| Autor: |
Jach F; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de.; Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062 Dresden, Germany., Block T; Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstraße 30, 48149 Münster, Germany., Prots Y; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de., Schmidt M; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de., Bobnar M; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de., Pöttgen R; Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstraße 30, 48149 Münster, Germany., Ruck M; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de.; Faculty of Chemistry and Food Chemistry, Technische Universität Dresden, 01062 Dresden, Germany., Höhn P; Max-Planck-Institute for Chemical Physics of Solids, Nöthnitzer Straße 40, 01187 Dresden, Germany. Franziska.Jach@tu-dresden.de. |
| Abstrakt: |
While a negative oxidation state occurs rarely for metals in general, this is commonly known for metal carbonyl anions, i.e. carbonyl metalates. Although CO and CN - are isoelectronic, cyanidometalates usually do not exhibit metal centers with negative oxidation states. However, we report on the electron-rich tetrahedral tetracyanidoferrate(-II) anion [Fe(CN) 4 ] 6- , which was stabilized in (Sr 3 N) 2 [Fe(CN) 4 ] (space group R 3 c , a = 702.12(2) pm, c = 4155.5(2) pm). Microcrystalline powders were synthesized by a solid-state route, single crystals were obtained from Na metal flux. In comparison to classical cyanidometalates, C-N distances are longer and stretching frequencies are lower as indicated by X-ray diffraction, IR and Raman spectroscopy. Weak C-N, strong Fe-C bonds as well as the anion geometry resemble the isoelectronic tetrahedral carbonyl ferrate [Fe(CO) 4 ] 2- . 57 Fe Mössbauer spectroscopic measurements reveal a negative isomer shift in agreement with substantially delocalized d electrons due to strong π back-bonding. These results point to a very similar bonding situation of both 18 e tetracyanido and tetracarbonyl ferrates including non-innocent redox-active ligands and a d 10 closed shell configuration on iron. Hereby, new tetracyanidoferrate(-II) provides a missing link for a more in-depth understanding of the chemical bonding trends of highly-reduced cyanidometalates in the quest for even higher reduced transition metals in this exceptional class of compounds. |
