LIQUID-CRYSTAL MEDIUM

Abstract

The present invention relates to liquid-crystal (LC) media as defined in claim 1, having negative dielectric anisotropy and to the use thereof for optical, electro-optical and electronic purposes, in particular in LC displays.

Claims

1. A liquid crystal medium comprising a) one or more compounds of the formula I ##STR00368## in which Ar denotes a methylene group or an aromatic hydrocarbon group having 6 to 40 C atoms or a heteroaromatic hydrocarbon group having 4 to 40 C atoms; Sp denotes a spacer group; R.sup.S denotes H, alkyl having 1 to 12 C atoms or alkenyl having 2 to 12 C atoms; Z.sup.S denotes —O—, —C(O)O—, —(CH.sub.2).sub.z— or —(CH.sub.2).sub.zO—, or a single bond; HA denotes ##STR00369## R.sup.H denotes H, O.sup.•, CH.sub.3, OH or OR.sup.S; R.sup.S1, R.sup.S2, R.sup.S3 and R.sup.S4, identically or differently, denote alkyl having 1 to 6 C atoms; G denotes H or R.sup.S or a group Z.sup.S-HA; z is an integer from 1 to 6, and q is 2, 3 or 4; and b) one or more compounds selected from the group of compounds of the formulae IIA, IIB, IIC, and c) in addition, one or more compounds of the formula IID: ##STR00370## in which R.sup.2A, R.sup.2B, R.sup.2C and R.sup.2D each, independently of one another, denote H, an alkyl or alkenyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF.sub.3 or at least monosubstituted by halogen, where one or more CH.sub.2 groups in these radicals may each be replaced by —O—, —S—, ##STR00371##  —C≡C—, —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; L.sup.1 and L.sup.2 each, independently of one another, denote F, Cl, CF.sub.3 or CHF.sub.2; Y denotes H, F, Cl, CF.sub.3, CHF.sub.2, or CH.sub.3; Z.sup.2, Z.sup.2B and Z.sup.2D each, independently of one another, denote a single bond, —CH.sub.2CH.sub.2—, —CH═CH—, —CF.sub.2O—, —OCF.sub.2—, —CH.sub.2O—, —OCH.sub.2—, —COO—, —OCO—, —C.sub.2F.sub.4—, —CF═CF—, or —CH═CHCH.sub.2O—; (O) denotes O or a single bond; p denotes 0, 1 or 2; q denotes 0 or 1; and v denotes 1, 2, 3, 4, 5, or 6; wherein (i) the one or more compounds of formula IID includes at least one compound of the formula IID-10 or (ii) the medium further comprises at least one compound of the formula CL: ##STR00372## in which R.sup.2D and (O) have the meanings defined for formula IID, and alkyl denotes n-alkyl having 1 to 5 C atoms, R.sup.L denotes H, a straight chain or branched alkyl or alkoxy radical having 1 to 15 C atoms, or a straight chain or branched alkenyl radical having 2 to 15 C atoms, where one or more CH.sub.2 groups in these radicals may each be replaced, independently of one another, by ##STR00373##  —C≡C—, —CF.sub.2O—, —OCF.sub.2—, —CH═CH—, —O—, —CO—O—, or —O—CO— in such a way that O atoms are not linked directly to one another, and in which, in addition, one or more H atoms may each be replaced by halogen, X.sup.L denotes F, Cl, CN, CHF.sub.2, CF.sub.3, OCF.sub.3, or, identically or differently, has one of the meanings of R.sup.L, and Y.sup.L denotes H, F, Cl or CH.sub.3.

2. The liquid crystal medium according to claim 1, wherein the total concentration of the one or more compounds of the formula I is in the range of from 1000 ppm to 5000 ppm.

3. The liquid crystal medium according to claim 1, wherein the medium comprises one or more compounds of formula I selected from the compounds of the formulae I-1, 1-2 and I-3: ##STR00374## in which R.sup.H has the meanings given in claim 1, Sp on each occurrence, identically or differently, denotes a spacer group, and W denotes linear or branched, optionally unsaturated alkylene having 1 to 12 C atoms, in which one or more non-adjacent —CH.sub.2— groups may each be replaced with —O—.

4. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of the formula ST-3 ##STR00375## in which R.sup.ST denotes H, an alkyl or alkoxy radical having 1 to 15 C atoms, where, in addition, one or more CH.sub.2 groups in these radicals may each be replaced, independently of one another by —C≡C—, —CF.sub.2O—, —OCF.sub.2—, —CH═CH—, ##STR00376##  —O—, —CO—O—, or —O—CO— in such a way that O atoms are not linked directly to one another, and in which one or more H atoms may each be replaced by halogen, ##STR00377##  on each occurrence, identically or differently, denotes ##STR00378## ZST denotes —CO—O—, —O—CO—, —CF.sub.2O—, —OCF.sub.2—, —CH.sub.2O—, —OCH.sub.2—, —CH.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 p denotes 0, 1 or 2.

5. The liquid crystal medium according to claim 1, wherein the medium comprises one or more compounds of formula IID as defined in claim 1, in which Z.sup.2D denotes a single bond.

6. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of the formula III ##STR00379## in which R.sup.31 and R.sup.32 each, independently of one another, denote H, an alkyl or alkoxy radical having 1 to 15 C atoms, where one or more CH.sub.2 groups in these radicals may each be replaced, independently of one another, by ##STR00380##  —C≡C—, —CF.sub.2O—, —OCF.sub.2—, —CH═CH—, by —O—, —CO—O—, or —O—CO— in such a way that O atoms are not linked directly to one another, and in which one or more H atoms may each be replaced by halogen, A.sup.31 on each occurrence, independently of one another, denotes a) 1,4-cyclohexenylene or 1,4-cyclohexylene radical, in which one or two non-adjacent CH.sub.2 groups may each be replaced by —O— or —S—, b) a 1,4-phenylene radical, in which one or two CH groups may each be replaced by N, or c) a radical from the group spiro[3.3]heptane-2,6-diyl, 1,4-bicyclo[2.2.2]-octylene, naphthalene-2,6-diyl, decahydronaphthalene-2,6-diyl, 1,2,3,4-tetrahydronaphthalene-2,6-diyl, phenanthrene-2,7-diyl and fluorene-2,7-diyl, where the radicals a), b) and c) may be mono- or polysubstituted by halogen atoms, Z.sup.31 on each occurrence independently of one another denotes —CO—O—, —O—CO—, —CF.sub.2O—, —OCF.sub.2—, —CH.sub.2O—, —OCH.sub.2—, —CH.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, n denotes 0, 1 or 2, L.sup.31 and L.sup.32 each, independently of one another, denote F, Cl, CF.sub.3, or CHF.sub.2, and W denotes O or S.

7. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of the formula IV ##STR00381## in which R.sup.41 denotes an unsubstituted alkyl radical having 1 to 7 C atoms or an unsubstituted alkenyl radical having 2 to 7 C atoms, and R.sup.42 denotes an unsubstituted alkyl radical having 1 to 7 C atoms or an unsubstituted alkoxy radical having 1 to 6 C atoms, or an unsubstituted alkenyl radical having 2 to 7 C atoms.

8. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds selected from the group of compounds of the formulae IV-3-3 to IV-3-5: ##STR00382##

9. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds selected from the compounds of the formulae IV-1-1 to IV-1-5 ##STR00383##

10. The medium according to claim 1, wherein the medium comprises one or more compounds selected from the group of compounds of the formulae CL-3-1 to CL-3-12 ##STR00384## ##STR00385##

11. The medium according to claim 1, wherein the medium has a birefringence in the range of from 0.085 to 0.110.

12. A liquid crystal display comprising the liquid crystal medium as defined in claim 1.

13. The liquid crystal display of claim 12, wherein the display is a VA, IPS or FFS type display.

14. A method of generating an electro-optical effect comprising using the liquid crystal medium according to claim 1 in a VA, IPS, FFS, PS-VA, PS-IPS or PS-FFS display.

15. A process of preparing a liquid crystal medium according to claim 1, comprising: mixing one or more compounds of formula I with one or more compounds selected from the group of the formulae IIA, IIB and/or IIC, one or more compounds of the formula IID and, and, if the one or more compounds of the formula IID do not include at least one compound of formula IID-10, one or more compounds of formula CL, as defined in claim 1, and optionally with a polymerizable compound or further liquid crystal compounds or additives.

Description

EXAMPLES

[0456] The present invention is illustrated in detail by the following non-restrictive working examples.

[0457] The following abbreviations and symbols are used: [0458] V.sub.0 threshold voltage, capacitive [V] at 20° C., [0459] n.sub.e extraordinary refractive index at 20° C. and 589 nm, [0460] n.sub.o ordinary refractive index at 20° C. and 589 nm, [0461] Δn optical anisotropy at 20° C. and 589 nm, [0462] ε.sub.⊥ dielectric permittivity perpendicular to the director at 20° C. and 1 kHz, [0463] ε.sub.∥ dielectric permittivity parallel to the director at 20° C. and 1 kHz, [0464] Δε dielectric anisotropy at 20° C. and 1 kHz, [0465] cl.p., T(N,I) clearing point [° C.], [0466] γ.sub.1 rotational viscosity at 20° C. [m.Math.Pas], [0467] K.sub.1 elastic constant, “splay” deformation at 20° C. [pN], [0468] K.sub.2 elastic constant, “twist” deformation at 20° C. [pN], [0469] K.sub.3 elastic constant, “bend” deformation at 20° C. [pN].

[0470] Unless explicitly noted otherwise, all concentrations in the present application are quoted in percent by weight and relate to the corresponding mixture as a whole, comprising all solid or liquid-crystalline components, without solvents.

[0471] Unless explicitly noted otherwise, all temperature values indicated in the present application, such as, for example, for the melting point T(C,N), the transition from the smectic (S) to the nematic (N) phase T(S,N) and the clearing point T(N,I), are quoted in degrees Celsius (° C.). 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.

[0472] All physical properties are and have been determined in accordance with “Merck Liquid Crystals, Physical Properties of Liquid Crystals”, Status November 1997, Merck kGaA, Germany, and apply for a temperature of 20° C., and Δn is determined at 589 nm and Δε at 1 kHz, unless explicitly indicated otherwise in each case.

[0473] The term “threshold voltage” for the present invention relates to the capacitive threshold (V.sub.0), also known as the Freedericks threshold, unless explicitly indicated otherwise. In the examples, the optical threshold may also, as generally usual, be quoted for 10% relative contrast (V.sub.10).

[0474] Unless stated otherwise, the process of polymerising the polymerisable compounds in the PSA displays as described above and below is carried out at a temperature where the LC medium exhibits a liquid crystal phase, preferably a nematic phase, and most preferably is carried out at room temperature.

[0475] Unless stated otherwise, methods of preparing test cells and measuring their electrooptical and other properties are carried out by the methods as described hereinafter or in analogy thereto.

[0476] The display used for measurement of the capacitive threshold voltage consists of two plane-parallel glass outer plates with a distance of 25 μm, each of which has on the inside an electrode layer and an unrubbed polyimide alignment layer on top, which effect homeotropic alignment of the liquid-crystal molecules.

[0477] The display or test cell used for measurement of the tilt angles consists of two plane-parallel glass outer plates at a separation of 4 μm, each of which has on the inside an electrode layer and a polyimide alignment layer on top, where the two polyimide layers are rubbed antiparallel to one another and effect a homeotropic edge alignment of the liquid-crystal molecules.

[0478] The polymerisable compounds are polymerised in the display or test cell by irradiation with UV light of defined intensity for a prespecified time, with a voltage simultaneously being applied to the display (usually 10 V to 30 V alternating current, 1 kHz). In the examples, unless indicated otherwise, a fluorescent lamp and an intensity of 0 to 20 mW/cm.sup.2 is used for polymerisation. The intensity is measured using a standard meter (Ushio Accumulate UV meter with central wavelength of 313 nm).

[0479] The transmission measurements are performed in test cells with fishbone electrode layout (from Merck Ltd., Japan; 1 pixel fishbone electrode (ITO, 10×10 mm, 47.7° angle of fishbone with 3 μm line/3 μm space), 3.2 μm cell gap, AF-glass, tilt angle 1°).

[0480] The storage stability in the bulk (LTS.sub.bulk) of the media according to the invention at a given temperature T is determined by visual inspection. 2 g of the media of interest are filled into a closed glass vessel (bottle) of appropriate size placed in a refrigerator at a predetermined temperature. The bottles are checked at defined time intervals for the occurrence of smectic phases or crystallisation. For every material and at each temperature two bottles are stored. If crystallisation or the appearance of a smectic phase is observed in at least one of the two correspondent bottles the test is terminated and the time of the last inspection before the one at which the occurrence of a higher ordered phase is observed is recorded as the respective storage stability.

EXAMPLES

[0481] The following stabilisers of formula I are used:

##STR00367##

[0482] The nematic LC host mixtures H1 to H88 and Mixture Examples N1 to N88 have the compositions and the properties given in the following tables.

Mixture H1

[0483]

TABLE-US-00007 B(S)-2O-O6 2.0% CCY-3-O2 8.0% CCY-3-O1 3.0% CLOY-3-O2 15.0% CLY-3-O2 12.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CCY-5-O2 4.0% CC-3-V1 15.0% CC-4-V1 16.0% CC-3-O3 1.0% CC-3-5 6.0% CCZC-3-3 4.0% CCZC-3-5 4.0% Σ 100.0%

Mixture Example N1

[0484]

TABLE-US-00008 H1 99.94% T.sub.(N,I). [°C.]: 125.4 ST-3a-1 0.03% Δn (589 nm, 25° C.): 0.0904 I-1-1a 0.03% Δε (1 kHz, 25° C.): −3.7 Σ 100.0% K.sub.1 [pN], 25° C.): K.sub.3 [pN], (25° C.): 26.2 γ.sub.1 [mPa .Math. s], (25° C.): 206

Mixture H2

[0485]

TABLE-US-00009 B(S)-2O-O4 4.0% B(S)-2O-O5 5.0% B(S)-2O-O6 2.5% Y-4O-O4 3.0% PY-3-O2 7.5% CLY-3-O2 9.0% CLY-3-O3 6.0% CPY-3-O2 4.5% CC-2-3 6.0% CC-3-5 4.5% CC-3-V 32.0% CC-3-V1 8.0% CLP-V-1 8.0% Σ 100.0%

Mixture Example N2

[0486]

TABLE-US-00010 H2 99.87% T.sub.(N,I) [° C.]: 76 ST-3a-1 0.03% Δn (589 nm, 25° C.): 0.0969 I-1-1a 0.10% n.sub.e (25° C., 589.3 nm]: 1.5800 Σ 100.0% n.sub.o (25° C., 589.3 nm]: 1.4831 Δε (1 kHz, 25° C.): −2.7 ε.sub.|| (1 kHz, 25° C.): 3.4 ε.sub.⊥ (1 kHz, 25° C.): 6.1 K.sub.1 [pN], (25° C.): 15.1 K.sub.3 [pN], (25° C.): 14.1 γ.sub.1 [mPa .Math. s], (25° C.): 57 V.sub.0 [V], (25° C.): 2.39

[0487] Low temperature stability (LTS) tests of the host mixtures H1 and H2 and of the mixtures N1 and N2 according to the invention are performed as described above. The results are summarized in the following table.

TABLE-US-00011 Mixture LTS.sub.bulk (−30° C.) [h] H1 96 N1 >240 H2 120 N2 168

[0488] The addition of a compound of formula I to a host medium significantly increases the LTS. By increasing the amount of the compound I-1-1a in Mixture Example N2 to 1200 ppm, the LTS is further increased.

[0489] Mixture H3

TABLE-US-00012 B(S)-2O-O4 4.0% B(S)-2O-O5 5.0% Y-4O-O4 8.0% CY-3-O2 5.5% CCY-3-O2 2.0% CLY-3-O2 9.0% CLY-3-O3 6.0% CPY-3-O2 2.5% CC-3-4 6.0% CC-3-5 5.0% CC-3-V 25.0% CC-3-V1 5.0% CCP-3-1 10.0% CLP-V-1 7.0% Σ 100.0%

Mixture Example N3

[0490]

TABLE-US-00013 H3 99.87% T.sub.(N,I) [° C.]: 80 ST-3a-1 0.03% Δn (589 nm, 25° C.): 0.0922 I-4-2a 0.01% n.sub.e (25° C., 589.3 nm]: 1.5751 Σ 100.0% n.sub.o (25° C., 589.3 nm]: 1.4829 Δε (1 kHz, 25° C.): −3.1 ε.sub.|| (1 kHz, 25° C.): 3.5 ε.sub.⊥ (1 kHz, 25° C.): 6.6 K.sub.1 [pN], (25° C.): 16.3 K.sub.3 [pN], (25° C.): 15.5 γ.sub.1 [mPa .Math. s], (25° C.): 82 V.sub.0 [V], (25° C.): 2.37

[0491] The host mixture H3 and mixture N3 are cooled to −40° C. After 24 h a smectic phase is observed in host mixture H3, whereas the mixture N3 according to the invention is nematic.

[0492] Mixture H4

TABLE-US-00014 B(S)-(c5)1O-O2 2.0% CCY-3-O2 8.0% CCY-3-O1 3.0% CLOY-3-O2 15.0% CLY-3-O2 12.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CCY-5-O2 4.0% CC-3-V1 15.0% CC-4-V1 16.0% CC-3-O3 1.0% CC-3-5 6.0% CCZC-3-3 4.0% CCZC-3-5 4.0% Σ 100.0%

Mixture Example N4

[0493]

TABLE-US-00015 H1 99.92% T.sub.(N,I). [° C.]: 125 ST-3a-1 0.03% Δn (589 nm, 25° C.): 0.0906 I-1-1a 0.05% Δε (1 kHz, 25° C.): −3.7 Σ 100.0% K.sub.1 [pN], (25° C.): 24.1 K.sub.3 [pN], (25° C.): 24.9 γ.sub.1 [mPa .Math. s], (25° C.): 209

[0494] Mixture H5

TABLE-US-00016 CC-3-V1 10.0% CC-4-V1 16.0% CC-3-O3 8.0% CC-3-5 5.0% Y-4O-O4 5.5% CY-5-O2 2.0% CCY-3-O2 8.0% CCY-5-O2 2.5% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CLY-3-O3 1.0% CCZC-3-3 4.0% CCZC-3-5 4.0% Σ 100.0%

Mixture Example N5

[0495]

TABLE-US-00017 H1 99.87% T.sub.(N,I) [° C.]: 103.5 ST-3a-1 0.02% Δn (589 nm, 25° C.): 0.0833 I-1-1a 0.11% n.sub.e (25° C., 589.3 nm]: 1.5583 Σ 100.0% n.sub.o (25° C., 589.3 nm]: 1.4750 Δε (1 kHz, 25° C.): −3.8 ε.sub.|| (1 kHz, 25° C.): 3.3 ε.sub.⊥ (1 kHz, 25° C.): 7.1 K.sub.1 [pN], (25° C.): 21.2 K.sub.3 [pN], (25° C.): 21.2 γ.sub.1 [mPa .Math. s], (25° C.): 151 V.sub.0 [V], (25° C.): 2.50

[0496] Mixture H6

TABLE-US-00018 CC-3-V1 10.0% CC-4-V1 14.0% CC-3-O3 8.0% CC-3-5 13.5% CCOY-2-O2 3.5% CCOY-3-O2 9.0% CLOY-3-O2 15.0% CLY-3-O2 10.0% CLY-4-O2 5.0% CLY-5-O2 4.0% CLY-3-O3 1.0% CCZC-3-3 4.0% CCZC-3-5 3.0% Σ 100.0%

Mixture Example N6

[0497]

TABLE-US-00019 H1 99.92% T.sub.(N,I) [° C.]: 115 ST-3a-1 0.03% Δn (589 nm, 25° C.): 0.0836 I-1-1a 0.05% Δε (1 kHz, 25° C.): −3.8 Σ 100.0% K.sub.1 [pN], (25° C.): 25.3 K.sub.3 [pN], (25° C.): 24.8 γ.sub.1 [mPa .Math. s], (25° C.): 180 V.sub.0 [V], (25° C.): 2.80

[0498] Mixture H7

TABLE-US-00020 CC-3-V1 10.0% CC-4-V1 16.0% CC-3-O3 8.0% CC-3-5 5.0% Y-4O-O4 5.5% CEY-5-O2 2.0% CCY-3-O2 8.0% CCY-5-O2 2.5% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CLY-3-O3 1.0% CCZC-3-3 4.0% CCZC-3-5 4.0% Σ 100.0%

Mixture Example N7

[0499]

TABLE-US-00021 H1 99.87% T.sub.(N,I) [° C.]: 103 ST-3a-1 0.02% Δn (589 nm, 25° C.): 0.0832 I-1-1a 0.11% n.sub.e (25° C., 589.3 nm]: 1.5582 Σ 100.0% n.sub.o (25° C., 589.3 nm]: 1.4750 Δε (1 kHz, 25° C.): −3.8 ε.sub.|| (1 kHz, 25° C.): 3.3 ε.sub.⊥ (1 kHz, 25° C.): 7.1 K.sub.1 [pN], (25° C.): 21.0 K.sub.3 [pN], (25° C.): 21.1 γ.sub.1 [mPa .Math. s], (25° C.): 152 V.sub.0 [V], (25° C.): 2.51

[0500] The Mixture Examples N8 to N88 consist of the host mixtures H8 to H88 below, and 1000 ppm of the compound I-1-1a each. The mixtures are distinguished by a particularly high LTS.

[0501] Mixture H8

TABLE-US-00022 B(S)-2O-O6 2.0% T.sub.(N,I). [° C.]: 122 CCY-3-O2 8.0% Δn (589 nm, 25° C.): 0.0898 CAIY-3-O2 3.0% Δε (1 kHz, 25° C.): −3. CLOY-3-O2 15.0% K.sub.1 [pN], (25° C.): 21.1 CLY-3-O2 12.0% K.sub.3 [pN], (25° C.): 21.9 CLY-4-O2 5.0% γ.sub.1 [mPa .Math. s], (25° C.): 200 CLY-5-O2 5.0% CCY-5-O2 4.0% CC-3-V1 15.0% CC-4-V1 16.0% CC-3-O3 1.0% CC-3-5 6.0% CC-1-3 2.0% CCZC-3-3 4.0% CCZC-3-5 4.0% Σ 100.0%

[0502] Mixture H9

TABLE-US-00023 B(S)-2O-O4 4.0% cl. p. [° C.]: 123 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.0972 CC-3-V 2.0% Δε [1 kHz, 20° C.]: −3.9 CC-3-V1 10.0% γ.sub.1 [mPa s, 20° C.]: 228 CC-4-V1 15.0% CC-3-5 13.0% CCP-3-1 5.0% CCY-3-O2 10.0% CCY-5-O2 6.5% CLOY-3-O2 8.5% CCOY-2-O3 4.0% CLY-3-O2 9.5% CLY-4-O2 5.0% CLY-5-O2 5.0% Σ 100.0%

[0503] Mixture H10

TABLE-US-00024 B(S)-2O-O4 4.0% cl. p. [° C.]: 76 B(S)-(c5)1O-O2 5.0% Δn [589 nm, 20° C.]: 0.0957 CC-3-V 10.5% Δε [1 kHz, 20° C.]: −6.1 CC-3-V1 10.0% γ.sub.1 [mPa s, 20° C.]: 115 CC-3-4 12.0% CC-3-5 6.5% CCY-3-O2 11.0% CLOY-3-O2 1.0% CLY-3-O2 10.0% CLY-4-O2 4.5% COB(S)-2-O4 11.0% Y-4O-O4 14.5% Σ 100.0%

[0504] Mixture H11

TABLE-US-00025 B(S)-2O-O4 4.0% cl. p. [° C.]: 75 B(S)-(c5-3en)1O-O2 5.0% Δn [589 nm, 20° C.]: 0.0944 CC-3-V 10.5% Δε [1 kHz, 20° C.]: −6.0 CC-3-V1 10.0% γ.sub.1 [mPa s, 20° C.]: 112 CC-3-4 12.0% CC-3-5 6.5% CCY-3-O2 11.0% CLOY-3-O2 1.0% CLY-3-O2 10.0% CLY-4-O2 4.5% COB(S)-2-O4 11.0% Y-4O-O4 14.5% Σ 100.0%

[0505] Mixture H12

TABLE-US-00026 CLP-3-O1 8.0% cl. p. [° C.]: 125.5 B(S)-2O-O4 3.68% Δn [589 nm, 20° C.]: 0.1064 B(S)-2O-O5 2.76% ε.sub.|| [1 kHz, 20° C.]: 3.2 B(S)-2O-O6 3.68% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-3-V1 9.2% Δε [1 kHz, 20° C.]: −3.8 CC-4-V1 12.88% K.sub.1 [pN, 20° C.]: 32.1 CC-3-4 1.84% K.sub.3 [pN, 20° C.]: 50.2 CC-3-5 9.2% V.sub.0 [V, 20° C.]: 3.84 CCP-3-1 5.52% CCP-V2-1 7.82% CCY-3-O2 8.28% CLOY-3-O2 14.26% CLY-3-O2 8.28% CLY-5-O2 4.6% Σ %

[0506] Mixture H13

TABLE-US-00027 B(S)-2O-O4 4.0% cl. p. [° C.]: 120.1 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.0969 CC-3-V 2.%0 ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CC-4-V1 15.0% Δε [1 kHz, 20° C.]: −4.0 CC-3-5 13.0% γ.sub.1 [mPa s, 20° C.]: 236 CCP-3-1 5.0% K.sub.1 [pN, 20° C.]: 27.3 CCY-3-O2 10.0% K.sub.3 [pN, 20° C.]: 27.5 CCY-5-O2 6.5% V.sub.0 [V, 20° C.]: 2.74 CLOY-3-O2 12.5% CLY-3-O2 9.5% CLY-4-O2 5.0% CLY-5-O2 5.0% Σ 100.0%

[0507] Mixture H14

TABLE-US-00028 B(S)-2O-O4 3.0% cl. p. [° C.]: 121.2 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0972 CC-3-V 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CC-4-V1 9.0% Δε [1 kHz, 20° C.]: −3.8 CC-3-5 12.0% γ.sub.1 [mPa s, 20° C.]: 232 CCP-3-1 12.0% K.sub.1 [pN, 20° C.]: 28.7 CCY-3-O2 9.0% K.sub.3 [pN, 20° C.]: 29.0 CCY-5-O2 2.0% V.sub.0 [V, 20° C.]: 2.90 CLOY-3-O2 12.5% CLY-3-O2 9.0% CLY-5-O2 5.0% CLY-3-O3 4.0% CLY-4-O2 4.0% CC-3-O3 4.5% Σ 100.0%

[0508] Mixture H15

TABLE-US-00029 B(S)-2O-O4 4.0% cl. p. [° C.]: 74.8 B(S)-2O-O5 5.0% Δn [589 nm, 20° C.]: 0.0963 CC-3-V 10.5% ε.sub.|| [1 kHz, 20° C.]: 4.3 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 10.3 CC-3-4 12.0% Δε [1 kHz, 20° C.]: −6.0 CC-3-5 6.5% γ.sub.1 [mPa s, 20° C.]: 110 CCY-3-O2 11.0% K.sub.1 [pN, 20° C.]: 16.4 CLOY-3-O2 1.0% K.sub.3 [pN, 20° C.]: 13.8 CLY-3-O2 10.0 V.sub.0 [V, 20° C.]: 1.58 CLY-4-O2 4.5 COB(S)-2-O4 11.0% Y-4O-O4 14.5 Σ 100.0%

[0509] Mixture H16

TABLE-US-00030 B(S)-2O-O4 3.0% cl. p. [° C.]: 121.1 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0971 CC-3-V 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 8.5% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CC-4-V1 9.0% Δε [1 kHz, 20° C.]: −3.8 CC-3-O3 4.0% γ.sub.1 [mPa s, 20° C.]: 229 CC-3-5 11.5% K.sub.1 [pN, 20° C.]: 28.3 CCP-3-1 12.0% K.sub.3 [pN, 20° C.]: 28.0 CCY-3-O2 10.0% V.sub.0 [V, 20° C.]: 2.86 CCY-5-O2 1.5% CLOY-3-O2 12.5% CLY-3-O2 9.0% CLY-3-O3 4.0% CLY-4-O2 4.0% CLY-5-O2 4.5% Σ 100.0%

[0510] Mixture H17

TABLE-US-00031 B(S)-2O-O4 2.0% cl. p. [° C.]: 120.3 CC-3-O3 5.0% Δn [589 nm, 20° C.]: 0.0906 CC-3-V 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CC-4-V1 12.5% Δε [1 kHz, 20° C.]: −3.7 CC-3-5 12.0% CCP-3-1 2.0% γ.sub.1 [mPa s, 20° C.]: 247 CCY-3-O1 2.5% K.sub.1 [pN, 20° C.]: 25.9 CCY-3-O2 9.0% K.sub.3 [pN, 20° C.]: 26.2 CCY-5-O2 3.0% V.sub.0 [V, 20° C.]: 2.79 CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-5-O2 5.0% CLY-3-O3 4.5% CLY-4-O2 4.0% CCZPC-3-5 2.5% Σ 100.0%

[0511] Mixture H18

TABLE-US-00032 B(S)-2O-O4 4.0% cl. p. [° C.]: 75.5 B(S)-2O-O5 5.0% Δn [589 nm, 20° C.]: 0.0960 CC-3-V 3.5% ε.sub.|| [1 kHz, 20° C.]: 4.6 CC-3-V1 9.5% ε.sub.⊥ [1 kHz, 20° C.]: 11.5 CC-3-4 12.0% Δε [1 kHz, 20° C.]: −7.0 CC-3-5 5.5% γ.sub.1 [mPa s, 20° C.]: 141 CCY-3-O2 11.0% K.sub.1 [pN, 20° C.]: 16.7 CCY-4-O2 10.5% K.sub.3 [pN, 20° C.]: 14.9 CLOY-3-O2 6.5% V.sub.0 [V, 20° C.]: 1.53 CLY-3-O2 10.0% COB(S)-2-O4 6.5% Y-4O-O4 16.0% Σ 100.0%

[0512] Mixture H19

TABLE-US-00033 B(S)-2O-O4 4.0% cl. p. [° C.]: 110.4 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1023 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 12.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-3-V1 8.0% Δε [1 kHz, 20° C.]: −3.6 CC-4-V1 11.0% γ.sub.1 [mPa s, 20° C.]: 164 CC-3-5 12.0% K.sub.1 [pN, 20° C.]: 24.4 CCP-3-1 9.0% K.sub.3 [pN, 20° C.]: 23.2 CCY-3-O2 9.0% V.sub.0 [V, 20° C.]: 2.71 CLOY-3-O2 8.5% CLP-V-1 5.0% CLY-3-O2 9.0% COB(S)-2-O4 5.5% Σ 100.0%

[0513] Mixture H20

TABLE-US-00034 B(S)-2O-O4 4.0% cl. p. [° C.]: 73.3 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1077 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 4.3 B-2O-O5 4.0% ε.sub.⊥ [1 kHz, 20° C.]: 11.3 CC-3-V 33.5% Δε [1 kHz, 20° C.]: −7.0 CCY-3-O2 9.0% γ.sub.1 [mPa s, 20° C.]: 131 CLOY-3-O2 5.0% K.sub.1 [pN, 20° C.]: 14.5 CLY-3-O2 7.0% K.sub.3 [pN, 20° C.]: 14.5 CLY-4-O2 1.5% V.sub.0 [V, 20° C.]: 1.52 COB(S)-2-O4 10.0% CY-3-O2 15.0% LY-3-O2 3.0% Σ 100.0%

[0514] Mixture H21

TABLE-US-00035 B(S)-2O-O4 4.0% cl. p. [° C.]: 109.9 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1031 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-V 6.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CC-3-V1 12.0% Δε [1 kHz, 20° C.]: −4.6 CC-4-V1 15.0% γ.sub.1 [mPa s, 20° C.]: 186 CC-3-5 12.0% K.sub.1 [pN, 20° C.]: 25.4 CCP-3-1 2.0% K.sub.3 [pN, 20° C.]: 24.5 CCY-3-O2 8.0% V.sub.0 [V, 20° C.]: 2.43 CLOY-3-O2 10.0% CLY-3-O2 7.0% CLY-3-O3 6.0% CLY-4-O2 5.0% COB(S)-2-O4 6.0% Σ 100.0%

[0515] Mixture H22

TABLE-US-00036 B(S)-2O-O4 4.0% cl. p. [° C.]: 112.9 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1028 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 14.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CC-3-V1 11.0% Δε [1 kHz, 20° C.]: −3.6 CC-4-V1 7.0% γ.sub.1 [mPa s, 20° C.]: 165 CC-3-5 10.0% K.sub.1 [pN, 20° C.]: 24.2 CCP-3-1 12.0% K.sub.3 [pN, 20° C.]: 23.3 CCP-V2-1 3.0% V.sub.0 [V, 20° C.]: 2.68 CCY-3-O2 9.0% CLOY-3-O2 5.5% CLY-3-O2 9.0% CLY-4-O2 1.0% COB(S)-2-O4 7.5% Σ 100.0%

[0516] Mixture H23

TABLE-US-00037 B(S)-2O-O4 4.0% cl. p. [° C.]: 111.8 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.1030 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-3-V1 10.0% Δε [1 kHz, 20° C.]: −3.8 CC-4-V1 14.5% γ.sub.1 [mPa s, 20° C.]: 169 CC-3-4 3.0% K.sub.1 [pN, 20° C.]: 25.6 CC-3-5 10.0% K.sub.3 [pN, 20° C.]: 24.2 CCP-3-1 7.5% V.sub.0 [V, 20° C.]: 2.65 CCP-3-3 1.0% CCP-V2-1 1.0% CCY-3-O2 7.0% CLOY-3-O2 6.0% CLY-3-O2 7.0% CLY-5-O2 5.0% COB(S)-2-O4 9.5% Σ 100.0%

[0517] Mixture H24

TABLE-US-00038 B(S)-2O-O4 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 B(S)-2O-O5 2.5% ε.sub.⊥ [1 kHz, 20° C.]: 6.3 CC-3-V 5.5% Δε [1 kHz, 20° C.]: −3.3 CC-3-V1 8.0% γ.sub.1 [mPa s, 20° C.]: 203 CC-4-V1 12.0% K.sub.1 [pN, 20° C.]: 28.2 CC-3-4 2.0% K.sub.3 [pN, 20° C.]: 27.7 CC-3-5 12.0% V.sub.0 [V, 20° C.]: 3.04 CCP-3-1 10.0% CCVC-3-V 3.0% CCY-3-O2 8.0% CCY-5-O2 4.5% CLOY-3-O2 9.5% CLY-3-O2 9.0% CLY-4-O2 5.0% CLY-5-O2 5.0% Σ 100.0%

[0518] Mixture H25

TABLE-US-00039 B(S)-2O-O4 4.0% cl. p. [° C.]: 115.7 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0959 B(S)-2O-O6 1.5% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 10.5% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-3-V1 8.5% Δε [1 kHz, 20° C.]: −3.6 CC-4-V1 7.0% γ.sub.1 [mPa s, 20° C.]: 210 CC-3-5 12.5% K.sub.1 [pN, 20° C.]: 25.2 CCOC-3-3 3.0% K.sub.3 [pN, 20° C.]: 25.7 CCP-3-1 10.5% V.sub.0 [V, 20° C.]: 2.81 CCY-3-O2 8.0% LTS bulk [h, −20° C.]: 192 CCY-5-O2 5.0% CLOY-3-O2 12.5% CLY-3-O2 9.0% CLY-5-O2 5.0% Σ 100.0%

[0519] Mixture H26

TABLE-US-00040 B(S)-2O-O4 4.0% cl. p. [° C.]: 112.3 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1025 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 7.5% ε.sub.⊥ [1 kHz, 20° C.]: 7.1 CC-3-V1 10.0% Δε [1 kHz, 20° C.]: −3.9 CC-4-V1 14.0% γ.sub.1 [mPa s, 20° C.]: 178 CC-3-4 3.0% K.sub.1 [pN, 20° C.]: 25.2 CC-3-5 9.5% K.sub.3 [pN, 20° C.]: 24.0 CCP-3-1 6.5% V.sub.0 [V, 20° C.]: 2.61 CCP-V2-1 2.5% CCY-3-O2 8.0% CLOY-3-O2 7.5% CLY-3-O2 8.0% CLY-5-O2 6.0% COB(S)-2-O4 6.5% Σ 100.0%

[0520] Mixture H27

TABLE-US-00041 B(S)-2O-O4 4.5% cl. p. [° C.]: 116.9 B(S)-2O-O5 4.5% Δn [589 nm, 20° C.]: 0.1038 B(S)-2O-O6 2.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-V 1.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.9 CC-3-V1 10.5% Δε [1 kHz, 20° C.]: −4.6 CC-4-V1 15.0% γ.sub.1 [mPa s, 20° C.]: 239 CC-3-5 12.0% K.sub.1 [pN, 20° C.]: 26.7 CCP-3-1 5.5% K.sub.3 [pN, 20° C.]: 27.2 CCY-3-O2 10.5% V.sub.0 [V, 20° C.]: 2.56 CCY-5-O2 6.0% CLOY-3-O2 13.0% CLY-3-O2 9.0% CLY-5-O2 5.0% PGIY-2-O4 1.5% Σ 100.0%

[0521] Mixture H28

TABLE-US-00042 B(S)-2O-O4 3.0% Cl. p. [° C.]: 102.8 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1047 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.6 CC-3-V 26.5% ε.sub.⊥ [1 kHz, 20° C.]: 7.7 CC-3-V1 10.0% Δε [1 kHz, 20° C.]: −4.1 CC-3-5 5.0% γ.sub.1 [mPa s, 20° C.]: 162 CCG-V-F 3.0% K.sub.1 [pN, 20° C.]: 19.5 CCY-3-O2 7.0% K.sub.3 [pN, 20° C.]: 22.4 CLOY-3-O2 11.0% V.sub.0 [V, 20° C.]: 2.45 CLY-3-O2 7.0% CLY-4-O2 5.0% CLY-5-O2 4.5% CPY-3-O2 11.0% Σ 100.0%

[0522] Mixture H29

TABLE-US-00043 B(S)-2O-O4 3.0% Cl. p. [° C.]: 105.1 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1014 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.6 CC-3-V 18.5% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CC-3-V1 10.0% Δε [1 kHz, 20° C.]: −4.2 CC-4-V1 8.0% γ.sub.1 [mPa s, 20° C.]: 180 CCG-V-F 3.0% K.sub.1 [pN, 20° C.]: 20.6 CC-3-5 5.0% K.sub.3 [pN, 20° C.]: 22.9 CCY-3-O2 9.0% V.sub.0 [V, 20° C.]: 2.44 CLOY-3-O2 13.5% CLY-3-O2 8.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CPY-3-O2 5.0% Σ 100.0%

[0523] Mixture H30

TABLE-US-00044 B(S)-2O-O4 4.0% Cl. p. [° C.]: 114.1 B(S)-2O-O5 1.0% Δn [589 nm, 20° C.]: 0.1028 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.1 CC-4-V1 11.5% Δε [1 kHz, 20° C.]: −3.0 CC-3-5 10.0% γ.sub.1 [mPa s, 20° C.]: 179 CCP-3-1 7.5% K.sub.1 [pN, 20° C.]: 24.0 CCP-3-3 4.5% K.sub.3 [pN, 20° C.]: 24.8 CCP-V2-1 7.0% V.sub.0 [V, 20° C.]: 3.04 CCY-3-O1 1.5% CCY-3-O2 7.0% CCY-5-O2 2.5% CLOY-3-O2 4.0% CLY-3-O2 6.0% CLY-4-O2 1.5% CLY-5-O2 4.0% CPY-3-O2 3.0% CY-3-O2 3.0% CP-3-O2 8.0% Σ 100.0%

[0524] Mixture H31

TABLE-US-00045 B(S)-2O-O4 4.0% Cl. p. [° C.]: 118.8 B(S)-2O-O5 1.0% Δn [589 nm, 20° C.]: 0.1028 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 5.9 CC-4-V1 8.0% Δε [1 kHz, 20° C.]: −2.9 CC-3-5 10.0% γ.sub.1 [mPa s, 20° C.]: 198 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 25.5 CCP-3-3 6.0% K.sub.3 [pN, 20° C.]: 26.8 CCP-V2-1 11.5% V.sub.0 [V, 20° C.]: 3.22 CCY-3-O2 8.5% CLOY-3-O2 9.0% CLY-3-O2 7.0% CLY-5-O2 5.0% CP-3-O2 8.0% Σ 100.0%

[0525] Mixture H32

TABLE-US-00046 CC-3-O1 18.5% cl. p. [° C.]: 94.1 CCOC-3-3 4.0% Δn [589 nm, 20° C.]: 0.0803 CCPC-33 3.5% ε.sub.|| [1 kHz, 20° C.]: 4.1 CCY-3-O1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 9.8 CCY-3-O3 4.0% Δε [1 kHz, 20° C.]: −5.7 CCY-4-O2 8.0% γ.sub.1 [mPa s, 20° C.]: 294 CCY-5-O2 6.0% K.sub.1 [pN, 20° C.]: 16.2 CCZC-3-3 2.5% K.sub.3 [pN, 20° C.]: 18.6 CCZC-4-3 4.0% V.sub.0 [V, 20° C.]: 1.91 CCZC-4-5 4.0% CLOY-3-O2 24.0% CY-3-O2 7.5% Y-4O-O4 6.0% Σ 100.0%

[0526] Mixture H33

TABLE-US-00047 B(S)-2O-O4 4.0% Cl. p. [° C.]: 100.3 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1027 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.7 CC-3-V 24.0% ε.sub.⊥ [1 kHz, 20° C.]: 8.8 CC-3-V1 10.0% Δε [1 kHz, 20° C.]: −5.2 CC-3-5 5.0% γ.sub.1 [mPa s, 20° C.]: 159 CCY-3-O1 6.0% K.sub.1 [pN, 20° C.]: 20.5 CCY-3-O2 7.0% K.sub.3 [pN, 20° C.]: 19.3 CCY-5-O2 1.5% V.sub.0 [V, 20° C.]: 2.03 CLOY-3-O2 4.0% CLY-3-O2 7.0% CLY-3-O3 6.0% CLY-4-O2 5.0% CLY-5-O2 5.0% COB(S)-2-O4 5.0% CPY-3-O2 0.5% Y-4O-O4 4.0% Σ 100.0%

[0527] Mixture H34

TABLE-US-00048 CC-3-V1 12.0% cl. p. [° C.]: 127.1 CC-3-5 12.5% Δn [589 nm, 20° C.]: 0.0873 CCOC-3-3 4.0% ε.sub.|| [1 kHz, 20° C.]: 2.9 CCOC-4-3 2.0% ε.sub.⊥ [1 kHz, 20° C.]: 5.5 CCP-3-1 16.0% Δε [1 kHz, 20° C.]: −2.5 CCY-3-O2 10.0% γ.sub.1 [mPa s, 20° C.]: 281 CCY-5-O2 5.0% K.sub.1 [pN, 20° C.]: 26.7 CCZC-3-3 4.0% K.sub.3 [pN, 20° C.]: 28.7 CCZC-3-5 4.0% V.sub.0 [V, 20° C.]: 3.56 CLOY-3-O2 21.5% CLP-V-1 5.0% CP-3-O2 4.0% Σ 100.0%

[0528] Mixture H35

TABLE-US-00049 CC-3-V1 12.0% cl. p. [° C.]: 131.3 CC-3-5 12.5% CCOC-3-3 4.0% CCZC-3-3 4.0% CCP-3-1 16.0% CCZPC-3-5 3.5% CCY-3-O2 10.0% CCY-5-O2 5.0% CLOY-3-O2 26.0% CLY-3-O2 5.0% CP-3-O2 2.0% Σ 100.0%

[0529] Mixture H36

TABLE-US-00050 B(S)-2O-O5 5.0% cl. p. [° C.]: 114 CC-3-V 5.7% Δn [589 nm, 20° C.]: 0.0952 CC-3-V1 12.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-O3 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-3-5 12.0% Δε [1 kHz, 20° C.]: −3.7 CCP-3-1 15.0% γ.sub.1 [mPa s, 20° C.]: 213 CCY-3-O2 9.0% K.sub.1 [pN, 20° C.]: 25.6 CCY-5-O2 4.1% K.sub.3 [pN, 20° C.]: 26.2 CLOY-3-O2 14.0% V.sub.0 [V, 20° C.]: 2.80 CLY-3-O2 10.0% CLY-4-O2 5.0% LY-3-O2 2.0% Y-4O-O4 1.2% Σ 100.0%

[0530] Mixture H37

TABLE-US-00051 CC-3-2V1 4.0% cl. p. [° C.]: 115 CC-3-V 24.0% Δn [589 nm, 20° C.]: 0.0917 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 5.7 CCP-V-1 15.0% ε.sub.⊥ [1 kHz, 20° C.]: 3.1 CCP-V2-1 8.0% Δε [1 kHz, 20° C.]: 2.6 CCZPC-3-5 3.0% γ.sub.1 [mPa s, 20° C.]: 121 CCQU-3-F 3.0% K.sub.1 [pN, 20° C.]: 17.4 CCVC-3-V 6.0% K.sub.3 [pN, 20° C.]: 21.8 CCY-3-1 3.0% V.sub.0 [V, 20° C.]: 2.76 CDUQU-3-F 5.0% CLOY-3-O2 2.5% CLP-V-1 6.0% CY-3-O2 1.0% DGUQU-4-F 4.0% CP-3-O2 5.0% PGP-1-2V 2.5% Σ 100.0%

[0531] Mixture H38

TABLE-US-00052 B(S)-2O-O4 3.0% cl. p. [° C.]: 101.8 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0952 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.5 CC-3-V 13.0% ε.sub.⊥ [1 kHz, 20° C.]: 8.6 CC-3-V1 8.0% Δε [1 kHz, 20° C.]: −5.1 CC-3-O3 5.0% K.sub.1 [pN, 20° C.]: 22.3 CC-3-5 12.0% K.sub.3 [pN, 20° C.]: 22.6 CCP-3-1 1.0% V.sub.0 [V, 20° C.]: 2.23 CCY-3-O1 1.2% CCY-3-O2 11.0% CCY-3-O3 1.0% CCY-5-O2 6.8% CCZC-3-5 0.8% CLOY-3-O2 15.0% CLY-3-O2 8.2% CLY-4-O2 2.0% CLY-5-O2 3.0% Y-4O-O4 3.0% Σ 100.0%

[0532] The medium H38 contains 400 ppm of the compound ST-3b-1.

[0533] Mixture H39

TABLE-US-00053 B(S)-2O-O4 1.5% cl. p. [° C.]: 109.6 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.0985 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.5 CC-3-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 8.4 CC-4-V1 12.0% Δε [1 kHz, 20° C.]: −4.9 CC-3-5 12.0% K.sub.1 [pN, 20° C.]: 24.1 CCP-V2-1 7.5% K.sub.3 [pN, 20° C.]: 24.4 CCPC-33 2.5% V.sub.0 [V, 20° C.]: 2.36 CCY-3-O2 10.0% CCY-5-O2 5.0% CLOY-3-O2 15.5% CLY-3-O2 9.0% CLY-3-O3 0.5% CLY-5-O2 5.0% Y-4O-O4 6.0% Σ 100.0%

[0534] Mixture H40

TABLE-US-00054 CC-3-V1 11.0% Δn [589 nm, 20° C.]: 0.0793 CC-3-5 14.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CCOC-3-3 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CCOC-4-3 3.0% Δε [1 kHz, 20° C.]: −4.0 CCP-3-1 6.0% K.sub.1 [pN, 20° C.]: 24.1 CCY-3-O2 12.5% K.sub.3 [pN, 20° C.]: 27.4 CLOY-3-O2 15.5% V.sub.0 [V, 20° C.]: 2.77 CLY-3-O2 9.0% CP-3-O2 2.0% Y-4O-O4 3.0% BCN-35 15.0% CC-3-V 4.0% Σ 100.0%

[0535] Mixture H41

TABLE-US-00055 CC-3-V 20.0% cl. p. [° C.]: 83.9 CCOC-4-3 4.0% Δn [589 nm, 20° C.]: 0.0781 CCZPC-3-3 3.5% ε.sub.|| [1 kHz, 20° C.]: 4.3 CCY-3-O1 7.0% ε.sub.⊥ [1 kHz, 20° C.]: 9.3 CCY-3-O3 4.0% Δε [1 kHz, 20° C.]: −5.1 CCY-4-O2 8.0% CCY-5-O2 7.0% CCZC-3-3 2.5% CCZC-3-5 2.0% CCZC-4-3 3.0% CCZC-4-5 3.0% CLOY-3-O2 21.0% Y-4O-O4 15.0% Σ 100.0%

[0536] Mixture H42

TABLE-US-00056 B(S)-2O-O4 4.0% cl. p. [° C.]: B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: B(S)-2O-O6 0.5% ε.sub.|| [1 kHz, 20° C.]: CC-3-V 4.5% ε.sub.⊥ [1 kHz, 20° C.]: CC-3-V1 12.0% Δε [1 kHz, 20° C.]: CC-4-V1 10.0% γ.sub.1 [mPa s, 20° C.]: CCG-V-F 2.0% γ.sub.1 [mPa s, 20° C.]: CC-3-5 12.0% K.sub.1 [pN, 20° C.]: CCP-3-1 11.0% K.sub.3 [pN, 20° C.]: CCY-3-O2 8.0% V.sub.0 [V, 20° C.]: CLOY-3-O2 12.5% LTS bulk [h, −20° C.]: CLY-3-O2 10.0% LTS bulk [h, −30° C.]: CLY-4-O2 5.0% LTS bulk [h, −10° C.]: CLY-5-O2 4.5% Σ 100.0%

[0537] Mixture H43

TABLE-US-00057 B(S)-2O-O4 5.0% cl. p. [° C.]: 104.5 CC-3-V1 12.0% Δn [589 nm, 20° C.]: 0.0941 CC-4-V1 10.0% ε.sub.|| [1 kHz, 20° C.]: 3.5 CC-3-5 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 8.4 CCP-3-1 4.0% Δε [1 kHz, 20° C.]: −4.9 CCY-3-O2 11.0% γ.sub.1 [mPa s, 20° C.]: 224 CCY-5-O2 8.0% K.sub.1 [pN, 20° C.]: 22.5 CCZC-3-3 4.0% K.sub.3 [pN, 20° C.]: 24.3 CLOY-3-O2 16.5% V.sub.0 [V, 20° C.]: 2.35 CLY-3-O2 10.0% CY-3-O2 4.0% CP-3-O2 1.0% Y-4O-O4 4.5% Σ 100.0%

[0538] Mixture H44

TABLE-US-00058 B(S)-2O-O4 3.0% Δn [589 nm, 20° C.]: 0.0890 B(S)-2O-O5 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.5 B(S)-2O-O6 4.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.1 B-2O-O5 1.0% Δε [1 kHz, 20° C.]: −3.6 CC-3-V 25.0% K.sub.1 [pN, 20° C.]: 17.6 CC-3-V1 8.0% K.sub.3 [pN, 20° C.]: 16.7 CC-4-V1 8.0% V.sub.0 [V, 20° C.]: 2.27 CC-3-5 12.0% CCY-3-O2 10.0% CLOY-3-O2 4.5% CLY-3-O2 10.0% CLY-3-O3 5.0% Y-4O-O4 5.5% Σ 100.0%

[0539] Mixture H45

TABLE-US-00059 CC-3-O1 15.0% Δn [589 nm, 20° C.]: 0.0784 CCOC-4-3 4.0% ε.sub.|| [1 kHz, 20° C.]: 4.4 CCY-3-O1 7.0% ε.sub.⊥ [1 kHz, 20° C.]: 10.3 CCY-3-O2 2.0% Δε [1 kHz, 20° C.]: −5.9 CCY-3-O3 7.0% K.sub.1 [pN, 20° C.]: 14.1 CCY-4-O2 8.0% K.sub.3 [pN, 20° C.]: 14.9 CCY-5-O2 8.0% V.sub.0 [V, 20° C.]: 1.68 CCZC-3-3 2.5% LTS bulk [h, −20° C.]: 1000 CCZC-3-5 2.0% CCZC-4-3 3.0% CCZC-4-5 3.0% CLOY-3-O2 15.0% CY-5-O2 14.5% Y-4O-O4 9.0% Σ 100.0%

[0540] Mixture H46

TABLE-US-00060 CC-3-O1 17.5% Δn [589 nm, 20° C.]: 0.0770 CCOC-4-3 4.0% ε.sub.|| [1 kHz, 20° C.]: 4.3 CCPC-33 3.5% ε.sub.⊥ [1 kHz, 20° C.]: 9.7 CCY-3-O1 7.0% Δε [1 kHz, 20° C.]: −5.4 CCY-3-O3 4.0% K.sub.1 [pN, 20° C.]: 14.1 CCY-4-O2 8.0% K.sub.3 [pN, 20° C.]: 15.1 CCY-5-O2 7.0% V.sub.0 [V, 20° C.]: 1.77 CCZC-3-3 2.5% LTS bulk [h, −20° C.]: 1000 CCZC-3-5 2.0% CCZC-4-3 3.0% CCZC-4-5 3.0% CLOY-3-O2 15.0% CY-5-O2 14.5% Y-4O-O4 9.0% Σ 100.0%

[0541] Mixture H47

TABLE-US-00061 B(S)-2O-O6 3.5% cl. p. [° C.]: 124.9 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1001 CC-3-V 15.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.9 CC-4-V1 4.0% Δε [1 kHz, 20° C.]: −3.7 CC-3-4 3.5% γ.sub.1 [mPa s, 20° C.]: 199 CC-3-5 5.0% K.sub.1 [pN, 20° C.]: 26.0 CCP-3-1 5.0% K.sub.3 [pN, 20° C.]: 23.5 CCP-V2-1 5.5% V.sub.0 [V, 20° C.]: 2.67 CCY-3-O1 5.5% CCY-3-O2 7.0% CCY-5-O2 6.0% CLY-3-O2 7.0% CLY-3-O3 6.0% CLY-4-O2 5.0% CLY-5-O2 5.0% COB(S)-2-O4 3.5% CCOC-3-3 1.0% CLOY-3-O2 1.5% Σ 100.0%

[0542] Mixture H48

TABLE-US-00062 B(S)-2O-O5 4.0% cl. p. [° C.]: 84.2 BCN-35 20.0% Δn [589 nm, 20° C.]: 0.0751 CC-3-O1 20.0% ε.sub.|| [1 kHz, 20° C.]: 4.8 CCOC-4-3 4.0% ε.sub.⊥ [1 kHz, 20° C.]: 12.1 CCY-3-O1 7.0% Δε [1 kHz, 20° C.]: −7.3 CCY-3-O3 5.0% K.sub.1 [pN, 20° C.]: 14.6 CCY-4-O2 8.5% K.sub.3 [pN, 20° C.]: 16.6 CLOY-3-O2 20.0% V.sub.0 [V, 20° C.]: 1.59 Y-4O-O4 11.5% Σ 100.0%

[0543] Mixture H49

TABLE-US-00063 B(S)-2O-O4 1.0% cl. p. [° C.]: 116.3 CC-3-V 3.5% Δn [589 nm, 20° C.]: 0.0898 CC-3-V1 12.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-4-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.3 CC-3-5 12.5% Δε [1 kHz, 20° C.]: −3.2 CCP-3-1 10.0% γ.sub.1 [mPa s, 20° C.]: 242 CCY-3-O2 10.0% K.sub.1 [pN, 20° C.]: 26.0 CLOY-3-O2 25.0% K.sub.3 [pN, 20° C.]: 28.5 CLY-3-O2 10.0% V.sub.0 [V, 20° C.]: 3.14 CCP-3-2V 6.0% Σ 100.0%

[0544] Mixture H50

TABLE-US-00064 ACC-2-3 5.0% cl. p. [° C.]: 117.4 B(S)-2O-O4 2.5% Δn [589 nm, 20° C.]: 0.0903 CC-3-V 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 12.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CC-4-V1 10.0% Δε [1 kHz, 20° C.]: −3.5 CC-3-5 12.0% γ.sub.1 [mPa s, 20° C.]: 239 CCP-3-1 11.75% K.sub.1 [pN, 20° C.]: 28.0 CCY-3-O2 10.0% K.sub.3 [pN, 20° C.]: 28.3 CLOY-3-O2 23.25% V.sub.0 [V, 20° C.]: 3.01 CLY-3-O2 10.0% Σ 100.0%

[0545] Mixture H51

TABLE-US-00065 B(S)-2O-O4 2.5% cl. p. [° C.]: 116.7 CC-3-V 3.25% Δn [589 nm, 20° C.]: 0.0899 CC-3-V1 12.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-4-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CC-3-5 12.5% Δε [1 kHz, 20° C.]: −3.3 CCL-3-2 6.0% γ.sub.1 [mPa s, 20° C.]: 232 CCP-3-1 9.75% CCY-3-O2 11.0% CLOY-3-O2 23.0% CLY-3-O2 10.0% Σ 100.0%

[0546] Mixture H52

TABLE-US-00066 B(S)-2O-O4 4.0% cl. p. [° C.]: 120.4 B(S)-2O-O5 2.0% Δn [589 nm, 20° C.]: 0.0967 B(S)-2O-O6 2.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V 4.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-3-V1 11.0% Δε [1 kHz, 20° C.]: −3.6 CC-4-V1 9.75% γ.sub.1 [mPa s, 20° C.]: 224 CC-3-5 11.0% K.sub.1 [pN, 20° C.]: 27.8 CCL-3-2 3.0% K.sub.3 [pN, 20° C.]: 26.5 CCP-3-1 4.0% V.sub.0 [V, 20° C.]: 2.87 CCP-V2-1 9.0% CCY-3-O2 8.75% CCZC-3-5 3.0% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-5-O2 4.5% Σ 100.0%

[0547] Mixture H53

TABLE-US-00067 B(S)-2O-O4 4.0% cl. p. [° C.]: 107 CC-3-V 11.5% Δn [589 nm, 20° C.]: 0.0841 CC-3-V1 14.0% ε.sub.|| [1 kHz, 20° C.]: 3.0 CC-4-V1 12.0% ε.sub.⊥ [1 kHz, 20° C.]: 5.4 CCC-3-V 5.0% Δε [1 kHz, 20° C.]: −2.5 CC-3-O3 8.0% γ.sub.1 [mPa s, 20° C.]: 140 CC-3-5 5.0% K.sub.1 [pN, 20° C.]: 23.5 CCP-3-1 6.75% K.sub.3 [pN, 20° C.]: 24.1 CCY-3-O2 10.0% V.sub.0 [V, 20° C.]: 3.31 CLOY-3-O2 13.75% CLY-3-O2 9.0% CP-3-O2 1.0% Σ 100.0%

[0548] Mixture H54

TABLE-US-00068 B(S)-2O-O4 3.75% cl. p. [° C.]: 121 CC-3-V1 9.0% Δn [589 nm, 20° C.]: 0.0948 CC-4-V1 9.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-V-V1 5.5% ε.sub.⊥ [1 kHz, 20° C.]: 6.5 CC-3-O3 4.0% Δε [1 kHz, 20° C.]: −3.4 CC-3-5 11.5% γ.sub.1 [mPa s, 20° C.]: 218 CCP-3-1 12.0% K.sub.1 [pN, 20° C.]: 27.1 CCY-3-O2 10.0% K.sub.3 [pN, 20° C.]: 27.2 CCY-5-O2 1.5% V.sub.0 [V, 20° C.]: 2.98 CLOY-3-O2 12.5% CLY-3-O2 9.0% CLY-3-O3 3.75% CLY-4-O2 4.0% CLY-5-O2 4.5% Σ 100.0%

[0549] Mixture H55

TABLE-US-00069 B(S)-2O-O4 2.5% cl. p. [° C.]: 119 CC-1V-V1 5.0% Δn [589 nm, 20° C.]: 0.0939 CC-3-V 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 8.75% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-4-V1 1.75% Δε [1 kHz, 20° C.]: −3.6 CC-3-O3 4.0% γ.sub.1 [mPa s, 20° C.]: 227 CC-3-5 11.5% K.sub.1 [pN, 20° C.]: 26.2 CCP-3-1 9.0% K.sub.3 [pN, 20° C.]: 27.9 CCY-3-O2 10.0% V.sub.0 [V, 20° C.]: 2.95 CCY-5-O2 1.5% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-3-O3 4.0% CLY-4-O2 5.0% CLY-5-O2 5.0% Σ 100.0%

[0550] Mixture H56

TABLE-US-00070 CC-3-O3 8.9% Cl. p. [° C.]: 103.7 CC-2-3 8.7% Δn [589 nm, 20° C.]: 0.0816 CCY-3-O2 9.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-5 12.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CCY-5-O2 9.0% Δε [1 kHz, 20° C.]: −4.0 CC-3-V 1.2% γ.sub.1 [mPa s, 20° C.]: 205 CCY-3-O1 8.0% K.sub.1 [pN, 20° C.]: 22.4 CC-3-V1 8.0% K.sub.3 [pN, 20° C.]: 23.1 CLY-3-O2 9.0% V.sub.0 [V, 20° C.]: 2.54 CCY-3-O3 5.0% CC-3-2V1 2.8% Y-4O-O4 2.3% CLOY-3-O2 15.1% CY-1-O2 1.0% Σ 100.0%

[0551] Mixture H57

TABLE-US-00071 B(S)-2O-O5 3.0% Cl. p. [° C.]: 98.1 CC-3-V1 10.0% Δn [589 nm, 20° C.]: 0.0839 CC-4-V1 8.5% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-O3 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CC-3-5 5.0% Δε [1 kHz, 20° C.]: −4.1 CCY-3-O2 8.0% γ.sub.1 [mPa s, 20° C.]: 186 CCY-5-O2 3.0% K.sub.1 [pN, 20° C.]: 22.9 CCZC-3-3 3.5% K.sub.3 [pN, 20° C.]: 23.6 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.54 CLY-3-O2 9.0% LTS bulk [h, −20° C.]: 456 CLY-5-O2 5.0% CWC-3-3 15.0% Y-4O-O4 7.0% Σ 100.0%

[0552] Mixture H58

TABLE-US-00072 CC-3-V1 10.0% Cl. p. [° C.]: 103.4 CC-4-V1 16.0% Δn [589 nm, 20° C.]: 0.0841 CC-3-O3 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-5 6.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.4 CCY-3-O2 8.0% Δε [1 kHz, 20° C.]: −4.0 CCY-5-O2 3.0% γ.sub.1 [mPa s, 20° C.]: 191 CCZC-3-3 4.0% K.sub.1 [pN, 20° C.]: 22.1 CCZC-3-5 2.5% K.sub.3 [pN, 20° C.]: 22.3 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.49 CLY-3-O2 9.0% CLY-4-O2 2.5% CLY-5-O2 5.0% CCY-V-O2 5.0% Y-4O-O4 6.0% Σ 100.0%

[0553] Mixture H59

TABLE-US-00073 CC-3-V1 10.0% Cl. p. [° C.]: 103.1 CC-4-V1 16.0% Δn [589 nm, 20° C.]: 0.0844 CC-3-O3 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-5 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CCY-3-O2 8.0% Δε [1 kHz, 20° C.]: −3.9 CCY-V-O1V 3.0% γ.sub.1 [mPa s, 20° C.]: 194 CCZC-3-3 4.0% K.sub.1 [pN, 20° C.]: 21.7 CCZC-3-5 4.0% K.sub.3 [pN, 20° C.]: 21.8 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.50 CLY-3-O2 9.0% LTS bulk [h, −20° C.]: 1000 CLY-3-O3 1.0% CLY-4-O2 5.0% CLY-5-O2 3.5% CY-5-O2 4.5% Y-4O-O4 4.0% Σ 100.0%

[0554] Mixture H60

TABLE-US-00074 B(S)-2O-O4 4.0% Cl. p. [° C.]: 117.6 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1019 B(S)-2O-O6 1.5% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CC-4-V1 15.5% Δε [1 kHz, 20° C.]: −3.7 CC-3-5 12.0% γ.sub.1 [mPa s, 20° C.]: 211 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 29.5 CCP-3-3 2.25% K.sub.3 [pN, 20° C.]: 30.0 CCP-V2-1 5.5% V.sub.0 [V, 20° C.]: 3.01 CCY-3-O2 9.0% CLOY-3-O2 12.0% CLY-3-O2 9.0% CLY-5-O2 3.25% LPOY-3-O2 5.0% Σ 100.0%

[0555] Mixture H61

TABLE-US-00075 CC-3-V1 10.0% Cl. p. [° C.]: 100.5 CC-4-V1 16.0% Δn [589 nm, 20° C.]: 0.0849 CC-3-O3 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-5 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.4 CCY-3-O2 8.0% Δε [1 kHz, 20° C.]: −4.0 CCY-5-O2 2.5% γ.sub.1 [mPa s, 20° C.]: 180 CCZC-3-3 4.0% K.sub.1 [pN, 20° C.]: 21.2 CCZC-3-5 4.0% K.sub.3 [pN, 20° C.]: 20.6 CLOY-V-O2 15.0% V.sub.0 [V, 20° C.]: 2.40 CLY-3-O2 9.0% CLY-3-O3 1.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CY-5-O2 2.0% Y-4O-O4 5.5% Σ 100.0%

[0556] Mixture H62

TABLE-US-00076 B(S)-2O-O4 4.0% Cl. p. [° C.]: 119.5 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0934 CC-3-V 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-4-V1 10.0% Δε [1 kHz, 20° C.]: −3.6 CC-3-4 2.0% γ.sub.1 [mPa s, 20° C.]: 231 CC-3-5 9.0% K.sub.1 [pN, 20° C.]: 27.2 CCP-3-1 3.5% K.sub.3 [pN, 20° C.]: 26.2 CCP-V2-1 5.5% V.sub.0 [V, 20° C.]: 2.86 CCY-3-O2 9.0% LTS bulk [h, −20° C.]: 1000 CCZC-3-3 2.0% CCZC-3-5 4.0% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-5-O2 5.0% CWC-3-3 5.0% Σ 100.0%

[0557] Mixture H63

TABLE-US-00077 B(S)-2O-O4 4.0% Cl. p. [° C.]: 120 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1029 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-4-V1 15.0% Δε [1 kHz, 20° C.]: −3.6 CC-3-5 10.5% γ.sub.1 [mPa s, 20° C.]: 222 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 28.4 CCP-3-3 2.5% K.sub.3 [pN, 20° C.]: 27.8 CCP-V2-1 10.0% V.sub.0 [V, 20° C.]: 2.94 CWCY-3-O2 5.0% CLOY-3-O2 15.0% CLY-3-O2 7.0% CLY-5-O2 5.0% CPY-3-O2 1.0% Σ 100.0%

[0558] Mixture H64

TABLE-US-00078 CC-3-V1 10.0% Cl. p. [° C.]: 105 CC-4-V1 16.0% Δn [589 nm, 20° C.]: 0.0838 CC-3-O3 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-5 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CWCY-3-O2 8.0% Δε [1 kHz, 20° C.]: −4.0 CCY-5-O2 2.5% γ.sub.1 [mPa s, 20° C.]: 207 CCZC-3-3 4.0% K.sub.1 [pN, 20° C.]: 22.8 CCZC-3-5 4.0% K.sub.3 [pN, 20° C.]: 22.8 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.54 CLY-3-O2 9.0% CLY-3-O3 1.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CY-5-O2 2.0% Y-4O-O4 5.5% Σ 100.0%

[0559] Mixture H65

TABLE-US-00079 CC-3-V1 10.0% Cl. p. [° C.]: 102.8 CC-4-V1 10.5% Δn [589 nm, 20° C.]: 0.0860 CC-3-O3 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-5 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CCS-3-2 10.0% Δε [1 kHz, 20° C.]: −3.9 CCY-3-O2 8.0% γ.sub.1 [mPa s, 20° C.]: 187 CCY-5-O2 2.5% K.sub.1 [pN, 20° C.]: 23.1 CCZC-3-3 2.0% K.sub.3 [pN, 20° C.]: 21.9 CCZC-3-5 2.25% V.sub.0 [V, 20° C.]: 2.49 CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-3-O3 3.0% CLY-4-O2 3.0% CLY-5-O2 5.0% Y-4O-O4 6.75% Σ 100.0%

[0560] Mixture H66

TABLE-US-00080 CC-4-V1 16.0% Cl. p. [° C.]: 100.1 CC-3-O3 8.0% Δn [589 nm, 20° C.]: 0.0821 CC-3-5 5.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCY-3-O2 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CCY-5-O2 2.5% Δε [1 kHz, 20° C.]: −4.1 CCZC-3-3 4.0% γ.sub.1 [mPa s, 20° C.]: 235 CCZC-3-5 4.0% K.sub.1 [pN, 20° C.]: 21.5 CLOC-3-2 10.0% K.sub.3 [pN, 20° C.]: 19.9 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.32 CLY-3-O2 9.0% CLY-3-O3 1.0% CLY-4-O2 5.0% CLY-5-O2 5.0% CY-5-O2 2.0% Y-4O-O4 5.5% Σ 100.0%

[0561] Mixture H67

TABLE-US-00081 B(S)-2O-O4 4.0% Cl. p. [° C.]: 119.5 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1118 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CC-4-V1 15.0% Δε [1 kHz, 20° C.]: −3.6 CC-3-5 10.5% γ.sub.1 [mPa s, 20° C.]: 218 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 27.5 CCP-3-3 1.5% K.sub.3 [pN, 20° C.]: 27.1 CCP-V2-1 10.0% V.sub.0 [V, 20° C.]: 2.89 CLOY-3-O2 14.0% CLY-3-O2 7.0% CLY-5-O2 5.0% CWCY-V-O4 8.0% Σ 100.0%

[0562] Mixture H68

TABLE-US-00082 CP-3-O2 20.2% Cl. p. [° C.]: 73.7 CCY-3-O2 9.0% Δn [589 nm, 20° C.]: 0.1640 CCP-3-1 4.3% ε.sub.|| [1 kHz, 20° C.]: 5.8 PGIGI-3-F 5.4% ε.sub.⊥ [1 kHz, 20° C.]: 2.8 CCY-5-O2 7.4% Δε [1 kHz, 20° C.]: 3.1 CPTP-3-2 10.0% γ.sub.1 [mPa s, 20° C.]: 57 CPY-3-O2 9.0% K.sub.1 [pN, 20° C.]: 15.5 PP-1-2V1 6.0% K.sub.3 [pN, 20° C.]: 12.9 CLP-V-1 5.0% V.sub.0 [V, 20° C.]: 2.39 B(S)-2O-O5 4.0% B(S)-2O-O4 3.0% B(S)-2O-O6 1.7% CLOY-3-O2 15.0% Σ 100.0%

[0563] Mixture H69

TABLE-US-00083 CP-3-O2 20.2% Cl. p. [° C.]: 73 CCY-3-O2 9.0% Δn [589 nm, 20° C.]: 0.1638 CCP-3-1 4.3% ε.sub.|| [1 kHz, 20° C.]: 5.8 PGIGI-3-F 5.4% ε.sub.⊥ [1 kHz, 20° C.]: 2.8 CCY-5-O2 7.4% Δε [1 kHz, 20° C.]: 3.1 CPTP-3-2 10.0% γ.sub.1 [mPa s, 20° C.]: 56 CPY-3-O2 9.0% PP-1-2V 6.0% CLP-V-1 5.0% B(S)-2O-O5 4.0% B(S)-2O-O4 3.0% B(S)-2O-O6 1.7% CLOY-3-O2 15.0% Σ 100.0%

[0564] Mixture H70

TABLE-US-00084 B(S)-2O-O4 4.0% Cl. p. [° C.]: 120.1 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.1008 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CC-4-V1 15.75% Δε [1 kHz, 20° C.]: −3.5 CC-3-5 11.0% γ.sub.1 [mPa s, 20° C.]: 221 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 28.2 CCP-3-3 3.0% K.sub.3 [pN, 20° C.]: 26.9 CCP-V2-1 6.75% V.sub.0 [V, 20° C.]: 2.92 CCQPC-2-3 3.0% LTS bulk [h, −20° C.]: 432 CCY-3-O2 6.0% CLOY-3-O2 15.0% CLY-3-O2 7.0% CLY-5-O2 3.5% Σ 100.0%

[0565] Mixture H71

TABLE-US-00085 B(S)-2O-O4 4.0% Cl. p. [° C.]: 116.5 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.1012 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-3-V1 11.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.8 CC-4-V1 15.0% Δε [1 kHz, 20° C.]: −3.6 CC-3-5 11.0% γ.sub.1 [mPa s, 20° C.]: 221 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 29.1 CCY-3-O2 6.0% K.sub.3 [pN, 20° C.]: 28.3 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.95 CLY-3-O2 7.0% CLY-5-O2 5.0% CPY-3-O2 1.5% CCEP-3-1 10.0% Σ 100.0%

[0566] Mixture H72

TABLE-US-00086 B(S)-2O-O4 4.0% Cl. p. [° C.]: 114.6 B(S)-2O-O5 3.5% Δn [589 nm, 20° C.]: 0.1011 CC-3-V1 10.0% ε.sub.|| [1 kHz, 20° C.]: 3.1 CC-4-V1 13.75% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CC-3-5 11.0% Δε [1 kHz, 20° C.]: −3.5 CCP-3-1 8.0% γ.sub.1 [mPa s, 20° C.]: 214 CCP-3-3 3.0% K.sub.1 [pN, 20° C.]: 26.8 CCY-3-O2 6.0% K.sub.3 [pN, 20° C.]: 27.7 CEC-1V-V1 8.0% V.sub.0 [V, 20° C.]: 2.98 CLOY-3-O2 15.0% CLY-3-O2 7.0% CLY-5-O2 5.0% CPY-3-O2 5.75% Σ 100.0%

[0567] Mixture H73

TABLE-US-00087 B(S)-2O-O4 4.0% Cl. p. [° C.]: 75 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1023 B(S)-2O-O6 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.6 CC-3-V 46.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-3-V1 2.75% Δε [1 kHz, 20° C.]: −3.5 CLOY-3-O2 1.0% γ.sub.1 [mPa s, 20° C.]: 80 CLY-3-O3 6.0% K.sub.1 [pN, 20° C.]: 13.8 CLY-4-O2 2.5% K.sub.3 [pN, 20° C.]: 13.9 CPY-2-O2 9.0% V.sub.0 [V, 20° C.]: 2.12 CPY-3-O2 9.0% CY-3-O4 8.5% PGIY-2-O4 3.75% Σ 100.0%

[0568] Mixture H74

TABLE-US-00088 B(S)-2O-O4 3.0% Cl. p. [°C.]: 118.9 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1048 B(S)-2O-O6 3.0% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-4-V1 11.5% Δε [1 kHz, 20° C.]: −3.9 CC-3-5 11.0% γ.sub.1 [mPa s, 20° C.]: 211 CCP-3-1 8.0% K.sub.1 [pN, 20° C.]: 28.9 CCP-3-3 3.0% K.sub.3 [pN, 20° C.]: 29.0 CCP-V2-1 8.5% V.sub.0 [V, 20° C.]: 2.90 CCY-3-O2 9.0% CLOY-3-O2 12.5% CLY-3-O2 7.0% CLY-5-O2 5.0% B(S)-4O-O5 2.5% CP-3-O2 2.0% Σ 100.0%

[0569] Mixture H75

TABLE-US-00089 B(S)-2O-O5 3.0% cl. p. [°C.]: 99.2 CC-3-V 21.0% Δn [589 nm, 20° C.]: 0.0906 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-4-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CC-3-4 1.5% Δε [1 kHz, 20° C.]: −4.0 CC-3-5 8.0% γ.sub.1 [mPa s, 20° C.]: 152 CCY-3-O2 9.0% K.sub.1 [pN, 20° C.]: 20.5 CLOY-3-O2 12.0% K.sub.3 [pN, 20° C.]: 20.8 CLY-3-O2 9.0% V.sub.0 [V, 20° C.]: 2.41 CLY-3-O3 6.0% LTS bulk [h, −20° C.]: 1000 CLY-5-O2 5.0% COB(S)-2-O4 5.0% CVCOY-3-O2 1.75% Y-4O-O4 2.75% Σ 100.0%

[0570] Mixture H76

TABLE-US-00090 CC-3-V 34.5% cl. p. [°C.]: 87.7 CC-3-V1 7.0% Δn [589 nm, 20° C.]: 0.0931 CCY-3-O2 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.5 CLOY-3-O2 6.5% ε.sub.⊥ [1 kHz, 20° C.]: 6.6 CLY-3-O2 9.0% Δε [1 kHz, 20° C.]: −3.1 CLY-3-O3 6.0% γ.sub.1 [mPa s, 20° C.]: 113 CLY-4-O2 5.0% K.sub.1 [pN, 20° C.]: 16.0 CLY-5-O2 5.0% K.sub.3 [pN, 20° C.]: 18.5 CY-3-O2 12.0% V.sub.0 [V, 20° C.]: 2.59 PYP-2-3 5.5% CCU-2-F 1.5% Σ 100.0%

[0571] Mixture H77

TABLE-US-00091 CC-3-V 12.0% cl. p. [°C.]: 96 CC-3-V1 8.0% Δn [589 nm, 20° C.]: 0.0836 CC-4-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CCC-3-V 5.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CC-3-4 4.0% Δε [1 kHz, 20° C.]: −3.9 CC-3-5 8.0% γ.sub.1 [mPa s, 20° C.]: 147 CCP-3-1 0.75% K.sub.1 [pN, 20° C.]: 20.5 CCY-3-O2 9.0% K.sub.3 [pN, 20° C.]: 20.6 CCY-5-O2 2.0% V.sub.0 [V, 20° C.]: 2.44 CLOY-3-O2 15.0% LTS bulk [h, −20° C.]: 1000 CLY-3-O2 9.0% CLY-3-O3 5.0% CLY-5-O2 5.0% COB(S)-2-O4 1.0% Y-4O-O4 8.25% Σ 100.0%

[0572] Mixture H78

TABLE-US-00092 B(S)-2O-O5 3.0% cl. p. [°C.]: 96.2 CC-3-V 17.5% Δn [589 nm, 20° C.]: 0.0937 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-4-V1 12.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CC-3-4 4.0% Δε [1 kHz, 20° C.]: −3.9 CC-3-5 8.0% γ.sub.1 [mPa s, 20° C.]: 149 CCY-3-O2 9.0% K.sub.1 [pN, 20° C.]: 21.4 CCY-5-O2 2.5% K.sub.3 [pN, 20° C.]: 21.2 CLOY-3-O2 15.0% V.sub.0 [V, 20° C.]: 2.45 CLY-3-O2 9.0% CLY-5-O2 5.0% B(S)-2O-OiPr 6.5% Y-4O-O4 0.5% Σ 100.0%

[0573] Mixture H79

TABLE-US-00093 B(S)-2O-O4 3.0% cl. p. [°C.]: 98.5 B(S)-2O-O5 3.0% Δn [589 nm, 20° C.]: 0.0917 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-V 7.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.8 CC-3-V1 6.0% Δε [1 kHz, 20° C.]: −4.4 CC-4-V1 7.0% γ.sub.1 [mPa s, 20° C.]: 156 CC-2-3 4.5% K.sub.1 [pN, 20° C.]: 22.3 CC-3-O3 7.0% K.sub.3 [pN, 20° C.]: 19.9 CC-3-4 5.0% V.sub.0 [V, 20° C.]: 2.25 CC-3-5 8.0% CCY-3-1 2.0% CCY-3-O1 3.0% CCY-3-O2 6.0% CCY-5-O2 8.0% CLOY-3-O2 4.0% CLY-3-O2 9.0% CLY-3-O3 3.0% CLY-5-O2 3.5% CNI(F)-5-O2 7.0% Σ 100.0%

[0574] Mixture H80

TABLE-US-00094 B(S)-2O-O4 4.0% cl. p. [°C.]: 99 B(S)-2O-O5 2.5% Δn [589 nm, 20° C.]: 0.0938 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.4 CC-3-V 27.5% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CC-3-V1 8.0% Δε [1 kHz, 20° C.]: −4.1 CC-3-O3 2.0% γ.sub.1 [mPa s, 20° C.]: 155 CC-3-5 8.0% K.sub.1 [pN, 20° C.]: 21.1 CCP-3-1 2.0% K.sub.3 [pN, 20° C.]: 22.4 CCY-3-O2 11.0% V.sub.0 [V, 20° C.]: 2.46 CCY-5-O2 2.0% CLOY-3-O2 14.0% CLY-3-O2 9.0% CLY-5-O2 5.0% DCY-3-O2 1.0% Σ 100.0%

[0575] Mixture H81

TABLE-US-00095 B(S)-2O-O4 4.0% cl. p. [°C.]: 97.9 B(S)-2O-O5 2.0% Δn [589 nm, 20° C.]: 0.0935 B(S)-2O-O6 4.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-V 27.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.5 CC-3-V1 8.0% Δε [1 kHz, 20° C.]: −4.2 CC-3-5 10.5% γ.sub.1 [mPa s, 20° C.]: 155 CCP-3-1 2.0% K.sub.1 [pN, 20° C.]: 21.3 CCY-3-O2 11.0% K.sub.3 [pN, 20° C.]: 22.4 CCY-5-O2 1.5% CLOY-3-O2 15.0% CLY-3-O2 9.0% CLY-5-O2 5.0% LOY-3-O2 1.0% Σ 100.0%

[0576] Mixture H82

TABLE-US-00096 B(S)-2O-O5 3.0% cl. p. [°C.]: 98.5 CC-3-V 22.0% Δn [589 nm, 20° C.]: 0.0902 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-O3 4.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.3 CC-3-4 4.5% Δε [1 kHz, 20° C.]: −4.0 CC-3-5 8.0% γ.sub.1 [mPa s, 20° C.]: 154 CCY-3-O1 3.0% K.sub.1 [pN, 20° C.]: 20.9 CCY-3-O2 9.0% K.sub.3 [pN, 20° C.]: 21.0 CLOY-3-O2 12.0% V.sub.0 [V, 20° C.]: 2.41 CLY-3-O2 9.0% LTS bulk [h, −20° C.]: 1000 CLY-3-O3 4.0% CLY-5-O2 4.0% COB(S)-2-O4 5.0% CPY-3-O2 1.5% LOY-3-O2 3.0% Σ 100.0%

[0577] Mixture H83

TABLE-US-00097 B(S)-2O-O5 3.0% cl. p. [°C.]: 100.5 CC-3-V 28.0% Δn [589 nm, 20° C.]: 0.0914 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-4-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CCP-3-1 2.0% Δε [1 kHz, 20° C.]: −3.8 CCY-3-O2 9.0% γ.sub.1 [mPa s, 20° C.]: 144 CLOY-3-O2 12.0% K.sub.1 [pN, 20° C.]: 19.9 CLY-3-O2 8.0% K.sub.3 [pN, 20° C.]: 21.1 CLY-3-O3 5.0% V.sub.0 [V, 20° C.]: 2.47 CLY-5-O2 5.0% LTS bulk [h, −20° C.]: 912 COB(S)-2-O4 5.0% CCNI(F)-3-O4 3.5% Y-4O-O4 1.5% Σ 100.0%

[0578] Mixture H84

TABLE-US-00098 B(S)-2O-O5 3.0% cl. p. [°C.]: 100.1 CC-3-V 25.0% Δn [589 nm, 20° C.]: 0.0912 CC-3-V1 8.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-4-V1 10.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CC-3-5 3.0% Δε [1 kHz, 20° C.]: −3.9 CCP-3-1 1.0% γ.sub.1 [mPa s, 20° C.]: 148 CCY-3-O2 9.0% K.sub.1 [pN, 20° C.]: 19.9 CLOY-3-O2 12.0% K.sub.3 [pN, 20° C.]: 21.0 CLY-3-O2 8.0% V.sub.0 [V, 20° C.]: 2.45 CLY-3-O3 5.0% LTS bulk [h, −20° C.]: 1000 CLY-5-O2 5.0% COB(S)-2-O4 5.0% CCZY-3-O2 3.5% Y-4O-O4 2.5% Σ 100.0%

[0579] Mixture H85

TABLE-US-00099 B(S)-2O-O5 3.0% cl. p. [°C.]: 94.4 B(S)-2O-O6 2.0% Δn [589 nm, 20° C.]: 0.0899 CC-3-V 30.0% ε.sub.|| [1 kHz, 20° C.]: 3.3 CC-3-V1 8.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.2 CC-3-5 8.0% Δε [1 kHz, 20° C.]: −3.9 CCY-3-O2 9.0% γ.sub.1 [mPa s, 20° C.]: 141 CLOY-3-O2 15.0% K.sub.1 [pN, 20° C.]: 19.9 CLY-3-O2 9.0% K.sub.3 [pN, 20° C.]: 21.2 CLY-3-O3 3.0% V.sub.0 [V, 20° C.]: 2.47 CLY-4-O2 5.0% LTS bulk [h, −20° C.]: 672 CLY-5-O2 5.0% PY-1-O2 1.5% Y-4O-O4 1.5% Σ 100.0%

[0580] Mixture H86

TABLE-US-00100 B(S)-2O-O4 4.0% Cl. p. [°C.]: 76 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1014 B(S)-(c5-3en)1O-O4 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.6 CC-3-V 46.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.0 CC-3-V1 2.75% Δε [1 kHz, 20° C.]: −3.5 CLOY-3-O2 1.0% γ.sub.1 [mPa s, 20° C.]: 82 CLY-3-O3 6.0% CLY-4-O2 2.5% CPY-2-O2 9.0% CPY-3-O2 9.0% CY-3-O4 8.5% PGIY-2-O4 3.75% Σ 100.0%

[0581] Mixture H87

TABLE-US-00101 B(S)-2O-O4 4.0% Cl. p. [°C.]: 77 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1031 B(S)-2O-O6 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.2 CC-3-V 46.0% ε.sub.⊥ [1 kHz, 20° C.]: 6.7 CC-3-V1 2.75% Δε [1 kHz, 20° C.]: −3.5 CLOY-3-O2 1.0% γ.sub.1 [mPa s, 20° C.]: 81 CLY-3-O3 6.0% CLY-4-O2 2.5% CPY-2-O2 9.0% CPY-3-O2 9.0% CY-3-O4 8.5% PPY-3-O2 2.0% PGIY-2-O4 1.75% Σ 100.0%

[0582] Mixture H88

TABLE-US-00102 B(S)-2O-O4 4.0% Cl. p. [°C.]: 76 B(S)-2O-O5 4.0% Δn [589 nm, 20° C.]: 0.1025 B(S)-2O-O6 3.5% ε.sub.|| [1 kHz, 20° C.]: 3.5 CC-3-V 46.0% ε.sub.⊥ [1 kHz, 20° C.]: 7.1 CC-3-V1 2.75% Δε [1 kHz, 20° C.]: −3.6 CLOY-3-O2 1.0% γ.sub.1 [mPa s, 20° C.]: 78 CLY-3-O3 6.0% CLY-4-O2 2.5% CPY-2-O2 9.0% CPY-3-O2 9.0% CY-3-O4 8.5% PPY-3-O2 2.0% PEPY-3-O2 1.75% Σ 100.0%