Liquid crystal display device
US-2016131947-A1 · May 12, 2016 · US
US10858591B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10858591-B2 |
| Application number | US-201715585312-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 3, 2017 |
| Priority date | Jun 6, 2016 |
| Publication date | Dec 8, 2020 |
| Grant date | Dec 8, 2020 |
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A stabilizer represented by formula I, wherein M represents cyclopentyl, cyclobutyl or cyclopropyl; Z 1 and Z 2 each independently represent a single bond, —CH 2 —, —CH 2 CH 2 —, —O—, —CH 2 O—, —OCH 2 — or —COO—; represents one or two of and n represents 0, 1 or 2.
Opening claim text (preview).
The invention claimed is: 1. A liquid crystal composition comprising a stabilizer represented by formula I, and, one or more of compounds represented by formulas II-1 to II-14, wherein M represents cyclopentyl, cyclobutyl or cyclopropyl; Z 1 and Z 2 each independently represent a single bond; represents one or two of and n represents 1 or 2; wherein R0, R0′, R1, R1′, R2, R2′, R3, R3′ each independently represent an alkyl group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, or an alkoxy group having a carbon atom number of 1-10, wherein any —CH 2 — can be substituted by —O—, and any hydrogen can be substituted by F; and the (F)s each independently represent H or F. 2. The liquid crystal composition according to claim 1 , characterized in that said stabilizer represented by formula I is selected from the following structures: wherein M represents cyclopentyl, cyclobutyl or cyclopropyl; represents and Z 1 represents a single bond. 3. The liquid crystal composition according to claim 2 , characterized in that said stabilizer represented by formula I-a is selected from the following structures: said stabilizer represented by formula I-b is selected from the following structures: 4. The liquid crystal composition according to claim 1 , characterized in that in said liquid crystal composition, the total content in mass percentage of the compound represented by formula I is 0.001-5%; the total content in mass percentage of the compounds represented by formulas II-1 to II-10 is 1-60%; and the total content in mass percentage of the compounds represented by formulas II-11 to 11-14 is 0-30%; wherein R0 and R2 each independently represent an alkyl group having a carbon atom number of 1-5 or an alkenyl group having a carbon atom number of 2-5, and R1 and R3 each independently represent an alkyl or alkoxy group having a carbon atom number of 1-5. 5. The liquid crystal composition according to claim 1 , characterized in that said liquid crystal composition is a positive liquid crystal composition and further comprises one or more compounds represented by formula III: wherein R 4 represents an alkyl group having a carbon atom number of 1-10, a fluorinated alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorinated alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorinated alkenyl group having a carbon atom number of 2-10, an alkenoxy group having a carbon atom number of 3-8 or a fluorinated alkenoxy group having a carbon atom number of 3-8, and any one or more CH 2 in R 4 may be substituted by cyclopentyl, cyclobutyl or cyclopropyl; each independently represent one or two of m represents 1 or 2; Z 3 and Z 4 each independently represent a single bond, —CF 2 O—, —CH 2 CH 2 — or —CH 2 O—; and Y 2 represents F, a fluorinated alkyl group having a carbon atom number of 1-5, a fluorinated alkoxy group having a carbon atom number of 1-5, a fluorinated alkenyl group having a carbon atom number of 2-5, or a fluorinated alkenoxy group having a carbon atom number of 3-8. 6. The liquid crystal composition according to claim 5 , characterized in that said one or more compounds represented by formula III are one or more of compounds represented by formulas III-1 to 111-22: wherein X 1 and X 2 each independently represent H or F, and cannot both be F or H; R 4 each independently represents an alkyl group having a carbon atom number of 1-10, a fluorinated alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorinated alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorinated alkenyl group having a carbon atom number of 2-10, an alkenoxy group having a carbon atom number of 3-8 or a fluorinated alkenoxy group having a carbon atom number of 3-8, and any CH 2 in R 4 may be substituted by cyclopentyl, cyclobutyl or cyclopropyl; the (F)s each independently represent H or F; and Y 2 each independently represents F, a fluorinated alkyl group having a carbon atom number of 1-5, a fluorinated alkoxy group having a carbon atom number of 1-5, a fluorinated alkenyl group having a carbon atom number of 2-5, or a fluorinated alkenoxy group having a carbon atom number of 3-8. 7. The liquid crystal composition according to claim 1 , characterized in that said liquid crystal composition is a negative liquid crystal composition and further comprises one or more compounds represented by formula IV: wherein R 5 and R 6 each independently represent an alkyl group having a carbon atom number of 1-10, a fluorinated alkyl group having a carbon atom number of 1-10, an alkoxy group having a carbon atom number of 1-10, a fluorinated alkoxy group having a carbon atom number of 1-10, an alkenyl group having a carbon atom number of 2-10, a fluorinated alkenyl group having a carbon atom number of 2-10, an alkenoxy group having a carbon atom number of 3-8 or a fluorinated alkenoxy group having a carbon atom number of 3-8, and any CH 2 in R 5 and R 6 may be substituted by cyclopentyl, cyclobutyl or cyclopropyl; Z 5 and Z 6 each independently represent a single bond, —CH 2 CH 2 —, —CH 2 O—; each independently represent one of m represents 1 or 2; and n represents 0, 1 or 2. 8. The liquid crystal composition according to claim 7 , cha
Ph-Ph · CPC title
Cyclobutane rings · CPC title
Cy-Ph-Ph-Cy · CPC title
the liquid crystal having negative dielectric anisotropy · CPC title
Cy-Ph-Ph-Ph · CPC title
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