Nematic liquid crystal composition and liquid crystal display element using the same
US-10323186-B2 · Jun 18, 2019 · US
US11414599B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11414599-B2 |
| Application number | US-202016855447-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 22, 2020 |
| Priority date | Jun 9, 2015 |
| Publication date | Aug 16, 2022 |
| Grant date | Aug 16, 2022 |
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The present invention relates to polymerizable compounds, to processes and intermediates for the preparation thereof, to liquid-crystal media comprising them, and to the use of the polymerizable compounds and liquid crystalline media for optical, electro-optical and electronic purposes, in particular in liquid crystalline displays, especially in liquid crystalline displays of the polymer sustained alignment type.
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The invention claimed is: 1. A liquid crystalline medium comprising one or more compounds of formulae I1-3-1, I1-3-2, I1-4-1 or I1-4-2 wherein L a is a straight-chain alkoxy group with 1 to 12 C atoms or a branched alkoxy group with 3 to 12 atoms, and is optionally fluorinated, P denotes acrylate or methacrylate, and all groups P that are present have the same meaning, Sp, is —(CH 2 ) p2 —O—, —(CH 2 ) p2 —O—, —(CH 2 ) p2 —CO—O—, or —(CH 2 ) p2 —O—CO—, wherein p2 is 2, 3, 4, 5 or 6, and the O-atom or the CO-group, respectively, is connected to the aromatic ring, one or more compounds of the formulae CY and/or PY: in which the individual radicals have the following meanings: a denotes 1 or 2, b denotes 0 or 1, denotes R 1 and R 2 each, independently of one another, denote alkyl having 1 to 12 C atoms, where, in addition, one or two non-adjacent CH 2 groups may be replaced by —O—, —CH═CH—, —CO—, —O—CO— or —CO—O— in such a way that 0 atoms are not linked directly to one another, Z X denotes —CH═CH—, —CH 2 O—, —OCH 2 —, —CF 2 O—, —OCF 2 —, —O—, —CH 2 —, —CH 2 CH 2 — or a single bond, L 1-4 each, independently of one another, denote F, CI, OCF 3 , CF 3 , CH 3 , CH 2 F, CHF 2 and one or more compounds of formulae AN1 or ZK1: in which alkyl denotes a straight-chain alkyl radical having 1-6 C atoms, and alkenyl denotes a straight-chain alkenyl radical having 2-7 C atoms, in which alkyl and alkyl* each, independently of one another, denote a straight-chain alkyl radical having 1-6 C atoms. 2. The liquid crystalline medium according to claim 1 , further comprising one or more additional compounds of the following formulae: in which the individual radicals, on each occurrence identically or differently, each, independently of one another, have the following meaning: is is R A1 is alkenyl having 2 to 9 C atoms or, if at least one of the rings X, Y and Z denotes cyclohexenyl, also one of the meanings of R A2 , R A2 is alkyl having 1 to 12 C atoms, in which, in addition, one or two non-adjacent CH 2 groups may be replaced by —O—, —CH═CH—, —CO—, —OCO— or —COO— in such a way that 0 atoms are not linked directly to one another, Z x is —CH 2 CH 2 —, —CH═CH—, —CF 2 O—, —OCF 2 —, —CH 2 O—, —OCH 2 —, —CO—O—, —O—CO—, —C 2 F 4 —, —CF=CF—, —CH═CH—CH 2 O—, or a single bond, L 1-4 each, independently of one another, are H, F, Cl, OCF 3 , CF 3 , CH 3 , CH 2 F or CHF 2 H, x is 1 or 2, z is 0 or 1. 3. The liquid crystalline medium according to claim 1 , further comprising one or more additional compounds of the following formula: in which the individual radicals have the following meanings: denotes denotes R 3 and R 4 each, independently of one another, denote alkyl having 1 to 12 C atoms, in which, in addition, one or two non-adjacent CH 2 groups may be replaced by —O—, —CH═CH—, —CO—, —O—CO— or —CO—O— in such a way that 0 atoms are not linked directly to one another, Z Y denotes —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 a single bond. 4. The liquid crystalline medium according to claim 1 , wherein the polymerizable compounds of formula I1-3-1, I1-3-2, I1-4-1 or I1-4-2 are polymerized. 5. A process of preparing an liquid crystalline medium of claim 1 , comprising mixing one or more mesogenic or liquid-crystalline compounds with one or more compounds of formula I1-3-1, I1-3-2, I1-4-1 or I1-4-2 and optionally with further liquid-crystalline compounds and/or additives. 6. A liquid crystalline display comprising a liquid crystalline medium as defined in claim 1 . 7. The liquid crystalline display of claim 6 , which is a PSA display. 8. The liquid crystalline display of claim 7 , which is a PS-VA, PS-OCB, PS-IPS, PS-FFS, PS-UB-FFS, PS-poli-VA or PS-TN display. 9. A liquid crystalline display of comprising two substrates, at least one which is transparent to light, an electrode provided on each substrate or two electrodes provided on only one of the substrates, and located between the substrates a layer of an liquid crystalline medium according to claim 1 , wherein the polymerizable compounds are polymerized between the substrates of the display. 10. A process for the production of a liquid crystalline display according to claim 9 , comprising providing the liquid crystalline medium comprising one or more polymerizable compounds between the substrates of the display, and polymerizing the polymerizable compounds. 11. A process for preparing a compound of formula by esterification of a compound of the formula wherein L is on each occurrence identically or differently F, CI, —CN, P—Sp—, or straight chain alkyl having 1 to 25 C atoms, or branched or cyclic alkyl having 3 to 25 C atoms, wherein one or more non-adjacent CH 2 -groups are optionally replaced by —O—, —S—, —CO—, —CO—O—, —O—CO—O—CO—O— in such a manner that O- and/or S-atoms are not directly connected with each other, and wherein one or more H atoms are each optionally replaced by F or CI, or L has the meaning of L a , Sp is a spacer group that is optionally substituted by one or more groups P, or a single bond, P is a polymerizable group, r1, r3, r7 are independently of each other 0, 1, 2 or 3, r2 is 0, 1, 2, 3 or 4, r4, r5, r6 are independently of each other 0, 1 or 2, with r1+r7≥1, r1+r2+r3 1, r4+r5 1, r1+r3+r4 1, R denotes H, and Pg denotes OH, and wherein one R is H and
characterised by the chemical structure of the liquid crystal components {, e.g. by a specific unit} · CPC title
Ph-Ph · CPC title
Compounds containing at least two rings in which the different rings are directly linked (covalent bond) · CPC title
by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds · CPC title
containing a triphenylene ring system · CPC title
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