Excited-State N Atoms Transform Aromatic Hydrocarbons into N -Heterocycles in Low-Temperature Plasmas.

The direct formation of N -heterocycles from aromatic hydrocarbons has been observed in nitrogen-based low-temperature plasmas; the mechanism of this unusual nitrogen-fixation reaction is the topic of this paper. We used homologous aromatic compounds to study their reaction with reactive nitrogen species (RNS) in a dielectric barrier discharge ionization (DBDI) source. Toluene (C 7 H 8 ) served as a model compound to study the reaction in detail, which leads to the formation of two major products at "high" plasma voltage: a nitrogen-replacement product yielding protonated methylpyridine (C 6 H 8 N + ) and a protonated nitrogen-addition (C 7 H 8 N + ) product. We complemented those studies by a series of experiments probing the potential mechanism. Using a series of selected-ion flow tube experiments, we found that N + , N 2 + , and N 4 + react with toluene to form a small abundance of the N -addition product, while N( 4 S) reacted with toluene cations to form a fragment ion. We created a model for the RNS in the plasma using variable electron and neutral density attachment mass spectrometry in a flowing afterglow Langmuir probe apparatus. These experiments suggested that excited-state nitrogen atoms could be responsible for the N -replacement product. Density functional theory calculations confirmed that the reaction of excited-state nitrogen N( 2 P) and N( 2 D) with toluene ions can directly form protonated methylpyridine, ejecting a carbon atom from the aromatic ring. N( 2 P) is responsible for this reaction in our DBDI source as it has a sufficient lifetime in the plasma and was detected by optical emission spectroscopy measurements, showing an increasing intensity of N( 2 P) with increasing voltage.