• Korean Journal of Materials Research
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• v.4 no.6
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• pp.695-703
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• 1994

Some 4-(4-alkyloxybenzoyloxy)-4'-(S)-$\alpha$-chloro-alkanoyloxybiphenyls have been synthesized and their mesomorphic properties were studied. They show a ferroelectric chiral smectic C phase in addition to the chiral nematic and smectic A phase. We obtained a large spontaneous polarization exceeding $10^{-7}\textrm{cm}^2$ in new biphenyl ester series.

• Journal of the Korean Chemical Society
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• v.48 no.6
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• pp.599-608
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• 2004

New two kinds of methacrylate monomers having a benzene ring inserted between spacer and methacryloyl group and the chiral center connected to the terminal of the mesogenic structures were synthesized. In these two series the effects for the formation of the liquid crystals in regard to the length changes of the spacers and mesogenic groups were investigated. The first series did not show any liquid crystalline phases in the intermediate compounds nor in the end products. However, the methacrylates of second series showed the liquid crystalline phases in the intermediate compounds as well as in the final products regardless of the length of the spacers.

• Korean Chemical Engineering Research
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• v.45 no.2
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• pp.155-159
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• 2007

A series of new dimesogenic compounds having two identical, terminal Schiff base type mesogens and a central tetramethylene spacer were synthesized. Their thermotropic and mesomorphic properties of the compounds were investigated by differential scanning calorimetry and polarizing microscopy. The compounds with X= -F, -Cl, -Br, -CN and $-OCH_3$ were enantiotropically nematic liquid crystal. In contrast, the compounds with X= -I and $-CF_3$ were non-liquid crystal. The nematic forming efficiency of the groups was in the order of -CN > $-OCH_3$ > -Br > -Cl > -F.

• Journal of the Korean Chemical Society
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• v.48 no.5
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• pp.499-503
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• 2004

We designed and synthesized compounds which have negative dielectric anisotropy (N type) for VA-LCD mode. Due to the large dipole moments toward the minor axis of molecule and anisotropy of polarizability, they can be used as N type LC. F atom and NCS group and propyl group were introduced as substituents on bicyclohexylbenzene core unit and alkyl chains (propyl~heptyl) were introduced on terminal part. All of the synthesized compounds showed negative dielectric anisotropy as expected.

• Elastomers and Composites
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• v.45 no.4
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• pp.286-290
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• 2010

Liquid-crystalline (LC) monomer, which was functionalized with a coumarin group on their extremity, was synthesized by UV light irradiation in their LC phases. LC monomer was converted into the dimers by the cycloaddition reaction of the coumarin group, and the LC phases were maintained after photodimerization reaction. The dimers showed LC phases in the wider temperature range than those of the corresponding monomer. Structures of the compound were identified by FT IR and $^1H$ NMR spectroscopies. Their phase transition temperatures and thermal stability were also investigated by differential scanning calorimetry (DSC), gel permeating chromatography (GPC) and polarized optical microscopy (POM). From optical polarizing microscopy, the prepared polymer shows enantiotropic liquid crystallinity with smectic and nematic textures.

• Journal of the Korean Graphic Arts Communication Society
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• v.16 no.2
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• pp.37-44
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• 1998

• Journal of the Korean Chemical Society
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• v.45 no.1
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• pp.67-75
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• 2001

A new homologous series with the general formula in which n is the longitudinal alkyloxy group, n=1-10, was synthesized. The thermotropic and liquid crystalline properties were studied by differential scanning calorimetry and on the hot-stage of a polarizing microscope. All of the new compounds were monotropic and texture observations proved that all investigated homologues with n=1-10 exhibited nematic phases. Also, the compounds showed pronounced alternation effects in the homologous series with constant lateral bridging group, oxydecamethyleneoxy, but increasing longitudinal chains, n.

• Journal of the Korean Chemical Society
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• v.52 no.5
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• pp.583-587
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• 2008

• Korean Journal of Materials Research
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• v.2 no.6
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• pp.398-407
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• 1992

Cholesteryl S-alkoxybenzene thiocarbonates was synthesized and their liquid crystal transition temperature were determined. Those compounds exhibit enantiotropic cholesteric mesophases. The cholestric-isotropic transition temperatures decrease gradually with increasing alkoxy chain length and mesophase transition were investigated by differential scanning calorimetry.

• Journal of the Korean Chemical Society
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• v.45 no.6
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• pp.562-569
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• 2001

A homologous series of new H-shaped twin liquid crystal molecules (PPPA-n) with flexible spacers, oxypolymethyleneoxy, has been prepared by esterification of acid chloride of $\alpha$,$\omega$-bis(2,5-dicar-boxyphenoxy) alkanes with p-phenylphenol. The length of spacer was varied from oxyethyleneoxy (n=2) to oxydecamethyleneoxy (n=10). Their thermodynamic data were measured by differential scanning calorimetry and liquid crystalline properties were investigated by a hot-stage polarizing microscope.