The electronic spectra of the octahedral
TeCl62- and TeBr62-
complexes are reported and assigned. The s → p transition a1gσ*
→ T1uσ* gives rise to three spin-allowed bands in TeCl62-
(32,880; 34,480; 35,680 cm-1) and TeBr62-
(28,470; 29,730; 30,850 cm-1).
These data are taken as evidence that the excited singlet states are
distorted to lower symmetry, probably C2v. The lowest
allowed halide →
Te(IV) charge transfer transitions are at 44,170 cm-1 and
somewhat higher than 52,000 cm-1 in
TeCl62- ;
analogous transitions appear at 37,000 and 42,600 cm-1 in
TeBr62-. The observed spectral data indicate that
the “inert” 5s2 Te(IV) electrons, which reside in the a1gσ*
level, are partially delocalized to the halide
ligands.