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 language | English |
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Pages (from-to) | 1016-1017 |
Number of pages | 2 |
Journal | Organometallics |
Volume | 12 |
Issue number | 4 |
DOIs | |
State | Published - 1993 |
Scopus Subject Areas
- Physical and Theoretical Chemistry
- Organic Chemistry
- Inorganic Chemistry