Complexes of lanthanoids with neutral π donor ligands

The synthesis, structures and reactions of lanthanoid complexes with alkenes, alkynes and arenes have been reviewed. Whilst the discussion is centred on neutral π donors, including intramolecular π-arene-lanthanoid bonding, some formal [Sm III (C 5 Me 5 ) 2 (π-donor) − ] complexes, derived from Sm(C 5 Me 5 ) 2 and neutral π donors, have been included, especially examples which readily dissociate into the reactants. Metal-carbon bond lenghts for lanthanoid(II or III) complexes have been convenientljy analysed and compared by subtraction of the appropriate lanthanoid ionic radius for the formal coordination number. Derived values in the approximate range 1.70–2.10 A are typical, with higher values often associated with intramolecular π-areneLn coordination or dimerization through intermolecular π-areneLn bonding. Lower values, 1.40–1.70 A, can carry implications of charge transfer, e.g. Ln II L 0 → Ln III (L) −1 or may be partly a geometric consequence of other bonding in the molecule. The significantly covalent arene-lanthanoid(0) complexes have stronger bonding than in Ln(II or III)-(π donor) derivatives and occupy a unique place in organolanthanoid chemistry.