Liquid-crystalline medium

US9701905B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9701905-B2
Application numberUS-201314651837-A
CountryUS
Kind codeB2
Filing dateNov 22, 2013
Priority dateDec 13, 2012
Publication dateJul 11, 2017
Grant dateJul 11, 2017

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Abstract

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The application relates to a liquid-crystalline medium comprising at least one dichroic dye having a rylene structure which absorbs red light. The application furthermore relates to a device, preferably a device for the regulation of the passage of energy through a light-transmitting area, which contains the liquid-crystalline medium.

First claim

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The invention claimed is: 1. A liquid-crystalline medium comprising at least one dichroic dye F having a rylene structure whose longest-wave absorption maximum is at a wavelength of greater than 600 nm, and which is selected from the group consisting of compounds of formulae (F-I), (F-II), (F-III), (F-IV) and (F-V), wherein n is 1, 2, 3, 4, 5, 6, 7 or 8, Z F1 is, each independently, a single bond, —C(═O)O—, —OC(═O)—, —C(═O)S—, —SC(═O)—, —CF 2 —, —CF 2 —CF 2 —, —CF 2 O—, —OCF 2 — or —O—, R F1 is, each independently, an alkyl or alkoxy group having 1 to 10 C atoms, or an alkenyl or alkynyl group having 2 to 10 C atoms, or a cycloalkyl group having 3 to 10 C atoms, which are optionally substituted by one or more radicals R FA , or an aryl or heteroaryl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , R F2 , R F3 , R F4 , R F5 , R F6 are each independently, H, F, Cl, Br, OR FA , OCH 2 R FA , SR FA , SCH 2 R FA , C(═O)OR FA , an alkyl or alkoxy group having 1 to 10 C atoms, or an alkenyl or alkynyl group having 2 to 10 C atoms, or a cycloalkyl group having 3 to 10 C atoms, which are optionally substituted by one or more radicals R FA , or an aryl or heteroaryl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , or an aralkyl or heteroaralkyl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , or an aryloxy or heteroaryloxy group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , R FA is, each independently, F, Cl, Br, —OCF 2 R FB , —CF 2 O—R FB , an alkyl or alkoxy group having 1 to 10 C atoms, or an alkenyl or alkynyl group having 2 to 10 C atoms, or a cycloalkyl group having 3 to 10 C atoms, where the said groups are optionally substituted by one or more radicals R FB , or an aryl or heteroaryl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FB , and R FB is, each independently, F or an aliphatic, aromatic or heteroaromatic organic radical having 1 to 20 C atoms; and one or more compounds of formula (I) wherein R 11 is H, F, Cl, CN, NCS, R 1 —O—CO—, R 1 —CO—O—, an alkyl, alkoxy or thioalkoxy group having 1 to 10 C atoms, or an alkenyl, alkenyloxy or thioalkenyloxy group having 2 to 10 C atoms, in which one or more H atoms in the above-mentioned groups are optionally replaced by F, Cl or CN, and in which one or more CH 2 groups in the above-mentioned groups are optionally replaced by O, S, —O—CO— or —CO—O—, R 1 is an alkyl group having 1 to 10 C atoms, in which one or more hydrogen atoms are optionally replaced by F or Cl, and in which one or more CH 2 groups are optionally replaced by O or S, Z 11 is —CO—O—, —O—CO—, —CF 2 —CF 2 —, —CF 2 —O—, —O—CF 2 —, —CH 2 —CH 2 —, —CH═CH—, —CF═CF—, —CF═CH—, —CH═CF—, —C≡C—, —OCH 2 —, —CH 2 O—or a single bond, A 11 is and X is, each independently, F, Cl, CN or an alkyl, alkoxy or alkylthio group having 1 to 10 C atoms, in which one or more hydrogen atoms in the above-mentioned groups are optionally replaced by F or Cl, and in which one or more CH 2 groups in the above-mentioned groups are optionally replaced by O or S. 2. The liquid-crystalline medium according to claim 1 , wherein the degree of anisotropy R of the dye F is greater than 0.4. 3. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F absorbs predominantly light in the wavelength range from 600 to 2000 nm. 4. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F is present in a concentration of 0.1% by weight to 10% by weight. 5. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F is a fluorescent dye. 6. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F contains a single rylene chromophore, which is the only rylene chromophore in the dichroic dye F. 7. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F contains a single chromophore, which is the only a chromophore in the dichroic dye F. 8. The liquid-crystalline medium according to claim 1 , which, besides the dichroic dye F, comprises two or three further dichroic dyes, where at least one of the two or three further dichroic dyes absorbs green to yellow light and at least one other of the two or three further dichroic dyes absorbs blue light. 9. The liquid-crystalline medium according to claim 1 , which, in addition to the dichroic dye F, comprises one or more further dichroic dyes which are selected from the group consisting of azo compounds, anthraquinones, methine compounds, azomethine compounds, merocyanine compounds, naphthoquinones, tetrazines, perylenes, terrylenes, quaterrylenes, higher rylenes and pyrromethenes. 10. The liquid-crystalline medium according to claim 1 , which comprises exclusively dichroic dyes which are rylene dyes selected from the group consisting of compounds of formulae (F-I), (F-II), (F-III), (F-IV) and (F-V). 11. The liquid-crystalline medium according to claim 1 , which has a dielectric anisotropy of greater than 3. 12. A process for preparing the liquid-crystalline medium according to claim 1 , comprising first mixing the one or more compounds of formula (I) with one of more further compounds suitable for forming a liquid crystalline medium without the dichroic dye, and subsequently adding the dichroic dye to said liquid-crystalline medium and dissolving the dichroic dye therein. 13. An electrically switchable LC device of the guest-host type, containing at least one liquid-crystalline medium according to claim 1 in a switching layer. 14. The liquid-crystalline medium according to claim 1 , wherein the dichroic dye F is a compound of formula (F-I) wherein n is 1, 2, 3, 4, 5, 6, 7 or 8; Z F1 is, each independently, a single bond, —C(═O)O—, —OC(═O)—, —C(═O)S—, —SC(═O)—, —CF 2 —, —CF 2 —CF 2 —, —CF 2 O—, —OCF 2 — or —O—; R F1 is, each independently, an alkyl or alkoxy group having 1 to 10 C atoms, or an alkenyl or alkynyl group having 2 to 10 C atoms, or a cycloalkyl group having 3 to 10 C atoms, which are optionally substituted by one or more radicals R FA , or an aryl or heteroaryl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA ; R F2 , R F3 are each independently, H, F, Cl, Br, OR FA , OCH 2 R FA , SR FA , SCH 2 R FA , C(═O)OR FA , an alkyl or alkoxy group having 1 to 10 C atoms, or an alkenyl or alkynyl group having 2 to 10 C atoms, or a cycloalkyl group having 3 to 10 C atoms, which are optionally substituted by one or more radicals R FA , or an aryl or heteroaryl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , or an aralkyl or heteroaralkyl group having 6 to 30 aromatic ring atoms, which are optionally substituted by one or more radicals R FA , or an aryloxy or heteroaryloxy group having 6 to 30 arom

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What does patent US9701905B2 cover?
The application relates to a liquid-crystalline medium comprising at least one dichroic dye having a rylene structure which absorbs red light. The application furthermore relates to a device, preferably a device for the regulation of the passage of energy through a light-transmitting area, which contains the liquid-crystalline medium.
Who is the assignee on this patent?
Merck Patent Gmbh
What technology area does this patent fall under?
Primary CPC classification C09K19/606. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Jul 11 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).