Please use this identifier to cite or link to this item:
|Scopus||Web of Science®||Altmetric|
|Title:||Studies on the mechanism of the peroxyoxalate chemiluminescence reaction Part 1. Confirmation of 1 2-dioxetanedione as an intermediate using 13C nuclear magnetic resonance spectroscopy|
|Citation:||Analytica Chimica Acta, 2004; 502(2):141-147|
|Publisher:||Elsevier Science BV|
|Richard Bos, Neil W. Barnett, Gail A. Dyson, Kieran F. Lim, Richard A. Russell and Simon P. Watson|
|Abstract:||A simple model peroxyoxalate chemiluminescence system was monitored directly across a range of temperatures (from −80 to +20 °C) using 13C nuclear magnetic resonance spectroscopy. These experiments were made possible by the utilisation of 13C doubly labelled oxalyl chloride, which was reacted with anhydrous hydrogen peroxide in dry tetrahydrofuran. Ab initio quantum calculations were also performed to estimate the 13C nuclear magnetic resonance (NMR) shift of the most commonly postulated key intermediate 1,2-dioxetanedione and this data, in concert with the spectroscopic evidence, confirmed its presence during the reaction.|
|Keywords:||Peroxyoxalate chemiluminescence intermediate; 1,2-Dioxetanedione; Nuclear magnetic resonance spectroscopy; Ab initio quantum calculations|
|Description:||Copyright © 2003 Elsevier B.V. All rights reserved.|
|Appears in Collections:||Adelaide Graduate Centre publications|
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.