Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Oxygen and oxidants enhance the sensitivity of cells to radiation. To understand this effect at the mechanistic level, the redox dependences for the reactivity of weakly reducing alpha-monoalkoxyalkyl radicals of 1,4-dioxane and tetrahydrofuran with a series of oxidants, for example, quinones, viologens, and nitro-arenes, with one-electron reduction potentials E71 values ranging from -80 to -640 mV, have been determined using the technique of pulse radiolysis. The second-order rate constants for these reactions with the alpha-monoalkoxyalkyl radicals of 1,4-dioxane and tetrahydrofuran are in the range (0.03-1.5) x 109 and (1.0-6.6) x 109 dm3 mol(-1) s(-1), respectively. The reactions of the alpha-alkoxyalkyl radicals of 1,4-dioxane with quinones and viologens involve an outer-sphere electron transfer, in contrast to a reaction with the nitro-arenes to give adducts. The resulting long-lived nitroaromatic adduct radicals were found to react with the reductant, TMPD, probably leading to the formation of hydroxylamine-type products. In cells, adducts formed on reaction of deoxyribose sugar radical with oxidants and subsequent reactions with reductants may contribute to the mechanisms involved in radiosensitization by oxygen and those oxidants that interact through adduct formation.

Original publication

DOI

10.1021/jp807994b

Type

Journal article

Journal

J Phys Chem B

Publication Date

19/02/2009

Volume

113

Pages

2207 - 2211

Keywords

Calixarenes, Dioxanes, Free Radicals, Furans, Oxidants, Oxidation-Reduction, Quinones, Viologens