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Showing 1 to 4 of 4 for “"Fe complexes"”.

  1. Synthesis and stabilities of mononuclear iron (II) dicarbonyls derived from neutral NNS ligands : structural models of the apo-active site of mono-iron (Hmd) hydrogenase

    … and characterization of iron dicarbonyl complexes derived from tridentate ortho-substituted Schiff base pyridine/thioether ligands ([subscript R]NNS) and (Fe(CO)₄(Br)₂). Two general synthetic routes are reported for the isolation of such iron carbonyls. First, metalation of [subscript …

    texas Repository record for Synthesis and stabilities of mononuclear iron (II) dicarbonyls derived from neutral NNS ligands : structural models of the apo-active site of mono-iron (Hmd) hydrogenase (opens in a new tab)

  2. Chemical Modification of Cellulose Fibers and their Orientation in Magnetic Field

    … by modifying the cellulose fibers with a ferromagnetic entity and subjecting to a magnetic field. Chemically modified cellulose fibers (CLF) were oriented in dilute polylactic acid by subjecting the fiber and matrix to a magnetic field of ≈ 4T (Tesla). CLF and Microcrystalline cellulose …

    toronto-retro Repository record for Chemical Modification of Cellulose Fibers and their Orientation in Magnetic Field (opens in a new tab)

  3. The gas chromatographic separation properties of azulene and the synthesis and characterization of bulky bis-pyrazolylpyridine metal-ligand complexes.

    … of bulky tridentate ligand-metal complexes. Azulene is an aromatic molecule with interesting properties, most notably a permanent dipole moment of 1.08 D. This degree of polarity in the absence of heteroatoms is quite rare and offers potential for use in unique gas chromatographic …

    baylor Repository record for The gas chromatographic separation properties of azulene and the synthesis and characterization of bulky bis-pyrazolylpyridine metal-ligand complexes. (opens in a new tab)

  4. Free radical formation and DNA damage in the cytotoxicity of alkylaminoanthraquinone antitumour agents.

    … uptake between the agents did not account for differences in cytotoxicity and DNA strand breakage observed. The 1,4 substitution pattern of MIT, CI941 and 1,4AQ appears to prevent metabolic activation. In further studies;- i) MIT and CI941 were more potent inhibitors of 3 MCF-7 topoisomerase I …

    de-montfort Repository record for Free radical formation and DNA damage in the cytotoxicity of alkylaminoanthraquinone antitumour agents. (opens in a new tab)