Chelating Lewis acids with a geminal arrangement of two acceptor functions have been shown to coordinate halide, thiolate, or benzoate anions. The remarkable efficacy of the chelating coordination of hydride ions by two aluminum atoms by the formation of persistent carbocations through C-H bond activation is also known. However, often the acceptor atoms occupy geminal positions at a bridging carbon atom, which results in relatively strained four-membered heterocycles upon coordination of single-atom donors.
Therefore, a team of scientists led by Werner Uhl of the University of Münster (Germany) were very much interested in synthesizing compounds that have larger spacers between the acceptor functions in order to obtain more flexible backbones and hence better coordinating properties. The twofold hydroalumination of silicon-centered dialkynes was employed as a facile route for the preparation of such compounds, as reported in the European Journal of Inorganic Chemistry.
During the double hydroalumination of dialkynylsilanes, mixed alkenyl–alkynyl compounds resulting from the reduction of only one C?C triple bond were obtained as intermediates, two of which were isolated and characterized. Hydroalumination of the remaining C?C triple bond yielded dialkenyl species that were ideally preorganized to be applied as chelating Lewis acids, which was demonstrated by the chelation of chloride ions. In addition, an alkenyl–alkynylsilane intermediate gave a silacyclobutene derivative by 1,1-carbalumination; this is the second time such a reaction has been observed. The mechanism of this reaction was investigated by quantum chemical calculations.
This study reports an easy way to synthesize chelating Lewis acids with two geminal acceptor aluminum atoms. The chelating coordination of chloride ions by both aluminum atoms to give a six-membered ClAl2C2Si heterocycle was demonstrated.
More information: Werner Uhl, Hydroalumination of Bis(alkynyl)silanes: Generation of Chelating Lewis Acids, Their Application in the Coordination of Chloride Ions and a 1,1-Carbalumination Reaction, European Journal of Inorganic Chemistry, http://dx.doi.org/ … ic.201100890
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