• 제목/요약/키워드: natural reaction

검색결과 1,743건 처리시간 0.032초

Facile Synthesis of Natural Moracin Compounds using Pd(OAc)2/P(tBu)3-HBF4 as a Sonogashira Coupling Reagent

  • Lee, Jae Jun;Yun, So-Ra;Jun, Jong-Gab
    • Bulletin of the Korean Chemical Society
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    • 제35권12호
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    • pp.3453-3458
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    • 2014
  • An efficient and practical synthesis of natural moracins, which have diverse range of biological properties including anticancer, antioxidant, and antibacterial activities, has been achieved using $Pd(OAc)_2/P(^tBu)_3-HBF_4$ as a Sonogashira coupling reagent which solved the unreactive problems in case of higher electron density of haloaryl compounds in the reaction. Lowering electron density of halophenol with acetylation and changing Sonogashira coupling reagent from $PdCl_2(PPh_3)_2$ to $Pd(OAc)_2/P(^tBu)_3-HBF_4$ smoothly produce the benzofuran structures in the syntheses of moracins M, N and S. The electron deficient halobenzaldehyde, however, easily forms the benzofuran using original Sonogashira conditions, and utilized for the first synthesis of moracin Y.

A Theoretical Synthesis of Poly(methyl methacrylate) (PMMA) by the Molecular Orbitals Calculation

  • Kim, Jong-Too;Kim, Ui-Rak;Akira Imamura
    • Macromolecular Research
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    • 제8권6호
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    • pp.292-297
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    • 2000
  • The theoretical synthesis of the isotactic and syndiotactic poly(methyl methacrylate) were carried out as a model for real polymerization reactions following the normal chain reaction processes by repeating the uniform localization of wave functions with inclusion of the interaction between the end group of the cluster and an attaching molecule by the elongation method, and then, the calculated value was compared with the usual PM$_3$ calculation. The results revealed that a reaction of cluster with monomer molecules has made it possible to calculate the electronic structure and total energy of polymer with nearly infinite length and a matrix of constant dimension. The isotactic poly(methyl methacrylate) is more stable than syndiotactic one. The same tendency have been found between the experimentally measured properties and a calculated total energy to explain the chain motion in isotatic and syndiotactic poly(methyl methacrylate).

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Indium(III) Chloride Mediated Michael Addition of Indoles to Ketene S,S-Acetals: Synthesis of Bis- and Tris-indolylketones

  • Singh, Thokchom Prasanta;Khan, Ruhima;Noh, Young Ri;Lee, Sang-Gyeong;Singh, Okram Mukherjee
    • Bulletin of the Korean Chemical Society
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    • 제35권10호
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    • pp.2950-2954
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    • 2014
  • A series of bis and tris-indolylketones and meridianin alkaloids are prepared by one pot Michael reaction of indole and ketene S,S-acetals under solvent-free condition using mild Lewis acid $InCl_3$.

Recognition of substrates by membrane potential

  • Yun, Kyu-sik;Tak, Tae-moon;Kim, Jong-ho
    • 한국막학회:학술대회논문집
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    • 한국막학회 1998년도 춘계 총회 및 학술발표회
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    • pp.31-35
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    • 1998
  • 1. INTRODUCTION : Recognition and binding of organic substrates by biological molecules are of vital importance in biophysics and biophysical chemistry. Most studies of the application focused on the development of biosensors, which detected reaction products generated by the binding between enzymes and substrates. Other types of biosensors in which membrane proteins (e.g., nicotinic acetylcholine receptor, auxin receptor ATPase, maltose bining protein, and glutmate receptor) were utilized as a receptor function were also developed. In the previous study[1], the shifts in membrane potential, caused by the injection of substrates into a permeation cell, were measured using immobilized glucose oxidase membranes. It was suggested that the reaction product was not the origin of the potential shifts, but the changes in the charge density in the membrane due to the binding between the enzyme and the substrates generated the potential shifts. In this study, $\gamma$-globulin was immobilized (entrapped) in a poly($\gamma$-amino acid) network, and the shifts in the membrane potential caused by the injection of some amino acids were investigated.

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Model-system으로서의 몬트모릴로나이트의 층간화합물에 관한 연구 (I) (A Study of Intercalations-complexes of Montmorillonite as Model-Systems)

  • 조성준;김종옥
    • 자연과학논문집
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    • 제5권1호
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    • pp.77-86
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    • 1992
  • 양이온 교환반응에 의해 몬트모릴로나이트내의 금속 양이온을 긴 chain을 갖는 유기 양이온 tenside로 치환시킴으로써 물성이 다른 몬트모닐롤나이트의 층간화합물을 형성하게 된다. 이러한 층간화합물은 공업적으로 아주 광범위하게 이용되는가 하면, model-systems로서 물질의 거동을 밝혀내는 학문적 연구에 또한 많이 이용되기도 한다. 따라서 본 연구에서는 이러한 몬트모릴로나이트의 층간화합물을 형성하여 여러 상이한 조건하에서의 이들의 거동에 대하여 연구했다.

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Borate 완충용액에서 아연의 부식에 대한 대류와 대기의 영향 (Hydrodynamic and Atmospheric Effects on Corrosion of Zinc in Borate Buffer Solution)

  • 정세진;김연규
    • 대한화학회지
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    • 제55권4호
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    • pp.575-580
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    • 2011
  • Borate 완충용액에서 전극의 회전속도와 용액에 녹아 있는 $O_2$가 Zn-RDE의 부식에 미치는 영향을 조사하였다. 아연의 부식은 RDE의 회전속도와 산소의 양에 크게 영향을 받았으며, 부식 반응구조로 가역적 1-전자 전이에 이어서 일어나는 불균등화 반응(disproportion reaction)을 제안하였다.

Interlayered colored iron compounds prepared by reactions of nanoirons with bidentate chelating ligands in laponite

  • Kim, Dong Hwan;Kim, Youhyuk
    • 한국결정성장학회지
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    • 제31권2호
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    • pp.69-72
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    • 2021
  • The reaction of ammonium ferric sulfate with sodium borohydride in laponite sol yields nanoiron colloidal solution. This solution in air forms transparent yellow brown solution. The resulting solution reacts with bidentate chelating ligands. The reaction products are characterized by UV-Vis absorption spectroscopy and X-ray diffraction. All compounds show metal to ligand charge transfer band in the region of 400~650 nm in UV-Vis absorption spectra. This indicates the formation of iron-ligand complex by air oxidation of nanoiron. Also, XRD patterns exhibit that the iron-ligand complex is intercalated in the interlayer of laponite.

Stoichiometry, Thermal Stability and Reducibility of Perovskite-Type Mixed Oxide LaBO$_3$ (B = Fe, Co, Ni)

  • Park, Il-Hyun;Lee, Hyung-Pyo
    • Bulletin of the Korean Chemical Society
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    • 제9권5호
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    • pp.283-288
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    • 1988
  • The titled properties on reduction of the perovskite $LaBO_3$ (B = Fe, Co, Ni) have been investigated by means of temperature-programmed reduction, isothermal reduction and X-ray diffraction methods. Nominal composition of $LaFeO_{3.18},\;LaCoO_{3.00}\;and\;LaNiO_{2.92}$ are determined. Reduction reaction of these mixed oxides differed according to B-site transition metal and thermal stability on reduction decreased as following order: $LaFeO_{3.18}$ > $LaCoO_{3.00}$ > $LaNiO_{2.92}$. From the results of isothermal reaction, kinetics on reduction of the perovskite has been discussed in detail.

Ferroptosis-Like Death in Microorganisms: A Novel Programmed Cell Death Following Lipid Peroxidation

  • Min Seok Kwun;Dong Gun Lee
    • Journal of Microbiology and Biotechnology
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    • 제33권8호
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    • pp.992-997
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    • 2023
  • Ferroptosis is a new kind of programmed cell death of which occurrence in microorganisms is not clearly verified. The elevated level of reactive oxygen species (ROS) influences cellular metabolisms through highly reactive hydroxyl radical formation under the iron-dependent Fenton reaction. Iron contributes to ROS production and acts as a cofactor for lipoxygenase to catalyze poly unsaturated fatty acid (PUFA) oxidation, exerting oxidative damage in cells. While ferroptosis is known to take place only in mammalian cells, recent studies discovered the possible ferroptosis-like death in few specific microorganisms. Capacity of integrating PUFA into intracellular membrane phospholipid has been considered as a key factor in bacterial or fungal ferroptosis-like death. Vibrio species in bacteria and Saccharomyces cerevisiae in fungi exhibited certain characteristics. Therefore, this review focus on introducing the occurrence of ferroptosis-like death in microorganisms and investigating the mode of action underlying the cells based on contribution of lipid peroxidation and iron-dependent reaction.

망간산화물(NMO, MnO2, Mn2O3)을 이용한 저온에서의 NH3-SCR의 반응속도 연구 (A Reaction Kinetic for Selective Catalytic Reduction of NOx with NH3 over Manganese Oxide (NMO, MnO2, Mn2O3) at Low Temperature)

  • 김민수;홍성창
    • 청정기술
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    • 제24권4호
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    • pp.307-314
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    • 2018
  • 본 연구에서는 NMO (Natural Manganese Ore), $MnO_2$, $Mn_2O_3$ 촉매를 산소 존재 하에 저온에서 $NH_3$를 환원제로 이용하여 질소산화물(NOx)을 제거하는 선택적 촉매 환원법에 사용되었다. NMO의 경우, 안정성 실험에서 질소산화물 전환율이 423 K에서 100시간 후에도 변하지 않는 것을 확인하였다. 동력학 실험의 경우, 열 및 물질전달이 영향을 주지 않는 영역에서 수행하였다. 정상상태에서의 반응속도 연구는 저온 SCR반응에서 암모니아에 대하여 0차이고 일산화질소에 대해서는 0.41 ~ 0.57차였으며 산소에 대해서는 0.13 ~ 0.26차인 것을 확인하였다. 온도가 증가할 때, 암모니아와 산소 농도의 결과에 따라 반응차수가 감소함을 확인하였다. 촉매 표면에 해리흡착 된 암모니아와 가스상 일산화질소(E-R 모델)와의 반응 및 흡착 된 일산화질소(L-H 모델)와의 반응을 확인하였다.