Advanced search
Start date
Betweenand
(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Peroxyoxalate High-Energy Intermediate is Efficiently Decomposed by the Catalyst Imidazole

Full text
Author(s):
Boaro, Andreia ; Bartoloni, Fernando Heering
Total Authors: 2
Document type: Journal article
Source: Photochemistry and Photobiology; v. 92, n. 4, p. 546-551, JUL-AUG 2016.
Web of Science Citations: 1
Abstract

The peroxyoxalate reaction is a highly efficient chemiluminescence system, its chemiexcitation process involving the intermolecular interaction between an activator (ACT) and the high-energy intermediate (HEI) of the reaction. Typically, the HEI is generated through the reaction of an oxalate ester with H2O2, in the presence of a basic/nucleophilic catalyst, such as imidazole (IMI-H). IMI-H, besides catalyzing the formation of the HEI, is also known to decompose this peroxidic intermediate. Despite that, up to now, no rate constant value has been determined for such significant interaction. Through kinetic measurements, we have observed that IMI-H is roughly four times more efficient than 9,10-diphenylanthracene (DPA), a classic ACT, in catalyzing the decomposition of the HEI by a bimolecular electron transfer reaction through a Chemically Initiated Electron Exchange Luminescence-like process. For instance, when IMI-H and DPA are at the same concentration, 78% of the generated HEI is actually consumed by the nonemissive bimolecular interaction with IMI-H. We have obtained an average singlet excited state formation quantum yield, at infinite ACT concentration, of (5.5 +/- 0.5)x10(-2)Emol(-1), determined at five different IMI-H concentrations. This ultimately suggests that the yield of formation of HEI actually does not depend on the IMI-H concentration. (AU)

FAPESP's process: 12/13807-7 - New tools for the study of electron transfer reactions in PS II model systems
Grantee:Fernando Heering Bartoloni
Support Opportunities: Regular Research Grants