Infrared spectroscopy of the microhydrated nitrate ions NO(3)(-)(H2O)(1-6)

We present infrared photodissociation spectra of the microhydrated nitrate ions NO(3)(-)(H(2)O)(1-6), measured from 600 to 1800 cm(-1). The assignment of the spectra is aided by comparison with calculated B3LYP/aug-cc-pVDZ harmonic frequencies, as well as with higher-level calculations. The IR spect...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Molecules, spectroscopy, kinetics, environment, & general theory, 2009-07, Vol.113 (26), p.7584-7592
Hauptverfasser: Goebbert, Daniel J, Garand, Etienne, Wende, Torsten, Bergmann, Risshu, Meijer, Gerard, Asmis, Knut R, Neumark, Daniel M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:We present infrared photodissociation spectra of the microhydrated nitrate ions NO(3)(-)(H(2)O)(1-6), measured from 600 to 1800 cm(-1). The assignment of the spectra is aided by comparison with calculated B3LYP/aug-cc-pVDZ harmonic frequencies, as well as with higher-level calculations. The IR spectra are dominated by the antisymmetric stretching mode of NO(3)(-), which is doubly degenerate in the bare ion but splits into its two components for most microhydrated ions studied here due to asymmetric solvation of the nitrate core. However, for NO(3)(-)(H(2)O)(3), the spectrum reveals no lifting of this degeneracy, indicating an ion with a highly symmetric solvation shell. The first three water molecules bind in a bidentate fashion to the terminal oxygen atoms of the nitrate ion, keeping the planar symmetry. The onset of extensive water-water hydrogen bonding is observed starting with four water molecules and persists in the larger clusters.
ISSN:1520-5215
DOI:10.1021/jp9017103