Mass spectra of Nb+ and Rh+ complexes with argon ligands exhibit 'magi
c' peaks Nb+Ar4 and Rh+Ar6, similar to observations for V+Ar4 and Co+A
r6, indicating coordinative saturation. A consistent explanation is ob
tained by assuming that the rare gas ligands seek out electron density
minima in the valence shell of the ion, which permit a closer approac
h to the metal core and a stronger charge-induced dipole bond. Ab init
io density functional calculations, which predict stable square planar
complexes for the d(4) ions and octahedral for the d(8) species, supp
ort this interpretation and show that rare gas complexes of d(4) metal
ions fit perfectly well into the coordination chemical framework base
d on the Jahn-Teller effect. (C) 1997 Elsevier Science B.V.