Abstract
Several Pd(II) and Pt(II) complexes of tripropylarsines (AsR3; R = Pr, iPr) [MCl2(AsR3)2], [M2Cl2(m-Cl)2(AsR3)2], [Pd2Me2(m-Cl)2(AsR3)2], [Pd2X2(m-Pz)2(AsR3)2] (X = Cl or Me, Pz = pyrazolate), [Pd2Cl2(m-Y)2(AsR3)2] (Y = OAc or SPh), [MCl(S2CNEt2)(AsR3)] and [PdCp(Cl)(AsiPr3)] (M = Pd or Pt) were prepd. All the complexes were characterized by elemental analyses, IR and 1H NMR spectroscopy. The stereochem. of the complexes was deduced from the spectroscopic data. The structures of [Pd2Me2(m-X)2(AsiPr3)2] (X = Cl or Pz) were established by single crystal x-ray diffraction analyses. Both of the complexes have sym-trans configuration. Strong trans influence of the Me group is reflected on the Pd-X bond distances. [on SciFinder(R)]
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