Diverse Reactions of Formazanate/Formazan with Tetrylenes: Reduction, C-H Bond Activation, Substitution and Addition
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Updated: Jul 21, 2025
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Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions
Published on: July 17, 2020
Da Jin1, Xiaofei Sun1, Vanitha R Naina1
1Institute of Inorganic Chemistry, Karlsruhe Institute of Technology (KIT), Engesserstraße 15, 76131, Karlsruhe, Germany.
Abstract:
The reactivity of the formazanate potassium salt [LtBu K(thf)] (LtBu= PhNNC(4-t BuPh)NNPh) with the group 14 chlorotetrylenes [{PhC(t BuN)2 }ECl] (E=Si, Ge, Sn) was investigated. Three corresponding compounds with unique configurations were formed, demonstrating the diverse reactivity of the system. In addition to the anticipated salt metathesis reactions of the potassium salt with the chlorine function of tetrylenes, unexpected reduction/insertion steps into the N=N bond of the formazanate (Si, Ge) and subsequent C-H activation (Ge) were also observed. Furthermore, when the neutral formazan ligand [LtBu H] was exposed to silylenes [{PhC(t BuN)2 }SiCl] and [LPh SiNMePy], substitution and addition reactions occurred. These discoveries significantly enrich the diversity of formazanate/formazan redox chemistry, opening up new avenues for exploration in this field.
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