Heterometallic Lanthanide Group 12 Metal Iodides

Neodymium tri-iodide reacts with Group 12 metal (M; M = Zn, Cd, Hg) iodides to form heterometallic compounds.
These Lewis acidic M cleave Nd−I bonds to give either ionic {[(THF)5NdI2][MI3THF]; M = Zn, Cd} or charge-neutral {(THF)5NdI(μ2I)HgI3} compounds. Differences in structure are interpreted primarily in terms of M−L bond
strengths, rather than Nd−L bond strengths. Experiments with Yb indicate that if there is any excess iodide present
in these syntheses then the most readily isolated product is a triiodide salt, i.e., [(THF)5YbI2][I3]. In conventional
solvents the presence of Lewis acid is not required for iodide displacementfrom pyridine, “YbI3” crystallizes as
[(py)5YbI2][I]. These compounds are potentially useful as heterometallic sources of lanthanide-doped iodide matrixes,
they illustrate the ease with which iodides are displaced from lanthanide coordination spheres, and they underscore
the complexity associated with using lanthanide iodides as Lewis acid catalysts.