Further Exploring the “Sting of the Scorpion”: Hydride Migration and Subsequent Rearrangement of Norbornadiene to Nortricyclyl on Rhodium(I)
A new boron-based flexible scorpionate ligand based upon 7-azaindole, Li[Ph(H)B(azaindolyl)2] (Li[ Ph Bai]), has been prepared. This ligand, together with the previously reported ligand K[HB(azaindolyl)3] (K[Tai]), have been used to prepare a range of monovalent group 9 transition-metal complexes. T...
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Published in: | Organometallics 2009-09, Vol.28 (17), p.5222-5232 |
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Main Authors: | , , , , |
Format: | Article |
Language: | eng |
Online Access: | Get full text |
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Summary: | A new boron-based flexible scorpionate ligand based upon 7-azaindole, Li[Ph(H)B(azaindolyl)2] (Li[ Ph Bai]), has been prepared. This ligand, together with the previously reported ligand K[HB(azaindolyl)3] (K[Tai]), have been used to prepare a range of monovalent group 9 transition-metal complexes. The complexes [M(COD){κ3 N,N,H-Ph(H)B(azaindolyl)2}] (where M = rhodium, iridium and COD = 1,5-cyclooctadiene) and [Rh(NBD){κ3 N,N,H-HB(R)(azaindolyl)2}] (where NBD = 2,5-norbornadiene and R = Ph, azaindolyl) have been prepared. Structural characterization of [M(COD){κ3 NNH-Ph(H)B(azaindolyl)2}] (where M = rhodium, iridium) and [Rh(NBD){κ3 N,N,H-HB(azaindolyl)3}] reveal strong interactions of the B−H functional group with the metal centers, particularly in the case of [Ir(COD){κ3 N,N,H-Ph(H)B(azaindolyl)2}]. The complex [Rh(NBD){κ3 N,N,H-HB(azaindolyl)3}] undergoes a further reaction, resulting from hydride migration from boron to the norbornadiene group. Subsequent rearrangement results in the formation of the rhodium−nortricyclyl complex [Rh(nortricyclyl){κ4 N,N,B,N-B(azaindolyl)3}], providing the first nitrogen-based metallaboratrane complex to contain the tetradentate (κ4 N,N,B,N) coordination mode. |
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ISSN: | 0276-7333 1520-6041 |