Liquid crystal composition
US-2015060734-A1 · Mar 5, 2015 · US
US9599760B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9599760-B2 |
| Application number | US-201514806082-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jul 22, 2015 |
| Priority date | Dec 26, 2014 |
| Publication date | Mar 21, 2017 |
| Grant date | Mar 21, 2017 |
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A composition for an optical film, including a first liquid crystal compound represented by the following Chemical Formula 1 and a second liquid crystal compound represented by the following Chemical Formula 2, wherein a difference between a solubility parameter of the first liquid crystal compound and a solubility parameter of the second liquid crystal compound is about 2.50 to about 2.90 wherein in Chemical Formulae 1 and 2, X, R 1 to R 3 , Z, n, m, and p are the same as described in the detailed description.
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What is claimed is: 1. A composition for an optical film, comprising: a first liquid crystal compound represented by Chemical Formula 1 and a second liquid crystal compound represented by Chemical Formula 2, wherein a difference between a solubility parameter of the first liquid crystal compound and a solubility parameter of the second liquid crystal compound is about 2.50 to about 2.90: wherein, in Chemical Formula 1 or 2, X is a hydrogen-bonding functional group, R 1 to R 3 are independently hydrogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C1 to C10 alkoxy group, a halogen atom, a substituted or unsubstituted C1 to C10 halogen-containing group, or a combination thereof, Z is a single bond, —C(═O)O—, —(O═C)O—, or —O(C═)O—, n is 4 to 8, m is 0 or 1, and p is 3 to 6. 2. The composition for an optical film of claim 1 , wherein the X of Chemical Formula 1 is a cyano group, a substituted or unsubstituted C1 to C10 cyano-containing group, a hydroxy group, substituted or unsubstituted C1 to C10 hydroxy-containing group, a carboxyl group, a substituted or unsubstituted C1 to C10 carboxyl-containing group, or a combination thereof. 3. The composition for an optical film of claim 1 , wherein the first liquid crystal compound is represented by Chemical Formula 1a and the second liquid crystal compound is represented by Chemical Formula 2a: wherein, in Chemical Formula 1a or 2a, X is a cyano group, a substituted or unsubstituted C1 to C10 cyano-containing group, a hydroxy group, substituted or unsubstituted C1 to C10 hydroxy-containing group, a carboxyl group, a substituted or unsubstituted C1-C10 carboxyl-containing group, or a combination thereof, n is 4 to 8, and p is 3 to 6. 4. The composition for an optical film of claim 3 , wherein the first liquid crystal compound is represented by Chemical Formula 1aa and the second liquid crystal compound is represented by one of Chemical Formulae 2aa to 2ad: 5. The composition for an optical film of claim 1 , further comprising a solvent, wherein an amount of the first liquid crystal compound and the second liquid crystal compound in the composition is about 5 to about 50 percent by weight based on the total weight of the composition, and the remaining amount is the solvent. 6. The composition for an optical film of claim 5 , wherein a mole ratio of the first liquid crystal compound and the second liquid crystal compound is about 1:0.7 to about 1:2. 7. The composition for an optical film of claim 1 , further comprising a photoinitiator. 8. The composition for an optical film of claim 7 , wherein an amount of the photoinitiator is about 0.1 to about 2 percent by weight based on the total amount of the composition. 9. An optical film comprising a substrate, and a liquid crystal layer positioned on the substrate, wherein the liquid crystal layer comprises a first liquid crystal compound represented by Chemical Formula 1 and a second liquid crystal compound represented by Chemical Formula 2, and wherein a difference between a solubility parameter of the first liquid crystal compound and a solubility parameter of the second liquid crystal compound is about 2.50 to about 2.90: wherein, in Chemical Formula 1 or 2, X is a hydrogen-bonding functional group, R 1 to R 3 are independently hydrogen, a substituted or unsubstituted C1 to C10 alkyl group, a substituted or unsubstituted C1 to C10 alkoxy group, a halogen atom, a substituted or unsubstituted C1 to C10 halogen-containing group, or a combination thereof, Z is a single bond, —C(═O)O—, —(O═C)O— or —O(C═O)—, n is 4 to 8, M is 0 or 1, and p is 3 to 6. 10. The optical film of claim 9 , wherein the X of Chemical Formula 1 comprises a cyano group, a substituted or unsubstituted C1 to C10 cyano-containing group, a hydroxy group, a substituted or unsubstituted C1 to C10 hydroxy-containing group, a carboxyl group, a substituted or unsubstituted C1 to C10 carboxyl-containing group, or a combination thereof. 11. The optical film of claim 9 , wherein the first liquid crystal compound is represented by Chemical Formula 1a and the second liquid crystal compound is represented by Chemical Formula 2a: wherein, in Chemical Formula 1a or 2a, X is a cyano group, a substituted or unsubstituted C1 to C10 cyano-containing group, a hydroxy group, a substituted or unsubstituted C1 to C10 hydroxy-containing group, a carboxyl group, a substituted or unsubstituted C1-C10 carboxyl-containing group, or a combination thereof, n is 4 to 8, and p is 3 to 6. 12. The optical film of claim 11 , wherein the first liquid crystal compound is represented by Chemical Formula 1aa and the second liquid crystal compound is represented by one of Chemical Formulae 2aa to 2ad: 13. The optical film of claim 9 , wherein the first liquid crystal compound and the second liquid crystal compound are aligned in a direction perpendicular to the length direction of the substrate. 14. The optical film of claim 9 , wherein the liquid crystal layer has in-plane retardation R 0 of 0 nanometers≦R 0 ≦1 nanometer for incident light of about 550 nanometers wavelength. 15. The optical film of claim 14 , wherein the liquid crystal layer has thickness direction retardation R th of 50 nanometers≦R th ≦500 nanometers for incident light of about 550 nanometers wavelength. 16. The optical film of claim 9 , wherein the liquid crystal has a refractive index satisfying Relationship Equation 1: n z >n x =n y Relationship Equation 1 wherein, in Relationship Equation 1, n x is a refractive index of the liquid crystal at a slow axis, n y is a refractive index of the liquid crystal at a fast axis, and n z is a refractive index in a direction perpendicular to n x and n y . 17. A compensation film comprising: the optical film of claim 9 , and a retardation film positioned on at least one side of the optical film. 18. The compensation film of claim 17 , wherein the retardation film comprises a λ/4 retardation film, a λ/2 retardation film, or a combination thereof. 19. An anti-reflective film, comprising: the compensation film of claim 17 , and a polarizer positioned on the compensation film. 20. A display device comprising a display panel and the optical film of claim 9 . 21. A display device comprising a display panel and the compensation film of claim 17 . 22. A display device comprising a display panel and the anti-reflective film of claim 19 .
the chain containing -COO- or -OCO- groups · CPC title
Birefringent or phase retarding elements (G02B5/3008, G02B5/3016 take precedence; systems for polarisation control G02B27/286; manufacturing phase modulating patterns by lithographic processes G03F7/001) · CPC title
involving passive liquid crystal elements (optical properties of liquid crystals G02F1/0063; polarising elements associated with active liquid crystal devices G02F1/133528) · CPC title
Anti-reflection coatings · CPC title
chain containing -COO- or -OCO- groups · CPC title
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