Abstract
The reactions of (Cl)Rh(PR 3) 3 (R = Me, Et) with the anionic thiapentadienide reagent lithium 2,3-dimethyl-5-thiapentadienide have been investigated. In each case, the kinetic product exhibits a thiapentadienyl bonding mode in which the sulfur atom is σ-bonded to rhodium; however, ligand rearrangement yields thermodynamic isomers in which the carbon end of the thiapentadienyl chain is σ-bonded to rhodium.
| Original language | English |
|---|---|
| Pages (from-to) | 805-808 |
| Number of pages | 4 |
| Journal | Organometallics |
| Volume | 24 |
| Issue number | 5 |
| DOIs | |
| State | Published - Feb 28 2005 |
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