-O2 7.00% CY-3-O2 14.00% CY-3-O4 8.00% CY-5-O2 9.00% PYP-2-3 3.00%
is purified using the process according to the invention.

Example 53

(173) A liquid-crystalline mixture, for example for FFS applications, of the composition

(174) TABLE-US-00059 CCQU-3-F 8.00% CCP-V2-1 7.00% CCP-V-1 10.00% CC-3-V 32.50% PGP-2-2V 10.00% PUQU-3-F 12.50% PGUQU-5-F 4.00% PGUQU-4-F 5.00% PGUQU-3-F 5.00% APUQU-3-F 6.00%
is purified using the process according to the invention.

Example 54

(175) A liquid-crystalline mixture, for example for FFS applications, of the composition

(176) TABLE-US-00060 APUQU-3-F 1.00% BCH-3F.F.F 17.00% CC-3-V 35.00% CC-3-V1 6.00% CCP-3F.F.F 2.50% CCP-V-1 12.00% CCP-V2-1 8.50% CPGP-5-2 3.00% CPGP-5-3 2.50% DPGU-4-F 4.00% PGUQU-3-F 4.00% PGUQU-4-F 2.00% PGUQU-5-F 2.00% PPGU-3-F 0.50%
is purified using the process according to the invention.

Example 55

(177) A liquid-crystalline mixture, for example for PM-VA applications, of the composition

(178) TABLE-US-00061 CH-35 3.00% CH-43 3.00% CLY-3-O2 3.25% CPY-2-O2 10.00% CY-3-O2 15.00% CH-33 3.00% CCY-5-O2 4.00% CCY-4-O2 6.00% CCY-3-O3 6.00% CCY-3-O2 6.00% CCY-3-1 2.00% CCY-2-1 8.75% CY-3-O4 20.00% CCPC-33 3.75% CCH-34 4.75% CCPC-34 1.50%
is purified using the process according to the invention.

Example 56

(179) A liquid-crystalline mixture, for example for PS-FFS applications, of the composition

(180) TABLE-US-00062 APUQU-3-F 5.99% BCH-3F.F 5.49% CC-3-V 24.94% CC-3-V1 7.98% CCGU-3-F 5.98% CCP-30CF.sub.3 2.99% CCP-V-1 16.96% CCP-V2-1 13.96% CCQU-3-F 2.49% CCQU-5-F 4.99% PGUQU-4-F 4.49% PPGU-3-F 0.50% PUQU-3-F 2.99% RM-41 0.25%
is purified using the process according to the invention.

(181) The following mixtures are likewise purified using the process according to the invention:

Example 57

(182) TABLE-US-00063 CY-3-O4 14.00% Clearing point [° C.]: 106.0 CCY-3-O2 8.00% Δn [589 nm, 20° C.]: 0.1597 CCY-4-O2 7.00% ε.sub.∥ [1 kHz, 20° C.]: 3.9 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.5 CCY-5-O2 5.00% Δε [1 kHz, 20° C.]: −4.6 CPY-2-O2 10.00% K.sub.1 [pN, 20° C.]: 16.6 CPY-3-O2 8.00% K.sub.3 [pN, 20° C.]: 17.6 PYP-2-3 14.00% V.sub.0 [20° C., V]: 2.08 PYP-2-4 14.00% γ.sub.1 [mPa .Math. s, 20° C.]: 316 CCH-301 8.00% PGP-2-3 6.00%

Example 57a

(183) The mixture according to Example 57 additionally comprises 0.025% of STAB-35.

Example 58

(184) TABLE-US-00064 CY-3-O2 13.00% Clearing point [° C.]: 111 CY-5-O2 9.00% CY-5-O4 8.00% CCY-3-O2 6.00% CCY-3-O3 5.00% CCY-4-O2 5.00% CCY-5-O2 3.50% CPY-2-O2 7.00% CPY-3-O2 3.00% CCH-34 17.50% CCP-3-1 4.50% CH-35 3.00% CH-43 3.00% CH-45 0.50% CCPC-33 3.00% CCPC-34 3.00% CCPC-35 3.00%

Example 59

(185) TABLE-US-00065 CC-3-V 37.00% Clearing point [° C.]: 75.2 CCY-3-O1 5.00% Δn [589 nm, 20° C.]: 0.1014 CCY-3-O2 5.00% Δε [1 kHz, 20° C.]: −3.7 CCY-4-O2 4.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CLY-3-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.4 CPY-2-O2 9.00% K.sub.1 [pN, 20° C.]: 13.2 CPY-3-O2 10.00% K.sub.3 [pN, 20° C.]: 15.2 CY-3-O2 11.50% V.sub.0 [20° C., V]: 2.13 PY-3-O2 11.50%

Example 60

(186) TABLE-US-00066 CC-3-V 40.00% Clearing point [° C.]: 100.3 CC-3-V1 5.00% Δn [589 nm, 20° C.]: 0.1059 CCP-30CF3 4.00% Δε [1 kHz, 20° C.]: 3.9 CCP-V-1 13.00% ε.sub.∥ [1 kHz, 20° C.]: 6.7 CCP-V2-1 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 2.8 CCVC-3-V 4.00% K.sub.1 [pN, 20° C.]: 14.9 CDUQU-3-F 2.00% K.sub.3 [pN, 20° C.]: 17.0 CPGP-5-2 5.00% V.sub.0 [20° C., V]: 2.07 CPGP-5-3 1.50% γ.sub.1 [mPa .Math. s, 20° C.]: 74 DGUQU-4-F 2.00% DPGU-4-F 3.00% PGP-2-3 4.00% PGP-2-4 4.00% PPGU-3-F 0.50% PUQU-3-F 8.00%

Example 61

(187) TABLE-US-00067 CY-3-O4 23.00% Clearing point [° C.]: 71.3 CCY-3-O1 6.00% Δn [589 nm, 20° C.]: 0.1197 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −7.0 CCY-3-O3 7.00% ε.sub.∥ [1 kHz, 20° C.]: 5.0 CCY-4-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 12.0 CCY-5-O2 5.00% K.sub.1 [pN, 20° C.]: 11.7 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 13.2 CPY-3-O2 10.00% V.sub.0 [20° C., V]: 1.44 CCY-2-1 3.50% γ.sub.1 [mPa .Math. s, 20° C.]: 246 PYP-2-4 8.50% PY-1-O4 8.00% Y-4O-O4 8.00%

Example 62

(188) TABLE-US-00068 PUQU-3-F 9.00% Clearing point [° C.]: 75.9 PGUQU-3-F 7.00% Δn [589 nm, 20° C.]: 0.1131 PGUQU-4-F 5.00% Δε [1 kHz, 20° C.]: 6.1 CPGU-3-OT 4.50% K.sub.1 [pN, 20° C.]: 11.9 PPGU-3-F 0.50% K.sub.3 [pN, 20° C.]: 13.6 CDUQU-3-F 0.05% V.sub.0 [20° C.]: 1.14 CC-3-V 49.95% γ.sub.1 [mPa .Math. s, 20° C.]: 57 CCP-V-1 12.00% PGP-2-3 8.00% PGP-2-4 4.00%

Example 63

(189) TABLE-US-00069 PUQU-3-F 8.00% Clearing point [° C.]: 75.4 PGUQU-3-F 7.00% Δn [589 nm, 20° C.]: 0.1191 PGUQU-4-F 4.00% Δε [1 kHz, 20° C.]: 6.1 PPGU-3-F 0.50% K.sub.1 [pN, 20° C.]: 12.6 CPGU-3-OT 7.00% K.sub.3 [pN, 20° C.]: 12.5 CC-3-V 49.50% V.sub.0 [20° C., V]: 1.52 CCP-3-1 1.50% γ.sub.1 [mPa .Math. s, 20° C.]: 57 CCP-V-1 6.00% PP-1-2V1 2.50% PGP-2-3 8.50% PGP-2-4 5.50%

Example 64

(190) TABLE-US-00070 CY-3-O4 12.00% Clearing point [° C.]: 102.5 CY-5-O4 12.00% Δn [589 nm, 20° C.]: 0.1605 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −5.6 CCY-4-O2 7.00% ε.sub.∥ [1 kHz, 20° C.]: 4.0 CCY-3-O3 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 9.6 CPY-2-O2 12.00% K.sub.1 [pN, 20° C.]: 16.9 CPY-3-O2 12.00% K.sub.3 [pN, 20° C.]: 17.1 PYP-2-3 15.00% V.sub.0 [V, 20° C.]: 1.84 PYP-2-4 15.00% γ.sub.1 [mPa .Math. s, 20° C.]: 401

Example 65

(191) TABLE-US-00071 BCH-32 8.00% Clearing point [° C.]: 80.6 CC-3-V 28.00% Δn [589 nm, 20° C.]: 0.1194 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −3.9 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 4.0 CLY-3-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.9 CPY-2-O2 10.00% K.sub.1 [pN, 20° C.]: 13.0 CPY-3-O2 10.00% K.sub.3 [pN, 20° C.]: 14.0 PGIY-2-O4 8.00% V.sub.0 [20° C.]: 2.0 PY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 120 Y-4O-O4 8.00%

Example 66

(192) TABLE-US-00072 CY-3-O2 15.00% Clearing point [° C.]: 80.1 CY-5-O2 7.00% Δn [589 nm, 20° C.]: 0.1026 CCY-3-O1 4.00% Δε [1 kHz, 20° C.]: −3.5 CCY-3-O2 2.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CCY-4-O2 6.00% K.sub.1 [pN, 20° C.]: 13.9 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 13.8 CPY-3-O2 8.00% V.sub.0 [20° C.]: 2.11 PYP-2-4 6.50% γ.sub.1 [mPa .Math. s, 20° C.]: 132 CCH-23 15.00% CCH-34 5.00% CCH-35 4.00% CCH-301 6.00% BCH-32 7.50%

Example 67

(193) TABLE-US-00073 APUQU-2-F 3.00% Clearing point [° C.]: 100.1 APUQU-3-F 2.50% Δn [589 nm, 20° C.]: 0.1046 CC-3-2V1 3.00% CC-3-V 37.00% CC-3-V1 5.00% CCP-V-1 13.00% CCP-V2-1 7.50% CCVC-3-V 5.00% CDUQU-3-F 2.00% CPGP-5-2 4.00% DGUQU-4-F 2.00% PGP-2-3 5.00% PGP-2-4 4.50% PPGU-3-F 0.50% PUQU-3-F 6.00%

Example 68

(194) TABLE-US-00074 PCH-3 6.00% Clearing point [° C.]: 86.0 CC-5-V 20.00% Δn [589 nm, 20° C.]: 0.1612 PCH-301 14.00% Δε [1 kHz, 20° C.]: 1.8 PCH-302 15.00% ε.sub.∥ [1 kHz, 20° C.]: 4.7 PPTUI-3-2 15.00% ε.sub.⊥ [1 kHz, 20° C.]: 2.9 PPTUI-3-4 15.00% CCP-V-1 8.00% CCP-V2-1 7.00%

Example 68a

(195) The mixture according to Example 68 additionally comprises 2% of R-5011.

Example 69

(196) TABLE-US-00075 CY-3-O4 13.00% Clearing point [° C.]: 92.0 CC-4-V 17.00% Δn [589 nm, 20° C.]: 0.1598 CC-3-V1 8.00% Δε [1 kHz, 20° C.]: −1.9 CCP-V-1 12.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CCP-V2-1 12.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.3 PPTUI-3-2 10.00% PTP-302FF 10.00% PTP-502FF 10.00% CPTP-302FF 4.00% CPTP-502FF 4.00%

Example 70

(197) TABLE-US-00076 CY-3-O4 12.50% Clearing point [° C.]: 75.4 CY-5-O2 10.00% Δn [589 nm, 20° C.]: 0.1077 CCY-3-O1 4.50% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CLY-3-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-2-O2 10.00% V.sub.0 [20° C.]: 2.30 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 112.9 CC-3-V 27.40% BCH-32 3.50% PP-1-2V1 9.00% CDUQU-3-F 0.10%

Example 71

(198) TABLE-US-00077 CY-3-O2 15.00% Clearing point [° C.]: 75.8 CY-3-O4 2.50% Δn [589 nm, 20° C.]: 0.1021 CY-5-O2 10.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O1 5.00% ε.sub.∥ [1 kHz, 20° C.]: 3.6 CCY-4-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-2-O2 7.00% K.sub.1 [pN, 20° C.]: 13.4 CPY-3-O2 7.00% K.sub.3 [pN, 20° C.]: 13.5 CCY-2-1 6.00% V.sub.0 [20° C.]: 2.14 CCY-3-1 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 128 CCH-23 15.50% CCH-34 5.00% BCH-32 13.00% PP-1-4 3.00%

Example 72

(199) TABLE-US-00078 CC-3-V 33.00% Clearing point [° C.]: 80.2 CCY-3-O1 6.00% Δn [589 nm, 20° C.]: 0.1116 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −4.1 CCY-4-O2 2.50% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CPY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 14.5 CLY-3-O2 8.00% K.sub.3 [pN, 20° C.]: 16.1 PY-1-O4 1.50% V.sub.0 [20° C.]: 2.09 PY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 119 PY-4-O2 8.00% CY-3-O2 3.00%

Example 73

(200) TABLE-US-00079 BCH-32 2.00% Clearing point [° C.]: 79.7 BCH-52 2.50% Δn [589 nm, 20° C.]: 0.1036 CCY-2-1 9.50% Δε [1 kHz, 20° C.]: −3.7 CCY-3-1 9.50% ε.sub.∥ [1 kHz, 20° C.]: 4.8 CCY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.5 CCY-5-O2 10.00% K.sub.1 [pN, 20° C.]: 13.9 CPY-2-O2 12.00% K.sub.3 [pN, 20° C.]: 14.1 CY-3-O4 15.00% V.sub.0 [20° C.]: 2.06 CY-5-O4 15.50% PCH-53 10.50% APUQU-3-F 3.50%

Example 74

(201) TABLE-US-00080 BCH-32 0.50% Clearing point [° C.]: 79.2 BCH-52 0.50% Δn [589 nm, 20° C.]: 0.1037 CCY-2-1 5.00% Δε [1 kHz, 20° C.]: −3.8 CCY-3-1 5.00% ε.sub.∥ [1 kHz, 20° C.]: 6.2 CCY-3-O2 13.00% ε.sub.⊥ [1 kHz, 20° C.]: 10.0 CCY-5-O2 13.00% K.sub.1 [pN, 20° C.]: 14.8 CPY-2-O2 12.00% K.sub.3 [pN, 20° C.]: 14.5 CY-3-O4 19.50% V.sub.0 [20° C.]: 2.12 CY-5-O4 19.50% PCH-53 5.00% APUQU-3-F 7.00%

Example 75

(202) TABLE-US-00081 CY-3-O2 27.50% Clearing point [° C.]: 80.0 CCY-4-O2 26.50% Δn [589 nm, 20° C.]: 0.0911 CPY-3-O2 13.50% Δε [1 kHz, 20° C.]: −3.6 CC-3-V 25.00% ε.sub.∥ [1 kHz, 20° C.]: 4.4 CCH-34 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.1 APUQU-3-F 2.50%

Example 76

(203) TABLE-US-00082 APUQU-3-F 7.00% Clearing point [° C.]: 88.0 CC-3-V 35.00% Δn [589 nm, 20° C.]: 0.1150 CC-3-V1 5.00% Δε [1 kHz, 20° C.]: −2.2 CCP-30CF.sub.3 5.00% ε.sub.∥ [1 kHz, 20° C.]: 1.0 CCP-V-1 12.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.1 CPGP-5-2 1.00% K.sub.1 [pN, 20° C.]: 14.3 DPGU-4-F 8.00% K.sub.3 [pN, 20° C.]: 14.7 PGP-2-2V 12.00% V.sub.0 [20° C.]: 1.53 PUQU-3-F 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 66 CC-2-V1 5.00%

Example 77

(204) TABLE-US-00083 BCH-32 6.00% Clearing point [° C.]: 101.6 CC-3-V 39.50% Δn [589 nm, 20° C.]: 0.1111 CCP-3-1 6.50% Δε [1 kHz, 20° C.]: 6.9 CCP-30CF.sub.3 1.00% K.sub.1 [pN, 20° C.]: 15.3 CCP-V-1 16.00% K.sub.3 [pN, 20° C.]: 17.3 CDUQU-3-F 9.50% V.sub.0 [20° C.]: 1.57 CPGP-5-2 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 89 CPGP-5-3 1.00% LTS [bulk, −30° C.]: >1000 h PGU-2-F 7.50% PGUQU-3-F 3.50% PGUQU-4-F 2.00% PGUQU-5-F 3.50% PPGU-3-F 1.00%

Example 78

(205) TABLE-US-00084 BCH-32 5.00% Clearing point [° C.]: 102.5 CC-3-V 35.00% Δn [589 nm, 20° C.]: 0.1207 CC-3-V1 5.00% Δε [1 kHz, 20° C.]: 7.3 CCP-V-1 15.00% K.sub.1 [pN, 20° C.]: 15.2 CDUQU-3-F 8.00% K.sub.3 [pN, 20° C.]: 16.6 CPGP-4-3 3.00% V.sub.0 [20° C.]: 1.53 CPGP-5-2 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 96 CPGP-5-3 3.00% LTS [bulk, −30° C.]: >1000 h CPGU-3-OT 4.50% PGU-2-F 5.50% PGU-3-F 5.50% PGUQU-3-F 2.50% PPGU-3-F 0.50% PUQU-3-F 4.50%

Example 79

(206) TABLE-US-00085 BCH-32 6.00% Clearing point [° C.]: 101 CC-3-V 34.50% Δn [589 nm, 20° C.]: 0.1210 CC-3-V1 6.00% Δε [1 kHz, 20° C.]: 7.3 CCP-V-1 15.00% K.sub.1 [pN, 20° C.]: 15.1 CDUQU-3-F 6.50% K.sub.3 [pN, 20° C.]: 16.5 CPGP-4-3 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 92 CPGP-5-2 3.00% LTS [bulk, −30° C.]: >1000 h CPGP-5-3 1.50% CPGU-3-OT 5.00% PGU-2-F 5.50% PGU-3-F 4.50% PGUQU-3-F 4.00% PPGU-3-F 0.50% PUQU-3-F 5.00%

Example 80

(207) TABLE-US-00086 APUQU-3-F 5.00% Clearing point [° C.]: 104.4 BCH-3F.F 2.50% Δn [589 nm, 20° C.]: 0.0947 CC-3-V 40.00% Δε [1 kHz, 20° C.]: 7.2 CCGU-3-F 6.00% K.sub.1 [pN, 20° C.]: 15.5 CCP-3-1 2.50% K.sub.3 [pN, 20° C.]: 18.3 CCP-30CF.sub.3 7.00% V.sub.0 [20° C.]: 1.55 CCP-V-1 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 93 CCP-V2-1 6.00% CDUQU-3-F 10.00% CPGP-5-2 2.00% DPGU-4-F 2.50% PPGU-3-F 0.50% PUQU-3-F 4.00%

Example 81

(208) TABLE-US-00087 APUQU-3-F 5.00% Clearing point [° C.]: 104.5 CC-3-V 39.00% Δn [589 nm, 20° C.]: 0.0942 CCGU-3-F 10.00% Δε [1 kHz, 20° C.]: 7.2 CCP-3-1 3.00% K.sub.1 [pN, 20° C.]: 15.3 CCP-30CF.sub.3 7.50% K.sub.3 [pN, 20° C.]: 18.5 CCP-V-1 13.00% V.sub.0 [20° C.]: 1.54 CCP-V2-1 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 94 CDUQU-3-F 8.00% CPGP-5-2 2.00% PPGU-3-F 0.50% PUQU-3-F 7.00%

Example 82

(209) TABLE-US-00088 APUQU-3-F 5.00% Clearing point [° C.]: 104.5 CC-3-V 34.50% Δn [589 nm, 20° C.]: 0.0940 CC-3-V1 4.50% Δε [1 kHz, 20° C.]: 7.3 CCGU-3-F 10.00% K.sub.1 [pN, 20° C.]: 15.5 CCP-3-1 3.00% K.sub.3 [pN, 20° C.]: 18.7 CCP-30CF.sub.3 7.50% V.sub.0 [20° C.]: 1.54 CCP-V-1 11.50% γ.sub.1 [mPa .Math. s, 20° C.]: 97 CCP-V2-1 4.00% CCQU-3-F 4.00% CDUQU-3-F 6.50% CPGP-5-2 2.00% PPGU-3-F 0.50% PUQU-3-F 7.00%

Example 83

(210) TABLE-US-00089 BCH-3F.F.F 12.00% Clearing point [° C.]: 101.2 CC-3-V 8.00% Δn [589 nm, 20° C.]: 0.1079 CC-3-V1 9.00% Δε [1 kHz, 20° C.]: 6.8 CC-4-V 10.00% K.sub.1 [pN, 20° C.]: 14.2 CCGU-3-F 4.00% K.sub.3 [pN, 20° C.]: 17.0 CCP-1F.F.F 4.50% V.sub.0 [20° C.]: 1.53 CCP-30CF.sub.3 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 100 CCP-3F.F.F 8.00% CCP-V-1 13.00% CCP-V2-1 6.00% CPGP-5-2 3.00% CPGU-3-OT 1.50% PGP-2-2V 3.00% PPGU-3-F 1.00% PUQU-3-F 9.00%

Example 84

(211) TABLE-US-00090 APUQU-2-F 5.50% Clearing point [° C.]: 80.5 APUQU-3-F 3.00% Δn [589 nm, 20° C.]: 0.1017 CC-3-V 36.00% Δε [1 kHz, 20° C.]: 9.2 CC-3-V1 6.50% ε.sub.∥ [1 kHz, 20° C.]: 12.9 CCP-30CF.sub.3 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.7 CCP-V-1 11.50% K.sub.1 [pN, 20° C.]: 11.8 CDUQU-3-F 5.00% K.sub.3 [pN, 20° C.]: 12.8 DPGU-4-F 5.50% V.sub.0 [20° C.]: 1.20 PGP-2-2V 2.00% γ.sub.1 [mPa .Math. s, 20° C.]: 53 PGU-2-F 7.50% PUQU-3-F 9.50%

Example 84a

(212) The mixture according to Example 84 additionally comprises 0.4% of RM-1.

Example 85

(213) TABLE-US-00091 BCH-32 3.00% Clearing point [° C.]: 109.8 CCH-23 15.00% Δn [589 nm, 20° C.]: 0.1028 CCH-34 3.00% Δε [1 kHz, 20° C.]: −3.7 CCH-35 7.00% ε.sub.∥ [1 kHz, 20° C.]: 3.3 CCP-3-1 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CCY-3-1 8.00% K.sub.1 [pN, 20° C.]: 20.4 CCY-3-O2 12.00% K.sub.3 [pN, 20° C.]: 20.6 CCY-4-O2 10.00% CCY-5-O2 5.50% CPY-2-O2 5.00% CPY-3-O2 11.00% CY-3-O2 8.00% PY-3-O2 5.50%

Example 86

(214) TABLE-US-00092 CC-3-V1 10.00% Clearing point [° C.]: 74.6 CCH-23 18.50% Δn [589 nm, 20° C.]: 0.1032 CCH-35 8.00% Δε [1 kHz, 20° C.]: −3.0 CCP-3-1 7.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CCY-3-O2 12.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.3 CPY-3-O2 10.50% K.sub.1 [pN, 20° C.]: 15.0 CY-3-O2 15.50% K.sub.3 [pN, 20° C.]: 16.1 PY-3-O2 10.50% V.sub.0 [20° C.]: 2.45 PYP-2-3 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 103

Example 86a

(215) The mixture from Example 86 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.3% of RM-1.

Example 87

(216) TABLE-US-00093 CDUQU-3-F 7.00% Clearing point [° C.]: 100 CCP-V-1 2.00% Δn [589 nm, 20° C.]: 0.0714 CCQU-3-F 5.00% Δε [1 kHz, 20° C.]: 8.3 CCQU-5-F 5.00% ε.sub.∥ [1 kHz, 20° C.]: 12.0 CCZU-3-F 13.50% ε.sub.⊥ [1 kHz, 20° C.]: 3.8 CCZU-5-F 4.00% K.sub.1 [pN, 20° C.]: 11.4 PUQU-3-F 1.00% K.sub.3 [pN, 20° C.]: 15.8 CC-5-V 7.00% V.sub.0 [20° C.]: 1.23 CCG-V-F 7.50% γ.sub.1 [mPa .Math. s, 20° C.]: 118 CCH-301 14.00% CCP-2F.F.F 5.00% CCP-30CF.sub.3.F 7.00% CCP-3F.F.F 7.00% CCP-5F.F.F 7.00% CCPC-33 1.50% CCPC-34 2.00% CH-33 1.50% CH-35 1.50% CH-43 1.50%

Example 88

(217) TABLE-US-00094 APUQU-2-F 8.00% Clearing point [° C.]: 88.9 APUQU-3-F 8.00% Δn [589 nm, 20° C.]: 0.0987 CC-3-V 30.00% Δε [1 kHz, 20° C.]: 5.9 CC-3-V1 8.50% ε.sub.∥ [1 kHz, 20° C.]: 8.9 CCP-3-1 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 2.9 CCP-V-1 16.00% K.sub.1 [pN, 20° C.]: 13.4 CCP-V2-1 11.00% K.sub.3 [pN, 20° C.]: 16.1 PP-1-2V1 6.00% V.sub.0 [20° C.]: 1.59 PUQU-3-F 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 56

Example 89

(218) TABLE-US-00095 CC-3-V 28.50% Clearing point [° C.]: 74.6 CC-3-V1 7.00% Δn [589 nm, 20° C.]: 0.1040 CCY-3-O2 12.50% Δε [1 kHz, 20° C.]: −3.0 CCY-4-O2 5.25% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CPY-3-O2 9.75% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CY-3-O2 15.00% K.sub.1 [pN, 20° C.]: 13.2 CY-3-O4 4.75% K.sub.3 [pN, 20° C.]: 15.5 CY-5-O2 1.00% V.sub.0 [20° C.]: 2.40 PCH-301 3.25% γ.sub.1 [mPa .Math. s, 20° C.]: 98 PPGU-3-F 0.50% PYP-2-3 12.50%

Example 89a

(219) The mixture from Example 89 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.3% of RM-1.

Example 90

(220) TABLE-US-00096 CC-3-V 15.00% Clearing point [° C.]: 74.4 CC-3-V1 9.00% Δn [589 nm, 20° C.]: 0.1086 CCH-23 8.00% Δε [1 kHz, 20° C.]: −3.2 CCH-34 7.50% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CCY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CCY-5-O2 8.00% K.sub.1 [pN, 20° C.]: 14.3 CPY-2-O2 3.00% K.sub.3 [pN, 20° C.]: 15.7 CPY-3-O2 8.50% V.sub.0 [20° C.]: 2.33 CY-3-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 102 PY-3-O2 16.00% PYP-2-3 8.00%

Example 90a

(221) The mixture from Example 90 additionally comprises 0.3% of RM-1.

Example 91

(222) TABLE-US-00097 CC-3-V 29.00% Clearing point [° C.]: 103 CC-3-V1 9.00% Δn [589 nm, 20° C.]: 0.1176 CC-3-2V1 7.00% Δε [1 kHz, 20° C.]: 4.8 CCP-V-1 7.00% ε.sub.∥ [1 kHz, 20° C.]: 7.6 CCP-V2-1 7.50% ε.sub.⊥ [1 kHz, 20° C.]: 2.9 PP-1-2V1 3.00% K.sub.1 [pN, 20° C.]: 18.0 PGP-1-2V 4.00% K.sub.3 [pN, 20° C.]: 19.6 PGP-2-2V 6.00% V.sub.0 [20° C.]: 2.04 PGP-3-2V 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 CCP-30CF.sub.3 5.00% CCGU-3-F 4.00% PGUQU-4-F 3.50% CDUQU-3-F 3.00% DGUQU-4-F 4.00% CPGU-3-OT 4.00%

Example 91a

(223) The mixture from Example 91 additionally comprises 0.001% of STAB-35.

Example 92

(224) TABLE-US-00098 PGUQU-3-F 8.00% Clearing point [° C.]: 82.5 PGUQU-4-F 9.00% Δn [589 nm, 20° C.]: 0.2143 PGUQU-5-F 9.00% Δε [1 kHz, 20° C.]: 65.8 PGU-2-F 7.00% ε.sub.∥ [1 kHz, 20° C.]: 73.4 PGU-3-F 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 PGP-2-3 8.00% PGP-2-4 8.00% ME2N.F 12.00% ME3N.F 12.00% BCH-3F.F 7.00% BCH-5F.F 7.00% DPGU-4-F 5.00%

Example 93

(225) TABLE-US-00099 CC-3-V 10.50% Clearing point [° C.]: 100.8 CC-3-V1 5.50% Δn [589 nm, 20° C.]: 0.0999 CCP-V-1 6.50% Δε [1 kHz, 20° C.]: 9.1 PUQU-3-F 7.00% ε.sub.∥ [1 kHz, 20° C.]: 12.6 CCGU-3-F 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.5 APUQU-3-F 2.50% K.sub.1 [pN, 20° C.]: 13.4 CCP-30CF.sub.3 8.00% K.sub.3 [pN, 20° C.]: 17.0 CCP-50CF.sub.3 5.00% V.sub.0 [pN, 20° C.]: 1.28 CCP-30CF.sub.3.F 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 126 CCQU-3-F 10.00% CCP-1F.F.F 9.00% CCP-3F.F.F 11.00% PGP-2-2V 6.00% CDU-2-F 1.00%

Example 94

(226) TABLE-US-00100 CY-3-O2 10.50% Clearing point [° C.]: 79.7 PY-1-O4 5.00% Δn [589 nm, 20° C.]: 0.1113 PY-3-O2 7.50% Δε [1 kHz, 20° C.]: −4.4 PY-4-O2 4.00% K.sub.1 [pN, 20° C.]: 14.5 CCY-3-O1 5.50% K.sub.3 [pN, 20° C.]: 16.7 CCY-3-O2 5.00% V.sub.0 [20° C.]: 2.05 CCY-4-O2 4.00% CLY-3-O2 9.00% CPY-2-O2 9.00% CPY-3-O2 9.00% CC-3-V 23.50% CC-3-V1 7.00% CBC-33F 1.00%

Example 95

(227) TABLE-US-00101 DU-2-N 2.50% Clearing point [° C.]: 94.0 ME2N.F 8.00% Δn [589 nm, 20° C.]: 0.2530 ME3N.F 8.00% Δε [1 kHz, 20° C.]: 47.6 ME4N.F 16.00% ε.sub.∥ [1 kHz, 20° C.]: 55.7 ME5N.F 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.1 HP-3N.F 5.00% K.sub.1 [pN, 20° C.]: 11.3 HP-4N.F 5.00% K.sub.3 [pN, 20° C.]: 13.8 HP-5N.F 2.50% V.sub.0 [20° C.]: 0.51 PTP-102 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 464 PPTUI-3-2 20.00% PPTUI-3-4 20.00%

Example 95a

(228) The mixture according to Example 95 additionally comprises 5% of RM-41.

Example 96

(229) TABLE-US-00102 CCY-3-O1 7.50% Clearing point [° C.]: 81.5 CCY-4-O2 3.50% Δn [589 nm, 20° C.]: 0.1082 CLY-3-O2 7.00% Δε [1 kHz, 20° C.]: −2.7 CPY-2-O2 10.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CPY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.1 PYP-2-3 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 88 CC-3-V 45.00% K.sub.1 [pN, 20° C.]: 13.4 PY-1-O4 4.00% K.sub.3 [pN, 20° C.]: 15.3 PY-3-O2 2.00% V.sub.0 [20° C., V]: 2.53 Y-4O-O4 2.00%

Example 97

(230) TABLE-US-00103 CCY-3-O1 7.50% Clearing point [° C.]: 81 CCY-4-O2 5.00% Δn [589 nm, 20° C.]: 0.1054 CLY-3-O2 7.00% Δε [1 kHz, 20° C.]: −2.6 CPY-2-O2 10.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CPY-3-O2 8.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.0 PYP-2-3 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 86 CC-3-V 45.50% K.sub.1 [pN, 20° C.]: 13.3 PY-1-O4 5.00% K.sub.3 [pN, 20° C.]: 15.1 Y-4O-O4 2.50% V.sub.0 [20° C., V]: 2.54

Example 98

(231) TABLE-US-00104 CC-3-2V1 4.00% Clearing point [° C.]: 100 CC-3-V 37.50% Δn [589 nm, 20° C.]: 0.1047 CC-3-V1 5.00% Δε [1 kHz, 20° C.]: 3.9 CCP-V-1 13.00% ε.sub.∥ [1 kHz, 20° C.]: 6.6 CCP-V2-1 7.50% ε.sub.⊥ [1 kHz, 20° C.]: 2.7 CCVC-3-V 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 72 CDUQU-3-F 1.00% K.sub.1 [pN, 20° C.]: 15.1 CPGP-5-2 3.00% K.sub.3 [pN, 20° C.]: 17.4 DGUQU-4-F 2.00% V.sub.0 [20° C., V]: 2.07 PGP-2-3 5.00% PGP-2-4 3.00% PGUQU-3-F 4.00% PGUQU-4-F 3.50% PPGU-3F 0.50% PUQU-3F 5.00%

Example 99

(232) TABLE-US-00105 APUQU-2-F 1.50% Clearing point [° C.]: 100 APUQU-3-F 5.00% Δn [589 nm, 20° C.]: 0.1056 CC-3-2V1 4.00% Δε [1 kHz, 20° C.]: 4.0 CC-3-V 36.00% ε.sub.∥ [1 kHz, 20° C.]: 6.8 CC-3-V1 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 2.8 CCP-V-1 13.00% γ.sub.1 [mPa .Math. s, 20° C.]: 71 CCP-V2-1 9.50% K.sub.1 [pN, 20° C.]: 15.4 CCVC-3-V 4.00% K.sub.3 [pN, 20° C.]: 17.7 CDUQU-3-F 3.00% V.sub.0 [20° C., V]: 2.07 DGUQU-4-F 2.00% PGP-1-2V 5.50% PGP-2-2V 7.00% PPGU-3-F 0.50% PUQU-3-F 4.00%

Example 100

(233) TABLE-US-00106 CC-3-V1 9.00% Clearing point [° C.]: 74.7 CCH-23 18.00% Δn [589 nm, 20° C.]: 0.0982 CCH-34 3.00% Δε [1 kHz, 20° C.]: −3.4 CCH-35 7.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCP-3-1 5.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CCY-3-O2 11.50% γ.sub.1 [mPa .Math. s, 20° C.]: 108 CPY-2-O2 8.00% K.sub.1 [pN, 20° C.]: 14.9 CPY-3-O2 11.00% K.sub.3 [pN, 20° C.]: 15.9 CY-3-O2 15.50% V.sub.0 [20° C., V]: 2.28 PY-3-O2 11.50%

Example 100a

(234) The mixture according to Example 100 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.45% of RM-1.

Example 101

(235) TABLE-US-00107 CC-3-V 15.00% Clearing point [° C.]: 85 CPGP-4-3 2.00% Δn [589 nm, 20° C.]: 0.1981 CPGP-5-2 2.00% Δε [1 kHz, 20° C.]: 9.9 CPTP-301 6.00% ε.sub.|| [1 kHz, 20° C.]: 13.6 DGUQU-4-F 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.7 PCH-301 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 123 PGP-2-2V 14.50% K.sub.1 [pN, 20° C.]: 15.1 PGUQU-3-F 7.50% K.sub.3 [pN, 20° C.]: 15.1 PGUQU-4-F 7.00% V.sub.0 [20° C., V]: 1.29 PGUQU-5-F 6.00% PP-1-2V1 12.00% PTP-102 6.00% PTP-201 6.00% PUQU-3-F 6.00%

Example 102

(236) TABLE-US-00108 CC-3-V 28.00% Clearing point [° C.]: 84.8 CC-3-V1 3.00% Δn [589 nm, 20° C.]: 0.1078 CCP-3-1 3.00% Δε [1 kHz, 20° C.]: −4.1 CCY-3-O2 9.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-4-O2 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CLY-3-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 122 CLY-3-O3 6.00% K.sub.1 [pN, 20° C.]: 14.8 CPY-2-O2 7.00% CPY-3-O2 9.00% PY-3-O2 8.00% PY-4-O2 4.00% PYP-2-4 2.50% Y-4O-O4 5.50%

Example 102a

(237) The mixture according to Example 102 additionally comprises 0.04% of

(238) ##STR00398##
and
0.01% of

(239) ##STR00399##

Example 103

(240) TABLE-US-00109 CC-3-V 28.00% Clearing point [° C.]: 80 CC-3-V1 5.00% Δn [589 nm, 20° C.]: 0.1082 CCP-3-1 2.50% Δε [1 kHz, 20° C.]: −4.1 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.8 CCY-4-O2 2.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.9 CLY-3-O2 6.50% γ.sub.1 [mPa .Math. s, 20° C.]: 113 CLY-3-O3 6.50% K.sub.1 [pN, 20° C.]: 14.5 CPY-2-O2 9.00% CPY-3-O2 10.00% PY-3-O2 10.00% PY-4-O2 5.00% Y-4O-O4 5.00%

Example 103a

(241) The mixture according to Example 103 additionally comprises 0.04% of

(242) ##STR00400##
and
0.01% of

(243) ##STR00401##

Example 104

(244) TABLE-US-00110 CC-3-V 29.00% Clearing point [° C.]: 75.1 CC-3-V1 5.00% Δn [589 nm, 20° C.]: 0.1075 CCP-3-1 3.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.8 CLY-3-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CLY-3-O3 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 103 CPY-2-O2 9.00% K.sub.1 [pN, 20° C.]: 14.3 CPY-3-O2 10.00% PY-3-O2 10.00% PY-4-O2 7.00% Y-4O-O4 5.00%

Example 104a

(245) The mixture from Example 104 additionally comprises 0.04% of

(246) ##STR00402##
and
0.015% of

(247) ##STR00403##

Example 105

(248) TABLE-US-00111 CC-3-V 29.00% Clearing point [° C.]: 80.1 CCY-3-O1 8.00% Δn [589 nm, 20° C.]: 0.1052 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −4.7 CCY-4-O2 2.00% ε.sub.|| [1 kHz, 20° C.]: 3.9 CLY-3-O2 8.50% ε.sub.⊥ [1 kHz, 20° C.]: 8.7 CLY-3-O3 7.50% γ.sub.1 [mPa .Math. s, 20° C.]: 125 CPY-2-O2 10.00% K.sub.1 [pN, 20° C.]: 14.0 CPY-3-O2 7.50% CY-3-O2 6.50% PY-3-O2 10.00% Y-4O-O4 5.00%

Example 105a

(249) The mixture according to Example 105 additionally comprises 0.04% of

(250) ##STR00404##
and
0.02% of

(251) ##STR00405##

Example 106

(252) TABLE-US-00112 CC-3-V 37.00% Clearing point [° C.]: 75.2 CCY-3-O1 5.00% Δn [589 nm, 20° C.]: 0.1012 CCY-3-O2 5.00% Δε [1 kHz, 20° C.]: −3.8 CCY-4-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CLY-3-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CPY-2-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 97 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 13.3 CY-3-O2 12.00% K.sub.3 [pN, 20° C.]: 15.3 PY-3-O2 11.00% V.sub.0 [20° C., V]: 2.12

Example 106a

(253) The mixture according to Example 106 additionally comprises 0.04% of

(254) ##STR00406##
and
0.015% of

(255) ##STR00407##

Example 107

(256) TABLE-US-00113 CY-3-O2 15.00% Clearing point [° C.]: 80.4 CY-5-O2 12.50% Δn [589 nm, 20° C.]: 0.1038 CCY-3-O1 2.50% Δε [1 kHz, 20° C.]: −3.3 CCY-4-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 137 CCY-2-1 6.00% K.sub.1 [pN, 20° C.]: 14.2 CCY-3-1 6.00% K.sub.3 [pN, 20° C.]: 14.2 CCH-23 15.00% V.sub.0 [20° C., V]: 2.18 CCH-34 5.00% CCH-301 1.50% BCH-32 15.50%

Example 107a

(257) The mixture according to Example 107 additionally comprises 0.01% of

(258) ##STR00408##

Example 108

(259) TABLE-US-00114 CY-3-O2 15.00% Clearing point [° C.]: 100 CY-3-O4 20.00% Δn [589 nm, 20° C.]: 0.0968 CY-5-O2 7.50% Δε [1 kHz, 20° C.]: −5.9 CCY-3-O2 6.50% ε.sub.|| [1 kHz, 20° C.]: 4.0 CCY-3-O3 6.50% ε.sub.⊥ [1 kHz, 20° C.]: 9.9 CCY-4-O2 6.50% γ.sub.1 [mPa .Math. s, 20° C.]: 324 CCY-5-O2 6.50% K.sub.1 [pN, 20° C.]: 15.1 CPY-2-O2 5.50% K.sub.3 [pN, 20° C.]: 17.2 CPY-3-O2 5.00% V.sub.0 [20° C., V]: 1.80 CC-4-V 3.00% CH-33 3.00% CH-35 2.00% CH-43 3.00% CH-45 2.00% CCPC-33 4.00% CCPC-34 4.00%

Example 109

(260) TABLE-US-00115 CY-3-O2 11.00% Clearing point [° C.]: 101 CY-3-O4 18.00% Δn [589 nm, 20° C.]: 0.1662 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −6.1 CCY-3-O3 6.00% ε.sub.|| [1 kHz, 20° C.]: 4.2 CCY-4-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 10.3 CCY-5-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 363 CPY-3-O2 6.00% K.sub.1 [pN, 20° C.]: 16.5 CC-4-V 3.00% K.sub.3 [pN, 20° C.]: 22.00 CPTP-3-1 5.00% V.sub.0 [20° C., V]: 2.00 PTP-302FF 10.00% PTP-502FF 10.00% CPTP-302FF 5.00% CPTP-502FF 5.00% CCPC-33 3.00%

Example 110

(261) TABLE-US-00116 CY-3-O2 8.00% Clearing point [° C.]: 101 CY-3-O4 13.00% Δn [589 nm, 20° C.]: 0.0970 CCY-3-O2 6.50% Δε [1 kHz, 20° C.]: −2.1 CPY-2-O2 3.50% ε.sub.|| [1 kHz, 20° C.]: 3.2 CPY-3-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.3 CCH-301 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 136 CC-4-V 12.00% K.sub.1 [pN, 20° C.]: 14.8 CC-5-V 8.00% K.sub.3 [pN, 20° C.]: 18.3 CCP-V-1 13.00% V.sub.0 [20° C., V]: 3.11 CCP-V2-1 13.00% BCH-32 5.00% CCPC-33 5.00%

Example 111

(262) TABLE-US-00117 CY-3-O4 12.00% Clearing point [° C.]: 101 CC-4-V 13.00% Δn [589 nm, 20° C.]: 0.1660 CC-5-V 9.50% Δε [1 kHz, 20° C.]: −2.1 CCP-V-1 10.50% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCP-V2-1 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.5 PTP-102 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 151 CPTP-3-1 5.00% K.sub.1 [pN, 20° C.]: 16.2 CPTP-3-2 5.00% K.sub.3 [pN, 20° C.]: 19.8 PTP-302FF 9.50% V.sub.0 [20° C., V]: 3.25 PTP-502FF 9.50% CPTP-302FF 6.50% CPTP-502FF 6.50%

Example 112

(263) TABLE-US-00118 CY-3-O2 15.00% Clearing point [° C.]: 71.9 CCY-3-O1 6.00% Δn [589 nm, 20° C.]: 0.1203 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −8.1 CCY-3-O3 5.50% ε.sub.|| [1 kHz, 20° C.]: 5.2 CCY-4-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 13.3 CCY-5-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 253 CPY-2-O2 1.50% K.sub.1 [pN, 20° C.]: 13.2 CPY-3-O2 10.00% K.sub.3 [pN, 20° C.]: 15.7 CLY-3-O2 8.00% V.sub.0 [20° C., V]: 1.46 PY-3-O2 6.00% PY-1-O4 8.00% PY-4-O2 8.00% Y-4O-O4 8.00%

Example 113

(264) TABLE-US-00119 CC-3-V1 8.00% Clearing point [° C.]: 75.5 CCH-23 18.00% Δn [589 nm, 20° C.]: 0.0978 CCH-34 4.00% Δε [1 kHz, 20° C.]: −3.5 CCH-35 7.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCP-3-1 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CCY-3-O2 12.50% γ.sub.1 [mPa .Math. s, 20° C.]: 111 CPY-2-O2 8.00% K.sub.1 [pN, 20° C.]: 14.9 CPY-3-O2 11.00% K.sub.3 [pN, 20° C.]: 15.8 CY-3-O2 15.50% V.sub.0 [20° C., V]: 2.26 PY-3-O2 11.00%

Example 113a

(265) The mixture according to Example 113 additionally comprises 0.3% of RM-1.

Example 114

(266) TABLE-US-00120 BCH-32 1.50% Clearing point [° C.]: 74.8 CC-3-V 15.50% Δn [589 nm, 20° C.]: 0.1035 CC-3-V1 11.00% Δε [1 kHz, 20° C.]: −3.1 CCH-23 12.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCH-34 3.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CCY-3-O2 11.50% γ.sub.1 [mPa .Math. s, 20° C.]: 95 CCY-5-O2 0.50% K.sub.1 [pN, 20° C.]: 14.1 CPY-2-O2 8.50% K.sub.3 [pN, 20° C.]: 15.4 CPY-3-O2 12.00% V.sub.0 [20° C., V]: 2.36 CY-3-O2 9.50% PY-3-O2 11.50% PYP-2-3 3.00%

Example 115a

(267) The mixture according to Example 115 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.3% of RM-1.

Example 116

(268) TABLE-US-00121 CC-3-V 30.50% Clearing point [° C.]: 79.8 CC-3-V1 4.50% Δn [589 nm, 20° C.]: 0.1022 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O3 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 CLY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 114 CPY-2-O2 8.00% K.sub.1 [pN, 20° C.]: 14.5 CPY-3-O2 11.00% K.sub.3 [pN, 20° C.]: 16.7 CY-3-O2 15.00% V.sub.0 [20° C., V]: 2.14 PY-3-O2 8.00%

Example 117

(269) TABLE-US-00122 CY-3-O2 15.00% Clearing point [° C.]: 80.4 CY-5-O2 12.50% Δn [589 nm, 20° C.]: 0.1038 CCY-3-O1 2.50% Δε [1 kHz, 20° C.]: −3.3 CCY-4-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 137 CCY-2-1 6.00% K.sub.1 [pN, 20° C.]: 14.2 CCY-3-1 6.00% K.sub.3 [pN, 20° C.]: 14.2 CCH-23 15.00% V.sub.0 [20° C., V]: 2.18 CCH-34 5.00% CCH-301 1.50% BCH-32 15.50%

Example 118

(270) TABLE-US-00123 CY-3-O2 15.00% Clearing point [° C.]: 80.5 CY-3-O4 4.00% Δn [589 nm, 20° C.]: 0.1025 CY-5-O2 6.50% Δε [1 kHz, 20° C.]: −3.4 CCY-3-O1 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-3-O3 2.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 141 CPY-2-O2 7.00% K.sub.1 [pN, 20° C.]: 14.0 CPY-3-O2 7.00% K.sub.3 [pN, 20° C.]: 14.1 CCY-2-1 6.00% V.sub.0 [20° C., V]: 2.16 CCY-3-1 6.00% CCH-23 15.50% CCH-34 5.00% BCH-32 13.00% PP-1-4 2.00%

Example 119

(271) TABLE-US-00124 PGUQU-3-F 4.00% Clearing point [° C.]: 85.4 CCQU-3-F 7.50% Δn [589 nm, 20° C.]: 0.1028 PUQU-3-F 15.50% Δε [1 kHz, 20° C.]: 9.9 APUQU-2-F 4.00% ε.sub.|| [1 kHz, 20° C.]: 13.3 APUQU-3-F 7.50% ε.sub.⊥ [1 kHz, 20° C.]: 3.4 CC-3-V 27.50% γ.sub.1 [mPa .Math. s, 20° C.]: 82 CCP-3-V1 6.00% K.sub.1 [pN, 20° C.]: 12.6 CCP-V-1 13.00% K.sub.3 [pN, 20° C.]: 15.3 CCP-V2-1 10.00% V.sub.0 [20° C., V]: 1.19 PPGU-3-F 0.50% BCH-3F.F 4.50%

Example 119a

(272) The mixture according to Example 119 additionally comprises 0.01% of

(273) ##STR00409##

Example 120

(274) TABLE-US-00125 CC-3-V 30.50% Clearing point [° C.]: 80.1 CC-3-V1 4.50% Δn [589 nm, 20° C.]: 0.1033 CCY-3-O1 6.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CLY-3-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 CPY-2-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 113 CPY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 14.4 CY-3-O2 15.00% K.sub.3 [pN, 20° C.]: 17.0 PY-3-O2 8.00% V.sub.0 [20° C., V]: 2.16

Example 120a

(275) The mixture from Example 120 additionally comprises 0.3% of

(276) ##STR00410##

Example 121

(277) TABLE-US-00126 CC-3-V 28.50% Clearing point [° C.]: 74.6 CC-3-V1 7.00% Δn [589 nm, 20° C.]: 0.1040 CCY-3-O2 12.50% Δε [1 kHz, 20° C.]: −3.0 CCY-4-O2 5.25% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-3-O2 9.75% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CY-3-O2 15.00% γ.sub.1 [mPa .Math. s, 20° C.]: 98 CY-3-O4 4.75% K.sub.1 [pN, 20° C.]: 13.2 CY-5-O2 1.00% K.sub.3 [pN, 20° C.]: 15.5 PCH-301 3.25% V.sub.0 [20° C., V]: 2.4 PPGU-3-F 0.50% PYP-2-3 12.50%

Example 121a

(278) The mixture from Example 121 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate. BASF) and 0.45% of RM-1.

Example 122

(279) TABLE-US-00127 CC-3-V 36.50% Clearing point [° C.]: 75 CC-3-V1 2.00% Δn [589 nm, 20° C.]: 0.1015 CCY-3-O1 8.00% Δε [1 kHz, 20° C.]: −3.7 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-4-O2 2.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CLY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 97 CLY-3-O3 2.00% K.sub.1 [pN, 20° C.]: 13.8 CPY-2-O2 10.00% K.sub.3 [pN, 20° C.]: 15 CPY-3-O2 3.00% V.sub.0 [20° C., V]: 2.14 CY-3-O2 5.50% PY-3-O2 13.00% PY-1-O4 3.50%

Example 123

(280) TABLE-US-00128 BCH-32 4.50% Clearing point [° C.]: 75.5 CCH-23 14.00% Δn [589 nm, 20° C.]: 0.0938 CCH-301 7.00% Δε [1 kHz, 20° C.]: −2.5 CCH-34 9.00% ε.sub.|| [1 kHz, 20° C.]: 3.3 CCH-35 5.50% ε.sub.⊥ [1 kHz, 20° C.]: 5.8 CCP-3-1 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 89 CY-3-O2 5.00% K.sub.1 [pN, 20° C.]: 13.5 CY-V-O2 7.00% K.sub.3 [pN, 20° C.]: 14.5 CCY-3-O1 5.00% V.sub.0 [20° C., V]: 2.54 CCY-3-O2 9.00% CPY-V-O2 10.00% PCH-302 5.00% PY-V2-O2 9.00%

Example 124

(281) TABLE-US-00129 BCH-32 1.50% Clearing point [° C.]: 75 CC-3-V 37.00% Δn [589 nm, 20° C.]: 0.0960 CCP-3-1 8.00% Δε [1 kHz, 20° C.]: −2.6 CY-3-O2 15.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-O1 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.0 CCY-3-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 79 CPY-3-O2 8.50% K.sub.1 [pN, 20° C.]: 13.0 PCH-302 5.50% K.sub.3 [pN, 20° C.]: 16.0 PY-V-O2 8.00% V.sub.0 [20° C., V]: 2.6

Example 125

(282) TABLE-US-00130 BCH-32 1.00% Clearing point [° C.]: 75 CC-3-V 41.00% Δn [589 nm, 20° C.]: 0.0948 CCP-3-1 8.50% Δε [1 kHz, 20° C.]: −2.3 CY-3-O2 13.00% ε.sub.|| [1 kHz, 20° C.]: 3.2 CCY-3-O1 6.50% ε.sub.⊥ [1 kHz, 20° C.]: 5.5 CCY-3-O2 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 70 CPY-3-O2 6.00% K.sub.1 [pN, 20° C.]: 13.4 PCH-302 7.00% K.sub.3 [pN, 20° C.]: 16.5 PY-1V-O2 8.50% V.sub.0 [20° C., V]: 2.84

Example 126

(283) TABLE-US-00131 PY-3-O2 7.50% Clearing point [° C.]: 74 PY-1V-O2 4.00% Δn [589 nm, 20° C.]: 0.1094 CY-3-O2 14.50% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O1 3.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O2 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-2-O2 7.50% γ.sub.1 [mPa .Math. s, 20° C.]: 85 CPY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 12.9 CC-3-V 37.00% K.sub.3 [pN, 20° C.]: 14.6 BCH-32 8.00% V.sub.0 [20° C., V]: 2.34 PPGU-3-F 0.50%

Example 127

(284) TABLE-US-00132 PY-3-O2 8.00% Clearing point [° C.]: 74.5 PY-3V-O2 5.00% Δn [589 nm, 20° C.]: 0.1086 CY-3-O2 11.50% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O1 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O2 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-2-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 87 CPY-3-O2 7.00% K.sub.1 [pN, 20° C.]: 12.9 CC-3-V 37.50% K.sub.3 [pN, 20° C.]: 14.1 BCH-32 6.50% V.sub.0 [20° C., V]: 2.30 PPGU-3-F 0.50%

Example 128

(285) TABLE-US-00133 PY-V2-O2 12.00% Clearing point [° C.]: 76 CY-V-O2 9.00% Δn [589 nm, 20° C.]: 0.1087 CCY-3-O1 9.00% Δε [1 kHz, 20° C.]: −3.1 CCY-V2-O2 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-V-O2 10.50% γ.sub.1 [mPa .Math. s, 20° C.]: 83 CC-3-V 36.50% K.sub.1 [pN, 20° C.]: 12.4 BCH-32 6.50% K.sub.3 [pN, 20° C.]: 14.7 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.28

Example 129

(286) TABLE-US-00134 PY-V2-O2 11.50% Clearing point [° C.]: 75.5 CY-3-O2 11.00% Δn [589 nm, 20° C.]: 0.1074 CCY-3-O1 9.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 12.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 87 CC-3-V 37.00% K.sub.1 [pN, 20° C.]: 13.0 BCH-32 6.00% K.sub.3 [pN, 20° C.]: 14.7 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.29

Example 130

(287) TABLE-US-00135 PY-1V-O2 10.50% Clearing point [° C.]: 72 CY-3-O2 18.00% Δn [589 nm, 20° C.]: 0.1068 CCY-3-O1 7.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 78 CC-3-V 41.00% K.sub.1 [pN, 20° C.]: 12.6 BCH-32 3.00% K.sub.3 [pN, 20° C.]: 14.6 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.30

Example 131

(288) TABLE-US-00136 PY-V2-O2 10.50% Clearing point [° C.]: 75 CY-3-O2 10.00% Δn [589 nm, 20° C.]: 0.1070 CCY-3-O1 6.00% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 9.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CPY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 90 CC-3-V 35.00% K.sub.1 [pN, 20° C.]: 12.7 BCH-32 6.50% K.sub.3 [pN, 20° C.]: 14.5 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.23 Y-4O-O4 2.50% LTS (bulk) [−20° C.]: >1000 h LTS (bulk) [−30° C.]: >1000 h

Example 132

(289) TABLE-US-00137 PY-1V-O2 10.00% Clearing point [° C.]: 73.5 CY-3-O2 18.00% Δn [589 nm, 20° C.]: 0.1084 CCY-3-O1 6.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 CC-3-V 40.00% K.sub.1 [pN, 20° C.]: 12.8 BCH-32 3.50% K.sub.3 [pN, 20° C.]: 14.9 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.3

Example 133

(290) TABLE-US-00138 PY-V2-O2 11.50% Clearing point [° C.]: 74.5 CY-3-O2 10.00% Δn [589 nm, 20° C.]: 0.1071 CCY-3-O1 4.50% Δε [1 kHz, 20° C.]: −3.4 CCY-3-O2 11.00% ε.sub.|| [1 kHz, 20° C.]: 3.8 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.1 CPY-3-O2 12.50% γ.sub.1 [mPa .Math. s, 20° C.]: 91 CC-3-V 34.50% K.sub.1 [pN, 20° C.]: 12.7 BCH-32 6.00% K.sub.3 [pN, 20° C.]: 14.6 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.2 Y-4O-O4 2.50%

Example 134

(291) TABLE-US-00139 PY-V2-O2 14.00% Clearing point [° C.]: 74.5 CY-3-O2 10.50% Δn [589 nm, 20° C.]: 0.1075 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CPY-2-O2 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 90 CC-3-V 36.50% K.sub.1 [pN, 20° C.]: 11.7 BCH-32 2.50% K.sub.3 [pN, 20° C.]: 14.1 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.21

Example 135

(292) TABLE-US-00140 PY-3V-O2 10.50% Clearing point [° C.]: 74.5 CY-3-O2 15.00% Δn [589 nm, 20° C.]: 0.1073 CCY-3-O1 7.50% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CPY-2-O2 11.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 84 CC-3-V 40.50% K.sub.1 [pN, 20° C.]: 12.8 BCH-32 3.00% K.sub.3 [pN, 20° C.]: 14.1 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.29

Example 136

(293) TABLE-US-00141 CC-3-V 36.50% Clearing point [° C.]: 73 CY-3-O2 10.00% Δn [589 nm, 20° C.]: 0.1081 CCY-3-O1 6.50% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 11.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 90 PY-3-O2 4.00% K.sub.1 [pN, 20° C.]: 13.2 PY-3V-O2 6.50% K.sub.3 [pN, 20° C.]: 15.0 PY-1-O4 4.50% V.sub.0 [20° C., V]: 2.25 PYP-2-3 3.00% PP-1-2V1 3.50%

Example 137

(294) TABLE-US-00142 PY-V2-O2 7.00% Clearing point [° C.]: 75.5 CY-3-O2 10.00% Δn [589 nm, 20° C.]: 0.1086 CY-1V2-O2 6.00% Δε [1 kHz, 20° C.]: −2.7 CCY-3-O1 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-3-O2 2.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.2 CPY-2-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 85 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 12.8 CC-3-V 37.00% K.sub.3 [pN, 20° C.]: 14.5 BCH-32 10.50% V.sub.0 [20° C., V]: 2.45 PPGU-3-F 0.50% LTS (bulk) [−20° C.]: >1000 h

Example 138

(295) TABLE-US-00143 PY-V-O2 5.00% Clearing point [° C.]: 75 PY-V2-O2 5.00% Δn [589 nm, 20° C.]: 0.1087 PY-3-O2 3.00% Δε [1 kHz, 20° C.]: −3.1 CY-V-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CY-3-O2 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CCY-3-O1 3.50% γ.sub.1 [mPa .Math. s, 20° C.]: 83 CCY-3-O2 7.00% K.sub.1 [pN, 20° C.]: 12.6 CCY-4-O2 5.00% K.sub.3 [pN, 20° C.]: 14.2 CPY-2-O2 8.00% V.sub.0 [20° C., V]: 2.28 CPY-3-O2 10.00% LTS (bulk) [−20° C.]: >1000 h CC-3-V 38.00% BCH-32 6.00% PPGU-3-F 0.50% Y-4O-O4 2.00%

Example 139

(296) TABLE-US-00144 PY-V2-O2 5.50% Clearing point [° C.]: 75.5 PY-3-O2 8.00% Δn [589 nm, 20° C.]: 0.1075 CY-V-O2 6.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O1 5.50% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-3-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CCY-4-O2 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 88 CPY-2-O2 8.00% K.sub.1 [pN, 20° C.]: 12.6 CPY-3-O2 9.00% K.sub.3 [pN, 20° C.]: 14.0 CC-3-V 35.00% V.sub.0 [20° C., V]: 2.26 BCH-32 8.00% LTS (bulk) [−20° C.]: >1000 h PPGU-3-F 0.50% LTS (bulk) [−30° C.]: >1000 h Y-4O-O4 2.00%

Example 140

(297) TABLE-US-00145 PY-V-O2 5.50% Clearing point [° C.]: 74.5 PY-3-O2 4.50% Δn [589 nm, 20° C.]: 0.1098 CY-3-O2 11.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O2 10.50% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-3-O2 11.00% γ.sub.1 [mPa .Math. s, 20° C.]: 85 CC-3-V 37.00% K.sub.1 [pN, 20° C.]: 12.9 BCH-32 8.00% K.sub.3 [pN, 20° C.]: 14.5 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.31 Y-4O-O4 2.00% LTS (bulk) [−20° C.]: >1000 h LTS (bulk) [−30° C.]: >1000 h

Example 141

(298) TABLE-US-00146 PY-3-O2 6.00% Clearing point [° C.]: 75 PY-V2-O2 6.00% Δn [589 nm, 20° C.]: 0.1079 CY-3-O2 12.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O1 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-3-O2 9.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-2-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 91 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 13.1 CC-3-V 35.50% K.sub.3 [pN, 20° C.]: 14.9 BCH-32 7.00% V.sub.0 [20° C., V]: 2.29 PPGU-3-F 0.50% LTS (bulk) [−20° C.]: >1000 h LTS (bulk) [−30° C.]: >1000 h

Example 142

(299) TABLE-US-00147 PY-3-O2 6.00% Clearing point [° C.]: 75 PY-1V2-O2 6.50% Δn [589 nm, 20° C.]: 0.1088 CY-3-O2 13.00% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 12.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 93 CC-3-V 36.00% K.sub.1 [pN, 20° C.]: 13.5 BCH-32 6.00% K.sub.3 [pN, 20° C.]: 15.6 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.32

Example 143

(300) TABLE-US-00148 PY-3-O2 4.50% Clearing point [° C.]: 75 PY-V2-O2 6.00% Δn [589 nm, 20° C.]: 0.1078 CY-3-O2 10.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O1 2.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-3-O2 11.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-2-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 88 CPY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 13.0 CC-3-V 36.00% K.sub.3 [pN, 20° C.]: 14.8 BCH-32 8.00% V.sub.0 [20° C., V]: 2.31 PPGU-3-F 0.50% LTS (bulk) [−30° C.] >1000 h Y-4O-O4 2.00%

Example 143a

(301) The mixture according to Example 143 additionally comprises 0.01% of

(302) ##STR00411##

Example 144

(303) TABLE-US-00149 BCH-32 6.00% Clearing point [° C.]: 77 CCH-23 16.00% Δn [589 nm, 20° C.]: 0.0953 CCH-301 3.50% Δε [1 kHz, 20° C.]: −2.5 CCH-34 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.3 CCH-35 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.8 CCP-3-1 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 96 CY-3-O2 15.00% K.sub.1 [pN, 20° C.]: 14.6 CCY-3-O1 5.00% K.sub.3 [pN, 20° C.]: 15.6 CCY-3-O2 7.00% V.sub.0 [20° C., V]: 2.66 CPY-3-O2 8.50% LTS (bulk) [−20° C.] >1000 h PCH-302 6.00% LTS (bulk) [−30° C.] >1000 h PY-V2-O2 9.00%

Example 145

(304) TABLE-US-00150 BCH-32 4.00% Clearing point [° C.]: 76 CC-3-V 34.50% Δn [589 nm, 20° C.]: 0.0955 CCP-3-1 10.00% Δε [1 kHz, 20° C.]: −2.5 CY-3-O2 14.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.9 CCY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 CPY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 13.4 PCH-302 4.50% K.sub.3 [pN, 20° C.]: 16.2 PY-V2-O2 9.00% V.sub.0 [20° C., V]: 2.66 LTS (bulk) [−20° C.]: >1000 h LTS (bulk) [−30° C.]: >1000 h

Example 146

(305) TABLE-US-00151 BCH-32 6.50% Clearing point [° C.]: 76.5 CCH-23 16.00% Δn [589 nm, 20° C.]: 0.0933 CCH-301 4.50% Δε [1 kHz, 20° C.]: −2.5 CCH-34 8.00% ε.sub.∥ [1 kHz, 20° C.]: 3.3 CCH-35 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.8 CCP-3-1 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 96 CY-3-O2 15.00% K.sub.1 [pN, 20° C.]: 14.3 CCY-3-O1 5.50% K.sub.3 [pN, 20° C.]: 15.0 CCY-3-O2 8.00% V.sub.0 [20° C., V]: 2.57 CPY-3-O2 9.00% PCH-302 4.50% PY-V2-O2 8.50%

Example 147

(306) TABLE-US-00152 Y-4O-O4 7.00% Clearing point [° C.]: 75.5 PY-1-O4 2.00% Δn [589 nm, 20° C.]: 0.1062 CCY-3-O1 2.50% Δε [1 kHz, 20° C.]: −2.2 CCY-3-O2 8.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CPY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.5 PYP-2-3 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 90 CCH-23 19.00% K.sub.1 [pN, 20° C.]: 14.5 CCH-34 6.00% K.sub.3 [pN, 20° C.]: 14.2 CCH-35 6.00% V.sub.0 [20° C., V]: 2.70 PCH-302 8.00% BCH-32 7.00% CCP-3-1 10.00% PY-V2-O2 6.00%

Example 148

(307) TABLE-US-00153 BCH-32 7.00% Clearing point [° C.]: 75 CCH-23 16.00% Δn [589 nm, 20° C.]: 0.0930 CCH-301 3.50% Δε [1 kHz, 20° C.]: −2.5 CCH-34 6.50% ε.sub.∥ [1 kHz, 20° C.]: 3.3 CCH-35 6.50% ε.sub.⊥ [1 kHz, 20° C.]: 5.8 CCP-3-1 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 93 CY-3-O2 7.50% K.sub.1 [pN, 20° C.]: 13.7 CY-V1-O2 7.00% K.sub.3 [pN, 20° C.]: 14.1 CCY-3-O1 6.00% V.sub.0 [20° C., V]: 2.52 CCY-3-O2 9.00% LTS (bulk) [−20° C.] >1000 h CPY-3-O2 7.00% PCH-302 5.00% PY-V2-O2 9.50%

Example 149

(308) TABLE-US-00154 BCH-32 7.00% Clearing point [° C.]: 74 CCH-23 15.00% Δn [589 nm, 20° C.]: 0.0921 CCH-301 4.00% Δε [1 kHz, 20° C.]: −2.5 CCH-34 8.00% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CCH-35 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.9 CCP-3-1 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 95 CY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 13.4 CY-V1-O2 7.00% K.sub.3 [pN, 20° C.]: 14.1 CCY-3-O1 9.00% V.sub.0 [20° C., V]: 2.49 CCY-3-O2 7.00% CPY-1V-O1 7.00% PCH-302 4.00% PY-V2-O2 8.00%

Example 150

(309) TABLE-US-00155 BCH-32 7.00% Clearing point [° C.]: 77 CCH-23 13.00% Δn [589 nm, 20° C.]: 0.0935 CCH-301 3.00% Δε [1 kHz, 20° C.]: −2.4 CCH-34 10.00% ε.sub.∥ [1 kHz, 20° C.]: 3.3 CCH-35 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.7 CCP-3-1 10.50% γ.sub.1 [mPa .Math. s, 20° C.]: 97 CY-3-O2 8.50% K.sub.1 [pN, 20° C.]: 14.1 CY-V1-O2 5.50% K.sub.3 [pN, 20° C.]: 14.6 CCY-3-O1 10.00% V.sub.0 [20° C., V]: 2.62 CCY-3-O2 6.00% CPY-1V-O1 5.50% PCH-302 6.00% PY-V2-O2 9.00%

Example 151

(310) TABLE-US-00156 CY-3-O2 9.50% Clearing point [° C.]: 75 PY-V-O2 9.50% Δn [589 nm, 20° C.]: 0.1101 CCY-3-O2 9.00% Δε [1 kHz, 20° C.]: −3.0 CCY-4-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CPY-2-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CPY-3-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 100 CCH-34 10.00% K.sub.1 [pN, 20° C.]: 13.4 CCH-23 21.00% K.sub.3 [pN, 20° C.]: 14.3 PYP-2-3 7.00% V.sub.0 [20° C., V]: 2.31 CCP-3-1 3.00% PCH-301 10.50%

Example 152

(311) TABLE-US-00157 PY-3-O2 11.00% Clearing point [° C.]: 75 PY-1V-O2 8.00% Δn [589 nm, 20° C.]: 0.1100 CY-3-O2 5.00% Δε [1 kHz, 20° C.]: −3.4 CCY-3-O2 9.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-2-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 107 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 14.3 CCH-34 10.00% K.sub.3 [pN, 20° C.]: 15.2 CCH-23 21.00% V.sub.0 [20° C., V]: 2.24 CCP-3-1 4.00% PCH-301 9.00%

Example 153

(312) TABLE-US-00158 CY-3-O2 10.00% Clearing point [° C.]: 75 PY-V-O2 9.00% Δn [589 nm, 20° C.]: 0.1099 CCY-3-O2 9.00% Δε [1 kHz, 20° C.]: −3.2 CCY-4-O2 7.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CCH-34 11.00% K.sub.1 [pN, 20° C.]: 13.2 CCH-23 20.00% K.sub.3 [pN, 20° C.]: 14.1 PYP-2-3 7.00% V.sub.0 [20° C., V]: 2.24 CCP-3-1 1.00% PCH-301 10.00%

Example 154

(313) TABLE-US-00159 CY-3-O2 12.50% Clearing point [° C.]: 74 PY-3-O2 4.00% Δn [589 nm, 20° C.]: 0.1026 PY-V-O2 5.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O2 9.00% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CCY-4-O2 2.00% γ.sub.1 [mPa .Math. s, 20° C.]: 102 CPY-2-O2 7.00% K.sub.1 [pN, 20° C.]: 13.5 CPY-3-O2 9.00% K.sub.3 [pN, 20° C.]: 14.1 CCH-34 10.00% V.sub.0 [20° C., V]: 2.22 CCH-23 21.00% LTS (bulk) [−20° C.]: >1000 h BCH-32 5.50% PCH-301 8.00% PYP-2-3 1.00%

Example 155

(314) TABLE-US-00160 PY-3-O2 12.00% Clearing point [° C.]: 75 PY-V-O2 5.00% Δn [589 nm, 20° C.]: 0.1112 CCY-3-O2 10.00% Δε [1 kHz, 20° C.]: −3.1 CCY-4-O2 9.50% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CPY-2-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 107 CCH-34 5.50% K.sub.1 [pN, 20° C.]: 13.7 CCH-23 21.00% K.sub.3 [pN, 20° C.]: 14.4 PYP-2-3 4.50% V.sub.0 [20° C., V]: 2.29 CCH-35 4.00% PCH-301 12.00% BCH-32 1.50%

Example 156

(315) TABLE-US-00161 PY-V-O2 8.00% Clearing point [° C.]: 74.8 CY-3-O2 5.50% Δn [589 nm, 20° C.]: 0.1073 CY-V-O2 11.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O1 4.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 CPY-V-O4 7.00% K.sub.1 [pN, 20° C.]: 12.1 CC-3-V 37.00% K.sub.3 [pN, 20° C.]: 14.6 BCH-32 7.00% V.sub.0 [20° C., V]: 2.30 PPGU-3-F 0.50%

Example 157

(316) TABLE-US-00162 PY-3-O2 5.00% Clearing point [° C.]: 76 PY-V2-O2 6.50% Δn [589 nm, 20° C.]: 0.1082 CY-3-O2 12.00% Δε [1 kHz, 20° C.]: −3.2 CCY-3-O1 5.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-V-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 89 CPY-V-O4 10.00% K.sub.1 [pN, 20° C.]: 12.6 CC-3-V 35.00% K.sub.3 [pN, 20° C.]: 14.6 BCH-32 7.00% V.sub.0 [20° C., V]: 2.26 PPGU-3-F 0.50%

Example 157a

(317) The mixture according to Example 157 additionally comprises 0.01% of

(318) ##STR00412##

Example 157b

(319) The mixture according to Example 157 additionally comprises 0.01% of

(320) ##STR00413##

Example 158

(321) TABLE-US-00163 PY-V-O2 5.00% Clearing point [° C.]: 73.5 PY-V2-O2 5.00% Δn [589 nm, 20° C.]: 0.1074 PY-3-O2 3.00% Δε [1 kHz, 20° C.]: −2.9 CY-V-O2 4.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CY-3-O2 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CCY-3-O1 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 78 CCY-3-O2 6.00% K.sub.1 [pN, 20° C.]: 12.5 CCY-4-O2 5.00% K.sub.3 [pN, 20° C.]: 14.0 CPY-2-O2 7.50% V.sub.0 [20° C., V]: 2.33 CPY-3-O2 10.00% CC-3-V 39.00% BCH-32 7.00% PPGU-3-F 0.50% Y-4O-O4 2.00%

Example 159

(322) TABLE-US-00164 PY-V-O2 5.00% Clearing point [° C.]: 75 CY-3-O2 8.00% Δn [589 nm, 20° C.]: 0.1078 CY-V-O2 11.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O1 4.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-3-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 84 CPY-V-O4 5.00% K.sub.1 [pN, 20° C.]: 11.9 CPY-V-O2 7.00% K.sub.3 [pN, 20° C.]: 14.4 CC-3-V 35.50% V.sub.0 [20° C., V]: 2.30 BCH-32 9.00% PPGU-3-F 0.50%

Example 160

(323) TABLE-US-00165 APUQU-2-F 9.00% Clearing point [° C.]: 77.5 APUQU-3-F 8.50% Δn [589 nm, 20° C.]: 0.1087 CC-3-V 43.50% Δε [1 kHz, 20° C.]: 9.9 CCP-30CF.sub.3 7.50% ε.sub.∥ [1 kHz, 20° C.]: 13.7 CCP-V-1 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.8 DPGU-4-F 3.50% γ.sub.1 [mPa .Math. s, 20° C.]: 68 PGP-2-2V 4.00% K.sub.1 [pN, 20° C.]: 12.4 PGUQU-4-F 4.50% K.sub.3 [pN, 20° C.]: 13.1 PUQU-3-F 8.50% V.sub.0 [20° C., V]: 1.18 PY-3V-O2 4.00% LTS (bulk) [−20° C.]: >1000 h LTS (bulk) [−30° C.]: >1000 h

Example 161

(324) TABLE-US-00166 PY-1V-O2 4.50% Clearing point [° C.]: 73.5 PY-V2-O2 5.00% Δn [589 nm, 20° C.]: 0.1074 CY-3-O2 10.00% Δε [1 kHz, 20° C.]: −2.8 CY-V-O2 4.50% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CCY-3-O2 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 78 CPY-2-O2 9.00% K.sub.1 [pN, 20° C.]: 12.5 CPY-3-O2 10.00% K.sub.3 [pN, 20° C.]: 14.3 CC-3-V 39.50% V.sub.0 [20° C., V]: 2.40 BCH-32 8.00% PPGU-3-F 0.50%

Example 162

(325) TABLE-US-00167 PY-V2-O2 5.50% Clearing point [° C.]: 74 PY-3-O2 6.00% Δn [589 nm, 20° C.]: 0.1074 CY-V2-O2 5.00% Δε [1 kHz, 20° C.]: −2.9 CY-3-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-3-O1 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CCY-3-O2 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 85 CCY-4-O2 6.00% K.sub.1 [pN, 20° C.]: 12.6 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 13.9 CPY-3-O2 12.00% V.sub.0 [20° C., V]: 2.30 CC-3-V 36.50% BCH-32 8.50% PPGU-3-F 0.50% Y-4O-O4 2.00%

Example 163

(326) TABLE-US-00168 PY-V2-O2 6.00% Clearing point [° C.]: 74.5 PY-3-O2 6.00% Δn [589 nm, 20° C.]: 0.1086 CY-1V2-O2 4.50% Δε [1 kHz, 20° C.]: −2.9 CY-3-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O1 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CCY-3-O2 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 86 CCY-4-O2 6.00% K.sub.1 [pN, 20° C.]: 12.8 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 14.2 CPY-3-O2 12.00% V.sub.0 [20° C., V]: 2.33 CC-3-V 37.00% BCH-32 8.00% PPGU-3-F 0.50% Y-4O-O4 2.00%

Example 164

(327) TABLE-US-00169 PY-V2-O2 6.50% Clearing point [° C.]: 74 CY-3-O2 11.00% Δn [589 nm, 20° C.]: 0.1068 CY-V2-O2 6.50% Δε [1 kHz, 20° C.]: −2.8 CCY-3-O1 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O2 2.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-2-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 85 CPY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 12.3 CC-3-V 36.00% K.sub.3 [pN, 20° C.]: 14.1 BCH-32 9.50% V.sub.0 [20° C., V]: 2.35 PPGU-3-F 0.50%

Example 165

(328) TABLE-US-00170 PCH-504FF 10.00% Clearing point [° C.]: 72 PCH-502FF 8.00% Δn [589 nm, 20° C.]: 0.1216 PCH-304FF 4.00% Δε [1 kHz, 20° C.]: −4.0 CCP-V2-1 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.9 BCH-32 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.9 CCH-35 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 125 CC-5-V 7.00% K.sub.1 [pN, 20° C.]: 14.6 CC-3-V1 10.00% K.sub.3 [pN, 20° C.]: 14.7 CPY-2-O2 10.00% V.sub.0 [20° C., V]: 2.03 CPY-3-O2 13.00% PY-V2-O2 20.00%

Example 166

(329) TABLE-US-00171 CY-3-O2 24.00% Clearing point [° C.]: 81 PY-1V2-O2 7.00% Δn [589 nm, 20° C.]: 0.1019 CCY-3-O3 4.00% Δε [1 kHz, 20° C.]: −3.1 CCY-3-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-3-O2 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 126 CCP-3-3 9.00% K.sub.1 [pN, 20° C.]: 14.9 CCP-3-1 9.00% K.sub.3 [pN, 20° C.]: 16.0 BCH-32 5.00% V.sub.0 [20° C., V]: 2.39 CCH-34 10.00% LTS (bulk) [−20° C.]: >1000 h CCH-25 10.00% PCH-301 5.00%

Example 167

(330) TABLE-US-00172 CY-3-O2 18.00% Clearing point [° C.]: 80.5 PY-1V2-O2 6.00% Δn [589 nm, 20° C.]: 0.0949 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −3.1 CCY-4-O2 4.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CPY-2-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 113 CCH-34 8.00% K.sub.1 [pN, 20° C.]: 14.9 CCH-23 22.00% K.sub.3 [pN, 20° C.]: 16.0 CCP-3-3 7.00% V.sub.0 [20° C., V]: 2.41 CCP-3-1 7.00% LTS (bulk) [−20° C.]: >1000 h PCH-301 3.00%

Example 168

(331) TABLE-US-00173 CY-1V-O1V 20.00% Clearing point [° C.]: 82.5 PY-1V2-O2 7.00% Δn [589 nm, 20° C.]: 0.0987 CY-3-O2 5.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-4-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 109 CCH-34 10.00% K.sub.1 [pN, 20° C.]: 14.9 CC-3-V1 11.00% K.sub.3 [pN, 20° C.]: 18.9 CC-2-V1 11.00% V.sub.0 [20° C., V]: 2.66 CCP-3-1 8.00% LTS (bulk) [−20° C.]: >1000 h PCH-301 2.00% CCVC-3-V 6.00%

Example 169

(332) TABLE-US-00174 CY-1V-O1V 20.00% Clearing point [° C.]: 81 PY-1V2-O2 5.00% Δn [589 nm, 20° C.]: 0.0953 CY-3-O2 7.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 106 CCH-34 10.00% K.sub.1 [pN, 20° C.]: 14.5 CC-3-V1 11.00% K.sub.3 [pN, 20° C.]: 18.6 CC-2-V1 11.00% V.sub.0 [20° C., V]: 2.63 CCP-3-1 8.00% LTS (bulk) [−20° C.]: >1000 h PCH-301 2.00% CCVC-3-V 6.00%

Example 170

(333) TABLE-US-00175 CY-1V-O1V 20.00% Clearing point [° C.]: 81.5 PY-1V2-O2 6.00% Δn [589 nm, 20° C.]: 0.0947 CY-3-O2 6.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O2 7.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-O1 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-3-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CCH-34 10.00% K.sub.1 [pN, 20° C.]: 14.6 CC-3-V1 12.00% K.sub.3 [pN, 20° C.]: 18.6 CC-2-V1 12.00% V.sub.0 [20° C., V]: 2.64 CCP-V2-1 4.00% CCP-V-1 4.00% CCVC-3-V 6.00%

Example 171

(334) TABLE-US-00176 CY-1V-O1V 20.00% Clearing point [° C.]: 80.5 PY-1V2-O2 5.00% Δn [589 nm, 20° C.]: 0.0962 CY-3-O2 12.00% Δε [1 kHz, 20° C.]: −3.4 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 112 CCH-34 7.00% K.sub.1 [pN, 20° C.]: 14.3 CC-3-V1 11.00% K.sub.3 [pN, 20° C.]: 18.5 CC-2-V1 11.00% V.sub.0 [20° C., V]: 2.45 CCP-3-1 6.00% CCVC-3-V 8.00%

Example 172

(335) TABLE-US-00177 CY-1V-O1V 20.00% Clearing point [° C.]: 81.5 PY-1V2-O2 7.00% Δn [589 nm, 20° C.]: 0.0932 CY-3-O2 7.50% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 10.50% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-4-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-3-V2 11.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CC-3-V1 11.00% K.sub.1 [pN, 20° C.]: 14.9 CC-2-V1 11.00% K.sub.3 [pN, 20° C.]: 19.0 CCP-3-1 6.00% V.sub.0 [20° C., V]: 2.55 CCVC-3-V 6.00% LTS (bulk) [−20° C.] >1000 h

Example 173

(336) TABLE-US-00178 CY-3-O2 12.00% Clearing point [° C.]: 80.0 PY-1V2-O2 11.00% Δn [589 nm, 20° C.]: 0.0950 CCY-3-O2 10.00% Δε [1 kHz, 20° C.]: −3.1 CCY-4-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.3 CPY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CCH-34 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 111 CCH-23 22.00% K.sub.1 [pN, 20° C.]: 15.1 CCP-3-3 3.00% K.sub.3 [pN, 20° C.]: 16.6 CCP-3-1 7.00% V.sub.0 [20° C., V]: 2.46 PCH-301 7.00% LTS (bulk) [−20° C.] >1000 h

Example 174

(337) TABLE-US-00179 CY-1V-O1V 18.00% Clearing point [° C.]: 80.5 PY-1V2-O2 4.00% Δn [589 nm, 20° C.]: 0.0943 CY-3-O2 15.00% Δε [1 kHz, 20° C.]: −3.6 CCY-3-O2 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 7.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CPY-3-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 112 CCH-34 7.00% K.sub.1 [pN, 20° C.]: 14.2 CC-3-V1 11.00% K.sub.3 [pN, 20° C.]: 18.2 CC-2-V1 11.00% V.sub.0 [20° C., V]: 2.37 CCP-3-1 3.00% CCVC-3-V 9.00%

Example 175

(338) TABLE-US-00180 CY-1V-O1V 18.00% Clearing point [° C.]: 80.5 PY-1V2-O2 3.00% Δn [589 nm, 20° C.]: 0.0946 CY-3-O2 16.00% Δε [1 kHz, 20° C.]: −3.7 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CPY-3-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 113 CC-3-V2 7.00% K.sub.1 [pN, 20° C.]: 14.2 CC-3-V1 11.00% K.sub.3 [pN, 20° C.]: 18.7 CC-2-V1 11.00% V.sub.0 [20° C., V]: 2.39 CCP-3-1 3.00% CCVC-3-V 9.00%

Example 176

(339) TABLE-US-00181 PY-3-O2 11.00% Clearing point [° C.]: 75 PY-V2-O2 6.50% Δn [589 nm, 20° C.]: 0.1105 CCY-3-O2 9.00% Δε [1 kHz, 20° C.]: −3.1 CCY-4-O2 3.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-3-O1 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CPY-2-O2 6.50% γ.sub.1 [mPa .Math. s, 20° C.]: 105 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 13.9 CCH-34 10.00% K.sub.3 [pN, 20° C.]: 14.3 CCH-23 21.00% V.sub.0 [20° C., V]: 2.28 PYP-2-3 6.00% LTS (bulk) [−20° C.] >1000 h CCP-3-1 3.00% PCH-301 9.00%

Example 177

(340) TABLE-US-00182 PY-3-O2 11.00% Clearing point [° C.]: 74 PY-1V2-O2 7.50% Δn [589 nm, 20° C.]: 0.1107 CCY-3-O2 9.00% Δε [1 kHz, 20° C.]: −3.0 CCY-3-O1 5.50% ε.sub.|| [1 kHz, 20° C.]: 3.4 CPY-2-O2 6.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.4 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CCH-34 10.00% K.sub.1 [pN, 20° C.]: 14.0 CCH-23 21.00% K.sub.3 [pN, 20° C.]: 14.8 PYP-2-3 5.50% V.sub.0 [20° C., V]: 2.37 CCP-3-1 4.00% LTS (bulk) [−20° C.] >1000 h PCH-301 10.00%

Example 178

(341) TABLE-US-00183 PY-3-O2 11.00% Clearing point [° C.]: 74 PY-1V2-O2 8.00% Δn [589 nm, 20° C.]: 0.1119 CY-3-O2 3.00% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 9.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-2-O2 6.50% γ.sub.1 [mPa .Math. s, 20° C.]: 108 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 14.3 CCH-34 10.00% K.sub.3 [pN, 20° C.]: 15.0 CCH-23 21.00% V.sub.0 [20° C., V]: 2.26 PYP-2-3 5.00% LTS (bulk) [−20° C.] >1000 h CCP-3-1 4.00% PCH-301 6.50%

Example 179

(342) TABLE-US-00184 CC-3-V 39.00% Clearing point [° C.]: 74.5 CC-3-V1 3.00% Δn [589 nm, 20° C.]: 0.1017 CCP-V-1 8.00% Δε [1 kHz, 20° C.]: 3.2 CCP-V2-1 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 64 PGP-2-2V 3.50% K.sub.1 [pN, 20° C.]: 13 PP-1-2V1 9.00% K.sub.3 [pN, 20° C.]: 15.4 PPGU-3-F 1.00% V.sub.0 [20° C., V]: 2.13 PUQU-3-F 15.50% CCY-3-O2 9.00%

Example 180

(343) TABLE-US-00185 BCH-32 5.00% Clearing point [° C.]: 75.3 CC-3-V 41.50% Δn [589 nm, 20° C.]: 0.0989 CC-3-V1 8.50% Δε [1 kHz, 20° C.]: −1.9 CCH-35 2.00% ε.sub.|| [1 kHz, 20° C.]: 3.2 CCP-3-1 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.0 CCY-3-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 69 CPY-2-O2 5.50% K.sub.1 [pN, 20° C.]: 14.2 CPY-3-O2 12.50% K.sub.3 [pN, 20° C.]: 15.5 PY-3-O2 15.00% V.sub.0 [20° C., V]: 3.02

Example 180a

(344) The mixture according to Example 180 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.3% of RM-1.

Example 181

(345) TABLE-US-00186 CCY-3-O1 8.00% Clearing point [° C.]: 74.9 CCY-4-O2 7.50% Δn [589 nm, 20° C.]: 0.1123 CPY-2-O2 10.00% Δε [1 kHz, 20° C.]: −3.7 CPY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CC-3-V 15.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 PY-1-O4 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 121 PY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 13.2 PY-4-O2 5.00% K.sub.3 [pN, 20° C.]: 15.5 CC-3-V1 9.00% V.sub.0 [20° C., V]: 2.15 CCY-3-O2 6.50% PCH-301 15.00%

Example 181a

(346) The mixture according to Example 181 additionally comprises 0.01% of

(347) ##STR00414##

Example 182

(348) TABLE-US-00187 CY-3-O2 10.00% Clearing point [° C.]: 100 CY-3-O4 20.00% Δn [589 nm, 20° C.]: 0.0865 CY-5-O4 20.00% Δε [1 kHz, 20° C.]: −5.4 CCY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.9 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 9.3 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 347 CCY-5-O2 6.00% K.sub.1 [pN, 20° C.]: 15.6 CH-33 3.00% K.sub.3 [pN, 20° C.]: 16.6 CH-35 3.50% V.sub.0 [20° C., V]: 1.84 CH-43 3.50% CH-45 3.50% CCPC-33 4.00% CCPC-34 4.50% CCPC-35 4.00%

Example 183

(349) TABLE-US-00188 CY-3-O2 15.00% Clearing point [° C.]: 91 CY-5-O2 12.00% Δn [589 nm, 20° C.]: 0.105 CCY-3-O1 4.00% Δε [1 kHz, 20° C.]: −4.5 CCY-3-O2 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 106 CCY-3-O3 4.00% V.sub.0 [20° C., V]: 1.32 CCY-4-O2 4.00% CLY-3-O2 10.00% CLY-3-O3 2.00% CPY-2-O2 8.00% CC-3-V 24.00% PGP-2-5 5.00%

Example 184

(350) TABLE-US-00189 CY-3-O2 14.00% Clearing point [° C.]: 84.7 CY-3-O4 4.00% Δn [589 nm, 20° C.]: 0.1068 CY-5-O2 7.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O1 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 138 CCY-3-O2 5.00% K.sub.1 [pN, 20° C.]: 14.1 CCY-4-O2 8.00% K.sub.3 [pN, 20° C.]: 16.2 CCY-5-O2 3.00% V.sub.0 [20° C., V]: 2.13 CPY-2-O2 9.00% CPY-3-O2 9.00% PYP-2-3 6.00% CC-3-V 22.00% CC-3-V1 3.50% CCP-V-1 5.00% PPGU-3-F 0.50%

Example 185

(351) TABLE-US-00190 CY-3-O2 15.00% Clearing point [° C.]: 80.4 CY-5-O2 12.50% Δn [589 nm, 20° C.]: 0.1038 CCY-3-O1 2.50% Δε [1 kHz, 20° C.]: −3.3 CCY-4-O2 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CPY-3-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 137 CCY-2-1 6.00% K.sub.1 [pN, 20° C.]: 14.2 CCY-3-1 6.00% K.sub.3 [pN, 20° C.]: 14.2 CCH-23 15.00% V.sub.0 [20° C., V]: 2.18 CCH-34 5.00% CCH-301 1.50% BCH-32 15.50%

Example 185a

(352) The mixture according to Example 185 additionally comprises 0.25% of RM-35

(353) ##STR00415##
and
0.025% of

(354) ##STR00416##

Example 186

(355) TABLE-US-00191 CC-3-V 34.00% Clearing point [° C.]: 100 CC-3-V1 2.50% Δn [589 nm, 20° C.]: 0.1003 CCP-V-1 10.00% Δε [1 kHz, 20° C.]: 9.1 PUQU-3-F 7.00% ε.sub.|| [1 kHz, 20° C.]: 12.3 PGUQU-3-F 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.2 CPGU-3-OT 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 99 CCGU-3-F 4.00% K.sub.1 [pN, 20° C.]: 14.2 APUQU-3-F 8.00% K.sub.3 [pN, 20° C.]: 17.3 CCP-3F.F.F 4.50% CCP-30CF.sub.3 4.00% CCP-50CF.sub.3 3.00% CCQU-3-F 10.00% CBC-33 3.00%

Example 186a

(356) The mixture according to Example 186 additionally comprises 0.03% of

(357) ##STR00417##

Example 186b

(358) The mixture according to Example 186 additionally comprises 0.03% of

(359) ##STR00418##

Example 187

(360) TABLE-US-00192 Y-4O-O4 4.50% Clearing point [° C.]: 100 PYP-2-3 2.00% Δn [589 nm, 20° C.]: 0.1716 CC-3-V 25.00% Δε [1 kHz, 20° C.]: −1.5 CC-4-V 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCP-V-1 14.00% ε.sub.⊥ [1 kHz, 20° C.]: 4.9 PTP-302FF 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 114 CPTP-302FF 10.00% K.sub.1 [pN, 20° C.]: 15.2 CPTP-302FF 10.00% K.sub.3 [pN, 20° C.]: 18.5 PPTUI-3-2 14.50% V.sub.0 [20° C., V]: 3.76

Example 188

(361) TABLE-US-00193 CCH-23 25.00% Clearing point [° C.]: 70.3 CC-3-V 4.50% Δn [589 nm, 20° C.]: 0.0737 PCH-53 25.00% Δε [1 kHz, 20° C.]: −1.1 CCY-2-1 12.00% ε.sub.|| [1 kHz, 20° C.]: 2.8 CCY-3-1 12.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.9 CCY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 11.7 CCY-3-O3 5.00% K.sub.3 [pN, 20° C.]: 13.1 CBC-33F 4.50%

Example 189

(362) TABLE-US-00194 CC-3-V1 10.25% Clearing point [° C.]: 74.7 CCH-23 18.50% Δn [589 nm, 20° C.]: 0.1027 CCH-35 6.75% Δε [1 kHz, 20° C.]: −3.1 CCP-3-1 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-1 2.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CCY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CPY-2-O2 6.00% K.sub.1 [pN, 20° C.]: 15.4 CPY-3-O2 9.75% K.sub.3 [pN, 20° C.]: 16.8 CY-3-O2 11.50% V.sub.0 [20° C., V]: 2.46 PP-1-2V1 3.75% PY-3-O2 13.00%

Example 189a

(363) The mixture according to Example 189 additionally comprises 0.01% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.3% of RM-1.

Example 190

(364) TABLE-US-00195 BCH-3F.F 10.00% Clearing point [° C.]: 99.6 BCH-3F.F.F 12.00% Δn [589 nm, 20° C.]: 0.1122 CBC-33 3.00% Δε [1 kHz, 20° C.]: 10.1 CBC-33F 3.00% ε.sub.|| [1 kHz, 20° C.]: 13.8 CCGU-3-F 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.6 CCH-34 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 164 CCH-35 6.50% K.sub.1 [pN, 20° C.]: 11.8 CCP-1F.F.F 10.00% K.sub.3 [pN, 20° C.]: 15.9 CCP-2F.F.F 10.00% V.sub.0 [20° C., V]: 1.14 CCP-3-1 2.50% CCP-3F.F.F 8.00% CPGP-4-3 3.00% CPGP-5-2 2.00% CPGP-5-3 1.00% PUQU-2-F 1.00% PUQU-3-F 10.00%

Example 191

(365) TABLE-US-00196 CBC-53F 3.00% Clearing point [° C.]: 115.5 CC-3-2V1 1.00% Δn [589 nm, 20° C.]: 0.1106 CC-3-V 25.00% Δε [1 kHz, 20° C.]: 7.0 CC-3-V1 5.00% ε.sub.∥ [1 kHz, 20° C.]: 9.9 CCGU-3-F 5.50% ε.sub.⊥ [1 kHz, 20° C.]: 2.9 CCP-30CF.sub.3 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 118 CCP-30CF.sub.3.F 8.00% K.sub.1 [pN, 20° C.]: 17.4 CCP-40CF.sub.3 3.00% K.sub.3 [pN, 20° C.]: 20.4 CCP-50CF.sub.3 3.00% V.sub.0 [20° C., V]: 1.66 CCP-V-1 8.00% CCP-V2-1 12.00% CPGU-3-OT 5.00% PGUQU-3-F 4.00% PGUQU-4-F 4.00% PGUQU-5-F 2.00% PP-1-2V1 3.00% PPGU-3-F 0.50% PUQU-2-F 1.00% PUQU-3-F 3.00%

Example 192

(366) TABLE-US-00197 APUQU-2-F 2.50% Clearing point [° C.]: 85.8 APUQU-3-F 5.00% Δn [589 nm, 20° C.]: 0.1106 PUQU-3-F 10.00% Δε [1 kHz, 20° C.]: 8.6 PGUQU-3-F 5.00% ε.sub.∥ [1 kHz, 20° C.]: 12.6 PGUQU-4-F 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 4.0 PGUQU-5-F 2.00% γ.sub.1 [mPa .Math. s, 20° C.]: 92 DPGU-4-F 4.00% K.sub.1 [pN, 20° C.]: 13.0 PPGU-3-F 0.50% K.sub.3 [pN, 20° C.]: 15.3 CDUQU-3-F 0.05% V.sub.0 [20° C., V]: 1.30 CC-3-V 39.95% CCP-V-1 9.00% CCP-V2-1 8.00% CCP-3-1 2.00% PGP-2-3 3.00% CY-3-O2 5.00% CCY-3-O2 5.00%

Example 193

(367) TABLE-US-00198 APUQU-2-F 2.50% Clearing point [° C.]: 85.8 APUQU-3-F 5.00% Δn [589 nm, 20° C.]: 0.1105 PUQU-3-F 12.50% Δε [1 kHz, 20° C.]: 10.6 PGUQU-3-F 5.00% ε.sub.∥ [1 kHz, 20° C.]: 14.8 PGUQU-4-F 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 4.2 PGUQU-5-F 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 98 DPGU-4-F 4.00% K.sub.1 [pN, 20° C.]: 12.7 PPGU-3-F 0.50% K.sub.3 [pN, 20° C.]: 15.1 CDUQU-3-F 0.05% CC-3-V 34.95% CCP-V-1 7.00% CCP-V2-1 6.00% CCP-3-1 2.50% CCPC-33 2.00% CY-3-O2 5.00% CCY-3-O2 5.00%

Example 194

(368) TABLE-US-00199 APUQU-2-F 3.00% Clearing point [° C.]: 85.7 APUQU-3-F 5.00% Δn [589 nm, 20° C.]: 0.1097 PUQU-3-F 12.00% Δε [1 kHz, 20° C.]: 8.7 PGUQU-3-F 5.00% ε.sub.∥ [1 kHz, 20° C.]: 12.4 PGUQU-4-F 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.7 PGUQU-5-F 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 PPGU-3-F 0.50% K.sub.1 [pN, 20° C.]: 12.9 CDUQU-3-F 0.05% K.sub.3 [pN, 20° C.]: 15.7 CC-3-V 38.95% V.sub.0 [20° C., V]: 1.29 CCP-V-1 10.50% CCP-V2-1 9.00% PGP-2-3 2.00% CCY-3-O2 3.50% CPY-3-O2 3.50%

Example 195

(369) TABLE-US-00200 APUQU-2-F 3.00% Clearing point [° C.]: 85.7 APUQU-3-F 5.00% Δn [589 nm, 20° C.]: 0.1097 PUQU-3-F 12.00% Δε [1 kHz, 20° C.]: 8.7 PGUQU-3-F 5.00% ε.sub.∥ [1 kHz, 20° C.]: 12.4 PGUQU-4-F 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.7 PGUQU-5-F 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 82 PPGU-3-F 0.50% K.sub.1 [pN, 20° C.]: 12.9 CDUQU-3-F 0.05% K.sub.3 [pN, 20° C.]: 15.7 CC-3-V 38.95% V.sub.0 [20° C., V]: 1.29 CCP-V-1 10.50% CCP-V2-1 9.00% PGP-2-3 2.00% CCY-3-O2 3.50% CPY-3-O2 3.50%

Example 196

(370) TABLE-US-00201 CC-3-V 35.00% Clearing point [° C.]: 84.6 CCY-3-O1 9.00% Δn [589 nm, 20° C.]: 0.1010 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −4.0 CCY-4-O2 5.00% ε.sub.∥ [1 kHz, 20° C.]: 3.6 CLY-3-O3 11.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 CPY-2-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 114 CPY-3-O2 4.00% K.sub.1 [pN, 20° C.]: 14.5 CY-3-O2 6.50% PY-3-O2 12.00%

Example 196a

(371) The mixture according to Example 196 additionally comprises 0.04% of

(372) ##STR00419##
and
0.015% of

(373) ##STR00420##

Example 197

(374) TABLE-US-00202 CC-3-V 33.00% Clearing point [° C.]: 84 CCY-3-O1 7.00% Δn [589 nm, 20° C.]: 0.1111 CCY-3-O2 7.00% Δε [1 kHz, 20° C.]: −4.0 CCY-4-O2 5.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CLY-3-O3 11.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 CPY-2-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 119 CPY-3-O2 8.00% K.sub.1 [pN, 20° C.]: 14.8 PP-1-2V1 1.50% PY-1-O4 8.50% PY-3-O2 10.00%

Example 197a

(375) The mixture according to Example 197 additionally comprises 0.04% of

(376) ##STR00421##
and
0.015% of

(377) ##STR00422##

Example 198

(378) TABLE-US-00203 APUQU-2-F 4.00% Clearing point [° C.]: 85.6 APUQU-3-F 7.00% Δn [589 nm, 20° C.]: 0.1021 PUQU-3-F 5.00% Δε [1 kHz, 20° C.]: 6.9 PGUQU-3-F 4.00% ε.sub.∥ [1 kHz, 20° C.]: 10.0 PGUQU-4-F 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.1 PGUQU-5-F 3.00% γ.sub.1 [mPa .Math. s, 20° C.]: 71 CCP-V-1 16.00% K.sub.1 [pN, 20° C.]: 13.1 CC-3-V 40.00% K.sub.3 [pN, 20° C.]: 15.3 CC-3-V1 4.00% V.sub.0 [20° C., V]: 1.45 CC-4-V 3.00% PGP-2-3 4.00% PGP-2-4 1.00% PPGU-3-F 1.00% CCOC-4-3 5.00%

Example 198a

(379) The mixture according to Example 198 additionally comprises 0.25% of RM-41

(380) ##STR00423##

Example 198b

(381) The mixture according to Example 198 additionally comprises 0.3% of RM-17

(382) ##STR00424##

Example 199

(383) TABLE-US-00204 Y-4O-O4 12.00% Clearing point [° C.]: 101 CY-3-O2 14.00% Δn [589 nm, 20° C.]: 0.1504 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −6.2 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 4.5 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 10.7 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 281 CPY-2-O2 2.50% K.sub.1 [pN, 20° C.]: 15.7 PTP-302FF 10.00% K.sub.3 [pN, 20° C.]: 19.9 CPTP-302FF 10.00% V.sub.0 [20° C., V]: 1.90 CPTP-502FF 10.00% CC-4-V 2.50% CCP-V-1 11.50% CCPC-33 4.50%

Example 200

(384) TABLE-US-00205 Y-4O-O4 12.00% Clearing point [° C.]: 100 CCY-3-O1 5.00% Δn [589 nm, 20° C.]: 0.1496 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −4.1 CCY-3-O3 6.00% ε.sub.∥ [1 kHz, 20° C.]: 4.0 CCY-4-O2 2.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.1 CC-4-V 15.00% γ.sub.1 [mPa .Math. s, 20° C.]: 180 CCP-V-1 11.00% K.sub.1 [pN, 20° C.]: 16.1 CCP-V2-1 5.00% K.sub.3 [pN, 20° C.]: 18.5 BCH-32 5.00% V.sub.0 [20° C., V]: 2.25 PTP-302FF 10.00% PTP-502FF 3.00% CPTP-302FF 10.00% CPTP-502FF 10.00%

Example 201

(385) TABLE-US-00206 Y-4O-O4 10.00% Clearing point [° C.]: 100 CCY-3-O1 2.50% Δn [589 nm, 20° C.]: 0.1515 PTP-302FF 10.00% Δε [1 kHz, 20° C.]: −2.1 PTP-502FF 3.50% ε.sub.∥ [1 kHz, 20° C.]: 3.5 CPTP-302FF 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.6 CPTP-502FF 3.50% γ.sub.1 [mPa .Math. s, 20° C.]: 125 CC-4-V 15.00% K.sub.1 [pN, 20° C.]: 16.6 CC-3-V1 8.00% K.sub.3 [pN, 20° C.]: 18.7 CCP-V-1 12.00% V.sub.0 [20° C., V]: 3.13 CCP-V2-1 12.00% BCH-32 5.00% CPTP-3-1 5.00% CPTP-3-2 3.50%

Example 202

(386) TABLE-US-00207 Y-4O-O4 12.00% Clearing point [° C.]: 101 CY-3-O2 6.00% Δn [589 nm, 20° C.]: 0.1218 CY-3-O4 15.00% Δε [1 kHz, 20° C.]: −6.2 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 4.5 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 10.7 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 302 CLY-3-O2 5.00% K.sub.1 [pN, 20° C.]: 15.7 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 18.9 CPY-3-O2 8.00% V.sub.0 [20° C., V]: 1.83 CPTP-302FF 4.00% CPTP-502FF 4.00% CCP-V-1 11.00% CCPC-33 4.50% CCPC-34 4.50%

Example 203

(387) TABLE-US-00208 Y-4O-O4 15.00% Clearing point [° C.]: 101 CCY-3-O2 5.00% Δn [589 nm, 20° C.]: 0.1216 CCY-3-O3 5.00% Δε [1 kHz, 20° C.]: −4.0 CCY-4-O2 5.00% ε.sub.∥ [1 kHz, 20° C.]: 4.0 CLY-3-O2 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.0 CPY-2-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 167 CPY-3-02 8.00% K.sub.1 [pN, 20° C.]: 16.1 CPTP-302FF 5.00% K.sub.3 [pN, 20° C.]: 17.3 CPTP-502FF 5.00% V.sub.0 [20° C., V]: 2.19 CC-4-V 13.50% CCP-V-1 11.50% CCP-V2-1 10.00% BCH-32 5.00%

Example 204

(388) TABLE-US-00209 Y-4O-O4 10.00% Clearing point [° C.]: 100 CCY-3-O2 5.00% Δn [589 nm, 20° C.]: 0.1203 CCY-3-O3 3.50% Δε [1 kHz, 20° C.]: −2.0 CPY-3-O2 5.50% ε.sub.∥ [1 kHz, 20° C.]: 3.4 PTP-302FF 3.50% ε.sub.⊥ [1 kHz, 20° C.]: 5.4 CPTP-302FF 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 117 CPTP-502FF 5.00% K.sub.1 [pN, 20° C.]: 15.6 CCH-301 5.00% K.sub.3 [pN, 20° C.]: 18.5 CC-4-V 15.00% V.sub.0 [20° C., V]: 3.17 CC-3-V1 8.00% CCP-V-1 13.00% CCP-V2-1 13.00% BCH-32 5.00% CPTP-3-1 3.50%

Example 205

(389) TABLE-US-00210 BCH-32 16.00% Clearing point [° C.]: 105 BCH-52 6.50% Δn [589 nm, 20° C.]: 0.1503 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −4.2 CCY-3-O2 8.00% ε.sub.∥ [1 kHz, 20° C.]: 3.8 CCY-3-O3 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.0 CCY-4-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 297 CCY-5-O2 7.00% K.sub.1 [pN, 20° C.]: 18.3 CY-3-O4 13.00% K.sub.3 [pN, 20° C.]: 17.3 PY-3-O2 5.50% V.sub.0 [20° C., V]: 2.13 PY-4-O2 9.00% PYP-2-3 8.00% PYP-2-4 8.00%

Example 205a

(390) The mixture according to Example 205 additionally comprises 0.015% of

(391) ##STR00425##
and
0.015% of

(392) ##STR00426##

Example 206

(393) TABLE-US-00211 CC-3-V 35.50% Clearing point [° C.]: 79.8 CCY-3-O2 6.00% Δn [589 nm, 20° C.]: 0.0962 CCY-3-O3 6.00% Δε [1 kHz, 20° C.]: −3.4 CCY-4-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-5-O2 3.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CPY-2-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 111 CPY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 13.3 CY-3-O4 10.00% K.sub.3 [pN, 20° C.]: 15.2 CY-5-O2 9.00% V.sub.0 [20° C., V]: 2.23 PGIGI-3-F 5.00%

Example 207

(394) TABLE-US-00212 CC-3-V 31.50% Clearing point [° C.]: 79.6 CCP-V-1 5.00% Δn [589 nm, 20° C.]: 0.1044 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −3.4 CCY-3-O3 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-4-O2 5.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CPY-2-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 115 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 13.3 CY-3-O4 7.00% K.sub.3 [pN, 20° C.]: 15.2 CY-5-O2 7.00% V.sub.0 [20° C., V]: 2.24 PGIGI-3-F 5.00% PY-3-O2 7.00%

Example 208

(395) TABLE-US-00213 CC-3-V 36.50% Clearing point [° C.]: 84.9 CCP-V-1 3.00% Δn [589 nm, 20° C.]: 0.1054 CCY-3-O1 6.50% Δε [1 kHz, 20° C.]: −3.5 CCY-3-O2 3.50% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CLY-3-O3 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 108 CPY-2-O2 11.00% K.sub.1 [pN, 20° C.]: 14.4 CPY-3-O2 9.00% K.sub.3 [pN, 20° C.]: 15.7 CY-3-O2 3.00% V.sub.0 [20° C., V]: 2.24 PY-3-O2 13.50%

Example 209

(396) TABLE-US-00214 CC-3-V 39.00% Clearing point [° C.]: 75.2 BCH-3F.F.F 8.00% Δn [589 nm, 20° C.]: 0.1298 PGU-2-F 6.00% Δε [1 kHz, 20° C.]: 18.3 PGU-3-F 6.00% ε.sub.|| [1 kHz, 20° C.]: 22.6 APUQU-2-F 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 4.3 APUQU-3-F 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 99 PGUQU-3-F 6.00% K.sub.1 [pN, 20° C.]: 10.9 PGUQU-4-F 6.00% K.sub.3 [pN, 20° C.]: 11.1 PGUQU-5-F 6.00% V.sub.0 [20° C., V]: 0.81 DPGU-4-F 9.00%

Example 210

(397) TABLE-US-00215 CC-3-V 38.50% Clearing point [° C.]: 74.9 CCY-3-O1 4.50% Δn [589 nm, 20° C.]: 0.1012 CCY-3-O2 4.00% Δε [1 kHz, 20° C.]: −3.7 CCY-4-O2 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CLY-3-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.4 CPY-2-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 94 CPY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 13.4 PY-1-O4 7.50% K.sub.3 [pN, 20° C.]: 14.4 PY-3-O2 6.00% V.sub.0 [20° C., V]: 2.08 Y-4O-O4 4.50% LTS (bulk) [−20° C.] >1000 h

Example 210a

(398) The mixture according to Example 210 additionally comprises 0.25% of

(399) ##STR00427##
and
0.25% of

(400) ##STR00428##

Example 211

(401) TABLE-US-00216 CC-3-V 40.50% Clearing point [° C.]: 74.8 CC-3-V1 5.00% Δn [589 nm, 20° C.]: 0.1073 CCPC-33 3.00% Δε [1 kHz, 20° C.]: −1.9 CCY-3-O2 9.00% ε.sub.|| [1 kHz, 20° C.]: 3.2 CPY-2-O2 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 5.2 CPY-3-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 63 PP-1-2V1 6.00% K.sub.1 [pN, 20° C.]: 12.6 PY-3-O2 7.00% K.sub.3 [pN, 20° C.]: 14.1 PYP-2-3 8.00% V.sub.0 [20° C., V]: 2.86 Y-4O-O4 3.00%

Example 211a

(402) The mixture according to Example 211 additionally comprises 0.04% of

(403) ##STR00429##
and
0.02% of

(404) ##STR00430##

Example 212

(405) TABLE-US-00217 APUQU-2-F 2.50% Clearing point [° C.]: 97.5 APUQU-3-F 7.00% Δn [589 nm, 20° C.]: 0.1000 PGUQU-3-F 4.00% Δε [1 kHz, 20° C.]: 8.0 PGUQU-4-F 4.00% ε.sub.|| [1 kHz, 20° C.]: 11.1 PUQU-3-F 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.1 CCP-V-1 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 93 CCP-V2-1 14.00% K.sub.1 [pN, 20° C.]: 15.3 CCGU-3-F 3.50% K.sub.3 [pN, 20° C.]: 17.6 CCQU-3-F 10.00% V.sub.0 [20° C., V]: 1.45 PCH-302 6.50% CC-3-V 25.00% CC-3-V1 8.00% CCP-30CF.sub.3 5.00% PPGU-3-F 0.50%

Example 212a

(406) The mixture according to Example 212 additionally comprises 0.25% of

(407) ##STR00431##

Example 213

(408) TABLE-US-00218 CY-3-O2 18.50% Clearing point [° C.]: 80 CCY-3-O2 11.00% Δn [589 nm, 20° C.]: 0.0896 CCY-4-O2 9.00% Δε [1 kHz, 20° C.]: −3.4 CPY-2-O2 7.50% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-3-O2 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CCH-34 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 117 CCH-35 9.00% K.sub.1 [pN, 20° C.]: 14.4 CC-3-V 10.00% K.sub.3 [pN, 20° C.]: 15.1 CCH-301 9.00% V.sub.0 [20° C., V]: 2.23 CCH-303 5.00% PYP-2-3 3.00%

Example 213a

(409) The mixture according to Example 213 additionally comprises 0.2% of

(410) ##STR00432##

Example 214

(411) TABLE-US-00219 CY-3-O2 10.50% Clearing point [° C.]: 79.7 PY-1-O4 5.00% Δn [589 nm, 20° C.]: 0.1113 PY-3-O2 7.50% Δε [1 kHz, 20° C.]: −4.4 PY-4-O2 4.00% K.sub.1 [pN, 20° C.]: 14.5 CCY-3-O1 5.50% K.sub.3 [pN, 20° C.]: 16.7 CCY-3-O2 5.00% V.sub.0 [20° C., V]: 2.05 CCY-4-O2 4.00% CLY-3-O2 9.00% CPY-2-O2 9.00% CPY-3-O2 9.00% CC-3-V 23.50% CC-3-V1 7.00% CBC-33F 1.00%

Example 215

(412) TABLE-US-00220 APUQU-3-F 3.00% Clearing point [° C.]: 90.5 CC-3-V1 7.75% Δn [589 nm, 20° C.]: 0.1057 CC-4-V 10.00% Δε [1 kHz, 20° C.]: 7.4 CC-5-V 9.25% γ.sub.1 [mPa .Math. s, 20° C.]: 91 CCGU-3-F 7.00% K.sub.1 [pN, 20° C.]: 13.6 CCH-34 3.00% K.sub.3 [pN, 20° C.]: 15.5 CCP-30CF.sub.3 2.50% V.sub.0 [20° C., V]: 1.43 CCP-V-1 14.00% CCP-V2-1 9.50% PCH-301 11.00% PGP-2-2V 2.00% PGUQU-3-F 5.00% PPGU-3-F 0.50% PUQU-3-F 12.00% APUQU-2-F 3.50%

Example 216

(413) TABLE-US-00221 CC-3-V 27.00% Clearing point [° C.]: 74.9 CCY-3-1 9.50% Δn [589 nm, 20° C.]: 0.1093 CCP-3-1 8.00% Δε [1 kHz, 20° C.]: −3.8 CLY-3-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CPY-2-O2 10.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CPY-3-O2 10.50% γ.sub.1 [mPa .Math. s, 20° C.]: 108 CY-3-O2 15.00% K.sub.1 [pN, 20° C.]: 14.1 PY-3-O2 13.50% K.sub.3 [pN, 20° C.]: 15.8 V.sub.0 [20° C., V]: 2.16

Example 217

(414) TABLE-US-00222 CC-3-V 16.00% Clearing point [° C.]: 85.4 CC-3-V1 5.00% Δn [589 nm, 20° C.]: 0.1060 CCH-34 7.00% Δε [1 kHz, 20° C.]: −3.7 CCP-3-1 1.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-3-O1 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.4 CCY-3-O2 7.50% γ.sub.1 [mPa .Math. s, 20° C.]: 114 CCY-3-O3 2.00% K.sub.1 [pN, 20° C.]: 13.4 CCY-4-O2 5.00% K.sub.3 [pN, 20° C.]: 14.5 CPY-2-O2 10.00% V.sub.0 [20° C., V]: 2.09 CPY-3-O2 9.00% CY-3-O2 10.00% CY-3-O4 6.50% CY-5-O4 6.00% PYP-2-3 5.50% PYP-2-4 3.50%

Example 217a

(415) The mixture according to Example 217 additionally comprises 0.04% of

(416) ##STR00433##

Example 218

(417) TABLE-US-00223 CCH-23 12.00% Clearing point [° C.]: 110.7 CCH-34 10.00% Δn [589 nm, 20° C.]: 0.1002 CCP-3-1 7.00% Δε [1 kHz, 20° C.]: −2.9 CCY-3-1 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.2 CCY-3-O1 1.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.1 CCY-3-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 147 CCY-3-O3 7.50% K.sub.1 [pN, 20° C.]: 17.3 CCY-4-O2 9.00% K.sub.3 [pN, 20° C.]: 18.3 CPGP-4-3 2.00% V.sub.0 [20° C., V]: 2.65 CPY-2-O2 8.00% CPY-3-O2 8.00% CY-3-O2 1.50% CY-3-O4 3.00% PCH-301 10.00% PYP-2-3 1.50%

Example 218a

(418) The mixture according to Example 218 additionally comprises 0.04% of

(419) ##STR00434##

Example 219

(420) TABLE-US-00224 BCH-32 1.50% Clearing point [° C.]: 74.3 CC-3-V 19.50% Δn [589 nm, 20° C.]: 0.1089 CC-3-V1 5.50% Δε [1 kHz, 20° C.]: −3.8 CCP-3-1 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCP-3-3 4.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CLY-3-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 115 CPY-2-O2 10.50% K.sub.1 [pN, 20° C.]: 13.7 CPY-3-O2 10.50% K.sub.3 [pN, 20° C.]: 16.1 CY-3-O2 15.00% V.sub.0 [20° C., V]: 2.18 CY-5-O2 9.00% PY-3-O2 10.00%

Example 220

(421) TABLE-US-00225 CY-3-O2 15.00% Clearing point [° C.]: 74.7 CY-5-O2 6.50% Δn [589 nm, 20° C.]: 0.1082 CCY-3-O2 11.00% Δε [1 kHz, 20° C.]: −3.0 CPY-2-O2 5.50% ε.sub.|| [1 kHz, 20° C.]: 3.6 CPY-3-O2 10.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CC-3-V 28.50% γ.sub.1 [mPa .Math. s, 20° C.]: 97 CC-3-V1 10.00% K.sub.1 [pN, 20° C.]: 12.9 PYP-2-3 12.50% K.sub.3 [pN, 20° C.]: 15.7 PPGU-3-F 0.50% V.sub.0 [20° C., V]: 2.42

Example 221

(422) TABLE-US-00226 PGUQU-3-F 5.00% Clearing point [° C.]: 84.8 CCQU-3-F 8.00% Δn [589 nm, 20° C.]: 0.1035 CCQU-5-F 4.00% Δε [1 kHz, 20° C.]: 10.1 PUQU-3-F 13.50% ε.sub.|| [1 kHz, 20° C.]: 13.5 APUQU-2-F 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.4 APUQU-3-F 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 86 CC-3-V 25.50% K.sub.1 [pN, 20° C.]: 12.3 CC-3-V1 6.00% K.sub.3 [pN, 20° C.]: 15.0 CCP-V-1 13.00% V.sub.0 [20° C., V]: 1.17 CCP-V2-1 6.00% PPGU-3-F 0.50% BCH-3F.F 7.50% BCH-2F.F 2.00%

Example 221a

(423) The mixture according to Example 221 additionally comprises 0.25% of

(424) ##STR00435##

Example 222

(425) TABLE-US-00227 CY-3-O2 12.00% Clearing point [° C.]: 85.4 CY-5-O2 12.00% Δn [589 nm, 20° C.]: 0.1039 CCY-3-O3 5.00% CCY-4-O2 5.00% CPY-2-O2 10.00% CPY-3-O2 10.00% CCY-2-1 4.00% CC-3-V 16.00% CCH-23 10.00% CCH-34 4.00% CCP-V-1 4.00% PGP-2-5 2.00% CPGP-5-2 3.00% CPGP-5-3 3.00%

Example 223

(426) TABLE-US-00228 CC-3-V 41.50% Clearing point [° C.]: 74.5 CCY-3-O1 2.50% Δn [589 nm, 20° C.]: 0.0984 CCY-3-O2 11.50% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O3 5.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CPY-2-O2 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CPY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 89 CY-3-O2 9.50% K.sub.1 [pN, 20° C.]: 13.2 PY-3-O2 7.00% K.sub.3 [pN, 20° C.]: 15.2 PY-4-O2 3.00% V.sub.0 [20° C., V]: 2.29 PYP-2-3 3.00%

Example 223a

(427) The mixture according to Example 223 additionally comprises 0.001% of Irganox® 1076 (octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, BASF) and 0.4% of

(428) ##STR00436##

Example 224

(429) TABLE-US-00229 CC-3-V 30.50% Clearing point [° C.]: 80.1 CC-3-V1 4.50% Δn [589 nm, 20° C.]: 0.1033 CCY-3-O1 6.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 8.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CLY-3-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.6 CPY-2-O2 8.00% γ.sub.1 [mPa .Math. s, 20° C.]: 113 CPY-3-O2 12.00% K.sub.1 [pN, 20° C.]: 14.4 CY-3-O2 15.00% K.sub.3 [pN, 20° C.]: 17.0 PY-3-O2 8.00% V.sub.0 [20° C., V]: 2.16

Example 225

(430) TABLE-US-00230 CC-3-V 41.50% Clearing point [° C.]: 74.5 CCY-3-O1 2.50% Δε [1 kHz, 20° C.]: −3.3 CCY-3-O2 11.50% K.sub.1 [pN, 20° C.]: 13.2 CCY-3-O3 5.00% K.sub.3 [pN, 20° C.]: 15.2 CPY-2-O2 5.00% V.sub.0 [20° C., V]: 2.29 CPY-3-O2 12.00% CY-3-O2 9.50% PY-3-O2 7.00% PY-4-O2 3.00% PYP-2-3 3.00%

Example 226

(431) TABLE-US-00231 CC-3-V 26.00% Clearing point [° C.]: 80.5 CCY-3-O2 6.00% Δn [589 nm, 20° C.]: 0.1040 CCY-3-O3 6.00% Δε [1 kHz, 20° C.]: −4.0 CCY-4-O2 6.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-5-O2 6.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CPY-2-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 133 CPY-3-O2 6.00% K.sub.1 [pN, 20° C.]: 13.6 PYP-2-3 7.00% K.sub.3 [pN, 20° C.]: 15.4 CY-3-O2 15.00% V.sub.0 [20° C., V]: 2.07 CY-5-O2 12.00% LTS (bulk) [−20° C.] >1000 h BCH-32 4.00%

Example 226a

(432) The mixture according to Example 226 additionally comprises 0.3% of

(433) ##STR00437##

Example 227

(434) TABLE-US-00232 CC-3-V 26.50% Clearing point [° C.]: 84.6 CC-3-V1 2.00% Δn [589 nm, 20° C.]: 0.1076 CCH-34 2.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-3-O3 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CCY-4-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 129 CPY-2-O2 10.00% K.sub.1 [pN, 20° C.]: 13.9 CPY-3-O2 10.00% K.sub.3 [pN, 20° C.]: 15.4 CY-3-O2 10.50% V.sub.0 [20° C., V]: 2.06 PYP-2-3 9.00% Y-4O-O4 5.00%

Example 227a

(435) The mixture according to Example 227 additionally comprises 0.04% of

(436) ##STR00438##
and
0.015% of

(437) ##STR00439##

Example 228

(438) TABLE-US-00233 APUQU-3-F 1.50% Clearing point [° C.]: 110.1 CC-3-V 34.00% Δn [589 nm, 20° C.]: 0.1208 CC-3-V1 5.00% Δε [1 kHz, 20° C.]: 6.2 CCP-30CF.sub.3 4.50% ε.sub.|| [1 kHz, 20° C.]: 9.2 CCP-V-1 10.50% ε.sub.⊥ [1 kHz, 20° C.]: 3.0 CCP-V2-1 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CCVC-3-V 3.50% K.sub.1 [pN, 20° C.]: 16.3 CPGP-5-2 4.50% K.sub.3 [pN, 20° C.]: 18.9 CPGP-5-3 4.50% V.sub.0 [20° C., V]: 1.70 DGUQU-4-F 3.00% PGP-2-3 4.00% PGP-2-4 2.00% PGUQU-3-F 5.00% PGUQU-4-F 3.50% PGUQU-5-F 3.00% PPGU-3-F 0.50% PUQU-3-F 5.00%

Example 229

(439) TABLE-US-00234 APUQU-3-F 1.50% Clearing point [° C.]: 110 CC-3-V 35.50% Δn [589 nm, 20° C.]: 0.1257 CCP-30CF.sub.3 4.00% Δε [1 kHz, 20° C.]: 6.3 CCP-V-1 12.00% ε.sub.|| [1 kHz, 20° C.]: 9.3 CCP-V2-1 4.50% ε.sub.⊥ [1 kHz, 20° C.]: 3.0 CCVC-3-V 4.00% γ.sub.1 [mPa .Math. s, 20° C.]: 104 CPGP-5-2 5.00% K.sub.1 [pN, 20° C.]: 16.1 CPGP-5-3 5.00% K.sub.3 [pN, 20° C.]: 18.7 DGUQU-4-F 3.00% V.sub.0 [20° C., V]: 1.69 PGP-2-3 4.00% PGP-2-4 2.00% PGUQU-3-F 5.00% PGUQU-4-F 3.50% PGUQU-5-F 3.00% PPGU-3-F 0.50% PUQU-3-F 5.00% PP-1-2V1 2.50%

Example 230

(440) TABLE-US-00235 CY-3-O2 5.00% Clearing point [° C.]: 102 CY-3-O4 15.00% Δn [589 nm, 20° C.]: 0.2503 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O3 6.00% ε.sub.|| [1 kHz, 20° C.]: 4.3 CPY-2-O2 3.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.3 PTP-102 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 392 PPTUI-3-2 15.00% K.sub.1 [pN, 20° C.]: 19.5 PPTUI-3-4 11.00% K.sub.3 [pN, 20° C.]: 24.0 PTP-302FF 12.00% V.sub.0 [20° C., V]: 2.57 PTP-502FF 12.00% CPTP-302FF 5.00% CPTP-502FF 5.00%

Example 231

(441) TABLE-US-00236 CC-3-V 35.00% Clearing point [° C.]: 79.6 CCP-3-1 7.50% Δn [589 nm, 20° C.]: 0.1095 CCPC-33 2.00% Δε [1 kHz, 20° C.]: −2.6 CCY-3-O2 7.00% ε.sub.|| [1 kHz, 20° C.]: 3.5 CCY-4-O2 7.50% ε.sub.⊥ [1 kHz, 20° C.]: 6.1 CPY-2-O2 8.50% γ.sub.1 [mPa .Math. s, 20° C.]: 92 CPY-3-O2 9.00% K.sub.1 [pN, 20° C.]: 14.5 PP-1-2V1 5.50% PY-3-O2 8.00% PYP-2-3 5.00% Y-4O-O4 5.00%

Example 231a

(442) The mixture according to Example 231 additionally comprises 0.04% of

(443) ##STR00440##
and
0.02% of

(444) ##STR00441##

Example 232

(445) TABLE-US-00237 CY-3-O4 25.00% Clearing point [° C.]: 81.2 CY-5-O2 9.00% Δn [589 nm, 20° C.]: 0.1531 CCY-3-O2 7.00% Δε [1 kHz, 20° C.]: −5.0 CCY-3-O3 4.50% ε.sub.|| [1 kHz, 20° C.]: 4.1 CPY-2-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 9.1 CPY-3-O2 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 298 PYP-2-3 14.00% K.sub.1 [pN, 20° C.]: 13.1 PYP-2-4 10.00% K.sub.3 [pN, 20° C.]: 15.9 CCP-V-1 3.00% V.sub.0 [20° C., V]: 1.89 BCH-32 2.00% PP-1-2V1 3.50% PGP-2-3 2.00%

Example 232a

(446) The mixture according to Example 232 additionally comprises 10% of

(447) ##STR00442##

Example 233

(448) TABLE-US-00238 CC-3-V 29.00% Clearing point [° C.]: 80.1 CCY-3-O1 8.00% Δn [589 nm, 20° C.]: 0.1033 CCY-3-O2 6.00% Δε [1 kHz, 20° C.]: −4.5 CCY-4-O2 2.00% ε.sub.|| [1 kHz, 20° C.]: 4.0 CLY-3-O2 8.50% ε.sub.⊥ [1 kHz, 20° C.]: 8.4 CLY-3-O3 7.50% γ.sub.1 [mPa .Math. s, 20° C.]: 98 CPY-2-O2 10.00% K.sub.1 [pN, 20° C.]: 13.2 CPY-3-O2 7.50% K.sub.3 [pN, 20° C.]: 14.6 CY-3-O2 6.50% V.sub.0 [20° C., V]: 1.91 PY-3-O2 10.00% Y-4O-O4 5.00%

Example 233a

(449) The mixture according to Example 233 additionally comprises 0.04% of

(450) ##STR00443##
and
0.02% of

(451) ##STR00444##

Example 234

(452) TABLE-US-00239 CC-3-V 34.00% Clearing point [° C.]: 79.7 CCPC-33 1.00% Δn [589 nm, 20° C.]: 0.1095 CCY-3-1 4.00% Δε [1 kHz, 20° C.]: −3.5 CCY-3-O2 10.00% ε.sub.|| [1 kHz, 20° C.]: 3.7 CCY-4-O2 9.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CPY-2-O2 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 105 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 14.0 PP-1-2V1 1.50% PY-3-O2 10.00% PYP-2-3 6.00% Y-4O-O4 5.00%

Example 234a

(453) The mixture according to Example 234 additionally comprises 0.04% of

(454) ##STR00445##
and
0.02% of

(455) ##STR00446##

Example 235

(456) TABLE-US-00240 CC-3-V 19.00% Clearing point [° C.]: 80.2 CCY-3-O1 5.00% Δn [589 nm, 20° C.]: 0.1104 CCY-3-O2 7.00% Δε [1 kHz, 20° C.]: −3.7 CCY-3-O3 12.00% ε.sub.|| [1 kHz, 20° C.]: 3.6 CCY-4-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CPY-2-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 143 CPY-3-O2 10.00% K.sub.1 [pN, 20° C.]: 12.9 CY-3-O2 12.00% K.sub.3 [pN, 20° C.]: 14.5 CY-3-O4 3.50% V.sub.0 [20° C., V]: 2.09 PP-1-3 7.00% PP-1-4 7.00%

Example 236

(457) TABLE-US-00241 CY-3-O2 15.00% Clearing point [° C.]: 79.1 CY-5-O2 9.50% Δn [589 nm, 20° C.]: 0.0944 CCY-3-O1 4.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-3-O3 4.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 120 CCY-5-O2 4.00% K.sub.1 [pN, 20° C.]: 13.4 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 15.4 CPY-3-O2 9.00% V.sub.0 [20° C., V]: 2.06 PYP-2-4 2.00% CC-3-V 32.00%

Example 236a

(458) The mixture according to Example 236 additionally comprises 0.015% of

(459) ##STR00447##

Example 237

(460) TABLE-US-00242 CY-3-O2 15.00% Clearing point [° C.]: 79.1 CY-5-O2 9.50% Δn [589 nm, 20° C.]: 0.0944 CCY-3-O1 4.00% Δε [1 kHz, 20° C.]: −4.0 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-3-O3 4.50% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CCY-4-O2 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 120 CCY-5-O2 4.00% K.sub.1 [pN, 20° C.]: 13.4 CPY-2-O2 8.00% K.sub.3 [pN, 20° C.]: 15.4 CPY-3-O2 9.00% V.sub.0 [20° C., V]: 2.06 PYP-2-4 2.00% CC-3-V 32.00%

Example 237a

(461) The mixture according to Example 237 additionally comprises 0.015% of

(462) ##STR00448##

Example 238

(463) TABLE-US-00243 APUQU-3-F 4.00% Clearing point [° C.]: 85.7 CC-3-V 41.00% Δn [589 nm, 20° C.]: 0.1004 CC-3-V1 6.50% Δε [1 kHz, 20° C.]: 6.8 CCP-V-1 12.00% ε.sub.∥ [1 kHz, 20° C.]: 9.8 CCP-V2-1 11.00% ε.sub.⊥ [1 kHz, 20° C.]: 3.0 CPGP-5-3 2.50% γ.sub.1 [mPa .Math. s, 20° C.]: 69 PGUQU-3-F 5.00% K.sub.1 [pN, 20° C.]: 13.0 PGUQU-4-F 4.00% K.sub.3 [pN, 20° C.]: 16.6 PGUQU-5-F 3.50% V.sub.0 [20° C., V]: 1.47 PUQU-3-F 10.50%

Example 239

(464) TABLE-US-00244 CC-3-V 32.50% Clearing point [° C.]: 74.7 CC-3-V1 1.50% Δn [589 nm, 20° C.]: 0.1090 CCY-3-O1 8.50% Δε [1 kHz, 20° C.]: −3.8 CCY-3-O2 5.50% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CLY-3-O2 10.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CPY-3-O2 9.50% γ.sub.1 [mPa .Math. s, 20° C.]: 102 PY-3-O2 10.50% K.sub.1 [pN, 20° C.]: 13.8 CY-3-O2 14.00% K.sub.3 [pN, 20° C.]: 15.7 PYP-2-3 8.00% V.sub.0 [20° C., V]: 2.15

Example 240

(465) TABLE-US-00245 CC-3-V 33.00% Clearing point [° C.]: 80.2 CCY-3-O1 6.00% Δn [589 nm, 20° C.]: 0.1116 CCY-3-O2 8.00% Δε [1 kHz, 20° C.]: −4.1 CCY-4-O2 2.50% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CPY-2-O2 8.00% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CPY-3-O2 12.00% γ.sub.1 [mPa .Math. s, 20° C.]: 119 CLY-3-O2 8.00% K.sub.1 [pN, 20° C.]: 14.5 PY-1-O4 1.50% K.sub.3 [pN, 20° C.]: 16.1 PY-3-O2 10.00% V.sub.0 [20° C., V]: 2.09 PY-4-O2 8.00% CY-3-O2 3.00%

Example 240a

(466) The mixture according to Example 240 additionally comprises 0.008% of

(467) ##STR00449##

Example 241

(468) TABLE-US-00246 BCH-3F.F 5.00% Clearing point [° C.]: 101 BCH-3F.F.F 8.50% Δn [589 nm, 20° C.]: 0.0925 CC-3-V1 10.00% Δε [1 kHz, 20° C.]: 5.3 CC-4-V 12.50% ε.sub.∥ [1 kHz, 20° C.]: 8.3 CCG-V-F 9.00% γ.sub.1 [mPa .Math. s, 20° C.]: 119 CCP-2F.F.F 3.50% K.sub.1 [pN, 20° C.]: 14.2 CCP-3-1 4.50% K.sub.3 [pN, 20° C.]: 19.9 CCP-3F.F.F 10.00% V.sub.0 [20° C., V]: 1.73 CCP-V-1 12.00% CCP-V2-1 7.00% ECCP-5F.F 13.00% PUQU-3-F 5.00%

Example 242

(469) TABLE-US-00247 APUQU-2-F 4.00% Clearing point [° C.]: 86.4 APUQU-3-F 6.00% Δn [589 nm, 20° C.]: 0.1030 PUQU-3-F 10.00% Δε [1 kHz, 20° C.]: 7.0 CCQU-3-F 2.00% ε.sub.∥ [1 kHz, 20° C.]: 10.1 CCP-V-1 13.00% γ.sub.1 [mPa .Math. s, 20° C.]: 71 CCP-V2-1 7.00% K.sub.1 [pN, 20° C.]: 13.2 PGUQU-3-F 6.00% K.sub.3 [pN, 20° C.]: 15.8 CC-3-V 40.00% V.sub.0 [20° C., V]: 1.45 CC-3-V1 5.50% PGP-2-3 3.00% CPGP-5-2 3.00% PPGU-3-F 0.50%

Example 242a

(470) The mixture according to Example 242 additionally comprises 0.25% of RM-41

(471) ##STR00450##

Example 243

(472) TABLE-US-00248 Y-4O-O4 9.00% Clearing point [° C.]: 96 CY-3-O4 12.00% Δn [589 nm, 20° C.]: 0.0796 CCY-3-O1 5.00% Δε [1 kHz, 20° C.]: −2.3 CCY-3-O2 5.50% ε.sub.∥ [1 kHz, 20° C.]: 3.4 CCY-3-O3 5.50% ε.sub.⊥[1 kHz, 20° C.]: 5.7 CC-4-V 15.00% K.sub.1 [pN, 20° C.]: 14.8 CC-5-V 5.50% K.sub.3 [pN, 20° C.]: 16.6 CC-3-V1 6.50% V.sub.0 [20° C., V]: 2.85 CCP-V-1 11.00% CCP-V2-1 10.00% CH-33 3.00% CH-35 3.00% CCPC-33 4.50% CCPC-34 4.50%

Example 244

(473) TABLE-US-00249 Y-4O-O4 11.50% Clearing point [° C.]: 95 CCY-3-O1 4.00% Δn [589 nm, 20° C.]: 0.1697 CCY-3-O2 5.00% Δε [1 kHz, 20° C.]: −4.4 CCY-3-O3 2.50% ε.sub.∥ [1 kHz, 20° C.]: 4.1 CPY-3-O2 4.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.5 CC-4-V 10.00% γ.sub.1 [mPa .Math. s, 20° C.]: 193 CCP-V-1 6.00% K.sub.1 [pN, 20° C.]: 16.8 CCP-V2-1 12.00% K.sub.3 [pN, 20° C.]: 19.5 BCH-32 5.00% V.sub.0 [20° C., V]: 2.23 PTP-302FF 12.00% PTP-502FF 12.00% CPTP-302FF 8.00% CPTP-502FF 8.00%

Example 245

(474) TABLE-US-00250 CY-3-O2 10.00% Clearing point [° C.]: 80.7 PY-1-O4 5.00% Δn [589 nm, 20° C.]: 0.1123 PY-3-O2 6.50% Δε [1 kHz, 20° C.]: −4.2 PY-4-O2 3.00% ε.sub.∥ [1 kHz, 20° C.]: 3.8 CCY-3-O1 5.00% ε.sub.⊥ [1 kHz, 20° C.]: 8.0 CCY-3-O2 5.00% γ.sub.1 [mPa .Math. s, 20° C.]: 150 CCY-4-O2 3.00% K.sub.1 [pN, 20° C.]: 14.6 CLY-3-O2 8.00% K.sub.3 [pN, 20° C.]: 15.2 CPY-2-O2 10.00% V.sub.0 [20° C., V]: 2.01 CPY-3-O2 10.00% CCH-301 8.50% CCH-23 12.00% CCH-34 4.50% CCH-35 3.00% BCH-32 6.50%

Example 246

(475) TABLE-US-00251 PCH-3N.F.F 7.00% Clearing point [° C.]: 91 CP-1V-N 18.00% Δn [589 nm, 20° C.]: 0.2003 CP-V2-N 16.00% Δε [1 kHz, 20° C.]: 10.3 CC-4-V 12.00% ε.sub.∥ [1 kHz, 20° C.]: 14.3 CCP-V-1 9.00% ε.sub.⊥ [1 kHz, 20° C.]: 4.0 PPTUI-3-2 18.00% PPTUI-3-4 20.00%

Example 247

(476) TABLE-US-00252 BCH-32 8.00% Clearing point [° C.]: 96 CC-3-V 24.50% Δn [589 nm, 20° C.]: 0.1195 CCP-V-1 8.00% Δε [1 kHz, 20° C.]: −2.7 CCY-2-1 2.00% ε.sub.∥ [1 kHz, 20° C.]: 3.3 CCY-3-O1 6.00% CCY-3-O3 2.00% CLY-3-O2 5.00% CLY-3-O3 5.00% CPY-2-O2 6.50% CPY-3-O2 6.00% CY-3-O2 6.00% CY-3-O4 3.00% CY-5-O2 5.00% PYP-2-3 6.50% PYP-2-4 6.50%

Example 247a

(477) The mixture according to Example 247 additionally comprises 0.03% of

(478) ##STR00451##
and
0.4% of

(479) ##STR00452##

Example 248

(480) TABLE-US-00253 BCH-32 2.00% Clearing point [° C.]: 80 CC-3-V 31.00% Δn [589 nm, 20° C.]: 0.1083 CCY-3-O1 4.50% Δε [1 kHz, 20° C.]: −3.9 CCY-3-O2 6.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CCY-4-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 120 CLY-3-O2 8.00% K.sub.1 [pN, 20° C.]: 12.7 CPY-2-O2 7.50% K.sub.3 [pN, 20° C.]: 15.1 CPY-3-O2 10.00% V.sub.0 [20° C., V]: 2.07 CY-3-O2 6.25% PY-3-O2 5.75% PY-1-O4 6.00% PY-4-O2 6.00%

Example 248a

(481) The mixture according to Example 248 additionally comprises 0.005% of

(482) ##STR00453##

Example 249

(483) TABLE-US-00254 CC-3-V 37.00% Clearing point [° C.]: 75.2 CCY-3-O1 5.00% Δn [589 nm, 20° C.]: 0.1016 CCY-3-O2 5.00% Δε [1 kHz, 20° C.]: −3.7 CCY-4-O2 4.00% ε.sub.∥ [1 kHz, 20° C.]: 3.7 CLY-3-O2 7.00% γ.sub.1 [mPa .Math. s, 20° C.]: 99 CPY-2-O2 9.00% V.sub.0 [20° C., V]: 2.13 CPY-3-O2 10.00% CY-3-O2 11.50% PY-3-O2 11.50%

Example 249a

(484) The mixture according to Example 249 additionally comprises 0.015% of

(485) ##STR00454##

Example 249b

(486) The mixture according to Example 249 additionally comprises 0.005% of

(487) ##STR00455##

Example 250

(488) TABLE-US-00255 PUQU-3-F 8.00% Clearing point [° C.]: 96.3 APUQU-2-F 6.00% Δn [589 nm, 20° C.]: 0.0994 APUQU-3-F 6.00% Δε [1 kHz, 20° C.]: 9.6 CDUQU-3-F 6.00% γ.sub.1 [mPa .Math. s, 20° C.]: 87 DPGU-4-F 6.00% K.sub.1 [pN, 20° C.]: 14.5 CCGU-3-F 4.00% K.sub.3 [pN, 20° C.]: 16.6 CC-3-V 36.00% V.sub.0 [20° C., V]: 1.29 CC-3-V1 8.00% CCP-V-1 12.00% CCP-V2-1 6.00% CBC-33F 1.50% PPGU-3-F 0.50%