• Title of article

    Facile access to enantiomerically pure bis(sulfoxide) chelates of late transition metals

  • Author/Authors

    Daniel R. Evans، نويسنده , , Mingsheng Huang، نويسنده , , W. Michael Seganish، نويسنده , , James C. Fettinger، نويسنده , , Tracie L. Williams، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2003
  • Pages
    4
  • From page
    462
  • To page
    465
  • Abstract
    Herein contains a report detailing the synthesis and characterization of six, chiral, late-transition metal complexes all chelated using RS,RS-bis(p-tolylsulfinyl)ethane, RS,RS-BTSE. All complexes revealed S-ligation to the metal with an expected contraction of the sulfinyl-oxygen bond length when compared to free sulfoxide. The presented data serve to illustrate three attractive, yet unexplored, aspects of the bis(sulfoxide) bidentate ligand: (i) bidentate sulfoxide ligands, when chelated to a metal, give rise to complexes that are pseudo-C2 symmetric in terms of both sterics and electronics, (ii) the sulfoxides, unlike typical N-, P-, and O-based ligands, present the coordination sphere with a significant amount of steric and electronic mismatch, and (iii) the data support the fact that sulfoxides are moderate σ-donors and good-to-excellent π-acceptors – an aspect that should afford such metal chelates with a wide degree of reactivity. Finally, X-ray crystallographic experiments, coupled with an extensive CCDC search, provide an opportunity to establish the following ligand-ranking scheme for bidentate ligands spanned by an ethylene bridge, R2N–
  • Journal title
    Inorganic Chemistry Communications
  • Serial Year
    2003
  • Journal title
    Inorganic Chemistry Communications
  • Record number

    1316008