Abstract
Abstract
Electron paramagnetic resonance (EPR) spectroscopy is the ideal method of choice when detecting and studying the wide variety of paramagnetic oxygen-centred radicals. For simple diatomic radicals, such as the superoxide (O2−) or peroxy $$ ({\text{ROO}}^{\bullet})$$(ROO∙) species, the CW EPR profile (in particular the g-values) of these species can appear similar and indeed indistinguishable in some cases. Experiments using 17O-enriched oxygen, revealing a rich 17O hyperfine pattern, are therefore essential to distinguish between the two species. However, in many cases, particularly involving TiO2 photocatalysis, the peroxy-type $$ ({\text{ROO}}^{\bullet})$$(ROO∙) radicals or other intermediate species such as the [O2−…organic]-type adducts can be transient in nature and once again can produce similar g-values. In general terms, these reactive oxygen species (ROS) are formed and detected at low-temperature conditions. Hence, the application of EPR spectroscopy to studies of surface-stabilised oxygen-centred radicals must be performed under carefully selected conditions in order to confidently distinguish between the differing types of diatomic radicals, such as O2−, $$ {\text{ROO}}^{\bullet}$$ROO∙ or [O2−…organic].
Publisher
Springer Science and Business Media LLC
Cited by
19 articles.
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