4 years ago

Silyl Chalconium Ions: Synthesis, Structure and Application in Hydrodefluorination Reactions

Silyl Chalconium Ions: Synthesis, Structure and Application in Hydrodefluorination Reactions
Thorben Sieling, Natalie Kordts, Marc Schmidtmann, Saskia Rathjen, Sandra Künzler, Henning Großekappenberg, Thomas Müller
Silylated chalconium ions based on peri-naphthalene and acenaphthene scaffolds are synthesized and introduced as versatile amphiphilic reagents. The investigation of their spectroscopic, structural and bonding properties revealed that their silyl Lewis acidity is controlled by the nature of the chalcogen donor and by the carbon backbone. This opens the perspective for an effective fine tuning and control of their reactivity. Their use as amphiphilic CATalyst was exemplarily demonstrated in hydrodefluorination reactions. More information can be found in the Full Paper by T. Müller et al. (DOI: 10.1002/chem.201700995).

Publisher URL: http://onlinelibrary.wiley.com/resolve/doi

DOI: 10.1002/chem.201702049

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