Literature DB >> 15783194

Sulfoxide carbon-sulfur bond activation.

Joseph M O'Connor1, Kevin D Bunker, Arnold L Rheingold, Lev Zakharov.   

Abstract

The alkynylsulfoxide, TMSCCSO(p-tolyl) (TMS = trimethylsilyl, tolyl = C6H4Me), undergoes reaction with (eta5-C5H5)Co(PPh3)2 at room temperature to give the cobaltosulfoxide complex, (C5H5)Co(PPh3)(eta1-CCTMS)[eta1-(S)-SO(p-tolyl)], which was characterized by X-ray crystallography. Exposure of this cobaltosulfoxide complex to oxygen gas leads to the formation of the corresponding metallosulfone complex, (C5H5)Co(PPh3)(eta1-CCTMS)[eta1-(S)-SO2(p-tolyl)], which was characterized by X-ray crystallography. Alternatively, in solution at room temperature, the metallosulfoxide is converted to a 1:4 mixture of the equatorial-equatorial and equatorial-axial bridging cobalt-thiolato dimers, {(C5H5)Co[mu-S(p-tolyl)]}2, respectively. The equatorial-equatorial isomer was characterized by X-ray crystallography.

Entities:  

Year:  2005        PMID: 15783194     DOI: 10.1021/ja050160g

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Cobalt 1,3-Diisopropyl-1H-imidazol-2-ylidene Complexes: Synthesis, Solid-State Structures, and Quantum Chemistry Calculations.

Authors:  Carmen L Vélez; Phineus R L Markwick; Ryan L Holland; Antonio G Dipasquale; Arnold L Rheingold; Joseph M O'Connor
Journal:  Organometallics       Date:  2010-11-23       Impact factor: 3.876

2.  Probing the Hydrogenation of Vinyl Sulfoxides Using para-Hydrogen.

Authors:  Ben J Tickner; Rachel R Parker; Adrian C Whitwood; Simon B Duckett
Journal:  Organometallics       Date:  2019-11-14       Impact factor: 3.876

  2 in total

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