Abstract
The reaction of the hetero-ring anion [C2But2P2Sb]- with [{M(η4-1,5-C8H12)Cl}2], M = Rh, Ir, leads to the formation of [M(η5-C2But2P2Sb)(η4-1,5-C8H12)], M = Rh 7, Ir 8. Treatment of CoCl2 with either an equimolar mixture of [C2But2P2Sb]- and [C5Me5]-, or two equivalents of [C2But2P2Sb]- affords the compounds [Co(η5-C5Me5)(η4-C2But2HP2Sb)], 11, and [Co(η5-C2But2P2Sb)(η4-C2But2HP2Sb)], 12, which represent the first examples of diphosphastibacyclopentadiene complexes; the X-ray crystal structures of 7 and 11 are reported.
| Original language | English |
|---|---|
| Pages (from-to) | 89-94 |
| Number of pages | 6 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 534 |
| Issue number | 1-2 |
| DOIs | |
| Publication status | Published - 28 Apr 1997 |
| Externally published | Yes |
Keywords
- Antimony
- Diphosphastibacyclopentadiene
- Diphosphastibolyl
- Low coordination
- Phosphorus
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