Abstract

We present two organometallic precursor approaches leading to the hitherto-unknown dioxo monocarbodiimides (Ln(2)O(2)CN(2)) of the late lanthanides Ho, Er, and Yb as well as yttrium. One involves insertion of CO(2), and the other one is a straightforward route using a molecular single-source precursor. To this end the reactivity of the activated amido lanthanide compound [(Cp(2)ErNH(2))(2)] towards carbon dioxide absorption under supercritical conditions was studied. Selective insertion of CO(2) into the amido complex yielded the single-source precursor [Er(2)(O(2)CN(2)H(4))Cp(4)], which was characterized by vibrational spectroscopy and thermal and elemental analyses. Ammonolysis of this amorphous compound at 700 degrees C affords Er(2)O(2)CN(2). To gain deeper insight into the structural characteristics of the amorphous precursor, a similar molecular carbamato complex was synthesized and fully characterized. X-ray structure analysis of the dimeric complex [Cp(4)Ho(2){mu-eta(1):eta(2)-OC(OtBu)NH}] shows an unusual bonding mode of the tert-butylcarbamate ligand, which acts as both a bridging and side-on chelating group. Ammonolysis of this compound also yielded dioxo monocarbodiimides, and therefore the crystalline carbamato complex turned out to be an alternative precursor for the straightforward synthesis of Ln(2)O(2)CN(2). Analogously, the dioxo monocarbodiimides of Y, Ho, Er, and Yb were synthesized by this route. The crystal structures were determined from X-ray powder diffraction data and refined by the Rietveld method (Ln=Ho, Er). Further spectroscopic characterization and elemental analysis evidenced the existence of phase-pure products. The dioxo monocarbodiimides of holmium and erbium crystallize in the trigonal space group P[over]3m1. According to X-ray powder diffraction, they adopt the Ln(2)O(2)CN(2) (Ln=Ce-Gd) structure type.

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