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Free radical products in X-irradiated Rochelle salt: low temperature ENDOR and DFT studies

机译:X射线辐射的罗谢尔盐中的自由基产物:低温ENDOR和DFT研究

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摘要

Single crystals of Rochelle salt, [(-)OOC-CHOH-CHOH-COO(-), Na(+) K(+)]center dot 4H(2)O, X-irradiated at 10 K, have been examined using EPR, ENDOR and EIE spectroscopic techniques to characterize the radiation induced radicals stable at that temperature and their reactions upon warming. The one-electron gain product was observed and from the hyperfine interaction with a beta-proton it was unambiguously centered at the C(4) position of the tartrate moiety. An additional nearly isotropic hyperfine structure of about 21 MHz was tentatively assigned to interaction with a sodium ion exhibiting a close contact to O(3) in the crystal. Evidence was obtained that the one-electron reduced radical had become protonated at one of the C(4) bonded carboxyl oxygens, most probably O(4). No evidence for the corresponding C(1)-centered reduction product was found. Two resonance lines (R2, A1) were shown by EIE to belong to a species formed by decarboxylation at C(3), a secondary oxidation product. Two other resonance lines (K1, K2) were assigned to two varieties of another decarboxylation radical, centered at C(2), distinguished by differences in the potassium ion coordination. Furthermore, one other resonance line (A2) was tentatively ascribed to a third decarboxylation radical, centered at the opposite end of the tartrate moiety. The precursor of these products, that is, the one-electron loss product, was not observed after X-irradiation at 10 K. Thermally induced free radical reactions followed by EPR in the temperature range of 12-119K indicate that a water molecule or a hydroxyl ion is eliminated from the one-electron reduction product radical and that a C(3)-centered radical is formed. The reduction and oxidation reaction pathways of hydroxy acid derivatives are discussed.
机译:罗谢尔盐单晶[(-)OOC-CHOH-CHOH-COO(-),Na(+)K(+)]中心点4H(2)O,已用EPR进行了X射线辐照,ENDOR和EIE光谱技术来表征在该温度下稳定的辐射诱导自由基及其在变暖时的反应。观察到单电子增益产物,并且从与β质子的超精细相互作用中,它明确地位于酒石酸部分的C(4)位置。大约21 MHz的另一个近似各向同性的超精细结构被暂时分配给与钠离子相互作用,该钠离子与晶体中的O(3)紧密接触。获得的证据表明,单电子还原的自由基已在C(4)键合的羧基氧之一(最可能为O(4))上质子化。找不到相应的以C(1)为中心的还原产物的证据。 EIE显示两条共振线(R2,A1)属于通过在二级氧化产物C(3)上进行脱羧反应而形成的物质。其他两个共振线(K1,K2)被分配到另一个以C(2)为中心的另一个脱羧基的两个变体,以钾离子配位的差异来区分。此外,另一个共振线(A2)被暂时归因于第三脱羧基团,该第三脱羧基团以酒石酸盐部分的相反端为中心。在10 K X辐射后未观察到这些产物的前体,即单电子损失产物。在12-119K的温度范围内热诱导的自由基反应以及随后的EPR表明,水分子或从单电子还原产物自由基中消除了氢氧根离子,并形成了一个以C(3)为中心的自由基。讨论了羟基酸衍生物的还原和氧化反应途径。

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