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Item Pulse Radiolysis Study of the Reaction of Solvated Electrons with Sulphur Hexafluoride in Methanolic Solution(Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (12), 1977) Johnson, David W; Salmon, G. ArthurThe rate constant for the reaction of e–s with SF6 in deaerated methanolic solution has been determined to be k3=(1.88 ± 0.06)× 1010 dm3 mol–1 s–1. The product of this reaction, ·SF5, has an absorption spectrum with a maximum at 300 nm with ε= 1300 dm3 mol–1 cm–1 and decays by mixed first- and second-order kinetics.Item Solvation Spectra Part 52.1—The Aquation of Silver Atoms and Cations: a Radiation and Electron Spin Resonance Study(Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (10), 1977) Brown, D. Robert; Symons, Martyn C. RExposure of a range of aqueous solutions containing AgI cations to 60Co γ-rays at 77 K gave AgII and AgO together with other paramagnetic products. The AgII centres have [graphic omitted] configurations, which means that linear solvation for Ag+ is unlikely, since this would lead to a [graphic omitted] configuration. A range of distinct AgO centres displaying low (∼80 %) atom character was detected. Their yield was enhanced, but their distribution largely unaltered, when certain additives, such as potassium fluoride, were used to give glassy solids. However, their distribution varied with dose and with temperature. The major initial product exhibited an extra 6 G doublet splitting due to hyperfine coupling to a single proton. On further irradiation, this centre was superceded by others exhibiting no resolved coupling to protons but, in some cases, well defined g and A anisotropy. For all the AgO centres, gav was less than the free-spin value. When water enriched in 17O was used, superhyperfine coupling was detected for some of the AgO centres. From the apparent anisotropic and isotropic coupling constants, delocalisation of ∼5% per water molecule was deduced. The intensities indicated the presence of several equivalent water ligands but solvation numbers could not be derived accurately. These results for AgO are significant for two reasons; (1) they show that solvation is not lost in aqueous glasses when the charge on an ion is neutralised. This contrasts with the fact that when small neutral molecules become charged, solvation is acquired, even at 77 K. (2) They indicate the presence of a range of discrete AgI solvates in solution rather than a single preferred unit.