Liquid-crystal medium
The present invention relates to liquid-crystal (LC) media as defined in claim 1 , to the use thereof for optical, electro-optical and electronic purposes, in particular in LC displays, and to LC displays containing said LC media. The invention in particular relates to LC media with improved response time that enable energy saving displays.
1 . A liquid crystal medium comprising
a) one or more compounds of the formula I:
in which
R 1 and R 2 , 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, alkoxy, alkenyl or alkenyloxy having 3 to 15 C atoms, where one or more CH2 groups in these radicals may each be replaced, independently of one another, by
C≡C—, —CF 2 O—, —OCF 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 one or more H atoms may each be replaced by halogen,
Z 1 denotes —CF 2 O—, —OCF 2 —, —CH 2 O—, —OCH 2 —, —CO—O—, —O—CO—, —C 2 H 4 —, —CH═CH—, —C═C— or a single bond,
L 1 and L 2 , each, independently of one another, denote F, Cl, CF 3 or CHF 2 ,
Y denotes H, F, Cl, CF 3 , CHF 2 or CH 3 ;
b) one or more compounds selected from the group of compounds of formulae IID-7
in which alkyl on each occurrence, identically or differently, denotes a straight-chain alkyl radical having 1-6 C atoms, and
(O) denotes O or a single bond; and
c) one or more compounds selected from the group of compounds of III-2-1, III-2-2, III-2-3, III-2-4, III-2-5, III-2-6, III-2-7, III-2-8, III-2-9, and III-2-10, and one or more compounds selected from the group of compounds of formulae III-3-1, III-3-2, III-3-4, III-3-5, and III-3-6
in which
alkyl and alkyl* each, independently of one another, denote a straight-chain alkyl radical having 1-6 C atoms,
alkenyl and alkenyl* each, independently of one another, denote a straight-chain alkenyl radical having 2-6° C. atoms,
alkoxy and alkoxy* each, independently of one another, denote a straight-chain alkoxy radical having 1-6 C atoms,
R 32 denotes ethyl, n-propyl, or n-butyl, and
L 31 and L 32 each, independently of one another, denote F, Cl, CF 3 or CHF 2 ;
wherein the medium has a negative dielectric anisotropy.
2 . 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 the formulae I-1 to I-17
in which
alkyl and alkyl* each, independently of one another, denote a straight-chain alkyl radical having 1-6 C atoms,
alkenyl denotes a straight-chain alkenyl radical having 2-6 C atoms, and cycloalkyl denotes a straight chain or branched alkyl group having 1 to 10 C atoms in which a CH 2 group is replaced by
3 . 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 IIA, IIB, IIC and IID, in which the compounds of formula IID are not of formula IID-7,
in which
R 2A , R 2B , R 2C and R 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 2 groups in these radicals may each be replaced, independently of one another, by
—C≡C—, —CF 2 O—, —OCF 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 one or more H atoms may each be replaced by halogen,
L 1 and L 2 each, independently of one another, denote F, Cl, CF 3 or CHF 2 ,
Y denotes H, F, Cl, CF 3 , CHF 2 or CH 3 ,
Z 2 , Z 2B and Z 2D each, independently of one another, denote a single bond, —CH 2 CH 2 —, —CH═CH—, —CF 2 O—, —OCF 2 —, —CH 2 O—, —OCH 2 —, —COO—, —OCO—, —C 2 F 4 —, —CF═CF— or —CH═CHCH 2 O—,
(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.
4 . The medium according to claim 1 , wherein the medium further comprises one or more compounds selected from the group of compounds of formula IID-1
in which alkyl on each occurrence, identically or differently, denotes a straight-chain alkyl radical having 1-6 C atoms, and (O) denotes O or a single bond.
5 . The liquid crystal medium according to claim 1 , wherein the medium further comprises one or more compounds selected from formula III-1
in which the groups occurring have the meanings defined in claim 1 .
6 . The liquid crystal medium according to claim 3 , wherein the medium comprises one or more compounds of formula IIA and said one or more compounds of formula IIA are selected from the group of compounds of the formulae IIA-18, IIA-40 and IIA-42:
in which
alkyl on each occurrence, identically or differently, denotes a straight-chain alkyl radical having 1-6 C atoms, and
(O) denotes O or a single bond.
7 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds of the formula IV
in which
R 41 denotes an unsubstituted alkyl radical having 1 to 7 C atoms or an unsubstituted alkenyl radical having 2 to 7 C atoms,
R 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 comprises one or more compounds selected from the group of compounds of the formulae IV-1, IV-2, IV-3 and IV-4
in which
alkyl and alkyl′, independently of one another, denote alkyl having 1 to 7 C atoms, alkenyl and alkenyl′ independently of one another, denote an alkenyl radical having 2 to 5 C atoms, and
alkoxy denotes alkoxy having 1 to 5 C atoms.
9 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds of the formula IVa,
in which
R 41 and R 42 each, independently of one another, denote a straight-chain alkyl, alkoxy, alkenyl, alkoxyalkyl or alkoxy radical having up to 12 C atoms, and
denotes
Z 4 denotes a single bond, —CH 2 CH 2 —, —CH═CH—, —CF 2 O—, —OCF 2 —, —CH 2 O—, -OCH 2 —, —COO—, —OCO—, —C 2 F 4 —, —C 4 H 8 —, or —CF═CF—.
10 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds of the formula IVb-1 to IVb-3
in which
alkyl and alkyl* each, independently of one another, denote a straight-chain alkyl radical having 1 to 6 C atoms, and
alkenyl and alkenyl* each, independently of one another, denote a straight-chain alkenyl radical having 2 to 6 C atoms.
11 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds of the formula V
in which
R 51 , R 52 independently denote 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,
identically or differently, denote
Z 51 and Z 52 , identically or differently, denote-CH 2 —CH 2 —, —CH 2 —O—, —CH═CH—, —C≡C—, —COO- or a single bond, and
n is 1 or 2.
12 . The liquid crystal medium according to claim 11 , wherein the medium comprises one or more compounds selected from the group of compounds of the formulae V-1 to V-16
in which R 51 and R 52 have the meanings defined in claim 11 .
13 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds of the formula VIII
in which
R 81 and R 82 , identically or differently, denote H, halogen, CN, SCN, 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, alkoxy, alkenyl or alkenyloxy having 3 to 15 C atoms, where one or more CH 2 groups in these radicals may each be replaced, independently of one another, by
—C≡C—, —CF 2 O—, —OCF 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 one or more H atoms may each be replaced by halogen,
A 0 , A 81 , and A 82 , each, independently of one another, denote phenylene-1,4-diyl, in which one or two CH groups may each be replaced by N and one or more H atoms may each be replaced by halogen, CN, CH 3 , CHF 2 , CH 2 F, CF 3 , OCH 3 , OCHF 2 or OCF 3 , cyclohexane-1,4-diyl, in which one or two non-adjacent CH 2 groups may each be replaced, independently of one another, by O or S and one or more H atoms may each be replaced by F, 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 81 and Z 82 , each, independently of one another, denote —CF 2 O—, —OCF 2 —, —CH 2 O—, —OCH 2 —, —CO—O—, —O—CO—, —C 2 H 4 —, —C 2 F 4 , —CF 2 CH 2 —, —CH 2 CF 2 —, —CFHCFH—, —CFHCH 2 —, —CH 2 CFH—, —CF 2 CFH—, —CFHCF 2 —, —CH═CH—, —CF═CH—, —CH═CF—, —CF═CF—, —C═C— or a single bond;
n denotes 0, 1, 2 or 3, and
m denotes 0, 1, 2 or 3.
14 . The liquid crystal medium according to claim 1 , wherein the medium comprises one or more compounds selected from the group of compounds of the formulae PI and PII
in which
R 2 and R 3 denote H, an alkyl or alkoxy radical having 1 to 12 C atoms, an alkenyl radical having 2 to 12 C atoms, where one or more CH 2 groups in these radicals are optionally replaced 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;
independently of one another denote
L 21 , L 22 ,
L 31 and L 32 independently of each other, denote H or F,
Y 2 and Y 3 identically or differently, denote H or CH 3 ,
X 2 and X 3 independently of each other, denote halogen, halogenated alkyl or halogenated alkoxy with 1 to 3 C-atoms or halogenated alkenyl or halogenated alkenyloxy with 2 or 3 C-atoms,
Z 3 denotes —CH 2 CH 2 —, —CF 2 CF 2 —, —COO—, trans- —CH═CH—, trans-CF═CF—, —CH 2 O— or a single bond, and
l, m, n and o are, independently of each other, 0 or 1.
15 . The liquid crystal medium according to claim 1 , wherein the medium comprises at least one chiral dopant.
16 . The liquid crystal medium according to claim 1 , wherein the medium comprises one, two, three or more polymerizable compounds.
17 . The liquid crystal medium according to claim 1 , wherein the medium comprises one, two, three or more stabilizers.
18 . A liquid crystal display comprising the liquid crystal medium according to claim 1 .
19 . The liquid crystal display of claim 18 , wherein the display is a VA, IPS, FFS, PS-VA, PS-IPS or PS-FFS type display.
20 . A method of generating an electro-optical effect comprising applying a voltage to a liquid crystal display according to claim 18 .
21 . 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 compounds of the formula IID-7, one or more compounds selected from the group of compounds of III-2-1, III-2-2, III-2-3, III-2-4, III-2-5, III-2-6, III-2-7, III-2-8, III-2-9, and III-2-10, and one or more compounds selected from the group of compounds of formulae III-3-1, III-3-2, III-3-4, III-3-5, and III-3-6, and optionally with a polymerizable compound or a chiral dopant or a stabilizer or further liquid crystal compounds or additives.
22 . The liquid crystal medium according to claim 1 , wherein the total concentration of compounds of formulae III-2-1, III-2-2, III-2-3, III-2-4, III-2-5, III-2-6, III-2-7, III-2-8, III-2-9, III-2-10, III-3-1, III-3-2, III-3-4, III-3-5, and III-3-6 is in the range of from 7% to 20%.
23 . The liquid crystal medium according to claim 3 , wherein the medium comprises one or more compounds selected from the group of compounds of the formulae IIB and IID.