Structural properties of bis(hexacarbonyldicobalt) complexes with heteroatoms next to the former triple bonds: a contribution to the mechanism of the Pauson-Khand reaction

The bis(hexacarbonyldicobalt) complexes of cyclic diynes with sila-, thia- and selena-substituted acetylene units have been isolated. The structural features of these complexes have been elucidated by means of X-ray diffraction analyses on single crystals. In three cases (24′, 25′ and 29′) the X-ray...

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Hauptverfasser: Werz, Daniel B. (VerfasserIn) , Schulte, Jan Hilko (VerfasserIn) , Rausch, Bernhard J. (VerfasserIn) , Gleiter, Rolf (VerfasserIn) , Rominger, Frank (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: April 26, 2004
In: European journal of inorganic chemistry
Year: 2004, Heft: 12, Pages: 2585-2593
ISSN:1099-0682
DOI:10.1002/ejic.200300862
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejic.200300862
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejic.200300862
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Verfasserangaben:Daniel B. Werz, J. Hilko Schulte, Bernhard J. Rausch, Rolf Gleiter, and Frank Rominger

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520 |a The bis(hexacarbonyldicobalt) complexes of cyclic diynes with sila-, thia- and selena-substituted acetylene units have been isolated. The structural features of these complexes have been elucidated by means of X-ray diffraction analyses on single crystals. In three cases (24′, 25′ and 29′) the X-ray investigations show bis(pentacarbonyldicobalt) complexes instead of bis(hexacarbonyldicobalt) ones. Their empty coordination sites are each occupied by divalent chalcogen moieties from the opposite side of the molecule affording distorted C2Co2 cores. These results corroborate the possibility of intramolecular activation in Pauson−Khand reactions of chalcogen-containing substrates. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) 
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