US2022228065A1PendingUtilityA1

Liquid-crystalline medium and liquid-crystal display comprising the same

Assignee: MERCK PATENT GMBHPriority: Sep 8, 2017Filed: Mar 28, 2022Published: Jul 21, 2022
Est. expirySep 8, 2037(~11.1 yrs left)· nominal 20-yr term from priority
C09K 19/3402C09K 2019/3027C09K 19/32C09K 19/3098C09K 19/3458C09K 2019/122C09K 2019/0466C09K 2019/3408C09K 2019/301C09K 2019/3422C09K 19/12C09K 2019/3016C09K 19/586C09K 19/3491C09K 19/0403C09K 19/3441C09K 19/30
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Claims

Abstract

The invention relates to a liquid-crystalline medium, preferably having a nematic phase and dielectric anisotropy of 0.5 or more, which comprises one or more compounds of formula YXin whichthe parameters have the meanings 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 YX for the improvement of the transmission and/or response times of a liquid-crystalline medium which comprises one or more additional mesogenic compounds.

Claims

exact text as granted — not AI-modified
1 - 17 . (canceled) 
     
     
         18 . A compound of formula YX 
       
         
           
           
               
               
           
         
         in which 
       
       
         
           
           
               
               
           
         
       
       denote independently of each other denote 
       
         
           
           
               
               
           
         
         n denotes 0 or 1, 
         R Y  denotes alkyl, alkoxy, fluorinated alkyl or fluorinated alkoxy having 1 to 7 C atoms, alkoxyalkyl or fluorinated alkenyl having 2 to 7 C atoms, 
         X Y  denotes F, Cl, NCS, fluorinated alkyl, fluorinated alkenyl, fluorinated alkoxy or fluorinated alkenyloxy, the latter four groups having 1 to 4 C atoms, preferably F, CF 3  or OCF 3 , and 
         Z Y  denotes a single bond, —CH═CH—, —C≡C—, —CH 2 —CH 2 —, —CF 2 —O—, CH 2 —O— or —CO—O—; 
         except that compounds wherein 
         n denotes 1, 
         Z Y  denotes a single bond, 
       
       
         
           
           
               
               
           
         
       
       A denotes 
       
         
           
           
               
               
           
         
       
       denotes 
       
         
           
           
               
               
           
         
       
       and
 X Y  denotes F, 
 or 
 n denotes 1, 
 Z Y  denotes a single bond, 
 
       
         
           
           
               
               
           
         
       
       denotes 
       
         
           
           
               
               
           
         
       
       denotes 
       
         
           
           
               
               
           
         
       
       and
 X Y  denotes OCF 3 , 
 or 
 n denotes 0, 
 Z Y  denotes a single bond, 
 
       
         
           
           
               
               
           
         
       
       denotes 
       
         
           
           
               
               
           
         
       
       and
 X Y  denotes F or OCF 3 , 
 are excluded. 
 
     
     
         19 . The compound of  claim 18 , wherein the compound is selected from the group of compounds of formulae YX-1, YX-2, YX-3, YX-4 and YX-5: 
       
         
           
           
               
               
           
         
       
       in which
 R Y  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, and 
 X Y  denotes F, Cl, CN, NCS, fluorinated alkyl, fluorinated alkenyl, fluorinated alkoxy or fluorinated alkenyloxy, the latter four groups preferably having 1 to 4 C atoms, preferably F, CF 3  or OCF 3 . 
 
     
     
         20 . The compound according to  claim 18 , wherein the compound is selected from the group consisting of: 
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
       
       wherein n is an integer from 1 to 6. 
     
     
         21 . A process for the preparation of a liquid-crystalline medium comprising one or more compounds of formula YX according to  claim 18 , wherein one or more compounds of formula YX are mixed with one or more additional mesogenic compounds. 
     
     
         22 . A process for the preparation of a compound of formula YX according to  claim 18 , comprising:
 nucleophilic addition of a metallated aryl derivative resulting in a corresponding tertiary alcohol,   dehydration of the tertiary alcohol to give a cyclohexylene-cyclohexenylenephenylene compound, and   hydrogenation of the cyclohexylene-cyclohexenylene-phenylene compound to the respective bicyclohexylene-phenylene compound.   
     
     
         23 . The process of  claim 18  wherein the nucleophilic addition of a metallated aryl derivative resulting in the corresponding tertiary alcohol is a Grignard reagent to a bicyclohexyl ketone.

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