Abstract
A theoretical treatment is proposed for the relaxation induced by the dipolar interaction between two spins separated by several bonds about which jump motions occur among three sites, two of them at least being equivalent. The influence of the internal and overall molecular motions upon the carbon-13 longitudinal relaxation is discussed for the model of n-butylamine coordinated to a paramagnetic ion having a comparatively long T 1e like Mn2+. The 13C paramagnetic dipolar relaxation appears to be mainly dependent upon the ratios of the transition rates among the different conformers. A computer program has been written to analyse the 13C longitudinal dipolar relaxation in terms of internal motions and transient conformations for flexible and partially rigid molecules such as butylamine, allylamine and benzylamine coordinated to Mn(AA)2 and Gd(DPM)3. The extension of these calculations to complexes where the nuclear relaxation is governed by the electron spin relaxation times is examined for the example of...
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