Disentangling the Contribution of Multiple Isomers to the Infrared Spectrum of the Protonated Water Heptamer
- Publication date
- 2015
- Publisher
Abstract
We use infrared/infrared double-resonance population labeling (IR<sup>2</sup>MS<sup>2</sup>) spectroscopy in the spectral region of the free and hydrogen-bonded OH stretching fundamentals (2880–3850 cm<sup>-1</sup>) to identify the number and to isolate the vibrational signatures of individual isomers contributing to the gas-phase IR spectra of the cryogenically cooled protonated water clusters H<sup>+</sup>(H<sub>2</sub>O)<sub>n</sub>·H<sub>2</sub>/D<sub>2</sub> with n = 7–10. For n = 7, four isomers are identified and assigned. Surprisingly, the IR<sup>2</sup>MS<sup>2</sup> spectra of the protonated water octa-, nona-, and decamer show no evidence for multiple isomers. The present spectra support the prediction that the quasi-2D to 3D structural transition occurs in between n = 8 and 9 in the cold cluster regime. However, the same models have difficulty explaining the remarkable size dependence of the isomer population reported here