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Methylrhenium trioxide

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(Redirected from Methyltrioxorhenium)
Methylrhenium trioxide
Names
IUPAC name
Methyl(trioxo)rhenium(VII)
Other names
Methyltrioxorhenium(VII)
Identifiers
3D model (JSmol)
Abbreviations MTO
ChemSpider
ECHA InfoCard 100.202.821 Edit this at Wikidata
UNII
  • InChI=1S/CH3.3O.Re/h1H3;;;; ☒N
    Key: PQTLALPZRPFYIT-UHFFFAOYSA-N ☒N
  • InChI=1/CH3.3O.Re/h1H3;;;;/rCH3O3Re/c1-5(2,3)4/h1H3
    Key: PQTLALPZRPFYIT-YHFCCQKIAF
  • C[Re](=O)(=O)=O
Properties
CH3ReO3
Molar mass 249.239 g·mol−1
Appearance white powder
Melting point 112 °C (234 °F; 385 K)
highly soluble in water
Hazards
GHS labelling:
GHS03: OxidizingGHS07: Exclamation mark
Warning
H272, H315, H319, H335, H413
P210, P220, P221, P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P370+P378, P403+P233, P405, P501
Safety data sheet (SDS) External MSDS
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Methylrhenium trioxide, also known as methyltrioxorhenium(VII), is an organometallic compound with the formula CH3−ReO3. It is a volatile, colourless solid that has been used as a catalyst in some laboratory experiments. In this compound, rhenium has a tetrahedral coordination geometry with one methyl and three oxo ligands. The oxidation state of rhenium is +7.

Synthesis

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Methylrhenium trioxide is commercially available. It can be prepared by many routes, a typical method is the reaction of rhenium heptoxide and tetramethyltin:[1]

Re2O7 + (CH3)4Sn → CH3ReO3 + (CH3)3Sn−O−ReO3

Analogous alkyl and aryl derivatives are known. Compounds of the type R−ReO3 are Lewis acids, forming both 1:1 and 1:2 adducts with halides and amines.

Uses

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Methylrhenium trioxide serves as a heterogeneous catalyst for a variety of transformations. Supported on alumina/silica, it catalyzes olefin metathesis at 25 °C.

In solution, methylrhenium trioxide catalyses for the oxidations with hydrogen peroxide. Terminal alkynes yield the corresponding carboxylic acid or ester, internal alkynes yield diketones, and alkenes give epoxides. Methylrhenium trioxide also catalyses the conversion of aldehydes and diazoalkanes into an alkene,[2] and the oxidation of amines to N-oxides with sodium percarbonate.[3]

References

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  1. ^ Herrmann, W. A.; Kratzer R. M.; Fischer R. W. (1997). "Alkylrhenium Oxides from Perrhenates: A New, Economical Access to Organometallic Oxide Catalysts". Angew. Chem. Int. Ed. Engl. 36 (23): 2652–2654. doi:10.1002/anie.199726521.
  2. ^ Hudson, Andrew; Betz, Daniel; Kühn, Fritz E.; Jiménez-Alemán, Guillermo H.; Boland, Wilhelm (2013-09-16). "Methyltrioxorhenium". Encyclopedia of Reagents for Organic Synthesis. John Wiley & Sons, Ltd. doi:10.1002/047084289x.rn00017.pub3. ISBN 978-0-471-93623-7.
  3. ^ Jain, Suman L.; Joseph, Jomy K.; Sain, Bir (2006). "Rhenium-Catalyzed Highly Efficient Oxidations of Tertiary Nitrogen Compounds to N-Oxides Using Sodium Percarbonate as Oxygen Source". Synlett: 2661–2663. doi:10.1055/s-2006-951487.