• 제목/요약/키워드: Cinnamoyl group

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Resorcinol계 Photoresist의 합성과 그 감광 특성 (Synthesis and Photocharacteristics of Resorcinols Photoresist)

  • 근장현;김승진;박홍수
    • 공업화학
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    • 제5권4호
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    • pp.662-668
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    • 1994
  • Photoresist로의 응용을 위하여 감광성 관능기를 가진 폴리머인 polyresorcinol-formaldehyde glycidyl ether의 cinnamoyl ester(RGEFC)를 제조하였다. RGEFC의 감광 특성은 노광 전후의 유기용매에 대한 용해도 차이로서 결정하였는데, 유리판상에 도포한 각종 시료를 제반조건하에서 노광한 다음, 도포시에 사용한 같은 용매에 담그어 잔막수득량을 계산하였다. 필름의 감도와 밀접한 관계를 가지는 수득량은 수지의 중합도, 증감제의 종류 및 첨가농도에 따라 좌우되었으며, 그 감도는 폴리머의 중합도에 의존되어 중합도가 커질수록 증가되었다. 사용된 증감제 중 RGEFC에 대한 가장 효과적인 증감제는 2, 6-dichloro-4-nitroaniline이었다.

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우피소근의 polyoxypregnane 화합물의 Aldehyde Oxidase 및 지질과산화 억제효과 (Inhibitory Effects of Polyoxypregnane Constituents from the Roots of Cynanchum caudatum on the Aldehyde Oxidase Activity and Lipid Peroxidation)

  • 이동웅;이남재
    • 약학회지
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    • 제44권3호
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    • pp.257-262
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    • 2000
  • The roots of Cynanhum caudatum (Asclepiadaceae) have been used in folk medicine in Japan and China for the prevention and treatment of various geriatric diseases and also as a cardiotonic agent. Constituents of this plant have mainly been examined for glycosides: besides two steroidal alkaloids, gagaminine and gagamine which was firstly isolated by us, more than 35 polyoxypregnane glycosides and aglycones have also been identified. Gagaminine inhibits potently the hepatic aldehyde oxidase activity and lipid peroxidation in vitro. The present work deals with the comparison of antioxidative activities of gagamine, a new pregnane alkaloid, three isolated polyoxypregnanes containing a keto group at C-20 with those of gagaminine, a potent antioxidant, in order to explain the structure-activity relationships. The results of this study further prove that the cinnamoyl group of gagaminine is very important for the inhibition on the aldehyde oxidase activity while the nicotinoyl group is necessary for anti-lipid peroxidation. Besides that, the keto compounds having no ester group at C-12 were found to be more active than the others except gagaminine.

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Characteristics of Organic Thin Film Transistors with UVtreated Surface of Synthesized Gate Insulator

  • Bong, Kang-Wook;Park, Jae-Hoon;Kang, Jong-Mook;Kim, Hye-Min;Lee, Hyun-Jung;Yi, Mi-Hye;Choi, Jong-Sun
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2007년도 7th International Meeting on Information Display 제7권2호
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    • pp.1295-1297
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    • 2007
  • In this study, we report that the characteristics of OTFTs can be improved by the UV exposure of the surface of the synthesized photo-reactive gate insulator, and be optimized by controlling the exposure time. As a gate dielectric, the modified PVP was prepared by substituting hydroxyl group in PVP with cinnamoyl group. The synthesis details and the effects of the modified PVP on the device performance are discussed.

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Structure-Activity Relationships of Gagaminine and Its Derivatives on the Inhibition of Hepatic Aldehyde Oxidase Activity and Lipid Peroxidation

  • Lee, Dong-Ung;Shin, Uk-Seob;Huh, Keun
    • Archives of Pharmacal Research
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    • 제21권3호
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    • pp.273-277
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    • 1998
  • In order to determine the structure-activity relationships for antioxidative effects of gagaminine, a steroidal alkaloid isolated from the roots of Cynanchum wilfordi (Asclepiadaceae), two derivatives identified as sarcostin and penupogenin were prepared from gagaminine by hydrolysis and reduction. These compounds were evaluated for the inhibitory effects on the aidehyde oxidase activity and on lipid perbxidation in vitro. Furthermore, their effects were compared with those of gagaminine and the related compounds, cinnamic acid and nicotinic acid. The results of this study prove that the cinnamoyl group in the structure of gagaminine is critical in inhibition of the aldehyde oxidase activity while the nicotinoyl group may be necessary for anti-lipid peroxidation of the compound.

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Photosensitive Polymers: Effects of Photoreactive Group and UV-Exposure on Alignment of Liquid-Crystals on the Film Surface

  • Ree, Moon-Hor;Kim, Sang-Il;Lee, Seung-Woo
    • 한국정보디스플레이학회:학술대회논문집
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    • 한국정보디스플레이학회 2000년도 제1회 학술대회 논문집
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    • pp.41-42
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    • 2000
  • Photosensitive polyimides containing cinnamoyl and coumarin side groups were synthesized in a high molecular weight, giving a good quality of films. Nematic liquid-crystal (LC) molecules on the film were aligned along the direction with an angle of $97-99^{\circ}$ respect to the polarization of ultraviolet (UV) light. The LC alignment was induced mainly by the photoaligned polymer chains made by the first UV-exposure even though the film was treated by multiple exposures with changing the polarization of UV light. From these results, it is concluded that the LC alignment on the film is induced by the photodimerization rather than the trans-cis photoisomerization.

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Trihydric Phenol계 Photoresist의 합성과 그 감광 특성 (Synthesis and Photocharacteristics of Trihydric Phenol Photoresist)

  • 홍의석;고재용;박홍수
    • 한국응용과학기술학회지
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    • 제13권1호
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    • pp.47-54
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    • 1996
  • Cinnamoyl ester(PGEFC) of poly(phloroglucinol-formaldehyde) glycidyl ether which has photosensitive functional group was prepared to apply to photoresist. Photosensitivity of PGEFC was estimated by the solubility difference in organic solvent before and after exposure to light. The yield of residual film was calculated by immersing the sample-coated quartz plates in the solvent which was used in coating. The yield of the residual film which was closely related to the sensitivity of the film, was affected by the degree of polymerization of the backbone resin, sensitizers and their concentration. The sensitivity was depended upon the degree of polymerization. Most of effective sensitizer for PGEFC among the sensitizers was 2, 6-dichloro-4-nitroaniline.

광감성 폴리비닐플루오로신나메이트의 액정 배향에 관한 연구 (Studies of Liquid Crystal Alignment on the Photosensitive Polyvinylfluorocinnamate)

  • 김동수;안원술;하기룡
    • 폴리머
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    • 제31권5호
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    • pp.393-398
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    • 2007
  • 편광 푸리에 변환 적외선 분광법(polarized fourier transform infrared spectroscopy)과 자외선 분광법(ultraviolet spectroscopy)을 이용하여 액정 디스플레이 (liquid crystal display, LCD)의 배향막으로 사용 가능한 Polyvulylfluoroclnnamate(PVCN-F) 필름의 편광 자외선(Polarized UV, PUV) 조사 및 러빙에 따른 액정의 배향 메커니즘에 관한 연구를 수행하였다. UV의 조사시간이 증가함에 따라 PVCN-F cinnamoyl group의 C=C기들의 cycloaddition 반응으로 인하여 $1638cm^{-1}$에서 나타나는 vinylene -C=C- FT-IR 흡수 피크들의 면적이 감소하고, $1712cm^{-1}$에서 나타나는 conjugated C=O 신축진동에 의한 피크가 nonconjugated C=O 신축진동 피크인 $1734cm^{-1}$로 이동함을 확인하였다. 또한 PUV가 조사된 PVCN-F 배향막을 사용하여 제조된 액정 셀에서는 조사된 PUV의 극성 방향과 수직으로 액정이 배향함을 확인하였고, 러빙 방법으로 제조된 PVCN-F 배향막을 사용한 액정 셀에서는 액정이 러빙 방향과 수평으로 배향됨을 dichroic dye(이색성 염료)의 첨가 없이 편광 FT-IR 스팩트럼을 사용하여 확인하였다.

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.