• Elastomers and Composites
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• 제40권1호
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• pp.37-44
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• 2005

새로운 형태의 액정성 폴리우레탄을 2,6-bis(${\omega}$-hydroxyalkoxy)naphthalene (BHNm; m= 5, 6, 8, 11)과 2,5-tolylene diisocyanate 또는 1,4-phenylene diisocyanate의 중부가 반응에 의해 합성하였다. 폴리우레탄의 고유 점성도는 0.28-0.43 dL/g 였다. 열적 성질은 DSC 및 편광현미경에 의해 측정되었다. 단량체 BHNm과 메틸치환기를 가진 2,5-tolylene diisocyanate에 의해 합성된 폴리우레탄은 모두 단방성 액정성을 나타내었다. 그러나 BHNm와 1,4-phenylene diisocyanate를 합성한 폴리우레탄에서는 DSC와 편광현미경으로 조사 결과 전혀 액정성을 나타내지 않았다.

• Elastomers and Composites
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• 제48권2호
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• pp.141-147
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• 2013

메소겐(Mesogen) 단위가 포함되어 있지 않는 para- 형태의 1,4-phenylene diisocyanate (1,4-PDI)와 2,6-bis(${\omega}$-hydroxypentoxy)naphthalene (BHN5) 또는 1,4-bis(${\omega}$-hydroxypentoxy)benzene (BHB5)을 단일과 공중합폴리우레탄을 부가중합에 의해 합성하였다. 모든 공중합폴리우레탄에서는 전단변형의 측정에서 단방성 액정상을 나타내었다. 예를 들면, 고유점도가 $[\eta]$=0.32 dL/g인 폴리우레탄 Poly(50/50, mol%)은 $223^{\circ}C{\sim}211^{\circ}C$에서 냉각 시 액정성을 나타내었다. 그러나 두 개의 단일폴리우레탄에서는 DSC (Differental Scanning calorimeter) 측정 및 편광현미경 관찰에서도 액정상을 전혀 관찰 할 수 없었다. 합성된 폴리우레탄의 액정성은 시차주사열량분석기, 편광현미경과 X-ray에 의해 확인하였다.

• 한국염색가공학회지
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• 제8권1호
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• pp.56-63
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• 1996

A number of thermotropic liquid crystalline polyurethanes with mesogenic unit were synthesized by polyaddition of a para-type diisocyanate such as 1, 4-phenylene diisocyanate(1,4-PDI) with 4, 4'-bis($\omega$-hydorxyalkoxy) biphenyls($BP{m}$) in DMF. The thermal and liquid crystab line properties were examined by differential scanning calorimetry(DSC), polarized optical microscopy, and wide-angle X-ray scattering(WAXS). Intrinsic viscosities of the polymers exbibited two endothermic peaks correspondinding to phase transitions of melting and isotropization. For example, polyurethane(1,4-PDI/($BP{11}$) ) was found to display a liquid crystalline phase between 177 to 205$^{\circ}C$. In order to know how the hydrogen bonding interaction affects the formation of mesophases in polyurethane 1, 4-PDI/($BP{8}$) / thermal processing FT-IR measurements were carried out. It was found that the stretches regarded as shift to higher frequency region with increasing temperature which showed grdually their liquid crystalline phase

• 한국염색가공학회지
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• 제7권4호
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• pp.8-15
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• 1995

A series of thermotropic Polyurethanes mesogenic unit were synthesized by polyaddition of a para-type diisocyanate such as 2,5-tolylene diisocyanate(2,5-TDI) with 4-4'-bis($\omega$-hydroxyalkoxy) biphenls(BPm: $HOCmH_{2m}OC_{6}H_{4}OC_{m}H_{2m}OH$ : m is the carbon number of the hydroxyalkoxy group) in DMF. Intrinsic viscosities of the polymers were in the range of 0.41~0.99dL/g DSC thermograms for these polymers exhibited two endothermic peaks corresponding to phase transitions of melting and isotropization. For examplem polyurethane 2,5-TDI/BPll with [η]=0.99 prepared from 2.5-TDI and 4,4'-bis[11-hydroxyundecaoxy biphenyl(BP11) a liquid crystalline phase from 156 to 173$^{\circ}C$. The thermotropic properites of liquid crystalline polyurethanes have been investigated by wide-angle X-ray scatter(WAXS), infrared (IR) spectroscopy, and differential scanning calorimetry (DSC). The mesomorphic behavior of the polyurethanes was concluded to be greatly dependent on the intermolecular hydrogen bonds through the urethane.