Liquid-crystalline medium and liquid-crystal display comprising the same and compounds
US-2022267676-A1 · Aug 25, 2022 · US
US11795398B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11795398-B2 |
| Application number | US-202017624721-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 2, 2020 |
| Priority date | Jul 5, 2019 |
| Publication date | Oct 24, 2023 |
| Grant date | Oct 24, 2023 |
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The invention relates to a liquid-crystalline medium having a nematic phase comprising one or more compounds of formula X wherein the parameters have the meaning given in the text, to the use thereof in an electro-optical display, particularly in an active-matrix display based on the IPS or FFS effect, to displays of this type which contain a liquid-crystalline medium of this type and to the use of the compounds of formula X for improvement of the transmission and/or response times of a liquid-crystalline medium which comprises one or more additional mesogenic compounds, as well as to the compounds of formula X.
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The invention claimed is: 1. A liquid crystalline medium having a nematic phase and a dielectric anisotropy (Δε) of 0.5 or more, comprising: one or more compounds selected from formulae X-2-2 and X-2-4 in which R 1X denotes H, an alkyl radical having 1 to 15 C atoms, wherein 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, Y 1 denotes Cl, CF 3 , CHF 2 , OCF 3 , CN or NCS, and one or more additional compounds. 2. The medium according to claim 1 , further comprising one or more compounds of formula B and/or formula S, in which denotes denotes n denotes 1 or 2, denotes alkyl, alkoxy, fluorinated alkyl, fluorinated alkoxy, alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl and X 1 denotes F, Cl, fluorinated alkyl, fluorinated alkenyl, fluorinated alkoxy, or fluorinated alkenlyoxy, in which denotes denotes n denotes 1 or 2, R 1 denotes alkyl, alkoxy, fluorinated alkyl, fluorinated alkoxy, alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl, and X 1 denotes F, Cl, fluorinated alkyl, fluorinated alkenyl, fluorinated alkoxy, or fluorinated alkenlyoxy. 3. The medium according to claim 1 , further comprising one or more compounds of formula I: in which denotes denotes n denotes 0 or 1, R 11 and R 12 independently of each other denote alkyl, alkoxy, fluorinated alkyl or fluorinated alkoxy, alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 C atoms, and R 11 alternatively denotes R 1 and R 12 alternatively denotes X 1 , R 1 denotes alkyl, alkoxy, fluorinated alkyl, or fluorinated alkoxy, or alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 C atoms, and X 1 denotes F, Cl, fluorinated alkyl, fluorinated alkenyl, fluorinated alkoxy, or fluorinated alkenyloxy. 4. The medium according to claim 1 , further comprising one or more compounds selected from the group of compounds of formulae II and III in which R 2 denotes alkyl, alkoxy, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms, or alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 C atoms, on each appearance, independently of one another, denote L 21 and L 22 denote H or F, X 2 denotes halogen, halogenated alkyl or alkoxy having 1 to 3 C atoms, or halogenated alkenyl or alkenyloxy having 2 or 3 C atoms, m denotes 0, 1, 2 or 3, R 3 denotes alkyl, alkoxy, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms, alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 C atoms, on each appearance, independently of one another, are L 31 and L 32 , independently of one another, denote H or F, X 3 denotes halogen, halogenated alkyl or alkoxy having 1 to 3 C atoms, or halogenated alkenyl or alkenyloxy having 2 or 3 C atoms, F, Cl, —OCF 3 , —OCHF 2 , —O—CH 2 CF 3 , —O—CH═CF 2 , —O—CH═CH 2 , or —CF 3 , 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 n denotes 0, 1, 2 or 3. 5. The liquid-crystalline medium according to claim 1 , further comprising one or more dielectrically neutral compounds selected from the group of formulae IV and V: in which R 41 and R 42 , independently of one another, denote alkyl, alkoxy, fluorinated alkyl, or fluorinated alkoxy having 1 to 7 C atoms, or alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 C atoms, independently of one another and, if occurs twice, also these independently of one another, denote Z 41 and Z 42 , independently of one another and, if Z 41 occurs twice, also these independently of one another, denote —CH 2 CH 2 —, —COO—, trans-CH═CH—, trans-CF═CF—, —CH 2 O—, —CF 2 O—, —C≡C— or a single bond, p denotes 0, 1 or 2, R 51 and R 52 , independently of one another, denote alkyl, alkoxy, fluorinated alkyl, or fluorinated alkoxy having 1 to 7 C atoms, or alkenyl, alkenyloxy, alkoxyalkyl, or fluorinated alkenyl having 2 to 7 atoms, if present, each, independently of one another, denote Z 51 to Z 53 each, independently of one another, denote —CH 2 —CH 2 —, —CH 2 —O—, —CH═CH—, —C≡C, —COO— or a single bond, and i and j each, independently of one another, denote 0 or 1. 6. The liquid-crystalline medium according to claim 5 , further comprising one or more compounds selected from the group of formulae VI to IX:
Constructional arrangements; {Manufacturing methods}(G02F1/135, G02F1/136 take precedence) · CPC title
containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings · CPC title
in which at least two rings are linked by a carbon chain containing carbon to carbon double bonds · CPC title
at least two benzene rings directly linked, e.g. biphenyls · CPC title
having oxygen as hetero atom (sugars C09K19/0422) · CPC title
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