Nature of the transient species formed in pulse radiolysis of n-allylthiourea in aqueous solutions

Nature of the transient species formed in pulse radiolysis of n-allylthiourea in aqueous solutions Reactions of e− aq, OH radicals and H atoms were studied with n-allylthiourea (NATU) using pulse radiolysis. Hydrated electrons reacted with NATU (k = 2.8×109 dm3 mol−1 s−1) giving a transient species which did not have any significant absorption above 300 nm. It was found to transfer electrons to methyl viologen. At pH 6.8, the reduction potential of NATU has been determined to be −0.527 V versus NHE. At pH 6.8, OH radicals were found to react with NATU, giving a transient species having absorption maxima at 400–410 nm and continuously increasing absorption below 290 nm. Absorption at 400–410 nm was found to increase with parent concentration, from which the equilibrium constant for dimer radical cation formation has been estimated to be 4.9×103 dm3 mol−1. H atoms were found to react with NATU with a rate constant of 5 × 109 dm3 mol−1 s−1, giving a transient species having an absorption maximum at 310 nm, which has been assigned to H-atom addition to the double bond in the allyl group. Acetoneketyl radicals reacted with NATU at acidic pH values and the species formed underwent reaction with parent NATU molecule. Reaction of Cl.− 2 radicals (k = 4.6 × 109 dm3 mol−1 s−1) at pH 1 was found to give a transient species with λ max at 400 nm. At the same pH, reaction of OH radicals also gave transient species, having a similar spectrum, but the yield was lower. This showed that OH radicals react with NATU by two mechanisms, viz., one-electron oxidation, as well as addition to the allylic double bond. From the absorbance values at 410 nm, it has been estimated that around 38% of the OH radicals abstract H atoms and the remaining 62% of the OH radicals add to the allylic double bond. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Research on Chemical Intermediates Springer Journals

Nature of the transient species formed in pulse radiolysis of n-allylthiourea in aqueous solutions

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Publisher
Brill Academic Publishers
Copyright
Copyright © 2006 by VSP
Subject
Chemistry; Inorganic Chemistry; Physical Chemistry; Catalysis
ISSN
0922-6168
eISSN
1568-5675
D.O.I.
10.1163/156856706775012996
Publisher site
See Article on Publisher Site

Abstract

Reactions of e− aq, OH radicals and H atoms were studied with n-allylthiourea (NATU) using pulse radiolysis. Hydrated electrons reacted with NATU (k = 2.8×109 dm3 mol−1 s−1) giving a transient species which did not have any significant absorption above 300 nm. It was found to transfer electrons to methyl viologen. At pH 6.8, the reduction potential of NATU has been determined to be −0.527 V versus NHE. At pH 6.8, OH radicals were found to react with NATU, giving a transient species having absorption maxima at 400–410 nm and continuously increasing absorption below 290 nm. Absorption at 400–410 nm was found to increase with parent concentration, from which the equilibrium constant for dimer radical cation formation has been estimated to be 4.9×103 dm3 mol−1. H atoms were found to react with NATU with a rate constant of 5 × 109 dm3 mol−1 s−1, giving a transient species having an absorption maximum at 310 nm, which has been assigned to H-atom addition to the double bond in the allyl group. Acetoneketyl radicals reacted with NATU at acidic pH values and the species formed underwent reaction with parent NATU molecule. Reaction of Cl.− 2 radicals (k = 4.6 × 109 dm3 mol−1 s−1) at pH 1 was found to give a transient species with λ max at 400 nm. At the same pH, reaction of OH radicals also gave transient species, having a similar spectrum, but the yield was lower. This showed that OH radicals react with NATU by two mechanisms, viz., one-electron oxidation, as well as addition to the allylic double bond. From the absorbance values at 410 nm, it has been estimated that around 38% of the OH radicals abstract H atoms and the remaining 62% of the OH radicals add to the allylic double bond.

Journal

Research on Chemical IntermediatesSpringer Journals

Published: Jan 1, 2006

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