• Applied Chemistry for Engineering
• /
• v.19 no.6
• /
• pp.661-667
• /
• 2008

In this study, cholesteric liquid crystal (CLC) was synthesized and applied as a polarizing component on the optical film of back light units (BLU) for LCDs. After mixing CLC with nematic liquid crystal, this mixture was fulfilled in the module consisting of two films and then its amplifying efficiency and polarizing ability for a planarly emitted light were examined to apply as a BLU polarizer film for increasing the brightness of light. The properties of CLC compound were tested by UV/Visible spectroscopy and polarizing optical microscopy (POM). Flexible spacer was made by linear carboxylic acid group of cholesteric derivatives between cholesterol mesogen units for one-axis orientation in each layer. The CLC containing film could be used as a module to increase the ability of polarization and to enhance brightness of BLU and to widen wavelength range by stacking the films.

• Applied Chemistry for Engineering
• /
• v.28 no.2
• /
• pp.230-236
• /
• 2017

We synthesized liquid crystalline polymers containing isosorbide group as a cholesteric derivative and methylene group for controlling the transition temperature to the liquid crystal phase. Effects of the concentration of the isosorbide group and the position of the methylene group on the properties of the liquid crystalline polymer were investigated. Among all the synthesized polymers, polymers (MnHI-x) with a methylene group in the main chain showed higher melting transition temperature and thermal stability than those (SnBI-x) with a methylene group in the side chain. All the synthesized polymers showed an enantiotropic liquid crystal phase. The polymers having 10 mol% isosorbide as a cholesteric liquid crystal phase derivative showed nematic phase, and those having 20 mol% or more isosorbide showed a cholesteric or chiral smectic phase. Thus, we can conclude that the isosorbide group plays a role as a cholesteric liquid crystal phase derivative.

• Polymer(Korea)
• /
• v.33 no.3
• /
• pp.207-212
• /
• 2009

The precursor polyimide of the photoreactive polyimides(PI-SP6 and PI-SP12) was prepared from a derivative of 2, 2, 2-trifluoroethane dianhydride and 3,3'-dihydroxy-4,4'-diaminobiphenyl. PI-SP6 and PI-SP12 were then prepared by the polymer reactions of the precursor polyimide with photoreactive 2-styrylpyridine alkylene (hexylene and dodecylene) derivatives, respectively. The photoreactive polymers were soluble in organic solvents. The polymers showed the initial decomposition temperatures around $350^{\circ}C$. The glass transition temperatures of PI-SP6 and PI-SP12 were found to be $130^{\circ}C$ and $85^{\circ}C$, respectively. This result means that the latter polymer is more flexible than the former polymer. Their transmittance in the film state was 90% at $250^{\circ}C$, which indicates that the photosensitive polyimides with thermal stability have high optical transparency even at the high temperature. The respective dichroic ratios of PI-SP6 and PI-SP12 were found to be 0.01 and 0.03 at an exposure energy of $1.5\;J/cm^2$. This result suggests that the latter polymer with larger flexibility compared to the former polymer is more effective for the photoalignment.