Abstract
The eta (2)(3e)-vinyl complex [Mo{=C(Ph)CHPh}{P(OMe)(3)}(2)Cp] is oxidized by [FeCp2](+), [CPh3](+), or B(C6F5)(3) to form the 17-electron. cation [Mo{=C(Ph)CHPh}{P(OMe)(3))(2)Cp](+) which on warming loses H to form the cationic eta (2)(4e)-alkyne complex [Mo(eta (2)-PhC CPh){P(OMe)(3))(2)Cp](+). In the case of the borane there is evidence for a competing reaction between the eta (2)-vinyl complex and the acid (H2O)B(C6F5)(3), a resulting in the formation of a labile trans-stilbene complex.
Original language | English |
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Pages (from-to) | 231-233 |
Number of pages | 3 |
Journal | Organometallics |
Volume | 20 |
Issue number | 2 |
Publication status | Published - 22 Jan 2001 |
Keywords
- RHENIUM ALKYNE COMPLEXES
- ETA-2-VINYL COMPLEXES
- COORDINATED LIGANDS
- INSERTION REACTIONS
- MOLECULAR-STRUCTURE
- CRYSTAL-STRUCTURES
- BOND-CLEAVAGE
- TUNGSTEN
- REACTIVITY
- METALLACYCLOPROPENE