Abstract

The heterovalent (2 Ln2+, 2 Ln3+) tetranuclear (DME)4Ln4Se(SePh)8 clusters (Ln = Sm, Yb, Nd(III)/Yb(II), Sm(III)/Yb(II); DME = dimethoxyethane) can be prepared either by the reduction of Se−C bonds with Ln or by the reaction of Ln(SePh)2 with elemental Se in DME. The Sm(II) compound is difficult to isolate because it slowly redissolves after precipitation. The Yb4 compound and Nd2Yb2 compounds are considerably more stable, and can be isolated in higher yield. For the Ln = Sm4, Yb4, Sm2Yb2, and Nd2Yb2 clusters, low-temperature structural characterization reveals a square array of four metal ions with a crystallographically imposed disorder that renders the Ln(II) and Ln(III) sites indistinguishable; the Nd2Yb2 compound also crystallizes in a lattice-solvated unit cell in which there are distinct Ln(II)/Ln(III) metal ions. Connecting the four metals in all structures is a selenido ligand that caps the square array of Ln ions, and pairs of SePh ligands that bridge each of the four edges, with a chelating DME...

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.