Abstract
The new chiral arylplatinum(II) compounds [2,6-bis(1-(dimethylamino)ethyl)phenyl]chloroplatinum(II) (4) and (-)-[(1R,1′R)-bis(1-(dimethylamino)propyl)phenyl]chloroplatinum(II) (5) have been synthesized. The transmetallation of the corresponding aryllithium compounds does not affect either stereogenic centres of the organic ligand while the rate of the transmetallation is shown to be influenced by the size of the benzylic substituents. The X-ray crystal structure of 5 is reported from which the absolute configuration of both stereogenic centres of the organic ligand was determined to be (R).
| Original language | English |
|---|---|
| Pages (from-to) | 1-7 |
| Number of pages | 7 |
| Journal | Journal of Organometallic Chemistry |
| Volume | 551 |
| Issue number | 1-2 |
| Publication status | Published - 30 Jan 1998 |
Keywords
- (-)-[(1R,1′R)-bis(1-(dimethylamino)propyl)phenyl]chloroplatinum(II)
- Arylplatinum(II)
- Chiral monoanionic aryldiamine ligands
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