Login / Signup

Infrared Spectroscopy and Anharmonic Vibrational Analysis of (H2O-Krn)+ (n = 1-3): Hemibond Formation of the Water Radical Cation.

Jing-Min LiuTomoki NishigoriToshihiko MaeyamaQian-Rui HuangMarusu KatadaJer-Lai KuoAsuka Fujii
Published in: The journal of physical chemistry letters (2021)
The hemibond is a nonclassical covalent bond formed between a radical (cation) and a closed shell molecule. The hemibond formation ability of water has attracted great interest, concerning its role in ionization of water. While many computational studies on the water hemibond have been performed, clear experimental evidence has been hardly reported because the hydrogen bond formation overwhelms the hemibond formation. In the present study, infrared photodissociation spectroscopy is applied to (H2O-Krn)+ (n = 1-3) radical cation clusters. The observed spectra of (H2O-Krn)+ are well reproduced by the anharmonic vibrational simulations based on the hemibonded isomer structures. The firm evidence of the hemibond formation ability of water is revealed.
Keyphrases
  • density functional theory
  • high resolution
  • molecular dynamics simulations
  • molecular dynamics
  • single molecule
  • raman spectroscopy
  • simultaneous determination
  • monte carlo