Simple analytical approximation of the longitudinal electronic relaxation rate of Gd(iii) complexes in solutions

Literature Information

Publication Date 2004-04-01
DOI 10.1039/B316249D
Impact Factor 3.676
Authors

Pascal H. Fries


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Abstract

More and more sophisticated theoretical models have been developped for a correct description of the relaxation of the electronic spin S = 7/2 of the Gd(III) paramagnetic complexes used as contrast agents in magnetic resonance imaging (MRI). Both the static zero field splitting (ZFS) modulated by the random rotation of the complex and the transient ZFS due to the very fast distortion of this entity must be included in these models. This leads to rather complicated analytical expressions, from which it is difficult to evaluate the respective effects of the physically relevant parameters. However, in the Redfield limit of the theory of electronic spin relaxation, we show that the longitudinal relaxation function G∥(t) has a quasi-monoexponential decay characterized by a unique relaxation rate 1/T1e, which has a simple expression in terms of the applied magnetic field B0, of the static and transient ZFS parameters, and of the rotational and vibrational correlation times. For the typical investigated Gd(III) complexes, this expression is shown to have a very satisfactory accuracy for B0 < 10 T. The various physical parameters as well as the range of validity of the relaxation approximation are discussed in detail.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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