Abstract
Competing steric pressures within the coordination sphere of 2-(2′-X-naphth-1′-yl)-3,4-dimethyl-5-phenyl-η5- phospholyl(pentamethylcyclopentadienyl)ruthenium(II) complexes (X = OMe (1), OH (3), OTf (4), PPh2(O) (5), PPh2 (6)) give rise to a well-defined and predictable axial chirality about the phospharuthenocene- naphthyl bond. Crystal structure analysis of the platinum complex cis-[Pt(6)Cl2] (7) shows a very different geometry from that found in cis-[Pt(1)(PEt3)Cl2] (2) because of the leverage exerted on the Pt coordination sphere by the (2′-PPh2-naphth-1′- yl) functionality.
| Original language | English |
|---|---|
| Pages (from-to) | 2964-2970 |
| Number of pages | 7 |
| Journal | Organometallics |
| Volume | 26 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 4 Jun 2007 |
| Externally published | Yes |
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