Zalibera Michal, Rapta Peter, Stasko Andrej, Brindzová Lucia, Brezová Vlasta
Institute of Physical Chemistry and Chemical Physics, Faculty of Chemical and Food Technology, Slovak University of Technology in Bratislava, Radlinského 9, SK-812 37 Bratislava, Slovak Republic.
Free Radic Res. 2009 May;43(5):457-69. doi: 10.1080/10715760902846140.
Thermal decomposition of potassium persulphate (K2S2O8) was studied in detail by the EPR spin trapping technique in dimethylsulphoxide (DMSO), employing 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), 5-ethoxycarbonyl-5-methyl-1-pyrroline-N-oxide (EMPO) and 5-(diisopropoxyphosphoryl)-5-methyl-1-pyrroline-N-oxide (DIPPMPO) as spin traps. DMPO and/or its derivatives exclusively trapped the primary formed SO4*- radical anions producing stable spin adducts with half-lives exceeding 2 h at room temperature. High-resolution EPR spectra of these adducts showed unusually rich hyperfine structure due to the interaction of the unpaired electron with all magnetically active nuclei of the spin trap moiety. In contrast to aprotic DMSO solvent, *DMPO-OH adducts dominated in mixed DMSO/water solutions with water content higher than 50%. The thermal decomposition of K2S2O8 in DMSO represents an effective source of free radicals for the radical scavenging capacity (RSC) determination assay, applicable to hydrophilic as well as hydrophobic antioxidants. Efficiency of the assay is demonstrated with a series of cereal samples.
采用 5,5 - 二甲基 - 1 - 吡咯啉 - N - 氧化物(DMPO)、5 - 乙氧羰基 - 5 - 甲基 - 1 - 吡咯啉 - N - 氧化物(EMPO)和 5 - (二异丙氧基磷酰基) - 5 - 甲基 - 1 - 吡咯啉 - N - 氧化物(DIPPMPO)作为自旋捕获剂,利用电子顺磁共振(EPR)自旋捕获技术在二甲基亚砜(DMSO)中对过硫酸钾(K₂S₂O₈)的热分解进行了详细研究。DMPO 及其衍生物专门捕获最初形成的 SO₄•- 自由基阴离子,在室温下生成半衰期超过 2 小时的稳定自旋加合物。这些加合物的高分辨率 EPR 光谱显示,由于未成对电子与自旋捕获部分的所有磁活性核相互作用,具有异常丰富的超精细结构。与非质子性 DMSO 溶剂不同,在水含量高于 50%的 DMSO/水混合溶液中,*DMPO - OH 加合物占主导。K₂S₂O₈ 在 DMSO 中的热分解是用于自由基清除能力(RSC)测定试验的有效自由基来源,适用于亲水性和疏水性抗氧化剂。用一系列谷物样品证明了该试验的有效性。