• 제목/요약/키워드: Phenyl cinnamate

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Maleimide계 폴리머를 이용한 액정배향특성 (Liquid Crystal Aligning Capabilities on the Photopolymer Based Maleimide)

  • 이윤건;황정연;서대식;김준영;이재호;김태호
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2001년도 추계학술대회 논문집
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    • pp.358-361
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    • 2001
  • A new photoalignment material PM15CA, poly{N-(phenyl)maleimide-co-3-[4-(pentyloxy) cinnamate]propyl-2-hydroxy-1-methacrylate}, was synthesized and the electro-optical (EO) characteristics in the vertical-aligned (VA) liquid crystal display (LCD) photo-aligned on the photopolymer surface were studied. Excellent voltage-transmittance(V-T) characteristics in the VA-LCD photoaligned with polarized UV exposure of oblique direction on the pohotopolymer surfaces for 1 min can be achieved. The transmittance of the VA-LCD photoaligned on the photopolymer surface decreased with increasing UV exposure time. We suggest that the decrease of transmittance in the VA-LCD photoaligned on the photopolymer surface is attributed to the dissociation of the ester linkage in the photodimerized cinnamate structure with increasing UV exposure time

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Maleimide계 폴리머를 이용한 액정배향특성 (Liquid Crystal Aligning Capabilities on the Photopolymer Based Maleimide)

  • 이윤건;황정연;서대식;김준영;이재호;김태호
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2001년도 추계학술대회 논문집 Vol.14 No.1
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    • pp.358-361
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    • 2001
  • A new photoalignment material PMI5CA, poly{N-(phenyl)maleimide-co-3-[4-(pentyloxy) cinnamate]propyl-2-hydroxy-1-methacrylate}, was synthesized and the electra-optical (EO) characteristics in the vertical-aligned (VA) liquid crystal display (LCD) photo-aligned on the photopolymer surface were studied. Excellent voltage-transmittance(V-T) characteristics in the VA-LCD photoaligned with polarized UV exposure of oblique direction on the pohotopolymer surfaces for 1 min can be achieved. The transmittance of the VA-LCD photoaligned on the photopolymer surface decreased with increasing UV exposure time. We suggest that the decrease of transmittance in the VA-LCD photoaligned on the photopolymer surface is attributed to the dissociation of the ester linkage in the photodimerized cinnamate structure with increasing UV exposure time

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Structure-Reactivity Correlations in Nucleophilic Displacement Reactions of Y-Substituted-Phenyl X-Substituted-Cinnamates with Z-Substituted-Phenoxides

  • Son, Yu-Jin;Kim, Eun-Hee;Kang, Ji-Sun;Um, Ik-Hwan
    • Bulletin of the Korean Chemical Society
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    • 제34권8호
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    • pp.2455-2460
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    • 2013
  • Second-order rate constants ($k_N$) have been measured spectrophotometrically for the nucleophilic displacement reactions of 4-nitrophenyl X-substituted-cinnamates (4a-4e) and Y-substituted-phenyl cinnamates (5a-5e) with Z-substituted-phenoxide anions in 80 mol % $H_2O$/20 mol % DMSO at $25.0{\pm}0.1^{\circ}C$. The Hammett plot for the reactions of 4a-4e with 4-chlorophenoxide (4-$ClPhO^-$) consists of two intersecting straight lines, which might be taken as a change in the rate-determining step (RDS). However, it has been concluded that the nonlinear Hammett plot is not due to a change in the RDS but is caused by stabilization of the ground state of substrates possessing an electron-withdrawing group in the cinnamoyl moiety through resonance interactions, since the Yukawa-Tsuno plot exhibits an excellent linear correlation with ${\rho}X=0.89$ and r = 0.58. The Br${\o}$nsted-type plot for the reactions of 4-nitrophenyl cinnamate (4c) with Z-substituted-phenoxides is linear with ${\beta}_{nuc}=0.76$. The Br${\o}$nsted-type plot for the reactions of Y-substituted-phenyl cinnamates (5a-5d) with 4-chlorophenoxides (4-$ClPhO^-$) is also linear with ${\beta}_{lg}=-0.72$. The Hammett plot correlated with ${\sigma}^-$ constants for the reactions of 5a-5d results in a much better linear correlation than that correlated with ${\sigma}^o$ constants, indicating that a partial negative charge develops on the O atom of the leaving aryloxide. Thus, the reactions have been concluded to proceed through a concerted mechanism.

Poly[N-(phenyl)maleimide]계 광폴리머를 이용한 액정배향효과 (Effects of Liquid Crystal Alignment on the Photopolymer based Poly[N-(phenyl)maleimide])

  • 황정연;서대식;김준영;이재호;김태호
    • 한국전기전자재료학회논문지
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    • 제14권10호
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    • pp.845-849
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    • 2001
  • The new phto-alignment material PMI5CA, poly{N-(phenyl)maleimide-co-3-[4-(pentyloxy) cinamate]porpyl-2-hydroxy-1-methacrylate}, was synthesized and the electro-optical (EO)characteristics in the vertical-aligned(VA) liquid crystal display (LCD) photo-aligned on the photopolymer surface were studied. Excellent Voltage-transmittance(V-T) characteristics in the VA-LCD photoaligned with polarized UV exposure of oblique direction on the pohotopolymer surface for 1 min can be achieve. The transmittance of the VA-LCD photoaligned on the photopolymer surface decreased with increasing UV exposure time. We suggest that decrease of transmittance in the VA-LCD photoaligned on the photopolymer surface is attributed to the dissociation of the ester linkage in the photodimerized cinnamate structure with increasing UV exposure time.

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Electroluminescent Property of Tetrahydrochrysene as a Potential Emitting Layer in Organic Electroluminescent Device

  • Hwang, Kwan-Jin;Kim, Jin-Guk;Lee, Seung-Hee;Kwon, Oh-Kwan;Kim, Young-Kwan
    • Journal of Photoscience
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    • 제7권2호
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    • pp.59-61
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    • 2000
  • As a potential electroluminescent material, tetrahydrochrysene (THC) is prepared using the dehydrocyclization following the acyloin condensation of methyl-3-phenyl propionate as key step from trans-mehyl cinnamate in 3 steps. THC showed emission at 428 and 456 nm after the photo- and electro-excitation, respectively. The luminance of THC doped on PVK was about /$25 cdm^2$ at 30 voltage with 70 nm of thickness. The results suggests that a new fluorescent organic dye, THC can be used organic electroluminescent device.

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New candidate for skin depigmentation: The inhibitory effect and cytotoxicity of small molecule compounds at in vitro cell culture

  • Rho, H.S;Kim, K.J.;Hwang, J.S.;H.J., Shin;Chang, H.K.;Chang, I.S.;Lee, O.S.
    • 대한화장품학회:학술대회논문집
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    • 대한화장품학회 2003년도 IFSCC Conference Proceeding Book II
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    • pp.174-183
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    • 2003
  • To obtain effective and safe topical depigmenting agents, we synthesized hydroxybenzoates, alkoxybenzoates, and 3,4,5-trimethoxycinnamate containing a thymol moiety and screened then for high-level inhibitory activity against melanin synthesis. Among them, 5-methyl-2-(methylethyl)phenyl (2Ε)-3-(3,4,5-trimethoxyphenyl)prop-2-enoate (Melasolv)$^{TM}$ 4h, showed the most potent depigmenting effect ($IC_{50}$/ = 10$\mu$M) with low cytotoxicity ($IC_{50}$/ = 200$\mu$M). To find the inhibition mechanism of our candidate, various in vitro tests were performed such as DPPH assay, tyrosinase activity in mushroom or in culture cell and expression of tyrosinase, TRP-l and TRP-2. The result of this study suggested that 4h inhibited melanin synthesis by reducing the expression of tyrosinase and TRP-l at the transcriptional level in melan-a melanocytes.s.

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