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  • 1
    ISSN: 1434-4475
    Keywords: Tetrachloro tin(IV) ; Diazabutadiene ; Mössbauer ; Far-infrared
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Abhängigkeit des Logarithmus der Fläche unter der Zinn-119-Mössbauer-Resonanz (A in verschiedenen Temperaturen werden zuA 77 normalisiert) von der Temperatur wurde für Tetrachlor[1,4-di(p-methoxyphenyl)-2,3-dimethyl-1,4-diazabutadien]zinn(IV) gemessen. Der Anstieg lnA gegenT von −2.46·10−2K−1 spricht für eine monomere Struktur. In den Vibrations-Spektren stimmen die wichtigsten Dehnungsschwingungen mit einercis-oktaedrischen Konfiguration von C2v-Symmetrie überein.
    Notes: Summary The dependence of the logarithm of the area under the tin-119 Mössbauer resonance (A at different temperatures are normalized toA 77) vs. temperature is measured for tetrachloro[1,4-di(p-methoxyphenyl)-2,3-dimethyl-1,4-diazabutadiene] tin(IV). The slope of the plot of lnA vs.T is −2.46·10−2K−1, suggesting a monomeric structure. In the vibrational spectra the significant stretching vibrations agree with acis octahedral configuration of C2v symmetry.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0268-2605
    Keywords: palladium ; platinum ; imidazoline ; DNA ; cyclometallated complexes ; cytotoxic activity ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In this paper we describe the synthesis and chemical characterization of three new Pd(II)-imidazoline complexes: [PdCl2 (C6H5-CH2-C3H5N2)2] (2), [PdCl(SEt2) (C6H4-C3H5N2)] (5) and [Pd(C6H4-C3H5N2) (μ-Br)]2 (6). We have also analyzed the DNA modifications and in vitro antileukaemic activity of these compounds and of their previously reported analogs [Pd Cl2 (C6H5-C3H5N2)2] (1), [Pd (C6H4-C3H5N2) (μ-OAc)]2 (3), [Pd (C6H4-C3H5N2) (μ-Cl)]2 (4) and [Pt(C6H4-C3H5N2)(μ-Cl] (7). All these compounds modify the DNA secondary structure since they alter the melting temperature (Tm) of the DNA. Circular dichroism spectra indicated, moreover, that compounds 3, 5 and 6 induced higher modification on the double helix than compounds 1, 2 and 4. While compounds 1, 2 and 5 seem to induce slight changes in the electrophoretic mobility of the open and covalently closed circular forms of pUC8 DNA at high ri (input molar ratio of Pd or Pt to nucleotides), compounds 3, 6 and 7 do not modify at any ri the tertiary structure of the plasmid DNA. Antileukaemic tests suggest that compounds 1, 4 and 7 exhibit important cytotoxic activity since their IC50 values against HL-60 human leukaemic cells were below 10 μg ml-1. © 1997 John Wiley & Sons, Ltd.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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