Coherent D2 rotational tunneling and incoherent D2 dynamics in a solid non-classical RuD2 complex studied by 2H solid state NMR spectroscopy

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Publication Date
DOI 10.1039/A904155I
Impact Factor 3.676
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Abstract

The 2H solid state NMR spectra and T1 relaxation data of a transition metal η2-dideuterium complex, namely trans-[Ru(D2)Cl(PPh2CH2CH2PPh2)2]PF6, have been measured in the temperature regime from 5.4 to 320 K. In the Ru–D2 sample, coherent and incoherent exchange processes on the time scale of the quadrupolar interaction have been found, leading at low temperatures to a tunnel splitting of the 2H NMR spectrum. With increasing temperature a slight increase of the tunnel splitting is observed, in conjunction with a strong increase of the incoherent exchange process, which finally, at temperatures above 20 K, destroys the tunnel splitting and determines the spectral line shape. For the description of the experimental spectra a Liouville formulation of the Alexander–Binsch NMR line shape theory, adapted for exchanging deuterons, is employed. It is shown that the whole evaluation of the 2H magnetization takes place in four 2D and two 4D subspaces of the 81D Liouville space, leading to a drastic simplification of the numerical efforts in the simulation of the spectral line shapes. The height of the tunnel barrier calculated from the value of the tunnel splitting is 270 meV (6.22 kcal mol-1). The incoherent exchange rates extracted from the spectra and from T1 relaxation data are analyzed in terms of a Bell tunneling model, with a temperature dependent effective potential.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
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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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