Lewis Acid-Mediated One-Electron Reduction of Nitrous Oxide.

Abstract

The one-electron reduction of nitrous oxide (N2 O) was achieved using strong Lewis acids E(C6 F5 )3 (E=B or Al) in combination with metallocenes. In the case of B(C6 F5 )3 , electron transfer to N2 O required a powerful reducing agent such as Cp*2 Co (Cp*=pentamethylcyclopentadienyl). In the presence of Al(C6 F5 )3 , on the other hand, the reactions could be performed with weaker reducing agents such as Cp*2 Fe or Cp2 Fe (Cp=cyclopentadienyl). The Lewis acid-mediated electron transfer from the metallocene to N2 O resulted in cleavage of the N-O bond, generating N2 and the oxyl radical anion [OE(C6 F5 )3 ]⋅- . The latter is highly reactive and engages in C-H activation reactions. It was possible to trap the radical by addition of the Gomberg dimer, which acts as a source of the trityl radical.