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  • 1
    ISSN: 1432-1327
    Keywords: Syntheses ; Enantiomeric ruthenium complexes ; DNA binding modes ; Enantioselectivity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Δ - and Λ-[Ru(bpy)2(HPIP)](PF6)2 (Δ-1 and Λ-1; bpy =2,2′-bipyridine, HPIP=2-(2-hydroxyphenyl)imidazo[4,5-f][1,10]phenan-throline), Δ- and Λ-[Ru(bpy)2(HNAIP)](PF6)2 (Δ-2 and Λ-2; HNAIP=2-(2-hydroxy-1-naphthyl)imidazo[4,5-f][1,10]phenanthroline), Δ- and Λ-[Ru(bpy)2 (HNOIP)](PF6)2 (Δ-3 and Λ-3; HNOIP=2-(2-hydroxy-5-nitrophenyl)imidazo[4,5-f][1,10]phenanthroline), and Δ- and Λ-[Ru(bpy)2(DPPZ)](PF6)2 (Δ-4 and Λ-4; DPPZ=dipyridophenazine), have been synthesized. Binding behavior of these chiral complexes to calf thymus DNA (CT-DNA) has been investigated by electronic absorption, steady-state emission, and circular dichroism spectroscopies, as well as by viscosity measurements and equilibrium dialysis binding studies. Several points came from the results. (1) The DNA-binding properties were distinctly different for the [Ru(bpy)2L]2+ (L=HPIP, HNAIP, HNOIP) series of ruthenium(II) complexes, which indicates that the photophysical behavior of the complexes on binding to DNA can be modulated through ligand design. (2) Different binding rates of individual enantiomers of complexes 1 and 4 to DNA were observed through dialysis experiments. The Λ enantiomer bound more rapidly than the Δ enantiomer and their different intercalative binding geometries were suggested to be responsible. (3) Both Δ-2 and Λ-2 bound weakly to CT-DNA; Δ-2 may bind through a partial intercalation mode, whereas Λ-2 may bind in the DNA groove. (4) There was no noticeable enantioselectivity for complexes 1, 3, and 4 on binding to CT-DNA. Both of their enantiomers can intercalate into DNA base pairs. It is noted that Δ-3 and Λ-3 exhibited almost identical spectral changes on addition of CT-DNA, and a similar binding manner of the isomers to the double helix was proposed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of superconductivity 13 (2000), S. 73-76 
    ISSN: 1572-9605
    Keywords: Y1−x Ba2Cu3O1−y ; nonstoichiometry ; microstructural defect ; flux pinning
    Source: Springer Online Journal Archives 1860-2000
    Topics: Electrical Engineering, Measurement and Control Technology , Physics
    Notes: Abstract Considerably improved flux pinning and critical current density J c values have been achieved in Y-deficient Y-123 superconductors by directional solidification in air. In comparison with the regular Y-123 composition, Y-deficient one also has an orthorhombic structure and Y-123 main crystal phase remains in it. Whereas with the shortage of Y, Y1−x Ba2Cu3O7−y can be regarded as (YBa2Cu3)1−x O7−t(Ba2Cu3) x O t−y or (YBa2Cu3O7−z )(□ x YO z−y ), so there may develop several kinds of microstructure defects as pinning sites in the system, such as highly dense, fine-scale, and faultlike defects, as well as localized superstructure, which are able to induce the increasing in flux pinning and J c values in higher external magnetic fields. This kind of simple nonstoichiometric route could lead to a commercial technique for flux-pinning enhancement in Y-123 bulk materials.
    Type of Medium: Electronic Resource
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