Two-center three-electron bonding in ClNH{sub 3} revealed via helium droplet infrared laser Stark spectroscopy: Entrance channel complex along the Cl + NH{sub 3} → ClNH{sub 2} + H reaction

• Published in: The Journal of chemical physics 2016-04, Vol.144 (16)
• Main Authors: Moradi, Christopher P., Douberly, Gary E., Xie, Changjian, Guo, Hua, Kaufmann, Matin
• Format: Article
• Language: English
• Subjects: AMMONIUM COMPOUNDS; BONDING; CALCULATION METHODS; CHLORINE COMPOUNDS; COMPLEXES; DIPOLE MOMENTS; DOPED MATERIALS; DROPLETS; HELIUM; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; LASER SPECTROSCOPY
• ISSN: 0021-9606; 1089-7690

Pyrolytic dissociation of Cl{sub 2} is employed to dope helium droplets with single Cl atoms. Sequential addition of NH{sub 3} to Cl-doped droplets leads to the formation of a complex residing in the entry valley to the substitution reaction Cl + NH{sub 3} → ClNH{sub 2} + H. Infrared Stark spectroscopy in the NH stretching region reveals symmetric and antisymmetric vibrations of a C{sub 3v} symmetric top. Frequency shifts from NH{sub 3} and dipole moment measurements are consistent with a ClNH{sub 3} complex containing a relatively strong two-center three-electron (2c–3e) bond. The nature of the 2c–3e bonding in ClNH{sub 3} is explored computationally and found to be consistent with the complexation-induced blue shifts observed experimentally. Computations of interconversion pathways reveal nearly barrierless routes to the formation of this complex, consistent with the absence in experimental spectra of two other complexes, NH{sub 3}Cl and Cl–HNH{sub 2}, which are predicted in the entry valley to the hydrogen abstraction reaction Cl + NH{sub 3} → HCl + NH{sub 2}.