Liquid-crystal display
US-8940375-B2 · Jan 27, 2015 · US
US9982194B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9982194-B2 |
| Application number | US-201514674518-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 31, 2015 |
| Priority date | Dec 20, 2011 |
| Publication date | May 29, 2018 |
| Grant date | May 29, 2018 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The invention relates to liquid-crystalline media which can be used, in particular, for electro-optical displays having active-matrix addressing based on the ECB effect and for IPS (in-plane switching) displays or FFS (fringe field switching) displays.
Opening claim text (preview).
What is claimed is: 1. A liquid-crystalline medium comprising: (i) at least one compound of the formula I, in which R 1 and R 1* each, independently of one another, denote an alkyl or alkoxy radical having 1 to 15 C atoms, where, in addition, one or more CH 2 groups in these radicals may each be replaced, independently of one another, by —C≡C—, —CF 2 O—, —CH═CH—, , , —O—, —CO—O—, —O—CO— in such a way that O atoms are not linked directly to one another, and in which, in addition, one or more H atoms may be replaced by halogen, Z 1 denotes a single bond, —CH 2 CH 2 —, —CH═CH—, —CH 2 O—, —OCH 2 —, —CF 2 O—, —OCF 2 —, —COO—, —OCO—, —C 2 F 4 —, —CF═CF—, —CH═CHCHO—, L 1 and L 2 each, independently of one another, denote F, Cl, CF 3 or CHF 2 ; (ii) one or more compounds selected from the group consisting of compounds of the formulae L-1 to L-11, CCH-nOm, P-4, and EY, in which R, R 1 and R 2 each, independently of one another, denote H, an alkyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF 3 or at least monosubstituted by halogen, where, in addition, one or more CH 2 groups in these radicals may be replaced by —O—, —S—, , —C≡C—, —CF 2 O—, —OCF 2 —, —OC—O— or —O—CO— in such a way that O atoms are not linked directly to one another, alkyl denotes an alkyl radical having 1-6 C atoms, and s denotes 1 or 2; in which n and m each, independently of one another, denote 1, 2, 3, 4, 5 or 6, wherein R 1 is an alkyl or alkoxy radical having 1 to 15 C atoms, wherein one or more CH 2 groups in these radicals are optionally replaced, independently of one another, by —C≡C—, —CF 2 O, —CH═CH—, —O—, —CO—O—, —O—CO— in such a way that O atoms are not linked directly to one another, and wherein, in addition, one or more H atoms may be replaced by halogen; in which R 1 and R 1* each, independently of one another, denote an alkyl or alkoxy radical having 1 to 15 C atoms, where, in addition, one or more CH 2 groups in these radicals may each be replaced, independently of one another, by —C≡C—, —CF 2 O—, —CH═CH—, , , —O—, —CO—O—, —O—CO— in such a way that O atoms are not linked directly to one another, and in which, in addition, one or more H atoms may be replaced by halogen, L 1 and L 2 each, independently of one another, denote F, Cl, CF 3 or CHF 2 ; and (iii) at least two compounds selected from the group of compounds of formulae IIA, IIB and IIC, in which R 2A and R 2B each, independently of one another, denote H, an alkyl or alkenyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF 3 or at least monosubstituted by halogen, where, in addition, one or more CH 2 groups in these radicals may be replaced by —O—, —S—, —C≡C—, —CF 2 O—, —OCF 2 —, —OC—O— or —O—CO— in such a way that O atoms are not linked directly to one another, R 2c each, independently of one another, denote H, an alkyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF 3 or at least monosubstituted by halogen, where, in addition, one or more CH 2 groups in these radicals may be replaced by —O—, —S—, —C≡C—, —CF 2 O—, —OCF 2 —, —OC—O— or —O—CO— in such a way that O atoms are not linked directly to one another, L 1-4 each, independently of one another, denote F or Cl, Z 2 and Z 2′ 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—, —CH═CHCH 2 O—, p denotes 1 or 2, q denotes 1 or 2, and v denotes 1 to 6. 2. The liquid-crystalline medium according to claim 1 , wherein the proportion of one or more compounds of the formula I in the mixture as a whole is 10-45% by weight. 3. The liquid-crystalline medium according to claim 1 further comprising one or more compounds selected from the compounds of formulae BC, CR, PH-1, PH-2 and BF, in which R B1 , R B2 , R CR1 , R CR2 , R 1 , R 2 each, independently of one another, denote H, an alkyl radical having up to 15 C atoms which is unsubstituted, monosubstituted by CN or CF 3 or at least monosubstituted by halogen, where, in addition, one or more CH 2 groups in these radicals may be replaced by —O—, —S—, —C≡C—, —CF 2 O—, —OCF 2 —, —OC—O— or —O—CO— in such a way that O atoms are not linked directly to one another, c is 0, 1 or 2. 4. The liquid-crystalline medium according to claim 1 further comprising one or more additives selected from the group consisting of stabilisers, antioxidants, UV absorbers, nanoparticles, microparticles, and a combination thereof. 5. The liquid-crystalline medium according to claim 1 further comprising one or more additives selected from the following compounds: in which n=1, 2, 3, 4, 5, 6 or 7 6. The liquid-crystalline medium according to claim 1 further comprising one or more BHT derivatives. 7. The liquid-crystalline medium according to claim 1 , wherein the liquid-crystalline medium comprises at least one compound of formula I selected from the group consisting of formulae I-1 through I-145:
linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters {or ethers} · CPC title
Ph-Ph-Ph · CPC title
containing compounds with benzene rings directly linked · CPC title
Compounds comprising 1,4-cyclohexylene and 2,3-difluoro-1,4-phenylene · CPC title
Ph-Ph · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.