The Journal of Chemical Physics · 1966 · 271 citations · 21 references
Natural SciencesChemistryPhysicsCondensed Matter PhysicsPhysical ChemistrySpectroscopyExchange InteractionsIntermolecular ForcesMolecular Angular MomentumMolecular InteractionsRelaxation MechanismsSpin DynamicsMolecular Perturbation TheoryRelaxation In LiquidsRotational Correlation TimeRotational RelaxationSpin ExchangeSpin Exchange InteractionsSpin RelaxationSpin Relaxation Mechanisms
In Part I of this series the residual linewidths for vanadyl acetylacetonate in toluene were found to be proportional to (T/η), where η is the viscosity, and independent of applied field. Since the solutions are dilute, spin exchange is not important. The residual linewidth is attributed to a spin—rotational relaxation mechanism, and calculations based on a perturbation theory of spin—rotational interactions and Hubbard's theory of spin—rotational relaxation yield results in reasonably good agreement with experiment. This relaxation mechanism is probably significant for many dilute S = ½ systems in liquids. For systems with weak anisotropic intermolecular interactions, e.g. ClO2 in CCl4, the correlation time τω for angular momentum and the spin—rotational contribution to the linewidth appear to be larger than those predicted by Hubbard's theory.
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Paramagnetic Relaxation Times for Titanium and Chrome Alum
J. H. Van Vleck · Physical Review · 1940 · 875 citations
The Coupling of Angular Momentum Vectors in Molecules
J. H. Van Vleck · Reviews of Modern Physics · 1951 · 607 citations
Natural Sciences, Chemistry, Physics +11