LIQUID-CRYSTAL MEDIUM

Abstract

A liquid-crystal (LC) material having negative dielectric anisotropy and the use thereof for optical, electro-optical and electronic purposes, such as for example in LC displays, in particular energy saving displays based on the ECB, IPS or FFS effect, where the liquid crystal medium contains one or more compounds of formula I

##STR00001##

and one or more compounds compounds of formulae IIA, IIB, IIC and IID

##STR00002##

Claims

1. A liquid crystal medium comprising a) one or more compounds of formula I ##STR00505## in which R.sup.1 and R.sup.2, identically or differently, denote H, halogen, straight chain alkyl or alkoxy having 1 to 15 C atoms, straight chain alkenyl or alkenyloxy having 2 to 15 C atoms or branched alkyl or alkoxy or alkenyl or alkenyloxy having 3 to 15 C atoms, where one or more CH.sub.2 groups in these radicals may each be replaced, independently of one another, by ##STR00506## CC, CF.sub.2O, OCF.sub.2, CHCH, O, COO or OCO in such a way that O atoms are not linked directly to one another, and in which one or more H atoms may be replaced by halogen, A.sup.0, A.sup.1, and A.sup.2, each, independently of one another, denote phenylene-1,4-diyl, in which one or two CH groups may be replaced by N and one or more H atoms may be replaced by halogen, CN, CH.sub.3, CHF.sub.2, CH.sub.2F, CF.sub.3, OCH.sub.3, OCHF.sub.2 or OCF.sub.3, or denote cyclohexane-1,4-diyl, in which one or two non-adjacent CH.sub.2 groups may be replaced, independently of one another, by O and/or S and one or more H atoms may be replaced by F, or denote cyclohexene-1,4-diyl, bicyclo[1.1.1]-pentane-1,3-diyl, bicyclo[2.2.2]octane-1,4-diyl, spiro[3.3]heptane-2,6-diyl, tetrahydropyran-2,5-diyl or 1,3-dioxane-2,5-diyl, Z.sup.1 and Z.sup.2, each, independently of one another, denote CF.sub.2O, OCF.sub.2, CH.sub.2O, OCH.sub.2, COO, OCO, C.sub.2H.sub.4, C.sub.2F.sub.4, CF.sub.2CH.sub.2, CH.sub.2CF.sub.2, CFHCFH, CFHCH.sub.2, CH.sub.2CFH, CF.sub.2CFH, CFHCF.sub.2, CHCH, CFCH, CHCF, CFCF, CC or a single bond, m denotes 0, 1, 2 or 3, and n denotes 0, 1, 2 or 3; and b) one or more compounds selected from the group of compounds of formulae IIA, IIB, IIC and IID ##STR00507## in which R.sup.2A, R.sup.2B, R.sup.2C and R.sup.2D identically or differently, denote H, straight chain alkyl or alkoxy having 1 to 15 C atoms, straight chain alkenyl or alkenyloxy having 2 to 15 C atoms or branched alkyl or alkoxy or alkenyl or alkenyloxy having 3 to 15 C atoms, where one or more CH.sub.2 groups in these radicals may each be replaced, independently of one another, by ##STR00508## CC, CF.sub.2O, OCF.sub.2, CHCH, by O, COO or OCO in such a way that O atoms are not linked directly to one another, and in which one or more H atoms may be replaced by halogen, 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, CHCH, CF.sub.2O, OCF.sub.2, CH.sub.2O, OCH.sub.2, COO, OCO, C.sub.2F.sub.4, CFCF or CHCHCH.sub.2O, (O) denotes O or a single bond, p denotes 0, 1 or 2, q denotes 0 or 1, and v denotes an integer from 1 to 6.

2. The liquid crystal medium according to claim 1, wherein the total amount of the one or more compounds selected from the group of compounds of formulae IIA, IIB, IIC and IID is in the range of 9% to 70%.

3. The liquid crystal medium according to claim 1, wherein the one or more compounds of formula I are selected from the group of compounds of formulae I-1 to I-6 ##STR00509## in which R.sup.1 and R.sup.2 have the meanings given for formula I, L is halogen, CN, CH.sub.3, CHF.sub.2, CH.sub.2F, CF.sub.3, OCH.sub.3, OCHF.sub.2 or OCF.sub.3, and r, s and t independently are 0, 1, 2, 3, or 4.

4. The liquid crystal medium according to claim 3, wherein the group ##STR00510## in the formulae I-1 to 1-6 denotes ##STR00511##

5. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of formula III ##STR00512## 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 ##STR00513## CC, CF.sub.2O, OCF.sub.2, CHCH, by O, COO or OCO in such a way that O atoms are not linked directly to one another, and in which one or more H atoms may 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 be replaced by O or S, b) a 1,4-phenylene radical, in which one or two CH groups may be replaced by N, or c) a radical selected from the group consisting of 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, n denotes 0, 1 or 2, Z.sup.31 on each occurrence independently of one another denotes COO, OCO, 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, CHCHCH.sub.2O, C.sub.2F.sub.4, CH.sub.2CF.sub.2, CF.sub.2CH.sub.2CFCF, CHCF, CFCH, CHCH, CC or a single bond, 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.

6. The liquid crystal medium according to claim 5, wherein W in formula III denotes S.

7. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of formula IV ##STR00514## 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 consisting of compounds of formulae IV-3-1 and IV-3-2: ##STR00515## in which alkyl denotes n-alkyl having 1 to 7 C-atoms.

9. The liquid crystal medium according to claim 1, wherein the medium further comprises one or more compounds of the formula V ##STR00516## in which R.sup.51 and R.sup.52 denote, each independently, alkyl having 1 to 7 C atoms, alkoxy having 1 to 7 C atoms, or alkoxyalkyl, alkenyl or alkenyloxy having 2 to 7 C atoms, ##STR00517## identically or differently, denote ##STR00518## Z.sup.51 and Z.sup.52, identically or differently, denote CH.sub.2CH.sub.2, CH.sub.2O, CHCH, CC, COO or a single bond, and n is 1 or 2.

10. The liquid crystal medium according to claim 1, wherein the medium has a birefringence of 0.105 or more.

11. The liquid crystal medium according to claim 1, wherein the medium comprises a polymerisable compound.

12. A liquid crystal display comprising the liquid crystal medium according to claim 1.

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

14. An energy saving display for gaming comprising the liquid crystal medium according to claim 1.

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 consisting of compounds of formulae IIA, IIB, IIC and IID, and optionally with a polymerisable compound or further liquid crystal compounds or additives.

Description

EXAMPLES

[0522] The present invention is illustrated in detail by the following non-restrictive working examples.

[0523] The following abbreviations and symbols are used: [0524] V.sub.0 threshold voltage, capacitive [V] at 20 C., [0525] n.sub.e extraordinary refractive index at 20 C. and 589 nm, [0526] n.sub.o ordinary refractive index at 20 C. and 589 nm, [0527] n optical anisotropy at 20 C. and 589 nm, [0528] .sub. dielectric permittivity perpendicular to the director at 20 C. and 1 kHz, [0529] .sub. dielectric permittivity parallel to the director at 20 C. and 1 kHz, [0530] dielectric anisotropy at 20 C. and 1 kHz, [0531] cl.p., T(N,I) clearing point [ C.], [0532] .sub.1 rotational viscosity at 20 C. [mPa.Math.s], [0533] K.sub.1 elastic constant, splay deformation at 20 C. [pN], [0534] K.sub.2 elastic constant, twist deformation at 20 C. [pN], [0535] K.sub.3 elastic constant, bend deformation at 20 C. [pN].

[0536] 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.

[0537] 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.

[0538] 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 n is determined at 589 nm and at 1 kHz, unless explicitly indicated otherwise in each case.

[0539] 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).

[0540] 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.

[0541] 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.

[0542] The display used for measurement of the capacitive threshold voltage consists of two plane-parallel glass outer plates with a distance of 25 m, 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.

[0543] 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 m, 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.

[0544] 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).

[0545] The transmission measurements are performed in test cells with fishbone electrode layout (from Merck Ltd., Japan; 1 pixel fishbone electrode (ITO, 1010 mm, 47.7 angle of fishbone with 3 m line/3 m space), 3.2 m cell gap, AF-glass, tilt angle 1).

[0546] 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.

MIXTURE EXAMPLES

[0547] The Mixture Examples M1 to M75 and P1 to P10 have the compositions and physical properties indicated in the following tables:

TABLE-US-00006 Mixture Example M1 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90.4 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1203 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6079 CC-3-V 7.5% n.sub.o [589 nm, 20 C.]: 1.4876 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 4.5% .sub.1 [mPa s, 20 C.]: 107 CCP-3-1 5.5% K.sub.1 [pN, 20 C.]: 19.8 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.2 CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00007 Mixture Example M2 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 89.7 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1194 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6067 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4873 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.1 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 110 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.8 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.1 CLY-5-O2 3.0% CPY-3-O2 11.5% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00008 Mixture Example M3 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 92.3 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1196 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6077 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4881 CC-3-V1 10.0% [1 kHz, 20 C.]: 3.1 CC-3-4 4.0% .sub. [1 kHz, 20 C.]: 3.4 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.5 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 108 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 20.0 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.3 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 7.5% PYS-3-2 7.5% 100.0%

[0548] In the following table, key parameters of the mixtures M1 to M3 are summarized.

TABLE-US-00009 K.sub.avg. .sub.1 .sub.1/K.sub.11 n [pN] [mPas] [mPas/pN] M1 3.0 0.120 16.0 107 5.4 M2 3.1 0.119 16.0 110 5.5 M3 3.1 0.120 16.1 109 5.4

[0549] By using a compound of the formula I in a medium with negative dielectric anisotropy, it was surprisingly found that a favourably low rotational viscosity (.sub.1) and at the same time a very low ratio .sub.1/K.sub.1 can be achieved which improves the response time of a display.

TABLE-US-00010 Mixture Example M4 B(S)-(c3)1O-O2 4.0% T.sub.(N,I) [ C.]: 91.6 B(S)-2O-O5 4.0% n [589 nm, 25 C.]: 0.1200 B(S)-2O-O6 3.0% n.sub.e [25 C., 589.3 nm]: 1.6080 CC-3-V 7.5% n.sub.o [25 C., 589.3 nm]: 1.4880 CC-3-V1 8.0% [1 kHz, 25 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 25 C.]: 3.3 CC-5-V 10.0% .sub. [1 kHz, 25 C.]: 6.3 CC-3-5 4.5% .sub.1 [mPa .Math. s, 25 C.]: 111 CCP-3-1 5.5% CLY-3-O2 9.0% CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0%

TABLE-US-00011 Mixture Example M5 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 91.6 B(S)-2O-O5 4.0% n [589 nm, 25 C.]: 0.1204 B(S)-(c5)1O-O2 3.0% n.sub.e [25 C., 589.3 nm]: 1.6084 CC-3-V 7.5% n.sub.o [25 C., 589.3 nm]: 1.4880 CC-3-V1 8.0% [1 kHz, 25 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 25 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 25 C.]: 6.4 CC-3-5 4.5% .sub.1 [mPa .Math. s, 25 C.]: 112 CCP-3-1 5.5% CLY-3-O2 9.0% CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0%

TABLE-US-00012 Mixture Example M6 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 89.9 B(S)-2O-O5 4.0% n [589 nm, 25 C.]: 0.1231 B(S)-2O-O6 3.0% n.sub.e [25 C., 589.3 nm]: 1.6119 CC-3-V 7.5% n.sub.o [25 C., 589.3 nm]: 1.4888 CC-3-V1 8.0% [1 kHz, 25 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 25 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 25 C.]: 6.4 CC-3-5 4.5% .sub.1 [mPa .Math. s, 25 C.]: 111 CCP-3-1 5.5% CLY-3-O2 9.0% CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-(c5)-2 5.0% PY-1-O2 10.0%

TABLE-US-00013 Mixture Example M7 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 91.6 B(S)-2O-O5 4.0% n [589 nm, 25 C.]: 0.1200 B(S)-2O-O6 3.0% n.sub.e [25 C., 589.3 nm]: 1.6080 CC-3-V 7.5% n.sub.o [25 C., 589.3 nm]: 1.4880 CC-3-V1 8.0% [1 kHz, 25 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 25 C.]: 3.3 CC-5-V 10.0% .sub. [1 kHz, 25 C.]: 6.3 CC-3-5 4.5% K.sub.1 [pN, 25 C.]: 17.3 CLP-V-1 5.5% K.sub.3 [pN, 25 C.]: 16.4 CLY-3-O2 9.0% .sub.1 [mPa .Math. s, 25 C.]: 109 CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0%

TABLE-US-00014 Mixture Example M8 B(S)-2O-O5 3.5% T.sub.(N,I) [ C.]: 76.6 B-2O-O5 2.0% n [589 nm, 20 C.]: 0.1079 CC-3-V 34.5% n.sub.e [589 nm, 20 C.]: 1.5920 CC-3-V1 3.5% n.sub.o [589 nm, 20 C.]: 1.4841 CCY-3-O2 6.0% [1 kHz, 20 C.]: 3.9 CCY-4-O2 5.0% .sub. [1 kHz, 20 C.]: 3.9 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.8 CLY-3-O3 6.0% .sub.1 [mPa s, 20 C.]: 95 CPY-2-O2 9.5% K.sub.1 [pN, 20 C.]: 14.0 CPY-3-O2 5.0% K.sub.3 [pN, 20 C.]: 14.0 CY-3-O2 4.0% PGIY-2-O4 3.0% PUS-3-2 5.0% Y-4O-O4 7.0% 100.0%

TABLE-US-00015 Mixture Example M9 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 88.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1195 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6068 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4873 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.1 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 109 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.6 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.0 CLY-5O2 3.0% CPY-3-O2 11.5% PUS-2-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00016 Mixture Example M10 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 88.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1192 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6064 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.1 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 108 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.3 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.2 CLY-5-O2 3.0% CPY-3-O2 11.5% PUS-2-1 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00017 Mixture Example M11 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 79.4 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1179 B(S)-2O-O6 2.5% n.sub.e [589 nm, 20 C.]: 1.6055 CC-3-V 35.5% n.sub.o [589 nm, 20 C.]: 1.4876 CC-3-V1 4.0% [1 kHz, 20 C.]: 3.8 CCP-3-1 3.0% .sub. [1 kHz, 20 C.]: 3.7 CLY-3-O2 5.0% .sub. [1 kHz, 20 C.]: 7.5 CLY-3-O3 3.5% .sub.1 [mPa s, 20 C.]: 97 CPY-2-O2 7.5% K.sub.1 [pN, 20 C.]: 14.8 CPY-3-O2 9.5% K.sub.3 [pN, 20 C.]: 15.2 CY-3-O2 10.0% CY-5-O2 1.5% PGIY-2-O4 5.0% PUS-3-2 4.0% PY-1-O2 1.0% 100.0%

TABLE-US-00018 Mixture Example M12 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1418 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6402 CPP-3-2 6.0% n.sub.o [589 nm, 20 C.]: 1.4984 CC-3-V 34.0% [1 kHz, 20 C.]: 2.8 CCY-3-O2 4.0% .sub. [1 kHz, 20 C.]: 3.7 CCY-4-O2 2.0% .sub. [1 kHz, 20 C.]: 6.6 COB(S)-2-O4 8.5% .sub.1 [mPa s, 20 C.]: 89 CPY-2-O2 4.0% K.sub.1 [pN, 20 C.]: 15.9 CPY-3-O2 3.0% K.sub.3 [pN, 20 C.]: 13.8 PGIY-2-O4 1.5% PP-1-2V1 11.5% PUS-3-2 10.5% Y-4O-O4 3.0% 100.0%

TABLE-US-00019 Mixture Example M13 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1425 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6382 CPP-3-2 1.0% n.sub.o [589 nm, 20 C.]: 1.4957 CC-3-V 39.5% [1 kHz, 20 C.]: 2.1 CC-3-V1 6.0% .sub. [1 kHz, 20 C.]: 3.5 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 5.6 CPY-3-O2 3.5% .sub.1 [mPa s, 20 C.]: 75 PP-1-2V1 5.0% K.sub.1 [pN, 20 C.]: 15.8 PUS-3-2 10.0% K.sub.3 [pN, 20 C.]: 13.2 PYP-2-3 14.5% 100.0%

TABLE-US-00020 Mixture Example M14 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74.1 B(S)-2O-O5 4.5% n [589 nm, 20 C.]: 0.1418 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6392 CC-3-V 39.5% n.sub.o [589 nm, 20 C.]: 1.4974 CCY-3-O2 4.0% [1 kHz, 20 C.]: 2.6 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 3.6 CPY-2-O2 2.5% .sub. [1 kHz, 20 C.]: 6.1 CPY-3-O2 6.0% .sub.1 [mPa s, 20 C.]: 83 PGIY-2-O4 1.0% K.sub.1 [pN, 20 C.]: 16.2 PP-1-2V1 12.0% K.sub.3 [pN, 20 C.]: 14.2 PUS-3-2 10.0% PYP-2-3 4.0% 100.0%

TABLE-US-00021 Mixture Example M15 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 76.6 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1400 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6371 CPP-3-2 5.5% n.sub.o [589 nm, 20 C.]: 1.4971 CC-3-V 33.5% [1 kHz, 20 C.]: 2.2 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 3.4 CCY-3-O2 2.0% .sub. [1 kHz, 20 C.]: 5.6 COB(S)-2-O4 8.5% .sub.1 [mPa s, 20 C.]: 81 CPY-3-O2 4.0% K.sub.1 [pN, 20 C.]: 16.7 PGIY-2-O4 1.5% K.sub.3 [pN, 20 C.]: 14.7 PP-1-2V1 12.0% PUS-3-2 5.0% PYP-2-3 8.0% 100.0%

TABLE-US-00022 Mixture Example M16 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 76 B(S)-2O-O5 5.0% n [589 nm, 20 C.]: 0.1405 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6402 CPP-3-2 11.5% n.sub.o [589 nm, 20 C.]: 1.4997 CC-3-V 39.5% [1 kHz, 20 C.]: 2.0 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 3.4 CPY-3-O2 3.0% .sub. [1 kHz, 20 C.]: 5.4 PGIY-2-O4 1.0% .sub.1 [mPa s, 20 C.]: 75 PP-1-2V1 12.0% K.sub.1 [pN, 20 C.]: 16.5 PUS-3-2 5.0% K.sub.3 [pN, 20 C.]: 13.7 PYP-2-3 6.5% 100.0%

TABLE-US-00023 Mixture Example M17 B(S)-2O-O4 4.5% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1382 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6356 CPP-3-2 5.0% n.sub.o [589 nm, 20 C.]: 1.4974 CC-3-V 35.0% [1 kHz, 20 C.]: 2.3 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 3.4 CPY-3-O2 3.5% .sub. [1 kHz, 20 C.]: 5.7 COB(S)-2-O4 8.5% .sub.1 [mPa s, 20 C.]: 78 PGIY-2-O4 4.0% K.sub.1 [pN, 20 C.]: 16.1 PP-1-2V1 12.0% K.sub.3 [pN, 20 C.]: 14.1 PUS-3-2 3.0% PYP-2-3 8.5% 100.0%

TABLE-US-00024 Mixture Example M18 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74.2 B(S)-2O-O5 5.0% n [589 nm, 20 C.]: 0.1398 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6385 CPP-3-2 7.0% n.sub.o [589 nm, 20 C.]: 1.4987 CC-3-V 41.0% [1 kHz, 20 C.]: 2.2 COB(S)-2-O4 9.0% .sub. [1 kHz, 20 C.]: 3.5 CPY-3-O2 4.0% .sub. [1 kHz, 20 C.]: 5.7 PGIY-2-O4 2.0% .sub.1 [mPa s, 20 C.]: 77 PP-1-2V1 11.0% K.sub.1 [pN, 20 C.]: 15.9 PUS-3-2 5.0% K.sub.3 [pN, 20 C.]: 13.5 PYP-2-3 8.0% 100.0%

TABLE-US-00025 Mixture Example M19 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 76.6 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1402 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6388 CPP-3-2 7.0% n.sub.o [589 nm, 20 C.]: 1.4986 CC-3-V 42.5% [1 kHz, 20 C.]: 2.0 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 3.5 CPY-2-O2 1.5% .sub. [1 kHz, 20 C.]: 5.5 CPY-3-O2 4.0% .sub.1 [mPa s, 20 C.]: 77 PGIY-2-O4 1.5% K.sub.1 [pN, 20 C.]: 14.4 PP-1-2V1 7.0% K.sub.3 [pN, 20 C.]: 13.5 PUS-3-2 10.0% PYP-2-3 6.0% 100.0%

TABLE-US-00026 Mixture Example M20 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 77.7 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1423 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6407 CPP-3-2 6.5% n.sub.o [589 nm, 20 C.]: 1.4984 CC-3-V 35.0% [1 kHz, 20 C.]: 1.9 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 3.4 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 5.4 CPY-3-O2 4.0% .sub.1 [mPa s, 20 C.]: 79 PP-1-2V1 7.5% K.sub.1 [pN, 20 C.]: 16.7 PUS-3-2 10.0% K.sub.3 [pN, 20 C.]: 14.1 PYP-2-3 8.5% 100.0%

TABLE-US-00027 Mixture Example M21 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75.1 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1422 B(S)-2O-O6 4.0% n.sub.e [589 nm, 20 C.]: 1.6406 CPP-3-2 4.0% n.sub.o [589 nm, 20 C.]: 1.4984 CC-3-V 41.5% [1 kHz, 20 C.]: 2.0 CC-3-V1 2.0% .sub. [1 kHz, 20 C.]: 3.5 COB(S)-2-O4 8.5% .sub. [1 kHz, 20 C.]: 5.5 CPY-3-O2 4.0% .sub.1 [mPa s, 20 C.]: 76 PP-1-2V1 6.0% K.sub.1 [pN, 20 C.]: 15.7 PUS-3-2 10.0% K.sub.3 [pN, 20 C.]: 13.3 PYP-2-3 12.0% 100.0%

TABLE-US-00028 Mixture Example M22 CC-3-V 32.0% T.sub.(N,I) [ C.]: 74 CC-3-V1 8.0% n [589 nm, 20 C.]: 0.1086 CCY-3-O1 6.0% n.sub.e [589 nm, 20 C.]: 1.5931 CCY-3-O2 11.0% n.sub.o [589 nm, 20 C.]: 1.4845 CCY-4-O2 5.0% [1 kHz, 20 C.]: 3.1 CPY-3-O2 10.5% .sub. [1 kHz, 20 C.]: 3.6 CY-3-O2 4.5% .sub. [1 kHz, 20 C.]: 6.6 PY-3-O2 18.0% K.sub.1 [pN, 20 C.]: 14.0 PUS-3-2 5.0% K.sub.3 [pN, 20 C.]: 15.7 100.0% LTS bulk [h, 20 C.]: 1000

TABLE-US-00029 Mixture Example M23 CCY-3-O1 3.5% T.sub.(N,I) [ C.]: 83 CLY-3-O2 10.0% n [589 nm, 20 C.]: 0.1059 CLY-3-O3 2.5% n.sub.e [589 nm, 20 C.]: 1.5879 CPY-2-O2 11.0% n.sub.o [589 nm, 20 C.]: 1.4820 CPY-3-O2 12.5% [1 kHz, 20 C.]: 3.4 CC-3-V 28.0% .sub. [1 kHz, 20 C.]: 3.5 CC-3-V1 10.5% .sub. [1 kHz, 20 C.]: 7.0 CY-3-O2 14.0% K.sub.1 [pN, 20 C.]: 15.0 CY-5-O2 5.0% K.sub.3 [pN, 20 C.]: 17.1 PUS-3-2 3.0% 100.0%

TABLE-US-00030 Mixture Example M24 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 96 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1197 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6069 CC-3-V 28.5% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.0 CC-5-V 9.0% .sub. [1 kHz, 20 C.]: 3.4 CCY-3-O2 7.5% .sub. [1 kHz, 20 C.]: 6.5 CLY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 110 CLY-5-O2 5.0% K.sub.1 [pN, 20 C.]: 19.7 CPY-3-O2 12.0% K.sub.3 [pN, 20 C.]: 18.5 PUS-3-2 9.0% Y-4O-O4 1.0% 100.0%

TABLE-US-00031 Mixture Example M25 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1202 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6076 CC-3-V 11.0% n.sub.o [589 nm, 20 C.]: 1.4874 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.0 CC-4-V1 16.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 5.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 108 CCP-3-1 5.5% K.sub.1 [pN, 20 C.]: 19.6 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.4 CLY-3-O3 1.5% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00032 Mixture Example M26 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1201 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6075 CC-3-V 11.5% n.sub.o [589 nm, 20 C.]: 1.4874 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.1 CC-4-V1 16.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 5.0% .sub. [1 kHz, 20 C.]: 6.5 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 109 CCP-3-1 4.5% K.sub.1 [pN, 20 C.]: 19.4 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.4 CLY-5-O2 2.0% CPY-3-O2 12.0% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00033 Mixture Example M27 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.5 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6090 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4892 CPP-3-2 1.0% n [589 nm, 20 C.]: 0.1198 CC-3-V 31.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 6.3 CC-4-V1 0.75% [1 kHz, 20 C.]: 3.0 CCP-3-1 8.0% .sub.1 [mPa s, 20 C.]: 109 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 19.2 CLY-5-O2 5.0% K.sub.3 [pN, 20 C.]: 19.0 CPY-2-O2 5.25% CPY-3-O2 9.0% PUS-3-2 5.0% PY-1-O2 4.5% 100.0%

TABLE-US-00034 Mixture Example M28 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.1 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6085 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4885 CPP-3-2 0.75% n [589 nm, 20 C.]: 0.1200 CC-3-V 28.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 6.4 CC-4-V1 6.0% [1 kHz, 20 C.]: 3.0 CCP-3-1 8.0% .sub.1 [mPa s, 20 C.]: 109 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 19.1 CLY-5-O2 5.0% K.sub.3 [pN, 20 C.]: 18.8 CPY-2-O2 4.25% LTS bulk [h, 20 C.]: 1000 CPY-3-O2 9.0% PUS-3-2 5.0% PY-1-O2 5.5% 100.0%

TABLE-US-00035 Mixture Example M29 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.8 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6080 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4882 CPP-3-2 0.5% n [589 nm, 20 C.]: 0.1198 CC-3-V 26.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 6.4 CC-4-V1 6.0% [1 kHz, 20 C.]: 3.0 CC-3-5 2.5% .sub.1 [mPa s, 20 C.]: 111 CCP-3-1 4.0% K.sub.1 [pN, 20 C.]: 19.3 CCP-3-3 3.0% K.sub.3 [pN, 20 C.]: 18.7 CLY-3-O2 9.0% LTS bulk [h, 20 C.]: 1000 CLY-5-O2 5.0% CPY-2-O2 5.0% CPY-3-O2 9.0% PUS-3-2 5.0% PY-1-O2 5.5% 100.0%

TABLE-US-00036 Mixture Example M30 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.2 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6078 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4875 CC-3-V 20.75% n [589 nm, 20 C.]: 0.1203 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 3.6 CC-4-V1 6.0% .sub. [1 kHz, 20 C.]: 6.6 CCG-V-F 3.0% [1 kHz, 20 C.]: 3.0 CC-3-5 8.0% .sub.1 [mPa s, 20 C.]: 116 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.6 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.4 CLY-5-O2 5.0% LTS bulk [h, 20 C.]: 1000 CPY-2-O2 4.75% CPY-3-O2 10.0% PUS-3-2 5.0% PY-1-O2 6.0% 100.0%

TABLE-US-00037 Mixture Example M31 CY-3-O2 14.5% T.sub.(N,I) [ C.]: 99.2 CCY-3-O2 7.0% n.sub.e [589 nm, 20 C.]: 1.5839 CCY-4-O2 7.0% n.sub.o [589 nm, 20 C.]: 1.4821 CCY-3-O3 4.5% n [589 nm, 20 C.]: 0.1018 CLY-2-O4 4.5% .sub. [1 kHz, 20 C.]: 3.5 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.7 CLY-3-O3 6.0% [1 kHz, 20 C.]: 4.2 CPY-3-O2 5.0% .sub.1 [mPa s, 20 C.]: 162 B(S)-2O-O5 3.0% K.sub.1 [pN, 20 C.]: 19.5 B(S)-2O-O4 3.0% K.sub.3 [pN, 20 C.]: 18.2 CC-3-V1 6.0% CC-4-V1 5.5% CCP-3-1 5.0% CCH-23 12.0% CC-3-4 8.0% PUS-3-2 3.0% 100.0%

TABLE-US-00038 Mixture Example M32 B(S)-2O-O4 3.0% T.sub.(N,I) [ C.]: 74.5 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6201 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4909 CC-3-V 36.5% n [589 nm, 20 C.]: 0.1292 CC-3-V1 1.0% .sub. [1 kHz, 20 C.]: 3.9 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.9 CLY-3-O3 5.25% [1 kHz, 20 C.]: 4.0 CPY-2-O2 6.25% .sub.1 [mPa s, 20 C.]: 98 CPY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 14.7 PGIY-2-O4 6.0% K.sub.3 [pN, 20 C.]: 14.3 PUS-3-2 5.0% PY-3-O2 15.0% 100.0%

TABLE-US-00039 Mixture Example M33 B-2O-O5 2.0% T.sub.(N,I) [ C.]: 76.5 CC-3-V 34.5% n.sub.e [589 nm, 20 C.]: 1.5921 CC-3-V1 3.5% n.sub.o [589 nm, 20 C.]: 1.4839 CCY-3-O2 6.0% n [589 nm, 20 C.]: 0.1082 CCY-4-O2 5.0% .sub. [1 kHz, 20 C.]: 3.9 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.8 CLY-3-O3 6.0% [1 kHz, 20 C.]: 3.9 CPY-2-O2 9.5% .sub.1 [mPa s, 20 C.]: 94 CPY-3-O2 5.0% K.sub.1 [pN, 20 C.]: 13.6 CY-3-O2 4.0% K.sub.3 [pN, 20 C.]: 13.9 PGIY-2-O4 3.0% Y-4O-O4 7.0% PUS-3-2 5.0% B(S)-2O-O5 3.5% 100.0%

TABLE-US-00040 Mixture Example M34 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 79.7 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6043 B(S)-2O-O6 2.5% n.sub.o [589 nm, 20 C.]: 1.4865 CC-3-V 35.5% n [589 nm, 20 C.]: 0.1178 CC-3-V1 4.0% .sub. [1 kHz, 20 C.]: 3.7 CCP-3-1 3.0% .sub. [1 kHz, 20 C.]: 7.5 CLY-3-O2 5.0% [1 kHz, 20 C.]: 3.8 CLY-3-O3 3.5% .sub.1 [mPa s, 20 C.]: 96 CPY-2-O2 7.5% K.sub.1 [pN, 20 C.]: 15.6 CPY-3-O2 9.5% K.sub.3 [pN, 20 C.]: 14.9 CY-3-O2 10.0% CY-5-O2 1.5% PGIY-2-O4 5.0% PUS-3-2 4.0% PY-1-O2 1.0% 100.0%

TABLE-US-00041 Mixture Example M35 CPP-3-2 5.85% T.sub.(N,I) [ C.]: 76.6 CC-3-V1 7.2% n.sub.e [589 nm, 20 C.]: 1.6120 CCH-23 15.3% n.sub.o [589 nm, 20 C.]: 1.4895 CC-3-4 5.85% n [589 nm, 20 C.]: 0.1225 CCY-3-O1 3.15% .sub. [1 kHz, 20 C.]: 3.5 CCY-3-O2 11.25% .sub. [1 kHz, 20 C.]: 6.0 CPY-2-O2 4.95% [1 kHz, 20 C.]: 2.5 CPY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 105 CY-3-O2 13.95% K.sub.1 [pN, 20 C.]: 14.7 CP-3-O1 4.05% K.sub.3 [pN, 20 C.]: 15.2 PP-1-2V1 4.5% PY-3-O2 4.95% PUS-3-2 10.0% 100.0%

TABLE-US-00042 Mixture Example M36 B(S)-2O-O5 4.5% T.sub.(N,I) [ C.]: 77.6 CPP-3-2 5.4% n.sub.e [589 nm, 20 C.]: 1.6224 CLY-3-O2 5.4% n.sub.o [589 nm, 20 C.]: 1.4930 CPY-2-O2 9.45% n [589 nm, 20 C.]: 0.1294 CPY-3-O2 9.45% .sub. [1 kHz, 20 C.]: 3.6 B(S)-2O-O4 4.05% .sub. [1 kHz, 20 C.]: 6.1 CC-3-V 42.75% [1 kHz, 20 C.]: 2.5 PY-1-O2 9.0% .sub.1 [mPa s, 20 C.]: 77 PUS-3-2 10.0% K.sub.1 [pN, 20 C.]: 14.5 100.0% K.sub.3 [pN, 20 C.]: 14.0

TABLE-US-00043 Mixture Example M37 B(S)-2O-O4 4.5% T.sub.(N,I) [ C.]: 75.6 B(S)-2O-O5 4.5% n.sub.e [589 nm, 20 C.]: 1.6452 CPP-3-2 8.1% n.sub.o [589 nm, 20 C.]: 1.4988 CC-3-V 13.5% n [589 nm, 20 C.]: 0.1464 CC-3-V1 6.75% .sub. [1 kHz, 20 C.]: 3.7 CC-4-V1 11.7% .sub. [1 kHz, 20 C.]: 6.1 CCP-3-1 9.0% [1 kHz, 20 C.]: 2.4 CLY-3-O2 2.25% .sub.1 [mPa s, 20 C.]: 91 CPY-3-O2 1.8% K.sub.1 [pN, 20 C.]: 15.8 PY-1-O2 10.8% K.sub.3 [pN, 20 C.]: 14.8 PY-3-O2 9.0% PYP-2-3 8.1% PUS-3-2 10.0% 100.0%

TABLE-US-00044 Mixture Example M38 B(S)-2O-O4 4.5% T.sub.(N,I) [ C.]: 75.2 B(S)-2O-O5 4.5% n.sub.e [589 nm, 20 C.]: 1.6053 CC-3-V 35.5% n.sub.o [589 nm, 20 C.]: 1.4890 CC-3-V1 9.0% n [589 nm, 20 C.]: 0.1163 CCP-3-1 3.0% .sub. [1 kHz, 20 C.]: 3.7 CCY-3-O1 8.0% .sub. [1 kHz, 20 C.]: 6.4 CCY-3-O2 7.5% [1 kHz, 20 C.]: 2.8 CLY-3-O2 5.0% .sub.1 [mPa s, 20 C.]: 76 PUS-3-2 10.0% K.sub.1 [pN, 20 C.]: 15.2 PY-1-O2 10.0% K.sub.3 [pN, 20 C.]: 15.0 PY-2-O2 3.0% 100.0%

TABLE-US-00045 Mixture Example M39 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74.2 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6066 CPP-3-2 4.5% n.sub.o [589 nm, 20 C.]: 1.4909 CC-3-V 32.5% n [589 nm, 20 C.]: 0.1157 CC-3-V1 6.0% .sub. [1 kHz, 20 C.]: 3.6 CCP-3-1 9.5% .sub. [1 kHz, 20 C.]: 6.4 CCY-3-O2 9.0% [1 kHz, 20 C.]: 2.8 CLY-3-O2 6.5% .sub.1 [mPa s, 20 C.]: 76 PUS-3-2 5.0% K.sub.1 [pN, 20 C.]: 14.6 PY-1-O2 9.0% K.sub.3 [pN, 20 C.]: 14.8 PY-2-O2 10.0% 100.0%

TABLE-US-00046 Mixture Example M40 B(S)-2O-O4 3.5% T.sub.(N,I) [ C.]: 75.1 B(S)-2O-O5 4.5% n.sub.e [589 nm, 20 C.]: 1.6065 CPP-3-2 5.0% n.sub.o [589 nm, 20 C.]: 1.4908 CC-3-V 32.5% n [589 nm, 20 C.]: 0.1157 CC-3-V1 6.5% .sub. [1 kHz, 20 C.]: 3.6 CCP-3-1 9.5% .sub. [1 kHz, 20 C.]: 6.3 CCY-3-O2 8.0% [1 kHz, 20 C.]: 2.7 CLY-3-O2 7.0% .sub.1 [mPa s, 20 C.]: 76 PUS-3-2 5.0% K.sub.1 [pN, 20 C.]: 14.6 PY-1-O2 10.0% K.sub.3 [pN, 20 C.]: 14.9 PY-2-O2 8.5% 100.0%

TABLE-US-00047 Mixture Example M41 B(S)-2O-O4 4.5% T.sub.(N,I) [ C.]: 75 B(S)-2O-O5 4.5% n.sub.e [589 nm, 20 C.]: 1.6048 CC-3-V 36.5% n.sub.o [589 nm, 20 C.]: 1.4891 CC-3-V1 8.0% n [589 nm, 20 C.]: 0.1157 CCP-3-1 4.0% .sub. [1 kHz, 20 C.]: 3.6 CCY-3-O1 7.0% .sub. [1 kHz, 20 C.]: 6.3 CCY-3-O2 8.0% [1 kHz, 20 C.]: 2.7 CLY-3-O2 4.5% .sub.1 [mPa s, 20 C.]: 75 PUS-3-2 10.0% K.sub.1 [pN, 20 C.]: 15.3 PY-1-O2 9.0% K.sub.3 [pN, 20 C.]: 15.1 PY-2-O2 4.0% 100.0%

Mixture Example M42

[0550] The mixture example M42 consists of 99.98% of the Mixture example M1 and 0.02% of a compound of the formula ST-12b-1

##STR00494##

Mixture Example M43

[0551] The mixture example M43 consists of 99.985% of the Mixture example M1 and 0.015% of a compound of the formula S1-1a

##STR00495##

Mixture Example M44

[0552] The mixture example M44 consists of 99.98% of the Mixture example M2 and 0.02% of a compound of the formula S2-1a

##STR00496##

TABLE-US-00048 Mixture Example M45 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.3 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1192 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6057 CC-3-V 21.5% n.sub.o [589 nm, 20 C.]: 1.4865 CC-3-V1 8.0% [1 kHz, 20 C.]: 2.9 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 6.0% .sub. [1 kHz, 20 C.]: 6.2 CCP-3-1 0.5% .sub.1 [mPa s, 20 C.]: 103 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 20.1 CLY-4-O2 5.0% K.sub.3 [pN, 20 C.]: 17.9 CPY-3-O2 12.0% PYS-3-2 9.0% PY-1-O2 3.0% 100.0%

TABLE-US-00049 Mixture Example M46 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95 B(S)-2O-O5 4.25% n [589 nm, 20 C.]: 0.1193 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6066 CC-3-V 30.5% n.sub.o [589 nm, 20 C.]: 1.4873 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.2 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 3.4 CCY-3-O2 8.0% .sub. [1 kHz, 20 C.]: 6.6 CLY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 108 CLY-5-O2 5.0% K.sub.1 [pN, 20 C.]: 20.1 CPY-3-O2 7.0% K.sub.3 [pN, 20 C.]: 18.2 PYS-3-2 12.0% Y-4O-O4 1.25% 100.0%

TABLE-US-00050 Mixture Example M47 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 97.8 B(S)-2O-O5 4.25% n [589 nm, 20 C.]: 0.1212 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6084 CC-3-V 7.25% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.3 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.6 CC-3-5 8.0% .sub.1 [mPa s, 20 C.]: 109 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 20.8 CLY-4-O2 5.0% K.sub.3 [pN, 20 C.]: 14.1 CLY-5-O2 5.0% CPY-3-O2 3.25% PYS-3-2 9.75% PY-1-O2 8.5% 100.0%

TABLE-US-00051 Mixture Example M48 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 92.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1199 B(S)-(c5)1O-O2 3.0% n.sub.e [589 nm, 20 C.]: 1.6079 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4880 CC-3-V1 10.0% [1 kHz, 20 C.]: 3.1 CC-3-4 4.0% .sub. [1 kHz, 20 C.]: 3.4 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.5 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 111 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 19.5 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.1 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 7.5% PYS-3-2 7.5% 100.0%

TABLE-US-00052 Mixture Example M49 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 91.5 B(S)-(c3) 1O-O2 4.0% n [589 nm, 20 C.]: 0.1200 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6079 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4881 CC-3-V1 10.0% [1 kHz, 20 C.]: 3.1 CC-3-4 4.0% .sub. [1 kHz, 20 C.]: 3.4 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.5 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 110 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 19.3 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.2 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 7.5% PYS-3-2 7.5% 100.0%

TABLE-US-00053 Mixture Example M50 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1195 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6059 CC-3-V 21.5% n.sub.o [589 nm, 20 C.]: 1.4864 CC-3-V1 8.0% [1 kHz, 20 C.]: 2.9 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 6.0% .sub. [1 kHz, 20 C.]: 6.2 CCP-3-1 0.5% .sub.1 [mPa s, 20 C.]: 106 CLY-3-O2 9.0% CLY-4-O2 5.0% CPY-3-O2 12.0% PYS-(c5)-2 9.0% PY-1-O2 3.0% 100.0%

TABLE-US-00054 Mixture Example M51 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1190 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6056 CC-3-V 21.5% n.sub.o [589 nm, 20 C.]: 1.4866 CC-3-V1 8.0% [1 kHz, 20 C.]: 2.9 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 6.0% .sub. [1 kHz, 20 C.]: 6.2 CCP-3-1 0.5% .sub.1 [mPa s, 20 C.]: 102 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 20.2 CLY-4-O2 5.0% K.sub.3 [pN, 20 C.]: 18.1 CPY-3-O2 12.0% PYS-3-1 9.0% PY-1-O2 3.0% 100.0%

TABLE-US-00055 Mixture Example M52 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.3 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1188 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6054 CC-3-V 21.5% n.sub.o [589 nm, 20 C.]: 1.4866 CC-3-V1 8.0% [1 kHz, 20 C.]: 2.9 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 6.0% .sub. [1 kHz, 20 C.]: 6.2 CCP-3-1 0.5% .sub.1 [mPa s, 20 C.]: 101 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 20.1 CLY-4-O2 5.0% K.sub.3 [pN, 20 C.]: 18.3 CPY-3-O2 12.0% PYS-2-1 4.0% PYS-2-2 5.0% PY-1-O2 3.0% 100.0%

TABLE-US-00056 Mixture Example M53 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90.9 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1206 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6087 CPP-3-2 2.0% n.sub.o [589 nm, 20 C.]: 1.4881 CC-3-V 7.0% [1 kHz, 20 C.]: 3.1 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 3.4 CC-4-V1 15.0% .sub. [1 kHz, 20 C.]: 6.5 CC-5-V 10.0% .sub.1 [mPa s, 20 C.]: 108 CC-3-5 6.0% K.sub.1 [pN, 20 C.]: 20.0 CCP-3-1 5.0% K.sub.3 [pN, 20 C.]: 18.1 CLY-3-O2 9.0% CPY-3-O2 12.0% PYS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00057 Mixture Example M54 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 91.4 B(S)-2O-O5 2.0% n [589 nm, 20 C.]: 0.1192 CC-3-V 17.5% n.sub.e [589 nm, 20 C.]: 1.6068 CC-3-V1 9.0% n.sub.o [589 nm, 20 C.]: 1.4876 CC-4-V1 2.0% [1 kHz, 20 C.]: 3.2 CC-5-V 7.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.6 CCY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 111 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 19.5 CLY-3-O3 0.5% K.sub.3 [pN, 20 C.]: 18.1 CLY-4-O2 5.0% CLY-5-O2 5.0% PYS-3-2 11.5% PY-1-O2 10.0% 100.0%

TABLE-US-00058 Mixture Example M55 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 93.8 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1199 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6090 CPP-3-2 3.0% n.sub.o [589 nm, 20 C.]: 1.4891 CC-3-V 28.0% [1 kHz, 20 C.]: 3.0 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 4.5% .sub. [1 kHz, 20 C.]: 6.3 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 104 CCP-3-3 3.0% K.sub.1 [pN, 20 C.]: 19.3 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.5 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 6.5% PYS-3-2 6.0% 100.0%

TABLE-US-00059 Mixture Example M56 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 73.4 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6401 B(S)-2O-O6 4.0% n.sub.o [589 nm, 20 C.]: 1.4997 CPP-3-2 8.0% n [589 nm, 20 C.]: 0.1404 CC-3-V 41.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 0.5% .sub. [1 kHz, 20 C.]: 5.4 COB(S)-2-O4 8.5% [1 kHz, 20 C.]: 2.0 PGIY-2-O4 1.0% .sub.1 [mPa s, 20 C.]: 70 PP-1-2V1 10.0% K.sub.1 [pN, 20 C.]: 15.6 PYP-2-3 11.0% K.sub.3 [pN, 20 C.]: 12.9 PYS-3-2 7.5% 100.0%

TABLE-US-00060 Mixture Example M57 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75.1 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6395 B(S)-2O-O6 4.0% n.sub.o [589 nm, 20 C.]: 1.4986 CPP-3-2 6.0% n [589 nm, 20 C.]: 0.1409 CC-3-V 40.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 4.0% .sub. [1 kHz, 20 C.]: 5.5 COB(S)-2-O4 9.0% [1 kHz, 20 C.]: 2.1 PP-1-2V1 6.5% .sub.1 [mPa s, 20 C.]: 71 PYP-2-3 7.0% K.sub.1 [pN, 20 C.]: 16.2 PYS-3-2 15.0% K.sub.3 [pN, 20 C.]: 12.9 100.0%

TABLE-US-00061 Mixture Example M58 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75.5 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6400 B(S)-2O-O6 4.0% n.sub.o [589 nm, 20 C.]: 1.4996 CPP-3-2 8.0% n [589 nm, 20 C.]: 0.1404 CC-3-V 40.5% .sub. [1 kHz, 20 C.]: 3.3 CC-3-4 2.75% .sub. [1 kHz, 20 C.]: 5.4 COB(S)-2-O4 9.5% [1 kHz, 20 C.]: 2.1 PP-1-2V1 8.0% .sub.1 [mPa s, 20 C.]: 21 PYP-2-3 4.25% K.sub.1 [pN, 20 C.]: 16.5 PYS-3-2 15.0% K.sub.3 [pN, 20 C.]: 12.7 100.0%

TABLE-US-00062 Mixture Example M59 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.5 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6089 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4886 CC-3-V 31.0% n [589 nm, 20 C.]: 0.1203 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 2.5% .sub. [1 kHz, 20 C.]: 6.3 CCP-3-1 8.0% [1 kHz, 20 C.]: 3.0 CLY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 103 CLY-4-O2 5.0% K.sub.1 [pN, 20 C.]: 18.0 CPY-2-O2 3.0% K.sub.3 [pN, 20 C.]: 18.4 CPY-3-O2 9.0% PY-1-O2 3.75% PYS-3-2 7.75% 100.0%

TABLE-US-00063 Mixture Example M60 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.3 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6088 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4888 CC-3-V 29.0% n [589 nm, 20 C.]: 0.1200 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-5 4.5% .sub. [1 kHz, 20 C.]: 6.4 CCP-3-1 8.0% [1 kHz, 20 C.]: 3.0 CLY-3-O2 9.0% .sub.1 [mPa s, 20 C.]: 106 CLY-4-O2 5.0% K.sub.1 [pN, 20 C.]: 19.3 CPY-2-O2 2.5% K.sub.3 [pN, 20 C.]: 18.6 CPY-3-O2 9.0% LTS bulk [h, 20 C.]: 1000 PY-1-O2 4.5% PYS-3-2 7.5% 100.0%

TABLE-US-00064 Mixture Example M61 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.7 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6099 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4894 CPP-3-2 4.0% n [589 nm, 20 C.]: 0.1205 CC-3-V 27.5% .sub. [1 kHz, 20 C.]: 3.4 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 6.4 CC-3-5 4.0% [1 kHz, 20 C.]: 3.0 CCP-3-1 8.0% .sub.1 [mPa s, 20 C.]: 108 CLY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 19.2 CLY-4-O2 5.0% K.sub.3 [pN, 20 C.]: 18.8 CPY-3-O2 9.5% PY-1-O2 7.0% PYS-3-2 5.0% 100.0%

TABLE-US-00065 Mixture Example M62 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.8 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6093 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4894 CPP-3-2 3.5% n [589 nm, 20 C.]: 0.1199 CC-3-V 25.0% .sub. [1 kHz, 20 C.]: 3.3 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 6.4 CC-4-V1 6.0% [1 kHz, 20 C.]: 3.0 CC-3-5 3.0% .sub.1 [mPa s, 20 C.]: 107 CCP-3-1 8.0% K.sub.1 [pN, 20 C.]: 19.3 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.5 CLY-4-O2 5.0% LTS bulk [h, 20 C.]: 1000 CPY-3-O2 9.25% PY-1-O2 7.25% PYS-3-2 5.0% 100.0%

TABLE-US-00066 Mixture Example M63 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 95.3 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6083 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4890 CPP-3-2 0.75% n [589 nm, 20 C.]: 0.1193 CC-3-V 18.75% .sub.|| [1 kHz, 20 C.]: 3.6 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 6.6 CC-4-V1 6.0% [1 kHz, 20 C.]: 3.1 CCG-V-F 3.0% .sub.1 [mPa s, 20 C.]: 114 CC-3-5 8.0% K.sub.1 [pN, 20 C.]: 19.8 CCP-3-1 8.0% K.sub.3 [pN, 20 C.]: 18.6 CLY-3-O2 9.0% LTS bulk [h, 20 C.]: 1000 CLY-4-O2 4.0% CPY-3-O2 10.0% PY-1-O2 8.5% PYS-3-2 5.0% 100.0%

TABLE-US-00067 Mixture Example M64 B(S)-2O-O4 3.0% T.sub.(N,I) [ C.]: 74.3 B(S)-2O-O5 4.0% n.sub.e [589 nm, 20 C.]: 1.6216 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4904 CC-3-V 36.5% n [589 nm, 20 C.]: 0.1312 CC-3-V1 1.75% .sub.|| [1 kHz, 20 C.]: 3.8 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.9 CLY-3-O3 6.0% [1 kHz, 20 C.]: 4.1 CPY-2-O2 2.5% .sub.1 [mPa s, 20 C.]: 95 CPY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 14.7 PYS-3-2 7.25% K.sub.3 [pN, 20 C.]: 14.2 PGIY-2-O4 6.0% PY-3-O2 15.0% 100.0%

TABLE-US-00068 Mixture Example M65 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 92.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1190 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6071 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4881 CC-3-V1 10.0% [1 kHz, 20 C.]: 2.9 CC-3-4 4.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.3 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 105 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 20.1 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.3 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 7.5% PGS-2-1 7.5% 100.0%

TABLE-US-00069 Mixture Example M66 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 91.8 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1199 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6087 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4888 CC-3-V1 10.0% [1 kHz, 20 C.]: 2.7 CC-3-4 4.0% .sub.|| [1 kHz, 20 C.]: 3.6 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.3 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 110 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 19.7 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.0 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 7.5% SGP-2-3 7.5% 100.0%

TABLE-US-00070 Mixture Example M67 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1196 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6068 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.2 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.6 CCP-3-5 6.0% .sub.1 [mPa s, 20 C.]: 111 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.9 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.3 CLY-5-O2 3.0% CPY-3-O2 11.5% PUS-3-2 3.0% PYS-3-2 2.0% PY-1-O2 10.0% 100.0%

TABLE-US-00071 Mixture Example M68 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 90.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1196 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6068 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.2 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.3 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CCP-3-5 6.0% .sub.1 [mPa s, 20 C.]: 109 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.9 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.5 CLY-5-O2 3.0% CPY-3-O2 11.5% PYS-3-2 3.0% PGS-3-2 2.0% PY-1-O2 10.0% 100.0%

TABLE-US-00072 Mixture Example M69 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 89.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1197 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6070 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4873 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.1 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.5 CCP-3-5 6.0% .sub.1 [mPa s, 20 C.]: 108 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 19.9 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.0 CLY-5-O2 3.0% CPY-3-O2 11.5% PUS-3-2 2.0% PGS-3-2 3.0% PY-1-O2 10.0% 100.0%

TABLE-US-00073 Mixture Example M70 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 97.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1207 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6079 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4872 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.3 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.7 CCC-3-V 6.0% .sub.1 [mPa s, 20 C.]: 121 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 20.8 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 19.0 CLOY-3-O2 3.0% CPY-3-O2 11.5% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00074 Mixture Example M71 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 87.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1216 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6093 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4876 CC-3-V1 8.0% [1 kHz, 20 C.]: 3.2 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.6 CCC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 111 CCP-V-1 3.5% K.sub.1 [pN, 20 C.]: 19.7 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 17.9 CLOY-3-O2 3.0% CPY-3-O2 11.5% PUS-3-2 5.0% PY-1-O2 10.0% 100.0%

TABLE-US-00075 Mixture Example M72 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 110.0 B(S)-2O-O5 3.0% n [589 nm, 20 C.]: 0.1204 B(S)-2O-O6 2.0% n.sub.e [589 nm, 20 C.]: 1.6077 CC-3-V 16.0% n.sub.o [589 nm, 20 C.]: 1.4873 CC-3-V1 4.0% [1 kHz, 20 C.]: 2.9 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.3 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.2 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 122 CCP-3-1 3.5% K.sub.1 [pN, 20 C.]: 22.5 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 20.6 CLY-5-O2 6.5% CPY-3-O2 11.5% PUS-3-2 3.0% PPY-1-O2 10.0% 100.0%

TABLE-US-00076 Mixture Example M73 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 94.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1205 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6087 CC-3-V 19.5% n.sub.o [589 nm, 20 C.]: 1.4882 CC-3-V1 2.0% [1 kHz, 20 C.]: 2.9 CC-2-3 14.0% .sub.|| [1 kHz, 20 C.]: 3.3 CC-3-5 8.0% .sub. [1 kHz, 20 C.]: 6.2 CCP-3-1 5.0% .sub.1 [mPa s, 20 C.]: 105 CCP-3-3 2.0% K.sub.1 [pN, 20 C.]: 20.0 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 17.7 CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 3.0% PPY-3-2 5.0% PYS-3-2 7.5% 100.0%

TABLE-US-00077 Mixture Example M74 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 92.5 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1247 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6122 CC-3-V 8.0% n.sub.o [589 nm, 20 C.]: 1.4875 CC-2-2V1 8.0% [1 kHz, 20 C.]: 3.0 CC-4-V1 15.0% .sub.|| [1 kHz, 20 C.]: 3.4 CC-5-V 10.0% .sub. [1 kHz, 20 C.]: 6.4 CC-3-5 6.0% .sub.1 [mPa s, 20 C.]: 118 LPP-3-1 3.5% K.sub.1 [pN, 20 C.]: 20.4 CLY-3-O2 9.0% K.sub.3 [pN, 20 C.]: 18.4 CLY-5-O2 3.0% CPY-3-O2 11.5% PUS-3-2 5.0% PY-1-O2 10.0% 2 100.0%

TABLE-US-00078 Mixture Example M75 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 93.0 B(S)-2O-O5 4.0% n [589 nm, 20 C.]: 0.1202 B(S)-2O-O6 3.0% n.sub.e [589 nm, 20 C.]: 1.6082 CC-3-V 22.0% n.sub.o [589 nm, 20 C.]: 1.4880 CC-3-V1 4.0% [1 kHz, 20 C.]: 2.8 CC-3-2V1 6.0% .sub.|| [1 kHz, 20 C.]: 3.3 CC-3-4 4.0% .sub. [1 kHz, 20 C.]: 6.1 CC-3-5 8.0% .sub.1 [mPa s, 20 C.]: 103 CCP-3-1 5.0% K.sub.1 [pN, 20 C.]: 20.6 CCP-3-3 2.0% K.sub.3 [pN, 20 C.]: 18.8 CLY-3-O2 9.0% CLY-4-O2 5.0% CPY-3-O2 9.0% PY-1-O2 2.5% PP-1-3 5.0% PYS-3-2 7.5% 100.0%

TABLE-US-00079 Mixture Example M76 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 73.8 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6130 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4903 CC-3-V 39.25% [1 kHz, 20 C.]: 0.1227 CC-3-V1 10.0% .sub.|| [1 kHz, 20 C.]: 3.6 CLY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 6.6 CPY-3-O2 6.5% .sub.1 [mPa s, 20 C.]: 3.1 PGIY-2-O4 6.0% K.sub.1 [pN, 20 C.]: 15.4 PGS-2-1 6.5% K.sub.3 [pN, 20 C.]: 14.4 PY-3-O2 10.75% 100.0%

TABLE-US-00080 Mixture Example M77 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6138 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4909 CC-3-V 41.0% n [589 nm, 20 C.]: 0.1229 CC-3-V1 9.0% .sub.|| [1 kHz, 20 C.]: 3.5 CLY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 6.4 CPY-3-O2 6.5% [1 kHz, 20 C.]: 2.9 PGIY-2-O4 4.5% K.sub.1 [pN, 20 C.]: 15.6 PGS-2-1 8.0% K.sub.3 [pN, 20 C.]: 14.3 PY-3-O2 10.0% 100.0%

TABLE-US-00081 Mixture Example M78 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 73.5 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6134 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4909 CC-3-V 42.5% n [589 nm, 20 C.]: 0.1225 CC-3-V1 6.5% .sub. [1 kHz, 20 C.]: 3.5 CLY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 6.4 CPY-3-O2 9.0% [1 kHz, 20 C.]: 2.9 PGIY-2-O4 0.75% K.sub.1 [pN, 20 C.]: 15.6 PGS-2-1 9.0% K.sub.3 [pN, 20 C.]: 14.2 PY-3-O2 11.25% 100.0%

TABLE-US-00082 Mixture Example M79 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6118 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4903 CC-3-V 44.5% n [589 nm, 20 C.]: 0.1215 CC-3-V1 9.0% .sub. [1 kHz, 20 C.]: 3.5 CLY-3-O2 4.5% .sub. [1 kHz, 20 C.]: 6.2 CPY-3-O2 7.0% [1 kHz, 20 C.]: 2.7 B(S)-4O-O5 4.0% K.sub.1 [pN, 20 C.]: 15.5 PGIY-2-O4 6.0% K.sub.3 [pN, 20 C.]: 13.6 PGS-2-1 8.0% PY-3-O2 5.0% 100.0%

TABLE-US-00083 Mixture Example M80 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6128 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4908 CPP-3-2 5.5% n [589 nm, 20 C.]: 0.1220 CC-3-V 40.5% .sub. [1 kHz, 20 C.]: 3.5 CC-3-V1 8.0% .sub. [1 kHz, 20 C.]: 6.2 CLY-3-O2 9.0% [1 kHz, 20 C.]: 2.7 CPY-3-O2 2.5% K.sub.1 [pN, 20 C.]: 15.2 PGIY-2-O4 6.0% K.sub.3 [pN, 20 C.]: 14.0 PY-3-O2 8.5% LTS bulk [h, 20 C.]: 216 PYS-3-2 8.0% 100.0%

TABLE-US-00084 Mixture Example M81 PY-3-O2 7.0% T.sub.(N,I) [ C.]: 75.1 LY-3-O2 5.0% .sub. [1 kHz, 20 C.]: 3.8 CLY-3-O2 6.0% .sub. [1 kHz, 20 C.]: 7.6 CPY-2-O2 7.0% [1 kHz, 20 C.]: 3.8 CPY-3-O2 9.0% K.sub.1 [pN, 20 C.]: 15.1 B(S)-2O-O4 4.0% K.sub.3 [pN, 20 C.]: 14.5 B(S)-2O-O5 4.0% B(S)-2O-O6 4.0% PGIY-2-O4 6.0% PYP-2-3 2.0% CC-3-V 34.0% CC-3-V1 6.0% PUS-3-2 6.0% 100.0%

TABLE-US-00085 Mixture Example M82 CPP-3-2 8.0% T.sub.(N,I) [ C.]: 75.5 PYP-2-3 10.5% n.sub.e [589 nm, 20 C.]: 1.6010 CCP-V-1 10.0% n.sub.o [589 nm, 20 C.]: 1.4870 CC-3-V 42.0% n [589 nm, 20 C.]: 0.1140 CC-3-V1 1.0% .sub. [1 kHz, 20 C.]: 3.5 CLP-V-1 5.0% .sub. [1 kHz, 20 C.]: 6.7 PY-2-O2 12.0% [1 kHz, 20 C.]: 3.2 PUS-3-2 3.5% K.sub.1 [pN, 20 C.]: 15.9 Y-4O-O4 1.0% K.sub.3 [pN, 20 C.]: 17.9 B(S)-2O-O5 4.0% LTS bulk [h, 20 C.]: 1000 B(S)-2O-O4 3.0% 100.0%

TABLE-US-00086 Mixture Example M83 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 73.2 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6131 B(S)-2O-O6 4.0% n.sub.o [589 nm, 20 C.]: 1.4917 PGIY-2-O4 4.5% n [589 nm, 20 C.]: 0.1214 PYP-2-3 3.0% .sub. [1 kHz, 20 C.]: 3.5 CC-3-V 42.0% .sub. [1 kHz, 20 C.]: 6.1 CC-3-V1 7.0% [1 kHz, 20 C.]: 2.6 CLY-3-O2 6.0% K.sub.1 [pN, 20 C.]: 15.3 CPP-3-2 7.0% K.sub.3 [pN, 20 C.]: 13.3 PY-3-O2 8.0% COB(S)-2-O4 4.5% PUS-3-2 5.0% 100.0%

TABLE-US-00087 Mixture Example M84 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 72.5 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6125 B(S)-2O-O6 2.0% n.sub.o [589 nm, 20 C.]: 1.4916 PGIY-2-O4 4.0% n [589 nm, 20 C.]: 0.1209 PYP-2-3 3.0% .sub. [1 kHz, 20 C.]: 3.5 CC-3-V 43.0% .sub. [1 kHz, 20 C.]: 6.2 CC-3-V1 6.0% [1 kHz, 20 C.]: 2.6 CLY-3-O2 5.0% K.sub.1 [pN, 20 C.]: 14.8 CPP-3-2 7.0% K.sub.3 [pN, 20 C.]: 13.0 PY-3-O2 9.0% LTS bulk [h, 20 C.]: 336 COB(S)-2-O4 7.0% PUS-3-2 5.0% 100.0%

TABLE-US-00088 Mixture Example M85 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 72.8 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6135 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4918 PGIY-2-O4 5.0% n [589 nm, 20 C.]: 0.1217 PYP-2-3 2.5% .sub. [1 kHz, 20 C.]: 3.6 CC-3-V 43.0% .sub. [1 kHz, 20 C.]: 6.3 CC-3-V1 5.0% [1 kHz, 20 C.]: 2.8 CLY-3-O2 7.0% K.sub.1 [pN, 20 C.]: 14.9 CPP-3-2 6.5% K.sub.3 [pN, 20 C.]: 13.2 PY-3-O2 9.0% LTS bulk [h, 20 C.]: 144 COB(S)-2-O4 5.0% PUS-3-2 5.0% 100.0%

TABLE-US-00089 Mixture Example M86 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 73.5 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6170 B(S)-2O-O6 2.0% n.sub.o [589 nm, 20 C.]: 1.4919 PGIY-2-O4 6.0% n [589 nm, 20 C.]: 0.1251 PYP-2-3 2.5% .sub. [1 kHz, 20 C.]: 3.6 CC-3-V 43.0% .sub. [1 kHz, 20 C.]: 6.6 CC-3-V1 3.0% [1 kHz, 20 C.]: 3.0 CLY-3-O2 7.0% K.sub.1 [pN, 20 C.]: 14.5 CPP-3-2 5.0% K.sub.3 [pN, 20 C.]: 12.9 PY-3-O2 9.5% LTS bulk [h, 20 C.]: 312 COB(S)-2-O4 5.5% PUS-3-2 5.5% CPY-3-O2 2.0% 100.0%

TABLE-US-00090 Mixture Example M87 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74.2 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6171 B(S)-2O-O6 2.0% n.sub.o [589 nm, 20 C.]: 1.4925 PGIY-2-O4 6.0% n [589 nm, 20 C.]: 0.1246 PYP-2-3 2.5% .sub. [1 kHz, 20 C.]: 3.6 CC-3-V 46.0% .sub. [1 kHz, 20 C.]: 6.6 CLY-3-O2 7.0% [1 kHz, 20 C.]: 2.9 CPP-3-2 5.5% K.sub.1 [pN, 20 C.]: 14.9 PY-3-O2 8.5% K.sub.3 [pN, 20 C.]: 13.1 COB(S)-2-O4 6.0% LTS bulk [h, 20 C.]: 312 PUS-3-2 5.5% CPY-3-O2 2.0% 100.0%

TABLE-US-00091 Mixture Example M88 PY-3-O2 13.0% T.sub.(N,I) [ C.]: 75.1 CLY-3-O2 7.0% n.sub.e [589 nm, 20 C.]: 1.6239 CLY-3-O3 4.0% n.sub.o [589 nm, 20 C.]: 1.4915 CPY-3-O2 10.0% n [589 nm, 20 C.]: 0.1324 B(S)-2O-O4 4.0% .sub. [1 kHz, 20 C.]: 3.8 B(S)-2O-O5 5.0% .sub. [1 kHz, 20 C.]: 7.6 B(S)-2O-O6 3.0% [1 kHz, 20 C.]: 3.8 PGIY-2-O4 6.0% K.sub.1 [pN, 20 C.]: 15.4 PYP-2-3 2.0% K.sub.3 [pN, 20 C.]: 14.5 CC-3-V 35.0% CC-3-V1 5.0% PUS-3-2 6.0% 100.0%

TABLE-US-00092 Mixture Example M89 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75.5 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6123 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4898 CC-3-V 46.5% n [589 nm, 20 C.]: 0.1225 CC-3-V1 2.0% .sub. [1 kHz, 20 C.]: 3.6 CLY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 6.5 CPY-3-O2 10.0% [1 kHz, 20 C.]: 2.9 PGIY-2-O4 6.0% K.sub.1 [pN, 20 C.]: 15.2 PUS-3-2 8.0% K.sub.3 [pN, 20 C.]: 14.3 PY-3-O2 6.5% LTS bulk [h, 20 C.]: 192 100.0%

TABLE-US-00093 Mixture Example M90 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 75 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6118 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4896 CC-3-V 40.25% n [589 nm, 20 C.]: 0.1222 CC-3-V1 9.0% .sub. [1 kHz, 20 C.]: 3.6 CLY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 6.4 CLY-3-O3 1.0% [1 kHz, 20 C.]: 2.8 CPY-3-O2 6.75% K.sub.1 [pN, 20 C.]: 15.3 PGIY-2-O4 6.0% K.sub.3 [pN, 20 C.]: 14.5 PUS-3-2 8.0% PY-3-O2 8.0% 100.0%

TABLE-US-00094 Mixture Example M91 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 74 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6105 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4895 CC-3-V 40.25% n [589 nm, 20 C.]: 0.1210 CC-3-V1 9.0% .sub. [1 kHz, 20 C.]: 3.6 CLY-3-O2 5.0% .sub. [1 kHz, 20 C.]: 6.6 CCOY-3-O2 5.0% [1 kHz, 20 C.]: 3.0 CPY-3-O2 6.75% K.sub.1 [pN, 20 C.]: 15.1 PGIY-2-O4 6.0% K.sub.3 [pN, 20 C.]: 14.2 PUS-3-2 8.0% PY-3-O2 8.0% 100.0%

TABLE-US-00095 Mixture Example M92 B(S)-2O-O4 4.0% T.sub.(N,I) [ C.]: 71.5 B(S)-2O-O5 5.0% n.sub.e [589 nm, 20 C.]: 1.6101 B(S)-2O-O6 3.0% n.sub.o [589 nm, 20 C.]: 1.4900 CC-3-V 39.25% n [589 nm, 20 C.]: 0.1201 CC-3-V1 10.0% .sub. [1 kHz, 20 C.]: 3.7 CCOY-3-O2 9.0% .sub. [1 kHz, 20 C.]: 7.2 CPY-3-O2 6.5% [1 kHz, 20 C.]: 3.5 PGIY-2-O4 6.0% K.sub.1 [pN, 20 C.]: 14.8 PGS-2-1 6.5% K.sub.3 [pN, 20 C.]: 14.4 PY-3-O2 10.75% 100.0%

[0553] Polymerisable Mixtures

[0554] The polymerisable mixtures P1 to P9 are prepared from the nematic mixtures given in Table 1 by adding a reactive mesogen (RM) selected from the group of compounds of the formulae RM-1, RM-17, RM-35, RM-64 and RM-171, in the amount given in Table 1 (% RM).

TABLE-US-00096 TABLE 1 Polymerisable Mixtures LC Mixture Host RM % RM P1 M1 RM-1 0.3 P2 M2 RM-17 0.3 P3 M3 RM-35 0.3 P4 M4 RM-64 0.3 P5 M5 RM1 0.25 P6 M6 RM-17 0.25 P7 M7 RM-35 0.25 P8 M8 RM-64 0.25 P9 M9 RM-171 0.35 [00497]RM-1 [00498]RM-17 [00499]RM-35 [00500]RM-64 [00501]RM-145 [00502]RM-163 [00503]RM-171

Mixture Example P10

[0555] The polymerisable mixture P10 consists of 99.434% of Mixture Example M1, 0.300% of RM-1, 0.200% of RM-145, 0.050% of RM-163, 0.001% of Irganox 1076 and 0.015% of the compound ST-3a-1.

##STR00504##

[0556] The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.

[0557] Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. The preceding preferred specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever. From the description, one skilled in the art can easily ascertain the essential characteristics of this invention and, without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and conditions.

[0558] The entire disclosures of all applications, patents and publications, cited herein and of corresponding application No. PCT/CN2022/100661, filed Jun. 23, 2022, are incorporated by reference herein.