Abstract
Niobium(V) and tantalum(V) amides [(η5-C5H4)-Si(CH3)2-NR]M[N(CH3)2]3 (R = C6H5) containing chelate-type C, N-Ligands are available in 45% (M = Nb) and 60% (M = Ta) isolated yield, respectively, from the homoleptic amides M[N(CH3)2]5 and the N-functionalized cyclopentadiene C5H5-Si(CH3)2-NHR by double amine elimination. The niobium and tantalum derivatives undergo an unprecedented photo-induced rearrangement at room temperature, yielding the imido complexes [(η5-C5H4)-Si(CH3)2-N(CH3)2]M( = NR)[N(CH3)2]2 as a result of Si-N bond cleavage.
| Original language | English |
|---|---|
| Pages (from-to) | 357-361 |
| Number of pages | 5 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 506 |
| Issue number | 1-2 |
| DOIs | |
| State | Published - 1996 |
Keywords
- Amide
- Amino-functionalized cyclopentadienyl
- Niobium
- Rearrangement
- Si-N Bond cleavage
- Tantalum
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