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Iron , nuclear spin relaxation times

Redfield limit, and the values for the CH2 protons of his- N,N-diethyldithiocarbamato)iron(iii) iodide, Fe(dtc)2l, a compound for which Te r- When z, rotational reorientation dominates the nuclear relaxation and the Redfield theory can account for the experimental results. When Te Ti values do not increase with Bq as current theory predicts, and non-Redfield relaxation theory (33) has to be employed. By assuming that the spacings of the electron-nuclear spin energy levels are not dominated by Bq but depend on the value of the zero-field splitting parameter, the frequency dependence of the Tj values can be explained. Doddrell et al. (35) have examined the variable temperature and variable field nuclear spin-lattice relaxation times for the protons in Cu(acac)2 and Ru(acac)3. These complexes were chosen since, in the former complex, rotational reorientation appears to be the dominant time-dependent process (36) whereas in the latter complex other time-dependent effects, possibly dynamic Jahn-Teller effects, may be operative. Again current theory will account for the observed Ty values when rotational reorientation dominates the electron and nuclear spin relaxation processes but is inadequate in other situations. More recent studies (37) on the temperature dependence of Ty values of protons of metal acetylacetonate complexes have led to somewhat different conclusions. If rotational reorientation dominates the nuclear and/or electron spin relaxation processes, then a plot of ln( Ty ) against T should be linear with slope Er/R, where r is the activation energy for rotational reorientation. This was found to be the case for Cu, Cr, and Fe complexes with Er 9-2kJ mol" However, for V, Mn, and... [Pg.10]

Representative and spectra are presented in Figures 5, 6, 7, and 8 for the Amax and Monterey samples. The quantitative reference (peak at 0.0 ppm) in each spectrum is hexamethyldisiloxane ((CH3)3-Si-0-Si(0113)3). A paramagnetic relaxation reagent (the paramagnetic relaxation reagents used were either tris(acetylacetonato) iron (III), Fe(acac)3, or tris(acetylacetonato) chromium (III), Cr(acac)3 at concentrations of 2-6 X lO M). was added to decrease spin lattice relaxation times (Ti s) and suppress nuclear Overhauser effects (5). In addition,... [Pg.45]

Another particularly interesting type of experiment gives information about the Co parent atom. At temperatures of < IK the Zeeman levels of Co I — 1) atoms in iron metal are not equally occupied as their separation is kT. Assuming that the spin-lattice relaxation times are longer than the total nuclear decay time, the preferential orientation of the nucleus... [Pg.307]


See other pages where Iron , nuclear spin relaxation times is mentioned: [Pg.10]    [Pg.130]    [Pg.192]    [Pg.6218]    [Pg.6217]    [Pg.156]    [Pg.293]    [Pg.309]    [Pg.97]    [Pg.1959]    [Pg.214]    [Pg.67]    [Pg.1958]    [Pg.430]    [Pg.108]    [Pg.289]    [Pg.331]    [Pg.183]   
See also in sourсe #XX -- [ Pg.10 ]




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