Department of Chemistry and TRIUMF, Simon Fraser University , Burnaby, BC V5A 1S6, Canada.
J Phys Chem A. 2014 Feb 20;118(7):1162-7. doi: 10.1021/jp411297s. Epub 2014 Feb 10.
Very little is known about the behavior of free H atoms and small organic radicals inside clathrate hydrate structures despite the relevance of such species to combustion of hydrocarbon hydrates. Muonium is an H atom analog, essentially a light isotope of hydrogen, and can be used to probe the chemistry of H atoms and transient free radicals. We demonstrate the first application of muon spin spectroscopy to characterize radicals in clathrate hydrates. Atomic muonium was detected in hydrates of cyclopentane and tetrahydrofuran, and muoniated free radicals were detected in the hydrates of cyclopentene and 2,5-dihydrofuran, indicating rapid addition of muonium to the organic guest. Muon avoided level-crossing spectra of the radicals in hydrates are markedly different to those of the same radicals in pure organic liquids at the same temperature, and this can be explained by limited mobility of the enclathrated radicals, leading to anisotropy in the hyperfine interactions.
尽管在烃类水合物的燃烧中,笼形水合物结构内的游离 H 原子和小型有机自由基的行为非常重要,但人们对此知之甚少。Muonium 是 H 原子的类似物,本质上是氢的轻同位素,可用于探测 H 原子和瞬态游离基的化学性质。我们首次将 muon 自旋光谱学应用于表征笼形水合物中的自由基。在环戊烷和四氢呋喃的水合物中检测到原子 muonium,在环戊烯和 2,5-二氢呋喃的水合物中检测到 muoniated 游离基,表明 muonium 快速添加到有机客体中。在相同温度下,笼形水合物中自由基的 muon 避免交叉能级光谱与相同自由基在纯有机液体中的光谱明显不同,这可以通过包合自由基的有限迁移性来解释,导致超精细相互作用的各向异性。