A comparison of pulse and CW EPR T2-relaxation measurements of an inhomogeneously broadened nitroxide spin probe undergoing Heisenberg spin exchange 2. The intercept discrepancy

IF 2 3区 化学 Q3 BIOCHEMICAL RESEARCH METHODS
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引用次数: 0

Abstract

Experimental confirmation of a theoretical prediction of a non-linear broadening of the spin packets of nitroxide free radicals due to Heisenberg spin exchange at low concentrations, C, is presented. A recent demonstration that spectra with resolved proton hyperfine structure may be analyzed efficiently and accurately was utilized to confirm the theory. As C0, a plot of the spin-packet line width (SPW) curves downward due to the presence of proton hyperfine couplings that increase the number of distinguishable quantum spin states. At higher C, the broadening is linear with C and the results for the spin exchange rate constant determined from the slope of the broadening of the average spin-packet line width and electron spin echo measurements are in agreement. It is shown that applying modest digital smoothing does not change the values of the SPW. An example of a practical application of these methods to published work is presented, allowing an enigma to be resolved.
对进行海森堡自旋交换的不均匀拓宽亚硝基自旋探针进行的脉冲和连续波 EPR T2- 弛豫测量的比较 2.截距差异
实验证实了在低浓度 C 下海森堡自旋交换导致硝化自由基自旋包非线性拓宽的理论预测。为了证实这一理论,最近进行了一次演示,证明可以高效、准确地分析质子超频结构的光谱。当 C→0 时,自旋包线宽(SPW)曲线向下弯曲,这是由于质子超细耦合的存在增加了可区分的量子自旋态的数量。在较高的 C 值下,展宽与 C 值呈线性关系,根据平均自旋电子包线宽展宽斜率确定的自旋交换率常数与电子自旋回波测量结果一致。结果表明,应用适度的数字平滑不会改变 SPW 的值。本文还介绍了将这些方法实际应用于已发表论文的实例,从而解开了一个谜团。
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来源期刊
CiteScore
3.80
自引率
13.60%
发文量
150
审稿时长
69 days
期刊介绍: The Journal of Magnetic Resonance presents original technical and scientific papers in all aspects of magnetic resonance, including nuclear magnetic resonance spectroscopy (NMR) of solids and liquids, electron spin/paramagnetic resonance (EPR), in vivo magnetic resonance imaging (MRI) and spectroscopy (MRS), nuclear quadrupole resonance (NQR) and magnetic resonance phenomena at nearly zero fields or in combination with optics. The Journal''s main aims include deepening the physical principles underlying all these spectroscopies, publishing significant theoretical and experimental results leading to spectral and spatial progress in these areas, and opening new MR-based applications in chemistry, biology and medicine. The Journal also seeks descriptions of novel apparatuses, new experimental protocols, and new procedures of data analysis and interpretation - including computational and quantum-mechanical methods - capable of advancing MR spectroscopy and imaging.
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