156 research outputs found

    Feststellung und Prüfung des Jahresabschlusses der Aktiengesellschaft im Gemeinsamen Markt

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    Feststellung und Prüfung des Jahresabschlusses der Aktiengesellschaft im Gemeinsamen Markt : Kommissionsvorschlag e. 5. Richtlinie zur Angleichung d. Gesellschaftsrechts (IV. Kap.) / Hans-Jürgen Sonnenberger ; Michael Coester. - In: Die Aktiengesellschaft. 19. 1974. S. 177-18

    Verkehrssitten im Schuldvertrag

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    Französisches Handels- und Wirtschaftsrecht

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    Einführung in das französische Recht

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    Einführung in das französische Recht / Hans Jürgen Sonnenberger ; Eugen Schweinberger. - 2., völlig neu bearb. Aufl. - Darmstadt : Wiss. Buchges., 1986. - XVII, 232 S. - [1. Aufl. 1972

    Reduction Chemistry of Neptunium cyclopentadienide complexes: from structure to understanding

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    Neptunium complexes in the formal oxidation states II, III, and IV supported by cyclopentadienyl ligands are explored, and significant differences between Np and U highlighted as a result. A series of neptunium(III) cyclopentadienyl (Cp) complexes [Np(Cp)3], its bis-acetonitrile adduct [Np(Cp)3(NCMe)2], plus its KCp adduct K[Np(Cp)4] and [Np(Cp')3] (Cp' = C5H4SiMe3) have been made and characterised providing the first single crystal x-ray analyses of NpIII Cp complexes. In all NpCp3 derivatives there are three Cp rings in eta5-coordination around the NpIII centre; additionally in [Np(Cp)3] and K[Np(Cp)4] one Cp ring establishes a mu-eta1-interaction to one C atom of a neighbouring NpCp3 unit. The solid state structure of K[NpCp4] is unique in containing two different types of metal-Cp coordination geometries in the same crystal. NpIIICp4 units are found exhibiting four units of eta5-coordinated Cp rings like in the known complex [NpIV(Cp)4], the structure of which is now reported. A detailed comparison of the structures gives evidence for the change of ionic radii of ca. -8 pm associated with change in oxidation state between NpIII and NpIV. The rich redox chemistry associated with the syntheses is augmented by the reduction of [Np(Cp')3] by KC8 in the presence of 2.2.2 cryptand to afford the putative neptunium(II) K(2.2.2 cryptand)[Np(Cp')3] that is thermally unstable above -10 °C like its U and Th congeners. Together, these spontaneous and controlled redox reactions of organo-neptunium complexes, along with information from structural characterisation, show the relevance of organometallic Np chemistry to understanding fundamental structure and bonding in the minor actinides.JRC.G.I.5-Advanced Nuclear Knowledg
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