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Reorientation of the Alkyne Moiety in Fe3(CO)9(RC2R) Clusters Induced by a Two-Electron Electrochemical Reduction

  • Domenico Osella
  • , Roberto Gobetto
  • , Paolo Montangero
  • , Piero Zanello
  • , Arnaldo Cinquantini

Research output: Contribution to journalArticlepeer-review

Abstract

The redox chemistry of alkyne-trimetal clusters has been investigated by electrochemical and spectroscopic techniques. The closo-Fe3(CO)9(RC2R) series undergoes two near reversible one-electron reduction steps. The bulk of spectroscopic data of the electrolytically generated [Fe3(CO)9(EtC2Et)]2 dianion strongly suggests that the orientation of the alkyne moiety relative to the metallic triangle is changed from perpendicular to parallel. On the contrary the cathodic reduction of the nido series FeCo2(CO)9(EtC2Et), Os3(CO)10(EtC2Et), and H2M3(CO)9(EtC2Et) (M = Ru, Os) is totally irreversible and is associated to cluster breakdown.

Original languageEnglish
Pages (from-to)1247-1253
Number of pages7
JournalOrganometallics
Volume5
Issue number6
DOIs
Publication statusPublished - 1 Jun 1986
Externally publishedYes

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