Components for high-frequency technology, and liquid-crystalline media

US9790426B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9790426-B2
Application numberUS-201013497806-A
CountryUS
Kind codeB2
Filing dateSep 14, 2010
Priority dateSep 25, 2009
Publication dateOct 17, 2017
Grant dateOct 17, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A component for high-frequency technology or for the microwave range and millimeter wave range of the electromagnetic spectrum. The component contains a liquid-crystal compound of the formula I in which the parameters have the respective meanings given in the claims or in the text, or a liquid-crystal medium which itself comprises one or more compounds of this formula I. Also, the corresponding, novel liquid-crystal media, the use and preparation thereof, and the production and use of the components. The components are particularly suitable as phase shifters in the microwave and millimeter wave range, for microwave and millimeter wave array antennae and very particularly for so-called tuneable reflectarrays.

First claim

Opening claim text (preview).

The invention claimed is: 1. Component which operates in the microwave range or millimeter wave range of the electromagnetic spectrum, wherein the component is selected from the group consisting of the following components: wireless and radiowave antenna arrays; microwave antenna arrays; and devices selected from the group consisting of the following devices: phase shifters; varactors; and matching circuit adaptive filters; and wherein the component comprises a liquid-crystal medium, wherein the medium comprises two or more compounds of the formula I, wherein the concentration of all of the compounds of formula I is 30 to 95% by weight, based on the total weight of the medium, in which R 11 and R 12 , independently of one another, denote unfluorinated alkyl having 1 to 15 C atoms, or unfluorinated alkenyl having 2 to 15 C atoms, R 13 denotes ethyl or cycloalkyl having 3 to 6 carbon atoms, provided that: the liquid-crystal medium contains one or more compounds of the formula I-2 and contains one or more compounds of the formula I-3 wherein A 1 denotes cycloalkyl having 3 to 6 C atoms; and wherein the liquid-crystal medium additionally comprises one or more components selected from the group of the following components, components B and D to E, a strongly dielectrically positive component, component B, which has a dielectric anisotropy of 10 or more, a component, component D, which has a dielectric anisotropy in the range from more than −5.0 to less than 10.0 and comprises one or more compounds of the following formula IV: in which R 41 and R 42 , independently of one another, denote unfluorinated alkyl or unfluorinated alkoxy, each having 1 to 15 C atoms, or unfluorinated alkenyl, unfluorinated alkenyloxy or unfluorinated alkoxyalkyl, each having 2 to 15 C atoms, or cycloalkyl, alkylcycloalkyl, cycloalkenyl, alkylcycloalkenyl, alkylcycloalkylalkyl or alkylcycloalkenylalkyl, each having up to 15 C atoms, L 41 to L 44 on each appearance, in each case independently of one another, denote H, alkyl having 1 to 5 C atoms, F or Cl, provided that at least two of the substituents L 41 to L 44 are not H, and P denotes an integer in the range from 7 to 14; and a component, component E, which has a dielectric anisotropy in the range from more than −5.0 to less than 10.0 and comprises one or more compounds of the formulae V to IX: in which L 51 denotes R 51 or X 51 , L 52 denotes R 52 or X 52 , R 51 and R 52 , independently of one another, denote H, unfluorinated alkyl or unfluorinated alkoxy having 1 to 17 C atoms or unfluorinated alkenyl, unfluorinated alkenyloxy or unfluorinated alkoxyalkyl having 2 to 15 C atoms, X 51 and X 52 , independently of one another, denote H, F, Cl, —CN, —NCS, —SF 5 , fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, unfluorinated or fluorinated alkenyloxy or unfluorinated or fluorinated alkoxyalkyl having 2 to 7 C atoms, and  independently of one another, denote L 61 denotes R 21 and, in the case where Z 61 and/or Z 62 denote trans-CH═CH— or trans-CF═CF—, alternatively denotes X 21 , L 62 denotes R 62 and, in the case where Z 61 and/or Z 62 denote trans-CH═CH— or trans-CF═CF—, alternatively denotes X 62 , R 61 and R 62 , independently of one another, denote H, unfluorinated alkyl or unfluorinated alkoxy having 1 to 17 C atoms or unfluorinated alkenyl, unfluorinated alkenyloxy or unfluorinated alkoxyalkyl having 2 to 15 C atoms, X 61 and X 62 , independently of one another, denote F or Cl, —CN, —NCS, —SF 5 , fluorinated alkyl or alkoxy having 1 to 7 C atoms or fluorinated alkenyl, alkenyloxy or alkoxyalkyl having 2 to 7 C atoms, one of Z 61 and Z 62 denotes trans-CH═CH—, trans-CF═CF— or —C≡C— and the other, independently thereof, denotes trans-CH═CH—, trans-CF═CF— or a single bond, and  independently of one another, denote L 71 denotes R 71 or X 71 , L 72 denotes R 72 or X 72 , R 71 and R 72 , independently of one another, denote H, unfluorinated alkyl or unfluorinated alkoxy having 1 to 17 C atoms or unfluorinated alkenyl, unfluorinated alkenyloxy or unfluorinated alkoxyalkyl having 2 to 15 C atoms, X 71 and X 72 , independently of one another, denote H, F, Cl, —CN, —NCS, —SF 5 , fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, unfluorinated or fluorinated alkenyloxy or unfluorinated or fluorinated alkoxyalkyl having 2 to 7 C atoms, and Z 71 to Z 73 , independently of one another, denote trans-CH═CH—, trans-CF═CF—, —C≡C— or a single bond, and  independently of one another, denote R 81 and R 82 , independently of one another, denote H, unfluorinated alkyl or alkoxy having 1 to 15 C atoms or unfluorinated alkenyl, alkenyloxy or alkoxyalkyl having 2 to 15 C atoms, one of Z 81 and Z 82 denotes trans-CH═CH—, trans-CF═CF— or —C≡C— and the other, independently thereof, denotes trans-CH═CH—, trans-CF═CF— or a single bond, and  independently of one another, denote L 91 denotes R 91 or X 91 , L 92 denotes R 92 or X 92 , R 91 and R 92 , independently of one another, denote H, unfluorinated alkyl or alkoxy having 1 to 15 C atoms or unfluorinated alkenyl, alkenyloxy or alkoxyalkyl having 2 to 15 C atoms, X 91 and X 92 , independently of one another, denote H, F, Cl, —CN, —NCS, —SF 5 , fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms or fluorinated alkenyl, unfluorinated or fluorinated alkenyloxy or unfluorinated or fluorinated alkoxyalkyl having 2 to 7 C atoms, and Z 91 to Z 93 , independently of one another, denote trans-CH═CH—, trans-CF═CF—, —C≡C— or a single bond,  independently of one another, denote and where compounds of the formula IIIA where R 31 and R 32 denote unfluorinated alkyl or unfluorinated alkoxy, each having 1 to 15 C atoms, or unfluorinated alkenyl, unfluorinated alkenyloxy

Assignees

Inventors

Classifications

  • Ph-C≡C-Ph-C≡C-Ph · CPC title

  • by controlled diffraction or phased-array beam steering (controlled diffraction for optical switching G02F1/31) · CPC title

  • C09K19/18Primary

    the chain containing carbon-to-carbon triple bonds, e.g. tolans · CPC title

  • used in the High Frequency technical field · CPC title

  • containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane rings · CPC title

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What does patent US9790426B2 cover?
A component for high-frequency technology or for the microwave range and millimeter wave range of the electromagnetic spectrum. The component contains a liquid-crystal compound of the formula I in which the parameters have the respective meanings given in the claims or in the text, or a liquid-crystal medium which itself comprises one or more compounds of this formula…
Who is the assignee on this patent?
Manabe Atsutaka, Goebel Mark, Klass Dagmar, and 3 more
What technology area does this patent fall under?
Primary CPC classification C09K19/18. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 17 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).