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Tris(dimethylamino)silylium ion: structure and reactivity of a dimeric silaguanidinium
Nina Kramer1, Hubert Wadepohl, Lutz Greb
1Anorganisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 275, 69120 Heidelberg, Germany. greb@uni-heidelberg.de.
Abstract:
Although several strategies for the stabilization of silylium ions have been established, "π-stabilization" with directly attached π-donor heteroatoms at silicon has not been developed yet. Hydride abstraction from (Me2N)3SiH generates dicationic [(Me2N)3Si+]2 in solution and in the solid state - constituting the dimer of an elusive silaguanidinium ion. This compound can be synthesized on a gram scale and is compatible with common organic solvents. However, it readily undergoes spontaneous electrophilic silylation of electron-rich aromatic compounds or initiates a catalytic hydro-defluorination reaction.
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