Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Electronic Resource  (4)
  • 1960-1964  (2)
  • 1955-1959  (2)
Material
  • Electronic Resource  (4)
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 177 (1956), S. 852-853 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] (I) Proposed structure of (CBHi9)2Rh2Cla. The dotted lines representing bonds between the olefinic double bonds and the metal are intended to imply a scheme of bonding such as has been suggested in the ion [C2H4PtCl33~ (see ref. 4) Cl C8H1 Rh (II) A novel derivative C8H12RhC5H5 (III), in ...
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 177 (1956), S. 1042-1043 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Recently, van der Kerk and his co-workers1'2 have suggested that (la) contributes strongly to the structure of methyl derivatives (R = Me) but that its importance decreases rapidly on ascending the homologous series. They consider the dipolar form (la) to be responsible for the antifungal and ...
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 76 (1964), S. 621-628 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An Hand zweier vierzähniger Liganden, die Phosphor und Arsen enthalten, wurde der Einfluß der Liganden-Gestalt auf die Koordinationszahl und die Geometrie von Komplexverbindungen untersucht. Beide Liganden bilden fünffach koordinierte Komplexe mit trigonal-bipyramidaler Struktur [Fe(II), Co(I), Co(II), Rh(I), Ni(II), Pd(II), Pt(II)], können aber auch sechsfach koordinierte Komplexe mit oktaedrischer Struktur bilden [Fe(II), Ru(II), Os(II), Co(III), Rh(III), Pd(IV), Pt(IV)]. Die magnetischen Eigenschaften dieser Verbindungen lassen sich ebenso wie ihre Stereochemie mit der Ligandenfeldtheorie erklären: Bei Metall-Ionen mit einer d6-Elektronenkonfiguration sollte eine geringe Gesamtfeldstärke die Bildung paramagnetischer, fünffach koordinierter Komplexe begünstigen, während eine hohe Gesamtfeldstärke zur Bildung sechsfach koordinierter, diamagnetischer Komplexe führen sollte.  -  Die Untersuchungen haben gezeigt, daß die Tendenz mehrzähniger Liganden, alle Donator-Atome zu betätigen, nicht so groß ist, wie allgemein angenommen. Beispielsweise ließen sich Cr(III)-Komplexe isolieren, in denen die vierzähnigen Liganden nur dreizähnig sind, und Hg(II)-Komplexe, in denen nur zwei der vier Donator-Atome mit dem zentralen Metallatom verbunden sind.
    Additional Material: 7 Tab.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 0570-0833
    Keywords: Tetradentate ligands ; P ligands ; Arsenic ligands ; Phosphorus ; Arsenic ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The effect of ligand shape on coordination numbers and geometry of coordination compounds has been studied using two tetradentate ligands containing phosphorus and arsenic. These tend to form five-coordinate complexes with trigonal bipyramidal structure [Fe(II), Co(I), Co(II), Rh(I), Ni(II), Pd(II), Pt(II)], but can also form six-coordinate complexes with octahedral structure [Fe(II), Ru(II), Os(II), Co(III), Rh(III), Pd(IV), Pt(IV)]. The magnetic properties and the stereochemistry of the complexes are explained by ligand field theory which predicts that, for metal ions with d6-electronic configuration, a low overall field strength should favor the formation of five-coordinate paramagnetic complexes while a high overall field strength should favor the formation of six-coordinate diamagnetic complexes. - This work provides further indication that the tendency of polydentate ligands to use all the potential donor atoms is not as pronounced as is generally believed. This is shown by the isolation of chromium(III) complexes in which the tetradentate ligands are, in fact, acting as tridentate, and by the isolation of mercury(II) complexes where only two of the four donor atoms of the polydentate ligand are actually bonded to the central metal atom.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...