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The Effect of Spin Relaxation on ENDOR Spectra Recorded at High Magnetic Fields and Low Temperatures

✍ Scribed by B Epel; A Pöppl; P Manikandan; S Vega; D Goldfarb


Publisher
Elsevier Science
Year
2001
Tongue
English
Weight
168 KB
Volume
148
Category
Article
ISSN
1090-7807

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✦ Synopsis


A simple theoretical model that describes the pulsed Davies electron-nuclear double resonance (ENDOR) experiment for an electron spin S ‫؍‬ 1 2 coupled to a nuclear spin I ‫؍‬ 1 2 was developed to account for unusual W-band (95 GHz) ENDOR effects observed at low temperatures. This model takes into account the thermal polarization along with all internal relaxation processes in a fourlevel system represented by the electron-and nuclear-spin relaxation times T 1e and T 1n , respectively, and the cross-relaxation time, T 1x . It is shown that under conditions of sufficiently high thermal spin polarization, nuclei can exhibit asymmetric ENDOR spectra in two cases: the first when t mix ӷ T 1e and T 1n , T 1x ӷ T 1e , where ENDOR signals from the ␣ manifold are negative and those of the ␤ manifold positive, and the second when the cross-and/or nuclear-relaxation times are longer than the repetition time (t mix Ӷ T 1e Ӷ t R and T 1n , T 1x > t R ). In that case the polarization of the ENDOR signals becomes opposite to the previous case, the lines in the ␣ manifolds are positive, and those of the ␤ manifold are negative. This case is more likely to be encountered experimentally because it does not require a very long mixing time and is a consequence of the saturation of the nuclear transitions. Using this model the experimental t mix and t R dependencies of the W-band 1 H ENDOR amplitudes of [Cu(imidazole) 4 ]Cl 2 were reproduced and the values of T 1e and T 1x ӷ T 1e were determined. The presence of asymmetry in the ENDOR spectrum is useful as it directly provides the sign of the hyperfine coupling. The presented model allows the experimentalist to adjust experimental parameters, such as t mix and t R , in order to optimize the desired appearance of the spectrum.


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The ESR and ENDOR spectra and hyperfine coupling constants (hfi) of the tertiary butoxyl spin adduct of 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) change markedly, but reversibly, with increase in temperature from 140 to 280 K, and the spectra can be cycled repeatedly between these temperature limits.