(Cyclopentadienyl)trioxorhenium(VII) - No match for methyltrioxorhenium (MTO)

Manuel Högerl, Fritz E. Kühn

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

Together with a further improvement of the synthesis of (cyclopentadienyl)trioxorhenium(VII), CpReO3, its reaction chemistry and catalytic activity is also revisited in greater detail. However, in spite of the high catalytic activity of the homologous methyltrioxorhenium(VII) (MTO) and the related CpMo(O2)X, (X = R, Hal, etc.) it is seen that CpReO3 suffers greatly from the lability of the Cp-Re bond under oxidative conditions and in the presence of electron donor ligands. (Cyclopentadienyl)trioxo-rhenium(VII) although accessible very conveniently, neither matches the rich reaction chemistry of its pentamethylcyclopentadienyl derivative, Cp*ReO3 nor the catalytic versatility of MTO.

Original languageEnglish
Pages (from-to)1444-1447
Number of pages4
JournalZeitschrift fur Anorganische und Allgemeine Chemie
Volume634
Issue number8
DOIs
StatePublished - Jul 2008

Keywords

  • Cyclopentadiene
  • Homogeneous catalysis
  • Lewis-bases
  • Methyltrioxorhenium
  • Organometallics

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