• 제목/요약/키워드: Covalent

검색결과 367건 처리시간 0.022초

Noncovalent Modification of Carbon Nanofibers Using 2-Naphthalenethiol for Catalyst Supports in PEM Fuel Cells

  • Oh, Hyung-Suk;Kim, Han-Sung
    • Journal of Electrochemical Science and Technology
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    • 제1권2호
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    • pp.92-96
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    • 2010
  • A new synthesis method for the preparation of Pt electrocatalysts on carbon nanofibers (CNFs) is reported. In this method, Pt electrocatalysts are loaded onto 2-naphthalenethiol (NT) functionalized CNFs. The noncovalent functionalization of CNFs by NT is the effective way for better distribution of Pt particles and higher electrocatalytic activity in polymer electrolyte membrane fuel cells. It was found that the presence of NT acts as a poison to catalysts. Therefore, it is necessary to remove NT through the heat treatment at $400^{\circ}C$.

고압력하에서의 $\alpha-quartz$$\alpha-quartz$$GeO_2$의 상전이에 관한 분자동력학시뮬레이션 (Molecular Dynamic Simulations of the Phase Transition of $\alpha-quartz$ and $\alpha-quartz-type$-type $GeO_2$ under High Pressure)

  • 김대원;노광수;최희락;성태현
    • 한국세라믹학회지
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    • 제34권7호
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    • pp.713-721
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    • 1997
  • Molecular dynamic (MD) simulations with new interatomic potential function including the covalent bond were performed on the phase transition of $\alpha$-quartz-type GeO2 under high pressure. The optimized crystal structure and the pressure dependence of the lattice constant showed higher reproducibility than the previous models and were in very good agreement with the experimental data. A phase transition of $\alpha$-quartz and $\alpha$-quartz-type GeO2 by simulation was found approximately 24 GPa and 6-7 GPa, respectively. This phase transition involved an abrupt volume shrinkage and showed 4-6 coordination mixed structure with the increasing in the coordination number of cation.

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압출성형에 의한 식물세포벽의 수용화 (Solubilization of Plant Cell Walls by Extrusion)

  • 황재관;김종태;홍석인;김철진
    • 한국식품영양과학회지
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    • 제23권2호
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    • pp.358-370
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    • 1994
  • Plant cell walls consist of a variety of chemical constituents such as cellulose, humicelluloses, pertins, lignin, glycoproteins, etc. These components are strongly linked through hydrogen , covalent, ionic and hydrophobic bondings, which thus confers the self-protection capability on plants. Some processing by-products (hulls, brans, pomaces) of cereal, fruits and vegetables are very limited in further utilization due to their compact structural rigidity. In view of the fact that the plant cell walls are essentially composed of dietary fiber components , solubilization of the strong intermolecular linkage s can contribute to increasing the soluble dietary fiber content and thus diversifying the functional and physiological role of plant cell walls as dietary fiber sources. This article reviews the chemical constituents of cereals, fruits & vegetables and brown seaweeds with reference to their intermoleuclar linkages. An particular emphasis will be placed on the solubilizing phenomena of rigid plant cell walls by extrusion and the resulting change of functional properties. It is suggested that underutilized food resources, typically exemplified by various food processing by-products and surplus seaweeds, can be successfully modified toward improved functional performance by extrusion.

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Asymmetric Ring Opening of Terminal Epoxides Catalyzed by Chiral Co(III)-BF3 Salen Complex Immobilized on SBA-16

  • Kim, Yong-Suk;Lee, Choong-Young;Kim, Geon-Joong
    • Bulletin of the Korean Chemical Society
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    • 제30권8호
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    • pp.1771-1777
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    • 2009
  • The homogeneous B$F_3$ containing chiral Co(III) salen complexes were anchored non-covalently on the surfaces of mesoporous SBA-16 silica containing aluminum species. The Brönsted and Lewis acidic sites are attributed to the immobilization of fluorine functionalized chiral salen complexes on the supports. The FT-IR, UV, ESCA, and NMR analyses were performed to determine the structure of synthesized chiral salen catalysts. These heterogeneous catalysts could be applied in asymmetric ring opening of terminal epoxides by water and phenol derivatives. They showed very high enantioselectivity and yield more than 98% in the catalytic synthesis of optically active products.

Synthesis and Characterization of Cobalt(II)/(III), Nickel(II) and Copper(II) Complexes of New 14, 15 and 16-Membered Macrocyclic Ligands

  • El-Tabl, Abdou Saad
    • Bulletin of the Korean Chemical Society
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    • 제25권12호
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    • pp.1757-1763
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    • 2004
  • A new series of nickel(II), cobalt(II)/(III) and copper(II) complexes of 14, 15 and 16-membered of macrocyclic ligands have been prepared and characterized by elemental analyses, IR, UV-VIS and $^1H-NMR$ spectra, magnetic susceptibilities, conductivities, DTA and ESR measurements. Molar conductances in DMF solution indicate that, the complexes are nonelectrolytes except (9-12) complexes. The electronic spectra show that, all complexes are square planar or distorted octahedral geometry. The ESR spectra of solid complexes (4), (8) and (11) show square planar of axial type symmetry $(d_{x2-y2})$ with considerable covalent bond character. However, complex (12) shows a spectrum of octahedral geometry with $d_{z2}$ ground state. Complex (12) shows exploitation in reducing the amount of electron adducts formed in DNA during irradiation with low radiation products.

Synthesis and Physicochemical Properties of Schiff Base Macrocyclic Ligands and Their Transition Metal Chelates

  • Rafat, Fouzia;Siddiqi, K.S.
    • 대한화학회지
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    • 제55권6호
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    • pp.912-918
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    • 2011
  • Tetraaza Schiff base macrocyclic ligands, $L^1$,$L^2$ and their transition metal chelates have been synthesized and characterized by elemental analyses, IR, electronic, EPR and $^1H$ NMR spectra, TGA and magnetic measurements. The molar conductance of one milli-molar solution of the complexes measured in DMF indicates that the divalent metal complexes are nonelectrolyte while those of trivalent metal ion, are 1:1 electrolytic in the same solvent. The reduction of Racah parameter from the free ion value confirms the presence of considerable covalence of metal ligand sigma bond in the Co(II) and Mn(II) complexes. The EPR spectra of Cu(II) complexes at room temperature shows axial symmetry indicating a $d_x{^2}_{-y}{^2}$ ground state with significant covalent character. The thermal analysis suggests that the complexes do not contain water molecules because only the metal is left as residue.

Modulation of Phytotropin Receptors by Fluoride and ATP

  • Nam, Myung-Hee;Kang, Bin-G.
    • BMB Reports
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    • 제28권6호
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    • pp.552-555
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    • 1995
  • Treatment of microsomal vesicles isolated from etiolated Pisum sativum L cv. Alaska epicotyl tissue with agents inhibiting protein dephosphorylation, namely NaF and/or ATP, resulted in increased binding of the phytotropin NPA to the putative auxin efflux carriers localized on the plasma membrane. The phytotropin effect was especially conspicuous if the vesicles were simultaneously treated with Triton X-100. Kinetic analysis of the binding indicated the existance of two distinct sites for NPA, each having different affinities. Increased binding of the phytotropin to the membrane where protein dephosphorylation was inhibited was attributable to the increased ligand affinity of both sites. Treatment of tissue segments with flubride was found to enhance in vivo auxin transport. Implications of covalent modification of the auxin efflux carrier complex for the regulation of membrane transport of auxin molecules are discussed.

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Mono and Multilayer Assembly of Zeolite Microcrystals on Substrates

  • Yoon, Kyung-Byung
    • Bulletin of the Korean Chemical Society
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    • 제27권1호
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    • pp.17-26
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    • 2006
  • We have shown that zeolite microcrystals can be readily organized in the form of uniformly oriented monoand multilayers on various substrates by well-defined chemical linkages based on covalent, ionic, and hydrogen bondings between the microcrystals and the substrates. This finding establishes the fact that micrometer-scale building blocks can be readily organized into organized entities through interconnection of the surface-tethered large number of functional groups. Since zeolite crystals have highly regular and uniform nanochannels and nanopores within them, the resulting mono and multilayers of zeolite microcrystals bear great potential to be utilized in various novel applications.

Quartz Crystal Microbalance 시스템을 이용한 저밀도 지질단백질측정용 면역센서의 개발 (Development of Quartz Crystal Microbalance-Based Immunosensor for the Determination of Low-Density Lipoprotein)

  • 김상현;윤현철;감학성
    • KSBB Journal
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    • 제13권4호
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    • pp.337-342
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    • 1998
  • Immunosensor for the determination of LDL(Low-Density Lipoprotein), a good indicator for the diagnosis of atherosclerosis and hypercholesterolemia, was developed by using quartz crystal microbalance(QCM). The immunosensor consists of flow-through cell, oscillating circuit, oscilloscope, and frequency counter. FIA(Flow Injection Analysis) was applied to the QCM system for the measurement of LDL in liquid phase. Antibody showing binding affinity against LDL was immobilized on the gold electrode of a quartz crystal by covalent coupling via polyethylenimine / glutaredehyde. LDL was injected and bound to the antibody immobilized on the QCM immunosensor. The response of the immunosensor (F0 - F1) was found to be proportional to the LDL concentration from 200 $\mu\textrm{g}$/ml to 800 $\mu\textrm{g}$/ml. Operational conditions for the operation of immunosensor were also investigated in terms of sensitivity and non-specific binding.

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뫼스바우어 분광법에 의한 준강자성체 $Fe_7Se_8$의 결정학적 특성 및 자기적 특성 (Crystallographic and Magnetic Properties of the Ferrimagnetic $Fe_7Se_8$ by M$\ddot{o}$ssbauer Spectroscopy)

  • 조용호;김효준;이동욱;김응찬;남효덕
    • 한국전기전자재료학회논문지
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    • 제11권1호
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    • pp.62-66
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    • 1998
  • M$\ddot{o}$ssbauer spectra of ferrimagnetic $Fe_2SE_8$ prepared with $^{57}Fe$ enriched iron have been taken at 298 K and below 78K, and Fe\ulcornerSe\ulcorner has been studied by X-ray diffraction. The crystal structure is found to be a "3c" hexagonal superstructure of the NiAs structure. Three sets of six-line hyperfine patterns were obtained and assigned to three magnetically nonequivalent sites of a superstructure of the crystal. The iron ions at all three sites are found to be in a highly covalent ferrous state. It is shown that the results obtained at the low temperature region are well consistent with Okazaki's "3c" superstructure model.uperstructure model.

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