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  • 97.10  (1)
  • Gold(I) complexes  (1)
  • Key words Solid state electrochemistry  (1)
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  • 1
    ISSN: 1433-0768
    Schlagwort(e): Key words Solid state electrochemistry ; Mössbauer ; Magnetic susceptibility ; X-ray powder diffraction ; Iron(III)-cadmium(II) hexacyanoferrates
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Coprecipitates of CdII, KI and FeIII with hexacyanoferrate ions [Fe(CN)6]4− have been studied by solid-state electrochemistry (voltammetry of immobilized microparticles), magnetic susceptibility measurements, X-ray powder diffraction, electron spin resonance, Mössbauer and diffuse reflectance spectroscopy. Most suprisingly, all experimental results point to the formation of a continuous series of complex mixed phases without the formation of phase mixtures. Although CdII and FeIII ions differ too much in their ionic radii to allow the formation of simple substitution mixed hexacyanoferrates, they are capable of forming different kinds of complex insertion and substitution mixed crystals because of the zeolitic structure of both the iron and the cadmium hexacyanoferrate. Low cadmium concentrations can be found in the zeolitic cavities of iron hexacyanoferrate (Prussian blue), and they start to widen the lattice and facilitate, at higher concentrations, the direct substitution of high-spin iron(III) ions by cadmium ions. In cases of an excess of cadmium, the formation of cadmium hexacyanoferrate with iron(III) ions in the interstitials of the zeolitic structure is observed. These mixed phases show strong charge transfer bands in the visible range and have the appearance of “diluted” Prussian blue. For the first time, this indicates that the charge transfer between the carbon-coordinated low-spin iron(II) ions and the high-spin iron(III) ions can also occur when the latter are situated in the cavities of a host hexacyanoferrate. In Prussian blue the interstitial iron(III) ions are responsible for a very strong charge transfer interaction between the low-spin iron(II) ions and the nitrogen-coordinated high-spin iron(III) ions. Upon substitution of the very small amount of interstitial iron(III) ions in Prussian blue by potassium and cadmium ions the Kubelka-Munk function diminishes by more than 30%, indicating a tremendous decrease in iron(III)-iron(II) interaction.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    The European physical journal 334 (1989), S. 491-510 
    ISSN: 1434-601X
    Schlagwort(e): 25.55 ; 97.10
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract The22Ne(α, γ)26Mg and22Ne(α, n)25Mg reactions were investigated forE α(lab) from 0.71 to 2.25 MeV. Neon gas enriched to 99% in22Ne was recirculated in a differentially pumped gas target system of the extended type. Theγ-ray transitions were observed with Ge(Li) detectors and the neutrons with3He ionization chambers. A previously known resonance at ER(lab)=2.05 MeV was verified and 15 new resonances were found in the energy range covered, with the lowest at ER(lab)=0.83 MeV. Information on resonance energies, widths, strengths,γ-ray branching ratios, as well asJ π assignments, is reported. The energy range investigated corresponds to the important temperature range ofT 9 from 0.3 to 1.4 (109 K), for which the astrophysical rates were determined for both reactions. The results show that the ratios of the rates for22Ne(α, n)25Mg and22Ne(α, γ)26Mg are significantly smaller than the previously adopted values, e.g., by at least a factor of 60 nearT 9=0.65. Thus, the22Ne(α, n)25Mg reaction will likely play a smaller role as a neutron source fors-process nucleosynthesis, than has frequently been assumed.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 1021-1026 
    ISSN: 0044-2313
    Schlagwort(e): Gold(I) complexes ; N-thiocarbamoyl benzamidine ligands ; X-ray structure ; linear coordination ; intermolecular hydrogen bonds ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Gold(I) Complexes of N-Thiocarbamoyl Benzamidines: Synthesis and StructuresBy reaction of tetrachlorogold(III) acid with N-thiocarbamoyl benzamidines HL complexes of composition AuI(HL)Cl have been obtained. The molecular structures of three complexes have been determined by single crystal X-ray diffraction methods. All complexes show linear coordination in which the ligand HL coordinates by the S atom and the second coordination site of gold(I) is occupied by a chloro ligand. The bond lengths in the coordinated ligands HL do not change appreciably in comparison with the free ligands. In all investigated structures intermolecular hydrogen bonds of the type N—H … Cl are formed.
    Notizen: Durch Umsetzung von Tetrachlorogold(III)-säure mit N-Thiocarbamoylbenzamidinen HL wurden Komplexverbindungen der Zusammensetzung AuI(HL)Cl erhalten. Die Molekülstrukturen von drei Komplexen wurden durch Röntgenkristallstrukturanalyse bestimmt. Alle Komplexe weisen eine lineare Koordination auf, wobei der Ligand HL über das Schwefel-Atom koordiniert und die zweite Koordinationsstelle am Gold(I) durch einen Chloro-Liganden besetzt ist. Die Bindungslängen in den koordinierten Liganden HL ändern sich gegenüber denen der freien Liganden nur geringfügig. In allen untersuchten Strukturen liegen intermolekulare Wasserstoffbrückenbindungen des Typs N—H … Cl vor.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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