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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 3 (1997), S. 1005-1008 
    ISSN: 0947-6539
    Keywords: alkali metals ; calcium ; ketyl radicals ; radicals ; samarium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The use of hexamethylphosphoramide (HMPA) or other sterically demanding groups as stabilizing ligands allows the successful isolation of a series of structurally characterizable complexes of ketyl radicals with alkali, alkaline earth, and lanthanide metal. It has been demonstrated that the stability and reactivity of the ketyl radicals strongly depend on both the nature of the metals to which they are bound and the steric and electronic properties of the ancillary ligands, as well as the structure of their parent ketones.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0044-8249
    Keywords: Arene ; Calcium ; Radikale ; Reduktionen ; Strukturaufklärung ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 30 (1995), S. 684-692 
    ISSN: 1076-5174
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Bis(triphenylphosphine)iminium salts of a series of high-nuclear and anionic ruthenium carbonyl cluster complexes were characterized by use of the negative-ion fast atom bombardment mass spectrometry. With a m-nitrobenzyl alcohol matrix, all of the monoanionic cluster complexes gave relatively intense intact anion peaks [A]- and all of the dianionic cluster complexes examined gave protonated monoanion peaks [HA]-. In some cases weak adduct ions were observed, which arose from the reaction of the cluster anions with the matrix during the bombardment process. The predominant fragmentation process of intact ions was found to be sequential loss of CO ligands and no loss of methyl, allyl or iodo ligand was observed. However, dissociation of bromo ligand from [Ru6C(CO)16Br]- and fragmentation of acetyl groups in [Ru5C(CO)13I2(COMe)]- and 6C(CO)16(COMe)- were noted. Degradation of cluster metal frameworks of [HRu10C(CO)24]- and [Ru10C(CO)24]2- into [HRu6C(CO)16]- was observed. These fragmentation and degradation patterns are comparable to their reactions in solution.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 1011-1016 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Charge transfer complexes of the type [ML2]2-[RV]2+ are prepared from viologens (RV2+) and dianionic metal dithiolenes ([ML2]2-; M=Zn, Cd, Hg; L=a substituted 1,2-ethenedithiolate). The solid state structure consists of separated pseudocolumns of tetrahedral metal dithiolenes and twisted viologens. While there is no evidence for short contacts within a column, an intercolumnar interaction is indicated by Zn-H and S-H distances of 3.27 and 2.87 Å, respectively. UV-VIS spectra exhibit an ion pair charge transfer band in the range of 460-660 nm (∊=400-1900). Its location is predominatly determined by the nature of the ethenedithiolate ligand inducing shifts of 70-200 nm while the metal has only a weak influence. Formation constants of the 1:1 ion pairs are in the range of 100-600 1 mol-1. Spectrophotometric analysis reveals the presence of further adducts with different composition.
    Notes: Charge-Transfer-Komplexe des Typs [ML2]2-[RV]2+ werden aus Viologenen (RV2+) und dianionischen Metalldithiolenen ([ML2]2-; M=Zn, Cd, Hg; L=ein substituiertes 1,2-Ethendithiolat) synthetisiert. Die Festkörperstruktur besteht aus getrennten Pseudosäulen tetraedrischer Metalldithiolene und verdrillter Viologene. Für intrakolumnare Wechselwirkungen gibt es keine Hinweise, für interkolumnare sprechen dagegen die kurzen Zn-H- und S-H-Abstände von 3.27 und 2.87 Å. UV-VIS-Spektren enthalten eine Ionenpaar-Charge-Transfer-Bande im Bereich von 460-660 nm (∊=400-1900). Deren Lage wird hauptsächlich durch die Natur des Ethendithiolat-Liganden festgelegt, welcher Verschiebungen von 70-200 nm induziert. Das Zentralmetall übt nur einen schwachen Einfluß aus. Die Bildungskonstanten der 1:1-Ionenpaare liegen im Bereich von 100-600 1 mol-1. Spektrophotometrische Analysen deuten auf das Vorliegen weiterer Ionenassoziate unterschiedlicher Zusammensetzung.
    Additional Material: 5 Ill.
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  • 5
    ISSN: 0570-0833
    Keywords: arenes ; calcium ; radicals ; reductions ; structure elucidation ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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