Lanthanide Clusters with Internal Ln: Fragmentation and the Formation of Dimers with Bridging Se2- and Se22- Ligands

Abstract

Reactions of "LnI(x)(SePh)(3-x)" (Ln = Dy, Ho) with elemental S/Se give (THF)14Ln10S6(Se2)6I6. The compounds are composed of a Ln6S6 double cubane core, with two twisted "Ln2(SeSe)3" units condensed onto opposing rectangular sides of the Ln6S6 fragment. This deposition of Ln2Se6 totally encapsulates the two central Ln's with chalcogen atoms (four S and four Se atoms), excluding neutral THF donors or iodides from the two primary coordination spheres. Reactions of Ln(10) clusters with a stronger Lewis base result in fragmentation and, in the case of Ln = Er, the isolation of (py)6Er2(Se2)(S0.8Se0.2)I2, with two Ln(III) ions spanned by E2- and (EE)2- ligands. The related homochalcogen dimers (py)6Ln2(Se2)(Se)Br2 (Ln = Ho, Yb) were prepared to establish that such molecules could be prepared rationally, and to confirm the isolability of E2- ligands coordinated to only two sterically unconstrained Ln ions.