Reactivity of the [η2-bis(tert-butylsulfonyl)acetylene](carbonyl)(η5-cyclopentadienyl)cobalt complex towards electron-rich and -poor ccetylenes

The electron-rich aminoacetylenes Et2NC2R (2a-c, R = SPh, PPh2, and Ph, respectively) react smoothly with [η2-bis(tert-butylsulfonyl)acetylene](carbonyl)(η5-cyclopentadienyl)co-balt (1) to form the donor-acceptor stabilized (η4-cyclobutadiene)cobalt complexes 3a-c in good yields. However, treatment...

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Hauptverfasser: Goswami, Avijit (VerfasserIn) , Stäb, Tobias (VerfasserIn) , Rominger, Frank (VerfasserIn) , Gleiter, Rolf (VerfasserIn) , Siebert, Walter (VerfasserIn)
Dokumenttyp: Article (Journal) Festschrift
Sprache:Englisch
Veröffentlicht: August 24, 2005
In: European journal of inorganic chemistry
Year: 2005, Heft: 20, Pages: 4086-4089
ISSN:1099-0682
DOI:10.1002/ejic.200500308
Schlagworte:
Online-Zugang:Resolving-System, lizenzpflichtig, Volltext: https://doi.org/10.1002/ejic.200500308
Verlag, lizenzpflichtig, Volltext: https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejic.200500308
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Verfasserangaben:Avijit Goswami, Tobias H. Staeb, Frank Rominger, Rolf Gleiter, and Walter Siebert

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520 |a The electron-rich aminoacetylenes Et2NC2R (2a-c, R = SPh, PPh2, and Ph, respectively) react smoothly with [η2-bis(tert-butylsulfonyl)acetylene](carbonyl)(η5-cyclopentadienyl)co-balt (1) to form the donor-acceptor stabilized (η4-cyclobutadiene)cobalt complexes 3a-c in good yields. However, treatment of the electron-poor borylacetylenes 2d-f with the cobalt complex 1 does not lead to the expected (η4-cyclobutadiene)cobalt complexes. Analogously, the reaction of bis(1-phenylethynyl)sulfide (2g) with two equivalents of 1 gives rise to the sulfur-bridged bis[η4-(cyclobutadiene)cobalt] complex 3g. The new cobalt complexes were characterized by NMR spectroscopy, mass spectrometry, and by X-ray structure analysis for 3a, which reveals almost equal C-C bond lengths within the cyclobutadiene ring. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) 
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