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Reactivity of FeMoO4 in CsCl Fluxes and Formation of the Salt-Inclusion Type of Compounds

Weber, Anna K. ; Panthöfer, Martin ; Möller, Angela (2022)
Reactivity of FeMoO4 in CsCl Fluxes and Formation of the Salt-Inclusion Type of Compounds.
In: Inorganic Chemistry, 61 (26)
doi: 10.1021/acs.inorgchem.2c01195
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

The reactivity of FeMoO₄ in CsCl fluxes has been investigated by thermal analysis and chemical reactions in evacuated silica ampules. The products have been characterized by ex situ X-ray diffraction methods. Metathesis reactions involving CsCl lead to the formation of Cs₂Fe₂(MoO₄)₃ and the salt adduct Cs₂FeCl₄·CsCl. A side reaction has been observed, which is associated with a decomposition of [MoO₄]²⁻ in CsCl fluxes yielding Cs₂Mo₄O₇·CsCl, which contains the rare pyromolybdate anion, [Mo₂O₇]²⁻, located in the center of a ∞₂[CsCl] hetero-honeycomb arrangement. This salt-inclusion type of compound has been studied further in terms of its formation starting from Cs₂MoO₄, MoO₃, and CsCl. The intermediate adduct phase, Cs₂MoO₄·MoO₃, contains uncharged ∞1[MoO₂O₂/₂] chains that react with CsCl at elevated temperatures to Cs₂Mo₂O₇·CsCl. Furthermore, the site preference for alkaline-metal cations (K+, Rb+, and Cs+) has been evaluated for a mixed substitution series. In accordance with the Pearson concept, the polarizability of the respect cation outweighs any size differences for the occupancy of the salt-intergrowth motif, the honeycomb part of the structure.

Typ des Eintrags: Artikel
Erschienen: 2022
Autor(en): Weber, Anna K. ; Panthöfer, Martin ; Möller, Angela
Art des Eintrags: Bibliographie
Titel: Reactivity of FeMoO4 in CsCl Fluxes and Formation of the Salt-Inclusion Type of Compounds
Sprache: Englisch
Publikationsjahr: 16 Juni 2022
Verlag: American Chemical Society
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Inorganic Chemistry
Jahrgang/Volume einer Zeitschrift: 61
(Heft-)Nummer: 26
DOI: 10.1021/acs.inorgchem.2c01195
Kurzbeschreibung (Abstract):

The reactivity of FeMoO₄ in CsCl fluxes has been investigated by thermal analysis and chemical reactions in evacuated silica ampules. The products have been characterized by ex situ X-ray diffraction methods. Metathesis reactions involving CsCl lead to the formation of Cs₂Fe₂(MoO₄)₃ and the salt adduct Cs₂FeCl₄·CsCl. A side reaction has been observed, which is associated with a decomposition of [MoO₄]²⁻ in CsCl fluxes yielding Cs₂Mo₄O₇·CsCl, which contains the rare pyromolybdate anion, [Mo₂O₇]²⁻, located in the center of a ∞₂[CsCl] hetero-honeycomb arrangement. This salt-inclusion type of compound has been studied further in terms of its formation starting from Cs₂MoO₄, MoO₃, and CsCl. The intermediate adduct phase, Cs₂MoO₄·MoO₃, contains uncharged ∞1[MoO₂O₂/₂] chains that react with CsCl at elevated temperatures to Cs₂Mo₂O₇·CsCl. Furthermore, the site preference for alkaline-metal cations (K+, Rb+, and Cs+) has been evaluated for a mixed substitution series. In accordance with the Pearson concept, the polarizability of the respect cation outweighs any size differences for the occupancy of the salt-intergrowth motif, the honeycomb part of the structure.

Fachbereich(e)/-gebiet(e): DFG-Sonderforschungsbereiche (inkl. Transregio)
DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche
07 Fachbereich Chemie
07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Anorganische Chemie
DFG-Sonderforschungsbereiche (inkl. Transregio) > Sonderforschungsbereiche > SFB 1487: Eisen, neu gedacht!
Hinterlegungsdatum: 09 Nov 2023 08:05
Letzte Änderung: 09 Nov 2023 08:05
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