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Reactivity of Diarylnitrenium Ions.

Agnes KüttGunnar JeschkeLauri ToomJaak NerutChristopher A Reed
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
Hydride abstraction from diarylamines with the trityl ion is explored in an attempt to generate a stable diarylnitrenium ion, Ar2 N+ . Sequential H-atom abstraction reactions ensue. The first H-atom abstraction leads to intensely colored aminium radical cations, Ar2 NH.+ , some of which are quite stable. However, most undergo a second H-atom abstraction leading to ammonium ions, Ar2 NH2 + . In the absence of a ready source of H-atoms, a unique self-abstraction reaction occurs when Ar=Me5 C6 , leading to a novel iminium radical cation, Ar=N.+ Ar, which decays via a second self H-atom abstraction reaction to give a stable iminium ion, Ar=N+ HAr. These products differ substantially from those derived via photochemically produced diarylnitrenium ions.
Keyphrases
  • molecular dynamics
  • electron transfer
  • ionic liquid
  • room temperature
  • perovskite solar cells