• Title/Summary/Keyword: Unsaturated side chains

Search Result 4, Processing Time 0.018 seconds

Synthesis and Properties of Ionic Liquids:Imidazolium Tetrafluoroborates with Unsaturated Side Chains

  • Min, Gwan-Hong;Yim, Tae-eun;Lee, Hyun-Yeong;Huh, Dal-Ho;Lee, Eun-joo;Mun, Jun-young;Oh, Seung M.;Kim, Young-Gyu
    • Bulletin of the Korean Chemical Society
    • /
    • v.27 no.6
    • /
    • pp.847-852
    • /
    • 2006
  • Imidazolium tetrafluoroborate ionic liquids having unsaturated aliphatic side chains were synthesized and characterized. Most of them are liquid at room temperature and all of them are stable up to $300{^{\circ}C}$. Some imidazolium tetrafluoroborates with an allylic side chain showed much wider voltage windows on the platinum electrode, better conductivities, and lower viscosities compared with the corresponding ionic liquids containing the saturated side chains.

Analysis of the Urushiol in Korean Lacquer (한국산 옻칠의 우루시올 성분 분석)

  • Kim, Jung-Bae
    • The Korean Journal of Food And Nutrition
    • /
    • v.19 no.3
    • /
    • pp.267-270
    • /
    • 2006
  • In Korea, for a long time Rhus verniciflua has traditionally been used as an herbal medicines plants. A stem of Rhus verniciflua has been used to treat gastrointestinal trouble with in form of boiled chicken as a folk medicine. But it has been recognized as an extremely active allergen causing skin reactions. The chief allergenic component, urushiol, is found within the oleoresinous sap of Rhus verniciflua. Most components of urushiol have unsaturated side chains. These unsaturated side chains of urushiol are important to polymerization of these natural products. The urushiol components in Korean lacquer were isolated by reversed phase HPLC. The molecular weight of purified urushiol was determined as 340 from mass analysis. This compound was identified as Heptadecatetraenyl catechol (MW 340).

Degradation characteristics of the FRP material for using as a PCB substrate (PCB 기판용 FRP 재료의 열화특성)

  • Park Jong Kwan
    • Journal of the Institute of Electronics Engineers of Korea SD
    • /
    • v.41 no.12
    • /
    • pp.1-6
    • /
    • 2004
  • In this study, heat and discharge treatments are arbitrary simulated for finding out the initiations and processes of surface degradation on the surface of polymer for using as a PCB substrate. Thermal-treatment changed the surface to the hydrophobic one with the increase of contact angle and surface potential decay, respectively. The XPS spectrum showed that the increased hydrophobicity in thermal treatment was originated from the continuous decrease of side-chains caused by secessions of oxygen groups and the increase of unsaturated double bond in carbon chains. Also, thermal-treatment caused the discoloration on the point of treated surface. These phenomena were attributed to the generation of ether group. In the chemical change by discharge treatment, a lot of side-chains occurred on the treated surface, and so the hydrophilicity increased as time elapsed.

Structure-Activity Relationship of Xanthones from Mesua daphnifolia and Garcinia nitida towards Human Estrogen Receptor Nagative Breast Cancer Cell Line

  • Ee, G.C.L.;Lim, C.K.;Rahmat, A.
    • Natural Product Sciences
    • /
    • v.11 no.4
    • /
    • pp.220-224
    • /
    • 2005
  • Extensive chemical studies on the stem bark extracts of two Guttifereous plants namely Mesua daphnifolia and Garcinia nitida have led to the isolation of eight xanthones. Mesua daphnifolia gave cudraxanthone G (1), ananixanthone (2), 1,3,5-trihydroxy-4-methoxyxanthone (3) and euxanthone (4) while Garcinia nitida gave inophyllin B (5), 1,3,7-trihydroxy-2,4-bis (3-methylbut-2-enyl)xanthone (6), 3-isomangostin (7) and rubraxanthone (8). All these compounds were assayed against the MDA-MB-231 (human estrogen receptor negative breast cancer) cells. A structure-activity relationship study showed that structurally, all the 1, 3-oxygenated xanthones which carried unsaturated prenyl side chains (either 3-methylbut-2-enyl or 1,1-dimethyl-2-propenyl) at carbones C-2 and C-4 in the xanthone ring A are essential for the outstanding activities in the assay.