Advertisement

Organometallic compounds of the transition elements. Classification of ligands and theories of bonding

  • P. Powell

Abstract

While organometallic compounds of the Main Group elements are most conveniently classified from the position of the metal in the Periodic Table, it is useful to classify d-block transition metal complexes from the organic ligands which they contain. In Table 6.1 ligands are listed according to the number of electrons which they formally contribute to the metal—ligand bonding. While there is usually no doubt as to the total number of valence electrons in a complex, confusion in counting electrons can arise if attempts are made to take into account any polarization of the metal—ligand bonds, by assigning an oxidation state to the metal, for example. A Metal—hydrogen bond can be thought of as arising from M and H+, M. or M+ and H. In all cases the same essentially covalent bond results, which contains the same number of electrons (two), independent of the final polarization M+—H or M—H+. It is therefore recommended that in counting electrons, all metal—ligand bonds are treated as covalent. Thus an M—H bond is considered as arising from a metal atom M. and the radical H., so that H. is formally a one electron donor. Metal alkyls and less conventionally metal halides are treatedsimilarly. A metal cyclopentadienyl bond M—C5H5 is also considered as arising from M . and cyclopentadienyl radical C5 5 . rather than from M+ and C5H 5 , making C5H5 formally a five electron ligand.

Keywords

Transition Element Organometallic Compound Iron Carbonyl Frontier Orbital Molecular Orbital Theory 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Albright, T.A. (1982) Acc. Chem. Research, 15, 149.CrossRefGoogle Scholar
  2. Albright, T.A. and Whangbo, M-H. (1985) Orbital Interactions in Chemistry, Wiley, Chichester.Google Scholar
  3. Green, J.C. (1981) Gas phase photoelectron spectra of dand/block organometallic compounds.Struct. Bonding, 43, 37.CrossRefGoogle Scholar
  4. Hoffmann, R. (1982) Nobel lecture. Angew. Chem. (Int. edn.), 21, 71.Google Scholar
  5. Mingos, D.M.P. (1982) Comprehensive Organometallic Chemistry, (Vol. 3, Chapter 1).Google Scholar
  6. Muetterties, E.L., Bleeke, J.R., Wucherer, E.J. and Albright, T.A. (1982) Structural, stereochemical and electronic features of arene metal complexes. Chem. Revs, 82, 499.CrossRefGoogle Scholar
  7. Stone, F.G.A. (1984) Isolobal relationships. Angew. Chem. (Int. edn.), 23, 89.CrossRefGoogle Scholar

Copyright information

© P. Powell 1988

Authors and Affiliations

  • P. Powell
    • 1
  1. 1.Royal Holloway and Bedford New CollegeUniversity of LondonEngland

Personalised recommendations