Article Dans Une Revue Organometallics Année : 2020

Synthesis of Norbornene-Based Phosphine-Stabilized Silylium Ions Behaving as Masked Frustrated Lewis Pairs

Résumé

A novel architecture of phosphine-stabilized silylium ions is described. The peculiar moderate flexible framework allows an efficient donation of the phosphine group toward the electron deficient silicon center thus providing a very good stabilization of the corresponding silylium ions. The P-Si interaction was studied in solution and in the solid state by NMR spectroscopy and X-ray diffraction analysis, respectively. The reactivity of silylium ions is easily improved using less donating phosphine ligands. Of particular interest, thanks to the flexible ligand framework, phosphine-stabilized silylium ion 5f behaves as a frustrated Lewis pair instead of a simple Lewis acid and exhibits an original ambiphilic reactivity with carbonyl derivatives that allows the synthesis of seven-to nine-membered ring heterocycles.

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hal-03408869 , version 1 (29-10-2021)

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Aymeric Dajnak, Eddy Maerten, Nathalie Saffon-Merceron, Antoine Baceiredo, Tsuyoshi Kato. Synthesis of Norbornene-Based Phosphine-Stabilized Silylium Ions Behaving as Masked Frustrated Lewis Pairs. Organometallics, 2020, 39 (18), pp.3403-3412. ⟨10.1021/acs.organomet.0c00489⟩. ⟨hal-03408869⟩
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