Abstract
The tetranuclear acetylide compounds Cp*WOs3(CO)11(CCR) (R = Ph, Bu, CH2OMe), depending on the substituents of the acetylide ligand, undergo reversible C–C bond scission and C–H activation to afford the carbido–alkylidyne cluster Cp*WOs3(CO)10(μ4-C)(μ-CPh) and the carbido–vinylidene clusters Cp*WOs3(CO)9(μ4-C)(μ-H)(μ-CCHR′) (R′ = Pr, OMe), respectively.
| Original language | English |
|---|---|
| Pages (from-to) | 5483-5485 |
| Journal | Organometallics |
| Volume | 14 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 1 Dec 1995 |
| Externally published | Yes |
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