Rhenium(VII) oxide
Rhenium(VII) oxide is the inorganic compound with the formula Re2O7. This yellowish solid is the anhydride of HOReO3. Perrhenic acid, Re2O7·2H2O, is closely related to Re2O7. Re2O7 is the raw material for all rhenium compounds, being the volatile fraction obtained upon roasting the host ore.[1]
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Names | |
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Other names
Rhenium heptoxide | |
Identifiers | |
3D model (JSmol) |
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ECHA InfoCard | 100.013.857 ![]() |
PubChem CID |
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CompTox Dashboard (EPA) |
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Properties | |
Re2O7 | |
Molar mass | 484.40298 g/mol |
Appearance | yellow crystalline powder |
Density | 6.103 g/cm3, solid |
Melting point | 360 °C (680 °F; 633 K) |
Boiling point | sublimes |
Hazards | |
EU classification (DSD) (outdated) |
not listed |
Related compounds | |
Related compounds |
Manganese(VII) oxide; technetium(VII) oxide; perrhenic acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Structure
Solid Re2O7 consists of alternating octahedral and tetrahedral Re centres. Upon heating, the polymer cracks to give molecular (nonpolymeric) Re2O7. This molecular species closely resembles manganese heptoxide, consisting of a pair of ReO4 tetrahedra that share a vertex, i.e., O3Re-O-ReO3.[2]
Synthesis and reactions
Rhenium(VII) oxide is formed when metallic rhenium or its oxides or sulfides are oxidized at 500-700 °C in air.[3]
Re2O7 dissolves in water to give perrhenic acid. It is a precursor to methylrhenium trioxide ("MTO"), a catalyst for oxidations.[4]
Uses
Hydrogenation catalyst
Rhenium(VII) oxide finds some use in organic synthesis as a catalyst for ethenolysis,[5] carbonyl reduction and amide reduction.[6]
References
- Hans Georg Nadler "Rhenium and Rhenium Compounds" Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2000. doi:10.1002/14356007.a23_199
- Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.
- Schmidt, Max; Schmidbaur, Hubert (1967). "Trimethylsilyl Perrhenate". Inorganic Syntheses. 9: 149–151. doi:10.1002/9780470132401.ch40. ISBN 9780470132401.
- W. A. Herrmann and F. E. Kuhn (1997). "Organorhenium Oxides". Acc. Chem. Res. 30 (4): 169–180. doi:10.1021/ar9601398.
- Lionel Delaude, Alfred F. Noels. "Metathesis". Kirk-Othmer Encyclopedia of Chemical Technology. Wiley.CS1 maint: uses authors parameter (link)
- Nishimura, Shigeo (2001). Handbook of Heterogeneous Catalytic Hydrogenation for Organic Synthesis (1st ed.). New York: Wiley-Interscience. pp. 42–43, 182, 389–390, & 408. ISBN 9780471396987.