eprintid: 17997
rev_number: 29
userid: 1419
dir: disk0/00/01/79/97
datestamp: 2013-04-08 17:33:27
lastmod: 2021-06-12 22:55:21
status_changed: 2013-04-08 17:33:27
type: article
metadata_visibility: show
item_issues_count: 0
eprint_status: archive
creators_name: Myshakin, EM
creators_name: Jordan, KD
creators_name: Robertson, WH
creators_name: Weddle, GH
creators_name: Johnson, MA
creators_email: 
creators_email: jordan@pitt.edu
creators_email: 
creators_email: 
creators_email: 
creators_id: 
creators_id: JORDAN
creators_id: 
creators_id: 
creators_id: 
title: Dominant structural motifs of NO<sup>-</sup>·(H<inf>2</inf>O)<inf>n</inf> complexes: Infrared spectroscopic and ab initio studies
ispublished: pub
divisions: sch_as_chemistry
full_text_status: public
abstract: Infrared spectra of the NO-·(H2O)n=1-5 clusters are obtained by argon predissociation spectroscopy. Thus, the spectrum of NO-·H2O revealed a free OH band and two intense red-shifted IHB bands, consistent with two asymmetric isomers with single H-bonded Cs structures. The NO- anion favors the formation of cyclic hydrates in contrast to O2-, which encourages more open hydration motifs.
date: 2003-03-15
date_type: published
publication: Journal of Chemical Physics
volume: 118
number: 11
pagerange: 4945 - 4953
refereed: TRUE
issn: 0021-9606
id_number: 10.1063/1.1545771
citation:   Myshakin, EM and Jordan, KD and Robertson, WH and Weddle, GH and Johnson, MA  (2003) Dominant structural motifs of NO<sup>-</sup>·(H<inf>2</inf>O)<inf>n</inf> complexes: Infrared spectroscopic and ab initio studies.  Journal of Chemical Physics, 118 (11).  4945 - 4953.  ISSN 0021-9606     
document_url: http://d-scholarship-dev.library.pitt.edu/17997/1/licence.txt