Mesogenic compound, liquid-crystal medium and liquid crystal display

US2016115388A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016115388-A1
Application numberUS-201414785500-A
CountryUS
Kind codeA1
Filing dateMar 21, 2014
Priority dateApr 19, 2013
Publication dateApr 28, 2016
Grant date

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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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Abstract

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The instant invention relates to mesogenic compounds of formula I-Z to mesogenic media, preferably exhibiting a blue phase, comprising a component, component A, consisting of one or more compounds of formula I-Z, and, preferably, a second component, component B, consisting of one or more compounds selected from the group of compounds of formulae I-M and I-U, wherein the parameters are as specified in the text, preferably stabilised by a polymer, and their use in electro-optical light modulation elements and their respective use in displays, as well as to such displays.

First claim

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1 . Mesogenic compound of formula I-Z wherein R 1 is alkyl with 1 to 9 C-atoms, which is straight chain or branched, unsubstituted, mono- or poly-substituted by F, Cl or CN, and in which one or more CH 2 groups are optionally replaced, in each case independently from one another, by —O—, —S—, —NR 01 —, —SiR 01 R 02 —, —CO—, —COO—, —OCO—, —OCO—O—, —S—CO—, —CO—S—, —CY 01 ═CY 02 — or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, L 1 is H or F, X 1 is F, CN or CF 3 , Y 01 and Y 02 are, independently of each other, F, Cl or CN, and alternatively one of them may be H, and R 01 and R 02 are, independently of each other, H or alkyl with 1 to 12 C-atoms. 2 . Mesogenic medium exhibiting a blue phase, comprising a component A, consisting of one or more compounds of formula I-Z wherein R 1 is alkyl with 1 to 9 C-atoms, which is straight chain or branched, unsubstituted, mono- or poly-substituted by F, Cl or CN, and in which one or more CH 2 groups are optionally replaced, in each case independently from one another, by —O—, —S—, —NR 01 —, —SiR 01 R 02 —, —CO—, —COO—, —OCO—, —OCO—O—, —S—CO—, —CO—S—, —CY 01 ═CY 02 — or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, L 1 is H or F, X 1 is F, CN or CF 3 , Y 01 and Y 02 are, independently of each other, F, Cl or CN, and alternatively one of them may be H, and R 01 and R 02 are, independently of each other, H or alkyl with 1 to 12 C-atoms. 3 . Mesogenic medium according to claim 2 , characterized in that it comprises one or more chiral dopants. 4 . Mesogenic medium according to claim 2 , characterized in that it comprises a second component, component B, consisting of one or more compounds selected from the group of of compounds of formulae I-M and I-U wherein R 1 , L 1 and X 1 have the respective meanings given in claim 2 . 5 . Mesogenic medium according to claim 2 , characterized in that it comprises one or more compounds selected from the group of formulae I-A, I-E, I-N and I-T wherein R 0 has the meaning of R 1 , R 1 has the meaning given in claim 2 , and L 01 to L 03 , L 1 , L 11 and L 12 are independently of one another H or F. 6 . Mesogenic medium according to claim 2 , characterized in that it comprises one or more compounds of formula II wherein L 21 to L 23 are, independently of each other, H or F, R 2 is alkyl, which is straight chain or branched, is unsubstituted, mono- or poly-substituted by F, Cl or CN, preferably by F, and in which one or more CH 2 groups are optionally replaced, in each case independently from one another, by —O—, —S—, —NR 01 —, —SiR 01 R 02 —, —CO—, —COO—, —OCO—, —OCO—O—, —S—CO—, —CO—S—, −CY 01 ═CY 02 — or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, Y 01 and Y 02 are, independently of each other, F, Cl or CN, and alternatively one of them may be H, R 01 and R 02 are, independently of each other, H or alkyl with 1 to 12 C-atoms. 7 . Medium according to claim 2 , characterized in that it comprises one or more compounds of formula III wherein R 3 has the meaning given for R 1 in claim 2 . 8 . Medium according to claim 2 , characterized in that it comprises one or more compounds selected from the group of compounds of formulae IV and V wherein R 4 and R 5 are, independently of each other, alkyl, which is straight chain or branched, preferably has 1 to 20 C-atoms, is unsubstituted, mono- or poly-substituted by F, Cl or CN, preferably by F, and in which one or more CH 2 groups are optionally replaced, in each case independently from one another, by —O—, —S—, —CO—, —COO—, —OCO—, —OCO—O—, —S—CO—, —CO—S— or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, L 5 is H or F, n and m are, independently of one another, 0 or 1. 9 . Medium according to at least claim 2 , characterized in that it comprises a polymerisable component, which comprises one or more polymerisable compounds. 10 . Medium according to claim 2 , characterized in that it comprises one or more compounds of formula M1 wherein the parameters have the following meanings: P 1 and P 2 each, independently of one another, a polymerisable group, Sp 1 and Sp 2 each, independently of one another, a single bond or a spacer group, and, wherein alternatively also one or more of P 1 -Sp 1 - and P 2 -Sp 2 - may be R aa , provided that at least one of P 1 -Sp 1 - and P 2 -Sp 2 - present in the compound is not R aa , R aa H, F, Cl, CN or linear or branched alkyl having 1 to 25 C-atoms, wherein one or more non-adjacent —CH 2 — groups, independently of each another, may be replaced by —C(R 0 )═C(R 00 )—, —C≡C—, —N(R 0 )—, —O—, —S—, —CO—, —CO—O—, —O—CO—, —O—CO—O— in such a way that neither O- nor S-atoms are directly linked to one another, and wherein also one or more H-atoms may be replaced by F, Cl, CN or P 1 -Sp 1 -, R 0 , R 00 each, at each occurrence independently of one another, H or alkyl having 1 to 12 C-atoms, R y and R z each, independently of one another, H, F, CH 3 or CF 3 , L at each occurrence independently of one another, F, Cl, CN, SCN, SF 5 or linear or branched, optionally mono- or poly-fluorinated, alkyl, alkoxy, alkenyl, alkinyl, alkylcarbonyl, alkoxycarbonyl, alkylcarbonyloxy or alkoxycarbonyloxy having 1 to 12 C-atoms, and r 0, 1, 2, 3 or 4. 11 . Medium according to claim 2 , characterized in that it comprises one or more compounds of formula M2 wherein the parameters have the following meanings: P 1 and P 2 each, independently of one another, a polymerisable group, Sp 1 and Sp 2 each, independently of one another, a single bond or a spacer group, and, wherein alternatively also one or more of P 1 -Sp 1 - and P 2 -Sp 2 - may be R aa , provided that at least one of P 1 -Sp 1 - and P 2 -Sp 2 - present in the compound is not R aa , R aa H, F, Cl, CN or linear or branched alkyl having 1 to 25 C-atoms, wherein one or more non-adjacent —CH 2 — groups, independently of each another, may be replaced by —C(R 0 )═C(R 00 )—, —C≡C—, —(R 0 )—, —O—, —S—, —CO—, —CO—O—, —O—CO—, —O—CO—O— in such a way that neither O- nor S-atoms are directly linked to one another, and wherein also one or more H-atoms may be replaced by F, Cl, CN or P 1 -Sp 1 -, R 0 , R 00 each, at each occ

Assignees

Inventors

Classifications

  • Uncondensed pyrimidines · CPC title

  • Heterocyclic compounds · CPC title

  • Blue phase · CPC title

  • characterised by the electro-optical or magneto-optical effect, e.g. field-induced phase transition, orientation effect, guest-host interaction or dynamic scattering · CPC title

  • stabilizing the alignment; Polymer stabilized alignment · CPC title

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What does patent US2016115388A1 cover?
The instant invention relates to mesogenic compounds of formula I-Z to mesogenic media, preferably exhibiting a blue phase, comprising a component, component A, consisting of one or more compounds of formula I-Z, and, preferably, a second component, component B, consisting of one or more compounds select…
Who is the assignee on this patent?
Merck Patent Gmbh
What technology area does this patent fall under?
Primary CPC classification C09K19/3458. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Apr 28 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).