Mechanistic Study of the Solvent-Induced Fragmentation of Cp3Co3(CO)2

Craig E. Barnes, Jeffery A. Orvis

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

The cluster complex Cp3Co3(CO)2 (1) undergoes a unique, solvent-induced, two-step fragmentation reaction to give the di- and tetranuclear complexes Cp2-Co2(CO)2 (2) and Cp4Co4(CO)2 (3). The mechanism of this reaction is shown to involve initial, reversible attack of solvent (benzene or THF) on 1, causing fragmentation to 2 and a solvated, mononuclear intermediate, CpCo-(sol)n. This intermediate subsequently reacts with a second molecule of 1 to form 3. The mononuclear species shows a surprising selectivity in its reactions with trapping agents depending upon the nature of the coordinated solvent.

Original languageEnglish
Pages (from-to)1016-1017
Number of pages2
JournalOrganometallics
Volume12
Issue number4
DOIs
StatePublished - 1993

Scopus Subject Areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry
  • Inorganic Chemistry

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