Chemical and Electrochemical Oxidation of Diferrocenyltelluride
Abstract The halogenation of diferrocenyltelluride, Fc 2 Te, with XeF 2 , PhICl 2 and I 2 afforded the diferrocenyltellurium dihalides Fc 2 TeX 2 (X=F, Cl, I). Halide exchange of Fc 2 TeCl 2 with KBr yielded Fc 2 TeBr 2 . The oxidation of Fc 2 Te with NO[SbF 6 ] and K[B(C 6 F 5 ) 4 ] provided the triferrocenyltelluronium salt [Fc 3 Te][B(C 6 F 5 ) 4 ] and the dinuclear nitrosyl iron complex Fe 2 (μ‐TeFc) 2 (NO) 4 . The new compounds were comprehensively characterized by multinuclear NMR spectroscopy ( 125 Te, 19 F, 13 C, 1 H), UV/vis absorption spectroscopy, cyclic voltammetry, LIFDI‐TOF mass spectrometry and single crystal X‐ray diffraction.
Authors
- Jens Beckmann (ORCID: https://orcid.org/0000-0002-8548-1821)
- Corina Stoian (ORCID: https://orcid.org/0000-0002-9795-4702)
- Mathias H. Linden
- Pim Puylaert (ORCID: https://orcid.org/0000-0003-3397-2677)
- Harto Lindén
- Nils Schmidt
Institutions
- University of Bremen (DE)
- Sachtleben Bergbau (Germany) (DE)
Publication Details
- Journal
- European Journal of Inorganic Chemistry
- Published
- 2025-01-10
- DOI
- https://doi.org/10.1002/ejic.202400709
- Primary Topic
- Organoselenium and organotellurium chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Deutsche Forschungsgemeinschaft
- Universität Bremen