期刊
CHEMICAL SCIENCE
卷 13, 期 33, 页码 9693-9700出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d2sc02783f
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资金
- Deutsche Forschungsgemeinscha
- Alexander von Humboldt Foundation
This study reports the reduction of bulky ferrocenyl-based NHC-stabilised aluminium(iii) diiodide in different hydrocarbon solvents, with different outcomes observed in hexane and aromatic solvents. Reduction in hexane led to C-H activation, while reduction in aromatic solvents resulted in unknown Birch-type reductions of solvent molecules.
We report the reduction of bulky ferrocenyl-based NHC-stabilised aluminium(iii) diiodide [Fc*(NHC)AlI2] (Fc* = 2,5-bis(3,5-di-tert-butylphenyl)-1-ferrocenyl) in different hydrocarbon solvents (hexane, benzene, toluene, and p-xylene), which results in different outcomes. Reduction in hexane with an equivalent amount of KC8 generates the diiododialane [(Fc*(NHC)AlI)(2)], whereas complete reduction in hexane leads to an unusual C-H activation at an N-Me group of one NHC unit. In contrast, reaction in aromatic solvents result in hitherto unknown Birch-type reductions of the corresponding solvent molecules by transient aluminium radicals of the type [LAlR2], which is ultimately bound to two aluminium centers.
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