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首页> 外文期刊>The journal of physical chemistry, A. Molecules, spectroscopy, kinetics, environment, & general theory >EPR Line Shifts and Line Shape Changes Due to Heisenberg Spin Exchange and Dipole?Dipole Interactions of Nitroxide Free Radicals in Liquids: 9. An Alternative Method to Separate the Effects of the Two Interactions Employing ~(15)N and ~(14)N
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EPR Line Shifts and Line Shape Changes Due to Heisenberg Spin Exchange and Dipole?Dipole Interactions of Nitroxide Free Radicals in Liquids: 9. An Alternative Method to Separate the Effects of the Two Interactions Employing ~(15)N and ~(14)N

机译:由于海森堡自旋交换和液体中一氧化氮自由基的偶极-偶极相互作用而引起的EPR线位移和线形变化:9.分离〜(15)N和〜(14)N两种相互作用影响的另一种方法

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A method to separate the effects of Heisenberg spin exchange (HSE) and dipole?dipole (DD) interactions on EPR spectra of nitroxide spin probes in solution by employing ~(15)N and ~(14)N nitroxide spin probes in parallel experiments is developed theoretically and tested experimentally. Comprehensive EPR measurements are reported of 4-oxo-2,2,6,6-tetramethylpiperidine-d_(16);1-~(15)N-1-oxyl (perdeuterated ~(15)N Tempone; 15pDT), in 70 wt % aqueous glycerol as functions of concentration and temperature. The method, termed the relative broadening constant method (RBCM), is demonstrated by using the present results together with those in the literature that employed perdeuterated ~(14)N Tempone (14pDT) under identical conditions. In principle, the separation of DD and HSE is dependent on the model of diffusion and molecular-kinetic parameters; however, within present day experimental uncertainties, the RBCM method turns out to be insensitive to the model. The earlier methods to separate DD and HSE by measuring the dispersion component introduced by the two interactions shows general agreement with the RBCM; however, there are discrepancies larger than estimated uncertainties due to random errors. Thus, further support is found for Salikhov’s recent theory of the effects of DD and HSE on EPR spectra (Appl. Magn. Reson. 2010, 38, 237); however, detailed confirmation is still lacking. The RBCM affords a possible approach to separate HSE and DD in spectra complicated by slow motion and/or overlap with other resonance lines, allowing the method to be used in situations more complicated than low-viscosity simple liquids.
机译:一种通过并行实验使用〜(15)N和〜(14)N氮氧化物自旋探针来分离Heisenberg自旋交换(HSE)和偶极?偶极(DD)相互作用对溶液中氮氧化物自旋探针的EPR谱的影响的方法是理论上的发展和实验测试。据报道在70中对4-oxo-2,2,6,6-四甲基哌啶-d_(16); 1-〜(15)N-1-氧基(全氘代〜(15)N Tempone; 15pDT)进行了全面的EPR测量wt%甘油水溶液的浓度和温度的函数。通过使用本研究结果以及在相同条件下采用全氘(〜14)N Tempone(14pDT)的文献中的方法,证明了该方法称为相对扩展常数方法(RBCM)。原则上,DD和HSE的分离取决于扩散模型和分子动力学参数。然而,在目前的实验不确定性下,RBCM方法对模型不敏感。通过测量两个相互作用引入的色散成分来分离DD和HSE的较早方法显示出与RBCM的总体一致;但是,由于随机误差,存在的差异大于估计的不确定性。因此,萨利霍夫最近关于DD和HSE对EPR光谱的影响的理论得到了进一步的支持(Appl。Magn。Reson。2010,38,237)。但是,仍然缺乏详细的确认。 RBCM提供了一种可能的方法,可将光谱中由慢速运动和/或与其他共振线重叠的HSE和DD分离,从而使该方法可用于比低粘度简单液体更复杂的情况。

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