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The spectral forms of transient ESR spectra of radical pairs andthe origin of the antiphase structure

机译:自由基对的瞬时ESR光谱的光谱形式和后期结构的起源

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We show that transient electron spin resonance (ESR) spectra of short lived radical pairs can be written formally as a superposition of Lorentzian-like lines and the corresponding dispersive lines. The coefficients to these spectral components depend strongly on the frequency and amplitude of the microwave (mw) field and consequently a variety of spectral forms may result. The coefficients, and thus the spectral form, are determined by the interradical interaction induced rate of change of the longitudinal and transversal electron spin polarization. The ongitudinal polarization is responsible for the well known chemically induced dynamic electron polarization (CIDEP) which changes the intensity of the lines without affecting the line shape. The transversal polarization is shown to be responsible for the antiphase structure (APS) in accordance with our previous proposition [J. Chem. Phys. 109, 8743 (1998)]. A simple one re-encounter model calculation illustrates and explains qualitatively most of the observed APS characteristics. Numerical calculations are used to discuss anomalously large APS splitting.
机译:我们表明,短寿命自由基对的瞬态电子自旋共振(ESR)光谱可以形式上像洛伦兹样线和相应的分散线的叠加形式书写。这些频谱成分的系数在很大程度上取决于微波(mw)场的频率和幅度,因此可能会产生各种频谱形式。系数以及由此的光谱形式由自由基间相互作用引起的纵向和横向电子自旋极化的变化率确定。径向偏振是众所周知的化学感应动态电子偏振(CIDEP)的原因,它可以改变线的强度而不影响线的形状。根据我们先前的观点,横向极化被证明是造成反相结构(APS)的原因[J.化学物理109,8743(1998)]。一种简单的重新遇到模型计算可以从质量上说明和解释大多数观察到的APS特征。数值计算用于讨论异常大的APS分裂。

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