Mono(alkyne)cobalt complexes and electron-rich alkynes: the formation of an alkyne-bridged dinuclear cobalt complex by a one-pot procedure

[η2-Bis(tert-butylsulfonyl)acetylene](carbonyl)(η5-trimethylsilylcyclopentadienyl)cobalt (2c) proved to be reactive towards bis(telluro)- and bis(seleno)-substituted alkynes 3 and 4, respectively, to yield push-pull-substituted CpCo-stabilized cyclobutadiene complexes. By utilizing the unsymmetrical...

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Hauptverfasser: Werz, Daniel B. (VerfasserIn) , Gleiter, Rolf (VerfasserIn) , Rominger, Frank (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: August 17, 2004
In: European journal of inorganic chemistry
Year: 2004, Heft: 20, Pages: 4021-4027
ISSN:1099-0682
DOI:10.1002/ejic.200400339
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejic.200400339
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejic.200400339
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Verfasserangaben:Daniel B. Werz, Rolf Gleiter, and Frank Rominger

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520 |a [η2-Bis(tert-butylsulfonyl)acetylene](carbonyl)(η5-trimethylsilylcyclopentadienyl)cobalt (2c) proved to be reactive towards bis(telluro)- and bis(seleno)-substituted alkynes 3 and 4, respectively, to yield push-pull-substituted CpCo-stabilized cyclobutadiene complexes. By utilizing the unsymmetrical diyne 6 and the symmetrical bis(thio)-substituted triyne 7 it was shown that only the most electron-rich triple bond was attacked by the electrophilic compound 2c. In the case of 7 a dinuclear CpCo-stabilized cyclobutadiene complex 14 bridged by one acetylene moiety was obtained. All the reactions could be carried out at room temperature under rather mild conditions. X-ray investigations of 8, 12, 14a, and 15 show almost equal C−C bond lengths in the cyclobutadiene moieties. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004) 
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