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dc.contributor.authorCopperthwaite, Richard G.-
dc.contributor.authorLloyd, John-
dc.date.accessioned2025-05-09T06:40:12Z-
dc.date.available2025-05-09T06:40:12Z-
dc.date.issued1978-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/18895-
dc.description.abstractThe first-order rate constants for the decomposition of Na[ClO3] and Na[ClO4] when studied by X-p.e.s. are shown to have a linear dependence on the intensity of the ionising radiation used. A simple steady-state model, which emphasises the rôle of molecular excitons in the decomposition process, is constructed to explain this behaviour. Variable temperature studies in the range 293–113 K indicate that the rate of photo-induced decomposition of Na[ClO3] increases as the temperature is lowered, and analysis of the mode of decomposition suggests that the temperature-dependence arises from thermal deactivation of the molecular exciton, [ClO*3]–.en_US
dc.language.isoenen_US
dc.publisherJournal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1978, 74 (09-12)en_US
dc.subjectChemistryen_US
dc.subjectX-ray photoelectron spectroscopyen_US
dc.subjectJournal of the Chemical Society : Faraday Transaction - Ien_US
dc.titleX-ray photoelectron spectroscopic (X-p.e.s.) studies on in situ photoinduced decomposition of inorganic molecular ions. Part 2.—Na[ClOx] system: mechanistic (x= 3, 4) and variable-temperature (x= 3) investigationsen_US
dc.typeArticleen_US
Appears in Collections:Journal Articles (before-1995)

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