Abstract
A series of low-coordinate tin and lead cationic complexes have been synthesized using the bulky β-diketiminate ligand [{N(2,6-iPr2C6H3)C(Me)}2CH]− (BDI) to stabilize the metal center. Two different routes to [(BDI)Sn]+[X]− and [(BDI)Pb]+[X]− were explored (X = B(C6F5)4, AlCl4, MeB(C6F5)3): abstraction of the chloride with a Lewis acid from (BDI)SnCl and (BDI)PbCl and abstraction of a methyl group with a borane from (BDI)SnMe and (BDI)PbMe. The crystal structures of the tin and lead cations were determined; in both, solvent molecules were found to coordinate to the metal center. In the case of [(BDI)Pb]+[B(C6F5)4]−, a dichloromethane molecule was found. Density functional theory (DFT) calculations showed that this could be due to crystal packing. In the case of [(BDI)Sn]+[MeB(C6F5)3]−, an ether molecule was coordinated to the tin metal center. DFT calculations revealed a significant energy gain for the coordinated ether as opposed to the free molecules.
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