期刊
ORGANOMETALLICS
卷 30, 期 6, 页码 1334-1339出版社
AMER CHEMICAL SOC
DOI: 10.1021/om100712a
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资金
- EPSRC [EP/E032575/1]
A series of low-coordinate tin and lead cationic complexes have been synthesized using the bulky beta-diketiminate ligand [{N(2,6-'Pr2C6H3)C(Me)}(2)CH](-) (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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