Abstract

Careful studies are described of the ESR line shapes and saturation behavior for the peroxylamine disulfonate (PADS) radical dissolved in a range of glycerol-water mixtures. This permitted studies where the rotational correlation time τR ranged from 3 × 10−12 sec to < 10−6 sec. The unsaturated line shapes for 10−10 < τR < 10−9 sec are, as in Paper I, readily interpreted in terms of anisotropic rotational diffusion, but for τR < 10−10 sec anomalous behavior of the linewidths, which could be attributed to nonsecular spectral densities, occurs. Supporting experiments at 35 GHz, and also on 17O-labeled PADS, are in excellent agreement with values of τR and N = 4.7 (the ratio of the two components of the axially symmetric diffusion tensor), and they supply further information on the anomalous behavior of the nonsecular spectral densities. A phenomenological treatment based on the memory function approach was found to qualitatively reproduce some observed features. The saturation studies were performed over both the motional narrowing and slow-tumbling regions. The motional narrowing results could be analyzed in a straightforward manner to yield values of We, the electron-spin flip rate, which are found to exhibit a weak dependence on τR, roughly as τR−(1/4) for the glycerol solvents. The stochastic Liouville method is applied to an analysis of slow-tumbling saturated spectra and generally reasonable agreement with experiment is achieved for the simplifying assumptions utilized. The rotationally invariant We obtained from the slow-tumbling analyses are found to agree with the values of We extrapolated from the motional-narrowing region. Other aspects of the slow-tumbling saturation experiments and analysis are discussed.

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