Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/10557
Title: Infrared-Induced Rotamerization of Oxalic Acid Monomer in Argon Matrix
Authors: Maçôas, Ermelinda M. S. 
Fausto, Rui 
Pettersson, Mika 
Khriachtchev, Leonid 
Räsänen, Markku 
Issue Date: 3-Aug-2000
Publisher: American Chemical Society
Citation: The Journal of Physical Chemistry A. 104:30 (2000) 6956-6961
Abstract: Infrared-induced conformational isomerization of oxalic acid monomer isolated in an argon matrix at 7.5 K was studied by infrared spectroscopy. For the first time, three conformational states of this molecule were identified experimentally and their vibrational spectra are assigned. In good agreement with density functional theory predictions, all the observed conformers exhibit a trans OC−CO axis, differing in the relative conformation of their O−C−O−H axes. In the most stable conformer (belonging to the C2h symmetry point group), two intramolecular OH···O hydrogen bonds are present. The second (Cs) most stable conformer shows a single OH···O bond, and the third one (C2h) does not exhibit any intramolecular hydrogen bond. Using narrowband tunable irradiation in the near-infrared region it was possible to promote very efficiently conformer interconversions, which was followed spectroscopically.
URI: http://hdl.handle.net/10316/10557
ISSN: 1089-5639
DOI: 10.1021/jp000634s
Rights: openAccess
Appears in Collections:FCTUC Química - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat
Infrared-Induced Rotamerization of Oxalic Acid Monomer in Argon Matrix.pdf76.17 kBAdobe PDFView/Open
Show full item record

Page view(s)

80
checked on Oct 16, 2019

Download(s)

125
checked on Oct 16, 2019

Google ScholarTM

Check

Altmetric

Dimensions


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.